Effect of second-trimester sonographic cervical length on the risk of spontaneous preterm delivery in different risk groups: A prospective observational multicenter study.


Journal

Acta obstetricia et gynecologica Scandinavica
ISSN: 1600-0412
Titre abrégé: Acta Obstet Gynecol Scand
Pays: United States
ID NLM: 0370343

Informations de publication

Date de publication:
Sep 2021
Historique:
revised: 12 05 2021
received: 06 02 2021
accepted: 28 05 2021
pubmed: 8 6 2021
medline: 11 9 2021
entrez: 7 6 2021
Statut: ppublish

Résumé

The aim of the study is to compare the effect of cervical length measured with transvaginal ultrasound in the second trimester on the risk of spontaneous preterm delivery (PTD) between different risk groups of asymptomatic women with a singleton pregnancy. This is a pre-planned exploratory analysis of the CERVIX study, a prospective blinded multicenter diagnostic accuracy study. Asymptomatic women with a singleton pregnancy were consecutively recruited at their second-trimester routine ultrasound examination at seven Swedish ultrasound centers. Cervical length was measured with transvaginal ultrasound at 18-20 weeks (Cx1; n = 11 072) and 21-23 weeks (Cx2, optional; n = 6288). The effect of cervical length on the risk of spontaneous PTD and its discriminative ability was compared between women with: (i) previous spontaneous PTD, late miscarriage or cervical conization (high-risk group; n = 1045); (ii) nulliparae without risk factors (n = 5173); (iii) parae without risk factors (n = 4740). Women with previous indicated PTD were excluded (n = 114). Main outcome measures were: effect of cervical length on the risk of spontaneous PTD expressed as odds ratio per 5-mm decrease in cervical length with interaction analysis using logistic regression to test whether the effect differed between groups, area under the receiver operating characteristic curve (AUC), sensitivity, specificity, number needed to screen to detect one spontaneous PTD. The effect of cervical length at Cx2 on the risk of spontaneous PTD <33 weeks was similar in all groups (odds ratios 2.26-2.58, interaction p value 0.91). The discriminative ability at Cx2 was superior to that at Cx1 and was similar in all groups (AUC 0.69-0.76). Cervical length ≤25 mm at Cx2 identified 57% of spontaneous preterm deliveries <33 weeks in the high-risk group with number needed to screen 161. The number needed to screen for groups (ii) and (iii) were 1018 and 843. The effect of cervical length at 21-23 weeks on the risk of spontaneous PTD <33 weeks is similar in high- and low-risk pregnancies. The differences in number needed to screen should be considered before implementing a screening program.

Identifiants

pubmed: 34096036
doi: 10.1111/aogs.14203
doi:

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1644-1655

Subventions

Organisme : The Swedish National Patient Insurance Company (LÖF)
Organisme : The Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement
ID : ALF-718591
Organisme : The Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement
ID : ALFGBG-717501
Organisme : The Swedish Research Council
ID : 2014-06998
Organisme : Forskning och Utbildning (FoU) Södra Älvsborg

Informations de copyright

© 2021 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG).

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Auteurs

Tove Wikström (T)

Center of Perinatal Medicine and Health, Department of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Obstetrics, Sahlgrenska University Hospital, Gothenburg, Sweden.

Henrik Hagberg (H)

Center of Perinatal Medicine and Health, Department of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Obstetrics, Sahlgrenska University Hospital, Gothenburg, Sweden.

Bo Jacobsson (B)

Center of Perinatal Medicine and Health, Department of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Obstetrics, Sahlgrenska University Hospital, Gothenburg, Sweden.

Pihla Kuusela (P)

Södra Älvsborg Hospital, Borås, Sweden.

Jan Wesström (J)

Center for Clinical Research Dalarna, Falu Hospital, Falun, Sweden.

Peter Lindgren (P)

Department of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden.
Center for Fetal Medicine, Karolinska University Hospital, Stockholm, Sweden.

Helena Fadl (H)

Department of Obstetrics and Gynecology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

Ulla-Britt Wennerholm (UB)

Center of Perinatal Medicine and Health, Department of Obstetrics and Gynecology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Obstetrics, Sahlgrenska University Hospital, Gothenburg, Sweden.

Lil Valentin (L)

Department of Obstetrics and Gynecology, Skåne University Hospital, Malmö, Sweden.
Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.

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