Objective. To generate a national picture of performance in the area of preventive and developmental services for children aged 4 to 35 months using 4 composite quality measures in the areas of 1) anticipatory guidance and parental education, 2) screening for family psychosocial risks, 3) screening for smoking and drug and alcohol use in the home, and 4) provision of family-centered care.
Methods. Data from the National Survey on Early Childhood Health (N = 2068) were used to calculate the 4 composite performance measures, which, taken together, represent 23 topics included in the American Academy of Pediatrics health supervision guidelines. The reliability and degree of redundancy within and across these 4 measures were evaluated. Four methods for scoring these measures were used. Quality scores for subgroups of children were calculated, and logistic regression analysis was performed to examine the association of demographic, health, and health system variables with receiving recommended care.
Results. Regardless of the scoring method used, performance is highest in areas of family-centered care and screening for smoking and drug and alcohol use in the home. Performance is lowest in the areas of anticipatory guidance and education and assessment for family psychosocial risks. Using a scoring method that takes into account parent preferences for guidance and beliefs about discussing psychosocial topics, composite quality measure scores ranged from 13.5% to 59.6% of parents of young children receiving recommended care. Overall, 94.0% of parents reported 1 or more unmet needs for parenting guidance, education, and screening by pediatric clinician(s) in 1 or more of the content of care areas evaluated. Uninsured children and children aged 18 to 35 months are disproportionately represented among the 15.3% of children whose parents indicated an unmet need in each of the 4 areas of care. Although the reliability of each composite measure was high, no single item in any composite was highly correlated with the remaining combined items. Performance on any 1 composite measure for a child was only somewhat predictive of performance for the other measures. There are significant variations in performance on the basis of child age, race, insurance status, maternal education, marital status, and parent language as well as other factors.
Conclusions. National results using 4 complementary composite quality measures confirm the need for improving the quality of preventive and developmental services for young children in the United States. The 4 measures identify areas of care and subgroups of children for whom improvements in quality are most needed. The measures provide a parsimonious yet comprehensive assessment across distinct health supervision topics and 4 essential aspects of preventive and developmental services. Until valid measures of outcomes of preventive and developmental services are identified or 1 single process of care measure is shown to be highly predictive of these outcomes, assessing multiple aspects of recommended care will be necessary to assess performance of health care providers or systems of care.
Health care quality measurement, disclosure, and improvement are subjects of significant and growing national interest, as exemplified in recent reports such as Crossing the Quality Chasm by the Institute of Medicine.1–3 Health systems in general and medical practices in particular are being encouraged or required to assess and improve the quality of care that they provide and to make performance information available to their patients and those who pay for health care services.2,4–9 To date, much of the evidence on quality has been about adult care and treatment of illness. Less is known about pediatric care overall and preventive and developmental health care in particular. Consequently, we still fall short of capturing information about the provision and impact of the core of pediatric primary care health supervision. However, through recent advances, health care quality measurement and improvement methods for children’s health care are now available.10–18
The majority of health care expenditures for children are spent on <15% of all children aged 0 to 18, those who have chronic conditions or special health care needs.19–21 However, care for most children is largely composed of routine services to promote their healthy development, prevent injuries, and screen for illness and other threats to health. This is especially the case for young children. Currently, rates of immunization and rates of doctor visits for well-child checkups are the primary focus of health care quality measurement, reporting, and improvement efforts in the area of preventive care for young children,22 yet these quality measures do not provide information regarding whether the broader range of recommended preventive and developmental services outlined by pediatricians in the Guidelines for Health Supervision III have actually occurred.23–25
