Evidence map›Paper›PMID 26931488›Full record

ArticleMalaria journal2016

Reactive case-detection of malaria in Pailin Province, Western Cambodia: lessons from a year-long evaluation in a pre-elimination setting.

John Hustedt, Sara E Canavati, Chandary Rang, Ruth A Ashton, Nimol Khim, Laura Berne, Saorin Kim, Siv Sovannaroth, Po Ly, Didier Ménard and 3 more

4 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Malaria journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% 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.

NCT03511443 naunknown statusnot on this mapstarted 2017, after this paper: background citation

Evaluation of the Performance of a Highly-sensitive Rapid Diagnostic Test (RDT) Versus Conventional RDT, Compared With PCR as the Gold Standard, in Reactive Case Detection of Malaria Infections in Rakhine State, Myanmar

TypeinterventionalSponsorUniversity Research Co, LLCRan2017 to 2018Enrolled1,980ConditionsMalaria Diagnosis, Malaria,FalciparumArmshsRDT
NCT03783299 phase4completednot on this mapstarted 2017, after this paper: background citation

Assessing the Effectiveness of Targeted Active Case Detection Among High Risk Populations in Southern Lao PDR

TypeinterventionalSponsorUniversity of California, San FranciscoRan2017 to 2018Enrolled39,968ConditionsPlasmodium Falciparum MalariaArmsStandard RDT and HS-RDT, Artemether-lumefantrine, Primaquine Phosphate
NCT04416945 nawithdrawnnot on this mapstarted 2020, after this paper: background citation

Targeting High-risk Populations With Enhanced Reactive Case Detection: a Study to Assess the Effectiveness and Feasibility for Reducing Plasmodium Falciparum and P. Vivax Malaria in Southern Lao Peoples Democratic Republic

TypeinterventionalSponsorUniversity of California, San FranciscoRan2020 to 2021Enrolled0ConditionsPlasmodium Falciparum Malaria, Plasmodium Vivax MalariaArmsHousehold Reactive Case Detection, RACD of cases' co-workers/co-travelers, Case Management and Follow-up
NCT05052502 nacompletednot on this mapstarted 2020, after this paper: background citation

Targeting High-risk Populations With Enhanced Reactive Focal Mass Drug Administration: A Study to Assess the Effectiveness and Feasibility for Plasmodium Falciparum and Plasmodium Vivax Malaria in Thailand

TypeinterventionalSponsorUniversity of California, San FranciscoRan2020 to 2022Enrolled14,977ConditionsPlasmodium Falciparum Malaria, Plasmodium Vivax MalariaArmsCase Management and Follow-up, Reactive focal mass drug administration (rfMDA)
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

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  15. Malaria infection prevalence and sensitivity of reactive case detection in Zanzibar.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2020
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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

13 authors at 5 institutions in 3 countries.

