Abstract
Background: Disability-related considerations have largely been absent from the COVID-19 response, despite evidence that people with disabilities are at elevated risk for acquiring COVID-19. We evaluated clinical outcomes in patients who were admitted to hospital with COVID-19 with a disability compared with patients without a disability.
Methods: We conducted a retrospective cohort study that included adults with COVID-19 who were admitted to hospital and discharged between Jan. 1, 2020, and Nov. 30, 2020, at 7 hospitals in Ontario, Canada. We compared in-hospital death, admission to the intensive care unit (ICU), hospital length of stay and unplanned 30-day readmission among patients with and without a physical disability, hearing or vision impairment, traumatic brain injury, or intellectual or developmental disability, overall and stratified by age (≤ 64 and ≥ 65 yr) using multivariable regression, controlling for sex, residence in a long-term care facility and comorbidity.
Results: Among 1279 admissions to hospital for COVID-19, 22.3% had a disability. We found that patients with a disability were more likely to die than those without a disability (28.1% v. 17.6%), had longer hospital stays (median 13.9 v. 7.8 d) and more readmissions (17.6% v. 7.9%), but had lower ICU admission rates (22.5% v. 28.3%). After adjustment, there were no statistically significant differences between those with and without disabilities for in-hospital death or admission to ICU. After adjustment, patients with a disability had longer hospital stays (rate ratio 1.36, 95% confidence interval [CI] 1.19–1.56) and greater risk of readmission (relative risk 1.77, 95% CI 1.14–2.75). In age-stratified analyses, we observed longer hospital stays among patients with a disability than in those without, in both younger and older subgroups; readmission risk was driven by younger patients with a disability.
Interpretation: Patients with a disability who were admitted to hospital with COVID-19 had longer stays and elevated readmission risk than those without disabilities. Disability-related needs should be addressed to support these patients in hospital and after discharge.
A successful public health response to the COVID-19 pandemic requires accurate and timely identification of, and support for, high-risk groups. There is increasing recognition that marginalized groups, including congregate care residents, racial and ethnic minorities, and people experiencing poverty, have elevated incidence of COVID-19.1,2 Older age and comorbidities such as diabetes are also risk factors for severe COVID-19 outcomes.3,4 One potential high-risk group that has received relatively little attention is people with disabilities.
The World Health Organization estimates there are 1 billion people with disabilities globally.5 In North America, the prevalence of disability is 20%, with one-third of people older than 65 years having a disability.6 Disabilities include physical disabilities, hearing and vision impairments, traumatic brain injury and intellectual or developmental disabilities.5,6 Although activity limitations experienced by people with disabilities are heterogeneous,5,6 people with disabilities share high rates of risk factors for acquiring COVID-19, including poverty, residence in congregate care and being members of racialized communities.7–9 People with disabilities may be more reliant on close contact with others to meet their daily needs, and some people with disabilities, especially intellectual developmental disabilities, may have difficulty following public health rules. Once they acquire SARS-CoV-2 infection, people with disabilities may be at risk for severe outcomes because they have elevated rates of comorbidities.10 Some disabilities (e.g., spinal cord injuries and neurologic disabilities) result in physiologic changes that increase vulnerability to respiratory diseases and may mask symptoms of acute respiratory disease, which may delay diagnosis.11–13 There have also been reports of barriers to high-quality hospital care for patients with disabilities who have COVID-19, including communication issues caused by the use of masks and restricted access to support persons.14–17
Some studies have suggested that patients with disabilities and COVID-19 are at elevated risk for severe disease and death, with most evaluating intellectual or developmental disability.13,18–26 Yet, consideration of disability-related needs has largely been absent from the COVID-19 response, with vaccine eligibility driven primarily by age and medical comorbidity, limited accommodations made for patients with disabilities who are in hospital, and disability data often not being captured in surveillance programs.14–17 To inform equitable pandemic supports, there is a need for data on patients with a broad range of disabilities who have COVID-19. We sought to evaluate standard clinical outcomes in patients admitted to hospital with COVID-1927 (i.e., in-hospital death, intensive care unit [ICU] admission, hospital length of stay and unplanned 30-d readmission) for patients with and without a disability, overall and stratified by age. We hypothesized that patients with a disability would have worse outcomes because of a greater prevalence of comorbidities,10 physiologic characteristics that increase morbidity risk11–13 and barriers to high-quality hospital care.14–17
Methods
Study design and data sources
We conducted a retrospective cohort study using data from 5 academic and 2 community-based teaching hospitals in Toronto and Mississauga, Ontario, Canada, that are part of GEMINI, a hospital research collaborative.28 Data were collected from clinical and administrative information systems by GEMINI.29 Key data elements have 98%–100% accuracy compared with medical record review done manually.29 Data included demographics, diagnoses, vital signs, laboratory test results and use of hospital resources.
