Title
Identifying multidrug resistant tuberculosis transmission hotspots using routinely collected data
Date Issued
01 May 2012
Access level
open access
Resource Type
journal article
Author(s)
Manjourides J.
Lin H.
Shin S.
Jeffery C.
Pagano M.
Cohen T.
Socios en Salud Sucursal Peru
Socios en Salud Sucursal Peru
Publisher(s)
Elsevier B.V.
Abstract
In most countries with large drug resistant tuberculosis epidemics, only those cases that are at highest risk of having MDRTB receive a drug sensitivity test (DST) at the time of diagnosis. Because of this prioritized testing, identification of MDRTB transmission hotspots in communities where TB cases do not receive DST is challenging, as any observed aggregation of MDRTB may reflect systematic differences in how testing is distributed in communities. We introduce a new disease mapping method, which estimates this missing information through probability-weighted locations, to identify geographic areas of increased risk of MDRTB transmission. We apply this method to routinely collected data from two districts in Lima, Peru over three consecutive years. This method identifies an area in the eastern part of Lima where previously untreated cases have increased risk of MDRTB. This may indicate an area of increased transmission of drug resistant disease, a finding that may otherwise have been missed by routine analysis of programmatic data. The risk of MDR among retreatment cases is also highest in these probable transmission hotspots, though a high level of MDR among retreatment cases is present throughout the study area. Identifying potential multidrug resistant tuberculosis (MDRTB) transmission hotspots may allow for targeted investigation and deployment of resources. © 2012 Elsevier Ltd. All rights reserved.
Start page
273
End page
279
Volume
92
Issue
3
Language
English
OCDE Knowledge area
Enfermedades infecciosas
Sistema respiratorio
Subjects
Scopus EID
2-s2.0-84862777983
PubMed ID
Source
Tuberculosis
ISSN of the container
14729792
Sponsor(s)
JM received support from National Institutes of Health T32AI07358 ; CJ received support from National Institutes of Health R01EB0006195 ; MP received support from National Institutes of Health P01CA134294 ; TC received support from U19 A1076217 , U54 GM088558-01 and DP2OD006663 from the Office of the Director, US National Institutes of Health.
Sources of information:
Directorio de Producción Científica
Scopus