The guidelines recommend that pediatric clinicians 1) provide anticipatory guidance and education (AGPE) to parents on a wide range of topics related to promoting a child’s physical, social, cognitive, and emotional health and development; 2) provide family-centered care (FCC); 3) regularly screen for parent and family psychosocial risks (FA); and 4) screen for smoking and drug and alcohol use in the home (SDA). The American Academy of Pediatrics (AAP) recommendations for preventive and developmental pediatric care further outline a schedule for 1 to 7 visits (depending on age) a year for children under 5 to address not only measurement of growth and development but also developmental/behavioral assessments and anticipatory guidance in areas such as injury prevention, violence prevention, sleep positioning, and nutritional counseling.23,26 It is understood that some recommendations enjoy a greater degree of professional consensus and scientific evidence of impact on child developmental outcomes than others.27 Also, while many guideline topics are intended to be addressed for all children, many others are flexible, with the content determined by the needs of the child and the relationship between the family and the practitioner.23
The Child and Adolescent Health Measurement Initiative convened an expert panel between 1998 and 2000 to guide the selection of a subset of topics for inclusion in the parent-reported Promoting Healthy Development Survey (PHDS) and PHDS-Plus, an expanded version of the PHDS.11,16 (The PHDS, PHDS-Plus, and a reduced-item pediatric practice-level version of the PHDS are available at no cost by contacting the primary author or online at www.cahmi.org.) The PHDS and PHDS-Plus survey yield composite measures across several areas of preventive and developmental services for young children as well as topic-specific assessments for children aged 0 to 9 months, 10 to 18 months, and 19 to 48 months. Topics selected for inclusion in the survey were 1) appropriate for all children in the specified age group; 2) supported by scientific evidence or professional consensus; 3) important to parents (as derived from cognitive interviews and focus groups); 4) reliably and validly reported by parents; 5) not measured in another reliable, valid, or more efficient way, including through administrative data, medical chart reviews, and surveys of pediatricians; and 6) parsimonious (eg, topic is not already largely represented by another, related topic included in the PHDS). The PHDS and PHDS-Plus also take into account parents’ perceived needs for guidance and information by asking whether parents desired to talk about topics that had not been discussed. The National Survey of Early Childhood Health (NSECH) incorporated the majority of the survey items from the PHDS, making assessments of quality possible at the national level.
This article describes each of the 4 composite quality measures and complementary methods for constructing summary, national composite measures of quality in health supervision from the NSECH data. In addition, we evaluate the degree to which the 4 composite measures of quality and the specific topics included in each measure contribute distinct, statistically nonredundant performance information. Variations in composite measure scores across subgroups of children are presented to highlight aspects of care and populations of children for which preventive and developmental services may be most in need of improvement. Data from the administration of the PHDS-Plus in 1 state Medicaid program were used to illustrate the impact of alternative scoring methods on assessing the performance of individual pediatric practices.
Data from NSECH conducted by the National Center for Health Statistics in 2000 (N = 2068) were used to calculate national estimates of performance on 4 composite quality-of-care measures for young children. Sampling and administration methods for the NSECH are summarized by Blumberg et al in this issue of Pediatrics. Table 1 describes the NSECH study sample. All data are weighted to the US population of children aged 4 to 35 months.
Data from the PHDS-Plus collected in 1 state Medicaid program were used to illustrate the use of 1 of the 4 composite measures at the practice level. A random sample was drawn of 5004 children who were enrolled in Medicaid, would be 3 to 48 months of age at the time of survey administration, for whom telephone contact information was available, and who had been continuously enrolled in Medicaid for at least 1 year or since birth. The PHDS-Plus telephone survey was administered to the parent or guardian of the child in the household who knows the most about the child’s health and medical care using a standardized telephone interview. Data were collected by a third-party survey vendor until 2000 surveys were completed. Overall, 65.0% of parents were able to be contacted, and 96.3% of these completed the survey, for a final response rate of 62.6%. The pediatric provider assigned to the child in enrollment data were linked to the survey data, providing practice-specific data for 18 sites, with sample sizes ranging from 25 to 151. Data are analyzed for the 11 practices for which at least 30 surveys were completed.
Content of Care Assessed
Four composite measures of quality that were developed and tested in the PHDS and fielded in both the NSECH and the PHDS-Plus were evaluated. Performance measures were calculated in 4 areas: AGPE, FA, SDA, and FCC. Appendix 1 provides a complete list of survey topics included in each of the quality composites.
For AGPE, parents were asked whether at anytime in the last 12 months, over the course of visits that their child may have had, their child’s clinician(s) discussed with them each of a set of age-appropriate topics. Parents whose child’s clinician had not discussed the topic were asked whether a discussion would have been helpful. For FA and SDA topics, parents were asked whether their child’s clinician asked about a topic. All parents were also asked whether they believe that pediatric providers should discuss the topic with parents. The second question captures parents’ normative views on discussion of these topics.
