Increased risk of adverse drug reactions by higher linezolid dose per weight in multidrug-resistant tuberculosis.

MDR-TB adverse drug reactions anaemia drug concentrations leukopenia linezolid peripheral neuropathy thrombocytopenia

Journal

International journal of antimicrobial agents
ISSN: 1872-7913
Titre abrégé: Int J Antimicrob Agents
Pays: Netherlands
ID NLM: 9111860

Informations de publication

Date de publication:
13 Aug 2024
Historique:
received: 10 04 2024
revised: 12 07 2024
accepted: 02 08 2024
medline: 16 8 2024
pubmed: 16 8 2024
entrez: 15 8 2024
Statut: aheadofprint

Résumé

Linezolid treatment has a high risk of toxicity and adverse drug reactions (ADR) are frequent. Few studies have investigated risk factors of major ADRs separately, therefore, we aimed to evaluate major ADRs including peripheral neuropathy in relation to risk factors and drug concentration levels of linezolid in a high-resource setting for multidrug-resistant tuberculosis (MDR-TB). We conducted a retrospective cohort study including participants treated with a linezolid-containing MDR-TB regimen in Sweden 1992-2018. Data was collected from medical records. ADRs were classified according to Common Terminology Criteria for Adverse Events (version 5.0). Of all participants (n=132), 43.2% were female and the median age 28 years. The median linezolid treatment was 6.5 months (IQR 3.0-12.7) with a median daily dose of 9.6 mg/kg/day. Any ADR was seen in 58.3% (n=77) of participants, with 35.6% having peripheral neuropathy (n=47), 27.3% anaemia (n=36), 22.0% leukopenia (n=36) while 6.1% (n=8) had optic neuritis. The median time for peripheral neuropathy was 3.6 months (IQR 2.1-5.9) and 8.3 months (6.2-10.7) for optic neuritis. A >2.0 mg/L trough concentration (n=40) was associated with anaemia (p=0.0038) and thrombocytopenia (p=0.009) but not with peripheral neuropathy. In multivariable analysis, a dose ≥12 mg/kg/day was associated with time to peripheral neuropathy (HR 2.89, 95%CI 1.08-7.74, p=0.035), anaemia (HR 6.62, 95%CI 2.22-19.8, p=0.001) and leukopenia (HR 5.23, 95% CI 1.48-18.5, p=0.010). Linezolid ADRs were frequent in a high-resource setting. Structured, regular follow-up for ADRs and adjusting dosing according to body weight followed-up by monitoring of drug concentrations early may reduce toxicity.

Identifiants

pubmed: 39146999
pii: S0924-8579(24)00218-8
doi: 10.1016/j.ijantimicag.2024.107302
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107302

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Competing Interests JJ is heading the Swedish national advisory board on MDR-TB and other difficult to treat cases and JB, LDF and TS are also members of the advisory board. JW is the scientific secretary in the EUCAST steering committee on antimycobacterial susceptibility testing, which is an unpaid position. JWA has been giving lectures on an infectious diseases conference on therapeutic drug monitoring for linezolid and received an educational fee from Pfizer. JB received a payment fee for lectures on Post-COVID by Astra Zeneca and Novartis. JK, AO, MS, MM, and RG have no conflict of interest to declare.

Auteurs

Johanna Kuhlin (J)

Karolinska Institutet, Department of Medicine, Solna, Division of Infectious Diseases, Stockholm, Sweden; Karolinska University Hospital, Department of Infectious Diseases, Stockholm, Sweden. Electronic address: Johanna.kuhlin@ki.se.

Lina Davies Forsman (LD)

Karolinska Institutet, Department of Medicine, Solna, Division of Infectious Diseases, Stockholm, Sweden; Karolinska University Hospital, Department of Infectious Diseases, Stockholm, Sweden. Electronic address: lina.davies.forsman@ki.se.

Aisha Osman (A)

Karolinska Institutet, Department of Medicine, Solna, Division of Infectious Diseases, Stockholm, Sweden. Electronic address: aisha-deeqa.osman@hotmail.com.

Magdalena Skagerberg (M)

Karolinska University Hospital, Department of Infectious Diseases, Stockholm, Sweden. Electronic address: Magdalena.skagerberg@regionstockholm.se.

Jerker Jonsson (J)

Public Health Agency of Sweden, Department of Public Health Analysis and Data Management, Stockholm, Sweden. Electronic address: jerker.jonsson@folkhalsomyndigheten.se.

Ramona Groenheit (R)

Public Health Agency of Sweden, Department of Microbiology, Stockholm, Sweden. Electronic address: Ramona.groenheit@folkhalsomyndigheten.se.

Mikael Mansjö (M)

Public Health Agency of Sweden, Department of Microbiology, Stockholm, Sweden. Electronic address: Mikael.mansjo@folkhalsomyndigheten.se.

Jim Werngren (J)

Public Health Agency of Sweden, Department of Microbiology, Stockholm, Sweden. Electronic address: jim.werngren@folkhalsomyndigheten.se.

Jan-Willem Alffenaar (JW)

University of Sydney, Faculty of Medicine and Health, Sydney, NSW, Australia; Westmead Hospital, Research and Education Network, Sydney, NSW, Australia; The University of Sydney, Institute for Infectious Diseases (Sydney ID), Sydney, NSW, Australia. Electronic address: Johannes.alffenaar@sydney.edu.au.

Thomas Schön (T)

Linköping University, Department of Biomedical and Clinical Sciences, Linköping, Sweden; Linköping University Hospital, Department of Microbiology, Linköping, Sweden; Kalmar County Hospital, Department of Clinical Microbiology and Infectious Diseases, Kalmar, Sweden. Electronic address: Thomas.schon@liu.se.

Judith Bruchfeld (J)

Karolinska Institutet, Department of Medicine, Solna, Division of Infectious Diseases, Stockholm, Sweden; Karolinska University Hospital, Department of Infectious Diseases, Stockholm, Sweden. Electronic address: Judith.bruchfeld@ki.se.

Classifications MeSH