BioMed Research International
Volume 2016 (2016), Article ID 7845438, 9 pages
http://dx.doi.org/10.1155/2016/7845438

Research Article

Different Multimorbidity Measures Result in Varying Estimated Levels of Physical Quality of Life in Individuals with Multimorbidity: A Cross-Sectional Study in the General Population

Aline Ramond-Roquin,1,2,3,4 Jeannie Haggerty,⁵ Mireille Lambert,² Jose Almirall,² and Martin Fortin1,2

¹Département de Médecine de Famille et de Médecine d’Urgence, Université de Sherbrooke, 3001 12e Avenue Nord, Sherbrooke, Québec, Canada J1H 5H3
²Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay-Lac-Saint-Jean, 305 Saint-Vallier, Chicoutimi, Canada
³Département de Médecine Générale, Université d’Angers, L’Université Nantes Angers Le Mans, 1 rue Haute de Reculée, 49045 Angers Cedex 01, France
⁴Laboratoire d’Ergonomie et d’Épidémiologie en Santé au Travail, Université d’Angers, L’Université Nantes Angers Le Mans, 1 rue Haute de Reculée, 49045 Angers Cedex 01, France
⁵Faculty of Medicine, McGill University, Montreal, Canada

Received 26 October 2015; Revised 8 February 2016; Accepted 21 February 2016

Academic Editor: Renè Melis

Copyright © 2016 Aline Ramond-Roquin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Introduction. Multimorbidity adversely affects health-related quality of life. Methodological factors may impact the magnitude of this relationship. Objective. To evaluate how physical health-related quality of life varies in individuals with multimorbidity depending on the length of the list of candidate conditions considered. Methods. Secondary analysis from PRECISE, a cohort study of the general adult population of Quebec, Canada. Multimorbidity was measured using the 21-chronic condition list from the Disease Burden Morbidity Assessment, and physical health-related quality of life was measured using the physical component summary (PCS) of SF-12v2. The PCS was calculated, (a) using 2 or more conditions from the 21-condition list (MM2+, 21) and then from a reduced 6-condition list (MM2+, 6) and (b) using three or more conditions from each list (MM3+, 21, and MM3+, 6). Results. The analysis included 1,710 individuals (mean age 51.3, 40.5% men). Multimorbidity prevalence ranged from 63.8% (MM2+, 21 conditions) to 3.8% (MM3+, 6 conditions). The mean [95% CI] PCS dropped from 45.7 [CI: 45.0–46.3] (MM2+, 21) to 40.2 [CI: 38.7–41.8] (MM2+, 6) and from 44.2 [CI: 43.4–44.9] (MM3+, 21) to 34.8 [CI: 31.9–37.6] (MM3+, 6). Conclusion. The length of the list of candidate conditions considered has a great impact on the estimations of physical health-related quality of life.

1. Introduction

Prevalence of multimorbidity, which refers to the cooccurrence of multiple chronic conditions in the same individual, has increased over the last decades in the general population [1–3]. Because of its association with multiple negative consequences at the individual, healthcare systems, and societal levels, multimorbidity is now acknowledged by some as a research priority [4–6]. Outcomes associated with multimorbidity still need to be explored.

Health-related quality of life, which is a multidimensional concept that refers to physical, psychological, and social domains of health, is adversely affected by the presence of multimorbidity [7–9]. The increasing number of concurrent chronic conditions has been found to be strongly associated with lower scores of health-related quality of life [10–15]. This association seems to be exacerbated in younger people and in the most deprived populations and perhaps to a lesser extent in women [10, 11, 16, 17]. The physical component of health-related quality of life seems to be more affected by multimorbidity than the mental component [18, 19].

Studies aiming to quantify the impact of multimorbidity on the quality of life show wide heterogeneity in terms of the intensity of this association [18]. It has been suggested that the lack of a uniform way to measure multimorbidity may explain a significant part of this variability. However, these studies also presented other important methodological differences (population studied, measure of quality of life, etc.) which prevented the evaluation of the own impact of multimorbidity measure on the heterogeneity observed.

Multimorbidity can be measured using either simple count of conditions or weighted measures which take into account the severity of each existing condition [20]. The use of weighted measures of multimorbidity seems to reveal a stronger association with health-related quality of life, probably because higher scores do not necessarily mean higher number of chronic conditions [21]. However, most operational definitions of multimorbidity in the literature have been based on a simple count of conditions. In such cases, a minimal number of conditions are required to be considered as “multimorbid,” often two or more conditions (MM2+) or three or more conditions (MM3+) in a single individual [22].

