Evidence map›Paper›PMID 31100064›Full record

ArticlePLoS medicine2019

Plasmodium vivax morbidity after radical cure: A cohort study in Central Vietnam.

Thanh Vinh Pham, Hong Van Nguyen, Angel Rosas Aguirre, Van Van Nguyen, Mario A Cleves, Xa Xuan Nguyen, Thao Thanh Nguyen, Duong Thanh Tran, Hung Xuan Le, Niel Hens and 4 more

Open access · goldAbstract read
In one paragraph

Article in PLoS medicine, 2019. 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
0.7field-weighted citation impact, top 26% 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, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Magnitude and patterns of severeFrontiers in medicine · 2023
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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

14 authors at 7 institutions in 7 countries.

Thanh Vinh PhamNational Institute of Malariology, Parasitology and Entomology (NIMPE), Hanoi, Vietnam.ORCID 0000-0002-7822-7059
Hong Van NguyenNational Institute of Malariology, Parasitology and Entomology (NIMPE), Hanoi, Vietnam.ORCID 0000-0002-4212-7056
Angel Rosas AguirreResearch Institute of Health and Society (IRSS), Université Catholique de Louvain (UCL), Brussels, Belgium.ORCID 0000-0002-3271-7028
Van Van NguyenProvincial Health Services, Tam Ky City, Quang Nam Province, Vietnam.
Mario A ClevesDepartment of Pediatrics, University of Arkansas for Medical Sciences (UAMS), College of Medicine, Little Rock, Arkansas, United States of America.
Xa Xuan NguyenNational Institute of Malariology, Parasitology and Entomology (NIMPE), Hanoi, Vietnam.
Thao Thanh NguyenProvincial Malaria Station, Tam Ky City, Quang Nam Province, Vietnam.
Duong Thanh TranNational Institute of Malariology, Parasitology and Entomology (NIMPE), Hanoi, Vietnam.
Hung Xuan LeNational Institute of Malariology, Parasitology and Entomology (NIMPE), Hanoi, Vietnam.
Niel HensCenter for Statistics, I-BioStat, Hasselt University, Hasselt, Belgium.ORCID 0000-0003-1881-0637
Anna Rosanas-UrgellDepartment of Biomedical Sciences, Institute of Tropical Medicine (ITM), Antwerp, Belgium.ORCID 0000-0002-0432-5203
Umberto D'AlessandroMedical Research Council Unit The Gambia (MRCG), the London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0001-6341-5009
Niko SpeybroeckResearch Institute of Health and Society (IRSS), Université Catholique de Louvain (UCL), Brussels, Belgium.
Annette ErhartMedical Research Council Unit The Gambia (MRCG), the London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0002-0522-4965
National Institute of Malariology, Parasitology and Entomology · VNLondon School of Hygiene & Tropical Medicine · GBFund for Scientific Research · BEInstituut voor Tropische Geneeskunde · BEUCLouvain · BEUniversity of Antwerp · BEUniversity of Arkansas for Medical Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn Vietnam, the importance of vivax malaria relative to falciparum during the past decade has steadily increased to 50%. This, together with the spread of multidrug-resistant Plasmodium falciparum, is a major challenge for malaria elimination. A 2-year prospective cohort study to assess P. vivax morbidity after radical cure treatment and related risk factors was conducted in Central Vietnam. METHODS AND

findingsThe study was implemented between April 2009 and December 2011 in four neighboring villages in a remote forested area of Quang Nam province. P. vivax-infected patients were treated radically with chloroquine (CQ; 25 mg/kg over 3 days) and primaquine (PQ; 0.5 mg/kg/day for 10 days) and visited monthly (malaria symptoms and blood sampling) for up to 2 years. Time to first vivax recurrence was estimated by Kaplan-Meier survival analysis, and risk factors for first and recurrent infections were identified by Cox regression models. Among the 260 P. vivax patients (61% males [159/260]; age range 3-60) recruited, 240 completed the 10-day treatment, 223 entered the second month of follow-up, and 219 were followed for at least 12 months. Most individuals (76.78%, 171/223) had recurrent vivax infections identified by molecular methods (polymerase chain reaction [PCR]); in about half of them (55.61%, 124/223), infection was detected by microscopy, and 84 individuals (37.67%) had symptomatic recurrences. Median time to first recurrence by PCR was 118 days (IQR 59-208). The estimated probability of remaining free of recurrence by month 24 was 20.40% (95% CI [14.42; 27.13]) by PCR, 42.52% (95% CI [35.41; 49.44]) by microscopy, and 60.69% (95% CI [53.51; 67.11]) for symptomatic recurrences. The main risk factor for recurrence (first or recurrent) was prior P. falciparum infection. The main limitations of this study are the age of the results and the absence of a comparator arm, which does not allow estimating the proportion of vivax relapses among recurrent infections.

conclusionA substantial number of P. vivax recurrences, mainly submicroscopic (SM) and asymptomatic, were observed after high-dose PQ treatment (5.0 mg/kg). Prior P. falciparum infection was an important risk factor for all types of vivax recurrences. Malaria elimination efforts need to address this largely undetected P. vivax transmission by simultaneously tackling the reservoir of P. falciparum and P. vivax infections.

Indexed as

AdolescentAdultAntimalarialsChildChild, PreschoolChloroquineDrug Administration ScheduleFemaleHumansIncidenceMalaria, VivaxMaleMiddle AgedPlasmodium vivaxPrimaquineProgression-Free SurvivalAntimalarialsChloroquinePrimaquine

Identifiers

PMID31100064
PMCPMC6524795
OpenAlexW2946622009

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.