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Da-Cheng-Qi Decoction Combined with Conventional Treatment for Treating Postsurgical Gastrointestinal Dysfunction

机译:大成齐汤与常规治疗合并治疗后期胃肠功能障碍

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摘要

Aim. To assess the current clinical evidence of the effectiveness of Da-Cheng-Qi Decoction (DCQD) for the treatment of Postoperative gastrointestinal dysfunction (PGD). Methods. Randomized controlled trails (RCTs) of Da-Cheng-Qi Decoction (DCQD) to PGD were searched from available major electronic databases to September 2016. The intervention must be a modified DCQD or DCQD integrated to Western Medicine (WM) compared with WM or placebo or blank. The main outcome index was clinical effectiveness and improvement of major symptoms. Data extraction, data analysis, and methodological quality assessment are conducted according to the Cochrane Handbook for Systematic Review of Interventions, version 5.0.2. RevMan 5.3 software was applied to our data analyses. Results. Seven RCTs involving 494 participants were recruited and identified. The methodological quality of all trials were assessed and generally of low-level. Those studies were published between 2004 and 2013. All 7 studies which used herbals (modified DCQD) integrate WM in test group compared with WM as the intervention and only one study (Sunyouxu 2013) integrates placebo to Western Medicine as the control group intervention. The treatment course was 1 week to 2 weeks. Evaluation of intervention effectiveness consists of the clinical effective rate indicator and the PGD symptoms indicator including time of borborygmus, time of gastrointestinal exhaust, and time of defecate. The clinical effectiveness results are beneficial to the test group. Conclusion. DCQD could improve PGD symptoms and promotion clinical effectiveness.
机译:目的。评估目前大峰汤汤(DCQD)治疗术后胃肠功能障碍(PGD)的临床证据。方法。从可用的主要电子数据库中搜索了Da-Cheng-Qi汤(DCQD)的随机控制路径(RCT)到2016年9月。与WM或安慰剂相比,干预必须是综合到西药(WM)的改进的DCQD或DCQD或空白。主要结果指数是主要症状的临床效果和改善。数据提取,数据分析和方法质量评估是根据Cochrane手册进行的,用于系统审查的干预措施,版本5.0.2。 Revman 5.3软件应用于我们的数据分析。结果。招募并确定了涉及494名参与者的七个RCT。所有试验的方法论质量评估,通常是低水平的。这些研究结果发表2004年和2013年所有的7项研究,其使用的草药之间(修改大承气汤)与WM的介入,只有一项研究(Sunyouxu 2013)集成安慰剂西药作为对照组相比,干预试验组集成WM。治疗课程为1周至2周。干预效果的评估包括临床有效率指示剂和PGD症状指标,包括Borborygmus的时间,胃肠道排气的时间和排序的时间。临床效果结果对测试组有益。结论。 DCQD可以提高PGD症状和促进临床效果。

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