BC Cancer Agency`s approach to improving the quality of

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Cette présentation a été effectuée le 23 novembre 2010, au cours de la journée « Les données
clinico-administratives et d’enquête essentielles à la qualité des services : l’exemple du cancer »
dans le cadre des 14es Journées annuelles de santé publique (JASP 2010). L’ensemble des
présentations est disponible sur le site Web des JASP, à l’adresse http://www.inspq.qc.ca/
archives.
BC Cancer Agency
BC
Cancer Agency’ss approach to approach to
improving the quality of care in oncology Dr David Levy
D
D id L
President
BC Cancer Agency Mandate
g y
To provide a province‐wide, population‐based cancer control program for BC & the Yukon
14es Journées annuelles de santé publique
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BCCA mission is to: • To reduce the incidence of cancer • To reduce the mortality rate of people with cancer • To improve the quality of life of people living T i
th
lit f lif f
l li i
with cancer
Whitehorse, Yukon
• Central Agency office
•Cancer Research Centre (Vanc. Vict)
•Regional Cancer Centres
•Community Cancer Centres
•Community Cancer Clinics
•70 regional pharmacies – chemo
•Networks:
•hereditary cancer
•cervical cytology
•colposcopy clinics
•screening mammography centres
•palliative care
•surgical oncology council & network
BCCA Cancer Centre and
University Cancer Research
Centre
BCCA Cancer Centre and
Research Centre
Consultative Clinic
Screening
Mammography
Centres, Cervical
Cytology Screening
Program
Dawson
Creek
Prince Rupert
Terrace
Prince
George
Kitimat
Kamloops
Vernon
Powell River
Kelowna
Penticton
Nelson
Vancouver
Campbell River
Comox
Port Alberni
Nanaimo
Vancouver Island
(Victoria)
Chilliwack Trail
Fraser
Valley
(Surrey)
14es Journées annuelles de santé publique
Cranbrook
Creston
Abbotsford
2
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Treatment
Referral
Prevention
Screening
Diagnostics
Treatment
The Patient
Screening g
data
Population data
EMR
Registry data
End of life Care
Chemotherapy data
Radiology reports
Pathology
reports
Survivorship
Surgical data Death data
Radiotherapy data Symptom Screening
BCCA Clinical Surveillance & Outcomes Data Environment
BCCA Clinical, Surveillance & Outcomes Data Environment
External Data Sources 14es Journées annuelles de santé publique
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Ministryy of Health:
•DAD - Hospital discharge/admissions data
•Diagnoses, surgical procedures, 30 day mortality,
•co-morbidity
•MSP - Billing data
•Surgical information/diagnostic info
•SPR - Surgery wait times
•Cancer Surgery wait times*
Vital Statistics:
Death information
Challenges (1)
• Filling the gaps in the pathway:
– Collection of performance status, co‐morbidity and stage
– Meaningful surgical data, across the province
– Need for synoptic reporting of pathology and radiology
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Challenges (2)
g ( )
Why is BC Why
is BC
performance better?
I do not know
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I do know
• It is only important if you measure it*
• Up‐to‐date protocols and their measured adherence, results in consistent high‐quality oncology care across a province
• Tumour tissue, linked to outcome data and treatment parameters is a very important research resource
21st
century
health
care
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Prevention
Screening
Treatment
Referral
Diagnostics
Survivorship
Treatment
The Patient
What data is important to patients?
End of life Care
How do we measure recurrence??
Challenge (3)
g ( )
• Rising number of cancer cases
• Cancer can be a chronic disease
• Fiscally challenged healthcare systems
• Increasing public and patient expectation
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Sustainable cancer control systems
y
• Delivery of Quality care ‐ overtly
– Safe,
– Effective, – Efficient
• Patients expect high‐quality care, outcomes and experience Patient survey 2006
y
• 6,000 patients in BC receiving ambulatory cancer treatment
• 26,000 patients receiving ambulatory cancer care in Alberta Manitoba Nova Scotia
care in Alberta, Manitoba, Nova Scotia, Ontario, and Saskatchewan.
