Paediatrics
| Page | Contents |
|---|---|
| 15.01 | • Paediatric life support • Newborn life support • Intraosseous infusion• Anaphylaxis |
| 15.02 | Infections • Traffic light assessment of kids • Meningitis• Encephalitis |
| 15.03 | Infections • Measles• Mumps• Rubella • Erythema infectiosum• HFMD • Roseola infantum• Chickenpox • HIV in children |
| 15.04 | Respiratory disorders • Upper respiratory tract infections - Croup- Epiglottitis - Bacterial tracheitis- Diphtheria • Lower respiratory tract infections - Bronchiolitis- VIW - Pneumonia- Whooping cough • Asthma• Cystic fibrosis [02.04] |
| 15.05 | Cardiovascular disorders • Ventricular septal defect (VSD) • Atrial septal defect (ASD) • Patent ductus arteriosus • Coarctation of the aorta • Congenital aortic valve stenosis • Eisenmenger's syndrome |
| 15.06 | Cardiovascular disorders • Tetralogy of Fallot (ToF) • Transposition of great arteries (TGA) • Ebstein's anomaly• Kawasaki disease • Murmurs and heart sounds in children |
| 15.07 | GI disorders • Abdominal pain• Neuroblastoma • Coeliac disease• Malnutrition • Diarrhoea & vomiting |
| 15.08 | GI disorders • Appendicitis• Intussusception • Pyloric stenosis• Hirschsprung • Oesophageal atresia |
| 15.09 | GI disorders • Congenital diaphragmatic hernia • Inguinal hernia• Imperforate anus • Mid-gut malrotation • Gastroschisis & omphalocele • Meckel's diverticulum • Infant feeding problems |
| 15.10 | Renal & urological disorders • UTIs• Nephrotic syndrome • Acute glomerulonephritis |
| 15.11 | Renal & urological disorders • Phimosis• Cryptorchidism • Hypospadias• Horseshoe kidney • Wilms' tumour (nephroblastoma) • Haemolytic uraemic syndrome (HUS) • Nocturnal enuresis |
| 15.12 | Neurological disorders • Epilepsy• Status epilepticus • Brain tumours |
| 15.13 | Neurological disorders • Neural tube defects • Autism spectrum disorder |
| 15.14 | Haemonc disorders • Anaemia• Iron deficiency • Sickle cell disease • Hereditary spherocytosis • Henoch-Schonlein purpura |
| 15.15 | Haemonc disorders • Immune thrombocytopaenia • Acute lymphoblastic leukaemia • Primary immunodeficiencies • Severe combined immunodeficiency |
| 15.16 | Endocrine disorders • Diabetes mellitus + MODY• DKA • Hypothyroidism |
| 15.17 | Endocrine disorders • Hyperthyroidism • Inherited metabolic diseases • Glycogen storage disorders • Phenylalanine ketonuria • Lysosomal storage diseases |
| 15.18 | Endocrine disorders • Precocious puberty • Congenital adrenal hyperplasia • Genetic disorders summary |
| 15.19 | Developmental disorders • Developmental milestones • Speech delay• Cerebral palsy • Muscular dystrophies (incl Duchenne) • Global developmental delay |
| 15.20 | Genetic disorders • Down + other trisomies • Klinefelter• Triple X• Turner |
| 15.21 | Genetic disorders • Cri du chat• DiGeorge • Williams• Achondroplasia • Marfan• Noonan• Fragile X |
| 15.22 | Neonates • Neonatal sepsis• Seizures • Respiratory distress• Jaundice |
| 15.23 | Neonates • Necrotising entercolitis • Hypoglycaemia• Hypotonia • Minor problems, including skin issues |
| 15.24 | Miscellaneous • Non-accidental injury • Screening schedule (perinatal) • Sudden infant death syndrome - Brief unexplained resolved event • Vaccination schedule |