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. Author manuscript; available in PMC: 2014 Feb 1.
Published in final edited form as: Med Decis Making. 2012 Oct 25;33(2):235–243. doi: 10.1177/0272989X12464434

Evidence of spillover effects of illness among household members: EQ-5D scores from a US population sample

Eve Wittenberg 1, Grant Ritter 2, Lisa A Prosser 3
PMCID: PMC3606811  NIHMSID: NIHMS449900  PMID: 23100461

Introduction

Health affects more than just the solitary individual who participates in health-promoting activities or suffers from an acute or chronic condition. Social network research has shown that individuals share their obesity, smoking and happiness with their family members, friends and neighbors.1 More directly, taking care of an ill or disabled individual imposes a burden on the care giver that has been well-documented, both in health effects and quality of life.26 It has also been suggested that an ill individual exerts a psychic or emotional toll on family members who care about the patient, distinct from the toll of caregiving.7,8 Less often noted is the opposite, positive benefit of care taking.9 In sum, research has clearly established that our conceptualization of health effects extends beyond one individual to include those surrounding him or her, including those physically present and those emotionally connected. The implications of this “spillover” of health to surrounding individuals include the consideration of others’ health and well-being in clinical decision making, and the inclusion of the costs and benefits of multiple individuals in analyses of health interventions. The landscape of health decision making is altered by the conceptualization of health as a family affair and important research priorities come to the fore from this perspective. This paper reports on an analysis of US population data that includes a utility-based measure of the effect of chronic illness on household members. We provide EQ-5D utility estimates of this “spillover” effect of illness on surrounding individuals.

Documented spillover effects are varied and often condition-specific, ranging from specific symptomology (e.g., anxiety10, sleep disturbance11), to psychological well-being12 and physical health.5,13 The effects have been measured in the context of a variety of specific health conditions and family or caregiving relationships, such as family caregivers of stroke patients6, spouses14, parents15, children16 and siblings17 of cancer patients18, and family members and caregivers of individuals with mental illness (e.g., bipolar disorder19, schizophrenia20, and dementia10). A separate literature has attempted to quantify the spillover effect of illness for inclusion in economic evaluation.21 Health utility is a quantitative measure of quality of life that can be used to assess patient reported outcomes and to calculate the outcome measure used in cost utility analysis, quality adjusted life years (QALYs). Health utility is a subjective measure of the value assigned to living in a particular health state, measured on a scale of 0 to 1 where 0 is the value of being dead and 1 is the value of being in full or optimal health.22 Utility measures are “preference based,” meaning they reflect individuals’ subjective preferences, or opinions, about living in a particular state of health, compared with objective measures of quality of life that report symptoms or functioning. The uniform scale on which utilities are measured allows comparison of outcomes across conditions and populations. Limitations of utility measurement methods have been noted.23

Utility measures of spillover effects offer the opportunity for integration of this component of outcomes into decision analyses and cost-effectiveness analyses. Specific situations in which spillover effects are critical inputs for decision analysis have been identified, including for measurement reasons, such as utilities for health states of very young children in which the parent proxy cannot reasonably separate their own utility from that of the child24, or for face validity reasons, such as living organ transplant in which both donor and recipient are integral to the decision.25 The study reported here estimated the spillover disutility of all chronic conditions experienced by a sample of the US population, measured using one utility instrument(the EuroQol-5D (EQ-5D)). These values will inform economic evaluations based on QALYs.

Methods

Data

We analyzed four years of Medical Expenditure Panel Survey (MEPS) data in which EQ-5D scores were collected. MEPS is a set of household-based, in-person interview surveys of the non-institutionalized US population conducted by the Agency for Healthcare Research and Quality, collecting data at five time points over a two-year span.26,27 This study used household component data from panels beginning in 2000, 2001 and 2002, plus EQ-5D responses collected in a supplemental paper questionnaire administered once annually in 2000–2003 to all MEPS panelists active at that time. The resulting data included all family medical condition data over five reporting periods (“rounds” 1–5) and two EQ-5D administrations in each of these three panels (at approximately rounds 2 and 4; see Technical Appendix for study design diagram). The EQ-5D score represents community-perspective utility for a health state described by the respondent completing the EQ-5D instrument, meaning the values that a representative sample of the general population would assign for that described health state.22 These values are recommended for use in societal perspective cost-effectiveness analysis.22,28

Our sample consisted of 24,188 adults, representing 14,043 households and including 11,867 children (EQ-5D data were collected from adults only; children supply household medical condition data for the analysis but are not included in the sample). Individuals with missing EQ-5D data were excluded, as were individuals in households where an ill person left the household before the second administration of the EQ-5D (643 adults in 447 households). MEPS data are publicly available and unidentified and approval from applicable Institutional Review Boards was granted.

