B 小鼠、大鼠和兔生殖实验中,应用25倍人用剂量的头孢唑林,未观察到头孢唑林对上述动物生殖功能和胎仔的有害影响。孕妇妊娠晚期,每8小时静脉注射头孢克洛2g 治疗肾盂肾炎,未发现药物所致胎儿毒性反应。头孢唑林能够转运通过胎盘,进入脐带血和羊水中。妊娠晚期给予500mg头孢唑林,脐带血清药物浓度可达母体血清药物浓度的35%~69%,羊水中药物浓度在用药后2.5小时可达8μg/ml。7例23~32周龄妊娠孕妇静脉注射头孢唑林2g,水肿与非水肿胎儿平均血药浓度分别为18.04μg/ml 和21.02μg/ml,表明水肿并不影响胎儿体内药物转运。一次性静脉注射头孢唑林2g,4小时后乳汁中平均药物浓度达1.2~1.5μg/ml,乳/血药浓度比值为0.02。肌内注射头孢唑林500mg,每日1次或3次,未能在乳汁中检测到药物。 [1]ht p://www.ehs.lil y.com/msds/msds_cefazolin_sodium.html [2]ht p://www.emea.eu.int/pdfs/vet/mrls/012696en.pdf [3]Bernard B,Barton L,Abate M,et al.Maternal-fetal transfer of cefazo lin in thefirst twenty weeks of pregnancy.J Infect Dis.1977;136∶377-82 [4]Brown CEL,Christmas JT,Bawdon RE.Placental transfer of cefazolin and piperacil in in pregnancies remote from term complicated by Rh iso immunization.Am J Obstet Gynecol 1990;163∶938-43 [5]Sanchez-Ramos L,McAlpine KJ,Adair CD,et al.Pyelonephritis in pregnancy:once-a-day ceftriaxone versus multiple doses of cefazolin.A randomized,double-blind trial.Am J Obstet Gynecol.1995;172∶129-33 [6]Yoshioka H,Cho K,Takimato M,et al.Transfer of cefazolin into hu man milk.J Pediatr 1979;94∶151-2
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