Objectives
1. Describe the agent that causes HIV disease and the history of HIV.
2. Define AIDS by using the current terminology from the Centers for Disease Control and Prevention.
3. Explain the differences between HIV infection, HIV disease, and AIDS.
4. Describe the progression of HIV infection.
5. Discuss how HIV is and is not transmitted.
6. Describe patients who are at risk for HIV infection.
7. Discuss the pathophysiologic features of HIV disease.
8. List signs and symptoms that may be indicative of HIV disease.
9. Discuss the laboratory and diagnostic tests related to HIV disease.
10. Discuss the issues related to HIV antibody testing.
11. Describe the multidisciplinary approach in caring for a patient with HIV disease.
12. List opportunistic infections associated with advanced HIV disease (AIDS).
13. Discuss the nurse's role in assisting the HIV-infected patient with coping, grieving, reducing anxiety, and minimizing social isolation.
14. Discuss the importance of adherence to HIV treatment.
15. Discuss the use of effective prevention strategies in the counseling of patients.
16. Define the nurse's role in the prevention of HIV infection.
Key Terms
http://evolve.elsevier.com/Cooper/foundationsadult/
As early as 1979, physicians in New York and California were identifying cases of Pneumocystis jiroveci (formerly Pneumocystis carinii) pneumonia, an unusual pulmonary disease caused by a fungus that primarily infects people who have suppressed immune systems. The fungus is found commonly in the environment but does not normally affect people who are healthy. During the time when the acquired immunodeficiency syndrome (AIDS) epidemic was at its peak, the majority of people with advanced AIDS developed this lung infection. The use of prophylactic antibiotics has significantly decreased the number of cases of this condition among patients with AIDS (PubMed Health, 2009). Also during the height of the epidemic, physicians noted an increase in the number of people with Kaposi's sarcoma, a rare cancer of the skin and mucous membranes characterized by blue, red, or purple raised lesions (Figure 55-1) that occurred mainly in men of Mediterranean descent. Of interest was that these two diseases were occurring at alarming rates in clusters of young homosexual men whose immune systems were failing. Researchers at the Centers for Disease Control and Prevention (CDC), a division of the U.S. Public Health Service that investigates and reports on various diseases, soon learned that this immune disorder was also affecting people who used injection drugs and patients with hemophilia. Later, the immune disorder was also identified in heterosexual men and women.
The origins of human immunodeficiency virus (HIV) remain somewhat obscure, and why HIV gave rise to the AIDS pandemic only in the twentieth century has not yet been determined. The earliest case of HIV infection has been dated to 1959. It was identified in the Democratic Republic of Congo through different methods of molecular clock analysis. It has also been estimated that HIV began to radiate from its source in approximately the 1930s (Buonaguro et al., 2007). The escalating pandemic probably resulted from the combination of significant cultural and sociobehavioral changes, the use of nonsterile needles for parenteral injections and vaccinations, and the unintended contamination of products used for medical treatments.
HIV/AIDS has been recognized as a clinical syndrome since the early 1980s. Several researchers have, however, identified patients who might have fit the CDC's Case Surveillance definition before that time. The unusual and rapid deterioration and death in 1969 of a 15-year-old boy (Robert R.) in St. Louis from aggressive, disseminated Kaposi's sarcoma suggests that his might have been the first confirmed death from HIV infection in the United States (Garry et al., 1988). This patient had no international travel experience, which suggests that other individuals were infected with HIV as well. This also implies that HIV might have existed in some form in the United States since at least the 1960s.
HIV is known as zoonotic, an organism that has been able to cross from an animal species to humans. A similar virus (called simian immunodeficiency virus) was noted in primates and probably crossed into humans by way of the hunting and consumption of these animals in Africa. Other examples of zoonotic transmission include severe acute respiratory distress syndrome, anthrax, rabies, hantavirus, and West Nile virus (World Health Organization [WHO], 2009). HIV began to spread in the middle to late 1970s, but because of the long incubation period, the viral epidemic progressed undetected in most countries. When the virus began causing widespread disease in the 1980s, it provoked fear among laypeople and health care providers alike. It was also a challenging time for health care workers because they knew they were observing a new pathogen whose route of transmission was not completely understood. In spite of the stigmas and fears that emerged (and still exist to some extent today), nurses were at the forefront of providing care to affected patients. Nurses met the challenges of providing and coordinating services, organizing community-based organizations, teaching about prevention, and helping patients deal with a terminal disease.
The CDC (1981) published a notation about some patients with signs and symptoms that later would be attributed to AIDS. The signs and symptoms listed were related to the development of opportunistic infections. Such infections occur when the body's immune system has been weakened. Since that time, AIDS has become known as one of the most challenging infectious diseases of the twentieth and twenty-first centuries. In 1982, the CDC issued a statement that blood and other body fluids may be vehicles for transmitting the disease and that precautions must be used with all blood and body fluids.
The discovery of a second HIV strain was both major and alarming, inasmuch as it was the first clue that HIV could mutate rapidly. This capability for rapid mutation, often referred to as genetic promiscuity, has become the trademark of this virus. It represents an immense challenge for scientists as they search for treatment and vaccine strategies. HIV type 1 (HIV-1) is found worldwide and is the prevalent strain in most places, including the United States, Europe, and Central Africa. HIV-1 and HIV type 2 (HIV-2) are spread in the same ways and have similar signs and symptoms. Infection with either of these viral strains also results in opportunistic infections. Most people with HIV-1 infection develop profound immunodeficiency and high viral loads, which result in death, but most cases of HIV-2 infection result in long-term nonprogression (Rowland-Jones and Whittle, 2007). Patients with HIV-2 tend to be less infectious during the initial stage of the infection than those with HIV-1 infection. As the HIV-2 infection progresses, however, the patient's ability to infect other people increases. The prevalence of HIV-2 infection is greater in parts of Africa and in the countries surrounding Africa than elsewhere in the world. This is thought to be related to commercial trading relationships and immigration. Reports of cases of HIV-2 infections in the United States have increased, mainly in refugees and immigrants from countries with high rates of HIV-2.
HIV-1 is much more virulent (toxic) than HIV-2. People with HIV-2 infection tend to have a normal life span similar to their uninfected population cohort. Also, in contrast to HIV-1, HIV-2 does not increase mortality risks in patients between the ages of 55 and 80 years (Rowland-Jones and Whittle, 2007). Patients infected with HIV-2 develop problems with immunodeficiency more slowly. However, such patients who are also malnourished, without adequate access to health care, and without clean water have an increased mortality risk in comparison with healthier HIV-2– infected patients.
Since the first cases of AIDS were reported in 1981, the CDC has revised the case definition three times in response to improved laboratory and diagnostic methods (CD4+ and viral test results), additional clinical conditions, increased knowledge of the natural history of HIV disease, and improved clinical management (CDC, 2008). The current definition, used by all states and U.S. territories, allows the disease to be consistently monitored for public health purposes. These revisions to the AIDS surveillance case definition took into account the advances in diagnostic methods and treatment to provide more accurate information on the numbers of life-threatening illnesses and deaths that are opportunistic (caused by normally nonpathogenic organisms in a host whose resistance has been decreased by such disorders as HIV disease) among HIV-infected individuals.
It was not until 1987, after the CDC reported three cases of occupationally acquired HIV infection in health care providers, that universal guidelines for blood and body fluid precautions, or standard precautions, were developed for the prevention of occupational exposure. These guidelines forever changed the way health care personnel protect themselves and other people from the spread of bloodborne pathogens. That same year, the Association of Nurses in AIDS Care was established to address the needs of individuals with HIV disease and to provide a professional forum for nurses, who often faced discrimination as a result of providing care to HIV-infected patients.
By that time, a broad spectrum of individuals, including children, adults, and people from all socioeconomic groups, were affected by this disorder (see Life Span Considerations box). Nurses became instrumental in establishing education and treatment standards, in collaboration with community-based organizations. Today, nurses constitute the largest group of health care professionals who care for individuals with HIV disease, which stresses the importance of prevention and influencing policymakers. HIV nursing provides lessons that can be useful in other patient populations as well: the importance of patient education, adherence to medical regimens, prevention, and health-promoting behaviors.
Throughout the world, HIV is one of the leading causes of death and results in more deaths than does any other disease caused by infection. As of 2011, approximately 34.2 million people were infected with HIV (CDC, n.d.). Approximately 2.5 million new diagnoses were made, and 330,000 children were infected with HIV in 2011. Almost all of those people reside in countries with low or middle incomes.
Sub-Saharan Africa has been hit especially hard (WHO, 2013a). This region contains more than 69% of the world's population with HIV but only 12% of the total world population (Henry J. Kaiser Family Foundation, 2013). In 2011, 17.3 million children in that region had lost one or both of their parents to AIDS. Death related to AIDS is associated largely with poor access to prevention and treatment services (Henry J. Kaiser Family Foundation, 2013). Since 2005, the number of people infected with HIV has steadily declined (AVERT, n.d.). This decreasing infection rate is thought to be related to increased access to antiretroviral treatments. Managing and treating this disease will remain a challenge for years to come, especially in the sub-Saharan region of Africa.
In the United States approximately 50,000 new cases of HIV are diagnosed each year. More than 1.1 million people in the United States are currently living with HIV/AIDS (CDC, 2013a). Between 2003 and 2006, the number of new HIV/AIDS cases in the United States stabilized, but the number of people who were living with the disease increased. At the end of 2006, almost 500,000 people were infected and living with HIV/AIDS (CDC, 2008). California, Florida, and New York accounted for most of the patients with AIDS diagnoses (CDC, 2008).
Beginning in 1996, the use of highly active antiretroviral therapy (HAART) in people with HIV infection increased greatly in the United States. Since that time, fewer people with HIV infection have developed AIDS. New HIV and AIDS cases affect various racial groups, ethnic groups, geographic areas, and demographic populations; thus this epidemic has affected nonwhite people, women, heterosexuals, and people who use injection drugs. However, people with HIV are living longer (CDC, 2008).
In 2010, the CDC reported that the population of men who have sex with other men constitutes the biggest proportion of HIV/AIDS patients, accounting for 78% of the total number of HIV infections in male patients 13 years of age and older (CDC, 2013b). The HIV infection rates among this population decreased from 71% in 1983 to 44% in 1996. Holmberg (1996) predicted that this rate would continue to decrease to approximately 25%. Instead of decreasing, however, the number of new HIV infections in men who have sex with men has not continued the hoped-for decline. In response the CDC is implementing a system of “High Impact HIV Prevention” by targeting at-risk populations with direct measurable strategies (CDC, 2013c).
During the first 25 years of this epidemic, the distribution of new cases on the basis of ethnicity and race changed (see Cultural Considerations box). Disproportionate numbers of Hispanic Americans and African Americans have been infected with HIV. In 2006, although African Americans made up only 13% of the population in the United States, they accounted for almost half of the total number of HIV/AIDS cases that were diagnosed. African American adults and adolescents are 10 times more likely to receive a diagnosis of AIDS than are white adults and adolescents. The primary risk factor for African American men who developed HIV was sexual contact. In 2005, African American men who have sex with men (MSM) were much more likely than other MSM to be infected with HIV. Another risk factor for African American men is engaging in high-risk heterosexual behavior (CDC, 2013d).
Some African American men who engage in sex with other men identify themselves as heterosexuals because of the stigma and homophobia issues. Many African American MSM are secretive about their homosexuality or choose not to identify their sexual orientation. Prevention programs are challenged when people do not identify themselves as engaging in risky behaviors or having increased risk factors.
Initially the face of HIV/AIDS was predominately homosexual men and people who used injection drugs. Rates of transmission of the disease to women have been startling. Currently, an estimated 25% of HIV/AIDS sufferers are women (Womenshealth.gov, 2011a). HIV was the leading cause of mortality in African American women between 25 and 34 years of age. African American women are 23 times more likely to be diagnosed with AIDS than are white American women. Young people between ages 13 and 29 reflected an estimated 39% of new infections in the United States.
Although Hispanic Americans account for 16% of the population, they accounted for almost 20% of new HIV infections in 2009 (U.S. Department of Health and Human Services [HHS], 2012). Many socioeconomic and cultural factors have contributed to this epidemic and associated prevention challenges in the U.S. Hispanic and Latino communities. For Hispanic men and women, the primary risk factor for developing HIV is sex with men. Rates of other sexually transmitted infections (STIs), including chlamydia, gonorrhea, and syphilis, are also higher among Hispanic Americans than among non-Hispanic white Americans (CDC, 2013e). Transient Hispanic populations often have difficulty receiving access to health care because of social structure, language barriers, and migration patterns (CDC, 2008). The predicaments caused by poverty limit access to appropriate health care, housing, and HIV prevention. All these factors may directly or indirectly increase risk factors for HIV infection in the Hispanic population.
