Transplant and Oncology Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Curr Opin Infect Dis. 2011 Aug;24(4):344-9. doi: 10.1097/QCO.0b013e328348b379.
Infection remains a major cause of morbidity and mortality following transplantation, and antimicrobial prophylaxis regimens continue to improve. This review summarizes the important studies on prophylaxis following solid organ transplant (SOT) and hematopoietic stem cell transplantation (HSCT) published in the last 18 months.
Many transplant centers use 100 days of antivirals to prevent cytomegalovirus (CMV) disease after SOT. Randomized trials comparing 100-day regimens to 200 days in high-risk kidney recipients and 12 months in lung transplant patients showed distinct advantages of longer duration CMV prophylaxis. Prevention of hepatitis B virus after transplant is changing as regimens with low dose or no hepatitis B immunoglobulin are being evaluated. International consensus guidelines on the prevention of infection after stem cell transplantation are summarized and newer studies on the prevention of invasive fungal infection in this population are reviewed.
In organ transplantation, routine antibacterial, antiviral, and antifungal regimens need to be tailored to address donor-transmitted infections, serological risk status of recipients, and measurable antifungal drug levels. Recent studies indicate that longer duration prophylaxis for CMV may have advantages in high-risk SOT recipients. After HSCT, regimens require adjustment based on immunological risks associated with transplant type and presence of graft vs. host disease.
感染仍然是移植后发病率和死亡率的主要原因,抗菌预防方案仍在不断改进。本综述总结了过去 18 个月中发表的关于实体器官移植(SOT)和造血干细胞移植(HSCT)后预防的重要研究。
许多移植中心使用 100 天的抗病毒药物预防 SOT 后的巨细胞病毒(CMV)病。在高危肾移植受者中比较 100 天方案与 200 天方案以及在肺移植患者中比较 12 个月方案的随机试验表明,更长时间 CMV 预防的明显优势。随着低剂量或无乙型肝炎免疫球蛋白的方案的评估,移植后乙型肝炎病毒的预防正在发生变化。总结了关于干细胞移植后感染预防的国际共识指南,并综述了该人群中侵袭性真菌感染预防的最新研究。
在器官移植中,常规的抗菌、抗病毒和抗真菌方案需要根据供体传播感染、受者的血清学风险状况和可测量的抗真菌药物水平进行调整。最近的研究表明,高危 SOT 受者的 CMV 更长时间预防可能具有优势。在 HSCT 后,根据与移植类型相关的免疫风险以及移植物抗宿主病的存在,需要调整方案。