Glycopeptide pharmacokinetics in current paediatric cardiac surgery practice

被引:4
作者
Shime, Nobuaki
Kato, Yuko
Kosaka, Tadashi
Kokufu, Takatoshi
Yamagishi, Masaaki
Fujita, Naohisa
机构
[1] Kyoto Prefectural Univ Med, Dept Intens Care & Anaesthesiol, Kamigyo Ku, Kyoto 6028566, Japan
[2] Kyoto Prefectural Univ Med, Dept Pharm, Kyoto, Japan
[3] Kyoto Prefectural Univ Med, Dept Pediat Cardiac Surg, Kyoto, Japan
[4] Kyoto Prefectural Univ Med, Dept Lab Med, Kyoto, Japan
[5] Kyoto Prefectural Univ Med, Dept Infect Control & Prevent, Kyoto, Japan
关键词
paediatric cardiac surgery; cardiopulmonary bypass; antimicrobial prophylaxis; teicoplanin; vancomycin;
D O I
10.1016/j.ejcts.2007.07.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To examine the evolution of serum concentrations of prophylactic glycopeptides administered during state-of-the-art cardiopulmonary bypass (CPB) and vigorous haemodiafiltration in paediatric patients undergoing cardiac surgery. Methods: We enrolled infants and children < 3 years of age who, based on the preoperative microbiological screening, age and surgical complexity, were at high risk of methicillin-resistant Staphylococcus aureus (MRSA) infection. Antimicrobial prophylaxis with glycopeptides was administered to 22 patients, randomly assigned to vancomycin (VAN; n = 11) versus teicoplanin (TEC; n = 11). Fixed doses of each drug (15 mg/kg for VAN and 8 mg/kg for TEC) were administered immediately before the operation, at the time of priming of the extracorporeal circuit, upon admission to the intensive care unit and for 48 h thereafter, q. 8 h for VAN, and once daily for TEC. Vigorous haemodiafiltration was applied during and briefly after CPB. Results: The second dose of drug added to the prime prevented a fall in serum drug concentrations at the onset of CPB in both groups. A 77% decrease in VAN, versus 53% in TEC concentrations, was observed after the conclusion of CPB. Serum concentrations of TEC > 10 mu g/ml were observed throughout the treatment period in 91% of patients, while 55% of patients assigned to VAN had serum concentrations consistently > 5 p mu g/ml (p=0.08). Therapeutic serum concentrations were maintained throughout the intraoperative period, particularly with TEC, administered before the first surgical incision, followed by a supplemental bolus in the priming fluid of CPB. Postoperative surgical wound infections occurred in neither group. Conclusions: The prophylactic use of glycopeptides in paediatric patients at high risk of MRSA infection undergoing cardiac surgery was safe and effective. TEC might be the drug of choice, since stable, therapeutic serum concentrations were easily maintained throughout the treatment period. (c) 2007 European Association for Cardio-Thoracic Surgery. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:577 / 581
页数:5
相关论文
共 25 条
[1]   Risk factors for surgical site infections after pediatric cardiovascular surgery [J].
Allpress, AL ;
Rosenthal, GL ;
Goodrich, KM ;
Lupinetti, FM ;
Zerr, DM .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2004, 23 (03) :231-234
[2]   The therapeutic monitoring of antimicrobial agents [J].
Begg, EJ ;
Barclay, ML ;
Kirkpatrick, CJM .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1999, 47 (01) :23-30
[3]   Effects of ultrafiltration and peritoneal dialysis on proinflammatory cytokines during cardiopulmonary bypass surgery in newborns and infants [J].
Dittrich, S ;
Aktuerk, D ;
Seitz, S ;
Mehwald, P ;
Schulte-Mönting, J ;
Schlensak, C ;
Kececioglu, D .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2004, 25 (06) :935-940
[4]   The society of thoracic surgeons practice guideline series: Antibiotic prophylaxis in cardiac surgery, part I: Duration [J].
Edwards, FH ;
Engelman, RM ;
Houck, P ;
Shahian, DM ;
Bridges, CR .
ANNALS OF THORACIC SURGERY, 2006, 81 (01) :397-404
[5]  
FREEMAN CD, 1993, ANN PHARMACOTHER, V27, P594
[6]   Timing of vancomycin prophylaxis for cardiac surgery patients and the risk of surgical site infections [J].
Garey, Kevin W. ;
Dao, Thanh ;
Chen, Hua ;
Amrutkar, Paresh ;
Kumar, Nandan ;
Reiter, Margaret ;
Gentry, Layne O. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 58 (03) :645-650
[7]   PHARMACOKINETICS OF INTRAVENOUS VANCOMYCIN IN PEDIATRIC CARDIOPULMONARY BYPASS-SURGERY [J].
HATZOPOULOS, FK ;
STILECALLIGARO, IL ;
RODVOLD, KA ;
SULLIVANBOLYAI, J ;
DELNIDO, P ;
LEVITSKY, S .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1993, 12 (04) :300-304
[8]   Continuous ultrafiltration attenuates the pulmonary injury that follows open heart surgery with cardiopulmonary bypass [J].
Huang, HM ;
Yao, TJ ;
Wang, W ;
Zhu, DM ;
Zhang, W ;
Chen, H ;
Fu, WD .
ANNALS OF THORACIC SURGERY, 2003, 76 (01) :136-140
[9]   Pharmacokinetics of vancomycin administered as prophylaxis before cardiac surgery [J].
Kitzes-Cohen, R ;
Farin, D ;
Piva, G ;
Ivry, S ;
Sharony, R ;
Amar, R ;
Uretzky, G .
THERAPEUTIC DRUG MONITORING, 2000, 22 (06) :661-667
[10]   EFFECT OF CARDIOPULMONARY BYPASS ON VANCOMYCIN AND NETILMICIN DISPOSITION [J].
KLAMERUS, KJ ;
RODVOLD, KA ;
SILVERMAN, NA ;
LEVITSKY, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (05) :631-635