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Impact of Positive End Maximum Voluntary Ventilation and Dyspnea Index in Patients After Valvular Heart Surgery

Respiration Disorders Clinical Trial

Official title:
Comparison Between the Manual Respiratory Exercises and Respiratory Pressure Meter

Clinical Trial Summary

Pulmonary mechanics are further disturbed after cardiothoracic surgery that manifests like restrictive pathology, which may persist for weeks to months postoperatively. This experimental aimed to investigate the efficacy of a positive end-expiratory pressure device on maximum expiratory pressure, maximum voluntary ventilation, and dyspnea index in patients who underwent valve surgery.

Clinical Trial Description

Thirty male and female adolescent patients who underwent valve surgery aged 12-18 years old, recruited from the national heart institute enrolled in this experimental. They were assigned into two matched groups: Experimental group consisted of 15 patients, received positive end-expiratory pressure (PEEP) with a mouthpiece in addition to routine chest physiotherapy (postural drainage, percussion, vibration, and deep breathing exercises). Control group consisted of 15 patients, received routine chest physiotherapy alone. The program continued for four weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05267067
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date September 2, 2020
Completion date February 1, 2021
View Details
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