Calculation of Composite Measures
Four different scoring methods were used to construct composite scores on the basis of topics in AGPE, FA, SDA, and FCC.
Method 1: All or Nothing
This method provides information on how consistently comprehensive the care is that young children receive. It is calculated as the proportion of parents who reported that all topics in each of the areas of AGPE, FA, or SDA are addressed or each of the 4 aspects of FCC is “always” provided.
Method 2: Preference Sensitive.
This method provides information about how consistently thorough and/or responsive pediatric clinicians are to parents’ perceived needs and preferences for care. It is calculated as the proportion of parents who reported either that all topics in a content area were addressed by pediatric clinicians or that all topics not discussed were also not perceived by parents as being helpful to discuss (in the AGPE composite) or as not being appropriate for discussion between providers and parents (in the FA and the SDA composites). The “preference sensitive” version of the FCC composite considers FCC to be provided when parents reported that it “usually” or “always” occurred on each item.
Method 3: Unmet Need
This method provides information on missed opportunities for pediatric clinicians to provide aspects of recommended care that parents perceive that they need or believe should occur. For AGPE, it is calculated as the proportion of parents who reported that at least 1 AGPE topic that would have been helpful was not addressed. For FA and SDA, it is the proportion of parents who reported that they were not asked about a topic about which they believe that providers should ask. The “unmet need” version of the FCC quality measure identifies a child as having an unmet need when the parent reported that the aspect of care “never” occurs.
Method 4: Mean Coverage
This method provides information on how many of the topics included in the survey pediatric clinicians tend to address with parents of young children. It is calculated as the average proportion of composite measure topics that parents report were addressed by pediatric clinicians.
All topics within each quality composite measure were weighted equally in the construction of the measures. Table 2 summarizes the scoring methods used to construct the 4 quality measures in each content of care area (AGPE, FA, SDA, and FCC). In addition to the 4 composite measures, a global composite measure of the proportion of children whose care met the “all or nothing” or the “preference sensitive” scoring criteria for each of the 4 measures was calculated, weighting each measure equally.
Performance scores for the 4 composite quality measures were calculated using each of the 4 scoring methods described above. Using scores derived from the “preference sensitive” scoring method, positive and negative predictive values for the topical composite measures were calculated to show whether the provision of recommended care in 1 topical area is associated with the provision of recommended care in another topical area. The positive predictive value (PPV) is the probability that the child will meet criteria for having received high quality care in one topical area, given that the child has met criteria for receiving high quality care in another topical area. The negative predictive value (NPV) is the probability that the child will not meet criteria for receiving high-quality care in 1 area, given that the child has not met criteria for receiving high-quality care in another topical area. Internal consistency of each composite measure was evaluated using standardized Cronbach’s α. Mean correlation among items in each composite and item total correlations were analyzed.
Scores that were based on the “preference sensitive” method were used to examine variation in performance by child and parent factors. χ2 or F tests were used at a .05 level of significance. Adjusted odds ratios from logistic regression analysis show which demographic, child health, and health system factors are associated with higher or lower composite scores. Independent variables included in this analysis were child’s age, race/ethnicity, gender, insurance status, and risk for developmental and behavioral delays using the Parents Evaluation of Developmental Status, which uses parent concerns to identify children who are at risk.28 Other factors included were maternal educational level, marital status, language in which the survey was administered (English or Spanish), geographic region of the United States, whether the child always saw the same provider for well-child care, and whether the parent reported that the child had a well-child visit in the past 12 months. Collinearity among independent variables was assessed before regression analysis and was not found to be problematic.
AGPE scores were calculated using both the “all or nothing” and the “preference sensitive” scoring methods. Correlation in scores across practices was evaluated using Spearman’s ρ correlation coefficient, and the relative spread in scores across practices for each version of the AGPE measure was assessed using the coefficient of variation statistic (standard deviation across practices divided by the grand mean across practices multiplied by 100%). Adjusted standard errors and tests of significance were obtained using Stata 7.0 statistical software to account for the complex survey sampling design.
