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Laryngeal Paralysis: Pathophysiology, Diagnosis, and Surgical Repair


John F. Griffin IV, DVM D. J. Krahwinkel, DVM, MS, DACVS, DACVA, DACVECC
University of Tennessee

ABSTRACT:

Dysfunction of the recurrent laryngeal nerves causes laryngeal paralysis in dogs and cats. Paralysis of the cricoarytenoideus dorsalis muscle results in an inability to abduct the arytenoid cartilages during inspiration.The resulting cross-sectional area of the glottis is inadequate for normal respiration.The most common clinical signs of laryngeal paralysis in dogs and cats are stridor, exercise intolerance, respiratory distress, and a change in phonation. A variety of surgical procedures have been used to successfully treat laryngeal paralysis in dogs and cats. Arytenoid lateralization appears to give the best clinical outcome.

aryngeal paralysis results when the abductor muscles of the larynx are disrupted. The larynx does not open during inspiration because the arytenoid cartilages fail to retract. The disease may be unilateral but more often occurs bilaterally. Laryngeal paralysis is a common, important cause of upper respiratory obstruction in dogs1 and is increasingly being recognized in cats.2 Although laryngeal paralysis was once thought to be an isolated clinical entity, recent reports suggest that the condition is only one manifestation of a generalized neuromuscular disorder.3,4 This article provides a metaanalytical overview of the current literature on laryngeal paralysis, describes recent advances in diagnostic techniques, and reviews surgical procedures used for correction. A review of laryngeal paralysis in cats is also provided.

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EPIDEMIOLOGY Laryngeal paralysis is most often diagnosed in geriatric large- and giant-breed dogs but can also occur in a number of small breeds. 5,6 Most studies 3,712 report that male

dogs are more commonly affected than female dogs. Reported canine male:female ratios range from 3.7:1 to 1:1.11,12 The mean age range of dogs treated surgically for laryngeal paralysis is 9.5 to 12.2 years of age.3,712 Labrador retrievers are most commonly affected with acquired laryngeal paralysis.1 Other commonly affected large and giant breeds include the St. Bernard, Irish setter, and Afghan hound.3,712 One report 1 described the prevalence of laryngeal paresis and paralysis in a population of dogs undergoing general anesthesia at a university veterinary teaching hospital. The investigators performed laryngoscopy on 250 dogs, assigning each dog a subjective score of 0 (i.e., normal) to 4 (i.e., completely paralyzed). One-quarter of the dogs examined had some degree of laryngeal paresis. Laryngeal scores were significantly and directly related to age, body weight, and body condition score. Labrador retrievers and rottweilers were at least twice as likely to be affected as other breeds. No effort was made to standardize the anesthetic protocol. This could be important because the most commonly used anesthetic drugs depress laryngeal motion.13
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Stridor Exercise intolerance

Respiratory distress Change in phonation Cyanosis Cough or gag Fever Collapse

20

40

60

80

Percentage of cases
Figure 1. Graph depicting the most common clinical

signs of laryngeal paralysis in dogs. These figures represent data from several retrospective studies.612

LARYNGEAL PARALYSIS IN IMMATURE DOGS Laryngeal paralysis occurs in immature Bouvier des Flandres, Siberian huskies, dalmatians, rottweilers, Leonbergers, and bullterriers.6,1418 Laryngeal paralysis has also been reported in a young Afghan hound, a cocker spaniel, a dachshund, and a miniature pinscher.6,14 Hereditary laryngeal paralysis was first described in the Bouvier des Flandres and is transmitted as an autosomal dominant trait in this breed.14,19,20 This can be seen as a single clinical entity or as part of a polyneuropathy. 3 Microscopic, degenerative lesions of the nucleus ambiguous of the brain stem have been described.19 However, these changes alone fail to explain the distal distribution of neurogenic atrophy and common peroneal nerve changes in an 8-month-old male Bouvier des Flandres in another report.3 Less is known about hereditary laryngeal paralysis in other canine breeds. Laryngeal paralysis in young Siberian huskies and husky crossbreeds is thought to occur most often as a single clinical entity in dogs with blue eyes and white faces with freckles. 21 Preliminary breeding studies have been unable to describe the mode of heritability. Five rottweilers (three of which were related) with laryngeal paralysispolyneuropathy complex had an onset of clinical signs at 9 to 13 weeks of age.17 Four had bilateral cataracts, one had megaesophagus, and all five had inspiratory stridor. Mild to moderate muscular weakness was noted, with the hindlimbs more severely
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affected than the forelimbs. No sex predilection was identified. Fourteen dalmatians with lar yngeal paralysis polyneuropathy complex had an onset of clinical signs at 2 to 12 months of age.16 Nine dogs had polyneuropathy, manifested as weakness, hypotonia, and hyporeflexia, principally distal to the elbow and stifle. Nine dogs had megaesophagus. The mean observation period between onset of clinical signs and euthanasia or death was 3.7 months. No sex predilection was identified. Laryngeal paralysis was seen in Leonbergers 1 year of age and older.22 Clinical signs included exercise intolerance, weakness, gait abnormalities, change in phonation, and dyspnea. Affected dogs had distal limb muscle atrophy, decreased spinal and cranial nerve reflexes, and decreased to absent movement of the laryngeal and pharyngeal muscles. Electromyogram studies suggested denervation of distal muscles. Nerve conduction velocities were decreased. Peripheral nerve biopsies showed a loss of axons and a shift toward smaller diameter myelinated fibers. Laryngeal paralysis appears to follow an Xlinked pattern of inheritance in Leonbergers.

