• Cleft Palate Craniofac. J. · Mar 2003

    Management of infants with Pierre Robin sequence.

    • Silke Wagener, Sukh S Rayatt, Andy J Tatman, Peter Gornall, and Rona Slator.
    • Birmingham Children's Hospital, Birmingham, England.
    • Cleft Palate Craniofac. J. 2003 Mar 1;40(2):180-5.

    ObjectiveSeveral methods of treating babies with Pierre Robin sequence have been described since the condition itself was first documented in 1923. The main aim of treatment has been to relieve upper airway obstruction. Treatment methods used range from positioning of the baby to invasive surgery. The aim of this article was to describe the assessment, treatment, and monitoring methods used for babies referred with Pierre Robin sequence (PRS).Setting/PatientsFrom December 1995 to May 2000, 22 consecutive patients were admitted to Birmingham Children's Hospital with PRS. Their airway and nutritional status were assessed and continuously monitored.InterventionsTreatment concentrated on the relief of airway obstruction with a nasopharyngeal airway (NPA) and nutritional support of the babies until they grew out of their respiratory and feeding difficulties.Main Outcome MeasuresOutcome measures were oxygen saturation, growth of the babies, and the need for surgery.ResultsAll babies were managed successfully with an NPA and nutritional support. No baby required surgery, and the majority showed good weight gain.ConclusionRelieving airway obstruction by NPA is an effective and safe treatment for babies with PRS until they have grown out of their respiratory and feeding difficulties. It avoids the need for surgery and can be used on neonatal wards using the monitoring described.

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