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Predicting symptom complexity: Using autoregressive integrated moving average (ARIMA) models to create responsive clinic scheduling.

2021· article· en· W3170529957 on OpenAlexaffabout
Linda Watson, Siwei Qi, Andrea DeIure, Claire Link, April Hildebrand, Lindsi Chmielewski, Louise Smith, Dean Ruether, Krista Rawson

Bibliographic record

VenueJournal of Clinical Oncology · 2021
Typearticle
Languageen
FieldMedicine
TopicGlobal Cancer Incidence and Screening
Canadian institutionsAlberta Health Services
Fundersnot available
KeywordsAutoregressive integrated moving averageMedicineBayesian information criterionStatisticsMean squared errorMean absolute percentage errorAutocorrelationMoving averageAutoregressive modelBayesian probabilityTime seriesMathematics

Abstract

fetched live from OpenAlex

e13529 Background: Increasing cancer incidence, coupled with a trend in treating patients for longer periods of time, presents challenges in addressing all patients’ symptoms/concerns within the allotted time for ambulatory clinic appointments. Consequently, the ability to forecast and monitor the percentage of cancer patients with different symptom complexity levels is extremely valuable. Symptom complexity is a summary score that weighs the severity of all patient reported symptom scores at one time point. If a clinic could predict how many patients may need more time due to complex symptom management needs, clinic-scheduling templates could be adjusted to include a set number of longer appointments. Methods: Auto Regressive Integrated Moving Average (ARIMA) models were utilized to forecast the percentage of patients with a high symptom complexity level within one cancer clinic in Alberta, Canada. Goodness-of-fit measures such as Bayesian information criterion (BIC) and Ljung-Box test were used to determine optimal form for the ARIMA model. Following model selection, the autocorrelation function (ACF) was performed. These tests together verified that chosen AR, MA and differencing (I) were appropriate. Model performance on the historical data for model fit was summarized by Mean Absolute Error (MAE) and Root Squared Mean Error (RSME). Forecasting accuracy was assessed using mean absolute prediction error by comparing the forecasts with actual clinic data. Results: Of the multiple model structures tested, ARIMA (0, 0, 1) was selected, with the lowest BIC and non-significant Ljung-Box test. We obtained forecasts of the percentage of patients with high symptom complexity levels, with an MAE at 4.0%. To assess forecast accuracy, we calculated the absolute prediction error by comparing the forecasted percentages of patients with high symptom complexity levels to actual clinic visit data and the mean absolute prediction error was 5.9%. Conclusions: This forecasting model has important implications, allowing clinics to adjust scheduling templates to provide a select number of longer timeslots and therefore, be better prepared to meet the symptom management needs of cancer patients who are considered highly complex. This model could be applied to other clinical populations to allow for a tailored scheduling approach based on each clinic’s symptom complexity forecasting.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.008
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Simulation or modeling · Consensus signal: Simulation or modeling
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.421
Threshold uncertainty score0.838

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.008
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.459
GPT teacher head0.523
Teacher spread0.064 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designSimulation or modeling
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2021
Admission routes2
Has abstractyes

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