Evidence map›Paper›PMID 38458578›Full record

ArticleJournal of biomedical informatics2024

FedFSA: Hybrid and federated framework for functional status ascertainment across institutions.

Sunyang Fu, Heling Jia, Maria Vassilaki, Vipina K Keloth, Yifang Dang, Yujia Zhou, Muskan Garg, Ronald C Petersen, Jennifer St Sauver, Sungrim Moon and 8 more

Abstract read
In one paragraph

Article in Journal of biomedical informatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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  5. Quantifying the Uncertainty and Risk Contributions of Activities of Daily Living Features in Dementia Prediction.Proceedings. IEEE International Conference on Healthcare Informatics · 2026
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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

18 authors.

Sunyang FuMayo Clinic, Rochester, MN, United States; University of Texas Health Science Center, Houston, TX, United States. Electronic address: sunyang.fu@uth.tmc.edu.
Heling JiaMayo Clinic, Rochester, MN, United States. Electronic address: Jia.Heling@mayo.edu.
Maria VassilakiMayo Clinic, Rochester, MN, United States. Electronic address: Vassilaki.Maria@mayo.edu.
Vipina K KelothYale University, New Haven, CT, United States. Electronic address: vipina.kuttichikeloth@yale.edu.
Yifang DangUniversity of Texas Health Science Center, Houston, TX, United States. Electronic address: Yifang.Dang.1@uth.tmc.edu.
Yujia ZhouUniversity of Texas Health Science Center, Houston, TX, United States. Electronic address: Yujia.Zhou@uth.tmc.edu.
Muskan GargMayo Clinic, Rochester, MN, United States. Electronic address: Garg.Muskan@mayo.edu.
Ronald C PetersenMayo Clinic, Rochester, MN, United States. Electronic address: peter8@mayo.edu.
Jennifer St SauverMayo Clinic, Rochester, MN, United States. Electronic address: StSauver.Jennifer@mayo.edu.
Sungrim MoonMayo Clinic, Rochester, MN, United States. Electronic address: sungrim.moon@nih.gov.
Liwei WangMayo Clinic, Rochester, MN, United States. Electronic address: Liwei.Wang@uth.tmc.edu.
Andrew WenUniversity of Texas Health Science Center, Houston, TX, United States. Electronic address: Andrew.Wen@uth.tmc.edu.
Fang LiUniversity of Texas Health Science Center, Houston, TX, United States. Electronic address: Fang.Li@uth.tmc.edu.
Hua XuYale University, New Haven, CT, United States. Electronic address: hua.xu@yale.edu.
Cui TaoUniversity of Texas Health Science Center, Houston, TX, United States. Electronic address: Cui.Tao@uth.tmc.edu.
Jungwei FanMayo Clinic, Rochester, MN, United States. Electronic address: Fan.Jung-wei@mayo.edu.
Hongfang LiuMayo Clinic, Rochester, MN, United States; University of Texas Health Science Center, Houston, TX, United States. Electronic address: Hongfang.Liu@uth.tmc.edu.
Sunghwan SohnMayo Clinic, Rochester, MN, United States. Electronic address: Sohn.Sunghwan@mayo.edu.

