Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-08T07:30:20.483Z Has data issue: false hasContentIssue false

Impairment in Health-Related Quality of Life among Community-Dwelling Stroke Survivors

Published online by Cambridge University Press:  02 June 2021

Raed A. Joundi*
Affiliation:
Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Canada
Scott B. Patten
Affiliation:
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Canada
Aysha Lukmanji
Affiliation:
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Canada
Jeanne V. A. Williams
Affiliation:
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Canada
Eric E. Smith
Affiliation:
Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Canada
*
Correspondence to: Raed A. Joundi, Department of Clinical Neurosciences, Health Sciences Building, University of Calgary, 3330 Hospital Drive NW, Calgary, AlbertaCanada. Email: [email protected]
Rights & Permissions [Opens in a new window]

Abstract:

Introduction:

Health utility instruments are increasingly being used to measure impairment in health-related quality of life (HRQoL) after stroke. Population-based studies of HRQoL after stroke and assessment of differences by age and functional domain are needed.

Methods:

We used the Canadian Community Health Survey linked with administrative databases to determine HRQoL using the Health Utilities Index Mark 3 (HUI3) among those with prior hospitalization or emergency department visit for stroke and compared to controls without stroke. We used multivariable linear regression to determine the difference in HUI3 between those with stroke and controls for the global index and individual attributes, with assessment for modification by age (<60, 60–74, and 75+ years) and sex, and we combined estimates across survey years using random effects meta-analysis.

Results:

Our cohort contained 1240 stroke survivors and 123,765 controls and was weighted to be representative of the Canadian household population. Mean health utility was 0.63 (95% confidence interval [CI] 0.58, 0.68) for those with stroke and 0.83 (95% CI 0.82, 0.84) for controls. There was significant modification by age, but not sex, with the greatest adjusted reduction in HUI3 among stroke respondents aged 60–74 years. Individual HUI3 attributes with the largest reductions in utility among stroke survivors compared to controls were mobility, cognition, emotion, and pain.

Conclusions:

In this population-based study, the reduction in HUI3 among stroke survivors compared to controls was greatest among respondents aged 60–74, and in attributes of mobility, cognition, emotion, and pain. These results highlight the persistent impairment of HRQoL in the chronic phase of stroke and potential targets for community support.

Résumé :

RÉSUMÉ :

Détérioration de la qualité de vie liée à la santé chez les personnes qui ont survécu à un accident vasculaire cérébral et qui vivent dans la collectivité.

Introduction :

On utilise de plus en plus des instruments de mesure de l’utilité afin d’évaluer la détérioration de la qualité de vie liée à la santé (QVLS) à la suite d’un accident vasculaire cérébral (AVC). Il existe peu d’études en population sur la QVLS après un AVC et peu de données sur l’évaluation des différences par tranche d’âge et par domaine fonctionnel.

Méthode :

L’équipe de recherche a utilisé le formulaire d’Enquête sur la santé dans les collectivités canadiennes lié à des bases de données administratives afin de déterminer la QVLS à l’aide du système de classification Health Utilities Index Mark 3 (HUI3) chez les personnes ayant déjà été hospitalisées ou traitées au service des urgences pour un AVC, puis a comparé les résultats avec ceux de témoins n’ayant pas subi d’AVC. Les différences sur l’HUI3 entre les malades ayant subi un AVC et les témoins ont été établies à l’aide d’une régression linéaire plurifactorielle en ce qui concerne le score total et les attributs individuels, puis affinées par une évaluation des modifications selon l’âge (< 60 ans; 60-74 ans; et 75+ ans) et le sexe; a suivi une mise en commun des estimations pour toutes les années d’enquête à l’aide d’une méta-analyse à effets aléatoires.

Résultats :

La cohorte comptait 1240 survivants d’un AVC et 123 765 témoins, et a été pondérée de manière à être représentative de la population vivant en ménage au Canada. La valeur moyenne de l’utilité était de 0,63 (IC à 95 % : 0,58-0,68) parmi les survivants d’un AVC et de 0,83 (0,82-0,84) parmi les témoins. Par ailleurs, une différence significative liée à l’âge, mais non au sexe, a été observée chez les survivants d’un AVC âgés de 60 à 74 ans, différence qui a entraîné la baisse la plus importante du score rajusté sur l’HUI3. Enfin, les attributs individuels évalués sur l’HUI3, ayant subi les diminutions les plus notables de la valeur d’utilité parmi les survivants d’un AVC comparativement aux témoins étaient la mobilité, la fonction cognitive, l’état émotionnel et la douleur.

