Skip to main content
Log in

Effectiveness and Safety of Chinese Medicine for Idiopathic Pulmonary Fibrosis: A Systematic Review and Meta-Analysis

  • Evidence-Based Integrative Medicine
  • Published:
Chinese Journal of Integrative Medicine Aims and scope Submit manuscript

Abstract

Objective

To evaluate the effectiveness and safety of Chinese medicine (CM) for Idiopathic pulmonary fibrosis (IPF) patients.

Methods

To screened relevant articles, PubMed, Cochrane Library, Excerpta Medica Datase (EMBASE), China National Knowledge Infrastructure (CNKI), Chinese VIP Information (VIP), Wanfang Database and Chinese Biomedical Database (CBM) were searched in English or Chinese until December 2015 for randomized controlled trials, which compared CM treatment (CM group) with Western medicine or placebo (control group) on IPF. The outcome measures included acute exacerbation, pulmonary function, the St George's respiratory questionnaire (SGRQ) scores, 6-minute walk test (6MWT) distance, adverse events and mortality.

Results

This meta-analysis included 25 randomized controlled trials involving 1,471 patients. Compared with the control group, CM group was superiori in reducing the risk of exacerbation [relative risk (RR)=0.40, 95% CI 0.22 to 0.72, P<0.05], improving in forced expiratory volume in one second (FEV1) [standard mean difference (SMD)=0.62, 95% CI 0.40 to 0.84, P<0.01] and diffusion capacity for carbon monoxide (DLCO, SMD=0.40, 95% CI 0.22 to 0.58, P<0.01), but there was no significant difference in vital capacity (VC, SMD=0.10, 95% CI–0.12 to 0.31, P>0.05). This meta-analysis also revealed that CM therapy significantly decreased the SGRQ score (SMD=–0.60, 95% CI–1.14 to–0.05, P<0.05) and improved 6MWT distance (SMD=0.59, 95% CI 0.34 to 0.84, P<0.01), compared with the control group. Meanwhile, CM therapy was associated with a low incidence of adverse effects (RR=0.19, 95% CI 0.08 to 0.43, P<0.01). However, there was no significant difference in mortality (RR=0.24, 95% CI 0.05 to 1.10, P>0.05) between CM and control groups.

Conclusions

The pooled outcomes suggest that CM treatment appears benefit in reducing the risk of exacerbation, improving lung function and decreasing the incidence of adverse effects and enhancing the quality of life. However, the outcomes were limited because of the low quality of the included studies. More rigorous clinic trials need to be carried out to provide sufficient and accurate evidence in the future.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Mejia M, Carrillo G, Rojas-Serrano J, Estrada A, Suarez T, Alonso D, et al. Idiopathic pulmonary fibrosis and emphysema: decreased survival associated with severe pulmonary arterial hypertension. Chest 2009;136:10–15.

    PubMed  Google Scholar 

  2. Kreuter M, Ehlers-Tenenbaum S, Schaaf M, Oltmanns U, Palmowski K, Hoffmann H, et al. Treatment and outcome of lung cancer in idiopathic interstitial pneumonias. Sarcoidosis Vasc Diffuse Lung Dis 2015;31:266–274.

    PubMed  Google Scholar 

  3. Patel NM, Lederer DJ, Borczuk AC, Kawut SM. Pulmonary hypertension in idiopathic pulmonary fibrosis. Chest 2007;132:998–1006.

    PubMed  Google Scholar 

  4. Lee JS, Collard HR, Anstrom KJ, Martinez FJ, Noth I, Roberts RS, et al. Anti-acid treatment and disease progression in idiopathic pulmonary fibrosis: an analysis of data from three randomised controlled trials. Lancet Respir Med 2013;1:369–376.

    PubMed  PubMed Central  Google Scholar 

  5. King TE Jr, Pardo A, Selman M. Idiopathic pulmonary fibrosis. Lancet 2011;378:1949–1961.

    PubMed  Google Scholar 

  6. Baddini-Martinez J, Baldi BG, Costa CH, Jezler S, Lima MS, Rufino R, et al. Update on diagnosis and treatment of idiopathic pulmonary fibrosis. J Bras Pneumol 2015;41:454–466.

    PubMed  PubMed Central  Google Scholar 

  7. Zhou JX. The ambroxol combined with ligustrazine in the treatment of 52 patients with idiopathic pulmonary fibrosis. J Clin Pulm Med (Chin) 2013;18:85–86.

    Google Scholar 

  8. Zhou XM, Wen GY, Zhao Y, Liu YM, Li JX. Inhibitory effects of alkaline extract of Citrus reticulata on pulmonary fibrosis. J Ethnopharmacol 2013;146:372–378.

    PubMed  Google Scholar 

  9. He HY, Tang HY, Gao LL, Wu Y, Feng ZQ, Lin HL, et al. Tanshinone IIA attenuates bleomycin-induced pulmonary fibrosis in rats. Mol Med Rep 2015;11:4190–4196.

