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Title: Practice Management Series


1
Practice Management Series
  • ASCO
  • Clinical Practice Series

2
Practice Management Curriculum
  • Adapting to Changes in Medicare
  • Generating Practice Efficiencies
  • Health Information Technology in Practice

3
Adapting to Changes in Medicare2006
  • Topics for today
  • The 2006 Oncology Demonstration Project
  • Physician fee schedule changes
  • Drug administration coding
  • Part D

4
2006 Oncology Demonstration Project
  • A one-year demonstration project, effective
    1/1/06
  • Purpose is to identify and assess, in
    office-based oncology practices, certain oncology
    services that positively affect outcomes in the
    Medicare population.
  • Capture the spectrum of services oncologists
    provide to Medicare beneficiaries with certain
    cancer diagnoses
  • Determine the extent to which practice guidelines
    parallel care that hematologists/oncologists
    provide

5
2006 Oncology Demonstration Project
  • Replaces the 2005 chemotherapy demonstration
    project
  • Calendar year 2005 G-codes (G0921 G0932) have
    been eliminated, effective 12/31/05

6
G-Codes
  • CMS has established 81 new G-codes in three
    reporting categories
  • 1. Primary focus of the E M visit (G9050
    G9055)
  • 2. Whether current patient management adheres to
    clinical practice guidelines (G9056 G9062)
  • 3. Current disease state (G9063 G9130)
  • Reporting is no longer specific to chemotherapy
    administration services now associated with E
    M services for established patients with cancer

7
Who Can Participate?
  • Office-based hematologists and oncologists
  • Medicare-designated physician specialties
    hematology (specialty code 82), medical oncology
    (specialty 83), and hematology/oncology
    (specialty 90)
  • Check with your carrier to be sure your
    physicians are identified with the correct
    specialty designation

8
Who Can Participate?
  • Midlevel providers (NPs, PAs) who may bill
    independently for Medicare services are not
    eligible to participate in the demonstration
  • ASCOs interpretation of the carrier instructions
    is that visits performed in compliance with
    Medicares incident-to rules may be billed under
    the demonstration

9
How Does it Work?
  • Office-based hematologists and oncologists can
    participate for services furnished in 2006 when
  • E M services level 2 thru 5 (99212 99215) are
    provided to established patients with a primary
    diagnosis of cancer in one of 13 major diagnostic
    categories
  • Participation is voluntary and the physician
    participates by filing a claim for services with
    their Medicare carrier

10
13 Diagnostic Categories
  • Head Neck Cancer (140.0 149.9, 161.0 161.9)
  • Esophageal Cancer (150.0 150.9)
  • Gastric Cancer (151.0 151.9)
  • Colon Cancer (153.0 153.9)
  • Rectal Cancer (154.0, 154.1)
  • Pancreatic Cancer (157.0, 157.1, 157.3, 157.8,
    157.9)
  • Lung Cancer (both non-small cell and small cell)
    (162.2 162.9)
  • Female breast cancer (invasive) (174.0 174.9)
  • Ovarian Cancer (183.0)
  • Prostate cancer (185)
  • Non-Hodgkins Lymphoma (202.00 202.08, 202.80
    202.98)
  • Multiple Myeloma (203.00, 203.01)
  • Chronic myelogenous leukemia (205.10, 205.11)

11
Payment Requirements
  • To qualify for payment, providers must submit one
    G-code from each of the three reporting
    categories when billing for an E M service for
    established patients, 99212 99215
  • Claims must be assigned
  • Place of service must be office (place of
    service code 11)
  • Patients enrolled in Medicare Advantage plans are
    not eligible

12
Payment Requirements
  • Providers reporting data for all three categories
    with a qualifying visit will receive
    demonstration payment of 23
  • Allowances are as follows
  • G9050 G9055 7.67
  • G9056 G9062 7.67
  • G9063 G9130 7.66
  • The usual Part B coinsurance and deductible apply
  • Effective date is 1/1/06 carrier implementation
    date is 1/17/06 carriers will hold claims until
    1/17/06

13
E M Visits
  • The demonstration applies to E M visits with
    patients who have a diagnosis in one of the 13
    listed categories where the primary focus of the
    visit is management of the cancer, its
    complications, and the complications of its
    treatment
  • Eligible visits should have an ICD-9 code on the
    claim for one of the included cancers that
    cancer should be the first listed cancer
    diagnosis on the claim form
  • The cancer does not need to be the first list
    diagnosis of any kind

14
E M Visits
  • The E M service may be furnished on the same
    day that chemotherapy is provided to a patient or
    it may be the only service a patient receives on
    that day
  • If a medically necessary E M service is
    provided on the same day as chemotherapy
    administration, attach modifier -25 to the E M
    service

