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External validation of models to predict the outcome of pregnancies of unknown location: a multicentre cohort study
OBJECTIVE: To validate externally five approaches to predict ectopic pregnancy (EP) in pregnancies of unknown location (PUL): the M6P and M6NP risk models, the two‐step triage strategy (2ST, which incorporates M6P), the M4 risk model, and beta human chorionic gonadotropin ratio cut‐offs (BhCG‐RC). D...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821217/ https://www.ncbi.nlm.nih.gov/pubmed/32931087 http://dx.doi.org/10.1111/1471-0528.16497 |
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author | Christodoulou, E Bobdiwala, S Kyriacou, C Farren, J Mitchell‐Jones, N Ayim, F Chohan, B Abughazza, O Guruwadahyarhalli, B Al‐Memar, M Guha, S Vathanan, V Gould, D Stalder, C Wynants, L Timmerman, D Bourne, T Van Calster, B |
author_facet | Christodoulou, E Bobdiwala, S Kyriacou, C Farren, J Mitchell‐Jones, N Ayim, F Chohan, B Abughazza, O Guruwadahyarhalli, B Al‐Memar, M Guha, S Vathanan, V Gould, D Stalder, C Wynants, L Timmerman, D Bourne, T Van Calster, B |
author_sort | Christodoulou, E |
collection | PubMed |
description | OBJECTIVE: To validate externally five approaches to predict ectopic pregnancy (EP) in pregnancies of unknown location (PUL): the M6P and M6NP risk models, the two‐step triage strategy (2ST, which incorporates M6P), the M4 risk model, and beta human chorionic gonadotropin ratio cut‐offs (BhCG‐RC). DESIGN: Secondary analysis of a prospective cohort study. SETTING: Eight UK early pregnancy assessment units. POPULATION: Women presenting with a PUL and BhCG >25 IU/l. METHODS: Women were managed using the 2ST protocol: PUL were classified as low risk of EP if presenting progesterone ≤2 nmol/l; the remaining cases returned 2 days later for triage based on M6P. EP risk ≥5% was used to classify PUL as high risk. Missing values were imputed, and predictions for the five approaches were calculated post hoc. We meta‐analysed centre‐specific results. MAIN OUTCOME MEASURES: Discrimination, calibration and clinical utility (decision curve analysis) for predicting EP. RESULTS: Of 2899 eligible women, the primary analysis excluded 297 (10%) women who were lost to follow up. The area under the ROC curve for EP was 0.89 (95% CI 0.86–0.91) for M6P, 0.88 (0.86–0.90) for 2ST, 0.86 (0.83–0.88) for M6NP and 0.82 (0.78–0.85) for M4. Sensitivities for EP were 96% (M6P), 94% (2ST), 92% (N6NP), 80% (M4) and 58% (BhCG‐RC); false‐positive rates were 35%, 33%, 39%, 24% and 13%. M6P and 2ST had the best clinical utility and good overall calibration, with modest variability between centres. CONCLUSIONS: 2ST and M6P performed best for prediction and triage in PUL. TWEETABLE ABSTRACT: The M6 model, as part of a two‐step triage strategy, is the best approach to characterise and triage PULs. |
format | Online Article Text |
id | pubmed-7821217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78212172021-01-29 External validation of models to predict the outcome of pregnancies of unknown location: a multicentre cohort study Christodoulou, E Bobdiwala, S Kyriacou, C Farren, J Mitchell‐Jones, N Ayim, F Chohan, B Abughazza, O Guruwadahyarhalli, B Al‐Memar, M Guha, S Vathanan, V Gould, D Stalder, C Wynants, L Timmerman, D Bourne, T Van Calster, B BJOG Original Articles OBJECTIVE: To validate externally five approaches to predict ectopic pregnancy (EP) in pregnancies of unknown location (PUL): the M6P and M6NP risk models, the two‐step triage strategy (2ST, which incorporates M6P), the M4 risk model, and beta human chorionic gonadotropin ratio cut‐offs (BhCG‐RC). DESIGN: Secondary analysis of a prospective cohort study. SETTING: Eight UK early pregnancy assessment units. POPULATION: Women presenting with a PUL and BhCG >25 IU/l. METHODS: Women were managed using the 2ST protocol: PUL were classified as low risk of EP if presenting progesterone ≤2 nmol/l; the remaining cases returned 2 days later for triage based on M6P. EP risk ≥5% was used to classify PUL as high risk. Missing values were imputed, and predictions for the five approaches were calculated post hoc. We meta‐analysed centre‐specific results. MAIN OUTCOME MEASURES: Discrimination, calibration and clinical utility (decision curve analysis) for predicting EP. RESULTS: Of 2899 eligible women, the primary analysis excluded 297 (10%) women who were lost to follow up. The area under the ROC curve for EP was 0.89 (95% CI 0.86–0.91) for M6P, 0.88 (0.86–0.90) for 2ST, 0.86 (0.83–0.88) for M6NP and 0.82 (0.78–0.85) for M4. Sensitivities for EP were 96% (M6P), 94% (2ST), 92% (N6NP), 80% (M4) and 58% (BhCG‐RC); false‐positive rates were 35%, 33%, 39%, 24% and 13%. M6P and 2ST had the best clinical utility and good overall calibration, with modest variability between centres. CONCLUSIONS: 2ST and M6P performed best for prediction and triage in PUL. TWEETABLE ABSTRACT: The M6 model, as part of a two‐step triage strategy, is the best approach to characterise and triage PULs. John Wiley and Sons Inc. 2020-10-07 2021-02 /pmc/articles/PMC7821217/ /pubmed/32931087 http://dx.doi.org/10.1111/1471-0528.16497 Text en © 2020 The Authors. BJOG: An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Christodoulou, E Bobdiwala, S Kyriacou, C Farren, J Mitchell‐Jones, N Ayim, F Chohan, B Abughazza, O Guruwadahyarhalli, B Al‐Memar, M Guha, S Vathanan, V Gould, D Stalder, C Wynants, L Timmerman, D Bourne, T Van Calster, B External validation of models to predict the outcome of pregnancies of unknown location: a multicentre cohort study |
title | External validation of models to predict the outcome of pregnancies of unknown location: a multicentre cohort study |
title_full | External validation of models to predict the outcome of pregnancies of unknown location: a multicentre cohort study |
title_fullStr | External validation of models to predict the outcome of pregnancies of unknown location: a multicentre cohort study |
title_full_unstemmed | External validation of models to predict the outcome of pregnancies of unknown location: a multicentre cohort study |
title_short | External validation of models to predict the outcome of pregnancies of unknown location: a multicentre cohort study |
title_sort | external validation of models to predict the outcome of pregnancies of unknown location: a multicentre cohort study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821217/ https://www.ncbi.nlm.nih.gov/pubmed/32931087 http://dx.doi.org/10.1111/1471-0528.16497 |
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