Independent of whether a weighted measure or a simple count is used, an important aspect of its measurement is the list of conditions screened as present or not in a given individual. This methodological aspect applies to every study on multimorbidity. Many different lists of potential conditions have been proposed, with a median number of 14 conditions [20], with some being as short as six conditions [9, 19] and others as long as 40 [17, 23]. It is known that differences in the list of conditions considered to measure multimorbidity have a considerable influence on estimates of the prevalence of multimorbidity [24]. However, the influence of the list of conditions on the estimated level of the physical component of health-related quality of life in individuals with multimorbidity has yet to be investigated.

2. Objectives

This study aimed to evaluate how estimates of physical health-related quality of life vary in individuals with multimorbidity depending on the length of the list of candidate conditions, using different operational definitions of multimorbidity.

3. Methods

3.1. Study Design and Setting

This cross-sectional study builds on a secondary analysis of data collected for a larger project, the Program of Research on the Evolution of a Cohort Investigating Health System Effects (PRECISE) [25]. This project aimed to examine the effects of the transformation of primary healthcare services on a population’s health. The PRECISE study was conducted in four local healthcare networks in Quebec, Canada, located in metropolitan, urban, rural, and remote settings. Details of the method and sampling strategies used are described in the study protocol reported elsewhere [25].

3.2. Population Recruitment

The present study included a randomly selected sample recruited from March to April 2010 in the general population by random digital dialing. Once contact was made, staff selected the eligible adult in the household with the most recent birthday to ensure random selection. Participants had to be community-dwelling adults, aged between 25 and 75 years, without major cognitive impairment, able to respond to written and oral questions in English or French, and to reside in one of the four networks identified.

3.3. Data Collection

At recruitment, participants reported on sociodemographic information: age, gender, household income, education level, perceived financial situation, house ownership, presence or absence of medical insurance, and possession of a retirement plan. We produced a data-driven classification of socioeconomic status based on the last five variables and classified individuals into four clusters: elite group, middle-high, middle-low, and low. This aimed to capture the multidimensional nature of socioeconomic status into a single variable. Definitional criteria for the four socioeconomic clusters are described elsewhere [26].

Two weeks after recruitment, participants completed a self-administered questionnaire (paper or online) or a questionnaire administered by telephone that included sections to measure (1) multimorbidity and (2) physical health-related quality of life.

Measurement of Multimorbidity. The instrument comprised a list of 21 chronic conditions adapted from the Disease Burden Morbidity Assessment (DBMA). It has been validated to measure multimorbidity, including validation in a population from Quebec, with a good predictive value for health-related quality of life [8, 27, 28]. To determine the presence of a condition, for 20 out of 21 conditions, the instruction to the participants was as follows: “Please, indicate if you have been told by a health professional that you have any of the following illnesses.” For the 21st condition, “overweight,” the participant was invited to self-report his or her height and weight, from which we calculated the Body Mass Index (BMI). We considered the presence of overweight when the BMI was higher than 24.9 Kg/m² [29]. The number of conditions for each individual was first summed up based on the full list of 21 conditions (shown in the results section). We then summed up the number of conditions based on a reduced list of six conditions (out of 21) to correspond to a list previously used in the literature to study health-related quality of life and multimorbidity [9, 19]. Any missing value was considered as an absent condition. We also applied successively two operational definitions of multimorbidity, MM2+ then MM3+. Therefore, multimorbidity was successively measured in four different ways in this study: MM2+ (21); MM2+ (6); MM3+ (21); and MM3+ (6). Given that the list of six conditions was a sublist of the 21 conditions, it follows that, for each of the operational definitions of multimorbidity, the individuals considered as multimorbid according to the 6-condition list constituted a subsample of those considered as multimorbid according to the 21-condition list.

Measurement of Physical Health-Related Quality of Life. The physical component of health-related quality of life was measured using the SF-12, version 2 [30, 31], a short form version of SF-36 [32], a generic instrument validated in a Canadian population [33]. The physical component summary is calculated from weighted scores of both the mental and the physical dimensions of the SF-12v2. The physical component summary ranges from 0 to 100, with a population-normed mean of 50 and a standard deviation of 10, where a 5-point difference is considered clinically significant [34]. Lower scores refer to lower physical quality of life.