15
E M Visits
  • As always, the physician should appropriately
    document the patients record to support the
    level of E M service billed
  • E M visits should not be upcoded because of
    the additional documentation required by the
    demonstration project

16
Documentation Requirements
  • For each qualifying visit, physicians must
    identify three appropriate G-codes, one from each
    category
  • Primary focus of visit (G9050 G9055)
  • Adherence to guidelines (G9056 G9062)
  • Current disease state (G9063 G9130)

17
Documentation Requirements
  • Physician must also supply documentation in the
    patient chart to support billing for the
    demonstration project
  • The primary requirement is to identify the source
    of the guideline consulted
  • The title of the specific guideline that was
    consulted is not required

18
Documentation Requirements
  • Suggested phrases for documentation
  • Demonstration project ASCO
  • Demonstration project NCCN
  • Demonstration project ASCO NCCN, or Both
  • Demonstration project No guideline available,
    or None
  • Demonstration project Clinical trial, or CT

19
Documentation Requirements
  • Physicians do not have to provide additional
    documentation in the patient chart beyond these
    elements
  • Local Medicare carriers have been advised that
    further documentation requirements are not to be
    imposed
  • Notify ASCO if your carrier adds documentation
    requirements

20
An Alternative Approach
  • CMS has also suggested using a documentation
    template, or flowsheet, designed to fulfill all
    requirements under the demonstration project
  • http//www.asco.org/asco/downloads/Medlearn_Articl
    e_Demo_Documentation_and_Reporting.pdf
  • If such a template is used, physicians do not
    have to provide any additional documentation in
    the patient record
  • Again, local carriers are instructed not to
    impose additional documentation requirements

21
Documentation Templates from ASCO
  • ASCO has prepared 13 diagnosis-specific templates
    for use with the Demonstration Project
  • In addition to the codes, each template includes
    a list of appropriate practice guidelines (both
    ASCO and NCCN)
  • To access the ASCO templates, go to
  • www.asco.org/2006demo

22
Coding Guidance Primary Focus of the Visit
  • Physician should determine the single code that
    best identifies the primary focus of the E M
    visit on that particular day
  • CMS recognizes that many different issues are
    addressed in most E M visits physicians should
    make what to them seems the best choice for that
    day

23
Primary Focus of the Visit
  • G9050 Oncology Work-up Evaluation
  • G9051 Oncology Treatment Decision/Treatment
    Management
  • G9052 Oncology Surveillance for Disease
  • G9053 Oncology Expectant Management of Patient
  • G9054 Oncology Supervision Palliative
  • G9055 Oncology Visit Unspecified

24
Coding Guidance Guideline Adherence
  • Treating physician should choose the single code
    that best reflects whether or not patient
    management adheres to practice guidelines, and if
    not, the best listed reason why not

25
Oncology Practice Guidelines
  • G9056 Management Adheres to Guidelines
  • G9057 Management Differs from Guidelines as a
    Result of Enrollment in Clinical Trial
  • G9058 Management Differs from Guidelines because
    the Physician Disagrees with the Guidelines
  • G9059 Management Differs from the Guidelines
    because the Patient Opts for Different Treatment
  • G9060 Management Differs from Guidelines for
    Reasons Associated with Patient Illness
  • G9061 Patients Condition Not Addressed by
    Guidelines
  • G9062 Management Differs from Guidelines for
    Other Reasons

26
G9056 Management Adheres to Guidelines
Focus of the Visit What to Look For
G9050 Oncology work-up evaluation Compare tests obtained to those recommended in guidelines
G9051 Oncology treatment decision/treatment management Compare chemotherapy, hormonal therapy, immunotherapy, and radiotherapy treatments offered or provided to those recommended in guidelines
G9052 Oncology surveillance for disease Compare surveillance approach, such as tests and frequency of tests, to that recommended in guidelines
27
G9056
Focus of the Visit What to Look For
G9053 Oncology expectant management of patient Compare expectant management approach, such as tests and frequency of tests, to that recommended in guidelines
G9054 Oncology supervision of palliative therapies Compare management of patients primary symptom, complaint, or complication in that visit to that recommended in guidelines
G9055 Oncology visit unspecified Compare relevant management to relevant guidelines
28
G9057 Management Differs from Guidelines as a
Result of Enrollment in Clinical Trial
  • Code is reserved for patients who are on an
    IRB-approved clinical trial that dictates the
    care being provided in that visit
  • Will most often be relevant to visits in which
    the primary focus is treatment but may also
    include clinical trials focused on evaluation,
    surveillance, expectant management or palliation

29
G9057
  • If the primary focus of the visit is the subject
    of the clinical trial, this code should be
    submitted if the primary focus of the visit is
    other than that being evaluated in the clinical
    trial, the treating physician should determine if
    that management adheres to guidelines.