Study population
We included adults 18 years of age or older with COVID-19 who were admitted to an inpatient medical service (e.g., general medicine or respirology) or medical–surgical ICU and discharged between Jan. 1 and Nov. 30, 2020 (at 3 of the hospitals, data were available only from Jan. 1 to July 31, 2020). We identified COVID-19 diagnoses using International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10-CA) codes U07.1 and U07.2,27,30 with U07.1 having 98% sensitivity, 99% specificity and 92% positive predictive value for COVID-19 detection compared with results for polymerase chain reaction (PCR) tests.31
We identified a disability using published algorithms to ascertain physical disability,32 hearing and vision impairments,33,34 traumatic brain injury35 and intellectual or developmental disability36,37 in administrative data (Table 1). These algorithms include diagnoses associated with need for accommodations when accessing health care,32 functional limitations37,38 and adverse health outcomes.39 Other similar algorithms have shown a specificity of 100% and positive predictive value of 80% compared with data from disability service providers.40 We considered dementia and psychiatric disorders as comorbidities rather than including them as part of the “disability” definition because both are strong risk factors for death from COVID-1941,42 and are common in some groups with disability.43,44 We considered disability to be present if 1 or more disability diagnoses were recorded in the index hospital admission or any previous admission to a general medicine service at 1 of the GEMINI hospitals after Apr. 1, 2010 (the beginning of the GEMINI database; before 2019, GEMINI collected data only on general medicine admissions).
Outcomes
We chose outcomes that were standard clinical indicators of severe COVID-19 outcomes among patients admitted to hospital: in-hospital death, ICU admission, total length of hospital stay and unplanned readmission to a medical service or medical–surgical ICU at any GEMINI hospital within 30 days of discharge but excluding interfacility transfers.27 We considered readmissions to be unplanned if they occurred through an emergency department.
Covariates
We measured age, sex, transfer from an acute care hospital, long-term care facility residence and comorbidity, which we ascertained through specific conditions (i.e., chronic obstructive pulmonary disease, coronary artery disease, dementia, diabetes mellitus, heart failure, hypertension and psychiatric disorders) using the Clinical Classification Software Refined (Agency for Healthcare Research and Quality)45 and via the Charlson Comorbidity Index.46 We used postal codes to ascertain neighbourhood-level income and visible minority quintiles (Postal CodeOM Conversion File Plus, Statistics Canada; www150.statcan.gc.ca/n1/en/catalogue/82F0086X).47 We ascertained vital signs, laboratory test results and mortality prediction scores at admission (modified Acute Physiology and Chronic Health Evaluation [mAPACHE]48 and ISARIC Coronavirus Clinical Characterisation Consortium 4C [ISARIC-4C]49).
Statistical analysis
We reported baseline characteristics, vital signs, laboratory test results and mortality prediction scores at admission of patients admitted to hospital with COVID-19 with and without a disability using descriptive statistics and compared them using standardized differences.50
We modelled in-hospital death, ICU admission and unplanned 30-day readmission using modified Poisson regression,51 which uses a robust error variance to estimate relative risks (RRs). We used negative binomial regression, which estimates rate ratios, to model length of hospital stay. Since age is a strong predictor of disability6 and adverse COVID-19 outcomes,3 we derived overall models and models in patients 64 years of age or younger and 65 years or older separately. We selected this age threshold because risk of death associated with COVID-19 is elevated in patients who are older than 65 years of age3 and Ontario residents become eligible for Old Age Security pension and the Ontario Drug Benefit at this age. We created the following sequential models that were adjusted for confounders: age, sex and residence in long-term care;1–4,7–10 model 1 variables and medical comorbidity, dementia and psychiatric disorders (although these are correlated with disability,10,43,44 we wanted to isolate risk associated with disability from that associated with chronic illness broadly); model 2 variables and predicted mortality risk using mAPACHE scores; and model 3 variables and neighbourhood-level income and visible minority quintiles (for overall models only, because these could accommodate more variables).
