Transversus abdominis plane block as a component of anesthesia in kidney transplantation

A. Shabunin, E. P. Rodionov, P. Drozdov, A. A. Malyshev, B. A. Smolev, A.  A. Efanov, S.  A. Fedorishchev, R. I. Malashenko, S. А. Astapovich, E. A. Lidzhieva
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Abstract

Aim. To evaluate the safety and efficacy of the transversus abdominis plane block in kidney transplantation from deceased donor.Material and methods. The first stage included a retrospective comparative analysis of the results using the transversus abdominis plane block in renal transplantation. Group I (n=30) included patients who underwent transversus abdominis plane block after kidney transplantation; in comparative group II (n=58) the TAP-block wasn’t performed. We assessed the daily requirement for trimeperidine on the first day after kidney transplantation. The second stage was a prospective randomized placebo-controlled study. The patients were randomly divided into 2 groups with respect to whether the transversus abdominis plane block was provided with an active drug, or placebo was used; so the sodium chloride 0.9% was injected into the transversus abdominis plane in the intermuscular fascial plane between the internal oblique and transversus abdominis muscle in patients of Group III (n=31), and a local anesthetic was injected in patients of Group IV (n=34).) The daily requirements for trimeperidine, tramadol were assessed as well as the pain severity according to visual analogue scale at 1, 6, 12, 24 hours after surgery, the incidence of adverse events in the gastrointestinal tract; and several laboratory parameters (cortisol, interleukin-1, interleukin-6) related to pain syndrome were analyzed.Results. As a result of pseudorandomization, 17 cases were included in each of two retrospective stage, which were comparable in terms of patients' main characteristics (p>0.05). The daily requirement for trimeperidine in the transversus abdominis plane block group (Group I) was lower than in the comparison group with a trend toward statistical significance (p=0.07). The median daily dose of trimeperidine in Group III (placebo control) was 59.5 mg (interquartile range: 51.5–72.0), which was higher than in Group IV (45.5 mg; interquartile range: 38.5–62.0) (p=0.039). The postoperative pain severety assessed by visual analogue scale was also statistically significantly higher in group III at the timepoint of 12 hours after surgery, making 4.0 points (interquartile range: 2.5–5.0) versus 1.5 points (interquartile range: 0.5–2.5) in group VI (p=0.015). There were no differences between the groups in pain severity at 1, 6, and 24 hours after surgery. The daily requirement for tramadol was also statistically significantly higher in Group III, amounting to 50 mg (interquartile range: 0–100) versus 0 (interquartile range: 0–55 mg) in the active drug Group IV (p=0.045).Conclusion. Our study showed that the use of the transversus abdominis plain block was safe and effective, yielding encouraging results, which demonstrated a clinically significant reduction in the need for opioid analgesics and in the incidence of adverse events in the postoperative period after transversus abdominis plane block which contributes to the early activation of patients. Therefore, further studies are needed to improve the package of multimodal perioperative analgesia after kidney transplantation.
腹横肌平面阻滞作为肾移植手术麻醉的一部分
目的评估腹横肌平面阻滞在死亡供体肾移植中的安全性和有效性。第一阶段包括对肾移植中使用腹横肌平面阻滞的结果进行回顾性比较分析。第一组(30 人)包括肾移植后接受腹横肌平面阻滞的患者;第二组(58 人)未进行腹横肌平面阻滞。我们评估了肾移植术后第一天的曲美哌啶日需求量。第二阶段是一项前瞻性随机安慰剂对照研究。根据腹横肌平面阻滞是使用活性药物还是安慰剂,将患者随机分为两组;因此,第三组患者(31 人)在腹内斜肌和腹横肌之间的肌筋膜间腹横肌平面注射 0.9% 氯化钠,第四组患者(34 人)注射局麻药。)术后1、6、12、24小时,根据视觉模拟量表评估了曲美匹定和曲马多的每日需求量、疼痛严重程度、胃肠道不良反应发生率,并分析了与疼痛综合征相关的几项实验室指标(皮质醇、白细胞介素-1、白细胞介素-6)。由于采用了假随机方法,两个回顾性阶段各纳入了 17 例患者,患者的主要特征具有可比性(P>0.05)。腹横肌平面阻滞组(I组)的曲美哌啶日需求量低于对比组,且有统计学意义(P=0.07)。第三组(安慰剂对照组)曲美哌啶的日剂量中位数为 59.5 毫克(四分位距:51.5-72.0),高于第四组(45.5 毫克;四分位距:38.5-62.0)(P=0.039)。根据视觉模拟量表评估的术后疼痛严重程度,第三组在术后 12 小时的时间点也明显高于第六组,第三组为 4.0 分(四分位间范围:2.5-5.0),而第六组为 1.5 分(四分位间范围:0.5-2.5)(P=0.015)。两组在术后 1、6 和 24 小时的疼痛严重程度没有差异。据统计,第三组的曲马多每日需求量也明显较高,达到 50 毫克(四分位数间距:0-100),而第四组的活性药物需求量为 0(四分位数间距:0-55 毫克)(P=0.045)。我们的研究表明,使用腹横肌平面阻滞是安全有效的,取得了令人鼓舞的结果,表明腹横肌平面阻滞术后阿片类镇痛药的需求量和不良事件的发生率均有显著的临床减少,这有助于患者的早期激活。因此,还需要进一步研究,以改进肾移植术后围术期多模式镇痛的一揽子方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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