Evidence map›Paper›PMID 30143045›Full record

Observational studyCardiovascular diabetology2018

Development of predictive risk models for major adverse cardiovascular events among patients with type 2 diabetes mellitus using health insurance claims data.

James B Young, Marjolaine Gauthier-Loiselle, Robert A Bailey, Ameur M Manceur, Patrick Lefebvre, Morris Greenberg, Marie-Hélène Lafeuille, Mei Sheng Duh, Brahim Bookhart, Carol H Wysham

Abstract readObservational Study
In one paragraph

Observational study in Cardiovascular diabetology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 3 pooled it
–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

20 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Prognostic models for all-cause and cardiovascular mortality in type 2 diabetes: Systematic review.Diabetic medicine : a journal of the British Diabetic Association · 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

10 authors.

James B YoungCleveland Clinic Foundation Lerner College of Medicine of Case Western Reserve University, Cleveland, OH, USA.
Marjolaine Gauthier-LoiselleAnalysis Group, Inc., 1000 De La Gauchetière Ouest, Suite 1200, Montreal, QC, H3B 4W5, Canada. Marjolaine.Gauthier-Loiselle@analysisgroup.com.ORCID 0000-0002-9439-595X
Robert A BaileyJanssen Scientific Affairs, LLC, Raritan, NJ, USA.
Ameur M ManceurAnalysis Group, Inc., 1000 De La Gauchetière Ouest, Suite 1200, Montreal, QC, H3B 4W5, Canada.
Patrick LefebvreAnalysis Group, Inc., 1000 De La Gauchetière Ouest, Suite 1200, Montreal, QC, H3B 4W5, Canada.
Morris GreenbergAnalysis Group Inc., Boston, MA, USA.
Marie-Hélène LafeuilleAnalysis Group, Inc., 1000 De La Gauchetière Ouest, Suite 1200, Montreal, QC, H3B 4W5, Canada.
Mei Sheng DuhAnalysis Group Inc., Boston, MA, USA.
Brahim BookhartJanssen Scientific Affairs, LLC, Raritan, NJ, USA.
Carol H WyshamRockwood Clinic, Spokane, WA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere exist several predictive risk models for cardiovascular disease (CVD), including some developed specifically for patients with type 2 diabetes mellitus (T2DM). However, the models developed for a diabetic population are based on information derived from medical records or laboratory results, which are not typically available to entities like payers or quality of care organizations. The objective of this study is to develop and validate models predicting the risk of cardiovascular events in patients with T2DM based on medical insurance claims data.

methodsPatients with T2DM aged 50 years or older were identified from the Optum™ Integrated Real World Evidence Electronic Health Records and Claims de-identified database (10/01/2006-09/30/2016). Risk factors were assessed over a 12-month baseline period and cardiovascular events were monitored from the end of the baseline period until end of data availability, continuous enrollment, or death. Risk models were developed using logistic regressions separately for patients with and without prior CVD, and for each outcome: (1) major adverse cardiovascular events (MACE; i.e., non-fatal myocardial infarction, non-fatal stroke, CVD-related death); (2) any MACE, hospitalization for unstable angina, or hospitalization for congestive heart failure; (3) CVD-related death. Models were developed and validated on 70% and 30% of the sample, respectively. Model performance was assessed using C-statistics.

resultsA total of 181,619 patients were identified, including 136,544 (75.2%) without prior CVD and 45,075 (24.8%) with a history of CVD. Age, diabetes-related hospitalizations, prior CVD diagnoses and chronic pulmonary disease were the most important predictors across all models. C-statistics ranged from 0.70 to 0.81, indicating that the models performed well. The additional inclusion of risk factors derived from pharmacy claims (e.g., use of antihypertensive, and use of antihyperglycemic) or from medical records and laboratory measures (e.g., hemoglobin A1c, urine albumin to creatinine ratio) only marginally improved the performance of the models.

conclusionThe claims-based models developed could reliably predict the risk of cardiovascular events in T2DM patients, without requiring pharmacy claims or laboratory measures. These models could be relevant for providers and payers and help implement approaches to prevent cardiovascular events in high-risk diabetic patients.

Indexed as

Administrative Claims, HealthcareElectronic Health RecordsAgedAged, 80 and overCardiovascular DiseasesClinical Decision-MakingDatabases, FactualData MiningDecision Support TechniquesDiabetes Mellitus, Type 2FemaleHumansMaleMiddle AgedPrimary PreventionPrognosisCardiovascular diseaseHealth insurance claimsRisk predictionType 2 diabetes mellitus

Identifiers

PMID30143045
PMCPMC6109303

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.