Clinical Trials Directory

Trials / Completed

CompletedNCT02894788

Postoperative Intensive Care Surveillance

POSTOPERATIVE INTENSIVE CARE SURVEILLANCE. A Tool to Optimize ICU-beds Management?

Status
Completed
Phase
Study type
Observational
Enrollment
2,498 (actual)
Sponsor
Istituto Clinico Humanitas · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Several score systems were created to stratify perioperative risk and predict mortality. The study rises from the needing of a rapid and simple system to identify the patient worthy of Postoperative Intensive Surveillance. In the first phase Authors retrospectively investigated on patients underwent to elective surgery searching for determining factors (DFs) for postoperative ICU admission. Later, Researchers prospectively studied how DFs could predict the admission in ICU of consecutive patients scheduled for elective surgery during a three-months period and created an index, named PoIS (Post-operative Intensive Surveillance), based on the results of this analysis. Authors used surgical invasiveness (SI), Diabetes Mellitus (DM), Myocardiopathy (MCP), Cerebrovascular Disease (CVD), Body Mass Index (BMI), age, serum creatinine level (sCr), Tiffenau Index (TI) and male sex for the development of the original model. Authors classified SI from G1 (lowest) to G5 (highest). The results show that the power of prediction of postoperative morbidity of PoIS and POSSUM resulted coincident and better than the American Society of Anesthesiology scoring system.

Conditions

Interventions

TypeNameDescription
OTHERICU admission

Timeline

Start date
2015-03-01
Primary completion
2015-08-01
Completion
2015-09-01
First posted
2016-09-09
Last updated
2016-09-09

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT02894788. Inclusion in this directory is not an endorsement.