Conclusions :

D’après cette étude en population, la diminution la plus forte du score sur l’HUI3 parmi les survivants d’un AVC par rapport aux témoins a été enregistrée dans la tranche d’âge de 60 à 74 ans, et les attributs les plus touchés étaient la mobilité, la fonction cognitive, l’état émotionnel et la douleur. Ces résultats font ressortir la détérioration constante de la QVLS durant la phase chronique de l’AVC et les cibles potentielles de soutien communautaire.

Type
Original Article
Copyright
© The Author(s), 2021. Published by Cambridge University Press on behalf of Canadian Neurological Sciences Federation

Background

Stroke is the second most common cause of death Reference Lozano, Naghavi and Foreman1 and a leading cause of disability worldwide. It is estimated that the prevalence of disability due to stroke will increase by 24% between now and 2030. Reference Feigin, Krishnamurthi and Parmar2 Patient-reported physical and social well-being have been recognized as important outcomes after stroke. Reference Carod-Artal and Egido3,Reference De Wit, Theuns and Dejaeger4 There has been increasing interest in the use of health utility scores to capture health-related quality of life (HRQoL) in stroke survivors Reference Rebchuk, O’Neill, Szefer, Hill and Field5,Reference Reeves, Lisabeth and Williams6 as utility scales provide an assessment of HRQoL that reflects the preference valuation of health states by community members. Prior studies have shown reduced HRQoL in patients with stroke using measures such as the EuroQol-5 Dimension (EQ-5D) Reference De Wit, Theuns and Dejaeger4,Reference Delcourt, Zheng and Chen7Reference Cadilhac, Andrew and Lannin11 and Health Utilities Index Mark 3 (HUI3), Reference Haacke, Althaus, Spottke, Siebert, Back and Dodel12Reference Pickard, Johnson and Feeny14 and more recently major clinical trials in stroke have incorporated HRQoL assessments. Reference Goyal, Demchuk and Menon15,Reference Berkhemer, Fransen and Beumer16

The EQ-5D and HUI3 both correlate strongly with the Barthel index and Rankin scale, Reference Pickard, Johnson and Feeny14 although contain additional important domains such as mood and cognition. Prior studies have assessed the HUI3 in stroke, Reference Edwards Jodi, Koehoorn, Boyd Lara and Levy Adrian13,Reference Pickard, Johnson and Feeny14,Reference Grootendorst, Feeny and Furlong17,Reference Kapral, Fang and Hill18 although many are outdated, relied on self-report of stroke, and did not assess differences by age. There is also a lack of population-based studies on HRQoL after stroke comparing to controls without stroke.

An updated understanding of post-stroke dysfunction and HRQoL is needed to design and implement programs to better address the needs of stroke survivors. To overcome the limitations of prior survey research that relied on patient-reported stroke history, we linked the Canadian Community Health Survey (CCHS) to population-based universal healthcare administrative databases to ascertain physician-diagnosed stroke cases, and then compared HRQoL to those without a stroke linkage. We assessed differences by age, sex, and health attribute. We hypothesized that younger individuals with stroke would suffer greater losses in HRQoL compared to older individuals, and that impairments would be most pronounced in domains of mobility, cognition, and emotional health.

Methods

Study Sample: Canadian Community Health Survey

The CCHS is an annual cross-sectional survey, representing 97% of the Canadian population aged 12 years and older. The survey randomly samples households nationwide and selects one respondent from each household. The CCHS collects information about health status, health determinants, and health care utilization of the household population. We used CCHS years 2009, 2010, 2013, 2014, and 2015 as the HUI3 was a mandatory component of the questionnaire in these years. Interviews are conducted using computer-assisted personal and telephone interview software. 19 Before releasing the CCHS for use, data are assessed for quality and compared to previous cycles to avoid errors. Approximately 3% of the Canadian population is excluded from the survey target population, which includes those living on Indigenous reserves, those living in foster care, full time members of the Canadian Armed Forced, the institutionalized population and the remote Région du Nunavik and Région des Terres-Cries-de-la-Baie-James. Data were collected by Statistics Canada using a multistage sample allocation strategy to support estimation at the health region and provincial level. 19

While the CCHS contains an item on the questionnaire regarding a history of stroke diagnosis, self-report of stroke is subject to recall bias and there is a large discordance between individual self-report and medical diagnosis of stroke derived from administrative data. Reference Wu, Lai, Gau, Wang and Tsai20,Reference Muggah, Graves, Bennett and Manuel21 The CCHS has recently been linked to administrative databases of hospital discharge and emergency department visits, 22 allowing more accurate determination of stroke cases.

