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Vison  for  Canadian  Rare  Disease  
Networks
Cystic  Fibrosis  in  British  Columbia
30  March  2017
Health  Care  Environment  in  British  Columbia
2
CF  Clinics
•Island  Health
• Royal  Jubilee
• Victoria  General
•Vancouver  Coastal  Health
• St.  Paul’s  Hospital
•Provincial  Health  Services
• BC  Children’s  Hospital
Provincial  Health  Services  Authority
Provincial  Health  Services  Authority  (PHSA)
• PHSA  plans,  manages  and  evaluates  specialty  and  province-­wide  health  care  
services  across  BC,  working  with  the  five  geographic  health  authorities  to  meet  local  
and  provincial  needs
• It  is  responsible  for  managing  and  governing  well-­known  specialized  agencies  and  
services:  
-­ BC  Cancer  Agency   -­ BC Renal  Agency  
-­ BC  Centre  for  Disease  Control   -­ BC  Transplant  
-­ BC  Children’s  Hospital -­ Perinatal  Services  BC
-­ BC  Mental  Health  Substance  Use  Services   -­ Cardiac  Services  BC  
-­ BC  Women’s  Hospital +  Health  Centre   -­ Stroke  Services  BC
• It  plans,  coordinates,  evaluates  and,  in  some  cases  funds  specialized  services  
delivered  by  the  regional  health  authorities.  PHSA’s  role  supports  the  accessibility,  
quality,  efficiency  and  effectiveness  of  province-­wide  programs  and  services.  
3
Current  system  challenges  and  opportunities
• Increasing  numbers  of  individuals  living  with  CF  across  the  province
• Increasing  clinical  complexity  and  the  existence  of  co-­morbid  medical  conditions
• New  drugs  with  patients  requiring  access  and  subsequent  close  monitoring  and  
reporting  to  ensure  ongoing  funding/approvals.    More  of  these  drugs  are  in  the  
pipeline.
• Clinics  and  the  model  of  care  were  never  purpose  built  to  support  the  current  
needs  of  patients
• Technology  has  enabled  opportunities  for  virtual  care  models
• Transitions  of  care  are  increasingly  necessary  (pediatric  to  adult)  and  a  need  to  
define  role  and  sharing  of  care  with  other  specialists  and  GPs
4
Adults  Living  with  Cystic  Fibrosis  in  B.C.
5
Children  Living  with  Cystic  Fibrosis  in  B.C.
6
• In  2013,  the  MOH  sponsored  KPMG  to  develop  a  Business  Case  after  Cystic  Fibrosis  
Canada  and  clinicians  had  highlighted  concerns.    Limited  action  arose  from  this.    
• In  2014  Cystic  Fibrosis  Canada  again  met  with  the  provincial  government  to  address  
funding  issues  which  resulted  in  the  BC  Minister  of  Health  requesting  the  Health  Authority  
senior  leaders  to  meet  and  discuss  options.    Again  there  was  limited  resulting  action  with  
no  lead  organization.
• In  2015,  following  further  correspondence  with  the  Ministry  of  Health,  Provincial  Health  
Services  Authority  (PHSA)  was  asked  to  take  an  active  role  in  pulling  key  stakeholders    
together.    This  included  clinicians  and  leadership  from  existing  clinics,  patients  and  CF  
Canada.      
• In  2015,  as  well,  clinicians  were  successful  in  receiving  funding  through  Doctors  of  BC  -­ 3  
phases,  3  years  to  establish  standards  of  care  and  care  pathways.
• In  2016,  presentations  were  made  to  senior  staff  at  the  Ministry  of  Health  to  outline  
ongoing  challenges  and  problem  solve.
Background  for  Work  in  B.C.
What  is  Needed?
• Application  of  standards  of  care  – care  provided  in  CF  clinics  and  in  primary  and  
acute  care  environments  varies,  as  there  are  few  currently  applied  standards
• Increased  support  for  individuals  transitioning  to  adult  care  and  through  primary  and  
acute  care  – outside  of  the  4  CF  clinics;;  there  is  limited  awareness  in  emergency  
rooms,  inpatient  units,  and  in  primary  care  settings  around  the  province  surrounding  
CF  treatment
• Improved  provincial  access  to  specialized  care  and  increased  use  of  
technology/virtual  care  – a  third  of  patients  reside  outside  of  Victoria  and  the  Lower  
Mainland  and  only  have  access  to  specialized  care  by  travelling  to  CF  clinics  or  
through  very  limited  outreach
• Increased  shared  care  with  “CF  aware”  specialists  and  allied  health  
• Increased  availability  of  provincial  patient  care,  performance  and  operational  data  –
relevant  data  to  support  individual  patient  care  management,  planning,  and  research  
is  not  systematically  collected 8
Who  needs  to  be  involved?