30
G9057
  • NOTE NCCN guidelines specify participation in a
    clinical trial as a recommended management
    strategy. For the purposes of this
    demonstration, if management differs from that
    specified in guidelines due to the patients
    enrollment on an IRB-approved clinical trial,
    G9057 should be reported as described above.

31
Coding Guidance Disease Status
  • Physician providing the E M service on that day
    should determine the single code that best
    represents the disease status of the patients
    cancer.
  • Disease status code should be relevant to the
    cancer that is the first listed cancer diagnosis
    on the claim form.
  • Disease status should be based on the best
    available data at the time of the visit. No
    additional diagnostic tests or evaluations should
    be performed for the purpose of further
    determining disease status for the purposes of
    this demonstration project.

32
Disease Status Codes
Lung cancer, non-small cell, small cell (162.2 162.9) G9063 G9070
Female breast cancer (174.0 174.9) G9071 G9076
Prostate cancer (185) G9077 G9083
Colon cancer (153.0 153.9) G9084 G9089
Rectal cancer (154.0, 154.1) G9090 G9095
Esophageal cancer (150.0 150.9) G9096 G9099
33
Disease Status Codes
Gastric cancer (151.0 151.9) G9100 G9104
Pancreatic cancer (157.0 157.3, 157.8, 157.9) G9105 G9108
Head and neck cancer (140.0 149.9, 161.0 161.9) G9109 G9112
Ovarian cancer (183.0) G9113 G9117
Non-Hodgkins lymphoma (202.00 202.08, 202.80 202.98) G9118 G9122
Chronic myelogenous leukemia (205.10, 205.11) G9123 G9127
Multiple myeloma (203.00, 203.01) G9128 G9130
34
Demo Project FAQs
  • How do I enroll in the demonstration project?
  • There is no separate enrollment process.
    Reporting one G-code form each category for an E
    M visit for a patient with a qualifying
    diagnosis will automatically enroll you in the
    demonstration project. Participation is
    voluntary.
  • Can I bill for the demonstration project in the
    hospital outpatient department?
  • No. CMS has stated that the demonstration can
    only be billed in the office setting (place of
    service 11).

35
Demo Project FAQs
  • Will the patient be responsible for a 20
    Medicare co-pay?
  • Yes.
  • Will non-Medicare secondary payers recognize the
    demonstration project and cover the 20 co-pay?
  • All official Medigap plans will cover the 20
    co-pay. Other secondary insurers may cover the
    co-pay. Check with individual payers.

36
Demo Project FAQs
  • Is patient consent required for the demonstration
    project?
  • No. Physicians are not required to obtain
    patient consent to participate in the
    demonstration project. However, physicians may
    choose to provide some explanation of the
    additional co-pay to their patients.

37
Demo Project FAQs
  • Is a physician required to select the G-codes for
    the demonstration or can this be done by a nurse
    reviewing the patients chart?
  • CMS has clearly noted its intent to tie the
    demonstration project to a physician service and
    has designed reporting requirements around the
    physicians evaluation and management of the
    patient. Therefore, ASCO recommends that the
    physician take primary responsibility for
    selecting and reporting the appropriate
    demonstration codes, based on his/her evaluation
    of the patient. Physicians also need to continue
    to comply with the E M documentation
    requirements for their level 2 5 office visits.

38
2006 Physician Fee Schedule
  • Conversion factor
  • Payment for covered outpatient drugs and
    biologicals
  • Diagnostic imaging
  • Physician self-referral prohibition
  • HCPCS changes

39
Conversion Factor
  • CF was scheduled to decrease 4.4 on 1/1/06
  • Before the holiday break, the House and Senate
    both approved a conference report to freeze the
    conversion factor at 2005 levels BUT the Senate
    struck three unrelated provisions on a point of
    order and now the House must re-pass the report
  • House is expected to re-pass the report, but this
    is not guaranteed
  • Timing is unclear, probably late January or
    February
  • Freeze on CF will likely be retroactive to
    1/1/06 impact on claims processing unclear at
    this time

40
Payment for Covered Outpatient Drugs and
Biologicals
  • Average Sales Price (ASP)
  • ASP calculation methodology remains unchanged
  • ASP updates continue to be provided quarterly,
    generally about 15 days before the beginning of
    the quarter

41
Payment for Covered Outpatient Drugs and
Biologicals
  • Intravenous infusion of immunoglobulin
  • Temporary code (G0332) established to describe
    additional pre-administration services related to
    IVIG administration
  • Intended to cover substantial additional
    resources that are associated with locating and
    acquiring adequate IVIG product and preparing for
    an office infusion of IVIG in the current
    environment.
  • G0332 may be billed once per day in association
    with a patient encounter for administration of
    IVIG.

