Abstract Presentations 5. Karin Lisspers, Sweden Breathing and - - PowerPoint PPT Presentation

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Abstract Presentations 5. Karin Lisspers, Sweden Breathing and - - PowerPoint PPT Presentation

Abstract Presentations 5. Karin Lisspers, Sweden Breathing and feeling well through universal access to right care Predicting hospitalization of Swedish patients due to COPD exacerbation with machine learning. Presented by: Karin Lisspers,


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Breathing and feeling well through universal access to right care

Abstract Presentations

  • 5. Karin Lisspers, Sweden
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Breathing and feeling well through universal access to right care

Predicting hospitalization of Swedish patients due to COPD exacerbation with machine learning.

Presented by: Karin Lisspers, Uppsala university karin.lisspers@regiondalarna.se

Karin Lisspers1, Björn Ställberg1, Kjell Larsson2, Christer Janson1, Mario Müller3, Mateusz Łuczko3, Bine Kjoeller Bjerregaard3, Gerald Bacher4, Björn Holzhauer4, Pankaj Goyal4, Gunnar Johansson1

1 Uppsala university, 2 Karolinska Institute, 3 IQVIA, 4 Novartis Pharma AG

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Disclosure

Declaration of Interest:

KaL, BS, KjL, CJ and GJ are members of the steering committee on the ARCTIC study, which is funded by Novartis. KaL and CJ have during last five years participated in educational activities and lectures with AstraZeneca, Novartis, TEVA and Chiesi and advisory boards with AstraZeneca, Novartis, Boehringer Ingelheim and GlaxoSmithKline. BS reports receiving funding from AstraZeneca, Novartis, Boehringer Ingelheim, GlaxoSmithKline, Meda, Teva, and Chiesi

  • utside the submitted work.

KjL has during the last five years served in an advisory board and/or served as speaker and/or participated in education arranged by AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Orion, Novartis, Mylan, Sanofi and Teva. GJ served on advisory boards arranged by AstraZeneca, Novo Nordisk and Takeda. GB, BH, PG are employees and shareholders of Novartis. MM, ML, BKB are employees of IQVIA. IQVIA have received funding from Novartis to conduct the study.

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Study objective

  • To develop a model that predicts short term (within 10 days) risk

factors for hospitalization due to severe exacerbations of COPD, using Swedish patient level data.

Background

  • COPD exacerbations negatively

impact disease severity, progression, mortality and may lead to hospitalizations.

Rationale/clinical need

  • Tools that predict impending exacerbations

could be used for pre-emptive intervention to prevent exacerbations and thus improve long-term COPD outcomes.

Background, rationale and objectives

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Patient population

  • Large retrospective cohort study in Sweden

spanning a time period between 2000- 20131,2.

  • Data extracted from electronic medical

records (EMR) from 52 primary care centers and linked with national health registries.

  • Most COPD patients are treated in primary

care in Sweden.

Study time period

1. Lisspers K et al. Economic burden of COPD in a Swedish cohort: the ARCTIC study. Int J Chron Obstruct Pulmon Dis. 2018;13:275‐285. 2. Lisspers K et al. Gender differences among Swedish COPD patients: results from the ARCTIC, a real-world retrospective cohort study. NPJ Prim Care Respir Med. 2019;29(1):45.

Lookback period (≥365 days) Prediction period Jun 2006 or later Observation period Identification period for COPD diagnosis

10 days 10 days 10 days 10 days 10 days 10 days 10 days

Oct 2013 or before Jun 2005 2000

Data before 2005 was used for “whole patient history” features.

The ARCTIC dataset

Data from 2005 contains data from National Prescribed Drug Register.

Study design

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Prediction factors

  • Patient demographics
  • History of previous exacerbations
  • Comorbidities
  • Medications
  • Laboratory tests and measurements
  • Contacts to the healthcare system
  • Seasonal variables

Model selection

Following methods were tested:

  • 1. Logistic regression
  • 2. Random forest
  • 3. Gradient Boosted trees

Final model (Gradient Boosted trees) was selected using cross-validation on the training data.

Validation

  • All models were developed on 75% of cohort (5,867 patients) and validated on the remaining

unseen 25% of cohort (1,956 patients).

  • Validation analyses showed superior predictive performance as compared to a random classifier:
  • AUROC score = 0.86 (compared to AUROC = 0.50 for a random classifier)
  • AUPRC score = 0.08 (12.5 times more effective than a random classifier)

AUROC=Area Under the Receiver Operating Characteristics; AUPRC = Area Under the Precision-Recall Curve

Methods

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Previous severe exacerbations* are prediction factors for future COPD hospitalization

0% 20% 40% 60% 80% 100% 2 4 6 8 10 12 14 16 18 20 22 24 Number of severe exacerbations* before prediction point per patient

Severe Exacerbations, 1-180 days before prediction point Severe Exacerbations, all time before prediction point Proportion of records with severe exacerbations* 10 days after prediction point

Top most important prediction features

1. Number of severe exacerbations* (last 180 days) 2. Number of severe exacerbations* (whole history) 3. First COPD diagnosis as outpatient 4. Number of COPD related healthcare contacts (whole history) 5. Charlson Comorbidity Index (CCI) 6. First COPD diagnosis as inpatient

The risk for hospitalization within the next 10 days increases with the number of previous severe exacerbations*.

* Severe exacerbations were defined as exacerbation where a hospital stay was required.

Results

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To identify patients at risk of severe exacerbations focus consultations on:

  • History of exacerbations
  • Setting of first COPD-diagnosis
  • COPD-related contacts to healthcare system
  • Comorbidities

Clinical information on patients’ history from EMRs and national registries can predict severe exacerbations (hospitalizations).

Conclusions