Evidence map›Paper›PMID 42062929›Full record

ArticleBMC infectious diseases2026

Prevalence and factors associated with hematological adverse events in RR-TB patients on linezolid-based regimens in Uganda: a multicenter retrospective cohort study.

Esther Apio, Joseph Baruch Baluku, Denis Bwayo, John Peter Masaba, Erias Kirabo, Jasper Kebesu, Oreb Nankunda, Julius Imalingat, Richard Katuramu

Abstract readMulticenter Study
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Esther ApioDepartment of Internal Medicine, Busitema University, Tororo, Uganda. esterapio@gmail.com.
Joseph Baruch BalukuDivision of Pulmonology, Kiruddu National Referral Hospital, Kampala, Uganda.
Denis BwayoDepartment of Internal Medicine, Busitema University, Tororo, Uganda.
John Peter MasabaDepartment of Internal Medicine, Busitema University, Tororo, Uganda.
Erias KiraboDepartment of Internal Medicine, Busitema University, Tororo, Uganda.
Jasper KebesuDepartment of Internal Medicine, Busitema University, Tororo, Uganda.
Oreb NankundaDepartment of Internal Medicine, Busitema University, Tororo, Uganda.
Julius ImalingatDepartment of Internal Medicine, Busitema University, Tororo, Uganda.
Richard KaturamuDepartment of Internal Medicine, Busitema University, Tororo, Uganda.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLinezolid (LZD) is a cornerstone of rifampicin-resistant tuberculosis (RR-TB) treatment, yet its hematological adverse events (AEs), particularly anemia, leukopenia, and thrombocytopenia, remain understudied in resource-limited settings like Uganda. With a high RR-TB burden and comorbidities such as HIV and malnutrition, understanding the prevalence and risk factors of these hematological AEs is critical to improving treatment adherence and outcomes.

aimThis study aimed to determine the prevalence of hematological AEs and identify factors associated with hematological AEs among RR-TB patients receiving LZD-based regimens in Uganda. METHODOLOGY: A multicenter retrospective cohort study was conducted using medical records of RR-TB patients treated with LZD at four Ugandan hospitals (Mbale RRH, Iganga General Hospital, Moroto RRH, and St. Kizito Matany Hospital) from 2020 to 2024. Hematological AEs were defined as anemia (Hb < 12 g/dL in women or < 13 g/dL in men), thrombocytopenia (platelets < 150 × 10³/µL), and leukopenia (WBC < 3.7 × 10⁹/L). Sociodemographic, clinical, and treatment-related data were extracted. A modified Poisson regression model with robust standard errors was used to estimate adjusted prevalence ratios (aPR) and 95% confidence intervals (CI).

resultsAmong 412 patients, 62.9% (259/412) had at least one hematological AE at baseline or during follow-up, and 36.4% (150/412) had hematological AEs first detected after LZD initiation. Among patients with available baseline CBC, 40.0% (98/245) developed incident hematological AEs. First detected anemia, thrombocytopenia, and leukopenia occurred in 21.4% (88/412), 14.8% (61/412), and 13.8% (57/412) of patients, respectively. Rural residence (aPR 1.60, 95% CI 1.11-2.33) and divorced or widowed marital status (aPR 4.10, 95% CI 1.58-10.77) were independently associated with hematological AEs. Patients with hematological AEs had lower treatment success (83.0% vs. 93.5%) and higher loss to follow-up (15.1% vs. 5.9%) than those without AEs.

conclusionHematological AEs were frequent among RR-TB patients receiving LZD in Uganda and were associated with reduced treatment success and increased loss to follow-up, while mortality remained low. Rural residence and divorced or widowed marital status were independently associated with these events, highlighting the need for targeted monitoring in higher-risk groups. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Antitubercular AgentsHematologic DiseasesLinezolidTuberculosis, Multidrug-ResistantAdolescentAdultAnemiaFemaleHumansLeukopeniaMaleMiddle AgedPrevalenceRetrospective StudiesRifampinRisk FactorsAntitubercular AgentsLinezolidRifampinHematological AEsLinezolidMulticenter retrospective cohort studyRifampicin-resistant tuberculosisUganda

Identifiers

PMID42062929
PMCPMC13289349

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.