Measuring family HRQoL spillover effects using direct health utility assessment.

Lisa A Prosser, Kara Lamarand, Acham Gebremariam, Eve Wittenberg
Author Information
  1. Lisa A Prosser: Child Health Evaluation and Research Unit, Division of General Pediatrics, University of Michigan Health System, Ann Arbor, MI (LAP, KL, AG)
  2. Kara Lamarand: Child Health Evaluation and Research Unit, Division of General Pediatrics, University of Michigan Health System, Ann Arbor, MI (LAP, KL, AG)
  3. Acham Gebremariam: Child Health Evaluation and Research Unit, Division of General Pediatrics, University of Michigan Health System, Ann Arbor, MI (LAP, KL, AG)
  4. Eve Wittenberg: Center for Health Decision Science, Harvard School of Public Health, Boston, MA (EW)

Abstract

BACKGROUND: Applications of cost-effectiveness analysis do not typically incorporate effects on caregiver quality of life despite increasing evidence that these effects are measurable.
METHODS: Using a national sample of US adults, we conducted 2 cross-sectional surveys during December 2011 and January 2012. One version asked respondents to value their own experience as the family member of a person with a chronic illness (experienced sample), and the other version asked respondents to value hypothetical scenarios describing the experience of having a family member with a chronic illness (community sample). Conditions included Alzheimer's disease/dementia, arthritis, cancer, and depression. Using standard gamble questions, respondents were asked to value the spillover effects of a family member's illness. We used regression analysis to evaluate the disutility (loss in health-related quality of life) of having a family member with a chronic illness by condition and relationship type, controlling for the respondent's own conditions and sociodemographic characteristics.
RESULTS: For the experienced sample (n = 1389), regression analyses suggested that greater spillover was associated with certain conditions (arthritis, depression) compared with other conditions (Alzheimer's disease, cancer). For the community sample (n = 1205), regression analyses indicated that lower spillover was associated with condition (cancer) but not the type of relationship with the ill family member (parent, child, spouse).
CONCLUSIONS: The effects of illness extend beyond the individual patient to include effects on caregivers of patients, parents of ill children, spouses, and other close family and household members. Cost-effectiveness analyses should consider the inclusion of health-related quality of life spillover effects in addition to caregiving time costs incurred by family members of ill individuals.

Keywords

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Grants

  1. K02 HS014010/AHRQ HHS
  2. R01 NR011880/NINR NIH HHS
  3. 5R01NR011880/NINR NIH HHS

MeSH Term

Adolescent
Adult
Aged
Caregivers
Chronic Disease
Cost of Illness
Cost-Benefit Analysis
Cross-Sectional Studies
Family
Female
Health Status
Humans
Male
Middle Aged
Quality of Life
Regression Analysis
Socioeconomic Factors
United States
Young Adult

Word Cloud

Created with Highcharts 10.0.0familyeffectssampleillnessspilloverqualitylifememberanalysisaskedrespondentsvaluechroniccancerregressionhealth-relatedconditionsanalysesillcost-effectivenessUsingversionexperienceexperiencedcommunityAlzheimer'sarthritisdepressionconditionrelationshiptypen=associatedcaregiversmembershealthutilityBACKGROUND:ApplicationstypicallyincorporatecaregiverdespiteincreasingevidencemeasurableMETHODS:nationalUSadultsconducted2cross-sectionalsurveysDecember2011January2012OnepersonhypotheticalscenariosdescribingConditionsincludeddisease/dementiastandardgamblequestionsmember'susedevaluatedisutilitylosscontrollingrespondent'ssociodemographiccharacteristicsRESULTS:1389suggestedgreatercertaincompareddisease1205indicatedlowerparentchildspouseCONCLUSIONS:extendbeyondindividualpatientincludepatientsparentschildrenspousesclosehouseholdCost-effectivenessconsiderinclusionadditioncaregivingtimecostsincurredindividualsMeasuringHRQoLusingdirectassessment

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