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Respiratory Disease In Childhood. Nick Connolly Paediatric SpR NHS Tayside. Respiratory problems in children. Neonatal respiratory problems Respiratory problems in older children Chronic Acute. Scenario .
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Respiratory Disease In Childhood Nick Connolly Paediatric SpR NHS Tayside
Respiratory problems in children Neonatal respiratory problems Respiratory problems in older children Chronic Acute
Scenario An infant born at 30 weeks gestation develops respiratory distress at age 2 hours
Respiratory Distress Syndrome • Relative Surfactant deficiency • 1% all births • Predominantly in preterm – inverse relationship with gestation
Surfactant • Phospholipid • Apoproteins • Secreted at 30-32/40 • Lack of surfactant results in atelectasis and impairment of gas exchange • Production stimulated by steroids
Further problems • Ventilated • Sudden deterioration requiring increased oxygen • No breath sounds on the right side of chest
Pneumothorax • Air in pleural space • Increased incidence with IPPV, CPAP and ventilation • Other risk factors – RDS (stiff lungs) • Spontaneous - occurs in around 1% vaginal deliveries, 1.5% caesarean sections
Chronic Lung Disease • Oxygen requirement beyond 36 weeks corrected gestation plus evidence of pulmonary parenchymal disease on CXR • Generally follows RDS • Barotrauma, volume trauma, high inspired oxygen • Healing stage associated with continued lung growth over 2-3 years – often wheezy
Scenario New born full-term infant with severe breathing difficulty after birth ?Dextrocardia
Diaphragmatic Hernia Incidence:1/2400 Associated pulmonary hypoplasia Commonest- Posterolateral (Bochdalek), left-sided Avoid bag-mask IPPV? Respiratory support Surgical
Weight(length/height)..plotted! ?clubbing Chest shape Auscultation Examination
Cystic fibrosis A 1 year-old child presenting with a prolonged history of cough, loose stools and failure to thrive A newborn infant with a raised immuno-reactive trypsin level on neonatal screening who is also found to be homozygous for the ΔF508 deletion
Cystic Fibrosis • Autosomal recessive • Carrier incidence roughly 1 in 25 people • Mutations in the CFTR gene • Multisystem disorder • Respiratory infections are prominent
Differential diagnosis Immune deficiency Ciliary dyskinesia Asthma Kartagener’s/ immotile cilia syndrome- rare
Scenario NM is a 7 month old infant with cystic fibrosis who was admitted with 2 chest infections. He grew Staphylococcus aureus on his respiratory secretions
Cystic Fibrosis Team Clinician Specialist nurse Clinical psychologist Social worker Physiotherapist Dietician
A 7-year child presents to your clinic with a 3-month history of cough worse at night or during active play Diagnosis: ASTHMA
Asthma – Diagnosis in ChildrenSIGN Guideline May 2008 Clinical Features that increase probability: • One or more : wheeze, cough, chest tightness, difficulty breathing • Atopy(personal or family history) • Widespread wheeze on auscultation • Response to Rx
Asthma – Diagnosis in ChildrenSIGN Guideline May 2008 High Probability – diagnosis of asthma likely (trial of Rx – further Ix if poor response) Low Probability – consider Ix & ? Referral Intermediate Probability: ?watchful waiting ?spirometry(response) ? Rx & evaluate
Management Stage 1: Treat with inhaled beta-agonists when needed Stage 2: Treat with regular inhaled steroids Stage 3A: Regular inhaled steroids + Long acting beta agonists Stage 3B: Stage 3A + Leukotriene antagonists
Passive Smoking • Reduces birthweight by 250g • 4500 pregnancy losses p.a. • 30% increase in Perinatal Mortality • Teratogenic : airways, cleft lip/palate • Glue ear • Carcinogenic • 4 million children live with smoking parent • Increase likelihood of asthma attack
Acute asthma Cough and wheeze worsening over hours or days
Treatment Oxygen Nebulised bronchodilator Oral prednisolone IV salbutamol IV aminophylline IV magnesium Ventilatory support
Scenario • 6 week old presented with increased work of breathing and possible apnoes • URTI symptoms over last 2 days
Bronchiolitis • Viral infection – RSV • Usually under 18 months old • More severe in younger babies, ex prem, family of smokers • Tachypnoea, poor feeding, irritating cough • Apnoea in small babies • Treatment is supportive • Increased incidence of wheezing episodes in the next ?10 years
Scenario 10 year old girl with cough, high fever and sputum production Previously very well Clinical examination: Dullness on percussion Vocal fremitus and resonance Bronchial breathing
Pneumonia Neonates: GBS, E.coli, Klebsiella, Staph aureus Infants: Strep pneumoniae, Chlamydia School age: Strep pneumoniae, Staph aureus, Gr A strep, Bordetella, Mycoplasma, Legionella
Scenario A 2-year old child presenting with barking cough and difficulty in breathing of sudden onset
Differential Diagnosis Inhaled foreign body Laryngomalacia Epiglottitis and bacterial tracheitis Allergy Croup