Effects of a single dose of rocuronium in patients with different body fat percentages: A randomised controlled trial

IF 2.9 4区 医学 Q2 Medicine Clinical and Experimental Pharmacology and Physiology Pub Date : 2024-01-09 DOI:10.1111/1440-1681.13836
Guanghui An, Yan Qiu, Zheliang Zhou, Xueying Ding, Cheng Li
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Abstract

The pharmacodynamics in patients with high body fat percentage might be similar to those in obese patients. This randomised controlled clinical trial observed the effects of rocuronium in patients with different percent body fats (PBFs). Fifty-four patients who underwent elective urological or pelvic surgery under general anaesthesia at Shanghai General Hospital were included in the present study; 51 patients were included for data analysis. Patients with normal PBF (<25%) were given a single dose of rocuronium calculated based on total body weight (N-TBW, control group). Patients with a higher PBF (≥25%) were given a single dose of rocuronium calculated based on total body weight (H-TBW). Patients with higher PBF and rocuronium were dosed based on fat-free mass (H-FFM). A train of four (TOF)-Watch acceleromyography monitor was used to measure the effects of the rocuronium. H-TBW (91.9 ± 28.8 s) had significantly shorter onset time than N-TBW and H-FFM (p = 0.003). H-TBW had significantly longer clinical duration time and pharmacological duration time than the other groups (p = 0.000 and 0.000, respectively); the TOF ratio0.25–0.9 time was significantly different among the three groups (p = 0.005). There were no significant differences in the recovery time (p = 0.103) or recovery index (p = 0.159) among the three groups. The effects of rocuronium dosed based on FFM in patients with high PBFs are similar to those in normal patients. A single dose of rocuronium calculated based on TBW might shorten the onset time, prolong the clinical and pharmacological duration times, and prolong the recovery time.

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单剂量罗库溴铵对不同体脂百分比患者的影响:随机对照试验
高体脂百分比患者的药效学可能与肥胖患者相似。本随机对照临床试验观察了罗库溴铵在不同体脂百分比(PBF)患者中的作用。本研究共纳入了 54 名在上海总医院全身麻醉下接受择期泌尿外科或盆腔手术的患者,其中 51 名患者接受了数据分析。PBF正常(<25%)的患者按总重量(N-TBW,对照组)计算给予单剂量的罗库溴铵。对 PBF 较高(≥25%)的患者按总重量(H-TBW)计算给予单剂量罗库溴铵。PBF 和罗库溴铵较高的患者则根据去脂体重(H-FFM)计算剂量。使用四组(TOF)-Watch 加速造影监视器来测量罗库溴铵的效果。H-TBW(91.9 ± 28.8 秒)的起始时间明显短于 N-TBW 和 H-FFM(p = 0.003)。H-TBW 的临床持续时间和药理持续时间明显长于其他组(分别为 p = 0.000 和 0.000);三组的 TOF ratio0.25-0.9 时间明显不同(p = 0.005)。三组恢复时间(p = 0.103)和恢复指数(p = 0.159)无明显差异。在高 PBFs 患者中,根据 FFM 给药的罗库溴铵效果与正常患者相似。根据 TBW 计算的单剂量罗库隆铵可能会缩短起始时间,延长临床和药理学持续时间,并延长恢复时间。
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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
128
审稿时长
6 months
期刊介绍: Clinical and Experimental Pharmacology and Physiology is an international journal founded in 1974 by Mike Rand, Austin Doyle, John Coghlan and Paul Korner. Our focus is new frontiers in physiology and pharmacology, emphasizing the translation of basic research to clinical practice. We publish original articles, invited reviews and our exciting, cutting-edge Frontiers-in-Research series’.
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