Predictors of receiving therapy among very low birth weight 2-year olds eligible for Part C early intervention in Wisconsin
© McManus et al.; licensee BioMed Central Ltd. 2013
Received: 14 August 2012
Accepted: 2 July 2013
Published: 11 July 2013
The Individuals with Disabilities Education Act (Part C) authorizes states to establish systems to provide early intervention services (e.g., therapy) for children at risk, with the incentive of federal financial support. This study examines family and neighborhood characteristics associated with currently utilizing physical, occupational, or speech therapy among very low birthweight (VLBW) 2-year-old children who meet Wisconsin eligibility requirements for early intervention services (EI) due to developmental delay.
This cross-sectional analysis used data from the Newborn Lung Project, a regional cohort study of VLBW infants hospitalized in Wisconsin’s newborn intensive care units during 2003–2004. We included the 176 children who were age two at follow-up, and met Wisconsin state eligibility requirements for EI based on developmental delay. Exact logistic regression was used to describe child and neighborhood socio-demographic correlates of parent-reported receipt of therapy.
Among VLBW children with developmental delay, currently utilizing therapy was higher among children with Medicaid (aOR = 5.3, 95% CI: 1.3, 28.3) and concomitant developmental disability (aOR = 5.2, 95% CI: 2.1, 13.3) and lower for those living in a socially more disadvantaged neighborhood (aOR=0.48, 95% CI: 0.21, 0.98, per tertile).
Among a sample of VLBW 2-year olds with developmental delays who are EI-eligible in WI, 4 out of 5 were currently receiving therapy, per parent report. Participation in Medicaid positively influences therapy utilization. Children with developmental difficulties who live in socially disadvantaged neighborhoods are at highest risk for not receiving therapy.
KeywordsVery low birth weight Early intervention Physical therapy Neighborhood disadvantage
Children born very low birth weight (<1,500 grams, VLBW) are at heightened risk for significant developmental difficulties [1, 2]. To mitigate disability associated with very low birth weight, the World Health Organization and the March of Dimes  advocate for bolstering infant and child health and education initiatives (e.g., early intervention) for all children born very low birth weight.
In the U.S, the Individuals with Disabilities Education Act (IDEA), Part C, authorizes states to establish systems to provide early intervention (EI) services for children with developmental delays and disabilities, with the incentive of federal financial support . EI is not a single program, but rather includes different packages of services that vary within and across states with regard to delivery models and provider disciplines . Due to the flexibility of EI service delivery models, measuring which children receive what type of EI services is difficult. To address this methodologic challenge, we focus our study on a narrow aspect of EI service delivery –physical, occupational, or speech therapy. Indeed, data from the National Early Intervention Longitudinal Study (NEILS), an observational cohort of children enrolled in over 20 EI programs across the United States, suggests that 14% of parents report wanting more physical, occupational, or speech therapy services for their children . This suggests that research focusing on predictors of therapy utilization among EI-eligible children is justified to better understand, in a sample of infants at high risk for poor developmental outcomes, what proportion receives therapy services. Moreover, some studies suggest that therapy services may improve cognitive and motor skills among very low birth weight infants [7, 8]. Thus, understanding predictors of therapy services among this vulnerable population has important clinical and programmatic implications. For example, given the recent national evidence suggesting overall difficulties in access to EI [9, 10], shedding light on predictors of a specific aspect of EI services (i.e., therapy) seems critical to improving our understanding of access disparities.
We focus our inquiry on specific therapy services among a sample of VLBW infants eligible for EI in Wisconsin. Our assumption is that EI is the most common source of physical, occupational, and speech therapy services. Thus, our results about therapy services may translate to predictors of EI therapy since we restrict our inquiry to an EI-eligible population. However, the extent to which our results capture therapy services received outside of EI (e.g., clinic-based therapies) among this high-risk, EI-eligible sample might suggest barriers to accessing EI as these vulnerable young children should be (i.e., according to IDEA mandates) receiving EI-based versus clinic-based therapy.
As summarized briefly below, health insurance, race, and socioeconomic status have all been shown to be associated with use of developmental and therapeutic services. Although there is some evidence about the role of neighborhood socioeconomic context as a predictor of use of developmental and therapeutic services, there has been less attention to this potentially important contextual factor.
