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Drug eluting and bare metal stents in people with and without diabetes: Collaborative network meta-analysis

  • Christoph Stettler
  • , Sabin Allemann
  • , Simon Wandel
  • , Adnan Kastrati
  • , Marie Claude Morice
  • , Albert Schömig
  • , Matthias E. Pfisterer
  • , Gregg W. Stone
  • , Martin B. Leon
  • , José Suárez De Lezo
  • , Jean Jacques Goy
  • , Seung Jung Park
  • , Manel Sabaté
  • , Maarten J. Suttorp
  • , Henning Kelbaek
  • , Christian Spaulding
  • , Maurizio Menichelli
  • , Paul Vermeersch
  • , Maurits T. Dirksen
  • , Pavel Cervinka
  • Marco De Carlo, Andrejs Erglis, Tania Chechi, Paolo Ortolani, Martin J. Schalij, Peter Diem, Bernhard Meier, Stephan Windecker, Peter Jüni*
*Šī darba korespondējošais autors
  • University of Bern
  • Imperial College London
  • Technical University of Munich
  • Institut Hospitalier Jacques Cartier
  • University of Basel
  • Columbia University
  • Hospital Universitario Reina Sofía
  • Clinique Cecil
  • University of Ulsan
  • Hospital de La Santa Creu I Sant Pau
  • St. Antonius Ziekenhuis
  • University of Copenhagen
  • Université Paris Cité
  • San Camillo Hospital
  • Middelheim General Hospital
  • Onze Lieve Vrouwe Gasthuis
  • Masaryk University
  • University of Pisa
  • Azienda Ospedaliera Careggi
  • University of Bologna
  • Leiden University

Zinātniskās darbības rezultāts: Devums žurnālamZinātniskais raksts (žurnālā)koleģiāli recenzēts

258 Atsauces (Scopus)

Kopsavilkums

Objective: To compare the effectiveness and safety of three types of stents (sirolimus eluting, paclitaxel eluting, and bare metal) in people with and without diabetes mellitus. Design: Collaborative network meta-analysis. Data sources: Electronic databases (Medline, Embase, the Cochrane Central Register of Controlled Trials), relevant websites, reference lists, conference abstracts, reviews, book chapters, and proceedings of advisory panels for the US Food and Drug Administration. Manufacturers and trialists provided additional data. Review methods: Network meta-analysis with a mixed treatment comparison method to combine direct within trial comparisons between stents with indirect evidence from other trials while maintaining randomisation. Overall mortality was the primary safety end point, target lesion revascularisation the effectiveness end point. Results: 35 trials in 3852 people with diabetes and 10 947 people without diabetes contributed to the analyses. Inconsistency of the network was substantial for overall mortality in people with diabetes and seemed to be related to the duration of dual antiplatelet therapy (P value for interaction 0.02). Restricting the analysis to trials with a duration of dual antiplatelet therapy of six months or more, inconsistency was reduced considerably and hazard ratios for overall mortality were near one for all comparisons in people with diabetes: sirolimus eluting stents compared with bare metal stents 0.88 (95% credibility interval 0.55 to 1.30), paclitaxel eluting stents compared with bare metal stents 0.91 (0.60 to 1.38), and sirolimus eluting stents compared with paclitaxel eluting stents 0.95 (0.63 to 1.43). In people without diabetes, hazard ratios were unaffected by the restriction. Both drug eluting stents were associated with a decrease in revascularisation rates compared with bare metal stents in people both with and without diabetes. Conclusion: In trials that specified a duration of dual antiplatelet therapy of six months or more after stent implantation, drug eluting stents seemed safe and effective in people both with and without diabetes.

OriģinālvalodaAngļu
Lapas (no-līdz)668-672
Lapu skaits5
ŽurnālsBMJ
Sējums337
Izdevuma numurs7671
DOIs
Publikācijas statussPublicēts - 20 sept. 2008

ANO IAM

Šis izpildes rezultāts palīdz sasniegt šādus ANO ilgtspējīgas attīstības mērķus (IAM)

  1. 3. IAM — Laba Veselība un Labbūtība
    3. IAM — Laba Veselība un Labbūtība

OECD Zinātnes nozare

  • 3.1 Medicīnas bāzes zinātnes, tai skaitā farmācija

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