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Published on: July 4, 2018
Intra-Abdominal Pressure as a Marker of Enteral Nutrition Intolerance in Critically Ill Patients. The PIANE Study
M Luisa Bordejé1, Juan C Montejo2, M Lidón Mateu3
1ICU, Hospital Universitario Germans Trias i Pujol, Carretera del Canyet s/n, 08916 Badalona, Spain. luisabordeje@gmail.com.
Insights
Elevated intra-abdominal pressure (IAP) correlates with gastrointestinal (GI) complications in patients receiving enteral nutrition (EN). However, IAP alone is not a reliable predictor of EN intolerance in critically ill individuals.
Area of Science:
- Critical Care Medicine
- Gastroenterology
- Clinical Nutrition
Background:
- Enteral nutrition (EN) is crucial for critically ill patients.
- Gastrointestinal (GI) complications can impede EN delivery.
- Intra-abdominal pressure (IAP) is a potential factor influencing GI tolerance.
Purpose of the Study:
- To investigate the association between elevated IAP and EN-related GI complications.
- To evaluate IAP's utility as a predictor of EN intolerance.
Main Methods:
- Prospective, observational, multicenter study of ICU patients on mechanical ventilation requiring EN for ≥5 days.
- IAP measured via urinary catheter; GI complications monitored daily.
- Comparison of patients with and without GI complications.
Main Results:
- 247 patients recruited; 128 experienced GI complications.
- Patients with GI complications had longer EN, mechanical ventilation, and ICU stays.
- A higher IAP was associated with EN intolerance (p < 0.003), with 14 mmHg showing low sensitivity/specificity.
Conclusions:
- Elevated IAP is associated with EN intolerance in critically ill patients.
- IAP alone is not a sufficient predictor for identifying patients at risk of EN intolerance.
Abstract:
To determine whether elevated intra-abdominal pressure (IAP) is associated with a higher rate of enteral nutrition-related gastrointestinal (GI) complications; to assess the value of IAP as a predictor of enteral nutrition (EN) intolerance. Intensive Care Unit (ICU) patients on mechanical ventilation requiring at least 5 days of EN were recruited for a prospective, observational, non-interventional, multicenter study. EN was performed and GI complications were managed with an established protocol. IAP was determined via a urinary catheter. Patients who developed any GI complications were considered as presenting EN intolerance. Variables related to EN, IAP and GI complications were monitored daily. Statistical analysis compared patients without GI complications (group A) vs. GI complications (group B). 247 patients were recruited from 28 participating ICUs (group A: 119, group B: 128). No differences between groups were recorded. Patients in group B (p < 0.001) spent more days on EN (8.1 ± 8.4 vs. 18.1 ± 13.7), on mechanical ventilation (8.0 ± 7.7 vs. 19.3 ± 14.9) and in the ICU (12.3 ± 11.4 vs. 24.8 ± 17.5). IAP prior to the GI complication was (14.3 ± 3.1 vs. 15.8 ± 4.8) (p < 0.003). The best IAP value identified for EN intolerance was 14 mmHg but it had low sensitivity and specificity. Although a higher IAP was associated with EN intolerance, IAP alone did not emerge as a good predictor of EN intolerance in critically ill patients.
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