Pamela Schwartz Schwarzman Animal Medical Center, New York, NY, USA The popularity of brachycephalic breeds has risen significantly in recent years. In particular, French Bulldogs have increased by 300% through kennel club registrations over the past 10 years in the United Kingdom.1 The English Bulldog, French Bulldog, and Pug have especially increased in popularity and are classified as “extreme brachycephalic breeds.”2,3 Extreme brachycephalic breeds have been noted to die at a younger age than other breeds, with a higher proportion of deaths related to upper respiratory disorders.2 Despite the increase in popularity of brachycephalic breeds, many owners are unaware of the conformation‐associated health risks related with these breeds, which may result in unrealistic expectations when pursuing treatment.1, 4–6 Brachycephalic obstructive airway syndrome (BOAS) is a term that describes several conformational abnormalities leading to respiratory distress, which often requires surgical intervention to alleviate clinical signs.5,7,8 Several anatomical changes have been documented to be associated with brachycephalic breeds. Anatomic abnormalities associated with BOAS include macroglossia, stenotic nares, aberrant nasopharyngeal turbinates, elongated soft palate, excessively thickened soft palate, hypoplastic trachea, and redundant pharyngeal folds.7, 9–11 Macroglossia in brachycephalic breeds creates lower air‐to‐soft tissue ratios within the oropharyngeal and nasopharyngeal regions, which can contribute to upper airway obstruction.12 Although one study documents increased nasal mucosal contact points and more prevalent aberrant turbinates in brachycephalic dogs, no correlation could be made between these findings and brachycephalic airway syndrome due to lack of knowledge of these dogs’ clinical signs.11 It is also unknown if the thickening of the soft palate is a primary structural abnormality or a secondary change; however, it is considered a component in severe BOAS.9,10 Combinations of this altered anatomy lead to increased resistance during inspiration.10 Brachycephalic dogs must create a higher negative pressure distal to the resistance, through labored breathing, to maintain appropriate oxygen levels.10 Secondary manifestations of increased airway resistance include everted laryngeal saccules, tonsillar eversion and hyperplasia, and laryngeal collapse.7,10 Gastrointestinal disease is common in many brachycephalic breeds and is likely associated with negative intra‐thoracic pressure generated during inspiration.7,13,14 It is not completely understood which anatomic change or a combination thereof leads to the most severe clinical signs. A thorough clinical history should be obtained, which can provide significant insight into any underlying problems. It is imperative to identify signs of both respiratory and gastrointestinal disease. It should be noted that lack of clinical signs does not equate to lack of conformational changes. One study evaluating brachycephalic dogs without clinical signs of upper airway disease found that all dogs had obvious redundancy or moderate to severe elongation of the soft palate.15 Another study found that the degree of nasopharyngeal occlusion by the soft palate evaluated by computed tomography (CT) was not correlated to the severity of clinical signs.16 The severity of respiratory signs influences the severity of gastrointestinal signs and vice versa. Brachycephalic dogs exhibiting respiratory signs have evidence of gastrointestinal disease (esophageal, gastric, or duodenal) on histologic evaluation whether or not gastrointestinal signs or endoscopically visible lesions are present. Gastroesophageal reflux can contribute to upper respiratory problems by producing upper esophageal, pharyngeal, and laryngeal inflammation.17 It is shown that treatment of upper gastrointestinal disease prior to anesthesia can decrease the complication rate associated with corrective upper respiratory surgery and improve prognosis.18 Due to the progressive nature of BOAS and increased risk of post‐operative complications when dogs present for surgery on an emergent basis, it is paramount that dogs have early surgical intervention, prior to severe clinical signs and development of irreversible secondary changes.7,19 Studies document the presence of severe secondary changes in dogs younger than one year of age.20 One study, where all dogs were at least one year of age, documented that performing surgery at a younger age was associated with an increased likelihood of a poorer prognosis after surgery.8 This is likely related to more severe disease in this population and supports performing surgery as early as possible. Dogs that have surgery at a younger age have significantly fewer complications, with the odds of developing complications increasing with each year of age.7 Although the benefit of prophylactic surgery is not fully known, the author recommends and routinely performs laryngeal examination, and if warranted, corrective airway surgery, under the same anesthetic episode of surgical sterilization. The author recommends surgical intervention prior to obvious clinical signs to improve quality of life and to attempt to slow the progression of diseases, between the age of six months and one year. How to determine which patient would benefit from corrective surgery, including which procedures, remains controversial. This is generally based on clinical signs and laryngeal examination findings. The prognosis appears to be related to the severity of airway pathology present and not the surgical procedure(s) performed. The author routinely performs surgical correction of all identifiable abnormalities of the nares, palate, saccules, and tonsils. Although most dogs improve after surgery, it is known that clinical signs, such as snoring while sleeping, stertor/stridor while awake, and dyspnea, can persist after surgery.21 Decreasing risk factors that can be controlled, such as obesity, are paramount.4,17,22 Therefore, lifelong lifestyle changes are warranted despite surgery, such as weight management to maintain a slim body condition and avoidance of extreme heat. A numeric scoring system, the BOAS index, has been established in three breeds (Pug, French Bulldog, and Bulldog) to reflect the severity of the disease and to assess the outcome after surgery.22 This requires whole‐body barometric plethysmography (WBBP), which is noninvasive, but may not be available to most clinicians. A preoperative brachycephalic risk (BRisk) score has been developed to predict the risk of major complications or death objectively and accurately in dogs undergoing corrective surgery for BOAS. There are six variables that are each independent predictors of outcome that make up the BRisk score: breed, history of airway surgery, additional planned procedures (other than airway surgery), body condition score, admission clinical findings regarding the severity of airway compromise, and admission rectal temperature. Dogs with a BRisk score >3 are 9.1 times greater risk for a negative outcome than dogs with a low score (<3). This score can help clinicians set realistic expectations and assist owners in their decision‐making process.4 A general physical examination and a minimum database should be performed. Blood samples should be collected for complete blood count and serum biochemical analysis to screen overall health. Venous or arterial blood gas samples provide important information about pH, blood oxygen, and carbon dioxide (pv‐/paCO2) concentrations prior to general anesthesia, which can be serially monitored during surgery and in the postoperative period. Brachycephalic dogs are noted to have lower arterial blood oxygen and higher arterial CO2 levels than non‐brachycephalic breeds.23 Three‐view thoracic radiographs are obtained to evaluate for the presence of pneumonia, pulmonary