Published in J Pediatr Nurs on August 25, 2011
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The under reporting of recruitment strategies in research with children with life-threatening illnesses: A systematic review. Palliat Med (2016) 0.75
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Racial, ethnic, and cultural differences in the dementia caregiving experience: recent findings. Gerontologist (2001) 1.97
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Effect of race on cultural justifications for caregiving. J Gerontol B Psychol Sci Soc Sci (2005) 1.60
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Positive aspects of Alzheimer's caregiving: the role of race. J Gerontol B Psychol Sci Soc Sci (2004) 1.35
Ethnicity and time to institutionalization of dementia patients: a comparison of Latina and Caucasian female family caregivers. J Am Geriatr Soc (2004) 1.34
Understanding factors associated with work loss for families caring for CSHCN. Pediatrics (2009) 1.24
The well-being of parental caregivers of children with activity limitations. Matern Child Health J (2008) 1.18
Household language use and health care access, unmet need, and family impact among CSHCN. Pediatrics (2009) 1.14
Adjustment of caregivers of pediatric patients with brain tumors: a cross-sectional analysis. Psychooncology (2009) 1.12
Quality of life of caregivers. Neuropsychol Rev (2004) 1.08
Partners in care: together for kids: Florida's model of pediatric palliative care. J Palliat Med (2008) 1.06
Health among caregivers of children with health problems: findings from a Canadian population-based study. Am J Public Health (2008) 1.04
One gets so afraid: Latino families and asthma management--an exploratory study. J Pediatr Health Care (2007) 0.93
Economic impact on families caring for children with special health care needs in New Hampshire: the effect of socioeconomic and health-related factors. Matern Child Health J (2005) 0.92
The effect of poverty and caregiver education on perceived need and access to health services among children with special health care needs. Am J Public Health (2006) 0.92
Assessing quality of life in Mexican-American children with asthma: impact-on-family and functional status. J Pediatr Psychol (2000) 0.90
Elder care among Mexican American families. Clin Nurs Res (1998) 0.90
Family support in pediatric palliative care: how are families impacted by their children's illnesses? J Palliat Med (2010) 0.88
The care of my child with cancer: a new instrument to measure caregiving demand in parents of children with cancer. J Pediatr Nurs (2002) 0.87
PTSD and psychological distress in Icelandic parents of chronically ill children: does social support have an effect on parental distress? Scand J Psychol (2006) 0.81
Patterns of informal care among Puerto Rican, African American, and white stroke survivors. Ethn Health (2009) 0.78
A programmable prompting device improves adherence to highly active antiretroviral therapy in HIV-infected subjects with memory impairment. Clin Infect Dis (2005) 2.25
Measuring the transition readiness of youth with special healthcare needs: validation of the TRAQ--Transition Readiness Assessment Questionnaire. J Pediatr Psychol (2009) 1.59
Risk and promotive factors in families, schools, and communities: a contextual model of positive youth development in adolescence. Pediatrics (2007) 1.43
Internet use and eHealth literacy of low-income parents whose children have special health care needs. J Med Internet Res (2011) 1.39
A family-centered, community-based system of services for children and youth with special health care needs. Arch Pediatr Adolesc Med (2007) 1.16
Agreement was not found in adolescents' quality of life rated by parents and adolescents. J Clin Epidemiol (2008) 1.16
Pediatric palliative care: describing hospice users and identifying factors that affect hospice expenditures. J Palliat Med (2009) 1.08
The role of race and ethnicity in the State Children's Health Insurance Program (SCHIP) in four states: are there baseline disparities, and what do they mean for SCHIP? Pediatrics (2003) 1.08
Partners in care: together for kids: Florida's model of pediatric palliative care. J Palliat Med (2008) 1.06
Disclosing medical errors to patients: it's not what you say, it's what they hear. J Gen Intern Med (2009) 1.05
