Evidence map›Paper›PMID 37224506›Full record

ArticleJMIR diabetes2023

An "All-Data-on-Hand" Deep Learning Model to Predict Hospitalization for Diabetic Ketoacidosis in Youth With Type 1 Diabetes: Development and Validation Study.

David D Williams, Diana Ferro, Colin Mullaney, Lydia Skrabonja, Mitchell S Barnes, Susana R Patton, Brent Lockee, Erin M Tallon, Craig A Vandervelden, Cintya Schweisberger and 5 more

Open access · goldAbstract read
In one paragraph

Article in JMIR diabetes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.0field-weighted citation impact, top 5% of its field
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

11 citing papers in PubMed, 16 citations in OpenAlex.

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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

15 authors at 5 institutions in 3 countries.

David D WilliamsHealth Services and Outcomes Research, Children's Mercy - Kansas City, Kansas City, MO, United States.ORCID https://orcid.org/0000-0003-0501-3751
Diana FerroDepartment of Endocrinology, Children's Mercy - Kansas City, Kansas City, MO, United States.ORCID https://orcid.org/0000-0003-1774-7509
Colin MullaneyCyft, Inc, Cambridge, MA, United States.ORCID https://orcid.org/0009-0005-4051-7068
Lydia SkrabonjaCyft, Inc, Cambridge, MA, United States.ORCID https://orcid.org/0009-0000-0796-2016
Mitchell S BarnesDepartment of Endocrinology, Children's Mercy - Kansas City, Kansas City, MO, United States.ORCID https://orcid.org/0009-0006-2339-6660
Susana R PattonCenter for Healthcare Delivery Science, Nemours Children's Health, Jacksonville, FL, United States.ORCID https://orcid.org/0000-0002-8902-6965
Brent LockeeDepartment of Endocrinology, Children's Mercy - Kansas City, Kansas City, MO, United States.ORCID https://orcid.org/0009-0008-3746-0541
Erin M TallonDepartment of Endocrinology, Children's Mercy - Kansas City, Kansas City, MO, United States.ORCID https://orcid.org/0000-0003-1353-6632
Craig A VanderveldenDepartment of Endocrinology, Children's Mercy - Kansas City, Kansas City, MO, United States.ORCID https://orcid.org/0000-0003-1185-7563
Cintya SchweisbergerDepartment of Endocrinology, Children's Mercy - Kansas City, Kansas City, MO, United States.ORCID https://orcid.org/0000-0002-8915-6700
Sanjeev MehtaJoslin Diabetes Center, Boston, MA, United States.ORCID https://orcid.org/0000-0001-6059-4611
Ryan McDonoughDepartment of Endocrinology, Children's Mercy - Kansas City, Kansas City, MO, United States.ORCID https://orcid.org/0000-0003-1909-3027
Marcus LindDepartment of Medicine, NU-Hospital Group, Uddevalla, Sweden.ORCID https://orcid.org/0000-0002-3796-9283
Leonard D'AvolioCyft, Inc, Cambridge, MA, United States.ORCID https://orcid.org/0009-0008-7309-9677
Mark A ClementsDepartment of Endocrinology, Children's Mercy - Kansas City, Kansas City, MO, United States.ORCID https://orcid.org/0000-0002-2368-0331
Children's Mercy Hospital · USCytel (United States) · USJoslin Diabetes Center · USNemours Children's Health System · USSahlgrenska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough prior research has identified multiple risk factors for diabetic ketoacidosis (DKA), clinicians continue to lack clinic-ready models to predict dangerous and costly episodes of DKA. We asked whether we could apply deep learning, specifically the use of a long short-term memory (LSTM) model, to accurately predict the 180-day risk of DKA-related hospitalization for youth with type 1 diabetes (T1D).

objectiveWe aimed to describe the development of an LSTM model to predict the 180-day risk of DKA-related hospitalization for youth with T1D.

methodsWe used 17 consecutive calendar quarters of clinical data (January 10, 2016, to March 18, 2020) for 1745 youths aged 8 to 18 years with T1D from a pediatric diabetes clinic network in the Midwestern United States. The input data included demographics, discrete clinical observations (laboratory results, vital signs, anthropometric measures, diagnosis, and procedure codes), medications, visit counts by type of encounter, number of historic DKA episodes, number of days since last DKA admission, patient-reported outcomes (answers to clinic intake questions), and data features derived from diabetes- and nondiabetes-related clinical notes via natural language processing. We trained the model using input data from quarters 1 to 7 (n=1377), validated it using input from quarters 3 to 9 in a partial out-of-sample (OOS-P; n=1505) cohort, and further validated it in a full out-of-sample (OOS-F; n=354) cohort with input from quarters 10 to 15.

resultsDKA admissions occurred at a rate of 5% per 180-days in both out-of-sample cohorts. In the OOS-P and OOS-F cohorts, the median age was 13.7 (IQR 11.3-15.8) years and 13.1 (IQR 10.7-15.5) years; median glycated hemoglobin levels at enrollment were 8.6% (IQR 7.6%-9.8%) and 8.1% (IQR 6.9%-9.5%); recall was 33% (26/80) and 50% (9/18) for the top-ranked 5% of youth with T1D; and 14.15% (213/1505) and 12.7% (45/354) had prior DKA admissions (after the T1D diagnosis), respectively. For lists rank ordered by the probability of hospitalization, precision increased from 33% to 56% to 100% for positions 1 to 80, 1 to 25, and 1 to 10 in the OOS-P cohort and from 50% to 60% to 80% for positions 1 to 18, 1 to 10, and 1 to 5 in the OOS-F cohort, respectively.

conclusionsThe proposed LSTM model for predicting 180-day DKA-related hospitalization was valid in this sample. Future research should evaluate model validity in multiple populations and settings to account for health inequities that may be present in different segments of the population (eg, racially or socioeconomically diverse cohorts). Rank ordering youth by probability of DKA-related hospitalization will allow clinics to identify the most at-risk youth. The clinical implication of this is that clinics may then create and evaluate novel preventive interventions based on available resources.

Indexed as

AIartificial intelligencedeep learningdiabetic ketoacidosisDKAlong short-term memoryLSTMmachine learningnatural language processingNLPrecurrent neural networkRNNT1Dtype 1 diabetes

Identifiers

PMID37224506
PMCPMC10394604
OpenAlexW4378172515

What OpenQuestion holds

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LicenceCC BY
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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.