Evaluating cut-off levels for progesterone, β human chorionic gonadotropin and β human chorionic gonadotropin ratio to exclude pregnancy viability in women with a pregnancy of unknown location: A prospective multicenter cohort 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:
Jan 2022
Historique:
revised: 13 09 2021
received: 11 06 2021
accepted: 07 11 2021
pubmed: 25 11 2021
medline: 4 2 2022
entrez: 24 11 2021
Statut: ppublish

Résumé

There is no global agreement on how to best determine pregnancy of unknown location viability and location using biomarkers. Measurements of progesterone and β human chorionic gonadotropin (βhCG) are still used in clinical practice to exclude the possibility of a viable intrauterine pregnancy (VIUP). We evaluate the predictive value of progesterone, βhCG, and βhCG ratio cut-off levels to exclude a VIUP in women with a pregnancy of unknown location. This was a secondary analysis of prospective multicenter study data of consecutive women with a pregnancy of unknown location between January 2015 and 2017 collected from dedicated early pregnancy assessment units of eight hospitals. Single progesterone and serial βhCG measurements were taken. Women were followed up until final pregnancy outcome between 11 and 14 weeks of gestation was confirmed using transvaginal ultrasonography: (1) VIUP, (2) non-viable intrauterine pregnancy or failed pregnancy of unknown location, and (3) ectopic pregnancy or persisting pregnancy of unknown location. The predictive value of cut-off levels for ruling out VIUP were evaluated across a range of values likely to be encountered clinically for progesterone, βhCG, and βhCG ratio. Data from 2507 of 3272 (76.6%) women were suitable for analysis. All had data for βhCG levels, 2248 (89.7%) had progesterone levels, and 1809 (72.2%) had βhCG ratio. The likelihood of viability falls with the progesterone level. Although the median progesterone level associated with viability was 59 nmol/L, VIUP were identified with levels as low as 5 nmol/L. No single βhCG cut-off reliably ruled out the presence of viability with certainty, even when the level was more than 3000 IU/L, there were 39/358 (11%) women who had a VIUP. The probability of viability decreases with the βhCG ratio. Although the median βhCG ratio associated with viability was 2.26, VIUP were identified with ratios as low as 1.02. A progesterone level below 2 nmol/L and βhCG ratio below 0.87 were unlikely to be associated with viability but were not definitive when considering multiple imputation. Cut-off levels for βhCG, βhCG ratio, and progesterone are not safe to be used clinically to exclude viability in early pregnancy. Although βhCG ratio and progesterone have slightly better performance in comparison, single βhCG used in this manner is highly unreliable.

Identifiants

pubmed: 34817062
doi: 10.1111/aogs.14295
pmc: PMC9564682
doi:

Substances chimiques

Chorionic Gonadotropin 0
Chorionic Gonadotropin, beta Subunit, Human 0
Progesterone 4G7DS2Q64Y

Types de publication

Evaluation Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

46-55

Subventions

Organisme : Internal funds KU Leuven
ID : C24/15/037
Organisme : Imperial Health Charity
ID : RFPrD1920/116
Organisme : NIHR Imperial Biomedical Research Centre
ID : IS-BRC-1215-20013
Organisme : NIHR Collaboration for Leadership in Applied Health Research and Care North West London South London
ID : RDIP033
Organisme : Fonds Wetenschappelijk Onderzoek
ID : G0B4716N

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

Shabnam Bobdiwala (S)

Department of Obstetrics and Gynaecology, Tommy's National Centre for Miscarriage Research, Queen Charlotte's & Chelsea Hospital, Imperial College London, London, UK.

Christopher Kyriacou (C)

Department of Obstetrics and Gynaecology, Tommy's National Centre for Miscarriage Research, Queen Charlotte's & Chelsea Hospital, Imperial College London, London, UK.

Evangelia Christodoulou (E)

Department of Development & Regeneration, KU Leuven, Leuven, Belgium.
Department of Cancer Epidemiology, DKFZ, Heidelberg, Germany.

Jessica Farren (J)

Department of Gynaecology, St Mary's Hospital, London, UK.

Nicola Mitchell-Jones (N)

Department of Gynaecology, Chelsea and Westminster NHS Trust, London, UK.

Maya Al-Memar (M)

Department of Obstetrics and Gynaecology, Tommy's National Centre for Miscarriage Research, Queen Charlotte's & Chelsea Hospital, Imperial College London, London, UK.

Francis Ayim (F)

Department of Gynaecology, Hillingdon Hospital NHS Trust, London, UK.

Baljinder Chohan (B)

Department of Gynaecology, Wexham Park Hospital, London, UK.

Emma Kirk (E)

Department of Gynaecology, Royal Free NHS Foundation Trust, London, UK.

Osama Abughazza (O)

Department of Gynaecology, Royal Surrey County Hospital, Guildford, UK.

Bramara Guruwadahyarhalli (B)

Department of Gynaecology, Chelsea and Westminster NHS Trust, London, UK.

Sharmistha Guha (S)

Department of Gynaecology, Chelsea and Westminster NHS Trust, London, UK.

Veluppillai Vathanan (V)

Department of Gynaecology, Wexham Park Hospital, London, UK.

Debbie Gould (D)

Department of Gynaecology, St Mary's Hospital, London, UK.

Catriona Stalder (C)

Department of Obstetrics and Gynaecology, Tommy's National Centre for Miscarriage Research, Queen Charlotte's & Chelsea Hospital, Imperial College London, London, UK.

Dirk Timmerman (D)

Department of Development & Regeneration, KU Leuven, Leuven, Belgium.
Department of Gynecology, University Hospital Leuven, Leuven, Belgium.

Ben Van Calster (B)

Department of Development & Regeneration, KU Leuven, Leuven, Belgium.

Tom Bourne (T)

Department of Obstetrics and Gynaecology, Tommy's National Centre for Miscarriage Research, Queen Charlotte's & Chelsea Hospital, Imperial College London, London, UK.
Department of Development & Regeneration, KU Leuven, Leuven, Belgium.

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Classifications MeSH