Am J Health-Syst Pharm
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


American Journal of Health-System Pharmacy, Vol. 64, Issue 8, 837-841
Copyright © 2007 by American Society of Health-System Pharmacists
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Trissel, L. A.
Right arrow Articles by Angeles, C. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Trissel, L. A.
Right arrow Articles by Angeles, C. H.

Practice Reports

Effect of two work practice changes on the microbial contamination rates of pharmacy-compounded sterile preparations

Lawrence A. Trissel, Joseph A. Gentempo, Lisa M. Saenz, Monica Y. Woodard and Carol H. Angeles

LAWRENCE A. TRISSEL, B.S.PHARM., FASHP, is Consultant, TriPharma Research, Cashiers, NC; at the time this study was conducted, Mr. Trissel was Director, Clinical Pharmaceutics Research, The University of Texas M. D. Anderson Cancer Center, Houston. JOSEPH A. GENTEMPO, M.S., is Pharmacist Trainer; LISA M. SAENZ, CPHT, is Pharmacy Technician Trainer; MONICA Y. WOODARD, CPHT, is Pharmacy Technician; and CAROL H. ANGELES, CPHT, is Pharmacy Technician, Division of Pharmacy, The University of Texas M. D. Anderson Cancer Center, Houston.

Address correspondence to Mr. Trissel at TriPharma Research, P.O. Box 265, Cashiers, NC 28717-0265.


Purpose. Using a multiple-step testing medium-risk-level compounding test procedure, the evaluation of two work-practice changes to determine if the changes could effectively reduce the potential for contamination occurrence was conducted.

Summary. Along with training and evaluation of aseptic sterile compounding techniques, each individual pharmacist and pharmacy technician at M. D. Anderson Cancer Center must successfully demonstrate aseptic preparation competency annually by performing the complicated multistep aseptic transfers of growth medium with no resulting growth of microorganisms. The multistep aseptic transfers are designed to simulate manual compounding of the most complicated medium-risk-level preparations anticipated as specified in the United States Pharmacopeia‘s chapter 797. An evaluation of two modest and simple work-practice changes was conducted: The use of bare hands and nonsterile gloves with only initial disinfection with 70% isopropyl alcohol (IPA) during years 1 and 2 (group A) was compared with the use of nonsterile chemotherapy gloves with initial and repeated disinfection with IPA for year 3 (group B) and the use of sterile gloves with initial and repeated disinfection with IPA for year 4 (group C). The process involved multiple discrete manipulations, including reconstitution of dry-growth medium; transfers of growth medium from vials and ampules using syringes, needles, a dispensing pin, and a filter straw; and transfers to an empty plastic i.v. bag. For groups B and C, significant reductions in contaminated samples were found compared with group A.

Conclusion. The use of protective chemotherapy gloves that were repeatedly disinfected with IPA decreased the contamination rate of pharmacy-compounded sterile preparations.

Index terms: Alcohols, isopropyl; Compounding; Contamination; Disinfectants; Gloves; Pharmacy; Sterile products

 






HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 by the American Society of Health-System Pharmacists.