3.4. Data Analysis

We first studied the sociodemographic characteristics and the number of chronic conditions in the whole population, then in individuals with multimorbidity, using successively each of the four multimorbidity measures. We then looked at an assumption underlying the main analyses; namely, whether there was a statistically significant association between multimorbidity and physical health-related quality of life, adjusted for sociodemographic covariates, for each of the four multimorbidity measures.

To evaluate how estimates of physical health-related quality of life vary with the length of the list of candidate conditions considered, we estimated the average level (mean values and 95% confidence intervals) of the physical component of health-related quality of life in individuals with multimorbidity and highlighted the resulting variation using the 21-condition list or the 6-condition list. We conducted these analyses successively using each of the two operational definitions of multimorbidity. Finally, we repeated all these analyses stratifying by age, gender, and socioeconomic status, in order to determine if the variations observed were consistent within each of these subgroups of individuals. For the stratified analysis, age was considered in three groups (25–44 years old, 45–64 years old, and 65–75 years old), based on previous literature on multimorbidity [35].

Categorical variables were described with absolute numbers and percentages. Quantitative variables were described using means and standard deviations (SD). Confidence intervals (95% CI) around estimated means of physical health-related quality of life were calculated using standard errors of the means, with appropriate statistics in the case of small samples. Analysis of covariance (ANCOVA) was used to characterize the association between multimorbidity and physical health-related quality of life, with modelling physical health-related quality of life according to multimorbidity status and sociodemographic covariates. All analyses were done using the SPSS version 20 software.

The study was approved by the ethics committee of the Centre de Santé et de Services Sociaux de Chicoutimi, as well as the research ethics committee of Hôpital Charles Lemoyne, QC, Canada.

4. Results

A total of 1,710 individuals participated in the PRECISE study and their data were included in these analyses. Among the study population, mean (SD) age was 51.3 (SD 12.5) years and there were 693 (40.5%) men. The main sociodemographic characteristics of the participants are presented in Table 1.

Table 1: Sociodemographic characteristics of the study population ().

Study population

Age, mean (SD) 22 missing
51.3 (12.5)

Males, (%):
693 (40.5)

Annual household income (CAN), (%) 46 missing

    Less than 20,000
196 (11.5)

    20,000 to 49,999
699 (40.9)

    50,000 or more
769 (45.0)

Education level, (%) 8 missing

    Less than high school
376 (22.0)

    Completed high school
521 (30.5)

    College/university
805 (47.1)

Socioeconomic status, (%) 66 missing

    Low
230 (13.5)

    Middle-low
345 (20.2)

    Middle-high
733 (42.9)

    Elite group
336 (19.6)

SD: standard deviation; Socioeconomic classes were derived from a data-driven combination of the following variables: education level, perceived financial situation, house ownership, presence or absence of medical insurance, and possession of a retirement plan.

Regarding chronic conditions, absence of overweight was imputed to 57 individuals due to missing values. For every other condition, there was either 0 or 1 missing value. Prevalence of each individual chronic condition in the study population is shown in Table 2. Considering the 21-condition list, 272 individuals (15.9%) reported no chronic condition, and the mean number of chronic conditions was 2.9 (SD 2.4). Alternatively, when the 6-condition list was considered, 1,016 individuals (59.4%) reported no chronic condition and the mean number of chronic conditions was 0.6 (SD 0.8).

Table 2: Prevalence of each individual chronic condition in the study population ().

(%)

Angina/coronary artery disease
124 (7.3)

Asthma
176 (10.3)

Chronic obstructive pulmonary disease
66 (3.9)

Diabetes
145 (8.5)

Hypertension
477 (27.9)

Stroke
21 (1.2)

Back pain
353 (20.6)

Osteoarthritis
361 (21.1)

Rheumatoid arthritis
44 (2.6)

Osteoporosis
94 (5.5)

Other illnesses of joints or limbs, lasting for 6 months or more
205 (12.0)

Cancer (within the past 5 years)
65 (3.8)

Cholesterol, elevated
439 (25.7)

Colon problem
123 (7.2)

Congestive heart failure
37 (2.2)

Depression
221 (12.9)

Hard of hearing
213 (12.5)

Overweight
1000 (58.5)

Stomach problem
356 (20.8)

Thyroid disorder
198 (11.6)

Vision problem
137 (8.0)

Conditions in bold are common to the two lists: full list (21 conditions) and reduced list (6 conditions).