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Impact in BC
p
• Further investment in supportive care
• Challenge to clinical approach v holistic approach to care
• Requires investment in patient‐driven R
i i
t
ti
ti t d i
priorities rather than clinician‐driven
• Q? Who is the healthcare service for?
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BC – Provincial Breast Health Strategy
gy
• Low uptake of screening‐ 53% of 50‐69 year olds
• Women receive mixed messages
• Delays in resolution of abnormal D l
i
l ti
f b
l
mammograms
BC Screening Mammography
• 300,000 screens each year
• 7.3% are abnormal = 21,737 women
• 5 weeks to diagnosis
(nowomen
biopsy)
94% of
with
an abnormal
b
l screen
do NOT have cancer
• 7 weeks to diagnosis (biopsy)
approx 3,600
14es Journées annuelles de santé publique
100% of those
women think they
may have cancer
until diagnostic
results
67.9%
39.6%
11
BC Breast Cancer Waits
Breast Cancer
300
250
More than half wait
more
than 2 months
# of days
200
150
100
50
0
1
3
5
7
9
11 13 15 17 19 21 23 25 27 29 31 33 35 37 39 41 43 45 47 49 51
Breast Cancer Cases Reviewed (n=51)
In BC healthcare appears
• Not patient focussed
• Long waits
• Difficult to navigate
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Current pathway
Pathway?
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Pathway design
• What
Wh t needs
d to
t happen
h
• The skills needed
• Metrics for quality, timeliness, experience
• Funding follows the patient
Clinical Pathway: A Highway
Roadmap
Clinic
appointment
7 days
14es Journées annuelles de santé publique
Support and
Information
h
here
14
Screening
Diagnostics
The Patient
Screening g
data
Population data
Survivorship
Treatment
Referral
Prevention
Radiology reports
Treatment
End of life Care
Chemotherapy data
EMR Surgical data Pathology
Outcomes and Surveillance Integrated reports
Radiotherapy Systems (OaSIS)
Registry data
Death data
data Symptom Screening
In conclusion
• Sustainable cancer control:
– Will be driven by protocolized care
– Patient experience of healthcare is now more p
, g
,
important, as good clinical outcomes are assured, and must be measured
– Clinicians need to change delivery models of healthcare to focus on improving experience
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Thank you
Hub and Spoke Model for delivery of care
SC
SC
SC
SC
SC
DIC
DIC
Full Service
Screening and
Diagnostic (Biopsy)
Facility
SC
Surgery
Pathology
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CANCER CENTRES,
CHILDREN’S HOSPITAL
Cancer Treatment Data
VITAL STATISTICS
Sibling Cohort
CANCER REGISTRY
Survivor Cohort, Patient ID,
Diagnosis, Death Follow-up
MEDICAL INSURANCE
PLAN
Health Utilization Data,
General Population Sample
EDUCATION MINISTRIES
Education Data
BC CANCER AGENCY
Oncology Scheduling,
Screening Data
CAYACS SURVIVOR
RESEARCH RESOURCE
STATCAN
Income and Employment
Info
PHARMANET
Prescription Drug Info
Development of outcome
indicators analysis files
indicators,
I. Health
Outcomes
II. Health Care
Outcomes
III. Education
Outcomes
IV. Income and
Employment
V. Knowledge
Translation
BC C/A/YA Cancer Survivors
Childhood, Adolescent, and
Young Adult (CAYACS)
Research Program
70% of childhood
survivors are over
For all five-year survivors of a cancer or tumour diagnosed under age
age of 20
25 years in British Columbia, Canada, from 1970, using population
registers and linked databases, the CAYACS Program aims to:
• Develop a resource for survivorship research
After
25 years,
40% have
• Determine risks of long term problems in multiple domains
5.2% have
blto these
• Examine patterns and
d quality
l off health
h l h care in relation
l problems
h
developed
risks a
needing
second cancer
Survivors,
hospitalization
one third less
likely to
marry
14es Journées annuelles de santé publique
BC C/A/YA Cancer Survivors
17
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