Analysis

We used multivariable regression analysis to estimate the independent spillover effect of household members’ chronic conditions on an index adult’s EQ-5D score. We modeled the spillover effect in two ways for purposes of confirmation: (a) a “static” model predicting an adult’s EQ-5D score at the second administration as a function of household members’ pre-existing and newly-occurring chronic conditions; and (b) a “change-score” model predicting the change in an adult’s EQ-5D score between the first and second administration as a function of household members’ chronic conditions occurring in the intervening period. Both models controlled for other known predictors of individual utility that were available in the MEPS data (the index adult’s own chronic conditions, age (continuous), race (White), gender (female), marital status (married=1), and household income (“low household income” = annual income <US$20,000=1)), and household composition. Both models utilized the longitudinal nature of the MEPS data to predict the association between household chronic illness and individual utility.

For the “static” model, the dependent variable was the index adult’s EQ-5D score at the second administration (“EQ-5D time 2”). This variable was modeled in continuous form using Duan’s two-stage approach to account for the high frequency of 1.0 scores in the data.29 The main independent variables of interest were indicators for categories of chronic conditions among the index adult’s household members, representing conditions that could impose spillover effects on the index adult’s utility. Reported chronic conditions are coded by MEPS using three-digit International Statistical Classification of Diseases and Related Health Problems, ninth edition (ICD-9) coding (see Technical Appendix for ICD-9 code categorization). We defined chronic conditions as those with duration of 12 months or expected lasting physical impairment, with distinctions for pediatric and adult conditions, per Hwang.30 Disease categories without any reported chronic conditions or with a prevalence of less than 1% for children or adults in the sample were excluded from the regression analysis in order to maximize statistical power to detect effects. Chronic conditions were categorized as “existing” or “new” based on when the condition was first reported in MEPS: existing chronic conditions were those first reported in rounds 1 or 2 of MEPS, or within approximately the first 12 months of the panel; new chronic conditions were those first reported in round 3 of the panel, or just prior to the administration of the second EQ-5D, our dependent variable. Household members were defined as children (< 18 years of age) or adults (18+ years of age). Thus, each index adult in our analytic sample had indicator variables for existing and newly-occurring chronic conditions by ICD-9 category among child and adult household members.

For the confirmatory, “change-score” model, an EQ-5D difference score was created for each index adult (“EQ-5D difference”), defined as the EQ-5D score at the second administration minus the EQ-5D score at the first administration. This variable was truncated to 0.05 increments to create a discrete outcome with a symmetric and approximately normal distribution (albeit with a high peak at 0, indicating no change between administrations) for linear modeling. Since EQ-5D scores tend to cluster at distinct values the data can be considered approaching discrete, and our transformation makes the gaps between these distinct values more uniform. We conducted a sensitivity test by modeling the outcome with a negative binomial distribution with similar results (not presented here). This model included the same set of new and existing condition categories and control variables.

Regression analyses used general estimating equations (GEE) to control for clustering at the household level. Additional analyses tested for possible confounding of the spillover variables due to the occurrence of new chronic conditions in the index adult (as a result of the household members’ conditions) by comparing models including and excluding the index adult’s own newly-occurring conditions. These analyses yielded similar results for the spillover variables and therefore only the analyses including these variables are presented here. The primary analysis did not distinguish between one or more children or adults in a household, nor between one or more conditions in any ICD-9 category; stratified analyses investigated the spillover effect of multiple chronic conditions occurring simultaneously in the household, within adults, children, and both types of household members. Model fit was assessed for the logistic model using the Likelihood ratio test, and for the linear models with an R-squared statistic. All analyses were conducted using SAS version 9.2 (SAS Institute, Cary, North Carolina).

