Cost-effectiveness of 3-months isoniazid and rifapentine compared to 9-months isoniazid for latent tuberculosis infection: a systematic review.

Cost-effectiveness Isoniazid Preventive treatment Rifapentine Systematic review Tuberculosis

Journal

BMC public health
ISSN: 1471-2458
Titre abrégé: BMC Public Health
Pays: England
ID NLM: 100968562

Informations de publication

Date de publication:
07 12 2022
Historique:
received: 25 05 2022
accepted: 29 11 2022
entrez: 8 12 2022
pubmed: 9 12 2022
medline: 15 12 2022
Statut: epublish

Résumé

We conducted a systematic review examining the cost effectiveness of a 3-month course of isoniazid and rifapentine, known as 3HP, given by directly observed treatment, compared to 9 months of isoniazid that is directly observed or self-administered, for latent tuberculosis infection. 3HP has shown to be effective in reducing progression to active tuberculosis and like other short-course regimens, has higher treatment completion rates compared to standard regimens such as 9 months of isoniazid. Decision makers would benefit from knowing if the higher up-front costs of rifapentine and of the human resources needed for directly observed treatment are worth the investment for improved outcomes. We searched PubMed, Embase, CINAHL, LILACS, and Web of Science up to February 2022 with search concepts combining latent tuberculosis infection, directly observed treatment, and cost or cost-effectiveness. Studies included were in English or French, on human subjects, with latent tuberculosis infection, provided information on specified anti-tubercular therapy regimens, had a directly observed treatment arm, and described outcomes with some cost or economic data. We excluded posters and abstracts, treatment for multiple drug resistant tuberculosis, and combined testing and treatment strategies. We then restricted our findings to studies examining directly-observed 3HP for comparison. The primary outcome was the cost and cost-effectiveness of directly-observed 3HP. We identified 3 costing studies and 7 cost-effectiveness studies. The 3 costing studies compared directly-observed 3HP to directly-observed 9 months of isoniazid. Of the 7 cost-effectiveness studies, 4 were modelling studies based in high-income countries; one study was modelled on a high tuberculosis incidence population in the Canadian Arctic, using empiric costing data from that setting; and 2 studies were conducted in a low-income, high HIV-coinfection rate population. In five studies, directly-observed 3HP compared to self-administered isoniazid for 9 months in high-income countries, has incremental cost-effectiveness ratios that range from cost-saving to $5418 USD/QALY gained. While limited, existing evidence suggests 3HP may not be cost-effective in low-income, high HIV-coinfection settings. Cost-effectiveness should continue to be assessed for programmatic planning and scale-up, and may vary depending on existing systems and local context, including prevalence rates and patient expectations and preferences.

Sections du résumé

BACKGROUND
We conducted a systematic review examining the cost effectiveness of a 3-month course of isoniazid and rifapentine, known as 3HP, given by directly observed treatment, compared to 9 months of isoniazid that is directly observed or self-administered, for latent tuberculosis infection. 3HP has shown to be effective in reducing progression to active tuberculosis and like other short-course regimens, has higher treatment completion rates compared to standard regimens such as 9 months of isoniazid. Decision makers would benefit from knowing if the higher up-front costs of rifapentine and of the human resources needed for directly observed treatment are worth the investment for improved outcomes.
METHODS
We searched PubMed, Embase, CINAHL, LILACS, and Web of Science up to February 2022 with search concepts combining latent tuberculosis infection, directly observed treatment, and cost or cost-effectiveness. Studies included were in English or French, on human subjects, with latent tuberculosis infection, provided information on specified anti-tubercular therapy regimens, had a directly observed treatment arm, and described outcomes with some cost or economic data. We excluded posters and abstracts, treatment for multiple drug resistant tuberculosis, and combined testing and treatment strategies. We then restricted our findings to studies examining directly-observed 3HP for comparison. The primary outcome was the cost and cost-effectiveness of directly-observed 3HP.
RESULTS
We identified 3 costing studies and 7 cost-effectiveness studies. The 3 costing studies compared directly-observed 3HP to directly-observed 9 months of isoniazid. Of the 7 cost-effectiveness studies, 4 were modelling studies based in high-income countries; one study was modelled on a high tuberculosis incidence population in the Canadian Arctic, using empiric costing data from that setting; and 2 studies were conducted in a low-income, high HIV-coinfection rate population. In five studies, directly-observed 3HP compared to self-administered isoniazid for 9 months in high-income countries, has incremental cost-effectiveness ratios that range from cost-saving to $5418 USD/QALY gained. While limited, existing evidence suggests 3HP may not be cost-effective in low-income, high HIV-coinfection settings.
CONCLUSION
Cost-effectiveness should continue to be assessed for programmatic planning and scale-up, and may vary depending on existing systems and local context, including prevalence rates and patient expectations and preferences.

Identifiants

pubmed: 36476206
doi: 10.1186/s12889-022-14766-6
pii: 10.1186/s12889-022-14766-6
pmc: PMC9727859
doi:

Substances chimiques

Isoniazid V83O1VOZ8L

Types de publication

Systematic Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2292

Informations de copyright

© 2022. The Author(s).