CCHS Sharelink

CCHS Sharelink is a CCHS sub-sample with about 85% of total respondents, who agreed to have their responses linked to administrative records. Statistics Canada created sample weights for CCHS Sharelink to retain population representativeness. CCHS Sharelink resembles CCHS in sociodemographic characteristics. 22 Linkages were performed by Statistics Canada and included the Canadian Institutes of Health Discharge Abstract Database (CIHI-DAD) for hospitalizations and the National Ambulatory Care Reporting System (NACRS) for emergency department visits. The DAD is an administrative database which collects demographic, diagnostic, and treatment information from all admitted patients in Canada, excluding the province of Quebec. NACRS collects similar information for visits to the emergency department. CIHI-DAD was linked back to 1999–2000 and NACRS to 2002–2003.

Case Definition

We first excluded respondents from Quebec, as Quebec does not contribute data to CIHI-DAD. We also excluded respondents under 40, due to very few stroke cases in that age group. All cases of first stroke were identified in CIHI-DAD and NACRS from 1999 to 2015 using International Statistical Classification of Diseases and Related Health Problems, Tenth Revision, Canada (ICD-10-CA) codes (ischemic stroke: I63.x, I64.x, H34.1; intracerebral hemorrhage [ICH]: I61.x). ICD-9 codes [ischemic stroke: 434.01, 434.11, 434.91, 436; ICH: 431] were used to obtain cases prior to 2003. These case definitions used have high validity in Canada. Reference Porter, Mondor, Kapral, Fang and Hall23,Reference Kokotailo and Hill24 Individuals who had a prior episode of stroke captured in the administrative databases and who participated in the CCHS in the selected years were included in the stroke cohort. Control subjects without prior identification of stroke comprised the remainder of individuals in the CCHS in the selected years.

Covariates

Covariates were obtained from the CCHS, including age, sex, year of survey, province of respondent, rural residence, ethnicity, education level, total household income quartile, marital status, and self-reported body mass index (BMI), smoking status, hypertension, diabetes, heart disease, chronic obstructive pulmonary disease (COPD), arthritis, and asthma. Age was categorized as <60, 60–74, and 75+. Categorization of the remainder of variables can be seen in Table 1. Due to known biases in self-report of BMI, we employed a correction suggested by Statistics Canada. Reference Shields, Connor Gorber, Janssen and Tremblay25 Chi-square test was used to assess differences in proportions between those with and without stroke. All numerical estimates were rounded as per Statistics Canada confidentiality policies.

Table 1: Weighted percentages and means of sample characteristics by stroke status

CI = confidence interval; COPD = chronic obstructive pulmonary disease; HUI3 = Health Utilities Index Mark 3.

Proportions are obtained by following Statistics Canada procedures on weighting and rounding and categories may not always sum to 100.

Health Utilities Index Mark 3

The HUI3 is a generic, preference-based measure of health status, which includes the attributes of vision, hearing, speech, ambulation, dexterity, emotion, cognition and pain, with five or six levels for each attribute (Supplemental Table 1) and incorporates utility weights based on standard gamble studies in a general population sample. The HUI3 has been validated for use in the Canadian stroke population. Reference Grootendorst, Feeny and Furlong17 The summary index ranges from −0.36 (state worse than dead) through 0 (similar to dead) to 1 (perfect health) Reference Horsman, Furlong, Feeny and Torrance26 and is obtained by multiplying each individual attribute rank by its multi-attribute weight, and then using the following equation: HUI3 score = 1.371*(Vision*Hearing*Speech*Dexterity*Mobility*Emotion*Cognition*Pain) − 0.371. The single attribute weights were used when analyzing individual attributes. Reference Feeny, Furlong and Torrance27

Analysis

HUI3 index score means with 95% confidence intervals (CIs) were stratified by age and sex and t-tests were used to evaluate the difference between those with and without stroke. Chi-squared tests were used to compare proportions across categories of global impairment Reference Feng, Bernier, McIntosh and Orpana28 [none (1), mild (0.89–0.99), moderate (0.7–0.88), severe (>0–0.69), or equal to or worse than dead (0 or below)]. We used multivariable linear regression to determine the association between history of stroke and mean difference in HUI3 score using the multi-attribute weights, separately for each CCHS survey year. Because the CCHS uses a multi-stage sampling procedure and several sampling frames, a replicate bootstrap weighting procedure is recommended to deal with design effects. A set of 500–1000 bootstrap weights provided by Statistics Canada were used to account for clustering and variation in selection probabilities. These bootstrap weights also include adjustments for non-response to help minimize selection bias. We used bootstrap weights for the linear regression in each survey year separately, and then combined the coefficients at the survey level using random effects meta-analysis.

To assess for the presence of modification by age or sex, we first ran a simple model with mean HUI3 as the outcome, stroke as the exposure, and age and sex included as interaction terms, using the Wald test to assess for a significant interaction (p < 0.05). Age was categorized as <60, 60–74, and 75 and older, with <60 serving as the reference group. As this model demonstrated modification by age, we then fit individual age-specific models, with the simple model adjusted for only sex. The full model included sex and the remainder of the covariates. All covariates demonstrated evidence of confounding in at least one age- and year-specific model defined as a change in the stroke-HUI3 regression coefficient by >10%. As NACRS cases were predominantly from provinces Ontario, Alberta, and British Columbia, we conducted a sensitivity analysis excluding stroke cases identified by NACRS only. We also did a sensitivity analysis excluding those with self-reported stroke from the control group.

