Abstract
Objective. To estimate the prevalence of communication vulnerability (CV) and its association with various health measures among working-age Australians with musculoskeletal conditions (MSK). The various vulnerability characteristics may lead to inadequate communication between consumers and healthcare professionals.
Methods. Prevalence of CV among 18–64 year olds, with or without MSK, was analyzed using the Australian Bureau of Statistics’ National Health Survey 2007–08 data. Associations between CV and measures of health complexity (accumulating multimorbidity and risk factors) and health burden (poorer self-rated health, psychological distress, and pain restricting work) in the MSK population were estimated using logistic regression. Further analyses were conducted for each vulnerability characteristic to determine the degree of association (crude and adjusted) with measures of interest.
Results. CV were more prevalent in working-age Australians with MSK (65%) than those without (51%). Adjusted for age and sex among working-age Australians with at least 1 MSK, those with 1 or more CV were more likely to have multimorbidity [adjusted OR (aOR) = 1.8, 95% CI 1.5–2.2], lifestyle risk factors (aOR = 2.1, 95% CI 1.5–2.8), poorer self-rated health (aOR = 3.4, 95% CI 2.7–4.2), greater psychological distress (aOR = 2.9, 95% CI 2.3–3.7), and pain restricting employment (aOR = 1.7, 95% CI 1.4–2.1) compared with those without CV.
Conclusion. For working-age people, there is an association between MSK and CV. For those with MSK, CV were associated with increased likelihood of health complexity and burden. These findings have policy and clinical relevance. Research is needed to determine whether interventions that address these specific CV characteristics reduce the burden of disease within these populations.
Communication between consumers and health professionals is increasingly being recognized as important1. Poor communication contributes to serious adverse events2, poorer health status3, and decreased medication adherence4. Additionally, communication underpins a key tenet of patient-centered care, tailoring interactions to individual’s needs, preferences, and perspectives5.
Particular characteristics of individuals — such as speech, sensory, and cognitive impairments; limited English proficiency; sexual, cultural, and/or religious differences; and/or limited health literacy — may complicate clinical management and increase the potential for inadequate consumer—professional communication6,7. Blackstone, et al termed these characteristics “communication vulnerabilities”7 (CV). People with CV experience health inequalities8 and difficulties navigating healthcare systems, in addition to being underserved by them9,10.
CV affect health in various ways2. For example:
Speech and sensory impairments and limited local language proficiency create difficulties for both consumers and health professionals when clarifying concerns, achieving understanding, and discussing health information2,6.
Cognitive, intellectual, or psychological impairments impede memory, the ability to develop new skills, or to understand, prevent, and manage diseases or medications11.
Poor health literacy affects the capacity to obtain, process, and understand basic health information and services12.
For this analysis, we focused on musculoskeletal conditions (MSK) such as osteoarthritis (OA), inflammatory arthritis, or osteoporosis. MSK are grouped together as an Australian National Health Priority Area13 because they are common14 and typically require complex care by multiple health professionals, polypharmacy, physical therapy, and/or surgery15. Increasingly, people with MSK experience coexisting chronic health conditions (termed “multimorbidity”). In this context, effective communication is particularly important because multimorbidity affects quality of life16 and contributes to adverse events and outcomes, and increases healthcare use17,18. Given these factors, a nationally representative population with MSK is a logical starting place to better understand the implications of CV. Establishing an association between CV and measures of health burden among this broad and already complex patient population may have policy and clinical implications.
Health complexity issues have been identified in older people19, but less so in working-age populations. Yet many chronic health conditions affect workforce participation and social roles, potentially creating additional social and economic burdens among individuals and society.
We therefore focused on the working-age population (ages 18–64 years) and aimed to estimate (1) the prevalence of CV among those with and without MSK, and (2) among those with MSK, the association between any, and specific, CV characteristics and measures of health. These measures include complexity (the presence of multimorbidity or disease risk factors), and burden (poorer self-rated health, distress, or pain restricting work).
MATERIAL AND METHODS
This analysis used the nationally representative Australian Bureau of Statistics’ (ABS) National Health Survey 2007–08 (NHS07-08) data20. The survey covers a wide range of self-reported personal health information across all age groups, including health status, health-related risk factors, and healthcare use.
