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Effect of Delaying Replacement of Parenteral Nutrition Intravenous Administration Sets: Preclinical Experiments and a Dynamic Laboratory Model of Microbial Colonization.
Gavin, Nicole Clare; McMillan, David; Keogh, Samantha; Choudhury, Md Abu; Ray-Barruel, Gillian; Rickard, Claire M.
Afiliación
  • Gavin NC; National Centre of Research Excellence in Nursing, Menzies Health Institute Queensland, Griffith University, Queensland, Australia.
  • McMillan D; Alliance for Vascular Access Teaching and Research Group, Menzies Health Institute Queensland, Griffith University, Queensland, Australia.
  • Keogh S; Cancer Care Services, Royal Brisbane and Women's Hospital, Queensland, Australia.
  • Choudhury MA; Alliance for Vascular Access Teaching and Research Group, Menzies Health Institute Queensland, Griffith University, Queensland, Australia.
  • Ray-Barruel G; Inflammation and Healing Research Cluster, School of Health and Sports Sciences, University of the Sunshine Coast, Queensland, Australia.
  • Rickard CM; Alliance for Vascular Access Teaching and Research Group, Menzies Health Institute Queensland, Griffith University, Queensland, Australia.
JPEN J Parenter Enteral Nutr ; 42(6): 987-997, 2018 08.
Article en En | MEDLINE | ID: mdl-30133843
ABSTRACT

BACKGROUND:

Recommendations prescribe daily intravenous administration set (IVAS) replacement for parenteral nutrition (PN) comprising intravenous fat emulsions (IVFE) due to risk of micro-organism growth and resultant central-line associated bloodstream infections (CLABSIs), but system disconnection for this practice may allow contamination and CLABSIs. MATERIALS AND

METHODS:

Laboratory experiments and model development were used to simulate PN administration after contamination from healthcare workers' hands. This study observed the growth of micro-organisms known to cause CLABSIs in a variety of PN and other IV fluids and developed a model to investigate the effect of delaying IVAS replacement on microbial growth for up to 7 days.

RESULTS:

Micro-organisms grew at different rates and were affected by solution type. In static experiments, growth was supported in IVFE and all-in-one PN, but suppressed in 50% glucose. Growth patterns were consistent over time for Staphylococcus epidermidis, Staphylococcus aureus, and Candida albicans in IVFE, all-in-one PN, and 0.9% sodium chloride in both static and dynamic experiments. C. albicans grew exponentially to clinically significant numbers in all-in-one PN and IVFE IVAS after 30 hours, but negligible growth of S. epidermidis or S. aureus occurred for 7 days.

CONCLUSION:

All-in-one PN and IVFE support the C. albicans growth after minimal initial contamination, with micro-organisms migrating from the fluid bag to the central venous access device. Improved aseptic nontouch technique during clinical practice is vital to prevent contamination. Daily IVAS replacement of for all-in-one PN and IVFE should continue until the safety of prolonging IVAS replacement is confirmed by randomized trials.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Staphylococcus aureus / Staphylococcus epidermidis / Candida albicans / Contaminación de Equipos / Nutrición Parenteral / Emulsiones Grasas Intravenosas Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: JPEN J Parenter Enteral Nutr Año: 2018 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Staphylococcus aureus / Staphylococcus epidermidis / Candida albicans / Contaminación de Equipos / Nutrición Parenteral / Emulsiones Grasas Intravenosas Tipo de estudio: Clinical_trials / Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: JPEN J Parenter Enteral Nutr Año: 2018 Tipo del documento: Article País de afiliación: Australia