As expected, a clinically and statistically significant association between multimorbidity status and physical health-related quality of life was observed for each of the four multimorbidity measures, adjusting for age, gender, and socioeconomic status. Depending on the multimorbidity measures, adjusted regression parameters associated with multimorbidity ranged from 8.57 to 10.92 ( for each parameter).

Prevalence of multimorbidity as well as level of physical health-related quality of life in those considered as multimorbid largely varied depending on the multimorbidity measure used (Figures 1 and 2). Using the MM2+ definition, individuals with multimorbidity defined by the 21-condition list (, 63.8% of the total population) had a mean physical component summary (95% CI) of 45.7 (CI: 45.0–46.3), while the group defined by the 6-condition list (, 13.8% of the total population) scored 40.2 (CI: 38.7–41.7) on average. Using the MM3+ definition, individuals with multimorbidity defined by the 21-condition list (, 48.9% of the total population) had a mean physical component summary (95% CI) of 44.2 (CI: 43.4–44.9), while the group defined by the 6-condition list (, 3.8% of the total population) scored 34.8 (CI: 31.9–37.6) on average.

(a)

(b)

Figure 1: Prevalence of multimorbidity, depending on the multimorbidity measure. Operational definitions of multimorbidity: MM2+: having two or more chronic conditions; MM3+: having three or more chronic conditions.

Figure 2: Estimates of the average level (mean values and 95% confidence intervals) of the physical component of health-related quality of life in individuals with multimorbidity, depending on the multimorbidity measure. Operational definitions of multimorbidity: MM2+: having two or more chronic conditions; MM3+: having three or more chronic conditions.

Regarding sociodemographic variables, using a reduced list of conditions led to the selection of a subgroup of older and more deprived individuals, with a higher proportion of men (Table 3). This was true for both operational definitions of multimorbidity (MM2+ and MM3+).

Table 3: Main characteristics of the individuals with multimorbidity, depending on the multimorbidity measure.

Measure of multimorbidity
MM2+
MM3+

21 conditions ()
6 conditions ()
21 conditions ()
6 conditions ()

Age: mean (SD)
55.0 (11.4)
59.0 (9.7)
56.3 (10.6)
59.5 (8.7)

Males: (%)
455 (41.7)
111 (46.8)
352 (42.1)
33 (50.0)

Socioeconomic status: (%)

    Low
165 (15.1)
50 (22.4)
137 (16.4)
17 (28.3)

    Middle-low
227 (20.8)
47 (21.1)
176 (21.1)
13 (21.7)

    Middle-high
456 (41.8)
96 (43.0)
346 (41.4)
28 (46.7)

    Elite group
200 (18.3)
30 (13.5)
143 (17.1)
2 (3.3)

Chronic conditions: mean number (SD)

    As documented by the 21-c. list
4.2 (2.1)
6.1 (2.3)
4.8 (1.2)
7.8 (2.4)

    As documented by the 6-c. list
0.9 (0.9)
2.3 (0.6)
1.1 (0.9)
3.2 (0.5)

SD: standard deviation; Socioeconomic classes were derived from a data-driven combination of the following variables: education level, perceived financial situation, house ownership, presence or absence of medical insurance, and possession of a retirement plan; 21-condition list; 6-condition list.

Missing data for each variable are not reported in this table because their number differed depending on the group considered. They ranged from 2 missing values (age, MM3+, 6 conditions) to 43 missing values (socioeconomic status, MM2+, 21 conditions).

Analyses stratified by age, gender, and socioeconomic level revealed similar patterns in the variations of estimates of quality of life within each of the subgroups of individuals successively considered (Figures 3(a), 3(b), and 3(c)). Using the 6-condition list consistently resulted in lower estimates of average physical health-related quality of life compared to using the 21-condition list. As in the main analysis, the variations observed in the stratified analyses were larger with the MM3+ operational definition than with the MM2+ operational definition.

(a)

(b)

(c)

Figure 3: Estimates of the average level (mean values and 95% confidence intervals) of the physical component of health-related quality of life in individuals with multimorbidity, depending on the multimorbidity measure, stratified by age (a), gender (b), and socioeconomic status (c). Operational definitions of multimorbidity: MM2+: having two or more chronic conditions; MM3+: having three or more chronic conditions. Estimates were not computed in the case of multimorbidity measured as MM3+ based on the 6-condition list for young people “25–44 years” and for the “elite” group, due to insufficient subsample size (4 and 2 individuals, resp.).