Detailed information about ABS sampling, survey design, and response rate is available elsewhere20.
Population
Our study focused on working-age adults (18–64 years, regardless of current employment status) with and without chronic MSK. “Musculoskeletal conditions” included OA, inflammatory arthritis, other arthritis or arthropathies, soft tissue disorders, gout, back pain, or other MSK not otherwise defined. MSK were considered “chronic” if self-reported as current and present for at least 6 months.
Exposure
Within the analyses, the presence of any 1 as well as specific “CV characteristics” were the exposures. Where possible, relevant NHS07-08 data were matched to the specific “CV characteristic” as defined by Blackstone, et al7. The specific characteristics included in Blackstone, et al’s established definition were speech; vision; hearing and cognitive impairments; limited English proficiency; religious, cultural, or sexual identity differences; and poor health literacy. Each characteristic increased the possibility for inadequate communication in health settings7. Within the NHS07-08, the majority of these characteristics, or a proxy, were available (Table 1). The proxy for poor health literacy was low education attainment (Yr 10 level or less). Migration from a country where English was not the primary spoken language was the proxy for English proficiency. Data concerning religious, cultural, or sexual identity difference were unavailable and thus not included in this analysis. To ensure that vision impairments included only severe conditions, minor conditions were excluded (presbyopia, short or long sightedness, color blindness, or astigmatism).
Measures of accumulated health complexity
The presence of selected comorbidities (chronic conditions designated as Australian National Health Priority Areas)13 and biomedical or lifestyle risk factors constituted “health complexity” (Table 1). Although sometimes considered a chronic health condition, obesity (i.e., a body mass index of 30 kg/m2 or greater) was considered a risk factor in our study.
Measures of health burden
Measures of “health burden” included poorer self-rated health, distress, and pain restricting work. Poorer self-rated health was composed of a response of either “fair” or “poor” to the Medical Outcomes Study Short Form-12, question 2, overall rating of health21. Distress was defined as Kessler Psychological Distress Scale-10 (K-10) score of either high (> 22 points) or very high (30–50 points) severity of distress experienced in the 4 weeks prior to interview22. A response of “moderately” or “extremely” to bodily pain interfering on normal work during the previous 4 weeks constituted “pain restricting work”.
Analyses
Figure 1 illustrates the populations used in the analyses: the working-age sample population (A); those with any MSK (B); those with any of the specific (I–VI) CV characteristics (C); and those with CV alongside MSK (D). Weighted population prevalence23 of any (C), and specific (I–VI) CV were estimated among the working-age sample with MSK (i.e., D ÷ B) and without MSK [i.e., (C – D) ÷ (A – B)]. Proportions were compared using the chi-square test.
For the variables “poorer self-rated health” and “pain restricting work”, the proportional odds assumption was violated. As these variables could not be treated as ordered categories, an ordinal logistic regression model was not appropriate. It was also not possible to treat the K-10 scores (measuring distress) as a continuous outcome because of non-normal distribution, and neither was it possible to transform the data to approximate normality.
Within those with MSK (B, in Figure 1), multiple logistic regression was used to assess the association between any CV (D, in Figure 1; i.e., exposure) and complexity or burden measures (i.e., outcomes) compared with those with MSK but no CV (B–D, in Figure 1). Further analyses were undertaken to determine whether the strength of associations varied for each specific (I–VI) CV.
All models were estimated using the ABS-generated replicant weights to account for the survey design. Crude and adjusted OR (aOR) and 95% CI are reported. Model 1 adjusts for age and sex. Model 2 further adjusts for quintiles of equivalized household income20 and occupation as classified by the Australian and New Zealand Standard Classification of Occupations20. All statistical analyses were performed using Stata (version 10.1).
RESULTS
Prevalence
Of the 20,800 NHS07-08 survey respondents, 12,604 were working-age adults. Overall, 55.6% of the working-age sample had at least 1 CV characteristic. Of the working-age with at least 1 MSK (n = 4555), 65.0% had a CV compared with 50.9% among those without MSK (p < 0.01; Table 2). The most common CV were low education attainment (32.9%), migration from a country where English is not the primary spoken language (18.9%), and hearing impairment (9.0%; Table 2).