In 1996 researchers incorrectly predicted that HIV cases would increase among people who use injection drugs (Holmberg, 1996). The biggest increase in new HIV cases has occurred in heterosexual populations. In 1983, heterosexuals made up 5% of new HIV cases. By 2009 this number had grown to 27% (HHS, 2012). Drugs that are not injected also affect the spread of HIV because drug users often engage in high-risk behaviors when they are under the influence (CDC, 2008).
As treatment for HIV has advanced, the progression from HIV to AIDS has slowed, resulting in a decreased mortality rate among people infected with HIV. Data from 2006 indicate that although the number of AIDS cases has remained stable, the death rate has decreased (CDC, 2008). Advanced treatment options mean that people are living longer after their AIDS diagnoses. Unfortunately, in countries where HIV-infected people are without adequate access to health care, HIV infection is still one of the leading causes of death.
Despite significant research into the modes of transmission of HIV, considerable fear and misinformation about HIV transmission, perhaps more than for any other disease, still exists. Health care providers and patients must be knowledgeable about modes of transmission and behaviors that put them at risk for HIV infection. Modes of transmission have remained constant throughout the course of the HIV pandemic. Health care providers also need to remember that transmission of HIV occurs through sexual practices, not sexual preferences.
The patterns in the spread of HIV changed considerably during the first two decades of the epidemic in the United States. Worldwide, sexual intercourse is by far the most common mode of HIV transmission, but in the United States, as many as half of all new HIV infections are now associated either directly or indirectly with injection drug use: that is, using HIV-contaminated needles to inject drugs or having sexual contact with an HIV-infected drug user. Overall, in comparison to the 1980s, HIV infections have stabilized in several key populations such as MSM, people who use injection drugs, heterosexuals, and infants. The number of estimated pediatric AIDS cases diagnosed each year has declined since 1992. This decline is associated with the increased compliance with universal counseling and testing of pregnant women and the use of zidovudine (Retrovir, ZDV, AZT) by HIV-infected pregnant women and their newborns.
HIV is an obligate virus, which means it must have a host organism to survive. The virus cannot live long outside the human body. HIV transmission depends on the presence of the virus, the infectiousness of the virus, the susceptibility of the uninfected recipient, and any conditions that may increase the recipient's risk for infection. HIV is transmitted from human to human through infected blood, semen, cervicovaginal secretions, and breast milk. If these infected fluids are introduced into an uninfected person, HIV can be transmitted to that person. In addition to the aforementioned body fluids, HIV is also found in pericardial, synovial, cerebrospinal, peritoneal, and amniotic fluids. Vertical transmission (transmission from a mother to a fetus) of HIV can occur during pregnancy, during delivery, or through postpartum breastfeeding (transmitted in the breast milk). Conditions that affect the likelihood of infection include the duration and frequency of exposure, the amount of virus inoculated into the recipient, the virulence of the organism, and the recipient's defense capability (immune system). Although HIV has been found in other body fluids such as saliva, urine, tears, and feces, there has been no evidence that these substances are vehicles of transmission, unless the fluids contain visible blood.
HIV is generally transmitted by behaviors and not by casual contacts, such as hugging, dry kissing, shaking hands, or sharing food and utensils. HIV is not transmitted by domestic animals or insects; through coughing or sneezing; or through sharing objects such as pencils, computer keyboards, or telephones. The three most common modes of HIV transmission are anal or vaginal intercourse, contaminated injecting drug equipment and paraphernalia, and transmission from mother to child.
Once infected, an individual is capable of transmitting HIV to other people at any time throughout the disease spectrum, even when the infected host appears healthy and has no obvious signs of the infection. In HIV infection, the viral load (amount of measurable HIV virions in the blood) peaks quickly after infection and during the later stages of the disease. During these periods, a recipient's unprotected exposure to an infected host increases the likelihood of transmission. However, it is important to remember that HIV can be transmitted during the entire disease spectrum.
Sexual intercourse remains the most common mode of transmission of HIV in the world today and is responsible for the majority of the world's total AIDS cases. Sexual activity provides the potential for the exchange of semen, cervicovaginal secretions, and blood. Important risk factors are the presence of HIV in one or both partners and the occurrence of behaviors that put one or both partners at risk for transmission. Some individuals become infected with HIV after a single unprotected sexual encounter, whereas others remain free from infection after hundreds of such encounters.
Although the majority of HIV transmissions in the United States occur among MSM via receptive anal intercourse, heterosexual transmission via anal intercourse is becoming increasingly prevalent. Heterosexual couples may prefer this method of sexual expression or use it because it eliminates the risk of pregnancy. Unfortunately, the most risky sexual activity is unprotected receptive anal intercourse. Because the rectum is generally tighter and the rectal mucosa is less lubricated than the vagina, the rectal mucosa may be torn, providing an excellent portal for the virus to enter the blood stream.
During any form of sexual intercourse (anal, vaginal, oral), the risk of infection is considerably higher for the receptive partner, although infection can be transmitted to an insertive partner as well. The receptive partner generally has prolonged exposure to semen (National Institute of Allergy and Infectious Diseases, 2009). Other factors that may increase the risk of sexual transmission include ulcerating genital diseases, such as herpes simplex virus (HSV) and syphilis; chancres secondary to STIs; intact (uncircumcised) foreskin; sex that is “forceful or vigorous”; immunosuppression due to drug use; and drug use that may lead to high-risk behavior. Infection risk for HIV can also be increased during intercourse when the infected partner has a high viral load (Benotsch et al., 2012; Cohen, 2012; Gray et al., 2012). The viral load is often increased in the primary and late stages of infection (Klimas et al., 2008). Oral-genital transmissions have been reported, and the HIV transmission risk increases if the receiving partner already has an STI that has caused open sores, such as HSV infection.
HIV may be transmitted by exposure to contaminated blood through the accidental or intentional sharing of injecting equipment and paraphernalia. Such equipment includes syringes, needles, cookers (spoons or bottle caps used for mixing the drug), and filtering devices (such as cotton balls). People who use injection drugs are the population with the second highest rates of HIV exposure, following MSM (CDC, 2006). Although typically seen in large metropolitan areas, injection drug use occurs in smaller cities and rural areas as well. Such drugs are not limited to illicit drugs; HIV can be transmitted via contaminated equipment used to inject steroids, vitamins, and insulin.
People who use injection drugs confirm needle placement in a vein by drawing back blood into the syringe; the substance is then injected into the vein. They may also draw blood back into the syringe and inject numerous times (“booting”). This ensures that no substance remains in the syringe. Other factors that put people who use illicit injection drugs at risk for HIV include poor nutritional status, poor hygiene, and impaired judgment due to mood-altering substances. People who use illicit injection drugs are also less likely to use condoms during sexual intercourse and may engage in sexual activity in exchange for drugs. The long-term effects of illicit injection drug use include increased risk for other diseases, such as hepatitis B, hepatitis C, and other bloodborne illnesses.
Since 1985, blood banks in the United States have screened all donated blood for HIV-1 antibodies and, since 1992, for HIV-2 antibodies. Blood banks have also implemented procedures to identify blood donors who might be at high risk for being infected with HIV. Blood from donors who are deemed to be at high risk or that yields test results positive for HIV is discarded. In addition to HIV, blood is currently screened for human T-lymphotropic virus types 1 and 2 (HTLV-1 and HTLV-2), hepatitis B virus, West Nile virus, Trypanosoma cruzi infection (Chagas disease), and hepatitis C virus (U.S. Food and Drug Administration [FDA], 2013a).
Every year, a small number of blood donations come from donors who are infected with HIV but in whom the HIV antibody was undetected. When a blood donor has not yet undergone seroconversion (a change in serologic test results from negative to positive as antibodies develop in reaction to an infection), the current HIV antibody test cannot detect the infection. In the past, there was a 22-day window during which the donor could donate infected blood in which HIV would not be detected by the HIV-1 and HIV-2 antibody test. Since 1995, however, blood has also been screened for HIV-1 p24 antigen. With this addition, this window has been reduced to 16 days. In 1999, the nucleic acid amplification test was introduced; this test detects HIV-1 RNA and has reduced the window to only 11 days. By 2003, after 25 million donations, only three people were infected with HIV after receiving a blood product transfusion. The blood came from two separate donors, and the blood tested negative for HIV with all currently available HIV tests (Donnegan, 2003). Currently, a person's risk for acquiring HIV through a blood transfusion is estimated to be about 1 per 1.5 million (CDC, 2010). Before 1985, people who received replacement clotting factors for blood coagulation difficulties (e.g., hemophilia) were at increased risk of contracting HIV. Since 1985, a recombinant technique is used to manufacture the clotting factors or the clotting factors are treated with chemicals or heated to kill the HIV.
Almost 25,000 adults who developed AIDS before 2003 were health care workers. This number represents 5% of all AIDS cases among adults who had a known occupation.
The CDC distinguishes between two types of HIV seroconversion. When the infection is “documented,” it means that the individual had a documented exposure related to occupation and developed HIV disease. A “possible” infection indicates that the individual worked in a high-risk setting with exposure to blood or other body fluids related to occupation; however, no exposure event was documented.
In the United States through 2001, of the 57 health care workers who were infected with HIV as a result of a documented occupational exposure, 26 (46%) developed AIDS (CDC, 2011). Of all health care workers with HIV, most did not have a documented exposure, and the infection is thought to result from high-risk sexual behavior. No confirmed work-related exposures in health care workers have been reported since 1999.
Most of the health care workers who have been infected with HIV are nurses. The second largest group is laboratory clinicians, and the third largest group is physicians (nonsurgical). Other health care workers with possible exposures included emergency medical technicians, health care aides, housekeepers, and maintenance workers. Most of the infections occurred after a needlestick injury with resulting puncture wound. Exposures are thought to be underreported because such reporting is voluntary. If a health care worker does have a needlestick that results in exposure to a known source of HIV infection, the risk for contracting HIV is low, at approximately 0.3%.
Needlesticks that occur when a health care worker is exposed to patients with known HIV infection are known as percutaneous exposures. If the exposure involves a hollow-bore needle filled with blood that had previously been placed in the patient's vein or artery, then the transmission risk of HIV is increased. The transmission risk also is increased if the health care worker suffers a deep injury at the time of the exposure. Scalpels, suture needles, and smaller gauge injection needles also pose a risk for transmission, but that risk is much lower. If only the mucous membranes are exposed during the incident, then the risk for seroconversion is only 0.09%. There is a low risk for seroconverting if the health care worker's skin is not intact and is exposed to blood or body fluids.
Unfortunately, postexposure antiviral therapy is hepatotoxic. When antiviral therapy is given to a health care worker after a documented exposure, it may result in severe hepatitis that may necessitate liver transplantation.
HIV infection can be transmitted from a mother to her infant during pregnancy, at the time of delivery, or after birth through breastfeeding. In the United States, it is estimated that approximately 30% of infected mothers transmit HIV to their infants and that approximately 50% to 70% of the transmissions occur late in utero or during birth. The rate of vertical transmission varies around the world; in France the rate is approximately 11%, but it is nearly 50% in parts of Africa. Factors such as the stage of maternal HIV disease (transmission is more likely to occur during the initial and later stages of infection, when more of the virus is circulating in the mother's blood and body fluids), a decreased CD4+ cell count or high viral load, the presence or absence of STIs, and the mother's nutritional status all play a role in vertical transmission. Factors that increase the risk of transmission during delivery include extreme prematurity; lack of health care; gestational complications that lead to extended labor; the mixing of maternal and fetal blood; newborn ingestion of maternal blood, amniotic fluid, or vaginal secretions; skin excoriation in the newborn; and being the first child born in a multiple gestation.
Clinical trials have demonstrated that the administration of zidovudine therapies to pregnant women who are HIV positive can reduce transmission to approximately 2% of infants. Studies on the outcomes of the infants whose mothers had these antiviral therapies have not found significantly different outcomes from infants born to HIV-positive women who did not receive the antiviral therapies during pregnancy (Marino, 2012).
In addition to drug therapy, substantial advances have been made in understanding the pathophysiology, treatment, and monitoring of HIV infection. These advances have resulted in changes in the standard of care for patients, including pregnant women, with HIV infection. More aggressive combination drug regimens that provide maximal viral suppression are now recommended. Although pregnancy alone is not a reason to defer treatment, the use of anti-HIV drugs during pregnancy requires special consideration. Unfortunately, no long-term data regarding the long-term effects on the fetus exist. Because of this, offering antiretroviral therapy (ART) to HIV-infected women—whether primarily to treat HIV infection or to reduce the likelihood of perinatal transmission—should be accompanied by a discussion of the known and unknown short- and long-term benefits and potential risks. Because of the findings of ACTG 076, zidovudine should be a part of this treatment regimen.