Comprehensive health insurance for low-income children is provided through state Medicaid programs . Children’s Medicaid mandates Early and Periodic Screening, Diagnosis, and Treatment (EPSDT) to meet the unique physical, emotional, and developmental needs of low income children . The role of Medicaid in facilitating access to therapy services for very young children is not clear. While some previous studies suggest children enrolled in Medicaid have fewer unmet therapy needs [13, 14] than those with private insurance, other studies suggest Medicaid enrolled children are less likely to access EI [10, 15].
In theory, insurance status (Medicaid participation versus having private insurance) should not be expected to influence therapy utilization for infants and toddlers eligible for early intervention since eligibility for early intervention is not contingent on health insurance access. However, in recent years, financing mechanisms  for early intervention have evolved to include more third-party billing and rising family fees, which are waived for children enrolled in Medicaid. Given the current financial crisis of early intervention programming  understanding the influence of source of insurance on therapy utilization among children eligible for early intervention has important implications for potentially improving efficiency of early intervention service delivery.
Research consistently shows that poor and minority children are at greater risk for developmental difficulties. For example, EI enrollment data from the National Longitudinal Study of Early Intervention  suggest that poor and minority children are over-represented in EI compared to the general population of infants and toddlers. Moreover, studies on EI utilization indicate that poor and minority children also have higher levels of unmet need for EI services than their non-poor and non-minority counterparts [10, 15, 19, 20].
Neighborhood socioeconomic conditions have been associated with a range of health, health care, and access outcomes among children . Less is known about whether neighborhood socioeconomic context (i.e., neighborhood social disadvantage) may contribute to access to early intervention services. Some research demonstrated that neighborhood poverty is associated with longer time from referral to initiation of early intervention services . But is neighborhood socioeconomic context associated with utilization of any intervention services? Neighborhood socioeconomic context (i.e., neighborhood social disadvantage) may affect access to early intervention services through characteristics of both the service environment (e.g., fewer services, poor transportation options) and the social environment (e.g., social norms, information networks).
To generate understanding of factors that affect utilization of early intervention therapy services, we take advantage of an existing regional cohort to study an early intervention-eligible subgroup (i.e., VLBW children with developmental delay) of a statewide cohort of VLBW children in Wisconsin. We hypothesize that, among two-year-olds born VLBW and eligible for early intervention therapy services due to developmental delay, children not currently receiving therapy will be more likely to be living in neighborhoods characterized by social disadvantage (i.e. an indicator for lack of adequate health and developmental resources).
Understanding social disparities in utilization of therapy services among VLBW children eligible for early intervention has important policy and programmatic implications for improving outreach and therapeutic service delivery to high-risk families.
The Newborn Lung Project is a regional cohort of infants born VLBW in 2003–2004 and hospitalized in any of the 16 Newborn Intensive Care Units in Wisconsin. The principal investigator of the Newborn Lung Project (MP) granted permission to the first author (BMM) to access and analyze the data. The original cohort recruited 979 infants for whom de-identified clinical data and follow-up contact information were collected. At age 2–3, 719 children had parent questionnaire and child developmental assessment data collected. In the present analysis, data for 26 Spanish-only speaking families were omitted because the developmental assessment was not available in Spanish. Of the 693 remaining children, 191 were age 2 and met Wisconsin early intervention eligibility criteria (i.e., performance more than 1.5 standard deviations below the mean on a developmental assessment) . The 191 included only 6 Hispanic and 5 Asian, Hawaiian, or multi-racial children. Due to these small numbers, we restrict our analyses to white and black, non-Hispanic children (n=176).
Developmental performance was measured using the Pediatric Evaluation of Disability Index (PEDI) . The PEDI is a functional assessment appropriate for children ages 6 months to 7 years. Social, motor, and self-care items are scored dichotomously by parents based upon the child’s ability to perform the task in most situations (1) or unable to perform the task in most situations (0). Raw scores are converted to a normalized, age standardized T-score (mean=50, SD=10). Children were included in the sample analyzed here if they had a PEDI score (in motor, self-care, or social domain) of <35. According to Wisconsin mandates for early intervention, the PEDI is an accepted tool to determine eligibility for early intervention .
