Stool specimens are frequently collected in children to identify parasites and other organisms that cause diarrhea, to assess gastrointestinal function, and to check for occult (hidden) blood. Ideally, stool should be collected without contamination with urine, but in children wearing diapers this is difficult unless a urine bag is applied. Children who are toilet trained should urinate first, flush the toilet, then defecate in the toilet, a bedpan (preferably one that is placed on the toilet to avoid embarrassment), or a commercial potty hat.
Stool specimens should be large enough to obtain an ample sampling, not merely a fecal fragment. Specimens are placed in an appropriate container, which is covered and labeled. If several specimens are needed, the containers are marked with the date and time and kept in a specimen refrigerator. Care is exercised in handling the specimen because of the risk of contamination.
Whether the specimen is collected by the nurse or others, the nurse is responsible for making certain that specimens, such as serial examinations and fasting specimens, are collected on time and the proper equipment is available. Collecting, transporting, and storing specimens can have a major impact on laboratory results.
Venous blood samples can be obtained by venipuncture or by aspiration from a peripheral or central access device (see Evidence-Based Practice box). Withdrawing blood specimens through peripheral lock devices in small peripheral veins has met with varying degrees of success. Although it avoids an additional venipuncture for the child, attempting to aspirate blood from the peripheral lock may shorten the life of the device. When using an IV infusion site for specimen collection, consider the type of fluid being infused. For example, a specimen collected for glucose level would be inaccurate if removed from a catheter through which glucose-containing solution was being administered.
Arterial blood samples are sometimes needed for blood gas measurement, although noninvasive techniques, such as transcutaneous oxygen monitoring and pulse oximetry, are used frequently. Arterial samples may be obtained by arterial puncture using the radial, brachial, or femoral arteries; by deep heel puncture; or from indwelling arterial catheters. Adequate circulation should be assessed before arterial puncture by observing capillary refill or performing the Allen test, a procedure that assesses the circulation of the radial, ulnar, or brachial arteries. Because unclotted blood is required, only heparinized collection tubes are used. In addition, no air bubbles should enter the tube, since they can alter blood gas concentration. Crying, fear, and agitation also affect blood gas values; therefore every effort is made to comfort the child. The nurse should pack the sample in ice to reduce blood cell metabolism and take it to the laboratory for immediate analysis.
Capillary blood samples are taken from children by a finger stick. A common method for taking peripheral blood samples from infants younger than 6 months of age is by a heel stick. Before the blood sample is taken, the heel is warmed for 3 minutes. The area is cleansed with alcohol, the infant’s foot firmly restrained with the free hand, and the heel punctured with an automatic lancet device (Clinical and Laboratory Standards Institute, 2006). An automatic device delivers a more precise puncture depth and is less painful than using a lance (Vertanen, Fellman, Brommels, and others, 2001). A surgical blade of any kind is contraindicated. An example of a safe device is the BD Quickheel Safety Lancet. The Tenderfoot Preemie device was compared with the Monolet lancet and was found to be safer than the lancet and required fewer heel punctures, less collection time, and lower recollection rates (Kellam, Sacks, Wailer, and others, 2001). Shepherd, Glenesk, Niven, and others (2006) reported the Tenderfoot device was more effective and safer than a lancet for newborn screening tests. Although obtaining capillary blood gases is a common practice, these measures may not accurately reflect arterial values.
The most serious complications of infant heel puncture are necrotizing osteochondritis from lancet penetration of the underlying calcaneus bone, infection, or abscess (Meehan, 1998). To avoid osteochondritis, the puncture should be no deeper than 2 mm and should be made at the outer aspect of the heel. The boundaries of the calcaneus can be marked by an imaginary line extending posteriorly from a point between the fourth and fifth toes and running parallel to the lateral aspect of the heel and another line extending posteriorly from the middle of the great toe and running parallel to the medial aspect of the heel (Fig. 22-11). Repeated trauma to the walking surface of the heel can cause fibrosis and scarring that may interfere with locomotion.
The specimens are quickly collected, and pressure is applied to the puncture site with dry gauze until bleeding stops. The arm is kept extended, not flexed, while pressure is applied for a few minutes after venipuncture in the antecubital fossa to reduce bruising. The site is covered with an adhesive bandage. In young children, adhesive bandages pose an aspiration hazard; they should be avoided or removed as soon as the bleeding stops. Applying warm compresses to ecchymotic areas increases circulation, helps remove extravasated blood, and decreases pain.
No matter how or by whom the specimen is collected, children, even some older ones, fear the loss of their blood. This is particularly true for children whose condition requires frequent blood specimens. They mistakenly believe that blood removed from their bodies is a threat to their lives. Explaining to them that their body is continuously producing blood provides them with a measure of reassurance. When the blood is drawn, a comment such as “Just look how red it is. You–re really making a lot of nice red blood,” confirms this information and affords them an opportunity to express their concern. An adhesive bandage gives them added reassurance that the vital fluids will not leak out.
Children also dislike the discomfort associated with venous, arterial, or capillary punctures. Children have identified these procedures as the ones most frequently causing pain during hospitalization and arterial punctures as being one of the most painful of all procedures experienced (Van Cleve, Johnson, and Pothier, 1996). The ones most distressed by venipunctures are toddlers, followed by school-age children and then adolescents. Consequently nurses need to institute pain reduction techniques to lessen the discomfort of these procedures (see Atraumatic Care box).
Collection of sputum or nasal discharge is sometimes required for diagnosis of respiratory infections, especially tuberculosis and respiratory syncytial virus (RSV). Older children and adolescents are able to cough and supply sputum specimens when given proper directions. It must be made clear to them that a coughed specimen, not mucus that is cleared from the throat, is needed. It is helpful to demonstrate a deep cough. Infants and small children are unable to follow directions to cough and will swallow any sputum produced; therefore gastric washings (lavage) may be used to collect a sputum specimen. Sometimes a satisfactory specimen can be obtained using a suction device such as a mucus trap if the catheter is inserted into the trachea and the cough reflex is elicited. A catheter inserted into the back of the throat is not sufficient. For children with a tracheostomy, a specimen is easily aspirated from the trachea or major bronchi by attaching a collecting device to the suction apparatus.
Nasal washings are usually obtained to diagnose an infection of RSV. The child is placed supine, and 1 to 3 ml sterile normal saline is instilled with a sterile syringe (without needle) into one nostril. The contents are aspirated using a small, sterile bulb syringe and are placed in a sterile container. Another method uses a syringe with 5 cm (2 inches) of 18- to 20-gauge tubing. The saline is quickly instilled and then aspirated to recover the nasal specimen. To prevent additional discomfort, all of the equipment should be ready before beginning the procedure.
Other respiratory secretion collection methods include nasopharyngeal swabs to diagnose Bordetella pertussis and throat cultures. The nurse swabs both the tonsils and the posterior pharynx when obtaining a throat culture. The swab stick is inserted into the culture tube. Some culture kits require squeezing an ampule to release the culture medium.
Nurses must have an understanding of the safe dosage of medications they administer to children, as well as the expected action, possible side effects, and signs of toxicity (Kennedy, 1996). Unlike with adult medications, there are few standardized pediatric dosage ranges, and with a few exceptions, drugs are prepared and packaged in average adult-dosage strengths.
Factors related to growth and maturation significantly alter an individual’s capacity to metabolize and excrete drugs. Immaturity or defects in any of the important processes of absorption, distribution, biotransformation, or excretion can significantly alter the effects of a drug. Newborn and preterm infants with immature enzyme systems in the liver (where most drugs are broken down and detoxified), lower plasma concentrations of protein for binding with drugs, and immaturely functioning kidneys (where most drugs are excreted) are particularly vulnerable to the harmful effects of drugs. Beyond the newborn period, many drugs are metabolized more rapidly by the liver, necessitating larger doses or more frequent administration. This is particularly important in pain control, since the dosage of analgesics may need to be increased or the interval between doses decreased.
Various formulas involving age, weight, and body surface area as the basis for calculations have been devised to determine children’s drug dosage. Because the administration of medication is a nursing responsibility, nurses need knowledge of not only drug action and patient responses, but also some resources for estimating safe dosages for children. The method most often used to determine children’s dosage is based on a specific dose per kilogram of body weight, such as 0.1 mg/kg.
The most reliable method for determining children’s dosage is to calculate the proportional amount of body surface area (BSA) to body weight. The ratio of BSA to weight varies inversely with length; therefore the infant who is shorter and weighs less than an older child or adult has relatively more surface area than would be expected from the weight. The usual determination of BSA requires the use of the West nomogram or an electronic calculator (widely available on the internet). The BSA is estimated from the height and weight of the child.
Administering the correct dosage of a drug is a shared responsibility between the practitioner who orders the drug and the nurse who carries out that order. Children react with unexpected severity to some drugs, and ill children are especially sensitive to drugs. When a dose is ordered that is outside the usual range or when there is some question regarding the preparation or the route of administration, the nurse should always check with the prescribing practitioner before proceeding with the administration, since the nurse is legally liable for any drug administered.
Even when it has been determined that the dosage is correct for a particular child, many drugs are potentially hazardous or lethal. Most facilities have regulations requiring specified drugs to be double-checked by another nurse before they are given to the child. Among drugs that require such safeguards are antiarrhythmics, anticoagulants, chemotherapeutic agents, electrolytes, and insulin. Others frequently included are epinephrine, opioids, and sedatives. Even if this precaution is not mandatory, nurses are wise to take such precautions. Errors in decimal point placement may occur and result in a tenfold or greater dosage error.
The oral route is preferred for administering medications to children because of the ease of administration. Most are dissolved or suspended in liquid preparations. Although some children are able to swallow or chew solid medications at an early age, solid preparations are not recommended for young children because of the danger of aspiration.
Most pediatric medications come in palatable and colorful preparations for ease of administration. Some have a slightly unpleasant aftertaste, but most children will swallow these liquids with little if any resistance. The nurse can taste a minute amount of an oral preparation to ascertain whether it is palatable or bitter. Complaints of dislike from the child can be accepted and the taste camouflaged whenever possible. Most pediatric units have preparations available for this purpose (see Atraumatic Care box).
The devices available to measure medicines are not always sufficiently accurate for measuring the small amounts needed in pediatric nursing practice. Although molded plastic calibrated cups offer reasonable accuracy in measuring moderate doses of liquids, paper cups are likely to have irregular shapes or crumpled bottoms. Considerable amounts of thick medication may remain in the cup. Measures of less than a teaspoon are impossible to determine accurately with a cup.
The teaspoon is an inaccurate measuring device and is subject to error. Teaspoons vary greatly in capacity, and different persons using the same spoon will pour different amounts. Therefore a drug ordered in teaspoons should be measured in milliliters; the established standard is 5 ml per teaspoon. A convenient hollow-handled medicine spoon is available to accurately measure and administer the drug. Household measuring spoons can also be used when other devices are not available. A device called the Medibottle has been shown to be more effective in delivering oral medication to infants than the oral syringe (Kraus, Stohlmeyer, Hannon, and others, 2001).
