- Research article
- Open Access
Racial and socioeconomic disparities in multimorbidity and associated healthcare utilisation and outcomes in Brazil: a cross-sectional analysis of three million individuals
BMC Public Health volume 21, Article number: 1287 (2021)
Evidence is limited on racial/ethnic group disparities in multimorbidity and associated health outcomes in low- and middle-income countries hampering effective policies and clinical interventions to address health inequalities.
This study assessed race/ethnic and socioeconomic disparities in the prevalence of multimorbidity and associated healthcare utilisation, costs and death in Rio de Janeiro, Brazil. A cross-sectional analysis was carried out of 3,027,335 individuals registered with primary healthcare (PHC) services. Records included linked data to hospitalisation, mortality, and welfare-claimant (Bolsa Família) records between 1 Jan 2012 and 31 Dec 2016. Logistic and Poisson regression models were carried out to assess the likelihood of multimorbidity (two or more diagnoses out of 53 chronic conditions), PHC use, hospital admissions and mortality from any cause. Interactions were used to assess disparities.
In total 13,509,633 healthcare visits were analysed identifying 389,829 multimorbid individuals (13%). In adjusted regression models, multimorbidity was associated with lower education (Adjusted Odds Ratio (AOR): 1.26; 95%CI: 1.23,1.29; compared to higher education), Bolsa Família receipt (AOR: 1.14; 95%CI: 1.13,1.15; compared to non-recipients); and black race/ethnicity (AOR: 1.05; 95%CI: 1.03,1.06; compared to white). Multimorbidity was associated with more hospitalisations (Adjusted Rate Ratio (ARR): 2.75; 95%CI: 2.69,2.81), more PHC visits (ARR: 3.46; 95%CI: 3.44,3.47), and higher likelihood of death (AOR: 1.33; 95%CI: 1.29,1.36). These associations were greater for multimorbid individuals with lower educational attainment (five year probability of death 1.67% (95%CI: 1.61,1.74%) compared to 1.13% (95%CI: 1.02,1.23%) for higher education), individuals of black race/ethnicity (1.48% (95%CI: 1.41,1.55%) compared to 1.35% (95%CI: 1.31,1.40%) for white) and individuals in receipt of welfare (1.89% (95%CI: 1.77,2.00%) compared to 1.35% (95%CI: 1.31,1.38%) for non-recipients).
The prevalence of multimorbidity and associated hospital admissions and mortality are greater in individuals with black race/ethnicity and other deprived socioeconomic groups in Rio de Janeiro. Interventions to better prevent and manage multimorbidity and underlying disparities in low- and middle-income country settings are needed.
Noncommunicable diseases (NCDs) remain the leading cause of death and disability worldwide. However, 77% of NCD deaths and 82% of NCD DALYs lost globally are in low- and middle-income countries (LMICs) . The estimated economic burden of leading NCDs between 2011 and 2030 is USD $47 trillion (2010 USD $) with nearly half (USD $21 trillion) in LMICs . Appropriate prevention and management of risk factors and chronic conditions is essential to address the NCD burden .
Multimorbidity (two or more chronic conditions) strains health systems attempting to manage the growing burden of NCDs. Multimorbid individuals report worse quality of life  and increased functional decline , incur higher healthcare costs , and are at increased risk of death . Individuals with deprived socioeconomic status and low educational attainment have a higher prevalence of multimorbidity [7,8,9,10,11,12,13], including in LMICs [14,15,16]. Accumulation of risk factors, chronic stress, and poorer healthcare access in deprived socioeconomic groups drive these disparities. Multimorbidity onset can be up to 15 years earlier in deprived populations compared to affluent populations .
Research on multimorbidity in LMICs is extremely limited [18, 19] – particularly examining racial/ethnic and socioeconomic group disparities. Studies in high-income countries show higher rates of multimorbidity among Hispanics and African Americans in the USA [8,9,10,11], South-Asian and black individuals in the UK , and ethnic minorities in the Netherlands . Similarly, evidence from the USA  and cross-country studies in LMICs [14,15,16] show those with lower education have higher rates of multimorbidity. Studies from LMICs almost exclusively rely on household surveys which are subject to recall bias and are often underpowered to detect disparities.
