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ISRN Veterinary Science
Volume 2012 (2012), Article ID 238505, 15 pages
Imaging Evaluation of Dogs and Cats with Dysphagia
Department of Surgical and Radiological Sciences, Davis School of Veterinary Medicine, The University of California, Davis, CA 95616, USA
Received 15 August 2012; Accepted 19 September 2012
Academic Editors: A. Berman and M. Malkinson
Copyright © 2012 Rachel E. Pollard. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The current literature is reviewed in this paper regarding the application of diagnostic imaging in the evaluation of swallowing disorders of the dog. The applications of radiography, contrast radiography, and contrast videofluoroscopy are discussed with pertinent case examples provided for emphasis. The indications for image-guided interventions are also described.
Dysphagia, or difficulty with swallowing, is a clinical symptom that may arise from a variety of diseases. Traditionally, dysphagias are classified based on the location of the abnormality (Table 1) [1, 2]. Oropharyngeal dysphagias involving the oral phase of swallowing typically result in abnormal prehension and can be diagnosed by watching the patient eat. However, oropharyngeal dysphagias affecting the pharyngeal and cricopharyngeal phases of swallowing often present with clinically similar signs such as gagging, retching, and the necessity to attempt swallowing multiple times prior to success. Myotomy or myectomy may result in clinical improvement in patients with delayed or absence of opening of the upper esophageal sphincter but animals with disorders of pharyngeal contraction will become clinically worse with surgery . Moreover, animals with combined disease affecting both the pharyngeal and cricopharyngeal phases of swallowing may be poor surgical candidates.
Standard veterinary diagnostic imaging techniques can provide information regarding pharyngeal, cricopharyngeal, and esophageal anatomy . However, many disease processes more specifically affect function with little or no anatomic alteration. In addition, certain anatomical alterations such as hiatal hernias are transient such that the point-in-time imaging capabilities provided by plain radiography may not capture the abnormality. Functional and transient abnormalities are particularly common in dysphagic animals. Although radiographs with or without oral barium administration may help define certain causes for dysphagia, real-time imaging techniques such as contrast fluoroscopy provide a means for visualizing esophageal function allowing for detection of subtle and transient abnormalities .
2. Normal Swallowing Anatomy and Physiology
Swallowing is a complex physiologic process that propels a bolus of liquid of food from the oral cavity to the stomach. The actions involving the lapping of liquid and prehension and chewing of food are voluntary and require coordinated movements of the tongue and jaws. Once a bolus is propelled into the pharyngeal region, the swallowing reflex occurs involuntarily requiring input from the sensory and motor branches of the trigeminal, the hypoglossal, facial, and glossopharyngeal nerves . The pharynx contracts caudally against the base of the tongue to push the bolus toward the upper esophageal sphincter. Simultaneously, the epiglottis flips upward to cover the opening of the larynx to prevent aspiration. As the pharynx contracts, the paired cricopharyngeus and thyropharyngeus muscles that make up the upper esophageal sphincter relax to allow passage of the bolus into the proximal esophagus. Once the bolus has passed, the upper esophageal sphincter closes to prevent retrograde movement of the food or liquid and the epiglottis returns to its relaxed position so that normal respiration may resume.
The esophagus is a flexible tube responsible for the transport of a bolus from the upper esophageal sphincter to the stomach. Similar to the rest of the gastrointestinal tract the esophagus is a layered structure with the innermost surface being lined by mucosa. The submucosa, muscularis, and externally the adventitia are the remaining layers . In the dog, the muscularis layer consists of striated muscle. In the cat, the muscularis layer consists of striated muscle cranially but changes to smooth muscle in the caudal third resulting in the characteristic “herring bone” appearance on contrast esophagography. A bolus may be transported from the proximal esophagus to the lower esophageal sphincter by primary or secondary peristaltic waves . A primary peristaltic wave is a continuation of pharyngeal contraction that will propel the bolus directly to the stomach. If primary peristalsis fails then the bolus is transported to the stomach either by secondary peristalsis or with the ensuing primary peristaltic wave generated by the next bolus.
The lower esophageal sphincter is a focal narrowing of the esophagus at the junction with the stomach that is toned at rest to prevent retrograde movement of gastric contents. The sphincter is made up of a focal thickening of the muscularis layer of the esophagus, a confluence of gastric rugae at the gastroesophageal junction oriented transversely to the sphincter, and a muscular sling created by the diaphragm . A short segment of the esophagus resides on the abdominal side of the diaphragm where relatively positive intraabdominal pressure compresses it. When a bolus is transported caudad by the esophagus, the lower esophageal sphincter relaxes to allow passage into the stomach.
Survey radiography of the thorax and neck is often the first imaging step for the evaluation of the dysphagic animal. This should include three projections of the thorax (dorsoventral or ventrodorsal, right, and left lateral) and at least one lateral projection of the neck. Care should be taken to ensure that the radiograph of the neck is adequately positioned. More specifically, the lateral cervical study must not be rotated and the head should be extended as poor positioning can seriously compromise interpretation and frequently results in distortion of the anatomy.
The primary purpose of survey radiographs is to rule out gross anatomic alterations that would cause dysphagia. Foreign bodies in the pharynx or esophagus may or may not be radiographically apparent . Radiodense foreign bodies such as teeth , needles , and fish hooks  are typically readily identified with survey radiography. However, foreign bodies consisting of soft tissue dense material are harder to identify (Figure 1). Penetrating wood foreign bodies involving the pharynx and proximal esophagus have been reported in both dogs [8, 11] and cats  and may be hard to visualize. Radiographs obtained from dogs with penetrating wood foreign bodies in the pharynx and proximal esophagus rarely identify the stick and most commonly show soft tissue swelling and gas in the subcutaneous tissues, fascial planes, and mediastinum .
Pharyngeal and retropharyngeal masses of neoplastic and infectious origins can cause dysphagia but are often difficult to define using survey radiography [13–15]. However, esophageal masses may result in dysphagia and, particularly those involving the thoracic esophagus can be identified radiographically. Spirocerca lupi is a nematode that infests the canine esophagus resulting in radiographically apparent esophageal masses, caudal thoracic vertebral spondylitis, and aortic undulation [15, 16]. Transformation of Spirocerca granulomas into malignant sarcomas has been reported and also results in radiographically visible esophageal masses [17, 18]. Other types of neoplastic lesions reported to cause esophageal dysphagia include squamous cell carcinoma, leiomyoma, leiomyosarcoma, fibrosarcoma, osteosarcoma [19, 20], adenocarcinoma , and plasmacytoma .
Megaesophagus is another cause for esophageal dysphagia that can be diagnosed using survey radiography. Megaesophagus can be congenital or acquired . Acquired megaesophagus is classified as idiopathic or secondary to other diseases such as myasthenia gravis [24, 25] (with or without thymic neoplasia [26, 27]), hypoadrenocorticism [7, 28, 29], hypothyroidism [30–32], tetanus , and dysautonomia [34, 35] to name a few. Acquired megaesophagus can also be segmental forming oral to an obstructive process such as a stricture or vascular ring anomaly . Radiographic findings such as leftward deviation of the trachea and tracheal narrowing are findings associated with vascular ring anomalies that occur along with segmental esophageal dilation cranial to the heart base . When diffuse megaesophagus is found, contrast imaging is typically not indicated since a cause for esophageal dysphagia has been defined and contrast administration may result in aspiration . However, segmental megaesophagus should be further defined with contrast radiography in an attempt to differentiate stricture from vascular ring anomaly.
Survey radiographs will also help define if aspiration pneumonia is present. Aspiration pneumonia is common in dysphagic patients and typically involves the dependent aspect of the right and left cranial and right middle lung lobes. Since the right middle lung lobe is a common site for aspiration, the left lateral thoracic view is essential for complete assessment of the lung (Figure 2) . When megaesophagus is identified, the presence of aspiration pneumonia has a negative association with survival time . In cases where the cause for dysphagia is not clear on survey radiographs, barium contrast studies should be postponed if severe aspiration pneumonia is present, as aspiration of barium during the imaging procedure will further compromise lung function.
