Literature DB >> 25357033

Robin sequence: mortality, causes of death, and clinical outcomes.

Melinda A Costa1, Michael M Tu, Kariuki P Murage, Sunil S Tholpady, William A Engle, Roberto L Flores.   

Abstract

BACKGROUND: The authors report the cause of and risk factors for mortality in infants with Robin sequence and identify characteristics associated with quality-of-life outcomes.
METHODS: The authors performed an 11-year retrospective review of all infants with Robin sequence treated at a neonatal intensive care unit. Patient characteristics were correlated to mortality and quality-of-life measures. Emergency room visits and hospital admissions were used to assess quality-of-life outcomes. Significant variables were identified by means of univariate analysis.
RESULTS: One hundred eighty-one consecutive infants were identified. Patient characteristics included the following: isolated, 32.6 percent; syndromic, 31.5 percent; gastrointestinal, 38.1 percent; pulmonary, 32.6 percent; cardiac, 30.9 percent; central nervous system, 25.4 percent; and two or more organ system anomalies, 69.6 percent. Mortality was 16.6 percent; two deaths were related to airway obstruction problems. There were no deaths in isolated Robin sequence (p = 0.002). Mortality was statistically associated with cardiac anomalies (p < 0.001), central nervous system anomalies (p = 0.001), and two or more organ system abnormalities (p = 0.001). Variables associated with an increased rate of emergency room visits were cardiac anomalies (p = 0.04) and two or more organ system abnormalities (p = 0.04). The presence of two or more organ system abnormalities (p = 0.04) was associated with an increased hospital admission rate.
CONCLUSIONS: Mortality and negative quality-of-life measures in Robin sequence are not directly related to respiratory obstruction. Isolated Robin sequence confers no increased risk of mortality. There is a high incidence of cardiac and central nervous system anomalies, which are significantly associated with mortality. Cardiac and cranial imaging should be performed during the initial evaluation of infants with Robin sequence. CLINICAL QUESTION/LEVEL OF EVIDENCE: Risk, III.

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Mesh:

Year:  2014        PMID: 25357033     DOI: 10.1097/PRS.0000000000000510

Source DB:  PubMed          Journal:  Plast Reconstr Surg        ISSN: 0032-1052            Impact factor:   4.730


  6 in total

Review 1.  Surgical Management and Outcomes of Pierre Robin Sequence: A Comparison of Mandibular Distraction Osteogenesis and Tongue-Lip Adhesion.

Authors:  Rosaline S Zhang; Ian C Hoppe; Jesse A Taylor; Scott P Bartlett
Journal:  Plast Reconstr Surg       Date:  2018-08       Impact factor: 4.730

2.  Objective measurements for upper airway obstruction in infants with Robin sequence: what are we measuring? A systematic review.

Authors:  Robrecht J H Logjes; Joanna E MacLean; Noor W de Cort; Christian F Poets; Véronique Abadie; Koen F M Joosten; Cory M Resnick; Ivy K Trindade-Suedam; Carlton J Zdanski; Christopher R Forrest; Frea H Kruisinga; Roberto L Flores; Kelly N Evans; Corstiaan C Breugem
Journal:  J Clin Sleep Med       Date:  2021-08-01       Impact factor: 4.324

3.  Mortality in Robin sequence: identification of risk factors.

Authors:  Robrecht J H Logjes; Maartje Haasnoot; Petra M A Lemmers; Mike F A Nicolaije; Marie-José H van den Boogaard; Aebele B Mink van der Molen; Corstiaan C Breugem
Journal:  Eur J Pediatr       Date:  2018-02-28       Impact factor: 3.183

Review 4.  Robin sequence: what the multidisciplinary approach can do.

Authors:  Stephanie M Cohen; S Travis Greathouse; Cyrus C Rabbani; Joseph O'Neil; Matthew A Kardatzke; Tasha E Hall; William E Bennett; Ameet S Daftary; Bruce H Matt; Sunil S Tholpady
Journal:  J Multidiscip Healthc       Date:  2017-03-27

5.  Severity of Retrognathia and Glossoptosis Does Not Predict Respiratory and Feeding Disorders in Pierre Robin Sequence.

Authors:  Anne Morice; Véronique Soupre; Delphine Mitanchez; Francis Renault; Brigitte Fauroux; Sandrine Marlin; Nicolas Leboulanger; Natacha Kadlub; Marie-Paule Vazquez; Arnaud Picard; Véronique Abadie
Journal:  Front Pediatr       Date:  2018-11-20       Impact factor: 3.418

6.  A novel 1p33p32.2 deletion involving SCP2, ORC1, and DAB1 genes in a patient with craniofacial dysplasia, short stature, developmental delay, and leukoencephalopathy: A case report.

Authors:  Maoying Jiang; Shanlin Wang; Fei Li; Juan Geng; Yiting Ji; Ke Li; Xiaodong Jiang
Journal:  Medicine (Baltimore)       Date:  2020-11-06       Impact factor: 1.817

  6 in total

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