Brazil is an important setting for evaluating multimorbidity. It is a large middle-income country that has expanded universal health services in the context of stark disparities in health outcomes between socioeconomic and race/ethnic groups . Brazil’s GINI index of income inequality was 53 in 2019 - one of the most unequal in the world. More than half of Brazilians aged 25 or older have not completed secondary school . Nearly a third (32.9%) of black or pardo Brazilians earn less than US$5.50 a day (compared to 15.4% of white Brazilians), whilst 9.1% of black/pardo Brazilians are illiterate compared to 3.9% of white Brazilians . Primary health care (PHC), under the Family health Strategy, have been expanded nationally since the mid 1990s covering around 60% of the population in 2018 . PHC services are publicly-funded and free at the point of care, and include comprehensive preventative and acute care provided by multidisciplinary teams . With a sizeable private sector, PHC in Brazil generally covers low and middle-income populations. However, there are major health system fragilities  and growing NCD risk factors . Nationally, an estimated 42 million individuals (22–23% of adults) are multimorbid [26, 27], rising to 68% for those over 50 years of age , with higher rates of multimorbidity for those with lower education [26,27,28]. Brazilian studies utilising medical records with statistical power to examine disparities in multimorbidity prevalence and outcomes are scarce. This study uses a large dataset of three million individuals of all ages over the life course registered with PHC services in the city of Rio de Janeiro. It firstly assesses the prevalence of multimorbidity and associated risk factors, and secondly explores the association of multimorbidity with healthcare utilisation, patients’ healthcare costs, and death between race/ethnicity and socioeconomic groups.
A cross-sectional analysis of PHC registered individuals with linked welfare, PHC, hospitalisation, and mortality records.
PHC registration records of 3,027,335 individuals of all ages in Rio de Janeiro city were obtained - covering 47% of the city population. The study population is low-income as PHC services are focused in poorer areas. All individuals who registered with PHC up to 31 Dec 2016 were included. Records were linked to welfare claimant records (Cadastro Unico), PHC electronic medical records, hospitalisation admission records (Sistema de Informações Hospitalares; SIH), and mortality records (Sistema de Informações sobre Mortalidade; SIM) - all covering the five-year period from 1 Jan 2012 to 31 Dec 2016. Datasets were obtained from the Secretariat for Health in Rio de Janeiro and linked using tax numbers, date of birth, and phonetic matching of names. The linkage methods involved deterministic and probabilistic processes with manual review. Probabilistic matching varied from 8 to 15%, depending on the databases being linked. Details on the linkage are published elsewhere [29, 30].
From PHC registration records, individuals’ characteristics were collated including age, sex, race/ethnicity, highest educational attainment, and private insurance usage. Welfare claimant records identified individuals in receipt of welfare (conditional cash transfers; Bolsa Família) and monthly expenditures on medicines. From PHC consultations, hospitalisation admission records, and mortality records, ICD-10 codes and PHC procedure codes were obtained. There were 3,173,289 individuals in the original dataset (registered up to 31 Dec 2016), of which 145,954 (4.6%) were removed - 76,418 due to missing data on sex, race, date of birth or date of death; 67,170 duplicates; and 2366 records with deaths before 1 Jan 2012.
To assess multimorbidity, 53 chronic conditions were examined (Additional File 1 for conditions and ICD-10/procedure codes based on previous studies [17, 19, 31, 32]). Individuals were assigned chronic disease diagnoses based on criteria relating to timing of diagnoses (e.g. diagnoses within last 2 years), although for most conditions this was if any relevant diagnosis was ever recorded. Multimorbidity was defined as having two or more chronic disease diagnoses.
The resulting dataset contained PHC registered individuals and their chronic disease diagnoses, demographic and socioeconomic characteristics, counts of PHC consultations (all consultations including treatment and preventative care) and hospital admissions (emergency and elective) and mortality outcomes. Hospital admissions due to childbirth were excluded (ICD10 O00-O99.9, Z32-Z39.9). For a subset of the population (welfare claimants), household monthly expenditure on medicines was available. This was the reported monthly household expenditure on medicines (R$s). Demographic and socioeconomic characteristics were encoded as: sex (male; female); 5 year age groups; self-reported race/ethnicity (white; black; pardo (mixed race); Asian (Amarelo); or indigenous); the individual’s highest educational attainment (none, pre-school or literacy class; elementary School (Grades 1–4); elementary School (Grades 5+); high-school; higher education; or missing); if individual was in a Bolsa Família recipient household (yes; no); and if individual had private insurance (yes; no).
