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[头孢唑林与头孢呋辛作为心血管手术围手术期抗生素预防用药的前瞻性随机对照研究]

[A prospective, randomized comparative study between cefazolin and cefuroxime as perioperative antibiotic prevention in cardiovascular surgery].

作者信息

Geroulanos S, Oxelbark S, Turina M

出版信息

Schweiz Med Wochenschr. 1984 Mar 3;114(9):297-303.

PMID:6369532
Abstract

In a randomized prospective study, two different regimens of antibiotic prophylaxis have been tested: 4-day cefazolin prophylaxis (Kefzol, 0.5 g every 6 h) compared with 2-day cefuroxime administration (Zinacef, 1.5 g every 12 h). A total of 569 patients in the two groups were studied over a 10 months' period. Hematological, liver-function, serum creatinine and urea measurements were performed preoperatively and repeated daily for the first four days and after one week. At least five chest X-rays were taken during the hospitalization. Body temperature was measured regularly every two hours in the ICU and at least twice daily thereafter. The wounds were examined daily and the patients were carefully observed for other infections. Bacteriological examinations of the tips of all inserted catheters and pacemaker wires were undertaken on removal in the first four months of the trial. Swabs of any tracheal or wound secretion or pus were taken for bacteriological examinations, and blood cultures were performed for any suspected septicemia. Of the 569 patients, 3 had to be withdrawn from the study. Of the assessable patients, 285 received cefuroxime and 281 were given cefazolin. Seven patients (1.2%) died intra- or postoperatively. The total infection rate was 5.5%; 5.7% in the cefazolin group and 5.3% in the cefuroxime group. The overall wound infection rate was 1.8%; 2.5% in the cefazolin group and 1.1% in the cefuroxime group. Septicemia occurred in 0.5%, pneumonia in 11 patients (1.9%); 1.5% in the cefazolin and 2.5% in the cefuroxime group. Seven patients (1.2%) developed a urinary tract infection; 1.4% on the cefazolin group and 1.1% in the cefuroxime group.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项随机前瞻性研究中,对两种不同的抗生素预防方案进行了测试:4天的头孢唑林预防方案(头孢唑林,每6小时0.5克)与2天的头孢呋辛给药方案(头孢呋辛,每12小时1.5克)。在10个月的时间里,对两组共569名患者进行了研究。术前进行血液学、肝功能、血清肌酐和尿素测量,并在头四天每天重复测量,一周后再次测量。住院期间至少拍摄5次胸部X光片。在重症监护病房每两小时定期测量体温,此后每天至少测量两次。每天检查伤口,并仔细观察患者是否有其他感染。在试验的前四个月,对所有插入的导管尖端和起搏器导线进行移除时的细菌学检查。采集任何气管或伤口分泌物或脓液的拭子进行细菌学检查,对任何疑似败血症患者进行血培养。569名患者中,有3名不得不退出研究。在可评估的患者中,285名接受了头孢呋辛,281名接受了头孢唑林。7名患者(1.2%)在术中或术后死亡。总感染率为5.5%;头孢唑林组为5.7%,头孢呋辛组为5.3%。总体伤口感染率为1.8%;头孢唑林组为2.5%,头孢呋辛组为1.1%。败血症发生率为0.5%,肺炎患者11名(1.9%);头孢唑林组为1.5%,头孢呋辛组为2.5%。7名患者(1.2%)发生尿路感染;头孢唑林组为1.4%,头孢呋辛组为1.1%。(摘要截断于250字)

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