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1.
Arch Dis Child Fetal Neonatal Ed ; 91(1): F21-5, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16159956

ABSTRACT

OBJECTIVE: To describe the later health status of newborn infants who received extracorporeal membrane oxygenation (ECMO) for acute respiratory failure in the era after the UK ECMO trial. DESIGN: Prospective follow up study of newborn infants who received ECMO at a single centre between January 1997 and January 2001. SETTING: Departments of ECMO and Paediatric Intensive Care, University Hospitals of Leicester. PATIENTS: All babies who received ECMO within 14 days of birth. INTERVENTIONS: Neurodevelopment screening using the schedule for growing skills-II (SGS-II) assessment tool. MAIN OUTCOME MEASURES: Survival at 12 months of age by disease and functional development at follow up. RESULTS: A total of 145 neonates received ECMO for treatment of respiratory failure. Of these, 108 (75%) were alive at 1 year of age. There were no deaths in children treated for respiratory failure secondary to meconium aspiration syndrome (73/145). Ninety three (86% of survivors) infants attended a follow up visit at 11-19 months postnatal age. Eighty two were classed as normal, seven as having "impairment", and four as having "severe disability". CONCLUSIONS: Most newborn infants with acute respiratory failure treated with ECMO will have a normal neurodevelopment screening assessment at 11-19 months of postnatal age. There is no evidence to suggest that changes in neonatal practice since the UK ECMO trial have led to changes in outcome of infants undergoing ECMO therapy.


Subject(s)
Extracorporeal Membrane Oxygenation , Respiratory Insufficiency/therapy , Acute Disease , Child Development , Developmental Disabilities/etiology , Follow-Up Studies , Humans , Infant, Newborn , Motor Skills , Prognosis , Respiratory Insufficiency/psychology , Survival Rate
2.
J Postgrad Med ; 43(4): 106-8, 1997.
Article in English | MEDLINE | ID: mdl-10740738

ABSTRACT

Chordoma, a rare malignant tumour of early adulthood, rarely presents in children. We report such a case of rare malignant tumour which was diagnosed in the first decade of life.


Subject(s)
Chordoma/surgery , Spinal Neoplasms/surgery , Child, Preschool , Chordoma/diagnostic imaging , Chordoma/pathology , Colostomy , Female , Humans , Sacrococcygeal Region , Spinal Neoplasms/diagnostic imaging , Spinal Neoplasms/pathology , Tomography, X-Ray Computed
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