4. Contrast Radiography
If an anatomic abnormality other than megaesophagus is suspected on the survey study, contrast radiography may be indicated to help further define the origin of the problem. The type of contrast agent selected to perform contrast radiography depends on the suspected lesion type . Barium paste or cream is highly viscous and may adhere best to mucosal irregularities. However, due to the viscosity of the agents, barium paste and cream may not flow well around intraluminal lesions . Therefore, liquid barium (60% weight-volume) is the most common agent used for contrast radiography of the pharynx and esophagus . Dosage is related to body weight such that small to medium sized dogs should receive 15 mL boluses while larger dogs should receive 20–30 mL boluses of liquid barium orally . When perforation of the pharynx, cricopharynx, or esophagus is suspected, nonionic iodinated contrast agents are preferable to avoid the granulomatous reaction associated with leakage of barium into the cervical soft tissues or mediastinum . Esophageal perforation should be suspected when survey radiographs identify gas in the cervical soft tissues or mediastinum but no external wounds are present. Soft tissue swelling in the cervical region may indicate abscessation subsequent to perforation should it be combined with regional emphysema. Similarly, opacification and widening of the mediastinum may accompany pneumomediastinum when perforation of the thoracic esophagus has resulted in mediastinitis . In these instances, nonionic, iodinated contrast agents should be diluted 50 : 50 with sterile water and 10–15 mL boluses are administered orally .
Regardless of the type of contrast agent used, the animal is restrained in right lateral recumbency and liquid contrast agent is administered orally using a catheter-tipped syringe. Sedation should be avoided since tranquilizers result in significant alterations in swallowing function . However, should the animal be intractable, acepromazine may be administered in dogs recognizing that rapid esophageal transit times may result particularly at higher doses . Lateral and dorsoventral radiographs of the neck and thorax should be obtained during swallowing or as soon after swallowing as possible. Multiple swallows may be necessary and it is wise to obtain several views of any suspected abnormalities. When perforation is not suspected, kibble is then soaked in barium and administered orally . Additional lateral and dorsoventral radiographs of the neck and thorax should be obtained. Barium soaked kibble is particularly helpful when trying to identify esophageal strictures through which liquid barium may pass unimpeded. Mixing iodinated contrast agents with kibble is not advised since iodinated agents are typically used when perforation is suspected and esophageal leakage of kibble is undesirable .
Specific instances where contrast radiography is particularly useful include confirmation of an esophageal foreign body suspected on survey radiographs or in the case of a young animal with a suspected vascular ring anomaly (Figure 3). A full discussion of vascular ring anomalies is beyond the scope of this paper however it is important to recognize that a multitude of types exists. Approximately 95% of vascular ring anomalies resulting in megaesophagus and esophageal dysphagia originate from persistence of the right aortic arch . This can occur in isolation or in combination with other abnormal vessel development such as an aberrant left subclavian artery [44, 45]. Other infrequent types of vascular ring anomalies reported to cause esophageal dilation and dysphagia include persistent left cranial vena cava , double aortic arch , and left aortic arch with right ligamentum arteriosum . Contrast esophagography can prove useful for identifying a vascular ring anomaly but often cannot distinguish between the different types . Keep in mind that a single narrowed area in the esophagus may represent a peristaltic wave and strictures or vascular ring anomalies should only be diagnosed if persistent narrowing is present on several projections and abnormal dilation of the esophagus is present.
Contrast radiography can also be useful when a large soft tissue mass is present in the caudal mediastinum but the origin of the mass is unclear. Contrast medium can help identify the exact location of the esophagus in the mass. Additionally, it may identify irregularity of the esophageal mucosa, which would indicate an esophageal origin for the mass. Gastroesophageal intussusception is a disorder usually diagnosed in young dogs [49–53] and cats  in which the stomach telescopes into the esophageal lumen. Preexisting megaesophagus may predispose to intussusception. Survey radiographs often show a heterogenous caudal mediastinal mass with proximal gas dilation of the esophagus. The gastric shadow may be absent from the abdomen. Liquid barium administration (Figure 4) will help define rugal folds on the surface of the mass and confirm esophageal obstruction .
5. Contrast Enhanced Videofluoroscopy
In people, contrast enhanced videofluoroscopy is used to evaluate and classify oropharyngeal dysphagias and functional or transient disorders of the esophagus and lower esophageal sphincter [55–61]. In companion animals, the use of contrast videofluoroscopy is limited by cost and availability. However, for certain disorders, contrast videofluoroscopy is essential to reach a definitive diagnosis as to the cause of dysphagia. It is important to recognize that, although substantial data is present in the medical literature documenting the effect of bolus size [62–66], number , consistency [68–72], viscosity [73–75], and body positioning during the procedure [76–79] on the outcome of videofluoroscopy in people, very little information has been generated on these topics in veterinary patients. Moreover, substantial evidence is present indicating that age delays esophageal transit times  and pharyngeal bolus propulsion [81, 82] in people but this has not been investigated in dogs. This is most likely related to the radiation exposure to technical staff, who must restrain the animals in order to perform research in these areas and the difficulty associated with standardizing how much food or liquid an animal swallows at any given time.
When performing an esophagram, the animal is ideally fasted for 12 hours prior to the procedure. Liquid barium (60% weight-volume) is the most common contrast agent used but, similar to contrast radiography, nonionic iodinated agents diluted 50 : 50 with sterile water can be used in cases where perforation of the pharynx or esophagus is suspected. The animal is then positioned on the fluoroscopy table. Although most institutions position the animal in right lateral recumbency, a sternal or standing position can also be used. A recent report described the differences between sternal and lateral body positioning during contrast videofluoroscopy of swallowing in the dog and found that cervical esophageal transit times were significantly delayed in laterally recumbent dogs . However, a specific positioning device is necessary to minimize patient motion during sternally positioned studies (Figure 5) and, in the authors’ experience, motion remains problematic during these examinations. As with contrast radiography, sedation should be avoided when performing contrast enhanced videofluoroscopy due to the inherent alteration in swallowing function that results from tranquilization.
Regardless of body position, liquid barium should be administered orally in small (5–10 mL) boluses using a catheter-tipped syringe. At least three swallows should be observed and at least one bolus should be followed all the way to the stomach. Barium-soaked kibble should also be given orally and bolus propulsion observed fluoroscopically so as to rule out a functional abnormality that allows liquid passage but affects passage of solid foods.
Recording the study and performing frame-by-frame analysis can provide quantitative measures of swallowing function. The normal timing of the swallowing act has been reported (Figure 6) . Videos are viewed frame by frame where each frame represented 1/30th of a second. The frame in which the epiglottis is observed to close over the larynx is considered as the starting point for all time measurements. From this point, frames are counted until the observation of maximal contraction of the pharynx, opening of the upper esophageal sphincter, and closing of the upper esophageal sphincter. The swallow is considered completed when the epiglottis was observed to reopen. Once the number of frames to each point in the swallow are calculated, that number is divided by 30 to obtain the number of seconds from the initiation of the swallow to each particular event within that swallow (each frame represents 1/30th of a second in the NTSC system, the analog television system used in the United States). Normal values are listed in Table 2.
The contraction of the pharynx can also be assessed using frame-by-frame analysis to calculate the pharyngeal constriction ratio . From the digitized videofluoroscopic studies, a hold frame and a maximum contraction frame are selected. The hold frame is identified as a frame in which the larynx appeared at rest without rostral or caudal motion. The maximum contraction frame is identified as a frame in which the dorsal pharyngeal wall had reached its most ventral and caudal position. For the hold frame, a region of interest (ROI) is drawn around the air space beginning dorsal to the soft palate then rostrally to the hyoid apparatus and tympanic bulla, dorsally to the dorsal aspect of the pharyngeal wall, caudally along the dorsal aspect of the pharyngeal wall to the upper esophageal sphincter, and ventrally around the corniculate process of the arytenoid cartilage to include the vallecula, finally connecting the epiglottis to the starting point. The upper esophageal sphincter is specifically defined as the region in the cranial esophagus that remained the narrowest through the study . For the maximum contraction frame, an ROI is drawn around any residual barium or airspace identified within the pharyngeal area. The ROI’s are expressed in pixel numbers and the pharyngeal constriction ratio is calculated by dividing the number of pixels in the maximum contraction frame by the number of pixels in the hold frame. Normal pharyngeal constriction ratio in the dog is .
