Evidence map›Paper›PMID 35385826›Full record

ArticleThe American journal of tropical medicine and hygiene2022

Treatment of Bolivian Leishmania braziliensis Cutaneous and Mucosal Leishmaniasis.

Jaime Soto, Patricia Gutiérrez, Paula Soto, David Paz, Eduardo Cayhuara, Carmen Molina, Mia Sánchez, Jonathan Berman

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Inhaled Pentamidine for Bolivian Mucosal Leishmaniasis.The American journal of tropical medicine and hygiene · 2025
    Article
  4. Article
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

8 authors at 3 institutions in 2 countries.

Jaime SotoFUNDERMA (Fundación Nacional de Dermatología) and Hospital Dermatológico de Jorochito, Santa Cruz, Bolivia.
Patricia GutiérrezFUNDERMA (Fundación Nacional de Dermatología) and Hospital Dermatológico de Jorochito, Santa Cruz, Bolivia.
Paula SotoFUNDERMA (Fundación Nacional de Dermatología), Santa Cruz, Bolivia.
David PazHospital Dermatológico de Jorochito, Santa Cruz, Bolivia.
Eduardo CayhuaraPrograma Nacional de Leishmaniasis, Ministerio de Salud del Estado Plurinacional de, La Paz, Bolivia.
Carmen MolinaPrograma Nacional de Leishmaniasis, Ministerio de Salud del Estado Plurinacional de, La Paz, Bolivia.
Mia SánchezFUNDERMA (Fundación Nacional de Dermatología), Santa Cruz, Bolivia.
Jonathan BermanAB Foundation, North Bethesda, Maryland.
Fundación PROINPA · BOMinisterio de Salud · BOFast Track Drugs and Biologics · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although infection with Leishmania braziliensis is perhaps the key reason to treat New World cutaneous leishmaniasis (CL) and mucosal leishmaniasis (ML), the total literature contains relatively few reported cases. With the aim of supplementing the meager clinical information available, we searched the records of Jorochito (Dermatology) Hospital, Bolivia, for the years 1999-2020 and identified treatment records for 1,696 naive CL patients and 355 naive ML patients. Because follow-up was poor for this real-world treatment experience in the developing world, only 255 CL patients (15%) and 114 ML patients (32%) attended follow-up at Hospital. We therefore engaged in an Active Search for "lost" patients, located a further 542 CL patients (32%) and 142 ML patients (44%), thus eventually accomplished follow up on 697 CL patients (41%) and 256 ML patients (72%). Granular adverse event data derived from hospital records is listed for the 902 CL and 86 ML patients administered Glucantime intramuscularly, the 401 CL and 202 ML patients administered Glucantime intravenously, and the 163 CL and 89 ML patients administered miltefosine orally. Efficacy was obtained from hospital records for patients seen at hospital and from patient recall communicated by telephone for the patients found in the Active Search. The overall CL cure rate was 508 of 697 CL patients (73%) with follow-up: intramuscular Glucantime-196/293 (67%); intravenous Glucantime-90/126 (71%); intralesional Glucantime-34/54 (63%); oral miltefosine-52/69 (75%). The overall ML cure rate was 161 of 256 ML patients (63%) with follow-up: intramuscular Glucantime-26/48 (54%); intravenous Glucantime-66/104 (63%); intravenous amphotericin B deoxycholate-19/35 (54%); oral miltefosine-50/71 (70%). We offer this extensive adverse event and efficacy experience as useful guides for clinicians presented with a L. braziliensis infection. The cure rates also illustrate the quandary of New World CL and ML chemotherapy: sufficiently high to be useful but nevertheless needing augmentation with new agents.

Indexed as

Antiprotozoal AgentsLeishmania braziliensisLeishmaniasis, CutaneousLeishmaniasis, MucocutaneousBoliviaHumansMeglumine AntimoniateTreatment OutcomeAntiprotozoal AgentsMeglumine Antimoniate

Identifiers

PMID35385826
PMCPMC8991326
OpenAlexW4223484067

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.