Results

The MEPS sample was designed to be representative of the US adult population, with a mean age of 45 years, 54% female, 64% non-Hispanic white, and 60% married (Table 1). Half of the individuals (50%) lived in a household with at least one child under 18 years, and 89% lived with at least one other adult. Chronic conditions were present in almost one-third of the adults in the sample (31%), with 37% of adults living in a household with another adult with a chronic condition. Most commonly reported adult chronic conditions were hypertension, diabetes mellitus, joint diseases and mental disorders (primarily depression). Among children, respiratory conditions (e.g., asthma and allergies) were most common. The mean EQ-5D preference weight score among our sample was 0.86. Approximately half (46.9%) of the sample reported an EQ-5D preference weight of 1.0, and the remainder reported scores from −0.11 to 0.86.

Table 1.

Sample characteristics, adults in 2000–2003 MEPS Panels with complete EQ-5D data (n=24,188)

Mean (sd) Number (%)
Age (years) 45.2 (17.1)
White, non-Hispanic 15,480 (64.0)
Female 13,120 (54.2)
Married 14,421 (59.6)
Low annual household income (< US$20,000) 4,232 (17.5)
Have at least one chronic condition (self) 7,501 (31.0)
Household contains:
≥ 1 child 12,175 (50.3)
≥ 1 other adult 21,963 (88.5)
≥ 1 child with a chronic condition 2,042 (8.4)
≥ 1 other adult with a chronic condition 9,165 (36.9)
EQ-5D score, range 0.86 (0.17), [−0.11–1.0]

All characteristics are from round 2 except for marital status (round 4) and EQ-5D score (2nd administration);

sd= standard deviation; EQ-5D=EuroQol 5-dimensions.

In our “static” multivariable analysis, controlling for the respondent’s own conditions and sociodemographic and household characteristics, we found an association between lower EQ-5D scores and the presence of certain chronic conditions among household members. For the first part of the two-part model, which predicts the odds ratio of the index adult having an EQ-5D score of 1.0 versus less than 1.0, existing mental and respiratory conditions among adults and children in the household, and musculoskeletal system diseases among adults in the household, were associated with a statistically significant odds ratios (ORs): for existing mental disorders among other adults in household the OR multiplier was 0.71 (95% CI: 0.64,0.79), for existing respiratory diseases among other adults 0.85 (0.75,0.97), for existing mental disorders among children in the household 0.72 (0.62 0.82), for existing respiratory diseases among children 0.88 (0.81,0.96), and for existing musculoskeletal diseases among other adults 0.83 (0.75,0.93) (Table 2a). Some newly-occurring chronic conditions in the household predicted a further reduction in the odds ratio for the index adult’s EQ-5D score: for new mental disorders among household adults the OR multiplier was 0.79 (0.65,0.97), and among children the OR multiplier was 0.64 (0.48,0.86), while other adults’ nervous/sensory system diseases had an OR of 0.76 (0.61,0.96), and other adults’ musculoskeletal system diseases an OR of 0.78 (0.65,0.95). We found the largest effect from the index adult’s own existing and new chronic conditions, such as an OR of 0.27 for existing mental disorders in one’s self (0.24,0.30) (Table 2a). A comparative summary of the associations due to household members’ chronic conditions is presented in Figure 1. Being married and having an increase in household annual income were associated with statistically significant higher odds ratio of reporting an EQ-5D score of 1.0, while increased age, female gender, and low household annual income were significantly associated with lower odds ratio.