Descriptive statistics of receiving therapy among a sample (n=176) 2 year olds born very low birth weight and eligible for early intervention in Wisconsin A
No therapy (n=34)
Total Annual Income
Less than $30,000
$30,000 - $60,000
More than $60,000
HS Diploma /Equivalent or Less
Some post HS schooling
Bachelor Degree or more
Sex of the Child
Lives with both parents
Mom received prenatal care
Developmental delay only
Concomitant developmental disability
Child’s Age (chronological, in moths)
Mother’s age (years)
Birth weight (grams)
Severity of neonatal morbidityC
The primary outcome of interest, receipt of therapy, was collected by parent-report of whether the child currently receives physical, occupational, or speech therapy services (any services vs. no services).
Child and family characteristics
Parental education was categorized as high school (HS) (i.e., 12 years) or less, some college, and completion of a college degree (i.e., at least 16 years). Child’s race and ethnicity was grouped as white, non-Hispanic or black, non-Hispanic (hereafter referred to as black). Annual family income (USA$) was categorized as less than $30,000, $30,000 to $60,000, and greater than $60,000. We also included birthweight, sex of the child, child’s age, mother’s age at child’s birth, whether the child received Medicaid or private insurance, and family structure (single-parent versus two parent families). Severity of neonatal morbidity was measured using the Score for Neonatal Acute Physiology (SNAP) , an index ranging from 0–115 that comprises 6 physiologically-based items (pH, urine output, blood pressure, temperature, oxygen requirement, and seizures) with higher scores reflecting more severe morbidity. Child’s developmental status was categorized as developmental delay only or concomitant developmental disability (e.g., cerebral palsy or other neurological conditions). Descriptive statistics of these variables, by therapy status, are presented in Table 1.
We conceptualized neighborhood disadvantage as social characteristics of neighborhoods that were associated with disadvantage (i.e., low income, low maternal education, single family households, etc.) and because these factors have particular relevance for child development and family well-being. A neighborhood disadvantage index was created using principal component analysis (PCA) of 5 Census tract socio-demographic variables (U.S. Census Bureau, 2003): % families in poverty, % of households with income above state median, % females with bachelor’s degree or more, % single mothers, and % of mothers of young children unemployed. PCA  is a data reduction technique that determines how to combine variables into a single score that captures as much as possible of the overall variability in all the variables and has been previously used in perinatal epidemiologic research . Specifically, the 5 Census variables were first standardized (after reverse coding % females with bachelor’s degree or more and % of households with income above state median). An overall neighborhood disadvantage score (mean=0, SD=1, and alpha=0.86) was created as an average of these items weighted by the item loadings (whose elements measure the strength of the relationship between the variable and principal component). The linear index was then split into tertiles, and children were classified as living in either disadvantaged (highest third), moderately disadvantaged (middle third), or advantaged (lowest third) neighborhoods. The results of the PCA have been previously published . Item loadings ranged from 0.66 for unemployed mothers of young children to 0.90 for families living in poverty.
To test our study hypotheses, we fit a series of exact logistic regression models. Exact logistic regression is an appropriate method to obtain estimates and confidence intervals with small sub-group sample sizes.
First, we tested for significant bi-variate associations between each child and family characteristic and receipt of therapy services. Significant predictors (p <.05) were included in subsequent model building. In the bi-variate analyses, only family income, insurance type, developmental status, and neighborhood disadvantage were statistically significant. We describe the subsequent model building process including these covariates.
The first model included family income to describe its association with current receipt of therapy. The second model additionally included child’s developmental status (i.e., presence of a developmental disability versus developmental delay only), and Medicaid participation to describe their association, above and beyond family income. In the third model we added neighborhood disadvantage to examine its association after controlling for child and family attributes. We modeled neighborhood disadvantage as an ordinal variable. In the multivariable models we present, the interpretation of the neighborhood disadvantage covariate is the difference in odds of receiving therapy between children from a more socially disadvantaged neighborhood category to those from the preceding less socially disadvantaged one (e.g., disadvantaged versus moderate disadvantaged).
