Pathologic apnea is a cessation of respiratory effort or
airflow for 20s or of shorter duration when accompanied by bradycardia or hypoxemia. Types Central: Absence of airflow due to lack of ventilatory effect Obstructive Absence of airflow despite ventilatory effect. Mixed Initial central component followed by an obstructive component AOP reflects more of physiologic process rather than a pathologic entity.
In contrast apnea in term babies is mostly pathologic.
Apnea from birth to three days.
Apnea in later infancy, from more than three days to
one year. Apnea from birth to three days. Birth : Hypoxic or Ischemic brain injury Intrapartum maternal Drug/GA Early Onset sepsis. Central : Congenital CNS malformations, Seizures ischemic infarction/stroke, Temporal lobe lesions, Metabolic causes Intracranial hemorrhage, Inflammation secondary to pneumonia, sepsis, or meningitis. Positional : SUPC: Feeding related hypoventilation/Apnoea Obstructive :
Functional causes Syndromes of
laryngomalacia, oropharyngeal airway vocal cord paralysis or obstruction paresis, phrenic nerve injury, Pierre Robin sequence, stimulation of the laryngeal Treacher Collins syndrome, chemo reflex from reflux Goldenhar syndrome, problems with coordination Crouzon disease, of sucking, swallowing, and Down syndrome. breathing
Congenital Central Hypoventilation Syndrome.
CCHS / Ondines curse CCHS affects the CNS and ANS Mutation in the PHOX2B gene. PRAM and NPRAM mutations. Reduced or shallow breathing, mostly in sleep. Cardiac asystoles ,hypothermia , BP variations Hirschsprungs disease- NPARMs Eye:Strabismus, abnormal pupil dilation, absent or reduced depth perception. Growth hormone deficiency and congenital hyperinsulinemia. Tumors of neural crest origin. Apnea from >3 days to one year
Periodic Breathing is characterized by cycles in which a
few breaths of 5-10 s alternate with periods of apnea of a similar duration. PB, absent in the first few days of life, becomes frequent at 2-4 weeks of age, and is rare by six months Kelly et al.. CHIME Study Brockmann et al. A single center reviewed infants diagnosed with obstructive sleep apnea (OSA) by polysomnography. Causes of OSA in infancy were different than those found in older children. Gastroesophageal reflux (GER) 30% laryngomalacia in 24% and craniofacial anomalies in 16% Genetic conditions were identified in 53%, most frequently trisomy 21 ALTE BRUE A BRUE is an event Low risk infants are occurring in infants <1 year defined by: of age with one or more of the following: > 60 days of age cyanosis or pallor gestational age >32 weeks and >45 weeks of absent,decreased,or postconceptional age; irregular breathing event duration <1 min marked change in tone (hyper/hypotonia) no CPR altered level of no significant historical responsiveness features no concerning physical findings High risk infants Retrospective review of infants with ALTE 10 12 30
35 20 GER
RSV : Causes ANS dysfuntion Depends to previous Respiratory condition
Suspected Petrussis
Inborn errors of metabolism causing acute metabolic
encepalopathy. Evaluation Maternal, prenatal, intrapartum, resuscitation, and postpartum history. Feeding history General and Systemic examination Lab: Biochemistry and FBC. Neuroimaging EEG ENT consultation Genetics SALT assessment Management and Prevention Strategies ABC CPAP Management : Underlying Causes ?Caffiene