Another unreliable device for measuring liquids is the dropper, which varies to a greater extent than the teaspoon or measuring cup. Droppers are available in numerous sizes, but even with the standard USP dropper, the volume of a drop will vary according to the viscosity (thickness) of the liquid measured; viscous fluids produce much larger drops than thin liquids. Many medications are supplied with caps or droppers designed for measuring each specific preparation. These are accurate when used to measure that specific medication but are not reliable for measuring other liquids. Emptying dropper contents into a medicine cup invites additional error. Because some of the liquid clings to the sides of the cup, a significant amount of the drug can be lost.
The most accurate means for measuring small amounts of medication is the plastic disposable syringe, especially the tuberculin syringe for volumes less than 1 ml. Not only does the syringe provide a reliable measure, but it also serves as a convenient means for transporting and administering the medication. The medication can be placed directly into the child’s mouth from the syringe.
Young children and some older children have difficulty swallowing tablets or pills. Because a number of drugs are not available in pediatric preparations, the tablet needs to be crushed before it can be given to these children. Commercial devices* are available, or simple methods can be employed for crushing tablets. Not all drugs can be crushed (e.g., medication with an enteric or protective coating or formulated for slow release).
Children who must take oral medication for an extended period can be taught to swallow tablets or capsules. Training sessions include using verbal instruction, demonstration, reinforcement for swallowing progressively larger candy or capsules, no attention for inappropriate behavior, and gradual withdrawal of guidance once children can swallow their medication.
Because pediatric doses often require dividing adult preparations of medication, the nurse may be faced with the dilemma of accurate dosage. With tablets, only those that are scored can be halved or quartered accurately. If the medication is soluble, the tablet or contents of a capsule can be mixed in a small, premeasured amount of liquid and the appropriate portion given. For example, if half a dose is required, the tablet is dissolved in 5 ml water or flavored liquid and 2.5 ml is given.
Although administering liquids to infants is relatively easy, the nurse must be careful to prevent aspiration. With the infant held in a semireclining position, the medication is placed in the mouth from a spoon, plastic cup, dropper, or syringe (without needle). The dropper or syringe is best placed along the side of the infant’s tongue, and the liquid is administered slowly in small amounts, allowing the child to swallow between deposits.
Medicine cups can be used effectively for older infants who are able to drink from a cup. Because of the natural outward tongue thrust in infancy, medications may need to be retrieved from the lips or chin and refed. Allowing the infant to suck medication that has been placed in an empty nipple or inserting the syringe or dropper into the side of the mouth, parallel to the nipple, while the infant nurses are other convenient methods for giving liquid medications to infants. Medication is not added to the infant’s formula feeding because the child may subsequently refuse the formula. Dispose of any plastic covers that may be on the ends of syringes. These covers are small enough to be aspirated by young children.
The young child who refuses to cooperate or resists consistently despite explanation and encouragement may require mild physical coercion. If so, it is carried out quickly and carefully. Every effort is made to determine why the child resists, and the reasons for the coercion are explained to the child in such a way that the child will know that it is being carried out for his or her well-being and is not a form of punishment. There is always a risk in using even mild forceful techniques. A crying child can aspirate a medication, particularly when lying on the back. If the nurse holds the child in the lap with the child’s right arm behind the nurse, the left hand firmly grasped by the nurse’s left hand, and the head securely restrained between the nurse’s arm and body, the medication can be slowly poured into the mouth (Fig. 22-12).
Selecting the Syringe and Needle
The volume of medication prescribed for small children and the small amount of tissue available for injection require that a syringe be selected that can measure small amounts of solution. For volumes of less than 1 ml, the tuberculin syringe, calibrated in one-hundredth-milliliter increments, is appropriate. Minute doses may require the use of a 0.5-ml, low-dose syringe. These syringes, along with specially constructed needles, minimize the possibility of inadvertently administering incorrect amounts of a drug because of dead space, which allows fluid to remain in the syringe and needle after the plunger is pushed completely forward. A minimum of 0.2 ml solution remains in a standard needle hub; therefore, when very small amounts of two drugs are combined in the syringe, such as mixtures of insulin, the ratio of the two drugs can be altered significantly. Measures that minimize the effect of dead space are:
When two drugs are combined in the syringe, always draw them up in the same order to maintain a consistent ratio between the drugs.
Use the same brand of syringe (dead space may vary between brands).
Use one-piece syringe units (needle permanently attached to the syringe).
Dead space is also an important factor to consider when injecting medication, since flushing the syringe with an air bubble adds an additional amount of medication to the prescribed dose. This can be hazardous when very small amounts of a drug are given. Consequently, flushing is not advisable, especially when less than 1 ml of medication is given. Syringes are calibrated to deliver a prescribed drug dose, and the amount of medication left in the hub and needle is not part of the syringe barrel calibrations. Certain drugs such as iron dextran and diphtheria and tetanus toxoid may cause irritation when tracked into the subcutaneous tissue. The Z-track method is recommended for use in infants and children rather than an air bubble. Changing the needle after withdrawing the fluid from the vial is another technique to minimize tracking.
The needle length must be sufficient to penetrate the subcutaneous tissue and deposit the medication into the body of the muscle. The needle gauge should be as small as possible to deliver fluid safely. Smaller-diameter (25- to 30-gauge) needles cause the least discomfort, but larger diameters are needed for viscous medication and prevention of accidental bending of longer needles (Table 22-4).
Older children and adolescents usually pose few problems in selecting a suitable site for IM injections, but infants, with their small and underdeveloped muscles, have fewer available sites. It is sometimes difficult to assess the amount of fluid that can be safely injected into a single site. Usually 1 ml is the maximum volume that should be administered in a single site to small children and older infants. The muscles of small infants may not tolerate more than 0.5 ml. As the child approaches adult size, volumes approaching those given to adults may be used. However, the larger the amount of solution, the larger the muscle must be into which it is injected.
Major nerves and blood vessels must be avoided. The preferred site for infants is the vastus lateralis (the rectus femoris is not an acceptable site). The ventrogluteal site is relatively free of major nerves and blood vessels, is a relatively large muscle with less subcutaneous tissue than the dorsal site, has well-defined landmarks for safe site location, is less painful than the vastus lateralis, and is easily accessible in several positions. Cook and Murtagh’s (2006) research into IM injection sites in children indicates that the ventrogluteal site has not been associated with complications and is the preferred site in children of all ages (see Table 22-4). In clinical practice, this site has been safely used in children as young as newborns. The deltoid muscle, a small muscle near the axillary and radial nerves, can be used for small volumes of fluid in children as young as 18 months of age. Its advantages are less pain and fewer side effects from the injectate (as observed with immunizations), compared with the vastus lateralis (Ipp, Gold, Goldback, and others, 1989). Table 22-4 summarizes the three major injection sites and illustrates the location of the preferred IM injection sites for children.
Although injections that are executed with care seldom cause trauma to the child, there have been reports of serious disability related to IM injections in children. Repeated use of a single site has been associated with fibrosis of the muscle with subsequent muscle contracture. Injections close to large nerves, such as the sciatic nerve, have been responsible for permanent disability, especially when potentially neurotoxic drugs are administered. There are several reports of tissue damage from penicillin. One of the difficulties in administering the opaque preparations, such as penicillin G (Bicillin), is that aspirated blood cannot be detected at the bottom of the syringe, thus increasing the risk of injecting into a blood vessel. When such drugs are injected, great care must be used in locating the correct site. When aspirating, the nurse should look for blood at the top of the syringe near the plunger, since blood may be drawn up through the column of penicillin. One study of IM injection techniques revealed that the straighter the path of needle insertion (e.g., 90-degree angle), the less displacement and shear to tissue, causing less discomfort (Katsma and Smith, 1997).
A reported potential hazard with medication in glass ampules is the presence of glass particles in the ampule after the container is broken. When the medication is withdrawn into the syringe, the glass particles may also be withdrawn and subsequently injected into the patient. As a precaution, medication from glass ampules should be drawn up only through a needle with a filter or injected intravenously through a site in the tubing that is distal to an IV filter.
Most children are unpredictable and few are totally cooperative when receiving an injection. Even children who appear to be relaxed and constrained can lose control under the stress of the procedure. It is advisable to have someone available to help hold the child if needed. Because children often jerk or pull away unexpectedly, the nurse should carry an extra needle to exchange for a contaminated one so that the delay is minimal. The child, even a small one, is told that he or she is receiving an injection (preferably using a phrase such as “putting medicine under the skin”), and then the procedure is carried out as quickly and skillfully as possible to avoid prolonging the stressful experience. Invasive procedures such as injections are especially anxiety provoking in young children, who may associate any assault to the “behind” area with punishment. Because injections are painful, the nurse should employ excellent injection technique and effective pain reduction measures to reduce discomfort (see Nursing Care Guidelines box).
Small infants offer little resistance to injections. Although they squirm and may be difficult to hold in position, they can usually be restrained without assistance. The body of a larger infant can be securely held between the nurse’s arm and body (Fig. 22-13). To inject into the body of the muscle, the nurse firmly grasps the muscle mass between the thumb and fingers to isolate and stabilize the site. In obese children, however, it is preferable to first spread the skin with the thumb and index finger to displace subcutaneous tissue and then grasp the muscle deeply on each side.
FIG. 22-13 Holding small child for intramuscular injection. Note how nurse isolates and stabilizes muscle.
If the medication is given around the clock, the nurse must wake the child. Although it may seem to be easier to surprise the sleeping child and do it quickly, this can cause the child to fear going back to sleep. When awakened first, children know that nothing will be done unless they are forewarned. See Nursing Care Guidelines box for techniques that maximize safety and minimize discomfort.
A needless injection system delivers IM or subcutaneous injections without the use of a needle and eliminates the risk of accidental needle puncture. This needle-free injection system involves a carbon dioxide cartridge that provides the power to deliver the medication through the skin. Although it is not painless, it may reduce pain and also the anxiety of seeing the needle (Polillio and Killy, 1997).
Subcutaneous and intradermal injections are frequently administered to children, but the technique differs little from the method used with adults. Examples of subcutaneous injections include insulin, hormone replacement, allergy desensitization, and some vaccines. Tuberculin testing, local anesthesia, and allergy testing are examples of frequently administered intradermal injections (see Evidence-Based Practice box).
Techniques to minimize the pain associated with these injections include changing the needle if it pierced a rubber stopper on a vial, using 26- to 30-gauge needles (only to inject the solution), and injecting small volumes (up to 0.5 ml). The angle of the needle for the subcutaneous injection is typically 90 degrees. In children with little subcutaneous tissue, some practitioners insert the needle at a 45-degree angle. However, the benefit of using the 45-degree angle rather than the 90-degree angle remains controversial.
Although subcutaneous injections can be given anywhere there is subcutaneous tissue, common sites include the center third of the lateral aspect of the upper arm, the abdomen, and the center third of the anterior thigh. Some practitioners believe it is not necessary to aspirate before injecting subcutaneously; for example, this is an accepted practice in the administration of insulin. Automatic injector devices do not aspirate before injecting.
When giving an intradermal injection into the volar surface of the forearm, the nurse should avoid the medial side of the arm, where the skin is more sensitive.
The IV route for administering medications is frequently used in pediatric therapy. For some drugs it is the only effective route. This method is used for giving drugs to children who have poor absorption as a result of diarrhea, dehydration, or peripheral vascular collapse; who need a high serum concentration of a drug; who have resistant infections that require parenteral medication over an extended time; who need continuous pain relief; and who require emergency treatment.