Table 2 presents results on the 4 composite measures (AGPE, FA, SDA, and FCC) using each of the 4 scoring methods. Results are provided first for AGPE, then for FA and SDA, and finally for FCC. Table 2 shows that for AGPE, care for ∼10.8% of parents of young children met the “all or nothing” scoring criteria indicating reported discussion of all of the 10 to 12 age-appropriate topics. Care for a greater proportion of children (44.7%) met the “preference sensitive” scoring method criteria, which shows the proportion of parents who reported discussion of all AGPE topics or reported no need of discussion among unaddressed topics. The “mean coverage” scoring method (which shows the average percentage of AGPE topics addressed) shows that, on average, 62.0% of the 10 to 12 age-appropriate topics were discussed with parents of young children.
Results for FA show that few parents of young children reported that their child’s pediatric clinician discussed psychosocial topics such as parent emotional well-being and partner support in parenting. Only 2.7% of parents of young children reported discussions on each of the 5 topics in the FA composite. Approximately 13.9% reported discussions on all psychosocial topics or that they view topics not discussed as inappropriate for pediatric providers to address with parents. The proportion of children who received care that met criteria for screening for SDA is similar using the “all or nothing” method (41.0%) or the “preference sensitive” method (50.0%). Scores on the SDA composite measure are higher than for the AGPE or FA composite measures regardless of which scoring method was used. Unmet needs are most frequent in the areas of AGPE (55.3%) and FA (86.1%). The “mean coverage” scoring method shows that, on average, parents reported that pediatric providers discussed 52.0% of FA and 66.7% of SDA topics with parents of young children.
FCC is reported as “usually” or “always” received by 59.6% of parents of young children. Although 15.4% of young children always receive FCC (as indicated using “all or nothing” scoring), approximately one third of parents of young children (37.6%) reported never receiving at least 1 aspect of FCC, as indicated using the “all or nothing” method.
Few children met criteria for all 4 composite measures irrespective of the scoring method used. Overall, 6.1% of children met the “preference sensitive” scoring criteria for each of the 4 composite measures (data not shown). Virtually no parents reported that their child’s care (0.8%) met the performance criteria for all 4 composite measures using the “all or nothing” method. The “unmet need” scoring method reveals that 94.0% of parents reported 1 or more unmet needs in at least 1 of the 4 aspects of care assessed here, and 15.3% have 1 or more unmet needs in each of the 4 areas of care. Children whose parents indicated an unmet need in each area are more likely to be older (8.6% of those younger than 9 months, 18.6% of those older than 9 months) and uninsured (23.3% of those uninsured, 14.7% of those insured).
On the basis of 11 pediatric practices in 1 state Medicaid program, the practice-level performance scores on AGPE using the “all or nothing” and the “preference sensitive” scoring methods (Fig 1) are significantly correlated (Spearman’s ρ = .58). The highest and the lowest scoring practices are the same regardless of the scoring method used. Variation in scores across practices is 3 times greater when the “all or nothing” method is used (range: 10.0%–32.6%) than when the “preference sensitive” method is used (range: 57.5%–81.4%). The coefficient of variation is 36% for the “all or nothing” method and 11.7% for the “preference sensitive” method.
Internal Consistency of Composite Measures
Reliability of the 4 “preference sensitive” composite measures ranges from 0.51 to 0.82 (Table 3). Reliability for the AGPE composite measure is highest, ranging from 0.78 to 0.82 across each of the 3 age groups. Inter-item correlations show that the correlations of each individual topic with the full AGPE measure (excluding the topic in question) vary widely (range: 0.04–0.45) in each of the 3 age groups.
Association Among Composite Measures
Scores from the “preference sensitive” scoring method show that each of the 4 composite quality measures provides unique information about performance. The PPV ranges from 0.18 to 0.77, and the NPV ranges from 0.41 to 0.93 (Table 4).
Overall, the FA measure has the highest PPVs. Specifically, when a child’s health care meets the “preference sensitive” scoring criteria on the FA measure, there are 77%, 74%, and 63% probabilities that a child’s care meets performance criteria on the FCC, SDA, and AGPE composite measures, respectively. Similarly, when a child’s health care does not meet performance criteria for the FCC measure, there is a high probability that care also does not meet the “preference sensitive” criteria of any of the other 3 composite performance measures. As Table 4 shows, the NPV of FCC for AGPE is 0.73, for FA is 0.92, and for SDA is 0.56.
