SORA

Advancing, promoting and sharing knowledge of health through excellence in teaching, clinical practice and research into the prevention and treatment of illness

External validation of prognostic models to predict stillbirth using International Prediction of Pregnancy Complications (IPPIC) Network database: individual participant data meta-analysis.

Allotey, J; Whittle, R; Snell, KIE; Smuk, M; Townsend, R; von Dadelszen, P; Heazell, AEP; Magee, L; Smith, GCS; Sandall, J; et al. Allotey, J; Whittle, R; Snell, KIE; Smuk, M; Townsend, R; von Dadelszen, P; Heazell, AEP; Magee, L; Smith, GCS; Sandall, J; Thilaganathan, B; Zamora, J; Riley, RD; Khalil, A; Thangaratinam, S; IPPIC Collaborative Network (2022) External validation of prognostic models to predict stillbirth using International Prediction of Pregnancy Complications (IPPIC) Network database: individual participant data meta-analysis. Ultrasound Obstet Gynecol, 59 (2). pp. 209-219. ISSN 1469-0705 https://doi.org/10.1002/uog.23757
SGUL Authors: Thilaganathan, Baskaran Khalil, Asma

[img]
Preview
PDF Published Version
Available under License Creative Commons Attribution Non-commercial.

Download (391kB) | Preview
[img] Microsoft Word (.docx) (Supporting information) Published Version
Available under License Creative Commons Attribution Non-commercial.

Download (53kB)
[img]
Preview
PDF Accepted Version
Available under License Creative Commons Attribution Non-commercial.

Download (1MB) | Preview

Abstract

OBJECTIVE: Stillbirth is a potentially preventable complication of pregnancy. Identifying women at high risk of stillbirth can guide decisions on the need for closer surveillance and timing of delivery in order to prevent fetal death. Prognostic models have been developed to predict the risk of stillbirth, but none has yet been validated externally. In this study, we externally validated published prediction models for stillbirth using individual participant data (IPD) meta-analysis to assess their predictive performance. METHODS: MEDLINE, EMBASE, DH-DATA and AMED databases were searched from inception to December 2020 to identify studies reporting stillbirth prediction models. Studies that developed or updated prediction models for stillbirth for use at any time during pregnancy were included. IPD from cohorts within the International Prediction of Pregnancy Complications (IPPIC) Network were used to validate externally the identified prediction models whose individual variables were available in the IPD. The risk of bias of the models and cohorts was assessed using the Prediction study Risk Of Bias ASsessment Tool (PROBAST). The discriminative performance of the models was evaluated using the C-statistic, and calibration was assessed using calibration plots, calibration slope and calibration-in-the-large. Performance measures were estimated separately in each cohort, as well as summarized across cohorts using random-effects meta-analysis. Clinical utility was assessed using net benefit. RESULTS: Seventeen studies reporting the development of 40 prognostic models for stillbirth were identified. None of the models had been previously validated externally, and the full model equation was reported for only one-fifth (20%, 8/40) of the models. External validation was possible for three of these models, using IPD from 19 cohorts (491 201 pregnant women) within the IPPIC Network database. Based on evaluation of the model development studies, all three models had an overall high risk of bias, according to PROBAST. In the IPD meta-analysis, the models had summary C-statistics ranging from 0.53 to 0.65 and summary calibration slopes ranging from 0.40 to 0.88, with risk predictions that were generally too extreme compared with the observed risks. The models had little to no clinical utility, as assessed by net benefit. However, there remained uncertainty in the performance of some models due to small available sample sizes. CONCLUSIONS: The three validated stillbirth prediction models showed generally poor and uncertain predictive performance in new data, with limited evidence to support their clinical application. The findings suggest methodological shortcomings in their development, including overfitting. Further research is needed to further validate these and other models, identify stronger prognostic factors and develop more robust prediction models. © 2021 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

Item Type: Article
Additional Information: © 2021 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
Keywords: external validation, individual participant data, intrauterine death, prediction model, stillbirth, IPPIC Collaborative Network, external validation, individual participant data, intra-uterine death, prediction model, stillbirth, 1114 Paediatrics and Reproductive Medicine, Obstetrics & Reproductive Medicine
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Ultrasound Obstet Gynecol
ISSN: 1469-0705
Language: eng
Dates:
DateEvent
1 February 2022Published
18 August 2021Published Online
2 August 2021Accepted
Publisher License: Creative Commons: Attribution-Noncommercial 4.0
Projects:
Project IDFunderFunder ID
14/158/02National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
102215/2/13/2Wellcome Trusthttp://dx.doi.org/10.13039/100004440
PubMed ID: 34405928
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113578
Publisher's version: https://doi.org/10.1002/uog.23757

Actions (login required)

Edit Item Edit Item