Abstract
PURPOSE In the United States, children who have a usual source of care (USC) have better access to health care than those who do not, but little is known about how parental USC affects children’s access. We examined the association between child and parent USC patterns and children’s access to health care services.
METHODS We undertook a secondary analysis of nationally representative, cross-sectional data from children participating in the 2002–2007 Medical Expenditure Panel Survey (n = 56,302). We assessed 10 outcome measures: insurance coverage gaps, no doctor visits in the past year, less than yearly dental visits, unmet medical and prescription needs, delayed care, problems getting care, and unmet preventive counseling needs regarding healthy eating, regular exercise, car safety devices, and bicycle helmets.
RESULTS Among children, 78.6% had a USC and at least 1 parent with a USC, whereas 12.4% had a USC but no parent USC. Children with a USC but no parent USC had a higher likelihood of several unmet needs, including an insurance coverage gap (adjusted risk ratio [aRR] 1.33; 95% confidence interval [CI], 1.21–1.47), an unmet medical or prescription need (aRR 1.70; 95% CI 1.09–2.65), and no yearly dental visits (aRR 1.12; 95% CI 1.06–1.18), compared with children with a USC whose parent(s) had a USC.
CONCLUSIONS Among children with a USC, having no parent USC was associated with a higher likelihood of reporting unmet needs when compared with children whose parent(s) had a USC. Policy reforms should ensure access to a USC for all family members.
INTRODUCTION
The association between having a usual source of care (USC) and improved access to health care services is well established in both adult and child populations.1–10 Children with a USC have more consistent access to health care services,2,9,11–15 which likely contributes to better overall health outcomes.16,17 According to recent estimates, however, approximately 19% of adults and nearly 10% of children in the United States do not have a USC. Safety-net services are oversubscribed, and the availability of primary care is widely disparate,18 leaving many families with few options for maintaining a relationship with a USC.
Although previous research clearly supports the importance of the relationship between a child having a stable USC and that individual child’s access to and utilization of recommended care,1–10,19 little is known about whether a child’s receipt of health care is associated with his or her parents’ USC status. In fact, to our knowledge, no previous studies describe child-parent USC patterns or measure how parental USC status affects a child’s access to health care services. Further, the effect a child’s USC status has on access to health care has been documented without accounting for parental USC status.
It is known that children with health insurance have higher odds of unmet health care needs if their parents are uninsured.20–23 In addition, child health care service utilization patterns are highly associated with maternal utilization patterns.24,25 These relationships underscore the need to explore other possible mechanisms through which parental factors affect children’s access to care. Specifically, this study examines the association between child-parent USC patterns and children’s access to health care services. Our central research question was whether a child’s access to health care services varies in association with whether at least 1 parent has a USC. We hypothesized that children of parents without a USC would have higher rates of unmet health care needs when compared with children whose parents have a USC, independent of the child’s USC status.
METHODS
This study was a secondary analysis of data from the Medical Expenditure Panel Survey-Household Component (MEPS-HC).26 MEPS-HC collects data from a subsample of households from the National Health Interview Survey in the United States and utilizes a stratified and clustered random sample with weights that produce nationally representative estimates for the civilian, noninstitutionalized population.27–29
MEPS data are reported in yearly files, combining data from 2 overlapping panels for each year (eg, data for 2002 combines the overlapping panels of 2001–2002 and 2002–2003); the MEPS design and methodology are reported elsewhere.26–29 Each year of data constitutes a nationally representative sample, and pooling the data produces average annual estimates. We combined data from 2002–2007 and included all children aged 17 years and younger with positive full-year weights who had at least 1 parent residing in the same household, and for whom both the child’s and at least 1 parent’s USC status could be ascertained (n = 56,302), weighted to a population of nearly 70.9 million children.
We linked each child to 1 or both parents and then constructed child-parent USC variables (n = 17,612 linked to 1 parent; n = 38,690 linked to 2 parents). This linkage is possible for biological parents, adopted parents, and step-parents; MEPS does not include similar variables for linking foster parents or nonparent guardians.30 The sample size of 56,302 children excludes 2,049 children with no parent identified in the household and an additional 437 children for whom USC status could not be reliably ascertained for the child or parent(s).
