PURPOSE: This procedure statement outlines how BlueCross BlueShield of Tennessee, Inc., and its affiliated companies, ("the Plan") may initiate corrective actions if an applicant or participating Provider fails to comply with applicable medical management requirements set forth in section 1, below. The Plan’s medical management programs include Provider credentialing, utilization review, quality management and Member grievance resolution activities that are overseen by professional review committees. The Plan's Board of Directors has designated the Medical Management Committee and its subcommittees (the "Committees") as the professional review committees responsible for performing peer review activities in accordance with the Federal Health Care Quality Improvement Act (the "HCQIA"), TCA section 63-6-219 and other applicable laws governing the organization and operation of professional peer review or medical review committees (the "Peer Review Laws").
The Plan's staff has been authorized to provide necessary support services to the Committees. Members of the Board, Committee Members, staff Members and anyone providing information to those Committees are intended to be protected against liability to the fullest extent permitted by the Peer Review Laws. The terms of this Procedure statement have been incorporated by reference into the Plan’s Provider participation applications and agreements. As partial consideration for being
permitted to apply to become a participating Provider and, if applicable, selected to participate in the Plan, participating Providers agree that they shall not seek to hold the Plan or such individuals liable for acts taken in good faith in accordance with this Procedure statement.
This procedure only applies to matters that involve Committee actions. Matters that do not involve Committee actions include: the non-acceptance of a participation application because the Provider fails to satisfy the Plan’s pre-credentialing application standards (e.g. failure to provide evidence of licensure or insurance), the termination of a Provider's participation other than by reason of that Provider’s failure
to comply applicable participation requirements (e.g. the participation agreement is terminated without cause); and disputes related to claims payment or authorization decisions. Such matters must be resolved in accordance with the Plan’s Provider Dispute Resolution Procedure statement.
Records or information concerning the activities of the Committees shall be treated and maintained as privileged and confidential peer review records to the fullest extent permitted by the Peer Review Laws. Reports to the Committees, the Board of Directors or regulatory agencies concerning actions taken pursuant to this procedure statement shall not alter the status of such records or information as privileged and confidential information.
I. PARTICIPATION REQUIREMENTS
The Plan's Chief Medical Officer or his designee (the "Chief Medical Officer") will monitor participating Providers' performance to ensure that they comply with the Plan's participation requirements. The following is intended to provide a non-exclusive summary of those participation requirements:
medical management activities. Such cooperation includes returning telephone calls, responding to written inquiries or requests from the Plan, providing information and documents requested by the Plan and cooperating with Plan staff Members as they perform their medical management activities.
accordance with applicable Plan medical management program policies and procedures.
participating Providers, unless asked to do so by a Member-patient who has been advised of that Provider’s non-participating status.
participation agreements.
care, conduct and competence.
community (e.g., no allegations of moral turpitude).
requirements as set forth in the Plan’s Credential Process, including, without limitation:
1. The Provider's licenses or certifications must be in good standing.
and effect.
status such that the credentialing information submitted to the Plan is no longer accurate.
II. CORRECTIVE ACTIONS
A. Investigation
The Plan's staff will investigate and report any apparent non-compliance with the participation requirements to the Chief Medical Officer or his designee, after making a reasonable effort to obtain material facts concerning that matter. Providers must submit requested information and fully cooperate with those staff members as a condition of their continued participation in the Plan. Staff members or the Chief Medical Officer may, at their discretion:
2. Review material documents, including Members' medical records; or
the matter being investigated.
B. Bases of Actions
The Chief Medical Officer or a Committee may initiate a corrective action if a participating Provider does not comply with applicable participation requirements, and:
objectives of the Plan's medical management program.
concerning the Provider's alleged non-compliance.
after the investigation has been completed.
request an appeal concerning the imposition of the corrective action in accordance with this procedure statement.
C. Actions by the Chief Medical Officer
Upon determining that a participating Provider has not complied with the Plan's participation requirements, the Chief Medical Officer may initiate corrective actions including, without limitation:
taken to address identified problems. A summary of the counseling session and the plan of corrective action will be included in the Provider's credentialing file.
appropriate Committee for further consideration and action.
corrective action" including without limitation:
review, mandatory prior authorizations for specified treatments or services, mandatory consultation, preceptorship, continuing medical education, and/or closure of the Provider's practice to new Members.
b. Terminating the Provider's participation.
withhold, a one-time financial penalty (e.g. the cost of services incurred as a consequence of the Provider’s non-compliance) or the denial of fees for inappropriate or unauthorized services.
additional time to investigate allegations concerning a Provider's conduct, competence, practices or reputation, the summary suspension shall remain in effect pending the completion of that investigation. Such investigation mustbe
completed within fourteen (14) days after the imposition of the summary suspension.