Clinical signs

CLINICAL SIGNS Clinical signs of laryngeal paralysis in dogs include stridor, exercise intolerance, respiratory distress, change in phonation, cyanosis, cough or gag, fever, and collapsed (Figure 1). 612 Hyperthermia and heatstroke may be observed, resulting from inability to adequately ventilate through panting. Clinical signs occur inconsistently until laryngeal paresis develops into paralysis.1 Some animals also show other signs related to neuromuscular dysfunction, such as limb weakness or dysphagia. CAUSE AND PATHOPHYSIOLOGY The cause of laryngeal paralysis can be genetic, as mentioned previously, or acquired. The cause of the acquired form is most commonly described as idiopathic.7 Other causes of laryngeal paralysis include neoplasia, trauma, infection, or a surgical complication in the cervical or thoracic region.5,7,23 Myasthenia gravis has been implicated as a cause of laryngeal paralysis.24 The mechanism of idiopathic laryngeal paralysis in dogs is described as a progressive, noninflammatory, degenerative disease of the recurrent laryngeal nerves.25 Histopathologic characteristics of the recurrent laryngeal nerves include loss of axons, beading of myelin, and perineural fibrosis. Neurogenic atrophy of the cricoarytenoideus dorsalis muscle has been noted.
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Bilateral laryngeal paralysis occurs in 81% to 100% of dogs with laryngeal paralysis presenting for surgery.7,12 Dogs may have symmetric or asymmetric laryngeal paralysis.10 Everted laryngeal saccules, elongated soft palate, laryngeal edema, and moderate to severe laryngeal collapse may play a role in upper airway obstruction secondary to laryngeal paralysis.6 Patients with laryngeal paralysis commonly have diffusely inflamed laryngeal mucosa. The reason for this is unknown.

LARYNGEAL PARALYSIS AS ONE MANIFESTATION OF POLYNEUROPATHY Changes in distal tibial and common peroneal nerve biopsy samples in young and old dogs with laryngeal paralysis and polyneuropathy have been described.3 The predominant changes in teased nerve fiber studies were fiber degeneration or demyelination and remyelination. Electrophysiologic changes indicative of a dying back neuropathy (i.e., axonal degeneration specifically targeting the distal part of long and large diameter nerve fibers) were noted in all dogs. The study authors suggest that laryngeal paralysis is only one clinical sign of an underlying, more generalized polyneuropathy with variable clinical expression of neurologic signs.

laryngeal paralysis) usually responds to thyroid supplementation. A possible explanation for this disparity could be that laryngeal paralysis is usually diagnosed as an end-stage disease after irreversible atrophy of the cricoarytenoideus dorsalis muscle has already occurred.1 Dogs receiving adequate thyroid supplementation have reportedly developed laryngeal paralysis.5 Dogs with laryngeal paralysis are reportedly 21 times more likely to have megaesophagus compared with control groups. 24 Laryngeal paralysis was diagnosed in 11.8% of dogs with acquired megaesophagus. Concurrent megaesophagus is a negative prognostic indicator. It has been speculated that laryngeal paralysis associated dysphagia or megaesophagus predisposes patients to aspiration pneumonia.28 Reported instances of pneumonia at the time of presurgical evaluation ranged from 7% to 10%.9,10 Nearly one-quarter of dogs treated surgically for laryngeal paralysis developed aspiration pneumonia at some point.5

DIAGNOSIS Clinical suspicion is an important tool in diagnosing laryngeal paralysis.1 Clinical suspicion was reportedly 91.6% sensitive and 98.5% specific for severe laryngeal

Laryngeal paralysis is usually only one manifestation of generalized neuromuscular disease.


In one report,12 56% of dogs treated surgically for laryngeal paralysis had posterior weakness before or after surgery. Instances of confirmed neurologic disease range from 2% to 22% of dogs treated surgically for laryngeal paralysis.5,10,11 Many reports57,9,11,12 of surgical treatment of laryngeal paralysis did not include a complete neurologic examination as part of the minimum database. paralysis in 250 dogs anesthetized at a veterinary teaching hospital. This comparison used laryngoscopic observation as the definitive diagnostic procedure. The accepted standard of diagnosis is direct visualization of the arytenoid cartilages by laryngoscopy with the patient under light anesthesia6,7,9,11,12 (Figure 2). The presence of abnormal laryngeal function in clinical cases has been based on the subjective opinion of the surgeon. There is a reported 95% agreement between two observers in assigning 17 dogs a laryngeal paralysis score.1 A potential problem with diagnosing laryngeal paralysis is that anesthetic agents normally depress laryngeal movement. In normal dogs, anesthetic depths necessary to alleviate jaw tone to safely and easily visualize the larynx may prevent laryngeal motion.13,29 The paralysis may be bilateral (Figure 3) or unilateral (Figure 4). A comparison of various anesthetic protocols for laryngeal function in normal dogs has been reported.13
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CONCURRENT DISEASE The relationship between hypothyroidism and laryngeal paralysis is unclear; however, many dogs with laryngeal paralysis are concurrently hypothyroid. 3,11,26 Hypothyroidism could represent a causative or predisposing factor or could merely be coincidental.57,9,11,12 Resolution of laryngeal paralysis in supplemented hypothyroid dogs has been poorly described.27 In contrast, hypothyroid polyneuropathy (with no concurrent
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Arytenoid

Vocal folds

Figure 2. Drawing of the normal larynx as seen via

laryngoscopy. The arytenoid cartilages are adducted, and the vocal folds are obvious in the glottic opening. (Haines DK 2005
The University of Tennessee College of Veterinary Medicine) Figure 3. Laryngoscopic view of a patient with bilateral