Current recommendations call for routine HIV counseling and voluntary HIV testing of pregnant women and women considering pregnancy. An HIV-positive pregnant woman should be given information to make an informed decision about treatment options. The HIV transmission rates from mother to child have been reduced due to several recommended interventions, including ART, formula feeding, and cesarean section. In developed countries, this number has decreased from 25% (without interventions) to approximately 1% (CDC, 2013f). In countries where ART is not available and mothers continue to breastfeed, the infection rate by age 2 for children born to HIV-infected mothers can be as high as 45% (WHO, 2013b). Infants born to HIV-infected mothers have positive HIV antibody results as long as 15 to 18 months after birth. This finding is caused by maternal antibodies that cross the placenta during gestation and remain in the infant's circulatory system. HIV infection can be diagnosed earlier by means of an HIV viral culture or measuring the amount of HIV RNA or viral load through polymerase chain reaction (PCR) or branched-chain DNA (bDNA) testing.
HIV is classified as a “slow” retrovirus or a lentivirus. After infection with these types of viruses, a long time passes before specific signs and symptoms appear. HIV requires cells for replication. The virus takes over the host cell and reproduces viral copies of it. Retroviruses are made of RNA. Most organisms' genetic material is made up of DNA. The retrovirus uses reverse transcriptase, an enzyme, to make its RNA change to DNA. This process allows the virus to be incorporated into the host's genetic material.
HIV can cross over into the host in the dendritic immune cells that are located in the mucosal layer of the vulva, the vagina, the rectum, and the penis. The exterior layer of the dendritic cell passes the virus into the interior portion of the cell. The virus is released into the lymphatic system via tissue or lymph nodes. Then the virus binds to a CD4+ lymphocyte (a type of white blood cell; a protein on the surface of cells that normally helps the body's immune system combat disease), by which it can travel farther into the lymphatic system and begin the initial infectious cycle (HHS, 2009).
The attachment of the viral particle to the host cell's CD4+ receptor and co-receptor (CCR5 or CXCR4) is the first step in replication of the virus (Figure 55-2). The HIV virion enters the host cell when the virus binds to the cell. After binding to the cell, co-receptors are needed to continue the fusion process and to enable the viral particle to eject two copies of the virus's RNA. Inside the cell, HIV reverse transcriptase changes the viral RNA into DNA. A full copy of this DNA is created and broken down into smaller, more functional pieces that are moved to the nucleus of the cell. The HIV DNA moves into the nucleus of the cell, where viral integrase helps insert it into the DNA of the host. The inserted virus is called a provirus. After activation, the cell makes a new copy of HIV by using viral proteins. Afterward, there is an abnormal amount of immune activation, and this perpetuates the progress of the HIV infection because it creates more CD4+ cells that will be under attack by HIV and will eventually exhaust the immune system. The number of CD8+ T cells that are activated at this time is directly related to an increased risk of developing advanced HIV infection, or AIDS. However, the HIV can remain dormant for years if the CD4+ cell remains inactivated. It has been difficult to completely control HIV because of its ability to remain undetected. Patients with HIV are advised to continue taking their antiretroviral medications (National Institute of Allergy and Infectious Diseases, 2011).
New viral proteins are created when the infected CD4+ cell converts DNA into RNA. This process is called transcription. The process relies on the host cell and the viral genetic material. The new RNA is messenger RNA (mRNA), and it is returned from the nucleus back into the cytoplasm. In the cytoplasm, mRNA is used as a template to begin making HIV protein. This process is called translation. The protein sequence of the mRNA is changed back into RNA, and this makes up the outer envelope and inner core of HIV. After translation, the genetic materials become smaller and smaller pieces of viral material. The viral protease chunks the genetic products into smaller pieces so that they can infect more CD4+ host cells. This HIV protease is specific to this virus and is targeted by a class of medications called protease inhibitors that are used to manage HIV. The envelope's viral proteins are joined together inside the host cell's membrane, with the core proteins, RNA, and enzymes just inside the membrane.
HIV then “buds” by pinching off this cell. One infected CD4+ cell has the ability to quickly make thousands of cell copies. The CD4+ cell dies as a result of this replication process. As time goes on, so many CD4+ cells are destroyed that the immune system becomes dysfunctional and opportunistic infections develop within the host.
HIV replicates quickly after entering the host body. It can rapidly produce billions of copies, which infect CD4+ cells and the lymphatic system (see Figure 55-2). The viral load of the host during the early stage of the infection can be extremely high and increases risk of virus transmission to other people who are exposed. The severity and progression of the infection are related to the host's infection with other STIs, age, and immune response. Basic host immune defenses (cellular and humoral) help limit replication and slow progression of HIV. Unfortunately, these immune responses cannot completely eliminate HIV from the host. The host can continue to appear healthy even when infected with the virus (Table 55-1). Some patients live with the virus for at least 10 years without any treatment and appear healthy. They are referred to as long-term nonprogressors. Cheng and colleagues (2007) found that when HIV-infected patients who were also co-infected with another type of virus took ART, their CD4+ cell count was low. When older HIV-infected patients do not use ART, their rate of disease progression is much faster than in younger patients. This discrepancy is thought to be related to the facts that older patients have more pathogen exposure, an increased number of memory CD4+ cells (which are targeted by HIV), and fewer numbers of naïve CD4+ cells. Older patients tend to have more difficulty producing more CD4+ cells.
Table 55-1
Types of White Blood Cells and Their Involvement in HIV Disease
WHITE BLOOD CELL (WBC) TYPE | DESCRIPTION | ROLE IN HIV DISEASE |
Neutrophils | Normally constitute 50%-75% of all circulating leukocytes and are capable of phagocytosis Important in the inflammatory response and the first line of defense against infection Short life span | Neutropenia (WBC deficiency) commonly occurs in advanced HIV disease. Drug-induced neutropenia is common, especially with drugs used to treat P. jiroveci pneumonia, toxoplasmosis, CMV retinitis, or colitis and with NRTIs. |
Monocytes, macrophages | Constitute about 3%-7% of all WBCs Involved in the inflammatory response Capable of processing antigens for presentation to T cells Have CD4+ receptors Macrophages: distributed throughout tissue and capable of phagocytosis | Monocytes and macrophages serve as a reservoir for HIV. When activated by stimulation with interferon (inflammatory response), they produce neopterin. Neopterin levels are increased in HIV disease. |
Basophils, mast cells | Both: involved in acute inflammation Mast cells: breakdown releases histamine and other factors | In HIV infection, these cells may inhibit leukocyte migration. |
T helper cells (CD4+ or T4 cells) | Contain CD4+ receptors Considered the “conductor” of the immune system because of their secretion of cytokines, which control most aspects of the immune response | These cells are the major target of HIV. Progressive infection gradually destroys the available pool of T helper cells so that the overall CD4+ cell count drops. Lower CD4+ cell counts correspond to more immunodeficiency and the onset of opportunistic infections. Infection with HIV can impair T helper cell function without killing the cell. |
Cytotoxic T cells or cytotoxic T lymphocytes (CTLs; CD8+ cells) | Contain CD8+ receptors and produce cytokines in a more limited manner than do CD4+ cells Combat viral and bacterial infections and are involved in direct killing of target cells by binding to them and releasing a substance that can perforate the cell membrane | Numbers of these cells increase in HIV infection. This increase represents the cellular response to infection. The strength of this initial cellular response has been shown to predict progression to AIDS (i.e., better cell response implies slower disease progression). Cytotoxic T cells kill T helper cells infected with HIV. |
Natural killer (NK) cells | Large granular lymphocytes involved in cell-mediated immune response Able to kill target cells because target cells are coated with antibody that binds to receptors on the surface of NK cells, allowing the NK cell to attach Kill target cells by releasing a substance that triggers lysis (breakdown of cell wall) of cell | Counts and structure of these cells remain normal in patients with HIV infection, but they are functionally defective. |
B cells | Produce antibodies specific to an antigen Capable of being stimulated by T helper cells | B cells are involved in the humoral response to HIV infection and produce a variety of antibodies against HIV. They are present throughout the course of HIV disease. |
CMV, Cytomegalovirus; HIV, human immunodeficiency virus; NRTI, nucleoside reverse transcriptase inhibitor; WBC, white blood cell.
Many factors can increase HIV disease progression. People who use drugs and engage in high-risk sexual behavior are less likely to employ infection-preventive methods. Depression may impair their use of resources to help manage their infection (Kalichman, 2008). Poor coping mechanisms and high levels of emotional stress have a negative effect on HIV disease progression (Ironson and Hayward, 2008; Leserman, 2008; Temoshok et al., 2008).
The virus can make amazing numbers of copies of itself daily (Ho et al., 1995; Wei et al., 1995). HIV contained in blood plasma has a half-life of less than 2 days. While the virus continues to replicate, many millions of CD4+ cells are produced and destroyed each day. The viral load in the patient's blood determines how quickly the CD4+ cells are destroyed.
The HIV viral load in the blood can remain low or difficult to detect for weeks or even months after the initial exposure and infection (Figure 55-3). When the immune system responds, the viral load decreases quickly as the body effectively contains the infection. Normally, antigens that are deemed foreign intermingle with B cells. At this stage, antibodies are produced. T cells start a cell-based immune response. In the early stages of the infection, the antibodies are able to reduce the viral load. T cells are beckoned to the lymph nodes, where the virus is trapped (see Table 55-1). The virus replicates in the lymph system (nodes, tissue, spleen, and tonsils).
The lymphatic system carries the infection from one site to another. During this time, the HIV-infected person does not have any signs or symptoms. Over time, the lymphatic system is damaged by the HIV. The virus enters the blood, which increases the rate of disease progression. The body is not able to mount an adequate response to new infections. The immune system damage is apparent on examination of B cell dysfunction, but more important CD4+ cells are destroyed and their levels depleted (see Figure 55-2).
As the CD4+ cells are destroyed, the immune system fails. Immune dysfunction can occur when the CD4+ lymphocyte count falls below 500/mm3 of blood. When the count falls below 200/mm3, severe immune system dysfunction is apparent. This results in the development of possibly fatal opportunistic infections in the host.
Monocytes can be infected by HIV because some of them also have CD4+ receptors. When a monocyte is infected, it can change into a phagocyte (a cell that ingests and digests bacteria). When a phagocyte is infected with HIV, it merely works as a factory to create more HIV. An infected phagocyte can rupture as a result of a normal local inflammatory response. When this happens, the HIV is spread even deeper into the body. In this way, the skin, the lungs, bone marrow, the central nervous system, and lymph nodes become directly infected.
The term HIV disease (the state in which HIV enters the body under favorable conditions and multiplies, producing injurious effects) encompasses the immune system's progressive dysfunction that is produced by the viral activity within the host. HIV disease replaces the previous term AIDS-related complex (ARC) (Table 55-2). Acquired immunodeficiency syndrome (AIDS) (the end stage of HIV infection, in which the CD4+ cell count is 200/mm3 or lower) occurs as the disease progresses and the body is severely damaged by opportunistic infections. At this stage, the host's body can no longer protect itself and is injured (see Figure 55-2). The CD4+ cell count is 200/mm3 or less. People can live for years with the infection before they develop any signs or symptoms of HIV. The signs and symptoms include night sweats, weight loss, diarrhea, unexplainable fevers, and fatigue. The viral course of HIV depends on host factors. The host has an increased risk for morbidity and mortality when he or she has inadequate access to health care services, is of lower socioeconomic status, or is under the care of a health care provider with minimal experience in dealing with HIV.
Table 55-2
Proper Terms Related to HIV and AIDS
MISLEADING PHRASES | MORE ACCURATE PHRASES |
High-risk groups | High-risk behaviors |
Infection with AIDS | HIV infection |
AIDS test | HIV antibody test |
AIDS positive | HIV positive |
AIDS victim or patient | Person living with HIV or AIDS |
AIDS carrier | HIV-infected person |
AIDS, Acquired immunodeficiency syndrome; HIV, human immunodeficiency virus.
Progression from the early stages to end-stage HIV disease varies greatly. Three patterns have been found: typical progression, long-term nonprogression, and rapid progression. In the typical progression pattern, patients develop signs and symptoms several years after seroconversion. Many do not know they have been infected with HIV and can infect others. In the long-term nonprogression pattern, patients may not develop signs and symptoms even 30 years after seroconversion. The long-term nonprogression pattern is rare; it is thought to be longer because the immune response of affected patients is very intense, so that their viral load is lower. Also, there are genetic differences in their receptors (CCR5) on CD4+ lymphocytes that make it difficult for the HIV to attach. This allows their CD4+ and CD8+ cells to be maintained at nearly normal levels.
Approximately 5% to 10% of people who are infected with HIV are rapid progressers. In these patients, HIV infection progresses to an AIDS diagnosis within 3 years. Several common factors are found in rapid progressers: their cytotoxic T cells (CD8+ cells) are dysfunctional and unable to contain HIV, the level of virus remains very high throughout the infection, and HIV antibodies are minimal.
The term acquired immunodeficiency syndrome has been defined for surveillance and reporting purposes; it is not used alone to characterize serious disease caused by HIV infection (see Table 55-2).
