Current through Reg. 49, No. 38; September 20, 2024
(a) Each
managed care organization (MCO) subject to this section must develop a plan to
prevent and reduce waste, abuse, and fraud and submit that plan annually to the
Health and Human Services Commission (HHSC), Office of Inspector General (OIG)
for approval.
(b) The MCO is
responsible for investigating possible acts of waste, abuse, or fraud for all
services, including those that the MCO subcontracts to outside
entities.
(c) The plan submitted to
the HHSC-OIG must include the following information to be considered for
approval.
(1) A description of the MCO's
procedures for detecting possible acts of waste, abuse, and fraud by providers.
The description must address each of the following requirements:
(A) use of audits to monitor compliance and
assist in detecting and identifying CHIP program violations and possible waste,
abuse, and fraud overpayments through data matching, analysis, trending, and
statistical activities;
(B)
monitoring of service patterns for providers, subcontractors, and
recipients;
(C) use of a hotline or
another mechanism to report potential or suspected violations;
(D) use of random payment review of claims
submitted by providers for reimbursement to detect potential waste, abuse, or
fraud;
(E) use of edits or other
evaluation techniques to prevent payment for fraudulent or abusive
claims;
(F) use of routine
validation of MCO data; and
(G)
verification that MCO members actually received services that were
billed.
(2) A
description of the MCO's procedures for investigating possible acts of waste,
abuse, and fraud by providers. The procedures must satisfy the requirements in
subparagraphs (A) - (C) of this paragraph.
(A) The MCO must conduct a preliminary
investigation within 15 working days of the identification or reporting of
suspected or potential waste, abuse, or fraud.
(B) The preliminary investigation must
include the following:
(i) Determining if the
MCO has received any previous reports of incidences of suspected waste, abuse,
or fraud or conducted any previous investigations of the provider in question.
If so, the investigation should include a review of all materials related to
the previous investigations, the outcome of the previous investigations, and a
determination of whether the new allegations are the same or relate to the
previous investigation.
(ii)
Determining if the service provider has received any educational training from
the MCO in regard to the allegation.
(iii) Conducting a review of the provider's
billing pattern to determine if there are any suspicious indicators.
(iv) Reviewing the provider's payment history
for the past three years, if available, to determine if there are any
suspicious indicators.
(v)
Reviewing the policies and procedures for the program type in question to
determine if what has been alleged is a violation.
(C) If it is determined that suspicious
indicators of possible waste, abuse, or fraud exist, within 15 working days
from the conclusion of subparagraphs (A) and (B) of this paragraph, the MCO
must select a sample for further review. The sample must consist of a minimum
of 50 recipients or 15% of a provider's claims related to the suspected waste,
abuse, and fraud; provided, however, that if the MCO selects a sample based
upon 15% of the claims, the sample must include claims relating to at least 50
recipients. The MCO must:
(i) within 15
working days of the selection of the sample, request medical or dental records
and encounter data for the sample recipients.
(ii) review the requested medical or dental
records and encounter data within 45 working days of receipt of the records to:
(I) validate the sufficiency of service
delivery data and to assess utilization and quality of care;
(II) ensure that the encounter data submitted
by the provider is accurate; and
(III) evaluate if the review of other
pertinent records is necessary to determine if waste, abuse, or fraud has
occurred. If the review of additional records is necessary then conduct such
review.
(3) A description of the MCO's procedures for
detecting possible acts of waste, abuse, and fraud by recipients. The
description must address the following:
(A)
Review of claims when waste, abuse, or fraud is suspected or reported to
determine if:
(i) Treatment(s) and/or
medication(s) prescribed by more than one provider appears to be duplicative,
excessive, or contraindicated;
(ii)
Recipients are using more than one provider to obtain similar treatments and
/or medications;
(iii) Providers
other than the assigned Primary Care Provider (PCP) are treating the recipient,
and there is no evidence that the recipient was treated by the assigned PCP for
a similar or related condition; and
(iv) The recipient has a high volume of
emergency room visits with a non-emergent diagnosis.
(B) Review medical or dental records for the
recipients in question if claims review does not clearly determine if waste,
abuse, or fraud has occurred.
