The effect of neutropenia on the clinical pharmacokinetics of vancomycin in adults

万古霉素 中性粒细胞减少症 药代动力学 医学 分配量 剂量 治疗药物监测 发热性中性粒细胞减少症 内科学 外科 化疗 金黄色葡萄球菌 遗传学 生物 细菌
作者
Didi Bury,Rob ter Heine,E.M.W. van de Garde,Marten R. Nijziel,R. J. E. Grouls,Maarten J. Deenen
出处
期刊:European Journal of Clinical Pharmacology [Springer Science+Business Media]
卷期号:75 (7): 921-928 被引量:30
标识
DOI:10.1007/s00228-019-02657-6
摘要

There is accumulating evidence that neutropenic patients require higher dosages of vancomycin. To prevent sub-therapeutic drug exposure, it is of utmost importance to obtain adequate exposure from the first dose onwards. We aimed to quantify the effect of neutropenia on the pharmacokinetics of vancomycin. Data were extracted from a matched patient cohort of patients known with (1) hematological disease, (2) solid malignancy, and (3) patients not known with cancer. Pharmacokinetic analysis was performed using non-linear mixed effects modeling with neutropenia investigated as a binary covariate on clearance and volume of distribution of vancomycin. A total of 116 patients were included (39 hematologic patients, 39 solid tumor patients, and 38 patients not known with cancer). In total, 742 paired time-concentration observations were available for the pharmacokinetic analysis. Presence of neutropenia showed to significantly (p = 0.00157) increase the clearance of vancomycin by 27.7% (95% CI 10.2–46.2%), whereas it did not impact the volume of distribution (p = 0.704). This study shows that vancomycin clearance is increased in patients with neutropenia by 27.7%. Therefore, the vancomycin maintenance dose should be pragmatically increased by 25% in neutropenic patients at the start of treatment. Since the volume of distribution appeared unaffected, no adjustment in loading dose is required. These dose adjustments do not rule out the necessity of further dose individualization by means of therapeutic drug monitoring.
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