In additional analyses, we stratified overall models by sex; described overall outcomes by type of disability (physical only, hearing or vision only, traumatic brain injury, or intellectual or developmental only and multiple); re-ran overall models, including dementia, in our disability definition; and re-ran overall models while also controlling for the number of previous hospital admissions over the study period. We performed all analyses using R version 4.0.2 (https://www.R-project.org/).
Ethics approval
We obtained approval from the research ethics board at each participating site.
Results
Between Jan. 1 and Nov. 30, 2020, there were 1279 hospital admissions for COVID-19 at our sites. The median age of the patients was 66 (interquartile range [IQR] 54–79) years, 742 (58.0%) were male and 285 (22.3%) had a recorded disability. Among admissions for patients with a disability, 212 (74.4%) had a physical disability, 18 (6.3%) had a hearing or vision impairment, 24 (8.4%) had a traumatic brain injury or intellectual or developmental disability and 31 (10.9%) had multiple disabilities. We found that patients with a disability were older than those without a disability, were less likely to be male, and were more likely to be residents of long-term care facilities and have comorbidities (Table 2). Patients with disabilities also had higher baseline predicted risk of death (Appendix 1, Table S1, available at www.cmaj.ca/lookup/doi/10.1503/cmaj.211277/tab-related-content).
Outcomes
In unadjusted analyses, we found that patients with disabilities were more likely to die in hospital than those without disabilities (28.1% v. 17.6%; RR 1.57, 95% confidence interval [CI] 1.19–2.06); the risk of death was not significantly different between those with and without disability after adjusting for age, sex, residence in a long-term care facility, medical comorbidity, dementia and psychiatric disorders (RR 1.09, 95% CI 0.82–1.45). After stratification by age, we found that adjusted risk was not significantly elevated in patients with disabilities aged 64 years or younger (RR 1.06, 95% CI 0.50–2.67) or in patients aged 65 years or older (RR 1.08, 95% CI 0.80–1.46) when compared with those without disabilities (Figure 1).
We found that admission rates to the ICU were lower in patients with disabilities than those without disabilities (22.5% v. 28.3%) but found no significant differences in rates after adjustment overall (RR 1.00, 95% CI 0.75–1.33) or after age stratification (≤ 64 yr RR 1.00, 95% CI 0.66–1.52; ≥ 65 yr RR 0.97, 95% CI 0.65–1.47) (Figure 2).
Patients with disabilities had longer hospital stays than those without disabilities (median 13.9 [IQR 5.8–30.1] d v. 7.8 [IQR 3.6–16.8] d; rate ratio 1.53, 95% CI 1.34–1.75), and this effect persisted after adjusting for age, sex, residence in a long-term care facility, medical comorbidity, dementia and psychiatric disorders (adjusted rate ratio 1.36, 95% CI 1.19–1.56). We determined that rate ratios for length of stay between patients with and without disabilities were greater in those aged 64 years or younger (rate ratio 1.47, 95% CI 1.16–1.86) and 65 years or older (rate ratio 1.31, 95% CI 1.11–1.54). We found no differences in these results after further adjustment for predicted risk of death at admission (Figure 3).
Patients with disabilities were more likely to have unplanned 30-day readmissions than those without disabilities (17.6% v. 7.9%; RR 2.03, 95% CI 1.32–3.12), with the risk remaining elevated after we adjusted for age, sex, long-term care facility residence, medical comorbidity, dementia and psychiatric disorders (RR 1.77, 95% CI 1.14–2.75). After stratification by age, we found that the risk of unplanned 30-day admissions was greater in patients with disabilities than those without disabilities who were 64 years of age or younger (RR 2.85, 95% CI 1.51–5.35) but not in those who were 65 years of age or older (RR 1.02, 95% CI 0.54–1.93). We found no differences in these results after further adjustment for predicted risk of death at admission (Figure 4).
In sex-stratified analyses, unplanned readmission risk was higher among males with disabilities than males without disabilities (RR 1.78, 95% CI 1.02–3.08), but this difference was not observed among females. Results for other outcomes were consistent when analyzing both males and females separately (Appendix 1, Table S2 and Table S3). Hospital stays were longer among both males and females with disabilities than those without disabilities (Appendix 1, Table S3). Outcomes by type of disability showed highest risks for poor outcomes among patients with traumatic brain injury or intellectual or developmental disabilities, or multiple disabilities (Appendix 1, Table S4). We found no changes after we included dementia in our disability definition (Appendix 1, Table S5 and Table S6) and after controlling for number of previous hospital admissions (Appendix 1, Table S7).
