Evidence map›Paper›PMID 37252771›Full record

ArticleJMIR public health and surveillance2023

Prediction of Multimorbidity in Brazil: Latest Fifth of a Century Population Study.

Xi-Liang Li, Hang Huang, Ying Lu, Randall S Stafford, Simone Maria Lima, Caroline Mota, Xin Shi

Open access · goldAbstract read
In one paragraph

Article in JMIR public health and surveillance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
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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

7 authors at 4 institutions in 4 countries.

Xi-Liang LiSchool of Mathematics and Information Science, Shandong Technology and Business University, Yantai, China.ORCID 0000-0002-0513-5938
Hang HuangSchool of Statistics, Shandong Technology and Business University, Yantai, China.ORCID 0000-0003-4589-5779
Ying LuDepartment of Biomedical Data Science, School of Medicine, Stanford University, Stanford, CA, United States.ORCID 0000-0002-7698-8962
Randall S StaffordDepartment of Medicine, School of Medicine, Stanford University, Stanford, CA, United States.ORCID 0000-0003-1805-1271
Simone Maria LimaManagement Engineering Department, Universidade Federal de Pernambuco, Recife, Brazil.ORCID 0000-0001-9404-8221
Caroline MotaManagement Engineering Department, Universidade Federal de Pernambuco, Recife, Brazil.ORCID 0000-0001-9617-5726
Xin ShiSchool of Mathematics and Information Science, Shandong Technology and Business University, Yantai, China.ORCID 0000-0002-4930-7295
Shandong Institute of Business and Technology · CNStanford University · USUniversidade Federal de Pernambuco · BRManchester Metropolitan University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultimorbidity is characterized by the co-occurrence of 2 or more chronic diseases and has been a focus of the health care sector and health policy makers due to its severe adverse effects.

objectiveThis paper aims to use the latest 2 decades of national health data in Brazil to analyze the effects of demographic factors and predict the impact of various risk factors on multimorbidity.

methodsData analysis methods include descriptive analysis, logistic regression, and nomogram prediction. The study makes use of a set of national cross-sectional data with a sample size of 877,032. The study used data from 1998, 2003, and 2008 from the Brazilian National Household Sample Survey, and from 2013 and 2019 from the Brazilian National Health Survey. We developed a logistic regression model to assess the influence of risk factors on multimorbidity and predict the influence of the key risk factors in the future, based on the prevalence of multimorbidity in Brazil.

resultsOverall, females were 1.7 times more likely to experience multimorbidity than males (odds ratio [OR] 1.72, 95% CI 1.69-1.74). The prevalence of multimorbidity among unemployed individuals was 1.5 times that of employed individuals (OR 1.51, 95% CI 1.49-1.53). Multimorbidity prevalence increased significantly with age. People over 60 years of age were about 20 times more likely to have multiple chronic diseases than those between 18 and 29 years of age (OR 19.6, 95% CI 19.15-20.07). The prevalence of multimorbidity in illiterate individuals was 1.2 times that in literate ones (OR 1.26, 95% CI 1.24-1.28). The subjective well-being of seniors without multimorbidity was 15 times that among people with multimorbidity (OR 15.29, 95% CI 14.97-15.63). Adults with multimorbidity were more than 1.5 times more likely to be hospitalized than those without (OR 1.53, 95% CI 1.50-1.56) and 1.9 times more likely need medical care (OR 1.94, 95% CI 1.91-1.97). These patterns were similar in all 5 cohort studies and remained stable for over 21 years. A nomogram model was used to predict multimorbidity prevalence under the influence of various risk factors. The prediction results were consistent with the effects of logistic regression; older age and poorer participant well-being had the strongest correlation with multimorbidity.

conclusionsOur study shows that multimorbidity prevalence varied little in the past 2 decades but varies widely across social groups. Identifying populations with higher rates of multimorbidity prevalence may improve policy making around multimorbidity prevention and management. The Brazilian government can create public health policies targeting these groups, and provide more medical treatment and health services to support and protect the multimorbidity population.

Indexed as

MultimorbidityAdultAgedBrazilChronic DiseaseComorbidityCross-Sectional StudiesFemaleHumansMaleMiddle AgedBrazildemographic factorslogistic regression analysismultimorbiditynomogram predictionprevalence

Identifiers

PMID37252771
PMCPMC10265407
OpenAlexW4378746044

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.