Transcript Minority Health Conference Presentation

Assessing Cancer Registry Systems:
Challenges and Opportunities for Improving
Outreach in Rhode Island Minority Populations
The Rhode Island Latino Cancer
Control Task Force (LCCTF)
Bridging the Health Care Divide: Research
and Programs to Eliminate Cancer Disparities
American Cancer Society Conference
New Orleans, Louisiana
April 18-20, 2007
Building a Coalition
2000 General Assembly urges Rhode
Island cities and towns to create
municipal Cancer Control Task Forces.
 Established partnership among American
Cancer Society, RIDOH, RICAN
 13 coalitions were formed.
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Building a Coalition
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Neither one focused on dispair
populations.
 Hispanic/Latinos are the majority of the
minority groups in RI, representing almost
12% of the overall population.
 Among the Hispanic/Latino population,
Cancer was the leading cost of death
during the period of 1999-2004 in the
State of Rhode Island.
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Building a Coalition
The Formation of the Latino Cancer Control
Task Force will help:
 to determine the nature of cancer challenge in
our community,

to examine its causes, and
 to identify resources, gaps and opportunities,
in order to develop prioritized strategies that
will diminish the cancer deaths among the
Latino community in our state.
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Building a Coalition
October 20, 2005,
The Latino Cancer Control Task Force
(LCCTF) was created as a
volunteer-based Community group formed
in response to the need to reduce the
leading causes of cancer morbidity and
mortality among Hispanic/Latinos in
Rhode Island.
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The Latino Cancer Control Task Force
Mission Statement
The Latino Cancer Control Task Force aims to
reduce the impact of cancer in the Latino
community in Rhode Island
by facilitating cancer prevention through
outreach, public education, awareness, early
detection, access to care and advocacy,
and improving care and quality of life for cancer
patients, their families, and caregivers.
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The Latino Cancer Control Task Force
Goals and Objectives
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Advocacy. Being vigorous advocates for cancer
control, supporting public policy initiatives and
research, and developing strategic alliances with
governmental agencies, hospitals, nongovernmental
health promotion organizations, health
professionals, the community, and the media.
Outreach. Providing outreach targeting the different
populations, institutions, providers, policy makers,
advocates, community leaders and organizations to
increase knowledge and awareness of cancer
issues affecting Latinos.
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The Latino Cancer Control Task Force
Goals and Objectives

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Education. Preventing cancer by increasing
knowledge and awareness of cancer and by
encouraging healthier behaviors.
Services. Promoting the early detection of
cancer through public education and access
to screenings and treatment.
Quality of life. Improving patients' quality of
life and minimizing their suffering through
education, support, and palliative care.
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The Latino Cancer Control Structure
Co-Chairs
(2)
Secretary
Data
Analysis
Workgroup
Outreach
Workgroup
Treasurer
Policy &
Advocacy
Workgroup
Media
Workgroup
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LCCTF Projects
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Conduct an assessment on what resources are
available to the Hispanic/Latino population.
Assess how data is collected and interpreted by
regulatory offices.
Bring together Latino health professionals to educate
and create community awareness on the issues of
cancer prevention and early detection.
Trough our Advocacy workgroup support American
Cancer Society Legislative Policy Priorities.
Ensure fair access to screenings and treatment.
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LCCTF Accomplishments

Membership: LCCTF membership represents the vast
diversity of Latinos in RI.

Data Analysis: Data Analysis workgroup conducted a
survey to all RI Hospitals.

1st. Annual Conference “Mujeres Hablemos
Claro! La Salud del Seno” 183 registered, 126
attended, 60 new volunteers, 13 “De Amiga a Amiga” volunteers
trained.

Legislation Introduced by one of LCCTF members
Senator Juan Pichardo, asking to increase the funds for the
WCSP.
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LCCTF Data Systems Project
Assess how data is collected and
interpreted by regulatory offices

The Rhode Island Cancer Registry
System Study
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The RICR System Study -Objectives

Conduct an assessment of the Rhode Island
Cancer Registry (RICR) System

Determine how race and ethnicity information
of cancer patients is collected and reported

Identify strengths, limitations and
opportunities for improving CR information
quality and data utilization for population
targeting and outreach
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Main Questions

What are the start and end-points of the
RI CR?
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What is the guideline?
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Is there compliance with OMB 15?
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What are the implications of non-uniform
reporting?
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Other study findings

