Evidence map›Paper›PMID 23629932›Full record

ArticleThe American journal of tropical medicine and hygiene2013

Ultrasensitive real-time PCR for the clinical management of visceral leishmaniasis in HIV-Infected patients.

Israel Molina, Roser Fisa, Cristina Riera, Vicenç Falcó, Aleix Elizalde, Fernando Salvador, Manuel Crespo, Adrian Curran, Paulo López-Chejade, Silvia Tebar and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Blood Parasite Load as an Early Marker to Predict Treatment Response in Visceral Leishmaniasis in Eastern Africa.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Trial
  3. Frontiers in cellular and infection microbiology · 2018
    Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Molecular Tracking of theFrontiers in cellular and infection microbiology · 2021
    Review
  10. Review
  11. Recent advances and new strategies in Leishmaniasis diagnosis.Applied microbiology and biotechnology · 2020
    Review
  12. Heliyon · 2020
    Article
  13. Observational
  14. Molecular Diagnosis of Visceral Leishmaniasis.Molecular diagnosis & therapy · 2018
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. 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 3 institutions in 1 country.

Israel MolinaInfectious Disease Department, Universitat Autònoma de Barcelona, Barcelona, Spain. imolina@vhebron.net
Roser Fisa
Cristina Riera
Vicenç Falcó
Aleix Elizalde
Fernando Salvador
Manuel Crespo
Adrian Curran
Paulo López-Chejade
Silvia Tebar
Santiago Pérez-Hoyos
Esteban Ribera
Albert Pahissa
Vall d'Hebron Institut de Recerca · ESUniversitat Autònoma de Barcelona · ESUniversitat de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular methods have been proposed as an alternative tool for the diagnosis of visceral leishmaniasis (VL), but no data are available regarding use for monitoring clinical outcome. A prospective cohort study of human immunodeficiency virus-(HIV) and VL-coinfected patients was conducted in a university-affiliated hospital in Barcelona, Spain. Leishmania parasite load was monitored using a real-time polymerase chain reaction (PCR) at baseline and every 3 months. Cutoff values for PCR were determined using receiver operating characteristic (ROC) curves. Overall, 37 episodes were analyzed, and 25 of these episodes were considered as relapsing episodes. A significant decrease of parasite load measured 3 months after treatment could predict the clinical evolution of VL. A parasite load over 0.9 parasites/mL measured 12 months after treatment could predicts relapse with a sensitivity of 100% and a specificity of 90.9%. Monitoring parasite load by an ultrasensitive quantitative Leishmania PCR is useful to predict the risk of relapse after a VL episode in HIV-infected patients.

Indexed as

AdultAmphotericin BAntiprotozoal AgentsCD4 Lymphocyte CountCoinfectionFemaleHIV InfectionsHumansLeishmaniasis, VisceralMaleMiddle AgedProspective StudiesReal-Time Polymerase Chain ReactionRecurrenceROC CurveAmphotericin BAntiprotozoal Agentsliposomal amphotericin B

Identifiers

PMID23629932
PMCPMC3748463
OpenAlexW2097334775

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.