However, other composite performance measures are weaker predictors of high quality in other content areas. For example, there is only an 18% probability that children with care that meets the FCC “preference sensitive” criteria also receive care that meets the FA criteria. There is only a 20% probability that care that meets the AGPE also meets the FA “preference sensitive” scoring criteria. We also observed that the parent-reported occurrence of 1 or more well-child visits in the past year is not highly predictive of whether children received recommended content of care during those visits (PPV range: 0.10–0.42 for AGPE, FA, and SDA).
Variation in Care Across Subgroups of Children
Table 5 shows variation in scores using preference-sensitive criteria according to a child’s age; gender; race; insurance status; level of risk for developmental, behavioral, or social delays; having a consistent provider of well-child care; and geographic location. Variation is also observed according to the mother’s educational level, marital status, and interview language. Such variations are more evident for the AGPE and the SDA composite measures than for the other measures where performance is uniformly lower (FA) or higher (FCC). For the AGPE measure, care for non-Hispanic white children is most likely to meet scoring criteria. In contrast, non-Hispanic white children are less likely to meet criteria on the SDA measure. Children of lower educated mothers are less likely than those with more educated mothers to have high AGPE or FCC scores but more likely to have high SDA scores. Children of parents who are unmarried or whose parent interviewed in Spanish are less likely to meet criteria on the AGPE and FCC measures and more likely to meet criteria on the FA and SDA measures.
Using the “preference sensitive” scoring method, maternal education, marital status, and interview language are predictive of performance on the SDA measure after controlling for other factors using logistic regression analyses. Significant variation by race/ethnicity is also found for the FA and SDA measures but not for AGPE and FCC. Overall, differences by subgroup in meeting criteria for 1 or more of the composite quality measures generally remain significant after controlling for other factors. Exceptions include “regular provider for well-child care” and “insurance status” variables (Table 6).
A range of parent-reported performance measures can be used to evaluate the quality of key components of recommended preventive and developmental services for young children. Results from this national survey confirm substantial gaps between what is recommended and what parents report is provided for a number of health supervision areas for young children. Findings show significant variation in performance across content of care areas as well as within and across subgroups of children according to a child’s age, race/ethnicity, and insurance and health status; mother’s education, marital status, and language spoken; and other factors.
Regardless of which of the 4 scoring methods is used for each measure, we observed that parents generally reported receiving the highest quality of care in the areas of FCC and screening for SDA and the lowest quality of care in the areas of AGPE and FA. Results indicate that nearly all parents of young children have 1 or more unmet needs for guidance or education from pediatric clinicians in 1 or more areas of care.
The performance measures described here are complementary and generate a more comprehensive assessment of the various components of pediatric primary care than has been available until now. This more complete approach to performance monitoring avoids inaccuracies that occur when only 1 aspect of care, such as immunization or well-care visit rates, is used to measure performance. Moreover, we found that no single quality measure did a good job of predicting the quality of care that a child received as assessed by other measures. This finding underscores the value of multiple measures and the value of parent surveys such as the NSECH or PHDS, which make it feasible to collect data and to construct and analyze variations on multiple health care quality measures simultaneously. Just as a single measure does not provide a comprehensive picture of performance, a single method for scoring measures is similarly limited. A more complete understanding of performance is provided by scoring multiple aspects of care in alternative ways. A richer picture of performance within and across key recommended aspects of preventive and developmental services for children can be better achieved using the complementary scoring methods illustrated in this article than by selecting only 1 scoring method. For example, using all 4 methods, we can report that 1) 10.8% of parents of young children receive anticipatory guidance and education on all of a representative subset of topics that are recommended for discussion with all parents by pediatric clinicians; 2) 44.7% receive guidance and education on all of these topics or were comfortable having not discussed the unaddressed topics; 3) 55.3% have 1 or more unmet needs for guidance and education; and 4) on average, 62.0% of the AGPE topics evaluated are discussed with parents by pediatric clinicians.
Although alternative measure scoring methods yielded differences in the absolute value of performance, these different methods were largely consistent in identifying aspects of care for which performance is highest or in need of improvement. The methods were also consistent in identifying which subgroups of children are most likely to receive or not receive recommended services.
