Comparative Effectiveness of Nonsteroidal Anti-inflammatory Drug Treatment vs No Treatment for Patent Ductus Arteriosus in Preterm Infants.
Comparative Effectiveness of Nonsteroidal Anti-inflammatory Drug Treatment vs No Treatment for Patent Ductus Arteriosus in Preterm Infants.
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非甾体类抗炎药物治疗的比较有效性与在早产儿中没有专利导管的治疗。
DOI:
10.1001/jamapediatrics.2016.4354
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发表时间:
2017-03-06
期刊:
影响因子:
26.1
通讯作者:
Klebanoff MA
中科院分区:
文献类型:
--
作者:
Slaughter JL;Reagan PB;Newman TB;Klebanoff MA
Patent Ductus Arteriosus (PDA) is associated with increased mortality and worsened respiratory outcomes including bronchopulmonary dysplasia (BPD) in preterm infants. Nonsteroidal Anti-inflammatory Drugs (NSAIDs) are efficacious in closing PDA, but the effectiveness of NSAID-mediated PDA closure in improving mortality and preventing BPD is unclear. To determine the effectiveness of NSAID treatment for PDA in reducing mortality and moderate/severe BPD at 36-weeks postmenstrual age. Within a retrospective cohort of infants discharged between January 2006–December 2013, we performed an instrumental variable analysis that incorporated provider preference-based, institutional variation in NSAID treatment frequency to determine the effect of NSAID treatment for PDA on mortality and BPD. Neonatal Intensive Care Units (NICUs) within 25 United States’ Children’s Hospitals included in the Pediatric Health Information System. 12,018 infants born at ≤28-weeks-gestation who were admitted to the NICU on their birth date and hospitalized at least 3 days. Proportion of NSAID treated infants born at each infant’s institution within ±6-months of that infant’s birth. The primary composite outcome was death, moderate, or severe BPD at 36-weeks’ postmenstrual age. The instrument, the proportion of NSAID treated infants at each unique infant’s hospital within ±6-months of that infant’s birth, was significantly associated with NSAID treatment and not significantly associated with gestation, race, or gender. An individual infant’s chances of receiving NSAID treatment increased by 0.84 percentage points (95% CI: 0.8–0.9; p<0.001) for every 1 percentage point increase in the annual NSAID treatment percentage at a given hospital. Instrumental variable analysis demonstrated no significant association between NSAID treatment and the odds of mortality or BPD (OR 0.94 [95% CI: 0.70, 1.25]), mortality (0.73 [0.43, 1.13]), or BPD in survivors (1.01 [0.73, 1.45]). When we incorporated provider preference-based practice variation as an instrument to minimize the effect of unmeasured confounding, we detected no changes in the odds of mortality or moderate/severe BPD among similar ≤28-week gestation preterm infants following NSAID treatment for PDA initiated 2–28 days postnatally. Our findings are in agreement with available randomized trial evidence and support a conservative approach to PDA management.
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影响因子:
2.9
作者:
Benitz, W. E.
通讯作者:
Benitz, W. E.
影响因子:
2.9
作者:
Hermes-DeSantis, E. R.;Clyman, R. I.
通讯作者:
Clyman, R. I.
影响因子:
2
作者:
Lainwala, Shabnam;Hussain, Naveed
通讯作者:
Hussain, Naveed
DOI:
10.1164/rccm.201101-0055oc
发表时间:
2011-06-15
影响因子:
24.7
作者:
Laughon, Matthew M.;Langer, John C.;Walsh, Michele C.
通讯作者:
Walsh, Michele C.
DOI:
10.1177/0272989x11416512
发表时间:
2012-01
期刊:
Medical decision making : an international journal of the Society for Medical Decision Making
影响因子:
--
作者:
Newman TB;Vittinghoff E;McCulloch CE
通讯作者:
McCulloch CE