OAR 333-010-0020
Cancer Reporting Regulations: Reporting Requirements for Health Care Facilities


This rule describes the specific requirements for health care facilities. Such facilities include inpatient facilities, outpatient facilities acting under the license of a hospital, ambulatory surgical centers, privately owned treatment or diagnostic centers contracted to and acting as a department of a health care facility or any other facility in which patients are diagnosed or provided treatment for cancer or benign or borderline tumors of the brain and central nervous system.

(1)

Health care facilities must report to OSCaR each case of reportable cancer or reportable non-malignant condition, as defined in OAR 333-010-0000 (Cancer Reporting Regulations: Definitions)(16) and 333-010-0000 (Cancer Reporting Regulations: Definitions)(18) respectively, in patients admitted for diagnosis or any part of the first course of treatment for that cancer. OSCaR will make lists of reportable cancers and reportable non-malignant conditions available on the Oregon State Cancer Registry website: www.healthoregon.org/oscar.

(2)

Health care facilities must report cases of reportable cancer or reportable non-malignant conditions to OSCaR as stipulated in OAR 333-010-0020 (Cancer Reporting Regulations: Reporting Requirements for Health Care Facilities)(1) within 180 days of the date the case first receives cancer diagnostic or treatment services at the facility.

(3)

Health care facilities with an active follow-up program must annually report vital status, date of last patient contact, and, if available, cancer or tumor status of reportable cancers and reportable non-malignant conditions to OSCaR.

(4)

Health care facilities must report their cases of reportable cancer or reportable non-malignant conditions and any follow-up information to OSCaR in the electronic data exchange format and codes, Record Type A: Case Abstract, as specified by NAACCR, including the variables specified in the Reportable Cancer Data Items List. The OSCaR Reportable Data Items List will be available on the Oregon State Cancer Registry website: www.healthoregon.org/oscar.

(5)

OSCaR shall establish a system of confirmation of receipt of cases submitted by each health care facility.

(6)

Health care facilities reporting cases of reportable cancer or reportable non-malignant conditions to a health system cancer registry have discharged their reporting responsibilities provided that the health system registry reports those cases to OSCaR according to the requirements for health care facilities.

(7)

Health care facilities may also elect to contract with a private vendor or contractor to report cases of reportable cancer and reportable non-malignant conditions to OSCaR as outlined above in OAR 333-010-0020 (Cancer Reporting Regulations: Reporting Requirements for Health Care Facilities)(1) through (4).

(8)

Any health care facility designated as a Type A or Type B rural hospital by the Oregon Office of Rural Health, may elect to meet the cancer reporting requirements by conducting their own identification of cases of reportable cancer and reportable non-malignant conditions and mailing a copy of the relevant portions of the medical record for each case to the central cancer registry. The central cancer registry staff will abstract and report such cases and bill the hospital for this service at its cost. Type A or Type B rural hospitals which authorize the central cancer registry to abstract and report cases have fulfilled their abstracting and reporting requirements under these rules.

(9)

Upon application to OSCaR by a health care facility, OSCaR may grant to the facility an extension of time, not to exceed one year, in which to meet the reporting requirements. Such requests must be in writing and directed to the state central cancer registry manager, with a copy to the State Health Officer at the Division. On request, the central cancer registry staff shall provide technical assistance to facilities to meet the reporting requirements.

(10)

Intentionally left blank —Ed.

(a)

If cancer reports from a health care facility do not meet reporting requirements, OSCaR shall inform the facility in writing of the disparity between the facility’s reports and the reporting standards. OSCaR will then consult with the facility regarding its options for meeting the reporting standards, as defined in OAR 333-010-0020 (Cancer Reporting Regulations: Reporting Requirements for Health Care Facilities)(1) through (4). Options shall include, but are not limited to:

(A)

Further consultation and training;

(B)

Referral to contractors for reporting services;

(C)

Provision, at cost, of reporting services by OSCaR. By selecting this option, health care facilities will fulfill all reporting requirements as defined in OAR 333-010-0090 (Cancer Reporting Regulations: Fees).

(b)

If, after a minimum of 30 days from the receipt of the written notification, the facility cannot meet the reporting requirements, OSCaR may activate its reporting service for the facility. When activated, OSCaR may enter the facility, obtain the information and report it in conformance with the appropriate format and standards. In these instances, the facility shall reimburse OSCaR or its authorized representative for the cost of obtaining and reporting the information.

Source: Rule 333-010-0020 — Cancer Reporting Regulations: Reporting Requirements for Health Care Facilities, https://secure.­sos.­state.­or.­us/oard/view.­action?ruleNumber=333-010-0020.