    CAS  PubMed  PubMed Central  Google Scholar 

  10. Higgins JP, Altman DG, Gftzsche PC, Jlini P, Moher D, Oxman AD, et al. The Cochrane collaboration's tool for assessing risk of bias in random trials. BMJ 2011;343:d5928.

    PubMed  PubMed Central  Google Scholar 

  11. Tan Y, Dong Y, Dong HJ. Clinical study of nourishing deficiency and dredging collaterals method therapy in treatment of idiopathic pulmonary fibrosis. Lishizhen Med Mater Med Res (Chin) 2009;20:713–714.

    Google Scholar 

  12. Zhong Y. Clinical observation of 56 cases of idiopathic pulmonary fibrosis treated with Qishen Yiqi Decoction combined with inhaled budesonide. Chin J Mod Drug Appl (Chin) 2010;4:134–135.

    Google Scholar 

  13. Hou J, Dai LJ, Mu GH. To evaluate the efficacy of ligustrazin and salvia miltiorrhiza combined prednisone to treat idiopathic pulmonary fibrosis. J Postgrad Med (Chin) 2001;24:17–18.

    Google Scholar 

  14. Liu M, Zhao QL, Liu GY, Zhu ZG, Liu CW, Ding BB. Clinical observation of Xuefu Zhuyu Capsule combined with N-acetylcysteine in the treatment of idiopathic pulmonary fibrosis. Chin J Tradit Chin Med Pharm (Chin) 2015;30:473–476.

    CAS  Google Scholar 

  15. Ouyang XH, Hu CH. Clinical observation of ligustrazine on idiopathic pulmonary fibrosis. Pract Clin Med (Chin) 1998;14:36–537.

    Google Scholar 

  16. Weng H, Ma DF. Clinical observation of Qingjin Decoction on idiopathic pulmonary fibrosis. Gansu J Tradit Chin Med (Chin) 2011;24:40–41.

    Google Scholar 

  17. Wang K, Ren XL. Curative effect observation of Yiqi Yangyin prescription on idiopathic pulmonary fibrosis. Shaanxi J Tradit Chin Med (Chin) 2014;35:182–183.

    Google Scholar 

  18. Lv YY, Li GL, Zhang NZ, Yang C, Xu S, Dong JB. Clinical observation of combination of traditional Chinese medicine and Western medicine for idiopathic pulmonary fibrosis. Clin J Tradit Chin Med (Chin) 2013;25:18–19.

    Google Scholar 

  19. Liu Y. Clinical effect of ligustrazine combined with inhaled budesonide on idiopathic pulmonary fibrosis. Mod J Integr Tradit Chin West Med (Chin) 2015;24:2536–2538.

    CAS  Google Scholar 

  20. Hu XL. Clinical observation of effect of idiopathic fibrosis of the lung treated by supplementing qi and nourishing yin and picking lung collaterals [dissertation]. Beijing: Beijing University of Chinese Medicine; 2007.

    Google Scholar 

  21. Li YY, Zhang YP, Wang SC, Miao Q, Zhang Q, Wang B, et al. Yiqi Tongluo method in treating idiopathic pulmonary fibrosis: a clinical trial. Lishizhen Med Mater Med Res (Chin) 2014;25:630–632.

    Google Scholar 

  22. He M, Zhang XM, Shi LQ, Yuan HQ, Zhong X, Hao SY, et al. Correlation between curative effect of gingko flavonoid glycosides on IPF and immune cytokines. J Beijing Univ Tradit Chin Med (Chin) 2015;12:6–9.

    Google Scholar 

  23. Mi S. Clinical and animal experiments of effect of tonifying qi and purging stagnation method treatment of idiopathic pulmonary fibrosis [dissertation]. Beijing: Beijing University of Chinese Medicine; 2012.

    Google Scholar 

  24. Luo HL. Clinical and animal study on the treatment of Feixiantong on idiopathic pulmonary fibrosis [dissertation]. Beijing: China Academy of Chinese Medical Sciences; 2010.

    Google Scholar 

  25. Song P. Clinical observation of the effect of Qingfei Huatan method treating phlegm heat obstructing lung type of idiopathic pulmonary interstitial fibrosis with infection treated [dissertation]. Beijing: Beijing University of Chinese Medicine; 2013.

    Google Scholar 

  26. Du CP. Clinical study on treatment of idiopathic pulmonary fibrosis with the capsule of solving fibrosis [dissertation]. Harbin: Heilongjiang University of Chinese Medicine; 2009.

    Google Scholar 

  27. Xu MJ, Zhang XY, Shao FL. Clinical observation of idiopathic pulmonary fibrosis treatment using Huaxian Dingchuan Decoction. Food Nutr China (Chin) 2014;20:87–89.

    Google Scholar 

  28. Li ZH, Dong R, Xin FR, Zhang SS, Chen J, Su HP. Observation of curative effect of Yangyin Yifei Tongluo Wan on patients with idiopathic pulmonary Fibrosis. J Liaoning Univ Tradit Chin Med (Chin) 2015;17:163–165.

