Evidence map›Paper›PMID 35008062›Full record

ArticleThe American journal of tropical medicine and hygiene2022

Active Pharmacovigilance for Primaquine Radical Cure of Plasmodium vivax Malaria in Odisha, India.

Anupkumar R Anvikar, Prajyoti Sahu, Madan M Pradhan, Supriya Sharma, Naseem Ahmed, Chander P Yadav, Sreya Pradhan, Stephan Duparc, Penny Grewal Daumerie, Neena Valecha

Open access · hybridAbstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
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

10 authors at 4 institutions in 3 countries.

Anupkumar R AnvikarNational Institute of Malaria Research, Dwarka, New Delhi, India.
Prajyoti SahuNational Vector Borne Disease Control Programme (NVBDCP), Odisha, India.
Madan M PradhanNational Vector Borne Disease Control Programme (NVBDCP), Odisha, India.
Supriya SharmaNational Institute of Malaria Research, Dwarka, New Delhi, India.
Naseem AhmedNational Institute of Malaria Research, Dwarka, New Delhi, India.
Chander P YadavNational Institute of Malaria Research, Dwarka, New Delhi, India.
Sreya PradhanNational Vector Borne Disease Control Programme (NVBDCP), Odisha, India.
Stephan DuparcMedicines for Malaria Venture, Geneva, Switzerland.
Penny Grewal DaumerieMedicines for Malaria Venture, Geneva, Switzerland.
Neena ValechaNational Institute of Malaria Research, Dwarka, New Delhi, India.
National Institute of Malaria Research · INMedicines for Malaria Venture · CHNational Center for Disease Control · INVector & Vector-Borne Diseases Research Institute · TZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmodium vivax malaria elimination requires radical cure with chloroquine/primaquine. However, primaquine causes hemolysis in glucose-6-phosphate dehydrogenase-deficient (G6PDd) individuals. Between February 2016 and July 2017 in Odisha State, India, a prospective, observational, active pharmacovigilance study assessed the hematologic safety of directly observed 25 mg/kg chloroquine over 3 days plus primaquine 0.25 mg/kg/day for 14 days in 100 P. vivax patients (≥ 1 year old) with hemoglobin (Hb) ≥ 7 g/dL. Pretreatment G6PDd screening was not done, but patients were advised on hemolysis signs and symptoms using a visual aid. For evaluable patients, the mean absolute change in Hb between day 0 and day 7 was -0.62 g/dL (95% confidence interval [CI]: -0.93, -0.31) for males (N = 53) versus -0.24 g/dL (95%CI: -0.59, 0.10) for females (N = 45; P = 0.034). Hemoglobin declines ≥ 3 g/dL occurred in 5/99 (5.1%) patients (three males, two females); none had concurrent clinical symptoms of hemolysis. Based on G6PD qualitative testing after study completion, three had a G6PD-normal phenotype, one female was confirmed by genotyping as G6PDd heterozygous, and one male had an unknown phenotype. A G6PDd prevalence survey was conducted between August 2017 and March 2018 in the same region using qualitative G6PD testing, confirmed by genotyping. G6PDd prevalence was 12.0% (14/117) in tribal versus 3.1% (16/509) in nontribal populations, with G6PD Orissa identified in 29/30 (96.7%) of G6PDd samples. Following chloroquine/primaquine, notable Hb declines were observed in this population that were not recognized by patients based on clinical signs and symptoms.

Indexed as

AntimalarialsGlucosephosphate Dehydrogenase DeficiencyMalaria, VivaxChloroquineFemaleHemoglobinsHemolysisHumansMalePharmacovigilancePlasmodium vivaxPrimaquineProspective StudiesAntimalarialsChloroquineHemoglobinsPrimaquine

Identifiers

PMID35008062
PMCPMC8922502
OpenAlexW4205501978

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.