For each covariate, we report the odds ratio (and 95% confidence interval) of receiving therapy. All analyses were conducted in SAS v.9.2 . The institutional review board at the University of Wisconsin-Madison and all participating centers (St. Joseph’s Hospital, Milwaukee, WI; Aurora Sinai, Milwaukee, WI; St. Joseph’s, Marshfield, WI Meriter Hospital, Madison, WI; Children’s Hospital of Wisconsin, Milwaukee, WI; St. Mary’s Hospital, Madison, WI; St. Vincent’s Hospital, Green Bay, WI; Columbia-St. Mary’s Hospital, Milwaukee, WI; St. Luke’s Hospital, Racine, WI; Children’s Hospital of Wisconsin – Fox Valley, Neenah, WI; Waukesa Memorial Hospital, Waukesha, WI; Aurora Women’s Pavilion, West Allis, WI; Gunderson Lutheran Hospital, LaCrosse, WI; Aurora Bay Care, Green Bay, WI; St. Elizabeth’s Hospital, Affinity Health System, Appleton, WI; and Franciscan Skemp Hospital, LaCrosse, WI) approved this study. Parents of the study children provided written informed consent to participate.
Unadjusted and adjusted odds ratios (95% confidence interval) of receiving therapy for a sample of very low birth weight children (n=176), who, at age 2, meet Wisconsin state eligibility criteria A for early intervention due to developmental delay
Unadjusted OR (95% CI)
Adjusted OR (95% CI)
Medical and health service
3.15 (1.20, 8.25)
3.12 (1.11, 9.71)
1.06 (0.18, 5.70)
1.58 (0.22, 11.57)
$30,000 - $60,000
1.99 (0.70, 5.65)
1.58 (0.60, 4.34)
1.13 (0.37, 3.61)
1.42 (0.43, 4.96)
6.06 (2.71, 13.53)
4.84 (1.95, 12.52)
5.15 (2.1, 13.27)
4.66 (2.03, 10.74)
3.80 (0.92, 19.48)
5.26 (1.25, 28.33)
1.01 (0.61, 1.67)
0.48 (0.21, 0.98)
The results of Model 2 (Table 2) suggest that children with concomitant developmental disability (aOR=4.84, 95% CI: 2.0, 12.5) have increased odds of currently receiving therapy compared to VLBW children with developmental delay only. Moreover, adding disability status in Model 2 reduces the magnitude of the parameter estimate of being in the lowest income stratum from aOR=3.12 (Model 1) to aOR=1.06 (Model 2). This suggests that the lowest income children are also likely to have a concomitant disability, which explains (in part) their higher odds of receiving therapy services.
The results of Model 3 demonstrate that children living in a more socioeconomically disadvantaged neighborhood have lower odds of receiving therapy. Specifically, children living in more socioeconomically disadvantaged neighborhoods had 52% lower odds (aOR=0.48, 95% CI: 0.21, 0.98) of currently receiving therapy than their peers living in advantaged neighborhoods, after controlling for family socio-demographic characteristics and severity of child’s condition. Also of note, after controlling for children’s family and neighborhood socioeconomic characteristics, children participating in Medicaid have significantly higher odds (aOR=5.26, 95% CI: 1.25, 28.33) of receiving therapy than their privately insured counterparts.
Among an existing regional cohort of VLBW 2-year olds, we examined family and neighborhood correlates of current receipt of physical, occupational, or speech therapy among a sample with developmental delay who meet state eligibility criteria for receipt of early intervention services. Among this high-risk population eligible for EI services, overall receipt of therapy is high (80%) and children with concomitant developmental disability are more likely to receive therapy. Moreover, we found that children with Medicaid had higher odds of receiving therapy than their privately insured peers and children living in a more socioeconomically disadvantaged neighborhood had lower odds of accessing any therapy services.