edema, hypoplastic trachea, and/or hiatal hernia.14 French Bulldogs appear to have a high prevalence of hiatal hernia.24 The author routinely performs thoracic radiographs on the day of surgery, so the lungs are determined to be free of pneumonia prior to anesthesia (Figure 7.1). Pneumonia can complicate the balance between ventilation and perfusion and potentially worsen with anesthesia,25 therefore, consideration should be given to postponing corrective surgery in the presence of pneumonia. More advanced imaging, such as CT and endoscopy, can be considered but are likely limited to specialty hospitals, and cost may be prohibitive for some. The majority of anatomic abnormalities to be evaluated for surgery will be based on a lightly sedated oropharyngeal‐laryngeal examination. The author prefers to perform the pharyngeal‐laryngeal examination on the day of surgery, preventing a separate sedative episode, for which untreated brachycephalic patients may have difficulty recovering. Aberrant nasopharyngeal turbinates require CT and endoscopy for diagnosis and treatment, respectively.26,27 Upper gastrointestinal endoscopy may be considered for dogs with persistent gastrointestinal signs after corrective BOAS surgery if medical management techniques are considered unsuccessful. Medical treatment is recommended to decrease the risk of gastroesophageal reflux and aspiration pneumonia by decreasing perioperative upper gastrointestinal signs of nausea, vomiting, and regurgitation. There is an increased frequency of regurgitation after surgical treatment of BOAS, especially in dogs with preoperative regurgitation.28 Multimodal treatment with combinations of antiemetics, prokinetics, antiacid gastroprotectants, opioids, anxiolytics, and anti‐inflammatories are recommended. There is no known ideal protocol, and the combination of medications will depend on the severity of clinical signs, patient temperament, drug availability, and clinician comfort with certain protocols14 (Table 7.1). The effect of maropitanti in preventing nausea and vomiting when administered one hour prior to pre‐medication is well established.29,30 Maropitant also has the added value of reducing the minimum alveolar concentration of sevoflurane in dogs.31 The author administers maropitant prior to pre‐medication then every 24 hours while hospitalized and only if needed after the patient is discharged. Although reflux can be influenced by anesthesia, the high prevalence of presurgical gastrointestinal signs in addition to endoscopic changes suggests a chronic gastroesophageal reflux in brachycephalic breeds.13,17,32 Pre‐ and postoperative antiacid treatment improves digestive clinical signs and lesions in dogs undergoing corrective surgery for BOAS and is recommended in dogs without obvious clinical signs.32 The author typically gives omeprazole on the morning of surgery if no gastrointestinal signs are noted. If preoperative regurgitation is noted or suspected to occur frequently (multiple times weekly or daily), the author treats with omeprazole and cisapride for a minimum of two to four weeks prior to surgery until gastrointestinal signs are minimized or resolved. The postoperative effects of ileus, such as vomiting, decreased tolerance of oral diets, and prolonged recovery from surgery, can be considered detrimental in a brachycephalic patient. Because the side effects of ileus are similar to upper gastrointestinal signs in brachycephalic breeds, it may be difficult to distinguish between the worsening of preexisting GOR and the effects of postoperative ileus. Therefore, efforts should be made to mitigate any effects of postoperative ileus. Administration of both a gastroprotectant and prokinetic postoperatively minimized vomiting, regurgitation, and reflux in one study.18 Ultrasound can be utilized to evaluate intestinal motility in dogs with suspected ileus.33 The author administers omeprazole and cisapride for two to four weeks postoperative if frequent (multiple times daily) regurgitation is noted after surgery. Figure 7.1 Right and left lateral and ventrodorsal (VD) radiographic views of a French Bulldog obtained prior to BOAS surgery. Within the mediastinum there is a rounded soft‐tissue opacity present caudodorsally on the left lateral image and along the midline on the VD image. This is not visualized well on the right lateral image. This is consistent with a sliding hiatal hernia. There is scant fluid within the caudal esophagus on the right lateral image, which may indicate gastroesophageal reflux. There is no evidence of pneumonia detected. Nebulized epinephrine causes a clinically significant reduction in the BOAS index in preoperative dogs with a BOAS index of >70% and in dogs recovering from BOAS surgery purportedly through reduction of mucosal edema.34 While WBBP needed to measure the BOAS index may not be readily available to most, epinephrine nebulization has minimal side effects, so it can be performed without knowledge of the patient’s BOAS index. The most notable side effect in one study was nausea, which could be due to the medication itself or from stress during administration.34 Although nausea could be due to stress, it is also recognized as a clinical sign with underlying gastroesophageal reflux and may be associated with the brachycephalic population at hand. Nebulization should be discontinued should it present obvious stress to the patient. The author typically initiates epinephrine nebulization in the postoperative period immediately after extubation then every 6 hours for 24 hours, which is when most patients are being discharged. Some clinicians do not continue this treatment after 24 hours because of a rebound phenomenon of worsening stridor in children with croup after treatment with nebulized adrenaline. Although a rebound phenomenon has been suggested in children, a review of the literature established that no study has reported the symptoms as being worse than baseline, and the re‐emergence of symptoms is less marked when children receive nebulization concurrently with steroids.35 Table 7.1 A list of multimodal medications used most frequently in the perioperative period. Most literature suggests the use of corticosteroids during the perioperative period to reduce surgery‐induced and postoperative (panting) pharyngeal swelling and edema, however, controlled evidence is lacking. The author administers one dose of corticosteroids 20 minutes prior to surgery, and if postoperative obstruction is a concern related to pharyngeal edema, additional doses are repeated as needed. Sedative‐anxiolytic drugs in combination with opioids are recommended, however, the desired effect can also relax the smooth muscle of the nasopharyngeal and oropharyngeal region risking further obstruction.36 The author prefers drugs that are reversible with a short duration of action and can be administered as a constant infusion (butorphanol and dexmedetomidine), which allows for these drugs to be titrated quickly up or down to achieve the lowest dose required without excessive sedation. Brachycephalic breeds have lower than normal arterial oxygen concentrations at rest compared to non‐brachycephalic dogs.23 Preoxygenation for three minutes prior to general anesthesia increases the time to desaturation.37 Brachycephalic dogs may particularly benefit from preoxygenation as upper airway obstruction is common and intubation can be more difficult, delaying a patent airway.14 If a face mask to deliver oxygen is stressful, the mask can be removed to deliver oxygen from the end of the anesthetic tubing, allowing some distance between the pet and the oxygen delivery system if needed. Anxiolytic drugs are administered as needed preoperatively and induction should occur rapidly. The initial 12–24 hours of recovery is considered the high‐risk period for the brachycephalic patient, particularly because of the possibility of airway