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Congenital Diaphragmatic Hernia. The Post-Neonatal Period (Part II)

Title
Congenital Diaphragmatic Hernia. The Post-Neonatal Period (Part II)
Type
Article in International Scientific Journal
Year
2008
Authors
Rocha, GM
(Author)
Other
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Bianchi, RF
(Author)
Other
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Inês Azevedo
(Author)
FMUP
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Correia Pinto, J
(Author)
Other
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Guimarães H
(Author)
FMUP
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Journal
Vol. 18
Pages: 307-312
ISSN: 0939-7248
Publisher: Thieme
Indexing
Scientific classification
FOS: Medical and Health sciences > Other medical sciences
Other information
Authenticus ID: P-003-VRD
Abstract (EN): Purpose: The aim of this study was to describe the long-term functional impact of congenital diaphragmatic hernia repair on the survivors of a cohort of newborns. Methods: We analysed the multidisciplinary follow-up medical charts of 26 congenital diaphragmatic hernia survivors, treated at the Hospital de Sao Joao neonatal intensive care unit from January 1997 to December 2006. Results: The median age at follow-up was 51 (14-141) months. One (4%) patient had died by the age of three months old. Thirteen (50%) patients presented with at least one sequelae, six (23%) presented with two or more. Gastrointestinal problems were the most prevalent, with 6 (23%) children below the fifth percentile for weight and 3 (12%) with gastro-oesophageal reflux. Respiratory morbidity was present in 4 (15%) patients. Four (15%) patients exhibited neurological problems. No case of sensorineural hearing loss was diagnosed. Other findings included musculoskeletal anomalies (12%), recurrence of hernia (8%) and patch rejection (4%). Conclusion: Congenital diaphragmatic hernia survivors present with ongoing morbidities and mortality during infancy and childhood. They constitute a group of patients who require long-term regular follow-up in a multidisciplinary setting to provide adequate support and improve their quality of life.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 6
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