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Improving the Cost-efficiency of Preventive Chemotherapy: Impact of New Diagnostics on Stopping Decisions for Control of Schistosomiasis.
Coffeng, Luc E; Graham, Matthew; Browning, Raiha; Kura, Klodeta; Diggle, Peter J; Denwood, Matthew; Medley, Graham F; Anderson, Roy M; de Vlas, Sake J.
Affiliation
  • Coffeng LE; Department of Public Health, Erasmus Medical Center, University Medical Center Rotterdam, The Netherlands.
  • Graham M; Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, University of Oxford.
  • Browning R; Department of Statistics, University of Warwick.
  • Kura K; London Centre for Neglected Tropical Disease Research, School of Public Health, Imperial College London.
  • Diggle PJ; Medical Research Council Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, School of Public Health, Imperial College London.
  • Denwood M; Centre for Health Informatics, Computing, and Statistics, Lancaster University Medical School, United Kingdom.
  • Medley GF; Department of Veterinary and Animal Sciences, University of Copenhagen, Denmark.
  • Anderson RM; Department of Global Health and Development, Faculty of Public Health and Policy, London School of Hygiene and Tropical Medicine, United Kingdom.
  • de Vlas SJ; London Centre for Neglected Tropical Disease Research, School of Public Health, Imperial College London.
Clin Infect Dis ; 78(Supplement_2): S153-S159, 2024 Apr 25.
Article in En | MEDLINE | ID: mdl-38662699
ABSTRACT

BACKGROUND:

Control of schistosomiasis (SCH) relies on the regular distribution of preventive chemotherapy (PC) over many years. For the sake of sustainable SCH control, a decision must be made at some stage to scale down or stop PC. These "stopping decisions" are based on population surveys that assess whether infection levels are sufficiently low. However, the limited sensitivity of the currently used diagnostic (Kato-Katz [KK]) to detect low-intensity infections is a concern. Therefore, the use of new, more sensitive, molecular diagnostics has been proposed.

METHODS:

Through statistical analysis of Schistosoma mansoni egg counts collected from Burundi and a simulation study using an established transmission model for schistosomiasis, we investigated the extent to which more sensitive diagnostics can improve decision making regarding stopping or continuing PC for the control of S. mansoni.

RESULTS:

We found that KK-based strategies perform reasonably well for determining when to stop PC at a local scale. Use of more sensitive diagnostics leads to a marginally improved health impact (person-years lived with heavy infection) and comes at a cost of continuing PC for longer (up to around 3 years), unless the decision threshold for stopping PC is adapted upward. However, if this threshold is set too high, PC may be stopped prematurely, resulting in a rebound of infection levels and disease burden (+45% person-years of heavy infection).

CONCLUSIONS:

We conclude that the potential value of more sensitive diagnostics lies more in the reduction of survey-related costs than in the direct health impact of improved parasite control.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parasite Egg Count / Schistosoma mansoni / Schistosomiasis mansoni / Cost-Benefit Analysis Limits: Adolescent / Adult / Animals / Child / Female / Humans / Male Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parasite Egg Count / Schistosoma mansoni / Schistosomiasis mansoni / Cost-Benefit Analysis Limits: Adolescent / Adult / Animals / Child / Female / Humans / Male Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2024 Document type: Article Affiliation country: