Tae Chung Hyun, Kang Ki Joo, Min Byung-Hoon, Ahn Joong Hyun, Kim Seonwoo, Lee Jun Haeng, Rhee Poong-Lyul, Kim Jae J
Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Dig Liver Dis. 2014 Aug;46(8):710-5. doi: 10.1016/j.dld.2014.04.007. Epub 2014 Jun 2.
The incidence, risk factors and management strategy of paradoxical reaction to midazolam during endoscopy are yet to be clarified.
This single center prospective study included 4140 adult patients (2263 males, mean age of 57.7 ± 12.6) undergoing endoscopy under sedation with midazolam and pethidine between September 2011 and December 2011. The characteristics of patients with and without paradoxical reaction were compared. For patients who experienced paradoxical reaction and received flumazenil, their endoscopic images were reviewed to assess whether European Society of Gastrointestinal Endoscopy guidelines were met as quality indicator of endoscopy.
The incidence of paradoxical reaction was 1.4%. In multivariate analyses, male gender, unsuccessful sedation in previous endoscopy, upper endoscopy, higher dose of midazolam, and lower dose of pethidine were identified as independent risk factors for paradoxical reaction. Despite paradoxical reaction, endoscopic procedures were successfully completed in 93.3% of cases when flumazenil was administered. The rates of meeting quality indicator of endoscopy were 92.3% in patients receiving flumazenil for paradoxical reaction and 97.6% in patients without paradoxical reaction.
For patients with risk factors for paradoxical reaction, active use of pethidine with a dose reduction of midazolam might be helpful to prevent the occurrence of paradoxical reaction. Administration of flumazenil might be positively considered in cases of paradoxical reaction.
在内镜检查期间咪达唑仑反常反应的发生率、危险因素及管理策略尚待阐明。
这项单中心前瞻性研究纳入了2011年9月至2011年12月期间接受咪达唑仑和哌替啶镇静下内镜检查的4140例成年患者(2263例男性,平均年龄57.7±12.6岁)。比较了发生和未发生反常反应患者的特征。对于发生反常反应并接受氟马西尼治疗的患者,复查其内镜图像以评估是否符合欧洲胃肠内镜学会指南作为内镜检查质量指标。
反常反应的发生率为1.4%。多因素分析显示,男性、既往内镜检查镇静不成功、上消化道内镜检查、咪达唑仑剂量较高及哌替啶剂量较低被确定为反常反应的独立危险因素。尽管发生了反常反应,但在给予氟马西尼的情况下,93.3%的病例内镜检查仍成功完成。发生反常反应接受氟马西尼治疗的患者内镜检查质量指标符合率为92.3%,未发生反常反应的患者为97.6%。
对于有反常反应危险因素的患者,积极使用哌替啶并减少咪达唑仑剂量可能有助于预防反常反应的发生。在发生反常反应的情况下可积极考虑给予氟马西尼。