    Google Scholar 

  29. Lin L. Clinical and animal study on the treatment of Feixiantong on idiopathic pulmonary fibrosis [dissertation]. Beijing: China Academy of Chinese Medical Sciences; 2007.

    Google Scholar 

  30. Yu L. Curative effect observation of ophiopogon decoction on patients with idiopathic pulmonary fibrosis, pulmonary function and quality of life [dissertation]. Shenyang: Liaoning University of Chinese Medicine; 2010.

    Google Scholar 

  31. Sun ZT, Lian F, Wei BL, Liu ES, Li XJ, Feng JH. The clinical and empirical study of supplementing qi and activating blood for dispersing accumulation method on idiopathic pulmonary fibrosis. Liaoning J Tradit Chin Med (Chin) 2007;34:865–867.

    Google Scholar 

  32. Fan CZ, Mi S, Zhang YP, Fan MR, Miao Q, Zhang Q, et al. Effect of the qi-tonifying and stagnation-purging method on quality of life in IPF patients. World Chin Med (Chin) 2013;8:1433–1435.

    Google Scholar 

  33. Fan MR, Zhang YP, Miao Q, Zhang Q, Tao K, Yang YP, et al. Clinical trial of feitong oral liquid in treating idiopathic pulmonary fibrosis. Tradit Chin Drug Res Clin Pharmacol (Chin) 2013;24:317–322.

    Google Scholar 

  34. Zhang GC, Lin M, Le J, Qiu ZY, Zhou XM. Clinical research of Huqi Huoxue Decoction in treating idiopathic pulmonary fibrosis. China J Chin Med (Chin) 2014;29:1269–1270.

    Google Scholar 

  35. Lei ZG. Clinical effect observation of salvia, ligustrazine combined with prednisone on idiopathic pulmonary fibrosis. Zhejiang J Integr Tradit Chin West Med (Chin) 2002;12:626–627.

    Google Scholar 

  36. Sergew A, Brown KK. Advances in the treatment of idiopathic pulmonary fibrosis. Expert Opin Emerg Drugs 2015;20:537–552.

    CAS  PubMed  Google Scholar 

  37. Maharaj S, Shimbori C, Kolb M. Fibrocytes in pulmonary fibrosis: a brief synopsis. Eur Respir Rev 2013;22:552–557.

    PubMed  Google Scholar 

  38. Jones MG, Fletcher S, Richeldi L. Idiopathic pulmonary fibrosis: recent trials and current drug therapy. Respiration 2013;86:353–363.

    CAS  PubMed  Google Scholar 

  39. Richeldi L, Du Bois RM, Raghu G, Azuma A, Brown KK, Costabel U, et al. Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. N Engl J Med 2014;370:2071–2082.

    PubMed  Google Scholar 

  40. Pan YM, Fu HY, Kong Q, Xiao Y, Shou Q, Chen H, et al. Prevention of pulmonary fibrosis with salvianolic acid A by inducing fibroblast cell cycle arrest and promoting apoptosis. J Ethnopharmacol 2014;155:1589–1596.

    CAS  PubMed  Google Scholar 

  41. Xu GQ, Shi SS, Fu DS. Clinical research on treating idiopathic pulmonary fibrosis with the Xuanfuhua Decoction. Clin J Chin Med (Chin) 2016;8:18–20.

    CAS  Google Scholar 

  42. Ryerson CJ, Cottin V, Brown KK, Collard HR. Acute exacerbation of idiopathic pulmonary fibrosis: shifting the paradigm. Eur Respir J 2015;46:512–520.

    PubMed  Google Scholar 

  43. Fidler L, Shapera S. Acute exacerbation of idiopathic pulmonary fibrosis. Can Respir J 2015;22:308.

    PubMed  PubMed Central  Google Scholar 

  44. Zhang YY, Qiao SJ. Treating 30 cases of IPF with the Jinlong Dingchuan Prescription. Clin J Chin Med (Chin) 2015;7:105–106.

    CAS  Google Scholar 

  45. Yount SE, Beaumont JL, Chen SY, Kaiser K, Wortman K, Van Brunt DL, et al. Health-related quality of life in patients with idiopathic pulmonary fibrosis. Lung 2016;192:227–234.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

Wu Q, Zhou XM conceived and designed this study. Wu Q, Zhou Y, Feng FC performed the data extraction, analysis, interpretation and wrote the initial draft. Zhou XM assisted with data interpretation. All authors contributed to the final manuscript.

Corresponding author

Correspondence to Xian-mei Zhou.

Additional information

Supported by the National Natural Science Foundation of China (No. 81673936)

Electronic supplementary material

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wu, Q., Zhou, Y., Feng, Fc. et al. Effectiveness and Safety of Chinese Medicine for Idiopathic Pulmonary Fibrosis: A Systematic Review and Meta-Analysis. Chin. J. Integr. Med. 25, 778–784 (2019). https://doi.org/10.1007/s11655-017-2429-5

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11655-017-2429-5

Keywords

Navigation