Evidence map›Paper›PMID 39774499›Full record

ArticlePloS one2024

Assessing the value of deep neural networks for postoperative complication prediction in pancreaticoduodenectomy patients.

Mikkel Bonde, Alexander Bonde, Haytham Kaafarani, Andreas Millarch, Martin Sillesen

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In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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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

2 citing papers in PubMed.

  1. Article
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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

5 authors.

Mikkel BondeDep. of Organ Surgery and Transplantation, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Alexander BondeDep. of Organ Surgery and Transplantation, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Haytham KaafaraniDiv. of Trauma, Emergency Surgery and Surgical Critical Care, Massachusetts General Hospital/Harvard Medical School, Boston, Massachusetts, Unites States of America.
Andreas MillarchDep. of Organ Surgery and Transplantation, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Martin SillesenDep. of Organ Surgery and Transplantation, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0001-9494-5475

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPancreaticoduodenectomy (PD) for patients with pancreatic ductal adenocarcinoma (PDAC) is associated with a high risk of postoperative complications (PoCs) and risk prediction of these is therefore critical for optimal treatment planning. We hypothesize that novel deep learning network approaches through transfer learning may be superior to legacy approaches for PoC risk prediction in the PDAC surgical setting.

methodsData from the US National Surgical Quality Improvement Program (NSQIP) 2002-2018 were used, with a total of 5,881,881 million patients, including 31,728 PD patients. Modelling approaches comprised of a model trained on a general surgery patient cohort and then tested on a PD specific cohort (general model), a transfer learning model trained on the general surgery patients with subsequent transfer and retraining on a PD-specific patient cohort (transfer learning model), a model trained and tested exclusively on the PD-specific patient cohort (direct model), and a benchmark random forest model trained on the PD patient cohort (RF model). The models were subsequently compared against the American College of Surgeons (ACS) surgical risk calculator (SRC) in terms of predicting mortality and morbidity risk.

resultsBoth the general model and transfer learning model outperformed the RF model in 14 and 16 out of 19 prediction tasks, respectively. Additionally, both models outperformed the direct model on 17 out of the 19 tasks. The transfer learning model also outperformed the general model on 11 out of the 19 prediction tasks. The transfer learning model outperformed the ACS-SRC regarding mortality and all the models outperformed the ACS-SRC regarding the morbidity prediction with the general model achieving the highest Receiver Operator Area Under the Curve (ROC-AUC) of 0.668 compared to the 0.524 of the ACS SRC.

conclusionDNNs deployed using a transfer learning approach may be of value for PoC risk prediction in the PD setting.

Indexed as

Deep LearningNeural Networks, ComputerPancreatic NeoplasmsPancreaticoduodenectomyPostoperative ComplicationsAgedCarcinoma, Pancreatic DuctalFemaleHumansMaleMiddle AgedRisk Assessment

Identifiers

PMID39774499
PMCPMC11684602

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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.