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麻杏石甘汤治疗社区获得性肺炎的有效性和安全性:一项随机对照试验的系统评价和荟萃分析

Effectiveness and safety of Maxing Shigan Decoction for community-acquired pneumonia: a systematic review and meta-analysis of randomized controlled trials.

作者信息

Ling Yutong, Liu Xuehan, Zhang Bingrui, Xiao Qionghua, Shuai Zhihao, Bai Han, Cai Rui, Li Shuangsang, Yuan Mingyi, Zhang Yanxia

机构信息

Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.

Center for Evidence-Based Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Med (Lausanne). 2025 Aug 29;12:1639027. doi: 10.3389/fmed.2025.1639027. eCollection 2025.

Abstract

BACKGROUND AND OBJECTIVE

Community-acquired pneumonia (CAP) is an acute lung infection disease with high morbidity and mortality. The treatment of CAP has become more and more challenging due to the gradual increase of antibiotic resistance and adverse events. Relevant evidence indicates that Maxing Shigan Decoction (MXSG) may play a unique therapeutic advantage. Our aim is to evaluate the overall effectiveness and safety of MXSG for CAP.

METHODS

Eight databases (PubMed, Embase, the Cochrane Library, CNKI, Wanfang, VIP, Yiigle, and Sinomed) were searched from their inception to January 20, 2025. Randomized controlled trials evaluating the effectiveness and safety of MXSG alone or in combination with conventional western medicine (WM) for CAP were included. We conducted meta-analysis by RevMan 5.4 software or just performed qualitative analysis.

RESULTS

We included 81 RCTs with 6682 participants in total. Compared with western medicine (WM) alone, MXSG plus WM showed a more beneficial effect on reducing the duration of fever (MD = -1.58 days, 95% CI: -1.88 to -1.29, < 0.00001), cough (MD = -2.30 days, 95% CI: -2.61 to -1.99, < 0.00001), phlegm (MD = -2.40 days, 95% CI: -2.56 to -2.23, < 0.00001), dyspnea (MD = -2.11 days, 95% CI: -2.73 to -1.49, < 0.00001), pulmonary crepitation (MD = -2.13 days, 95% CI: -2.47 to -1.79, < 0.00001) and length of hospitalization (MD = -1.38 days, 95% CI: -2.54 to -0.23, = 0.02). Furthermore, MXSG plus WM was significantly superior to WM in promoting the absorption of lung inflammation (MD = -3.31 days, 95% CI: -4.17 to -2.46, < 0.00001) and improving forced expiratory volume in the first second (MD = 0.54 L, 95% CI: 0.21 to 0.87, = 0.001). The incidence of adverse events was 3.60% in MXSG plus WM group and 5.38% in WM group, but the difference was not significant ( = 0.06).

CONCLUSION

Moderate or low certainty of evidence suggested that compared with WM alone, MXSG combined with WM may have potential effectiveness on relieving the clinical symptoms, promoting the absorption of lung inflammation, improving lung function, and reducing hospitalization length with a good safety for patients with CAP. In the future, high-quality double-blind RCTs should be required to confirm the effectiveness and safety on CAP.

SYSTEMATIC REVIEW REGISTRATION

https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42023404693, identifier CRD42023404693.

摘要

背景与目的

社区获得性肺炎(CAP)是一种发病率和死亡率较高的急性肺部感染性疾病。由于抗生素耐药性和不良事件的逐渐增加,CAP的治疗变得越来越具有挑战性。相关证据表明,麻杏石甘汤(MXSG)可能发挥独特的治疗优势。我们的目的是评估MXSG治疗CAP的总体有效性和安全性。

方法

检索了8个数据库(PubMed、Embase、Cochrane图书馆、CNKI、万方、维普、医脉通和中国生物医学文献数据库)自建库至2025年1月20日的文献。纳入评估MXSG单独或联合西医常规治疗CAP有效性和安全性的随机对照试验。我们使用RevMan 5.4软件进行荟萃分析,或仅进行定性分析。

结果

共纳入81项随机对照试验,总计6682名参与者。与单纯西医治疗相比,MXSG联合西医治疗在缩短发热持续时间(MD=-1.58天,95%CI:-1.88至-1.29,P<0.00001)、咳嗽持续时间(MD=-2.30天,95%CI:-2.61至-1.99,P<0.00001)、咳痰持续时间(MD=-2.40天,95%CI:-2.56至-2.23,P<0.00001)、呼吸困难持续时间(MD=-2.11天,95%CI:-2.73至-1.49,P<0.00001)、肺部啰音持续时间(MD=-2.13天,95%CI:-2.47至-1.79,P<0.00001)和住院时间(MD=-1.38天,95%CI:-2.54至-0.23,P=0.02)方面显示出更有益的效果。此外,MXSG联合西医治疗在促进肺部炎症吸收(MD=-3.31天,95%CI:-4.17至-2.46,P<0.00001)和改善第1秒用力呼气量(MD=0.54L,95%CI:0.21至0.87,P=0.001)方面明显优于西医治疗。MXSG联合西医治疗组不良事件发生率为3.60%,西医治疗组为5.38%,但差异无统计学意义(P=0.06)。

结论

证据的确定性为中等或低等,表明与单纯西医治疗相比,MXSG联合西医治疗可能对缓解CAP患者的临床症状、促进肺部炎症吸收、改善肺功能和缩短住院时间具有潜在有效性,且安全性良好。未来,需要高质量的双盲随机对照试验来证实其对CAP的有效性和安全性。

系统评价注册

https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42023404693,标识符CRD42023404693。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baad/12425732/1fc24f2b87cb/fmed-12-1639027-g001.jpg

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