Interestingly, using a reduced list of conditions to measure multimorbidity resulted in selecting people with substantially higher numbers of chronic conditions (Table 3). For example, the mean number of conditions as documented in the list of 21 conditions was 4.2 (SD 2.1) in individuals considered as multimorbid based on the MM2+ (21) definition while it was 6.1 (SD 2.3) in those considered as multimorbid based on the MM2+ (6) definition.

5. Discussion

This study suggests that different measures of multimorbidity result in significant variations in estimates of physical health-related quality of life within the same population. Our results show that using a reduced list of conditions leads to lower levels of estimated physical health-related quality of life in individuals with multimorbidity, independent of age, gender, and socioeconomic status, and whichever operational definition of multimorbidity was used (MM2+ or MM3+).

In fact, using a reduced list of conditions leads to the selection of a subgroup of individuals with an especially high number of existing chronic conditions, in comparison to the whole population considered as multimorbid based on a longer list. Each condition an individual has, whether documented or not, impacts his or her quality of life. It is therefore not surprising that people considered as multimorbid based on a reduced list of conditions have a higher number of existing chronic conditions while reporting lower physical quality of life.

The two lists used in this study were chosen for their contrast in terms of number of candidate conditions and because the six conditions of the reduced list were also included in the full list of 21 conditions. However, not one of these lists captures the whole range of the potential chronic conditions [36]. The use of any limited list, regardless of its length, necessarily implies a certain amount of unmeasured variability, due to unlisted conditions, and introduces a systematic bias towards the selection of individuals with higher degrees of multimorbidity. In that sense, using an open list of conditions to measure multimorbidity would result in a more accurate representation of reality, while being associated with other important challenges, such as reproducibility of the measure or optimal granularity in recording.

Beyond number, the nature of conditions considered in any list influences the estimated level of health-related quality of life. Among the 21 conditions from our full list, our 6-condition list included some which are among those with the highest impact on health-related quality of life (chronic obstructive pulmonary disease and stroke) and some which are among those with the lowest impact (hypertension or diabetes) [15, 16, 37]. We therefore believe that the variation observed in our study does not primarily result from the nature of conditions considered in the lists, but rather from the number of candidate conditions itself.

In our study, estimated prevalence of multimorbidity varied as much as 3.8% to 63.8% depending on the measure used. Moreover, the variations observed in the estimates of quality of life were 5.5 point units (means 45.7 to 40.2) with MM2+ and 9.4 points (means 44.2 to 34.8), with MM3+. These variations are larger than what is considered as the minimal clinically important difference for this score, namely, 5 points [38]. This illustrates how such methodological issues have the potential to considerably impact results and indicates that careful methodological considerations are required when measuring multimorbidity. The variations resulting from the alternative use of any other multimorbidity measures might be of different intensity from those observed in our study, but more stringent measures of multimorbidity will necessarily tend to identify smaller and sicker subgroups.

In addition to the quality of life, many other outcomes have been associated with the number of chronic conditions, such as disability [10, 13], psychological distress [12, 39], mortality [40], healthcare utilization [12, 41], or costs [41]. We believe that the choice of multimorbidity measure, and especially the length of the list of conditions, may also induce substantial variations when estimating the outcomes in multimorbid patients. Although stringent measures may be relevant for clinical purposes, short lists of conditions should be avoided in epidemiological studies: the shorter the list, the more biased the estimates of multimorbidity prevalence and related outcomes.

This study was based on data from the PRECISE cohort that constituted a representative sample of the Quebec general population at baseline [25]. The sample included in this study underrepresented young and deprived individuals, who were not as many to return their questionnaire (data not shown). However, the aim of this study was not to provide estimates of the physical component of health-related quality of life to be extrapolated to the general population, but rather to document variation in estimates resulting from using different multimorbidity measures. It is unlikely that this response bias has contributed to the results in any way. Prevalence of certain chronic conditions and of multimorbidity, as well as health-related quality of life, has been shown to present substantial international variations [10, 42, 43]. However, the impact of chronic conditions on health-related quality of life seems to be quite similar across countries [44]. Therefore, although our estimates may be not generalized to other populations, some variation in health-related quality of life could also be observed, within other cultural environments, when using different multimorbidity measures. We had to rely on the self-reported presence of chronic conditions to measure multimorbidity and, hence, either overreporting or underreporting may have occurred. This might affect the prevalence of some conditions in the sample. However, we do not think that this possibility would have an important impact on the differences observed with the use of different lists of conditions, which is the main message of this study.