Insertion sites and observation of the IV infusion are discussed on p. 733. Several factors need to be considered in relation to IV medication. When a drug is administered intravenously, the effect is almost instantaneous and further control is limited. Most drugs for IV administration require a specified minimum dilution and/or rate of flow, and many are highly irritating or toxic to tissues outside the vascular system. In addition to the precautions and nursing observations related to IV therapy, factors to consider when preparing and administering drugs to infants and children by the IV route include:
Amount of drug to be administered
Minimum dilution of drug and whether child is fluid restricted
Type of solution in which drug can be diluted
Length of time over which drug can be safely administered
Rate of infusion that child and vessels can tolerate safely
Time that this or another drug is to be administered
Compatibility of all drugs that child is receiving intravenously
Before any IV infusion, the site of insertion is checked for patency. Medications are never administered with blood products. Only one antibiotic should be administered at a time.
IV infusion is suitable for children who can tolerate the necessary infusion rate and the extra fluid needed to administer the medication. For the very small infant or fluid-restricted child who is not able to tolerate the increased rate of fluids, special delivery systems, such as syringe pumps, are used. Regardless of the technique, the nurse must know the minimum dilutions for safe administration of IV medications to infants and children.
The peripheral lock, also known as an intermittent infusion device or saline or heparin lock, is an alternative to a keep-open infusion when extended access to a vein is required without the need for continuous fluid. It is most frequently employed for intermittent infusion of medication into a peripheral venous route. A short, flexible catheter is used as the lock device, and a site is selected where there will be minimal movement, such as the forearm. The catheter is inserted and secured in the same manner as for any IV infusion device, but the hub is occluded with a stopper or injection cap.
The type of device used may vary, and the care and use of the peripheral lock are carried out according to the protocol of the institution or unit. However, the general concept is the same. The catheter remains in place and is flushed with saline after infusion of the medication. See the Evidence-Based Practice box on flushing with normal saline or heparin.
Children may be discharged with a peripheral lock in place to continue receiving medications without hospitalization; this is usually reserved for children who require medications on a short-term basis and are referred to a home-based infusion company. Those with chronic illnesses who require repeated blood sampling or medications, long-term chemotherapy, or frequent hyperalimentation or antibiotic therapy are best managed with a central venous catheter.
Central venous access devices (VADs) have several different characteristics. Factors that can influence the type of VAD include the reason for placement of the catheter (diagnosis), length of therapy, risk to the patient in placement of the catheter, and availability of resources to assist the family in maintaining the catheter.
Short-term or nontunneled catheters are used in acute care, emergency, and intensive care units. These catheters are made of polyurethane and are placed in large veins such as the subclavian, femoral, or jugular. Insertion is by surgical incision or large percutaneous threading. A chest x-ray film should be taken to verify placement of the catheter tip before administration of fluids or medications.
Peripherally inserted central catheters (PICCs) can be used for short-term to moderate-length therapy. These catheters consist of silicone or polymer material and are placed by specially trained nurses, physicians, or interventional radiologists (Gamulka, Mendoza, and Connolly, 2005). The most common insertion site is above the antecubital area using the median, cephalic, or basilic vein. The catheter is threaded either with or without a guidewire into the superior vena cava. PICCs can be trimmed before insertion, and the decision can be made to insert the catheter midline, which is considered between the insertion site and the axilla. The midline has a dwell time of 2 to 4 weeks. If the catheter is threaded midline, total parenteral nutrition (TPN) or any other drug known to irritate a peripheral vein (e.g., chemotherapy drugs) should not be administered. The high concentration of glucose in TPN makes it irritating to the vessel; it should be infused through a central catheter.
The decision to insert a PICC needs to be made before several attempts at IV insertion are done. Once the antecubital veins have been punctured repeatedly, they are not considered candidates for this type of catheter. Because this catheter is the least costly and has less chance of complications than other central VADs, it is an excellent choice for many pediatric patients.
Long-term central VADs include tunneled catheters and implanted infusion ports (Table 22-5 and Fig. 22-14). They may have single, double, or triple lumens. Several lumens (multilumen) catheters allow more than one therapy to be administered at the same time. Reasons to use multilumen catheters include repeated blood sampling, TPN, administration of blood products or infusion of large quantities and/or concentrations of fluids, administration of incompatible drugs or fluids at the same time (through different lumens), and central venous pressure monitoring.
FIG. 22-14 Venous access devices. A, Blood being drawn from a central venous catheter. B, Child with external central venous catheter. C, Child with implanted port with Huber needle in place. D, Side view of implanted port.
With any of the central venous catheters, medication is easily instilled through the injection cap. Maintenance of the catheter includes dressing changes, flushing to maintain patency, and prevention of occlusion or dislodgment.
With the implanted device the port must be palpated for placement and stabilized, the overlying skin cleansed, and only special noncoring Huber needles used to pierce the port’s diaphragm on the top or side, depending on the style. To avoid repeated skin punctures, a special infusion set with a Huber needle and extension tubing with a Luer connection can be used (see Fig. 22-14). With this attached, the injection procedure is the same as for an intermittent infusion device or a central venous catheter. To prevent infection, meticulous aseptic technique must be used any time the devices are entered, including instillation of heparin or saline to prevent clotting (Harris and Maguire, 1999). There should be a protocol stating that the Huber needle needs to be changed at established intervals, usually 5 to 7 days.
The children and parents are taught the procedure for care of the VAD before discharge from the hospital, including preparation and injection of the prescribed medication, the flush, and dressing changes. A protective device may be recommended for some active children to prevent their accidentally dislodging the needle. Many children take responsibility for preparing and administering medications. Both verbal and written step-by-step instructions are provided for the learners (Table 22-6). See the Evidence-Based Practice box for VAD site care.
TABLE 22-6
PICC, Peripherally inserted central catheter; TPN, total parenteral nutrition.
*Patients < 6 months of age: 10 units/ml 5 ml every month or 10 units/ml 5 ml every day if accessed.
Modified from Texas Children’s Hospital, Houston.
Infection and catheter occlusion are two of the most common complications of central venous catheters. They require treatment with antibiotics for infection and a fibrinolytic agent, such as alteplase, for clots (Fisher, Deffenbaugh, Poole, and others, 2004; Shen, Li, Murdock, and others, 2003). Uncapping can be prevented by taping the cap securely to the catheter and the clamped line to the dressing. Leaks can be prevented by using a smooth-edged clamp only. Parents are cautioned to keep scissors away from the child to prevent accidental cutting of the catheter. If the catheter leaks, they are instructed to tape it above the leak and then clamp the catheter at the taped site. The child should be taken to the practitioner as soon as possible to prevent infection or clotting after a catheter leak.
When a child has an indwelling feeding tube or a gastrostomy, oral medications are usually given via that route. An advantage of this method is the ability to administer oral medications around the clock without disturbing the child. A disadvantage is the risk of occluding or clogging the tube, especially when giving viscous solutions through small-bore feeding tubes. The most important preventive measure is adequate flushing after the medication is instilled (see Nursing Care Guidelines box).
The rectal route for administration is less reliable but is sometimes used when the oral route is difficult or contraindicated. It is also used when oral preparations are unsuitable to control vomiting. Some of the drugs available in suppository form are acetaminophen, sedatives, analgesics (morphine), and antiemetics. The difficulty in using the rectal route is that, unless the rectum is empty at the time of insertion, the absorption of the drug may be delayed, diminished, or prevented by the presence of feces. Sometimes the drug is later evacuated, securely surrounded by stool.
The wrapping on the suppository is removed and the suppository lubricated with water-soluble jelly or warm water. Rectal suppositories are traditionally inserted with the apex (pointed end) foremost. Reverse contractions or the pressure gradient of the anal canal may help the suppository slip higher into the canal. Using a glove or finger cot, quickly but gently insert the suppository into the rectum, beyond both of the rectal sphincters. The buttocks are then held together firmly to relieve pressure on the anal sphincter until the urge to expel the suppository has passed—5 to 10 minutes. Sometimes the amount of drug ordered is less than the dosage available. The irregular shape of most suppositories makes the process of dividing them into a desired dose difficult if not dangerous. If the suppository must be halved, it should be cut lengthwise. However, there is no guarantee that the drug is evenly dispersed throughout the petrolatum base.
If medication is administered via a retention enema, the same procedure is used. Drugs given by enema are diluted in the smallest amount of solution possible to minimize the likelihood of being evacuated.
There are few differences between administering eye, ear, and nose medication to children and to adults. The major difficulty is in gaining children’s cooperation. Older children need only explanation and direction. Although the administration of optic, otic, and nasal medication is not painful, these drugs can cause unpleasant sensations that can be eliminated with various techniques.
To instill eye medication, the child is placed supine or sitting with the head extended, and the child is asked to look up. One hand is used to pull the lower lid downward; the hand that holds the dropper rests on the head so that it may move synchronously with the child’s head, thus reducing the possibility of trauma to a struggling child or of dropping medication on the face (Fig. 22-15). As the lower lid is pulled down, a small conjunctival sac is formed; the solution or ointment is applied to this area, never directly on the eyeball. Another effective technique is to pull the lower lid down and out to form a cup effect, into which the medication is dropped. The lids are gently closed to prevent expression of the medication, and the child is asked to look in all directions to enhance even distribution of the preparation. Excess medication is wiped from the inner canthus outward to prevent contamination to the contralateral eye.
Instilling eye drops in infants can be difficult, since they often clench the lids tightly closed. One approach is to place the drops in the nasal corner where the lids meet. The medication pools in this area, and when the infant opens the lids, the medication flows onto the conjunctiva. For young children, playing a game can be helpful, such as instructing the child to keep the eyes closed until the count of 3 and then open them, at which time the drops are quickly instilled. Ointment can be applied by gently pulling down the lower lid and placing the ointment in the lower conjunctival sac.
Ear drops are instilled with the child in the prone or supine position and the head turned to the appropriate side. For children younger than 3 years of age, the external auditory canal is straightened by gently pulling the pinna downward and straight back. The pinna is pulled upward and back in children older than 3 years of age. To place the drops deep in the ear canal without contaminating the tip of the dropper, place a disposable ear speculum in the canal and administer the drops through the speculum. After instillation, the child should remain lying on the unaffected side for a few minutes. Gentle massage of the area immediately anterior to the ear facilitates the entry of drops into the ear canal. The use of cotton pledgets prevents medication from flowing out of the external canal. However, the pledgets should be loose enough to allow any discharge to exit from the ear. Premoistening thecotton with a few drops of medication prevents the wicking action from absorbing the medication instilled in the ear.
Nose drops are instilled in the same manner as in the adult patient. Unpleasant sensations associated with medicated nose drops are minimized when care is taken to position the child with the head extended well over the edge of the bed or a pillow (Fig. 22-16). Depending on size, the infant can be positioned in the football hold (see Fig. 22-5, B); in the nurse’s arm with the head extended and stabilized between the nurse’s body and elbow, and the arms and hands immobilized with the nurse’s hands; or as shown in Fig. 22-16. After instillation of the drops, the child should remain in position for 1 minute to allow the drops to come in contact with the nasal surfaces.
