Update of transmission modelling and projections of gambiense human African trypanosomiasis in the Mandoul focus, Chad.

Diagnostics Elimination of transmission Gambiense human African trypanosomiasis (gHAT) Glossina Modelling Tsetse Validation Vector control

Journal

Infectious diseases of poverty
ISSN: 2049-9957
Titre abrégé: Infect Dis Poverty
Pays: England
ID NLM: 101606645

Informations de publication

Date de publication:
24 Jan 2022
Historique:
received: 14 10 2021
accepted: 03 01 2022
entrez: 25 1 2022
pubmed: 26 1 2022
medline: 27 1 2022
Statut: epublish

Résumé

In recent years, a programme of vector control, screening and treatment of gambiense human African trypanosomiasis (gHAT) infections led to a rapid decline in cases in the Mandoul focus of Chad. To represent the biology of transmission between humans and tsetse, we previously developed a mechanistic transmission model, fitted to data between 2000 and 2013 which suggested that transmission was interrupted by 2015. The present study outlines refinements to the model to: (1) Assess whether elimination of transmission has already been achieved despite low-level case reporting; (2) quantify the role of intensified interventions in transmission reduction; and (3) predict the trajectory of gHAT in Mandoul for the next decade under different strategies. Our previous gHAT transmission model for Mandoul was updated using human case data (2000-2019) and a series of model refinements. These include how diagnostic specificity is incorporated into the model and improvements to the fitting method (increased variance in observed case reporting and how underreporting and improvements to passive screening are captured). A side-by-side comparison of fitting to case data was performed between the models. We estimated that passive detection rates have increased due to improvements in diagnostic availability in fixed health facilities since 2015, by 2.1-fold for stage 1 detection, and 1.5-fold for stage 2. We find that whilst the diagnostic algorithm for active screening is estimated to be highly specific (95% credible interval (CI) 99.9-100%, Specificity = 99.9%), the high screening and low infection levels mean that some recently reported cases with no parasitological confirmation might be false positives. We also find that the focus-wide tsetse reduction estimated through model fitting (95% CI 96.1-99.6%, Reduction = 99.1%) is comparable to the reduction previously measured by the decline in tsetse catches from monitoring traps. In line with previous results, the model suggests that transmission was interrupted in 2015 due to intensified interventions. We recommend that additional confirmatory testing is performed in Mandoul to ensure the endgame can be carefully monitored. More specific measurement of cases, would better inform when it is safe to stop active screening and vector control, provided there is a strong passive surveillance system in place.

Sections du résumé

BACKGROUND BACKGROUND
In recent years, a programme of vector control, screening and treatment of gambiense human African trypanosomiasis (gHAT) infections led to a rapid decline in cases in the Mandoul focus of Chad. To represent the biology of transmission between humans and tsetse, we previously developed a mechanistic transmission model, fitted to data between 2000 and 2013 which suggested that transmission was interrupted by 2015. The present study outlines refinements to the model to: (1) Assess whether elimination of transmission has already been achieved despite low-level case reporting; (2) quantify the role of intensified interventions in transmission reduction; and (3) predict the trajectory of gHAT in Mandoul for the next decade under different strategies.
METHOD METHODS
Our previous gHAT transmission model for Mandoul was updated using human case data (2000-2019) and a series of model refinements. These include how diagnostic specificity is incorporated into the model and improvements to the fitting method (increased variance in observed case reporting and how underreporting and improvements to passive screening are captured). A side-by-side comparison of fitting to case data was performed between the models.
RESULTS RESULTS
We estimated that passive detection rates have increased due to improvements in diagnostic availability in fixed health facilities since 2015, by 2.1-fold for stage 1 detection, and 1.5-fold for stage 2. We find that whilst the diagnostic algorithm for active screening is estimated to be highly specific (95% credible interval (CI) 99.9-100%, Specificity = 99.9%), the high screening and low infection levels mean that some recently reported cases with no parasitological confirmation might be false positives. We also find that the focus-wide tsetse reduction estimated through model fitting (95% CI 96.1-99.6%, Reduction = 99.1%) is comparable to the reduction previously measured by the decline in tsetse catches from monitoring traps. In line with previous results, the model suggests that transmission was interrupted in 2015 due to intensified interventions.
CONCLUSIONS CONCLUSIONS
We recommend that additional confirmatory testing is performed in Mandoul to ensure the endgame can be carefully monitored. More specific measurement of cases, would better inform when it is safe to stop active screening and vector control, provided there is a strong passive surveillance system in place.

Identifiants

pubmed: 35074016
doi: 10.1186/s40249-022-00934-8
pii: 10.1186/s40249-022-00934-8
pmc: PMC8785021
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

11

Subventions

Organisme : Bill and Melinda Gates Foundation
ID : OPP1177824
Organisme : Bill and Melinda Gates Foundation
ID : INV-005121
Organisme : Bill and Melinda Gates Foundation
ID : OPP1184344
Organisme : Bill and Melinda Gates Foundation
ID : INV-008412
Organisme : Bill and Melinda Gates Foundation
ID : INV-001785
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/S01375X/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/S00243X/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/P005888/1
Pays : United Kingdom

Informations de copyright

© 2022. The Author(s).

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Auteurs

Kat S Rock (KS)

Mathematics Institute, University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK. k.s.rock@warwick.ac.uk.
Zeeman Institute for Systems Biology & Infectious Disease Epidemiology Research (SBIDER), University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK. k.s.rock@warwick.ac.uk.

Ching-I Huang (CI)

Mathematics Institute, University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK.
Zeeman Institute for Systems Biology & Infectious Disease Epidemiology Research (SBIDER), University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK.

Ronald E Crump (RE)

Mathematics Institute, University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK.
Zeeman Institute for Systems Biology & Infectious Disease Epidemiology Research (SBIDER), University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK.

Paul R Bessell (PR)

Independent Consultant, Edinburgh, UK.

Paul E Brown (PE)

Mathematics Institute, University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK.
Zeeman Institute for Systems Biology & Infectious Disease Epidemiology Research (SBIDER), University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK.

Inaki Tirados (I)

Department of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, UK.

Philippe Solano (P)

Institut de Recherche pour le Développement, UMR INTERTRYP IRD-CIRAD, Université de Montpellier, 34398, Montpellier, France.

Marina Antillon (M)

Swiss Tropical and Public Health Institute, Basel, Switzerland.
University of Basel, Basel, Switzerland.

Albert Picado (A)

Foundation for Innovative New Diagnostics (FIND), Geneva, Switzerland.

Severin Mbainda (S)

Programme National de Lutte contre la Trypanosomiase Humaine Africaine (PNLTHA), Moundou, Chad.

Justin Darnas (J)

Programme National de Lutte contre la Trypanosomiase Humaine Africaine (PNLTHA), Moundou, Chad.

Emily H Crowley (EH)

Mathematics Institute, University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK.
Zeeman Institute for Systems Biology & Infectious Disease Epidemiology Research (SBIDER), University of Warwick, Academic Loop Road, Coventry, CV4 7AL, UK.

Steve J Torr (SJ)

Department of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, UK.

Mallaye Peka (M)

Programme National de Lutte contre la Trypanosomiase Humaine Africaine (PNLTHA), Moundou, Chad.

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