Evidence map›Paper›PMID 27811064›Full record

SynthesisBMJ (Clinical research ed.)2016

Short term versus long term dual antiplatelet therapy after implantation of drug eluting stent in patients with or without diabetes: systematic review and meta-analysis of individual participant data from randomised trials.

Giuseppe Gargiulo, Stephan Windecker, Bruno R da Costa, Fausto Feres, Myeong-Ki Hong, Martine Gilard, Hyo-Soo Kim, Antonio Colombo, Deepak L Bhatt, Byeong-Keuk Kim and 6 more

Open access · hybridAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in BMJ (Clinical research ed.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 4 pooled it
10.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 4 syntheses or guidelines pooled it, 69 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 10 institutions in 6 countries.

Giuseppe GargiuloDepartment of Cardiology, Bern University Hospital, University of Bern, CH-3010 Bern, Switzerland.
Stephan WindeckerDepartment of Cardiology, Bern University Hospital, University of Bern, CH-3010 Bern, Switzerland.
Bruno R da CostaDepartment of Cardiology, Bern University Hospital, University of Bern, CH-3010 Bern, Switzerland.
Fausto FeresInstituto Dante Pazzanese de Cardiologia, São Paulo, Brazil.
Myeong-Ki HongDivision of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea.
Martine GilardDepartment of Cardiology, CHU de la Cavale Blanche, Brest, France.
Hyo-Soo KimDepartment of Internal Medicine, Cardiovascular Center, Seoul National University Hospital, Seoul, Korea.
Antonio ColomboInterventional Cardiology Unit, San Raffaele Scientific Institute, Milan, Italy.
Deepak L BhattBrigham and Women's Hospital Heart and Vascular Center and Harvard Medical School, Boston, MA, USA.
Byeong-Keuk KimDivision of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea.
Marie-Claude MoriceDepartment of Cardiology, CHU de la Cavale Blanche, Brest, France.
Kyung Woo ParkDepartment of Internal Medicine, Cardiovascular Center, Seoul National University Hospital, Seoul, Korea.
Alaide ChieffoInterventional Cardiology Unit, San Raffaele Scientific Institute, Milan, Italy.
Tullio PalmeriniDipartimento Cardio-Toraco-Vascolare, University of Bologna, Bologna, Italy.
Gregg W StoneColumbia University Medical Center/New York-Presbyterian Hospital and the Cardiovascular Research Foundation, New York, NY, USA.
Marco ValgimigliDepartment of Cardiology, Bern University Hospital, University of Bern, CH-3010 Bern, Switzerland marco.valgimigli@insel.ch.
Hôpital Maison Blanche · FRSan Raffaele University of Rome · ITSeoul National University Hospital · KRUniversity Hospital of Bern · CHUniversity of Bern · CHYonsei University · KRCardiovascular Research Foundation · USHarvard University · USInstituto Dante Pazzanese de Cardiologia · BRUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo compare clinical outcomes between short term (up to 6 months) and long term (12 months) dual antiplatelet therapy (DAPT) after placement of a drug eluting stent in patients with and without diabetes.

designIndividual participant data meta-analysis. Cox proportional regression models stratified by trial were used to assess the impact of diabetes on outcomes. DATA SOURCE: Medline, Embase, and Cochrane databases and proceedings of international meetings searched for randomised controlled trials comparing durations of DAPT after placement of a drug eluting stent. Individual patient data pooled from six DAPT trials. PRIMARY OUTCOME: Primary study outcome was one year risk of major adverse cardiac events (MACE), defined as cardiac death, myocardial infarction, or definite/probable stent thrombosis. All analyses were conducted by intention to treat.

resultsSix trials including 11 473 randomised patients were pooled. Of these patients, 3681 (32.1%) had diabetes and 7708 (67.2%) did not (mean age 63.7 (SD 9.9) and 62.8 (SD 10.1), respectively), and in 84 (0.7%) the information was missing. Diabetes was an independent predictor of MACE (hazard ratio 2.30, 95% confidence interval 1.01 to 5.27; P=0.048 At one year follow-up, long term DAPT was not associated with a decreased risk of MACE compared with short term DAPT in patients with (1.05, 0.62 to 1.76; P=0.86) or without (0.97, 0.67 to 1.39; P=0.85) diabetes (P=0.33 for interaction). The risk of myocardial infarction did not differ between the two DAPT regimens (0.95, 0.58 to 1.54; P=0.82; for those with diabetes and 1.15, 0.68 to 1.94; P=0.60; for those without diabetes (P=0.84 for interaction). There was a lower risk of definite/probable stent thrombosis with long term DAPT among patients with (0.26, 0.09 to 0.80; P=0.02) than without (1.42, 0.68 to 2.98; P=0.35) diabetes, with positive interaction testing (P=0.04 for interaction), although the landmark analysis showed a trend towards benefit in both groups. Long term DAPT was associated with higher rates of major or minor bleeding, irrespective of diabetes (P=0.37 for interaction).

conclusionsAlthough the presence of diabetes emerged as an independent predictor of MACE after implantation of a drug eluting stent, compared with short term DAPT, long term DAPT did not reduce the risk of MACE but increased the risk of bleeding among patients with stents with and without diabetes.

Indexed as

Drug-Eluting StentsCoronary StenosisCoronary ThrombosisDiabetes MellitusDrug Therapy, CombinationHumansMyocardial InfarctionPercutaneous Coronary InterventionPlatelet Aggregation InhibitorsRandomized Controlled Trials as TopicTime FactorsPlatelet Aggregation Inhibitors

Identifiers

PMID27811064
PMCPMC5094199
OpenAlexW2546874379

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.