For each of the individual attributes, we determined the proportions of respondents with and without stroke who had level 1, level 2, or level 3+ (see Supplemental Table 1 for description of all levels). We then determined the association between stroke and HUI3 for the eight individual attributes in the same fashion as the global analysis, using the single attribute weights.

Multiple Imputation

The HUI3 score was missing in 4.3% of controls and 8.5% of stroke respondents. The vast majority of cases were due to non-answer of one attribute on the HUI3. We conducted a multiple imputation analysis with ordinal regression to replace the missing HUI3 attribute values, using all covariates and the remaining seven attributes as predictors in the model. Visual inspection of the replaced values was done to ensure face validity. The linear regressions were then repeated with the imputed values.

Analyses were done in the Prairie Regional Data Centre at the University of Calgary using Stata 16.0 (College Station, TX). Threshold of significance for p-values was <0.05. Under Tri-Council guidelines, this analysis did not require approval by a research ethics board.

Results

There were 1240 people with prior stroke (91% with ischemic stroke and 9% with ICH), and 123,765 controls. Eleven percent of stroke records were identified from emergency room records only and the remainder from hospital admissions. Proxy interviews were conducted in 2.5% of controls and 13.0% of stroke respondents. The median time between stroke diagnosis and CCHS interview was 4.3 years (IQR 1.8–7.2). The I2 values in the meta-analyses ranged from 0% to 59.7%.

Compared to those without a history of stroke, those with stroke had older age, were more likely to be male, had a lower education, lower income and had a higher proportion of vascular risk factors. All baseline characteristics are shown in Table 1. Mean unadjusted HUI3 was lower for those with stroke, for females, and individuals at older age (Table 1). Compared to controls, there was a much lower proportion of stroke respondents with no or minimal impairment in health utility and a greater proportion with severe impairment (shown in Figure 1).

Figure 1: Weighted percentages in each Health Utilities Index Mark 3 (HUI3) index score category by stroke status.

In the linear regression, there was evidence of significant modification by age (p = 0.033 for age 60–74). There was no significant modification by sex (p = 0.34). In the stratified age- specific simple models, mean HUI3 difference between those with stroke and without stroke was greatest in those aged 60–74 years (−0.22, 95% CI −0.27 to −0.17), compared to those < 60 years (−0.17, 95% CI −0.24 to −0.10) and 75+ years (−0.13, 95% CI −0.19 to −0.07; Figure 2A). The age-specific pattern was similar in the fully adjusted model (Figure 2B), when excluding cases only identified in the emergency department, when excluding self-reported stroke from the control group, and when imputing missing HUI3 values (Supplemental Figure 1).

Figure 2: Adjusted mean difference in HUI3 index score for stroke respondents compared to controls, stratified by age group for simple (A) and full models (B).

Respondents with stroke had greater proportion of moderate to severe impairment in all HUI3 attributes compared to controls, especially mobility (level 3 or above 34%), cognition (46%), and pain (35%; Figure 3). There was no significant interaction by age or sex for any of the individual HUI3 attribute utilities. In the simple model, stroke was significantly associated with reductions in all attributes except hearing, with the greatest reductions occurring in attributes emotion, cognition, pain, and mobility (Figure 4A). In the fully adjusted model, dexterity, emotion, cognition, and mobility remained significantly impaired in those with stroke versus controls, with most impairment in cognition and mobility (shown in Figure 4B). Results were similar after imputation of missing HUI3 attribute scores (Supplemental Figure 2).

Figure 3: Weighted percentage of impairment for levels of each HUI3 attribute (higher level is worse impairment), among stroke respondents and controls. See Supplemental Table 1 for description of all levels.

Figure 4: Adjusted mean difference of individual HUI3 attribute weights for stroke respondents compared to controls, for simple (A) and full model (B), plotted in order of greater HUI3 difference. H indicates hearing; S, speech; V, vision; D, dexterity; E, emotion; C, cognition; P, pain; and M, mobility.

Discussion

In our study of nationally representative cross-sectional surveys linked with administrative data, history of stroke was associated with a lower HRQOL as measured by the HUI3. We found modification by age, whereby those between 60 and 74 years experienced a greater adjusted reduction in HUI3 with stroke compared to those < 60 or 75+. Individuals with stroke had the greatest impairment in attributes of emotion, cognition, pain, and mobility.

