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. 2000 Nov;83(5):435–438. doi: 10.1136/adc.83.5.435

Late presentation of upper airway obstruction in Pierre Robin sequence

A Wilson 1, D Moore 1, M Moore 1, A Martin 1, R Staugas 1, J Kennedy 1
PMCID: PMC1718546  PMID: 11040155

Abstract

A retrospective review was carried out of 11 consecutive patients with the Pierre Robin sequence referred to a tertiary paediatric referral centre over a five year period from 1993 to 1998. Ten patients were diagnosed with significant upper airway obstruction; seven of these presented late at between 24 and 51 days of age. Failure to thrive occured in six of these seven infants at the time of presentation, and was a strong indicator of the severity of upper airway obstruction. Growth normalised on treatment of the upper airway obstruction with nasopharyngeal tube placement. All children had been reviewed by either an experienced general paediatrician or a neonatologist in the first week of life, suggesting that clinical signs alone are insufficent to alert the physician to the degree of upper airway obstruction or that obstruction developed gradually after discharge home. The use of polysomnography greatly improved the diagnostic accuracy in assesssing the severity of upper airway obstruction and monitoring the response to treatment. This report highlights the prevalence of late presentation of upper airway obstruction in the Pierre Robin sequence and emphasises the need for close prospective respiratory monitoring in this condition. Objective measures such as polysomnography should be used, as clinical signs alone may be an inadequate guide to the degree of upper airway obstruction.



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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Benjamin B., Walker P. Management of airway obstruction in the Pierre Robin sequence. Int J Pediatr Otorhinolaryngol. 1991 Jul;22(1):29–37. doi: 10.1016/0165-5876(91)90094-r. [DOI] [PubMed] [Google Scholar]
  2. Bull M. J., Givan D. C., Sadove A. M., Bixler D., Hearn D. Improved outcome in Pierre Robin sequence: effect of multidisciplinary evaluation and management. Pediatrics. 1990 Aug;86(2):294–301. [PubMed] [Google Scholar]
  3. Caouette-Laberge L., Bayet B., Larocque Y. The Pierre Robin sequence: review of 125 cases and evolution of treatment modalities. Plast Reconstr Surg. 1994 Apr;93(5):934–942. [PubMed] [Google Scholar]
  4. Cohen M. M., Jr Robin sequences and complexes: causal heterogeneity and pathogenetic/phenotypic variability. Am J Med Genet. 1999 Jun 4;84(4):311–315. [PubMed] [Google Scholar]
  5. Deegan P. C., McGlone B., McNicholas W. T. Treatment of Robin sequence with nasal CPAP. J Laryngol Otol. 1995 Apr;109(4):328–330. doi: 10.1017/s0022215100130051. [DOI] [PubMed] [Google Scholar]
  6. Dennison W. M. The Pierre Robin syndrome. Pediatrics. 1965 Sep;36(3):336–341. [PubMed] [Google Scholar]
  7. Freed G., Pearlman M. A., Brown A. S., Barot L. R. Polysomnographic indications for surgical intervention in Pierre Robin sequence: acute airway management and follow-up studies after repair and take-down of tongue-lip adhesion. Cleft Palate J. 1988 Apr;25(2):151–155. [PubMed] [Google Scholar]
  8. Gilhooly J. T., Smith J. D., Howell L. L., Deschaine B. L., Richey S. L. Bedside polysomnography as an adjunct in the management of infants with Robin sequence. Plast Reconstr Surg. 1993 Jul;92(1):23–27. doi: 10.1097/00006534-199307000-00003. [DOI] [PubMed] [Google Scholar]
  9. Heaf D. P., Helms P. J., Dinwiddie R., Matthew D. J. Nasopharyngeal airways in Pierre Robin Syndrome. J Pediatr. 1982 May;100(5):698–703. doi: 10.1016/s0022-3476(82)80567-2. [DOI] [PubMed] [Google Scholar]
  10. Myer C. M., 3rd, Reed J. M., Cotton R. T., Willging J. P., Shott S. R. Airway management in Pierre Robin sequence. Otolaryngol Head Neck Surg. 1998 May;118(5):630–635. doi: 10.1177/019459989811800511. [DOI] [PubMed] [Google Scholar]
  11. Ogborn M. R., Pemberton P. J. Late development of airway obstruction in the Robin anomalad (Pierre Robin syndrome) in the newborn. Aust Paediatr J. 1985 Aug;21(3):199–200. doi: 10.1111/j.1440-1754.1985.tb02135.x. [DOI] [PubMed] [Google Scholar]
  12. Reimão R., Papaiz E. G., Papaiz L. F. Pierre Robin sequence and obstructive sleep apnea. Arq Neuropsiquiatr. 1994 Dec;52(4):554–559. doi: 10.1590/s0004-282x1994000400017. [DOI] [PubMed] [Google Scholar]
  13. Shprintzen R. J. The implications of the diagnosis of Robin sequence. Cleft Palate Craniofac J. 1992 May;29(3):205–209. doi: 10.1597/1545-1569_1992_029_0205_tiotdo_2.3.co_2. [DOI] [PubMed] [Google Scholar]
  14. Spier S., Rivlin J., Rowe R. D., Egan T. Sleep in Pierre Robin syndrome. Chest. 1986 Nov;90(5):711–715. doi: 10.1378/chest.90.5.711. [DOI] [PubMed] [Google Scholar]
  15. Tomaski S. M., Zalzal G. H., Saal H. M. Airway obstruction in the Pierre Robin sequence. Laryngoscope. 1995 Feb;105(2):111–114. doi: 10.1288/00005537-199502000-00001. [DOI] [PubMed] [Google Scholar]
  16. Vegter F., Hage J. J., Mulder J. W. Pierre Robin syndrome: mandibular growth during the first year of life. Ann Plast Surg. 1999 Feb;42(2):154–157. [PubMed] [Google Scholar]

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