OAR 410-141-3570
Managed Care Entity Encounter Claims Data Reporting


(1) MCEs shall meet the data content and submission standards as required by HIPAA 45 CFR Part 162, the Authority’s electronic data transaction rules (OAR 943-120-0100 (Definitions) through 943-120-0200 (Authority System Administration)), the Authority’s 837 technical specifications for encounter data, and the Authority’s encounter data submission guidelines that are subject to periodic revisions and available on the Authority’s web site.
(2) MCEs shall collect service information in standardized formats to the extent feasible and appropriate; if HIPAA standard, the MCE must utilize the HIPAA standards:
(a) MCEs shall submit encounter claims for all covered services, except for health-related services, provided to members as defined in OAR 410-120-0000 (Acronyms and Definitions) and 410-141-3500 (Definitions);
(b) MCEs shall submit encounter claims data including encounters for:
(A) Services where the MCE determined that liability exists; even if the MCE did not make any payment for a claim;
(B) Services where the MCE determined that no liability exists;
(C) Services to members provided by a provider under a subcontract, capitation, or special arrangement with another facility or program;
(D) Paid amounts regardless of whether the servicing provider is paid on a fee for service basis, on a capitated basis by the MCE, or the MCE’s subcontractor; and
(E) Services to members who also have Medicare coverage, if a claim has been submitted to the MCE.
(c) MCEs shall obtain a Coordination of Benefits Agreement (COBA) number and coordinate with COBA to receive direct crossover claims for dually eligible members with traditional Medicare pursuant to 42 CFR 438.3(t);
(d) MCEs shall report encounter claims data whether the provider is an in-network participating or out-of-network, non-participating provider.
(3) MCEs shall follow the DCBS standards for electronic data exchange as described in the Oregon Companion Guides available on the DCBS website.
(4) MCEs shall submit all valid unduplicated encounter claims: professional, dental, institutional, and pharmacy within 45 days of the date of adjudication:
(a) MCEs shall ensure all pharmacy encounter claims data meet the data content standards as required by the National Council for Prescription Drug Programs (NCPDP) as available on their web site or by contacting the National Council for Prescription Drug Programs organization;
(b) Submission Standards and Data Availability:
(A) MCEs shall only use the two types of provider identifiers, as allowed by HIPAA NPI standards 45 CFR 160.103 and as provided to the MCE by the Authority in encounter claims:
(i) The National Provider Identifiers (NPI) for a provider covered entity enrolled with the Authority; or
(ii) The Oregon Medicaid proprietary provider numbers for the Authority enrolled non-covered atypical provider entities.
(B) MCEs shall make an adjustment to any encounter claim within 30 days of discovering the data is incorrect, no longer valid, or some element of the claim not identified as part of the original claim needs to be changed;
(C) If the Authority discovers errors or a conflict with a previously adjudicated encounter claim except as specified in paragraph (E) below, the MCE must adjust or void the encounter claim within 30 days of notification by the Authority of the required action or as identified in paragraph (E) below;
(D) If the Authority discovers errors with a previously adjudicated encounter claim resulting from a federal or state mandate or request that requires the completeness and accuracy of the encounter data, the MCE must correct the errors within a timeframe specified by the Authority;
(E) If circumstances prevent the MCE from meeting requested timeframes for correction, the MCE may contact the Authority to determine an agreed upon specified date except as required in subsection 4(c)(D) below;
(F) MCEs retain liability for certifying encounter data as complete, truthful, and accurate. MCEs must ensure claims data received from providers, either directly or through a third-party submitter, is accurate, truthful, and complete by:
(i) Verifying accuracy and timeliness of reported data;
(ii) Screening data for completeness, logic, and consistency;
(iii) Submitting a complete and accurate Encounter Data Certification and Validation Report available on the Authority’s website.
(G) MCEs shall make all collected and reported data available upon request to the Authority and CMS as described in 42 CFR 438.242.