Viral replication occurs during the acute infection period. The viral load peaks at millions of copies of virus per milliliter of plasma. The viral load declines right before the appearance of detectable antibodies that can be measured in the blood. The viral set point, or stabilizing of the viral load, is reached 4 to 6 months after exposure. This viral set point is important in that some researchers believe it to be a prognostic indicator of long-term survival: that is, the lower the viral set point, the longer the individual will survive with HIV disease. Postexposure prophylaxis (PEP), begun as soon as possible after exposure, may help lower this viral set point. This theory is demonstrated in cases in which health care personnel initiate PEP medications after an exposure and do not undergo seroconversion.
Seroconversion, as defined previously, is the development of antibodies from HIV, which takes place approximately 5 days to 3 months after exposure (generally within 1 to 3 weeks). This process is accompanied by a flulike or mononucleosis-like syndrome consisting of fever, night sweats, pharyngitis, headache, malaise, arthralgias, myalgias, diarrhea, nausea, and a diffuse rash prominent on the trunk. These symptoms last approximately 1 to 2 weeks, although some symptoms may last for several months. Seroconversion illness occurs in approximately 89% of HIV-infected people. HIV antibodies appear in 95% of people within 3 months of infection, and seroconversion occurs in 99% within 6 months. The viral load during the period of seroconversion is extremely high, with a short-term drop in CD4+ cells. The CD4+ cell level quickly returns to normal as the immune system mounts an attack against the viral infection; as a result, viral loads exist at nearly undetectable levels in the blood. In most people with HIV infection, the acute retroviral illness is mild and may be mistaken for a cold or other minor viral infection (Table 55-3).
Table 55-3
Acute HIV Infection: Frequency of Associated Signs and Symptoms
SIGN OR SYMPTOM | FREQUENCY (%) |
Fever | 96 |
Headache | 32 |
Lymphadenopathy | 74 |
Nausea and vomiting | 27 |
Pharyngitis | 70 |
Hepatosplenomegaly | 14 |
Rash | 70 |
Weight loss | 13 |
Myalgia or arthralgia | 54 |
Thrush | 12 |
Diarrhea | 32 |
Neurologic symptoms | 12 |
Oral or genital ulcers | 5-20 |
HIV, Human immunodeficiency virus.
From the Department of Health and Human Services Panel on Antiretroviral Guidelines for Adults and Adolescents. Guidelines for the Use of Antiretroviral Agents in HIV-1 Infected Adults and Adolescents. Available at aidsinfo.nih.gov/contentfiles/lvguidelines/adultandadolescentgl.pdf.
The median time between HIV infection and the development of end-stage HIV disease, or AIDS, in an untreated individual is between 8 and 14 years. This phase of HIV disease is sometimes called the asymptomatic phase because the HIV-infected individual looks and feels healthy. Some individuals have vague symptoms of a viral infection, including fatigue, headaches, low-grade fever, and night sweats. Because many of the symptoms of early infection are nonspecific, a diagnosis of HIV infection might not be made. Consequently, individuals may continue to engage in risky sexual and drug-using behaviors. Although seemingly healthy, the HIV-infected individual can transmit HIV to others. Lack of knowledge of one's HIV antibody status puts one at risk for earlier development of more advanced disease because changes in behaviors, such as those that promote health, are not instituted. Furthermore, if an individual is aware of being infected with the virus, early intervention with antiretroviral medications may prolong the asymptomatic phase and prevent progression to AIDS.
The early symptomatic phase of HIV infection occurs when the CD4+ cell count drops below 500/mm3. Early symptoms include constitutional problems such as persistent, unexplained fevers; recurrent drenching night sweats; chronic diarrhea; headaches; and fatigue. These signs and symptoms become severe enough to affect activities of daily living. A physical examination may reveal persistent generalized lymphadenopathy; recurrent or localized infections; and neurologic manifestations, such as numbness and tingling or weakness in the extremities (Box 55-1).
One of the most common infections in individuals with early symptomatic disease is oral candidiasis (thrush), a fungal infection that is rare in healthy adults (Figure 55-4). Other infections that signal immune dysfunction include varicella-zoster virus (shingles), persistent vaginal candidiasis (yeast infections), and increased frequency of oral or genital HSV outbreaks. Oral hairy leukoplakia, a condition related to the Epstein-Barr virus, and oral thrush are early indicators of HIV disease and prognostic markers for disease progression. Because of this, dental health professionals have a key role in identifying cases of early HIV disease.
Persistent generalized lymphadenopathy is defined as enlargement (≥1 cm) of two or more lymph nodes, located in places other than the inguinal region, that persists for at least 3 months. This condition may be present for many years before AIDS is diagnosed.
Neurologic manifestations of HIV disease occur in more than 90% of individuals who are infected. Neurologic symptoms include peripheral neuropathies, headaches, aseptic meningitis, cranial nerve palsies, and myopathies. These conditions may be caused by the HIV infection itself or may be side effects related to antiretroviral medications.
Several cofactors may influence a more rapid progression of HIV disease. In very young children and very old adults, the disease progresses more quickly. Concurrent infections such as HSV, cytomegalovirus, or Epstein-Barr virus affect progression. Drug and alcohol use, including smoking, may suppress the immune system. Malnutrition is also known to affect immune function, but further study relative to HIV is needed.
Acquired immunodeficiency syndrome is the term used to describe the end stage, or terminal phase, of the spectrum of HIV infection. The CDC has developed specific diagnostic criteria that must be present to make this diagnosis. These conditions are more likely to occur with severe immunosuppression. As HIV disease progresses, the CD4+ lymphocyte count decreases, and the ratio of CD4+ to CD8+ cells (T helper cells to T suppressor cells), which is normally 2 to 1, gradually shifts, resulting in more CD8+ than CD4+. The amount of virus detectable in the blood increases rapidly and remains high despite pharmacologic interventions. The number of white blood cells may also decline, and the person's reactivity to skin tests, such as purified protein derivative (tuberculin), is decreased or absent. An individual is said to be anergic if no skin response is noted.
Without treatment, the median time from an AIDS diagnosis to death averages years, but this varies greatly. With the advent of more effective antiretroviral and opportunistic disease prophylaxis, the life span of an HIV-infected individual is difficult to predict. Morbidity in people with advanced HIV disease also varies widely. Some people are severely ill and die rather quickly, whereas others have only to make minor adjustments in their lifestyle to cope with medical regimens or physical symptoms, such as fatigue or pain. Significant advances in the management of HIV disease have made it resemble a chronic illness. The effects of therapy on mortality have been significant: The number of new AIDS cases reported to the CDC every year has leveled off. This can be attributed to effective prophylaxis for opportunistic infections and to the development of HAART.
Strong evidence shows that early intervention postpones the onset of severe immunosuppression. Nurses should encourage individuals at risk for HIV infection to seek HIV antibody testing, and educate them in how to decrease the risk of HIV transmission.
Patients need to understand the implications of an HIV antibody test (Box 55-2):
• The individual's blood is tested for the presence of antibodies to the HIV infection. This is referred to as enzyme-linked immunosorbent assay (ELISA) testing. If this screening results in positive findings the blood is tested with a more specific test such as the Western blot (CDC, 2014).
• Tests with indeterminate results are repeated at a later date, generally in 4 to 6 weeks. Consistently indeterminate results necessitate the use of a viral culture or the measurement of viral load by means of bDNA measurement, reverse transcriptase–polymerase chain reaction (RT-PCR), or nucleic acid sequence–based amplification (NASBA).
• The series of laboratory tests confirms the presence or absence of antibodies to HIV, but their presence does not mean the person has AIDS. The tests are not diagnostic of AIDS. AIDS is diagnosed according to the 2008 CDC definition.
• A result that is seronegative (the state of lacking HIV antibodies as confirmed by blood test) is not an assurance that the individual is free of HIV infection, inasmuch as seroconversion may not yet have occurred.
• A seronegative result does not mean that an individual is free from risk of infection. If an individual continues to engage in risky behaviors, such as unprotected sexual intercourse or use of contaminated needles or drug paraphernalia, transmission may occur (Box 55-3).
Monitoring CD4+ cells is one of the laboratory parameters used to track the progression of HIV disease. As the disease progresses, the number of CD4+ cells decreases. The more significant the loss, the more severe the immunosuppression becomes. The CD4+ cell count is the best marker of the immunodeficiency associated with HIV infection. As such, the CD4+ cell count influences making decisions about antiretroviral and prophylactic drug therapy and is used to evaluate specific complaints related to the risk for contracting particular opportunistic infections. For example, Mycobacterium avium complex and cytomegalovirus infections are rare in patients with CD4+ cell counts higher than 50/mm3. P. jiroveci pneumonia and cryptococcosis are unusual in patients with CD4+ cell counts higher than 200/mm3. The CD4+ cell count is not a perfect surrogate marker of immunodeficiency, and factors such as the patient's clinical status must always be taken into account.
The CD4+ cell count reflects the number of CD4+ cells per cubic millimeter (or per microliter) of blood. It does not indicate the total number of CD4+ cells in the body. Millions of new CD4+ cells are produced daily and cleared by normal body processes (unrelated to the virus). The absolute CD4+ cell count can vary greatly in the same individual, depending on the time of day the blood is drawn; which laboratory is used; and the presence of acute illness or other factors, such as alcohol. Therefore the nurse should continue to use the same laboratory, draw blood at the same time of day, and avoid testing on days when the patient is acutely ill or under abnormal stress. When using the CD4+ cell count to make important treatment decisions, such as initiating prophylaxis for opportunistic infections, the nurse should collect two separate samples a few weeks apart.
The ability to detect HIV viral load measurements in plasma is a significant advancement in the monitoring of HIV disease. Viral load or burden is a quantitative measure of HIV viral RNA in the peripheral circulation, or the level of virus in the blood.
Three quantitative assay tests are available to measure viral load levels: NASBA, RT-PCR, and bDNA. Even very small numbers of infected cells can be detected by identifying virions. These tests can be used only to identify HIV. These tests are helpful for identifying HIV in people who have a negative ELISA (antibody) result.
Important characteristics of viral load monitoring include the following:
• In all clinical stages of the illness, HIV virus detection techniques identify measurable amounts of viral RNA copies in the plasma of most HIV-infected individuals.
• Viral load can provide significant information used to predict the course of disease progression, initiate ART, measure the degree of antiretroviral effect achieved, and note the failure of a drug regimen.
• Plasma levels of HIV RNA fall dramatically after effective ART.
• Detection of HIV RNA in plasma does not indicate whether any virus is present in lymphoid or other tissues.
Viral load and CD4+ cell counts are distinct markers that provide different information. Viral load can indicate disease progression and long-term clinical outcome; CD4+ cell measurements can indicate the damage sustained by the immune system (the loss of CD4+ or T cells) and the short-term risk for developing opportunistic infections. Each is an independent predictor of clinical outcome, and in combination they can give a more complete indication of clinical status, treatment response, and prognosis. Coffin (1996) used a metaphor to describe the infected patient without symptoms: as a train rushing along a track, heading for a bridge that has been destroyed. The time the crash will occur is determined by two variables: (1) where the train is at a particular instant (CD4+), and (2) how fast it is going (viral load).
A baseline determination of viral burden is recommended, with subsequent measurements every 3 to 4 months, in conjunction with CD4+ cell monitoring and clinical evaluations such as a history and physical examination. Guidelines continue to be revised as the implications of viral measurement evolve and its interpretation and use become better understood. In the future, opportunistic infection prophylaxis may be based on viral load, as well as on CD4+ cell counts.
Drug resistance to HAART can make effective treatment of HIV challenging. In North America and Europe, approximately 8% to 16% of cases of HIV involve at least one resistant mutation (Li et al., 2011). HIV mutates easily, which makes it hard to treat and contain. After multiple genetic mutations, the replication of HIV is chaotic and disorderly, which makes it more resistant to medication treatment and has prevented the development of an effective vaccine. ART resistance results from a patient's inability to adhere to ART protocols. Assay tests can detect HIV genetic mutations that result in ART resistance. Results of these tests are available in less than a month. A list of ART-resistant mutations has been developed by the International AIDS Society–USA. Phenotyping is available to help estimate how well the specific strain of virus will respond to treatment in people who have been receiving ART for a long time. In order to perform phenotyping, the patient must have a high viral load (Panel on Antiretroviral Guidelines for Adults and Adolescents, 2013). Genotyping is less expensive to perform, and the results are often available faster than those of phenotyping. Genotyping is recommended for patients who have not received ART (US DHHS, 2011).
During the acute stage of HIV, resistance testing is important for administering appropriate ART to prevent extensive replication of HIV. Some health care providers identify baseline genetic mutations before starting ART. A patient-specific ART regimen can be created to avoid medications that would not work. Patients who are resistant to some ART medications may have cross-resistance issues with other ART medications. Resistant HIV strains are found in people who have undergone ART, as well as in other people who are newly infected and have not received treatment. Resistance to some ART drugs and the ability to transmit resistance to newly infected people are important issues for public health officials who are battling to control and prevent HIV infection.
