Active Case Finding for Malaria: A 3-Year National Evaluation of Optimal Approaches to Detect Infections and Hotspots Through Reactive Case Detection in the Low-transmission Setting of Eswatini

Author:

Hsiang Michelle S123,Ntshalintshali Nyasatu4,Kang Dufour Mi-Suk5,Dlamini Nomcebo6,Nhlabathi Nomcebo6,Vilakati Sibonakaliso6,Malambe Calsile6,Zulu Zulisile6,Maphalala Gugu7,Novotny Joseph4,Murphy Maxwell8,Schwartz Alanna8,Sturrock Hugh2,Gosling Roly2,Dorsey Grant8,Kunene Simon6,Greenhouse Bryan8

Affiliation:

1. Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas

2. Malaria Elimination Initiative, Global Health Group

3. Department of Pediatrics, University of California, San Francisco (UCSF)

4. Clinton Health Access Initiative, Eswatini Office, Mbabane

5. Division of Prevention Science, Department of Medicine, UCSF

6. Eswatini National Malaria Programme, Manzini

7. Eswatini National Reference Laboratory, Mbabane

8. Division of HIV, Infectious Diseases, and Global Medicine, Department of Medicine, UCSF

Abstract

Abstract Background Reactive case detection (RACD) is a widely practiced malaria elimination intervention whereby close contacts of index cases receive malaria testing to inform treatment and other interventions. However, the optimal diagnostic and operational approaches for this resource-intensive strategy are not clear. Methods We conducted a 3-year prospective national evaluation of RACD in Eswatini, a malaria elimination setting. Loop-mediated isothermal amplification (LAMP) was compared to traditional rapid diagnostic testing (RDT) for the improved detection of infections and for hotspots (RACD events yielding ≥1 additional infection). The potential for index case–, RACD-, and individual-level factors to improve efficiencies was also evaluated. Results Among 377 RACD events, 10 890 participants residing within 500 m of index cases were tested. Compared to RDT, LAMP provided a 3-fold and 2.3-fold higher yield to detect infections (1.7% vs 0.6%) and hotspots (29.7% vs 12.7%), respectively. Hotspot detection improved with ≥80% target population coverage and response times within 7 days. Proximity to the index case was associated with a dose-dependent increased infection risk (up to 4-fold). Individual-, index case–, and other RACD-level factors were considered but the simple approach of restricting RACD to a 200-m radius maximized yield and efficiency. Conclusions We present the first large-scale national evaluation of optimal RACD approaches from a malaria elimination setting. To inform delivery of antimalarial drugs or other interventions, RACD, when conducted, should utilize more sensitive diagnostics and clear context-specific operational parameters. Future studies of RACD’s impact on transmission may still be needed.

Funder

National Institutes of Health

National Institute of Allergy and Infectious Diseases

Burroughs Wellcome Fund

American Society of Tropical Medicine and Hygiene

Eswatini Ministry of Health

Bill & Melinda Gates Foundation

Horchow Family Fund Scholarship

Clinton Health Access Initiative

Eswatini National Malaria Program

Horchow Family Fund Scholarship Award

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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