Cancer Program Guidelines - Association of Community Cancer ...
Cancer Program Guidelines - Association of Community Cancer ...
Cancer Program Guidelines - Association of Community Cancer ...
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Chapter 3: <strong>Cancer</strong> Data Management and Registry Operations<br />
Guideline I<br />
A cancer registry will be maintained to meet and<br />
preferably exceed the minimum requirements <strong>of</strong> the<br />
Commission on <strong>Cancer</strong> <strong>of</strong> the American College <strong>of</strong><br />
Surgeons.<br />
Rationale<br />
A cancer registry is an important program component for<br />
the evaluation <strong>of</strong> cancer care. Accurate and timely collection<br />
<strong>of</strong> cancer patient data with appropriate follow-up is required<br />
by the Commission on <strong>Cancer</strong>. The cancer registry contributes<br />
to administrative and programmatic planning, patient<br />
treatment planning, research, staging, and continuity <strong>of</strong> care<br />
through data retrieval and monitoring <strong>of</strong> outcomes through<br />
annual analysis, and long-term follow-up.<br />
Characteristics<br />
A. Case abstracting is performed or supervised by a<br />
Certified Tumor Registrar (CTR).<br />
B. The institution’s <strong>Cancer</strong> Committee monitors the activities<br />
<strong>of</strong> the cancer registry.<br />
C. An accurate and current database is maintained.<br />
1. All standards <strong>of</strong> the Commission on <strong>Cancer</strong> are<br />
rigidly followed.<br />
2. Data submission to the National <strong>Cancer</strong> Data<br />
Base (NCDB) and all other required sources are<br />
accurate and timely.<br />
3. Continuous quality improvement <strong>of</strong> the registry<br />
and data is a regular function <strong>of</strong> the registry<br />
and is documented.<br />
D. Data are reported regularly to the medical and hospital<br />
staff members.<br />
1. The data are regularly, at least annually, presented<br />
to the <strong>Cancer</strong> Committee, which assures<br />
the quality <strong>of</strong> the registry.<br />
2. The <strong>Cancer</strong> Committee also receives an annual<br />
overview for each calendar year, which may<br />
occur as part <strong>of</strong> an annual report.<br />
E. <strong>Cancer</strong> registry data are confidential.<br />
1. Compliance with the Health Insurance Portability<br />
and Accountability Act <strong>of</strong> 1996 (HIPAA)<br />
regulations is assured.<br />
2. Legitimate usage <strong>of</strong> the registry data for patient<br />
management is assured and provided in a timely<br />
fashion.<br />
3. Usage <strong>of</strong> the registry data for other purposes<br />
is encouraged, but confidentiality must be<br />
maintained.<br />
4. Research use <strong>of</strong> the data should be approved by<br />
an Institutional Review Board.<br />
ACCC <strong>Cancer</strong> <strong>Program</strong> <strong>Guidelines</strong> Chapter 3 <strong>Cancer</strong> Data Management and Registry Operations 9