Evidence map›Paper›PMID 42706689›Full record

SynthesisThe Journal of international medical research2026

Indobufen-based dual antiplatelet therapy after percutaneous coronary intervention: A systematic review and network meta-analysis.

Aparna Gopinath, Jungwook Heo, Afifa Fatima, Amarsimha Yerrajonna, Hannah George, Riyazuddin Mohd, Tawfiq Turjman, Uchechi Blessing Azuwike, Dany Pierre Clitandre Bien-Aimé, Jean Antoni Sebastien Lefevre and 5 more

Abstract readSystematic ReviewNetwork Meta-AnalysisReview
In one paragraph

Synthesis in The Journal of international medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Aparna GopinathDepartment of Medicine, Government Medical College, Thiruvananthapuram, Kerala, India.
Jungwook HeoDepartment of Yuhan Life Bio, Biopharmaceutical Science Major, Yuhan University, Gyeonggi-do, South Korea.
Afifa FatimaDepartment of Medicine, Shadan Institute of Medical Sciences, Hyderabad, Telangana, India.
Amarsimha YerrajonnaDepartment of Medicine, Bon Secours Mercy Health, Toledo, Ohio, USA.
Hannah GeorgeDepartment of Medicine, Keele University, Newcastle-under-Lyme, Staffordshire, UK.
Riyazuddin MohdDepartment of Medicine, Deccan College of Medical Sciences, Hyderabad, Telangana, India.ORCID 0009-0008-1121-2566
Tawfiq TurjmanDepartment of Medicine, Furness General Hospital, Barrow-in-Furness, Cumbria, UK.ORCID 0000-0001-7609-7337
Uchechi Blessing AzuwikeDepartment of Medicine, Faculty of Medicine, University of Novi Sad, Novi Sad, Serbia.ORCID 0009-0003-1957-4688
Dany Pierre Clitandre Bien-AiméDepartment of Medicine, Université Notre Dame d'Haïti, Port-au-Prince, Haiti.
Jean Antoni Sebastien LefevreDepartment of Medicine, Université Notre Dame d'Haïti, Port-au-Prince, Haiti.
Lavinia RechDepartment of Medicine, Medical University of Graz, Graz, Austria.
Mihret Derbie AsfawDepartment of Medicine, Hayat Medical College, Addis Ababa, Ethiopia.
Joy Rita EkumbalDepartment of Medicine, University of Nairobi, Nairobi, Kenya.
Lima DalilDepartment of Medicine, Kabul Medical University, Kabul, Afghanistan.ORCID 0009-0003-7045-8965
Mirza Muhammad Hadeed KhawarDepartment of Medicine, Services Institute of Medical Sciences, Lahore, Punjab, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectiveIndobufen has been proposed as an aspirin substitute within dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI), but has been compared only with aspirin plus clopidogrel. We aimed to estimate the comparative safety and efficacy of indobufen-based DAPT against contemporary antiplatelet strategies after PCI.MethodsIn a systematic review and frequentist random-effects network meta-analysis, we searched PubMed/MEDLINE, Embase, and CENTRAL from inception to May 2026 for randomised controlled trials of adults undergoing PCI with drug-eluting stents that compared antiplatelet strategies mapping onto seven pre-specified nodes, with aspirin plus clopidogrel as the reference. Crude per-arm event counts were extracted in duplicate. The connected primary safety outcome was major bleeding (Bleeding Academic Research Consortium [BARC] type 3/5); efficacy outcomes (myocardial infarction, stent thrombosis, all-cause death, stroke) were analysed per component. Odds ratios (ORs) with 95% confidence intervals (CIs) and P-scores were estimated.ResultsEleven trials enrolling more than 55, 000 patients were included. Indobufen plus clopidogrel did not differ significantly from aspirin plus clopidogrel for major bleeding (OR 1.05, 95% CI 0.62-1.78), myocardial infarction (0.91, 0.29-2.89), stent thrombosis (1.27, 0.34-4.74), or stroke (0.96, 0.27-3.44). In a disconnected direct comparison, indobufen reduced BARC 2-5 bleeding (OR 0.62, 0.45-0.84). The significant between-strategy differences concerned others: aspirin plus ticagrelor showed higher major bleeding (2.07, 1.46-2.94) and clopidogrel monotherapy lower (0.38, 0.22-0.64). Every comparison across clusters depended on a single bridging trial, and no network contained closed loops, precluding assessment of inconsistency.ConclusionsIndobufen-based DAPT was comparable, not superior, to aspirin plus clopidogrel across bleeding and ischaemic outcomes, with no signal of increased ischaemic risk. Because only one randomised trial has directly tested indobufen and all comparisons with ticagrelor-based or monotherapy strategies rest on a single bridging trial, the findings primarily support indobufen as a reasonable aspirin-sparing alternative within clopidogrel-based DAPT. Its relative position against other contemporary bleeding-reduction strategies remains unproven. These results reinforce the need for individualised antiplatelet therapy guided by patient-specific ischaemic and bleeding risk.INPLASY registration number: INPLASY202680037.

Indexed as

Dual Anti-Platelet TherapyPercutaneous Coronary InterventionPlatelet Aggregation InhibitorsAspirinClopidogrelDrug-Eluting StentsDrug Therapy, CombinationHemorrhageHumansMyocardial InfarctionAspirinClopidogrelPlatelet Aggregation Inhibitorsantiplatelet de-escalationaspirinclopidogreldrug-eluting stentsdual antiplatelet therapyIndobufenmajor bleedingnetwork meta-analysisP2Y12 inhibitorspercutaneous coronary intervention

Identifiers

PMID42706689
PMCPMC13554619

What OpenQuestion holds

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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.