Our study utilized administrative data for our case definition of stroke due to greater reliability than self-reported stroke. Reference Muggah, Graves, Bennett and Manuel21 In a prior study, health utility scores were higher for cases identified by health administrative data, suggesting that milder cases are detected. Prevalence of stroke in health administrative data was also lower as compared to self-report, implying the potential for misclassification bias in survey data. Reference Muggah, Graves, Bennett and Manuel21 Furthermore, the CCHS questionnaire asks whether the individual experiences the “effects of stroke,” which may result in misclassification from individuals with mild or resolved deficits, or misattribution of certain symptoms to other conditions or older age.

In this study, health utility scores for those with stroke based on hospital records were similar to prior published utility values for those with self-reported “effects of stroke” in Canada, Reference Edwards Jodi, Koehoorn, Boyd Lara and Levy Adrian13,Reference Mittmann, Trakas, Risebrough and Liu29,Reference Guertin, Humphries, Feeny and Tarride30 although these studies did not directly model the difference with control subjects. We found a significant reduction in HUI3 in stroke respondents compared to controls after adjustment for demographic, social, and co-morbid factors. The reason for the greater reduction in HUI3 score among stroke respondents aged 60–74 is unclear, although may relate to greater capacity for plasticity and recovery in younger individuals, and greater resilience in the elderly. Reference Jeste, Savla and Thompson31 Although floor effects may have played a role in the elderly due to lower baseline HRQoL, the HUI3 does not demonstrate substantial floor effects. Reference Luo, Johnson, Shaw and Coons32,Reference Davison, Jhangri and Feeny33 Survival bias may also result in higher than expected health utility scores in the elderly with stroke. Our results are nevertheless a meaningful and practical representation of community-dwelling stroke survivors with implications for resource needs. Stroke among 60–74 may occur when productivity and opportunity cost remain high, yet the adaptive mechanisms are lower, suggesting the potential need for greater post-stroke supports among survivors in the community in this age group.

We found that stroke was associated with the greatest reductions in utility for emotion, cognition, pain, and mobility. Among stroke survivors, 41% have intermediate to high risk of depression, Reference Davison, Jhangri and Feeny33,Reference Swartz, Cayley and Lanctôt34,Reference Luo, Johnson, Shaw and Coons32 and symptoms of depression have been found to be predictive of impaired functioning and community re-integration and low quality of life post-stroke. Reference Kapoor, Lanctot, Bayley, Herrmann, Murray and Swartz35 Although best-practice guidelines endorse screening for post-stroke depression, Reference Eskes, Lanctôt and Herrmann3638 under-recognition and under-treatment remains common. Reference Swartz, Bayley and Lanctôt39 The association with pain impairment was attenuated after full adjustment, although over a third of respondents with stroke reported moderate to severe pain. Post-stroke pain is also under-recognized and estimates of post-stroke pain prevalence range from 10% to 30%. Post-stroke pain may be due to central pain or peripheral neuropathic pain and is associated with greater functional dependence, depression, and cognitive decline. Reference O’Donnell Martin, Diener, Sacco Ralph, Panju Akbar, Vinisko and Yusuf40Reference Harno, Haapaniemi and Putaala42 Finally, respondents with stroke had the greatest proportion of impairment in the cognitive attribute compared to all other attributes, with over half of respondents reporting some degree of impairment. In the Oxford Vascular Study, the incidence of dementia was 34% at 1 year and after severe stroke and 8.2% after minor stroke. Reference Pendlebury and Rothwell43 Individuals with stroke have faster declines in executive function and global cognition than controls. Reference Levine, Galecki and Langa44 Our study re-inforces the prominent and persistent impacts of emotional, cognitive, pain, and mobility disturbances on overall HRQoL among community dwellers in the chronic phase of stroke.

Our analysis has numerous strengths, particularly with the quality and reliability of the data and the availability of a large number of baseline variables. The linkages of CCHS with the DAD are of high quality, with few false links. Reference Sanmartin, Decady and Trudeau45 The CCHS provides a large sample size which can be generalized to the Canadian household population. There were some limitations to the study. First, self-reported variables may be associated with response biases, although variables like hypertension and diabetes have shown high reliability in self-report. Reference Muggah, Graves, Bennett and Manuel21 The wording of questions is modeled after items contained in the US Behavioral Risk Factor Survey and specifies that a self-reported chronic condition must represent a diagnosis from a health professional. Second, individuals with stroke underwent the survey at various times from the stroke, although this is a realistic portrayal of the heterogeneity of stroke survivors living in the community. Third, diagnosis of stroke was reliant on administrative data, although administrative data coding for acute stroke has a high positive predictive value in Canada. Reference Porter, Mondor, Kapral, Fang and Hall23 Finally, we could not identify individuals hospitalized with stroke prior to 1999, although this provided a 10-year window from the earliest survey year.

