Evidence map›Paper›PMID 31340851›Full record

Observational studyParasites & vectors2019

Clinical aspects of visceral leishmaniasis caused by L. infantum in adults. Ten years of experience of the largest outbreak in Europe: what have we learned?

Luis Horrillo, Alicia Castro, Belén Matía, Laura Molina, Jesús García-Martínez, Jerónimo Jaqueti, Isabel García-Arata, Eugenia Carrillo, Javier Moreno, José Manuel Ruiz-Giardin and 1 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Parasites & vectors, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 47 citations in OpenAlex.

  1. When macrophages have more than one thing to show.British journal of haematology · 2026
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  10. Deciphering Host-Parasite Interplay inACS infectious diseases · 2024
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  15. Immune response to viscerotropicFrontiers in immunology · 2024
    Review
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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 at 3 institutions in 1 country.

Luis HorrilloÁrea de Infecciosas, Servicio de Medicina Interna, Hospital Universitario de Fuenlabrada, Camino del Molino 2, 28942, Fuenlabrada, Madrid, Spain.
Alicia CastroÁrea de Infecciosas, Servicio de Medicina Interna, Hospital Universitario de Fuenlabrada, Camino del Molino 2, 28942, Fuenlabrada, Madrid, Spain.
Belén MatíaÁrea de Infecciosas, Servicio de Medicina Interna, Hospital Universitario de Fuenlabrada, Camino del Molino 2, 28942, Fuenlabrada, Madrid, Spain.
Laura MolinaÁrea de Microbiología, Servicio de Laboratorio Clínico, Hospital Universitario de Fuenlabrada, Camino del Molino 2, 28942, Fuenlabrada, Madrid, Spain.
Jesús García-MartínezÁrea de Microbiología, Servicio de Laboratorio Clínico, Hospital Universitario de Fuenlabrada, Camino del Molino 2, 28942, Fuenlabrada, Madrid, Spain.
Jerónimo JaquetiÁrea de Microbiología, Servicio de Laboratorio Clínico, Hospital Universitario de Fuenlabrada, Camino del Molino 2, 28942, Fuenlabrada, Madrid, Spain.
Isabel García-ArataÁrea de Microbiología, Servicio de Laboratorio Clínico, Hospital Universitario de Fuenlabrada, Camino del Molino 2, 28942, Fuenlabrada, Madrid, Spain.
Eugenia CarrilloCentro Nacional de Microbiología, WHO Collaborating Centre for Leishmaniasis, Majadahonda, Madrid, Spain.
Javier MorenoCentro Nacional de Microbiología, WHO Collaborating Centre for Leishmaniasis, Majadahonda, Madrid, Spain.
José Manuel Ruiz-GiardinÁrea de Infecciosas, Servicio de Medicina Interna, Hospital Universitario de Fuenlabrada, Camino del Molino 2, 28942, Fuenlabrada, Madrid, Spain.
Juan San MartínÁrea de Infecciosas, Servicio de Medicina Interna, Hospital Universitario de Fuenlabrada, Camino del Molino 2, 28942, Fuenlabrada, Madrid, Spain. juanvictor.san@salud.madrid.org.ORCID http://orcid.org/0000-0003-4457-5124
Hospital Universitario de Fuenlabrada · ESCentro Nacional de Microbiologia · ESUniversidad Rey Juan Carlos · ES

Funding

Red de Investigación Corporativa Enfermedades Tropicales (RICET) (RD12/0018/0008Red de Investigación Corporativa Enfermedades Tropicales (RICET) RD16/0027/0017)
6 · The paper itself

Abstract

backgroundAn outbreak of leishmaniasis caused by Leishmania infantum was declared in the southwest of the Madrid region (Spain) in June 2009. This provided a unique opportunity to compare the management of visceral leishmaniasis (VL) in immunocompetent adults (IC-VL), patients with HIV (HIV-VL) and patients receiving immunosuppressants (IS-VL).

methodsA cohort of adults with VL, all admitted to the Hospital Universitario de Fuenlabrada between June 2009 and June 2018, were monitored in this observational study, recording their personal, epidemiological, analytical, diagnostic, treatment and outcome variables.

resultsThe study population was made up of 111 patients with VL (10% HIV-VL, 14% IS-VL, 76% IC-VL). Seventy-one percent of the patients were male; the mean age was 45 years (55 years for the IS-VL patients, P = 0.017). Fifty-four percent of the IC-VL patients were of sub-Saharan origin (P = 0.001). Fever was experienced by 98% of the IC-VL patients vs 73% of the LV-HIV patients (P = 0.003). Plasma ferritin was > 1000 ng/ml in 77% of the IC-VL patients vs 17% of the LV-HIV patients (P = 0.007). Forty-two percent of patients fulfilled the criteria for haemophagocytic lymphohistiocytosis. RDT (rK39-ICT) serological analysis returned sensitivity and specificity values of 45% and 99%, respectively, and ELISA/iIFAT returned 96% and 89%, respectively, with no differences in this respect between patient groups. Fourteen (13.0%) patients with VL experienced treatment failure, eight of whom were in the IC-VL group. Treatment with < 21 mg/kg (total) liposomal amphotericin B (LAB) was associated with treatment failure in the IC-VL patients [P = 0.002 (OR: 14.7; 95% CI: 2.6-83.3)].

conclusionsIS-VL was more common than HIV-VL; the lack of experience in dealing with IS-VL is a challenge that needs to be met. The clinical features of the patients in all groups were similar, although the HIV-VL patients experienced less fever and had lower plasma ferritin concentrations. RDT (rK39-ICT) analysis returned a good specificity value but a much poorer sensitivity value than reported in other scenarios. The patients with HIV-VL, IS-VL and IC-VL returned similar serological results. Current guidelines for treatment seem appropriate, but the doses of LAB required to treat patients with HIV-VL and IS-VL are poorly defined.

Indexed as

AdultAgedAntigens, ProtozoanCoinfectionDelayed DiagnosisDisease OutbreaksFemaleHIV InfectionsHumansImmunocompetenceImmunosuppressive AgentsLeishmania infantumLeishmaniasis, VisceralLongitudinal StudiesMaleMiddle AgedAntigens, ProtozoanImmunosuppressive AgentsDiagnosisHIVImmunocompromised hostLeishmania infantumOutbreakTherapyVisceral leishmaniasis

Identifiers

PMID31340851
PMCPMC6657057
OpenAlexW2964058934

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.