arXiv:2611.07124v1 Announce Type: new Abstract: Machine-learning models predicting live birth after in vitro fertilisation (IVF) or intracytoplasmic sperm injection (ICSI) from routine clinical data report performance from near chance to near perfect. We systematically reviewed these models under PRISMA 2020, searching OpenAlex, Scopus and Web of Science to 22 October 2026, appraised them with PROBAST+AI and TRIPOD+AI, and pooled their discrimination with random-effects meta-analysis on the logit scale. We define what fixes the meaning of a model's output (decision point, endpoint, unit of analysis, data source) and map the 48 included studies by model family, decision point and validation design. Models evaluated only internally pooled to an area under the receiver operating characteristic curve (AUC) of 0.814, against 0.756 (95% prediction interval 0.546-0.889) for models evaluated on a later period or another centre, and 0.764 for studies not at high risk of bias; neither difference was significant, and heterogeneity was extreme. Models whose decision point was not stated pooled to 0.910, the only significant moderator in meta-regression. Against logistic regression fitted to the same data, the best machine-learning model gained a pooled 0.056 AUC (95% CI 0.017-0.090). Of 48 studies, 47 were at high or unclear risk of bias, only four assessed the calibration slope, and no model has evidence of clinical impact. The certainty of the pooled evidence is low to very low; the gains that survive validation came from staging predictions to decision points and local calibration, not deeper architectures. We provide a TRIPOD+AI-mapped checklist, a benchmark specification and a research agenda.
Machine Learning for Live-Birth Prediction After IVF/ICSI From Structured Clinical Data: A Systematic Review, Meta-Analysis, and Critical Appraisal
A PRISMA 2020 systematic review and random-effects meta-analysis of 48 studies, posted to arXiv as 2611.07124v1, found that machine-learning models predicting live birth after IVF or ICSI from routine clinical data pooled to an AUC of 0.814 when evaluated only internally, versus 0.756 (95% prediction interval 0.546-0.889) for models tested on a later period or another centre. The best machine-learning model gained a pooled 0.056 AUC (95% CI 0.017-0.090) over logistic regression fitted to the same data, but 47 of the 48 studies were at high or unclear risk of bias, only four assessed calibration slope, and no model has evidence of clinical impact. The authors report low to very low certainty of the pooled evidence and conclude that gains surviving validation came from staging predictions to decision points and local calibration rather than deeper architectures.
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