Funding

SUPPLEMENT TO ALZHEIMERS DISEASE PATIENT REGISTRYU01AG006786 · NIA · MAYO CLINIC ROCHESTER · PI GRAFF-RADFORD, JONATHAN, JACK, CLIFFORD R. · 1986 to 2023
$49.6M
Research Education ComponentP30AG062677 · NIA · MAYO CLINIC ROCHESTER · PI KEJAL KANTARCI · 2019 to 2026
$33.5M
Disease pathways in the population determined by amyloid, tau, and neurodegeneration imaging biomarkersR37AG011378 · NIA · MAYO CLINIC ROCHESTER · PI CLIFFORD R. JACK · 2018 to 2026
$6.8M
Validating the New Criteria for Preclinical Alzheimer's diseaseR01AG041851 · NIA · MAYO CLINIC ROCHESTER · PI JACK, CLIFFORD R., KNOPMAN, DAVID S · 2012 to 2021
$6.3M
Early Detection of Mild Cognitive Impairment, Alzheimer’s Disease and Other Dementias using EHRR01AG068007 · NIA · MAYO CLINIC ROCHESTER · PI Yonas E Geda, Sunghwan Sohn · 2020 to 2026
$3.8M
Development, Validation, and Application of an Imaging based CVD ScaleR01NS097495 · NINDS · MAYO CLINIC ROCHESTER · PI VEMURI, PRASHANTHI · 2016 to 2020
$2.9M
Interdisciplinary Infrastructure for Aging Research: Rochester Epidemiology ProjectR33AG058738 · NIA · MAYO CLINIC ROCHESTER · PI LEBRASSEUR, NATHAN K, OLSON, JANET E · 2020 to 2022
$2.4M
Facilitate Observational Studies of Alzheimer's Disease and Alzheimer's Disease-Related Dementias Using Ontology and Natural Language ProcessingRF1AG072799 · NIA · YALE UNIVERSITY · PI LIU, HONGFANG, TAO, CUI · 2021 to 2021
$2.4M
Facilitate Observational Studies of Alzheimer's Disease and Alzheimer's Disease-Related Dementias Using Ontology and Natural Language ProcessingR01AG072799 · NIA · YALE UNIVERSITY · PI HONGFANG LIU, Cui Tao · 2025 to 2026
$1.7M
Interdisciplinary Infrastructure for Aging Research: Rochester Epidemiology ProjectR21AG058738 · NIA · MAYO CLINIC ROCHESTER · PI LEBRASSEUR, NATHAN K, OLSON, JANET E · 2018 to 2019
$437k
NIA NIH HHS P30 AG062677NIA NIH HHS R01 AG041851NIA NIH HHS R01 AG068007NIA NIH HHS R01 AG072799NIA NIH HHS R21 AG058738NIA NIH HHS R33 AG058738NIA NIH HHS R37 AG011378NIA NIH HHS RF1 AG072799NIA NIH HHS U01 AG006786NINDS NIH HHS R01 NS097495
6 · The paper itself

Abstract

introductionPatients' functional status assesses their independence in performing activities of daily living, including basic ADLs (bADL), and more complex instrumental activities (iADL). Existing studies have discovered that patients' functional status is a strong predictor of health outcomes, particularly in older adults. Depite their usefulness, much of the functional status information is stored in electronic health records (EHRs) in either semi-structured or free text formats. This indicates the pressing need to leverage computational approaches such as natural language processing (NLP) to accelerate the curation of functional status information. In this study, we introduced FedFSA, a hybrid and federated NLP framework designed to extract functional status information from EHRs across multiple healthcare institutions.

methodsFedFSA consists of four major components: 1) individual sites (clients) with their private local data, 2) a rule-based information extraction (IE) framework for ADL extraction, 3) a BERT model for functional status impairment classification, and 4) a concept normalizer. The framework was implemented using the OHNLP Backbone for rule-based IE and open-source Flower and PyTorch library for federated BERT components. For gold standard data generation, we carried out corpus annotation to identify functional status-related expressions based on ICF definitions. Four healthcare institutions were included in the study. To assess FedFSA, we evaluated the performance of category- and institution-specific ADL extraction across different experimental designs.

resultsADL extraction performance ranges from an F1-score of 0.907 to 0.986 for bADL and 0.825 to 0.951 for iADL across the four healthcare sites. The performance for ADL extraction with impairment ranges from an F1-score of 0.722 to 0.954 for bADL and 0.674 to 0.813 for iADL across four healthcare sites. For category-specific ADL extraction, laundry and transferring yielded relatively high performance, while dressing, medication, bathing, and continence achieved moderate-high performance. Conversely, food preparation and toileting showed low performance.

conclusionNLP performance varied across ADL categories and healthcare sites. Federated learning using a FedFSA framework performed higher than non-federated learning for impaired ADL extraction at all healthcare sites. Our study demonstrated the potential of the federated learning framework in functional status extraction and impairment classification in EHRs, exemplifying the importance of a large-scale, multi-institutional collaborative development effort.

Indexed as

Activities of Daily LivingFunctional StatusAgedHumansInformation Storage and RetrievalLearningNatural Language ProcessingDeep learningElectronic health recordsFederated learningFunctional statusNatural language processing

Identifiers

PMID38458578
PMCPMC11005095

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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.