obstruction.7,25 Brachycephalic patients recovering from surgery should be placed in sternal recumbency, with the head slightly elevated, and remain intubated until their endotracheal tube is no longer tolerated.14,25,38 Opioids and anxiolytics should be used to obtain a calm state without excessive sedation (Table 7.1). Oxygen should be provided to any patient that shows increased respiratory effort. Clinicians should be prepared with induction drugs, endotracheal tubes, and a laryngoscope for emergency reintubation in the presence of upper airway obstruction. If a postoperative obstruction occurs after BOAS corrective surgery, the author typically reintubates, assessing the larynx for the cause of obstruction. The author will treat with additional corticosteroids and anxiolytics, allowing a more prolonged recovery. Temporary tracheostomy should be considered if additional treatment for postoperative swelling, pain, and anxiety is considered ineffective after re‐attempting extubation. Stenotic nares are a congenital malformation of the nasal cartilage, resulting in medial collapse and narrowing of the external nares39,40 (Figure 7.2). The decrease in the transverse diameter of the nares leads to increased negative upper airway pressures to overcome the increased resistance in airflow.40 There are several surgical techniques that have been described for the management of stenotic nares. All techniques can be performed with a scalpel blade, electrocautery, or CO2 laser. Figure 7.2 Stenotic nares. Source: © Pamela Schwartz. Several wedge resection (alarplasty or alaplasty) techniques (vertical, horizontal, lateral) have been described, removing wedge‐shaped portions of the wing of the nostril and underlying alar fold, requiring suture to appose the nasal epithelium39,40 (Figure 7.3a,b). When using a blade for these techniques, hemorrhage occurs rapidly, which may impair visibility.41 Hemorrhage is controlled during surgery with direct pressure using a sterile cotton‐tipped applicator or gauze and typically resolves once the wound is sutured. A punch resection alarplasty is similar to the wedge techniques but utilizes a dermatological punch biopsy toolii to remove a circular plug of tissue in the ala nasi, which is then sutured closed. With each of these techniques, the nares are widened by narrowing the thickness of the alar nasi, removing tissue to the level of the alar fold.42,43 The patient is placed in sternal recumbency with the chin elevated slightly. The most ventromedial aspect of the alar wing (alar fold) is grasped at the level of the proposed tissue to be removed (Figure 7.4). The author uses a rat tooth or Bishop Harmon forceps to hold this tissue in place, making a cut on either side using an 11‐blade to subsequently remove this triangular section of tissue. The author recommends starting a minimum of 1–2 mm from the edge of the alar fold, as the wedge can be difficult to close if there is not a substantial amount of tissue to move laterally to close. Hemostasis is obtained using a sterile cotton‐tipped applicator; however, bleeding will persist until the edges are sutured. The author prefers 4‐0 PDS on an RB‐1 needle (the editor prefers 4‐0 Monocryl on a reverse cutting needle) for closure, placing the most distal/ventral suture first, initially holding the edges closed without tying the knot, to ensure adequate patency of the nostril prior to closure. If needed, an additional wedge of tissue can be removed prior to closure. Two to three interrupted sutures are placed to appose the cut surfaces. Alapexy is a surgical technique used to fix the alae in an abducted position. This technique involves creating two elliptical incisions, one at the ventrolateral aspect of the alar skin and a corresponding incision in the skin lateral to the ala. These paired incised surfaces are then apposed using suture. This technique may be more time‐consuming than other alarplasty techniques due to the need for two incisions and a two‐layer closure.43 It is difficult to make comparisons regarding the effectiveness of different surgical techniques for stenotic nares since most are performed in combination with additional upper airway corrective surgery. Figure 7.3 (a) Preoperative image of stenotic nares. (b) Postoperative image of the same dog immediately after vertical alar wedge resection. Source: © Pamela Schwartz. Figure 7.4 The white lines outline the proposed vertical wedge to be resected in the preoperative image (a) and the resulting widening of the nares in the postoperative image (b). Source: © Kristin Coleman. Amputation of the alar skin and underlying cartilage (Trader’s technique) is the first noted corrective surgery for stenotic nares described by Trader in 1949.44 This technique may not be favored by some presumably due to hemorrhage associated with the technique, a resulting open wound, and the plethora of other techniques that are available. An advantage of this surgery is the larger amount of tissue that can be removed with the amputation technique compared to alarplasty techniques.40 A study revisited the Trader’s technique in immature Shih Tzus documenting the complete resolution of all clinical signs associated with stenotic nares, as well as a cosmetic outcome in all dogs.40 The author performs a modified Trader’s technique, utilizing a carbon dioxide laser instead of a blade, preventing the need to control hemorrhage with epinephrine‐soaked gauze strips in the immediate postoperative period. In the author’s opinion, this technique allows the most significant widening of the nares with cosmetic results (Figure 7.5). Figure 7.5 Preoperative stenotic nares and immediate postoperative photo after Trader’s technique using CO2 laser in three separate breeds. Source: © Pamela Schwartz. Figure 7.6 The CO2 laser is used to excise the alar fold holding the handpiece at an approximately 40–45° angle from the coronal plane. Source: © Pamela Schwartz. The laser‐assisted turbinectomy (LATE) is an endosurgical procedure developed for the removal of obstructive turbinate tissue to improve endonasal airway patency in brachycephalic dogs.27 CT and anterior and posterior rhinoscopy have identified intranasal anatomical variations in three brachycephalic breeds (Pug, French Bulldog, and English Bulldog).26 Abnormal configuration of the nasal conchal tissue is classified as rostral aberrant turbinates and caudal aberrant turbinates (Figure 7.7).26,27 Direct intraconchal contact points are responsible for obstruction of the intranasal passageway.26 The surgery results in decreased mucosal contact points in the nasal passages. The most common complication is transient intraoperative hemorrhage in 32.3% of dogs. Regrowth of turbinates requiring another surgical procedure has been noted in 15.8%.27 Postoperative complications include dyspnea, which may require temporary tracheostomy, especially when laryngeal collapse is present, postoperative regurgitation, and reverse sneezing which is self‐limiting.45 At the time of follow‐up, 40% of dogs had intermittent nasal noise when sniffing and excited, which was a different noise than noted preoperatively, and 20% of dogs had a BOAS index that remained >50%.45 The outcome of the LATE procedure, performed two to six months after conventional multilevel surgery, was assessed using the median BOAS index based on WBBP. The median BOAS index decreased from 66.7% to 42.3% after LATE.45 There can be several disadvantages when considering the LATE procedure. Specialty equipment for diagnostics and treatment (CT, endoscopy, diode laser), advanced training, and additional time are required, especially if being performed as part of a multilevel surgery strategy. The mean surgical time for the LATE procedure is 18 minutes with a range of 7–59 minutes.27 Due to the need for advanced training and specialty equipment required for this technique, it is not