Among the MSK sample, those with and without any CV differed on a number of demographic factors (Table 3). Those with any CV were older, a greater number reported income level in the lowest quintile, more were not currently working, and fewer were partnered parents with children (Table 3).
Adjusted for age and sex, higher odds of having 1 or more CV were observed for the working-age population with MSK compared with those without MSK (aOR = 1.4, 95% CI 1.2–1.6; Table 2, Model 1). Those with MSK were more likely to have hearing or vision impairments, cognitive disability, or lower education level than those without MSK, despite controlling for potential confounders (Table 4, Models 1 and 2). No difference was observed for speech impairment; however, speech impairment was uncommon (Table 2). People with MSK were less likely to have migrated to Australia during the previous 20 years than those without MSK (Table 2).
Measures of accumulated health complexity
Working-age people with at least 1 MSK who had any CV were more likely to have multimorbidity than those with MSK but no CV (aOR = 1.8, 95% CI 1.5–2.2; Table 4, Model 1). Among the MSK population, the presence of any CV was strongly associated with 2 or more, and 3 or more, comorbidities alongside MSK, even after adjusting for potential confounders compared with no CV (Table 4).
For the multimorbidity analyses, psychological disability was included as a cognitive impairment in the CV variable (i.e., part of the exposure). However, mental health was included as part of the multimorbidity outcome (Table 1). The overlap between the exposure and outcome (psychological disability and mental health, respectively) may have inadvertently inflated the associations between CV and comorbidities (Table 4). Therefore, a sensitivity analysis was undertaken by excluding mental health from the comorbidity count. Although reduced, associations between CV and 1 or more comorbidity alongside MSK remained significant (sensitivity analysis: Model 1, aOR = 1.5, 95% CI 1.2–1.8, p > 0.0001; Model 2, aOR = 1.3, 95% CI 1.0–1.6, p > 0.021). Removing mental health strengthened associations between CV and 2 or more comorbidities alongside MSK, although estimates were less precise (sensitivity analysis: Model 1, aOR = 4.7, 95% CI 2.8–7.7, p > 0.0001; Model 2, aOR = 3.4, 95% CI 2.0–5.9, p > 0.0001). When mental health was excluded from the count, there were too few people with 3 or more comorbidities to estimate associations.
For working-age people with MSK, CV increased the likelihood of accumulated lifestyle risk factors (Table 4). In contrast, CV was not associated with accumulated biomedical risk factors (Table 4).
Measures of health burden
Among people with MSK, the additional presence of any CV was strongly associated with all measures of health burden, including ratings of poorer health (aOR = 2.5, 95% CI 2.0–3.1), experiencing distress (aOR = 2.3, 95% CI 1.8–3.0), or pain restricting work (aOR = 1.4, 95% CI 1.2–1.8; Table 5, Model 2) compared with those with MSK but no CV. Additional adjustment for multimorbidity did not substantively change the associations observed between any CV and poor health (aOR = 2.3, 95% CI 1.8–2.9), psychological distress (aOR = 2.0, 95% CI 1.5–2.7), or pain restricting work (aOR = 1.4, 95% CI 1.1–1.7).
Associations with all health burden measures were observed for sensory impairments, low education attainment, and were strongest for cognitive disability (Table 5). Migration from a country where English was not the main spoken language was associated with poorer self-rated health and distress. When considered by duration since arrival, associations were significant only for longstanding migrants for distress and for midstanding to longstanding migrants for poorer self-rated health (Table 5).
DISCUSSION
In this population-representative study of working-age Australians, CV were more prevalent in those with at least 1 MSK compared with those with none. Almost two-thirds of working-age people with an MSK also had at least 1 CV. The associations between CV and MSK were independent of the effects of age, sex, income level, and occupation type. Moreover, among the MSK population, having a CV was associated with lifestyle risk factors, multimorbidity, poorer self-rated health, and experiencing psychological distress or pain restricting work when compared with those without a CV, even after controlling for age, sex, income, occupation, and multimorbidity. There were no differences in association for biomedical risk factors in the MSK population with or without CV.
