pedia2 20100513 neo 2 - respiratory disorders of nb
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Respiratory Disorders of theRespiratory Disorders of the
NewbornNewborn
Arnold M. Lintag, M.D.,
DPPS
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I. Transition to PulmonaryI. Transition to Pulmonary
RespirationRespiration
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II. First BreathII. First Breath
Problems with LBW infants
A. Compliant chest wall
B. FRC is small
C. Abnormalities in ventilation perfusion ratio
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III. Periodic BreathingIII. Periodic Breathing
Periodic Breathing
A. Pattern
B. Found in prematures up to 36th
week
C. Considered normal
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A. Due to primary disorders
B. Idiopathic Apnea of Prematurity
1. Upper airway obstruction
2. Immaturity
3. Mixed
C. Short apnea - central
D. Long apnea - mixed
IV. Apnea > 20 sec. plus bradycardiaIV. Apnea > 20 sec. plus bradycardia
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CNS
Respiratory
Infectious
Gastrointestinal
IVH, drugs, seizures, hypoxic injury, herniation,neuromuscular disorders
Pneumonia, obstructive airway lesions,atelectasis, extreme prematurity (
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Metabolic
Cardiovascular
Idiopathic
Glucose, calcium, PO2, sodium,
ammonia, organic acids, ambient temperature,hypothermia
Hypotension, hypertension, heart failure,anemia, hypovolemia, vagal tone
Immaturity of respiratory center, sleep state,upper airway collapse
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IV. ApneaIV. Apnea
E. Clinical manifestations
1. Rare on first day
2. Apnea with prematurity occurs on 2nd -
7th day of life
3. 2nd week - warrants investigation
F. Treatment:
1. Theophylline
2. Treat the underlying cause
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A. Incidence
1. 50% of all neonatal deaths
2. 60 to 80% < 28 wks.
3. 15-30% 32-36 wks.
4. 5% beyond term
5. Term - IDM
6. Preterm male
7. Reduced incidence - maternal hypertension,
PROM, opiate addiction, antenatal corticosteroid
use
V. Hyaline Membrane Disease orV. Hyaline Membrane Disease or
Respiratory Distress SyndromeRespiratory Distress Syndrome
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B. Pathophysiology
1. Insufficient amounts of surfactant
a. 20 weeks - good concentration - does
not reach surface of the lungs
b. 28-32 weeks - not enough amounts
reaching the surface
c. > 35 weeks - mature amounts
V. Hyaline Membrane Disease orV. Hyaline Membrane Disease or
Respiratory Distress SyndromeRespiratory Distress Syndrome
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B. Pathophysiology
2. Components of Surfactants
3. Surfactant synthesis depends on:
a. Normal pH
b. Temperature
c. perfusion
V. Hyaline Membrane Disease orV. Hyaline Membrane Disease or
Respiratory Distress SyndromeRespiratory Distress Syndrome
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4. Important synthesis maybe depressed by:
a. asphyxia c. pulmo. ischemia
b. hypoxemia
hypovolemia hypoglycemia cold
stress
d. epithelial lining maybe injured by high oxygen
V. Hyaline Membrane Disease orV. Hyaline Membrane Disease or
Respiratory Distress SyndromeRespiratory Distress Syndrome
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B. Pathophysiology
4. Ischemia -- necrosis -- damage
capillary endothelium -- transudation of
fluids into alveoli entrapping necrotic
tissue, RBG, proteins-- hyaline
membrane
V. Hyaline Membrane Disease orV. Hyaline Membrane Disease or
Respiratory Distress SyndromeRespiratory Distress Syndrome
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C. Clinical Manifestations:
1. Golden Period - 72 hours after delivery
2. Sign Symptoms of respiratory distress
which worsens3. Occasional rales, decreased breath sounds
V. Hyaline Membrane Disease orV. Hyaline Membrane Disease or
Respiratory Distress SyndromeRespiratory Distress Syndrome
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D. Prevention
1. Prenatal check-ups
2. L/S ratio
3. Betamethasone to mothers in their < 32nd
week of gestation and may deliver within 42-
72 hours. L/S ratio shows lung maturity
4. Surfactant Therapy
V. Hyaline Membrane Disease orV. Hyaline Membrane Disease or
Respiratory Distress SyndromeRespiratory Distress Syndrome
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E. Diagnosis: Chest X-ray -- white out appearanceF. Treatment
1. Mechanical ventilation
2. Supportivea. temperature
b. oxygenation
