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Manual Hyperinflation and Physical Therapy Program on Lung Recruitment Mechanically Ventilated Pediatric Patients (MHI)

N

New Ismailia National University

Status

Completed

Conditions

Mechanical Ventilation Complication
Physical Disability

Treatments

Device: rehabilitation of mechanically ventilated patients
Procedure: supportive care

Study type

Interventional

Funder types

Other

Identifiers

NCT06349785
P.T.REC/012/003858

Details and patient eligibility

About

The purpose of this study is to investigate the immediate combined effects of Manual Hyperinflation and standard Physical therapy program on lung recruitment and secretion mass in mechanically ventilated pediatric patients aged between 10-15 years 'old

Full description

In developing countries, lower respiratory tract infection is a major cause of death in children, with severely ill patients being admitted to the critical-care unit. While physical therapists commonly use the manual hyperinflation (MHI) technique for secretion mass clearance in critical-care patients, its efficacy has not been determined in pediatric patients.

Manual hyperinflation is a frequently maneuver used in critically ill intubated and mechanically ventilated patients. With MHI, patients are disconnected from the mechanical ventilator after which their lungs are temporarily ventilated with a manual ventilation bag. so, by applying a larger than normal volume at a low inspiratory pause and expiration with a high expiratory flow, MHI is suggested to mimic a normal cough.

Propagation of airway secretions from the smaller toward the larger airways, then allows for easy removed of airway secretions with the airway suction. finally, MHI could prevent airway plugging and even promote alveolar recruitment. so the aim of the study is to enhance lung recruitment using MHI combined with standard Physical therapy program

Enrollment

32 patients

Sex

All

Ages

10 to 15 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patients will be aged 10-15 years,
  • receiving mechanical ventilation via an endotracheal tube for at least 24 h
  • presenting with vital signs in the normal range.
  • All patients are suffering from lower respiratory tract infection like pneumonia, bronchitis and acute exacerbation of bronchiectasis

Exclusion criteria

  • Patients with history of thoracic surgery
  • Patients with pneumothorax or acute respiratory distress syndrome
  • Patients with severe acute head injury
  • Patients use inotropes and vasopressors drugs
  • Patients with severe Broncho pleural fistula, rib fracture, emphysema bullae, lung abscess, patients with history of preterm birth or heart disease.
  • Patients who requiring mechanical ventilation with a peak inspiratory pressure (PIP)

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

32 participants in 2 patient groups

study group A
Experimental group
Description:
Assigned Children in the study will receive manual hyperinflation and standard physical therapy program. Manual hyperinflation (MHI): Manual hyperinflation will be performed by single physical therapist using a silicone resuscitator bag . The resuscitator bag (maximum volume of 500 mL) was connected to a pressure manometer with an oxygen flow of 10 L. min-1 with the total duration of session in group A will be 15 minutes, daily for 2 weeks
Treatment:
Procedure: supportive care
Device: rehabilitation of mechanically ventilated patients
study group B
Active Comparator group
Description:
- Children in study group B will receive standard Physical therapy program including suction, percussion and vibration with total duration of session in group a will be 15 minutes, daily for 2 weeks
Treatment:
Procedure: supportive care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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