Can under-reporting be corrected?
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Start and End-Points - RICR
COLLECTION
AGGREGATION
LOCAL, REGIONAL AND NATIONAL REPORTING
DATA SYSTEM
Cancer
Patients
Cancer
Patients/Cancer
Families
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What is the Guideline?
The Rhode Island Department of Health requires health
providers to collect the following demographic
information about their patients:
What is your ethnic background?
Hispanic/Latino
Not Hispanic/Latino
What is your race? (please indicate all races that apply)
American Indian or Alaskan Native
Asian
Black or African American
Native Hawaiian or other Pacific Islander
White
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OMB 15
Is there compliance in the collection and
reporting of race and ethnicity?
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RICRS Assessment - Methods

Hospital Survey
14 acute care hospitals
 13 cancer registries
 hospital cancer registry data not a start or
end-point
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Key Informant Interviews
3 key informants
 public health, health care industry and
national voluntary health organization
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Hospital Cancer Registry Survey

Unit of Analysis: hospitals (information collected
via questionnaire)

Population of Interest: Rhode Islanders with
a diagnosis of primary cancer

Main Topics: forms used for cancer patient
intake, collection of cancer risk factors and
race/ethnicity information, content of database
and access to cancer registry data, feasibility of
CR and MR linkage, frequency of reports and
organizations receiving reports (22 questions)
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Participating Hospitals (N=14)
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Kent Hospital
Landmark Medical Center
Memorial Hospital of Rhode Island
Miriam Hospital
Naval Health Care New England
Newport Hospital
Rhode Island Hospital
Roger Williams Medical Center
South County Hospital
St. Joseph Hospital
Our Lady of Fatima Hospital
VA Medical Center
Westerly Hospital
Women & Infants Hospital
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Key Informant Interviews

Unit of Analysis: individual expertise in cancer
data systems (information collected via questionnaire)
 Population of Interest: US population with a
diagnosis of primary cancer
 Main Topics: reporting organizations, types/
format of information reported, risk factor and
race/ethnicity information quality, methods for
adjusting under-reporting, OMB compliance,
database content and access to cancer registry
data, feasibility of CR and MR linkage, frequency
of reports and agencies targeted (26 questions)
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Key Informants (N=3)

John Fulton, PhD
Director, Rhode Island Cancer Registry
Associate Director of Health
Rhode Island Department of Health

David Rousseau, PhD
Director, Cancer Information Systems
Hospital Association of Rhode Island

Jimmy Parson, PhD
Research and Analysis Manager
American Cancer Society, NHO
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Analysis
Hospital Survey

Since sample size was small, results are
presented as frequencies and percents

Because some questions asked for more than
1 response, some figures exceed the total
number of expected responses
Responses were converted into ordinal scales
(i.e.; all=100%; most=70-99%; some=40-69%;
a few=1-39%; none=0%)
Ordinal scales were grouped by topic in order
to summarize findings
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Analysis
Key Informant Interviews
Emphasis set on the qualitative aspects of
information
 Results not presented in frequencies or
percents
 Information used to gain a better insight into
hospital survey results and inform discussion
of findings and recommendations to 1) help
improve the quality of cancer registries and 2)
translate findings into improved outreach
practices
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Main Results -Hospital Survey
Summary
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14 Rhode Island hospitals have cancer registries
Requested participation of hospital cancer
registrars
Respondents signed consent form
1 initial mailing and two respondent follow-ups
11 hospital cancer registries responded (79%
response rate)
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Findings presented exclude non-respondents
Respondent follow-up ended 04-16-07
2 hospitals share the same reporting system
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Main Results -Hospital Survey (cont.)
Race/Ethnicity/Country of Origin

How is the race of a cancer patient determined?
(this was a multiple response question)
a. In 4 hospitals (36%) patient self-reports race
b. In 5 hospitals (45%) person filling form asks patient
c. In 1 hospital (9%) person filling form makes a
guess
d. In 4 hospitals (36%) information obtained from MR
e. 1 hospital (9%) uses medical history/physical exam

2 hospitals use a combination of methods b and d
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1 hospital use a combination of methods b and c
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Main Results -Hospital Survey (cont.)
Race/Ethnicity/Country of Origin

