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Current Literature: Bacterial Contamination of Ready‐to‐use 1‐L Feeding Bottles and Administration Sets in Severely Compromised Intensive Care Patients
Author(s) -
MathusVliegen LM,
Binnekade JM,
Haan KJ de
Publication year - 2000
Publication title -
nutrition in clinical practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.725
H-Index - 71
eISSN - 1941-2452
pISSN - 0884-5336
DOI - 10.1177/088453360001500607
Subject(s) - medicine , enterobacter cloacae , klebsiella oxytoca , contamination , enteral administration , intensive care unit , intensive care , parenteral nutrition , microbiological culture , enterobacteriaceae , emergency medicine , bacteria , surgery , intensive care medicine , biology , ecology , biochemistry , genetics , escherichia coli , gene
Objective: In intensive care patients, enteral feeding requires sterile feedings because of infectious complications and adequate supplements to meet nutritional needs. Heretofore, prepacked, large‐volume formula containers were developed, but bacterial contamination occurred in 4% to 15%. Our objective was to investigate the microbial contamination rate of 1‐L feeding bottles and newly designed administration sets over hanging times of 24 hours in the intensive care unit (ICU). Design and Setting: A prospective observational cohort study of patients admitted to the ICU of a university hospital. Patients: All consecutive patients fed via a nasojejunal tube for at least 4 days. Measurements: Cultures of feeding bottles, administration sets, and gastric and tracheobronchial aspirates at day 0, 1, 2, 4, and 7. Results: A total of 4% of feeding bottles and 74% of infusion sets contained >10(2) colony forming units (CFU)/mL. Gastric and bronchial aspirates were positive in 90% and 92%, respectively. Bacterial counts of feeding bottles were 10(2)‐10(5) CFU/mL, and the main bacteria isolated included Enterobacter cloacae, Klebsiella oxytoca , and enterococci. One‐third of all cultured bacteria in feeding bottles, administration sets, stomach, and lungs belonged to the Enterobacteriaceae family, which was held responsible for the nosocomial infections in the ICU. None of the 1‐L feeding bottles with a hanging time of 19 to 24 hours was contaminated. Only bottles that had to be exchanged because of need for a faster rate of infusion proved to be contaminated, apparently without clinical consequences. With time and the increasing severity of disease, the administration sets became contaminated at an increasingly faster rate and with higher bacterial counts mainly through retrograde growth of endogenous bacteria. The final step of bottle contamination might have been the bacterial transfer by nurses' hands. Conclusion: Despite an almost ideal design of the enteral nutrition delivery system, a 4% contamination rate of initially sterile feedings with clinically relevant bacteria and the fact that only manipulated systems showed bacterial growth are of concern. (Crit Care Med 28:67–73, 2000)