Emergency Classification According to Fingertip Circulation

Sponsor
Manisa Celal Bayar University (Other)
Overall Status
Completed
CT.gov ID
NCT05742113
Collaborator
(none)
1,490
1
1
24
62

Study Details

Study Description

Brief Summary

Dyspnea is one of the most common reasons for admission to the emergency department[1]. Oxygen saturation has great importance in determining the triage status of patients admitted to the hospital with dyspnea and planning the emergency treatment [2].

Peripheral perfusion index (PI), which shows tissue oxygenation is a noninvasive way of demonstrating tissue perfusion in critically ill patients. Studies have shown that PI is an accurate, fast and reliable pulse oximetry-based indicator of tissue perfusion [3-5]. PI shows the perfusion status of the tissue in the applied area for an instant and a certain time interval. The PI value ranges from 0.02% (very weak) to 20% (strong) [6].

Triage scales are used to distinguish emergency and non-emergency patients. The emergency triage system is used to quickly determine the care priorities of patients during admission to the emergency department[7,8].

It is important to make the triage classification for dyspnea in emergency services quickly and accurately to start the treatment protocols as early as. In this study, the investigators aimed to determine the relationship between perfusion index and the emergency triage classification in patients admitted to the emergency department with dyspnea.

Condition or Disease Intervention/Treatment Phase
  • Device: Masimo Radical-7
N/A

Detailed Description

Purpose: To determine the effect of PI measurement on the emergency triage classification in patients with dyspnea.

Methods: Adult patients who presented with dyspnea and whose perfusion index values were measured with Masimo Radical-7 device at the time of admission, at the first hour and the second hour of admission were included in the study. The PI and oxygen saturation measured by finger probes were compared and the superiority of their effects on the emergency triage classification was compared.

Study Design

Study Type:
Interventional
Actual Enrollment :
1490 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Masking Description:
no masking
Primary Purpose:
Diagnostic
Official Title:
DYSPNEA: PERFUSION INDEX and TRIAGE STATUS (the Name of the Project)
Actual Study Start Date :
Jan 1, 2019
Actual Primary Completion Date :
Jan 1, 2021
Actual Study Completion Date :
Jan 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Triage status red

the relationship between the perfusion index and the emergency triage classification in patients admitted to the emergency department with dyspnea.

Device: Masimo Radical-7
perfusion index measuring device

Outcome Measures

Primary Outcome Measures

  1. Perfusion index use for triage status [perfusion index measurement at the time of first admission to hospital]

    for determination of triage status of patients with dyspnea with using perfusion index

  2. Perfusion index use for triage status [perfusion index measurement at the time of the first hour after admission to hospital]

    for determination of triage status of patients with dyspnea with using perfusion index

  3. Perfusion index use for triage status [perfusion index measurement at the time of the second hour after admission to hospital]

    for determination of triage status of patients with dyspnea with using perfusion index

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult patients over the age of 18 who presented with dyspnea

  • whose perfusion index values were measured at the time of first admission (arrival time), at the first hour and the second hour of admission were included in the study

Exclusion Criteria:
  • Patients who applied due to the mechanism of trauma,

  • patients with known vascular disease (Buerger's disease, peripheral artery disease, etc.), -patients with COVID-19 PCR positivity

  • whose perfusion index measurement could not be completed due to hospitalization or discharge were excluded from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Manisa Celal Bayar University Manisa Turkey 45030

Sponsors and Collaborators

  • Manisa Celal Bayar University

Investigators

  • Principal Investigator: Cumhur M TULAY, Ass.Prof., Ass.Prof.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Manisa Celal Bayar University
ClinicalTrials.gov Identifier:
NCT05742113
Other Study ID Numbers:
  • 10.10.2018 and 20.478.486
  • Manisa Celal Bayar University
First Posted:
Feb 23, 2023
Last Update Posted:
Feb 23, 2023
Last Verified:
Feb 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
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Manisa Celal Bayar University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 23, 2023