Yield, Efficiency, and Costs of Mass Screening Algorithms for Tuberculosis in Brazilian Prisons.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
01 03 2021
Historique:
received: 24 09 2019
accepted: 13 02 2020
pubmed: 18 2 2020
medline: 29 4 2021
entrez: 18 2 2020
Statut: ppublish

Résumé

Tuberculosis (TB) is a major cause of morbidity and mortality among incarcerated populations globally. We performed mass TB screening in 3 prisons and assessed yield, efficiency, and costs associated with various screening algorithms. Between 2017 and 2018, inmates from 3 prisons in Brazil were screened for TB by symptom assessment, chest radiography, sputum testing by Xpert MTB/RIF fourth-generation assay, and culture. Chest radiographs were scored by an automated interpretation algorithm (Computer-Aided Detection for Tuberculosis [CAD4TB]) that was locally calibrated to establish a positivity threshold. Four diagnostic algorithms were evaluated. We assessed the yield (percentage of total cases found) and efficiency (prevalence among those screened) for each algorithm. We performed unit costing to estimate the costs of each screening or diagnostic test and calculated the cost per case detected for each algorithm. We screened 5387 prisoners, of whom 214 (3.9%) were diagnosed with TB. Compared to other screening strategies initiated with chest radiography or symptoms, the trial of all participants with a single Xpert MTB/RIF sputum test detected 74% of all TB cases at a cost of US$249 per case diagnosed. Performing Xpert MTB/RIF screening tests only on those with symptoms had a similar cost per case diagnosed (US$255) but missed 35% more cases (73 vs 54) as screening all inmates. In this prospective study in 3 prisons in a high TB burden country, we found that testing all inmates with sputum Xpert MTB/RIF was a sensitive approach, while remaining cost-efficient. These results support use of Xpert MTB/RIF for mass screening in TB-endemic prisons.

Sections du résumé

BACKGROUND
Tuberculosis (TB) is a major cause of morbidity and mortality among incarcerated populations globally. We performed mass TB screening in 3 prisons and assessed yield, efficiency, and costs associated with various screening algorithms.
METHODS
Between 2017 and 2018, inmates from 3 prisons in Brazil were screened for TB by symptom assessment, chest radiography, sputum testing by Xpert MTB/RIF fourth-generation assay, and culture. Chest radiographs were scored by an automated interpretation algorithm (Computer-Aided Detection for Tuberculosis [CAD4TB]) that was locally calibrated to establish a positivity threshold. Four diagnostic algorithms were evaluated. We assessed the yield (percentage of total cases found) and efficiency (prevalence among those screened) for each algorithm. We performed unit costing to estimate the costs of each screening or diagnostic test and calculated the cost per case detected for each algorithm.
RESULTS
We screened 5387 prisoners, of whom 214 (3.9%) were diagnosed with TB. Compared to other screening strategies initiated with chest radiography or symptoms, the trial of all participants with a single Xpert MTB/RIF sputum test detected 74% of all TB cases at a cost of US$249 per case diagnosed. Performing Xpert MTB/RIF screening tests only on those with symptoms had a similar cost per case diagnosed (US$255) but missed 35% more cases (73 vs 54) as screening all inmates.
CONCLUSIONS
In this prospective study in 3 prisons in a high TB burden country, we found that testing all inmates with sputum Xpert MTB/RIF was a sensitive approach, while remaining cost-efficient. These results support use of Xpert MTB/RIF for mass screening in TB-endemic prisons.

Identifiants

pubmed: 32064514
pii: 5736588
doi: 10.1093/cid/ciaa135
pmc: PMC7935388
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

771-777

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI130058
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI052073
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM136559
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Références

Emerg Infect Dis. 2017 Mar;23(3):496-499
pubmed: 28221118
Public Health. 2006 Oct;120(10):976-83
pubmed: 16965796
Epidemiol Infect. 2017 Sep;145(12):2491-2499
pubmed: 28756786
Lancet Glob Health. 2015 Jan;3(1):e10-2
pubmed: 25539957
Int J Tuberc Lung Dis. 2016 Aug;20(8):1072-7
pubmed: 27393542
Bull World Health Organ. 2010 Apr;88(4):273-80
pubmed: 20431791
PLoS Med. 2019 Jan 24;16(1):e1002737
pubmed: 30677013
Int J Tuberc Lung Dis. 2018 Oct 1;22(10):1166-1171
pubmed: 30236184
J Infect Dis. 2015 Apr 1;211 Suppl 2:S29-38
pubmed: 25765104
Int J Tuberc Lung Dis. 2007 Apr;11(4):398-404
pubmed: 17394685
BMC Infect Dis. 2015 Jan 22;15:24
pubmed: 25608746
Int J Tuberc Lung Dis. 2005 Jun;9(6):633-9
pubmed: 15971390
Lancet Infect Dis. 2019 Mar;19(3):e89-e95
pubmed: 30554997
PLoS Med. 2010 Dec 21;7(12):e1000381
pubmed: 21203587
PLoS One. 2013;8(1):e53644
pubmed: 23372662
Lancet Infect Dis. 2017 Apr;17(4):441-450
pubmed: 28063795
Lancet Infect Dis. 2018 Mar;18(3):261-284
pubmed: 29223583
Int J Tuberc Lung Dis. 2009 Oct;13(10):1247-52
pubmed: 19793429
Nature. 2006 Nov 23;444 Suppl 1:49-57
pubmed: 17159894
J Bras Pneumol. 2009 Jan;35(1):63-8
pubmed: 19219332
BMC Infect Dis. 2016 Oct 3;16(1):533
pubmed: 27716170
Lancet Infect Dis. 2018 Jul;18(7):e199-e210
pubmed: 29580818
PLoS One. 2008 May 07;3(5):e2100
pubmed: 18461123

Auteurs

Andrea da Silva Santos (ADS)

Faculty of Health Sciences, Federal University of Grande Dourados, Dourados, Brazil.

Roberto Dias de Oliveira (RD)

School of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.

Everton Ferreira Lemos (EF)

School of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.

Fabiano Lima (F)

School of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.

Ted Cohen (T)

Department of Epidemiology of Microbial Diseases, Yale University School of Public Health, New Haven, Connecticut, USA.

Olivia Cords (O)

Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, California, USA.

Leonardo Martinez (L)

Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, California, USA.

Crhistinne Gonçalves (C)

School of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.

Albert Ko (A)

Department of Epidemiology of Microbial Diseases, Yale University School of Public Health, New Haven, Connecticut, USA.

Jason R Andrews (JR)

Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, California, USA.

Julio Croda (J)

School of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Department of Epidemiology of Microbial Diseases, Yale University School of Public Health, New Haven, Connecticut, USA.
Oswaldo Cruz Foundation Mato Grosso do Sul, Campo Grande, Brazil.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH