What does NDCR mean in ONCOLOGY
The North Dakota Cancer Registry (NDCR) is an important tool for tracking cancer cases in the state of North Dakota. It collects data on all new cases of cancer, as well as deaths that are caused by the disease or related conditions. This information is then used to inform public policy and programs that aim to reduce the burden of cancer in the state. NDCR also provides valuable data for medical research, helping scientists better understand this often-devastating illness.
NDCR meaning in Oncology in Medical
NDCR mostly used in an acronym Oncology in Category Medical that means North Dakota Cancer Registry
Shorthand: NDCR,
Full Form: North Dakota Cancer Registry
For more information of "North Dakota Cancer Registry", see the section below.
Essential Questions and Answers on North Dakota Cancer Registry in "MEDICAL»ONCOLOGY"
What is the North Dakota Cancer Registry?
The North Dakota Cancer Registry (NDCR) is a statewide population-based cancer registry that collects data about all newly diagnosed cancer cases in the state. It also provides information about how many cases of each type of cancer have been reported in North Dakota, and where they are located. This helps health care providers make decisions about patient care, prevention efforts, research projects and public health programs in the state.
How is data collected by the NDCR?
Data for the NDCR is collected from hospitals, pathology laboratories, doctors’ offices, and other healthcare facilities throughout North Dakota. The data includes information about patient demographics, diagnosis and treatment of the cancer case.
Can anyone access NDCR data?
No, access to NDCR data is restricted to healthcare providers involved in patient care and public health professionals conducting research studies or developing public health programs.
What types of cancer are tracked by the NDCR?
The NDCR tracks seven major types of cancer; bladder, breast, colorectal (colon), kidney/renal pelvis (kidney), lung & bronchus (lung), melanoma (skin), non-Hodgkin lymphoma (NHL), prostate and thyroid. Additional rare cancers may also be tracked depending on availability of information about them.
Does the NDCR collect information on patients receiving treatments outside North Dakota?
No, only those patients living in North Dakota with a new diagnosis or treatment are tracked by the NDCR database.
How does NDCR contribute to public health programs?
The data collected by the NDCR allows public health professionals to study trends related to different types of cancers in order to develop better prevention methods and provide more accurate visions of public health status. For instance, researchers might use registry data to monitor disparities amongst various race/ethnic groups or geographic areas related to screenings rates and diagnoses rates for specific types of cancer.
Does NDCR provide any support for those with rare cancers?
Yes! The NCDR provides support resources such as education materials for both patients and healthcare providers regarding rare forms of cancer that do not have established disease-specific organizations available in their area. They can also connect individuals with similar diagnoses so they can share experiences as well as find ways to cope with their illness together.
Does NCDR offer services for family members who have a loved one diagnosed with cancer?
Yes! NCDR offers supports services such as counseling services for families dealing with a loved one's diagnosis as well as educational resources on diagnosis and treatment options available in North Dakota.
Does NCDR collaborate with other organizations to improve their research efforts?
Absolutely! NCDR works closely with organizations like American Cancer Society and National Cancer Institute among others in order to collaborate research efforts which may lead to additional insights regarding more effective treatments or preventative measures against certain diseases.
How often does NCDR release new reports based on their findings?
Reports based on NCDR findings are typically released twice per year – once during Summer months during an annual conference call featuring key findings from across all areas covered by NCDR research team members along with any updates or new initiatives released by state-level officials in charge.
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