Pharyngeal and cricopharyngeal origin dysphagias are difficult to identify and distinguish from one another without videofluoroscopic assessment and the measurements described above. Pharyngeal weakness is usually affiliated with neuromuscular diseases such as pseudorabies , myasthenia gravis , inflammatory myopathies [88, 89], congenital neurologic defects , and muscular dystrophy [91, 92]. It is also imperative to consider rabies in cases of pharyngeal weakness . Elevation of the pharyngeal constriction ratio but normal timing in regards to opening of the upper esophageal sphincter is the videofluoroscopic hallmark of pharyngeal weakness (Figure 7)  (Table 3). Cricopharyngeal dysfunction can be classified as achalasia (incomplete or absent opening of the upper esophageal sphincter) or dyssynchrony (delayed opening of the upper esophageal sphincter relative to bolus presentation) . Cricopharyngeal achalasia is most commonly a congenital disorder  the underlying mechanism behind which is unknown. Biopsy of the cricopharyngeus muscle performed on dogs suffering from this disease reveal hypertrophy, atrophy, inflammation, fibrosis, and normal muscle [95, 96]. Videofluoroscopic assessment of animals with cricopharyngeal achalasia reveals absent or minimal opening of the upper esophageal sphincter upon bolus presentation (Figure 8). Occasionally a hypertrophied cricopharyngeal muscle can be identified obstructing passage of the bolus into the proximal esophagus. Cricopharyngeal dyssynchrony can be seen in older dogs so a congenital origin is unlikely . However, inheritance of dyssynchrony has been demonstrated in the Golden Retriever breed . The diagnosis of cricopharyngeal dyssynchrony is made with contrast videofluoroscopy where opening of the upper esophageal sphincter is delayed resulting in elevation of pharyngeal constriction ratio  (Table 3). An upper esophageal sphincter opening time greater than two standard deviations from the normal mean is considered delayed/dyssynchronous .
Contrast videofluoroscopy is an excellent method for identification of segmental or subtle esophageal motility disorders that do not result in radiographically visible megaesophagus . The causes of reduced esophageal motility are likely similar to those of megaesophagus and some propose that reduced esophageal motility is a precursor to megaesophagus . Moreover, esophagitis, regardless of cause, can result in reduced esophageal motility [99, 100]. In addition to reduced motility, contrast videofluoroscopy may identify irregularities of the esophageal mucosa with prolonged mucosal adherence of barium consistent with esophagitis . Certain breeds appear to be predisposed to esophageal motility disorders including the Chinese Shar Pei, Bouvier des Flandres, and some breeds of terriers [91, 98, 101]. Additionally, redundancy of the esophagus has been reported as an incidental finding where gas and/or contrast material accumulates in a deviated section of the esophagus in the thoracic inlet region of young brachycephalic breeds . Age also effects esophageal motility in that young animals demonstrate reduced motility that frequently improves over time [98, 102].
Contrast videofluoroscopy can also enhance the detection and characterization of esophageal diverticuli and strictures. Diverticuli are uncommon causes of esophageal dysphagia but have sporadically been reported in both dogs [103–105] and cats [105–107]. Diverticuli may be congenital or acquired. Acquired diverticuli can be further characterized as traction (something pulling the esophageal wall out) or pulsion (something causing increased intraluminal pressure within the esophagus) in origin . Esophageal strictures can be congenital  but are most commonly acquired (Figure 9). In companion animals, the most common cause of esophageal stricture formation is gastroesophageal reflux associated with general anesthesia [105, 110–112]. However, esophageal stricture formation may also occur secondary to foreign bodies [103, 113], ingestion of caustic agents [111, 114], or vomiting/reflux unrelated to anesthesia . Iatrogenic esophageal stricture formation has been linked to administration of doxycycline in cats [116, 117]. Esophageal neoplasms were discussed previously in this paper and may also result in stricture formation . Regardless of the cause for the stricture, contrast videofluoroscopy will reveal a narrowed area of the esophagus with or without mucosal irregularity. The length of the stricture can also be defined. Dilation of the esophagus oral to the stricture may or may not be present. Some strictures are visible following liquid barium administration but many are not defined until barium soaked kibble is given.
Gastroesophageal dysphagias can result from a variety of abnormalities, many of which are transient (i.e., hiatal hernia), affect lower esophageal sphincter function, or both. Contrast enhanced videofluoroscopic esophagography can help diagnose and differentiate between these disorders. When gastroesophageal reflux or hiatal hernia is suspected, pressure may be applied to the abdomen while fluoroscopic assessment of the caudal esophagus and stomach is performed. Imaging the animal in sternal recumbency with a full stomach may also trigger reflux or hiatal herniation. In general, gastroesophageal reflux with or without hiatal herniation is difficult to identify without contrast videofluoroscopy. With videofluoroscopy, retrograde movement of contrast material from the stomach into the esophagus is visible. It is important to recognize that a small amount of reflux is normal but should be propelled back into the stomach rapidly .
Hiatal hernias involve cranial displacement of the abdominal esophagus, gastroesophageal junction, and cardia into the thoracic cavity on an intermittent or permanent basis [119, 120]. They can be classified into four distinct types. Type I is the most common and involves axial or “sliding” cranial displacement of the esophageal hiatus. Type II is a paraesophageal or “rolling” hernia. Type III is a combination of “sliding” and “rolling” of the hiatus. Type IV has been defined as a combination of Type III with herniation of abdominal organs other than the stomach [121–123]. Hiatal hernias are frequently congenital but can be seen secondary to trauma, upper airway obstruction, or tetanus [33, 124]. Contrast media in the esophagus and stomach help outline the lower esophageal sphincter making displacement more easily identified and “real-time” imaging over several minutes increases the likelihood of visualizing transient abnormalities (Figure 10). Transient disorders such as hiatal hernias and reflux may not occur during the contrast videofluoroscopic study and therefore should not be ruled out based on a negative imaging study.
Esophageal achalasia is a disorder characterized by reduced motility of the distal esophagus and failure of the lower esophageal sphincter to relax in coordination with presentation of a bolus. This disease is well documented in people [125–129] but is rare in dogs [130–133] and cats . Contrast videofluoroscopy is essential to diagnosis and reveals esophageal contraction against a closed lower esophageal sphincter . Retrograde movement of contrast in the esophagus results.
6. Image Guided Interventions
Therapeutic options for animals with esophageal dysphagias depend on the underlying etiology. While some diseases are medically managed, benign and malignant esophageal strictures prove difficult to effectively treat. Esophageal cancers are poorly responsive to chemotherapy and are in a bad location for radiation therapy due to potential radiation damage to the lung and heart . Thus, they have traditionally been treated with surgical resection [18, 118, 136, 137]. Surgical resection is limited by poor visibility during surgery and the need to preserve regional anatomic structures. Dehiscence or stricture formation can occur postoperatively. Similarly, benign esophageal strictures are challenging to treat. Complications related to surgery are similar to those reported with surgical resection of esophageal tumors. Using endoscopic guidance, balloon dilation of benign esophageal strictures is now frequently performed in companion animals but success rates are variable [111, 112, 138].
Palliative stenting has been reported in companion animals for the treatment of obstruction of the respiratory, urogenital, and cardiovascular systems [139–146]. Palliative stenting is well documented as a safe and effective method for treatment of esophageal obstruction in people [147–151]. Esophageal stenting for the treatment of benign strictures has been reported in dogs (Figure 11) as has palliative stenting for the treatment of esophageal neoplasia .