(c) Encounter Claims Data Corrections for “must correct” Encounter Claims:
(A) The Authority shall notify the MCE of the status of all encounter claims processed;
(B) Notification of all encounter claims processed that are in a “must correct” status shall be provided by the Authority to the MCE each week and for each subsequent week the encounter claim remains in a “must correct” status;
(C) The Authority may not necessarily notify the MCE of other errors; however, this information is available in the MCE’s electronic remittance advice supplied by the Authority;
(D) MCEs shall submit corrections to all encounter claims within 63 days from the date the Authority sends the MCE notice that the encounter claim remains in a “must correct” status;
(E) MCEs may not delete encounter claims with a “must correct” status as specified in section (3)(d) except when the Authority has determined the encounter claim cannot be corrected or for other reasons.
(5) Electronic Health Records (EHR) Systems OAR 410-165-0000 (Basis and Purpose) to 410-165-0140 (Oversight and Audits). In support of an eligible provider’s ability to demonstrate meaningful use as an EHR user, as described by 42 CFR 495.4 and 42 CFR 495.8, the MCE must:
(a) Submit encounter data in support of a qualified EHR user’s meaningful use data report to the Authority for validation as set forth in OAR 410-165-0080 (Meaningful Use);
(b) Respond within the timeframe determined by the Authority to any request for:
(A) Any suspected missing MCE encounter claims, or;
(B) MCE-submitted encounter claims found to be unmatched to an EHR user’s meaningful use report.
(6) MCEs shall comply with the following hysterectomy and sterilization standards as described in 42 CFR 441.250 to 441.259 and the requirements of OAR 410-130-0580 (Hysterectomies and Sterilization):
(a) MCEs shall submit a signed informed consent form to the Authority for each member that received either a hysterectomy or sterilization service within 30 days of the date of service; or immediately upon notification by the Authority that a qualifying encounter claim has been identified;
(b) The Authority in collaboration and cooperation with the MCE shall reconcile all hysterectomy or sterilization services with informed consents with the associated encounter claims by either:
(A) Confirming the validity of the consent and notifying the MCE that no further action is needed;
(B) Requesting a corrected informed consent form, or;
(C) Informing the MCE, the informed consent is missing or invalid and the payment must be recouped, and the associated encounter claim must be changed to reflect no payment made for services within the timeframe set by the Authority.
(7) Upon request by the Authority, MCEs shall furnish information regarding rebates for any covered outpatient drug provided by the MCE as follows:
(a) The Authority is eligible for the rebates authorized under Section 1927 of the Social Security Act (42 USC 1396r-8) as amended by section 2501 of the Patient Protection and Affordable Care Act (P.L. 111-148) and section 1206 of the Health Care and Education Reconciliation Act of 2010 (P.L. 111-152) for any covered outpatient drug provided by the MCE, unless the drug is subject to discounts under Section 340B of the Public Health Service Act;
(b) MCEs shall report prescription drug data as specified in section (3)(b).
(8) Encounter Pharmacy Data Rebate Dispute Resolution as governed by SSA Section 1927 42 U.S.C. 1396r-8 and as required by OAR 410-121-0000 (Foreword and Definition of Terms) through 410-121-0625 (Items Covered in the All-Inclusive Rate for Nursing Facilities). When the Authority receives an Invoiced Rebate Dispute from a drug manufacturer, the Authority shall send the Invoiced Rebate Dispute to the MCE for review and resolution within 15 days of receipt:
(a) The MCE shall assist in the dispute process as follows:
(A) By notifying the Authority that the MCE agrees an error has been made; and
(B) By correcting and re-submitting the pharmacy encounter data to the Authority within 45 days of receipt of the Invoiced Rebate Dispute.
(b) If the MCE disagrees with the Invoiced Rebate Dispute that an error has been made, the MCE shall send the details of the disagreement to the Authority’s encounter data liaison within 45 days of receipt of the Invoiced Rebate Dispute.

Source: Rule 410-141-3570 — Managed Care Entity Encounter Claims Data Reporting, https://secure.­sos.­state.­or.­us/oard/view.­action?ruleNumber=410-141-3570.