Prevalence of multimorbidity and associated risk factors
The prevalence of multimorbidity across race/ethnicity and socioeconomic groups was reported. The most common chronic conditions and those chronic conditions that contributed most to hospitalisations and deaths were reported. Logistic regression was employed to explore risk of multimorbidity by race/ethnicity and socioeconomic factors. Covariates were sex, age, race, educational group, Bolsa Família receipt, private insurance, and if individuals had any PHC use or hospitalisation. Adjusted odds ratios (AOR) were reported. Due to the high level of missing data on education (26.9%), analyses were conducted including the missing category for comparison.
Associations between multimorbidity, healthcare use, expenditures and death, and disparities across race/ethnic and socioeconomic groups
Regression modelling examined association between multimorbidity and PHC and hospital usage, health expenditures and mortality. Models were adjusted for sex, age, race/ethnicity, educational group, Bolsa Família receipt, and private insurance. Logistic regression was employed for death (binary outcome), Poisson models for counts (PHC consultations and hospital admissions), and linear regression for household health expenditures (subset of population with available data). AOR were reported for logistic regressions and adjusted rate ratios (ARR) reported for Poisson regression models.
The models were expanded with interactions to test whether the associations between multimorbidity and healthcare use, death and expenditures were different across race/ethnicity, educational attainment, and Bolsa Família status groups (i.e. three interactions per outcome). Post-regression probabilities (of death), rates (of PHC consultation and hospital admissions), and average household expenditures were predicted for the three socioeconomic groups and by multimorbidity status. These are interpreted relative to the five-year study period (i.e. five-year probability of death).
All analyses used robust standard errors and carried out in STATA® Statistical Software 15 (StataCorp LLC).
Overall prevalence estimates of multimorbidity from all PHC registrants were compared to estimates from a subsample of those that used PHC services. Potential biases from high levels of missing education data were tested through multiple imputation where 10 imputations were made based on individuals’ recorded age, sex, education status, race/ethnicity, Bolsa Família receipt, insurance coverage, and PHC and hospital usage.
There were 3,027,335 individuals in the dataset registered with PHC (Table 1). Of these, 1,722,477 (56.9%) had at least one consultation with PHC between 1 Jan 2012 and 31 Dec 2016 (PHC users) whilst 226,255 (7.5%) had at least one hospital admission. Over half (1,693,999; 56.0%) of the population was female. By race/ethnicity, 51.5% were pardo (mixed race), 35.8% white and 12.0% were black. Over one-fifth (21.3%) were Bolsa Família recipients. Most (1,633,095; 54.0%) had elementary (grades 1–4 or grades 5+) or high schooling, whilst 3.0% (91,656) had higher education and 16.1% (487,860) had no formal education. The mean number of PHC consultations and hospitalisations per individual over the five-year period were 4.3 and 0.12 respectively. In total, 39,385 (1.3%) individuals died. There were 881,632 individuals (29.1%) with data on expenditures and a mean household expenditure on medicines of R$ 9.9 per month (USD $ 3.3 in 2015).
Prevalence of multimorbidity and associated risk factors
To assess chronic condition diagnoses, 13,151,537 PHC consultations and 358,096 hospital admissions were analysed. The most common conditions were: hypertension (445,6901 individuals with diagnosis; 14.7%), diabetes mellitus (150,276; 5.0%), allergy (74,971; 2.5%), severe vision reduction (59,108; 2.0%), lipid metabolism disorders (52,991; 1.8%), and obesity (49,749; 1.6%) (Additional File 2). Over one-quarter of the population (835,151; 27.6%) had at least one chronic condition, whilst 12.9% (389,829) were multimorbid. Of multimorbid individuals, 228,153 (73.8%) had hypertension and 130,418 (33.5%) had diabetes mellitus (Additional File 3 and Additional File 4).