described here and can be referenced in Oechtering et al.27 Figure 7.7 (a) Retroflex endoscopy of a normal nonobstructed nasopharynx in a mesaticephalic breed of dog. (b) The appearance of obstructive caudal aberrant nasal turbinates in a brachycephalic breed of dog. Source: © Dr. Sarah Marvel. Traditional surgical correction objectives are aimed at trimming the length of the soft palate when the palate is elongated (staphylectomy), thus, relieving obstruction of the rima glottis.46 Staphylectomy may be performed using scissors (cut‐and‐sew technique), an energy‐sealing device, or CO2 laser. Staphylectomy using Harmonic Focus Shearsiii is associated with less hemorrhage and a shorter average surgical time compared to traditional sharp resection with sewing.46 CO2 laser also allows a shorter surgical time compared to incisional palate resection, however, a similar comparison was not made regarding its effect on hemorrhage.15 CO2 laser allows shorter surgical time and less use of an additional sealing device, suggestive of less bleeding compared to diode laser or electrocautery.47 Traditional landmarks for shortening the soft palate are the tip of the epiglottis and the middle to caudal third of the tonsillar crypt.15,48 Although some have suggested that trimming shorter than the traditional landmarks can lead to complications such as nasal regurgitation and rhinitis, more recent literature suggests otherwise.16,47,49 The author trims the soft palate shorter than the traditional recommendations. An extended palatoplasty described by Dunié‐Mérigot et al. and H‐pharyngoplasty described by Carabalona et al. are techniques to trim the soft palate beyond the traditional landmarks.47,49 Figure 7.8 Patient positioning with the maxilla suspended with tape. Source: © Pamela Schwartz. The positioning is as described for the laser staphylectomy. The editor prefers to have an assistant press ventrally on the endotracheal tube for additional working space in the oropharynx. The distal aspect of the soft palate is grasped with an Allis tissue forceps, or a stay suture can be used to retract the soft palate rostrally. Stay sutures are placed at the proposed start and end points of the soft palate at the level of the mid‐point of the tonsillar crypts, which are ideally two packs of 4‐0 Monocryl or Biosyn with a hemostat to elevate the site for suturing. The author prefers to place the first throw for the continuous suture and the end of the suture that is normally cut is left long as a stay suture. Curved Metzenbaum scissors are used to make small cuts across the soft palate, followed closely by suturing. This technique prevents the oral and nasopharyngeal mucosa from becoming widely separated from one another, which can be more challenging to manipulate within the small surgical field. This is continued until the entire amount of desired soft palate is excised. Hemorrhage is controlled using hemostats or electrocautery, and any bleeding will ultimately tamponade once the edges of the palate are closed. Figure 7.9 (a) Note the soft palate drapes over the endotracheal tube. (b) The tip of soft palate is grasped with Allis tissue forceps and retracted rostrally toward the base of the tongue for surgical planning. (c) A saline‐soaked gauze is placed caudal to the soft palate, covering the endotracheal tube. (d) During the use of the CO2 laser, a sterile tongue depressor is placed between the soft palate and the gauze as an additional barrier to protect against inadvertent damage to the endotracheal tube or surrounding soft tissue structures. Note the planned mark for staphylectomy made with the CO2 laser. Source: © Pamela Schwartz. Figure 7.10 The laser is used to mark the planned region of the staphylectomy site starting at the medial aspect of the tonsillar crypt. A curved line is drawn toward the pterygoid process then back down toward the opposite tonsillar crypt. Note the position of the laser is perpendicular to the soft palate at the pre‐determined line as opposed to a 45° angle from cranial to caudal, which would create more separation between the oral and nasopharyngeal mucosal surfaces. Source: © Pamela Schwartz. Figure 7.11 (a) After the first pass with the laser, the soft palate was deemed too long, and the procedure was repeated to remove the additional soft palate. (b) Immediately postoperative staphylectomy showing the level of the soft palate falling at the top of the arytenoid cartilage. Note the oral and nasal mucosal surfaces are not sutured. (c) The preoperative photo is included for direct comparison. Source: © Pamela Schwartz. Figure 7.12 Staphylectomy with the oral and nasal mucosal surfaces sutured. Source: © Pamela Schwartz. As staphylectomy does not address the thickness of the soft palate, additional techniques, such as the split staphylectomy and folded flap palatoplasty (FFP), have been designed to address both shortening and thinning of the soft palate simultaneously.50 Palatoplasty may be performed using electrocautery, CO2 laser, or diode laser; however, dogs have a more favorable outcome and fewer complications with CO2 or monopolar electrocautery in comparison to use with a diode laser.47 Compared with traditional staphylectomies, the suture placement associated with FFP is more rostral, and therefore, further away from the pharynx, which may result in less postoperative irritation and subsequently less pharyngeal inflammation and edema.41 The author prefers FFP when the soft palate is subjectively excessively thickened in addition to elongated. Figure 7.13 (a) Note three stay sutures at the distal end of the soft palate, one at the tip and two on either side of the first. (b) Monopolar electrocautery is used to mark a triangular or trapezoidal area to be incised. (c) The ventral mucosa and associated soft tissues of the soft palate are excised until the nasopharyngeal mucosa is approached. A small defect can be seen in the nasopharyngeal mucosa, which is sutured prior to closure. (d) The stay sutures are advanced rostrally, and the mucosal surfaces apposed. (e) Finished palatoplasty. Source: © Pamela Schwartz. Eversion of the laryngeal saccules is recognized as the first stage of laryngeal collapse20 (Figure 7.14). Everted saccules are positioned just rostral to the vocal folds.39 During the laryngeal examination, light anesthesia is important, as saccule eversion can be a dynamic process, and eversion can be missed if the patient is not breathing during the examination. If the saccules have been everted more chronically, it is possible that they will remain everted after general anesthesia, due to secondary changes such as elongation and thickening from fibrosis. The saccules can be removed using Metzenbaum scissors, a blade, or CO2 laser. The author prefers using scissors, due to ease and avoiding concerns related to using CO2 laser close to the endotracheal tube and vocal folds. One study reports a minimum of stage I laryngeal collapse in all dogs aged six months or less, further supporting the recommendation that dogs undergo surgical treatment as early as possible.20 Figure 7.14 The laryngeal saccules are bilaterally everted causing partial obstruction to the rima glottis. Eversion and enlargement of the palatine tonsils are also noted. Source: © Pamela Schwartz. Laryngeal collapse is commonly noted in dogs with BOAS and is described as a loss of cartilage rigidity, which allows medial deviation of the rostral laryngeal cartilages. Increased airway resistance and velocity and increased negative intraglottic luminal pressure lead to a gradual collapse of the rostral laryngeal opening.20,21,51,52 Three stages of laryngeal collapse have been described: stage I is eversion of the laryngeal saccules, stage II is loss of rigidity and medial displacement of the cuneiform process of the arytenoid cartilages, and stage III is collapse of the corniculate process of