Core competencies in hospital pharmacy - Intravenous admixtures

Hospital Pharmacy

Volumn 41, Issue 4, 2006, Pages 377-380

  Sanborn, Michael ^a  

^a Baylor Healthcare System   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DRUG FORMULATION; DRUG SCREENING; DRUG STABILITY; DRUG STORAGE; HOSPITAL PHARMACY; MEDICAL LITERATURE; REVIEW; TOTAL PARENTERAL NUTRITION; TRAINING;

EID: 33646228657     PISSN: 00185787     EISSN: None     Source Type: Journal    
DOI: 10.1310/hpj4104-377     Document Type: Review

References (18)

1. Institute for Safe Medication Practices. ISMP's List of High-Alert Medications. 2005. Available at: http://www. ismp.org/Tools/ highalertmedications. pdf. Accessed on February 20, 2006.
2. Flynn EA, Pearson RE, Barker KN. Observational study of accuracy in compounding I.V. admixtures at five hospitals. Am J Health Syst Pharm. 1997;54:904-912.
3. Pedersen CA, Schneider PJ, Scheckelhoff DJ. ASHP national survey of pharmacy practice in hospital settings: dispensing and administration-2005. Am J Health Syst Pharm. 2006;63:327-345.
4. Morris AM, Schneider PJ, Pederson CA, Mirtallo JM. National survey of quality assurance activities for pharmacy-compounded sterile preparations. Am J Health Syst Pharm. 2003;60:2567-2576.
5. American Society of Health-System Pharmacists. Best Practices for Hospital and Health-System Pharmacy. Bethesda, MD: The Society; 2005.
6. Pharmaceutical compounding-sterile preparations (general information chapter 797). In: The United States Pharmacopeia, 27th rev., and The National Formulary, 22nd ed. Rockville, MD: The United States Pharmacopeial Convention; 2004:2350-2370.
7. Kastango ES, Bradshaw BD. USP chapter 797: Establishing a practice standard for compounding sterile preparations in pharmacy. Am J Health Syst Pharm. 2004;61:1928-1938.
8. Trapskin PJ, Reagan R, Hite K, et al. The implementation of a personnel training and assessment program for new standards in the US Pharmacopeia general chapter 〈797〉 pharmaceutical compounding of sterile preparations. Hosp Pharm. 2006;41:43-48.
9. Kastango ES. Blueprint for implementing USP chapter 797 for compounding sterile preparations. Am J Health Syst Pharm. 2005;62:1271-1288.
10. Stein SM. Sterile preparation evolves: A USP 〈797〉 implementation story. Hosp Pharm. 2006;41:49-58.
11. Savage SW, Gomez TA, Burrell R. Implementation of USP 〈797〉: The gap analysis and plan. Hosp Pharm. 2005;40:184-188
12. Thomas M, Sanborn MD, Couldry, R. I.V. admixture contamination rates: Traditional practice site versus a class 1000 cleanroom. Am J Health Syst Pharm. 2005;62:2386-2392.
13. Schumock GT, Kafka PS, Tormo VJ. Design, construction, implementation, and cost of a hospital pharmacy clean-room. Am J Health Syst Pharm. 1998;55:458-463.
14. Tillett L. Barrier isolators as an alternative to a cleanroom. Am J Health Syst Pharm. 1999;56:1433-436
15. Thompson CA. Revisions continue on USP sterile-compounding chapter. Am J Health Syst Pharm. 2005;62:1856, 1858, 1861-1862.
16. Lee HE. Premixed intravenous admixtures: a positive development for hospital pharmacy. Am J Hosp Pharm. 1983;40:1043-1044.
17. National advisory group on standards and practice guidelines for patenteral nutrition. Safe practices for parenteral nutrition formulations. JPEN J Parenter Enteral Nutr. 1998;22:49-66.
18. American Society of Health-System Pharmacists. ASHP guidelines on the safe use of automated compounding devices for the preparation of parenteral nutrition admixtures. Am J Health Syst Pharm. 2000;57:1343-1348.