Evidence map›Paper›PMID 42121066›Full record

SynthesisBMC infectious diseases2026

Valve involvement in infective endocarditis among intravenous drug users: a systematic review and meta-analysis.

Minh H N Le, Hung H Phan, Vien T Truong, Minh P Tang, Phat K Nguyen, An Thuy Vo, Loc T Vu, Duy Chung, Chi N Duong, Quoc Bui and 10 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BMC infectious diseases, 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

20 authors.

Minh H N Le *Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA. d142111009@tmu.edu.tw.ORCID http://orcid.org/0000-0002-7728-1539
Hung H Phan *Cardiovascular Research Laboratories, Interventional Cardiology Department, Methodist Hospital, Merrillville, IN, 46410, USA.ORCID http://orcid.org/0009-0005-4103-6522
Vien T TruongDepartment of Cardiology, The Christ Hospital Health Network, Lindner Research Center, Cincinnati, OH, 45219, USA.
Minh P TangInternational Ph.D. Program in Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.ORCID http://orcid.org/0009-0002-9845-554X
Phat K NguyenInternational Master Program in Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-1309-6780
An Thuy VoFaculty of Pharmacy, Can Tho University of Medicine and Pharmacy, Can Tho City, 900000, Vietnam.ORCID http://orcid.org/0009-0004-4396-7761
Loc T VuCardiovascular Research Laboratories, Interventional Cardiology Department, Methodist Hospital, Merrillville, IN, 46410, USA.ORCID http://orcid.org/0000-0002-4448-9421
Duy ChungDepartment of Medicine, Northwest Medical Center, Tucson, AZ, 85741, USA.ORCID http://orcid.org/0000-0003-4877-6804
Chi N DuongDepartment of Biomedical & Nutritional Sciences, University of Massachusetts Lowell, Lowell, MA, 01854, USA.ORCID http://orcid.org/0000-0002-3117-8851
Quoc BuiDepartment of Medicine, South Texas Health System GME Consortium, College of Medicine, Texas A&M, Edinburg, TX, 78539, USA.ORCID http://orcid.org/0000-0001-6692-5602
Han H HuynhInternational Master Program for Translational Science, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.ORCID http://orcid.org/0000-0003-0083-4913
Trang D T LeMaster Program in Graduate Institute of Metabolism and Obesity Sciences, College of Nutrition, Taipei Medical University, Taipei, Taiwan.ORCID http://orcid.org/0000-0001-7324-0097
Hoai H LeCardiovascular Research Laboratories, Interventional Cardiology Department, Methodist Hospital, Merrillville, IN, 46410, USA.ORCID http://orcid.org/0000-0002-2018-1713
Hien Q KhaInternational Ph.D. Program in Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.ORCID http://orcid.org/0000-0002-7676-3843
Nhi H H LeCardiovascular Research Laboratories, Interventional Cardiology Department, Methodist Hospital, Merrillville, IN, 46410, USA.ORCID http://orcid.org/0000-0001-8487-874X
Dai Q PhanMien Dong Innovative Technology University, Dong Nai, 810000, Vietnam.
Dang NguyenHarvard T.H. Chan School of Public Health, Harvard University, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0002-9622-8370
Thach NguyenCardiovascular Research Laboratories, Interventional Cardiology Department, Methodist Hospital, Merrillville, IN, 46410, USA.ORCID http://orcid.org/0000-0002-1252-8174
Tuan VinhMedical Sciences Division, University of Oxford, Oxford, UK. tuan.vinh@hertford.ox.ac.uk.
Nguyen Quoc Khanh LeAIBioMed Research Group, Taipei Medical University, Taipei, 110, Taiwan. khanhlee@tmu.edu.tw.ORCID http://orcid.org/0000-0003-4896-7926

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntravenous drug use (IVDU) is a major risk factor for infective endocarditis (IE), with right-sided infective endocarditis (RSIE) most frequently observed. However, precise estimates of valve involvement and the relative risk (RR) of RSIE within the IVDU population remain unclear. This systematic review and meta-analysis aimed to quantify the prevalence of RSIE, left-sided IE (LSIE), both-sided IE, and valve-specific involvement in IVDUs while assessing the relative risk of right-sided versus left-sided IE within the IVDU population.

methodsA systematic search was conducted in PubMed, Embase, and Web of Science to identify studies reporting IE in IVDUs. Inclusion criteria followed the PICO framework, ensuring clear definitions of IVDU status and valve involvement. A random-effects model was used to calculate pooled prevalence estimates and RR ratios with 95% confidence intervals (CIs). Heterogeneity was assessed using the I² statistic, and sensitivity analyses were performed.

resultsA total of 14 studies involving 1,783 patients met the inclusion criteria. The pooled prevalence of right-sided infective endocarditis (RSIE) was 59% (95% CI: 54%-65%), left-sided infective endocarditis (LSIE) was 39% (95% CI: 33%-46%), and both-sided infective endocarditis was 8% (95% CI: 6%-12%). Among individual valves, the tricuspid valve was most commonly affected (59% (95% CI: 53%-64%)), followed by the mitral valve (21% (95% CI: 18%-26%)) and the aortic valve (16% (95% CI: 12%-20%)). Pulmonic valve involvement was rare (1% (95% CI: 0%-3%)). Overall, individuals who inject drugs (IVDUs) had a 1.49-fold increased risk of developing right-sided IE compared to left-sided IE (RR = 1.49 (95% CI: 1.15-1.95), p = 0.008).

conclusionThis SRMA confirms the predominance of right-sided IE, particularly tricuspid valve involvement, in IVDUs, with a significantly higher risk compared to left-sided IE. The findings underscore the need for targeted screening, early intervention, and IVDU-specific management strategies in IE care. Future research should focus on regional variations, microbiological patterns, and long-term outcomes in this high-risk population. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

EndocarditisHeart Valve DiseasesSubstance Abuse, IntravenousDrug UsersHumansPrevalenceRisk FactorsInfective endocarditisIntravenous drug useMeta-analysisRight-sided endocarditisTricuspid valve

Identifiers

PMID42121066
PMCPMC13343716

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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.