Comprehensive meta-analysis of safety and efficacy of bivalirudin versus heparin with or without routine glycoprotein IIb/IIIa inhibitors in patients with acute coronary syndrome

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Comprehensive meta-analysis of safety and efficacy of bivalirudin versus heparin with or without routine glycoprotein IIb/IIIa inhibitors in patients with acute coronary syndrome. / Navarese, Eliano Pio; Schulze, Volker; Andreotti, Felicita; Kowalewski, Mariusz; Kołodziejczak, Michalina; Kandzari, David E; Rassaf, Tienush; Gorny, Bartosz; Brockmeyer, Maximilian; Meyer, Christian; Berti, Sergio; Kubica, Jacek; Kelm, Malte; Valgimigli, Marco.

In: JACC-CARDIOVASC INTE, Vol. 8, No. 1 Pt B, 01.2015, p. 201-213.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Navarese, EP, Schulze, V, Andreotti, F, Kowalewski, M, Kołodziejczak, M, Kandzari, DE, Rassaf, T, Gorny, B, Brockmeyer, M, Meyer, C, Berti, S, Kubica, J, Kelm, M & Valgimigli, M 2015, 'Comprehensive meta-analysis of safety and efficacy of bivalirudin versus heparin with or without routine glycoprotein IIb/IIIa inhibitors in patients with acute coronary syndrome', JACC-CARDIOVASC INTE, vol. 8, no. 1 Pt B, pp. 201-213. https://doi.org/10.1016/j.jcin.2014.10.003

APA

Navarese, E. P., Schulze, V., Andreotti, F., Kowalewski, M., Kołodziejczak, M., Kandzari, D. E., Rassaf, T., Gorny, B., Brockmeyer, M., Meyer, C., Berti, S., Kubica, J., Kelm, M., & Valgimigli, M. (2015). Comprehensive meta-analysis of safety and efficacy of bivalirudin versus heparin with or without routine glycoprotein IIb/IIIa inhibitors in patients with acute coronary syndrome. JACC-CARDIOVASC INTE, 8(1 Pt B), 201-213. https://doi.org/10.1016/j.jcin.2014.10.003

Vancouver

Bibtex

@article{242b44aa98104fb5a2d361ce4ae671b2,
title = "Comprehensive meta-analysis of safety and efficacy of bivalirudin versus heparin with or without routine glycoprotein IIb/IIIa inhibitors in patients with acute coronary syndrome",
abstract = "OBJECTIVES: The aim of this meta-analysis was to compare the 30-day safety and efficacy of bivalirudin with those of heparin with or without routine administration of a glycoprotein IIb/IIIa inhibitor (GPI) in patients with acute coronary syndrome (ACS).BACKGROUND: Bivalirudin has been a mainstay of anticoagulation in patients with ACS compared with heparin. The extent to which trial results have been affected by the coadministration of heparin with a GPI, however, remains unclear.METHODS: A total of 13 randomized, controlled trials involving 24,605 patients were included.RESULTS: There was no significant difference in 30-day mortality or myocardial infarction rate with bivalirudin compared with heparin with or without routine GPI administration. A reduction of 30-day major bleeding was observed with bivalirudin compared with heparin that was significant when GPI was routinely administered (odds ratio [OR]: 0.52, 95% confidence interval [CI]: 0.45 to 0.60), p < 0.001) but not with provisionally administered GPI (OR: 0.66, 95% CI: 0.33 to 1.32; p = 0.24). The occurrence of stent thrombosis (ST) at 30 days was significantly increased with bivalirudin compared with heparin plus routinely administered GPI (OR: 1.67, 95% CI: 1.13 to 2.45, p = 0.02), but not compared with heparin plus provisionally administered GPI (OR: 2.08, 95% CI: 0.35 to 12.32, p = 0.42). The rate of acute ST (≤ 24 h), however, was almost 4.5-fold higher with bivalirudin compared with heparin with or without GPI, whereas the rate of subacute ST (24 h to 30 days) did not differ significantly.CONCLUSIONS: Overall, bivalirudin in ACS patients is associated with a significant reduction of major bleeding compared with heparin plus routinely administered GPI, but with a marked increase in ST rates compared with heparin with or without GPI.",
keywords = "Acute Coronary Syndrome/blood, Anticoagulants/adverse effects, Blood Platelets/drug effects, Chi-Square Distribution, Coronary Thrombosis/etiology, Hemorrhage/chemically induced, Heparin/adverse effects, Hirudins/adverse effects, Humans, Myocardial Infarction/etiology, Odds Ratio, Peptide Fragments/adverse effects, Platelet Aggregation Inhibitors/adverse effects, Platelet Glycoprotein GPIIb-IIIa Complex/antagonists & inhibitors, Randomized Controlled Trials as Topic, Recombinant Proteins/adverse effects, Risk Factors, Time Factors, Treatment Outcome",
author = "Navarese, {Eliano Pio} and Volker Schulze and Felicita Andreotti and Mariusz Kowalewski and Michalina Ko{\l}odziejczak and Kandzari, {David E} and Tienush Rassaf and Bartosz Gorny and Maximilian Brockmeyer and Christian Meyer and Sergio Berti and Jacek Kubica and Malte Kelm and Marco Valgimigli",
note = "Copyright {\textcopyright} 2015 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.",
year = "2015",
month = jan,
doi = "10.1016/j.jcin.2014.10.003",
language = "English",
volume = "8",
pages = "201--213",
journal = "JACC-CARDIOVASC INTE",
issn = "1936-8798",
publisher = "Elsevier Inc.",
number = "1 Pt B",

