A Chinese patent medicine, Shexiang Baoxin Pill, for Non-ST-elevation acute coronary syndromes: A systematic review. (24th December 2016)
- Record Type:
- Journal Article
- Title:
- A Chinese patent medicine, Shexiang Baoxin Pill, for Non-ST-elevation acute coronary syndromes: A systematic review. (24th December 2016)
- Main Title:
- A Chinese patent medicine, Shexiang Baoxin Pill, for Non-ST-elevation acute coronary syndromes: A systematic review
- Authors:
- Zhou, Zhou
Shen, Weixing
Yu, Lili
Xu, Cong
Wu, Qibiao - Abstract:
- Abstract: Ethnopharmacological relevance: Shexiang Baoxin Pill (SXBXP) is a well-known Chinese patent medicine, widely used for Non-ST-elevation acute coronary syndromes (NSTE-ACS). It is composed of seven materia medicas or extracts (Moschus, Radix Ginseng, Calculus Bovis, Cortex Cinnamomi, Styrax, Venenum Bufonis and Borneolum Syntheticum). Aim of the study: This study is aimed to systematically review the relevant randomised controlled trials (RCTs) to determine the efficacy and safety of SXBXP for long-term management of NSTE-ACS. Materials and methods: A systematic review and meta-analysis were carried out in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. All randomised controlled trials (RCTs) comparing long-term Shexiang Baoxin Pill with conventional treatment, with outcome measures relating to efficacy and safety were selected. Primary clinical outcome was the risk of cardiovascular events, secondary outcomes were hospitalizations, angina symptoms, electrocardiogram (ECG) measurements, and adverse events. Results: Eleven RCTs recruiting 1389 patients were included, the overall risk of bias of the included trials is high and the quality poor. Compared with conventional treatment alone, long-term Shexiang Baoxin Pill plus conventional treatment might be more effective in lowering the risk of cardiovascular events (RR=0.36, 95% CI 0.26–0.49, <0.00001), hospitalizations (RR=0.38, 95% CI 0.21–0.67, P =0.0009),Abstract: Ethnopharmacological relevance: Shexiang Baoxin Pill (SXBXP) is a well-known Chinese patent medicine, widely used for Non-ST-elevation acute coronary syndromes (NSTE-ACS). It is composed of seven materia medicas or extracts (Moschus, Radix Ginseng, Calculus Bovis, Cortex Cinnamomi, Styrax, Venenum Bufonis and Borneolum Syntheticum). Aim of the study: This study is aimed to systematically review the relevant randomised controlled trials (RCTs) to determine the efficacy and safety of SXBXP for long-term management of NSTE-ACS. Materials and methods: A systematic review and meta-analysis were carried out in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. All randomised controlled trials (RCTs) comparing long-term Shexiang Baoxin Pill with conventional treatment, with outcome measures relating to efficacy and safety were selected. Primary clinical outcome was the risk of cardiovascular events, secondary outcomes were hospitalizations, angina symptoms, electrocardiogram (ECG) measurements, and adverse events. Results: Eleven RCTs recruiting 1389 patients were included, the overall risk of bias of the included trials is high and the quality poor. Compared with conventional treatment alone, long-term Shexiang Baoxin Pill plus conventional treatment might be more effective in lowering the risk of cardiovascular events (RR=0.36, 95% CI 0.26–0.49, <0.00001), hospitalizations (RR=0.38, 95% CI 0.21–0.67, P =0.0009), and improving angina symptoms (RR=1.19, 95% CI 1.13–1.26, P<0.00001), ECG measurements (RR=1.25, 95% CI 1.13–1.39, P<0.00001). Overall rate of adverse events was not elevated (P=0.43). Conclusions: From the available evidence, SXBXP added to conventional treatment may have beneficial effects on the long-term outcomes of NSTE-ACS, without serious adverse events. However, given the high risk of bias and low quality of the included trials, currently, there is no adequate evidence to draw any conclusions about its routine use. Large, methodologically-sound trials are needed to further assess its effects. Graphical abstract: … (more)
- Is Part Of:
- Journal of ethnopharmacology. Volume 194(2016)
- Journal:
- Journal of ethnopharmacology
- Issue:
- Volume 194(2016)
- Issue Display:
- Volume 194, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 194
- Issue:
- 2016
- Issue Sort Value:
- 2016-0194-2016-0000
- Page Start:
- 1130
- Page End:
- 1139
- Publication Date:
- 2016-12-24
- Subjects:
- ACS acute coronary syndromes -- NSTE-ACS non-ST-elevation acute coronary syndromes -- STEMI ST-elevation myocardial infarction -- UA unstable angina -- AMI acute myocardial infarction -- ECG electrocardiogram -- RCT randomized controlled trials -- SXBXP Shexiang Baoxin Pill (Chinese patent medicine) -- PRISMA Preferred Reporting Items for Systematic Reviews and Meta-Analyses -- RR risk ratio -- CI confidence interval -- WMD weighted mean difference -- ESC European Society of Cardiology -- ISFC/WHO International Society and Federation of Cardiology/World Health Organization -- CSC/CMA Chinese Society of Cardiology of Chinese Medical Association
Ginsenoside Rb1 (PubChem CID: 118987129) -- Ginsenoside Rc (PubChem CID: 12855889) -- Ginsenoside Rg1 (PubChem CID: 441923) -- Resibufogenin (PubChem CID: 10063) -- Bufalin (PubChem CID: 9547215) -- Gamabufotalin (PubChem CID: 259803) -- Cinnamic acid (PubChem CID: 444539) -- Muscone (PubChem CID: 10947)
Acute coronary syndromes -- Shexiang Baoxin Pill -- Systematic review -- Meta-analysis -- Efficacy -- Safety
Ethnopharmacology -- Periodicals
Pharmacognosy -- Periodicals
Herbs -- Periodicals
Herbs -- Periodicals
Pharmacognosy -- Periodicals
Pharmacognosie -- Périodiques
Herbes -- Périodiques
615.1 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03788741 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jep.2016.11.024 ↗
- Languages:
- English
- ISSNs:
- 0378-8741
- Deposit Type:
- Legaldeposit
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