Our results regarding Medicaid use are consistent with a previous study from another state (i.e., Massachusetts)  suggesting that children with developmental risk enrolled in Medicaid have fewer unmet therapy needs. However, our findings differ from nationally representative samples  of children with developmental difficulties in which Medicaid enrollment did not influence receipt of services. This suggests that the impact of Medicaid on service use may vary from state to state. Our results are consistent with other research indicating that Medicaid participation can ameliorate access and navigation difficulties facing low-income families with children with developmental disabilities . Wisconsin and Massachusetts have both led the country in optimizing access to children’s Medicaid programming, which likely explains why Medicaid has a positive association with access to services in both of these states. This provides an optimistic message that high quality Medicaid programming may actually enhance the use of services among at risk children. But why are rates of utilization higher for Medicaid participants than those with private insurance? We consider two reasons. First, annual family participation fees are waived for children insured through Medicaid. Perhaps this removes a financial barrier to accessing early intervention services. Secondly, the EPSDT mandate for Medicaid might encourage pediatricians and family physicians to facilitate an early intervention referral for families. Regardless of the mechanism, as the states move toward restricting eligibility criteria for receipt for early intervention services, it will be important to ensure that children experiencing dual risk – social and developmental – receive necessary therapeutic services. Integrating Medicaid child health and early intervention mandates improve quality (e.g., care coordination) and prevent gaps in service delivery for low-income children living in socially vulnerable neighborhoods. However, we acknowledge that the association we find between Medicaid and therapy utilization could be due to the correlation between Medicaid and a host of child, family, and neighborhood adverse social characteristics (i.e., multicollinearity). Future research with larger sub-sample groups should investigate these associations further.
In the current study, children living in neighborhoods characterized by socioeconomic disadvantage are least likely to receive therapy, even after considering their family characteristics. Within the federal IDEA mandate, early intervention service delivery is largely driven by state and local funding and community advocacy . Thus, it is quite plausible that differences in service delivery are highly correlated with the socioeconomic and advocacy characteristics of communities above and beyond the attributes of their residents. Presumably, more advantaged communities have greater individual and community resource allocation to health and developmental services and higher maternal knowledge and advocacy around child development. Our findings are consistent with a previous study  in which children living in poorer neighborhoods were significantly more likely to have delays in receipt of therapy, perhaps due to limited resource allocation. However, we did not directly measure availability of services, only use of service, so future research should investigate how the availability of services, for example, the number of trained pediatric physical, occupational, and speech therapists, influences access to and utilization of therapy services. In addition, parents living in socially disadvantaged neighborhoods may choose not to access therapy services, perhaps due to a cultural stigma of having a child with a developmental delay or disability, or they do not perceive that the child needs or would benefit from therapy services.
Potential mechanisms to explain the association between family and neighborhood sociodemographic risk and unmet need include factors that influence access and adherence to intervention regimens. Previous research  suggests that unmet need for therapy services in the U.S. stems from difficulty obtaining referrals for specialty services, finding a skilled provider, and obtaining an adequate number of visits with these providers. Thus, it is plausible that, above and beyond the influence of family income and low maternal education, neighborhood social disadvantage may be an indicator of access and compliance challenges associated with unmet need among this vulnerable population. Indeed, our results suggest an interaction effect whereby the odds of receiving therapy does not differ by insurance type for children living in advantaged neighborhoods. However, for children living in more disadvantaged neighborhoods, insurance type is associated with receipt of therapy services. That is, participation in Medicaid may buffer the ill-effects of living in a socially disadvantaged neighborhood with regard to receipt of therapy services. However, an alternative explanation is that children living in socially disadvantaged neighborhoods who do not have Medicaid are insured through parental employer-sponsored health insurance. For these families, parental work schedules may be a barrier to accessing therapy services. Indeed, our results regarding the intersection between Medicaid participation, neighborhood social disadvantage, and receipt of therapy should be interpreted with the appropriate caution given the small sub-group sample sizes. Future research should explore these potential explanations with larger sample sizes.
We acknowledge several limitations to our study. First, this cross-sectional analysis is limited in its ability to ascribe causality, but rather describes relationships between family and neighborhood attributes and odds of receiving therapy. We acknowledge that parents of children with more therapy needs may be more motivated to apply for Medicaid. Indeed, participation in Medicaid may be a marker for more severe disability (though we did attempt to control for this) as well as maternal motivation and resources, and future research should explore this.