The “preference sensitive” scoring method used for most of the results presented here presumes that unaddressed guidance topics would not have benefited parents who reported that discussion would not have helped them. It is possible that they do not understand the potential benefits of such discussions. It is also possible that the young children of these parents may have pediatric clinicians who do not give effective guidance; if so, then these children are receiving higher scores than are actually appropriate given the intent of quality measurement. In addition to issues regarding the construction of the “preference sensitive” quality scores, we should note that in several areas, differences in scores across subgroups of children were somewhat large and potentially clinically meaningful but were not found to be statistically significant as a result of small actual sample sizes.
Regardless of the population group or the aspect of health care assessed, the quality of health care rarely can be represented accurately by either a single composite performance measure or by assessing whether a single recommended service is provided. This is especially true for children.29 For adults, we often have the option to evaluate health outcomes, which have the potential to provide a summary assessment of the quality of care provided overall. Health outcomes measures have the advantage of answering the question, “Did the expected outcome occur as a result of services provided?” without assessing the provision of each individual service that contributed to that outcome. Outcomes measurement is especially possible in areas of chronic illness care for adults and for some childhood chronic conditions, for which evidence linking care processes to both intermediate and longer term health outcomes is strong and risk adjustment methods to account for factors that are not responsive to health care interventions are also more fully developed (eg, blood sugar levels/glycated hemoglobin for people with diabetes).
For children’s preventive care, for which healthy development and avoidance of injury and illness are the desired outcomes and for which care guidelines are more often consensus based than evidence based, we are faced with special challenges in both accurately and efficiently measuring health care performance. In part, because of these and other challenges, child health care quality has not received the kind of attention that has been given to adult health care, and children’s issues have not been emphasized in many national quality measurement and improvement efforts.30 As evidenced in emerging national frameworks and reports on health care quality in America, the focus is on early detection and management of diseases in adults rather than on the promotion of healthy development and preventing illness and injury for children.1–3,31,32
Health care performance assessment efforts at the national, state, health system, and medical practice levels all face real constraints in the amount of information about performance that can be collected, included, or reasonably absorbed in performance reports to or about health care systems or providers. Choices must be made regarding what is most important, valid, and fair to evaluate for purposes of performance assessment, yet until better and more valid measures of the outcomes of preventive and developmental services are identified, assessing the multiple aspects of recommended care that expert consensus suggests contribute to these outcomes will be necessary to create the best possible assessment of performance of providers or systems of care. The 4 composite quality measures used in this article provide a relatively comprehensive yet parsimonious picture of performance in the area of preventive and developmental services for young children in America and were possible to develop and analyze using a single survey instrument. Although not exhaustive, the measures address 23 distinct preventive and developmental topics intended to be representative of the dozens of individual topics that are recommended to be addressed by pediatric clinicians.
As noted by Daley et al,7 “Voluntary, internal, nontransparent quality improvement efforts have yet to demonstrate that they can succeed in meeting expectations for higher levels of performance on the part of medical professionals.” As such, we expect efforts that require the routine assessment and communication of health care quality to grow.33–35 Methods such as those discussed here can provide pediatric clinicians with family-centered strategies for both evaluating and interpreting their overall performance and with the data that they and their patients need to understand and improve care. They are useful to differentiate performance among discrete aspects of care and to identify areas of care and subgroups of children for whom improvements in quality are most needed. Finally, these methods may also be useful for conducting the much-needed research to understand better the impact of the aspects of preventive and developmental services assessed here on child health and developmental outcomes, such as school readiness; prevention of injuries; avoidable illness; and other social, cognitive, emotional, and physical developmental and health outcomes for young children.
