Evidence for Transition Programs in Cystic Fibrosis...
Transcript of Evidence for Transition Programs in Cystic Fibrosis...
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Evidence for
Transition Programs
in Cystic Fibrosis
Care
Advanced Lung Disease
Program : Adult Cystic
Fibrosis
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Transfer Verses Transition
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Transition Planning in Pediatrics
Envisioning the future
Age of responsibility
Age of transition
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“When I was younger…. It was more like my mom’s
disease . It was mine but I didn’t really care.” Patient
“Proactive patients can make the transition smooth,
but some patients wait until they are sick to make
the transition, and that is hard.” Provider
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Differences in Current Programs at SUH
Adult Clinic
Group Practice Model
Mid Level Providers
Concurrent Clinics with Endocrine monthly
Weekly Teaching Sessions
Pediatric Clinic
Primary Care
Physician Model
Supportive Setting
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SUH Transition Plan 2012
Start at 8 years
Booklet with specific expectations
Explains how to prepare for parent and
patient
Medical Summary completed by the
patient
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SUH Communication and Coordination
between Adult/Pediatric Teams
Adult Coordinator attends weekly
Pediatric Meeting
Adult Coordinator attends weekly
inpatient rounds
Complete Adult and Pediatric Team meet
quarterly together
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SUH Adult Clinic Services
Support Group monthly with WebEx access
Referral to support services through Skype or face to face sessions
Weekly teaching sessions for new diagnosed patient or fallen away CF patients
Inpatient support : volunteer visitor, care packages, meals
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Transition Programs: Pediatrics to Adult:
Common Features
Patient preparation
Patient readiness assessment
Coordination of services
Benefits assessments
Medical summary
Primary and preventive care services
Patient follow up
Program evaluation
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Transition and Transfer
Models of care: separate clinics, separate
location
Barriers : patient/family , disease severity,
developmental delay
College patients either stay with pediatric
team until graduation or move to college
location site
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Difference between Pediatric or Adult
Clinic
Different cultures
Adult clinics may expand to include
subspecialists
Adult support may include emphasis on
thinking for the future
Patient concerns include infection control
and leaving Peds provider
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Suggestions for Transition Programs
Promote self care
Communicate and share responsibility
between teams members and patients
Insure visit to adult team and inpatient
unit
Individualize care for patients with special
needs
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CF and Transition to Adult Medical
Care
Barriers: confidence of Peds providers in
adult providers
Infection Control concerns
Insurance coverage: greater expenditures
over non CF expenses for health care
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Findings
Models of care base on clinical
experience or best practice approach
Validation is lacking based on evidence
for systematic study
Found increased hospitalization rates
within year after transfer
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Transition of Pediatric Chronic
Vulnerable Patients
National Initiative
Medical Home Concept
Disability financing
Vocational support
Provisions for work
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Transition with Vulnerable Population
Scope of problem
Written plan by age 14 years
Models: disease based, subspecialties
based, PCP based
Transition not based on age of patient
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Transition with Vulnerable population
Emphasis on medical summary
Plan should include services and how they will be financed
Barriers: for Peds provider: finding and securing adult clinicians, lack of support time for transition
Barriers: for adult provider: meeting psychosocial needs of chronically ill, facing disability and end of life issues with early relationship with patient
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Transition Program Assessment of
Pediatric to Adult CF Care
105 question Survey
195 US Cystic Fibrosis centers
Team participation
Method: email and phone call follow up
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CFF Transition Survey Findings
85% of CF patients are followed in centers
Median age to initiate transition discussion
was 17 years of age
Age of transition age was on average19
years with a range of 14 -30 years.
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CFF Transition Survey Findings
50% of programs did readiness
assessments
10% use a written list of self management
skills for the patient
80% of programs assigned a team
member to assess patient’s insurance
benefits
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Transition Survey Findings
80% of programs reviewed patients in
pediatric meeting
Minority of medical summaries include
assessment of patient self care skills or
review of communication problems with
provider team and patient
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Assessment of Satisfaction on Transition
Patient
Parents
Pediatric providers
Adult providers
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Evidence Based
Recommendations
Transfer and transition is a process
Development of trust is also a process
Disease severity will drive level of support
needed in transition
Patients may do better with transition than
parents or providers
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First Appointment in Clinic
Co Visit with Pediatrician if possible
Parent in the room until Fellow or Nurse
Practitioner come into the room
Parents may return when plan of care
discussed with Attending MD
Questions Questions Questions
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How can parents help patient
with Transition ?
Try to be a coach rather than a player
Encourage forward movement
Count to 10 before critical comments
Remember how you felt in the early years
of taking care of your child with this
diagnosis
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Come Ride with
Us to Better
Health Adult Cystic Fibrosis Clinic
Center for Advanced Lung Disease Program
Kathy Gesley Adult Coordinator [email protected]