410–141–3500
Definitions
410–141–3501
Administration of Oregon Integrated and Coordinated Health Care Delivery System Regulation
410–141–3505
Use of Subcontractors
410–141–3510
Provider Contracting and Credentialing
410–141–3515
Network Adequacy
410–141–3520
Record Keeping and Use of Health Information Technology
410–141–3525
Outcome and Quality Measures
410–141–3530
Sanctions
410–141–3540
Member Protections
410–141–3545
Coordinated Care Organization Behavioral Health Provider, Treatment and Facility Certification and Licensure
410–141–3550
Resolving Disputes between MCEs and the Authority
410–141–3555
Resolving Disputes between Health Care Entities and CCOs that Concern CCO Contact Award
410–141–3560
Resolving Contract Disputes Between Health Care Entities and CCOs
410–141–3565
Managed Care Entity Billing
410–141–3566
Telehealth Service and Reimbursement Requirements
410–141–3570
Managed Care Entity Encounter Claims Data Reporting
410–141–3575
MCE Member Relations: Marketing
410–141–3580
MCE Member Relations: Potential Member Information
410–141–3585
MCE Member Relations: Education and Information
410–141–3590
MCE Member Relations: Member Rights and Responsibilities
410–141–3600
MCE Assessment: Definitions
410–141–3601
MCE Assessment: General Administration
410–141–3605
MCE Assessment: Disclosure of Information
410–141–3610
MCE Assessment: Calculation, Report, Due Date, Verification
410–141–3615
MCE Assessment: Filing an Amended Report
410–141–3620
MCE Assessment: Determining the Date Filed
410–141–3625
MCE Assessment: Authority to Audit Records
410–141–3630
MCE Assessment: Determining Assessment Liability on Failure to File
410–141–3635
MCE Assessment: Financial Penalty for Failure to File a Report or Failure to Pay Assessment When Due
410–141–3640
MCE Assessment: Notice of Proposed Action
410–141–3645
MCE Assessment: Hearing Process
410–141–3650
MCE Assessment: Final Order of Payment
410–141–3655
Assessment: Remedies Available after Final Order of Payment
410–141–3700
CCO Application and Contracting Procedures
410–141–3705
Criteria for CCOs
410–141–3710
Contract Termination and Close-Out Requirements
410–141–3715
CCO Governance
410–141–3720
Service Area Change for Existing CCOs
410–141–3725
CCO Contract Renewal Notification
410–141–3730
Community Health Assessment and Community Health Improvement Plans
410–141–3735
Social Determinants of Health and Equity
410–141–3740
Traditional Health Workers
410–141–3800
CCO Enrollment for Children Receiving Health Services
410–141–3805
Mandatory MCE Enrollment Exceptions
410–141–3810
Disenrollment from MCEs
410–141–3815
CCO Enrollment for Temporary Out-of-Area Behavioral Health Treatment Services
410–141–3820
Covered Services
410–141–3825
Excluded Services and Limitations
410–141–3830
Prioritized List of Health Services
410–141–3835
MCE Service Authorization
410–141–3840
Emergency and Urgent Care Services
410–141–3845
Health-Related Services
410–141–3850
Transition of Care
410–141–3855
Pharmaceutical Services
410–141–3860
Integration and Coordination of Care
410–141–3865
Care Coordination Requirements
410–141–3870
Intensive Care Coordination
410–141–3875
MCE Grievances & Appeals: Definitions and General Requirements
410–141–3880
Grievances & Appeals: Grievance Process Requirements
410–141–3885
Grievances & Appeals: Notice of Action/Adverse Benefit Determination
410–141–3890
Grievances & Appeals: Appeal Process
410–141–3895
Grievances & Appeals: Expedited Appeal
410–141–3900
Grievances & Appeals: Contested Case Hearings
