TY - JOUR
T1 - Multiple-dose vials
T2 - Persistence of bacterial contaminants and infection control implications
AU - Longfield, R. N.
AU - Smith, L. P.
AU - Longfield, J. N.
AU - Coberly, J.
AU - Cruess, D.
PY - 1985
Y1 - 1985
N2 - Due to sporadic infections attributed to contaminated multiple-dose medication vials (MDV), some authorities have suggested discarding all MDV within 24 hours. We inoculated 11 commonly used medications with suspensions of 10 bacterial species previously associated with contaminated parenteral solutions and determined microbial persistence at both room and refrigerator temperature. At 22°C, atropine, curare, folic acid, NPH insulin and triamcinolone did not allow microbial persistence beyond 4 hours. Lidocaine and heparin were sterile by 24 hours. Regular insulin, immune serum globulin, and myochrysine allowed persistence for up to 7 days. At 4°C, bacterial persistence was significantly prolonged for all medications including those MDV requiring refrigeration. No organisms proliferated; however, F. meningosepticum and P. maltophilia were particularly persistent at both temperatures. The risk of persistent MDV contamination appears to be dependent upon specific pharmaceutical, microbe and storage temperature interactions. Recommendations for the refrigerations of MDV medications may require reevaluation on a product-by-product basis.
AB - Due to sporadic infections attributed to contaminated multiple-dose medication vials (MDV), some authorities have suggested discarding all MDV within 24 hours. We inoculated 11 commonly used medications with suspensions of 10 bacterial species previously associated with contaminated parenteral solutions and determined microbial persistence at both room and refrigerator temperature. At 22°C, atropine, curare, folic acid, NPH insulin and triamcinolone did not allow microbial persistence beyond 4 hours. Lidocaine and heparin were sterile by 24 hours. Regular insulin, immune serum globulin, and myochrysine allowed persistence for up to 7 days. At 4°C, bacterial persistence was significantly prolonged for all medications including those MDV requiring refrigeration. No organisms proliferated; however, F. meningosepticum and P. maltophilia were particularly persistent at both temperatures. The risk of persistent MDV contamination appears to be dependent upon specific pharmaceutical, microbe and storage temperature interactions. Recommendations for the refrigerations of MDV medications may require reevaluation on a product-by-product basis.
UR - http://www.scopus.com/inward/record.url?scp=0021923093&partnerID=8YFLogxK
U2 - 10.1017/S0195941700061415
DO - 10.1017/S0195941700061415
M3 - Article
AN - SCOPUS:0021923093
SN - 0195-9417
VL - 6
SP - 194
EP - 199
JO - Infection Control
JF - Infection Control
IS - 5
ER -