Williams D N, Raymond J L
Department of Medicine, Hennepin County Medical Center, Minneapolis, Minnesota, USA.
Clin Pharmacokinet. 1998 Jul;35(1):65-77. doi: 10.2165/00003088-199835010-00005.
Community-based parenteral anti-infective therapy (CoPAT) has, over the past 20 years, increased rapidly in many parts of the world including North America, Europe, South America and Australia. CoPAT is a multidisciplinary activity demanding close cooperation between nurses, pharmacists and physicians, as well as with the patient. The selection of an anti-infective drug for use outside the hospital setting must take into account not only the therapeutic effectiveness, cost effectiveness and safety of the drug, but also pharmacological factors such as the dosage schedule and the stability of the drug. Dosage schedules vary with pharmacokinetic factors (e.g. the use of drugs with long half-lives are favoured by CoPAT programmes) and pharmacodynamic features (e.g. once daily gentamicin therapy is attractive and practical because of concentration-dependent bactericidal killing and prolonged post-antibiotic effect). With selected drugs, the renal and, to a lesser degree, liver function of the patient will influence the dosage schedule. The mode of intravenous (i.v.) drugs administration will vary with volume considerations (limiting the use of syringe-infusion therapy for some drugs), stability issues (prevents drugs that are stable at room temperature for less than 24 hours from being used in multidose computerised delivery systems), as well as patient factors (ability to self administer an i.v. drug). Monitoring serum anti-microbial concentrations is undertaken to assure effectiveness and avoid toxicity, and is indicated for drugs with a narrow therapeutic window, such as the aminoglycosides. With the advent of the single daily dose administration of aminoglycosides, checking serum concentrations at the mid-point, i.e. 6 to 14 hours following administration of the first dose, is one approach. Because the toxic effects of vancomycin have been overstated, serum concentrations should only be obtained for defined indications primarily to assure therapeutic effectiveness.
在过去20年里,基于社区的肠外抗感染治疗(CoPAT)在世界许多地区,包括北美、欧洲、南美和澳大利亚迅速增加。CoPAT是一项多学科活动,需要护士、药剂师和医生以及患者之间密切合作。在医院外环境中选择抗感染药物时,不仅要考虑药物的治疗效果、成本效益和安全性,还要考虑药理学因素,如给药方案和药物稳定性。给药方案因药代动力学因素(例如CoPAT项目更倾向于使用半衰期长的药物)和药效学特征(例如由于浓度依赖性杀菌作用和抗生素后效应延长,庆大霉素每日一次治疗具有吸引力且实用)而有所不同。对于选定的药物,患者的肾功能以及在较小程度上肝功能会影响给药方案。静脉注射药物的给药方式会因容量因素(限制某些药物使用注射器输注疗法)、稳定性问题(防止在室温下稳定性低于24小时的药物用于多剂量计算机给药系统)以及患者因素(自我静脉注射药物的能力)而有所不同。监测血清抗菌浓度是为了确保有效性并避免毒性,适用于治疗窗较窄的药物,如氨基糖苷类药物。随着氨基糖苷类药物每日单次给药的出现,在给药后6至14小时的中点检查血清浓度是一种方法。由于万古霉素的毒性作用被夸大,仅应在明确指征下测定血清浓度,主要是为了确保治疗效果。