2002
DOI: 10.1054/clnu.2002.0545
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Is a 24-h cyclic closed enteral feeding system microbiologically safe in geriatric patients?

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Cited by 6 publications
(10 citation statements)
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References 29 publications
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“…Commercially available ''ready to hang'' closed enteral feeding systems are designed to limit handling procedures to the introduction of the giving set spike into the pack. Although this may reduce the risk of microbiological contamination resulting from poor handling procedures before feeding, retrograde contamination of the set may occur, the risk of contamination increasing with duration of feed (114). Ongoing training of ward staff and careful instruction of home caregivers by specialist nurses is an additional important component in reducing bacterial contamination.…”
Section: Bacterial Contamination Of Feedsmentioning
confidence: 99%
“…Commercially available ''ready to hang'' closed enteral feeding systems are designed to limit handling procedures to the introduction of the giving set spike into the pack. Although this may reduce the risk of microbiological contamination resulting from poor handling procedures before feeding, retrograde contamination of the set may occur, the risk of contamination increasing with duration of feed (114). Ongoing training of ward staff and careful instruction of home caregivers by specialist nurses is an additional important component in reducing bacterial contamination.…”
Section: Bacterial Contamination Of Feedsmentioning
confidence: 99%
“…Other approaches that can be potentially effective in the management of complications and reducing the rates of infections are reducing the time of exposure to the different sources of contamination, like reducing the time of exposure after opening the formula and decreasing feeding hang time. 33 Other common complications that were reported in these settings might also include the development of mechanical complications.…”
Section: Discussionmentioning
confidence: 99%
“…The distal end of the delivery set was inoculated before the beginning of each feeding session (a total of five times in 24.5 h), to simulate repeat contamination over time, due to the user contaminating the connector when reattaching to the feeding tube before each feeding session. The feed itself was not inoculated in this feeding system, as it is provided sterile and it was not a realistic scenario that the feed would be a source of contamination 20,21,29,33,59 (see Figure 1A). The inoculation of FS2 replicated that of FS1, except that the prepared powdered feed was inoculated directly with 1 ml of bacterial suspension and inverted to distribute the inoculum before the feeding session began, instead of inoculation of the foil seal of the feed container (see Figure 1B).…”
Section: Contamination Of the Enteral Feeding Systemsmentioning
confidence: 99%
“…The methodology employed is based on many studies published in the literature, 10,20,21,56 which have shaped the design and safe use of enteral feeding administration equipment over the last 40 years, and so the data produced can be considered to be robust and transferable to real-life clinical practice. However, other methods used previously 21,23,24,37,56,59 to swab a patient's enteral feeding equipment or take samples of feed from systems being used in clinical practice have been shown to produce data for similar evaluations of bacterial growth, although these data do not appear to differ significantly from that produced in laboratory tests. 20,23,59 The hygienic control testing provided evidence for the inherent presence and growth of the seven bacteria under investigation only, and the inoculated challenges provided data on the growth of the seven challenge bacteria only.…”
Section: Challenge Bacteria Fs1 Fs2mentioning
confidence: 99%