John HustedtMalaria Consortium Cambodia, Phnom Penh Office, House #91, St. 95, Boeung Trabek, Chamcar Morn, Phnom Penh, Cambodia. j.hustedt@malariaconsortium.org.
Sara E CanavatiMalaria Consortium Cambodia, Phnom Penh Office, House #91, St. 95, Boeung Trabek, Chamcar Morn, Phnom Penh, Cambodia. s.canavatidelatorre@kellogg.oxon.org.
Chandary RangMalaria Consortium Cambodia, 113 (6th floor of Parkway Square), Mao Tse Toung Blvd. Chamcar Morn, Phnom Penh, Cambodia. c.rang@malariaconsortium.org.
Ruth A AshtonMalaria Consortium Cambodia, Phnom Penh Office, House #91, St. 95, Boeung Trabek, Chamcar Morn, Phnom Penh, Cambodia. rashton@tulane.edu.
Nimol KhimInstitut Pasteur in Cambodia, 5, Blvd Monivong, Phnom Penh, Cambodia. knimol@pasteur-kh.org.
Laura BerneInstitut Pasteur in Cambodia, 5, Blvd Monivong, Phnom Penh, Cambodia. lberne@pasteur-kh.org.
Saorin KimInstitut Pasteur in Cambodia, 5, Blvd Monivong, Phnom Penh, Cambodia. ksaorin@pasteur-kh.org.
Siv SovannarothThe National Center for Parasitology, Entomology and Malaria Control, Ministry of Health, Corner street 92, Trapaing Svay village, Sankat Phnom Penh Thmey, Khan Sensok, Phnom Penh, Cambodia. sivsovannaroths@gmail.com.
Po LyThe National Center for Parasitology, Entomology and Malaria Control, Ministry of Health, Corner street 92, Trapaing Svay village, Sankat Phnom Penh Thmey, Khan Sensok, Phnom Penh, Cambodia. polyteng168@gmail.com.
Didier MénardInstitut Pasteur in Cambodia, 5, Blvd Monivong, Phnom Penh, Cambodia. dmenard@pasteur-kh.org.
Jonathan CoxMalaria Consortium Cambodia, Phnom Penh Office, House #91, St. 95, Boeung Trabek, Chamcar Morn, Phnom Penh, Cambodia. jonathan.cox@lshtm.ac.uk.
Sylvia MeekMalaria Consortium, Development House, 56-64 Leonard Street, London, EC2A 4LT, UK. s.meek@malariaconsortium.org.
Arantxa Roca-FeltrerFaculty of Tropical Medicine, Malaria Consortium Asia, Mahidol University, Room 805, 420/6 Rajavidhi Road, Bangkok, 10400, Thailand. a.roca@malariaconsortium.org.
Cambodia National Malaria Center · KHInstitut Pasteur du Cambodge · KHLondon School of Hygiene & Tropical Medicine · GBMahidol Oxford Tropical Medicine Research Unit · THMalaria Consortium · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs momentum towards malaria elimination grows, strategies are being developed for scale-up in elimination settings. One prominent strategy, reactive case detection (RACD), involves screening and treating individuals living in close proximity to passively detected, or "index" cases. This study aims to use RACD to quantify Plasmodium parasitaemia in households of index cases, and identify risk factors for infection; these data could inform reactive screening approaches and identify target risk groups.

methodsThis study was conducted in the Western Cambodian province of Pailin between May 2013 and March 2014 among 440 households. Index participants/index cases (n = 270) and surrounding households (n = 110) were screened for Plasmodium infection with rapid diagnostic tests (RDT), microscopy and real-time polymerase chain reaction (PCR). Participants were interviewed to identify risk factors. A comparison group of 60 randomly-selected households was also screened, to compare infection levels of RACD and non-RACD households. In order to identify potential risk factors that would inform screening approaches and identify risk groups, multivariate logistic regression models were applied.

resultsNine infections were identified in households of index cases (RACD approach) through RDT screening of 1898 individuals (seven Plasmodium vivax, two Plasmodium falciparum); seven were afebrile. Seventeen infections were identified through PCR screening of 1596 individuals (15 P. vivax, and 22 % P. falciparum/P. vivax mixed infections). In the control group, 25 P. falciparum infections were identified through PCR screening of 237 individuals, and no P. vivax was found. Plasmodium falciparum infection was associated with fever (p = 0.013), being a member of a control household (p ≤ 0.001), having a history of malaria infection (p = 0.041), and sleeping without a mosquito net (p = 0.011). Significant predictors of P. vivax infection, as diagnosed by PCR, were fever (p = 0.058, borderline significant) and history of malaria infection (p ≤ 0.001).

conclusionThis study found that RACD identified very few secondary infections when targeting index and neighbouring households for screening. The results suggest RACD is not appropriate, where exposure to malaria occurs away from the community, and there is a high level of treatment-seeking from the private sector. Piloting RACD in a range of transmission settings would help to identify the ideal environment for feasible and effective reactive screening methods.

Indexed as

Analysis of VarianceCambodiaCross-Sectional StudiesFamily CharacteristicsFemaleHumansMalaria, FalciparumMalaria, VivaxMalePlasmodium falciparumPlasmodium vivax

Identifiers

PMID26931488
PMCPMC4774174
OpenAlexW2288335923

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.