Using the Food and Drug Administration's Sentinel System for surveillance of TB infection

W. L. Walker*, K. M. Schmit, E. C. Welch, L. A. Vonnahme, A. Talwar, M. Nguyen, D. Stojanovic, A. J. Langer, N. M. Cocoros

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

BACKGROUND: We examined patterns in care for individuals treated for latent TB infection (LTBI) in the US Food and Drug Administration's Sentinel System. METHODS : Using administrative claims data, we identified patients who filled standard LTBI treatment prescriptions during 2008-2019. In these cohorts, we assessed LTBI testing, clinical management, and treatment duration. RESULT S : Among 113,338 patients who filled LTBI prescriptions, 80% (90,377) received isoniazid (INH) only, 19% (21,235) rifampin (RIF) only, and 2% (1,726) INH rifapentine (RPT). By regimen, the proportion of patients with documented prior testing for TBI was 79%, 54%, and 91%, respectively. Median therapy duration was 84 days (IQR 35-84) for the 3-month once-weekly INH RPTregimen, 60 days (IQR 30-100) for the 6- to 9-month INH regimen, and 30 days (IQR 2- 60) for the 4-month RIF regimen. CONCLUS IONS : Among the cohorts, INH-only was the most commonly prescribed LTBI treatment. Most persons who filled a prescription for LTBI treatment did not have evidence of completing recommended treatment duration. These data further support preferential use of shorter-course regimens such as INH RPT.

Original languageEnglish
Pages (from-to)1170-1176
Number of pages7
JournalInternational Journal of Tuberculosis and Lung Disease
Volume26
Issue number12
DOIs
Publication statusPublished - 1 Dec 2022
Externally publishedYes

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