Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 15 min ago
PreprintCC BY 4.0arXiv

Artificial intelligence surrogates for treatment effect estimation with before-and-after data

Abstract

Estimating the causal effects of medical treatments is difficult when clinically important outcomes are costly to measure or require long follow-up. Short-term or inexpensive surrogate outcomes offer a potential alternative, but surrogate biomarkers may be unavailable or difficult to identify. Advances in artificial intelligence (AI) have enabled increasingly accurate prediction of clinical outcomes from inexpensive, high-dimensional measurements, which creates an opportunity to use AI predictions themselves as surrogates. To this end, we develop a framework for estimating treatment effects from paired measurements obtained before and after treatment for each treated individual. A pretrained AI model is applied to the before and after measurements, and our estimator compares the resulting outcome predictions. We characterize the technical assumptions under which this within-person contrast identifies the average treatment effect on the treated, even when clinical outcomes are never observed for treated individuals. When these assumptions cannot be justified, we use prediction-powered inference to correct bias using a small number of observed clinical outcomes and obtain valid inference. Synthetic and real-world cardio-oncology experiments demonstrate the validity and accuracy of the approach.

Related

  1. Efficient Deep Gaussian Process Surrogates via Mini-Batch Latent MAP Estimation
    Chun-Yi Chang, Chih-Li Sung
    arXivPreprintCC BY 4.0Full textStatisticsarXiv
  2. Causal Mediation Analysis with High-Dimensional Surrogates: Identification, Estimation and Inference under Latent Factor Models
    Himani Yadav, Shi Bo, AmirEmad Ghassami +1
    arXivPreprintCC BY 4.0Full textStatisticsarXiv
  3. Causal Inference with Generative Artificial Intelligence: Application to Texts as Treatments
    Kosuke Imai, Kentaro Nakamura
    Journal of the American Statistical AssociationPeer-reviewedLicence not statedFull text26 citedStatisticsOpenAlex
  4. Differentially Private Average Treatment Effect Estimation by Propensity Score Blocking
    Duncan Stewardson, Grayson W. White, Adam Groce
    arXivPreprintCC BY 4.0Full textStatisticsarXiv
  5. The Akaike Information Criterion and Artificial Intelligence
    Hendrik Schäbe
    Reliability: Theory & ApplicationsPeer-reviewedCC BY-NCFull textStatisticsDOAJ
BibTeX
@misc{dean2026artificial,
  title = {{Artificial intelligence surrogates for treatment effect estimation with before-and-after data}},
  author = {Frances Dean and Anna Neufeld and Joshua Barrios and Geoffrey H Tison and Ahmed Alaa},
  howpublished = {arXiv},
  year = {2026},
  month = sep,
  doi = {10.48550/arxiv.2609.27180},
  eprint = {2609.27180},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2609.27180},
  note = {CC BY 4.0},
}
RIS
TY  - UNPB
TI  - Artificial intelligence surrogates for treatment effect estimation with before-and-after data
AU  - Frances Dean
AU  - Anna Neufeld
AU  - Joshua Barrios
AU  - Geoffrey H Tison
AU  - Ahmed Alaa
PY  - 2026
DA  - 2026/09/23
PB  - arXiv
DO  - 10.48550/arxiv.2609.27180
UR  - https://arxiv.org/abs/2609.27180
AB  - Estimating the causal effects of medical treatments is difficult when clinically important outcomes are costly to measure or require long follow-up. Short-term or inexpensive surrogate outcomes offer a potential alternative, but surrogate biomarkers may be unavailable or difficult to identify. Advances in artificial intelligence (AI) have enabled increasingly accurate prediction of clinical outcomes from inexpensive, high-dimensional measurements, which creates an opportunity to use AI predictions themselves as surrogates. To this end, we develop a framework for estimating treatment effects from paired measurements obtained before and after treatment for each treated individual. A pretrained AI model is applied to the before and after measurements, and our estimator compares the resulting outcome predictions. We characterize the technical assumptions under which this within-person contrast identifies the average treatment effect on the treated, even when clinical outcomes are never observed for treated individuals. When these assumptions cannot be justified, we use prediction-powered inference to correct bias using a small number of observed clinical outcomes and obtain valid inference. Synthetic and real-world cardio-oncology experiments demonstrate the validity and accuracy of the approach.
ER  -