Small Animal Surgical Emergencies. Группа авторов

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Small Animal Surgical Emergencies - Группа авторов

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rel="nofollow" href="#ulink_3c120444-565b-52ea-8b3e-4f7bd6251465">Figure 8.3) [41]. If these findings are present, then the impact of previous procedures (e.g., trocharization or orogastric intubation) should be taken into consideration, since these procedures may increase the number of false positive results.

Photo depicts right lateral abdominal radiograph showing gastric dilatation and volvulus. Photo depicts right lateral abdominal radiograph showing gastric dilatation and volvulus with gastric pneumatosis.

      Once GDV has been confirmed radiographically, gastric decompression should be attempted. Two methods commonly used are orogastric intubation and gastric trocharization. Orogastric intubation is the more common technique allowing for the removal of gas and fluid but can be more challenging to perform. Trocharization is a simple and rapid technique but allows relief of gaseous distension only. One study reported good success rates for both orogastric intubation (75.5% of dogs) and trocharization (86% of dogs), with no serious complications associated with either technique [42]. The techniques can be used concurrently and may be complimentary. The authors prefer to use trocharization.

Photo depicts (a) Once an area of tympany is identified, a 14- or 16-gauge over-the-needle catheter is placed percutaneously into the stomach. (b) An extension set has been placed into water to evaluate for bubbles to determine when the flow of gas has stopped. Photo depicts measuring stomach tube prior to orogastric intubation. Photo depicts bandage roll placed in dog's mouth as a gag and to facilitate passage of stomach tube, which is inserted through the hole in the center of the bandage.

      Some authors have suggested a role for management of ischemia–reperfusion injury to prevent subsequent complications [10, 25, 26]. Suggested interventions have included desferoxamine, dimethyl sulphoxide and allopurinol. All have been evaluated in experimental GDV, although none have been evaluated clinically [24, 26]. Lidocaine, however, has been evaluated retrospectively and prospectively as part of the management of GDV in dogs [10, 25]. Retrospective evaluation failed to show a survival benefit associated with lidocaine, but use was uncontrolled, and it is likely that lidocaine use was biased toward more seriously affected dogs [10]. In a prospective study, GDV dogs were treated with lidocaine and a historical population of dogs with GDV was used as a retrospective control [25]. Dogs received an intravenous bolus of lidocaine (2 mg/kg) immediately on presentation, followed by a lidocaine constant rate infusion (50 μg/kg/min) given over 24 hours. A reduced rate of arrhythmias and acute kidney injury, and shorter hospitalization time were reported with lidocaine therapy. Although it is unclear if other factors played a role in the decreased complication rate, the administration of lidocaine may be warranted in the management of GDV.

      While surgical intervention is considered mandatory for management of GDV, medical management of the condition, consisting of orogastric intubation, trocarization if necessary and treatment for shock, has been evaluated [44, 45]. A high mortality (66%) [44] and recurrence rate of 71–76% has been reported [44, 45]. The authors do not recommend medical management alone for the treatment of GDV.

      Anesthesia using a cardiovascular sparing protocol is recommended. Dogs should be preoxygenated. Premedication with a pure mu‐agonist opioid is useful if not already given. Fentanyl (2–5 ug/kg) is short acting, has a fast onset and can be used immediately prior to induction to reduce the dose of induction agent required. The

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