실험연구 : 토끼에서 Midazolam 과 Droperidol 이 Bupivacaine 의 심독성에 미치는 효과

Background : Unintended intravenous injection of bupivacaine causes severe cardiovascular compli- cation, which is known for its difficulty in resuscitation. This study was performed to evaluate the effects of pretreatment with midazolam and droperidol in the cardiac toxicity caused by inlravenous i...

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Veröffentlicht in:Korean journal of anesthesiology 2000-03, Vol.38 (3), p.503
Hauptverfasser: 강유진, Yoo Jin Kang, 김대우, Dae Woo Kim, 임용걸, Yong Gul Lim, 인장혁, Jang Hyeok In, 김용신, Yong Sin Kim, 양소영, So Young Yang
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container_issue 3
container_start_page 503
container_title Korean journal of anesthesiology
container_volume 38
creator 강유진
Yoo Jin Kang
김대우
Dae Woo Kim
임용걸
Yong Gul Lim
인장혁
Jang Hyeok In
김용신
Yong Sin Kim
양소영
So Young Yang
description Background : Unintended intravenous injection of bupivacaine causes severe cardiovascular compli- cation, which is known for its difficulty in resuscitation. This study was performed to evaluate the effects of pretreatment with midazolam and droperidol in the cardiac toxicity caused by inlravenous infusion of bupivacaine. Methods : Thirty rabbits were divided into three groups; saline- as a control, midazolam, and dro- peridol pretreated group. We observed the time intervals for the arrhythmia, 25% and 50% reduction in baseline mean arterial blood pressure, and arrest. We also checked the dose of infused bupivacaine to be required for arrest during continuous intravenous infusion of bupivacaine at the rate of I mg/kg/min. Results : The onset of dysrhythmia and the time to 50% reduction in baseline mean arterial blood pressure and arrest were significantly more delayed in the midazolam group than the control group (P < 0.05). With respect to the time to 25%, 50% reduction in baseline mean mterial blood pressure and arrest, the data of the droperidol group was significantly shorter than that of the control group (P < 0.05). Conclusions : Droperidol pretreatment hastened bupivacaine induced cardiac arrest in rabbits. Mida- zolam pretreatment exerted protective effects on arrhythmia and cardiac arrest. Thus midazolam would be a preferable agent as a supplement for regional anesthesia using bupivacaine. (Korean J Anesthesiol 2000; 38: 503~508)
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This study was performed to evaluate the effects of pretreatment with midazolam and droperidol in the cardiac toxicity caused by inlravenous infusion of bupivacaine. Methods : Thirty rabbits were divided into three groups; saline- as a control, midazolam, and dro- peridol pretreated group. We observed the time intervals for the arrhythmia, 25% and 50% reduction in baseline mean arterial blood pressure, and arrest. We also checked the dose of infused bupivacaine to be required for arrest during continuous intravenous infusion of bupivacaine at the rate of I mg/kg/min. Results : The onset of dysrhythmia and the time to 50% reduction in baseline mean arterial blood pressure and arrest were significantly more delayed in the midazolam group than the control group (P &lt; 0.05). With respect to the time to 25%, 50% reduction in baseline mean mterial blood pressure and arrest, the data of the droperidol group was significantly shorter than that of the control group (P &lt; 0.05). Conclusions : Droperidol pretreatment hastened bupivacaine induced cardiac arrest in rabbits. Mida- zolam pretreatment exerted protective effects on arrhythmia and cardiac arrest. Thus midazolam would be a preferable agent as a supplement for regional anesthesia using bupivacaine. (Korean J Anesthesiol 2000; 38: 503~508)</description><identifier>ISSN: 2005-6419</identifier><language>kor</language><publisher>대한마취통증의학회</publisher><subject>Anesthetics ; bupivacaine ; droperidol. 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This study was performed to evaluate the effects of pretreatment with midazolam and droperidol in the cardiac toxicity caused by inlravenous infusion of bupivacaine. Methods : Thirty rabbits were divided into three groups; saline- as a control, midazolam, and dro- peridol pretreated group. We observed the time intervals for the arrhythmia, 25% and 50% reduction in baseline mean arterial blood pressure, and arrest. We also checked the dose of infused bupivacaine to be required for arrest during continuous intravenous infusion of bupivacaine at the rate of I mg/kg/min. Results : The onset of dysrhythmia and the time to 50% reduction in baseline mean arterial blood pressure and arrest were significantly more delayed in the midazolam group than the control group (P &lt; 0.05). With respect to the time to 25%, 50% reduction in baseline mean mterial blood pressure and arrest, the data of the droperidol group was significantly shorter than that of the control group (P &lt; 0.05). Conclusions : Droperidol pretreatment hastened bupivacaine induced cardiac arrest in rabbits. Mida- zolam pretreatment exerted protective effects on arrhythmia and cardiac arrest. Thus midazolam would be a preferable agent as a supplement for regional anesthesia using bupivacaine. (Korean J Anesthesiol 2000; 38: 503~508)</description><subject>Anesthetics</subject><subject>bupivacaine</subject><subject>droperidol. 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subjects Anesthetics
bupivacaine
droperidol. Anesthetics
intravenous
local
midazolam
title 실험연구 : 토끼에서 Midazolam 과 Droperidol 이 Bupivacaine 의 심독성에 미치는 효과
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