Provider's conduct, competence, practices or reputation may result in an imminent danger to Members' health or welfare, or impair the Plan's reputation or operations, the suspension shall continue in effect unless the Provider's participation is reinstated following a hearing conducted in accordance with section III, below.
arrangements to have other Providers render services to Members who are under the care of the suspended Provider. The suspended Provider shall
cooperate in referring Members to such other Providers in accordance with this Corrective Action Plan and the terms of his or participation agreement.
Director of that group or IPA shall be notified, in writing, of the imposition of corrective actions pursuant to this section.
D. Actions by a Committee
1. Committee Meetings
If the Chief Medical Officer refers the matter to a Committee, that Committee shall consider information submitted to it concerning a Provider's non-compliance with the Plan's participation requirements during its next regularly scheduled meeting or at a special meeting called by the Chief Medical Officer to consider that matter.
Members of the Committee may participate in such meetings in person or by telephone conference call and may take actions by consent. Any meeting of a Committee concerning a Provider's alleged non-compliance shall be conducted in confidence and any information concerning such meetings shall be maintained as privileged and confidential information to the fullest extent permitted by applicable Peer Review Laws.
2. Committee Investigations
A Committee may direct the Chief Medical Officer or his designee to further investigate and submit additional information concerning a Provider's alleged non-compliance. The Committee may also request that the Provider submit specified information or attend a meeting to respond to questions concerning such alleged non-compliance. The Provider otherwise has no right to participate in Committee proceedings.
3. Corrective Actions
The Committee may take or direct the Chief Medical Officer to take
any of the corrective actions described in section C, above.
E. Notice of Corrective Action
The Chief Medical Officer or the Chairperson of the Committee shall immediately notify the Provider, by certified or overnight mail, of the imposition of a corrective action. If the Provider is a member of an IPA or medical group, a copy of that notice shall also be sent to the Medical Director of that IPA or medical group. That corrective action shall becomeeffective as of the
date of that letter, unless the Chief Medical Officer or Committee elect to defer the effective date of that action. The notice letter shall include:
1. A description of the corrective action,
licensing board or other entities as mandated by law if the Provider doesn't request an appeal or if that action is affirmed following exhaustion of the appeal process.
III. APPEAL PROCEDURES
award; shall limit review to whether or not the Plan’s action was arbitrary and capricious; may not award punitive or exemplary damages; may not vary or disregard the terms of the Provider's participation agreement, the certificate of coverage and other agreements, if applicable; and shall be bound by
controlling law; when issuing a decision concerning the matter at issue. Emergency relief such as injunctive relief may be awarded by an arbitrator/arbitration panel. A party shall make application for any such relief pursuant to the Optional Rules for Emergency Measures of Protection of the American Arbitration Association (most recent edition). The arbitrators’ award, order or judgment shall be final and binding upon the parties. That decision may be entered and enforced in any state or federal court of competent jurisdiction. The arbitration award may only be modified, corrected or vacated for the reasons set forth in the United States Arbitration Act (9 USC § 1).
B.Appeal of Non-Reportable Action by an Applicant
imposing the corrective action. A written response will be sent to the Provider within sixty (60) days of our receipt of the written appeal.
b. The Provider must comply with the terms and conditions of the corrective action while the appeal is pending, unless specifically directed otherwise by the Committee or Chief Medical Officer.
2. Binding Arbitration
If the Provider is still not satisfied with the Committee’s decision, he may make a written request that the matter be submitted to binding arbitration in accordance with the procedure set forth in paragraph III.A.2 above.
C. Appeal of a Potentially Reportable Action by Participating Providers or Applicants
b. The Provider may not be represented by an attorney and the meeting shall not be tape recorded or recorded by a court reporter.
c. After the conclusion of the meeting, the subcommittee will make a recommendation to the appropriate Committee or the Chief Medical Officer concerning continued imposition of the corrective action. The subcommittee’s recommendation will be considered at the next regularly scheduled Committee meeting unless the Chief Medical Officer calls a special meeting to consider that report. The Committee may accept, modify or reverse the subcommittee’s recommendation, at its discretion. The Provider shall not have the right to appeal or to otherwise participate in the Committee's deliberations concerning the subcommittee’s recommendation. The Committee shall notify the Provider of its decision within ten (10) working days after the date of that meeting.
a. Appointment of the Hearing Officer
If still dissatisfied with the Committee’s decision, the Provider may request a hearing. In that event, the Chief Medical Officer shall appoint a qualified
designee to serve as the Hearing Officer within thirty (30) working days after receiving that request. The Hearing Officer:
2. May not be in direct economic competition with
the Provider requesting the hearing.