Interpretation
We found that patients with disabilities who were admitted to hospital with COVID-19 had longer hospital stays and an elevated risk of unplanned 30-day readmission than patients without disabilities. These risks were not explained by sociodemographic factors, comorbidities or illness severity at baseline, although patients with disabilities had a greater predicted risk of death. The greater risk of 30-day readmission for patients with disabilities was mainly driven by patients younger than 65 years of age. Although we found no significant differences in hospital deaths or ICU admission after adjustment, it should be noted that the confidence intervals are wide and do not preclude a meaningful increase in risk that might be detected in a larger sample. Our findings suggest disability-related needs should be included in plans for COVID-19 response, in particular to support patients in hospital and to plan postdischarge supports, incuding community supports, to reduce risk of readmission to hospital.
Several population-based studies have evaluated COVID-19 mortality in people with disabilities.13,18–26 An ecological study conducted in the United States showed that counties with a higher prevalence of disability had higher mortality rates,18 and a retrospective cohort study in England that used census and mortality data reported that people with disabilities made up 58% of deaths.19 A 2020 retrospective study involving 576 patients with neurologic disabilities reported higher case-fatality rates,13 as did studies in the United Kingdom20–23 and US24–26 that involved patients with intellectual or developmental disabilities. We found no elevated risk of death in patients with disabilities in our cohort after adjustment. This difference from previous studies could be due to our adjustment for a wider range of covariates.18,22–26 Most of these studies evaluated overall risk of death rather than in patients admitted to hospital.18–25 Our sample population of patients in hospital, which was dominated by older, less healthy people, had a higher baseline mortality risk, making it less likely to detect differences between patients with and without disabilities. A 2020 study conducted in the US showed that disparities in case-fatality rates were larger in young patients with disabilities compared with those without intellectual or developmental disabilities.26 This is similar to our finding that disparities in unplanned readmission were more pronounced in younger patients. Our findings are also consistent with data obtained for other conditions (e.g., pneumonia) that showed that patients with disabilities were at elevated risk for poor outcomes.52,53 Our data show that disability, along with older age and medical comorbidities — also known risk factors for poor outcomes among patients with other acute conditions54 — should be a priority target for support strategies for COVID-19.
We expected worse COVID-19 outcomes in patients with disabilities given higher rates of comorbidity,10 physiologic changes related to some disabilities,11,13 and the correlation between age and disability.5,6 Longer hospital stays and higher risk of readmission among patients with disabilities may reflect slower recovery and increased vulnerability to recurrent illness because of physiologic differences.11–13
Studies should evaluate whether disparities reflect gaps in high-quality care for patients with disabilities. For example, communication failures contribute to patient harm,55,56 and pandemic conditions may have hindered communication more for patients with disabilities. Hospitals had restricted visitor policies that limited access for support persons who would ordinarily assist with communication.15 Facemasks and face shields also impede communication and may have a greater impact on people with disabilities.15 Pandemic restrictions have also affected access to outpatient clinical, interprofessional, personal care, meal and medication services for people with disabilities.57,58 These disruptions have had a profound impact on the physical, mental and social well-being of people with disabilities,59,60 and may contribute to readmission risk. The differential impact of disability at younger ages is notable. In younger groups, persons without a disability have higher baseline functioning, which results in a greater detectable difference in risk for poor outcomes.26 In older groups, differences between those with and without disabilities may be less pronounced because of greater comorbidity, frailty and physiologic changes related to aging at baseline.26
Our findings underscore the importance of prioritizing people with disabilities for COVID-19 vaccination. Vaccination is critical for preventing COVID-19 infection, admission to hospital and adverse clinical outcomes among patients with disabilities admitted to hospital. People with disabilities continue to experience barriers to vaccination access.61 Some groups of patients with disabilities, however, are at heightened risk for COVID-19 breakthrough infections and for adverse outcomes including hospital admission and death, even after being fully vaccinated.62
Limitations
Because our data were abstracted from 7 large urban or suburban hospitals, our findings may not be generalizable to other settings. However, our previous research27,28 showed that our cohort is similar to cohorts in studies conducted in the US and UK,63,64 and our data represent nearly 25% of contemporaneous COVID-19 hospital admissions in Ontario.27 A strength of our study is that we were able to identify disability from 11 years of data rather than in the index hospital record only.65 However, we were limited to a medical model of disability that relies on diagnoses rather than self-reported disability. We may have missed patients with undiagnosed disabilities or whose disabilities were not recorded for a hospital admission in a general medical service at one of the participating hospitals. However, any misclassification of patients with disabilities as not having a disability would likely result in underestimation of the risks, which means that the results reported herein are conservative. On the other hand, disability-related diagnoses vary in their impact on each person.65 This issue relates to the intersection of disability with chronic illness, some of which reflects aging.43 However, we stratified models by age and adjusted for comorbidity.
