PMID- 32915203 OWN - NLM STAT- MEDLINE DCOM- 20211110 LR - 20211110 IS - 1537-6591 (Electronic) IS - 1058-4838 (Linking) VI - 73 IP - 9 DP - 2021 Nov 2 TI - Higher Completion Rates With Self-administered Once-weekly Isoniazid-rifapentine Versus Daily Rifampin in Adults With Latent Tuberculosis. PG - e3459-e3467 LID - 10.1093/cid/ciaa1364 [doi] AB - BACKGROUND: Treatment of latent tuberculosis (LTBI) is important for tuberculosis (TB) prevention, and short course rifamycin-based therapies are preferred. Once-weekly isoniazid-rifapentine by self-administered therapy (3HP-SAT) has never been compared with 4 months of daily rifampin (4R). METHODS: Retrospective cohort study of adults >/=18 years of age initiating LTBI treatment with either 3HP-SAT or 4R in a United States (US)-based TB clinic between 11 April 2016 and 31 December 2018. We evaluated treatment completion through pharmacy fills and reviewed charts for reasons of noncompletion, including adverse events (AEs). The chi 2 test and a log-binomial multivariable model were used to compare treatment completion and AEs. RESULTS: Five hundred sixty individuals (42%) initiated 3HP-SAT and 773 (58%) initiated 4R. Median age was 38, 55% were female, and 89% were born outside of the US. Among those aged 18-49 years, treatment completion with 3HP-SAT was 79% compared to 68% with 4R (adjusted risk ratio [aRR], 1.17 [95% CI, 1.17-1.27]; P < .0001). Among individuals aged >/=50 years, treatment completion with 3HP-SAT was 87% compared to 64% with 4R (aRR, 1.35 [95% CI, 1.19-1.52]; P < .0001). Compared to 4R, there was no difference in risk of AEs in the 18-49 age group (aRR, 0.93 [95% CI, .58-1.48]; P = .75). Reduced risk of AEs was noted among patients aged >/=50 years who received 3HP-SAT (aRR, 0.37 [95% CI, .16-.85]; P = .02). CONCLUSIONS: 3HP-SAT was associated with higher LTBI treatment completion and lower rates of AEs compared to 4R in individuals aged 50 and older. Expanding 3HP-SAT as an option for patients with LTBI may enhance TB prevention strategies in the US. CI - (c) 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. FAU - Haas, Michelle K AU - Haas MK AD - Denver Health and Hospital Authority, Denver Public Health, Denver, Colorado, USA. AD - Division of Infectious Diseases, Department of Medicine, University of Colorado-Denver Anschutz Medical Campus, Aurora, Colorado, USA. FAU - Aiona, Kaylynn AU - Aiona K AD - Denver Health and Hospital Authority, Denver Public Health, Denver, Colorado, USA. FAU - Erlandson, Kristine M AU - Erlandson KM AD - Division of Infectious Diseases, Department of Medicine, University of Colorado-Denver Anschutz Medical Campus, Aurora, Colorado, USA. AD - Division of Geriatric Medicine, Department of Medicine, University of Colorado-Denver Anschutz Medical Campus, Aurora, Colorado, USA. FAU - Belknap, Robert W AU - Belknap RW AD - Denver Health and Hospital Authority, Denver Public Health, Denver, Colorado, USA. AD - Division of Infectious Diseases, Department of Medicine, University of Colorado-Denver Anschutz Medical Campus, Aurora, Colorado, USA. LA - eng PT - Journal Article PL - United States TA - Clin Infect Dis JT - Clinical infectious diseases : an official publication of the Infectious Diseases Society of America JID - 9203213 RN - 0 (Antitubercular Agents) RN - V83O1VOZ8L (Isoniazid) RN - VJT6J7R4TR (Rifampin) RN - XJM390A33U (rifapentine) SB - IM MH - Adult MH - Aged MH - Antitubercular Agents/therapeutic use MH - Drug Administration Schedule MH - Drug Therapy, Combination MH - Female MH - Humans MH - *Isoniazid/therapeutic use MH - *Latent Tuberculosis/drug therapy MH - Middle Aged MH - Retrospective Studies MH - Rifampin/analogs & derivatives/therapeutic use MH - United States/epidemiology OTO - NOTNLM OT - isoniazid OT - latent OT - rifampin OT - rifapentine OT - tuberculosis EDAT- 2020/09/12 06:00 MHDA- 2021/11/11 06:00 CRDT- 2020/09/11 12:12 PHST- 2020/05/06 00:00 [received] PHST- 2020/09/09 00:00 [accepted] PHST- 2020/09/12 06:00 [pubmed] PHST- 2021/11/11 06:00 [medline] PHST- 2020/09/11 12:12 [entrez] AID - 5904201 [pii] AID - 10.1093/cid/ciaa1364 [doi] PST - ppublish SO - Clin Infect Dis. 2021 Nov 2;73(9):e3459-e3467. doi: 10.1093/cid/ciaa1364.