3. Must be qualified to evaluate the issues likely to be presented during the hearing.
4. Shall be acting as member of the Committee while performing his or her duties.
b. Notice of Hearing
The Hearing Officer will contact the Provider to establish a mutually acceptable date, time, and place for the hearing; which shall be conducted not less than thirty (30) days after that date. The formal hearing shall be conducted within 120 days of appointment of the Hearing Officer unless both parties agreed to extend this time limit. If the parties are unable to agree, the Hearing Officer shall schedule the hearing. The Hearing Officer shall then issue a written notice of hearing to the Provider summarizing: 1) the scheduled time, date and place where the hearing will be conducted; 2) the applicable hearing procedure; 3) a detailed description of the basis of the corrective action, including any acts or omissions which the Provider is alleged to have committed (the "Allegations"); and 4) a statement concerning whether that action may be reportable to the State licensing agency or other entities as mandated by law in accordance with applicable Peer Review Laws.
c. Hearing Procedure
The hearing will be an informal proceeding. Formal rules of evidence or legal procedure will not be applicable during the hearing. The Hearing Officer may reschedule or continue the hearing at his or her discretion or upon reasonable request of the parties. The Provider may forfeit the right to a hearing, however, if he or she fails to appear at the
hearing without good cause, the right to schedule another hearing is also forfeited. In addition to any procedure adopted by the Hearing Officer:
1. The Provider has the right to be represented by an attorney or other representative. If the Provider elects to be represented, such representation shall be at his or her own expense.
2. The hearing will be recorded by a court reporter.
3. The Provider and the Plan must provide the other party with a list of witnesses expected to testify on its behalf during the hearing and any documentary evidence that it expects to present during the hearing, as soon as possible following issuance of the notice of hearing. Either party may amend that list at any time not less than ten (10) working days before the date of the hearing.
4.Each party has the right to inspect and copy any documentary information that the other party intends to present during the hearing, at the inspecting party's expense, upon reasonableadvance notice, at the location where such records are maintained.
5. During the hearing, each party has the right to:
6. Following the hearing, each party may obtain copies of the record of the hearing, upon payment of the charges for that record. Each party
shall also receive a copy of the Hearing Officer's report and recommendation.
d. Hearing Officers' Report
The Hearing Officer will issue a written report and recommendation within thirty (30) days after the conclusion of the hearing. That written report will set forth the Hearing Officer's recommendation concerning the imposition of the corrective action, if any, and the basis for that recommendation.
e. Action by the Committee
The Hearing Officer's report will be submitted to the appropriate Committee for consideration during its next regularly scheduled meeting, unless the
Chief Medical Officer calls a special meeting to consider that report. The Committee may accept, modify or reverse the Hearing Officer's recommendation, at its discretion. The Provider shall not have the right to appeal or to otherwise participate in the Committee's deliberations concerning the Hearing Officer's report. The Committee shall notify the Provider of its decision within ten (10) working days after the date of that meeting. The committee’s decision is the final internal action by BCBST. In the event the decision is an adverse decision as defined by applicable federal and/or state laws, BCBST will report to the appropriate agencies or Boards as required by the applicable federal or state laws.
f. Appeal of Decision
Any action based upon or related to the Committee's decision must be submitted to binding arbitration in accordance with paragraph III.A.2 above.
IV. REPORTING CORRECTIVE ACTIONS
A. Reporting to Regulatory Agencies
Certain actions must be reported in accordance with both state and federal law, including without limitation, HIPDB. The Chief Medical Officer will consult with the Plan's General Counsel prior to initiating any corrective action, if there is a question concerning whether it will be a reportable action.
1. The following actions must generally be reported:
c. A summary suspension that remains in effect for longer than fourteen (14) days.
with participation requirements that are not directly related to the Provider's professional conduct or competence.
B. INTERNAL REPORTING REQUIREMENTS
All corrective actions, whether reportable to a licensing board or not, must be reported to the following persons:
1. The involved Provider.
2. The Plan's General Counsel.