Two anesthetic protocols, intravenous thiopental alone and intramuscular acepromazine with intramuscular butorphanol plus isoflurane by mask, had the least effect on laryngeal motion. Intravenous propofol, intravenous ketamine plus intravenous diazepam, intramuscular acepromazine plus intravenous thiopental, or intramuscular acepromazine plus intravenous propofol aines 2005 The university of Tennessee College of Veterinary Medicine caused more depression of laryngeal motion. This study suggests that use of the latter anesthetic protocols could cause misdiagnosis of laryngeal paralysis. Another report29 suggests that intravenous thiopental and intravenous propofol are superior to intravenous ketamine plus intravenous diazepam because they more effectively alleviate jaw tone. Another study30 evaluated use of doxapram HCl (1.1 mg/kg IV ) as a respiratory stimulant in dogs anesthetized with acepromazine, butorphanol, and isoflurane. Depth of respiration increased in normal dogs, but ar ytenoid motion did not change in response to doxapram HCl injection. Dogs affected by laryngeal paralysis developed paradoxical arytenoid motion and a decrease in glottal area. The authors concluded that doxapram HCl administration may be useful in differentiating between normal and affected dogs. Affected dogs may experience extreme glottic constriction and require intubation during examination. Transnasal laryngoscopy in dogs has been recently
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laryngeal paralysis. The arytenoid cartilages are immobile and moderately inflamed, which is typical in patients with laryngeal paralysis.

described.31 This technique is an adaptation of the wellaccepted means of diagnosing laryngeal paralysis in horses. The authors were able to successfully assess normal and abnormal laryngeal function in dogs sedated with an opioid and acepromazine. This technique eliminated the need for general anesthesia to diagnose laryngeal paralysis. A 2.5-mm flexible endoscope was passed through the nasal passages of dogs treated with intranasal lidocaine. The technique successfully differentiated between three normal dogs and four dogs affected with laryngeal paralysis. All of the dogs resisted lidocaine application and initial placement of the endoscope. If no laryngeal motion was observed, the authors mechanically stimulated the laryngeal mucosa to differentiate normal from abnormal dogs. Normal dogs began moving the arytenoids, whereas affected dogs did not. Limitations of the technique include the need for a small, flexible endoscope and a large patient. Use of ultrasonography has been described for diagnosing laryngeal paralysis in dogs.32 With direct transoral lar yngoscopy used as a definitive diagnostic procedure, motion of the cuneiform processes of the arytenoid cartilages was correctly observed in 10 of 10 normal dogs and 29 of 30 dogs with unilateral or bilatNovember 2005

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eral laryngeal paralysis. The one instance of disagreement was when ultrasonography suggested unilateral involvement but laryngoscopy showed bilateral involvement. Advantages of this technique are that it is rapid and noninvasive and does not require sedation or anesthesia. Disadvantages are that it requires technical expertise and expensive equipment. Difficulties are encountered with large, obese dogs and very calm dogs with shallow breathing. Computer programs using the normalized glottal gap area have been used to quantitatively measure the glottal opening and thereby laryngeal function.13,33 This has enabled investigators to compare anesthetic agents used for diagnosis and the efficacy of surgical techniques in relieving upper airway obstruction. Historically, tidal breathing flowvolume loops (TBFVL) and arterial blood gas analysis have been used to characterize the type and severity of upper airway obstruction and response to surgical correction. 34,35 TBFVL has not been used clinically in any of the major surgical technique reviews.512 The logistical challenges of TBFVL likely preclude its clinical use because it requires a voluntary maximal tidal volume, which is difficult to achieve in animals. Blood gas analysis is probably not routinely conducted because it was shown that blood gas abnormalities are directly related to severity of clinical signs and are not specific for a particular disease.35 Electromyography of the cricoarytenoideus dorsalis

Figure 4. Laryngoscopic view of a patient with

unilateral laryngeal paralysis. Note the abduction of the left arytenoid cartilage.

gram should be considered. Conversely, dogs diagnosed with megaesophagus and/or aspiration pneumonia should be screened closely for laryngeal paralysis. 24 Serum acetylcholine receptor antibody tests could be considered to rule out myasthenia gravis, especially in dogs with megaesophagus. 24 Thyroid function tests should be conducted to rule out hypothyroidism.27

Although laryngeal paralysis most often affects geriatric large-breed dogs, it can affect young dogs of a number of breeds.
muscle has been successfully used to confirm laryngeal paralysis.6 However, this technology requires specialized equipment and a highly trained electrophysiologist. A complete neurologic examination should be performed on all dogs and cats with laryngeal paralysis. Patients with neurologic abnormalities in addition to laryngeal paralysis should be considered as candidates for electrophysiology and muscle and nerve biopsies. Alternatively, animals presenting with polyneuropathy should be carefully evaluated for laryngeal paralysis.3

EVALUATING FOR CONCURRENT DISEASE The possibility of concurrent disease makes additional diagnostic testing necessary in patients suspected of having laryngeal paralysis. Thoracic radiographs should be taken to rule out aspiration pneumonia, intrathoracic mass, and megaesophagus.5,9,10,24 Cervical radiographs have been recommended to rule out neoplasia.11 If dysphagia or regurgitation is reported, a barium esophaNovember 2005

MEDICAL TREATMENT Medical treatment of laryngeal paralysis involves symptomatic treatment of hypoxia, hyperthermia, excitement, and obesity. Oxygen therapy, cooling, exercise restriction, stress avoidance, and caloric restriction
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Arytenoid