Nasal spray dispensers are inserted into the naris vertically and then angled nasally to avoid trauma to the septum and to direct medication toward the inferior turbinate.
The nurse usually assumes the responsibility for preparing families to administer medications at home. The family should understand why the child is receiving the medication and the effects that might be expected, as well as the amount, frequency, and length of time the drug is to be administered. Instruction should be carried out in an unhurried, relaxed manner, preferably in an area away from a busy ward or office, following the same guidelines for teaching as outlined in the Nursing Care Guidelines box (p. 699).
The caregiver is carefully instructed regarding the correct dosage. Some persons have difficulty understanding medical terminology from the pharmacy; just because they nod or otherwise indicate an understanding, it cannot be assumed that the message is clear. It is important to ascertain their interpretation of a teaspoon, for example, and to be certain they have acceptable devices for measuring the drug. If the drug is packaged with a dropper, syringe, or plastic cup, the nurse should show or mark the point on the device that indicates the prescribed dose and demonstrate how the dose is drawn up into a dropper or syringe, measured, and the bubbles eliminated. If the nurse has any doubts about the parent’s ability to administer the correct dose, the parent should be asked to give a return demonstration. This is essential when the drug has potentially serious consequences from incorrect dosage, such as insulin or digoxin, or when more complex administration is required, such as parenteral injections. When teaching a parent to give an injection, the nurse must allot adequate time for instruction and practice.
Home modifications are often necessary because the availability of equipment or assistance can differ from the hospital setting. For example, the parent may need guidance in devising methods that allow for one person to hold the child and safely give the drug.
The time that the drug is to be administered is clarified with the parent. For instance, when a drug is prescribed in association with meals, the number of meals that the family is accustomed to eating influences the amount of drug the child receives. Does the child have meals twice a day or five times a day? When a drug is to be given several times during the day, together the nurse and parents can work out a schedule that accommodates the family’s routine. This is particularly significant if the drug must be given at equal intervals throughout a 24-hour period. For example, telling parents that the child needs 1 teaspoon of medicine four times a day is subject to misinterpretation, since parents may routinely schedule the doses at incorrect times. Instead, a preplanned schedule based on 6-hour intervals should be set up with the number of days required for therapeutic dosage listed. Modification should also be made to accommodate sleep schedules. Written instruction should accompany all drug prescriptions.
MEASUREMENT OF INTAKE AND OUTPUT
Accurate measurements of fluid intake and output (I&O) are essential to the assessment of fluid balance. Measurements from all sources—including gastrointestinal and parenteral I&O from urine, stools, vomitus, fistulas, nasogastric suction, sweat, and drainage from wounds—must be taken and considered. Although the practitioner usually indicates when I&O measurements are to be recorded, it is a nursing responsibility to keep an accurate I&O record on certain children, including those:
Infants or small children who are unable to use a bedpan or those who have bowel movements with every voiding require the application of a collecting device (p. 711). If collecting bags are not used, wet diapers or pads are carefully weighed to ascertain the amount of fluid lost. This includes liquid stool, vomitus, and other losses. The volume of fluid in milliliters is equivalent to the weight of the fluid measured in grams. The specific gravity as a measure of osmolality is determined with a refractometer or urine dipsticks and assists in assessing the degree of hydration (see FYI, p. 712).
Disadvantages of the weighed-diaper method of fluid measurement include (1) inability to differentiate one type of loss from another because of admixture, (2) loss of urine or liquid stool from leakage or evaporation (especially if the infant is under a radiant warmer), and (3) additional fluid in the diaper (superabsorbent disposable type) from absorption of atmospheric moisture (in high-humidity incubators).
Infants or children who are unable or not permitted to take fluids by mouth (NPO) have special needs. To ensure that they do not receive fluids, a sign can be placed in some obvious place, such as over their beds or on their shirts, to alert others to the NPO status. To prevent the temptation to drink, fluids should not be left at the bedside.
Oral hygiene, a part of routine hygienic care, is especially important when fluids are restricted or withheld (p. 701). For the young child who cannot brush the teeth or rinse the mouth without swallowing fluid, the mouth and teeth can be cleaned and kept moist by swabbing with saline-moistened gauze.
The child who is fluid restricted presents an equal challenge. Limiting fluids is often more difficult for the child than being NPO, especially when IV fluids are also eliminated. To make certain the child does not drink the entire amount allowed early in the day, the daily allotment is calculated to provide fluids at periodic intervals throughout the child’s waking hours. Serving the fluids in small containers gives the illusion of larger servings. No extra liquid is left at the bedside.
The site selected for PIV infusion depends on accessibility and convenience. Although it is possible to use any accessible vein in older children, the child’s developmental, cognitive, and mobility needs must be considered when selecting a site. Ideally in older children, the superficial veins of the forearm should be used, leaving the hands free. An older child can help select the site and thereby maintain some measure of control. For veins in the extremities it is best to start with the most distal site and avoid the child’s favored hand to reduce the disability related to the procedure. Restrict the child’s movements as little as possible—avoid a site over a joint in an extremity, such as the antecubital space. In small infants a superficial vein of the hand, wrist, forearm, foot, or ankle is usually most convenient and most easily stabilized (Fig. 22-17). Foot veins should be avoided in children learning to walk and in children already walking. Superficial veins of the scalp have no valves, insertion is easy, and they can be used in infants up to about 9 months of age, but they should be used only when other site attempts have failed. A transilluminator (Fig. 22-18) can aid in finding and evaluating veins for access (see Evidence-Based Practice box).
FIG. 22-18 Transilluminator: low-heat light-emitting diode (LED) light placed on the skin to illuminate veins; an opening allows cannulation of vein.
Selection of a scalp vein may require clipping the area around the site to better visualize the vein and provide a smoother surface on which to tape the catheter hub and tubing. Clipping a portion of the infant’s hair is upsetting to parents; therefore they should be told what to expect and reassured that the hair will grow in again rapidly (save the hair because parents often wish to keep it). Remove as little as possible, directly over the insertion site and taping surface. A rubber band slipped onto the head from brow to occiput will usually suffice as a tourniquet, although if the vessel is visible, a tourniquet may not be necessary.
Situations may occur in which rapid establishment of systemic access is vital, and venous access may be hampered by peripheral circulatory collapse, hypovolemic shock (secondary to vomiting or diarrhea, burns, or trauma), cardiopulmonary arrest, or other conditions (Dubick and Holcomb, 2000). Intraosseous infusion provides a rapid, safe, and lifesaving alternate route for administration of fluids and medications until intravascular access can be attained, especially in children who are 6 years of age and younger.
A large-bore needle, such as a bone marrow aspiration needle (e.g., Jamshidi) or an intraosseous needle (e.g., Cook), is inserted into the medullary cavity of a long bone, most often the proximal tibia. This procedure is usually reserved for children who are unconscious or for those who are receiving analgesia, since the procedure is painful. Local anesthesia should be used for a semiconscious patient. Observe the dependent tissue closely for swelling, since extravasation may be hidden under the leg and compartment syndrome may result.
For most IV infusions in children, a 22- to 24-gauge catheter may be used if therapy is expected to last less than 5 days. The smallest-gauge and shortest-length catheter that will accommodate the prescribed therapy should be chosen. The length of the catheter may be directly related to infection and/or embolus formation—the shorter the catheter, the fewer the complications (Maki, 1994). The gauge of the catheter should maintain adequate flow of the infusate into the cannulated vein while allowing adequate blood flow around the catheter walls to promote proper hemodilution of the infusate.
Determining the best catheter for the patient early in the therapy provides the best chance of avoiding catheter-related complications (Moureau, 1999). As the length of therapy increases, decisions regarding the type of infusion device (short peripheral, midline, peripherally inserted central catheter, or central venous catheter) should be explored. Guidelines such as flow charts or algorithms are available to help in these decisions (Catudal, 1999).
Over-the-needle IV catheters with hollow-bore needles carry a high risk for transmission of blood-borne pathogens from needlestick injuries. Safety catheters prevent accidental needlesticks with the use of over-the-needle IV catheters.
Needleless IV systems are designed to prevent needlestick injuries during administration of IV push medications and IV piggyback medications. Some needleless devices can be used with any tubing, whereas others require use of the entire IV delivery system for compatibility. Needleless IV systems rely on prepierced septa that are accessed by blunted plastic cannulas or systems that use valves that open and close a fluid path when activated by insertion of a syringe.
Blunt plastic cannulas and preslit injection port sites (Fig. 22-19) eliminate the need for steel needles and conventional injection port sites but remain accessible via hypodermic needles, a drawback except in emergent situations. Systems that do not permit needled access enhance safety by preventing health care workers from attempting to use needles. A syringe with a blue spike is available to access a single-dose vial (Fig. 22-19, A). The preslit injection port sites are identified by a white ring surrounding the port; this ring alerts users that the system is needleless (Fig. 22-19, B). Syringes are available with the blunt plastic cannula for accessing these sites (Fig. 22-19, C). A lever lock (Fig. 22-19, D) or threaded lock cannula (Fig. 22-19, E) attaches to an IV line, IV Y site, or peripheral intermittent infusion device. A preslit universal vial adapter (not pictured) provides access to standard multiple-dose vials, and syringe cannulas are then used to access the adapter. Valve technology allows syringes and IV tubing to connect directly in-line without the use of an adapter.
A variety of infusion pumps are available and used in nearly all pediatric infusions to accurately administer medication and minimize the possibility of overloading the circulation. It is important to calculate the amount to be infused in a given length of time, set the infusion rate, and monitor the apparatus frequently (at least every 1 to 2 hours) to make certain that the desired rate is maintained, the integrity of the system remains intact, the site remains intact (free of redness, edema, infiltration, or irritation), and the infusion does not stop. Continuous infusion pumps, although convenient and efficient, are not without risks. Overreliance on the accuracy of the machine can cause either too much or too little fluid to be infused; therefore its use does not eliminate careful periodic assessment by the nurse. Excess pressure can build up if the machine is set at a rate faster than the vein is able to accommodate (or continues to pump when the needle is out of the lumen).
To maintain the integrity of the IV line, adequate protection of the site is required. The catheter hub is firmly secured at the puncture site with a transparent dressing and commercial securement device (e.g., StatLock) (Fig. 22-20) or clear, nonallergenic tape. Transparent dressings are ideal because the insertion site is easily observed. Minimal tape should be used at the puncture site and on about 1 to 2 inches of skin beyond the site to avoid obscuring the insertion site for early detection of infiltration.
FIG. 22-20 StatLock securement devices enhance peripheral intravenous line dwell time and decrease phlebitis.
A protective cover is applied directly over the catheter insertion site to protect the infusion site. Easy access to the IV site for frequent (1- to 2-hour) assessments must be considered. Improvised plastic cups that are cut in half with the ridged edges covered with tape should not be used, since they have injured patients. A commercial site protector, I.V. House, is available in different sizes (Fig. 22-21). Its ventilation holes prevent moisture from accumulating under the dome (Lee and Vallino, 1996). This device is designed to protect the IV site; allow for visibility of the site; minimize use of padded boards, splints, or other restraints and tape; and maintain skin integrity. The connector tubing or extension tubing can be looped to make it small enough to fit under the protective cover to prevent accidental snagging of the catheter. It is important to safely secure the IV tubing to prevent infants and children from becoming entangled in the tubing or from accidentally pulling the catheter or needle out. Securing the tubing in this manner also eliminates movement of the catheter hub at the insertion site (mechanical manipulation). A colorful and interesting sticker can be applied to the protecting device to add a positive note to the procedure.