}

RIS

TY - JOUR

T1 - Comprehensive meta-analysis of safety and efficacy of bivalirudin versus heparin with or without routine glycoprotein IIb/IIIa inhibitors in patients with acute coronary syndrome

AU - Navarese, Eliano Pio

AU - Schulze, Volker

AU - Andreotti, Felicita

AU - Kowalewski, Mariusz

AU - Kołodziejczak, Michalina

AU - Kandzari, David E

AU - Rassaf, Tienush

AU - Gorny, Bartosz

AU - Brockmeyer, Maximilian

AU - Meyer, Christian

AU - Berti, Sergio

AU - Kubica, Jacek

AU - Kelm, Malte

AU - Valgimigli, Marco

N1 - Copyright © 2015 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

PY - 2015/1

Y1 - 2015/1

N2 - OBJECTIVES: The aim of this meta-analysis was to compare the 30-day safety and efficacy of bivalirudin with those of heparin with or without routine administration of a glycoprotein IIb/IIIa inhibitor (GPI) in patients with acute coronary syndrome (ACS).BACKGROUND: Bivalirudin has been a mainstay of anticoagulation in patients with ACS compared with heparin. The extent to which trial results have been affected by the coadministration of heparin with a GPI, however, remains unclear.METHODS: A total of 13 randomized, controlled trials involving 24,605 patients were included.RESULTS: There was no significant difference in 30-day mortality or myocardial infarction rate with bivalirudin compared with heparin with or without routine GPI administration. A reduction of 30-day major bleeding was observed with bivalirudin compared with heparin that was significant when GPI was routinely administered (odds ratio [OR]: 0.52, 95% confidence interval [CI]: 0.45 to 0.60), p < 0.001) but not with provisionally administered GPI (OR: 0.66, 95% CI: 0.33 to 1.32; p = 0.24). The occurrence of stent thrombosis (ST) at 30 days was significantly increased with bivalirudin compared with heparin plus routinely administered GPI (OR: 1.67, 95% CI: 1.13 to 2.45, p = 0.02), but not compared with heparin plus provisionally administered GPI (OR: 2.08, 95% CI: 0.35 to 12.32, p = 0.42). The rate of acute ST (≤ 24 h), however, was almost 4.5-fold higher with bivalirudin compared with heparin with or without GPI, whereas the rate of subacute ST (24 h to 30 days) did not differ significantly.CONCLUSIONS: Overall, bivalirudin in ACS patients is associated with a significant reduction of major bleeding compared with heparin plus routinely administered GPI, but with a marked increase in ST rates compared with heparin with or without GPI.

AB - OBJECTIVES: The aim of this meta-analysis was to compare the 30-day safety and efficacy of bivalirudin with those of heparin with or without routine administration of a glycoprotein IIb/IIIa inhibitor (GPI) in patients with acute coronary syndrome (ACS).BACKGROUND: Bivalirudin has been a mainstay of anticoagulation in patients with ACS compared with heparin. The extent to which trial results have been affected by the coadministration of heparin with a GPI, however, remains unclear.METHODS: A total of 13 randomized, controlled trials involving 24,605 patients were included.RESULTS: There was no significant difference in 30-day mortality or myocardial infarction rate with bivalirudin compared with heparin with or without routine GPI administration. A reduction of 30-day major bleeding was observed with bivalirudin compared with heparin that was significant when GPI was routinely administered (odds ratio [OR]: 0.52, 95% confidence interval [CI]: 0.45 to 0.60), p < 0.001) but not with provisionally administered GPI (OR: 0.66, 95% CI: 0.33 to 1.32; p = 0.24). The occurrence of stent thrombosis (ST) at 30 days was significantly increased with bivalirudin compared with heparin plus routinely administered GPI (OR: 1.67, 95% CI: 1.13 to 2.45, p = 0.02), but not compared with heparin plus provisionally administered GPI (OR: 2.08, 95% CI: 0.35 to 12.32, p = 0.42). The rate of acute ST (≤ 24 h), however, was almost 4.5-fold higher with bivalirudin compared with heparin with or without GPI, whereas the rate of subacute ST (24 h to 30 days) did not differ significantly.CONCLUSIONS: Overall, bivalirudin in ACS patients is associated with a significant reduction of major bleeding compared with heparin plus routinely administered GPI, but with a marked increase in ST rates compared with heparin with or without GPI.

KW - Acute Coronary Syndrome/blood

KW - Anticoagulants/adverse effects

KW - Blood Platelets/drug effects

KW - Chi-Square Distribution

KW - Coronary Thrombosis/etiology

KW - Hemorrhage/chemically induced

KW - Heparin/adverse effects

KW - Hirudins/adverse effects

KW - Humans

KW - Myocardial Infarction/etiology

KW - Odds Ratio

KW - Peptide Fragments/adverse effects

KW - Platelet Aggregation Inhibitors/adverse effects

KW - Platelet Glycoprotein GPIIb-IIIa Complex/antagonists & inhibitors

KW - Randomized Controlled Trials as Topic

KW - Recombinant Proteins/adverse effects

KW - Risk Factors

KW - Time Factors

KW - Treatment Outcome

U2 - 10.1016/j.jcin.2014.10.003

DO - 10.1016/j.jcin.2014.10.003

M3 - SCORING: Journal article

C2 - 25616926

VL - 8

SP - 201

EP - 213

JO - JACC-CARDIOVASC INTE

JF - JACC-CARDIOVASC INTE

SN - 1936-8798

IS - 1 Pt B

ER -