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Holding the baby: head downwards positioning for physiotherapy does not cause gastro-oesophageal reflux

G E Phillips1, S E Pike, M Rosenthal

  • 1Dept of Physiotherapy, Royal Brompton Hospital, London, UK.

Insights

Head-downwards physiotherapy positioning does not worsen gastro-oesophageal reflux (GOR) in infants with cystic fibrosis (CF). This study found no evidence to change current infant physiotherapy practices for GOR management.

Area of Science:

  • Pediatrics
  • Gastroenterology
  • Respiratory Therapy

Background:

  • Gastro-oesophageal reflux (GOR) is a concern in infants with cystic fibrosis (CF).
  • The head-downwards tipped position during physiotherapy has been suspected to exacerbate GOR.
  • Lower oesophageal pH monitoring is used to assess GOR events.

Purpose of the Study:

  • To investigate whether head-downwards tipped positioning during physiotherapy exacerbates GOR in infants.
  • To determine if current physiotherapy practices need modification for infants with respiratory disorders, particularly CF.

Main Methods:

  • Twenty-one infants (1-27 months) with respiratory disorders (11 with CF) underwent lower oesophageal pH monitoring.
  • Infants received two physiotherapy sequences (A/B or B/A) 12 hours apart, involving different positions and chest clapping.
  • Physiotherapy included gravity-assisted head-downwards tipping and non-tipped positions.

Main Results:

  • Head-downwards positioning did not induce or significantly aggravate GOR in either CF or non-CF infants.
  • A slight, non-significant increase in reflux was observed in CF infants during one physiotherapy sequence (Episode A).
  • The sitting position was more likely to show the lowest pH in CF subjects, but this did not indicate aggravated GOR.

Conclusions:

  • Head-downwards tipped positioning for physiotherapy does not induce or aggravate gastro-oesophageal reflux.
  • There is no evidence to support changing current infant physiotherapy methods regarding GOR.
  • Current physiotherapy techniques can be safely continued for infants with CF and other respiratory disorders.

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