Major strengths of our study included the large representative national sample, and although the NHS07-08 was not specifically designed to examine CV, there were comprehensive data available on a broad range of communication characteristics. This enabled the estimation of the proportion of the MSK working-age population with a broad range of CV defined as closely as possible to that stipulated by Blackstone, et al, or a proxy where no alternative was available7. Where possible, to address the limited information on the severity of the CV, these characteristics (and comorbidities or risk factors) were restricted to those present for at least 6 months and to those potentially functionally limiting.
Examining CV extends the focus beyond previously researched established barriers to healthcare based on skills and abilities, such as health literacy, and expands our understanding of factors contributing to health complexity and burden. Although MSK conditions are heterogeneous in terms of etiology, this patient population typically has complex medical needs. Combining MSK conditions enabled the examination of the potential implications added by CV among those managing these existing chronic conditions. The majority of CV characteristics are unlikely to spontaneously change, highlighting that the onus is on the healthcare systems and providers to consider and address the challenges raised by a range of CV. Especially in the MSK population, given associations exist between CV and measures of complexity and burden beyond that induced by MSK alone.
Differentiating associations by the duration since arrival for migrants from non-English–speaking countries revealed complex relationships. Migrants arriving in Australia less than 20 years prior to the survey (from non-English–speaking countries) were significantly less likely to report MSK. This may be because of (1) language difficulties delaying initial diagnosis in Australia or altering healthcare-seeking behavior, or (2) recent migrants generally being healthier24,25. The lack of MSK diagnosis and suggestive presence of a healthy migrant effect may not be simply interpreted as an absence of vulnerability or an indication of health equity25. Our findings support previous research24,26 suggesting that the apparent protective association appears to diminish with longer duration because migrants residing in Australia beyond 10 years reported poorer health and higher distress, even after controlling for age and sex. Additionally, rates of MSK among migrants born in non-English–speaking countries residing in Australia beyond 20 years exceeded rates of those born in Australia or who migrated from English-speaking countries.
The relationships between socioeconomic status (SES) factors (such as income and occupation), CV, and MSK are also complex. SES have the potential to be both (1) an outcome (e.g., either MSK or CV could restrict ability to work, thereby reducing capacity to earn income or gain employment), and (2) a confounder (e.g., an individual of low SES may engage in employment that results in increased risk of developing both back pain, such as manual work, and industrial deafness, such as a noisy workplace). Where lower SES is an outcome of MSK and/or CV, adjusting for SES would be inappropriate and would underestimate the true associations between CV and MSK. However, if SES is a confounder, adjusting for SES is appropriate.
To address both possibilities, Model 1 adjusts for age and sex, while Model 2 additionally adjusts for SES markers (income and occupation type). Adjustment for SES markers (Model 2) reduced the associations between CV and MSK, and reduced associations between CV and complexity and burden measures among those with MSK. However, some association remained, suggesting that these relationships are independent to those of age, sex, income, and occupation. Because education level was part of the exposure CV, this SES marker was not adjusted for.
Irrespective of their nature, the fact that associations exist is an important observation with relevance to healthcare contexts, and warrants confirmation in other populations. Additionally, further research can establish whether the relationships observed for CV among those with MSK are because of interaction effects and whether association between CV and disease complexity and burden measures differ for people with different types of MSK (such as inflammatory or noninflammatory arthritis).
These findings need to be interpreted in the context of the study limitations. A key limitation is the cross-sectional nature of the data; it is inappropriate to interpret the relationships observed between CV and MSK as causal in nature. However, our study was not intended to address the issue of causation.
A potential limitation is that the data are self-reported, which may result in non-reporting or overreporting of conditions. However, it has been demonstrated that self-reported diagnoses are valid27, even when people are cognitively impaired or disabled28. Further, where self-report is inaccurate, it is likely to result in underreporting28,29. Although it was possible to separate them, we combined conditions with and without general practitioner (GP) diagnosis. This was because even the GP diagnoses were not definitive diagnoses because this information was also self-reported.
Limitations of the NHS07-08 data itself included that there were hardly any respondents with speech impairments and no data regarding religious, cultural, and sexual difference. Therefore, conclusions cannot be drawn concerning these groups. Defining religious, cultural, and sexual difference is a challenge because it may vary with the social environment in which the study is conducted and with how people perceive themselves. By omitting this form of vulnerability, our study likely underestimates the prevalence of CV.
