Bos Jeannet C, van Hest Reinier M, Prins Jan M
*Department of Internal Medicine, Division of Infectious Diseases, Academic Medical Centre, University of Amsterdam; and†Department of Hospital Pharmacy, Division of Clinical Pharmacology, Academic Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.
Ther Drug Monit. 2017 Aug;39(4):387-398. doi: 10.1097/FTD.0000000000000418.
In sub-Saharan Africa (SSA), severe febrile illness accounts for a large majority of medical admissions. SSA patients may also suffer from cachexia and organ dysfunction resulting from tuberculosis, hepatitis B, and hypertension. It is hard to tell how these conditions influence the pharmacokinetics (PK) of antibiotics in this population. The aim of this systematic review was to summarize antibiotic PK data of SSA adult patient populations to clarify whether inappropriate drug concentrations that may also lead to antimicrobial resistance are likely to occur.
An electronic search was conducted in Ovid MEDLINE, Embase, and the African Index Medicus collecting studies from 1946 to May 2016. Reviewers independently selected studies reporting outcome data on volume of distribution (V), clearance, and half-life. Relevant information was abstracted and quality assessed.
Twelve studies were selected, addressing 6 antibiotic classes. There were 6 studies on fluoroquinolones and 1 on β-lactam antibiotics. Nine out of 12 originated from South Africa and 6 of those dealt with intensive care unit (ICU) populations. The quality of most studies was low. Studies on amikacin, teicoplanin, and ertapenem (n = 4) displayed a pattern of a large V with low drug concentrations. Fluoroquinolone PK changes were less prominent and more diverse whereas the probability of pharmacodynamic target attainment was low for the treatment of tuberculosis in South Africa. Interindividual variability of V was high for 10/12 studies.
Antibiotic PK data of SSA adult patient populations are scarce, but disease-induced inappropriate drug concentrations do occur. Data from non-ICU, severely ill patients, and β-lactam data are particularly lacking, whereas β-lactam antibiotics are commonly used, and typically vulnerable to disease-induced PK changes. Studies investigating the PK and pharmacodynamics of β-lactam antibiotics in severely ill, adult SSA patient populations are needed to improve local antibiotic dosing strategies.
在撒哈拉以南非洲地区(SSA),严重发热性疾病占医疗入院病例的绝大部分。SSA地区的患者还可能患有由结核病、乙型肝炎和高血压导致的恶病质和器官功能障碍。很难说这些情况如何影响该人群中抗生素的药代动力学(PK)。本系统评价的目的是总结SSA成年患者群体的抗生素PK数据,以阐明是否可能出现也可能导致抗菌药物耐药性的不适当药物浓度。
在Ovid MEDLINE、Embase和《非洲医学索引》中进行电子检索,收集1946年至2016年5月的研究。评审人员独立选择报告分布容积(V)、清除率和半衰期结果数据的研究。提取相关信息并进行质量评估。
共选择了12项研究,涉及6类抗生素。有6项关于氟喹诺酮类的研究和1项关于β-内酰胺类抗生素的研究。12项研究中有9项来自南非,其中6项涉及重症监护病房(ICU)人群。大多数研究的质量较低。关于阿米卡星、替考拉宁和厄他培南的研究(n = 4)显示出V大且药物浓度低的模式。氟喹诺酮类PK变化不太显著且更为多样,而在南非治疗结核病时达到药效学靶点的概率较低。12项研究中有10项V的个体间变异性较高。
SSA成年患者群体的抗生素PK数据稀缺,但确实会出现疾病导致的不适当药物浓度。尤其缺乏非ICU重症患者的数据和β-内酰胺类数据,而β-内酰胺类抗生素常用且通常易受疾病导致的PK变化影响。需要开展研究来调查SSA成年重症患者群体中β-内酰胺类抗生素的PK和药效学,以改进当地的抗生素给药策略。