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   <subfield code="a">Insulin/glucose infusion successfully resuscitates bupivacaine-induced sudden-onset circulatory collapse in dogs</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Mi-Hyun Kim, Kook-Hyun Lee, Chong-Soo Kim, Solmon Yang, Teserendorj Uugangerel, Chong-Min Kim, Byeong-Chul Kang]</subfield>
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   <subfield code="a">Une perfusion d'insuline et glucose permet la réanimation réussie de chiens après un collapsus circulatoire subit induit par bupivacaïne</subfield>
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   <subfield code="a">Purpose: In previous studies, insulin reversed the cardiac toxicity gradually induced by a continuous infusion of bupivacaine. In this randomized controlled study, we intended to simulate a more relevant clinical situation by injecting bupivacaine rapidly as a bolus to induce sudden-onset circulatory collapse in dogs. We then evaluated the insulin effect. Methods: Bupivacaine (10mg·kg−1 iv) was rapidly administered intravenously to 12 dogs. At the onset of circulatory collapse (defined as a mean arterial pressure [MAP] of 30mmHg), external chest compression was initiated. Insulin (2U·kg−1 iv) was given to the insulin-glucose (IG) group (n=6) and the same volume of 0.9% saline was given to the control (C) group (n=6). The primary outcome was successful resuscitation defined as both MAP≥60mmHg and sinus rhythm on an electrocardiogram that lasted≥60sec. Hemodynamic and blood variables were measured, including cardiac output and electrocardiogram intervals. Results: All IG dogs were successfully resuscitated within 15 (3)min, whereas none of the control dogs were resuscitated (P=0.002). After circulatory collapse, the average MAP was higher in group IG than in group C (P=0.006). Conclusion: Insulin effectively reversed the sudden-onset circulatory collapse in dogs caused by an intravenous bolus injection of bupivacaine.</subfield>
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