Evidence map›Paper›PMID 25101665›Full record

ArticlePLoS neglected tropical diseases2014

Visceral leishmaniasis and HIV co-infection in Bihar, India: long-term effectiveness and treatment outcomes with liposomal amphotericin B (AmBisome).

Sakib Burza, Raman Mahajan, Prabhat K Sinha, Johan van Griensven, Krishna Pandey, María Angeles Lima, Marta Gonzalez Sanz, Temmy Sunyoto, Sunil Kumar, Gaurab Mitra and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
7.1field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
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  11. Article
  12. Article
  13. Visceral Leishmaniasis-HIV Coinfection as a Predictor of IncreasedFrontiers in cellular and infection microbiology · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Miltefosine-Lopinavir Combination Therapy AgainstFrontiers in cellular and infection microbiology · 2019
    Article
  20. Review
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

13 authors at 4 institutions in 3 countries.

Sakib BurzaMédecins Sans Frontières, New Delhi, India; Institute of Tropical Medicine, Antwerp, Belgium.
Raman MahajanMédecins Sans Frontières, New Delhi, India.
Prabhat K SinhaRajendra Memorial Research Institute of Medical Sciences, Patna, Bihar, India.
Johan van GriensvenInstitute of Tropical Medicine, Antwerp, Belgium.
Krishna PandeyInstitute of Tropical Medicine, Antwerp, Belgium.
María Angeles LimaMédecins Sans Frontières, Barcelona, Spain.
Marta Gonzalez SanzMédecins Sans Frontières, New Delhi, India.
Temmy SunyotoMédecins Sans Frontières, New Delhi, India.
Sunil KumarSri Krishna Medical College and Hospital, Muzaffarpur, Bihar, India.
Gaurab MitraMédecins Sans Frontières, New Delhi, India.
Ranjeet KumarMédecins Sans Frontières, New Delhi, India.
Neena VermaInstitute of Tropical Medicine, Antwerp, Belgium.
Pradeep DasInstitute of Tropical Medicine, Antwerp, Belgium.
Instituut voor Tropische Geneeskunde · BEMédecins Sans Frontières · ESRajendra Memorial Research Institute of Medical Sciences · INShree Krishna Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVisceral Leishmaniasis (VL; also known as kala-azar) is an ultimately fatal disease endemic in the Indian state of Bihar, while HIV/AIDS is an emerging disease in this region. A 2011 observational cohort study conducted in Bihar involving 55 VL/HIV co-infected patients treated with 20-25 mg/kg intravenous liposomal amphotericin B (AmBisome) estimated an 85.5% probability of survival and a 26.5% probability of VL relapse within 2 years. Here we report the long-term field outcomes of a larger cohort of co-infected patients treated with this regimen between 2007 and 2012. METHODS AND PRINCIPAL

findingsIntravenous AmBisome (20-25 mg/kg) was administered to 159 VL/HIV co-infected patients (both primary infections and relapses) in four or five doses of 5 mg/kg over 4-10 days. Initial cure of VL at discharge was defined as improved symptoms, cessation of fever, improvement of appetite and recession of spleen enlargement. Test of cure was not routinely performed. Antiretroviral treatment (ART) was initiated in 23 (14.5%), 39 (24.5%) and 61 (38.4%) before, during and after admission respectively. Initial cure was achieved in all discharged patients. A total of 36 patients died during follow-up, including six who died shortly after admission. Death occurred at a median of 11 weeks (IQR 4-51) after starting VL treatment. Estimated mortality risk was 14.3% at six months, 22.4% at two years and 29.7% at four years after treatment. Among the 153 patients discharged from the hospital, 26 cases of VL relapse were diagnosed during follow-up, occurring at a median of 10 months (IQR 7-14) after discharge. After accounting for competing risks, the estimated risk of relapse was 16.1% at one year, 20.4% at two years and 25.9% at four years. Low hemoglobin level and concurrent infection with tuberculosis were independent risk factors for mortality, while ART initiated shortly after admission for VL treatment was associated with a 64-66% reduced risk of mortality and 75% reduced risk of relapse. SIGNIFICANCE: This is the largest cohort of HIV-VL co-infected patients reported from the Indian subcontinent. Even after initial cure following treatment with AmBisome, these patients appear to have much higher rates of VL relapse and mortality than patients not known to be HIV-positive, although relapse rates appear to stabilize after 2 years. These results extend the earlier findings that co-infected patients are at increased risk of death and require a multidisciplinary approach for long-term management.

Indexed as

AdolescentAdultAgedAmphotericin BAnti-HIV AgentsCD4 Lymphocyte CountChildCohort StudiesCoinfectionFemaleHIV InfectionsHumansLeishmaniasis, VisceralMaleMiddle AgedTreatment OutcomeAmphotericin BAnti-HIV Agentsliposomal amphotericin B

Identifiers

PMID25101665
PMCPMC4125300
OpenAlexW2101055145

What OpenQuestion holds

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LicenceCC BY
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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.