Hematologic abnormalities are common in HIV infections and may be caused by the HIV itself, by opportunistic infections, or by drug or radiation therapy. The white blood cell is often decreased, usually in conjunction with lymphopenia (decreased numbers of lymphocytes). Thrombocytopenia (decreased platelet count) may be caused by antiplatelet antibodies. Anemia is related to the chronic disease process and to HIV invasion of the bone marrow; it is a common adverse effect of antiretroviral agents.
Alterations in liver function tests are not uncommon. Abnormalities may be caused by viral hepatitis, alcohol abuse, opportunistic infections, neoplasms, or medications. Early identification of hepatitis B and hepatitis C viral infections is important because these infections may follow a more serious course in patients with HIV disease. Patients who are HIV-positive are often also seropositive for hepatitis B, inasmuch as both infections are bloodborne and sexually transmitted. In addition, about 25% of HIV-infected people in the United States are co-infected with hepatitis C, one of the most significant causes of chronic liver disease.
Syphilis testing is important because syphilis is more complicated and aggressive in HIV-infected patients. It is also more difficult to treat with standard therapies and more likely to advance quickly to neurosyphilis. If a person with HIV infection is seropositive for syphilis, assessment and treatment must be performed immediately.
Therapeutic management of HIV-infected patients focuses on monitoring HIV disease progression and immune function, preventing the development of opportunistic diseases, initiating and monitoring ART, detecting and treating opportunistic diseases, managing symptoms, and preventing complications of treatment.
HIV-positive individuals need to be linked to various resources, depending on their individual needs. Individuals often deny the infection, neglect their mental and physical health, and continue behaviors that put themselves and other people at risk. Interventions need to be sustained and reinforced; the emotional effect of such devastating news (“You are HIV-positive”) can overshadow any initial information or education provided. The nurse must stress safer behaviors and the need for medical and emotional support, such as assistance in family planning, treatment for substance abuse, treatment for STIs, treatment for tuberculosis, and immunizations.
A transdisciplinary care approach is most appropriate for patients with HIV disease because of their complex medical and psychosocial needs. The HIV-infected patient should be the primary member of this team, working along with a physician who specializes in HIV/AIDS, a social worker, a case manager, a dietitian, and a nurse. Other team members may include a dentist, a primary care provider (physician, osteopath, nurse practitioner, or physician assistant), a mental health worker, a substance abuse counselor, a nontraditional therapist (such as a massage therapist or acupuncturist), and the individual's family and significant other.
Probably the most difficult aspect of the medical management of HIV is dealing with the many opportunistic diseases that develop as the immune system degenerates. Although it is usually impossible to totally eradicate opportunistic diseases, the use of ART and prophylactic interventions can control their emergence or progression. However, these regimens must continue throughout the patient's life; otherwise, the disease will return. Advances in the diagnosis and treatment of opportunistic diseases have contributed significantly to increased life expectancy and decreased morbidity. Box 55-4 lists common opportunistic diseases associated with HIV disease.
Combination antiretroviral therapy (ART) is an important component in the management of HIV infection (Table 55-4). In 1987, zidovudine was the only medication available to treat patients with HIV disease; since then, the FDA has approved more than 30 antiretroviral medications. Seven different classes of ART are used to prevent the viral replication process: multiclass combination products, integrase inhibitors, fusion inhibitors, CCR5 co-receptor antagonists, nucleoside reverse transcriptase inhibitors (NRTIs) and nucleoside and nucleotide reverse transcriptase inhibitors, nonnucleoside reverse transcriptase inhibitors (NNRTIs), and protease inhibitors. Each class of medication interrupts HIV at different stages of the infectious process. In HAART, HIV is treated with three or more antiretroviral medications, usually two NNRTIs or NRTIs and a protease inhibitor. Sometimes another NRTI known as abacavir (Ziagen) is substituted for a protease inhibitor.
Table 55-4
Pros and Cons of Highly Active Antiretroviral Therapy (HAART)
PROs | CONs |
HIV, Human immunodeficiency virus.
Scientists have found that the most effective medication regimen is the use of cocktails (generally three or more compounds given together). Medication combinations make it much more difficult for the virus to develop resistance to the drugs. Such intervention may also slow the progression from asymptomatic or mildly symptomatic HIV infection to a more advanced disease. Therapies that can dramatically reduce the quantity of circulating virus in the blood have been developed; in many cases, blood circulating levels become undetectable. It is still possible for one individual to infect another with the virus despite having undetectable viral levels. Protease inhibitors directly reduce the ability of HIV to replicate, or make copies of itself, inside cells. As increasing numbers of therapeutic agents and clinical trial results become available, decisions about ART have become increasingly complex. For now, these combination therapies offer optimism for successful disease management and improvements in the quality and duration of life.
It is important to administer anti-HIV medications around the clock. For example, a medication ordered three times per day should be given as close as possible to every 8 hours, not three times while the patient is awake. Failure to take medications as prescribed result in reduced drug levels, which can ultimately cause the HIV virus to become resistant to the therapies. Communicating this teaching point to patients is crucial.
Considerations for ART include the following:
• Previous experience with ART may affect the efficacy of a proposed therapy because the virus may have become resistant to medications taken by the patient in the past (e.g., zidovudine, lamivudine).
• Certain combinations of antiretroviral drugs may reverse the resistance to a single drug. Recycling drugs previously taken can sometimes improve viral suppression. Incorrect dosing (timing) or incorrect usage (missed doses) can cause drug resistance.
• Drug incompatibilities, similar side effect profiles, and toxic effects must be considered in the choice of a regimen.
• The patient's commitment and ability to adhere to complex drug regimens must be considered. Inadequate adherence can lead to drug resistance and, ultimately, to drug failure. This point must be stressed to the patient. Adherence is paramount for survival and success of treatment.
Opinions differ as to when to initiate ART. The increasing number of antiretroviral agents and rapid evolution of new information have introduced extraordinary complexity into the treatment of HIV infection. A provider with expertise in HIV should supervise the care. Treatment should be offered to all patients with acute HIV syndrome (seroconversion illness), those in whom HIV seroconversion has occurred within the past 6 months, and all patients with symptoms attributed to HIV infection. In general, treatment should be offered to individuals with CD4+ cell counts of fewer than 350/mm3 or plasma HIV viral loads of copies exceeding 30,000/mL (bDNA method) or 55,000/mL (PCR method).
Health care providers are beginning to start ART in patients with higher CD4+ cell counts than before. This strategy results in fewer prescribed medications, the need to take them less often, and fewer side effects. The U.S. Public Health Service has provided guidelines for health care providers to help with decision making regarding ART. The National Institutes of Health's testing and treatment strategies have helped decrease morbidity and mortality rates for HIV-infected patients (Panel on Antiretroviral Guidelines for Adults and Adolescents, 2013).
Current HIV treatment is aimed at preventing the immune system damage that results from HIV replication. If HIV replication can be halted, then viral mutation can be prevented, and drug resistance issues can be decreased. ART is aimed at limiting viral loads to undetectable levels. With early ART, the patient's CD4+ cell counts will remain normal for a longer time. It is better to start ART when CD4+ cell counts are higher because they will drop less and recover more quickly (Paredes et al., 2000). The recommendation to treat a patient without symptoms should be based on the patient's willingness and readiness to begin therapy; the degree of existing immunodeficiency as determined by the CD4+ cell count; the risk of progression as determined by the CD4+ cell count and viral load; the potential benefits and risks of initiating therapy; and the likelihood, after counseling and education, of the patient's adherence to the prescribed treatment regimen. Once the decision has been made to begin ART, the goal should be maximal and durable suppression of viral load, restoration or preservation of immunologic function, improvement in quality of life, and reduction of HIV-related morbidity and mortality.
Clinical trials being conducted by the AIDS Clinical Trials Group and the National Institutes of Health in conjunction with universities, pharmaceutical companies, and other agencies may be important considerations for people with HIV disease. Patients may be able to participate in clinical trials or may benefit from the results of such research studies. Benefits include (1) access to new and potentially effective treatments for HIV disease before they are released to the public and (2) the chance to have physician visits and laboratory work paid for by the research study.
People with HIV disease often use nontraditional or complementary therapies, such as massage, acupuncture or acupressure, and biofeedback. Some patients use nutritional supplements or herbal remedies with the hope of alleviating the side effects of both the disease and the medications. Many patients prefer these therapies because of the limitations or side effects of approved drugs, mistrust of the health care system, easier access, lack of adequate insurance coverage, or the high cost of anti-HIV medications. These alternatives are best used in conjunction with approved therapeutic intervention.
Many patients may consider the use of complementary therapies. Alternative forms of therapy may be beneficial and should always be thoroughly explored. Patients should discuss their use with their health care team. It is important to educate the patient about selective review and use of complementary and alternative therapies. Their potential benefits and risks, along with the associated financial strain, should be evaluated carefully. Patients may need guidance to avoid expensive and particularly dangerous forms of alternative treatments. An open relationship and good communication with the patient build trust, creating a positive atmosphere for addressing difficult issues. They also reinforce the philosophy that the patient is an important participating member of the health care team.
Unfortunately, a vaccine for HIV is not yet available. This is because the virus easily mutates, many different viral strains exist, and poor adherence to ART has led to drug resistance issues. However, with greater understanding of the immune response to HIV and more effective ways to administer antigens, an aggressive push to create a vaccine is currently under way. Since the mid-1980s, many initiatives and partnerships among organizations worldwide have attempted to develop a vaccine for HIV. Researchers have taken many approaches: live attenuated vaccinations, live recombinant vaccines, and subunit vaccines (WHO, 2013c). The results have left the researchers surprised and disappointed. One initially promising study involving a vaccine that was supposed to increase cellular immune function (with an adenovirus used in place of HIV) showed that the vaccine offered no protection against HIV and in fact increased viral infection rates (Sekaly, 2008) (see Heath Promotion box). Another vaccine, referred to as HVTN-505, also proved to be ineffective; the study of it was suspended in 2013 (Knox, 2013).
The nurse should establish a comfort level in interacting with people with HIV disease. Patients must be treated in a nonjudgmental, empathetic, and caring manner regardless of their sexual practices or history of drug use. The nurse's attitudes, values, and beliefs should not interfere with the care of a patient with HIV disease. Patients are aware when their caregiver is not comfortable dealing with HIV disease. Knowledge of HIV transmission and competence in standard precautions and body substance isolation will minimize the fear of caring for HIV-infected patients. Boxes 55-5 and 55-6 and Table 55-5 list appropriate nursing assessments, activities, and interventions for HIV infection and disease.
Table 55-5
Nursing Activities in HIV Disease
HIV, Human immunodeficiency virus.
Nursing diagnoses and interventions for the patient with HIV disease include but are not limited to the following:
Health care needs can be unpredictable and assessment difficult because of the clinical diversity of HIV infection. HIV disease may necessitate alternating periods of long-term and acute care. The patient may fear isolation from the community or family and friends because of the social stigma associated with HIV disease.
The disease affects primarily young people who are at the most productive time in their lives, a time when they are expected to take control of their lives. For this reason, they often want an active role in the decision-making and planning stages of their care. Patients may experience bouts of serious, debilitating illness and then recover enough to function effectively for an unpredictable amount of time. People with HIV disease often prefer to stay at home as long as possible, and some prefer to die at home. Long-term care in an inpatient setting (e.g., long-term care facility) is not compatible with the social needs of young patients. Prolonged care is expensive. Patients who experience chronic diseases may find their insurance coverage is limited. In addition, the absence of insurance may affect availability and affordability of treatment options. Religious and community-based organization volunteers, such as AIDS project workers, provide support and care services for patients and families. Friends, family, and significant others are also important resources to be considered in the planning of care for the patient with HIV disease.
Adherence to a prescribed regimen (following a prescribed regimen of therapy or treatment for disease) is paramount to survival and the success of treatment. The nurse is in a unique position to help patients adapt and maintain vigilance in their treatment. Nurses must assist patients to understand that ART is a lifelong, complex undertaking. The ability to incorporate anti-HIV treatment into a lifestyle is affected by multiple factors, including treatment knowledge or misinformation, underlying psychiatric or psychological pathologic conditions, physical status, family and caregiver support, socioeconomic status, culture, fear of side effects, denial, and skills (memory, impaired function) necessary to adhere to a medical regimen.
Patients with a higher level of motivation to take their medications as ordered can have much better outcomes than do patients who are less compliant. Drug resistance to ART can develop over a weekend of missing doses. Typical adherence to ART is poor even when patients have to take only one or two pills each day. Results of one Veterans Affairs study indicated that only 76% of that population were up to date with their drug refills (Braithwaite et al., 2007).
Strategies that can assist nurses in increasing patient adherence include determining their own level of comfort with regard to HIV, learning to listen, having knowledge about the disease, using therapeutic communication skills, giving the patient and caregivers permission to grieve and feel sad, acknowledging frustration and helplessness, providing a safe environment, and seeking expert assistance as needed. All of these can help patients incorporate this difficult treatment into their lifestyle (Box 55-7).
