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Planned early delivery or expectant management for late preterm pre-eclampsia (PHOENIX): a randomised controlled trial.
Chappell, Lucy C; Brocklehurst, Peter; Green, Marcus E; Hunter, Rachael; Hardy, Pollyanna; Juszczak, Edmund; Linsell, Louise; Chiocchia, Virginia; Greenland, Melanie; Placzek, Anna; Townend, John; Marlow, Neil; Sandall, Jane; Shennan, Andrew.
Afiliación
  • Chappell LC; Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK. Electronic address: lucy.chappell@kcl.ac.uk.
  • Brocklehurst P; Birmingham Clinical Trials Unit, University of Birmingham, UK.
  • Green ME; Action on Pre-eclampsia, Evesham, UK.
  • Hunter R; Research Department of Primary Care and Population Health, University College London, London, UK.
  • Hardy P; Birmingham Clinical Trials Unit, University of Birmingham, UK.
  • Juszczak E; National Perinatal Epidemiology Unit Clinical Trials Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Linsell L; National Perinatal Epidemiology Unit Clinical Trials Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Chiocchia V; National Perinatal Epidemiology Unit Clinical Trials Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Greenland M; National Perinatal Epidemiology Unit Clinical Trials Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Placzek A; National Perinatal Epidemiology Unit Clinical Trials Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Townend J; National Perinatal Epidemiology Unit Clinical Trials Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Marlow N; UCL EGA Institute for Women's Health, University College London, London, UK.
  • Sandall J; Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.
  • Shennan A; Department of Women and Children's Health, School of Life Course Sciences, King's College London, London, UK.
Lancet ; 394(10204): 1181-1190, 2019 09 28.
Article en En | MEDLINE | ID: mdl-31472930
ABSTRACT

BACKGROUND:

In women with late preterm pre-eclampsia, the optimal time to initiate delivery is unclear because limitation of maternal disease progression needs to be balanced against infant complications. The aim of this trial was to determine whether planned earlier initiation of delivery reduces maternal adverse outcomes without substantial worsening of neonatal or infant outcomes, compared with expectant management (usual care) in women with late preterm pre-eclampsia.

METHODS:

In this parallel-group, non-masked, multicentre, randomised controlled trial done in 46 maternity units across England and Wales, we compared planned delivery versus expectant management (usual care) with individual randomisation in women with late preterm pre-eclampsia from 34 to less than 37 weeks' gestation and a singleton or dichorionic diamniotic twin pregnancy. The co-primary maternal outcome was a composite of maternal morbidity or recorded systolic blood pressure of at least 160 mm Hg with a superiority hypothesis. The co-primary perinatal outcome was a composite of perinatal deaths or neonatal unit admission up to infant hospital discharge with a non-inferiority hypothesis (non-inferiority margin of 10% difference in incidence). Analyses were by intention to treat, together with a per-protocol analysis for the perinatal outcome. The trial was prospectively registered with the ISRCTN registry, ISRCTN01879376. The trial is closed to recruitment but follow-up is ongoing.

FINDINGS:

Between Sept 29, 2014, and Dec 10, 2018, 901 women were recruited. 450 women (448 women and 471 infants analysed) were allocated to planned delivery and 451 women (451 women and 475 infants analysed) to expectant management. The incidence of the co-primary maternal outcome was significantly lower in the planned delivery group (289 [65%] women) compared with the expectant management group (338 [75%] women; adjusted relative risk 0·86, 95% CI 0·79-0·94; p=0·0005). The incidence of the co-primary perinatal outcome by intention to treat was significantly higher in the planned delivery group (196 [42%] infants) compared with the expectant management group (159 [34%] infants; 1·26, 1·08-1·47; p=0·0034). The results from the per-protocol analysis were similar. There were nine serious adverse events in the planned delivery group and 12 in the expectant management group.

INTERPRETATION:

There is strong evidence to suggest that planned delivery reduces maternal morbidity and severe hypertension compared with expectant management, with more neonatal unit admissions related to prematurity but no indicators of greater neonatal morbidity. This trade-off should be discussed with women with late preterm pre-eclampsia to allow shared decision making on timing of delivery.

FUNDING:

National Institute for Health Research Health Technology Assessment Programme.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Preeclampsia / Cesárea / Nacimiento Prematuro / Trabajo de Parto Inducido Tipo de estudio: Clinical_trials / Etiology_studies / Health_technology_assessment / Prognostic_studies Límite: Adult / Female / Humans / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Lancet Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Preeclampsia / Cesárea / Nacimiento Prematuro / Trabajo de Parto Inducido Tipo de estudio: Clinical_trials / Etiology_studies / Health_technology_assessment / Prognostic_studies Límite: Adult / Female / Humans / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Lancet Año: 2019 Tipo del documento: Article