(C)
For health care MCOs, use of edits or other evaluation techniques to identify
possible overuse or abuse of psychotropic or controlled medications by
recipients who are allegedly treated at least monthly by two or more
physicians. A physician includes: psychiatrists, pain management specialists,
anesthesiologists, and physical medicine and rehabilitation
specialists.
(4) A
description of the MCO's procedures for investigating possible acts of waste,
abuse, and fraud by recipients. The procedures must satisfy the requirements in
subparagraphs (A) - (B) of this paragraph, as applicable.
(A) An MCO must conduct a preliminary
investigation within 15 working days of the identification or reporting of
suspected or potential waste, abuse, or fraud.
(B) For a health care MCO, a preliminary
investigation must include the following:
(i)
Review of acute care and emergency room claims submitted by providers for the
recipient suspected of waste, abuse, or fraud.
(ii) Analysis of pharmacy claim data
submitted by providers for the recipient suspected of waste, abuse, or fraud to
determine possible abuse of controlled or non-controlled medications. If the
MCO does not have the data necessary to conduct the pharmacy claims review, the
MCO must request the data within 15 working days of the initial identification
or reporting of the suspected or potential waste, abuse, or fraud.
(iii) Analysis of claims submitted by
providers to determine if the diagnosis is appropriate for the medications
prescribed.
(5) A description of the MCO's internal
procedures for referring possible acts of waste, abuse, or fraud to the MCO's
Special Investigative Unit (SIU) and the mandatory reporting of possible acts
of waste, abuse, or fraud by providers or recipients to the HHSC-OIG. The
procedures must satisfy the requirements in subparagraphs (A) - (E) of this
paragraph.
(A) Assign an officer or director
the responsibility and authority for reporting all investigations resulting in
a finding of possible acts of waste, abuse, or fraud to the OIG. An officer
could be but is not limited to a Compliance Officer, a Manager of Government
Programs, or a Regulatory Compliance Analyst.
(B) Provide specific and detailed internal
procedures for officers, directors, managers, and employees to report possible
acts of waste, abuse, and fraud to the MCO's SIU. The procedures must include
but are not limited to:
(i) Guidance
regarding what information must be reported to the MCO's SIU.
(ii) A requirement that information must be
reported to the MCO's SIU within 24 hours of identification or reporting of
suspected waste, abuse, and fraud.
(C) Provide specific and detailed internal
procedures for the SIU to report investigations resulting in a finding of
waste, abuse, or fraud to the assigned officer or director. The procedures must
include but are not limited to:
(i) Guidance
regarding what information must be reported to the assigned officer or
director.
(ii) A requirement that
possible acts of waste, abuse, or fraud be reported to the assigned officer or
director must occur within 15 working days of making the
determination.
(D)
Utilizing the HHSC-OIG fraud referral form, the assigned officer or director
must report and refer all possible acts of waste, abuse or fraud to the
HHSC-OIG within 30 working days of receiving the reports of possible acts of
waste, abuse or fraud from the SIU. The report and referral must include an
investigative report identifying the allegation, statutes/regulations violated
or considered, and the results of the investigation; copies of program rules
and regulations violated for the time period in question; the estimated
overpayment identified; a summary of interviews conducted; the encounter data
submitted by the provider for the time period in question; and all supporting
documentation obtained as the result of the investigation. This requirement
applies to all reports of possible acts of waste, abuse, and fraud with the
exception of an expedited referral.
(E) An expedited referral is required when
the MCO has reason to believe that a delay may result in:
(i) harm or death to patients;
(ii) the loss, destruction, or alteration of
valuable evidence;
(iii) a
potential for significant monetary loss that may not be recoverable;
or
(iv) hindrance of an
investigation or criminal prosecution of the alleged offense.
(6) A description of
the MCO's procedures for educating recipients and providers and training
personnel to prevent waste, abuse, and fraud. The procedures must satisfy the
requirements in subparagraphs (A) - (H) of this paragraph.
(A) On an annual basis, the MCO must ensure
that waste, abuse and fraud training is provided to each employee and
subcontractor who is directly involved in any aspect of CHIP. At a minimum,
training is required for all individuals responsible for data collection,
provider enrollment or disenrollment, encounter data, claims processing,
utilization review, appeals or grievances, quality assurance, and
marketing.
