Diagnosis of patent ductus arteriosus by different echocardiographic methods in very preterm infants

不同超声心动图方法在极早产儿动脉导管未闭诊断中的应用

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Abstract

There is no consensus regarding the timing and diagnostic criteria for identifying hemodynamically significant patent ductus arteriosus (hsPDA). Our aim was to evaluate if the use of different diagnostic criteria at different times could be associated with a different incidence of hsPDA in very preterm infants. We studied 41 infants with gestational age < 32 weeks born in neonatal intensive care units (NICU) in Florence, Italy, or in Paris, France. They received the first echocardiography between 24 and 48 h of life and the second between 72 and 84 h to diagnose hsPDA using Florence and Paris criteria and PDA severity score. Concordance of diagnosis between criteria was evaluated with the Cohen unweighted κ statistic. The incidence of hsPDA diagnosed by the Florence (35%) or Paris (34%) criteria or by PDA severity score (35%) was similar. Concordance was substantial between Florence and Paris criteria and between Florence criteria and PDA severity score but was fair between Paris criteria and PDA severity score. Moreover, concordance significantly changed from the first to the second echocardiography. Conclusion: The studied diagnostic criteria showed important variations of concordance when applied at different times. This led to diagnose hsPDA in different patients at different times while leaving the overall percentage of hsPDA unchanged. Our results suggest that more attention should be paid to the choice of diagnostic criteria for individuating hsPDA in very preterm infants.  What is Known: • There is no consensus regarding the timing and diagnostic criteria for individuating hemodynamically significant patent ductus arteriosus (hsPDA) in preterm infant. • This implies large variations in its frequency and management diagnosis between centers. What is New: • This study evaluated for the first time how different diagnostic criteria used at different postnatal times may influence the diagnosis of hsPDA in very preterm infants.

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