ArticleFamilies, systems & health : the journal of collaborative family healthcare2013
Parent-reported outcomes of comprehensive care for children with medical complexity.
Article in Families, systems & health : the journal of collaborative family healthcare, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
12 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Systematic Review of Programs Treating High-Need and High-Cost People With Multiple Chronic Diseases or Disabilities in the United States, 2008-2014.Preventing chronic disease · 2015Pooled it
- Health-Related Quality of Life Outcomes of a Telehealth Care Coordination Intervention for Children With Medical Complexity: A Randomized Controlled Trial.Journal of pediatric health care : official publication of National Association of Pediatric Nurse Associates & PractitionersTrial
- Capturing caregivers' and families' experiences in a Complex Care Program: development of the Complex Care Program-Family Impact Questionnaire (CCP-FIQ).Journal of pediatric psychology · 2026Article
- Caring for children with medical complexity: Homecare nurses' point of view.Paediatrics & child health · 2025Article
- Pediatric primary care and subspecialist providers' comfort, attitudes and practices screening and referring for social determinants of health.BMC health services research · 2021Article
- Stakeholder perspectives: Communication, care coordination, and transitions in care for children with medical complexity.Journal for specialists in pediatric nursing : JSPN · 2021Article
- Looking into the life of technology-dependent children and their caregivers in Korea: lifting the burden of too many responsibilities.BMC pediatrics · 2020Article
- Creating a Pharmacotherapy Collaborative Practice Network to Manage Medications for Children and Youth: A Population Health Perspective.Children (Basel, Switzerland) · 2019Article
- Supporting Parent Caregivers of Children with Life-Limiting Illness.Children (Basel, Switzerland) · 2018Article
- Health Services and Health Care Needs Fulfilled by Structured Clinical Programs for Children with Medical Complexity.The Journal of pediatrics · 2016Article
- Children with medical complexity and Medicaid: spending and cost savings.Health affairs (Project Hope) · 2014Article
- Inequities in health care needs for children with medical complexity.Health affairs (Project Hope) · 2014Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
The Medical Home Clinic for Special Needs Children (MHCL) at Arkansas Children's Hospital provides comprehensive care oversight for children with medical complexity (CMC). The objective of this study is to evaluate parent perceptions of health care delivery outcomes after 12 months of enrollment in the MHCL. This is a prospective cohort study of parents of MHCL patients, who completed surveys at initial and 12-month visits. Surveys assessed parent health, child health and function, family stress, and overall satisfaction, using previously validated measures and scales. Paired analyses examined differences in measures between baseline and 12 months. One-hundred and twenty of 174 eligible parents completed the follow-up survey at 12 months. Respondents were 63% White/Caucasian, 90% biological parent, and 48% with an annual family income < $20,000. From baseline to 12 months, a greater number of respondents reported having a care plan (53% vs. 85%, p < .001); fewer respondents needed help with care coordination (78% vs. 31%, p < .001). No changes were seen in reports of having emotional needs met. Parents reported a decline in the physical subscale of the SF-12 Health-Related Quality of Life measure (49.1 vs. 46.4, p < .01), with those parents with ≥ 1 additional child with special needs reporting a marked decline (49.2 vs. 42.5, p < .001). No other changes in family impact were found. We conclude that comprehensive care oversight may improve care coordination for parents of CMC, but no association with improved parent health was found. Future studies should identify the factors that influence parental burden and tailor clinical interventions to address such factors.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.