the arytenoid cartilages and subsequent loss of the dorsal arch of the rima glottis with consistent crossing of the cuneiform cartilages medially.20,52,53 The best management of stage II or III laryngeal collapse is still controversial.52 Reported options for treatment of stage III collapse include arytenoid lateralization, permanent tracheotomy, and subtotal epiglottectomy in association with ablation of unilateral cartilage.52, 55–57 Arytenoid lateralization may be a useful treatment for stage II and III collapse in brachycephalic dogs with one study showing good long‐term results in dogs that survive; two dogs (16.7%) were euthanized postoperatively due to dyspnea secondary to minimal enlargement of the rima glottis.51 One study identified degenerative histologic characteristics and decreased load to failure and stiffness of the arytenoid cartilage in brachycephalic dogs compared to non‐brachycephalic dogs, which could result in failure after arytenoid lateralization, although further studies are warranted.58 Another study evaluated arytenoid lateralization for the treatment of combined laryngeal paralysis and laryngeal collapse, however, none of the dogs treated were brachycephalic.57 Subtotal epiglottectomy in association with ablation of unilateral cartilage shows promise with 12.5% requiring a temporary tracheostomy and variable outcome in the 75% of patients that were followed up at one year.52 Permanent tracheotomy in brachycephalic breeds is associated with major complications (80%) resulting in postoperative death in 53%.55 Because these are considered salvage procedures with higher complication and mortality rates, referral to a board‐certified surgeon is recommended. Temporary tracheostomy can be performed if needed prior to referral. Figure 7.15 (a) The left laryngeal saccule is exteriorized away from the vocal fold. (b) The laryngeal saccule is excised using Metzenbaum scissors cutting from ventral to dorsal. (c) Photo immediately after bilateral laryngeal saccule removal. The edges of the vocal folds can be visualized just caudal to the cut edges of the laryngeal saccules. Source: © Pamela Schwartz. Figure 7.16 Stage III laryngeal collapse is noted with the left cuneiform process of the arytenoid cartilage folded inward toward and crossing slightly rostral to the right cuneiform process. Source: © Pamela Schwartz. Historically, tonsillectomy was considered controversial.10 Eversion and enlargement of the palatine tonsils are suspected secondary changes due to increased negative airway pressure and can contribute to pharyngeal obstruction (Figure 7.14). One study documents everted tonsils in 56% of dogs with BOAS.59 Although the full advantage is not completely known, tonsillectomy has been documented as part of multilevel BOAS surgery strategy.8,45 Tonsillectomy can be performed using a blade, scissors, monopolar electrocautery, CO2 laser, or vessel‐sealing devices such as the LigaSure.iv Complications after tonsillectomy include hemorrhage, pharyngeal swelling, and postoperative aspiration of blood or fluid.60 A clamping technique combined with monopolar electrocautery has been associated with a high risk of bleeding compared to energy‐based vessel sealing devices.61,62 The author prefers CO2 laser, however, knowledge of anatomy is paramount to avoid hemorrhage and inadvertent damage to neighboring structures. The endotracheal tube is protected using saline‐soaked sponges and a sterile tongue depressor as needed. Safety glasses specific to the laser are required to be worn by all staff within the operating suite if utilizing CO2 laser. The tonsil is grasped with DeBakey or Allis tissue forceps and retracted from the tonsillar crypt (Figure 7.17a). Care is taken when manipulating the tonsil, as the tonsil is friable, and excessive manipulation can lead to hemorrhage or tearing of the tonsil. Retracting the edge of the tonsillar crypt dorsally helps to expose the tonsil and its attachments. The tonsil is then dissected free from its attachments while retracting it from the crypt (Figure 7.17b–g). The base of the tonsil is transected with scissors, a scalpel, electrocautery, laser, or vessel‐sealing device. The tonsillar artery may need ligation if scissors or a scalpel are utilized. The mucosal crypt is closed with a rapidly absorbable monofilament suture (Figure 7.18). The author prefers simple continuous closure with a small (4‐0) rapidly dissolving suture. Temporary tracheostomy is indicated in dogs that have continued airway obstruction despite corrective surgery for BOAS.18,63 Continued airway obstruction may be attributable to conformational changes that cannot be corrected (i.e., advanced laryngeal collapse), as well as pharyngeal swelling and edema from manipulation during surgery. Historically, temporary tubed tracheostomy has been associated with a high complication rate. Complications associated with temporary tubed tracheostomy may include coughing, occlusion of the tube with mucus or debris causing obstruction, inadvertent dislodgement of the tube, dyspnea, vomiting, pneumonia, subcutaneous emphysema, pneumomediastinum, sinus bradycardia, and death.64–67 One study reports a complication rate of 86%, with unsuccessful tube management in 19% of dogs ultimately leading to death or euthanasia.64 Another study evaluating temporary tracheostomy tube‐placement in dogs following corrective surgery for BOAS noted a high overall complication rate of 95.2% but successful management in 97.5%.67 Studies note that breed and age are risk factors with Bulldogs being less likely to have a successful outcome with temporary tubed tracheostomy, and the odds that a dog would require a temporary tracheostomy increasing with each year of age.63,64 An additional study found a correlation between dogs requiring a temporary tracheostomy after surgery and death or euthanasia in the postoperative period.68 The high complication rate and intensive management required for the successful management of traditional tubed tracheostomies have led to the development of novel techniques. Use of silicone tracheal stents or modified techniques with placement of a Penrose drain dorsal to the trachea continue to have high complication rates.65,66 A tubeless temporary tracheostomy technique has been developed by Dr. Heidi Hottinger (publication in progress) to potentially alleviate some of the complications associated with a tube tracheostomy for a variety of airway diseases, including BOAS. The goal of the tubeless temporary tracheostomy is to minimize handling and stress, as there is no tube maintenance. Only the surrounding skin is cared for using baby wipes initially every two hours and Aquaphor to decrease irritation from frequent cleaning of the skin. Suction, which can induce a vasovagal response, is not recommended, and any mucus can be cleaned with a sterile cotton‐tipped applicator only as needed. This technique has been used in over 60 patients in Dr. Hottinger’s and the editor’s clinic with the average time to discharge being one to two days. If pneumonia is present, the average hospital stay is extended to 3.3 days. Reported complications include mild to excessive mucoid discharge for the first one to two weeks (which then subsides) in up to 30% of cases, persistent stoma requiring outpatient surgical closure (usually only sedation needed) (20%), pneumonia, local dermatitis, dehiscence, and death (15%) within one week of surgery. Of the four cats in this population, there was a 25% risk of death (1 out of the 4). Of the cases that died or were euthanized, the majority were due to the primary disease process. A population of cases failed airway normalization (10%) and required conversion to a permanent tracheostomy. A tubed tracheostomy in comparison is much more labor‐intensive with some patients requiring interventions as frequently as every 15–60 minutes to combat the formation