Finally, relying on imperfect surrogates for measures not directly available in the NHS07-08 limits the strength of the conclusions regarding these particular characteristics. The proxy used for English language proficiency was migration from a country where English is not the primary spoken language, a commonly used surrogate for cultural and linguistic diversity and non-English first language30. We used this proxy because people migrating from non-English–speaking countries are potentially at risk of CV, irrespective of local language proficiency, because of unfamiliarity with navigating and accessing the healthcare system31. Research to determine whether English language proficiency or the commonly used proxies (language spoken at home and language of interview)31 are also associated with poorer health outcomes is needed.
In the absence of a direct measure of health literacy, we used low education attainment (Yr 10 level or less) as a proxy for limited health literacy32. The rationale for this is 2-fold: (1) direct measures of individual health literacy33,34,35,36,37 are logistically complex to administer within population health surveys, and (2) predictive models of health literacy32,38,39,40 are typically validated in elderly and/or clinical/administrative populations. As the sociodemographic factors predicting health literacy potentially differ with the age and source of the population32,40, predictive models may not be representative of working-age people who may face barriers to attending GP.
It is unclear whether the method of data collection (interviews) actually biased against persons with severe CV. Safeguards were present within NHS07-08; when prevented from responding (through illness, intellectual disability, or language difficulties), a person nominated by the respondents or an interpreter/interviewer fluent in the respondent’s language could respond on their behalf or act as an interpreter. Three attempts were made to reschedule with the participant and their nominated interpreter. Where rescheduling was not achieved, findings from these analyses may underestimate associations between CV and the measures of interest.
Previous research has also identified higher prevalence of specific CV (cognitive impairment, hearing loss, and limited health literacy)19 among specific MSK subgroups (systemic lupus erythematosus41 and rheumatoid arthritis42). Limited local language proficiency and health literacy are additionally implicated in patient-rated suboptimal shared decision-making communication with their clinicians43. Further, ethnicity is associated with differences in prescribing disease-modifying antirheumatic drugs44, and discord between patient and physician assessment of “disease control” for patients of low SES and ethnic minority groups45. The current study expands on this research by identifying that a broader range of CV characteristics are associated with poorer health outcomes, extending across MSK populations.
Taken together, these results suggest CV have implications for communicating information about disease prevention46 and treatment. Although the CV are personal characteristics, they have implications for health professionals. For example, health professionals caring for patients with severe CV may lack familiarity with using different modes of communication, even where patients have alternative modes of communication47, and may be reluctant to examine and diagnose issues above and beyond the communication characteristic itself48,49.
The associations between CV and lifestyle risk factors may suggest that current health promotion messages may be ineffective at reaching these groups46. If so, then health prevention and management information needs to be tailored to a Year 10 education level (or less, to be maximally inclusive) and to consider the linguistic, sensory, and cognitive contexts of people with MSK.
Comorbidities were more common among the MSK population with CV than those without a CV. This finding highlights the importance of interprofessional communication because managing MSK in the context of both CV and multimorbidity17,18 is likely to further complicate treatments and result in intensive healthcare services use, increasing the potential for communication failure and adverse outcomes.
The broad range of CV with potential health implications identified suggests that an equally broad range of policy measures that support strategies to improve communication are required. General communication may be improved with communication skills training4. Enlisting the aid of translators, interpreters, and speech pathologists, and presenting information at appropriate literacy levels and in linguistically appropriate formats may all additionally ease CV among those with MSK7.
If replicated by other studies, particularly those examining potential causal mechanisms, these results may indicate the need to further develop and implement evidence-based techniques to help overcome these potential communication barriers in healthcare settings. Given that low educational attainment and sensory and cognitive impairments were most common and strongly associated with measures of worse health burden, these communication characteristics require particular attention.
Acknowledgment
The 2007–2008 National Health Surveys data used within this manuscript were provided by the Australian Bureau of Statistics through its Microdata release program.
Footnotes
Supported by an Alice O’Brien, Arthritis and Osteoporosis Victoria, PhD scholarship to DL.
- Accepted for publication March 13, 2015.