Affiliation:
1. Pediatric Unit, Department of Human Pathology in Adult and Developmental Age 'Gaetano Barresi', University of
Messina, Via Consolare Valeria 1, 98124, Messina, Italy
Abstract
Abstract:
Apnea of prematurity is a common developmental defect affecting newborns, linked to
the immaturity of systems involved in controlling breathing, particularly, central and peripheral
chemoreceptors. Its severity, as well as its clinical manifestations, is inversely associated with gestational
age. Symptoms of immature control of breathing progressively improve with age, with a
resolution around 34-36 weeks of gestational age or 40-44 weeks in infants born at younger gestations.
Prevalence seems to be higher in females and same-gender twins. The role of genetics was
investigated: polymorphisms in genes encoding for adenosine receptors were associated with a
higher risk of developing apnea of prematurity and bronchopulmonary dysplasia. Continuous monitoring
of breathing patterns and vital signs is essential for the early detection of apnea episodes,
while respiratory polygraphy shows limited utility. It is essential to treat newborns with apnea or
other clinical manifestations of immature control of breathing to prevent the risk for long-term
morbidities, such as bronchopulmonary dysplasia or neurodevelopmental impairment. There is no
international consensus on the management of these premature infants. Nowadays, caffeine represents
the first line of pharmacological treatment in association with noninvasive ventilatory support
techniques. Furthermore, in the USA, doxapram is used in the case of refractory therapy with
caffeine. Among nonpharmacological strategies, transfusion, prone positioning, tactile and olfactory
stimulation, and kangaroo care were widely studied, but their efficacy is still unclear.
Publisher
Bentham Science Publishers Ltd.