APPENDIX 1: NSECH SURVEY ITEMS INCLUDED IN EACH OF THE COMPOSITE PERFORMANCE MEASURES
Anticipatory Guidance and Parental Education
Breastfeeding (4–9 months)
Sleeping positions (4–9 months)
Night waking and fussing (4–9, 10–18 months)
How child communicates his or her needs (4–9 months)
Burn prevention methods (eg, hot water temperature in the home) (4–9 months)
Sleeping with a bottle (10–18 months)
Taking child off the bottle (10–18 months)
Guidance and discipline techniques (10–18, 19–35 months)
Words and phrases that the child uses and understands (10–18, 19–35 months)
Toilet training (10–18, 19–35 months)
Bedtime routines (19–35 months)
Teaching child to avoid dangerous situations (eg, electrical sockets, the stove, climbing on things, running in the street) (19–35 months)
Things that child may start to do on his or her own (eg, washing, dressing) (19–35 months)
Use of syrup of ipecac if your child swallows poison (10–18, 19–35 months)
How child gets along with other children (19–35 months)
Issues related to food and feeding
Using a car seat
Child care arrangements
Importance of reading to child
Parent’s physical health
Emotional support for parent
Relationship with spouse or partner regarding parenting
Troubles paying for the child’s basic needs (eg, food, diapers)
Violence in the community
Smoking, Drug, and Alcohol Assessment
Smoking in the home
Drug and/or alcohol use in the home
Pediatric clinician takes time to understand the specific needs of child
Pediatric clinician respects the parent as an expert about his or her child
Pediatric clinician asks the parent how he or she is feeling as a parent
Pediatric clinician understands the parent and the child’s family and how they prefer to raise the child
This research was made possible by funding from The Gerber Foundation, the American Academy of Pediatrics Friends of Children Fund, the Maternal and Child Health Bureau in the Health Resources and Services Administration (5-U05MC-00010200), and the Commonwealth Fund.
- ↵Adams K, Corrigan JM, eds. Priority Areas for National Action: Transforming Health Care Quality. Washington, DC: National Academies Press; 2003
- ↵Institute of Medicine. Crossing the Quality Chasm: A New Health System for the 21st Century. Washington, DC: National Academy Press, 2001
- ↵The National Academies. Stronger Federal Leadership Needed to Reduce Medical Errors, Improve Care; Quality Initiatives in Government Programs Affect Entire Health Care Sector. The National Academies Press Release. Washington, DC: National Academies Press; 2002
- Lansky D. Improving quality through public disclosure of performance information. Health Aff (Millwood).2002;21 :52– 62
- Newhouse J. Why is there a quality chasm? Health Aff.2002;21 :13– 25
- ↵Daley J, Vogeli C, Blumenthal D, Kaushal R, Landon B, Normand S. Physician Clinical Performance Assessments: The State of the Art: Issues, Possibilities and Challenges for the Future. Boston, MA: Institute for Health Policy Massachusetts General Hospital; 2002
- ↵Child Health Toolbox: Measuring Performance in Child Health Programs. Uses of Performance Measurement. Rockville, MD: Agency for Healthcare Research and Quality; March2002. Available at: www.ahrq.gov/chtoolbx/uses.htm. Accessed February 11, 2004
- ↵Bethell C, Peck C, Schor E. Assessing health system provision of well-child care: the Promoting Health Development Survey. Pediatrics.2001;107 :1084– 1094
- CAHMI The Child and Adolescent Health Care Measurement Initiative. Available at: www.cahmi.org. Accessed February 11, 2004
- ↵Bethell C, Peck C, Abrams M, Halfon N, Sareen H, Collins KS. Partnering With Parents to Promote the Health Development of Young Children Enrolled in Medicaid. New York, NY: The Commonwealth Fund; 2002. Available at: www.cmwf.org/programs/child/bethell_partnering_bn_570.asp. Accessed February 12, 2004
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- ↵Blumberg SJ, Olson L, Frankel M, et al. Design and operation of the National Survey of Children With Special Health Care Needs, 2001. Vital Health Stat.2003;(41)
- ↵National Committee for Quality Assurance (NCQA). HEDIS 2002. Vol 2: Technical Specifications. Washington, DC: National Committee for Quality Assurance; 2002
- ↵American Academy of Pediatrics, Committee on Psychosocial Aspects of Child and Family Health. Guidelines for Health Supervision III. Elk Grove Village, IL: American Academy of Pediatrics; 1997 (updated 2002)
- Green M, ed. Bright Futures: Guidelines for Health Supervision of Infants, Children and Adolescents. 2nd ed. Arlington, VA: National Center for Education in Maternal and Child Health; 2002
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- Copyright © 2004 by the American Academy of Pediatrics