Table 2.

a&b. Static, 2-stage GEE model predicting index adult’s EQ-5D score at second administration time point:

a. stage 1 logistic model: odds ratios and 95% confidence intervals predicting EQ-5D score = 1.0 (n=24,188)

Variable Odds ratio 95% confidence interval
Index adult’s characteristics:
Intercept 1.806 -
Age 0.975* 0.973, 0.977
Female 0.792* 0.751, 0.835
White, non-Hispanic 0.956 0.911, 1.004
Married 1.198* 1.129, 1.271
Low annual household income (<US$20,000/year) 0.481* 0.451, 0.514
Increase in annual household income over US $20,000 threshold 1.520* 1.417, 1.631
Household contains:
  Child <18 years 1.000 0.946, 1.057
  Another adult 0.830* 0.784, 0.878
Existing chronic conditions (first reported at least 6 months prior to 2nd EQ-5D):
  Self-neoplasms (tumors) 0.817* 0.669, 0.998
  Self-diseases of the endocrine, metabolic systems and immunity disorders 0.555* 0.504, 0.611
  Self-mental disorders 0.265* 0.237, 0.297
  Self-diseases of the nervous/sensory systems 0.570* 0.507, 0.641
  Self-diseases of the circulatory system 0.740* 0.687, 0.798
  Self-diseases of the respiratory system 0.631* 0.553, 0.720
  Self-diseases of the musculoskeletal system 0.282* 0.253, 0.316
  Other adult-neoplasms (tumors) 0.843 0.699, 1.016
  Other adult-diseases of the endocrine, metabolic systems, and immunity disorders 0.960 0.875, 1.054
  Other adult-mental disorders 0.710* 0.638, 0.790
  Other adult-diseases of the nervous/sensory systems 0.903 0.805, 1.013
  Other adult-diseases of the circulatory system 0.998 0.924, 1.078
  Other adult-diseases of the respiratory system 0.852* 0.746, 0.973
  Other adult-diseases of the musculoskeletal system 0.834* 0.752, 0.925
  Child-mental disorders 0.716* 0.623, 0.823
  Child-diseases of the respiratory system 0.879* 0.809, 0.956
Newly-occurring chronic conditions (first reported within 3 months of 2nd EQ-5D)
  Self-neoplasms (tumors) 0.589* 0.414, 0.839
  Self-diseases of the endocrine, metabolic systems and immunity disorders 0.663* 0.510, 0.863
  Self-mental disorders 0.297* 0.237, 0.373
  Self-diseases of the nervous/sensory systems 0.550* 0.435, 0.695
  Self-diseases of the circulatory system 0.465* 0.379, 0.570
  Self-diseases of the respiratory system 0.587* 0.418, 0.825
  Self-diseases of the musculoskeletal system 0.345* 0.284, 0.418
  Other adult-neoplasms (tumors) 1.036 0.735, 1.460
  Other adult-diseases of the endocrine, metabolic systems, and immunity disorders 0.940 0.735, 1.202
  Other adult-mental disorders 0.793* 0.649, 0.968
  Other adult-diseases of the nervous/sensory systems 0.763* 0.605, 0.961
  Other adult-diseases of the circulatory system 0.906 0.746, 1.101
  Other adult-diseases of the respiratory system 0.948 0.703, 1.279
  Other adult-diseases of the musculoskeletal system 0.781* 0.645, 0.945
  Child-mental disorders 0.644* 0.484, 0.857
  Child-diseases of the respiratory system 0.857 0.727, 1.010
b. Stage 2 linear model: predicting index adult’s EQ-5D score <1.0; coefficients and 95% confidence intervals (n=12,852)

