改良外科医生辅助双侧腹横面阻滞对腰麻剖宫产术后首次镇痛时间的影响:随机安慰剂对照

A. Mamdouh
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引用次数: 1

摘要

背景:腹横肌平面阻滞(TAP阻滞)是剖宫产术中广泛应用的区域性镇痛技术之一。程序有不同的变体。本研究的目的是评估改良的外科医生辅助双侧TAP阻滞对剖宫产患者的镇痛效果。患者和方法:60名在脊麻下剖宫产的患者被随机分为两组,接受TAP阻滞,40ml 0.25%布比卡因(研究组)或40ml生理盐水作为安慰剂知情同意。所有患者将在术后每12小时静脉注射一次双氯芬酸75mg。术后,在最初的24小时内,每2小时通过视觉模拟疼痛量表(VAPS)进行一次评估。首次请求镇痛的时间将作为主要结果,所有患者将按需接受阿片类药物或VAPS>4,肌肉注射25mg哌替啶。此外,24小时内的总阿片类药物需求量将作为次要结果,以及术后并发症,如恶心、呕吐和腹胀。还将评估与TAP程序相关的并发症。结果:与研究组相比,安慰剂组在术后前24小时内首次提出镇痛要求的中位(四分位间距)时间明显更短;4h(4,6)和24h(10,24),p值均<0.001。对照组术后阿片类药物需求量(30/30{100%})显著高于研究组(13/30{43.3%})。安慰剂组阿片类剂量的中位数(四分位数间距)显著高于试验组;分别为2(2,2)和0(0,1)。在研究的所有方面,研究组的疼痛评分都较低(p<0.0001)。试验注册:Clinicaltrial.gov注册号:NCT04623632
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Effect of the Modified Surgeon Assisted Bilateral Transversus Abdominis Plane Block on Time Required for First Analgesic Dose after Cesarean Section under Spinal Anesthesia: Randomized placebo-control
Background: The transverses abdominis plane block (TAP block) is one of the widely used regional analgesic techniques in cesarean section. There are different variations of the procedure. The aim of the present study was to evaluate the analgesic effect of the modified surgeon assisted bilateral TAP block in patients undergoing cesarean section Patients&Methods: Sixty patients undergoing cesarean section under spinal anesthesia were randomized into two groups to receive either TAP block with 40 ml of bupivacaine 0.25%(study group) or 40 ml normal saline as placebo after obtaining informed consent. All patients will receive intravenous diclofencac75mg every 12 hrs postoperatively. Postoperatively, there was an assessment every 2hrs during the first 24hrs by the visual analogue pain scale (VAPS). Time to the first analgesic request will be measured as primary outcome and all patients will receive opioid on demand or VAPS > 4 with 25mg pethidine intramuscularly. Moreover, total opioid requirement in 24hrs will be measured as secondary outcome along with postoperative complications as nausea, vomiting and abdominal distention. Complications related to the TAP procedure will be also assessed. Results: The median (interquartile range) time to the first analgesic request in the first 24hrs postoperatively was significantly shorter in the placebo group compared to the study group; 4h (4, 6) and 24h (10, 24) with p value < 0.001. Postoperative opioid requirement was significantly higher in the control group (30/30{100%}) than the study group (13/30{43.3%}). The median (interquartile range) number of opioid doses was significantly higher in the placebo group compared with the study group; 2(2, 2) and 0(0, 1) respectively. At all points in the study, pain scores both were lower in the study group (p < 0.0001). Conclusion: The modified surgeon assisted bilateral TAP block is relatively new, safe and cost effective technique which provides adequate postoperative analgesia allowing for better maternal ambulation and better postoperative recovery. Trial registration: Clinicaltrial.gov registration number: NCT04623632
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