Lucy C. Chappell
Planned delivery or expectant management for late preterm pre-eclampsia: Study protocol for a randomised controlled trial (PHOENIX trial)
Chappell, Lucy C.; Green, Marcus; Marlow, Neil; Sandall, Jane; Hunter, Rachael; Robson, Stephen; Bowler, Ursula; Chiocchia, Virginia; Hardy, Pollyanna; Juszczak, Edmund; Linsell, Louise; Placzek, Anna; Brocklehurst, Peter; Shennan, Andrew
Authors
Marcus Green
Neil Marlow
Jane Sandall
Rachael Hunter
Stephen Robson
Ursula Bowler
Virginia Chiocchia
Pollyanna Hardy
Professor ED JUSZCZAK ED.JUSZCZAK@NOTTINGHAM.AC.UK
PROFESSOR OF CLINICAL TRIALS AND STATISTICS IN MEDICINE
Louise Linsell
Anna Placzek
Peter Brocklehurst
Andrew Shennan
Abstract
Background: Pre-eclampsia is a pregnancy disorder, characterised by hypertension and multisystem complications in the mother. The adverse outcomes of pre-eclampsia include severe hypertension, stroke, renal and hepatic injury, haemorrhage, fetal growth restriction and even death. The optimal time to instigate delivery to prevent morbidity when pre-eclampsia occurs between 34 and 37 weeks' gestation, without increasing problems related to infant immaturity or complications, remains unclear. Methods/design: The PHOENIX trial is a non-masked, randomised controlled trial, comparing planned early delivery (with initiation of delivery within 48 h of randomisation) with usual care (expectant management) in women with pre-eclampsia between 34 + 0 and 36 + 6 weeks' gestation. The primary objectives of the trial are to determine if planned delivery reduces adverse maternal outcomes, without increasing the short-term harm to infants (composite of perinatal deaths or neonatal unit admissions up to infant hospital discharge) or impacting long-term infant neurodevelopmental status at 2 years corrected age (Parent Report of Cognitive Abilities-Revised). Discussion: Current practice in the UK at the time of trial commencement for management of pre-eclampsia varies by gestation. Previous trials have shown that in women with pre-eclampsia after 37 weeks of gestion, delivery is initiated, as maternal complications are reduced without increasing fetal risks. Prior to 34 weeks of gestation, usual management aims to prolong pregnancy for fetal benefit, unless severe complications occur, necessitating preterm delivery. This trial aims to address the uncertainty for women where the balance of benefits and risks of delivery compared to expectant management are uncertain. Previous trials in this area have been undertaken, but have not provided a definitive answer, and the research question remains active. The results of this trial are expected to influence clinical practice internationally, through direct adoption and by incorporation into guidelines in countries with similar settings. Trial registration: ISRCTN01879376. Registered on 25 November 2013.
Citation
Chappell, L. C., Green, M., Marlow, N., Sandall, J., Hunter, R., Robson, S., Bowler, U., Chiocchia, V., Hardy, P., Juszczak, E., Linsell, L., Placzek, A., Brocklehurst, P., & Shennan, A. (2019). Planned delivery or expectant management for late preterm pre-eclampsia: Study protocol for a randomised controlled trial (PHOENIX trial). Trials, 20(1), Article 85. https://doi.org/10.1186/s13063-018-3150-1
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 18, 2018 |
Online Publication Date | Jan 28, 2019 |
Publication Date | 2019 |
Deposit Date | Jan 29, 2024 |
Publicly Available Date | Jan 31, 2024 |
Journal | Trials |
Electronic ISSN | 1745-6215 |
Publisher | Springer Verlag |
Peer Reviewed | Peer Reviewed |
Volume | 20 |
Issue | 1 |
Article Number | 85 |
DOI | https://doi.org/10.1186/s13063-018-3150-1 |
Public URL | https://nottingham-repository.worktribe.com/output/17088784 |
Publisher URL | https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-018-3150-1 |
Files
s13063-018-3150-1
(810 Kb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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