Cardiovascular mortality and oral antidiabetic drugs: protocol for a systematic review and network meta-analysis
Rashmi Goyat1, James Douglas Thornton2, Xi Tan1
1Department of Pharmaceutical Systems and Policy, School of Pharmacy, West Virginia University, Morgantown, West Virginia, USA.
Insights
This systematic review compares oral antidiabetic drugs (ADDs) for cardiovascular safety. It aims to determine which ADDs pose the greatest risk for cardiovascular mortality in diabetic patients.
Area of Science:
- Pharmacology
- Cardiology
- Endocrinology
Background:
- Cardiovascular diseases (CVD) are a major cause of death in diabetic individuals.
- Some antidiabetic drugs (ADDs) that lower HbA1c may increase CVD risk.
- Evaluating ADDs' cardiovascular safety is crucial due to high CVD prevalence in diabetes.
Purpose of the Study:
- To systematically review and network meta-analyze the cardiovascular safety of various oral antidiabetic drug classes.
- To compare the risks of cardiovascular events associated with different ADDs.
Main Methods:
- Systematic review and network meta-analysis of randomized clinical trials and observational studies up to January 2017.
- Searched four electronic databases; dual data selection and abstraction.
- Primary outcome: cardiovascular mortality; secondary outcomes: all-cause mortality, myocardial infarction, stroke, etc.
Main Results:
- The study will present a hierarchy of ADDs based on their potential to increase cardiovascular mortality.
- Results will be disseminated via conference presentation and peer-reviewed publication.
Conclusions:
- The findings will inform clinical decisions regarding ADD selection for diabetic patients, balancing glycemic control with cardiovascular risk.
- This research provides critical evidence for optimizing diabetes management to reduce cardiovascular morbidity and mortality.
Introduction:
Cardiovascular diseases are the leading cause of morbidity and mortality among individuals with diabetes. Despite the beneficial effects of antidiabetic drugs (ADDs) in terms of lowering haemoglobin A1c, several ADDs have been shown to increase the risk of cardiovascular events. Given the high prevalence of cardiovascular disease among individuals with diabetes, it is important to weigh the benefits of ADDs against their cardiovascular safety. Therefore, the objective of the current study is to conduct a systematic review with network meta-analysis to compare the effects of different oral pharmacological classes of ADDs on cardiovascular safety.
Methods And Analysis:
Randomised clinical trials (RCTs) and observational studies published in English up to 31 January 2017, and which include direct and/or indirect evidence, will be included. Studies will be retrieved by searching four electronic databases and cross-referencing. Dual selection and abstraction of data will occur. The primary outcome will be cardiovascular mortality. Secondary outcomes will include all-cause mortality, new event of acute myocardial infarction, stroke (haemorrhagic and ischaemic), hospitalisation for acute coronary syndrome and urgent revascularisation procedures. Risk of bias will be assessed using the Cochrane Risk of Bias assessment instrument for RCTs and the Strengthening the Reporting of Observational Studies in Epidemiology instrument for observational studies. Network meta-analysis will be performed using multivariate random-effects meta-regression models. The surface under the cumulative ranking curve will be used to provide a hierarchy of ADDs that increase cardiovascular mortality.
Dissemination:
The results of this study will be presented at a professional conference and submitted to a peer-reviewed journal.
Prospero Registration Number:
CRD42017051220.
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