Skeletal muscle and plasma concentrations of cefazolin during cardiac surgery in infants

被引:22
|
作者
Himebauch, Adam S. [1 ,2 ]
Nicolson, Susan C. [1 ]
Sisko, Martha [1 ]
Moorthy, Ganesh [2 ]
Fuller, Stephanie [3 ]
Gaynor, J. William [3 ]
Zuppa, Athena F. [1 ,2 ]
Fox, Elizabeth [2 ,4 ,5 ]
Kilbaugh, Todd J. [1 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Anesthesiol & Crit Care Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Ctr Clin Pharmacol, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Div Cardiothorac Surg, Dept Surg, Philadelphia, PA 19104 USA
[4] Univ Penn, Perelman Sch Med, Div Oncol, Dept Pediat, Philadelphia, PA 19104 USA
[5] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
来源
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY | 2014年 / 148卷 / 06期
关键词
SURGICAL SITE INFECTIONS; PEDIATRIC CARDIOVASCULAR-SURGERY; RISK-FACTORS; CARDIOPULMONARY BYPASS; ANTIBIOTIC PENETRATION; IN-VIVO; PHARMACOKINETICS; CHILDREN; TISSUE; MICRODIALYSIS;
D O I
10.1016/j.jtcvs.2014.06.064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To describe the pharmacokinetics and tissue disposition of prophylactic cefazolin into skeletal muscle in a pediatric population undergoing cardiac surgery. Methods: The subjects included 12 children, with a median age of 146 days (interquartile range, 136-174) and median weight of 5.5 kg (interquartile range, 5.2-7.3) undergoing cardiac surgery and requiring cardiopulmonary bypass with or without deep hypothermic circulatory arrest. Institutional cefazolin at standard doses of 25 mg/kg before incision and 25 mg/kg in the bypass prime solution were administered. Serial plasma and skeletal muscle microdialysis samples were obtained intraoperatively and the unbound cefazolin concentrations measured. Noncompartmental pharmacokinetic analyses were performed and the tissue disposition evaluated. Results: After the first dose of cefazolin, the skeletal muscle concentrations peaked at a median microdialysis collection interval of 30 to 38.5 minutes. After the second dose, the peak concentrations were delayed a median of 94 minutes in subjects undergoing deep hypothermic circulatory arrest. Skeletal muscle exposure to cefazolin measured by the area under concentration time curve 0-last measurement was less in the subjects who underwent deep hypothermic circulatory arrest than in those who received cardiopulmonary bypass alone (P = .04). The skeletal muscle concentrations of cefazolin exceeded the goal concentrations for methicillin-sensitive Staphylococcus aureus prophylaxis; however, the goal concentrations for gram-negative pathogens associated with surgical site infections were achieved only 42.1% to 84.2% and 0% to 11.2% of the intraoperative time in subjects undergoing cardiopulmonary bypass alone or deep hypothermic circulatory arrest, respectively. Conclusions: This cefazolin dosing strategy resulted in skeletal muscle concentrations that are likely not effective for surgical prophylaxis against gram-negative pathogens but are effective against methicillinsensitive S aureus in infants undergoing cardiac surgery.
引用
收藏
页码:2634 / 2641
页数:8
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