2017
DOI: 10.1097/pcc.0000000000001305
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Association of Response to Inhaled Nitric Oxide and Duration of Mechanical Ventilation in Pediatric Acute Respiratory Distress Syndrome*

Abstract: Objective Literature regarding appropriate use of inhaled nitric oxide (iNO) for pediatric acute respiratory distress syndrome (PARDS) is sparse. This study aims to determine if positive response to iNO is associated with decreased mortality and duration of mechanical ventilation in PARDS. Design Retrospective cohort study Setting Large pediatric academic medical center Patients or Subjects 161 children with PARDS and iNO exposure for ≥1 hour within 3 days of PARDS onset. Interventions Patients with ≥2… Show more

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Cited by 32 publications
(24 citation statements)
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References 40 publications
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“…Several small RCTs [289][290][291] and observational studies have described significant improvement in oxygenation after iNO therapy [292]. Many, but not all, of these studies include patients with sepsis [290,291,[293][294][295][296], and few analyze longer term, clinically relevant outcomes such as mortality. A 2016 Cochrane review indicated no mortality benefit from iNO administration (RR, 0.78; 95% CI, 0.51-1.18) in three RCTs [297].…”
mentioning
confidence: 99%
“…Several small RCTs [289][290][291] and observational studies have described significant improvement in oxygenation after iNO therapy [292]. Many, but not all, of these studies include patients with sepsis [290,291,[293][294][295][296], and few analyze longer term, clinically relevant outcomes such as mortality. A 2016 Cochrane review indicated no mortality benefit from iNO administration (RR, 0.78; 95% CI, 0.51-1.18) in three RCTs [297].…”
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confidence: 99%
“…The inability to control for these important confounding variables led to this study being criticized by the pediatric critical care community. (19) When examining the subjects enrolled in their study many of them (58%) were treated with antiarrhythmics which is unusual for PARDS and indicates a different study population than our study. The results for our primary outcome were similar; no significant difference in mortality.…”
Section: Discussionmentioning
confidence: 70%
“…A ≥20% improvement in mean daily OSI, within 72 hours of day 0 was determined a priori to be response to methylprednisolone. We selected this definition based on previous studies which had used OI/OSI as an outcome measure [20, 21].…”
Section: Methodsmentioning
confidence: 99%