Evidence map›Paper›PMID 41984477›Full record

ArticleJAMA network open2026

Machine Learning Model to Predict Postmastectomy Breast Reconstruction Complications.

Mohammed S Shaheen, Brennen T McManus, Clara M Cullen, Jung-Sheng Chen, Arash Momeni, Chang-Fu Kuo, Ping-Han Tsai, Kevin C Chung

Abstract read
In one paragraph

Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Mohammed S ShaheenSection of Plastic Surgery, Department of Surgery, University of Michigan Medical School, Ann Arbor.
Brennen T McManusSection of Plastic Surgery, Department of Surgery, University of Michigan Medical School, Ann Arbor.
Clara M CullenSection of Plastic Surgery, Department of Surgery, University of Michigan Medical School, Ann Arbor.
Jung-Sheng ChenDivision of Rheumatology, Allergy and Immunology, Department of Internal Medicine, New Taipei Municipal TuCheng Hospital, New Taipei City, Taiwan.
Arash MomeniDivision of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Stanford, California.
Chang-Fu KuoDivision of Rheumatology, Allergy and Immunology, Department of Internal Medicine, New Taipei Municipal TuCheng Hospital, New Taipei City, Taiwan.
Ping-Han TsaiDivision of Rheumatology, Allergy and Immunology, Department of Internal Medicine, New Taipei Municipal TuCheng Hospital, New Taipei City, Taiwan.
Kevin C ChungSection of Plastic Surgery, Department of Surgery, University of Michigan Medical School, Ann Arbor.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Postmastectomy breast reconstruction (PMBR) improves patients' quality of life, but patients often lack reliable, individualized information about complication risk. Machine learning (ML) can analyze complex clinical data to generate personalized risk estimates, facilitating shared decision-making. Objective: To develop and validate ML models trained on both structured data and manually abstracted variables from unstructured clinical notes to predict major complications after PMBR. Design, Setting, and Participants: This prognostic study used retrospective data from female patients aged 18 years or older who underwent unilateral or bilateral therapeutic mastectomy with immediate or delayed implant-based or autologous reconstruction at 2 academic centers in the US from 2012 to 2022. Demographic, treatment, and surgical variables were extracted from electronic health records with a 1-year postoperative follow-up period. Extreme gradient boosting (XGBoost) and random forest models were trained on 80% of the cohort (329 individuals) and tested on 20% of the cohort (82 individuals). Patients with bilateral prophylactic mastectomy, distant metastases, mixed autologous and implant-based reconstruction, or less than 12 months of follow-up were excluded. Of more than 4000 eligible patients, a random sample of 411 underwent manual health record review for variable abstraction. Data were analyzed from September through November 2024. Exposures: PMBR. Main Outcomes and Measures: Outcomes of interest were major complications, defined as unplanned reoperations or rehospitalizations within 1 year of reconstruction. Model performance was evaluated using the area under the receiver operating characteristic curve (AUROC) and area under the precision-recall curve (AUPRC). Results: The sample included 411 female patients (667 breasts) receiving implant-based (290 individuals [70.6%]) or autologous (121 individuals [29.4%]) PMBR, with a median (IQR) age of 51.3 (44.0-58.3) years. The overall major complication rate was 25.8% (106 individuals). The XGBoost model outperformed the random forest model, achieving an AUROC of 0.83 (95% CI, 0.72-0.94) and an AUPRC of 0.62 (95% CI, 0.55-0.69; baseline: 0.26) on the test set, compared with 0.74 (95% CI, 0.66-0.82) and 0.56 (95% CI, 0.50-0.62), respectively, for the random forest model. Top predictors of major complications included smoking, adjuvant radiotherapy, body mass index, age, and diabetes. Model performance remained consistent across reconstructive modalities. Conclusions and Relevance: In this prognostic study of PMBR outcomes, an internally validated ML model trained on both structured and unstructured clinical data was used to predict 1-year major complications. Such models support personalized risk assessment, inform decision-making, and provide a foundation for future externally validated and prospectively tested decision-support tools.

Indexed as

Machine LearningMammaplastyMastectomyPostoperative ComplicationsAdultBoosting Machine Learning AlgorithmsBreast NeoplasmsClassification AlgorithmsFemaleHumansMiddle AgedPrediction AlgorithmsPredictive Learning ModelsRandom ForestRetrospective StudiesRisk Assessment

Identifiers

PMID41984477
PMCPMC13084482

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.