Plasma and CSF pharmacokinetic characteristics of second-line anti-tuberculosis drugs in a patient with multidrug-resistant tuberculous meningitis
The treatment of multidrug-resistant tuberculous meningitis (MDR-TBM) presents significant challenges, as the ability of different anti-tuberculosis (anti-TB) drugs to penetrate the blood-brain barrier varies greatly. The pharmacokinetic characteristics of second-line anti-TB drugs including bedaquiline, cycloserine, moxifloxacin and contezolid remains unclear, particularly in cerebrospinal fluid (CSF). We report a case of a 30-year-old female who was diagnosed with MDR-TBM. Therapeutic drug monitoring (TDM) was used to determine whether each anti-TB drug’s peak concentration reached the effective range, and concentrations of each anti-TB drug in plasma and CSF of the patient after 5, 7, 9 and 12 h of medication was detected, the CSF/plasma concentration ratio of each anti-TB drug was also analyzed. TDM plays an important role in clinical individualized medication adjustment. Cycloserine, pyrazinamide, contezolid and moxifloxacin may have a high CSF permeability. This study provided valuable reference for the clinical management of MDR-TBM by measuring the plasma and CSF concentrations of anti-TB drugs.
Authors
- Y Chen (ORCID: https://orcid.org/0009-0006-1086-8243)
- Huijie Wang (ORCID: https://orcid.org/0000-0001-5020-5475)
- Jinlong Gao (ORCID: https://orcid.org/0000-0002-5386-0886)
- Xinjun Cai (ORCID: https://orcid.org/0009-0007-1841-6994)
- Jie Cao (ORCID: https://orcid.org/0000-0003-1555-7795)
- Jinmeng Li (ORCID: https://orcid.org/0000-0001-6589-3610)
- Xiaohong Pan (ORCID: https://orcid.org/0000-0003-3241-0250)
Institutions
- Hangzhou Normal University (CN)
- Integrated Chinese Medicine (China) (HK)
- Hangzhou Hospital of Traditional Chinese Medicine (CN)
Publication Details
- Journal
- BMC Infectious Diseases
- Published
- 2025-11-21
- DOI
- https://doi.org/10.1186/s12879-025-12052-5
- Primary Topic
- Infectious Diseases and Tuberculosis
- Type
- article
- Field-Weighted Citation Impact
- 0.00