The linkage between pediatric quality of life and health conditions: establishing clinically meaningful cutoff scores for the PedsQL. Value Health (2011) 1.04
Psychometric properties of the PROMIS ® pediatric scales: precision, stability, and comparison of different scoring and administration options. Qual Life Res (2013) 1.03
The effect of premium changes on SCHIP enrollment duration. Health Serv Res (2008) 1.02
Continuity of diabetes care is associated with avoidable hospitalizations: evidence from Taiwan's National Health Insurance scheme. Int J Qual Health Care (2009) 1.02
Information seeking behaviors of parents whose children have life-threatening illnesses. Pediatr Blood Cancer (2010) 0.99
Disparities in human papillomavirus vaccine series initiation among adolescent girls enrolled in Florida Medicaid programs, 2006-2008. J Adolesc Health (2010) 0.97
Factors associated with self-reported physical and mental health after hematopoietic cell transplantation. Biol Blood Marrow Transplant (2010) 0.96
Paediatric nurses' knowledge of palliative care in Florida: a quantitative study. Int J Palliat Nurs (2009) 0.95
Are effects from a brief multiple behavior intervention for college students sustained over time? Prev Med (2009) 0.95
Exploring factors influencing asthma control and asthma-specific health-related quality of life among children. Respir Res (2013) 0.95
A randomized trial of the impact of a programmable medication reminder device on quality of life in patients with AIDS. AIDS Patient Care STDS (2006) 0.93
Provider factors associated with disparities in human papillomavirus vaccination among low-income 9- to 17-year-old girls. Cancer (2012) 0.93
Efficacy of a brief image-based multiple-behavior intervention for college students. Ann Behav Med (2008) 0.91
Creating a crosswalk to estimate AIDS Clinical Trials Group quality of life scores in a nationally representative sample of persons in care for HIV in the United States. HIV Clin Trials (2005) 0.89
Factors affecting decisional conflict for parents with children enrolled in a paediatric palliative care programme. Int J Palliat Nurs (2010) 0.89
Spirituality of parents of children in palliative care. J Palliat Med (2011) 0.89
Brief integrative multiple behavior intervention effects and mediators for adolescents. J Behav Med (2010) 0.88
Family support in pediatric palliative care: how are families impacted by their children's illnesses? J Palliat Med (2010) 0.88
Health-Related Quality of Life of Young Adult Survivors of Childhood Cancer: A Review of Qualitative Studies. J Adolesc Young Adult Oncol (2011) 0.87
PROMIS(®) pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions. Qual Life Res (2015) 0.87
Relation between level or change of hemoglobin and generic and disease-specific quality of life measures in hemodialysis. Qual Life Res (2007) 0.86
Differential item functioning in quality of life measure between children with and without special health-care needs. Value Health (2011) 0.86
Factors that affect parent perceptions of provider-family partnership for children with special health care needs. Matern Child Health J (2009) 0.86
The relationships between asthma control, daytime sleepiness, and quality of life among children with asthma: a path analysis. Sleep Med (2013) 0.85
Measuring quality of life in pediatric palliative care: challenges and potential solutions. Palliat Med (2009) 0.85
Do Florida Medicaid providers' barriers to HPV vaccination vary based on VFC program participation? Matern Child Health J (2013) 0.84
The impact of community risks and resources on adolescent risky behavior and health care expenditures. J Adolesc Health (2006) 0.84
Assessing non-response bias in pediatric palliative care research. Palliat Med (2010) 0.84
Physicians' undecided attitudes toward posthumous reproduction: fertility preservation in cancer patients with a poor prognosis. J Support Oncol (2012) 0.83
Assessment of response shift using two structural equation modeling techniques. Qual Life Res (2012) 0.83
Handling missing quality of life data in HIV clinical trials: what is practical? Qual Life Res (2007) 0.83
Health care use and charges for adolescents enrolled in a title XXI program. J Adolesc Health (2002) 0.82
Coping Styles of Female Adolescent Cancer Patients with Potential Fertility Loss. J Adolesc Young Adult Oncol (2013) 0.82
Effects of an Integrated Care System on quality of care and satisfaction for children with special health care needs. Matern Child Health J (2012) 0.82