Variable Regression
coefficient
95% confidence interval
Index adult’s characteristics:
Intercept 0.8308 0.8177, 0.8439
Age −0.0007* −0.0009, −0.0004
Female 0.0059* 0.0007, 0.0111
White, non-Hispanic 0.0182* 0.0124, 0.0240
Married 0.0209* 0.0145, 0.0274
Low annual household income (<US$20,000/year) −0.0695* −0.0785, −0.0605
Increase in annual household income over US$20,000 threshold 0.0401* 0.0316, 0.0486
Household contains:
  Child <18 years −0.0098* −0.0161, −0.0035
  Another adult −0.0259* −0.0350, −0.0168
Existing chronic conditions (first reported at least 6 months prior to 2nd EQ-5D):
  Self-neoplasms (tumors) −0.0208* −0.0401, −0.0015
  Self-diseases of the endocrine, metabolic systems and immunity disorders −0.0264* −0.0351, −0.0177
  Self-mental disorders −0.0718* −0.0819, −0.0617
  Self-diseases of the nervous/sensory systems −0.0466* −0.0584, −0.0348
  Self-diseases of the circulatory system −0.0129* −0.0202, −0.0056
  Self-diseases of the respiratory system −0.0415* −0.0547, −0.0282
  Self-diseases of the musculoskeletal system −0.0578* −0.0668, −0.0489
  Other adult-neoplasms (tumors) 0.0148* 0.0004, 0.0292
  Other adult-diseases of the endocrine, metabolic systems, and immunity disorders −0.0081 −0.0172, 0.0010
  Other adult-mental disorders −0.0129* −0.0228, −0.0029
  Other adult-diseases of the nervous/sensory systems −0.0040 −0.0142, 0.0061
  Other adult-diseases of the circulatory system 0.0005 −0.0066, 0.0076
  Other adult-diseases of the respiratory system 0.0018 −0.0099, 0.0135
  Other adult-diseases of the musculoskeletal system −0.0115* −0.0208, −0.0022
  Child-mental disorders −0.0190* −0.0330, −0.0050
  Child-diseases of the respiratory system 0.0074 −0.0010, 0.0158
Newly-occurring chronic conditions (first reported within 3 months of 2nd EQ-5D)
  Self-neoplasms (tumors) −0.0172 −0.0471, 0.0127
  Self-diseases of the endocrine, metabolic systems and immunity disorders −0.0375* −0.0654, −0.0097
  Self-mental disorders −0.0501* −0.0717, −0.0286
  Self-diseases of the nervous/sensory systems −0.0245* −0.0449, −0.0041
  Self-diseases of the circulatory system −0.0307* −0.0487, −0.0128
  Self-diseases of the respiratory system −0.0418* −0.0776, −0.0060
  Self-diseases of the musculoskeletal system −0.0419* −0.0585, −0.0252
  Other adult-neoplasms (tumors) −0.0060 −0.0372, 0.0253
  Other adult-diseases of the endocrine, metabolic systems, and immunity disorders 0.0006 −0.0216, 0.0228
  Other adult-mental disorders −0.0210* −0.0417, −0.0003
  Other adult-diseases of the nervous/sensory systems 0.0153 −0.0032, 0.0337
  Other adult-diseases of the circulatory system 0.0002 −0.0158, 0.0163
  Other adult-diseases of the respiratory system 0.0083 −0.0157, 0.0322
  Other adult-diseases of the musculoskeletal system −0.0286* −0.0486, −0.0085
  Child-mental disorders −0.0004 −0.0331, 0.0322
  Child-diseases of the respiratory system −0.0050 −0.0251, 0.0152

(Likelihood ratio test p<0.0001)

GEE=general estimating equation

*

= statistically significant at p<=0.05

Increase in income is a reported change between the two EQ-5D administrations of at least $1,000 over or under the $20,000 threshold (downward=−1, no change=0, upward=1)

(R2 =0.1445)

GEE=general estimating equation

*

= statistically significant at p<=0.05

Figure 1.

Figure 1

Static regression model results: stage 1 (logistic) and stage 2 (linear) models predicting association between respondent’s EQ-5D score and existing and new chronic conditions in other household members, by ICD9 category. Models are adjusted for respondents’ own chronic conditions and sociodemographic characteristics, and household characteristics (stage 1: n=24,188; stage 2: n=12,852).

In the second part of the two-stage model, which included only adults reporting EQ-5D scores less than 1.0 (46.9% of sample; n=12,852), chronic conditions among household members were less consistently associated with a lower EQ-5D score for the index adult, with only existing mental disorders among adults or children associated with a reduction in the index adult’s EQ-5D score (adults −0.013 (95% CI: −0.0.023, −0.003); children −0.019 (−0.033, −0.005)) and musculoskeletal diseases among adults −0.012 (−0.021, −0.002). Existing neoplasms (tumors) in other adults in the household were significantly associated with an increase in EQ-5D score (0.015, (0.0004, 0.029)). Newly-occurring mental disorders and musculoskeletal diseases among adults were significantly associated with larger decrements in index adults’ EQ-5D scores (−0.021 (−0.042, −.0003) and −0.029 (−0.049, −0.009), respectively) (Table 2b). The index adult’s own existing and newly occurring chronic conditions were consistently associated with a statistically significant lower EQ-5D score, ranging from a decrement of 0.013 for existing diseases of the circulatory system (−0.02, −0.006) to 0.072 for existing mental disorders (−0.082, −0.062; Table 2b).

