The effect of vitamin C on pulmonary oedema in patients with severe preeclampsia: A single-centre, randomised, placebo-controlled, double-blind trial

To determine whether vitamin C in the first three days postpartum reduces pulmonary oedema (PE) assessed by lung ultrasound in patients with severe preeclampsia. Randomised, placebo-controlled, double-blind trial. Tertiary perinatal centre. Consecutively admitted patients with singleton pregnancies...

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Veröffentlicht in:Anaesthesia critical care & pain medicine 2021-02, Vol.40 (1), p.100800-100800, Article 100800
Hauptverfasser: Korenc, Monika, Zieleskiewicz, Laurent, Stopar Pintaric, Tatjana, Blajic, Iva, Ambrozic, Jana, Lucovnik, Miha
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Sprache:eng
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Zusammenfassung:To determine whether vitamin C in the first three days postpartum reduces pulmonary oedema (PE) assessed by lung ultrasound in patients with severe preeclampsia. Randomised, placebo-controlled, double-blind trial. Tertiary perinatal centre. Consecutively admitted patients with singleton pregnancies complicated by severe preeclampsia. Thirty-four patients received vitamin C (1.5 g/6 h) (n = 17) or placebo (n = 17) at days 1, 2, and 3 postdelivery. Mann-Whitney-U test was used to compare vitamin C vs placebo groups. A p ≤ 0.05 was considered statistically significant. Lung ultrasound was performed once daily in the first three days following delivery. Echo Comet Score (ECS) on day 1 postdelivery was the primary outcome studied and was obtained using the 28-rib interspaces technique. ECS on days 2 and 3 postdelivery were secondary outcomes. There was no significant difference in ECS on day 1 (median 23 (inter-quartile range (IQR) 21–61) vs 18 (IQR 8–35); p = 0.31). All ultrasound examinations on day 1 were performed within six hours from delivery. On days 2 and 3, ECS was significantly lower in vitamin C group compared to placebo (8 (IQR 3–14) vs 35 (IQR 15–78); p = 0.03 and 5 (IQR 3–10) vs 18 (IQR 18–44); p = 0.04, respectively). A single dose of intravenous vitamin C did not reduce PE in postpartum patients with severe preeclampsia on day 1 after delivery. Repeated doses, however, seem to have a delayed effect with a reduction in PE detected on ultrasound on days 2 and 3 following delivery. This trial is registered at ClinicalTrials.gov: ID NCT03451266 (https://clinicaltrials.gov/ct2/show/NCT03451266?term=NCT03451266&draw=2&rank=1).
ISSN:2352-5568
2352-5568
DOI:10.1016/j.accpm.2021.100800