Evidence map›Paper›PMID 41177884›Full record

ArticleMalaria journal2025

A cross-sectional survey of Plasmodium falciparum and Plasmodium vivax in India using rapid diagnostic test and microscopy across 12 sites of varying transmission, 2023-2024.

Prabin Dahal, Sauman Singh-Phulgenda, Shrikant Nema, Praveen Kumar Tripathi, Waseem Akram Malla, Diamond P Sinha, Ajeet Mohanty, Vani H Chalageri, B M Shrinivasa, Shri Pati Singh and 16 more

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Article in Malaria journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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5 · Who and what money

Authors and funding

26 authors.

Prabin Dahal *Infectious Diseases Data Observatory (IDDO), Oxford, UK.
Sauman Singh-Phulgenda *Infectious Diseases Data Observatory (IDDO), Oxford, UK.
Shrikant Nema *ICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Praveen Kumar TripathiICMR-National Institute of Malaria Research, Field, Unit, Ranchi, 834010, India.
Waseem Akram MallaICMR-National Institute of Malaria Research, Field Unit, Guwahati, 781036, India.
Diamond P SinhaICMR-National Institute of Malaria Research, Field Unit, Raipur, 492015, India.
Ajeet MohantyICMR-National Institute of Malaria Research, Field Unit, Goa, 403001, India.
Vani H ChalageriICMR-National Institute of Malaria Research, Field Unit, Bengaluru, 562110, India.
B M ShrinivasaICMR-National Institute of Malaria Research, Field Unit, Bengaluru, 562110, India.
Shri Pati SinghICMR-National Institute of Malaria Research, Field Unit, Raipur, 492015, India.
Piyoosh Kumar SinghICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Kuldeep SinghICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Ritesh RanjhaICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Rajendra Kumar BahariaICMR-National Institute of Malaria Research, Field Unit, Nadiad, 387003, India.
Rutuja ChhajedInfectious Diseases Data Observatory (IDDO), Oxford, UK.
Minu NainICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Aishika DasICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Roopal S KumarICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Apoorv GuptaICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Manju RahiICMR-Vector Control Research Centre, Puducherry, 605006, India.
Jennifer A FleggSchool of Mathematics and Statistics, University of Melbourne, Parkville, VIC, 3010, Australia.
Nitika NitikaICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Mehul DhordaInfectious Diseases Data Observatory (IDDO), Oxford, UK.
Anup R AnvikarICMR-National Institute of Malaria Research, New Delhi, 110077, India.
Philippe J GuérinInfectious Diseases Data Observatory (IDDO), Oxford, UK. philippe.guerin@ndm.ox.ac.uk.
Praveen K BhartiICMR-National Institute of Malaria Research, New Delhi, 110077, India. saprapbs@yahoo.co.in.

Funding

Gates Foundation INV-004713
6 · The paper itself

Abstract

backgroundIn India, Plasmodium falciparum and Plasmodium vivax remain in circulation. Accurate detection of the parasite species remains crucial for prompt initiation of treatment and reducing onward transmission.

methodsA cross-sectional study across 12 sites of varying malaria endemicities was conducted from September 2023 to April 2024. Febrile participants were tested for malaria using rapid diagnostic tests (RDTs) and microscopy. Malaria positivity proportions along with 95% confidence intervals (95% CI) were presented separately by parasite species. The diagnostic performance of the RDT was compared against microscopy.

resultsA total of 10,290 febrile participants were tested by both RDT and microscopy: 1,516 (14.7%, 95% CI 7.7-21.8%) malaria cases were identified by RDT and 1,436 (14.0%, 95% CI 6.9-21.1%) by microscopy. Of the 1,516 RDT positives, 1,105 (72.9%) had P. falciparum mono-infection, 290 (19.1%) had P. vivax mono-infection, and 121 (8.0%) had P. falciparum and P. vivax mixed infections. The sensitivity and specificity of RDT were 95.0% [95% CI 94-96%] and 99% [95% CI 98-99%], respectively, for detecting P. falciparum mono-infection, 83% [95% CI 78-87%] and 100% [95% CI 99-100%] for detecting P. vivax mono-infection, and 88% [95% CI 80-93%] and 100% for detecting a mixed infection of P. falciparum and P. vivax. Overall, 43 (0.4%) participants who were RDT negative were found to have malaria on subsequent microscopic examination.

conclusionApproximately 15% of the febrile participants tested were identified as malaria positive by RDT, of which nearly one-fifth were P. vivax mono-infections and 8% harboured P. falciparum and P. vivax mixed infections. Low sensitivity of the RDTs for identifying P. vivax underscores an urgent need for developing reliable diagnostics.

Indexed as

Diagnostic Tests, RoutineMalaria, FalciparumMalaria, VivaxMicroscopyPlasmodium falciparumPlasmodium vivaxAdolescentAdultAgedChildChild, PreschoolCross-Sectional StudiesFemaleHumansIndiaInfantIndiaMalaria eliminationPlasmodium falciparumPlasmodium vivaxSurveyTransmission

Identifiers

PMID41177884
PMCPMC12581485

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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.