How is the ethnicity of a cancer patient
determined? (multiple response question)
a. 3 hospitals (27%) present the patient with a
standard form and the question “Are you from
Hispanic or Latino origin”
b. 6 hospitals (56%) ask patients about their
ethnicity in a non-standard way
c. 2 hospitals (18%) reported “unknown”
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Key Informant Main Findings
TOPIC
Race/ethnicity
# of races
reported
HARI
yes
yes
most report 1 race
most report 1 race (“can
report up to six”)
most report 1 race
no
Information on
how ethnicity is
determined?
no
Target year for
helping partners
achieve OMB 15
compliance?
ACS
yes
Information on
how is race
determined?
Do you provide
guidance to
comply with
OMB 15?
RI CR
“Race and ethnicity
treated like all other
data items required
by law”
no
some; “this is a variable in
the NCAACCR data set, but
HEALTH does not require it”
no
When directed by feds
When required by state
When requested by hospitals
When required by RI HARI
“It’s being discussed but
no date yet”
no
a few
“We only look at race/
ethnicity data for
screening data and data
coming from CDC”
no response
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Start and End-Points - RICR
Cancer
Patients
Hospitals
CRs
Kent H.
1
Landmark MC
2
Memorial H RI
3
Miriam H.
4
Naval HC NE
5
Newport H.
6
Rhode Island H.
7
R. Williams MC
8
South County H.
9
Colorectal Screenings
in Health Plans
NCQA
21st Century
Oncology Services
ALA
BRFSS
YBRFS
CDC
NAACCR
NPCR
HARI
CBTRUS
ACS
CDC
RI CR
NAACCR
IACR
St .Joseph H.
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ACS
Divisions
ACS
Management
6 states
Our Lady of Fatima
VA MC
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Westerly H.
12
Women & Infants.
13
pathology labs,
surgical centers
Cancer
Patients/Cancer
Families?
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Compliance with OMB 15?

Findings from the hospital cancer registry survey
indicated lack of uniform collection of
information on race and ethnicity.
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Only a few hospitals ask patients to self-report
their race (27%) and ethnicity (27%) according to
the guideline
Only a few hospitals (36%) collect information on 2
or more races
The Key Informant Interview revealed that most
cancer data sources only report 1 race

There is no target date yet in RI for achieving
OMB 15 compliance with cancer data reporting
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Summary of Findings
1. Use of Intake Forms (IFs) specific to cancer
2. Use of IFs (cancer-specific and general)
3. Use of IFs to obtain cancer risk factor (CRF) information
4. Use of other forms to obtain CRF information
5. Collection of CRF information from all sources
6. Is reporting of CRF information a RI CR requirement?
7. Race information obtained at point of entry (POE)
8. Race information obtained from other sources
9. Ethnicity information obtained at POE
10. Ethnicity information obtained from other sources
11. RI CR mechanism to monitor OMB 15 compliance?
12. Collection of information on country of origin
13. IF/MR linkage
14. RI CR/MR linkage
15. Patient self-reporting of race and ethnicity
16. Collection of information of two or more races
17. Reporting of two or more races
18. Target date for OMB 15 compliance?
19. Cancer data available/IRB process in place
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Summary of Findings
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
16.
17.
18.
19.
45%
91%
30%
60%
90%
NO
60%
40%
56%
44%
NO
12%
100%
??
37%
27%
36%
9%
NO
91%
0%
10%
20%
Hospital Cancer Registry Survey
Key Informant Interview
30%
40%
50%
60%
70%
80%
90%
100%
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Implications of Non-Compliance

Undercount of multi-racial ethnic groups;
over count of non multi-racial ethnic groups
 Underestimates in cancer prevalence,
incidence and mortality
 Problem may not be limited to the RI CRS;
other RI/national data sets may be affected
 Difficult targeting and outreach of multiracial ethnic groups
 Misdirecting resources for targeting/outreach

Potential for unsound public health practice
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Can the Problem be Fixed?
Our recommendations:

Improve data quality at the point of entry
and monitor data quality collection and
reporting on key variables including race and
ethnicity

In the interim, promote use and refinement of
the Spanish Surname Algorithm to determine
the extent of the undercount of Hispanic
cancer cases and institutionalize dissemination
of more reliable cancer statistics
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Apply the Guideline Please
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Contact Information
Alvaro M Tinajero, MD, MPH, ScM
[email protected]
[email protected]
[email protected]
Mercedes (Betty) Bernal
[email protected]
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