The WHO defines palliative care as helping patients and families deal with possibly fatal illnesses and quality-of-life issues. The focus of palliative care is on preventing and relieving suffering by quickly identifying and treating pain. The goal of palliative care is to improve and maintain quality of life as much as possible by focusing on all physical, spiritual, psychological, social, and existential needs of the patient or the family that is dealing with a terminal illness (WHO, 2013a).
Palliative care is not seen as hastening the dying process or postponing death. Nurses realize that death is a natural process of life, but other people may believe that a patient's death signifies the failure of medicine and loss of hope. Palliative care is often delayed as a result of this false belief. Most hospice programs use a palliative care approach, with the understanding that impending death means a shift from curing to caring. Nurses must remember that the goal is to relieve suffering through management of pain and symptoms at any point in the patient's disease process.
For patients with HIV disease, it is important for palliative care not only to address the potential chronic debilitating conditions associated with HIV disease but also to address superimposed acute exacerbations of opportunistic infections and related symptoms. Intravenous therapy, blood transfusions, and antibiotic usage may be considered palliative in the end stage of HIV disease because these interventions help keep the patient comfortable and help maintain quality of life. In AIDS care, short-term aggressive, curative therapy is often important in treating acute infections such as pneumonia, but the overall goal remains palliation.
The complex needs of patients with HIV disease necessitate the services of a multidisciplinary team of physicians, nurses, social workers, dietitians, physical therapists, and clergy. The nurse is the “voice” and advocate for the patient who may or may not be able to communicate his or her treatment desires. Because of this unique role, it is important to be comfortable discussing treatment issues and options with patients, as well as respecting their decisions. Families and significant others of patients with end-stage HIV disease can experience disenfranchised grief, which occurs when a loss is not openly acknowledged, publicly mourned, or socially supported (Sherman, 2001). Symptoms such as pain, fatigue, anorexia, fever, shortness of breath, diarrhea, and insomnia are common among people who suffer disenfranchised grief. The nurse should become familiar with the causes and interventions necessary to alleviate these symptoms. The nurse must remember that symptoms such as pain are a subjective experience and must be treated appropriately until the patient indicates the treatment has worked. Although this phase of life is difficult for the patient and nurse, many nurses express significant satisfaction with these interactions, relationships, and their outcomes.
As the HIV pandemic has changed over time as a result of the use of ART and aggressive approaches to treatment, fewer patients with HIV infection are requiring hospice or palliative care. In some patients, however, HIV is not diagnosed until they are in a later stage of the disease process. These patients may choose palliative or hospice care instead of treatment.
People who have received a diagnosis of HIV infection deal with a complex set of psychosocial issues. Often, they are uncertain, fearful, depressed, and isolated. HIV infection can be treated, but it is incurable and contagious. Many infected people feel isolated and abandoned by friends and family because of the stigma associated with HIV. Like the health care costs associated with many chronic diseases, the expenses involved in treating HIV infection are daunting for many patients.
Nurses and health care providers must be empathetic during contact with patients. Listening is an important skill to help convey compassion. Therapeutic communication skills should be used to further develop rapport with a patient. The nurse should help the patient plan and decide about health care options. The patient has the right to be supported even when the decision seems imprudent.
Individuals who have been exposed to HIV infection but who are without any symptoms or complications live with uncertainty, anxiety, denial, and hopefulness (Box 55-8). The nurse's role in this stage of the disease process is to provide continued education about HIV disease and prevention and to assist in realistic goal setting. The nurse must make every effort to include the patient and the support system in planning care. Early in the care process, the nurse should assess past coping styles and support systems and continually reevaluate these issues. Healthy patterns of coping, such as talk therapy, relaxation, and meditation, should be encouraged. Relationships with family, friends, and significant others should be maintained and in fact may become stronger during the HIV crisis. However, prior family conflicts may worsen as a result of the stress of the illness. Families with poor communication skills are at particular risk for this outcome.
As HIV disease progresses through the clinical complications of infections and cancers, patients experience multiple losses, including the loss of energy; a self-care deficit that necessitates assistance with activities of daily living; and the loss of independence, employment, finances, and hope. The reality of death emerges. Nursing interventions should focus on a philosophy of facing life one day at a time and living each day to its fullest. This may be a time for strengthening personal and spiritual relationships and resolving any conflicts.
Anxiety and depression can become chronic, ultimately interfering with daily functioning, relationships, communication, and even the ability to make simple decisions. Although anxiety and depression are normal when a patient is dealing with a significant health care threat, the nurse should refer patients to mental health professionals for possible pharmacologic or verbal counseling when these feelings affect daily functioning for more than 2 weeks (US DHHS, 2011). Patients with HIV disease and depression should be assessed regularly for suicidal ideation, inasmuch as this phenomenon occasionally occurs in terminally ill patients. Early recognition of depression and anxiety is critical because most cases respond to medications, psychotherapy, or a combination.
Severe anxiety can cause individuals to believe they have no control over the events in their lives. Helping the patient develop a schedule of activities may decrease anxiety and feelings of powerlessness. The nurse should explore opportunities for spiritual support and comfort. Community support groups for patients and significant others may contribute to healthy coping. The nurse should arrange to spend time with the patient and the support system, in hopes that this will decrease anxiety and promote better coping.
The use of therapeutic communication and helping patients find meaning in life are critical nursing interventions. Assisting families and significant others in providing support to the terminally ill patient despite their own anger and grief is a unique nursing challenge. Such care, although emotionally draining, can provide great satisfaction.
The psychosocial aspects of HIV infection can be devastating. Feelings may include denial, fear, depression and anger. These are similar to those that may be seen in an individual who has been diagnosed with cancer. The first stressful issue faced by a patient with newly diagnosed HIV infection is disclosure of HIV status. A very real concern for HIV-positive patients is that family, significant others, and friends will be angry and may even reject or abandon the patients. Families and friends of a patient with newly diagnosed HIV infection may be misinformed about the disease. The patient and the family may benefit from sources of support such as a mental health provider with experience providing service to patients who are infected with HIV. Support groups for both patients and significant others are often also available. HIV-infected individuals who have been exposed through contaminated blood or who contract HIV from their partner may experience feelings of anger and hostility. Showing support and providing education about the disease may help alleviate some of these feelings.
Many patients with HIV infection benefit simply from having another person listen and explore in detail the feelings, unfounded fears, and treatment options. Many others, however, need the more structured support found in therapeutic relationships or formal support groups. Significant others and family members also may need assistance to provide support to their loved one. Formal counseling can help a patient address issues such as continued employment, health insurance concerns, preparations for disability, and feelings related to death. Referral to medical or clinical social workers and appropriate community agencies is part of the nurse's responsibility in addressing psychosocial needs. For some patients, it is appropriate to refer them to clergy.
Respect for the patient's right to confidentiality is particularly important for a patient with HIV disease. The confidentiality of the diagnosis must be carefully protected and shared only with caregivers who need to know for the purpose of assessment and treatment.
Health care workers should use standard precautions with each patient to prevent exposure to the patient's blood or bodily fluids. Not every infected patient may know that he or she is seropositive for HIV. When this information is shared by the patient, the information should be shared with other health care workers who are managing this patient's care.
The patient should be in control of who is told of the diagnosis, but laws dictate the reporting of an HIV diagnosis to appropriate health agencies. As with any patient seeking health care services, guidelines of the Health Insurance Portability and Accountability Act (HIPAA) must be followed. Partner notification laws must also be considered when HIV infection is diagnosed. The health care provider must follow laws in his or her state regarding partner notification.
Early intervention after detection of an HIV infection can promote health and limit or delay disability. Because the course of HIV infection is extremely variable, assessment is of primary importance. Nursing interventions are tailored to any patient needs noted during assessment. The nursing assessment of HIV disease should focus on the early detection of constitutional symptoms, opportunistic diseases, and psychosocial problems (Box 55-9).
HIV disease progression may be delayed by maintaining the health of the immune system. Useful interventions for an HIV-infected patient include (1) nutritional changes that maintain lean body mass, maintain weight in the range of ideal body weight, and ensure consumption of appropriate levels of vitamins and micronutrients; (2) elimination of smoking and drug use; (3) elimination or moderation of alcohol intake; (4) regular exercise; (5) stress reduction; (6) avoidance of exposure to new infectious agents; (7) mental health counseling; (8) involvement in support groups; and (9) safer sexual practices.
The patient should be taught to recognize clinical manifestations that may indicate progression of the disease; this will ensure that medical care is initiated promptly. Early manifestations that need to be reported include unexplained weight loss, night sweats, diarrhea, persistent fever, swollen lymph nodes, oral hairy leukoplakia, oral candidiasis (thrush; see Figure 55-4), and persistent vaginal yeast infections. In addition, the patient should report unusual headaches, changes in vision, nausea and vomiting, and numbness or tingling in the extremities. The nurse must give the patient as much information as needed to make health care decisions. These decisions dictate the appropriate medical and nursing interventions.
Nursing interventions become more complicated as the patient's immune system deteriorates and new problems arise to compound existing difficulties. The nursing focus should be on quality-of-life issues and symptom management, rather than on issues regarding a cure.
When opportunistic diseases develop, the nurse should provide symptom-based nursing interventions, education, and emotional support. For example, an acute case of P. jiroveci pneumonia necessitates intensive nursing interventions, including monitoring the respiratory status, administering medications and oxygen, positioning the patient to facilitate breathing, managing anxiety, promoting nutritional support, and helping the patient conserve energy to decrease oxygen demand. Because advanced HIV disease can lead to death, emotional support for the patient, caregiver, or significant other is particularly important (Nursing Care Plan 55-1).
Diarrhea is often a long-term problem for HIV-infected people. Damage to the intestinal villi, malabsorption, infections of the gastrointestinal tract, and the side effects of medications all contribute to a large number of cases of diarrhea. Nursing interventions include recommending dietary interventions (Table 55-6), encouraging adequate fluid intake to prevent dehydration, instructing the patient about skin care, and managing excoriation around the perianal area. In some cases, antidiarrheal agents may help control diarrhea and prevent further complications. The nurse should recommend the use of incontinence products to prevent soiling of the clothes and bed linens. In addition, the nurse should assess for factors that may trigger the diarrhea, such as anxiety, medications, or lactose intolerance.
Table 55-6
Nutritional Management: HIV Infection
HIV, Human immunodeficiency virus.
HIV wasting—the loss of lean body mass as a result of illness—has been a common clinical manifestation of HIV disease since early in the epidemic. Wasting is caused by disturbances in metabolism, which interfere with the effective use of nutrients, resulting in the loss of lean (muscle) body mass, often without reduction of body fat. This loss of lean body mass is a primary cause of functional decline in wasting, which results in increased risk of opportunistic infections, reduced quality of life, and reduced length of survival. A person with HIV is considered to have wasting syndrome when he or she has lost 10% of body weight and has had either diarrhea or weakness, and fever for 30 days. The person infected with HIV who has wasting syndrome is considered to have AIDS (Womenshealth.gov, 2011b).
The causes of wasting are probably multifactorial. Food intake may be inadequate because of mechanical difficulties (e.g., thrush or esophageal ulcers), loss of appetite (e.g., side effect of medications or neurologic disease), or psychological factors such as depression and anxiety. Absorption in the intestine may be decreased as a result of infections and a damaged mucosal barrier, which may lead to diarrhea. Some patients stop eating to decrease the number of bowel movements per day.
Wasting disturbs self-concept and self-image and can be one of the most difficult consequences of HIV infection to accept. Useful interventions for these disturbances include creating an atmosphere of acceptance and reassurance, encouraging a focus on past accomplishments and personal strengths, and facilitating the use of positive affirmations.
Decreased levels of testosterone have been reported in HIV-infected men. Testosterone has two distinct biologic properties: virilizing activity (androgenic effect) and protein building (anabolic effect). Because testosterone is an anabolic hormone, a deficiency may cause a loss of body cell mass, which contributes to HIV wasting. The role of gonadotropic hormones in women with wasting has not been studied sufficiently. Women with HIV wasting tend to lose a lot of body fat, but body cell mass is not significantly decreased. Conversely, men tend to lose a significant amount of lean body mass (e.g., exhibit skinny arms and legs), with preservation of fat, particularly in the truncal area.
With the advances in HIV treatment and opportunistic infection prophylaxis, serious malnutrition is less evident. However, nutrition does not return to normal after anti-HIV treatment begins. A syndrome of increased truncal obesity (visceral, abdominal), subcutaneous fat loss on the extremities and face (also called lipoatrophy), and metabolic abnormalities such as hyperlipidemia and insulin resistance have been reported in both men and women.
The management of wasting and lipodystrophy is difficult and generally requires multiple nursing interventions. Diminished appetite and weight must be assessed and documented. The nurse should encourage nutritional supplementation (see Table 55-6) and increased protein intake, provide enteral supplements (through nasogastric or gastric tubes if necessary), and assist with total parenteral nutrition when it is needed. Medications to stimulate appetite, such as dronabinol (Marinol), can help; unfortunately, these medications tend to increase body fat and not lean muscle mass. Testosterone (anabolic steroid) can be administered by mouth, intramuscularly, or transdermally to increase lean body mass and weight. The effect of testosterone can be enhanced by a low-weight resistance-training program (e.g., weight-lifting), which maintains muscle tone and improves appetite.
