- Location
- Remote - MN, United States of America
- Workplace
- Remote
- Type
- Internship
- Seniority
- Internship
- Source
- Workday
Description
Here at Savista, we enable our clients to navigate the biggest challenges in healthcare: quality clinical care with positive patient experiences and optimal financial results. We partner with healthcare organizations to problem solve and deliver revenue cycle improvement services that enable their success, support their patients, and nurture their communities, all while living our values of Commitment, Authenticity, Respect and Excellence (CARE).
This position is for a Student intern currently enrolled in the cancer information management program at the University of Cincinnati to complete the NCRA Practicum as indicated below:
Core Competency 1: Casefinding (approximately 12 hours)
Review source documents for potentially reportable cases to add to a suspense file.
Determine single versus multiple primaries.
Competency 2: Abstracting, Coding, and Staging (approximately 25 hours) Patient Identification
Verify and enter demographic information at diagnosis.
Identify primary payor.
Collect information on morbidities.
Assign accession and sequence numbers. Cancer Identification
Analyze medical record source documents to code primary cancer characteristics.
Analyze medical record source documents to interpret and code facility specific information.
Record pertinent information from source documents in text format to support all coded data items.
Clarify conflicting, ambiguous, or incomplete documentation. Staging Determine the stage of primary cancer:
TNM staging: Summary Stage, Specialty staging, Other staging Code other stage related elements: Site-specific factors, Mets at diagnosis
Core Competency 3: Analysis and Data Usage (approximately 5 hours)
Recommend data selection criteria for study requests.
Provide data for the evaluation of treatment, patient, and quality of life. Prepare reports to document research results and satisfy requests for data.
Process data requests according to privacy standards and institutional policy.
Provide information to support strategic planning, education, research, and marketing.
Monitor program adherence to evidence-based clinical practice guidelines.
Use benchmarking techniques to identify areas for improvement.
Generate data to identify the need for screening, prevention, or educational programs. Conduct statistical analyses.
Maintain data request log.
Core Competency 4: Registry Organization, Follow-Up, and Data Quality Assurance (approximately 10 hours) Registry Operations
Maintain knowledge of current trends, standards, and developments in oncology, cancer registry, and cancer program management.
Ensure program compliance with state/provincial and national registry rules, regulations, and standards.
Prepare and submit data to a central cancer registry.
Comply with applicable laws, regulations and policies regarding confidentiality, release of information, use of medical records, and research.
Maintain up-to-date policies and procedures. Case Validation and Finalization Interpret and resolve single-field, inter-field and interrecord edit errors.
Update or correct cases as necessary from a quality control review (e.g., internal or external review, including central registry).
Review Edit reports from external sources (e.g., NCDB, central registries) to improve the quality of facility data.
Identify education and training needs based on results of quality reviews.
Communicate results of quality assurance activities to appropriate entities.
Participate in quality studies conducted by standard setters (e.g., reliability studies).
Conduct follow-back activities. Follow-Up
Obtain follow-up information from physicians, patients, and/or other sources.
Enter follow-up information, such as: vital status, cancer status, date of last contact, first recurrence, progression of disease, and subsequent treatment.
Determine the need to submit additional information to central registries for previously reported patients. Data Quality Assurance
Develop and maintain the quality control plan.
Analyze the use of unknown and NOS data values.
Respond to inquiries from central registries.
Conduct casefinding audits to assess completeness of case reporting. Conduct re-abstracting audits to assess accuracy of data.
Perform visual review of text fields to assess accuracy of coded data.
Core Competency 5: Cancer Program Accreditation (approximately 5 hours)
Collaborate with committees (e.g., cancer committee, breast program leadership) to plan and schedule committee activities.
Coordinate and participate in committee meetings.
Prepare data and reports for presentation at committee meetings.
Document cancer program activities in committee meeting minutes.
Maintain supporting documentation necessary for accreditation.
Participate in accreditation survey site visits.
Coordinate resolution of deficiencies identified during accreditation surveys.
Participate in the application, approval, and evaluation processes for maintaining continuing education credits for cancer conferences (i.e., tumor boards).
Coordinate cancer conference activities.
Document cancer conference activities. This is a correct record of the completed practicum activities that I have witnessed. The student is aware that passing the five (5) core competency assessments is required to complete the practicum.
SAVISTA is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, age, veteran status, disability, national origin, sex, sexual orientation, religion, gender identity or any other federal, state or local protected class.