• Specialist  clinics
• Regional  Health  Authorities
• Provincial  Health  Services  Authority
• Patients/families
• CF  Canada
• Ministry  of  Health
9
How  Do  We  Get  There?
• Collaboration  which  brings  together  different  partners  with  a  
common  agenda  to  solve  large  complex  problems.  
• A  method  to  engage  partners  from  different  sectors  to  solve  the  
complex  problems.
• One  such  method,  which  approximates  the  approach  we  have  taken  
provincially,  is  the  “collective  impact”  model.    
• It  is  built  upon  five  interconnected  components  to  produce  strong  
alignment  and  lead  to  large  scale  system  results.
10
Necessary  Components
11
Stanford  Social  Innovation  Review,  2011
Our  Shared  Agenda
To  create  a  sustainable,  responsive  and  dynamic  CF  care  delivery  
system  in  British  Columbia
– That  is  patient-­centred
– That  responds  to  growth
– That  ensures  provincial  reach
– That  responds  to  new  drug  advances
– That  is  integrated,  consistent,  without  gaps  in  care
– That  optimizes  a  shared  care  model
– In  a  context  of  fiscal  restraint  and  competing  demands
12
Where  are  we  at?
• Provincial  Advisory  Group  with  membership  from  all  key  partners  
including  senior  level  leadership  
• An  accountability  structure  for  regular  reporting  
• Standards  of  care  and  clinical  pathways  
• Plan  for  a  data  capture  system  and  performance  metrics
• Provincial  Health  Services  Authority  providing  leadership  and  
serving  as  the  backbone  organization  with  dedicate  resources
• Commitment
13
14
Thank  You
pam.ramsay@phsa.ca

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RDD Conf Day1: Vison for Canadian Rare Disease Networks Cystic Fibrosis in British Columbia

  • 1. Vison  for  Canadian  Rare  Disease   Networks Cystic  Fibrosis  in  British  Columbia 30  March  2017
  • 2. Health  Care  Environment  in  British  Columbia 2 CF  Clinics •Island  Health • Royal  Jubilee • Victoria  General •Vancouver  Coastal  Health • St.  Paul’s  Hospital •Provincial  Health  Services • BC  Children’s  Hospital Provincial  Health  Services  Authority
  • 3. Provincial  Health  Services  Authority  (PHSA) • PHSA  plans,  manages  and  evaluates  specialty  and  province-­wide  health  care   services  across  BC,  working  with  the  five  geographic  health  authorities  to  meet  local   and  provincial  needs • It  is  responsible  for  managing  and  governing  well-­known  specialized  agencies  and   services:   -­ BC  Cancer  Agency   -­ BC Renal  Agency   -­ BC  Centre  for  Disease  Control   -­ BC  Transplant   -­ BC  Children’s  Hospital -­ Perinatal  Services  BC -­ BC  Mental  Health  Substance  Use  Services   -­ Cardiac  Services  BC   -­ BC  Women’s  Hospital +  Health  Centre   -­ Stroke  Services  BC • It  plans,  coordinates,  evaluates  and,  in  some  cases  funds  specialized  services   delivered  by  the  regional  health  authorities.  PHSA’s  role  supports  the  accessibility,   quality,  efficiency  and  effectiveness  of  province-­wide  programs  and  services.   3
  • 4. Current  system  challenges  and  opportunities • Increasing  numbers  of  individuals  living  with  CF  across  the  province • Increasing  clinical  complexity  and  the  existence  of  co-­morbid  medical  conditions • New  drugs  with  patients  requiring  access  and  subsequent  close  monitoring  and   reporting  to  ensure  ongoing  funding/approvals.    More  of  these  drugs  are  in  the   pipeline. • Clinics  and  the  model  of  care  were  never  purpose  built  to  support  the  current   needs  of  patients • Technology  has  enabled  opportunities  for  virtual  care  models • Transitions  of  care  are  increasingly  necessary  (pediatric  to  adult)  and  a  need  to   define  role  and  sharing  of  care  with  other  specialists  and  GPs 4
  • 5. Adults  Living  with  Cystic  Fibrosis  in  B.C. 5
  • 6. Children  Living  with  Cystic  Fibrosis  in  B.C. 6