Data collection occurred 8 years ago. As a result, the findings may not reflect current patterns of EI service delivery utilization. However, WI EI eligibility policy has not changed substantially during the last 8 years, which suggests the relevance of the study findings [23, 25].
About 1/3 of the original cohort was lost to follow-up. This has the potential to introduce bias if the children who were followed differ from children not followed on characteristics of interest. In unreported sensitivity analyses, we compared analyses with and without propensity score weights derived from measured birth characteristics and found no differences. While this suggests that minimal bias was introduced by differential follow-up, the possibility still exists that children lost to follow up differ on unmeasured variables.
The measurement of neighborhood disadvantage varies across studies. We chose one method (i.e. PCA) that was theoretically driven and methodologically robust to allow inclusion of a broad range of contextual factors while simultaneously addressing their mutlicollinearity. Future research should examine other ways of characterizing neighborhoods and also in understanding the mechanisms linking those neighborhood characteristics to service access.
We were limited in our data collection of therapy utilization to parent-report. We were not able to confirm receipt of therapy services using EI program administrative data (e.g., Individualized Family Service Plans or EI billing data). To our knowledge, the validity of parent report of EI therapy services has not been established. However, previous research [32–35] suggests that parent-report is a valid proxy for administrative health and developmental service utilization data. While these studies did not specifically examine parent-reported EI therapy, we are somewhat reassured that parents accurately report their children’s health and developmental service utilization. Related to this, we asked about current receipt of therapy services. Families responding affirmatively may actually receive clinic-based rather than EI-based services. If this were true, our findings may actually underestimate unmet need for EI therapy as infants and toddlers with developmental delays should be receiving therapy services through Part C EI rather than hospital or outpatient clinics.
Finally, our results may not be generalizable to EI programs in all states. States have flexibility in determining criteria for determining eligibility based upon a developmental delay. Given not only this cut-off (i.e., 1.5 SD below the mean in WI), but also that a parent-reported evaluation tool (i.e., the PEDI) can determine eligibility in WI, differences on these domains may limit applicability of our findings to other states.
Survival of VLBW children continues to increase with advances in NICU technology, which contributes to increasing numbers of children with developmental delays and disabilities . These life-long consequences for health, development, and quality of life can arguably be ameliorated most effectively with early and continuous intervention. Thus, understanding the types of early intervention service delivery young children with developmental difficulties access has important policy and programmatic implications for improving service delivery and developmental trajectories. Our results suggesting that Medicaid actually facilitates access to services provides hope that there are ways to do so, which should be examined in more detail for replication. However, our results that living in a disadvantaged neighborhood is associated with lower service utilization provides a more sober message that we need to also attend to specific barriers that appear to be occurring in disadvantaged neighborhoods.
Very low birth weight
Pediatric Evaluation of Disability Inventory
Score of Neonatal Acute Physiology.
The first author acknowledges support from the Robert Wood Johnson Health Foundation Health and Society Scholars program at UW-Madison. This research was supported by funding from the National Heart, Lung, and Blood Institute (HL038149).