Références

Bull World Health Organ. 2016 Dec 1;94(12):925-930
pubmed: 27994285
Clin Infect Dis. 2003 Dec 15;37(12):1686-92
pubmed: 14689352
Int J Tuberc Lung Dis. 2015 Jul;19(7):799-804
pubmed: 26056104
Ann Rheum Dis. 2018 Nov;77(11):1688-1689
pubmed: 29674320
Medicine (Baltimore). 2016 Aug;95(34):e4126
pubmed: 27559940
Clin Infect Dis. 2018 Sep 14;67(7):1072-1078
pubmed: 29617965
Scand J Caring Sci. 2012 Jun;26(2):313-23
pubmed: 22043979
Am Rev Respir Dis. 1978 Jun;117(6):991-1001
pubmed: 666111
J Int AIDS Soc. 2020 Oct;23(10):e25623
pubmed: 33073520
N Engl J Med. 2018 Aug 2;379(5):440-453
pubmed: 30067931
Am J Respir Crit Care Med. 2000 Sep;162(3 Pt 1):989-93
pubmed: 10988118
Lancet Infect Dis. 2017 May;17(5):e128-e143
pubmed: 28291721
Arch Intern Med. 2000 Mar 13;160(5):697-702
pubmed: 10724056
PLoS Med. 2009 Jul 21;6(7):e1000097
pubmed: 19621072
Lancet. 2015 Dec 5;386(10010):2344-53
pubmed: 26515679
Bull World Health Organ. 2015 Feb 1;93(2):118-24
pubmed: 25883405
Ann Intern Med. 2017 Nov 21;167(10):689-697
pubmed: 29114781
BMC Infect Dis. 2017 Feb 14;17(1):146
pubmed: 28196479
BMC Infect Dis. 2017 Apr 11;17(1):265
pubmed: 28399802
J Antimicrob Chemother. 2019 Jan 1;74(1):218-227
pubmed: 30295760
Am J Respir Crit Care Med. 2009 Jun 1;179(11):1055-60
pubmed: 19299495
Drug Alcohol Depend. 2002 May 1;66(3):283-93
pubmed: 12062463
Public Health Rep. 2019 May/Jun;134(1_suppl):71S-79S
pubmed: 31059418
MMWR Morb Mortal Wkly Rep. 2017 Apr 14;66(14):387-389
pubmed: 28406884
Clin Infect Dis. 2021 Sep 7;73(5):e1135-e1141
pubmed: 33289039
Intern Med J. 2017 Dec;47(12):1433-1436
pubmed: 29224209
Am Rev Respir Dis. 1967 Jun;95(6):935-43
pubmed: 6026165
Int J Tuberc Lung Dis. 2014 Jun;18(6):751
pubmed: 24903950
Eur Respir J. 2015 Apr;45(4):928-52
pubmed: 25792630
N Engl J Med. 2019 Mar 14;380(11):1001-1011
pubmed: 30865794
Pediatrics. 2004 Jun;113(6):e514-9
pubmed: 15173530
J Trop Med. 2011;2011:130976
pubmed: 22131996
Cochrane Database Syst Rev. 2015 May 29;(5):CD003343
pubmed: 26022367
BMJ. 2013 Mar 25;346:f1049
pubmed: 23529982
PLoS One. 2011;6(7):e22276
pubmed: 21789248
Int J Tuberc Lung Dis. 2018 Nov 1;22(11):1344-1349
pubmed: 30355415
Int J Tuberc Lung Dis. 2016 Aug;20(8):1065-71
pubmed: 27393541
MMWR Recomm Rep. 2020 Feb 14;69(1):1-11
pubmed: 32053584
MMWR Morb Mortal Wkly Rep. 2018 Jun 29;67(25):723-726
pubmed: 29953429
Am J Med. 2001 Jun 1;110(8):610-5
pubmed: 11382368
BMJ Open. 2021 May 13;11(5):e047514
pubmed: 33986067
JAMA. 2002 Jul 10;288(2):165-6
pubmed: 12095379
Int J Tuberc Lung Dis. 2013 Dec;17(12):1531-7
pubmed: 24200264
Addiction. 1999 Jul;94(7):1071-5
pubmed: 10707445
N Engl J Med. 2011 Dec 8;365(23):2155-66
pubmed: 22150035
Int J Tuberc Lung Dis. 2012 May;16(5):633-8
pubmed: 22410137

Auteurs

Wendy A Lai (WA)

University of Toronto Department of Family and Community Medicine, Toronto, Canada. wendy.lai@utoronto.ca.

Kaitlyn Brethour (K)

University of Ottawa Department of Chemistry and Biomolecular Science, Ottawa, Canada.

Olivia D'Silva (O)

University of Ottawa School of Epidemiology and Public Health, Ottawa, Canada.

Richard E Chaisson (RE)

Johns Hopkins Center for Tuberculosis Research, Baltimore, USA.

Alice A Zwerling (AA)

University of Ottawa School of Epidemiology and Public Health, Ottawa, Canada.

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