Effect of Prolonged Slow Expiration Technique on Blood Gases Among Pneumatic Neonates

November 24, 2023 updated by: Moshira Mohamed Metwally, Cairo University

Effect of Prolonged Slow Expiration Technique on Blood Gases Among Neonates With Pneumonia

Pneumonia is a medical condition that, if not treated promptly, can lead to life- threatening complications. The prolonged slow expiration technique is a new type of chest physiotherapy that helps infants discharge bronchial secretions which accumulated due to pneumonia.

Study Overview

Detailed Description

Pneumonia is an infective lung condition that is one of the most common risk factors for neonatal death. Pulmonary infections, most common caused by anaerobic bacterial infection, result in the accumulation of pus in the pleural cavity. Preterms, neonates with respiratory infections, and underdeveloped lungs all require the use of a prolonged slow expiration technique.

Prolonged slow expiration technique is the only chest clearance technique that provides both effective clearance and a soothing effect. Another recommendation for this technique is lack of application of emerging techniques of respiratory physiotherapy. Although the technique is effective, it is rarely in practice over the conventional methods of chest physiotherapy.

During prolonged slow expiration, intrathoracic pressure gradually rises due to thoracoabdominal compression, preventing bronchial collapse and flow disruption that occurs during forced expirations.

Study Type

Interventional

Enrollment (Actual)

32

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Giza, Egypt
        • Faculty of Physical Therapy

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

1 day to 2 months (Child)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age since birth till 2 months
  • Clinical findings of pneumonia: tachypnea, chest recession, fever, cyanosis and cough
  • Radiological diagnosis of pneumonia (x-ray): lober or segmental consolidation, nodular or coarse patchy infiltration, diffuse haziness and air bronchogram.
  • Neonates on oxygen therapy.

Exclusion Criteria:

  • Neonates with congenital cardiopathy.
  • Neonates with surgical incision in thorax or abdomen.
  • Neonates with neurological intervention.
  • Neonates with obstruction of upper air way.
  • Neonates with gastroesophageal reflux and laryngeal affection.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: Traditional chest physiotherapy
This group receives traditional chest physiotherapy that include postural drainage, percussion and vibration ( manually or by a vibrator) in each session which is twice daily from admission to neonatal intensive care unit till discharge

Postural drainage: the patient is positioned in postural drainage so that gravity had the maximum effect on the lung segment that needed to be drained, all lung zones are emphasised in positional initiatives for babies.

Percussion is the rhythmic striking of the chest wall with cupped hands for 1 to 2 minutes at a time.

Vibration is performed by placing fingers on the chest wall over the segment being drained and isometrically contracting the forearm and hand muscles to produce a vibratory motion.

Vibration is accomplished either through manual vibratory motion of the therapist's fingers on the infant's chest wall or through the use of a mechanical vibrator ( Foreo vibrator).

Other Names:
  • Postural drainage
  • Vibration
  • Percussion
  • Foreo Vibrator
Active Comparator: Prolonged slow expiration technique and traditional chest physiotherapy
This group receives traditional chest physiotherapy that include postural drainage, percussion and vibration ( manually or by a vibrator) plus prolonged slow expiration technique in each session which is twice daily from admission in neonatal intensive care unit till discharge.

Postural drainage: the patient is positioned in postural drainage so that gravity had the maximum effect on the lung segment that needed to be drained, all lung zones are emphasised in positional initiatives for babies.

Percussion is the rhythmic striking of the chest wall with cupped hands for 1 to 2 minutes at a time.

Vibration is performed by placing fingers on the chest wall over the segment being drained and isometrically contracting the forearm and hand muscles to produce a vibratory motion.

Vibration is accomplished either through manual vibratory motion of the therapist's fingers on the infant's chest wall or through the use of a mechanical vibrator ( Foreo vibrator).

Other Names:
  • Postural drainage
  • Vibration
  • Percussion
  • Foreo Vibrator
The therapist places one hand on the thorax below the suprasternal notch and the other hand over the upper abdomen while the neonate is supine. Both hands will have hypothenar contact with the thorax and abdomen. At the end of the expiratory phase, the therapist places a compression force with both hands. Compression at the end of expiration with hypothenar eminence is kept for 2 or 3 breathing cycles. This technique is repeated several times, with a rest time between applications of about 5 or 10 spontaneous breaths.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in arterial oxygen saturation (Sao2)
Time Frame: Change from Baseline SaO2 at 9 days
Arterial oxygen saturation is assessed by standardized international monitor and measured by %
Change from Baseline SaO2 at 9 days
Change in systolic and diastolic blood pressure
Time Frame: Change from baseline systolic and diastolic blood pressure at 9 days
Systolic and diastolic blood pressure are assessed by standardized international monitor and measured by millimeters of mercury ( mmHg)
Change from baseline systolic and diastolic blood pressure at 9 days
Change in heart rate (HR)
Time Frame: Change from baseline HR at 9 days
Heart rate is assessed by standardized international monitor and measured by beats per minute (BPM)
Change from baseline HR at 9 days
Change in temperature
Time Frame: Change from baseline temperature at 9 days
Temperature is assessed by thermometer and measured by degree(°)
Change from baseline temperature at 9 days
Change in power of hydrogen (PH)
Time Frame: Change from baseline PH at 9 days
PH is assessed by blood gases machine and it is a scale used to specify the acidity or basicity of blood
Change from baseline PH at 9 days
Change in partial pressure of carbon dioxide (PaCO2)
Time Frame: Change from baseline PaCO2 at 9 days
PaCO2 is assessed by blood gases machine and measured by mmHg and it serves as a marker of sufficient alveolar ventilation within the lungs
Change from baseline PaCO2 at 9 days
Change in bicarbonate (HCO3)
Time Frame: Change from baseline HCO3 at 9 days
HCO3 is assessed by blood gases machine and measured by milliequivalents per litre (mEq/L) and it is used to detect electrolyte imbalance
Change from baseline HCO3 at 9 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Elham Salem, Cairo university

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2023

Primary Completion (Actual)

August 3, 2023

Study Completion (Actual)

November 17, 2023

Study Registration Dates

First Submitted

February 26, 2023

First Submitted That Met QC Criteria

March 21, 2023

First Posted (Actual)

March 23, 2023

Study Record Updates

Last Update Posted (Actual)

November 29, 2023

Last Update Submitted That Met QC Criteria

November 24, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • NoP.T.REC/012/003676

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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