Drug-associated adverse events in the treatment of multidrug-resistant tuberculosis: an individual patient data meta-analysis

Autor: L Guglielmetti, Maia Kipiani, Petros Isaakidis, SK Brode, Jonathon R. Campbell, Parvaneh Baghaei, Payam Nahid, Rafael Laniado-Laborín, Lorenzo Guglielmetti, Zhiyi Lan, D Falzon, L Barkane, Vicky Chang, Dafne Paiva Rodrigues, D Menzies, R Singla, Denise Rodrigues, Z Lan, Noor Azlinda Ahmad, JR Campbell, R Laniado-Laborín, Jcm Brust, Nafees Ahmad, Christoph Lange, Andrea Benedetti, Dick Menzies, Zarir F Udwadia, P Nahid, Sarah K. Brode, A Benedetti, RR Kempker, P Baghaei, M Kipiani, Liga Kuksa, Rupak Singla, James C.M. Brust, Linda Barkane, Zarir F. Udwadia, Dennis Falzon, L Kuksa, P Isaakidis, Russell R. Kempker, Vwl Chang
Přispěvatelé: Centre d'Immunologie et de Maladies Infectieuses (CIMI), Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Rok vydání: 2020
Předmět:
Male
Collaborative Group for the Meta-Analysis of Individual Patient Data in MDR-TB treatment 2017
Antitubercular Agents
Clofazimine
chemistry.chemical_compound
0302 clinical medicine
Moxifloxacin
Levofloxacin
Tuberculosis
Multidrug-Resistant

030212 general & internal medicine
Diarylquinolines
Lung
ComputingMilieux_MISCELLANEOUS
Incidence
Pulmonary
Multidrug-Resistant
Aminosalicylic Acid
3. Good health
Infectious Diseases
6.1 Pharmaceuticals
Meta-analysis
Public Health and Health Services
Female
Infection
Fluoroquinolones
medicine.drug
Adult
Pulmonary and Respiratory Medicine
Canada
medicine.medical_specialty
Tuberculosis
Drug-Related Side Effects and Adverse Reactions
Clinical Sciences
Article
03 medical and health sciences
Rare Diseases
Internal medicine
medicine
Humans
Adverse effect
Tuberculosis
Pulmonary

Other Medical and Health Sciences
business.industry
Prevention
Linezolid
Evaluation of treatments and therapeutic interventions
Mycobacterium tuberculosis
medicine.disease
[SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology
Discontinuation
Emerging Infectious Diseases
Orphan Drug
Good Health and Well Being
030228 respiratory system
chemistry
Antimicrobial Resistance
Bedaquiline
business
Zdroj: Lancet Respir Med
The Lancet. Respiratory medicine, vol 8, iss 4
The Lancet Respiratory Medicine
The Lancet Respiratory Medicine, Elsevier, 2020, 8 (4), pp.383-394. ⟨10.1016/S2213-2600(20)30047-3⟩
ISSN: 2213-2600
2213-2619
DOI: 10.1016/s2213-2600(20)30047-3
Popis: We regret that this article is behind a paywall.
BACKGROUND: Treatment of multidrug-resistant tuberculosis requires long-term therapy with a combination of multiple second-line drugs. These drugs are associated with numerous adverse events that can cause severe morbidity, such as deafness, and in some instances can lead to death. Our aim was to estimate the absolute and relative frequency of adverse events associated with different tuberculosis drugs to provide useful information for clinicians and tuberculosis programmes in selecting optimal treatment regimens. METHODS: We did a meta-analysis using individual-level patient data that were obtained from studies that reported adverse events that resulted in permanent discontinuation of anti-tuberculosis medications. We used a database created for our previous meta-analysis of multidrug-resistant tuberculosis treatment and outcomes, for which we did a systematic review of literature published between Jan 1, 2009, and Aug 31, 2015 (updated April 15, 2016), and requested individual patient-level information from authors. We also considered for this analysis studies contributing patient-level data in response to a public call made by WHO in 2018. Meta-analysis for proportions and arm-based network meta-analysis were done to estimate the incidence of adverse events for each tuberculosis drug. FINDINGS: 58 studies were identified, including 50 studies from the updated individual patient data meta-analysis for multidrug-resistant tuberculosis treatment. 35 of these studies, with 9178 patients, were included in our analysis. Using meta-analysis of proportions, drugs with low risks of adverse event occurrence leading to permanent discontinuation included levofloxacin (1·3% [95% CI 0·3-5·0]), moxifloxacin (2·9% [1·6-5·0]), bedaquiline (1·7% [0·7-4·2]), and clofazimine (1·6% [0·5-5·3]). Relatively high incidence of adverse events leading to permanent discontinuation was seen with three second-line injectable drugs (amikacin: 10·2% [6·3-16·0]; kanamycin: 7·5% [4·6-11·9]; capreomycin: 8·2% [6·3-10·7]), aminosalicylic acid (11·6% [7·1-18·3]), and linezolid (14·1% [9·9-19·6]). Risk of bias in selection of studies was judged to be low because there were no important differences between included and excluded studies. Variability between studies was significant for most outcomes analysed. INTERPRETATION: Fluoroquinolones, clofazimine, and bedaquiline had the lowest incidence of adverse events leading to permanent drug discontinuation, whereas second-line injectable drugs, aminosalicylic acid, and linezolid had the highest incidence. These results suggest that close monitoring of adverse events is important for patients being treated for multidrug-resistant tuberculosis. Our results also underscore the urgent need for safer and better-tolerated drugs to reduce morbidity from treatment itself for patients with multidrug-resistant tuberculosis.
Databáze: OpenAIRE