External validation of and improvement upon a model for the prediction of placenta accreta spectrum severity using prospectively collected multicenter ultrasound data

医学 胎盘植入 多中心研究 超声波 背景(考古学) 胎盘 产科 放射科 试验预测值 前瞻性队列研究 妇科 外科 怀孕 内科学 随机对照试验 古生物学 胎儿 遗传学 生物
作者
Magdalena Kołak,Stephen Gerry,Hubert Huras,Ammar Al Naimi,Karin A. Fox,Thorsten Braun,Vedran Stefanović,Heleen J. van Beekhuizen,Olivier Morel,Alexander Paping,Charline Bertholdt,Pavel Calda,Zdeněk Laštůvka,Andrzej Jaworowski,Eglė Savukynė,Sally Collins
出处
期刊:Acta Obstetricia et Gynecologica Scandinavica [Informa]
标识
DOI:10.1111/aogs.14941
摘要

Abstract Introduction This study aimed to validate the Sargent risk stratification algorithm for the prediction of placenta accreta spectrum (PAS) severity using data collected from multiple centers and using the multicenter data to improve the model. Material and Methods We conducted a multicenter analysis using data collected for the IS‐PAS database. The Sargent model's effectiveness in distinguishing between abnormally adherent placenta (FIGO grade 1) and abnormally invasive placenta (FIGO grades 2 and 3) was evaluated. A new model was developed using multicenter data from the IS‐PAS database. Results The database included 315 cases of suspected PAS, of which 226 had fully documented standardized ultrasound signs. The final diagnosis was normal placentation in 5, abnormally adherent placenta/FIGO grade 1 in 43, and abnormally invasive placenta/FIGO grades 2 and 3 in 178. The external validation of the Sargent model revealed moderate predictive accuracy in a multicenter setting ( C ‐index 0.68), compared to its higher accuracy in a single‐center context ( C ‐index 0.90). The newly developed model achieved a C ‐index of 0.74. Conclusions The study underscores the difficulty in developing universally applicable PAS prediction models. While models like that of Sargent et al. show promise, their reproducibility varies across settings, likely due to the interpretation of the ultrasound signs. The findings support the need for updating the current ultrasound descriptors and for the development of any new predictive models to use data collected by different operators in multiple clinical settings.
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