6. Conclusion

Previous research had hypothesized that heterogeneity in multimorbidity measures may generate variability when studying quality of life in multimorbid individuals. This study demonstrated how different multimorbidity measures actually result in significant variation in the estimates of physical health-related quality of life within the same population. It argues for careful methodological consideration when measuring multimorbidity and its association with different outcomes. Standardization of the measure of multimorbidity is needed to allow the comparison of the results across different studies on multimorbidity.

In this regard, we recommend the use of a list of candidate conditions that is sufficiently long. Determining the ideal length is beyond the scope of this study, but it should be a compromise between lists that are too short, which will produce seriously biased estimates (6-condition lists being in this category) and lists that are too long, which can be difficult to manage. In order to reach a satisfying compromise, we suggest that both prevalence and impact for individuals and communities should be taken into account when choosing which conditions to include in the list.

Competing Interests

The authors declare that there are no competing interests regarding the publication of this paper.

Authors’ Contributions

Jeannie Haggerty and Martin Fortin designed the original study (PRECISE) and coordinated the data collection. Aline Ramond-Roquin, Mireille Lambert, and Jose Almirall suggested the research questions and designed the analysis with approval from the other authors. Aline Ramond-Roquin and Jose Almirall conducted the analysis of data. Aline Ramond-Roquin drafted the paper with Mireille Lambert and Jose Almirall under the guidance of Martin Fortin and Jeannie Haggerty. All the authors contributed to the writing by critically reviewing the paper and gave the final approval of the version submitted.

Acknowledgments

The authors would like to express their gratitude to the participants and thank Susie Bernier for her editorial assistance. This research was supported by the Canadian Institutes for Health Research (CIHR).

References

M. van den Akker, F. Buntinx, and J. A. Knottnerus, “Comorbidity or multimorbidity: what's in a name? A review of literature,” European Journal of General Practice, vol. 2, no. 2, pp. 65–70, 1996.

A. Uijen and E. van de Lisdonk, “Multimorbidity in primary care: prevalence and trend over the last 20 years,” European Journal of General Practice, vol. 14, supplement, pp. 28–32, 2008.

S. Fu, N. Huang, and Y.-J. Chou, “Trends in the prevalence of multiple chronic conditions in Taiwan from 2000 to 2010: a population-based study,” Preventing Chronic Disease, vol. 11, no. 10, Article ID 140205, 2014.

B. Starfield, “Global health, equity, and primary care,” Journal of the American Board of Family Medicine, vol. 20, no. 6, pp. 511–513, 2007.

Canadian Institute for Health Research, “Listening for Direction: A National Consultation on Health Services and Policy Issues. Secondary Listening for Direction: A National Consultation on Health Services and Policy Issues,” 2007, http://www.cihr-irsc.gc.ca/e/20461.html

E. Hummers-Pradier, M. Beyer, P. Chevallier et al., “Series: The research agenda for general practice/family medicine and primary health care in Europe. Part 4. Results: specific problem solving skills,” European Journal of General Practice, vol. 16, no. 3, pp. 174–181, 2010.

M. A. Testa and D. C. Simonson, “Assessment of quality-of-life outcomes,” The New England Journal of Medicine, vol. 334, no. 13, pp. 835–840, 1996.

E. A. Bayliss, J. L. Ellis, and J. F. Steiner, “Subjective assessments of comorbidity correlate with quality of life health outcomes: initial validation of a comorbidity assessment instrument,” Health and Quality of Life Outcomes, vol. 3, article 51, 2005.

E. I. Lubetkin, H. Jia, P. Franks, and M. R. Gold, “Relationship among sociodemographic factors, clinical conditions, and health-related quality of life: examining the EQ-5D in the U.S. general population,” Quality of Life Research, vol. 14, no. 10, pp. 2187–2196, 2005.

N. Garin, B. Olaya, M. V. Moneta et al., “Impact of multimorbidity on disability and quality of life in the Spanish older population,” PLoS ONE, vol. 9, no. 11, Article ID e111498, 2014.