Multimorbidity substantially increased with age (Fig. 1). Whilst on average the prevalence was 12.9%, it increased to 16.6% (379,919 individuals) for aged 18 years and over, 26.1% (337,657) for those aged 40 and over, and 37.0% (194,403) those age 60 and over (Additional File 5). There were differences by sex (15.4% of females were multimorbid; 9.6% of men) and race/ethnicity (16.0% of black, 13.9% of white, 13.1% of indigenous, 11.5% of pardo, and 11.0% of Asian). Disparities in the prevalence of multimorbidity by racial and educational groups widened with age (Fig. 2). The age at which a quarter of individuals had multimorbidity varied from 51 years for black individuals to 54 for pardo, 55 for white, and 57 for Asian (Amarelo).
In adjusted analyses, black individuals were 5% more likely to be multimorbid (AOR: 1.05; 95%CI: 1.03,1.06), whilst pardo individuals were 6% (AOR: 0.94; 95%CI: 0.93,0.95), Asian 11% (AOR: 0.89; 95%CI: 0.84,0.95), and indigenous individuals 19% (AOR: 0.82; 95%CI: 0.72,0.93) less likely to be multimorbid compared with white individuals (Additional File 6). The highest educated were 21% (AOR: 0.79; 95%CI: 0.77,0.81) less likely to be multimorbid than those with no education, whilst Bolsa Família recipients were 14% (AOR: 1.14; 95%CI: 1.13,1.15) more likely than non-recipients.
Associations between multimorbidity, healthcare utilisation, expenditures, death, and disparities across race/ethnic and socioeconomic groups
Nearly half (44%; 5,727,074) of all PHC consultations, 37% (133,526) of admissions, and a third (13,172) of deaths were in multimorbid individuals. Households of multimorbid individuals spent R$ 18.1 per month on medicines compared to R$ 8.9 for non-multimorbid individuals. Adjusted logistic and Poisson regression models found multimorbid individuals had 3.5 times as many PHC consultations (ARR: 3.46; 95%CI: 3.44,3.47), 2.7 times as many hospitalisations (ARR: 2.75; 95%CI: 2.69,2.81), and were 33% more likely to die (AOR: 1.33; 95%CI: 1.29,1.36) compared to non-multimorbid individuals (Additional File 7).
Additionally, there were significant interactions between multimorbidity and race/ethnicity and socioeconomic status (Fig. 3; Additional File 7). Predicted five-year PHC utilisation rates were higher in individuals with white race/ethnicity, lower educational attainment and those in recipient of welfare. Multimorbidity was associated with higher predicted hospitalisation rates among those with lower educational attainment and welfare recipients. Multimorbidity was associated with a greater risk of death among black Brazilians, those with lower educational attainment and welfare recipients.
In the subgroup regression analysis of 881,632 individuals with available data, multimorbid individuals spent $R 2.3 (95%CI: 1.9,2.7) more per month than those without multimorbidity (Additional File 8). The association of multimorbidity and higher expenditures on medicines was found across socioeconomic groups (Fig. 4), but the magnitude of increase varied. Individuals in black racial/ethnic, lower educational attainment and welfare recipients had smaller increases in expenditure associated with multimorbidity.
The prevalence of chronic conditions was on average twice as high among PHC users when compared to the whole registered population (Additional File 2). Prevalence estimates for only PHC users (1,722,477) showed very similar patterns across race/ethnicity and socioeconomic groups (Additional File 9). There were also similar effect estimates for risk of hospitalisation and death when examining PHC users only (Additional File 9). Multiple imputation of missing education data did not affect the main results (Additional File 10).
This study analyses multimorbidity and disparities using a large clinical dataset of three million individuals with 13.5 million linked healthcare records – a first for a middle-income country. More than one quarter of registered individuals had a chronic condition and 13% had multimorbidity. Multimorbidity prevalence increased with age: 17% for those aged 18 years and over, 26% for those aged 40 and over, and 37% those age 60 and over. Hypertension and diabetes were leading conditions. Disparities were pervasive with higher rates of multimorbidity and mortality in those with black race/ethnicity, lower educational attainment and those in receipt of welfare.