Music therapy in an integrated pediatric palliative care program. Am J Hosp Palliat Care (2009) 0.82
Anti-inflammatory medication adherence, healthcare utilization and expenditures among Medicaid and children's health insurance program enrollees with asthma. Pharmacoeconomics (2012) 0.82
Measuring quality of dental care: Caries prevention services for children. J Am Dent Assoc (2015) 0.81
The impact of insurance on satisfaction and family-centered care for CSHCN. Pediatrics (2009) 0.81
Relationships among symptoms, psychosocial factors, and health-related quality of life in hematopoietic stem cell transplant survivors. Support Care Cancer (2014) 0.81
The effect of Medicaid primary care provider reimbursement on access to early childhood caries preventive services. Health Serv Res (2014) 0.80
SF-6D utility index as measure of minimally important difference in health status change. J Am Pharm Assoc (2003) (2012) 0.79
Head-to-head comparisons of quality of life instruments for young adult survivors of childhood cancer. Support Care Cancer (2011) 0.79
Quality of Life Measurement for Children with Life-Threatening Conditions: Limitations and a New Framework. Child Indic Res (2011) 0.79
Using three legacy measures to develop a health-related quality of life tool for young adult survivors of childhood cancer. Qual Life Res (2011) 0.79
Assessing the congruence of transition preparedness as reported by parents and their adolescents with special health care needs. Matern Child Health J (2013) 0.79
The effect of renewal policy changes on SCHIP disenrollment. Health Serv Res (2008) 0.79
Health status and health-related quality of life in a pediatric palliative care program. J Palliat Med (2012) 0.79
The relationship between four health-related quality-of-life indicators and use of mammography and Pap test screening in US women. Qual Life Res (2015) 0.78
A brief image-based prevention intervention for adolescents. Psychol Addict Behav (2010) 0.78
Missing content from health-related quality of life instruments: interviews with young adult survivors of childhood cancer. Qual Life Res (2013) 0.78
A longitudinal study of a pediatric practice-based versus an agency-based model of care coordination for children and youth with special health care needs. Matern Child Health J (2008) 0.77
Congruence between parents' and adolescents' reports of special health care needs in a Title XXI program. J Pediatr Psychol (2003) 0.77
Does decisional conflict differ across race and ethnicity groups? A study of parents whose children have a life-threatening illness. J Palliat Med (2014) 0.77
Pediatric nurses' attitudes toward hospice and pediatric palliative care. Pediatr Nurs (2011) 0.77
Human papillomavirus vaccine administration among Medicaid providers who consistently recommended vaccination. Sex Transm Dis (2014) 0.76
Effect of a pediatric palliative care program on nurses' referral preferences. J Palliat Med (2009) 0.76
Developing a pediatric palliative care program: addressing the lack of baseline expenditure information. Am J Hosp Palliat Care (2008) 0.76
Influence of explanatory and confounding variables on HRQoL after controlling for measurement bias and response shift in measurement. Expert Rev Pharmacoecon Outcomes Res (2013) 0.76
Pediatricians' management practices for chronic pain. J Palliat Med (2010) 0.75
In reply to: Association between utility and treatment among patients with prostate cancer. Qual Life Res (2010) 0.75
Quality of Care for Chronic Conditions Among Disabled Medicaid Enrollees: An Evaluation of a 1915 (b) and (c) Waiver Program. Med Care (2015) 0.75
Association between perinatal medical expenses and a waiver to increase Florida healthy start services within Florida medicaid programs: 1998 to 2006. Matern Child Health J (2012) 0.75
Parents' experiences in choosing a health plan for their children with special health care needs. Matern Child Health J (2011) 0.75
Assessing the impact of an integrated care system on the healthcare expenditures of children with special healthcare needs. Am J Manag Care (2016) 0.75
Quality of life information and trust in physicians among families of children with life-limiting conditions. Patient Relat Outcome Meas (2010) 0.75
Effect of an integrated care system on utilization for CSHCN in Florida. Matern Child Health J (2014) 0.75