R. E. Mujica-Mota, M. Roberts, G. Abel et al., “Common patterns of morbidity and multi-morbidity and their impact on health-related quality of life: evidence from a national survey,” Quality of Life Research, vol. 24, no. 4, pp. 909–918, 2015.

C. B. Agborsangaya, D. Lau, M. Lahtinen, T. Cooke, and J. A. Johnson, “Health-related quality of life and healthcare utilization in multimorbidity: results of a cross-sectional survey,” Quality of Life Research, vol. 22, no. 4, pp. 791–799, 2013.

O. McDaid, M. J. Hanly, K. Richardson, F. Kee, R. A. Kenny, and G. M. Savva, “The effect of multiple chronic conditions on self-rated health, disability and quality of life among the older populations of Northern Ireland and the Republic of Ireland: a comparison of two nationally representative cross-sectional surveys,” BMJ Open, vol. 3, no. 6, Article ID e002571, 2013.

C. Brettschneider, H. Leicht, H. Bickel et al., “Relative impact of multimorbid chronic conditions on health-related quality of life—results from the multicare cohort study,” PLoS ONE, vol. 8, no. 6, Article ID e66742, 2013.

A. L. Stewart, S. Greenfield, R. D. Hays et al., “Functional status and well-being of patients with chronic conditions. Results from the Medical Outcomes Study,” The Journal of the American Medical Association, vol. 262, no. 7, pp. 907–913, 1989.

K.-I. Kim, J. H. Lee, and C.-H. Kim, “Impaired health-related quality of life in elderly women is associated with multimorbidity: results from the Korean national health and nutrition examination survey,” Gender Medicine, vol. 9, no. 5, pp. 309–318, 2012.

K. D. Lawson, S. W. Mercer, S. Wyke et al., “Double trouble: the impact of multimorbidity and deprivation on preference-weighted health related quality of life a cross sectional analysis of the Scottish Health Survey,” International Journal for Equity in Health, vol. 12, no. 1, article 67, 2013.

M. Fortin, L. Lapointe, C. Hudon, A. Vanasse, A. L. Ntetu, and D. Maltais, “Multimorbidity and quality of life in primary care: a systematic review,” Health and Quality of Life Outcomes, vol. 2, article 51, 2004.

I. T. M. Heyworth, M. L. Hazell, M. F. Linehan, and T. L. Frank, “How do common chronic conditions affect health-related quality of life?” The British Journal of General Practice: The Journal of the Royal College of General Practitioners, vol. 59, no. 568, pp. e353–e358, 2009.

C. Diederichs, K. Berger, and D. B. Bartels, “The measurement of multiple chronic diseases—A systematic review on existing multimorbidity indices,” Journals of Gerontology: Series A: Biological Sciences and Medical Sciences, vol. 66, no. 3, pp. 301–311, 2011.

M. Fortin, G. Bravo, C. Hudon et al., “Relationship between multimorbidity and health-related quality of life of patients in primary care,” Quality of Life Research, vol. 15, no. 1, pp. 83–91, 2006.

C. Harrison, H. Britt, G. Miller, and J. Henderson, “Examining different measures of multimorbidity, using a large prospective cross-sectional study in Australian general practice,” BMJ Open, vol. 4, no. 7, Article ID e004694, 2014.

K. Barnett, S. W. Mercer, M. Norbury, G. Watt, S. Wyke, and B. Guthrie, “Epidemiology of multimorbidity and implications for health care, research, and medical education: a cross-sectional study,” The Lancet, vol. 380, no. 9836, pp. 37–43, 2012.

M. Fortin, M. Stewart, M.-E. Poitras, J. Almirall, and H. Maddocks, “A systematic review of prevalence studies on multimorbidity: toward a more uniform methodology,” Annals of Family Medicine, vol. 10, no. 2, pp. 142–151, 2012.

J. Haggerty, M. Fortin, M.-D. Beaulieu et al., “At the interface of community and healthcare systems: a longitudinal cohort study on evolving health and the impact of primary healthcare from the patient's perspective,” BMC Health Services Research, vol. 10, article 258, 2010.

M. Fortin, J. Haggerty, J. Almirall, T. Bouhali, M. Sasseville, and M. Lemieux, “Lifestyle factors and multimorbidity: a cross sectional study,” BMC Public Health, vol. 14, no. 1, article 686, 2014.