Nutrition counseling is vital to ensure that individuals with HIV disease maintain a well-balanced diet, including supplements if necessary. The dietitian can assist in counseling, provide the patient with high-protein and high-calorie diets, and suggest meal plans that fit the patient's lifestyle. Smaller, more frequent meals can be less overwhelming than larger meals. Teaching about food safety is of paramount concern because enteric infections (e.g., cryptosporidiosis, microsporidiosis, and amebas) in HIV disease are often not treatable or are relapsing. In some cases, enteral or parenteral feeding becomes necessary.
Management of elevated triglyceride and lipid (cholesterol) levels is becoming common in HIV disease. As in other patient populations, these elevations can lead to cardiovascular disease and, in some cases, diabetes. Lipid-lowering agents such as the statins may be effective in treating this complication. However, because the liver metabolizes many of the antilipid agents, it is important to choose a drug that is safer than those that must pass through the liver to be activated; safer anticholesterol drugs include pravastatin (Pravachol), fluvastatin (Lescol), and possibly atorvastatin (Lipitor). A program of diet, exercise, and medications can safely lower lipids and reduce the chances of a cardiovascular event.
Insulin resistance or diabetes sometimes responds to oral hypoglycemic agents (e.g., metformin or rosiglitazone [Avandia]). In some cases, the anti-HIV therapy needs to be changed to a protease-sparing combination. Diet management, smoking cessation, weight loss, and exercise can help control the elevations in blood glucose that can occur with the use of anti-HIV medications.
Unfortunately, as with any overwhelming viral infection, HIV infection increases the patient's metabolic needs. This hypermetabolism and consequent higher energy expenditure frequently exceed the number of calories taken in by the patient. Malnutrition, weight loss, and generalized wasting are common problems in patients with HIV disease (see Nursing Care Plan 55-1). Many patients with HIV disease experience wasting. Malnutrition contributes to wasting, and wasting hastens the negative immune consequences of HIV infection. HIV wasting contributes to slower recovery from infection, impaired wound healing, increased risk of secondary infection, and decreased cardiac and respiratory function. Wasting can lead to an earlier death. The weight loss associated with HIV disease is often severe and debilitating, producing a vicious cycle of anorexia, malnutrition, loss of tissue mass, muscle wasting, profound fatigue, and increased susceptibility to infections and drug interactions. Although typically seen in later stages of HIV disease, malnutrition and wasting can occur in the early stages of HIV infection.
HIV-associated cognitive motor complex (previously known as “AIDS dementia”) is the term preferred by the WHO and the American Academy of Neurology to describe a common central nervous system complication of HIV disease. It occurs in 20% to 33% of all adults and as many as 50% of children with end-stage disease (AIDS). This condition is a complex combination of signs and symptoms, including dementia; impaired motor function; and, at times, characteristic behavioral changes that resemble those accompanying a stroke or head trauma. The disease generally does not cause alterations in the level of consciousness (National Institute of Mental Health, 2011). It is usually described as a triad of cognitive, motor, and behavioral dysfunction that slowly progresses over a period of weeks to months. The cognitive changes involve primarily a mental slowing and inattention. Affected patients typically lose their train of thought and complain of slowed thinking. They may miss appointments and find themselves making lists of tasks and chores that need completing. The signs and symptoms of motor dysfunction ordinarily develop after those of cognitive impairment. They include poor balance and coordination (e.g., falling and tripping, dropping things); slower manual activities (e.g., writing, eating); and, ultimately, leg weakness that can limit ambulation. This type of dementia can be diagnosed through a simple physical examination, neurologic testing, magnetic resonance imaging and computed tomography, and cerebrospinal fluid analysis.
Nursing interventions for neurocognitive dysfunction include the cautious administration of anti-HIV and psychotropic medications. Supervision of the patient, which includes a home safety assessment, is imperative. The nurse should ensure that orientation cues such as clocks and calendars are present, hallways and living areas are brightly lit, walkways are clear of electrical cords or throw rugs, and potentially dangerous objects (e.g., knives, poisons) are safely stored away from the patient.
Caring for patients with dementia is a collaborative effort between the health care provider and family. It is advisable to seek advice from a social worker, the home health care department, and a psychologist in developing a plan to care for an impaired individual.
AIDS-dementia, caused by HIV infection in the brain, is a common neurologic disorder associated with HIV. Dementia symptoms are sometimes reversible if a treatable cause can be diagnosed. Treatable causes include dehydration, depression, and medication toxicity or side effects. Clinical manifestations of AIDS dementia complex (ADC) include cognitive, behavioral, and motor abnormalities. Symptoms of ADC include decreased ability to concentrate, apathy, depression, social withdrawal, personality changes, confusion, hallucinations, altered levels of consciousness, and slowed response rates. ADC can lead to coma. Nursing interventions are focused on patient safety and caregiver support.
Neuropathies are diseases that affect the peripheral nervous system. They can affect sensory, motor, or autonomic nerves. The causes of neuropathies can be related to HIV disease itself or, more frequently, the side effects of many anti-HIV medications (e.g., stavudine [d4T, Zerit], and didanosine [ddI, Videx]). Symptoms include numbness, localized tingling, hypesthesia (diminished sensitivity to stimulation) or anesthesia, loss of sense of vibration and position (proprioception), and decreased or increased sensitivity to pain. In most cases, patients complain of numbness in the fingers, the hands, and the feet and pain on walking. Patients may also experience autonomic neuropathy. Symptoms such as mild positional hypotension, cardiovascular collapse, and chronic diarrhea are suggestive of autonomic neuropathy.
As new HIV medications with less neurotoxic side effects become available, fewer people are experiencing peripheral neuropathy. Older ART medications caused painful peripheral neuropathy, and people who have taken these medications in the past may develop this problem later.
With the advent of effective ART and better understanding of opportunistic infection prophylaxis, the frequency of such infections has decreased dramatically. Opportunistic infections still occur in severely immunocompromised patients, and so the nurse must become familiar with the recognition, treatment, and prophylaxis of these diseases. Opportunistic infections are typically seen in individuals who are nonadherent to their antiretroviral regimen, nonadherent to prophylactic regimens against opportunistic infections, or at the end stage of HIV disease and in individuals who do not consistently access the health care system. (See Table 55-3 and Box 55-4 for common opportunistic infections, treatment, and prevention.)
Because patients with HIV disease are living longer and more productive lives, attention to the promotion of health and healthy behaviors is important (see Health Care Promotion box). Patients should be encouraged to eat well-balanced meals, stop smoking or at least reduce the number of cigarettes smoked, get adequate sleep and rest periods if possible, use stress-reduction modalities (e.g., biofeedback, referral for counseling), obtain dental care regularly, and keep scheduled appointments with all health care providers. Attention to comorbid conditions, such as hypertension and diabetes, helps minimize additional health problems. The nurse should encourage patients to get all immunizations and keep them up to date; female patients should regularly receive gynecologic examinations. If hospitalizations are necessary, encourage the patient and significant others to participate in treatment decision making, and arrange for home care follow-up if indicated.
Although some pets can pose risks for transmission of opportunistic infections, they are, overall, therapeutic and healing for the patient. Only minor modifications need to be made for HIV-infected pet owners (e.g., birdcage and cat litter box cleaning). If possible, pet visits to the hospital or care facility should be arranged if a long separation is anticipated; the idea of benefit should not be dismissed just because this practice is not acceptable at the nurse's health care facility. The nurse should speak with managers and supervisors to obtain permission or help develop policies and procedures that allow the visitation of pets.
HIV disease is preventable. However, prevention requires the cooperation and efforts of public health care providers, medical providers, nurses in all specialties, families, communities, churches, and schools (Box 55-10). Education on prevention is the only truly effective “vaccine” available to curb the HIV pandemic. Many patients admitted to acute care facilities have unrecognized HIV disease or are at risk for HIV infection. Each patient's risk should be assessed, and those at risk should be counseled about HIV testing, the behaviors that put them at risk, and how to reduce or eliminate those risks. Today, every nurse is potentially an HIV nurse; that is, all nurses may find themselves responsible for teaching patients methods to reduce the risk of transmission. Nurses must be able to discuss, in a nonjudgmental way, behaviors related to sexual activity and substance use (e.g., condom application, using clean needles). Nurses should establish rapport with patients before asking sensitive, explicit questions related to behaviors typically not discussed.
Harm-reduction education is a fundamental element of HIV prevention methods. Harm reduction does not completely eliminate the risk of HIV transmission, but it minimizes the social harms and costs associated with certain behaviors. For example, attempts to quit smoking two packs of cigarettes per day all at once almost always result in failure. In a harm-reduction approach, the nurse can suggest that the patient reduce the number of cigarettes smoked from 40 to 30 a day. Although the ultimate goal is for the patient to stop smoking altogether, the patient has at least reduced the risk of long-term effects by limiting the number of cigarettes smoked. The same is true for HIV prevention. Encouraging patients to use protective barriers such as male and female condoms helps reduce the risk of HIV transmission.
An important part of preventing HIV transmission is HIV screening tests and follow-up education and counseling (see Box 55-3). However, patients must not be coerced into having an HIV screening test. The process of helping patients make the decision about whether to undergo testing and how to be tested is called test decision counseling. Nurses and health care providers should counsel their patients before and after HIV testing. HIV tests necessitate informed consent per state law before blood is collected. The informed consent is always accompanied by an explanation about the testing and implications of results. The limitations of the test must also be explained.
Performing HIV testing early in the course of the disease is important for increasing survival rates of HIV-infected patients and preventing the transmission to other people through high-risk behaviors. Guidelines from the CDC (2006) mandated that all patients in health care agencies be informed about HIV screening and then be screened for HIV. However, these patients are allowed to refuse the test. HIV antibody testing should be offered to all patients, regardless of patient-specific risk factors. Also, test results should be made available rapidly to the patient so that education can be given to the patient, if needed. The CDC's recommendations state that informed consent is not needed. However, patients may opt out of testing if they wish. In rare emergency situations in which health care providers need to know a patient's HIV status to make a decision regarding health care and the patient is unable to speak, the patient may be tested without his or her consent.
Increasing numbers of people with HIV can be identified with the current push for routine HIV screening. The FDA approved the use of ELISA testing for routine use during blood bank screenings. ELISA can identify antibodies for HIV-1 and HIV-2. Researchers who conducted a study in Cameroon found that ELISA was highly sensitive even with the wide variations in the genetic makeup of the HIV (Lee et al., 2007). The FDA has approved four rapid tests for HIV detection. Multispot and Oraquick can detect HIV-1 and HIV-2. Uni-Gold Recombigen and Reveal can identify only HIV-1 (Greenwald et al., 2006). OraQuick is the first in-home, over-the-counter HIV test approved by the FDA (US FDA, 2013b).
HIV antibody testing may take place in a physician's office or at designated HIV counseling and testing sites. Many patients feel more comfortable being tested by someone who knows their medical and social history, but others prefer to be tested in a location where they are unknown. The nurse should be aware of the various options for HIV antibody testing in his or her state or community in order to advise patients appropriately.
HIV antibody testing can be done one of two ways: confidentially or anonymously. In confidential testing, patients provide identifying information, including a name; an address; and often demographic information such as age, sex, race, and occupation. Using this information, care providers can locate and provide information to an individual who does not return for the test results or counseling. All records are strictly confidential, and testing in physicians' offices, clinics, and hospitals is conducted in a confidential manner. Health care providers who share or use this information inappropriately can be sued for negligence and invasion of privacy, and they may be disciplined by licensing boards for unauthorized disclosure or breach of confidentiality. Patients should be informed that the results of their HIV antibody test will be linked to the patient's medical record.
In anonymous testing, individuals are not asked to provide identifying information. Records are kept through assigned numbers, and the patient must retain this number to receive test results. It is not possible to locate and provide information to an individual who does not return for test results and counseling. In either form of testing, the nurse can perform pretest and post-test counseling.
Testing for HIV is an important part of the public health response to HIV disease. Risk assessment should be patient centered, a joint process between the nurse and patient. The patient should take “ownership” of the risk for HIV infection. The nursing assessment should include an evaluation of risky behaviors by the patient or a history of STIs. A patient will not get tested unless he or she perceives a need for testing and feels safe doing so. The nurse should help the patient assess the risks by asking some basic questions:
• Have you ever had a transfusion or used clotting factors? Was it before 1985?
• Have you ever shared needles, syringes, or other injecting equipment with anyone?
• Have you ever had a sexual experience in which your penis, vagina, rectum, or mouth came into contact with another person's penis, vagina, rectum, or mouth?
