Evidence map›Paper›PMID 41082563›Full record

SynthesisPLoS neglected tropical diseases2025

Leprosy relapse after multidrug therapy: Systematic review and meta-analysis.

Fabiane Veronica da Silva, Gutembergue Santos de Sousa, Eric Brito Ferraz, Pãmela Rodrigues De Souza Silva, Juliana Akie Takahashi, Omar Ariel Espinosa, Jack Roberto Silva Fhon, Roberta Olmo Pinheiro, Vilanice Alves de Araújo Püschel, Zélia Ferreira Caçador Anastácio and 1 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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

11 authors.

Fabiane Veronica da SilvaGraduate Program in Nursing at the Federal University of Mato Grosso, Avenida Fernando Correia, Cuiabá, Mato Grosso, Brazil.ORCID 0000-0002-6922-4120
Gutembergue Santos de SousaGraduate Program in Nursing at the Federal University of Mato Grosso, Avenida Fernando Correia, Cuiabá, Mato Grosso, Brazil.
Eric Brito FerrazGraduate Program in Nursing at the Federal University of Mato Grosso, Avenida Fernando Correia, Cuiabá, Mato Grosso, Brazil.
Pãmela Rodrigues De Souza SilvaGraduate Program in Nursing at the Federal University of Mato Grosso, Avenida Fernando Correia, Cuiabá, Mato Grosso, Brazil.
Juliana Akie TakahashiJBI Brazilian Centre for Evidence-based Practice - JBI Brazil, São Paulo, São Paulo, Brazil.
Omar Ariel EspinosaDepartment of Genomics, National Center for Medical Genetics and Genomics, Caja de Seguro Social, Panamá, Panamá.
Jack Roberto Silva FhonJBI Brazilian Centre for Evidence-based Practice - JBI Brazil, São Paulo, São Paulo, Brazil.
Roberta Olmo PinheiroLeprosy Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Vilanice Alves de Araújo PüschelJBI Brazilian Centre for Evidence-based Practice - JBI Brazil, São Paulo, São Paulo, Brazil.
Zélia Ferreira Caçador AnastácioResearch Center on Child Studies, University of Minho, Campus de Gualtar, Braga, Portugal.
Silvana Margarida Benevides FerreiraGraduate Program in Nursing at the Federal University of Mato Grosso, Avenida Fernando Correia, Cuiabá, Mato Grosso, Brazil.

Funding

Ministry of Science, Technology and Innovations (MCTI)National Council for Scientific and Technological Development (CNPq)
6 · The paper itself

Abstract

objectiveTo synthesize the scientific evidence regarding the prevalence of leprosy relapse following multidrug therapy.

methodA systematic review was conducted following the JBI methodology for prevalence studies and reported according to the guidelines, with the registration number CRD42020177141. The inclusion criteria were based on the mnemonics (Population, Condition, Context). Population: Individuals of any age or sex diagnosed with leprosy relapse and previously treated with paucibacillary or multibacillary multidrug therapy. Conditions: Leprosy relapse after multidrug therapy, measured as the proportion of cases. Context: Studies conducted within the healthcare service settings. The databases searched included Medline, Latin American and Caribbean Health Sciences Literature (LILACS), Embase, Cumulative Index to Nursing and Allied Health Literature (CINAHL), Scopus, WoS, and Caribbean Public Health Agency (CARPHA). The references were managed using Mendeley. A random-effects meta-analysis model was employed, and heterogeneity was assessed using Higgins' I² statistics.

resultsOf 26 studies (a combined sample of 71,385 participants), 19 were included in the meta-analysis. A higher prevalence of relapse was observed in working-age males, multibacillary cases with a high bacillary load, and those with established physical disabilities. The estimated prevalence of relapse across studies ranged from 0% to 10%, with a pooled estimate of 4% in India (95% CI: 0.03-0.05). The overall point estimate for relapse using regular multidrug therapy was 0.04 (95% CI: 0.02-0.05).

conclusionThe prevalence of relapse varied according to the geographic location and type of multidrug therapy, with substantial heterogeneity across studies. These findings suggest that factors such as individual patient characteristics, treatment adherence, and capacity for healthcare services may have influenced the outcomes observed in this review.

Indexed as

Leprostatic AgentsLeprosyDrug Therapy, CombinationFemaleHumansMalePrevalenceRecurrenceLeprostatic Agents

Identifiers

PMID41082563
PMCPMC12578349

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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.