Our change-score model showed a significant association between an occurrence of one chronic condition category among household members and an index adult’s change in EQ-5D score between measurement periods. While controlling for changes in individuals’ own conditions, sociodemographic characteristics, household characteristics, and all other chronic conditions in the household, the occurrence of new diseases of the musculoskeletal system among other adults in the household was significantly associated with a reduction in an index adult’s EQ-5D score by 0.007 (−0.012,−0.002) over time (Table 3). Some but not all categories of new conditions occurring for the index adult himself were significantly associated with a negative change in EQ-5D score over time.

Table 3.

Change-score, GEE model predicting difference in index adult’s EQ-5D scores between two administrations: EQ-5D score at second minus first administration (n=24,188)

Variable Regression
coefficient
95% confidence interval
Index adult’s characteristics:
Intercept 0.0058
Age −0.0001* −0.0002, −0.0001
Female 0 −0.0014, 0.0013
White, non-Hispanic 0.0011 −0.0006, 0.0028
Married 0.0016 −0.0003, 0.0035
Low annual household income (<US$20,000/year) −0.0010 −0.0041, 0.0020
Increase in annual household income over US$20,000 threshold 0.0011 −0.0018, 0.0040
Household contains:
  Child <18 years −0.0014 −0.0033, 0.0005
  Another adult 0.0001 −0.0027, 0.0028
Existing chronic conditions (first reported at least 6 months prior to 2nd EQ-5D):
  Self-neoplasms (tumors) −0.0039 −0.0099, 0.0022
  Self-diseases of the endocrine, metabolic systems and immunity disorders 0.0003 −0.0026, 0.0033
  Self-mental disorders 0.0028 −0.0007, 0.0063
  Self-diseases of the nervous/sensory systems 0.0001 −0.0036, 0.0038
  Self-diseases of the circulatory system 0.0002 −0.0021, 0.0025
  Self-diseases of the respiratory system 0.0029 −0.0016, 0.0074
  Self-diseases of the musculoskeletal system 0.0019 −0.0013, 0.0050
  Other adult-neoplasms (tumors) −0.0028 −0.0076, 0.0020
  Other adult-diseases of the endocrine, metabolic system, and immunity disorders −0.0010 −0.0038, 0.0019
  Other adult-mental disorders 0.0031 −0.0002, 0.0064
  Other adult-diseases of the nervous/sensory systems −0.0019 −0.0050, 0.0011
  Other adult-diseases of the circulatory system 0.0006 −0.0016, 0.0028
  Other adult-diseases of the respiratory system 0.0009 −0.0027, 0.0046
  Other adult-diseases of the musculoskeletal system −0.0021 −0.0051, 0.0010
  Child-mental disorders −0.0012 −0.0062, 0.0039
  Child-diseases of the respiratory system 0.0036* 0.0007, 0.0066
Newly-occurring chronic conditions (first reported within 3 months of 2nd EQ-5D)
  Self-neoplasms (tumors) −0.0130* −0.0248, −0.0013
  Self-diseases of the endocrine, metabolic systems and immunity disorders 0.0001 −0.0104, 0.0105
  Self-mental disorders 0.0010 −0.0071, 0.0090
  Self-diseases of the nervous/sensory systems −0.0057 −0.0126, 0.0012
  Self-diseases of the circulatory system −0.0054 −0.0120, 0.0012
  Self-diseases of the respiratory system −0.0136* −0.0251, −0.0021
  Self-diseases of the musculoskeletal system −0.0082* −0.0143, −0.0022
  Other adult-neoplasms (tumors) 0.0003 −0.0097, 0.0103
  Other adult-diseases of the endocrine, metabolic systems, and immunity disorders 0.0027 −0.0047, 0.0102
  Other adult-mental disorders −0.0001 −0.0069, 0.0066
  Other adult-diseases of the nervous/sensory systems −0.0034 −0.0099, 0.0030
  Other adult-diseases of the circulatory system −0.0006 −0.0065, 0.0053
  Other adult-diseases of the respiratory system −0.0008 −0.0130, 0.0114
  Other adult-diseases of the musculoskeletal system −0.0068* −0.0117, −0.0018
  Child-mental disorders 0.0014 −0.0106, 0.0133
  Child-diseases of the respiratory system 0.0011 −0.0050, 0.0073

(R2 =0.005)

GEE=general estimating equation

*

= statistically significant at p<=0.05

Households with multiple other adults or multiple children with chronic conditions totaled less than 1% of the analytic sample, hence the effect of multiple chronic conditions was omitted from our analysis.