Regardless of the stricture location, placement is typically performed with the animal under general anesthesia and under fluoroscopic guidance to assure that the stent is located within the narrowed region. Mesh, self-expanding metallic stents, are most commonly used because they are radiodense, easy to deploy, flexible, and can be reconstrained and repositioned prior to complete deployment . Deployment can be observed with fluoroscopy so that repositioning can occur as needed. The self-expanding mesh stents will shorten over time as they expand so this should be considered when the stent length is selected . As a consequence, esophageal stents should be placed eccentrically with the greater length oral to the lesion so that some degree of caudal migration is acceptable . Complication rates associated with esophageal stenting in people range from 26–52% [153, 154] and include tumor ingrowth into the stent mesh, overgrowth or granulation tissue at the stent margins, stent migration, bleeding, food bolus impaction, and esophageal injury during stent placement [150, 155].
- B. J. Watrous, “Clinical presentation and diagnosis of dysphagia,” Veterinary Clinics of North America—Small Animal Practice, vol. 13, no. 3, pp. 437–459, 1983.
- B. J. Watrous and P. F. Suter, “Normal swallowing in the dog: a cineradiographic study,” Veterinary Radiology and Ultrasound, vol. 20, no. 3–6, pp. 99–109, 1979.
- J. J. Warnock, S. L. Marks, R. Pollard, A. E. Kyles, and A. Davidson, “Surgical management of cricopharyngeal dysphagia in dogs: 14 cases (1989–2001),” Journal of the American Veterinary Medical Association, vol. 223, no. 10, pp. 1462–1468, 2003.
- B. J. Watrous, “The esophagus,” in Veterinary Diagnostic Radiology, D. E. Thrall, Ed., pp. 495–511, Saunders Elsevier, St. Louis, Mo, USA, 5th edition, 2007.
- W. Gengler, “Gagging,” in The Textbook of Veterinary Internal Medicine, S. J. Ettinger and E. C. Feldman, Eds., pp. 189–191, Saunders Elsevier, St Louis, Mo, USA, 2010.
- A. E. Jergens, “Diseases of the esophagus,” in The Textbook of Veterinary Internal Medicine, S. J. Ettinger and E. C. Feldman, Eds., pp. 1487–1499, Saunders Elsevier, St Louis, Mo, USA, 2010.
- S. J. Lifton, L. G. King, and C. A. Zerbe, “Glucocorticoid deficient hypoadrenocorticism in dogs: 18 cases (1986–1995),” Journal of the American Veterinary Medical Association, vol. 209, no. 12, pp. 2076–2081, 1996.
- L. G. Griffiths, R. Tiruneh, M. Sullivan, and S. W. J. Reid, “Oropharyngeal penetrating injuries in 50 dogs: a retrospective study,” Veterinary Surgery, vol. 29, no. 5, pp. 383–388, 2000.
- M. H. Kang, C. Y. Lim, and H. M. Park, “Nasopharyngeal tooth foreign body in a dog,” Journal of Veterinary Dentistry, vol. 28, no. 1, pp. 26–29, 2011.
- F. Billen, M. J. Day, and C. Clercx, “Diagnosis of pharyngeal disorders in dogs: a retrospective study of 67 cases,” Journal of Small Animal Practice, vol. 47, no. 3, pp. 122–129, 2006.
- I. P. Doran, C. A. Wright, and A. H. Moore, “Acute oropharyngeal and esophageal stick injury in forty-one dogs,” Veterinary Surgery, vol. 37, no. 8, pp. 781–785, 2008.
- S. R. Bright, R. J. Mellanby, and J. M. Williams, “Oropharyngeal stick injury in a Bengal cat,” Journal of Feline Medicine and Surgery, vol. 4, no. 3, pp. 153–155, 2002.
- A. Mas, L. Blackwood, P. Cripps et al., “Canine tonsillar squamous cell carcinoma—a multi-centre retrospective review of 44 clinical cases,” Journal of Small Animal Practice, vol. 52, no. 7, pp. 359–364, 2011.
- R. G. Helman and J. Oliver, “Pythiosis of the digestive tract in dogs from Oklahoma,” Journal of the American Animal Hospital Association, vol. 35, no. 2, pp. 111–114, 1999.
- J. D. Wray and A. S. Blunden, “Progressive dysphagia in a dog caused by a scirrhous, poorly differentiated perioesophageal carcinoma,” Journal of Small Animal Practice, vol. 47, no. 1, pp. 27–30, 2006.
- M. E. Mylonakis, T. Rallis, A. F. Koutinas et al., “Clinical signs and clinicopathologic abnormalities in dogs with clinical spirocercosis: 39 cases (1996–2004),” Journal of the American Veterinary Medical Association, vol. 228, no. 7, pp. 1063–1067, 2006.
- E. Ranen, G. Dank, E. Lavy, S. Perl, D. Lahav, and U. Orgad, “Oesophageal sarcomas in dogs: histological and clinical evaluation,” Veterinary Journal, vol. 178, no. 1, pp. 78–84, 2008.
- E. Ranen, E. Lavy, I. Aizenberg, S. Perl, and S. Harrus, “Spirocercosis-associated esophageal sarcomas in dogs: a retrospective study of 17 cases (1997–2003),” Veterinary Parasitology, vol. 119, no. 2-3, pp. 209–221, 2004.
- T. M. Jacobs and G. M. Rosen, “Photodynamic therapy as a treatment for esophageal squamous cell carcinoma in a dog,” Journal of the American Animal Hospital Association, vol. 36, no. 3, pp. 257–261, 2000.
- S. J. Withrow, “Esophageal cancer,” in Small Animal Clinical Oncology, S. J. Withrow and E. G. MacEwen, Eds., pp. 241–243, WB Saunders, Philadelphia, Pa, USA, 1996.
- M. Takiguchi, J. Yasuda, A. Hashimoto, K. Ochiai, and C. Itakura, “Esophageal/gastric adenocarcinoma in a dog,” Journal of the American Animal Hospital Association, vol. 33, no. 1, pp. 42–44, 1997.
- T. A. Hamilton and J. L. Carpenter, “Esophageal plasmacytoma in a dog,” Journal of the American Veterinary Medical Association, vol. 204, no. 8, pp. 1210–1211, 1994.
- A. R. McBrearty, I. K. Ramsey, E. A. Courcier, D. J. Mellor, and R. Bell, “Clinical factors associated with death before discharge and overall survival time in dogs with generalized megaesophagus,” Journal of the American Veterinary Medical Association, vol. 238, no. 12, pp. 1622–1628, 2011.
- G. D. Shelton, M. D. Willard, G. H. Cardinet III, and J. Lindstrom, “Acquired myasthenia gravis. Selective involvement of esophageal, pharyngeal, and facial muscles,” Journal of Veterinary Internal Medicine, vol. 4, no. 6, pp. 281–284, 1990.
- J. D. Wray and A. H. Sparkes, “Use of radiographic measurements in distinguishing myasthenia gravis from other causes of canine megaoesophagus,” Journal of Small Animal Practice, vol. 47, no. 5, pp. 256–263, 2006.
- K. Uchida, Y. Awamura, T. Nakamura, R. Yamaguchi, and S. Tateyama, “Thymoma and multiple thymic cysts in a dog with acquired myasthenia gravis,” Journal of Veterinary Medical Science, vol. 64, no. 7, pp. 637–640, 2002.
- M. F. C. Lainesse, S. M. Taylor, S. L. Myers, D. Haines, and J. D. Fowler, “Focal myasthenia gravis as a paraneoplastic syndrome of canine thymoma: improvement following thymectomy,” Journal of the American Animal Hospital Association, vol. 32, no. 2, pp. 111–117, 1996.
- J. W. Bartges and D. L. Nielson, “Reversible megaesophagus associated with atypical primary hypoadrenocorticism in a dog,” Journal of the American Veterinary Medical Association, vol. 201, no. 6, pp. 889–891, 1992.
- N. T. Whitley, “Megaoesophagus and glucocorticoid-deficient hypoadrenocorticism in a dog,” Journal of Small Animal Practice, vol. 36, no. 3, pp. 132–135, 1995.
