Adverse drug reactions, particularly liver disorders, drive interruptions in anti‐tuberculosis treatment: A retrospective cohort study
Eleanor G. Dixon, Evita Biraua, Edvards Brencsēns, Vitālijs Pašuks, Vija Riekstina, Anete Šperberga, Marisa D. Muckian, James W. Dear, Liga Kuksa, Derek J. Sloan, Helen R. Stagg

TL;DR
This study shows that liver-related side effects from anti-tuberculosis drugs are a major reason patients miss doses, leading to treatment interruptions.
Contribution
The study identifies hepatobiliary adverse drug reactions as the primary cause of missed doses in anti-TB treatment and quantifies their impact.
Findings
31% of patients missed doses due to adverse drug reactions.
Hepatobiliary disorders caused the longest and least frequent missed dose periods.
ADRs contributed to 20.9% of all missed doses in the study.
Abstract
Adverse drug reactions (ADRs) are a key driver of missed doses of anti‐tuberculosis (TB) therapy. We aimed to determine the relative burden of ADR‐driven missed doses, the missed dose patterns associated with ADRs, and the association between specific ADRs and missed doses. In this retrospective cohort study, adults (≥18 years) who began the standard 6‐month drug‐sensitive anti‐TB regimen in an outpatient facility in Riga, Latvia (May 2015–September 2022) and missed at least one dose of treatment were included. Data were collected from medical records and observed therapy records. Missed doses were subdivided into early discontinuation or sporadically missed. Descriptive analyses and lasagne plots were used. Across 174 patients, 54 (31.0%, CI: 24.2–37.9%) missed doses due to ADRs. Of 31 320 doses, 4217 (13.5%, CI: 13.1–13.9%) were missed, 20.9% (880/4217, CI: 19.6–22.1%) were due to…
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Taxonomy
TopicsDrug-Induced Hepatotoxicity and Protection · Pharmacogenetics and Drug Metabolism · Pharmacological Effects and Toxicity Studies
