TY - JOUR
T1 - Case-fatality rate of major bleeding events in patients on dual antiplatelet therapy after percutaneous coronary intervention
T2 - A systematic review and meta-analysis
AU - Tritschler, Tobias
AU - Patel, Anuj
AU - Kraaijpoel, Noémie
AU - Bhatt, Deepak L.
AU - de Luca, Giuseppe
AU - di Santo, Pietro
AU - Feres, Fausto
AU - Costa, Ricardo A.
AU - Hibbert, Benjamin
AU - Isshiki, Takaaki
AU - le Gal, Grégoire
AU - Castellucci, Lana A.
N1 - Funding Information: Drs. Tritschler, Le Gal, and Castellucci are members of the Canadian Venous Thromboembolism Research Network (CanVECTOR); the Network received grant funding from the Canadian Institutes of Health Research (funding reference: CDT‐142654). Dr. Tritschler held an Early Postdoc.Mobility Award from the Swiss National Science Foundation (SNSF P2ZHP3_177999) and a Fellowship Award from the CanVECTOR Network. Dr. Le Gal holds a mid‐career clinician scientist award from the Heart and Stroke Foundation of Ontario, and the Chair on the Diagnosis of Venous Thromboembolism, Department of Medicine, University of Ottawa. Dr. Castellucci holds a Heart and Stroke Foundation of Canada National New Investigator Award, and a Tier 2 research Chair in Thrombosis and Anticoagulation Safety from the University of Ottawa. The funders had no role in the study design, in the collection, analysis, and interpretation of data, in the writing of the manuscript, and in the decision to submit the article for publication. Publisher Copyright: © 2022 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis (ISTH).
PY - 2022/10/1
Y1 - 2022/10/1
N2 - Background: Assessment of the case-fatality rate (CFR) of major bleeding on dual antiplatelet therapy (DAPT) may improve balancing risks and benefits of different durations of DAPT following percutaneous coronary intervention (PCI). Objectives: To determine the CFR of major bleeding in patients on DAPT after PCI and to compare rates among different durations of DAPT. Methods: Medline, Embase, and CENTRAL were searched from inception to August 2021 for randomized trials that reported fatal bleeding among patients who were randomized to ≥1 month of DAPT following PCI. Summary estimates for CFRs of major bleeding were calculated using the random-effects inverse-variance method. Statistical heterogeneity was evaluated using the I2 statistic. Results: Of 2777 citations obtained by the search, 15 (48%) of 31 potentially eligible studies were excluded because fatal bleeding was not reported, leaving 16 studies that were included in the analysis. Overall, there were 823 major bleeding events including 91 fatal events in 48,884 patients who were assigned to receive DAPT during study follow-up. The CFR of major bleeding was 10.8% (95% confidence interval [CI], 7.1–16.2; I2 = 50%) in the entire study population, and 13.8% (95% CI, 6.5–27.1; I2 = 28%), 11.2% (95% CI, 6.7–18.0; I2 = 0%), and 5.8% (95% CI, 3.0–11.1; I2 = 0%) in those on short-term (≤6 months; n = 16,553), standard-term (12 months; n = 19,453), and long-term DAPT (>12 months; n = 10,238), respectively. Conclusion: Fatal bleeding is not reported in many studies evaluating DAPT after PCI. The CFR of major bleeding on DAPT is substantial and may be higher in the first 12 months of DAPT than during long-term DAPT.
AB - Background: Assessment of the case-fatality rate (CFR) of major bleeding on dual antiplatelet therapy (DAPT) may improve balancing risks and benefits of different durations of DAPT following percutaneous coronary intervention (PCI). Objectives: To determine the CFR of major bleeding in patients on DAPT after PCI and to compare rates among different durations of DAPT. Methods: Medline, Embase, and CENTRAL were searched from inception to August 2021 for randomized trials that reported fatal bleeding among patients who were randomized to ≥1 month of DAPT following PCI. Summary estimates for CFRs of major bleeding were calculated using the random-effects inverse-variance method. Statistical heterogeneity was evaluated using the I2 statistic. Results: Of 2777 citations obtained by the search, 15 (48%) of 31 potentially eligible studies were excluded because fatal bleeding was not reported, leaving 16 studies that were included in the analysis. Overall, there were 823 major bleeding events including 91 fatal events in 48,884 patients who were assigned to receive DAPT during study follow-up. The CFR of major bleeding was 10.8% (95% confidence interval [CI], 7.1–16.2; I2 = 50%) in the entire study population, and 13.8% (95% CI, 6.5–27.1; I2 = 28%), 11.2% (95% CI, 6.7–18.0; I2 = 0%), and 5.8% (95% CI, 3.0–11.1; I2 = 0%) in those on short-term (≤6 months; n = 16,553), standard-term (12 months; n = 19,453), and long-term DAPT (>12 months; n = 10,238), respectively. Conclusion: Fatal bleeding is not reported in many studies evaluating DAPT after PCI. The CFR of major bleeding on DAPT is substantial and may be higher in the first 12 months of DAPT than during long-term DAPT.
KW - bleeding
KW - case-fatality rate
KW - drug-eluting stent
KW - dual antiplatelet therapy
KW - meta-analysis
KW - percutaneous coronary intervention
UR - http://www.scopus.com/inward/record.url?scp=85141986374&partnerID=8YFLogxK
U2 - https://doi.org/10.1002/rth2.12834
DO - https://doi.org/10.1002/rth2.12834
M3 - Article
C2 - 36349260
SN - 2475-0379
VL - 6
JO - Research and practice in thrombosis and haemostasis
JF - Research and practice in thrombosis and haemostasis
IS - 7
M1 - e12834
ER -