of mucus plugs. Future studies are warranted to compare this technique to that of the traditional tubed tracheostomy. Figure 7.17 (a) The right tonsil is grasped with DeBakey Forceps and retracted. A sterile cotton‐tipped applicator is used to retract the tissue dorsally to expose the dorsomedial attachments of the tonsil. (b–f) CO2 laser is used to dissect the attachments of the tonsil, first rostromedially, retracting the tonsil while advancing more caudally to completely excise the tonsil. (g) The tonsillar crypt can be seen empty after tonsillectomy. Source: © Pamela Schwartz. Figure 7.18 (a) Everted tonsils preoperatively. (b) Immediately post bilateral tonsillectomy. Note the crypts are sutured closed. Source: © Pamela Schwartz. The patient is placed in dorsal recumbency with the neck extended. Rolled towels can be placed underneath the neck, which moves the trachea to a more superficial position. The fur is clipped from the ramus of the mandible to the thoracic inlet and aseptically prepped and draped (Figure 7.19). A ventral midline incision is made starting caudal to the thyroid cartilage, extending far enough to include the fourth and fifth tracheal rings (Figure 7.20a). Subcutaneous dissection is continued to expose the paired sternohyoid muscles (Figure 7.20b). The sternohyoid muscles are separated at their median raphe to expose the trachea (Figure 7.20c). To improve exposure, elevate the sternohyoid muscles to access the lateral aspects of the trachea, and bluntly dissect the dorsal fascial attachments. Dissection too dorsally could result in iatrogenic injury to the vagosympathetic trunk. If needed, a curved instrument can be placed dorsally to elevate the trachea to a more superficial position (Figure 7.20d). A transverse incision is made through the annular ligament using a blade between the third and fourth or fourth and fifth tracheal rings (Figure 7.20d). This incision should not exceed more than half of the tracheal circumference. Nonabsorbable stay sutures are placed encircling the cartilage cranial and caudal to the tracheostomy site, which can be manipulated to separate the edges during tube insertion. Suction all blood or mucus prior to tube insertion. To facilitate tube insertion into the caudal trachea, the caudal stay suture is tensioned, and the cranial cartilage can be flattened with a hemostat. Figure 7.19 Positioning for a temporary tracheostomy. Rolled towels are placed underneath the neck, which moves the trachea to a more superficial position. The fur is clipped from the ramus of the mandible to the thoracic inlet and aseptically prepped and draped. Source: © Heidi Hottinger. Figure 7.20 (a) A ventral midline incision is made starting caudal to the thyroid cartilage, extending far enough to include the fourth and fifth tracheal rings. (b) The sternohyoid muscles are noted. (c) The trachea is exposed. (d) A curved instrument is placed dorsally to elevate the trachea. A transverse incision is made through the annular ligament between the third and fourth or fourth and fifth tracheal rings, being sure to not transect through more than 50% of the circumference. Source: © Heidi Hottinger. If the tube is difficult to insert, the annular ligament incision can be extended slightly, or an ellipse of cartilage can be resected. Once the tube is placed, the sternohyoid muscles, subcutaneous tissue, and skin are apposed cranial and caudal to the tracheostomy tube. The tube is secured to the neck using umbilical tape, or there is a plethora of commercially available tracheal ties (Figure 7.21). The author recommends labeling the stay sutures with white tape (i.e., the cranial suture “up” and the caudal suture “down”) to easily identify them if a rapid tube exchange is required. In the postoperative period, the tube can be temporarily occluded to determine if the patient can tolerate breathing through the upper airway. Once the tube is removed, the tracheal stoma can be left open to heal by second intention. Figure 7.21 Cuffed and noncuffed tracheostomy tubes. Cuffed tubes are typically used if mechanical ventilation is needed. Note the open circles on either end of the flange, which are used to secure the tube around the patient’s neck. Source: © Pamela Schwartz. The patient is placed in dorsal recumbency with the neck extended. A rolled towel is placed underneath the neck to facilitate dorsiflexion, which moves the trachea to a more superficial position. The fur is clipped from the ramus of the mandible to the thoracic inlet and aseptically prepped and draped (Figure 7.19). A ventral midline incision is made starting caudal to the cricoid cartilage, extending far enough to include the fourth and fifth tracheal rings (Figure 7.20a). Subcutaneous dissection is continued to expose the paired sternohyoid muscles (Figure 7.20b). The sternohyoid muscles are separated at their median raphe to expose the trachea (Figure 7.20c). To improve exposure, elevate the sternohyoid muscles to access the lateral aspects of the trachea, and bluntly dissect the dorsal fascial attachments. Dissection too dorsally could result in iatrogenic injury to the vagosympathetic trunk. If needed, a curved instrument can be placed dorsally to elevate the trachea (Figure 7.20d). A transverse incision is made through the annular ligament using a blade between the second and third tracheal rings in brachycephalic dog breeds and between the third and fourth or fourth and fifth rings in normocephalic breeds (Figure 7.20d). This incision should not exceed more than half of the tracheal circumference. A tracheostomy tube is not placed; instead, the closure begins with the first two sutures engaging the commissures of the tracheostomy using a rapidly absorbable suture. The first suture is placed through the subcutis, medial edge of the sternohyoid muscle, and full thickness through the trachea, all in a single interrupted throw (Figure 7.22a–d). This is repeated on the opposite side. This adequately elevates the trachea as well as excludes the sternohyoid muscle from the field (Figure 7.23). Additional sutures are placed on either side of the stoma, engaging full‐thickness trachea to subcutis, moving lateral to medial until skin‐skin apposition is noted cranial and caudal to the tracheostomy site (Figure 7.24a,b). Suturing the trachea to the subcutis helps apply cranial and caudal tension on the stoma to widen it. The skin is then apposed cranial and caudal to the tracheostomy site, using absorbable interrupted skin sutures (Figure 7.25). Once the patient is extubated, flow‐by oxygen can be administered at the stoma site. Intubation of the tubeless tracheostomy site is not preferred, as it can disrupt the sutures. Closure consists of second‐intention healing and usually occurs within six to eight weeks postoperatively. Figure 7.22 The first suture is placed through the skin and subcutis (a), medial edge of the sternohyoid muscle (b), then full thickness through the trachea (c), all in a single interrupted throw (d). Source: © Heidi Hottinger. Figure 7.23 Placement of the first two sutures on either side of the tracheostomy site, which elevates the trachea and excludes the sternohyoideus muscles from the field. Source: © Heidi Hottinger. Figure 7.24 (a,b) Additional sutures are placed on either side of the stoma, engaging full‐thickness trachea to subcutis, moving lateral to medial until skin‐skin apposition is noted cranial and caudal to the tracheostomy site. Source: © Heidi Hottinger. Figure 7.25 The skin is apposed cranial and caudal to the tracheostomy site using absorbable interrupted skin sutures. Source: © Heidi Hottinger. Brachycephalic breeds have a higher risk of developing complications in the perianesthetic period but even more so in the postanesthetic period.25 The most common postoperative complications are vomiting, regurgitation, aspiration pneumonia, dyspnea, airway obstruction, and