333‑010‑0000
Cancer Reporting Regulations: Definitions
333‑010‑0020
Cancer Reporting Regulations: Reporting Requirements for Health Care Facilities
333‑010‑0030
Cancer Reporting Regulations: Reporting Requirements for Practitioners
333‑010‑0032
Cancer Reporting Regulations: Reporting Requirements for Clinical Laboratories
333‑010‑0035
Cancer Reporting Regulations: Patient Notification Requirement
333‑010‑0040
Cancer Reporting Regulations: Quality Standards
333‑010‑0050
Cancer Reporting Regulations: Confidentiality and Access to Data
333‑010‑0055
Cancer Reporting Regulations: Research Studies
333‑010‑0060
Cancer Reporting Regulations: Special Studies
333‑010‑0070
Cancer Reporting Regulations: Advisory Committee
333‑010‑0080
Cancer Reporting Regulations: Training and Consultation
333‑010‑0090
Cancer Reporting Regulations: Fees
333‑010‑0100
ScreenWise Breast and Cervical Cancer Program: Description of the ScreenWise Breast and Cervical Cancer Program
333‑010‑0105
Definitions
333‑010‑0110
Client Eligibility
333‑010‑0115
Client Enrollment
333‑010‑0120
Covered Services
333‑010‑0125
Excluded Services
333‑010‑0130
Standards of Care for Breast and Cervical Cancer Screening and Diagnostic Services
333‑010‑0135
Provider Enrollment
333‑010‑0140
Billing
333‑010‑0145
Claims and Data Submission
333‑010‑0150
Timely Submission of Claims and Data
333‑010‑0155
Payment
333‑010‑0160
Requirements for Financial, Clinical and Other Records
333‑010‑0165
Compliance with Federal and State Statutes
333‑010‑0170
Denial or Recovery of Reimbursement Resulting from Review or Audit
333‑010‑0175
Recovery of Overpayments to Providers Resulting from Review or Audit
333‑010‑0180
Provider Sanctions
333‑010‑0185
Provider Appeals
333‑010‑0190
Provider Appeals (Level 1) — Claims Reconsideration
333‑010‑0195
Provider Appeals (Level 2) — Contested Case Hearing
333‑010‑0197
Presumptive Eligibility for BCCTP
333‑010‑0200
ScreenWise WISEWOMAN Program: Description of the WISEWOMAN Program
333‑010‑0205
Definitions
333‑010‑0210
Client Eligibility
333‑010‑0215
Client Enrollment
333‑010‑0220
Provider Enrollment
333‑010‑0225
Standards of Care for WISEWOMAN Program Screening and Services
333‑010‑0230
Submission of Information by Ancillary Providers
333‑010‑0235
Covered Services
333‑010‑0240
Excluded Services
333‑010‑0245
Claims and Billing
333‑010‑0250
Payment
333‑010‑0255
Denial or Recovery of Reimbursement Resulting from Review or Audit
333‑010‑0260
Recovery of Overpayments to Providers Resulting from Review or Audit
333‑010‑0265
Client Data Submission
333‑010‑0270
Requirements for Financial, Clinical and Other Records
333‑010‑0275
Compliance with Federal and State Statutes
333‑010‑0280
Provider Sanctions
333‑010‑0285
Provider Appeals (Level 1) — Claims Reconsideration
333‑010‑0290
Provider Appeals (Level 2) — Contested Case Hearing
333‑010‑0300
Tobacco Prevention and Education Program: Definitions
333‑010‑0310
Tobacco Prevention and Education Program: Purpose and Intent
333‑010‑0320
Tobacco Prevention and Education Program: Framework for Grant Awards
333‑010‑0330
Tobacco Prevention and Education Program: Local Coalitions and Community-Based Programs
333‑010‑0350
Tobacco Prevention and Education Program: Statewide Public Awareness and Education Programs
333‑010‑0360
Tobacco Prevention and Education Program: Statewide and Regional Projects Programs
333‑010‑0370
Tobacco Prevention and Education Program: Reporting
333‑010‑0600
Childhood Diabetes Database: Definitions
333‑010‑0610
Childhood Diabetes Database: General Authority and Purpose
333‑010‑0620
Childhood Diabetes Database: Reporting Requirements for Schools
333‑010‑0630
Childhood Diabetes Database: Reporting Requirements for Practitioners
333‑010‑0640
Childhood Diabetes Database: Confidentiality and Access to Data
333‑010‑0650
Childhood Diabetes Database: Research Studies
333‑010‑0660
Childhood Diabetes Database: Advisory Committee
333‑010‑0700
Dental Pilot Projects: Purpose
333‑010‑0710
Dental Pilot Projects: Definitions
333‑010‑0720
Dental Pilot Projects: Application Procedure
333‑010‑0730
Dental Pilot Projects: Application Review Process
333‑010‑0740
Dental Pilot Projects: Project Application Provisional Approval or Denial
333‑010‑0750
Dental Pilot Projects: Provisional Approval
333‑010‑0760
Dental Pilot Projects: Minimum Standards
333‑010‑0770
Dental Pilot Projects: Informed Consent
333‑010‑0780
Dental Pilot Projects: Pilot Project Evaluation and Monitoring by Sponsor
333‑010‑0790
Dental Pilot Projects: Authority Responsibilities
333‑010‑0800
Dental Pilot Projects: Project Modifications
333‑010‑0810
Dental Pilot Projects: Discontinuation or Completion of Project
333‑010‑0820
Dental Pilot Projects: Suspension, Denial or Termination of Project
Last Updated

Jun. 8, 2021

Rule 333-010-0020’s source at or​.us