Our sample size was not sufficient to evaluate outcomes in patients with specific disabilities separately beyond descriptive analyses. We were also unable to include all covariates at once in the age-stratified multivariable models, given the smaller sample sizes available for these analyses. There may be a risk of type 1 error, given the number of comparisons. Although we adjusted for the most important predictors of poor outcomes for COVID-19,66 we did not have data on obesity or smoking, which are more common in people with disabilities,67 and income and ethnicity were measurable only at the neighbourhood level. We were able to capture readmissions only to GEMINI hospitals; however, more than 80% of readmissions in our region go to the original hospital of admission.68 We may have missed some patients with COVID-19 who were admitted to hospital for nonmedical reasons and were not cared for by a medical service or in an ICU, but the number of patients is likely small. Finally, the COVID-19 pandemic and response continue to rapidly evolve; our data reflect experiences during the first 2 major waves of the pandemic in Ontario, but the nature of the observed disparities may change as the pandemic progresses.
Conclusion
Our findings highlight the importance of a pandemic response that prioritizes the needs of patients with disabilities who have COVID-19, particularly when they are in hospital and after their hospital stay. For patients with sensory, intellectual or developmental disabilities especially, accommodations should be prioritized for those requiring support persons to assist with communication. Training for clinicians about the needs and rights of people with disabilities may also be useful. Higher unplanned readmission rates underscore the importance of a patient-oriented discharge process that helps patients plan how to manage at home with safe options for assistance with personal care. Our findings also show the need to include disability-related data in COVID-19 surveillance to track outcomes of COVID-19 prevention and intervention strategies. Future research should also evaluate the intersection of disability with gender, experiences of racism and other social determinants of health, which may further affect COVID-19 outcomes. Such efforts should be prioritized in the pandemic response to ensure equitable care for patients with disabilities who have COVID-19.
Footnotes
Competing interests: Amol Verma has received personal fees from Ontario Health, and personal grant funding from AMS Healthcare (Compassion and AI Fellowship) and St. Michael’s Hospital. Michael Fralick is a consultant for Proof Diagnostics, a company that has created a point-of-care testing device using CRISPR for COVID-19. He has also received grants from the Canadian Institutes of Health Research (CIHR) and support from grants from the Canadian Military for clinical trials to identify treatments for COVID-19. Fahad Razak has received personal fees from Ontario Health and is a member of the Ontario COVID-19 Science Advisory Table. Yona Lunsky has received a grant from CIHR for research on disability and health during COVID-19. She is a member of the Board of Directors for Special Olympics Canada. Margaret Herridge has received grants from CIHR. No other competing interests were declared.
This article has been peer reviewed.
Contributors: Yona Lunsky, Fahad Razak and Amol Verma were joint senior authors. This study was conceived by all of the authors and designed by Hilary Brown, Amol Verma, Fahad Razak and Yona Lunsky, with substantial input from all of the authors. Amol Verma, Michael Fralick, Janice Kwan, Adina Weinerman, Terence Tang and Fahad Razak contributed to data collection. Sudipta Saha conducted the data analysis. Hilary Brown and Amol Verma wrote the first draft of the manuscript. All of the authors contributed to the interpretation of the results, critically revised the manuscript for important intellectual content, gave final approval of the version to be published and agreed to be accountable for all aspects of the work.
Funding: This study was supported by Canadian Institutes of Health Research (CIHR) Grant VR4-172743. The development of the GEMINI data platform was supported with funding from the Canadian Cancer Society, the Canadian Frailty Network, the CIHR, the Canadian Medical Protective Association, Green Shield Canada Foundation, the Natural Sciences and Engineering Research Council of Canada, Ontario Health, the St. Michael’s Hospital Association Innovation Fund and the Department of Medicine at the University of Toronto, with in-kind support from partner hospitals and the Vector Institute. The funding source had no role in the design or conduct of the study; collection, management, analysis, or interpretation of the data; preparation, review, or approval of the manuscript; or decision to submit the manuscript for publication.
Data sharing: Data from this manuscript can be accessed upon request to the corresponding author, to the extent that is possible in compliance with local research ethics board requirements and data-sharing agreements.
- Accepted December 3, 2021.
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