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Safety of Airway Clearance in Non-hospitalized Infants With Acute Viral Bronchiolitis

G

Guadarrama Hospital

Status

Completed

Conditions

Bronchiolitis

Treatments

Other: Respiratory physiotherapy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Bronchiolitis is a disease that can occur in a mild form and moderate, and often does not require hospitalization. The technique of prolonged slow expiration followed by cough caused in children not hospitalized with mild and moderate bronchiolitis can improve clinical severity

Full description

Once each patient legal guardians has signed the informed consent document and it has been verified that the inclusion criteria are met, it will be assigned the same identification number (ID) that is related to its Clinical History (CH) by simple coding; custody of the file with the relationship of each ID with its CH will be the responsibility of the principal investigator.

Before starting the treatment protocol, a blind evaluator treats the was assigned the patient classifies the child according to the initial score of clinical severity proposed by Wang, in addition to the measurement of SO2 and heart rate measured through a pulse oximeter.

The protocol consists of 20 minutes of FR based on nasal washes in sitting, prolonged slow expiration: passive technique of expiratory help applied to the baby through a slow thoracic-abdominal pressure that begins at the end of a spontaneous expiration and continuing to the residual volume. The physiotherapist through the provoked cough or stimulation of the trachea achieves the expectoration of the sputum.

Care must be taken during the maneuvers of maintaining a position of the infant in supine decubitus in 30 degrees of slope, to avoid episodes of gastroesophageal reflux and decrease the risk of vomiting.

They are considered as criteria of cessation of the physiotherapeutic intervention, alterations abrupt of the respiratory rhythm (brady or tachypnea), stare, ocular revulsion, hiccups or hypertonia and changes in skin color (pallor or cyanosis). In addition to these clinical manifestations, it establishes that if the father or legal guardian demands it, the application of the protocol would be terminated.

In order to evaluate the immediate effect of the protocol, which is established as the effect evaluated 10 minutes immediately after the intervention was applied, the doctor again performs a measurement of SO2, heart rate and respiratory rate, and classify again according to the criteria of Wang's clinical severity scale and anotate any adverse event. At 20 minutes the same medical evaluator performs the same assessment.

Enrollment

265 patients

Sex

All

Ages

2 to 12 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients must meet the following inclusion criteria:

  • Have an age between 2 months and 12 months.
  • Have medical diagnosis of first episode of BQ of maximum 48 hours of evolution.
  • Not previously received respiratory physiotherapy since its diagnosis.
  • Have the informed consent signed by the child's legal guardians.

Exclusion criteria

The exclusion criteria are:

  • Acute BQ with score> 9 according to the Wang clinical scale.
  • Pathology associated cardiac, neurological or traumatic.
  • Previous hospitalizations for wheezing.
  • Medical diagnosis of recurrent sibilant.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

265 participants in 1 patient group

Respiratory physiotherapy
Other group
Description:
The protocol consists of 20 minutes of FR based on nasal washes in sitting, prolonged slow expiration: passive technique of expiratory help applied to the baby through a slow thoracic-abdominal pressure that begins at the end of a spontaneous expiration and continuing to the residual volume. The physiotherapist through the the provoked cough or stimulation of the trachea achieves the expectoration of the sputum.
Treatment:
Other: Respiratory physiotherapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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