The high burden of hypertension and diabetes identified in this study is concordant with Brazilian and international studies [33, 34], and the association between multimorbidity and hospitalisations, death and health expenditures is supported by recent systematic reviews [6, 35]. The race/ethnicity group and wider socioeconomic patterning of multimorbidity is also concordant with wider literature [2, 8,9,10,11,12,13,14, 24, 28, 34]. In this study, Bolsa Família receipt, lower education and belonging to a black or pardo race/ethnic groups are proxies for lower socioeconomic status. Lower socioeconomic status drives the accumulation of chronic conditions through poorer living standards and diets, lower healthcare access, exposure to pollutants and environmental stressors, diminished levels of health literacy and increased likelihood of unhealthier behaviours such as smoking, alcohol consumption, and low physical activity . In Rio de Janeiro, there is additionally increased neighbourhood violence  and national issues related to structural racism and restricted employment and educational opportunities . The results indicated that Black Brazilians had generally higher rates of multimorbidity, lower rates of PHC utilisation, and a higher risk of death than white Brazilians suggesting greater exposure to underlying risk factors and increased barriers to accessing healthcare [39, 40].
In this study, multimorbid individuals with black race/ethnicity and socioeconomically deprived had higher healthcare use and mortality. Little is known in LMICs about which factors increase mortality among individuals with multiple chronic conditions. Studies from the UK suggest behavioural factors are important [41, 42], but in Brazil and other LMICs deep social inequalities and barriers to accessing high-quality (and preventative) healthcare are likely also contributors. The finding that multimorbidity is associated with higher expenditures on medicines is concordant with previous evidence . However, multimorbidity-associated expenditures were greater in higher socioeconomic groups perhaps indicating forgone medicine consumption (due to cost) in lower socioeconomic groups or increased discretionary spend in higher socioeconomic groups where medicines are subsidised .
The findings from this study are pertinent to policymakers and clinicians in Brazil and other LMICs. Firstly, multimorbidity is highly prevalent, although likely underreported in clinical records – especially for conditions such as depression and chronic back pain. The estimated prevalence of multimorbidity in this study is lower than others in Brazil (22% of adults nationally [26, 27] and 68% for those over 50 years ), and differences may be due to over-reporting in surveys and under-reporting in clinical records. Secondly, disparities in multimorbidity reflect wider patterns of structural disadvantage and deprivation. Addressing inadequate access to high quality healthcare among deprived groups is vital [44, 45], in addition to addressing wider social determinants of multimorbidity . Thirdly, attention to reducing medicine costs in individuals with multimorbidity, especially among those with limited ability to pay, is an important priority. Finally, racial/ethnic inequalities persisted following statistical adjustment for socioeconomic indicators suggesting race/ethnicity may independently affect health outcomes - particularly the worse outcomes for black Brazilians. Given there are almost no biological explanations for these inequalities, this may highlight issues of racial divisions and structural racism.
Using clinical diagnoses from medical records is a major advancement for LMIC studies. Our study has sufficient statistical power to examine disparities in granular detail – not possible in previous studies . However, there are also limitations to consider. PHC-registered individuals may not use PHC (perhaps seeking alternative providers or forgoing healthcare) and therefore the estimated multimorbidity prevalence is likely an underestimate of the true prevalence. Additionally, diagnoses are determined from electronic medical records and the low prevalence of conditions such as chronic back pain and depression may be due to healthcare access issues or poor recording. Deprived populations experience greater barriers to healthcare suggesting underestimates are greater in deprived groups. The study population only covers PHC-registered individuals (just under half the population of Rio), and although the non-PHC covered population is likely to be wealthier due to PHC roll out in poorer areas, extrapolating findings from this study to the whole city is inappropriate. Also, data on race and educational attainment is self-reported with potential for misclassification , but biases are unlikely to be associated with multimorbidity or sufficiently large to negate the findings. As educational attainment was determined at the individual-level (as opposed to household or parental level), there may have been biases from including children in the analysis (because their educational attainment was related to their current schooling). However, the prevalence of multimorbidity was very low for children (less than 1.5%) and omitting children from analysis did not alter the results substantially. Moreover, multimorbidity was assessed cross-sectionally without the timing of diagnoses or time until outcomes accounted for. Better understanding of the temporal nature of multimorbidity, associated outcomes and mediating factors is an area for future work – especially in LMICs. This includes using longitudinal data to model multimorbidity over the life course and compare these between countries and settings. Another limitation was the large missing data for education, but sensitivity analyses suggest limited impact on the findings. Lastly, other socioeconomic factors such as income, wealth and housing were not available to analyse and could provide better understanding of the socioeconomic patterning of multimorbidity in Brazil.