Finger or toe areas are left unoccluded by dressings or tape to allow for assessment of circulation. The thumb is never immobilized because of the danger of contractures with limited movement later on. An extremity should never be encircled with tape. The use of roll gauze, self-adhering stretch bandages (Coban), and Ace bandages can cause the same constriction and hide signs of infiltration (Infusion Nurses Society, 2000a).
Traditionally, padded boards or splints have been used to partially immobilize the IV site. Padded boards or splints and restraints were appropriate when metal needles were inserted into the vein to prevent the sharp end from puncturing the vessel, especially at a joint. With the more recent use of soft, pliable catheters, arm or leg boards may not be necessary and have several disadvantages. They obscure the IV site, can constrict the extremity, may excoriate the underlying tissue and promote infection, can cause a contracture of a joint, restrict useful movement of the extremity, and are uncomfortable. Unfortunately, no research has been conducted to demonstrate their proposed benefit of increasing dwell time (patency of the IV line). Adequate securement should eliminate the need for padded boards in most circumstances. Older children who are alert and cooperative can usually be trusted to protect the IV site (see Evidence-Based Practice boxes).
When it comes time to discontinue an IV infusion, many children are distressed by the thought of catheter removal. Therefore they need a careful explanation of the process and suggestions for helping. Encouraging children to remove or help remove the tape from the site provides them with a measure of control and often fosters their cooperation. The procedure consists of turning off any pump apparatus, occluding the IV tubing, removing the tape, pulling the catheter out of the vessel in the opposite direction of insertion, and exerting firm pressure at the site. A dry dressing (adhesive bandage strip) is placed over the puncture site. The use of adhesive-removal pads can decrease the pain of tape removal, but the skin should be washed after use to avoid irritation. To remove transparent dressings (e.g., OpSite, Tegaderm), pull the opposing edges parallel to the skin to loosen the bond. Inspect the catheter tip to ensure the catheter is intact and that no portion remains in the vein.
The same precautions regarding maintenance of asepsis, prevention of infection, and observation for infiltration are carried out with patients of any age. However, infiltration is more difficult to detect in infants and small children than in adults. The increased amount of subcutaneous fat and the amount of tape used to secure the catheter often obscure the early signs of infiltration. When the fluid appears to be infusing too slowly or ceases, the usual assessment for obstruction within the apparatus—kinks, screw clamps, shutoff valve, and positioning interference (e.g., a bent elbow)—often locates the difficulty. When these actions fail to detect the problem, it may be necessary to carefully remove some of the dressing to obtain a clear view of the venipuncture site. Dependent areas, such as the palm and undersides of the extremity or the occiput and behind the ears, are examined.
Whenever possible, the IV infusion should be placed in an extremity to which the identification band (or bracelet) is not attached. Serious circulatory impairment can result from infiltrated solution distal to the band, which acts as a tourniquet, preventing adequate venous return. To check for return blood flow through the catheter, the tubing is removed from the infusion pump, and the bag is lowered below the level of the infusion site. Resistance during flushing or aspiration for blood return also indicates that the IV infusion may have infiltrated surrounding tissue. A good blood return, or lack thereof, is not always an indicator of infiltration in small infants. Flushing the catheter and observing for edema, redness, or streaking along the vein are appropriate for assessment of the IV.
IV therapy in pediatrics tends to be difficult to maintain because of mechanical factors such as vascular trauma resulting from the catheter, the insertion site, vessel size, vessel fragility, pump pressure, the patient’s activity level, operator skill and insertion technique, forceful administration of boluses of fluid, and infusion of irritants or vesicants through a small vessel (Pettit and Hughes, 1999). These factors cause infiltration and extravasation injuries. Infiltration is defined as inadvertent administration of a nonvesicant solution or medication into surrounding tissue. Extravasation is defined as inadvertent administration of vesicant solution or medication into surrounding tissue (Infusion Nurses Society, 2000a, 2000b). A vesicant or sclerosing agent causes varying degrees of cellular damage when even minute amounts escape into surrounding tissue. Guidelines are available for determining the severity of tissue injury by staging characteristics, such as the amount of redness, blanching, the amount of swelling, pain, the quality of pulses below infiltration, capillary refill, and warmth or coolness of the area (Infusion Nurses Society, 2000a, 2000b; Montgomery, Hanrahan, Korrman, and others, 1999).*
Treatment of infiltration or extravasation varies according to the type of vesicant. Guidelines are available outlining the sequence of interventions and specific treatment of infiltration or extravasation with antidotes (Oncology Nursing Society, 1998; Montgomery, Hanrahan, Korrman, and others, 1999).†
PIV catheters are the most commonly used intravascular device. Heavy cutaneous colonization of the insertion site is the single most important predictor of catheter-related infection with all types of short-term, percutaneously inserted catheters. Phlebitis, largely a mechanical rather than infectious process, remains the most important complication associated with the use of peripheral venous catheters.‡
Oxygen is administered for hypoxemia and may be delivered by mask, nasal cannula, tent, hood, face mask, or ventilator. Oxygen therapy is frequently administered in the hospital, although increasing numbers of children are receiving oxygen in the home. Oxygen delivered to infants is well tolerated by using a plastic hood (Fig. 22-22). The humidified oxygen should not be blown directly into the infant’s face. Older, cooperative infants and children can use a nasal cannula or prongs, which can supply a concentration of oxygen of about 50%. A mask is not well tolerated by children.
FIG. 22-22 Oxygen administered to infant by means of a plastic hood. Note oxygen analyzer (blue machine).
For children beyond early infancy, the oxygen tent is a satisfactory means for administration of oxygen (Fig. 22-23). A tent does not require any device to come into direct contact with the face, but the concentration of oxygen within the tent is difficult to control and to maintain above 30% to 50%. A major difficulty with the use of the tent is keeping the tent closed so that the oxygen concentration is maintained.
FIG. 22-23 The tent provides a comfortable method for oxygen administration. (From Wilson SF, Thompson JM: Respiratory disorders, St Louis, 1990, Mosby.)
To reduce oxygen loss, nursing care is planned carefully so that the tent is opened as little as possible. Because oxygen is heavier than air, loss will be greater at the bottom of the tent; therefore the tent is tucked in snugly without open edges. The bottom of the tent should be examined more often when the child is restless and fussy and liable to pull the covers loose. Some tents are even open at the top. Because of the rapidly diffusing qualities of carbon dioxide, the levels of the gas do not build up within these enclosures.
After the tent has been opened for an extended period, it is flushed with oxygen by increasing the flow meter for a few minutes to quickly raise the oxygen and mist concentration. The flow meter is then reset to the prescribed number of liters per minute.
The enclosed tent becomes warm; therefore some type of cooling mechanism is provided. The temperature inside the tent must be checked periodically to be certain that it is maintained at the desired level. Although the cool environment can reduce fever and airway inflammation, it can also produce hypothermia and cold stress. It is important to make certain that the child is kept warm and dry. Because oxygen is drying to the tissues, the gas is humidified, which causes moisture to condense on the tent walls.
In some instances the child can be removed from the oxygen tent for activities such as feeding and bathing, whereas in other cases the child is placed in the tent only during periods of rest. Still other children may require oxygen continuously and can be removed from the tent or incubator only if an oxygen source is held close to the child’s face. Any change in color, increased respiratory effort, or restlessness is an indication to return the child to the oxygen tent.
Oxygen Toxicity.: Prolonged exposure to high oxygen tensions can damage some body tissues and functions. The organs most vulnerable to the adverse effects of excessive oxygenation are the retina of the extremely preterm infant and the lungs of persons at any age.
Oxygen-induced carbon dioxide narcosis is a physiologic hazard of oxygen therapy that may occur in persons with chronic pulmonary disease, such as cystic fibrosis. In these patients the respiratory center has adapted to the continuously higher arterial carbon dioxide tension (Paco2) levels, and therefore hypoxia becomes the more powerful stimulus for respiration. When the arterial oxygen tension (Pao2) level is elevated during oxygen administration, the hypoxic drive is removed, causing progressive hypoventilation and increased Paco2 levels, and the child rapidly becomes unconscious. Carbon dioxide narcosis can also be induced by the administration of sedation in these patients.
Pulse oximetry is a continuous, noninvasive method of determining oxygen saturation (Sao2) to guide oxygen therapy. A sensor composed of a light-emitting diode (LED) and a photodetector is placed in opposition around a foot, hand, finger, toe, or earlobe, with the LED placed on top of the nail when digits are used (Fig. 22-24). The diode emits red and infrared lights that pass through the skin to the photodetector. The photodetector measures the amount of each type of light absorbed by functional hemoglobins. Hemoglobin saturated with oxygen (oxyhemoglobin) absorbs more infrared light than does hemoglobin not saturated with oxygen (deoxyhemoglobin). Pulsatile blood flow is the primary physiologic factor that influences accuracy of the pulse oximeter. In infants, reposition the probe at least every 3 to 4 hours to prevent pressure necrosis; poor perfusion and very sensitive skin may necessitate more frequent repositioning.
FIG. 22-24 Oximeter sensor on great toe. Note that sensor is positioned with light-emitting diode opposite photodetector. Cord is secured to foot to minimize movement of sensor.
Another noninvasive method is transcutaneous monitoring (TCM), which provides continuous monitoring of transcutaneous partial pressure of oxygen in arterial blood (tcPao2) and, with some devices, of carbon dioxide in arterial blood (tcPaco2). An electrode is attached to the warmed skin to facilitate arterialization of cutaneous capillaries. The site of the electrode must be changed every 3 to 4 hours to avoid burning the skin, and the machine must be calibrated with every site change. TCM is used frequently in neonatal intensive care units, but it may not reflect Pao2 in infants with impaired local circulation or in older infants whose skin is thicker.
Oximetry is insensitive to hyperoxia because hemoglobin approaches 100% saturation for all Pao2 readings greater than approximately 100 mm Hg, which is a dangerous situation for the preterm infant at risk for developing retinopathy of prematurity (see Chapter 9). Therefore the preterm infant being monitored with oximetry should have upper limits identified, such as 90% to 95%, and a protocol established for decreasing oxygen when saturations are high.
Oximetry offers several advantages over TCM. Oximetry (1) does not require heating the skin, thus reducing the risk of burns; (2) eliminates a delay period for transducer equilibration; and (3) maintains an accurate measurement regardless of the patient’s age or skin characteristics or the presence of lung disease.
Applying the sensor correctly is essential for accurate Sao2 measurements. Because the sensor must identify every pulse beat to calculate the Sao2, movement can interfere with sensing. Some devices synchronize the Sao2 reading with the heartbeat, thereby reducing the interference caused by motion. Sensors are not placed on extremities used for blood pressure monitoring or with indwelling arterial catheters, since pulsatile blood flow may be affected.