- Y. Bruchim, A. Kushnir, and M. H. Shamir, “L-thyroxine responsive cricopharyngeal achalasia associated with hypothyroidism in a dog,” Journal of Small Animal Practice, vol. 46, no. 11, pp. 553–554, 2005.
- E. Huber, W. Armbrust, J. L. Forster, et al., “Resolution of megaesophagus after treatment of concurrent hypothyroidism in a dog,” Schweizer Archiv für Tierheilkunde, vol. 143, pp. 512–514, 2001.
- A. Jaggy, J. E. Oliver, D. C. Ferguson, E. A. Mahaffey, and T. Glaus, “Neurological manifestations of hypothyroidism: a retrospective study of 29 dogs,” Journal of Veterinary Internal Medicine, vol. 8, no. 5, pp. 328–336, 1994.
- T. M. Dieringer and A. M. Wolf, “Esophageal hiatal hernia and megaesophagus complicating tetanus in two dogs,” Journal of the American Veterinary Medical Association, vol. 199, no. 1, pp. 87–89, 1991.
- D. A. Detweiler, D. S. Biller, J. J. Hoskinson, and K. R. Harkin, “Radiographic findings of canine dysautonomia in twenty-four dogs,” Veterinary Radiology and Ultrasound, vol. 42, no. 2, pp. 108–112, 2001.
- S. J. M. Niessen, J. Eastwood, J. B. A. Smyth, and G. B. Cherubini, “Five cases of canine dysautonomia in England (2004 to 2006),” Journal of Small Animal Practice, vol. 48, no. 6, pp. 346–352, 2007.
- J. W. Buchanan, “Tracheal signs and associated vascular anomalies in dogs with persistent right aortic arch,” Journal of Veterinary Internal Medicine, vol. 18, no. 4, pp. 510–514, 2004.
- S. T. Wallack, “Introduction to barium sulfate,” in The Handbook of Veterinary Contrast Radiography, S. T. Wallack, Ed., pp. 1–4, San Diego Veterinary Imaging, Solano Beach, Calif, USA, 2003.
- D. A. Kogan, L. R. Johnson, B. K. Sturges, K. E. Jandrey, and R. E. Pollard, “Etiology and clinical outcome in dogs with aspiration pneumonia: 88 cases (2004–2006),” Journal of the American Veterinary Medical Association, vol. 233, no. 11, pp. 1748–1755, 2008.
- T. R. O'Brien, “Esophagus,” in Radiographic Diagnosis of Abdominal Disorders in the Dog and Cat: Radiographic Interpretation, Clinical Signs, Pathophysiology, T. R. O'Brien, Ed., p. 141, WB Saunders, Philadelphia, Pa, USA, 1978.
- G. Seiler, U. Rytz, and L. Gaschen, “Radiographic diagnosis—cavitary mediastinal abscess,” Veterinary Radiology and Ultrasound, vol. 42, no. 5, pp. 431–433, 2001.
- E. Dvir, R. M. Kirberger, and D. Malleczek, “Radiographic and computed tomographic changes and clinical presentation of spirocercosis in the dog,” Veterinary Radiology and Ultrasound, vol. 42, no. 2, pp. 119–129, 2001.
- S. T. Wallack, “Iodinated esophagram-dog,” in The Handbook of Veterinary Contrast Radiography, S. T. Wallack, Ed., p. 52, San Diego Veterinary Imaging, Solano Beach, Calif, USA, 2003.
- F. Gaynor, R. E. Hoffer, M. F. Nichols et al., “Physiologic features of the canine esophagus: effects of tranquilization on esophageal motility,” American Journal of Veterinary Research, vol. 41, no. 5, pp. 727–732, 1980.
- J. Menzel and O. Distl, “Unusual vascular ring anomaly associated with a persistent right aortic arch and an aberrant left subclavian artery in German pinschers,” Veterinary Journal, vol. 187, no. 3, pp. 352–355, 2011.
- A. K. House, N. J. Summerfield, A. J. German, P. J. M. Noble, P. Ibarrola, and D. J. Brockman, “Unusual vascular ring anomaly associated with a persistent right aortic arch in two dogs,” Journal of Small Animal Practice, vol. 46, no. 12, pp. 585–590, 2005.
- T. Larcher, J. Abadie, F. A. Roux, J. Y. Deschamps, and M. Wyers, “Persistent left cranial vena cava causing oesophageal obstruction and consequent megaoesophagus in a dog,” Journal of Comparative Pathology, vol. 135, no. 2-3, pp. 150–152, 2006.
- M. L. Vianna and J. D. J. Krahwinkel Jr., “Double aortic arch in a dog,” Journal of the American Veterinary Medical Association, vol. 225, no. 8, pp. 1196–1224, 2004.
- K. Hurley, M. W. Miller, M. D. Willard, and H. W. Boothe, “Left aortic arch and right ligamentum arteriosum causing esophageal obstruction in a dog,” Journal of the American Veterinary Medical Association, vol. 203, no. 3, pp. 410–412, 1993.
- W. Roach and S. Hecht, “What is your diagnosis?” Journal of the American Veterinary Medical Association, vol. 231, no. 3, pp. 381–382, 2007.
- M. Pietra, F. Gentilini, S. Pinna, F. Fracassi, A. Venturini, and M. Cipone, “Intermittent gastroesophageal intussusception in a dog: clinical features, radiographic and endoscopic findings, and surgical management,” Veterinary Research Communications, vol. 27, supplement 1, pp. 783–786, 2003.
- K. L. Graham, M. S. Buss, C. R. Dhein, D. D. Barbee, and S. E. Seitz, “Gastroesophageal intussusception in a Labrador retriever,” Canadian Veterinary Journal, vol. 39, no. 11, pp. 709–711, 1998.
- A. Masloski and J. Besso, “What is your diagnosis? Gastroesophageal intussusception with megaesophagus in a dog,” Journal of the American Veterinary Medical Association, vol. 212, no. 1, pp. 23–24, 1998.
- E. L. Morris and G. H. Turnwald, “Gastroesophageal intussusception,” Journal of the American Veterinary Medical Association, vol. 176, no. 4, pp. 361–362, 1980.
- N. I. Martínez, W. Cook, G. C. Troy, and D. Waldron, “Intermittent gastroesophageal intussusception in a cat with idiopathic megaesophagus,” Journal of the American Animal Hospital Association, vol. 37, no. 3, pp. 234–237, 2001.
- J. E. Allen, C. White, R. Leonard, and P. C. Belafsky, “Comparison of esophageal screen findings on videofluoroscopy with full esophagram results,” Head and Neck, vol. 34, no. 2, pp. 264–269, 2012.
- Y. K. Cho, M. G. Choi, S. N. Oh et al., “Comparison of bolus transit patterns identified by esophageal impedance to barium esophagram in patients with dysphagia,” Diseases of the Esophagus, vol. 25, no. 1, pp. 17–25, 2012.
- J. Jou, J. Radowsky, R. Gangnon et al., “Esophageal clearance patterns in normal older adults as documented with videofluoroscopic esophagram,” Gastroenterology Research and Practice, vol. 2009, Article ID 965062, 6 pages, 2009.
- H. Imam, S. Shay, A. Ali, and M. Baker, “Bolus transit patterns in healthy subjects: a study using simultaneous impedance monitoring, videoesophagram, and esophageal manometry,” American Journal of Physiology, vol. 288, no. 5, pp. G1000–G1006, 2005.
- E. Fiorentino, D. Cabibi, F. Barbiera et al., “Hiatal hernia, gastro-oesophageal reflux and oesophagitis: videofluorographic, endoscopic and histopathological correlation,” Chirurgia Italiana, vol. 56, no. 4, pp. 483–488, 2004.
- S. Namaki, T. Tanaka, Y. Hara, H. Ohki, M. Shinohara, and Y. Yonhehara, “Videofluorographic evaluation of dysphagia before and after modification of the flap and scar in patients with oral cancer,” Journal of Plastic Surgery and Hand Surgery, vol. 45, no. 3, pp. 136–142, 2011.
- I. J. Cook, “Cricopharyngeal function and dysfunction,” Dysphagia, vol. 8, no. 3, pp. 244–251, 1993.
