ABSTRACT
We sought (1) to identify risk factors for meconium aspiration syndrome (MAS) among
infants born to women whose labors were complicated by thick-consistency meconium-stained
amniotic fluid (MSAF), and (2) to determine whether risk factors and infant prognosis
differ according to the time of onset of respiratory distress. We performed a secondary
analysis of a multicenter randomized trial of amnioinfusion (AI) for the prevention
of MAS among women with thick-consistency MSAF. MAS was defined as onset of respiratory
distress requiring oxygen supplementation within the first 4 hours of life. Patients
with respiratory symptoms with onset at ≥4 hours were treated as a separate outcome
category, “late-onset respiratory distress.” We developed peripartum and intrapartum
regression models to identify the risk of MAS and its subgroups. A tracing with marked
abnormalities was a significant risk factor for moderate/severe MAS, but not for mild
MAS or for late-onset respiratory distress. Meconium below the vocal cords and need
for resuscitation immediately after birth were risk factors for mild and moderate/severe
MAS as well as for late-onset respiratory distress. The risk of nonrespiratory comorbidities
varied directly according to the severity of the respiratory distress. Late-onset
respiratory distress shares several risk factors with MAS, as defined by Rossi et
al. The two conditions may represent different manifestations of the same disease
process.
KEYWORDS
Meconium-stained amniotic fluid - meconium aspiration syndrome
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William D FraserM.D. M.Sc.
Department of Obstetrics & Gynecology, Université de Montréal
3175 Chemin de la Côte Sainte-Catherine, Montreal (Quebec), Canada H3T 1C5
eMail: william.fraser@umontreal.ca