Ambient light from ceiling lights and phototherapy, as well as high-intensity heat and light from radiant warmers, can interfere with readings. Therefore the sensor should be covered to block these light sources. IV dyes; green, purple, or black nail polish; nonopaque synthetic nails; and possibly ink used for footprinting can also cause inaccurate Sao2 measurements. The dyes should be removed or, in the case of porcelain nails, a different area used for the sensor. Skin color, thickness, and edema do not affect the readings.
Aerosol therapy can be effective in depositing medication directly into the airway. The value of aerosolized water, or “mist therapy,” is controversial. This route of administration can be useful in avoiding the systemic side effects of certain drugs and in reducing the amount of drug necessary to achieve the desired effect. Bronchodilators, steroids, and antibiotics, suspended in particulate form, can be inhaled so that the medication reaches the small airways. Aerosol therapy is particularly challenging in children who are too young to cooperate with controlling the rate and depth of breathing. Administration of this therapy requires skill, patience, and creativity.
Medications can be aerosolized or nebulized with air or with oxygen-enriched gas. Handheld nebulizers are the most frequently used equipment. The medicated mist is discharged into a small plastic mask, which the child holds over the nose and mouth. To avoid particle deposition in the nose and pharynx, the child is instructed to take slow, deep breaths through an open mouth during the treatment. For home use an air compressor is necessary to force air through the liquid medication to form the aerosol. Compact, portable units can be obtained from health equipment companies. The metered-dose inhaler (MDI) is a self-contained, handheld device that allows for intermittent delivery of a specified amount of medication. Many bronchodilators are available in this form and are successfully used by children with asthma. For children under the age of 5 or 6 years, a spacer device attached to the MDI can help with coordination of breathing and aerosol delivery. It allows the aerosolized particles to remain in suspension longer. (See also Asthma, Chapter 23.)
Assessment of breath sounds and work of breathing should be done before and after treatments. Young children who become upset by having a mask held close to the face may become fatigued with fighting the procedure and may actually appear worse during and immediately after the therapy. It may be necessary to spend a few minutes calming the child after the procedure and allowing the vital signs to return to baseline to accurately assess changes in breath sounds and work of breathing.
Bronchial drainage is indicated whenever excessive fluid or mucus in the bronchi is not being removed by normal ciliary activity and cough. Positioning the child to take maximum advantage of gravity facilitates removal of secretions. Postural drainage can be effective in children with chronic lung disease characterized by thick mucus, such as cystic fibrosis.
Postural drainage is carried out three or four times daily and is more effective when it follows other respiratory therapy, such as bronchodilator or nebulization medication. Bronchial drainage is generally performed before meals (or 1 to 1½ hours after meals) to minimize the chance of vomiting and is repeated at bedtime. The duration of treatment depends on the child’s condition and tolerance; it usually lasts 20 to 30 minutes. Several positions facilitate drainage from all major lung segments (Fig. 22-25); all positions are not employed at each session. Children will usually cooperate for four to six positions. Older children can tolerate longer periods.
FIG. 22-25 Bronchial drainage positions for all major segments of child. For each position, model of tracheobronchial tree is projected beside child to show segmental bronchus (red) being drained and pathway of secretions out of bronchus. Drainage platform is horizontal unless otherwise noted. Red area on child’s chest indicates area to be cupped or vibrated by therapist. A, Apical segment of right upper lobe and apical subsegment of apical-posterior segment of left upper lobe. B, Posterior segment of right upper lobe and posterior subsegment of apical-posterior segment of left upper lobe. C, Anterior segments of both upper lobes. Child should be rotated slightly away from side being drained. D, Superior segments of both lower lobes. E, Posterior basal segments of both lower lobes. F, Lateral basal segments of right lower lobe. Left lateral basal segment would be drained by mirror image of this position (right side down). G, Anterior basal segment of left lower lobe. Right anterior basal segment would be drained by mirror image of this position (left side down). H, Medial and lateral segments of right middle lobe. I, Lingular segments (superior and inferior) of left upper lobe (homologue of right middle lobe). (From Chernick V, editor: Kendig’s disorders of the respiratory tract of children, ed 6, Philadelphia, 1998, Saunders.)
In the hospital an older child can be positioned over an elevated knee rest. Small children and infants can be positioned with pillows or on the therapist’s lap and legs. Infants should not be placed in the Trendelenburg position because they do not have an autonomic regulation of blood flow to the head. Special modifications of the techniques are required in children whose conditions contraindicate the standard positioning, such as head injuries, some types of surgical incisions or burns, and casts.
Chest physical therapy (CPT) usually refers to the use of postural drainage in combination with adjunctive techniques that are thought to enhance the clearance of mucus from the airway. These techniques include manual percussion, vibration, and squeezing of the chest; cough; forceful expiration; and breathing exercises. Special mechanical devices are also currently used to perform CPT (e.g., ThAIRapy Vest). Postural drainage in combination with forced expiration has been shown to be beneficial. Noninvasive inspiratory nasal pressure—support ventilation (PSV) during CPT has demonstrated a significant improvement in respiratory muscle performance and a reduction in oxygen desaturation (Fauroux, Boule, Lofaso, and others, 1999).
The most common technique used in association with postural drainage is manual percussion of the chest wall. The patient is dressed in a lightweight shirt and placed in a postural drainage position. The nurse then gently but firmly strikes the chest wall with a cupped hand (Fig. 22-26, A). For infants, special devices are available for percussing small areas (Fig. 22-26, B). A “popping,” hollow sound should be the result, not a slapping sound. The procedure should be done over the rib cage only and should be painless. Percussion can be performed with a soft circular mask (adapted to maintain air trapping) or a percussion cup marketed especially for the purpose of aiding in loosening secretions.
CPT is contraindicated when patients have pulmonary hemorrhage, pulmonary embolism, end-stage renal disease, increased intracranial pressure, osteogenesis imperfecta, or minimal cardiac reserves.
An artificial airway is usually used in association with mechanical ventilation and in children with upper airway obstruction. Endotracheal intubation can be accomplished by the nasal (nasotracheal), oral (orotracheal), or direct tracheal (tracheostomy) routes. Although it is more difficult to place, nasotracheal intubation is preferred to orotracheal intubation because it facilitates oral hygiene and provides more stable fixation, which reduces the complication of tracheal erosion and the danger of accidental extubation. Only uncuffed endotracheal tubes should be used in children younger than 8 years of age (Curley and Moloney-Harmon, 2001). Air or gas delivered directly to the trachea must be humidified.
A tracheostomy is a surgical opening in the trachea; the procedure may be done on an emergency basis or may be an elective one, and it may be combined with mechanical ventilation. Pediatric tracheostomy tubes are usually made of plastic or Silastic (Fig. 22-27). The most common types are the Hollinger, Jackson, Aberdeen, and Shiley tubes. These tubes are constructed with a more acute angle than adult tubes, and they soften at body temperature, conforming to the contours of the trachea. Because these materials resist the formation of crusted respiratory secretions, they are made without an inner cannula.
Children who have undergone a tracheostomy must be closely monitored for complications such as hemorrhage, edema, aspiration, accidental decannulation, tube obstruction, and the entrance of free air into the pleural cavity. The focus of nursing care is maintaining a patent airway, facilitating the removal of pulmonary secretions, providing humidified air or oxygen, cleansing the stoma, monitoring the child’s ability to swallow, and teaching while simultaneously preventing complications.
Because the child may be unable to signal for help, direct observation and use of respiratory and cardiac monitors are essential. Respiratory assessments include breath sounds and work of breathing, vital signs, tightness of the tracheostomy ties, and the type and amount of secretions. Large amounts of bloody secretions are uncommon and should be considered a sign of hemorrhage. The practitioner should be notified immediately if this occurs.
The child is positioned with the head of the bed raised or in the position most comfortable to the child, with the call light easily available. Suction catheters, suction source, gloves, sterile saline, sterile gauze for wiping away secretions, scissors, an extra tracheostomy tube of the same size with ties already attached, another tracheostomy tube one size smaller, and the obturator are kept at the bedside. A source of humidification is provided because the normal humidification and filtering functions of the airway have been bypassed. IV fluids ensure adequate hydration until the child is able to swallow sufficient amounts of fluids.
Suctioning.: The airway must remain patent and requires frequent suctioning during the first few hours after a tracheostomy to remove mucous plugs and excessive secretions. Proper vacuum pressure and suction catheter size are important to prevent atelectasis and decrease hypoxia from the suctioning procedure. Vacuum pressure should range from 60 to 100 mm Hg for infants and children and from 40 to 60 mm Hg for preterm infants. Unless secretions are thick and tenacious, the lower range of negative pressure is recommended. Tracheal suction catheters are available in a variety of sizes. The catheter selected should have a diameter one-half the diameter of the tracheostomy tube. If the catheter is too large, it can block the airway. The catheter is constructed with a side port so that the catheter is introduced without suction and removed while simultaneous intermittent suction is applied by covering the port with the thumb (Fig. 22-28). The catheter is inserted to 0.5 cm beyond or just to the end of the tracheostomy tube. The practice of instilling sterile saline in the tracheostomy tube before suctioning is not supported by research and is no longer recommended (see Evidence-Based Practice box).
FIG. 22-28 Tracheostomy suctioning. A, Insertion, port open. B, Withdrawal, port occluded. Note that catheter is inserted just slightly beyond end of tracheostomy tube.
The child is allowed to rest for 30 to 60 seconds after each aspiration to allow oxygen saturation to return to normal; then the process is repeated until the trachea is clear. Suctioning should be limited to about three aspirations in one period. Oximetry is used to monitor suctioning and prevent hypoxia.
In the acute care setting, aseptic technique is used during care of the tracheostomy. Secondary infection is a major concern, since the air entering the lower airway bypasses the natural defenses of the upper airway. Gloves are worn during the aspiration procedure, although a sterile glove is needed only on the hand touching the catheter. A new tube, gloves, and sterile saline solution are used each time.
Routine Care.: The tracheostomy stoma requires daily care. Assessments of the stoma area include observations for signs of infection and breakdown of the skin. The skin is kept clean and dry, and crusted secretions around the stoma may be gently removed with half-strength hydrogen peroxide. Hydrogen peroxide should not be used with sterling silver tracheostomy tubes because it tends to pit and stain the silver surface. The nurse should be aware of wet tracheostomy dressings, which can predispose the peristomal area to skin breakdown. Several products are available to prevent or treat excoriation. The Allevyn tracheostomy dressing is a hydrophilic sponge with a polyurethane back that is highly absorptive. Other possible barriers to help maintain skin integrity include the use of hydrocolloid wafers (e.g., DuoDERM CGF, Hollister Restore) under the tracheostomy flanges, as well as extra-thin hydrocolloid wafers under the chin.
The tracheostomy tube is held in place with tracheostomy ties made of a durable, nonfraying material. The ties are changed daily and when soiled. New ties are looped through the flanges and tied snugly in a triple knot at the side of the neck before the soiled ties are cut and removed. Some nurses have found that threading the ties through a piece of 0.25-inch surgical tubing cushions the ties; others have found the tubing to be irritating to the skin. The ties should be tight enough to allow just a fingertip to be inserted between the ties and the neck (Fig. 22-29). It is easier to ensure a snug fit if the child’s head is flexed rather than extended while the ties are being secured. Ties fastened with self-adhering closures are also available. These devices, such as the Dale tracheostomy tube holder, are made of a soft, cushioning, and slightly stretchy material that is very comfortable. They are becoming increasingly popular because of their ease of use and ability to maintain better skin integrity. However, nurses and family members must consider the safety factor and use them only on a child who will not pull and undo the fastener.