- C. M. Steele and P. H. H. M. van Lieshout, “Does barium influence tongue behaviors during swallowing?” American Journal of Speech—Language Pathology, vol. 14, no. 1, pp. 27–39, 2005.
- G. Chi-Fishman, M. Stone, and G. N. McCall, “Lingual action in normal sequential swallowing,” Journal of Speech, Language, and Hearing Research, vol. 41, no. 4, pp. 771–785, 1998.
- M. Stone and T. H. Shawker, “An ultrasound examination of tongue movement during swallowing,” Dysphagia, vol. 1, no. 2, pp. 78–83, 1986.
- S. M. Tasko, R. D. Kent, and J. R. Westbury, “Variability in tongue movement kinematics during normal liquid swallowing,” Dysphagia, vol. 17, no. 2, pp. 126–138, 2002.
- S. K. Daniels and A. L. Foundas, “Swallowing physiology of sequential straw drinking,” Dysphagia, vol. 16, no. 3, pp. 176–182, 2001.
- K. de Vault, J. Castell, and D. Castell, “How many swallows are required to establish reliable esophageal peristaltic parameters in normal subjects? An on-line computer analysis,” American Journal of Gastroenterology, vol. 82, no. 8, pp. 754–757, 1987.
- J. B. Hollis and D. O. Castell, “Effect of dry swallows and wet swallows of different volumes on esophageal peristalsis,” Journal of Applied Physiology, vol. 38, no. 6, pp. 1161–1164, 1975.
- E. M. Bisch, J. A. Logemann, A. W. Rademaker, P. J. Kahrilas, and C. L. Lazarus, “Pharyngeal effects of bolus volume, viscosity, and temperature in patients with dysphagia resulting from neurologic impairment and in normal subjects,” Journal of Speech and Hearing Research, vol. 37, no. 5, pp. 1041–1049, 1994.
- R. O. Dantas, M. K. Kern, B. T. Massey et al., “Effect of swallowed bolus variables on oral and pharyngeal phases of swallowing,” American Journal of Physiology, vol. 258, no. 5, pp. G675–G681, 1990.
- R. O. Dantas, W. J. Dodds, B. T. Massey, and M. K. Kern, “The effect of high- vs low-density barium preparations on the quantitative features of swallowing,” American Journal of Roentgenology, vol. 153, no. 6, pp. 1191–1195, 1989.
- C. L. Lazarus, J. A. Logemann, A. W. Rademaker et al., “Effects of bolus volume, viscosity, and repeated swallows in nonstroke subjects and stroke patients,” Archives of Physical Medicine and Rehabilitation, vol. 74, no. 10, pp. 1066–1070, 1993.
- K. H. Choi, J. S. Ryu, M. Y. Kim, J. Y. Kang, and S. D. Yoo, “Kinematic analysis of dysphagia: significant parameters of aspiration related to bolus viscosity,” Dysphagia, vol. 26, no. 4, pp. 392–398, 2011.
- O. Ekberg, M. Stading, D. Johansson, M. Blow, S. Ekman, and K. Wendin, “Flow properties of oral contrast medium formulations depend on the temperature,” Acta Radiologica, vol. 51, no. 4, pp. 363–367, 2010.
- S. G. Butler, A. Stuart, D. Castell, G. B. Russell, K. Koch, and S. Kemp, “Effects of age, gender, bolus condition, viscosity, and volume on pharyngeal and upper esophageal sphincter pressure and temporal measurements during swallowing,” Journal of Speech, Language, and Hearing Research, vol. 52, no. 1, pp. 240–253, 2009.
- J. M. Barkmeier, S. Bielamowicz, N. Takeda, and C. L. Ludlow, “Laryngeal activity during upright versus supine swallowing,” Journal of Applied Physiology, vol. 93, no. 2, pp. 740–745, 2002.
- E. Osmanoglou, I. R. van der Voort, K. Fach et al., “Oesophageal transport of solid dosage forms depends on body position, swallowing volume and pharyngeal propulsion velocity,” Neurogastroenterology and Motility, vol. 16, no. 5, pp. 547–556, 2004.
- J. A. Castell, C. B. Dalton, and D. O. Castell, “Effects of body position and bolus consistency on the manometric parameters and coordination of the upper esophageal sphincter and pharynx,” Dysphagia, vol. 5, no. 4, pp. 179–186, 1990.
- J. A. Castell, D. O. Castell, A. R. Schultz, and S. Georgeson, “Effect of head position on the dynamics of the upper esophageal sphincter and pharynx,” Dysphagia, vol. 8, no. 1, pp. 1–6, 1993.
- J. A. Logemann, B. R. Pauloski, L. Colangelo, C. Lazarus, M. Fujiu, and P. J. Kahrilas, “Effects of a sour bolus on oropharyngeal swallowing measures in patients with neurogenic dysphagia,” Journal of Speech and Hearing Research, vol. 38, no. 3, pp. 556–563, 1995.
- B. C. Sonies, L. J. Parent, K. Morrish, and B. J. Baum, “Durational aspects of the oral-pharyngeal phase of swallow in normal adults,” Dysphagia, vol. 3, no. 1, pp. 1–10, 1988.
- K. A. Kendall and R. J. Leonard, “Pharyngeal constriction in elderly dysphagic patients compared with young and elderly nondysphagic controls,” Dysphagia, vol. 16, no. 4, pp. 272–278, 2001.
- C. M. Bonadio, R. E. Pollard, P. A. Dayton, C. D. Leonard, and S. L. Marks, “Effects of body positioning on swallowing and esophageal transit in healthy dogs,” Journal of Veterinary Internal Medicine, vol. 23, no. 4, pp. 801–805, 2009.
- R. E. Pollard, S. L. Marks, A. Davidson, and W. J. Hornof, “Quantitative videofluoroscopic evaluation of pharyngeal function in the dog,” Veterinary Radiology and Ultrasound, vol. 41, no. 5, pp. 409–412, 2000.
- R. E. Pollard, S. L. Marks, R. Leonard, and P. C. Belafsky, “Preliminary evaluation of the pharyngeal constriction ratio (PCR) for fluoroscopic determination of pharyngeal constriction in dysphagic dogs,” Veterinary Radiology and Ultrasound, vol. 48, no. 3, pp. 221–226, 2007.
- R. Leonard, K. Kendall, and S. McKenzie, “UES opening and cricopharyngeal bar in nondysphagic elderly and nonelderly adults,” Dysphagia, vol. 19, no. 3, pp. 182–191, 2004.
- K. G. Braund, “Encephalitis and meningitis,” Veterinary Clinics of North America—Small Animal Practice, vol. 10, no. 1, pp. 31–56, 1980.
- K. Toyoda, K. Uchida, N. Matsuki et al., “Inflammatory myopathy with severe tongue atrophy in pembroke welsh corgi dogs,” Journal of Veterinary Diagnostic Investigation, vol. 22, no. 6, pp. 876–885, 2010.
- L. R. Ryckman, D. J. Krahwinkel, M. H. Sims, R. L. Donnell, P. F. Moore, and G. D. Shelton, “Dysphagia as the primary clinical abnormality in two dogs with inflammatory myopathy,” Journal of the American Veterinary Medical Association, vol. 226, no. 9, pp. 1519–1501, 2005.
- F. B. Hutt and A. de Lahunta, “A lethal glossopharyngeal defect in the dog,” Journal of Heredity, vol. 62, no. 5, pp. 291–293, 1971.
- M. E. Peeters, A. J. Venker-van Haagen, S. A. Goedegebuure, and W. T. Wolvekamp, “Dysphagia in Bouviers associated with muscular dystrophy; evaluation of 24 cases,” Veterinary Quarterly, vol. 13, no. 2, pp. 65–73, 1991.
- M. E. Peeters and G. J. Ubbink, “Dysphagia-associated muscular dystrophy: a familial trait in the bouvier des Flandres,” Veterinary Record, vol. 134, no. 17, pp. 444–446, 1994.
