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15 Head tilt and nystagmus

The vestibular system is responsible for balance and coordinating movements of the eyes, trunk and limbs with changes in head position. Head tilt and nystagmus are typically associated with unilateral vestibular disease and are relatively common presenting signs in canine emergency patients. Jerk nystagmus is typical of vestibular disease with the slow (pathological) phase towards the side of the lesion and the fast (corrective) phase away from the side of the lesion. Occasionally animals present with nystagmus due to cerebellar disease (paradoxical vestibular disease) or abnormalities in visual pathways. Other clinical signs associated with vestibular disease are listed in Box 15.1.

Box 15.1 Clinical signs of unilateral vestibular disease

Head tilt towards the side of the lesion
Nystagmus
Ataxia
Wide-based stance
Circling, leaning or falling towards the side of the lesion
Vomiting

Types of Unilateral Vestibular Disease

Vestibular disease may be the result of a lesion affecting either the central or the peripheral component of the vestibular system.

Central vestibular disease

The central component of the vestibular system is located in the brainstem and cerebellum. Nystagmus in central vestibular disease can be horizontal, rotatory, vertical or positional, with the fast phase towards or away from the lesion. Affected animals may well have additional clinical signs that reflect brain involvement, such as reduced mentation from depression through to coma, or ipsilateral paresis and proprioceptive deficits.

Peripheral vestibular disease

The peripheral components of the vestibular system are sensory receptors in the inner ear and the vestibular portion of vestibulocochlear nerve. Nystagmus in peripheral vestibular disease can be horizontal or rotatory, with the fast phase away from the side of the lesion. Affected animals may have normal mentation or they may be markedly disorientated; signs of brainstem abnormality are not expected unless there has been extension of inner ear disease. Paresis and proprioceptive deficits should not occur.

Horner’s syndrome (third eyelid protrusion, pupillary constriction, drooping of upper eyelid, enophthalmos) and facial nerve deficits (including ipsilateral drooping of and inability to move ear and lip, widened palpebral fissure, absent blinking) may occur with peripheral vestibular disease but are typically not recognized in the idiopathic form.

Paradoxical vestibular disease

Paradoxical vestibular disease refers to a syndrome of nystagmus, head tilt and circling due to cerebellar disease. Head tilt and circling occur contralateral to the side of the lesion and there are usually other more typical signs of cerebellar disease (e.g. head tremor, ipsilateral dysmetria).

Causes of Unilateral Vestibular Disease

The most common causes of central vestibular disease are brain tumours and inflammation (infectious or noninfectious). Trauma and metronidazole intoxication are other causes.

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The most common causes of peripheral vestibular disease are otitis media or interna, and idiopathic vestibular disease. Ototoxicity (e.g. due to topical medications), middle or inner ear trauma or tumours, and hypothyroidism are other possible causes. Nasopharyngeal polyps can cause peripheral vestibular disease in cats.

Clinical Tip

In the author’s experience, idiopathic peripheral vestibular disease is the form of vestibular disease seen most commonly in routine emergency practice. This disease is seen especially in older dogs but may also affect cats of any age. Diagnosis is made on the basis of compatible history and examination findings and by exclusion of other causes of peripheral disease. Although patients may present with really quite severe and often peracute clinical signs, they can improve remarkably over a period of several days (typically within 48–72 hours) with adequate supportive care. The prognosis is good with complete recovery common (may take up to 4 weeks and mild residual signs may persist), although recurrence may occur.
As the disease often occurs in older dogs, the major differential diagnosis on presentation is central vestibular disease secondary to a brain tumour. A thorough neurological examination to differentiate peripheral versus central signs is therefore essential in order not to inadvertently condemn these animals to having a worse prognosis. Owners can then be counselled appropriately and reassured about the rationale of giving their dog some time to improve.
It is noteworthy that animals with idiopathic peripheral vestibular disease do not usually have Horner’s syndrome or facial nerve deficits. In addition, there is no evidence for a beneficial effect from corticosteroid administration.

Approach to Unilateral Vestibular Disease

Signalment

Signalment may help to raise or lower the index of suspicion for certain differential diagnoses. For example, idiopathic peripheral vestibular disease is seen most often in older dogs and congenital vestibular disease is most likely in very young animals.

History

As always, a thorough history should be taken in all cases. Important pieces of information include:

Onset and progression – clinical signs are usually progressive with central disease
History of ear disease
Clinical signs consistent with ear disease
Non-vestibular potentially multifocal neurological signs suggestive of brain involvement
History of trauma
Medical therapy (e.g. potentially ototoxic topical therapy, metronidazole)
Clinical signs consistent with other diseases (e.g. hypothyroidism).

Major body system examination

In the majority of cases, the neurological system is the only system to be significantly affected. Animals with central vestibular disease due to a primary brain lesion may have potentially significant cardiovascular abnormalities and hyperthermia may be identified in some very disorientated dogs. A range of abnormalities may be identified following trauma.

Bilateral otoscopic examination should be performed in animals with peripheral vestibular signs. The tympanic membrane is often ruptured but if it remains intact it may not be possible to detect fluid in the middle ear. Myringotomy may need to be performed both for diagnostic purposes and to collect a fluid sample for cytology and microbiology. Most animals require heavy sedation or preferably general anaesthesia for a reliable otoscopic examination to be performed.

Emergency database

The emergency database is likely to be unremarkable in a lot of animals with vestibular disease. Dehydration may be identified in some animals and peripheral blood smear examination may reveal leucocytosis in some cases (e.g. otitis media or interna, inflammatory brain disease).

Diagnostic imaging

Central vestibular disease

Animals with signs of central vestibular disease require referral for advanced diagnostic imaging (computed tomography or magnetic resonance imaging) and cerebrospinal fluid analysis.

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Peripheral vestibular disease

Well-positioned plain radiographs of the skull designed to highlight the tympanic bullae may provide evidence of infection or neoplasia of the middle or inner ear. However, general anaesthesia is required and this should therefore only be undertaken in cases with signs suggestive of peripheral disease. Advanced diagnostic imaging modalities are considerably more sensitive so referral may be appropriate.

Treatment

Treatment of vestibular disease centres on addressing the underlying disorder if this is possible. For example, administration of toxic drugs should be discontinued and bacterial otitis should be treated with several weeks of systemic antibiosis (preferably based on culture and sensitivity testing).

Supportive care is also required with respect to intravenous fluid therapy in animals that are unable or unwilling to drink. Some dogs may also require assistance for toileting purposes and other nursing measures including well-padded bedding. Symptomatic anti-emetic treatment (maropitant, metoclopramide, ondansetron) is indicated in animals that are vomiting and may also help with nausea.

Animals presenting with head trauma must be stabilized as required (see Ch. 28).