We used the HUI3 to demonstrate the overall burden and degree of reduction in global HRQoL and specific attributes among community-dwelling stroke survivors compared to those without stroke. Emotion, cognition, pain, and mobility are particularly impacted among those with stroke. This knowledge could be used for future population-based assessments, measuring effects of interventions in improving HRQoL among stroke survivors, and monitoring of trends over time. Further studies should address whether the HUI3 or other measures of health utility add value to more standard stroke disability measures in routine clinical care or clinical trials.

Acknowledgements

The analysis was conducted at the Prairie Regional Data Centre, which is part of the Canadian Research Data Centre Network (CRDCN). The services and activities provided by the CRDCN are made possible by the financial or in-kind support of the Social Sciences and Humanities Research Council (SSHRC), the Canadian Institutes of Health Research (CIHR), the Canadian Foundation for Innovation (CFI), Statistics Canada, and participating universities whose support is gratefully acknowledged. The views expressed in this paper do not necessarily represent the CRDCN’s or that of its partners. The authors would like to thank Dina Lavorato and Stephanie Cantlay for their assistance in the Prairie Regional Data Centre.

Funding

RAJ is supported by a Fellowship Grant from the CIHR (MFE 164702).

Disclosures

EES reports royalties from UpToDate, consulting fees from Alnylam, Biogen, and Javelin. The other authors report no disclosures.

Statement of Authorship

RAJ was involved with project conception, analysis, and writing of the manuscript. SP was involved with project conception and critical revision of the manuscript. AL was involved with project conception and critical revision of the manuscript. JW was involved with analysis and critical revision of the manuscript ES was involved with project conception and critical revision of the manuscript.

Supplementary Material

To view supplementary material for this article, please visit https://doi.org/10.1017/cjn.2021.119.

