Optimizing cluster survey designs for estimating trachomatous inflammation-follicular within trachoma control programs.


Journal

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
ISSN: 1878-3511
Titre abrégé: Int J Infect Dis
Pays: Canada
ID NLM: 9610933

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 23 09 2021
revised: 21 12 2021
accepted: 22 12 2021
pubmed: 30 12 2021
medline: 3 3 2022
entrez: 29 12 2021
Statut: ppublish

Résumé

The World Health Organization recommends mass drug administration (MDA) with azithromycin to eliminate trachoma as a public health problem. MDA decisions are based on prevalence estimates from two-stage cluster surveys. There is a need to mathematically evaluate current trachoma survey designs. Our study aimed to characterize the effects of the number of units sampled on the precision and cost of trachomatous inflammation-follicular (TF) estimates. A population of 30 districts was simulated to represent the breadth of possible TF distributions in Amhara, Ethiopia. Samples of varying numbers of clusters (14-34) and households (10-60) were selected. Sampling schemes were evaluated based on precision, proportion of incorrect and low MDA decisions made, and estimated cost. The number of clusters sampled had a greater impact on precision than the number of households. The most efficient scheme depended on the underlying TF prevalence in a district. For lower prevalence areas (< 10%) the most cost-efficient design (providing adequate precision while minimizing cost) was 20 clusters of 20-30 households. For higher prevalence areas (> 10%), the most efficient design was 15-20 clusters of 20-30 households. For longer-running programs, using context-specific survey designs would allow for practical precision while reducing survey costs. Sampling 15 clusters of 20-30 households in suspected moderate-to-high prevalence districts and 20 clusters of 20-30 households in districts suspected to be near the 5% threshold appears to be a balanced approach.

Identifiants

pubmed: 34965463
pii: S1201-9712(21)01254-6
doi: 10.1016/j.ijid.2021.12.355
pii:
doi:

Substances chimiques

Azithromycin 83905-01-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

101-107

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Julia W Gallini (JW)

Department of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, USA.

Eshetu Sata (E)

Trachoma Control Program, The Carter Center, Addis Ababa, Ethiopia.

Mulat Zerihun (M)

Trachoma Control Program, The Carter Center, Addis Ababa, Ethiopia.

Berhanu Melak (B)

Trachoma Control Program, The Carter Center, Addis Ababa, Ethiopia.

Mahteme Haile (M)

Amhara Public Health Institute, Bahir Dar, Amhara, Ethiopia.

Taye Zeru (T)

Amhara Public Health Institute, Bahir Dar, Amhara, Ethiopia.

Demelash Gessese (D)

Trachoma Control Program, The Carter Center, Addis Ababa, Ethiopia.

Zebene Ayele (Z)

Trachoma Control Program, The Carter Center, Addis Ababa, Ethiopia.

Zerihun Tadesse (Z)

Trachoma Control Program, The Carter Center, Addis Ababa, Ethiopia.

E Kelly Callahan (EK)

Trachoma Control Program, The Carter Center, Atlanta, Georgia, USA.

Scott D Nash (SD)

Trachoma Control Program, The Carter Center, Atlanta, Georgia, USA. Electronic address: scott.nash@cartercenter.org.

Paul S Weiss (PS)

Department of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, USA.

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Classifications MeSH