Stratov I, Gottlieb T, Bradbury R, O'Kane G M
Department of Microbiology and Infectious Diseases, Concord Repatriation General Hospital, NSW, Australia.
J Infect. 1998 Mar;36(2):203-7. doi: 10.1016/s0163-4453(98)80014-5.
We performed a retrospective review of patient case records to identify risk factors for candidaemia and to assess incidence, management and outcome of candidaemia in an Australian teaching hospital. Between January 1994 and June 1996, 38 cases of candidaemia were identified. The incidence was 0.74 per 1000 admissions of 24 h duration, and 1.54 per 1000 admissions of 5 days or more. The mortality rate was 34%, with eight of 13 (62%) of these deaths attributable to candidaemia. Risk factors included underlying gastrointestinal disease (66%) and recent abdominal surgery (61%), while recent broad spectrum antibiotic use was a contributing factor in 95%. Twenty-nine patients (76%) had a vascular access device in situ at time of detection. This was the apparent source of candidaemia in 28 (97%). Twenty-six (90%) were being used for TPN administration. Of patients receiving TPN, 5.2% developed candidaemia. Standard central venous catheters (CVC) were present in 21 patients (55%), having been in situ for an average of 12.7 days. Eighteen (86%) had been in situ for 7 days or more. Management involved removal of any implicated intravascular device. Thirty of 33 early survivors received antifungal chemotherapy. Therapy with amphotericin B, fluconazole alone or amphotericin B followed by fluconazole was equally effective. Concurrent corticosteroid use and neutropaenia contributed to increased mortality. Candidaemia is not benign. Policies regarding regular changing of central lines, especially in the setting of TPN administration and control of broad spectrum antibiotic use are appropriate measures aimed to reduce incidence. Management involves removal of implicated lines and antifungal chemotherapy. Pre-emptive therapy for candida infection should be considered in selected patients with the likelihood of TPN-related central line sepsis. Fluconazole is an effective alternative to amphotericin B in non-neutropenic patients.
我们对患者病历进行了回顾性研究,以确定念珠菌血症的危险因素,并评估澳大利亚一家教学医院中念珠菌血症的发病率、治疗及转归情况。1994年1月至1996年6月期间,共确诊38例念珠菌血症。发病率为每1000例24小时住院患者中有0.74例,每1000例住院5天及以上患者中有1.54例。死亡率为34%,其中13例死亡中有8例(62%)归因于念珠菌血症。危险因素包括潜在的胃肠道疾病(66%)和近期腹部手术(61%),而近期使用广谱抗生素在95%的病例中是一个促成因素。29例患者(76%)在检测时体内有血管通路装置。这是28例(97%)念珠菌血症的明显来源。26例(90%)用于全胃肠外营养(TPN)给药。接受TPN治疗的患者中,5.2%发生了念珠菌血症。21例患者(55%)有标准中心静脉导管(CVC),平均留置时间为12.7天。18例(86%)留置时间达7天及以上。治疗措施包括移除任何有问题的血管内装置。33例早期存活患者中有30例接受了抗真菌化疗。两性霉素B、单独使用氟康唑或两性霉素B后序贯使用氟康唑的治疗效果相当。同时使用皮质类固醇和中性粒细胞减少会导致死亡率增加。念珠菌血症并非良性疾病。定期更换中心静脉导管的政策,尤其是在TPN给药情况下以及控制广谱抗生素的使用,是旨在降低发病率的适当措施。治疗包括移除有问题的导管和抗真菌化疗。对于有TPN相关中心静脉导管败血症可能性的特定患者,应考虑对念珠菌感染进行抢先治疗。在非中性粒细胞减少患者中,氟康唑是两性霉素B的有效替代药物。