  • 7. • In  2013,  the  MOH  sponsored  KPMG  to  develop  a  Business  Case  after  Cystic  Fibrosis   Canada  and  clinicians  had  highlighted  concerns.    Limited  action  arose  from  this.     • In  2014  Cystic  Fibrosis  Canada  again  met  with  the  provincial  government  to  address   funding  issues  which  resulted  in  the  BC  Minister  of  Health  requesting  the  Health  Authority   senior  leaders  to  meet  and  discuss  options.    Again  there  was  limited  resulting  action  with   no  lead  organization. • In  2015,  following  further  correspondence  with  the  Ministry  of  Health,  Provincial  Health   Services  Authority  (PHSA)  was  asked  to  take  an  active  role  in  pulling  key  stakeholders     together.    This  included  clinicians  and  leadership  from  existing  clinics,  patients  and  CF   Canada.       • In  2015,  as  well,  clinicians  were  successful  in  receiving  funding  through  Doctors  of  BC  -­ 3   phases,  3  years  to  establish  standards  of  care  and  care  pathways. • In  2016,  presentations  were  made  to  senior  staff  at  the  Ministry  of  Health  to  outline   ongoing  challenges  and  problem  solve. Background  for  Work  in  B.C.
  • 8. What  is  Needed? • Application  of  standards  of  care  – care  provided  in  CF  clinics  and  in  primary  and   acute  care  environments  varies,  as  there  are  few  currently  applied  standards • Increased  support  for  individuals  transitioning  to  adult  care  and  through  primary  and   acute  care  – outside  of  the  4  CF  clinics;;  there  is  limited  awareness  in  emergency   rooms,  inpatient  units,  and  in  primary  care  settings  around  the  province  surrounding   CF  treatment • Improved  provincial  access  to  specialized  care  and  increased  use  of   technology/virtual  care  – a  third  of  patients  reside  outside  of  Victoria  and  the  Lower   Mainland  and  only  have  access  to  specialized  care  by  travelling  to  CF  clinics  or   through  very  limited  outreach • Increased  shared  care  with  “CF  aware”  specialists  and  allied  health   • Increased  availability  of  provincial  patient  care,  performance  and  operational  data  – relevant  data  to  support  individual  patient  care  management,  planning,  and  research   is  not  systematically  collected 8
  • 9. Who  needs  to  be  involved? • Specialist  clinics • Regional  Health  Authorities • Provincial  Health  Services  Authority • Patients/families • CF  Canada • Ministry  of  Health 9
  • 10. How  Do  We  Get  There? • Collaboration  which  brings  together  different  partners  with  a   common  agenda  to  solve  large  complex  problems.   • A  method  to  engage  partners  from  different  sectors  to  solve  the   complex  problems. • One  such  method,  which  approximates  the  approach  we  have  taken   provincially,  is  the  “collective  impact”  model.     • It  is  built  upon  five  interconnected  components  to  produce  strong   alignment  and  lead  to  large  scale  system  results. 10
  • 11. Necessary  Components 11 Stanford  Social  Innovation  Review,  2011
  • 12. Our  Shared  Agenda To  create  a  sustainable,  responsive  and  dynamic  CF  care  delivery   system  in  British  Columbia – That  is  patient-­centred – That  responds  to  growth – That  ensures  provincial  reach – That  responds  to  new  drug  advances – That  is  integrated,  consistent,  without  gaps  in  care – That  optimizes  a  shared  care  model – In  a  context  of  fiscal  restraint  and  competing  demands 12
  • 13. Where  are  we  at? • Provincial  Advisory  Group  with  membership  from  all  key  partners   including  senior  level  leadership   • An  accountability  structure  for  regular  reporting   • Standards  of  care  and  clinical  pathways   • Plan  for  a  data  capture  system  and  performance  metrics • Provincial  Health  Services  Authority  providing  leadership  and   serving  as  the  backbone  organization  with  dedicate  resources • Commitment 13