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Development and validation of a risk prediction model of preterm birth for women with preterm labour symptoms (the QUIDS study): A prospective cohort study and individual participant data meta-analysis

Authors :
Stock, Sarah J.
Horne, Margaret
Bruijn, Merel
White, Helen
Boyd, Kathleen A.
Heggie, Robert
Wotherspoon, Lisa
Aucott, Lorna
Morris, Rachel K.
Dorling, Jon
Jackson, Lesley
Chandiramani, Manju
David, Anna L.
Khalil, Asma
Shennan, Andrew
van Baaren, Gert-Jan
Hodgetts-Morton, Victoria
Lavender, Tina
Schuit, Ewoud
Harper-Clarke, Susan
Mol, Ben W.
Riley, Richard D.
Norman, Jane E.
Norrie, John
Source :
PLoS Medicine. July 6, 2021, Vol. 18 Issue 7, e1003686
Publication Year :
2021

Abstract

Background Timely interventions in women presenting with preterm labour can substantially improve health outcomes for preterm babies. However, establishing such a diagnosis is very challenging, as signs and symptoms of preterm labour are common and can be nonspecific. We aimed to develop and externally validate a risk prediction model using concentration of vaginal fluid fetal fibronectin (quantitative fFN), in combination with clinical risk factors, for the prediction of spontaneous preterm birth and assessed its cost-effectiveness. Methods and findings Pregnant women included in the analyses were 22.sup.+0 to 34.sup.+6 weeks gestation with signs and symptoms of preterm labour. The primary outcome was spontaneous preterm birth within 7 days of quantitative fFN test. The risk prediction model was developed and internally validated in an individual participant data (IPD) meta-analysis of 5 European prospective cohort studies (2009 to 2016; 1,783 women; mean age 29.7 years; median BMI 24.8 kg/m.sup.2 ; 67.6% White; 11.7% smokers; 51.8% nulliparous; 10.4% with multiple pregnancy; 139 [7.8%] with spontaneous preterm birth within 7 days). The model was then externally validated in a prospective cohort study in 26 United Kingdom centres (2016 to 2018; 2,924 women; mean age 28.2 years; median BMI 25.4 kg/m.sup.2 ; 88.2% White; 21% smokers; 35.2% nulliparous; 3.5% with multiple pregnancy; 85 [2.9%] with spontaneous preterm birth within 7 days). The developed risk prediction model for spontaneous preterm birth within 7 days included quantitative fFN, current smoking, not White ethnicity, nulliparity, and multiple pregnancy. After internal validation, the optimism adjusted area under the curve was 0.89 (95% CI 0.86 to 0.92), and the optimism adjusted Nagelkerke R.sup.2 was 35% (95% CI 33% to 37%). On external validation in the prospective UK cohort population, the area under the curve was 0.89 (95% CI 0.84 to 0.94), and Nagelkerke R.sup.2 of 36% (95% CI: 34% to 38%). Recalibration of the model's intercept was required to ensure overall calibration-in-the-large. A calibration curve suggested close agreement between predicted and observed risks in the range of predictions 0% to 10%, but some miscalibration (underprediction) at higher risks (slope 1.24 (95% CI 1.23 to 1.26)). Despite any miscalibration, the net benefit of the model was higher than 'treat all' or 'treat none' strategies for thresholds up to about 15% risk. The economic analysis found the prognostic model was cost effective, compared to using qualitative fFN, at a threshold for hospital admission and treatment of [greater than or equal to]2% risk of preterm birth within 7 days. Study limitations include the limited number of participants who are not White and levels of missing data for certain variables in the development dataset. Conclusions In this study, we found that a risk prediction model including vaginal fFN concentration and clinical risk factors showed promising performance in the prediction of spontaneous preterm birth within 7 days of test and has potential to inform management decisions for women with threatened preterm labour. Further evaluation of the risk prediction model in clinical practice is required to determine whether the risk prediction model improves clinical outcomes if used in practice. Trial registration The study was approved by the West of Scotland Research Ethics Committee (16/WS/0068). The study was registered with ISRCTN Registry (ISRCTN 41598423) and NIHR Portfolio (CPMS: 31277).<br />Author(s): Sarah J. Stock 1,2,*, Margaret Horne 2, Merel Bruijn 2, Helen White 3, Kathleen A. Boyd 4, Robert Heggie 4, Lisa Wotherspoon 2, Lorna Aucott 5, Rachel K. Morris [...]

Details

Language :
English
ISSN :
15491277
Volume :
18
Issue :
7
Database :
Gale General OneFile
Journal :
PLoS Medicine
Publication Type :
Academic Journal
Accession number :
edsgcl.671194085
Full Text :
https://doi.org/10.1371/journal.pmed.1003686