Dependent Variables
Asking parents (or caregivers) about their perceptions of a child’s unmet need for care is one of the most common ways to assess unmet need.31 Accordingly, we used MEPS-HC items that pertained to parent-reported unmet health care needs to construct the following 6 unmet need variables: (1) insurance coverage gaps during the year, (2) no doctor visits in the past year, (3) less than yearly dental visits, (4) unmet medical and prescription needs, (5) delayed care, and (6) problems getting care. Yearly doctor visits were chosen because the American Academy of Pediatrics recommends yearly health care visits up to 21 years.32 For child dental care, the American Academy of Pediatric Dentistry recommends that yearly dental visits begin at the time of the first tooth and no later than 12 months of age.33 The delayed care variable combined MEPS-HC parental reports that a child did not always get care as soon as was wanted for an illness, injury, or condition that needed care right away and that a child did not always get an appointment for routine health care as soon as was wanted. The variable pertaining to problems getting care combined 3 MEPS-HC questions regarding a child having problems obtaining needed medical care, tests, prescriptions, referrals, or other treatments.
Because receipt of age-appropriate preventive services has an important impact on long-term health,34 we also constructed 4 composite outcomes pertaining to whether a child had not received anticipatory guidance regarding the importance of healthy eating, regular exercise, use of car safety devices (ie, seat belts, safety car seats, booster seats), and use of helmets while riding a bicycle or tricycle. We then assessed whether the child or parent had missed receiving guidance regarding at least 1 of the preventive counseling items in the past 2 years and during the child’s lifetime. Lastly, we assessed whether the child had not received guidance regarding any of the 4 preventive counseling items (missing all 4) in the past 2 years and during the child’s lifetime. Our analyses of the preventive counseling items excluded the 5,700 children in the MEPS-HC population that was younger than 2 years, because these questions were asked only of children aged 2 to 17 years.
Independent Variables
Among the MEPS-HC child sample (n = 56,302), we assessed the cross-sectional USC status of the child and parent(s) as the primary independent variable. We then created 6 mutually exclusive child-parent USC patterns (Table 1). These 6 groups were collapsed into 4 groups for univariate and multivariate analyses: (1) the child and 1 or both parent(s) have a USC (USC: yes child/yes parent[s]), (2) the child has a USC and 1 or both parents do not have a USC (USC: yes child/no parent), (3) the child does not have a USC and 1 or both parents have a USC (USC: no child/yes parent[s]), and (4) neither child nor parent has a USC (USC: no child/no parent).
Identification of the covariates that might influence children’s access to health care was guided by the conceptual model designed by Aday and Andersen35,36 and by MEPS-HC variables shown to be associated with children’s unmet health care needs.22 We used 2-tailed χ2 analyses to test univariate associations between these variables and each of the outcome variables. Ten independent variables were associated with at least 1 outcome (P <.10): household income, child’s age, child’s race/ethnicity, family composition, parental education, parental employment, region of residence, child’s insurance status, parent’s insurance status, and child’s health status. Thus, all covariates were included in logistic regression models with the exception of parental employment, which was found to have significant collinearity with parental education and household income variables.
Specifically, the household income groups were based on the MEPS-HC–constructed variable that divides families into 5 income groups based on earnings as a percentage of the federal poverty level, and in 2007 the federal poverty level for a family of 4 was $20,650.37 We created 1 child race/ethnicity variable that was based on self-reported responses to standard options provided by MEPS interviewers. Family composition refers to whether the child could be linked to 1 parent or 2 parents residing in the same household (it does not account for biological relationship between parent and child or the marriage status between the 2 parents).