Arytenoid

Vocal fold Vocal folds removed

Figure 5. Drawing of an endoscopic view of ventriculo-

cordectomy. The vocal cords have been removed bilaterally, leaving the most ventral ends uncut to prevent webbing. (Haines DK
2005 The University of Tennessee College of Veterinary Medicine)

Figure 6. Drawing of an endoscopic view of partial arytenoidectomy. A portion of the corniculate process of the arytenoid cartilage and vocal folds has been removed. (Haines DK 2005 The University of Tennessee College of Veterinary Medicine)

dkhaines 2005 The university of Tennessee College of Veterinary Medicine

are advised.36,37 Identification and treatment of concurrent disease may be beneficial. Some benefit may be dkhaines 2005 The university of Tennessee College of Veterinary Medicine gained by thyroid supplementation in hypothyroid dogs.27 Corticosteroids have been advocated to decrease laryngeal inflammation.36,37 There is no proven efficacious drug therapy for similar polyneuropathies in humans.38

SURGICAL TREATMENT A variety of surgical procedures are used to treat laryngeal paralysis. Some are aimed at enlarging the laryngeal opening by removing one or both of the vocal folds (i.e., ventriculocordectomy) and arytenoid cartilages (i.e., partial laryngectomy). Some procedures seek to lateralize one or both arytenoid cartilages (tieback), whereas others seek to widen the larynx by widening the thyroid cartilage (i.e., laryngofissure). A description and brief review of each of these techniques follow. Ventriculocordectomy Ventriculocordectomy has been described for treating laryngeal paralysis.9 The dog is anesthetized with an injectable agent and positioned in sternal recumbency with the head elevated. Alternately, a tracheostomy may be performed and the patient maintained under inhalant anesthesia. The mouth is opened with the aid of a denCOMPENDIUM

tal speculum and the tongue retracted cranially. An assistant elevates the soft palate and depresses the epiglottis with the blade of a laryngoscope, permitting visualization of the larynx. Long forceps and scissors or biopsy forceps are used to reach inside the laryngeal opening and remove the vocal folds from the larynx (Figure 5). To prevent laryngeal webbing, the most ventral one-quarter of the vocal fold should not be excised. Simple removal of the vocal folds in some patients provides enough of an airway that the animal does not need additional surgery.9 This is especially true for inactive animals. The complication of webbing may be minimized by using a ventral laryngotomy approach to the vocal folds. The folds are removed under direct visualization and the mucosa reapposed over the excised edges using a 4-0 monofilament absorbable suture.

Partial Arytenoidectomy Partial arytenoidectomy is often performed in combination with unilateral vocal cord excision as described above.8 One or both of the vocal folds are removed. Biopsy forceps are then used to remove the medial portions of the corniculate processes of the arytenoid cartilages (Figure 6). Surgeons should attempt to remove 2 to 3 mm of the medial border of this carNovember 2005

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Figure 7. Laryngoscopic view of a cat with bilateral laryngeal paralysis before and after partial arytenoidectomy.

Before arytenoidectomy.

After arytenoidectomy.

tilage. It is best to remove only cartilage on one side of the larynx to prevent webbing at the dorsal laryngeal opening. It may be necessary to use a rongeur to remove portions of the cartilage. A sufficient amount of laryngeal tissue is removed from one side to provide an adequate laryngeal opening (Figure 7). Hemorrhage is controlled by intermittently packing the larynx with gauze or saline or epinephrine sponges. Following the partial laryngeal excision, the larynx is packed with gauze for approximately 10 minutes to provide hemostasis. After hemorrhage has been controlled, the upper trachea is aspirated and lavaged, if necessary, to remove residual blood clots. The animal is maintained under anesthesia for another 10 minutes to ensure that additional hemorrhage does not occur. If a tracheostomy is used for these procedures, the tube is left in place for 24 to 48 hours to provide airway management until laryngeal swelling has subsided.

Laryngeal Tieback The objective of laryngeal tieback is to enlarge the laryngeal opening by surgically retracting the arytenoid
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cartilage on one side of the larynx.7,12 This is accomplished by dissecting the arytenoid cartilage from its attachments and retracting it caudolaterally to the dorsocaudal wing of the thyroid cartilage or the dorsocaudal aspect of the cricoid cartilage. The procedure may be done on the left or right side. The animal is anesthetized, and the surgical site over the lateral aspect of the larynx is prepared for aseptic surgery. The neck is extended over a small sandbag to elevate the larynx for increased surgical exposure. A skin incision is made from the level of the ramus of the mandible, ventral to the jugular vein, to a level just caudal to the bifurcation of the jugular vein. The subcutaneous musculature and connective tissues are separated and the jugular vein and its bifurcation retracted dorsally by Gelpi retractors. The thyropharyngeus muscle is incised at its attachment to the rim of the thyroid cartilage. The wing of the thyroid cartilage is reflected laterally by blunt dissection of the connective tissue on its medial border and separation of the cricothyroid articulation. The muscular process of the arytenoid cartilage can usually be palpated as a small protrusion on the lateral surface of the larynx. The cricoarytenoid muscle that
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Figure 9. Laryngoscopic view of a patient with bilateral

Arytenoid Cricoid

laryngeal paralysis before and after thyroarytenoid lateralization. Note the mild abduction of the arytenoid cartilage.

