Patent ductus arteriosus shunt elimination results in a reduction in adverse outcomes: a post hoc analysis of the PDA RCT cohort

被引:24
作者
Bussmann, Neidin [1 ]
Smith, Aisling [1 ]
Breatnach, Colm R. [1 ]
McCallion, Naomi [1 ,2 ]
Cleary, Brian [3 ,4 ]
Franklin, Orla [5 ]
McNamara, Patrick J. [6 ,7 ,8 ,9 ]
EL-Khuffash, Afif [1 ,2 ]
机构
[1] Rotunda Hosp, Dept Neonatol, Dublin, Ireland
[2] Royal Coll Surgeons Ireland, Dept Paediat, Dublin, Ireland
[3] Rotunda Hosp, Dept Pharm, Dublin, Ireland
[4] Royal Coll Surgeons Ireland, Sch Pharm, Dublin, Ireland
[5] Our Ladys Childrens Hosp Crumlin, Dept Paediat Cardiol, Dublin, Ireland
[6] Stead Family Childrens Hosp, Div Neonatol, Iowa City, IA USA
[7] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[8] Univ Iowa, Dept Cardiol, Iowa City, IA USA
[9] Univ Iowa, Cardiol, Iowa City, IA USA
关键词
CONTROLLED-TRIAL; PRETERM INFANTS; SEVERITY SCORE; IBUPROFEN; PLACEBO;
D O I
10.1038/s41372-021-01002-z
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective A post hoc appraisal of the PDA RCT to assess the relationship between early patent ductus arteriosus (PDA) shunt elimination and chronic lung disease or death (CLD/Death). Study design Infants <29 weeks were divided into four groups: intervention arm in whom PDA closure was achieved (n = 17); intervention arm in whom PDA closure was not achieved (n = 13); placebo arm (n = 30); low risk infants (n = 13). The main outcome measure was CLD/Death. Results The rates of CLD/Death were lower in the Intervention Success Group (29%) when compared to the Intervention Failure Group (85%) or the Placebo Group (60%, all p < 0.05). There was no difference in CLD/Death between the Intervention Success and Low Risk Groups (8%, p > 0.05). A persistent PDA beyond Day 8 was associated with CLD/Death (aOR 6.5 [1.7-25.5]). Conclusions Early shunt elimination in preterm infants with a PDA may reduce respiratory morbidity when compared to infants with prolonged shunt exposure.
引用
收藏
页码:1134 / 1141
页数:8
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