Reason for enrolment and relevant medical history | SUDI n=18 | Cause of CONI PLUS death | Age at death in weeks |
---|---|---|---|
Group 1: SUDI in extended family Relationship to CONI PLUS baby | |||
Aunt | Yes | SIDS | 3 |
Aunt and cousin | Yes | Pneumonitis | 3 |
Cousin | Yes | SIDS | 8 |
Uncle | Yes | SIDS | 28 |
Cousin | Yes | SIDS | 31 |
Aunt | Yes | Unascertained | 47 |
Group 2: Following ALTE Attributed cause for ALTE | |||
Unexplained | Yes | SIDS associated with coronary artery myocardial bridge | 8 |
Congenital anomaly | Hypertrophic cardiomyopathy (cleft palate and microcephaly contributing factors) | 9 | |
Congenital anomaly | Fibromuscular dysplasia | 10 | |
Congenital anomaly | Hypoplastic left heart | 14 | |
Infection | Tracheal stenosis with complete vascular ring | 14 | |
Unexplained | Yes | SIDS | 16 |
Congenital anomaly | Parainfluenza 3 bronchiolitis, severe development delay | 19 | |
Convulsions | Yes | Unascertained | 20 |
Unexplained | Yes | SIDS (intercurrent respiratory disease and unexplained recent and previous subdural haemorrhage) | 22 |
Congenital anomaly | Yes | Cytomegalovirus pneumonitis, systemic cytomegalovirus infection and residual aortic coarctation | 23 |
Congenital anomaly | Agenesis corpus callosum, bronchopneumonia | 25 | |
Congenital anomaly | Nemaline myopathy | 41 | |
Gastro-oesophageal reflux/feeding related | Spinal muscular atrophy type 1 | 42 | |
Congenital anomaly | Asphyxiating thoracic-dystrophy—Jarcho–Levin | 47 | |
Group 3: Death in previous sibling with known cause Sibling cause of death | |||
Myocarditis | Yes | Myocarditis | 3 days |
Congenital pneumonia | Ornithine transcarbamylase deficiency | 3 days | |
Congenital myopathy | Mitochondrial myopathy | 17 | |
Prematurity in two siblings | Yes | Unascertained, Jeune syndrome, agenesis corpus callosum, left microphthalmia, rotavirus infection | 25 |
Dandy–Walker syndrome | Dandy–Walker syndrome | 28 | |
Prematurity in two siblings | Spino-muscular atrophy | 31 | |
Prematurity | Yes | Unascertained | 43 |
Group 4: Prematurity | |||
28-week gestation, intrauterine growth restriction | Chronic lung disease | 33 | |
Group 6: Congenital anomaly/ill at birth | |||
Treacher Collins syndrome | Yes | Aspiration pneumonia | 4 |
Oesophageal atresia, tracheo-oesophageal fistula and duodenal atresia | Hypoxic ischaemic encephalopathy | 13 | |
Birth asphyxia | Yes | Hypoxic ischaemic encephalopathy | 16 |
Pierre Robin sequence | Yes | Upper respiratory tract obstruction | 18 |
Congenital contractures | Unspecified myopathy | 25 | |
Convulsions, neurodegenerative disorder | Epileptic encephalopathy | 26 | |
Cerebral palsy, global delay | Yes | H1N1 virus | 34 |
Fallot's tetralogy | Renal failure complicating Fallot's repair | 49 | |
22q deletion and atrial septal defect | Respiratory cyncytial virus bronchiolitis, congenital anomalies | 49 |
ALTE, apparent life threatening event; CONI PLUS, Care of Next Infant Plus; SIDS, sudden infant death syndrome; SUDI, sudden unexpected death in infancy.