Thyroid

Figure 8. Drawing demonstrating a thyroarytenoid

tieback with placement of two sutures from the muscular process of the arytenoid cartilage to the dorsocaudal border of the thyroid cartilage. (Haines DK
2005 The University of Tennessee College of Veterinary Medicine)

Before thyroarytenoid lateralization.

attaches at this point is making the dkhaines 2005 The university of usually Tennesseeatrophied, College of Veterinary Medicine process particularly prominent. Dissection begins under the muscular process with small blunt scissors, mosquito forceps, or a periosteal elevator, and the arytenoid cartilage is disarticulated from the cricoid cartilage immediately beneath the muscular process. When dissecting and placing sutures through the muscular process, surgeons should be extremely careful not to break the process, which is fairly easy to do in an elderly animal. This articulation is identified by the presence of articular cartilage. Once totally separated from the cricoid cartilage, the muscular process of the arytenoid cartilage is freely movable. To gain total mobility, it may be necessary to sever the sesamoidian band that connects the left and right arytenoid cartilages across the dorsal aspect of the larynx. This small band of tissue is approximately 1 mm in diameter and, when excised, allows the arytenoid to become totally mobilized. Two sutures of 0 (for large dogs) or 3-0 (for small dogs and cats) monofilament nonabsorbable suture with a sturdy half-circle taper point needle are placed through the muscular process of the arytenoid and through the dorsocaudal extremity of the wing of the thyroid cartilage8 (Figure 8). When these sutures are tied tightly, the arytenoid is pulled laterally, opening the larynx (Figure 9).
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After thyroarytenoid lateralization.

An alternative and more physiologic suturing technique involves placing the tieback suture from the muscular process of the arytenoid to the dorsocaudal border of the cricoid cartilage.13 Sutures from the arytenoid to the cricoid in this procedure approximate the same
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Figure 11. Laryngoscopic view of a patient with bilateral

Arytenoid Cricoid

laryngeal paralysis before and after cricoarytenoid lateralization. Note that the arytenoid is more lateralized than with the thyroarytenoid tieback in Figure 9.

Thyroid

Figure 10. Drawing illustrating a cricoarytenoid tieback with placement of two sutures from the muscular process of the arytenoid cartilage to the dorsocaudal aspect of the cricoid cartilage. (Haines DK 2005 The University of Tennessee College of Veterinary Medicine)

Before cricoarytenoid lateralization. dkhaines 2005 The university of Tennessee College of Veterinary Medicine

function and location as the cricoarytenoideus dorsalis muscle. This suture is more demanding to place because exposure of the dorsocaudal cricoid can be difficult. In placing these sutures, surgeons must be very careful to retract the esophagus dorsally to avoid injury when operating on the left side. Preferably, two simple sutures should be placed from the muscular process of the arytenoid to the caudal rim of the cricoid immediately lateral to the dorsal midline (Figure 10). For right-handed surgeons, the suture is passed from the cricoid cartilage cranial to the muscular process. For left-handed surgeons, the suture is passed from the muscular process caudally to the cricoid cartilage. After these sutures have been placed and one has been tied, the anesthetist should examine the larynx with a laryngoscope to ensure that the tieback procedure has resulted in proper lateralization of the arytenoid cartilage (Figure 11). It is very easy to overabduct the arytenoid cartilage with this procedure, resulting in dysfunction of the larynx after surgery due to inability of the epiglottis to totally close the abducted larynx. It is necessary to move the muscular process only a few millimeters caudally (Figure 11). The second suture is tied after the first has been confirmed to be properly placed. Absorbable sutures are used to reapproximate the severed thyropharyngeus muscle and the subcutaneous tissue. The skin is closed with monofilament nonabsorbable sutures.
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After cricoarytenoid lateralization.

Modified Castellated Laryngofissure A seldom-used technique is the modified castellated laryngofissure. The patient is anesthetized and placed in dorsal recumbency, with the neck arched ventrally, and the skin over the larynx is prepared for surgery.39,40
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Figure 12. Drawings of the castellated laryngofissure procedure. A, B, and C represent the three segments created by a step incision of the thyroid cartilage. (Haines DK 2005 The University of Tennessee College of Veterinary Medicine)

Basihyoid bone

Basihyoid bone

Step incision

Thyroid

Thyroid Cricothyroid ligament

Cricothyroid ligament

Cricoid

Cricoid

A step incision is made in the thyroid cartilage.

The step is distracted and sutured to widen the laryngeal opening.