References

Lozano, R, Naghavi, M, Foreman, K, et al. Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010. Lancet Lond Engl. 2012;380:2095–128.CrossRefGoogle ScholarPubMed
Feigin, VL, Krishnamurthi, RV, Parmar, P, et al. Update on the global burden of ischemic and hemorrhagic stroke in 1990–2013: the GBD 2013 study. Neuroepidemiology. 2015;45:161–76.CrossRefGoogle ScholarPubMed
Carod-Artal, FJ, Egido, JA. Quality of life after stroke: the importance of a good recovery. Cerebrovasc Dis Basel Switz. 2009;27(Suppl 1):204–14.CrossRefGoogle ScholarPubMed
De Wit, L, Theuns, P, Dejaeger, E, et al. Long-term impact of stroke on patients’ health-related quality of life. Disabil Rehabil. 2017;39:1435–40.CrossRefGoogle ScholarPubMed
Rebchuk, AD, O’Neill, ZR, Szefer, EK, Hill, MD, Field, TS. Health utility weighting of the modified Rankin scale: a systematic review and meta-analysis. JAMA Netw Open. 2020;3:e203767.CrossRefGoogle ScholarPubMed
Reeves, M, Lisabeth, L, Williams, L, et al. Patient-reported outcome measures (PROMs) for acute stroke: rationale, methods and future directions. Stroke. 2018;49:1549–56.CrossRefGoogle ScholarPubMed
Delcourt, C, Zheng, D, Chen, X, et al. Associations with health-related quality of life after intracerebral haemorrhage: pooled analysis of INTERACT studies. J Neurol Neurosurg Psychiatry. 2017;88:70–5.CrossRefGoogle ScholarPubMed
Xie, J, Wu, EQ, Zheng, Z-J, et al. Impact of stroke on health-related quality of life in the noninstitutionalized population in the United States. Stroke. 2006;37:2567–72.CrossRefGoogle ScholarPubMed
Dewilde, S, Annemans, L, Lloyd, A, et al. The combined impact of dependency on caregivers, disability, and coping strategy on quality of life after ischemic stroke. Health Qual Life Outcomes. 2019;17:31.CrossRefGoogle ScholarPubMed
Ramírez-Moreno, JM, Muñoz-Vega, P, Alberca, SB, Peral-Pacheco, D. Health-related quality of life and fatigue after transient ischemic attack and minor stroke. J Stroke Cerebrovasc Dis Off J Natl Stroke Assoc. 2019;28:276–84.CrossRefGoogle ScholarPubMed
Cadilhac, DA, Andrew, NE, Lannin, NA, et al. Quality of acute care and long-term quality of life and survival: the Australian stroke clinical registry. Stroke. 2017;48:1026–32.CrossRefGoogle ScholarPubMed
Haacke, C, Althaus, A, Spottke, A, Siebert, U, Back, T, Dodel, R. Long-term outcome after stroke: evaluating health-related quality of life using utility measurements. Stroke. 2006;37:193–8.CrossRefGoogle ScholarPubMed
Edwards Jodi, D, Koehoorn, M, Boyd Lara, A, Levy Adrian, R. Is health-related quality of life improving after stroke? Stroke. 2010;41:9961000.CrossRefGoogle Scholar
Pickard, AS, Johnson, JA, Feeny, DH. Responsiveness of generic health-related quality of life measures in stroke. Qual Life Res Int J Qual Life Asp Treat Care Rehabil. 2005;14:207–19.CrossRefGoogle ScholarPubMed
Goyal, M, Demchuk, AM, Menon, BK, et al. Randomized assessment of rapid endovascular treatment of ischemic stroke. N Engl J Med. 2015;372:1019–30.CrossRefGoogle ScholarPubMed
Berkhemer, OA, Fransen, PSS, Beumer, D, et al. A randomized trial of intraarterial treatment for acute ischemic stroke. N Engl J Med. 2015;372:1120.CrossRefGoogle ScholarPubMed
Grootendorst, P, Feeny, D, Furlong, W. Health utilities index mark 3: evidence of construct validity for stroke and arthritis in a population health survey. Med Care. 2000;38:290–9.CrossRefGoogle Scholar
Kapral, MK, Fang, J, Hill, MD, et al. Investigators of the registry of the Canadian stroke network. Sex differences in stroke care and outcomes: results from the Registry of the Canadian Stroke Network. Stroke. 2005;36:809814.CrossRefGoogle ScholarPubMed
Government of Canada. Statistics Canada. Canadian Community Health Survey – Annual Component (CCHS) [Internet]; 2019. Available at: https://www23.statcan.gc.ca/imdb/p2SV.pl?Function=getSurvey&SDDS=3226. Last accessed 11 June 2021.Google Scholar
Wu, C-S, Lai, M-S, Gau, SS-F, Wang, S-C, Tsai, H-J. Concordance between patient self-reports and claims data on clinical diagnoses, medication use, and health system utilization in Taiwan. PLoS One. 2014;9:e112257.CrossRefGoogle ScholarPubMed
Muggah, E, Graves, E, Bennett, C, Manuel, DG. Ascertainment of chronic diseases using population health data: a comparison of health administrative data and patient self-report. BMC Public Health. 2013;13:16.CrossRefGoogle ScholarPubMed
Government of Canada. Statistics Canada. Canadian Population Health Survey data linked to mortality, hospitalization and historical postal codes [Internet]; 2019. Available at: https://www.statcan.gc.ca/eng/rdc/data/cphs. Last accessed 11 June 2021.Google Scholar
Porter, J, Mondor, L, Kapral, MK, Fang, J, Hall, RE. How reliable are administrative data for capturing stroke patients and their care. Cerebrovasc Dis Extra. 2016;6:96106.CrossRefGoogle ScholarPubMed
Kokotailo, RA, Hill, MD. Coding of stroke and stroke risk factors using international classification of diseases, revisions 9 and 10. Stroke. 2005;36:1776–81.CrossRefGoogle ScholarPubMed
Shields, M, Connor Gorber, S, Janssen, I, Tremblay, MS. Bias in self-reported estimates of obesity in Canadian health surveys: an update on correction equations for adults. Health Rep. 2011;22:35–45.Google ScholarPubMed
Horsman, J, Furlong, W, Feeny, D, Torrance, G. The health utilities index (HUI®): concepts, measurement properties and applications. Health Qual Life Outcomes. 2003;1:54.CrossRefGoogle Scholar