- Taylor HG, Minich NM, Klein N, Hack M: Longitudinal outcomes of very low birthweight: Neuropsychological findings. J Int Neuropsychol Soc. 2004, 10: 149-163.PubMedGoogle Scholar
- Butler AS, Board on Health Sciences Policy: Neurodevelopmental, health, and family outcomes for infants born preterm. Preterm Birth: Causes, Consequences, and Prevention. Edited by: Behrman RE. 2006, Washington, DC: The National Academies Press, 346-397.Google Scholar
- Howson CP, Merialdi M, Lawn JE, Requejo JH, Say L: March of Dimes White Paper on Preterm Birth The Global and Regional Toll. 2009, White Plains, NY: March of Dimes FoundationGoogle Scholar
- PL 108–446. Individuals with Disabilities Education Act, Reauthorization. 2004, Available from: http://www.copyright.gov/legislation/pl108-446.pdf
- Spiker D, Hebbeler K, Wagner M, Cameto R, McKenna P: A framework for describing variation in state early intervention systems. Top Early Child Spec Educ. 2000, 20: 195-207. 10.1177/027112140002000401.View ArticleGoogle Scholar
- Bailey DB, Hebbeler K, Scarborough A, Spiker D, Mallik S: First experiences with early intervention: A national perspective. Pediatrics. 2004, 113: 887-896. 10.1542/peds.113.4.887.View ArticlePubMedGoogle Scholar
- Blauw-Hospers C, Hadders-Algra M: A systematic review of the effects of early intervention on motor development. Dev Med Child Neurol. 2005, 47: 421-432. 10.1017/S0012162205000824.View ArticlePubMedGoogle Scholar
- Spittle A, Orton J, Doyle LW, Boyd R: Early developmental intervention programs post hospital discharge to prevent motor and cognitive impairments in preterm infants. Cochrane Database Syst Rev. 2007, 2007:Google Scholar
- Feinberg E, Silverstein M, Donahue S: The impact of race on participation in Part C early intervention services. J Dev Behav Pediatr. 2011, 32 (4): 284-291. 10.1097/DBP.0b013e3182142fbd.View ArticlePubMedPubMed CentralGoogle Scholar
- Rosenberg SA, Zhang D, Robinson CC: Prevalence of Developmental Delays and Participation in Early Intervention Services for Young Children. Pediatrics. 2008, 121 (6): 1503-1509. 10.1542/peds.2007-1680.View ArticleGoogle Scholar
- Medicaid and CHIP Program Information: Retrived from: http://www.medicaid.gov/Medicaid-CHIP-Program-Information/By-Population/Children/Children.html
- The Commonwealth Fund: EPSDT: An Overview. 2005, Retrieved from: http://www.commonwealthfund.org/Content/Publications/Data-Briefs/2005/Sep/EPSDT--An-Overview.aspx Google Scholar
- Hill KS, Freeman LC, Yucel RM: Unmet need among children with special health care needs in Massachusetts. Matern Child Health J. 2008, 12: 650-661. 10.1007/s10995-007-0283-3.View ArticlePubMedGoogle Scholar
- Warfield ME, Gulley S: Unmet Need and Problems Accessing Specialty Medical and Related Services Among Children with Special Health Care Needs. Matern Child Health J. 2006, 10 (2): 201-216. 10.1007/s10995-005-0041-3.View ArticlePubMedGoogle Scholar
- Barfield WD, Clements KM, Lee KG, Kotelchuck M, Wilbur N, Wise PH: Using linked data to assess patterns of early intervention (EI) referral among very low birth weight infants. Matern Child Health J. 2008, 12 (1): 24-33. 10.1007/s10995-007-0227-y.View ArticlePubMedGoogle Scholar
- Greer M, Taylor A, Mackey Andrews SD: A Framework for Developing and Sustaining a Part C Finance System (NECTAC Notes No.23). 2007, Chapel Hill: The University of North Carolina, FPG Child Development Institute, National Early Childhood Technical Assistance CenterGoogle Scholar
- Infant and Toddlers Association: Part C Implementation: State Challenges and Responses. IDEA Infant and Toddler Coordinators Association. 2009, Retrieved from: http://www.ideainfanttoddler.org/pdf/2011_State_Challenges.pdf Google Scholar
- Hebbeler K, Spiker D, Mallik S, Scarborough A, Simeonsson R: National Early Intervention Longitudinal Study Demographic Characteristics of Children and Families Entering Early Intervention. 2003, Menlo Park, CA: SRI InternationalGoogle Scholar
- McManus BM, McCormick MC, Acevedo-Garcia D, Ganz M, Hauser-Cram P: The Effect of State Early Intervention (EI) Eligibility on EI Participation Among Children with Special Health Care Needs. Pediatrics. 2009, 124: S368-S374. 10.1542/peds.2009-1255G.View ArticlePubMedGoogle Scholar
