Evidence map›Paper›PMID 24752687›Full record

ArticleThe American journal of tropical medicine and hygiene2014

A new molecular surveillance system for leishmaniasis.

Kishor Pandey, Basu Dev Pandey, Arun Kumar Mallik, Jyoti Acharya, Kentaro Kato, Osamu Kaneko, Pedro Eduardo Ferreira

Abstract readEvaluation Study
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Emergence of cutaneous leishmaniasis in Nepal.Tropical medicine and health · 2021
    Article
  2. 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

7 authors.

Kishor PandeyDepartment of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Sukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal; Janakpur Zonal Hospital, Janakpur, Nepal; Department of Parasitology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden; Nanyang Technological University, School of Biological Sciences, Singapore.
Basu Dev PandeyDepartment of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Sukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal; Janakpur Zonal Hospital, Janakpur, Nepal; Department of Parasitology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden; Nanyang Technological University, School of Biological Sciences, Singapore.
Arun Kumar MallikDepartment of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Sukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal; Janakpur Zonal Hospital, Janakpur, Nepal; Department of Parasitology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden; Nanyang Technological University, School of Biological Sciences, Singapore.
Jyoti AcharyaDepartment of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Sukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal; Janakpur Zonal Hospital, Janakpur, Nepal; Department of Parasitology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden; Nanyang Technological University, School of Biological Sciences, Singapore.
Kentaro KatoDepartment of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Sukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal; Janakpur Zonal Hospital, Janakpur, Nepal; Department of Parasitology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden; Nanyang Technological University, School of Biological Sciences, Singapore.
Osamu KanekoDepartment of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Sukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal; Janakpur Zonal Hospital, Janakpur, Nepal; Department of Parasitology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden; Nanyang Technological University, School of Biological Sciences, Singapore.
Pedro Eduardo FerreiraDepartment of Protozoology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Sukraraj Tropical and Infectious Disease Hospital, Kathmandu, Nepal; Janakpur Zonal Hospital, Janakpur, Nepal; Department of Parasitology, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan; Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden; Nanyang Technological University, School of Biological Sciences, Singapore pedro.ferreira@ki.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Presently, global efforts are being made to control and eradicate the deadliest tropical diseases through the improvement of adequate interventions. A critical point for programs to succeed is the prompt and accurate diagnosis in endemic regions. Rapid diagnostic tests (RDTs) are being massively deployed and used to improve diagnosis in tropical countries. In the present report, we evaluated the hypothesis of, after use for diagnosis, the reuse of the Leishmania RDT kit as a DNA source, which can be used downstream as a molecular surveillance and/or quality control tool. As a proof of principle, a polymerase chain reaction-based method was used to detect Leishmania spp. minicircle kinetoplast DNA from leishmaniasis RDT kits. Our results show that Leishmania spp. DNA can be extracted from used RDTs and may constitute an important, reliable, and affordable tool to assist in future leishmaniasis molecular surveillance methods.

Indexed as

Endemic DiseasesAdultAgedDNA, KinetoplastDNA, ProtozoanEpidemiological MonitoringFemaleHumansLeishmaniaLeishmaniasisMaleMiddle AgedPolymerase Chain ReactionReagent Kits, DiagnosticReproducibility of ResultsTime FactorsDNA, KinetoplastDNA, ProtozoanReagent Kits, Diagnostic

Identifiers

PMID24752687
PMCPMC4047732

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.