A positive response to any of these questions requires further exploration with the patient. The nurse should be prepared to refer the patient to centers that provide testing and counseling services. All testing should include pretest and post-test counseling (see Boxes 55-3 and 55-9).
HIV infection in women has been frequently overlooked for several reasons. In the United States, the disease initially occurred mostly in men, and treatment models were developed accordingly. Providers did not assess the risks for women, and women did not seek testing and counseling because of denial or ignorance; thus interventions have not been implemented effectively. Heterosexual intercourse surpassed injection drug use as a vector for HIV transmission in women in the second decade of this pandemic and globally continues to be the highest risk factor in women. The CDC case definition includes at least one female-specific disease: cervical carcinoma. Women now need to be assessed for different manifestations, such as vaginal candidiasis, a common presenting condition for HIV-positive women (CDC, 1993).
HIV prevention has numerous barriers, not the least of which is a denial of risk, an attitude that “it won't happen to me.” Because the virus initially infected the MSM population in the United States, members of many other subpopulations have ignored their risks. Fear, misunderstanding, and the potential for social isolation and social stigma are significant barriers. Some individuals are so fearful that they no longer give blood or eat at a restaurant if they think a homosexual food handler works there. Such reactions reinforce the need for consistent, accurate information about the virus, the risks of transmission, and HIV disease itself.
Cultural and community attitudes, values, and norms can affect the success of prevention efforts. A community may be opposed to HIV/AIDS education in the local school district because of the fear that certain values will be compromised. Those values may include views on sexuality, abstinence, the use of condoms, the use of drugs, and the provision of instructions about cleaning needles and syringes. Community organizations, churches, educators, and leaders can determine the community's expectations or norms. Cooperative efforts are essential for successful prevention of HIV transmission. The issues related to the HIV epidemic—sex, drug use, death, and homosexuality—are not easy issues for most cultures or communities.
Fear of alienation and discrimination are significant additional barriers to prevention. Some individuals are reluctant even to pick up a pamphlet about HIV because they fear that someone will believe they are gay or using illicit drugs. Some people will not go to a physician or to a testing and counseling site for HIV testing for fear of being seen there by people they know. This fear is valid, particularly in rural parts of the country. Fear of discrimination includes fear of losing family, friends, prestige, job, housing, and insurance. Fortunately, many states have statutes to protect individuals with HIV disease from discrimination. Protection is also afforded by the Americans With Disabilities Act.
When patients have acute HIV disease and high viral loads, they are 10 times more likely to transmit HIV during sexual intercourse than during the chronic stage of HIV. Infection risk is also increased when sex is forceful or when mucosal membranes are disrupted (situations often associated with STIs). Most HIV infections are transmitted during the primary stage of the infection. This is when most people are unaware of their infection because they have no symptoms. Men are less likely to be infected with HIV during heterosexual intercourse than are women because women have more mucosal surface that can be exposed to infected body fluids in comparison to men. Male circumcision can also minimize a man's risk of becoming infected with HIV via heterosexual intercourse, according to the WHO (2013a).
Safer sexual activities reduce the risk of exposure to HIV through semen and cervicovaginal secretions. Abstaining from all sexual activity is the most effective way to accomplish this goal. Limiting sexual behavior to activities in which the mouth, penis, vagina, or rectum do not come into contact with the partner's mouth, penis, vagina, or rectum is also safe because there is no contact with blood, semen, or cervicovaginal secretions. These activities may include massage and masturbation. Insertive sex is considered safe only in a mutually monogamous relationship with a partner who is not infected with, or at risk of becoming infected with, HIV. The problem with mutual monogamy is that both partners need to follow all of the rules all of the time. Unfortunately, cases of HIV infection occur in individuals who are not aware that their partner has not remained monogamous. Serial monogamy (maintaining a monogamous relationship, often including unprotected intercourse, with one partner for a short time, followed by another relationship, and then another) also increases the risk of HIV exposure (Box 55-11).
ART can be provided to people who have been exposed to HIV through unwanted sexual intercourse (rape) or through injection drugs. The HHS has developed some recommendations regarding these types of nonoccupational exposures. When a person has been exposed to body fluids from an HIV-infected person during high-risk activity less than 72 hours before seeking treatment, the exposed person should receive a 28-day supply of ART. This is recommended even if the HIV-infected source of the exposure has an undetectable viral load. However, if the activity is deemed to be low-risk exposure to body fluids, or if the exposed person seeks health care after the 72-hour window, ART is not recommended. Cases should be examined on an individual basis to determine the need for PEP, counseling, treatment, and education about preventing future exposures (CDC, 2005a).
The use of barriers (Figure 55-5) reduces the risk of contact with HIV during sexual activity. Barriers should be used when a person engages in sexual activity with a partner whose HIV status is not definitely known or with a partner who is known to be infected with HIV. The most commonly used barrier is the male condom. Although not 100% effective, male condoms are very effective in the prevention of HIV transmission when used correctly and consistently. Other barriers include female condoms and latex dental dams. Female condoms consist of a vinyl sheath with two spring-form rings. The smaller ring is inserted into the vagina and holds the condom in place internally. The larger ring surrounds the opening to the condom. It keeps the condom in place externally while also protecting the external genitalia. The use of the female condom is complicated and cumbersome, and practice may be necessary to use this method effectively. Female condoms can also be used for anal sex, in both men and women. Dental dams or microwave-safe plastic wrap can be used to cover the external genitalia or anus during oral sexual activity (“rimming”). Although the risk of HIV transmission is significantly reduced with the use of latex barriers, other STIs, such as human papillomavirus, warts, and HSV, can still be transmitted.
The use of illicit or recreational drugs can cause immunosuppression, malnutrition, and emotional difficulties. Although using illicit drugs can increase a person's risk for acquiring HIV infection, drug use itself is not to blame. The major risks of HIV transmission are related to sharing injection equipment and having unsafe sexual experiences while under the influence of mood-altering chemicals. Essentially, people can reduce the risk of HIV infection by not using drugs. If drugs are injected, equipment should not be shared with other people. People should not engage in sexual activity while under the influence of any drug, including alcohol, that impairs decision making.
Abstaining from drugs is not always a viable option for a user who has no access to drug treatment services or who chooses not to quit. The risk of HIV for these individuals can be eliminated if they can find alternatives to injecting, such as smoking, snorting, or ingesting drugs. Risk can also be eliminated if the user does not share injection equipment, including needles, syringes, cookers, cotton, and rinse water. The safest tactic is for the user to have ready access to sterile equipment. Many states have laws that prohibit over-the-counter sale of needles and syringes, such as diabetic supplies. Some communities have needle exchange programs that supply sterile equipment to users to help reduce the risk of HIV transmission. The fear that needle exchange programs will result in increased illicit substance use has led to a lack of community support. However, studies have shown that in communities that have established exchange programs, drug use does not increase and rates of HIV infection are controlled (Wodak and Cooney, 2006).
As previously discussed, the risk of acquiring HIV through occupational exposure is low. The CDC and the Occupational Safety and Health Administration have instituted policies to protect employees from exposure to blood and other potentially infectious fluids (CDC, 2005b). The use of standard precautions and body substance isolation has been shown to reduce the risk of bloodborne pathogens, the risk of transmission of other diseases between the patient and the health care worker, and the risk of transmission between patients. Hand hygiene in the form of handwashing still remains the most effective means of preventing the spread of infection.
Results of epidemiologic and laboratory studies suggest that several factors might affect the risk of HIV transmission after an occupational exposure. In a retrospective study of health care workers who had percutaneous exposure to HIV, the CDC (2001) found that the risk of HIV infection was increased with exposure to a larger quantity of blood from the source patient, as indicated by (1) a device visibly contaminated with the patient's blood, (2) a procedure that involved a needle being placed directly in a vein or artery, or (3) a deep injury. The risk is also increased for exposure to blood from a patient with terminal illness, which possibly reflects the higher viral load of the patient late in the course of HIV disease (CDC, 2001). Information about primary HIV infection (seroconversion) indicates that a systemic infection does not occur immediately. This leaves a brief window of opportunity during which initiation of antiretroviral PEP might prevent or inhibit systemic infection by limiting the proliferation of the virus in the initial target cells or lymph nodes.
For best prophylactic effect, PEP must be initiated within 36 hours—but preferably within 1 to 4 hours—of the exposure. Depending on the type of exposure and many other variables, either a two- or a three-drug regimen is chosen (CDC, 2005a, 2005b). In addition to possible exposure to an antiretroviral-resistant strain of HIV, other factors that might contribute to failures include a high titer or large volume of inoculum exposure, delayed initiation or short duration of PEP, and factors related to the exposed health care personnel (e.g., immune status).
Completion of a 4-week course of therapy after an occupational exposure is fundamental. The medications used have many side effects, and health care workers may stop PEP prematurely because of these. It is important to consult with experts in occupational exposure if side effects (headache, nausea, vomiting, diarrhea) become unbearable. The use of PEP regimens has been associated with new-onset diabetes mellitus, hyperglycemia, hypertriglyceridemia, pancreatitis, elevated levels of lipids (cholesterol, low-density lipoproteins), and kidney stones. Despite these serious side effects, the exposed health care worker must continue therapy for 4 weeks or until it is determined that the source patient is not infected with HIV.
Hospitals or agencies should have policies that specifically address occupational HIV exposure, inasmuch as chemoprophylaxis must be undertaken immediately, even before testing of the source patient's and health care worker's blood for HIV or other bloodborne pathogens. Serial testing of the health care worker for HIV occurs immediately, 6 weeks, 3 months, and 6 months after the exposure.
Maintaining confidentiality for both the exposed health care worker and the source patient is of utmost importance. Many states and health care organizations have separate, distinct consent forms that are required before HIV antibody testing can be performed. Only in rare circumstances, such as the inability to give consent, can HIV antibody testing be completed without the patient's informed consent. Many ethical and legal issues surround HIV antibody testing; therefore, nurses must be informed of the applicable laws in the state in which they practice. In many states, charges of assault and battery can be brought against health care workers who perform HIV testing against a patient's will. Appropriate counseling and referrals should be made for the health care worker and patient when HIV testing is indicated.
HIV-infected people must be instructed not to give blood, donate organs, or donate semen for artificial insemination. They should not share razors, toothbrushes, or other household items that may contain blood or other body fluids. They should also avoid infecting sexual and needle-sharing partners, consider using birth control measures, and eliminate breastfeeding to avoid spreading the virus to infants.
During the HIV pandemic, much has been learned about transmission of the virus and ways to prevent infection. With no cure in sight, prevention of infection through education, prevention of mother-to-child transmission, and in some cases PEP or preexposure prophylaxis can limit the effect of this disease on the human population.
The dynamics of the pandemic have also changed dramatically. In the United States, HIV disease has the characteristics of any other chronic illness, in that (1) it has no cure, (2) it continues throughout the patient's life, (3) it causes increasing physical disability and dysfunction if not treated, and (4) it ultimately results in significant morbidity and mortality. Chronic diseases are characterized by acute exacerbations of cyclic problems that compound each other. Despite a significant decrease in the number of opportunistic infections, new complications have emerged. Health care providers today must address body composition changes, cardiac disease, neuropathies, and the long-term effects of the very medications that have kept HIV at bay.
Since the discovery of HIV, knowledge about the viral cycle, resulting immune response, and disease progression of HIV has made significant advances. New medication treatments are very effective and can help the host manage the disease by limiting replication of the virus, which can allow the immune system to continue to function. Rates of survival among patients with late-stage HIV (and who have access to HAART and are being cared for by health care providers with expertise in dealing with HIV) have increased dramatically. Patients who previously would have become disabled, quit jobs, and tended to end-of-life decisions are now reevaluating goals, returning to work, and rediscovering relative health. Now, couples with different HIV statuses have the option of having children with the use of sperm “washing” and in vitro fertilization.
For no other disease has there been such a rapid understanding and attempts at developing therapies as with HIV infection. The HIV research arena has provided insight into other diseases and scientific fields, including virology, immunology, and oncology. At this point, however, scientists' ability to develop new therapies depends on the patient's being nearly 100% adherent to regimens that are sometimes quite toxic. Adherence is poor even when therapy consists of only one pill per day. Even though treatment options for HIV have advanced, disease progression varies widely. Research is continuing into determining how psychological and social stressors alter immune system responses.
Women and people of color have become the fastest-growing segments of the population with HIV disease. Underdeveloped countries in Africa and Southeast Asia have been hardest hit; in fact, many villages have been destroyed because of HIV. The global threat of HIV is enormous, and nurses play a key role in the care and treatment of HIV-infected individuals. For the best possible outcomes, nurses must always seek guidance from HIV specialists when treating an individual with HIV disease because the care is very complex and multiple needs arise.
The field of HIV and AIDS nursing changes frequently, and nurses must constantly refresh their base of knowledge. Resources include local AIDS service organizations and state and regional AIDS education and training centers. As new therapies emerge, nurses are in a unique position to educate patients and the public about what is undoubtedly the most challenging infectious disease discovered in the twentieth century.