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  3. Revascularisation versus medical treatment in patients with stable coronary artery disease: network meta-analysis
 

Revascularisation versus medical treatment in patients with stable coronary artery disease: network meta-analysis

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BORIS DOI
10.7892/boris.54110
Publisher DOI
10.1136/bmj.g3859
PubMed ID
24958153
Description
OBJECTIVE

To investigate whether revascularisation improves prognosis compared with medical treatment among patients with stable coronary artery disease.

DESIGN

Bayesian network meta-analyses to combine direct within trial comparisons between treatments with indirect evidence from other trials while maintaining randomisation.

ELIGIBILITY CRITERIA FOR SELECTING STUDIES

A strategy of initial medical treatment compared with revascularisation by coronary artery bypass grafting or Food and Drug Administration approved techniques for percutaneous revascularization: balloon angioplasty, bare metal stent, early generation paclitaxel eluting stent, sirolimus eluting stent, and zotarolimus eluting (Endeavor) stent, and new generation everolimus eluting stent, and zotarolimus eluting (Resolute) stent among patients with stable coronary artery disease.

DATA SOURCES

Medline and Embase from 1980 to 2013 for randomised trials comparing medical treatment with revascularisation.

MAIN OUTCOME MEASURE

All cause mortality.

RESULTS

100 trials in 93 553 patients with 262 090 patient years of follow-up were included. Coronary artery bypass grafting was associated with a survival benefit (rate ratio 0.80, 95% credibility interval 0.70 to 0.91) compared with medical treatment. New generation drug eluting stents (everolimus: 0.75, 0.59 to 0.96; zotarolimus (Resolute): 0.65, 0.42 to 1.00) but not balloon angioplasty (0.85, 0.68 to 1.04), bare metal stents (0.92, 0.79 to 1.05), or early generation drug eluting stents (paclitaxel: 0.92, 0.75 to 1.12; sirolimus: 0.91, 0.75 to 1.10; zotarolimus (Endeavor): 0.88, 0.69 to 1.10) were associated with improved survival compared with medical treatment. Coronary artery bypass grafting reduced the risk of myocardial infarction compared with medical treatment (0.79, 0.63 to 0.99), and everolimus eluting stents showed a trend towards a reduced risk of myocardial infarction (0.75, 0.55 to 1.01). The risk of subsequent revascularisation was noticeably reduced by coronary artery bypass grafting (0.16, 0.13 to 0.20) followed by new generation drug eluting stents (zotarolimus (Resolute): 0.26, 0.17 to 0.40; everolimus: 0.27, 0.21 to 0.35), early generation drug eluting stents (zotarolimus (Endeavor): 0.37, 0.28 to 0.50; sirolimus: 0.29, 0.24 to 0.36; paclitaxel: 0.44, 0.35 to 0.54), and bare metal stents (0.69, 0.59 to 0.81) compared with medical treatment.

CONCLUSION

Among patients with stable coronary artery disease, coronary artery bypass grafting reduces the risk of death, myocardial infarction, and subsequent revascularisation compared with medical treatment. All stent based coronary revascularisation technologies reduce the need for revascularisation to a variable degree. Our results provide evidence for improved survival with new generation drug eluting stents but no other percutaneous revascularisation technology compared with medical treatment.
Date of Publication
2014
Publication Type
Article
Subject(s)
600 - Technology::610 - Medicine & health
300 - Social sciences, sociology & anthropology::360 - Social problems & social services
Language(s)
en
Contributor(s)
Windecker, Stephan
Universitätsklinik für Kardiologie
Departement Klinische Forschung, Forschungsgruppe Kardiologie
Stortecky, Stefan
Universitätsklinik für Kardiologie
Departement Klinische Forschung, Forschungsgruppe Kardiologie
Stefanini, Giulio
Universitätsklinik für Kardiologie
Departement Klinische Forschung, Forschungsgruppe Kardiologie
Da Costa, Bruno
Institut für Sozial- und Präventivmedizin (ISPM)
Departement Klinische Forschung, Core Facility, Clinical Trials Unit (CTU) Bern
Rutjes, Anne
Institut für Sozial- und Präventivmedizin (ISPM)
Di Nisio, Marcello
Siletta, Maria G
Maione, Ausilia
Alfonso, Fernando
Clemmensen, Peter M
Collet, Jean-Philippe
Cremer, Jochen
Falk, Volkmar
Filippatos, Gerasimos
Hamm, Christian
Head, Stuart
Kappetein, Arie Pieter
Kastrati, Adnan
Knuuti, Juhani
Landmesser, Ulf
Laufer, Günther
Neumann, Franz-Joseph
Richter, Dimitri
Schauerte, Patrick
Sousa Uva, Miguel
Taggart, David P
Torracca, Lucia
Valgimigli, Marco
Wijns, William
Witkowski, Adam
Kolh, Philippe
Jüni, Peter
Institut für Sozial- und Präventivmedizin (ISPM)
Departement Klinische Forschung, Core Facility, Clinical Trials Unit (CTU) Bern
Additional Credits
Universitätsklinik für Kardiologie
Institut für Sozial- und Präventivmedizin (ISPM)
Series
BMJ
Publisher
BMJ Publishing Group
ISSN
1756-1833
Access(Rights)
open.access
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