Examination of the Pressure Ulcers in Intensive Care Patients.

Sponsor
Kocaeli University (Other)
Overall Status
Completed
CT.gov ID
NCT05795777
Collaborator
(none)
176
1
16
11

Study Details

Study Description

Brief Summary

A pressure sore was localized skin and/or subcutaneous tissue injury, usually caused by pressure alone or a combination of shear and pressure, at bony prominences. Pressure sores, which are an indicator of the quality of health care, increase mortality, morbidity and cost. Pressure ulcers are the most common problem in intensive care patients and should be prevented. In the literature, the incidence of pressure ulcers in intensive care patients is between 1-59.9%.

A pressure sore is a localized injury to the skin and/or underlying soft tissue, usually over a bony prominence or associated with medical or other devices. This injury occurs when intense and/or prolonged pressure or pressure is accompanied by shear. Soft tissue tolerance to pressure and shear; temperature and humidity can affect nutrition, perfusion, concomitant conditions, and condition of soft tissue.

This study was carried out to determine the prevalence of pressure ulcers and influencing factors in patients hospitalized in the 3rd level intensive care unit of a university hospital.

Design: It is a descriptive, prospective, observational type study. Materials and Methods:

The sample of the study consisted of 176 patients aged 18 years and above, 24 hours after hospitalization in the intensive care units of a University Hospital. Patient Information Form and Braden Scale for Predicting Pressure Ulcer Risk, Glasgow Coma Scale were used to collecting data. Statistical Package in statistical analysis for the social sciences 20.0 program was used.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Due to the renovation initiated in the intensive care units, the work was started in November 2019, but the working time was extended due to the Covid 19 pandemic that developed immediately after. The sample of the study consisted of patients who met the inclusion criteria and accepted participation, among the patients who were hospitalized on Wednesday, which was determined as the middle of each week, between November 2019 and February 2021 in the 3rd-level intensive care units of a university hospital.

    Data Collection: "Personal Information Form" prepared by the researcher as a result of the literature review for data collection, "Braden Scale for Predicting Pressure Ulcer Risk" for evaluating pressure ulcers, "Glasgow Coma Score" for evaluating patient's consciousness status, and ulcer used by National Pressure Ulcer Advisory Panel and European Pressure Ulcer Advisory Panel staging classification was used.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    176 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    The Frequency of Pressure Ulcers In 3rd Level Intensive Care Unıts And Determinatıon of Affectıng Risk Factors
    Actual Study Start Date :
    Nov 1, 2019
    Actual Primary Completion Date :
    Feb 1, 2021
    Actual Study Completion Date :
    Mar 1, 2021

    Outcome Measures

    Primary Outcome Measures

    1. Data collection from patients [15 minutes]

      The sample of the study consisted of patients who were hospitalized in the tertiary intensive care unit of a university hospital between November 2019 and February 2021, who met the inclusion criteria and accepted to participate in the study. Data were collected from patients every Wednesday, which was determined as the middle of the week. Patients were evaluated with the Braden Scale for Predicting Pressure Ulcer Risk. The total score of the scale varies between 6-23 points. As the scores obtained from the scale decrease, the risk of developing pressure ulcers increases. A scale score of 9 or less indicates a high risk, and a scale score of 19-23 indicates no risk. Data collection from each patient took 15 minutes.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 92 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • over 18 years old

    • Hospitalized in the 3rd step intensive care unit

    • Being hospitalized for at least 24 hours

    • No pressure ulcers on the first hospitalization

    Exclusion Criteria:
    • hospitalization time not exceeding 24 hours

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Kocaeli Healt and Tecnology University Kocaeli Adana Turkey 41275

    Sponsors and Collaborators

    • Kocaeli University

    Investigators

    • Principal Investigator: Refiye Akpolat, Kocaeli Healt and Tecnology University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Refiye Akpolat, Assistant Proffesor, Kocaeli University
    ClinicalTrials.gov Identifier:
    NCT05795777
    Other Study ID Numbers:
    • 0000-0001-8907-0651
    First Posted:
    Apr 3, 2023
    Last Update Posted:
    Apr 3, 2023
    Last Verified:
    Mar 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Refiye Akpolat, Assistant Proffesor, Kocaeli University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 3, 2023