Morris Aisha M, Schneider Philip J, Pedersen Craig A, Mirtallo Jay M
College of Pharmacy and Health Sciences, Texas Southern University, Houston, USA.
Am J Health Syst Pharm. 2003 Dec 15;60(24):2567-76. doi: 10.1093/ajhp/60.24.2567.
The compliance of hospitals' quality assurance practices for pharmacy-compounded sterile preparations with the American Society of Health-System Pharmacists (ASHP) Guidelines on Quality Assurance for Pharmacy-Prepared Sterile Products was studied. A survey based on the 2000 ASHP guidelines was developed to determine current practices for compounding sterile preparations in hospital pharmacies. Practices were compared with those identified in a 1995 ASHP survey. The survey was mailed in July 2002 to a stratified random sample of 600 hospital pharmacy directors. There were a total of 182 usable responses, for a net response rate of 30.3%. Quality assurance practices for some quality domains showed low compliance with the 2000 ASHP guidelines. Only 5.2% of pharmacies that compounded risk level 1 preparations were compliant with garb requirements. Only 4.7% of pharmacies compounding risk level 3 preparations were compliant with recommendations for documentation. Compliance with guidelines on the use of resources to determine expiration dates was high (95.5%). Hospitals were moderately compliant with guidelines related to personnel training (62.7%) and labeling (61.1%). Although some improvements were observed, hospital pharmacies in 2002 were still not fully compliant with the ASHP Guidelines on Quality Assurance for Pharmacy-Prepared Sterile Products.
研究了医院药房配制的无菌制剂的质量保证实践与美国卫生系统药师协会(ASHP)《药房配制无菌产品质量保证指南》的符合情况。基于2000年ASHP指南开展了一项调查,以确定医院药房配制无菌制剂的现行做法。将这些做法与1995年ASHP调查中确定的做法进行了比较。该调查于2002年7月邮寄给600名医院药房主任的分层随机样本。总共收到182份有效回复,净回复率为30.3%。一些质量领域的质量保证实践对2000年ASHP指南的符合率较低。配制风险等级1制剂的药房中,只有5.2%符合着装要求。配制风险等级3制剂的药房中,只有4.7%符合文件记录建议。在使用资源确定有效期方面,对指南的符合率较高(95.5%)。医院在人员培训(62.7%)和标签(61.1%)相关指南方面的符合程度中等。尽管观察到一些改进,但2002年医院药房仍未完全符合ASHP《药房配制无菌产品质量保证指南》。