Discussion

Our findings provide empiric, population-level evidence of spillover effects of certain chronic conditions onto other household members. In a representative sample of the US population, and controlling for factors known to affect health utility, adults living in households with other family members chronically ill with mental health, respiratory and musculoskeletal conditions were more likely to report deficiencies in their own health utility, and to experience lower utility scores at the occurrence of chronic illness in the household. Though these effect sizes were small, their existence in a US population sample of adults provides compelling evidence that utility losses can be attributed to spillover effects from household members’ illnesses. Our findings confirmed that while one’s own health and income are the most important contributors to EQ-5D utility scores, household members’ health can exert a small effect on one’s utility above and beyond these individual-level characteristics.

The importance of spillover effects in cost effectiveness analysis and medical decision making has been noted.3,21,3134 Evaluation of the burden of disease or the effectiveness of interventions would be incomplete without consideration of the full spectrum of effects of disease on society, including both the affected individual (i.e., patient) and others.22 The questions raised by this acknowledgement are two-fold: how to measure spillover effects and how to incorporate them into analyses.35 How to measure effects has been addressed empirically and conceptually, with somewhat less attention devoted to how to incorporate effects. Empiric estimates of the spillover utility “toll” range from a high of 0.5 for family caregivers of cognitively impaired elderly persons36, to 0.07 for parents of children with activity limitations37 and 0.06 for family caregivers of elderly persons with dementia, stroke and other diseases.38 Some studies have failed to detect any effect, including samples of caregivers of individuals with depression39, rheumatoid arthritis40, and Alzheimer’s disease.41 Our results are near the lower end of this spectrum, possibly due to our population sample. Methods of measuring spillover effects include existing utility measures as we used with the EQ-5D, and instruments designed specifically to measure spillover, such as the Carer-Qol.42 Consensus largely holds at this point that spillover effects exist and should be included in evaluations.

Methods of inclusion of spillover effects into evaluations have yet to be formally compared. The calculation of QALYs at the family level may involve the combination of individual utilities, or an entirely separate family-based quality of life weighting measure. Evidence from the literature on combining utilities may be informative in this area, suggesting the inadequacy of simple summation across or within individuals.43 Consideration of the possibility of utility values outside of the 0–1 scale, both below zero and in excess of 1.0, may suggest ways in which an individual’s utility could be a combination of his/her own value and surrounding individuals’.44 The question of integration of spillover effects into cost-utility analysis remains important to the field, particularly as the evidence for the existence of these effects and their magnitude mounts.

Our results add evidence to the empiric literature demonstrating the existence of spillover. The caveats accompanying our findings show a general bias toward the null hypothesis of no effect, so may in fact add credibility to our conclusions. While most previous spillover literature has focused on specific diseases and specific caregiver populations, our study looked at spillover effects across conditions at the population level. Thus our sample included anyone living in a household with a chronically ill individual, regardless of caretaking responsibilities or familial ties. Our data also prevented consideration of ill family members who were not physically co-located with our sample adults. Our sample was thus broad in capturing spillover effects beyond caretaking, and exclusive of potentially important caregiver relationships, both of which would serve to bias our results toward underestimation of a spillover toll.

Our measure, the EQ-5D, is widely used and provides community-perspective utility values, useful for societal-perspective cost-utility analysis. The EQ-5D has acknowledged limitations in scope and depth, however, that may result in an underestimation of the effect of one person’s illness on another.45 Spillover effects on caregivers may evade the domains included in health related quality of life, occupying an entirely different “evaluative space” beyond that inhabited by evaluations focused on patients.46 It has also been suggested that family members and caretakers may find satisfaction from caretaking or experience emotional/spiritual benefits from handling adversity.7,9 Both of these suggestions imply that the EQ-5D may not fully capture the spillover effect, regardless of direction. Our findings persisted, however, despite these limitations in measurement inherent to our data, suggesting tenacity in our results.