Multimorbidity is prevalent and socioeconomically patterned in Brazil with higher multimorbidity and associated healthcare usage and mortality greater among more deprived socioeconomic groups. Interventions to better prevent and manage multimorbidity and underlying disparities in LMICs are needed. This includes actions targeted towards lower socioeconomic and racial/ethnic groups who have greater exposure to risk factors for chronic conditions and who experience higher barriers to accessing healthcare.
Availability of data and materials
The datasets analysed in this study were generated from linking routine healthcare and administrative datasets. Publicly-available datasets (anonymised and often aggregated) are available from Brazilian government websites: http://tabnet.datasus.gov.br/ and https://www.gov.br/pt-br/servicos/solicitar-cessao-de-dados-identificados-do-cadastro-unico. The specific versions of the datasets used in this analysis (individual-level records with names and tax numbers were linkage) were obtained from the Secretariat for Health in Rio de Janeiro. These linked datasets which were analysed in this study are not publicly available due the confidentiality and sensitivity of the linked individual-level data. However, the corresponding author is available to assist other researchers requesting approval from Brazilian authorities and obtaining appropriate ethical approval for re-use of these datasets.
Adjusted Odds Ratio
Adjusted Rate Ratio
International classification of diseases
low- and middle-income country
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This study was funded by the UK’s Joint Health Systems Research Initiative (DFID/MRC/Wellcome Trust/ESRC) grant number MR/P014593/1. JS was supported by an MRC fellowship (MR/T027517/1). AT supported by grant number CNPq 303267/2018-6. CMC was partially supported by research fellowship grants from the National Council for Scientific and Technological Development (Grant number 303295/2019–8) and Carlos Chagas Filho Foundation for Research Support in the State of Rio de Janeiro (Grant number E-26/200.003/2019). The funder had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
Ethics approval and consent to participate
Approval for this study was obtained from the Brazilian National Commission for Ethics in Research (Comissão Nacional de Ética em Pesquisa [CONEP])—number 2.689.528. Administrative permission to access and use the datasets in this study was obtained from the Secretariat for Health in Rio de Janeiro.
Consent for publication
BD was Undersecretary of Health Promotion, Surveillance, and Primary Care at the Secretaria Municipal de Saúde, Rio de Janeiro when this project was conceived.
VS is a Coordinator of Health Situation Analysis in the Health Surveillance Department, at the Secretaria Municipal de Saúde, Rio de Janeiro.
All other authors declare they have no conflicts of interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Chronic conditions with ICD-10 and primary care procedure Codes.
Individuals with diagnosed chronic conditions and prevalence estimates.
Chronic conditions ranked by number of diagnosed individuals for multimorbid individuals.
Leading combinations of chronic conditions in multimorbid individuals by contribution to multimorbid mortality and hospitalisations.
Prevalence of multimorbidity by demographic and socioeconomic groups for those aged 45–64 years and 65 year or more.
Logistic regression results on likelihood of any chronic condition or multimorbidity.
Supplementary regression results with socioeconomic interactions.
Linear regression results on household expenditures on medicines (subsample).
Sensitivity analysis showing regression results for PHC users only.
Sensitivity analysis with results from multiple imputation.
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Hone, T., Stokes, J., Trajman, A. et al. Racial and socioeconomic disparities in multimorbidity and associated healthcare utilisation and outcomes in Brazil: a cross-sectional analysis of three million individuals. BMC Public Health 21, 1287 (2021). https://doi.org/10.1186/s12889-021-11328-0
- Chronic conditions
- Middle-income country