Abstract | INTRODUCTION: METHODS: We investigated neonates with critical CHD who were started on prostaglandin E1 at 0.01 µg/kg/minute. We reviewed 154 consecutive patients who were separated into three anatomical groups: obstruction to systemic circulation, obstruction to pulmonary circulation, and inadequate mixing (d-transposition of the great arteries). Treatment failure rates and two commonly reported side effects, respiratory depression and seizure, were studied. RESULTS: A total of 26 patients (17%) required a dose increase in prostaglandin E1. Patients with pulmonary obstruction were more likely to require higher doses than patients with systemic obstruction (15/49, 31% versus 9/88, 10%, p = 0.003). Twenty-eight per cent of patients developed respiratory depression and 8% of patients needed mechanical ventilation. Prematurity (<37 week gestation) was the primary risk factor for respiratory depression. No patient required dose escalation or tracheal intubation while on transport. No patient had a seizure attributed to prostaglandin E1. CONCLUSIONS:
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Authors | Daniel Vari, Wendi Xiao, Shashank Behere, Ellen Spurrier, Takeshi Tsuda, Jeanne M Baffa |
Journal | Cardiology in the young
(Cardiol Young)
Vol. 31
Issue 1
Pg. 63-70
(Jan 2021)
ISSN: 1467-1107 [Electronic] England |
PMID | 33140712
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Alprostadil
(adverse effects)
- Ductus Arteriosus, Patent
(drug therapy)
- Heart Defects, Congenital
(drug therapy)
- Humans
- Infant
- Infant, Newborn
- Infusions, Intravenous
- Pulmonary Circulation
- Respiration, Artificial
- Transposition of Great Vessels
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