Routine tracheostomy tube changes are usually carried out weekly after a tract has been formed to minimize the formation of granulation tissue. The first change is usually performed by the surgeon; subsequent changes are performed by the nurse and, if the child is discharged home with the tracheostomy, by either a parent or a visiting nurse. Ideally, two caregivers participate in the procedure to assist with positioning the child.
Changing the tracheostomy tube is accomplished using sterile technique. Tube changes should occur before meals or 2 hours after the last meal. Continuous feedings should be turned off at least an hour before a tube change. The new, sterile tube is prepared by inserting the obturator and attaching new ties. The child is suctioned before the procedure to minimize secretions, then restrained and positioned with the neck slightly extended. One caregiver cuts the old ties and removes the tube from the stoma. The new tube is inserted gently into the stoma (using a downward and forward motion that follows the curve of the trachea), the obturator is removed, and the ties are secured. The adequacy of ventilation must be assessed after a tube change because the tube can be inserted into the soft tissue surrounding the trachea; therefore breath sounds and respiratory effort are carefully monitored.
Supplemental oxygen is always delivered with a humidification system to prevent drying of the respiratory mucosa. Humidification of room air for an established tracheostomy can be intermittent if secretions remain thin enough to be coughed or suctioned from the tracheostomy. Direct humidification via a tracheostomy mask can be provided during naps and at night so that the child is able to be up and around unencumbered during much of the day. Room humidifiers are also used successfully.
The inner cannula, if used, should be removed with each suctioning, cleaned with sterile saline and pipe cleaners to remove crusted material, dried thoroughly, and reinserted.
Emergency Care: Tube Occlusion and Accidental Decannulation.: Occlusion of the tracheostomy tube is life threatening, and infants and children are at greater risk than adults because of the smaller diameter of the tube. Maintaining patency of the tube is accomplished with suctioning and routine tube changes to prevent the formation of crusts that can occlude the tube.
Accidental decannulation also requires immediate tube replacement. Some children have a fairly rigid trachea, so the airway remains partially open when the tube is removed. However, others have malformed or flexible tracheal cartilage, which causes the airway to collapse when the tube is removed or dislodged. Because many infants and children with upper airway problems have little airway reserve, if replacement of the dislodged tube is impossible, a smaller-sized tube should be inserted. If the stoma cannot be cannulated with another tracheostomy tube, oral intubation should be performed.
Some children are unable to take nourishment by mouth because of anomalies of the throat, esophagus, or bowel; impaired swallowing capacity; severe debilitation; respiratory distress; or unconsciousness. These children are frequently fed by way of a tube inserted orally or nasally into the stomach (orogastric or nasogastric gavage) or duodenum-jejunum (enteral gavage), or by a tube inserted directly into the stomach (gastrostomy) or jejunum (jejunostomy). Such feedings may be intermittent or by continuous drip.
Feeding resistance, a problem that may result from any long-term feeding method that bypasses the mouth, is discussed in Chapter 9. During gavage or gastrostomy feedings, infants are given a pacifier. Nonnutritive sucking has several advantages, such as increased weight gain and decreased crying. However, to prevent the possibility of aspiration, only pacifiers with a safe design may be used. Using improvised pacifiers made from bottle nipples is not a safe practice.
Infants and children can be fed simply and safely by a tube passed into the stomach through either the nares or the mouth. The tube can be left in place or inserted and removed with each feeding. In older children it is usually less traumatic to tape the tube securely in place between feedings. When this alternative is used, the tube should be removed and replaced with a new tube according to hospital policy, specific orders, and the type of tube used. Meticulous hand washing is practiced during the procedure to prevent bacterial contamination of the feeding, especially during continuous-drip feedings (see Atraumatic Care box).
Not all feeding tubes are the same. Polyethylene and polyvinylchloride types lose their flexibility and need to be replaced frequently, usually every 3 or 4 days. The polyurethane and silicone tubes are indwelling and remain flexible; so that they can remain in place longer and afford more patient comfort. Use of these small-bore tubes for continuous feeding has reduced the incidence of complications such as pharyngitis, otitis media, and incompetence of the lower esophageal sphincter. Although the increased softness and flexibility of the tubes are advantages, they also have disadvantages such as difficult insertion (may require a stylet or metal guidewire), collapse of the tube during aspiration of gastric contents to test for correct placement, dislodgment during forceful coughing, and unsuitability for thick feedings. Traditional methods for verifying placement are less reliable with the small-bore tubes.
Infants will be easier to control if they are first wrapped in a mummy restraint (see Fig. 22-7). Even tiny infants with random movements can grasp and dislodge the tube. Preterm infants do not ordinarily require restraint, but if they do, a small blanket folded across the chest and secured beneath the shoulders is usually sufficient. Care must be taken so that breathing is not compromised.
Whenever possible, the infant should be held and provided a means of nonnutritive sucking during the procedure to associate the comfort of physical contact with the feeding. When this is not possible, gavage feeding is carried out with the infant or child on the back or toward the right side and the head and chest elevated. Feeding the child in a sitting position helps maintain the placement of the tube in the lowest position, thus increasing the likelihood of correct placement in the stomach (see Nursing Care Guidelines box).
Two standard methods of measuring tube length for insertion are (1) measuring from the nose to the bottom of the earlobe and then to the end of the xiphoid process or (2) measuring from the nose to the earlobe and then to a point midway between the xiphoid process and the umbilicus (Fig. 22-30, A). For very low—birth-weight infants, weight can be used to predict insertion length (Table 22-7). See Evidence-Based Practice box for placement verification techniques.
TABLE 22-7
Recommended Minimum Insertion Lengths for Orogastric Tubes in Very Low–Birth-Weight Infants
From Gallaher KJ, Cashwell S, Hall V, and others: Orogastric tube insertion length in very-low-birth-weight infants (<1500 grams), J Perinatal 13(2):128-131, 1993.
Feeding by way of a gastrostomy tube is a variation of tube feeding that is often used for children in whom passage of a tube through the mouth, pharynx, esophagus, and cardiac sphincter of the stomach is contraindicated or impossible. It is also used to avoid the constant irritation of a gastric tube in children who require tube feeding over an extended period. Placement of a gastrostomy tube may be performed with the patient under general anesthesia or percutaneously using an endoscope with the patient sedated and under local anesthesia (percutaneous endoscopic gastrostomy [PEG]). The tube is inserted through the abdominal wall into the stomach about midway along the greater curvature and, when surgically placed, is secured by a purse-string suture. The stomach is anchored to the peritoneum at the operative site. The tube used can be a Foley, wing-tip, or mushroom catheter. Immediately after surgery the catheter is left open and attached to gravity drainage for 24 hours or more.
Postoperative care of the wound site is directed toward prevention of infection and irritation. The area is cleansed at least daily or as often as needed to keep the area free of drainage. After healing takes place, meticulous care is needed to keep the area surrounding the tube clean and dry to prevent excoriation and infection. Daily applications of antibiotic ointment or other preparations may be prescribed to aid in healing and prevention of irritation. Care is exercised to prevent excessive pull on the catheter that might cause widening of the opening and subsequent leakage of highly irritating gastric juices. The tube is securely taped to the abdomen, leaving a small loop of tubing at the exit site to prevent tension on the site.
Granulation tissue may grow around a gastrostomy site (Fig. 22-31). This moist, beefy red tissue is not a sign of infection. However, if it continues to grow, the excess moisture can irritate the surrounding skin.
For children receiving long-term gastrostomy feeding, a skin-level device (e.g., MIC-KEY, Bard Button) offers several advantages. The small, flexible silicone device protrudes slightly from the abdomen, is cosmetically pleasing in appearance, affords increased comfort and mobility to the child, is easy to care for, and is fully immersible in water. The one-way valve at the proximal end minimizes reflux and eliminates the need for clamping. However, the button requires a well-established gastrostomy site and is more expensive than the conventional tube. In addition, the valve may become clogged. When functioning, the valve prevents air from escaping; therefore the child may require frequent bubbling. With some devices, during feedings the child must remain fairly still because the tubing easily disconnects from the opening if the child moves. With other devices, extension tubing can be securely attached to the opening (Fig. 22-32). The feeding is instilled at the other end of the tubing in a manner similar to that for a regular gastrostomy. The extension tubing may also have a separate medication port. Both the feeding and the medication ports have plugs attached. Some skin-level devices require a special tube to decompress the stomach (to check residual or release air).
FIG. 22-32 Child with skin-level gastrostomy device (MIC-KEY), which provides for secure attachment of extension tubing to gastrostomy opening.
Feeding of water, formula, or pureed foods is carried out in the same manner and rate as in gavage feeding. A mechanical pump may be used to regulate the volume and rate of feeding. After feedings, the infant or child is positioned on the right side or in the Fowler position, and the tube may be clamped or left open and suspended between feedings, depending on the child’s condition. A clamped tube allows more mobility but is appropriate only if the child can tolerate intermittent feedings without vomiting or prolonged backup of feeding into the tube. Sometimes a Y tube is used to allow for simultaneous decompression during feeding. If a Foley catheter is used as the gastrostomy tube, very slight tension is applied. The tube is securely taped to maintain the balloon at the gastrostomy opening to prevent leakage of gastric contents and to prevent the tube’s progression toward the pyloric sphincter, where it may occlude the stomach outlet. As a precaution, the length of the tube should be measured postoperatively and then remeasured each shift to be certain it has not slipped. A mark can be made above the skin level to further ensure its placement. When the gastrostomy tube is no longer needed, it is removed; the skin opening usually closes spontaneously by contracture.
Children at high risk for regurgitation or aspiration such as those with gastroparesis, mechanical ventilation, or brain injuries may require placement of a postpyloric feeding tube. Insertion of a nasoduodenal or nasojejunal tube is done by a trained practitioner because of the risk of misplacement and potential for perforation in tubes requiring a stylet. Accurate placement is verified by radiography. Small-bore tubes may easily clog. Flush tube when feeding is interrupted, before and after medication administration, and routinely every 4 hours or as directed by institutional policy. Tube replacement should be considered monthly to ensure optimal tube patency. Continuous feedings are delivered by mechanical pump to regulate volume and rate. Bolus feeds are contraindicated. Tube displacement is suspected in the child showing signs of feeding intolerance such as vomiting. Stop feedings and notify the practitioner.
TPN provides for the total nutritional needs of infants or children when feeding by the gastrointestinal tract is impossible, inadequate, or hazardous. Some common conditions include chronic intestinal obstruction, inadequate intestinal length, and prophylactically after surgery or during critical illness.
