Tuberculosis Diagnosis and Preventive Monotherapy Among Children and Adolescents Exposed to Rifampicin-Resistant Tuberculosis in the Household

Author:

Apolisi Ivy1,Cox Helen2,Tyeku Nolitha1,Daniels Johnny1,Mathee Shaheed3,Cariem Rabia4,Douglas-Jones Bianca1,Ngambu Noluvo3,Mudaly Vanessa3,Mohr-Holland Erika1,Isaakidis Petros5ORCID,Pfaff Colin1,Furin Jennifer6,Reuter Anja1

Affiliation:

1. Médecins Sans Frontières, Khayelitsha , Cape Town , South Africa

2. Institute of Infectious Disease and Molecular Medicine and Wellcome Centre for Infectious Disease Research, Division of Medical Microbiology, University of Cape Town , Cape Town , South Africa

3. Western Cape Province Department of Health , Cape Town , South Africa

4. City of Cape Town Department of Health , Cape Town , South Africa

5. Médecins Sans Frontières, Southern Africa Medical Unit , Cape Town , South Africa

6. Global Health and Social Medicine, Harvard Medical School , Boston, Massachusetts , USA

Abstract

AbstractBackgroundChildren and adolescents with household exposure to multidrug- or rifampicin-resistant tuberculosis (MDR/RR-TB) are at high risk of developing TB disease. Tuberculosis preventive therapy (TPT) is recommended, but programmatic experience is limited, particularly for adolescents.MethodsWe conducted a prospective cohort study to describe MDR/RR-TB diagnosis and TPT provision for individuals aged <18 years with MDR/RR-TB exposure. Participants were assessed for TB either in homes or health facilities, with referral for chest x-ray or specimen collection at clinician discretion. The TPT regimens included levofloxacin, isoniazid, or delamanid monotherapy for 6 months, based on source patient drug-resistance profile.ResultsBetween March 1, 2020 and July 31, 2021, 112 participants were enrolled; median age was 8.5 years, 57 (51%) were female, and 6 (5%) had human immunodeficiency virus. On screening, 11 (10%) were diagnosed with TB: 10 presumptive MDR/RR-TB and 1 drug-susceptible TB. Overall, 95 (94% of 101) participants started TPT: 79 with levofloxacin, 9 with isoniazid, and 7 with delamanid. Seventy-six (80%) completed TPT, 12 (13%) were lost to follow up, and 7 (7%) stopped TPT early due to adverse events. Potential adverse events were reported for 12 (13%) participants; none were serious. There were no further TB diagnoses (200 days median follow up).ConclusionsPost-MDR/RR-TB exposure management for children and adolescents resulted in significant MDR/RR-TB detection and both high TPT initiation and completion. Tuberculosis preventive monotherapy was well tolerated and there were no further TB diagnoses after initial assessment. Key factors supporting these outcomes included use of pediatric formulations for young children, monotherapy, and community-based options for assessment and follow up.

Funder

Médecins Sans Frontières

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

Reference38 articles.

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