Feeny, D, Furlong, W, Torrance, GW, et al. Multiattribute and single-attribute utility functions for the health utilities index mark 3 system. Med Care. 2002;40:113–28.CrossRefGoogle ScholarPubMed
Feng, Y, Bernier, J, McIntosh, C, Orpana, H. Validation of disability categories derived from Health Utilities Index Mark 3 scores. Health Rep. 2009;20:4350.Google ScholarPubMed
Mittmann, N, Trakas, K, Risebrough, N, Liu, BA. Utility scores for chronic conditions in a community-dwelling population. PharmacoEconomics. 1999;15:369–76.CrossRefGoogle Scholar
Guertin, JR, Humphries, B, Feeny, D, Tarride, J-É. Health Utilities Index Mark 3 scores for major chronic conditions: population norms for Canada based on the 2013 and 2014 Canadian Community Health Survey. Health Rep. 2018;29:12–9.Google ScholarPubMed
Jeste, DV, Savla, GN, Thompson, WK, et al. Older age is associated with more successful aging: role of resilience and depression. Am J Psychiatry. 2013;170:188–96.CrossRefGoogle ScholarPubMed
Luo, N, Johnson, JA, Shaw, JW, Coons, SJ. Relative efficiency of the EQ-5D, HUI2, and HUI3 index scores in measuring health burden of chronic medical conditions in a population health survey in the United States. Med Care. 2009;47:5360.CrossRefGoogle Scholar
Davison, SN, Jhangri, GS, Feeny, DH. Comparing the health utilities index mark 3 (HUI3) with the short form-36 preference-based SF-6D in chronic kidney disease. Value Health. 2009;12:340–5.CrossRefGoogle ScholarPubMed
Swartz, RH, Cayley, ML, Lanctôt, KL, et al. The “DOC” screen: feasible and valid screening for depression, obstructive sleep apnea (OSA) and cognitive impairment in stroke prevention clinics. PloS One. 2017;12:e0174451.CrossRefGoogle ScholarPubMed
Kapoor, A, Lanctot, KL, Bayley, M, Herrmann, N, Murray, BJ, Swartz, RH. Screening for post-stroke depression and cognitive impairment at baseline predicts long-term patient-centered outcomes after stroke. J Geriatr Psychiatry Neurol. 2019;32:40–8.CrossRefGoogle ScholarPubMed
Eskes, GA, Lanctôt, KL, Herrmann, N, et al. Canadian stroke best practice recommendations: mood, cognition and fatigue following stroke practice guidelines, update 2015. Int J Stroke Off J Int Stroke Soc. 2015;10:1130–40.CrossRefGoogle ScholarPubMed
Coutts, SB, Wein, TH, Lindsay, MP, et al. Canadian stroke best practice recommendations: secondary prevention of stroke guidelines, update 2014. Int J Stroke Off J Int Stroke Soc. 2015;10:282–91.CrossRefGoogle Scholar
Canadian Stroke Best Practices. Heart and Stroke Foundation of Canada. 1. Post Stroke Depression [Internet]. Available at: https://www.strokebestpractices.ca/en/recommendations/mood-cognition-and-fatigue-following-stroke/post-stroke-depression/. Last accessed 11 June 2021.Google Scholar
Swartz, RH, Bayley, M, Lanctôt, KL, et al. Post-stroke depression, obstructive sleep apnea, and cognitive impairment: rationale for, and barriers to, routine screening. Int J Stroke Off J Int Stroke Soc. 2016;11:509–18.CrossRefGoogle ScholarPubMed
O’Donnell Martin, J, Diener, H-C, Sacco Ralph, L, Panju Akbar, A, Vinisko, R, Yusuf, S. Chronic pain syndromes after ischemic stroke. Stroke. 2013;44:1238–43.CrossRefGoogle Scholar
Jönsson, A, Lindgren, I, Hallström, B, Norrving, B, Lindgren, A. Prevalence and intensity of pain after stroke: a population based study focusing on patients’ perspectives. J Neurol Neurosurg Psychiatry. 2006;77:590–5.CrossRefGoogle ScholarPubMed
Harno, H, Haapaniemi, E, Putaala, J, et al. Central poststroke pain in young ischemic stroke survivors in the Helsinki Young Stroke Registry. Neurology. 2014;83:1147–54.CrossRefGoogle ScholarPubMed
Pendlebury, ST, Rothwell, PM. Incidence and prevalence of dementia associated with transient ischaemic attack and stroke: analysis of the population-based Oxford Vascular Study. Lancet Neurol. 2019;18:248–58.CrossRefGoogle ScholarPubMed
Levine, DA, Galecki, AT, Langa, KM, et al. Trajectory of cognitive decline after incident stroke. JAMA. 2015;314:4151.CrossRefGoogle ScholarPubMed
Sanmartin, C, Decady, Y, Trudeau, R, et al. Linking the Canadian community health survey and the Canadian mortality database: an enhanced data source for the study of mortality. Health Rep. 2016;27:10–8.Google Scholar
Figure 0

Table 1: Weighted percentages and means of sample characteristics by stroke status

Figure 1

Figure 1: Weighted percentages in each Health Utilities Index Mark 3 (HUI3) index score category by stroke status.

Figure 2

Figure 2: Adjusted mean difference in HUI3 index score for stroke respondents compared to controls, stratified by age group for simple (A) and full models (B).

Figure 3

Figure 3: Weighted percentage of impairment for levels of each HUI3 attribute (higher level is worse impairment), among stroke respondents and controls. See Supplemental Table 1 for description of all levels.

Figure 4

Figure 4: Adjusted mean difference of individual HUI3 attribute weights for stroke respondents compared to controls, for simple (A) and full model (B), plotted in order of greater HUI3 difference. H indicates hearing; S, speech; V, vision; D, dexterity; E, emotion; C, cognition; P, pain; and M, mobility.

Supplementary material: PDF

Joundi et al. supplementary material

Joundi et al. supplementary material

Download Joundi et al. supplementary material(PDF)
PDF 135.1 KB