- A. E. Kyles, “Esophagus,” in Textbook of Small Animal Surgery, D. H. Slatter, Ed., pp. 573–592, WB Saunders, Philadelphia, Pa, USA, 3rd edition, 2002.
- J. Ladlow and R. J. Hardie, “Cricopharyngeal achalasia in dogs,” Compendium on Continuing Education for the Practicing Veterinarian, vol. 22, no. 8, pp. 750–755, 2000.
- V. Sokolovsky, “Cricopharyngeal achalasia in a dog,” Journal of the American Veterinary Medical Association, vol. 150, no. 3, pp. 281–285, 1967.
- I. R. Griffiths, I. D. Duncan, A. McQueen, et al., “Neuromuscular disease in dogs: some aspects of its investigation and diagnosis,” Journal of Small Animal Practice, vol. 14, no. 9, pp. 533–554, 1973.
- A. P. Davidson, R. E. Pollard, D. L. Bannasch, S. L. Marks, W. J. Hornof, and T. R. Famula, “Inheritance of cricopharyngeal dysfunction in golden retrievers,” American Journal of Veterinary Research, vol. 65, no. 3, pp. 344–349, 2004.
- N. H. Bexfield, P. J. Watson, and M. E. Herrtage, “Esophageal dysmotility in young dogs,” Journal of Veterinary Internal Medicine, vol. 20, no. 6, pp. 1314–1318, 2006.
- E. Han, “Diagnosis and management of reflux esophagitis,” Clinical Techniques in Small Animal Practice, vol. 18, no. 4, pp. 231–238, 2003.
- M. J. Mazzei, S. A. Bissett, K. M. Murphy, S. Hunter, and J. A. Neel, “Eosinophilic esophagitis in a dog,” Journal of the American Veterinary Medical Association, vol. 235, no. 1, pp. 61–65, 2009.
- R. Stickle, G. Sparschu, N. Love, and R. Walshaw, “Radiographic evaluation of esophageal function in Chinese Shar Pei pups,” Journal of the American Veterinary Medical Association, vol. 201, no. 1, pp. 81–84, 1992.
- N. Diamant, M. Szczepanski, and H. Mui, “Idiopathic megaesophagus in the dog: reasons for spontaneous improvement and a possible method of medical therapy,” Canadian Veterinary Journal, vol. 15, no. 3, pp. 66–71, 1974.
- P. Gianella, N. S. Pfammatter, and I. A. Burgener, “Oesophageal and gastric endoscopic foreign body removal: complications and follow-up of 102 dogs,” Journal of Small Animal Practice, vol. 50, no. 12, pp. 649–654, 2009.
- F. W. Hill, B. A. Christie, W. T. Reynolds, and R. B. Lavelle, “An oesophageal diverticulum in a dog,” Australian Veterinary Journal, vol. 55, no. 4, pp. 184–187, 1979.
- C. Adami, S. Di Palma, K. Gendron, and N. Sigrist, “Severe esophageal injuries occurring after general anesthesia in two cats: case report and literature review,” Journal of the American Animal Hospital Association, vol. 47, no. 6, pp. 436–442, 2011.
- L. Durocher, S. E. Johnson, and E. Green, “Esophageal diverticulum associated with a trichobezoar in a cat,” Journal of the American Animal Hospital Association, vol. 45, no. 3, pp. 142–146, 2009.
- T. Fukata, “Esophageal diverticulum-like pouch in a cat with allergic bronchitis,” Veterinary Medicine, vol. 79, no. 2, pp. 175–178, 1984.
- A. E. Jergen, “Diseases of the esophagus,” in Textbook of Veterinary Internal Medicine, S. J. Ettinger and E. C. Feldman, Eds., Saunders Elsevier, St. Louis, Mo, USA, 6th edition, 2005.
- E. Fox, K. Lee, C. R. Lamb, J. Rest, S. J. Baines, and D. Brockman, “Congenital oesophageal stricture in a Japanese shiba inu,” Journal of Small Animal Practice, vol. 48, no. 12, pp. 709–712, 2007.
- M. S. Leib, H. Dinnel, D. L. Ward, M. E. Reimer, T. L. Towell, and W. E. Monroe, “Endoscopic balloon dilation of benign esophageal strictures in dogs and cats,” Journal of Veterinary Internal Medicine, vol. 15, no. 6, pp. 547–552, 2001.
- B. H. Harai, S. E. Johnson, and R. G. Sherding, “Endoscopically guided balloon dilatation of benign esophageal strictures in 6 cats and 7 dogs,” Journal of Veterinary Internal Medicine, vol. 9, no. 5, pp. 332–335, 1995.
- K. K. Adamama-Moraitou, T. S. Rallis, N. N. Prassinos, and A. D. Galatos, “Benign esophageal stricture in the dog and cat: a retrospective study of 20 cases,” Canadian Journal of Veterinary Research, vol. 66, no. 1, pp. 55–59, 2002.
- M. S. Leib and L. L. Sartor, “Esophageal foreign body obstruction caused by a dental chew treat in 31 dogs (2000–2006),” Journal of the American Veterinary Medical Association, vol. 232, no. 7, pp. 1021–1025, 2008.
- R. L. Burk, D. A. Zawie, and M. S. Garvey, “Balloon catheter dilation of intramural esophageal strictures in the dog and cat: a description of the procedure and a report of six cases,” Seminars in Veterinary Medicine and Surgery, vol. 2, no. 4, pp. 241–247, 1987.
- S. A. Bissett, J. Davis, K. Subler, and L. A. Degernes, “Risk factors and outcome of bougienage for treatment of benign esophageal strictures in dogs and cats: 28 cases (1995–2004),” Journal of the American Veterinary Medical Association, vol. 235, no. 7, pp. 840–850, 2009.
- A. J. German, M. J. Canon, C. Dye et al., “Oesophageal strictures in cats associated with doxycycline therapy,” Journal of Feline Medicine and Surgery, vol. 7, no. 1, pp. 33–41, 2005.
- Y. L. McGrotty and C. M. Knottenbelt, “Oesophageal stricture in a cat due to oral administration of tetracyclines,” Journal of Small Animal Practice, vol. 43, no. 5, pp. 221–223, 2002.
- K. S. Hansen, C. Weisse, A. C. Berent et al., “Use of a self-expanding metallic stent to palliate esophageal neoplastic obstruction in a dog,” Journal of the American Veterinary Medical Association, vol. 240, no. 10, pp. 1202–1207, 2012.
- K. G. Miles, E. R. Pope, and A. E. Jergens, “Paraesophageal hiatal hernia and pyloric obstruction in a dog,” Journal of the American Veterinary Medical Association, vol. 193, no. 11, pp. 1437–1439, 1988.
- C. Prymak, H. M. Saunders, and R. J. Washabau, “Hiatal hernia repair by restoration and stabilization of normal anatomy. An evaluation in four dogs and one cat,” Veterinary Surgery, vol. 18, no. 5, pp. 386–391, 1989.
- J. M. Auger and S. M. Riley, “Combined hiatal and pleuroperitoneal hernia in a shar-pei,” Canadian Veterinary Journal, vol. 38, no. 10, pp. 640–642, 1997.
- K. M. Pratschke, J. M. L. Hughes, C. Skelly, and C. R. Bellenger, “Hiatal herniation as a complication of chronic diaphragmatic herniation,” Journal of Small Animal Practice, vol. 39, no. 1, pp. 33–38, 1998.
- R. K. Sivacolundhu, R. A. Read, and A. M. Marchevsky, “Hiatal hernia controversies—a review of pathophysiology and treatment options,” Australian Veterinary Journal, vol. 80, no. 1-2, pp. 48–53, 2002.
- D. Lorinson and R. M. Bright, “Long-term outcome of medical and surgical treatment of hiatal hernias in dogs and cats: 27 cases (1978–1996),” Journal of the American Veterinary Medical Association, vol. 213, no. 3, pp. 381–384, 1998.
- U. C. Ghoshal, S. B. Daschakraborty, and R. Singh, “Pathogenesis of achalasia cardia,” World Journal of Gastroenterology, vol. 18, no. 24, pp. 3050–3057, 2012.