death.25,28,49 The postoperative mortality rate is generally less than 5% but is reported to be as high as 7%.7,47,49,67,68 The most common cause of death is secondary to airway obstruction and aspiration pneumonia. Most dogs that undergo surgical correction of BOAS improve and have a good long‐term outcome, but it is important for owners to know that the anatomy cannot be normalized and many dogs will continue to have clinical signs.8,21,69 The author recommends that owners take normal brachycephalic precautions after surgery (avoiding extreme heat, maintaining a slim body condition) and recheck if a progression in clinical signs is noted or a whistling noise develops, which could indicate laryngeal collapse. The Norwich Terrier appears to have an obstructive airway syndrome that differs from that encountered by brachycephalic breeds. Similar to some brachycephalic breeds, half of Norwich Terriers lacked clinical signs despite the identification of severe obstruction on laryngeal examination.70 Differing from brachycephalic breeds, nasal and palate abnormalities are not common. The site of obstruction appears to be at the level of the larynx with narrowing noted caudal to the vocal folds that decreases the luminal diameter.70 The small size of the laryngeal opening presumably leads to airway obstruction and secondary changes such as redundancy of supra‐arytenoid tissue, everted laryngeal saccules, and laryngeal collapse. The role of surgery is unclear, although corrective surgery can be considered if secondary changes are present. The author anecdotally performed staphylectomy in a three‐year‐old Norwich Terrier with progressive respiratory signs. The elongated soft palate was a presumed secondary change, as CT and laryngeal examination documented a characteristic small laryngeal opening as well as stage II laryngeal collapse. Although the syndrome in Norwich Terriers differs from other brachycephalic breeds, they should be considered similarly challenging anesthetic candidates and should be watched carefully in the postanesthetic period.70 Much less is known regarding BOAS in cats, as it appears to be less common compared to dogs. Abnormalities of the nares appear to be the primary component of BOAS in cats.71–73 In some cases, stenotic external nares and a narrowed nasal vestibule are the primary causes of obstruction, whereas some cats appear to have ventral nasal obstruction resulting from redundant skin along the floor of the nares.71,73 One study evaluating Persian and Exotic Shorthair show cats identified moderate to severe stenotic nares in 86% and hypoplasia of the nose leather in 95% with the nose leather top positioned above the level of the lower eyelid in 93%. Despite these conformational abnormalities, few cat owners perceived any problems related to the airways.74 Because the obstruction is generally at the level of the nares, signs associated with BOAS in cats are mostly alleviated by the surgical intervention of the alar wings and alar folds. One study shows success in cats using a blade to remove the axial alar wing and alar fold bilaterally as reported for dogs.73 If obstruction is secondary to redundant skin along the floor of the nares, techniques used in dogs may be insufficient, as this anatomical abnormality is not addressed. In cats with obstruction from redundant skin along the floor of the nares, a single pedicle advancement flap allowed a reduction in stertorous breathing and no episodes of respiratory distress.71 In cats where the obstruction results from the alar folds and redundant skin, a combined surgery of “alar fold lift‐up” and “sulcus pull‐down” has been described as successful.70 Because of the paucity of information on cats, it is difficult to make direct comparisons between surgical techniques. There seems to be a low complication rate regardless of the surgical technique. The author prefers a modified Trader’s technique using a CO2 laser with or without suture as the first stage (Figure 7.26). Although the author has not needed to consider a second surgery on a cat, if the cat’s outcome is not perceived as successful once recovered, the author typically prepares owners for a single pedicle advancement flap if additional relief is needed. The cat is positioned in sternal recumbency with the head slightly elevated in a neutral position. Safety glasses specific to the laser are required to be worn by all staff within the operating suite if utilizing CO2 laser. The alar fold is grasped with Bishop Harmon forceps and retracted ventromedially. A sterile cotton‐tipped applicator is placed ventral to the alar fold within the nostril as a barrier to the blade or laser to protect the underlying nasal skin from inadvertent damage. The laser or blade is used to excise as much of the alar wing and alar fold as possible and, if needed, the skin just adjacent to the alar fold. This is left open to heal by second intention. Alternatively, a rapidly absorbable interrupted suture can be placed to help exteriorize the nasal mucosal surface, although this is rarely needed. Figure 7.26 Persian cat. (a) Stenotic nares preoperatively. (b) Nares postoperatively after a modified Trader’s technique. No sutures are placed. (c) Appearance of the nares after complete healing by second intention. Source: © Pamela Schwartz.
7
Brachycephalic Obstructive Airway Syndrome in Dogs and Cats
Introduction
Clinical signs in dogs with BOAS may include both respiratory and gastrointestinal signs. Reported clinical signs may include exercise intolerance, heat intolerance, sleep apnea, increased respiratory rate and effort, stertor or stridor, regurgitation, gagging, vomiting, nausea, dyspnea, and when severe, may progress to syncope, collapse, heat stroke, and death1,3,5–7,10,13 (Video 7.1). A correlation has been established between BOAS and gastrointestinal signs in the extreme brachycephalic breeds, with French Bulldogs having the highest prevalence of presurgical regurgitation and vomiting.13 It is important that veterinarians recognize that gastrointestinal signs are often a sequela of BOAS, requiring surgical intervention through corrective upper airway surgery. Gastroesophageal reflux, vomiting, or regurgitation can lead to aspiration pneumonia.7 There are clinical signs spanning from “normal” or a “normal variant” for a brachycephalic dog to a dog clinically affected with BOAS.3 A normalization phenomenon exists that describes the acceptance of some chronic and highly breed‐associated conditions as normal.6 In a questionnaire‐based study, 58% of owners reported a high frequency and severity of clinical signs in their dogs without perceiving them to have a breathing problem.6 Lack of recognition of clinical signs indicating disease may result in a lack of treatment until clinical signs progress and negatively affect an animal’s welfare and outcome.6 Since clinical signs are progressive, it is paramount that veterinarians recommend brachycephalic breeds seek early surgical intervention, even if not mentioned by the client as a concern, prior to the development of chronic and irreversible negative effects of BOAS or a respiratory crisis.3,6,7
Diagnostics
Perioperative Considerations
Perioperative treatment
Medication
Dosage
Timing and frequency
Maropitant
1 mg/kg IV or SQ
30–60 min prior to pre‐medication, then every 24 h
Metoclopromide
1 mg/kg IV bolus over 10 min
Once 30–60 min prior to pre‐medication
1 mg/kg/h IV CRI
During surgery and for 24 h postoperatively
Cisapride
0.25–0.5 mg/kg orally
Give every 8–12 h preopertively to minimize gastrointestinal signs. Continue postoperatively if regurgitation persists or worsens.
Pantoprozole
1 mg/kg IV
Every 12 h
Ondansetron
0.5–1 mg/kg IV (slowly)
Every 8–12 h postoperatively as needed
Dexamethasone SP
0.1 mg/kg IV
Given 20 min prior to surgery. This can be given again postoperatively if pharyngeal swelling is a concern.