Our analysis used complementary and confirmatory modeling approaches to test the strength and persistence of our findings. Our static model showed a clear though small spillover association between the existence of certain chronic conditions in a household and adults’ health utility. Our change-score analysis was designed to test for the association between an incident chronic condition among household members and individuals’ utility over a short time span, and found spillover for only one category of chronic conditions. We explored adaptation to spillover through the inclusion of both newly-occurring and pre-existing conditions in our analysis, and found some suggestive evidence that new conditions had a larger spillover effect than older ones, as is seen in individual-level adaptation to disease.47 (One spurious but possibly adaptive result was seen in our static model for adult household members’ existing neoplasms for individuals with EQ-5D scores below 1.0: these cancers had a significant positive spillover effect, suggesting that this condition increases the HRQOL of surrounding individuals. This result was not seen in newly occurring cancers among household members, nor in the index adult’s own existing cancer, though could possibly be evidence of adaptation to cancer.) Model caveats include design and data issues. We controlled for individual’s own conditions to exclude the possibility that that people with chronic conditions gravitate together in households, though our results are correlations not causal effects. The lack of substantial results in our change-score analysis compared to the static model reveals possible limitations in our study design, including the short time-frame between EQ-5D measures in the MEPS survey. This interim may have been insufficient to capture changes in utility in response to the incidence of a new condition in the household. Moreover, there is some temporal uncertainty in MEPS data collection, in that each interview is conducted within a 4–5 month time span while the EQ-5D instrument is included in a supplemental questionnaire mailed during a specific span. We categorized conditions conservatively to protect against errors in data temporality. In addition, MEPS does not contain the end date for chronic conditions, and we assumed that each reported conditions lasted until the end of our analytic time frame; this assumption may over-estimate the presence of chronic conditions in each household biasing our analysis against detection of an effect. And finally, most of our results fall below the level of minimally important differences for utilities48, though our goal was not to demonstrate clinical significance but rather analytic significance. Small utility effects may be relevant for policy decisions if accumulated across a population, or compared with similarly small differences. In sum, the combination of analyses that we conducted sheds additional light on the complex question of the existence of spillover effects for chronic conditions, and the presence of an effect in different modeling approaches and under different assumptions implies a strong case for our conclusions about the importance of this factor in health utility.

In conclusion, cost-effectiveness and comparative effectiveness research are informed by these results, suggesting that benefits from interventions should be measured across the family unit of the ill individual in order to fully capture the effects of a health intervention. Costs attributable to other family members are routinely included in analyses, and recommendations suggest the inclusion of all benefits, regardless of to whom they accrue.22 For conditions where there is substantial spillover, such as children’s illnesses, consideration should be given to evaluating HRQOL data from at minimum the primary family caretaker in addition to the affected “patient.” Nearly all the spillover estimates we observed inferred a negative effect from having an ill individual in the household, though positive effects have been observed in a few instances. A remaining question is how to incorporate our spillover effects into evaluations of interventions31, which would allow for a more complete picture of benefits accrued relative to resources expended.

Supplementary Material

Appendix Fig A
Appendix Fig B
Technical Appendix

Acknowledgments

The authors are grateful for research assistance provided by Gail Strickler, and programming provided by Galina Zolotusky and Acham Gebremariam.

This work was supported by awards numbers 5R01NR011880 from the National Institute of Nursing Research and 7 K02 HS014010 from the Agency for Health Care Research and Quality, both to EW. The content is solely the responsibility of the authors and does not necessarily represent the official views of the Agency for Health Care Research and Quality, the National Institute of Nursing Research, or the National Institutes of Health.

Footnotes

Preliminary results from this work were presented at the 33rd Annual Meeting of the Society for Medical Decision Making, Chicago, IL, October, 2011.

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Supplementary Materials

Appendix Fig A
Appendix Fig B
Technical Appendix

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