Other Surgical Options A skin incision is made over the larynx to the fourth dkhaines 2005 pedicle The university of Tennessee College of Veterinary Medicine Neuromuscular grafting has been investigated tracheal ring. The sternohyoideus muscle is divided to 41 in dogs. It is not commonly performed because it does expose the thyroid and cricoid cartilages. A tranot provide immediate relief of upper airway obstruction. cheotomy tube is inserted into a vertical incision dkhainesthe 2005 The university of Tennessee College of Veterinary Neuromuscular pedicle grafts require 36 to 44 weeks to between second and third tracheal rings. A stepMedicine return laryngeal movement to normal. Permanent traincision is made in the thyroid cartilage, and the larynx cheostomy has been recommended as a final alternative is opened (Figure 12). The vocal folds are removed in treating laryngeal paralysis.42 Permanent tracheostomy under direct visualization. The arytenoids are bilaterally can be problematic in dogs that like to swim. lateralized by monofilament mattress sutures placed through the thyroid cartilage and the arytenoid cartiCOMPARISON OF DIFFERENT lage dorsal to the vocal process, with the knot outside SURGICAL TECHNIQUES the laryngeal lumen. Two or three 3-0 monofilament A 2001 report5 provides the most comprehensive comnonabsorbable sutures are preplaced between the step parison of different surgical techniques. The findings and the cranial segment of the opposite cartilage incishow that both unilateral arytenoid lateralization and sion. The castellated cartilage incision is closed by partial laryngectomy offer superior clinical outcome over aligning the step against the cranial segment of the bilateral arytenoid lateralization. Complication rates opposite cartilage incision, thereby spreading the larynx between unilateral arytenoid lateralization (30%) and by the height of the step. The step is fixed in position partial laryngectomy (40%) were not significantly differby tightening the preplaced sutures. Sutures from the ent. However, dogs treated with partial laryngectomy thyroid around the basihyoid bone help secure the clowere significantly more likely to die of complications sure. Loose tissue and corner edges of cartilage are than were dogs treated with unilateral arytenoid lateraltrimmed away to prevent them from entering the ization. These complications included aspiration pneulumen of the larynx. The sternohyoideus and sternothymonia, respiratory distress, failure of surgical repair, and roideus muscles are tightly approximated to close the death. The complication rate may be higher than in laryngeal defect. The subcutaneous tissue and skin are some other studies because of a longer duration of folclosed routinely. The tracheostomy tube is removed in 3 low-up. There was not a significant difference in implant to 4 days.
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failure between dogs treated with thyroarytenoid lateralization and those treated with cricoarytenoid lateralization. Postoperative death rates were highest in dogs treated with bilateral arytenoid lateralization (67%) compared with unilateral arytenoid lateralization (14%) and partial laryngectomy (30%). Factors predisposing patients to death or complications were age, temporary tracheostomy placement, concurrent respiratory tract abnormalities, concurrent esophageal disease, postoperative megaesophagus, concurrent neoplastic disease, and concurrent neurologic disease. A common complication of the tieback procedure is persistent postoperative cough, especially after eating or drinking. This is because the arytenoid cannot adduct and the epiglottis does not completely close with swallowing. The most commonly recommended treatment of laryngeal paralysis in dogs is unilateral arytenoid lateralization.5 This procedure appears to offer good resolution of clinical

3 years of age in 31% of affected cats. Another study4 reported that clinical signs began in two of four cats younger than 1 year of age. Clinical signs of laryngeal paralysis in cats include tachypnea or dyspnea, stridor, exercise intolerance, change in phonation, dysphagia, weight loss, cough, anorexia, lethargy, cyanosis, and fever.2,4,45 As in dogs, laryngeal paralysis in cats may occur in conjunction with polyneuropathy.4 In one report,4 two of four affected cats had generalized neuromuscular disease. Little is known about the pathophysiology of laryngeal paralysis in cats. Based on the age of cats treated surgically for laryngeal paralysis, apparently, there are congenital and acquired causes. How often cats are affected with idiopathic laryngeal paralysis is unknown. In one report,2 75% of affected cats had bilateral laryngeal paralysis. Other causes of laryngeal paralysis include neoplasia, trauma, or a surgical complication in the cervical or thoracic region.46,47

Thorough evaluation for concurrent disease is important in establishing a therapeutic plan and prognosis for patients with laryngeal paralysis.
signs with fewer complications than partial laryngectomy.6,10 Unilateral arytenoid lateralization is technically easier and quicker than castellated laryngofissure.43 One report44 compared the two methods of unilateral arytenoid lateralization (i.e., thyroarytenoid versus cricoar ytenoid lateralization). It was shown that cricoarytenoid lateralization increased the size of the glottic opening compared with thyroarytenoid lateralization. Cricoarytenoid lateralization did not, however, result in improved clinical outcome but did require significantly less operative time (i.e., 25 minutes compared with 43 minutes).44 As in dogs, affected cats often have concurrent illness.2 Up to 25% have aspiration pneumonia. In one report,4 two of four cats were affected with generalized neuromuscular disease. Megaesophagus, FIV infection, and FeLV infection have been reported in affected cats.2,48 Diagnosis is made by direct visualization of the larynx in a lightly anesthetized cat.4 Veterinarians have successfully treated feline laryngeal paralysis with bilateral arytenoid lateralization,49 unilateral arytenoid lateralization,50 partial laryngectomy,4 and castellated laryngofissure.51 These methods in cats have not been meaningfully compared. Extrapolation of data from dogs suggests that unilateral arytenoid lateralization is the most effective, safe, and clinically practical surgical technique.37 Tieback procedures are more difficult in cats than in dogs because of the small size of the larynx. Dissection is more challenging, and suture placement must be precise.

LARYNGEAL PARALYSIS IN CATS Laryngeal paralysis is becoming more commonly recognized in cats.2,4 No sex or breed predilection has been identified. The median age of cats diagnosed with laryngeal paralysis is 11 years (range: 4 months to 17 years of age). Half of the affected cats in one report2 were domestic shorthair. Other breeds represented included domestic longhair, Siamese, Abyssinian, and Balinese. The same study reported that clinical signs began at younger than
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CONCLUSION Laryngeal paralysis is a common, important cause of upper respiratory obstruction in dogs and is increasingly being recognized in cats. Recent advances in diagnostic techniques should help veterinarians correctly identify
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CE Laryngeal Paralysis: Pathophysiology, Diagnosis, and Surgical Repair

the problem. Thorough evaluation for concurrent disease is crucial in providing excellent patient care. Several surgical alternatives seem to be acceptable, if not ideal, in treating the problem. Arytenoid tieback surgery appears to give the best overall results.