E. A. Bayliss, J. L. Ellis, and J. F. Steiner, “Seniors' self-reported multimorbidity captured biopsychosocial factors not incorporated into two other data-based morbidity measures,” Journal of Clinical Epidemiology, vol. 62, no. 5, pp. 550e1–557e1, 2009.

M.-E. Poitras, M. Fortin, C. Hudon, J. Haggerty, and J. Almirall, “Validation of the disease burden morbidity assessment by self-report in a French-speaking population,” BMC Health Services Research, vol. 12, article 35, 2012.

H. Canada and B. M. I. Chart, “Secondary BMI Chart,” http://www.hc-sc.gc.ca/fn-an/nutrition/weights-poids/guide-ld-adult/bmi_chart-graph_imc-eng.php

J. E. Ware, M. Kosinski, D. M. Turner-Bowker et al., How to Score Version 2 of he SF-12 Health Survey (with a Supplement Documenting Version 1), Quality Metric Incorporated, Lincoln, RI, USA, 2002.

N. C. Cheak-Zamora, K. W. Wyrwich, and T. D. McBride, “Reliability and validity of the SF-12v2 in the medical expenditure panel survey,” Quality of Life Research, vol. 18, no. 6, pp. 727–735, 2009.

J. E. Ware Jr., M. Kosinski, and S. D. Keller, “A 12-item short-form health survey: construction of scales and preliminary tests of reliability and validity,” Medical Care, vol. 34, no. 3, pp. 220–233, 1996.

W. M. Hopman, T. Towheed, T. Anastassiades et al., “Canadian normative data for the SF-36 health survey,” Canadian Medical Association Journal, vol. 163, no. 3, pp. 265–271, 2000.

R. N. Saris-Baglama, C. J. Dewey, G. B. Chisholm et al., QualityMetric Health Outcomes™ Scoring Software 4.0 User's Guide, QualityMetric Incorporated, Lincoln, RI, USA, 2010.

C. Hoffman, D. Rice, and H.-Y. Sung, “Persons with chronic conditions: their prevalence and costs,” The Journal of the American Medical Association, vol. 276, no. 18, pp. 1473–1479, 1996.

J. O'Halloran, G. C. Miller, and H. Britt, “Defining chronic conditions for primary care with ICPC-2,” Family Practice, vol. 21, no. 4, pp. 381–386, 2004.

H.-M. Wang, M. Beyer, J. Gensichen, and F. M. Gerlach, “Health-related quality of life among general practice patients with differing chronic diseases in Germany: cross sectional survey,” BMC Public Health, vol. 8, article 246, 2008.

G. Samsa, D. Edelman, M. L. Rothman, G. R. Williams, J. Lipscomb, and D. Matchar, “Determining clinically important differences in health status measures: a general approach with illustration to the Health Utilities Index Mark II,” PharmacoEconomics, vol. 15, no. 2, pp. 141–155, 1999.

J. M. Gunn, D. R. Ayton, K. Densley et al., “The association between chronic illness, multimorbidity and depressive symptoms in an Australian primary care cohort,” Social Psychiatry and Psychiatric Epidemiology, vol. 47, no. 2, pp. 175–184, 2012.

A. Menotti, I. Mulder, A. Nissinen, S. Giampaoli, E. J. M. Feskens, and D. Kromhout, “Prevalence of morbidity and multimorbidity in elderly male populations and their impact on 10-year all-cause mortalitym: the FINE study (Finland, Italy, Netherlands, elderly),” Journal of Clinical Epidemiology, vol. 54, no. 7, pp. 680–686, 2001.

C. Bähler, C. A. Huber, B. Brüngger, and O. Reich, “Multimorbidity, health care utilization and costs in an elderly community-dwelling population: a claims data based observational study,” BMC Health Services Research, vol. 15, no. 1, article 23, 2015.

T. Vos, R. M. Barber, B. Bell et al., “Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013,” The Lancet, vol. 386, no. 9995, pp. 743–800, 2013.

H.-H. König, H. Leicht, H. Bickel et al., “Effects of multiple chronic conditions on health care costs: an analysis based on an advanced tree-based regression model,” BMC Health Services Research, vol. 13, no. 1, article 219, 2013.

J. Alonso, M. Ferrer, B. Gandek et al., “Health-related quality of life associated with chronic conditions in eight countries: results from the International Quality of Life Assessment (IQOLA) Project,” Quality of Life Research, vol. 13, no. 2, pp. 283–298, 2004.