He Kun, Wang Yabing, Li Jianing, Bai Xiaoyin, Yang Zihan, Han Xianlin, Wu Dong
Department of Gastroenterology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Endocrinology, Beijing Friendship Hospital, Capital Medical College, Beijing, China.
Front Pharmacol. 2023 Feb 28;14:1131974. doi: 10.3389/fphar.2023.1131974. eCollection 2023.
The therapeutic value of neostigmine as a prokinetic drug in acute pancreatitis (AP), especially in non-mild AP, including moderately severe and severe AP remains controversial. This meta-analysis aimed to investigate the efficacy of neostigmine treatment in patients with non-mild AP. We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, China National Knowledge Infrastructure (CNKI), and Wanfang databases up to 24 December 2022 for RCTs comparing neostigmine plus conventional treatment versus the conventional treatment alone in patients with non-mild AP. Trial sequential analyses (TSA) were used to assess the risk of random errors and the results. Six RCTs with 318 participants were included. Compared with conventional treatment, patients who received neostigmine plus conventional treatment had a shorter time duration for their first defecation (MD: -1.74; 95% CI: -2.10 to -1.38; < 0.00001; = 205; RCTs = 4; low quality of evidence) and better relief time of abdominal symptoms (MD: -1.59, 95% CI: -2.07 to -1.11; < 0.00001; = 155; RCTs = 3; low quality of evidence) as primary outcomes, and a faster percentage decrease of IAP at 24 h ( = 0.0005; moderate quality of evidence) and a shorter length of ICU stay ( < 0.00001; moderate quality of evidence) as partial secondary outcomes. TSA suggested the sample size was limited, but the cumulative Z curves of the primary outcomes crossed the conventional boundary and the trial sequential monitoring boundary. For patients with non-mild AP, neostigmine promotes the recovery of gastrointestinal motility and may have positive effects on the improvement of a clinical prognosis. Further large-sample studies are needed for a definite conclusion. https://www.crd.york.ac.uk/prospero/; Identifier: CRD 42022381417.
新斯的明作为促动力药物在急性胰腺炎(AP),尤其是非轻度AP(包括中度重症和重症AP)中的治疗价值仍存在争议。本荟萃分析旨在研究新斯的明治疗非轻度AP患者的疗效。我们检索了截至2022年12月24日的Cochrane对照试验中央注册库(CENTRAL)、MEDLINE、Embase、中国知网(CNKI)和万方数据库,以查找比较新斯的明联合传统治疗与单纯传统治疗在非轻度AP患者中的随机对照试验(RCT)。采用试验序贯分析(TSA)评估随机误差风险和结果。纳入了6项RCT,共318名参与者。与传统治疗相比,接受新斯的明联合传统治疗的患者首次排便时间更短(MD:-1.74;95%CI:-2.10至-1.38;<0.00001;I²=205;RCTs=4;低质量证据),腹部症状缓解时间更好(MD:-1.59,95%CI:-2.07至-1.11;<0.00001;I²=155;RCTs=3;低质量证据)作为主要结局,24小时时腹内压(IAP)下降百分比更快(P=0.0005;中等质量证据)和ICU住院时间更短(<0.00001;中等质量证据)作为部分次要结局。TSA表明样本量有限,但主要结局的累积Z曲线越过了传统边界和试验序贯监测边界。对于非轻度AP患者,新斯的明可促进胃肠动力恢复,可能对改善临床预后有积极作用。需要进一步的大样本研究得出明确结论。https://www.crd.york.ac.uk/prospero/;标识符:CRD 42022381417。