21. OBrien JA, Hendriks JC: Inherited laryngeal paralysis: Analysis in the husky cross. Vet Q 8:301302, 1986. 22. Shelton GD, Podell M, Poncelet L, et al: Inherited polyneuropathy in Leonberger dogs: A mixed or intermediate form of Charcot-Marie-Tooth disease? Muscle & Nerve 27:471477, 2003. 23. Salisbury KS, Forbes S, Blevins WE: Peritracheal abscess associated with tracheal collapse and bilateral laryngeal paralysis in a dog. JAVMA 196:1273 1275, 1990. 24. Gaynor AR, Shofer FS, Washabau RJ: Risk factors for acquired megaesophagus in dogs. JAVMA 211:14061412, 1997. 25. OBrien JA, Harvey CE, Kelly AM, Tucker JA: Neurogenic atrophy of the laryngeal muscles of the dog. J Small Anim Pract 14:521532, 1973. 26. Harvey HJ, Irby NL, Watrous BJ: Laryngeal paralysis in hypothyroid dogs, in Kirk RW (ed): Current Veterinary Therapy VIII: Small Animal Practice. Philadelphia, WB Saunders, 1983, pp 694697. 27. Jaggy A, Oliver JE, Ferguson DC, et al: Neurological manifestations of hypothyroidism: A retrospective study of 29 dogs. J Vet Intern Med 8:328 336, 1994. 28. Holt D, Brockman D: Diagnosis and management of laryngeal disease of the dog and cat. Vet Clin North Am 24:855871, 1994. 29. Gross ME, Dodam JR, Pope ER, Jones BD: A comparison of thiopental, propofol, and diazepam-ketamine anesthesia for evaluation of laryngeal function in dogs premedicated with butorphanol and glycopyrrolate. JAAHA 38:503506, 2002. 30. Tobias K, Jackson AM, Harvey RC: Effects of doxapram HCl on laryngeal function of normal dogs and dogs with naturally occurring laryngeal paralysis. Vet Anesth Analg 31:258263, 2004. 31. Radlinsky MG, Mason DE, Hodgson D: Transnasal laryngoscopy for the diagnosis of laryngeal paralysis in dogs. JAAHA 40:211215, 2004. 32. Rudorf HR, Barr FJ, Lane JG: The role of ultrasound in the assessment of laryngeal paralysis in the dog. Vet Radiol Ultrasound 42(4):338343, 2001. 33. Lussier B, Flanders JA, Erb HN: The effect of unilateral arytenoid lateralization on rima glottidis area in canine cadaver larynges. Vet Surg 25:121126, 1996. 34. Amis TC, Smith MM, Gaber CE, Kurpershock C: Upper airway obstruction in canine laryngeal paralysis. Am J Vet Res 47(5):10071010, 1986. 35. Love S, Waterman AE, Lane JG: The assessment of corrective surgery for canine laryngeal paralysis by blood gas analysis: A review of 35 cases. J Small Anim Pract 28:597604, 1987. 36. Hedlund CS: Surgery of the upper respiratory system, in Fossum TW (ed): Small Animal Surgery. St Louis, Mosby, 1997, p 629. 37. Griffon DJ: Upper airway obstruction in cats: Diagnosis and treatment. Compend Contin Educ Pract Vet 22(10):897907, 2000. 38. Vrancken AF, van Schaik IN, Hughes RA, Notermans NC: Drug therapy for chronic idiopathic axonal polyneuropathy. Cochrane Database Syst Rev 2:CD003456, 2004. 39. Gourley IM, Paul H, Gregory C: Castellated laryngofissure and vocal fold resection for the treatment of laryngeal paralysis in the dog. JAVMA 182(10): 10841086, 1983. 40. Smith MM, Gourley IM, Kerpershoek CJ, Amis TC: Evaluation of a modified castellated laryngofissure for alleviation of upper airway obstruction in dogs with laryngeal paralysis. JAVMA 188(11):12791283, 1986. 41. Greenfield CL, Walshaw R, Kumar K, et al: Neuromuscular pedicle graft for restoration of arytenoid abductor function in dogs with experimentally induced laryngeal hemiplegia. Am J Vet Res 49(8):13601366, 1988. 42. Hedlund CS, Tangner CH, Waldron DR, Hobson HP: Permanent tracheostomy perioperative and long-term data from 34 cases. JAAHA 24:585 591, 1988.