Analyses
We determined the prevalence of different child-parent USC patterns. We then used 2-tailed χ2 tests to ascertain univariate associations between covariates and each of the 4 child-parent USC subgroups, and univariate associations between each of the child-parent subgroups and unmet need and preventive counseling outcomes. Finally, we used a series of logistic regression models to assess the adjusted associations between the 4 child-parent USC subgroups and the outcomes. Models were first built for the outcome of having no doctor visits in the past 12 months using forward selection modeling techniques. Covariates selected in this model were used for all remaining outcomes to achieve consistency in our examination and to facilitate comparisons of results across models, with 1 exception—child’s and parent’s insurance status were excluded from the model that assessed insurance coverage gap as the outcome. We reported measures of association as adjusted risk ratios (aRRs).38
We used SUDAAN 10.0.1 (Research Triangle Institute, Research Triangle Park, North Carolina) for all statistical analyses to account for the complex sampling design of the MEPS; α level was set at .05 for all multivariable analyses a priori. This study protocol was reviewed by the Oregon Health & Science University Institutional Review Board, which deemed the study exempt because the MEPS-HC is publicly available.
RESULTS
Among the study population of children, 78.6% had a USC and at least 1 parent had a USC, 12.4% had a USC but neither parent had a USC, 2.5% had no USC but at least 1 parent had a USC, and 6.5% had no USC and no parent had a USC (Table 1).
All characteristics of children and their parents were significantly different across the 4 child-parent USC subgroups (P <.05; Table 2). Most notably, the USC: yes child/yes parent(s) subgroup had the highest percentage of families earning more than 400% of the federal poverty level. A higher percentage of the USC: no child/no parent subgroup was Hispanic compared with all children. Children with unstable insurance coverage were also more likely to be in the USC: no child/no parent subgroup. Other characteristics disproportionately associated with the USC: no child/no parent subgroup included older age of the child, single-parent households, having parent(s) who did not complete high school, and having uninsured parents.
The percentage of children with unmet needs increased sharply as child-parent USC patterns deviated from the concordant pattern of both child and parent(s) having a USC (Table 3). In all cases, the USC: yes child/yes parent(s) subgroup had the lowest rates of unmet health care needs; children in the USC: no child/no parent subgroup had the highest rates. In univariate analyses, the USC: yes child/no parent subgroup had higher percentages of unmet health care needs than did the USC: yes child/yes parent(s) subgroup for all outcomes examined. The same pattern held true for the 4 preventive counseling items.
In multivariate analyses, the higher rates of unmet needs among children in the USC: yes child/no parent subgroup when compared with the USC: yes child/yes parent(s) subgroup achieved statistical significance in almost all cases. As shown in Table 4, the USC: yes child/no parent subgroup had a higher likelihood of an insurance coverage gap (aRR = 1.33; 95% confidence interval [CI], 1.21–1.47), having no doctor visits in the past 12 months (aRR = 1.11; 95% CI, 1.02–1.21), less than yearly dental visits (aRR = 1.12; 95% CI, 1.06–1.18), and unmet medical or prescription needs (aRR = 1.70; 95% CI, 1.09–2.65), when compared with the USC: yes child/yes parent(s) subgroup.
In Table 5, the USC: yes child/no parent subgroup was also at higher risk of having not received preventive counseling when compared with the USC: yes child/yes parent(s) subgroup in 3 of the 4 models. Although group differences in Tables 4 and 5 were not statistically significant for all outcomes, the observed trends suggest increased vulnerability as USC patterns deviated from both child and parent(s) having a USC.
DISCUSSION
In aggregated cross-sectional MEPS-HC data from 2002 to 2007, 9% of children (aged 17 years and younger and living with at least 1 parent) in the United States had no USC, and more than 18% of children had no parent in the household with a USC. In this study, the largest differences in children’s receipt of necessary health care were between children with a USC and those without a USC, which confirms previous evidence about the importance of a USC for children.1,3–9 This study revealed the new finding that parental USC status is also associated with children’s receipt of health care services, regardless of child’s USC status. Among children with a USC, those whose parent(s) lacked a USC had a higher likelihood of experiencing unmet health care needs.
