Patient empowerment improves follow‐up data collection after fetal surgery for spina bifida: institutional audit

Author:

Vergote S.12ORCID,Van der Stock J.12,Kunpalin Y.123,Bredaki E.123,Maes H.4,Banh S.3,De Catte L.12,Devlieger R.12ORCID,Lewi L.12ORCID,Devroe S.125,Spencer R.3,David A.123,De Vloo P.4,Van Calenbergh F.4,Deprest J. A.123ORCID

Affiliation:

1. Department of Development and Regeneration KU Leuven Leuven Belgium

2. Department of Obstetrics and Gynaecology University Hospitals Leuven Leuven Belgium

3. Institute for Women's Health University College London London UK

4. Department of Neurosurgery University Hospitals Leuven Leuven Belgium

5. Department of Anesthesiology University Hospitals Leuven Leuven Belgium

Abstract

ABSTRACTObjectivesTo define and grade fetal and maternal adverse events following fetal surgery for spina bifida and to report on the impact of engaging patients in collecting follow‐up data.MethodsThis prospective single‐center audit included 100 consecutive patients undergoing fetal surgery for spina bifida between January 2012 and December 2021. In our setting, patients return to their referring unit for further pregnancy care and delivery. On discharge, referring hospitals were requested to return outcome data. For this audit, we prompted patients and referring hospitals to provide data in cases of missing outcomes. Outcomes were categorized as missing, returned spontaneously or returned following additional request, by the patient and/or referring center. Postoperative maternal and fetal complications until delivery were defined and graded according to Maternal and Fetal Adverse Event Terminology (MFAET) and the Clavien–Dindo classification.ResultsThere were no maternal deaths, but severe maternal complications occurred in seven women (anemia in pregnancy, postpartum hemorrhage, pulmonary edema, lung atelectasis, urinary tract obstruction and placental abruption). No cases of uterine rupture were reported. Perinatal death occurred in 3% of fetuses and other severe fetal complications in 15% (perioperative fetal bradycardia/cardiac dysfunction, fistula‐related oligohydramnios, chorioamnionitis and preterm prelabor rupture of membranes (PPROM) before 32 weeks). PPROM occurred in 42% of patients and, overall, delivery took place at a median gestational age of 35.3 weeks (interquartile range, 34.0–36.6 weeks). Information provided following additional request, from both centers and patients but mainly from the latter, reduced missing data by 21% for gestational age at delivery, 56% for uterine‐scar status at birth and 67% for shunt insertion at 12 months. Compared with the generic Clavien–Dindo classification, the MFAET system ranked complications in a more clinically relevant way.ConclusionsThe nature and rate of severe complications following fetal surgery for spina bifida were similar to those reported in other large series. Spontaneous return of outcome data by referring centers was low, yet patient empowerment improved data collection. © 2023 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

Funder

Fonds Wetenschappelijk Onderzoek

Great Ormond Street Hospital for Children

National Institute for Health and Care Research

Publisher

Wiley

Subject

Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Reference23 articles.

1. European Surveillance of Congenital Anomalies (EUROCAT) database[Available from:www.eurocat‐network.eu].

2. The Association Between Race/Ethnicity and Major Birth Defects in the United States, 1999–2007

3. Fetal surgery for spina bifida: Past, present, future

4. A Randomized Trial of Prenatal versus Postnatal Repair of Myelomeningocele

5. The Management of Myelomeningocele Study: full cohort 30‐month pediatric outcomes;Farmer DL;Am J Obstet Gynecol,2018

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