Trifilio S, Verma A, Mehta J
Pharmacy Department, Northwestern Memorial Hospital, Chicago, IL 60611, USA.
Bone Marrow Transplant. 2004 Apr;33(7):735-9. doi: 10.1038/sj.bmt.1704423.
Antimicrobial agents are commonly used after hematopoietic stem cell transplant (HSCT) to prevent bacterial, viral and fungal infections. A pharmacy practice survey was undertaken to evaluate prevailing practices. The 31 centers evaluated transplanted over 3400 patients in 2001. Over half used bacterial prophylaxis; all with fluoroquinolones. A significantly higher proportion (90-100%) used fungal and viral prophylaxis. Most centers used fluconazole for fungal prophylaxis, but the dose used varied from 400 mg (the recommended dose) to 100 mg. Itraconazole and amphotericin preparations were used by some centers for allograft recipients because of their activity against aspergillosis. Most centers used brief viral prophylaxis for autograft recipients aimed at preventing HSV reactivation. Viral prophylaxis for allograft recipients was usually much more prolonged, reflecting concern over cytomegalovirus infections. Overall, there was significant deviation from recommended guidelines in many of the practices. Our survey suggests that substantial variation exists among transplant centers in their approach to antimicrobial prophylaxis after HSCT. This probably stems from the lack of definitive studies and strong recommendations in several areas, availability of newer agents that have not been adequately studied in the HSCT setting, and a desire to improve outcome before definitive studies are available for newer agents, a process that could take several years.
造血干细胞移植(HSCT)后通常会使用抗菌药物来预防细菌、病毒和真菌感染。开展了一项药学实践调查以评估当前的做法。2001年,接受评估的31个中心共为超过3400名患者进行了移植。超过半数的中心使用了细菌预防用药;均使用氟喹诺酮类药物。使用真菌和病毒预防用药的比例显著更高(90 - 100%)。大多数中心使用氟康唑进行真菌预防,但使用剂量从400毫克(推荐剂量)到100毫克不等。一些中心因伊曲康唑和两性霉素制剂对曲霉病有活性,而将其用于同种异体移植受者。大多数中心对自体移植受者进行短期病毒预防,旨在预防单纯疱疹病毒再激活。对同种异体移植受者的病毒预防通常持续时间长得多,这反映出对巨细胞病毒感染的担忧。总体而言,许多做法与推荐指南存在显著偏差。我们的调查表明,移植中心在HSCT后抗菌预防的方法上存在很大差异。这可能源于几个领域缺乏确定性研究和强有力的推荐,有一些在HSCT环境中未得到充分研究的新型药物可供使用,以及在新型药物有确定性研究结果(这一过程可能需要数年时间)之前希望改善治疗结果的愿望。