Our previous work has shown that insured children with uninsured parents have higher odds of unmet health care and preventive counseling needs when compared with insured children whose parents are insured.39 We have also shown that adults and children are both more likely to have unmet health care needs when they lack a USC, even if they have health insurance.40,41 In this study, we report on the importance of a USC for both parent and child, even while controlling for parental and child health insurance.
Policy Implications
The results of this study—showing that a child’s receipt of recommended health care services is associated not only with their own access to a USC but also their parents’ access to a USC—highlight the need to broaden the focus beyond expansions in the child health care workforce and quality improvements in child health care to consider the role that parental access to a USC plays in ensuring access to health care services for children. There is a clear need to advocate for policy changes that improve access to a USC for all family members. The Patient Protection and Affordable Care Act (PPACA) has a provision to increase the number of primary care clinicians,42 which is a step in the right direction. Specifically, the PPACA will provide resources for increasing training through additional primary care residency programs and numbers of nurse practitioners, as well as training more physician assistants to work in primary care settings. Scholarship and loan repayment programs will also be implemented for primary care clinicians who choose to work in underserved areas.43 Another possible policy change that could affect USC continuity is ensuring that a change in health insurance plans does not mean a change in one’s primary care clinician or site.
Furthermore, as more children and parents have discordant insurance coverage patterns (eg, child covered by public insurance, parents covered by employer-based private insurance),44 the need for both child and parents to have a USC will become even more important. Further studies are needed to determine which aspects of care are most likely to improve when everyone in the family has a USC, and whether child-parent USC concordance might mitigate the impact of fragmented family insurance coverage.
Practice Implications
In addition to advocating for the important policy changes outlined above, clinicians can develop practice-based interventions to assist parents in finding a stable USC for their children and for themselves. Some clinicians, such as family physicians and general practitioners, are in the unique position of providing primary care to all members of the same family. The patient-centered medical home holds promise as a model that can focus on coordinating care for entire families.10
Even clinicians who see only children or only adults could perform similar interventions if they are part of larger centers that can provide coordinated care for all family members. Interventions could also involve methods to track USC status for all family members. With widespread and expanding implementation of electronic health record systems, such processes and potential interventions could be computerized, and family records could be linked across USC sites.
Limitations
Although the MEPS-HC is representative of the civilian, noninstitutionalized population in the United States, the observational nature of the survey, as well as the cross-sectional analysis of the data, limits causal inferences. In addition, secondary analyses are limited by existing data. For example, we could obtain only the USC status and other items (ie, education, employment, insurance status) from parents residing in the respondent household. As with all studies that rely on self-report (or parental report), response bias is also a possibility. For example, a parent’s report regarding his or her child’s health care patterns may be biased because of the belief that a child’s unmet needs reflect poorly on the parents. We did not measure type of USC or assess the comprehensive nature of the USC to determine whether the USC met the criteria needed to be considered a medical home. We did not investigate the type of health insurance or the effect that a specific type of plan may have had on receipt of health care services. Lastly, it is possible that parents do not have a USC because they do not believe that access to the health care system ensures health for their children or themselves and not because they cannot obtain one.
When parents lack a USC, their child typically receives fewer recommended health care services and experiences more unmet needs regardless of the child’s USC and insurance status. Ensuring better access to necessary health care services will require comprehensive policy reforms that make it easier for all individuals to find and maintain a USC. Keeping the entire family in mind when crafting any new reforms will be essential to achieving a sustainable health care system and the best possible health outcomes for our children.
Acknowledgements
We wish to acknowledge the thousands of individuals who participated in the MEPS.
Footnotes
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Conflicts of interest: authors report none.
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Funding support: This project was directly supported by grants 1 K08 HS16181 and 1 R01 HS018569 from the Agency for Healthcare Research and Quality (AHRQ) and the Oregon Health & Science University Department of Medicine. This publication received indirect support from the Oregon Clinical and Translational Research Institute (OCTRI); grant number UL1 RR024140 from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH), and NIH Roadmap for Medical Research.
- Received for publication March 8, 2011.
- Revision received May 19, 2011.
- Accepted for publication June 22, 2011.
- © 2011 Annals of Family Medicine, Inc.