(B) The training must be
specific to the area of responsibility for the MCO and subcontractor staff
receiving the training and contain examples of waste, abuse or fraud in their
particular area of interest.
(C)
The MCO must ensure that general training is provided to all CHIP managed care
staff of the MCO and its subcontractors that are not directly involved with the
areas listed in subparagraph (A) of this paragraph. The general training must
provide information about the definition of waste, abuse, and fraud; how to
report suspected waste, abuse, and fraud and to whom the suspected waste,
abuse, and fraud is reported.
(D)
The organization must provide waste, abuse, and fraud training to all new MCO
and subcontractor staff that will be directly involved with any aspect of CHIP
within 90 days of the employee's employment date.
(E) Provide updates to all affected areas
when changes to policy and/or procedure may affect their area(s). The updates
must be provided within 20 working days of the changes occurring.
(F) Educate recipients, providers, and
employees about their responsibilities, the responsibility of others, the
definition of waste, abuse, and fraud and how and where to report it.
Appropriate methods of educating recipients, providers, and employees may
include but are not limited to newsletters, pamphlets, bulletins, and provider
manuals.
(G) The MCOs will maintain
a training log for all training pertaining to waste, abuse, and/or fraud in
CHIP. The log must include the name and title of the trainer, names of all
staff attending the training, and the date and length of the training. The log
must be provided immediately upon request to the HHSC-OIG, Office of the
Attorney General's (OAG)-Medicaid Fraud Control Unit (MFCU) and OAG-Civil
Medicaid Fraud Division (CMFD), and the United States Health and Human
Services-Office of Inspector General (HHS-OIG).
(H) Written standards of conduct, and written
policies and procedures that include a clearly delineated commitment from the
MCOs for detecting, preventing and investigating waste, abuse, and
fraud.
(7) The name,
title, address, telephone number, and fax number of the assigned officer or
director responsible for carrying out the plan;
(A) The person carrying out the plan should
be but is not limited to a Compliance Officer, a Manager of Government
Programs, Regulatory Compliance Analyst, Director of Quality Integrity or a
person in senior management.
(B)
When the person that is responsible for carrying out the plan changes, the
required information is to be reported to HHSC-OIG within 15 working days of
the change.
(8) A
description, process flow diagram, or chart outlining the organizational
arrangement of the MCO's personnel responsible for investigating and reporting
possible acts of waste, abuse, or fraud; and
(9) Advertising and marketing materials
utilized by the MCOs must be complete and accurately reflect the information
about the MCO. Marketing materials includes any informational materials
targeted to recipients.
(d) Each MCO must satisfy the requirements in
paragraphs (1) - (3) of this subsection related to investigations of waste,
abuse, and fraud conducted by the MCO's SIU.
(1) On a monthly basis, submit to the
HHSC-OIG a report listing all investigations conducted that resulted in no
findings of waste, abuse, or fraud. The report shall include the allegation,
the investigated recipient's or provider's CHIP number, the source, the time
period in question, and the date of receipt of the identification and/or
reporting of suspected and/or potential waste, abuse, or fraud.
(2) Maintain a log of all incidences of
suspected waste, abuse and fraud received by the MCO, regardless of the source.
The log shall contain the subject of the complaint, the source, the allegation,
the date the allegation was received, the recipient's or provider's CHIP
number, and the status of the investigation.
(3) The log should be provided at the time of
a reasonable request to the HHSC-OIG, OAG-MFCU, OAG-CMFD, and the HHS-OIG. A
reasonable request means a request made during hours that the business or
premises is open for business.
(e) MCOs must maintain the confidentiality of
any patient information relevant to an investigation of waste, abuse, or
fraud.
(f) MCOs must retain records
obtained as the result of an investigation conducted by the SIU for a minimum
period of five years or until all audit questions, appealed hearings,
investigations, or court cases are resolved.
(g) Failure of the provider to supply the
records requested by the MCO will result in the provider being reported to the
HHSC-OIG as refusing to supply records upon request and the provider may be
subject to sanction or immediate payment hold.