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Respiratory Distress in Neonates
Dr.Mohammad Saquib Mallick, FRCS Consultant Paediatric Surgeon , King Fahd Medical City. Riyadh
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Principles of Neonatal Surgery
Types of Newborns: Full-term: >38 weeks and weight > 2.5 kg preterm infant: <38 weeks with appropriate weight SGA: >38 weeks and weight< 2.5 kg VLBW: <32 weeks and <1.5 kg There are physiologic differences between all these infants
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Respiratory Distress The newborn suspected of having respiratory distress should be studied in a logical step by step manner. It is important to establish that the infant has a surgical problem before surgery is performed. Resuscitation must be done before operation Every condition will be dealt accordingly
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Respiratory Distress Causes Surgical Upper airway obstruction
Congenital diaphragmatic hernia Eventration of Diaphragm Esophageal atresia with TOF Pneumothorax Congenital lobar emphysema Congenital cystic adenomatoid malformation Pulmonary Sequestration
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Respiratory Distress Congenital Diaphragmatic Hernia
Incidence: 1:2000 to 5000, female more affected, prematurity and low BW, Left side
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Diaphragmatic Hernia Symptoms None to severe Polyhydramnios Presents birth to after many days Signs Scaphoid abdomen Audible bowel sound in the chest
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Diaphragmatic Hernia Diagnosis: Prenatal <25wks, prognosis bad
Clinical CXR 10% >after neonatal period
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Diaphragmatic Hernia
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Diaphragmatic Hernia Management Reussciataion and stabilization
Laparotomy Primary Patch by silo or muscle Laparoscopic repair
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Eventration of Diaphragm
Def: Abnormal elevation of diaphragm that results in paradoxical motion of affected hemidiaphragm during inspiration and expiration Cause: Congenital Acquired Symptoms: None Resp. distress Wheezing, repeated URI,
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Eventration of Diaphragm
Diagnosis: CXR Fluoroscopy or Real time US
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Eventration of Diaphragm
Management: Conservative plication
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Oesophageal atresia & TOF
Incidence: 1: 5000 live births, 50% associated with anomalies Types: Symptoms and Signs: Excessive salivation Respiratory Distress Inability to pass NG tube Choking and coughing on feeding VACTERL Syndrome
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Oesophageal atresia & TOF
Diagnosis – Clinical & CXR Management: Resuscitation Common type Right thoracotomy Division and repair of TOF Primary anastomosis Pure TOF Division and repair Isolated atresia >3 vertebra Staged surgery (gastrostomy and followed in 3-6 months by delayed repair. If fails then need esophageal replacement (stomach or colon)
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Respiratory Distress Pneumothorax:
The collection of air in the pleural cavity in neonates. Causes: Hyaline membrane disease Meconium aspiration Pulmonary hemorrhage Traumatic Rupture of cong.lung cyst
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Respiratory Distress Diagnosis: Clinical Radiological
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Respiratory Distress
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Respiratory Distress Treatment: 1, Decompression by inserting
chest tube 2, Treat the cause
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Respiratory Distress Congenital Lobar Emphysema:
“ massive over distension of a lobe or a segment of the lung that causes compression of normal lungs and medistinum“
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Respiratory Distress Etiology;
air trapping due to abnormalities in the bronchial cartilages. bronchial cartilage may be absent, hypoplastic, or dysplastic
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Respiratory Distress X-rays
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Respiratory Distress CT Scan:
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Respiratory Distress Management:
Surgical excision of of the involved lobe or lobes is the treatment of choice.
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QUESTIONS ?
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