Abstract: Background - BOAS Syndrome has no drug treatment option. Hypothesis/Objective - evaluate neuromuscular stimulant tetanus-toxin plus antibody-trapping decoy (Snoretox-1) in BOAS Syndrome. Animals - 14 BOAS Grade 2 or 3 dogs at home. Methods - injection bilaterally whilst under sedation into the centre of the rostral geniohyoid. 4 British Bulldogs received placebo then 50 Units/kg, 6 British Bulldogs received placebo then 25 Units/kg, and 6 Dogs (2 British, 2 French and 2 Pugs) 12.5 Units/kg without placebo. Dogs were graded utilizing the RFG scale, after a three-minute trot test, at multi-week intervals, until any improvement returned to baseline values. Results - All dogs at the 50 Units/kg and 25 Units/kg improved by at least one BOAS grade on the RFG scale. At 12.5 Units/kg some dogs had responses whilsts others did not. Non-parametric statistical analysis of the 50 and 25 units/kg dogs (Friedman χ² with Durbin-Conover post-hoc tests) showed that BOAS severity grade recorded after Snoretox-1 were significantly lower than after placebo at 12 weeks (p <.001), with return to baseline taking between 20 to 52 weeks. Feeding difficulty for up to 5 ½ weeks may occur with incorrect placement outside the rostral geniohyoid. Conclusions - Geniohyoid injection of the Snoretox-1 muscle toning therapeutic at 50 and 25 Units/kg decreased the severity of BOAS grading in BOAS dogs by one grade or more for a period of between 20 weeks and 52 weeks. Clinical Relevance - Snoretox-1 could offer a less invasive, well tolerated and effective treatment for BOAS.
Learning Objectives:
Upon completion, participant will be able to understand a new potential BOAS Syndrome therapeutic namely the Snoretox neuromuscular stimulant geniohyoid injection.
Upon completion, participant will be able to understand BOAS Syndrome and it's major complications.
Upon completion, participant will be able to understand current published data of potential mortality and major complication rate of surgery for BOAS syndrome.
Upon completion, participant will be able to understand how the new therapeutic is administered via direct injection into the geniohyoid under light sedation