Fetal electrocardiography ST-segment analysis for intrapartum monitoring: a critical appraisal of conflicting evidence and a way forward.

ST segment analysis acidemia cardiotocography cesarean delivery fetal blood sampling fetal death fetal distress fetal electrocardiogram fetal heart rate intrapartum fetal monitoring meta-analysis observational studies perinatal asphyxia randomized controlled trials real-world evidence

Journal

American journal of obstetrics and gynecology
ISSN: 1097-6868
Titre abrégé: Am J Obstet Gynecol
Pays: United States
ID NLM: 0370476

Informations de publication

Date de publication:
12 2019
Historique:
received: 26 10 2018
revised: 31 03 2019
accepted: 01 04 2019
pubmed: 14 4 2019
medline: 17 3 2020
entrez: 14 4 2019
Statut: ppublish

Résumé

In the past century, some areas of obstetric including intrapartum care have been slow to benefit from the dramatic advances in technology and medical care. Although fetal heart rate monitoring (cardiotocography) became available a half century ago, its interpretation often differs between institutions and countries, its diagnostic accuracy needs improvement, and a technology to help reduce the unnecessary obstetric interventions that have accompanied the cardiotocography is urgently needed. During the second half of the 20th century, key findings in animal experiments captured the close relationship between myocardial glycogenolysis, myocardial workload, and ST changes, thus demonstrating that ST waveform analysis of the fetal electrocardiogram can provide information on oxygenation of the fetal myocardium and establishing the physiological basis for the use of electrocardiogram in intrapartum fetal surveillance. Six randomized controlled trials, 10 meta-analyses, and more than 20 observational studies have evaluated the technology developed based on this principle. Nonetheless, despite this intensive assessment, differences in study protocols, inclusion criteria, enrollment rates, clinical guidelines, use of fetal blood sampling, and definitions of key outcome parameters, as well as inconsistencies in randomized controlled trial data handling and statistical methodology, have made this voluminous evidence difficult to interpret. Enormous resources spent on randomized controlled trials have failed to guarantee the generalizability of their results to other settings or their ability to reflect everyday clinical practice. The latest meta-analysis used revised data from primary randomized controlled trials and data from the largest randomized controlled trials from the United States to demonstrate a significant reduction of metabolic acidosis rates by 36% (odds ratio, 0.64; 95% confidence interval, 0.46-0.88) and operative vaginal delivery rates by 8% (relative risk, 0.92; 95% confidence interval, 0.86-0.99), compared with cardiotocography alone.

Sections du résumé

BACKGROUND
In the past century, some areas of obstetric including intrapartum care have been slow to benefit from the dramatic advances in technology and medical care. Although fetal heart rate monitoring (cardiotocography) became available a half century ago, its interpretation often differs between institutions and countries, its diagnostic accuracy needs improvement, and a technology to help reduce the unnecessary obstetric interventions that have accompanied the cardiotocography is urgently needed.
STUDY DESIGN
During the second half of the 20th century, key findings in animal experiments captured the close relationship between myocardial glycogenolysis, myocardial workload, and ST changes, thus demonstrating that ST waveform analysis of the fetal electrocardiogram can provide information on oxygenation of the fetal myocardium and establishing the physiological basis for the use of electrocardiogram in intrapartum fetal surveillance.
RESULTS
Six randomized controlled trials, 10 meta-analyses, and more than 20 observational studies have evaluated the technology developed based on this principle. Nonetheless, despite this intensive assessment, differences in study protocols, inclusion criteria, enrollment rates, clinical guidelines, use of fetal blood sampling, and definitions of key outcome parameters, as well as inconsistencies in randomized controlled trial data handling and statistical methodology, have made this voluminous evidence difficult to interpret. Enormous resources spent on randomized controlled trials have failed to guarantee the generalizability of their results to other settings or their ability to reflect everyday clinical practice.
CONCLUSION
The latest meta-analysis used revised data from primary randomized controlled trials and data from the largest randomized controlled trials from the United States to demonstrate a significant reduction of metabolic acidosis rates by 36% (odds ratio, 0.64; 95% confidence interval, 0.46-0.88) and operative vaginal delivery rates by 8% (relative risk, 0.92; 95% confidence interval, 0.86-0.99), compared with cardiotocography alone.

Identifiants

pubmed: 30980794
pii: S0002-9378(19)30532-0
doi: 10.1016/j.ajog.2019.04.003
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

577-601.e11

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

Auteurs

Isis Amer-Wåhlin (I)

Medical Management Centre, Department of Learning, Informatics, Management and Ethics, Department of Women and Child Health, Karolinska Institute, Stockholm, Sweden. Electronic address: isis.amer-wahlin@ki.se.

Austin Ugwumadu (A)

Department of Obstetrics & Gynaecology, St George's, University of London, London, UK.

Branka M Yli (BM)

Department of Obstetrics, Rikshospitalet Oslo University Hospital, Oslo.

Anneke Kwee (A)

Department of Obstetrics and Gynecology, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.

Susanna Timonen (S)

Department of Obstetrics and Gynecology, Turku University Hospital, Turku, Finland.

Vanessa Cole (V)

Department of Obstetrics and Gynaecology, Kingston Hospital, Galsworthy Road, Kingston-upon-Thames, UK.

Diogo Ayres-de-Campos (D)

Department of Obstetrics and Gynecology, and Reproductive Medicine, Santa Maria Hospital, University of Lisbon School of Medicine, Lisbon, Portugal.

Georges-Emmanuel Roth (GE)

Department of Obstetrics and Gynecology, CHRU of Strasbourg, Louis Pasteur University, Strasbourg, France.

Christiane Schwarz (C)

Lübeck University, Midwifery Research and Education Unit, Department of Obstetrics, Gynaecology & Reproductive Medicine, Lübeck Germany.

Luca A Ramenghi (LA)

Neonatal Intensive Care Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.

Tullia Todros (T)

Department of Obstetrics and Gynecology, Sant'Anna Hospital, University of Turin, Turin, Italy.

Virginie Ehlinger (V)

UMR 1027 INSERM, Team SPHERE, Toulouse III University, Toulouse, France.

Christophe Vayssiere (C)

UMR 1027 INSERM, Team SPHERE, Toulouse III University, Toulouse, France; Department of Obstetrics and Gynaecology, Paule de Viguier Hospital, CHU Toulouse, Toulouse, France.

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