TPN therapy involves IV infusion of highly concentrated solutions of carbohydrates, lipids, amino acids, vitamins, minerals, water, trace elements and other additives in a single container (Teitelbaum, Guenter, Howell, and others, 2005). The highly concentrated solutions require infusion into a vessel with sufficient volume and turbulence to allow for rapid dilution. The wide-diameter vessels selected are the superior vena cava and innominate or intrathoracic subclavian veins approached by way of the external or internal jugular veins. The highly irritating nature of concentrated glucose precludes the use of the small peripheral veins in most instances. However, dilute glucose-protein hydrolysates that are appropriate for infusing into peripheral veins are being used with increasing frequency. When peripheral veins are used, intralipid becomes the major calorie source. For long-term alimentation, VADs are commonly used (see p. 725).
The major nursing responsibilities are the same as for any IV therapy: control of sepsis, monitoring of the infusion rate, and assessment of the patient’s tolerance of the solution. The TPN solution must be prepared under sterile conditions. The infusion is maintained at a constant rate by an infusion pump. The TPN infusion rate should not be increased or decreased without the practitioner being informed, since alterations can cause hyperglycemia or hypoglycemia.
General assessments, such as vital signs, I&O measurements, and laboratory tests, facilitate early detection of infection or fluid and electrolyte imbalance. Additional amounts of potassium and sodium chloride are often required in hyperalimentation; therefore observation for signs of potassium or sodium deficit or excess is part of nursing care. This is rarely a problem except in children with reduced renal function or metabolic defects. Hyperglycemia may occur during the first day or two as the child adapts to the high-glucose load of the hyperalimentation solution. Although hyperglycemia occurs infrequently, insulin may be required to assist the body’s adjustment. To prevent hypoglycemia at the time the hyperalimentation is disconnected, the rate of the infusion and the amount of insulin are decreased gradually.
In addition to children’s physical needs, their developmental needs must also be considered during the often long-term use of TPN. Development should be regularly assessed to monitor the child’s progress, and appropriate interventions should be instituted to encourage expected milestones. Delays in the areas of gross motor and language skills are found most often; therefore special attention should be directed to these areas.
When alternative feedings are needed for an extended period, the family may need to learn how to feed the child with a nasogastric, gastrostomy, or TPN feeding regimen. The same principles discussed earlier in this chapter for compliance, especially in terms of education (p. 698), and in Chapter 21 for discharge planning and home care are applied. Because of the numerous skills the family must learn for home TPN, ample time must be allowed for the family to learn and perform the procedures under supervision before assuming full responsibility for the child’s care.
The family may be referred to community agencies that provide support and practical assistance. The Oley Foundation* is a nonprofit research and education organization that assists persons receiving enteral nutrition and home TPN.
The procedure for giving an enema to an infant or child does not differ essentially from that for an adult, except for the type and amount of fluid administered and the distance for inserting the tube into the rectum. Depending on the volume, a syringe with rubber tubing, an enema bottle, or an enema bag should be used (see Nursing Care Guidelines box).
An isotonic solution is used in children. Plain water is not used because, being hypotonic, it can cause rapid fluid shift and fluid overload. The Fleet enema (pediatric or adult sized) is not advised for children because of the harsh action of its ingredients (sodium biphosphate and sodium phosphate). Commercial enemas can be dangerous to patients with megacolon and to dehydrated or azotemic children. The osmotic effect of the Fleet enema may produce diarrhea, which can lead to metabolic acidosis. Other potential complications are extreme hyperphosphatemia, hypernatremia, and hypocalcemia, which may lead to neuromuscular irritability and coma (Walton, Thomas, Aly, and others, 2000).
Because infants and young children are unable to retain the solution after it is administered, the buttocks must be held together for a short time to retain the fluid. The enema is administered and expelled while the child is lying with the buttocks over the bedpan and with the head and back supported by pillows. Older children are usually able to hold the solution if they understand what to do and if they are not expected to hold it for too long. The nurse should have the bedpan handy or, for the ambulatory child, ensure that the bathroom is available before beginning the procedure. An enema is an intrusive procedure and thus threatening to the preschool child; therefore a careful explanation is especially important to ease possible fear.
A preoperative bowel preparation solution given orally or through a nasogastric tube is increasingly being used instead of an enema. The polyethylene glycol—electrolyte lavage solution (GoLYTELY) mechanically flushes the bowel without significant absorption, thereby avoiding potential fluid and electrolyte imbalance. Another effective oral cathartic is magnesium citrate solution.
Children may require stomas for various health problems. The most frequent causes in the infant are necrotizing enterocolitis and imperforate anus (less often, Hirschsprung disease). In the older child the most frequent causes are inflammatory bowel disease, especially Crohn disease (regional enteritis), and ureterostomies for distal ureter or bladder defects.
Care and management of ostomies in the older child differ little from the care of ostomies in the adult patient. The major emphasis in pediatric care is preparing the child for the procedure and teaching care of the ostomy to the child and family. The basic principles of preparation are the same as for any procedure (see p. 689). Simple, straightforward language is most effective, together with the use of illustrations and a replica model (e.g., drawing a picture of a child with a stoma on the abdomen and explaining it as “another opening where bowel movements [or any other term the child uses] will come out”). At another time the nurse can draw a pouch over the opening to demonstrate how the contents are collected. Using a doll to demonstrate the process is an excellent teaching strategy, and special books are available.*
Ostomy equipment consists of a one- or two-piece system with a hypoallergenic skin barrier to maintain peristomal skin integrity. The pouch should be large enough to contain a moderate amount of stool and flatus but not so large as to overwhelm the infant or child. A backing helps minimize the risk of skin breakdown from moisture trapped between the skin and pouch. Small clips or rubber bands should be avoided to prevent choking in the young child. Granulation tissue may grow around an ostomy site (see Fig. 22-31). This moist, beefy red tissue is not a sign of infection. However, if it continues to grow, the excess moisture can cause irritation of the surrounding skin.
Protection of the peristomal skin is a major aspect of stoma care. Well-fitting appliances are important to prevent leakage of contents. Before the appliance is applied, the skin is prepared with a skin sealant that is allowed to dry. Then stoma paste is applied around the base of the stoma or the back of the wafer. The sealant and paste work together to prevent peristomal breakdown.
In infants with a colostomy left unpouched, skin care is similar to that of any diapered infant. However, the peristomal skin is protected with a wafer barrier, such as a hydrocolloid dressing (e.g., DuoDERM) or a barrier substance (e.g., zinc oxide ointment [Desitin], or a mixture of the zinc oxide ointment and stoma [Stomahesive] powder). A gauze dressing may be applied over the stoma and wafer to absorb stomal drainage. If the skin becomes inflamed, denuded, or infected, the care is similar to the interventions used for diaper dermatitis (see Chapter 30). A product that helps protect healthy skin, heal excoriated skin, and minimize pain associated with skin breakdown is Proshield Plus. The skin protectant adheres to denuded weeping skin. Proshield Plus can be applied over topical antifungal and antibacterial agents if infection is present. “No-sting” barrier film is a skin sealant that has no alcohol base and can be used on open skin without stinging.
With young children, protection of the pouch from being pulled off is also an important consideration. One-piece outfits keep exploring hands from reaching the pouch, and the loose waist prevents any pressure on the appliance. Keeping the child occupied with toys during the pouch change is also helpful. As children mature, their participation in ostomy care is encouraged. Even preschoolers can assist by holding supplies, pulling paper backings from the appliance, and helping clean the stoma area. Toilet training for bladder control needs to begin at the appropriate time as for any other child.
Older children and adolescents should eventually have total responsibility for ostomy care just as they would for usual bowel function. During adolescence, concerns for body image and the ostomy’s impact on intimacy and sexuality emerge. The nurse should stress to teenagers that the presence of a stoma need not interfere with their activities. These youngsters can choose which ostomy equipment is best suited to their needs. Attractively designed and decorated pouch covers are well liked by teenagers.
An enterostomal therapy nurse specialist is an important member of the health care team and will have additional suggestions and skin care information and ostomy pouching options. Further information may be obtained by contacting the Wound, Ostomy and Continence Nurses Society.*
Because these children are almost always discharged with a functioning colostomy, preparation of the family should begin as early as possible in the hospital. The family is instructed in the application of the device (if used), care of the skin, and appropriate action in case skin problems develop. Early evidence of skin breakdown or stomal complications, such as ribbonlike stools, excessive diarrhea, bleeding, prolapse, or failure to pass flatus or stool, is brought to the attention of the physician, the nurse, or the stoma specialist. The same principles are applied as discussed earlier in this chapter for compliance, especially in terms of education (p. 699), and in Chapter 21 for discharge planning and home care.
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*Preparatory materials include Going to the Hospital and Going to the Doctor, available from Family Communications, Inc., 4802 Fifth Ave., Pittsburgh, PA 15213; (412) 687-2990; http://www.fci.org; Hospital Friends, available from the Centering Corporation, 7230 Maple St., Omaha, NE 68134; (866) 218-0101. Other resources include Berenstein Bears Go to the Doctor and Berenstein Bears Visit the Dentist (New York, Random House), available in most bookstores.
*This section was revised by Shannon McCord, MSN, RN, CPNP.
*Staging of pressure ulcers and guidelines for prevention and management of pressure ulcers can be found at http://wocn.org.
*Available from Hollister, Inc., 2000 Hollister Drive, Libertyville, IL 60048; (800) 323-4060; http://www.hollister.com.
†Available from ConvaTec, PO Box 5254, Princeton, NJ 08543-5254; (800) 422-8811; http://www.convatec.com.
*Lidocaine hydrochloride 2% jelly is available from International Medication Systems, Ltd., 1886 Santa Anita Ave., South El Monte, CA 91733; (800) 423-4136; http://www.ims-limited.com; and from AstraZeneca, 1800 Concord Pike, Wilmington, DE 19801; (800) 842-992; http://www.astrazeneca-us.com.
*Trademark Medical manufactures a pill crusher and has compiled a list of more than 190 medications that should not be crushed or chewed. Both are available from Trademark Medical, 449 Sovereign Court, St. Louis, MO 63011; (800) 325-9044; http://www.trademarkmedical.com.
*Guidelines for determining tissue injury severity are available from the Infusion Nurses Society, 315 Norwood Park South, Norwood, MA 02062; (781) 440-9408; fax: (781) 440-9409; http://www.ins1.org.
†Guidelines on interventions for infiltration and extravasation are available from the Oncology Nursing Society, 125 Enterprise Drive, Pittsburgh, PA 15275; (412) 859-6100; fax: (412) 859-6162; http://www.ons.org.
‡Guidelines for prevention of intravascular device—related infections are available from the Centers for Disease Control and Prevention, 1600 Clifton Road, Atlanta, GA 30333; (404) 639-1515; http://www.cdc.gov/ncidod/dhqp/gl_intravascular.html.
*214 Hun Memorial, MC-28, Albany Medical Center, Albany, NY 12208; (800) 776-OLEY; http://www.oley.org.
*Children with ileostomies are fitted immediately after surgery with an appliance to protect the skin from the proteolytic enzymes in the liquid stool. Infants may not be fitted with a pouch in the immediate postoperative period. When stomal drainage is minimal, a gauze dressing will suffice. Parents are usually given a choice of caring for the colostomy with or without an appliance. Pediatric appliances are available in a variety of sizes to ensure an adequate fit. Parents may find the following pamphlets helpful: A Parent’s Guide to Necrotizing Enterocolitis or Parent’s Guide to Ostomy Care for Children, available from ConvaTec.
*(888) 224-9626; http://www.wocn.org.