Butorphanol
0.4 mg/kg IM or IV
Once as a premedication
0.2–0.4 mg/kg IV bolus
Postoperatively as needed
0.1–0.4 mg/kg/h IV CRI
Intraoperatively and postoperatively
Epinephrine
0.05 mg/kg epinephrine is added to 0.9% saline to make a 5‐mL nebulization solution delivered as a flow by for 10 min
After extubation, then every 6 h for 24 h
Acepromazine
0.005–0.05 mg/kg IM or IV
As a pre‐medication only if needed, then as needed postoperatively
Trazodone
3–10 mg/kg PO
After extubation as needed every 6 h
Dexmedetomidine
1–3 mcg/kg IV bolus
Postoperatively as needed
1–3 mcg/kg/h IV CRI
Postoperatively as needed
Stenotic Nares
Vertical Alar Wedge Resection – Surgical Technique
Modified Trader’s Technique – Surgical Technique
Safety glasses specific to the laser are required to be worn by all staff within the operating suite if laser is utilized. The patient is placed in sternal recumbency with the chin elevated slightly. The most ventromedial aspect of the alar wing (alar fold) is grasped with rat‐toothed forceps and pulled ventromedially. A sterile cotton‐tipped applicator is placed ventral to the alar fold within the nostril as a barrier to the blade or laser to protect the underlying nasal skin from inadvertent damage. The laser or electrocautery is used to mark the planned region of alar amputation. The proposed line is evaluated and can be adjusted as needed prior to incising. A #11 blade or CO2 laser is used to excise the alar fold holding the blade or laser at an approximately 40–45° angle from the coronal plane (Figure 7.6; Video 7.2). The same procedure is repeated on the opposite side to make the resulting nares symmetrical. If a blade is utilized, hemostasis is achieved with direct pressure or electrocautery.
Laser‐Assisted Turbinectomy (LATE)
Soft Palate
CO 2 Laser Staphylectomy – Surgical Technique
Safety glasses specific to the laser are required to be worn by all staff within the operating suite. The patient should be positioned in sternal recumbency with the mouth opened by suspending the maxilla (Figure 7.8). The soft palate should be evaluated while the head and tongue are in a neutral position. Normally, the soft palate should not extend past the tip of the epiglottis or the mid‐to caudal aspect of the tonsillar crypt38 (Figure 7.9a). The tongue is grasped with a gauze sponge and pulled cranially by an assistant as needed throughout the surgery. A DeBakey forcep is used to grasp and retract the tip of the soft palate ventrally toward the base of the tongue to visualize the planned location of the incision (Figure 7.9b; Video 7.3). The DeBakey forcep is changed out for an Allis tissue forceps for continual traction, which will cause less hand fatigue than the DeBakey forceps. One or more saline‐soaked gauze are placed caudal to the soft palate covering the endotracheal tube to prevent damage from the laser (Figure 7.9c). A sterile tongue depressor is also used just caudal to the soft palate during laser used as an additional barrier to protect the endotracheal tube from inadvertent damage (Figure 7.9d).
The laser is used to mark the planned region of the staphylectomy site starting at and preserving the medial aspect of the tonsillar crypt. A curved line is drawn toward the pterygoid process then back down toward the opposite tonsillar crypt (Figure 7.9d). The soft palate with the proposed staphylectomy line can then be evaluated and adjusted as needed prior to cutting. Once this line is deemed satisfactory, the laser is used to perform the staphylectomy, placing the laser beam as perpendicular as possible to the tissue to avoid splitting the palate in a cranial to caudal direction, until the excess soft palate is excised (Figure 7.10). The saline‐soaked gauze is removed to assess the soft palate length. The procedure can be repeated if additional tissue needs to be excised until the shortness of the palate is deemed satisfactory (Figure 7.11). The author only sutures the oral and nasal mucosal surfaces if the distance between the two is subjectively too wide (>4 mm). If closure is performed, the author typically places as few simple interrupted sutures as needed using of 4‐0 Monocryl (Figure 7.12; Video 7.4).
Cut‐and‐Sew Staphylectomy Technique
Folded Flap Palatoplasty Technique Using Monopolar Electrocautery – Surgical Technique
The ventral tip of the soft palate is grasped with DeBakey forceps, and a stay suture is placed. The tip of the soft palate is pulled rostrally until the caudal opening of the nasopharynx is visible. The ventral mucosa of the soft palate is marked with monopolar electrocautery where the ventral tip of the soft palate meets it. Two additional stay sutures are then placed on either side of the most ventral stay suture for manipulation of the soft palate during dissection (Figure 7.13a). The stay sutures are pulled rostrally to help facilitate the area of tissue to be removed and subsequent cautery marks are made on the ventral mucosa to correspond with these stay sutures. The cautery marks are connected to make a triangular or trapezoidal shape marking the area to be incised (Figure 7.13b). Caution is used to spare the tonsillar crypts, making the most lateral aspect of the incision 2–4 mm axial to either tonsillar crypt. The ventral mucosa and associated soft tissues of the soft palate (connective tissue, part of the palatinus and levator veli palatini muscles) are excised until the oropharyngeal mucosa is approached (Figure 7.13c). If the nasopharyngeal mucosa is entered, dissection cannot continue further caudally and any defect within the nasopharyngeal mucosa should be closed. Once the planned excision is complete, the stay sutures are advanced, and the palate’s free edges can be trimmed as deemed necessary prior to closure. The most distal stay suture on the free end of the soft palate is brought up to the most rostral aspect of the ventral mucosa and sutured (Figure 7.13d; Video 7.5). Each mucosal surface lateral to this is then apposed using interrupted sutures (Figure 7.13e).
Eversion of the Laryngeal Saccules
Laryngeal Sacculectomy – Surgical Technique
The author prefers the patient remain intubated for removal of the saccules, having an assistant displace the endotracheal tube dorsally using an instrument, finger, or tongue depressor. Alternatively, the patient can be extubated briefly or the endotracheal tube can be temporarily replaced with a feeding tube to allow oxygen insufflation.20 The saccule is grasped at the most distal aspect (toward the rima glottis) and retracted rostrally using caution so as not to cause any inadvertent damage to the vocal folds, which are immediately caudal and in close proximity. The saccule is excised using curved Metzenbaum scissors starting ventrally and advancing dorsally using small cutting motions, which helps avoid inadvertent damage to the vocal folds (Figure 7.15a–c; Video 7.6). If hemorrhage is noted, it is controlled by direct pressure using a sterile cotton‐tipped applicator.
Advanced Laryngeal Collapse
Grade II or III laryngeal collapse has been diagnosed commonly with percentages as high as 63.9%8,21,54 (Figure 7.16; Video 7.7). Postoperative BOAS indices in dogs with advanced laryngeal collapse are higher than in dogs with only everted saccules, further supporting earlier surgical intervention.8 Multilevel corrective BOAS surgery should always be considered as the first choice for treatment, as long‐term outcome in dogs with laryngeal collapse is considered good, although clinical signs rarely resolve.21 Treatment for more advanced laryngeal collapse should only be considered if clinical signs worsen after multilevel surgery for BOAS.
Tonsillectomy
Tonsillectomy – Surgical Technique
Temporary Tracheostomy
Temporary Tracheostomy – Surgical Technique
Tubeless Temporary Tracheostomy – Surgical Technique
Postoperative Outcome
Norwich Terriers
Cats
Modified Trader’s Technique in Cats – Surgical Technique

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