INCREASED INTESTINAL PERMEABILITY IS ASSOCIATED WITH THE DEVELOPMENT OF MULTIPLE ORGAN DYSFUNCTION SYNDROME IN CRITICALLY ILL ICU PATIENTS

Citation
Cj. Doig et al., INCREASED INTESTINAL PERMEABILITY IS ASSOCIATED WITH THE DEVELOPMENT OF MULTIPLE ORGAN DYSFUNCTION SYNDROME IN CRITICALLY ILL ICU PATIENTS, American journal of respiratory and critical care medicine, 158(2), 1998, pp. 444-451
Citations number
42
Categorie Soggetti
Emergency Medicine & Critical Care","Respiratory System
ISSN journal
1073449X
Volume
158
Issue
2
Year of publication
1998
Pages
444 - 451
Database
ISI
SICI code
1073-449X(1998)158:2<444:IIPIAW>2.0.ZU;2-A
Abstract
We conducted a prospective, observational cohort study designed to com pare intestinal permeability (IP) and development of multiple organ dy sfunction syndrome (MODS) in a subset of critically ill patients in an intensive care unit (ICU). All patients with an expected ICU stay of 72 h or more were entered into the study, and IP was determined on a d aily basis whenever possible from the urinary fractional excretion of orally administered lactulose and mannitol (LMR). Forty-seven consecut ive patients were studied, and 28 developed MODS either at the time of admission or during their ICU course. These patients, as a group, had significantly worse IP at admission than did a non-MODS cohort (LnLMR : -2.10 +/- 1.10 versus -3.26 +/- 0.83). Those patients who developed MODS following admission also had a significantly greater admission IP than did the non-MODS group (-2.51 +/- 0.85). Differences in IP betwe en cohorts could not be explained by differences in the incidence of s ystemic inflammatory response syndrome (SIRS)/sepsis or shock. With mu ltivariate regression analysis, the only parameter present on admissio n that was predictive of subsequent MODS was IF. Differences in IP and the severity of organ dysfunction were also present (MODS severity mi ld: -3.01 +/- 0.72; moderate: -1.97 +/- 0.69; and severe: -1.12 +/- 0. 96). Patients who developed MODS had a persistently abnormal IP during their ICU stay, and a significantly delayed improvement in their IP c ompared with the non-MODS cohort. We conclude that the development of MODS is associated with an abnormal and severe derangement of IP that is detectable prior to the onset of the syndrome. This observation len ds credence to the premise that gastrointestinal (CI) dysfunction may be causally associated with the development of MODS in the critically ill patient.