c. acidosisd. electrolytes
e. blood glucose
3. Antibiotics
V. Hyaline Membrane Disease orV. Hyaline Membrane Disease orRespiratory Distress SyndromeRespiratory Distress Syndrome
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VI. Interstitial Pulmonary FibrosisVI. Interstitial Pulmonary Fibrosis
(Bronchopulmonary Dysplasia: Wilson Mikity
Syndrome
A. Found in prematures < 32 weeks
B. Found in terms with a history of Meconium
Aspiration
C. Clinical Manifestations
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D. Increasing dependency on O2
E. Roentgenogram: hyper lussent bubbly
appearance because several small areas of
atelectasis-cystic lesions
F. Treatment Supportive
VI. Interstitial Pulmonary FibrosisVI. Interstitial Pulmonary Fibrosis
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A. Usually in Cesarean deliveries
B. slow absorption of fetal lung fluids
VII. Transient Tachypnea of theVII. Transient Tachypnea of the
NewbornNewborn
C. Clinical Manifestation
1. Tachypneic
2. Cyanosis relieved by Oxygen
3. Recovers after 3 days
D. Treatment is supportive
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A. Pneumothorax
1. Incidence
a. 1 - 2%
b. males
c. term and postterm
d. Meconium aspiration
e. mechanical ventilation
f. vigorous resuscitation
g. RDS
VIII. Air Leak SyndromesVIII. Air Leak Syndromes
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A. Pneumothorax2. Pathogenesis
a. alveolar rupture - pulmonary interstitial
emphysema
VIII. Air Leak SyndromesVIII. Air Leak Syndromes
b. alveolar rupture - perivascular sheaths
pneumomediastinum
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A. Pneumothorax
3. Clinical Manifestations
a. asymptomatic - hyperresonance,
decreased breath sounds, crepitant rales
b. symptomatic - dyspnea, tachypnea, cyanosis
- displacement of the heart
towards the unaffected side
VIII. Air Leak SyndromesVIII. Air Leak Syndromes
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A. Pneumothorax
4. Diagnosis
Chest x-ray - hyperlucency on the affected
side
5. Treatment
a. supportive
b. observe if air leak is small
c. Chest tube attached to underwater seal
if severe
VIII. Air Leak SyndromesVIII. Air Leak Syndromes
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A. Fetal distress and hypoxia in term or
postterm
B. Pathogenesis
1. First Breath - aspirate
2. Small airway obstruction, ball-valve
effect
3. Chemical pneumonitis
IX. Meconium AspirationIX. Meconium Aspiration
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C. Clinical Manifestations
--- tachypnea, grunting, cyanosis, retractions
after delivery
D. Diagnosis
1. History
2. Chest X-ray: flattening of the diaphragm,
patchy infiltrates on both lungs
IX. Meconium AspirationIX. Meconium Aspiration
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E. Treatment:
1. Direct laryngoscopy and suction
2. Mechanical ventilation
3. Supportive
IX. Meconium AspirationIX. Meconium Aspiration
F. Complications:1. Pneumothorax
2. Persistent fetal circulation
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A. Found in term and post term infants with:
1. Birth asphyxia
2. MAS
3. Hypoglycemia
4. Polycythemia
5. Pulmonary hypoplasia --- diaphragmatic hernia
6. Oligohydramnios
7. Pleural effusions
8. Idiopathic
X. Persistent fetal CirculationX. Persistent fetal Circulation
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B. Pathophysiology
--- increased pulmonary vascular resistance -
persistence of R to L shunting
X. Persistent fetal CirculationX. Persistent fetal Circulation
C. Clinical Manifestations: (within 12 hours)
1. Tachypnea
2. Severe cyanosis
3. Retractions
4. Shock
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X. Persistent fetal CirculationX. Persistent fetal Circulation
D. Diagnosis
1. Hypoxia is labile and out of proportion -
chest roentgenograms
2. Unresponsive to oxygen by cannula or
hood
3. Right to left shunting by Doppler flow
studies in foramen ovale and ductus
arteriosus
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E. Treatment:
1. Treat underlying cause
2. Mechanical ventilation-hyperventilation-
decrease pCO2
3. Tolazoline-alpha adrenergic antagonist- increase fluids plus dopamine
4. Extracorporeal Membrane Oxygenation
X. Persistent fetal CirculationX. Persistent fetal Circulation
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XI. Pulmonary HemorrhageXI. Pulmonary Hemorrhage
A. Found in ICU patients with stormy
courses
B. Bleeding through endotracheal tube, nostrils,
month usually reddish and frothy
C. Indicative of a terminal course