- Wang CJ, Elliott MN, Rogowski J, Lim N, Schuster M: Factors influencing the enrollment of eligible extremely-low-birth-weight children in the Part C early intervention program. Acad Pediatr. 2009, 9 (4): 283-287. 10.1016/j.acap.2009.04.001.View ArticlePubMedPubMed CentralGoogle Scholar
- Dietz RD: The estimation of neighborhood effects in the social sciences: An interdisciplinary approach. Soc Sci Res. 2002, 31: 539-575. 10.1016/S0049-089X(02)00005-4.View ArticleGoogle Scholar
- Kim C, Disara K, Pfeiffer M, Kerker B, McVeigh KH: Effects of individual and neighborhood characteristics on the timeliness of provider designation for Early Intervention Services in New York City. J Dev Beh Ped. 2009, 30: 38-49. 10.1097/DBP.0b013e318196b0f0.View ArticleGoogle Scholar
- Shakelford J: State and Jurisdictional Eligibility Definitions for Infants and Toddlers with Disabilities Under IDEA. NECTAS Notes. 2006, 21: 43-47. Retrieved from: http://ectacenter.org/~pdfs/pubs/nnotes21.pdf Google Scholar
- Haley SM, Coster WJ, Ludlow LH, Haltiwanger JT, Andrellos PJ: PEDI Manual: Pediatric Evaluation of Disability Inventory (PEDI), version 1, development, standardization and administration manual. 1992, Boston, MA: New England Medical Center-PEDI Research GroupGoogle Scholar
- Guidelines for Best Practices in Determining Eligibility Based on Children’s Physical Development. Retrieved from: http://www.waisman.wisc.edu/birthto3/Txt/finemotor.html
- Richardson DK, Corcoran JD, Escobar GJ, Lee SK: SANP-II and SNAPPE-II: simplified newborn illness severity and mortality risk scores. J Pediatr. 2001, 138: 92-100. 10.1067/mpd.2001.109608.View ArticlePubMedGoogle Scholar
- Tabachnick BG, Fidell LS: Principal components and factor analysis, using multivariate statistics. 1996, Northridge, CA: California State University, Harper Collins College Publishers, 635-708.Google Scholar
- Buka SL, Brennan RT, Rich-Edwards JW, Raudenbush SW, Earls F: Neighborhood support and the birth weight of urban infants. AJE. 2003, 157 (1): 1-8. 10.1093/aje/kwf170.View ArticleGoogle Scholar
- McManus BM, Robert SA, Albanese A, Sadek-Bawadi M, Palta M: The relationship between neighborhood disadvantage and social function in Wisconsin 2- and 3- year olds born with very low birth weight. Arch Pediatr Adolesc Med. 2010, 185: e1-e7.Google Scholar
- SAS v9.2. 2002–2003, Cary, NC, USA: SAS Institute Inc
- Ngui EM, Flores G: Satisfaction With Care and Ease of Using Health Care Services Among Parents of Children With Special Health Care Needs: The Roles of Race/Ethnicity, Insurance, Language, and Adequacy of Family-Centered Care. Pediatrics. 2005, 117: 1184-1996.View ArticleGoogle Scholar
- Bussing R, Leon CE, Mason DM, Sinha K: Agreement between CASA parent reports and provider records of children’s ADHD services. J Behav Health Serv Res. 2003, 30 (4): 462-469. 10.1007/BF02287433.View ArticlePubMedGoogle Scholar
- D’Souza-Vazirani D, Minkovitz CS, Strobino DM: Validity of maternal report of acute health care use for children younger than 3 years. Arch Pediatr Adolesc Med. 2005, 159: 167-172. 10.1001/archpedi.159.2.167.PubMedGoogle Scholar
- Forrest CB, Riley AW, Vivier PM, Gordon NP, Starfield B: Predictors of children’s healthcare use: The value of child versus parental perspectives on healthcare needs. Medical Care. 2004, 42 (3): 232-238. 10.1097/01.mlr.0000115196.02425.05.View ArticlePubMedGoogle Scholar
- Hoagwood K, Horwitz S, Stiffman A, et al: Concordance between parent reports of children’s mental health services and service records: The services assessment for children and adolescents (SACA). J Child Fam Stud. 2000, 9 (3): 315-331. 10.1023/A:1026492423273.View ArticleGoogle Scholar
- Wilson-Costello D, Friedman H, Minich N, Fanaroff A, Hack M: Improved survival rates with increased neurodevelopmental disability for extremely low birth weight infants in the 1990’s. Pediatrics. 2005, 115: 997-1003. 10.1542/peds.2004-0221.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2431/13/106/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.