Early antituberculosis drug exposure in hospitalized patients with human immunodeficiency virus‐associated tuberculosis
Autor: | Lubbe Wiesner, Muki Shey, Robert J. Wilkinson, Helen McIlleron, Charlotte Schutz, Graeme Meintjes, Amy Ward, Paolo Denti, David A Barr, Rosie Burton, Gary Maartens, Saskia Janssen, Maxwell Chirehwa |
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Přispěvatelé: | Academic Medical Center, APH - Health Behaviors & Chronic Diseases, APH - Global Health, Wellcome Trust |
Rok vydání: | 2020 |
Předmět: |
Male
Antitubercular Agents HIV Infections 030226 pharmacology & pharmacy 0302 clinical medicine Pharmacology (medical) Pharmacology & Pharmacy 030212 general & internal medicine human immunodeficiency virus treatment Isoniazid 3. Good health TB tuberculosis Cohort Original Article Female 1115 Pharmacology and Pharmaceutical Sciences Life Sciences & Biomedicine pharmacokinetics medicine.drug Adult medicine.medical_specialty Tuberculosis PULMONARY TUBERCULOSIS Cmax METABOLISM Sepsis 03 medical and health sciences SEMIMECHANISTIC MODEL Pharmacokinetics Internal medicine medicine Humans COHORT RIFAMPIN Pharmacology Science & Technology SEPSIS business.industry MORTALITY HIV WORLDWIDE HIV Original Articles Pyrazinamide medicine.disease business Rifampicin |
Zdroj: | British Journal of Clinical Pharmacology British journal of clinical pharmacology, 86(5), 966-978. Wiley-Blackwell BRITISH JOURNAL OF CLINICAL PHARMACOLOGY |
ISSN: | 1365-2125 0306-5251 |
Popis: | AIMS Patients hospitalized at the time of human immunodeficiency virus-associated tuberculosis (HIV-TB) diagnosis have high early mortality. We hypothesized that compared to outpatients, there would be lower anti-TB drug exposure in hospitalized HIV-TB patients, and amongst hospitalized patients exposure would be lower in patients who die or have high lactate (a sepsis marker). METHODS We performed pharmacokinetic sampling in hospitalized HIV-TB patients and outpatients. Plasma rifampicin, isoniazid and pyrazinamide concentrations were measured in samples collected predose and at 1, 2.5, 4, 6 and 8 hours on the third day of standard anti-TB therapy. Twelve-week mortality was ascertained for inpatients. Noncompartmental pharmacokinetic analysis was performed. RESULTS Pharmacokinetic data were collected in 59 hospitalized HIV-TB patients and 48 outpatients. Inpatient 12-week mortality was 11/59 (19%). Rifampicin, isoniazid and pyrazinamide exposure was similar between hospitalized and outpatients (maximum concentration [Cmax ]: 7.4 vs 8.3 μg mL-1 , P = .223; 3.6 vs 3.5 μg mL-1 , P = .569; 50.1 vs 46.8 μg mL-1 , P = .081; area under the concentration-time curve from 0 to 8 hours: 41.0 vs 43.8 mg h L-1 , P = 0.290; 13.5 vs 12.4 mg h L-1 , P = .630; 316.5 vs 292.2 mg h L-1 , P = .164, respectively) and not lower in inpatients who died. Rifampicin and isoniazid Cmax were below recommended ranges in 61% and 39% of inpatients and 44% and 35% of outpatients. Rifampicin exposure was higher in patients with lactate >2.2 mmol L-1 . CONCLUSION Mortality in hospitalized HIV-TB patients was high. Early anti-TB drug exposure was similar to outpatients and not lower in inpatients who died. Rifampicin and isoniazid Cmax were suboptimal in 61% and 39% of inpatients and rifampicin exposure was higher in patients with high lactate. Treatment strategies need to be optimized to improve survival. |
Databáze: | OpenAIRE |
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