Written Care Plans for Children with Chronic Conditions: What Do Families Think? Linda Barnhart Shervin Churchill Jean Popalisky Nanci Villareale Purpose of Presentation Briefly describe Washington State Children with Special Health Care Needs Program Share results of Parent Survey on Written Care Plans June 24, 2006 CSHCN Program in Washington State The Children with Special Health Care Needs Program (CSHCN) is one of several programs in the Office of Maternal and Child Health in the Division of Community and Family Health. Develop and promote resource materials for families and professionals The CSHCN Program serves children with special health care needs and their families in many ways… ways… Support Public Health Nurses in Local Health Departments to provide: nursing assessment, interventions & care coordination 1 AAP Policy Statement on Care Coordination “A process that links children with special health care needs and their families to services and resources in a coordinated effort to maximize the potential of the children and provide them with optimal health care.” care.” Input from families Input from providers “Care Coordination for CSHCN in Washington State is fragmented.” fragmented.” WISE Grant 20012001-2005 finding “Care Coordination is needed but is timetime-consuming…” consuming…” Medical Home Survey of providers 2005 Receiving input from parents Kate’ Kate’s story “The agencies did not coordinate or communicate with each other… other… we were mired in paperwork.” paperwork.” Care Plan Survey for parents of children with special health care needs -- 2006 Objectives Methods Survey parents of children with special health care needs (CSHCN) to explore: Perceptions about written care plans (WCP) including purposes and uses Beliefs about developing and maintaining a WCP Resources that would be useful for parents WebWeb-based survey Parents of CSHCN, birth to 21 years Washington State residents Conducted FebFeb-March 2006 (9 weeks) Publicized through – Parent organizations and support groups – Public health nurses – Selected clinics at Children’ Children’s Hospital 2 Results – Sample Description Limitations Web based survey Available only in English SelfSelf-selected participants Impossible to calculate response rate Results are descriptive and qualitative, no statistical significance is associated with any of the reported results. Child Characteristics – Age Distribution 35 Place of residence: – Western WA: 79% – Central WA: 8% – Eastern WA: 13% Percent of parents 25 20 15% n=19 15 10 18% n=23 9% n=12 5 0 0-36 Months 37 mo - 5 yrs 6-10 yrs 11-14 yrs Female: 94% 3030-50 yrs old: 87% Post secondary education: 86% Child’ Child’s chronic condition description 30% n=39 28% n=37 30 134 respondents 15-21 yrs Main diagnosis Indicate if parent felt the child had – physical health needs – emotional or behavioral needs, and/or – developmental delay or developmental disability. How long child has had special health care needs How often their child’ child’s condition changes Age of Children Condition Classification by Parent* • Developmental delay 80% • Emotional/behavioral 54% • Physical health needs * Not mutually exclusive 51% Comparison with NS-CSHCN, WA sample: "Which of these statements best describes your child's health care needs?" 66% 70% 60% 50% 40% 37% 36% 33% 27% 30% Care Plan survey NS-CSHCN 20% 10% 6% 4% 1% 0% change all the time change only once in a while are usually stable 9-don’t know/other 3 ResultsResults- Questions on care planning Parent had main duty to coordinate the care of their child: 95% Had WCP at the time of the survey: Physical Health Needs* Emotional Behavioral* Developmental Delay* 31% 40% 35% 30% *Not mutually exclusive Who Developed the WCP? Parent alone developed WCP: 26%* Parent had help: 74%** – 34% had help from doctor’ doctor’s office – 28% had help from DDD – 24% had help from a school nurse or school personnel * Of those who had WCP’ WCP’s (n=40, 31% of sample) ** 44% had some help, 30% someone developed entire WCP Importance of written care plans to families and its uses* 86% believed it was important to have a WCP 67% thought a WCP would help the quality of health care their child receives in different settings such as home, school and health care settings * All survey participants, regardless of whether or not they had a WCP Proportion with WCP by age group Age Group: Percent with WCP 0 – 36 months 37 months – 5 years 6 – 10 years 11 – 14 years 15 – 21 years 18% 32% 21% 37% 48% How did the WCP help the parents? Helped keep all the important information in one place Did not have to repeat the information Helped all the health care providers understand the plan A few parents said the plan did not help them How families would use WCP’ WCP’s * Assist with transitions hospital to home, school, camp, or new doctor 74% * Educate health care professionals 73% * Facilitate communication between myself and health care professionals 77% * Keep a list of care givers and contacts 58% * Organize care for my child 73% 4 How families would use WCP’ WCP’s more ways … * Share with others involved in care of my child Development and maintenance of written care plans 77% * Summarize health information such as medications, therapies and treatments 79% * Summarize other information such as how my child communicates or his likes and dislikes 64% * Use as a tool to plan for the future 59% * Use in emergency situations 81% Development and maintenance of written care plans Who should be in charge of updating WCP? – Parent working with health care professional – Parent alone – Health care professional alone Who should be in charge of developing WCP? 77% 18% 2% Development and maintenance of written care plans – Parent working with health care professional – Parent alone – Health care professional alone 82% 15% 2% Development and maintenance of written care plans How often should the WCP be updated? – As child’ child’s needs change – Annually – Every 3 months – Every 6 months – Every time child in seen by doctor 57% 14% 9% 9% 7% Learning how to Develop a WCP Where should the WCP be? Electronic, on a private computer at home Electronic, on private computer at the doctor's office 36% On paper, at home 54% On paper, at the doctor's office in medical chart Web-based with password access for parent, doctor and others chosen by parent 41% • A form or forms that could be filled out 80% • Information from a health care provider 47% • Information from a parent with experience 44% 23% 56% 5 Learning how to Develop a WCP more ways … Theme from parent thoughts and comments General Perceptions: • A class for parents 46% Supportive of the idea of WCP’ WCP’s Thought WCP’ WCP’s would be beneficial • Web site with information about care plans 70% • Samples of written care plans 78% “This would be most helpful when seeing the different doctors my son sees every month.“ month.“ Theme from parent thoughts and comments “We find ourselves visiting a dizzying array of medical professionals … I realized there were tests called for long ago that never occurred. If a webweb-based site were developed that could alert me of the need for followfollow-up testing, perhaps … these important tests wouldn't be missed. “ --a --a parent Practical suggestions: (Potential bias of web survey population ) Who controls the plan Are WCP’ WCP’s somehow tied to funding? Recommended services may not be available Need for training Discussion and Recommendations Theme from parent thoughts and comments A few parents had concerns: concerns: Simple, brief, flexible Templates and examples would help WebWeb-based or on a computer for easy use & updates Training parents and professionals about WCP’ WCP’s as a Planning and Communication Tool Research where WCP’ WCP’s could be kept, where they could be secure and accessible 6 Resources and Information www.cshcn.org – Can find complete results of care plan survey – Care coordination resources www.doh.wa.gov/cfh/mch/cshcnhome2.htm – Links to resources and information about CSHCN in Washington State Contact information Washington State Department of Health Linda.Barnhart@doh.wa.gov Children’ Children’s Hospital & Regional Medical Center Jean.Popalisky@seattlechildrens.org 7