Evidence map›Paper›PMID 33064757›Full record

ArticlePloS one2020

Modified-Chronic Disease Score (M-CDS): Predicting the individual risk of death using drug prescriptions.

Marica Iommi, Simona Rosa, Michele Fusaroli, Paola Rucci, Maria Pia Fantini, Elisabetta Poluzzi

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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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

8 citing papers in PubMed.

  1. Article
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  3. General practice organisational models and heart failure medication adherence: multi-level evidence from a regional cohort in Emilia-Romagna, Italy.International journal for quality in health care : journal of the International Society for Quality in Health Care · 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

6 authors.

Marica IommiDepartment of Biomedical and Neuromotor Sciences-Hygiene and Biostatistics Unit, University of Bologna, Bologna, Italy.ORCID 0000-0003-4589-3474
Simona RosaDepartment of Biomedical and Neuromotor Sciences-Hygiene and Biostatistics Unit, University of Bologna, Bologna, Italy.
Michele FusaroliDepartment of Medical and Surgical Sciences-Pharmacology Unit, University of Bologna, Bologna, Italy.
Paola RucciDepartment of Biomedical and Neuromotor Sciences-Hygiene and Biostatistics Unit, University of Bologna, Bologna, Italy.
Maria Pia FantiniDepartment of Biomedical and Neuromotor Sciences-Hygiene and Biostatistics Unit, University of Bologna, Bologna, Italy.
Elisabetta PoluzziDepartment of Medical and Surgical Sciences-Pharmacology Unit, University of Bologna, Bologna, Italy.ORCID 0000-0002-7209-0426

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEstimating the morbidity of a population is strategic for health systems to improve healthcare. In recent years administrative databases have been increasingly used to predict health outcomes. In 1992, Von Korff proposed a Chronic Disease Score (CDS) to predict 1-year mortality by only using drug prescription data. Because pharmacotherapy underwent many changes over the last 3 decades, the original version of the CDS has limitations. The aim of this paper is to report on the development of the modified version of the CDS.

methodsThe modified CDS (M-CDS) was developed using 33 variables (from drug prescriptions within two-year before 01/01/2018) to predict one-year mortality in Bologna residents aged ≥50 years. The population was split into training and testing sets for internal validation. Score weights were estimated in the training set using Cox regression model with LASSO procedure for variables selection. The external validation was carried out on the Imola population. The predictive ability of M-CDS was assessed using ROC analysis and compared with that of the Charlson Comorbidity Index (CCI), that is based on hospital data only, and of the Multisource Comorbidity Score (MCS), which uses hospital and pharmaceutical data.

resultsThe predictive ability of M-CDS was similar in the training and testing sets (AUC 95% CI: training [0.760-0.770] vs. testing [0.750-0.772]) and in the external population (Imola AUC 95% CI [0.756-0.781]). M-CDS was significantly better than CCI (M-CDS AUC = 0.761, 95% CI [0.750-0.772] vs. CCI-AUC = 0.696, 95% CI [0.681-0.711]). No significant difference was found between M-CDS and MCS (MCS AUC = 0.762, 95% CI [0.749-0.775]).

conclusionsM-CDS, using only drug prescriptions, has a better performance than the CCI score in predicting 1-year mortality, and is not inferior to the multisource comorbidity score. M-CDS can be used for population risk stratification, for risk-adjustment in association studies and to predict the individual risk of death.

Indexed as

AlgorithmsComorbidityAgedAged, 80 and overArea Under CurveCerebrovascular DisordersChronic DiseaseDatabases, FactualDrug PrescriptionsFemaleHumansKaplan-Meier EstimateMaleMiddle AgedProportional Hazards ModelsRisk Factors

Identifiers

PMID33064757
PMCPMC7567358

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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.