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

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Respiration Disorders

Treatments

Other: respiratory exercises

Study type

Interventional

Funder types

Other

Identifiers

NCT05267067
Chest physiotherapy

Details and patient eligibility

About

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.

Full 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.

Enrollment

30 patients

Sex

All

Ages

12 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male patients
  • underwent valve surgery (repair or replacement) for mitral valve stenosis;
  • hemodynamically stable,
  • ages ranged from 12 to 18 years old-
  • BMI ranges from 18.5 to 24.9
  • reduced MEP, MVV and complaining from shortness of breath with exertion.

Exclusion criteria

  • Patients with previous cardiac surgery
  • congenital heart disease
  • neurological disorders
  • type1 diabetes mellitus
  • smoker
  • pacemaker implantation
  • atrial fibrillation
  • utilization of mechanical ventilation longer than 24 hours.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

30 participants in 2 patient groups

manual respirtory exercises
Active Comparator group
Description:
Using manual traditional respiratory exercises.
Treatment:
Other: respiratory exercises
Respiratory exercises with respiratory pressure meter
Active Comparator group
Description:
Using pressure respiratory meter in exercises.
Treatment:
Other: respiratory exercises

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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