410–141–3905
Grievances & Appeals: Expedited Contested Case Hearings
410–141–3910
Grievances & Appeals: Continuation of Benefits
410–141–3915
Grievances & Appeals: System Recordkeeping
410–141–3920
Transportation: NEMT General Requirements
410–141–3925
Transportation: Vehicle Equipment and Driver Standards
410–141–3930
Transportation: Out-of-Service Area and Out-of-State Transportation
410–141–3935
Transportation: Attendants for Child and Special Needs Transports
410–141–3940
Transportation: Secured Transports
410–141–3945
Transportation: Ground and Air Ambulance Transports
410–141–3955
Transportation: Member Service Modifications and Rights
410–141–3960
Transportation: Member Reimbursed Mileage, Meals, and Lodging
410–141–3965
Reports and Documentation
410–141–5000
FINANCIAL SOLVENCY REGULATION: Definitions
410–141–5005
FINANCIAL SOLVENCY REGULATION: CCO Financial Solvency Requirements
410–141–5010
FINANCIAL SOLVENCY REGULATION: Procedure for General Financial Reporting and for Determining Financial Solvency Matters
410–141–5015
FINANCIAL SOLVENCY REGULATION: Financial Statement Reporting
410–141–5020
FINANCIAL SOLVENCY REGULATION: Annual Audited Financial Statements and Auditor’s Report
410–141–5025
FINANCIAL SOLVENCY REGULATION: Qualifications of Independent Certified Public Accountant
410–141–5030
FINANCIAL SOLVENCY REGULATION: Notification of Adverse Financial Condition
410–141–5035
FINANCIAL SOLVENCY REGULATION: Accountant’s Letter of Qualifications
410–141–5040
FINANCIAL SOLVENCY REGULATION: Independent Certified Public Accountants Workpapers
410–141–5045
FINANCIAL SOLVENCY REGULATION: Corporate Governance Annual Disclosure Filing
410–141–5050
FINANCIAL SOLVENCY REGULATION: Requirements for Reinsurance
410–141–5055
FINANCIAL SOLVENCY REGULATION: Requirements for Obtaining Credit for Reinsurance
410–141–5060
FINANCIAL SOLVENCY REGULATION: Qualified Trust Agreements
410–141–5065
FINANCIAL SOLVENCY REGULATION: Letters of Credit
410–141–5070
FINANCIAL SOLVENCY REGULATION: Assets, Liabilities, Reserves
410–141–5075
FINANCIAL SOLVENCY REGULATION: Disallowance of Certain Reinsurance Transactions
410–141–5080
FINANCIAL SOLVENCY REGULATION: Transparency
410–141–5085
ASSET VALUATION AND PERMITTED INVESTMENTS: Definitions
410–141–5090
ASSET VALUATION AND PERMITTED INVESTMENTS: Calculation of Value
410–141–5095
ASSET VALUATION AND PERMITTED INVESTMENTS: Assets Other Than Securities
410–141–5100
ASSET VALUATION AND PERMITTED INVESTMENTS: Investments Used to Provide Compensating Balances
410–141–5105
ASSET VALUATION AND PERMITTED INVESTMENTS: Investment of Required Capitalization
410–141–5110
ASSET VALUATION AND PERMITTED INVESTMENTS: Investment in Mortgage Loans
410–141–5115
ASSET VALUATION AND PERMITTED INVESTMENTS: Investment in Real Property
410–141–5120
ASSET VALUATION AND PERMITTED INVESTMENTS: Investment in Corporate Stocks
410–141–5125
ASSET VALUATION AND PERMITTED INVESTMENTS: Loans
410–141–5130
ASSET VALUATION AND PERMITTED INVESTMENTS: Investments
410–141–5135
ASSET VALUATION AND PERMITTED INVESTMENTS: Personal Property
410–141–5140
ASSET VALUATION AND PERMITTED INVESTMENTS: “Prudent Investor” Standard
410–141–5145
ASSET VALUATION AND PERMITTED INVESTMENTS: Prohibited Conduct by Directors, Trustees, Officers, Agents or Employees
410–141–5150
ASSET VALUATION AND PERMITTED INVESTMENTS: Investment of Funds in Obligations That Are Not Investment Quality
410–141–5155
ASSET VALUATION AND PERMITTED INVESTMENTS: Approval by Board
