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Use of PARniv for Early Diagnosis of LVF in AECOPD

U

University of Monastir

Status

Completed

Conditions

Acute Heart Failure
COPD Exacerbation

Treatments

Diagnostic Test: non invasive ventilation

Study type

Observational

Funder types

Other

Identifiers

NCT05189119
pressure support /LVF/ AECOPD

Details and patient eligibility

About

Left ventricular failure (LVF) is a common cause of acute exacerbation of chronic obstructive pulmonary disease (AECOPD).

This association is frequently underestimated with regard to the difficulty of clinical diagnosis .

The investigators expect that the application of pressure support under NIV could be useful in this issue.

Full description

Acute heart failure (AHF) is a common cause of COPD exacerbation however its role is very often underestimated. Until now, the use of echocardiography and some invasive hemodynamic exploration techniques such as the Swan-ganz catheter has been stated as reference. Other noninvasive diagnostic methods have been studied, such as systolic time intervals and Valsalva maneuver, but their application still difficult in patients with COPD exacerbation, especially in emergency department (ED) settings. the study aimed to evaluate the performance of a new diagnostic technique based on the measurement of the PAR using non invasive ventilation (NIV) for the early identification of left ventricular failure (LVF) in patients presenting to the ED with acute COPD exacerbation

Enrollment

80 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with a history of COPD
  • consulted the emergency department for AECOPD defined by a respiratory rate >25c/min, SaO2 <90%, pH <7.35 and PaCO2 >6kPa were included.

Exclusion criteria

  • hemodynamic instability requiring the use of vasoactive drugs
  • patients with contraindications to NIV (Glasgow score <12, swallowing disorder or severe bronchial obstruction, vomiting, and those with upper airway obstruction or ongoing upper gastrointestinal bleeding and altered bronchial clearance)
  • non cooperative patients
  • who refused to give consent.

Trial design

80 participants in 2 patient groups

LVFgroup
Description:
patients with AECOPD and left ventricular failure
Treatment:
Diagnostic Test: non invasive ventilation
non LVF group
Description:
patients with AECOPD and whithout left ventricular failure
Treatment:
Diagnostic Test: non invasive ventilation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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