- L. H. Fontes, F. A. Herbella, T. N. Rodriguez, et al., “Progression of diffuse esophageal spasm to achalasia: incidence and predictive actors,” Diseases of the Esophagus. In press.
- V. Kushnir, G. S. Sayuk, and C. P. Gyawali, “Multiple rapid swallow responses segregate achalasia subtypes on high-resolutionmanometry,” Neurogastroenterology and Motility. In press.
- S. H. Chuah, P. I. Hsu, K. L. Wu, D. C. Wu, W. C. Tai, and C. S. Changchien, “2011 update on esophageal achalasia,” World Journal of Gastroenterology, vol. 18, no. 14, pp. 1573–1578, 2012.
- S. Ajani, N. B. Shah, and N. E. Vlahakis, “Achalasia: a diagnosis that's hard to swallow,” American Journal of Respiratory and Critical Care Medicine, vol. 185, no. 8, e893.
- P. A. Boria, C. R. L. Webster, and J. Berg, “Esophageal achalasia and secondary megaesophagus in a dog,” Canadian Veterinary Journal, vol. 44, no. 3, pp. 232–234, 2003.
- K. A. Ryer and J. Ryer, “Acquired achalasia: a case report,” Veterinary Medicine, Small Animal Clinician, vol. 75, no. 11, pp. 1703–1704, 1980.
- D. H. Clifford, E. D. Waddell, D. R. Patterson, C. F. Wilson, and H. L. Thompson, “Management of esophageal achalasia in miniature schnauzers,” Journal of the American Veterinary Medical Association, vol. 161, no. 9, pp. 1012–1021, 1972.
- H. W. Boothe, “Acquired achalasia (megaesophagus) in a dog: clinical features and response to therapy,” Journal of the American Veterinary Medical Association, vol. 173, no. 6, pp. 756–758, 1978.
- D. H. Clifford, F. K. Soifer, C. F. Wilson, E. D. Waddell, and G. L. Guilloud, “Congenital achalasia of the esophagus in four cats of common ancestry,” Journal of the American Veterinary Medical Association, vol. 158, no. 9, pp. 1554–1560, 1971.
- S. J. Withrow, “Tumors of the gastrointestinal tract,” in Small Animal Clinical Oncology, S. J. Withrow, Ed., pp. 477–479, Saunders, Edinburgh, UK, 4th edition, 2007.
- K. A. Johnson, J. E. Maddison, and G. S. Allan, “Correction of cervical esophageal stricture in a dog by creation of a traction diverticulum,” Journal of the American Veterinary Medical Association, vol. 201, no. 7, pp. 1045–1048, 1992.
- C. R. Gregory, I. M. Gourley, D. S. Bruyette, and L. J. Schultz, “Free jejunal segment for treatment of cervical esophageal stricture in a dog,” Journal of the American Veterinary Medical Association, vol. 193, no. 2, pp. 230–232, 1988.
- E. M. Hardie, R. T. Greene, R. B. Ford, et al., “Balloon dilation for treatment of esophageal stricture: a case report,” Journal of the American Animal Hospital Association, vol. 23, pp. 547–550, 1987.
- P. A. Sura and D. J. Krahwinkel, “Self-expanding nitinol stents for the treatment of tracheal collapse in dogs: 12 cases (2001–2004),” Journal of the American Veterinary Medical Association, vol. 232, no. 2, pp. 228–236, 2008.
- N. K. Lam, A. C. Berent, C. W. Weisse, C. Bryan, A. J. Mackin, and D. H. Bagley, “Endoscopic placement of ureteral stents for treatment of congenital bilateral ureteral stenosis in a dog,” Journal of the American Veterinary Medical Association, vol. 240, no. 8, pp. 983–990, 2012.
- A. C. Berent, C. Weisse, M. W. Beal, D. C. Brown, K. Todd, and D. Bagley, “Use of indwelling, double-pigtail stents for treatment of malignant ureteral obstruction in dogs: 12 cases (2006–2009),” Journal of the American Veterinary Medical Association, vol. 238, no. 8, pp. 1017–1025, 2011.
- M. S. Zaid, A. C. Berent, C. Weisse, and A. Caceres, “Feline ureteral strictures: 10 cases (2007–2009),” Journal of Veterinary Internal Medicine, vol. 25, no. 2, pp. 222–229, 2011.
- M. D. Schlicksup, C. W. Weisse, A. C. Berent, and J. A. Solomon, “Use of endovascular stents in three dogs with Budd-Chiari syndrome,” Journal of the American Veterinary Medical Association, vol. 235, no. 5, pp. 544–550, 2009.
- A. C. Berent, C. Weisse, K. Todd, M. P. Rondeau, and A. M. Reiter, “Use of a balloon-expandable metallic stent for treatment of nasopharyngeal stenosis in dogs and cats: six cases (2005–2007),” Journal of the American Veterinary Medical Association, vol. 233, no. 9, pp. 1432–1440, 2008.
- C. Weisse, A. Berent, K. Todd, C. Clifford, and J. Solomon, “Evaluation of palliative stenting for management of malignant urethral obstructions in dogs,” Journal of the American Veterinary Medical Association, vol. 229, no. 2, pp. 226–234, 2006.
- R. G. Newman, S. J. Mehler, B. E. Kitchell, and M. W. Beal, “Use of a balloon-expandable metallic stent to relieve malignant urethral obstruction in a cat,” Journal of the American Veterinary Medical Association, vol. 234, no. 2, pp. 236–239, 2009.
- M. Conio, A. Repici, G. Battaglia et al., “A randomized prospective comparison of self-expandable plastic stents and partially covered self-expandable metal stents in the palliation of malignant esophageal dysphagia,” American Journal of Gastroenterology, vol. 102, no. 12, pp. 2667–2677, 2007.
- D. Yakoub, R. Fahmy, T. Athanasiou et al., “Evidence-based choice of esophageal stent for the palliative management of malignant dysphagia,” World Journal of Surgery, vol. 32, no. 9, pp. 1996–2009, 2008.
- D. Xinopoulos, D. Dimitroulopoulos, I. Moschandrea et al., “Natural course of inoperable esophageal cancer treated with metallic expandable stents: quality of life and cost-effectiveness analysis,” Journal of Gastroenterology and Hepatology, vol. 19, no. 12, pp. 1397–1402, 2004.
- C. P. Selinger, P. Ellul, P. A. Smith, and N. C. Cole, “Oesophageal stent insertion for palliation of dysphagia in a district general hospital: experience from a case series of 137 patients,” Oxford Journals—Medicine, vol. 101, no. 7, pp. 545–548, 2008.
- R. Keller, D. Flieger, W. Fischbach, and S. U. Christl, “Self-expanding metal stents for malignant esophagogastric obstruction: experience with a new design covered nitinol stent,” Journal of Gastrointestinal and Liver Diseases, vol. 16, no. 3, pp. 239–243, 2007.
- F. W. Winkeibauer, R. Schöfl, B. Niederle, R. Wildling, S. Thurnher, and J. Lammer, “Palliative treatment of obstructing esophageal cancer with nitinol stents: value, safety, and long-term results,” American Journal of Roentgenology, vol. 166, no. 1, pp. 79–84, 1996.
- J. H. Kim, H. Y. Song, J. H. Shin et al., “Palliative treatment of unresectable esophagogastric junction tumors: balloon dilation combined with chemotherapy and/or radiation therapy and metallic stent placement,” Journal of Vascular and Interventional Radiology, vol. 19, no. 6, pp. 912–917, 2008.
- M. T. McLoughlin and M. F. Byrne, “Endoscopic stenting—where are we now and where can we go?” World Journal of Gastroenterology, vol. 14, no. 24, pp. 3798–3803, 2008.
- M. Y. V. Homs, E. W. Steyerberg, E. J. Kuipers et al., “Causes and treatment of recurrent dysphagia after self-expanding metal stent placement for palliation of esophageal carcinoma,” Endoscopy, vol. 36, no. 10, pp. 880–886, 2004.