410–141–5160
ASSET VALUATION AND PERMITTED INVESTMENTS: Record of Investments
410–141–5165
ASSET VALUATION AND PERMITTED INVESTMENTS: Prohibited Investments
410–141–5170
CAPITALIZATION: Capital and Surplus
410–141–5175
CAPITALIZATION: Impaired Capital and Surplus
410–141–5180
CAPITALIZATION: Dividend and Distribution Restrictions
410–141–5185
CAPITALIZATION: Restricted Reserve Account
410–141–5190
CAPITALIZATION: Surplus Notes
410–141–5195
CAPITALIZATION: Risk-based Capital (RBC) Definitions
410–141–5200
CAPITALIZATION: RBC Reports
410–141–5205
CAPITALIZATION: Company Action Level Event
410–141–5210
CAPITALIZATION: Regulatory Action Level Event
410–141–5215
CAPITALIZATION: Authorized Control Level Event
410–141–5220
CAPITALIZATION: Mandatory Control Level Event
410–141–5225
REPORTING AND APPROVAL OF CERTAIN TRANSACTIONS: Extraordinary Dividends and Other Distributions
410–141–5230
REPORTING AND APPROVAL OF CERTAIN TRANSACTIONS: Reports of Material Acquisitions And Dispositions Of Assets, and Changes to Ceded Reinsurance Agreements
410–141–5235
REPORTING AND APPROVAL OF CERTAIN TRANSACTIONS: Reports of Material Materiality and Reporting Standards for Asset Acquisitions and Dispositions
410–141–5240
REPORTING AND APPROVAL OF CERTAIN TRANSACTIONS: Materiality and Reporting Standards for Changes in Ceded Reinsurance Agreements
410–141–5245
EXAMINATIONS: CCO Production of Books and Records
410–141–5250
EXAMINATIONS: Authority Examinations of CCOs
410–141–5255
CCO ACQUISITIONS AND MERGERS: Purpose
410–141–5260
CCO ACQUISITIONS AND MERGERS: Activities Prohibited Unless Certain Provisions Satisfied
410–141–5265
CCO ACQUISITIONS AND MERGERS: Procedure For Acquiring Controlling Interest
410–141–5270
CCO ACQUISITIONS AND MERGERS: Information to Be Included in Form A
410–141–5275
CCO ACQUISITIONS AND MERGERS: Hearing, Request, Notice
410–141–5280
CCO ACQUISITIONS AND MERGERS: Determination Concerning Proposed Activity, Time For Decision, Grounds For Refusal
410–141–5285
CCO HOLDING COMPANY REGULATION: Definitions
410–141–5290
CCO HOLDING COMPANY REGULATION: Members of Holding Company Systems
410–141–5295
CCO HOLDING COMPANY REGULATION: Form and Contents of Registration Statement
410–141–5300
CCO HOLDING COMPANY REGULATION: Registration Statement Filing
410–141–5305
CCO HOLDING COMPANY REGULATION: Information Required to Be Disclosed
410–141–5310
CCO HOLDING COMPANY REGULATION: Presumption of Control
410–141–5315
CCO HOLDING COMPANY REGULATION: Disclaimer of Affiliation
410–141–5320
CCO HOLDING COMPANY REGULATION: Transactions Within Holding Company
410–141–5325
CCO HOLDING COMPANY REGULATION: Director and Officer Liability
410–141–5330
CCO HOLDING COMPANY REGULATION: Annual Enterprise Risk Report
410–141–5335
CCO HOLDING COMPANY REGULATION: Disclaimers and Termination of Registration
410–141–5340
CCO HOLDING COMPANY REGULATION: Forms
410–141–5345
CCO HOLDING COMPANY REGULATION: Forms
410–141–5350
CCO HOLDING COMPANY REGULATION: Forms
410–141–5355
CCO HOLDING COMPANY REGULATION: Forms
410–141–5360
CCO INSOLVENCY AND DISSOLUTION: Access to Funds and Transition of Members and Records
410–141–5365
CCO INSOLVENCY AND DISSOLUTION: Hazardous Operations
410–141–5370
CCO INSOLVENCY AND DISSOLUTION: Recovery From Parent Corporation Or Holding Company In The Event Of Liquidation Or Rehabilitation
410–141–5375
CCO INSOLVENCY AND DISSOLUTION: Voluntary Dissolution
410–141–5380
CIVIL PENALTIES
Last Updated

Jun. 8, 2021

Rule 410-141-3570’s source at or​.us