REFERENCES
1. Broome C, Burbidge HM, Pheiffer DU: Prevalence of laryngeal paresis in dogs undergoing general anesthesia. Aust Vet J 78(11):769772, 2000. 2. Schachter S, Norris CR: Laryngeal paralysis in cats: 16 cases (19901999). JAVMA 216(7):11001103, 2000. 3. Braund KG, Steinberg HS, Shores A, et al: Laryngeal paralysis in immature and mature dogs as one sign of a more diffuse polyneuropathy. JAVMA 194(12):17351740, 1989. 4. White RAS, Littlewood JD, Herrtage ME, Clarke DD: Outcome of surgery for laryngeal paralysis in four cats. Vet Rec 118(4):103104, 1986. 5. MacPhail CM, Monnet E: Outcome of and postoperative complications in dogs undergoing surgical treatment of laryngeal paralysis: 140 cases (19851998). JAVMA 218(12):19491955, 2001. 6. Harvey CE, OBrien JA: Treatment of laryngeal paralysis in dogs by partial laryngectomy. JAAHA 18:551556, 1982. 7. White RAS: Unilateral arytenoid lateralisation: An assessment of technique and long-term results in 62 dogs with laryngeal paralysis. J Small Anim Pract 30:543549, 1989. 8. Trout NJ, Harpster NK, Berg J, Carpenter J: Long-term results of unilateral ventriculocordectomy and partial arytenoidectomy for the treatment of laryngeal paralysis in 60 dogs. JAAHA 30:401407, 1994. 9. Holt D, Harvey CE: Idiopathic laryngeal paralysis: Results of treatment by bilateral vocal fold resection in 40 dogs. JAAHA 30:389395, 1994. 10. Ross JT, Matthiesen DT, Noone KE, Scavelli TA: Complications and longterm results after partial laryngectomy for the treatment of idiopathic laryngeal paralysis in 45 dogs. Vet Surg 20:169173, 1991. 11. Gaber CE, Amis TC, LeCouteur RA: Laryngeal paralysis in dogs: A review of 23 cases. JAVMA 186:377380, 1985. 12. Lahue TR: Treatment of laryngeal paralysis in dogs by unilateral cricoarytenoid laryngoplasty. JAAHA 25:317324, 1989. 13. Jackson AM, Tobias K, Long C, et al: Effects of various anesthetic agents on laryngeal motion during laryngoscopy in normal dogs. Vet Surg 33:102106, 2004. 14. Venker-van Haagen AJ, Hartman W, Goedegebuure SA: Spontaneous laryngeal paralysis in young Bouviers. JAAHA 14:714720, 1978. 15. OBrien JA, Hendriks JC: Inherited laryngeal paralysis in Siberian husky crosses. Proc Am Coll Vet Intern Med:142, 1985. 16. Braund KG, Shores A, Cochrane S, et al: Laryngeal paralysispolyneuropathy complex in young dalmatians. Am J Vet Res 55:534542, 1994. 17. Mahony OM, Knowles KE, Braund KG, et al: Laryngeal paralysispolyneuropathy complex in young rottweilers. J Vet Intern Med 12:330337, 1998. 18. Braund KG: Clinical Syndromes in Veterinary Neurology. St Louis, Mosby, 1994, pp 168170. 19. Venker-van Haagen AJ: Investigations of the pathogenesis of hereditary laryngeal paralysis in the Bouvier [PhD Thesis]. Utrecht, Netherlands, Proefschrift University, 1980. 20. Venker-van Haagen AJ, Boow J, Hartman W: Hereditary transmission of laryngeal paralysis in Bouviers. JAAHA 17:7576, 1981.

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Laryngeal Paralysis: Pathophysiology, Diagnosis, and Surgical Repair CE

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43. Petersen SW, Rosin E, Bjorling DE: Surgical options for laryngeal paralysis in dogs: A consideration of partial laryngectomy. Compend Contin Educ Pract Vet 13(10):15311539, 1991. 44. Griffiths LG, Sullivan M, Reid SWJ: A comparison of the effects of unilateral thyroarytenoid lateralization versus cricoarytenoid laryngoplasty on the area of the rima glottidis and clinical outcome in dogs with laryngeal paralysis. Vet Surg 30:359365, 2001. 45. Hardie EM, Kolata RJ, Stone EA, Steiss JE: Laryngeal paralysis in three cats. JAVMA 179:879882, 1981. 46. Rozanski EA, Stobie D: Laryngeal paralysis secondary to a cystic thyroid adenoma in a cat. Feline Pract 23(6):67, 1995. 47. Schaer M, Zaki FA, Harvey HJ, OReilly WH: Laryngeal hemiplegia due to neoplasia of the vagus nerve in a cat. JAVMA 174(5):513515, 1979. 48. Cribb AE: Laryngeal paralysis in a mature cat [correspondence]. Can Vet J 27:27, 1986. 49. Payne JT, Martin RA, Rigg DL: Abductor muscle prosthesis for correction of laryngeal paralysis in 10 dogs and one cat. JAAHA 26(6):599604, 1990. 50. White RN: Unilateral arytenoid lateralisation for the treatment of laryngeal paralysis in four cats. J Small Anim Pract 35(9):455458, 1994. 51. Campbell D, Holmberg DL: Surgical treatment of laryngeal paralysis in a cat. Can Vet J 25(11):414416, 1984.

4. A possible association exists between laryngeal paralysis and a. hypoadrenocorticism. b. hyperadrenocorticism. c. hypothyroidism. d. insulinoma. 5. Which anesthetic(s) is expected to have the least impact on laryngeal function? a. thiopental b. propofol c. diazepam plus ketamine d. All of the above have a similar effect on laryngeal function. 6. Administering doxapram to a dog with laryngeal paralysis would not be expected to cause _____________ during laryngeal examination. a. increased respiratory effort b. increased arytenoid abduction c. paradoxical arytenoid motion d. glottic constriction 7. Which statement regarding laryngeal paralysis is true? a. It is advisable to have an endotracheal tube ready when performing transnasal laryngoscopy because dogs may experience severe glottic constriction and require intubation during examination. b. Ultrasonography of the larynx correlates poorly with laryngeal function. c. Inappropriate choice of anesthetic protocols could lead to incorrect diagnosis of laryngeal paralysis. d. Hypothyroidism has been shown to cause laryngeal paralysis. 8. A common complication of partial arytenoidectomy is a. surgical repair failure. b. uncontrollable hemorrhage. c. epiglottic paralysis. d. laryngeal webbing. 9. Sutures can be passed between the ____________ cartilages to perform arytenoid lateralization. a. arytenoid and thyroid b. thyroid and cricoid c. arytenoid and cricoid d. a and c 10. The _____________ cartilage is cut in a stepwise fashion during castellated laryngofissure. c. arytenoid a. cricoid b. thyroid d. epiglottis

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1. Which has reportedly caused laryngeal paralysis in dogs? a. idiopathic nerve degeneration b. postsurgical complication c. neoplasia d. all of the above 2. Lar yngeal paralysis occurs most often in ___________ dogs. a. old, large-breed b. old, small-breed c. young, large-breed d. young, small-breed 3. Laryngeal paralysis in the Bouvier des Flandres is inherited as an _____________ trait. a. X-linked b. autosomal dominant c. autosomal recessive d. none of the above

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