The Tumor Registry is an important part of the cancer program. The registry is a collection of data of patients diagnosed and/or treated with cancer. The data includes patient demographics, extent of disease, treatment and lifetime follow-up. It is staffed by two full-time certified registrars who are trained in current cancer care methods, information collection, and statistical evaluation. The registrars are members of the National Cancer Registrars Association.
Since our 2004 reference date, the registrars have accessioned over 21,000 cases with approximately 1700 new cases diagnosed/treated in 2017. A follow-up rate of 90 percent is consistently maintained with a physician or patient follow-up letter.
Quality assurance is performed by a physician audit on at least 10% of yearly cases. This assures accuracy in staging in addition to establishing a link between the medical staff and registry.
Registry data may be used to:
Registry data is submitted to:
Researchers use these systems to determine cancer trends and treatment patterns, patient outcomes, educational and community screening guidelines.
NONDISCRIMINATION NOTICE STATEMENT
West Tennessee Healthcare (WTH) does not exclude, deny benefits to, or otherwise discriminate against any person on the grounds of race, color, national origin, age, religion, disability, Limited English Proficiency or sex, including discrimination based on gender identity, sexual orientation, sex stereotyping or pregnancy in admission to, participation in, or receipt of the services and benefits under any of its programs and activities, whether carried out by WTH directly or through a contractor or any other entity with which WTH arranges to carry out its programs and activities.
For further information about this policy, contact Amy Garner (731) 541-9914.