Literature DB >> 8913388

National survey of quality assurance activities for pharmacy-prepared sterile products in hospitals and home infusion facilities--1995.

J P Santell1, R F Kamalich.   

Abstract

The results of a survey of hospital pharmacy and home infusion facility activities for quality assurance in the preparation of sterile drug products are reported, and the hospital results are compared with those of a 1991 ASHP survey. A questionnaire was mailed in May and June 1995 to 778 hospital pharmacy directors and 203 home infusion pharmacy directors. Usable questionnaires were returned by 547 hospitals and 111 home infusion facilities, for an overall response rate of 67%. The percentages of hospitals with pharmacists involved in extemporaneous (70%) and batch (28%) preparation of sterile drug products have decreased since 1991, while the percentage with technicians who are not limited as to the types of sterile products they may prepare has increased. Some 16% of all sterile products compounded in hospitals were prepared by nonpharmacy personnel. Few respondents contracted with outside sources for compounding of sterile products. A need for educational programs on aseptic technique was identified by 83% of hospitals, and 84% of home infusion facilities indicated a need for education on environmental monitoring. Three fourths of respondents used the ASHP Technical Assistance Bulletin on Quality Assurance for Pharmacy-Prepared Sterile Products in developing their policies and procedures. Significant improvements in orientation and training techniques have occurred since 1991. Use of a laminar-airflow hood in a limited-access room has increased. The aspects of sterile product compounding most often modified since 1991 were, for hospitals, personnel training and evaluation (74%), facilities and equipment (48%), and garb policies (36%); for home infusion facilities, personnel training and evaluation (76%), facilities and equipment and garb policies (both 69%), and end-product testing and evaluation (66%). There have been advances in quality assurance procedures related to pharmacy-prepared sterile products, but opportunities for improvement remain.

Mesh:

Year:  1996        PMID: 8913388     DOI: 10.1093/ajhp/53.21.2591

Source DB:  PubMed          Journal:  Am J Health Syst Pharm        ISSN: 1079-2082            Impact factor:   2.637


  4 in total

1.  Survey of sterile admixture practices in canadian hospital pharmacies: part 1. Methods and results.

Authors:  Travis Warner; Cesilia Nishi; Ryan Checkowski; Kevin W Hall
Journal:  Can J Hosp Pharm       Date:  2009-03

2.  Use of a systematic risk analysis method to improve safety in the production of paediatric parenteral nutrition solutions.

Authors:  P Bonnabry; L Cingria; F Sadeghipour; H Ing; C Fonzo-Christe; R E Pfister
Journal:  Qual Saf Health Care       Date:  2005-04

Review 3.  Straight from the headlines: what is going on in compounding pharmacies, and how can clinical microbiologists help?

Authors:  Alice S Weissfeld
Journal:  J Clin Microbiol       Date:  2013-06-19       Impact factor: 5.948

4.  Incorporation of hands-on sterile technique instruction in an introductory pharmacy practice experience.

Authors:  Erika Cretton-Scott; Danielle Cruthirds; Lori Coward
Journal:  Am J Pharm Educ       Date:  2015-03-25       Impact factor: 2.047

  4 in total

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