Postural drainage and gastro-oesophageal reflux in infants with cystic fibrosis

Arch Dis Child. 1997 Feb;76(2):148-50. doi: 10.1136/adc.76.2.148.

Abstract

Gastro-oesophageal reflux is increased in cystic fibrosis and it is possible that postural drainage techniques may exacerbate reflux, potentially resulting in aspiration and further impairment of pulmonary function.

Aim: To evaluate the effects of physiotherapy with head down tilt (standard physiotherapy, SPT) on gastroesophageal reflux and to compare this with physiotherapy without head down tilt (modified physiotherapy, MPT).

Method: Twenty (mean age 2.1 months) infants with cystic fibrosis underwent 30 hour oesophageal pH monitoring during which SPT and MPT were carried out for two sessions each on consecutive days.

Results: The number of reflux episodes per hour, but not their duration, was significantly increased during SPT compared with MPT (SPT 2.5 (0.4) v MPT 1.6 (0.3), p = 0.007) and to background (1.1 (0.)1, p = 0.0005). Fractional reflux time was also increased during SPT (11.7 (2.6)%) compared with background (6.9 (1.3)%) p = 0.03) but not compared with MPT (10.7 (2.7)%). There was no significant difference between MPT and background for number of reflux episodes, their duration, or fractional reflux time.

Conclusions: SPT, but not MPT, was associated with a significant increase in gastro-oesophageal reflux in infants with cystic fibrosis.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Cystic Fibrosis / complications*
  • Cystic Fibrosis / rehabilitation
  • Drainage, Postural / adverse effects*
  • Esophagus / metabolism
  • Female
  • Gastroesophageal Reflux / etiology*
  • Head-Down Tilt / adverse effects
  • Humans
  • Hydrogen-Ion Concentration
  • Infant
  • Infant, Newborn
  • Male
  • Physical Therapy Modalities / adverse effects*
  • Single-Blind Method