42
Payment for Covered Outpatient Drugs and
Biologicals
  • New J-codes for IVIG
  • J1566 Injection, immune globulin, intravenous,
    lyophilized (powder), 500 mg.
  • J1567 Injection, immune globluin, intravenous,
    non-lyophilized (liquid), 500 mg.
  • Codes Q9941, Q9942, Q9943, Q9944 have been
    deleted

43
Diagnostic Imaging
  • Multiple procedure payment reduction
  • CMS finalized a proposal to reduce payment for
    the 2nd and subsequent imaging procedures within
    the same family
  • Procedure with the highest payment will be paid
    at the full amount payment for the technical
    component of additional procedures will be
    reduced
  • Professional component is not subject to this
    reduction
  • Two-year phase-in process 25 reduction in 2006,
    50 reduction in 2007
  • Reductions apply to office-based imaging only

44
Physician Self-Referral Prohibition
  • Nuclear medicine
  • Effective 1/1/07, nuclear medicine services
    (including PET scans) will be included in the
    definition of designated health services
    subject to the Stark law

45
HCPCS Changes
  • Many new codes and deleted codes
  • Watch out for new descriptions, new units of
    measure
  • Code changes are effective 1/1/06

46
Drug Administration Services
  • 2005 Medicare G-codes have been deleted effective
    12/31/05 and replaced with CPT codes
  • Definitions for 2006 CPT codes mirror the 2005
    Medicare G-codes for drug administration services
  • ASCOs coding cross-reference sheet contains the
    2006 CPT codes, the 2005 Medicare G-codes, and
    all definitions

47
Drug Administration Services
  • 2006 CPT codes should be recognized by private
    payers as CPT is the standard coding system
    recognized by HIPAA
  • Implementation dates may vary by payer
  • 2006 CPT codes for drug administration services
    are also being used in the hospital outpatient
    setting under the hospital outpatient prospective
    payment system
  • Combination of CPT codes and new C-codes
  • Payment still based on APCs

48
Drug Administration FAQs
  • Did CPT keep the terms initial, each
    additional, and additional sequential that
    were used with the Medicare G-codes?
  • Yes. The CPT book includes these same terms and
    there have been no changes in their definitions.

49
Drug Administration FAQs
  • Did CPT make any additional changes to the
    definition of an intravenous push?
  • No. The CPT Editorial Panel has defined an
    intravenous or intra-arterial push as an
    injection in which the healthcare professional
    who administers the substance or drug is
    continuously present to administer the injection
    and observe the patient, or an infusion of 15
    minutes or less.

50
Drug Administration FAQs
  • We are still very confused about concurrent
    infusions. Has there been any clarification or
    definition of a concurrent infusion?
  • The American Medical Association (AMA) defines a
    concurrent infusion as one in which multiple
    infusions are provided through the same
    intravenous line.
  • The concurrent infusion code (90768) is for
    non-chemotherapy infusions only.

51
Drug Administration FAQs
  • If a second drug is added to a bag for
    intravenous administration, can the
    administration of the second drug be reported?
  • No. More than one substance in a single bag is
    considered one infusate and one infusion. In
    this scenario, only one administration can be
    reported. The J-code for each substance is
    separately reportable.

52
Drug Administration FAQs
  • If two drugs are infused simultaneously but hung
    in two separate bags, would it still be a
    concurrent infusion?
  • Yes. Even if multiple drugs are hung separately,
    they administration is considered to be
    concurrent because the drugs are running
    simultaneously. In this situation you would
    report an initial or subsequent administration
    for the first drug and a concurrent
    administration for the second drug.

53
Drug Administration FAQs
  • What if two drugs are mixed in the same bag and
    administered for fifteen minutes?
  • If an infusion lasts 15 minutes or less, it meets
    the definition of a push and the appropriate push
    code (initial or subsequent) should be reported.
    In this situation, the infusion would be reported
    as one push however, each substance or drug
    would be separately reported.

54
Drug Administration FAQs
  • Can more than one concurrent administration code
    be reported?
  • A concurrent infusion can be billed once per
    patient encounter.
  • Is there a code for concurrent chemotherapy?
  • No. There is no code to report concurrent
    chemotherapy administrations. If a concurrent
    chemotherapy administration occurs, only one
    chemotherapy administration code can be reported.
    Each drug can be separately reported.

55
Drug Administration FAQs
  • Are there guidelines for reporting the duration
    of an infusion?
  • Yes. After the first hour of infusion, round
    infusion times to the nearest 30 minutes. For
    infusions of 30 minutes or less, round down. For
    infusions greater than 30 minutes, round up.

56
Drug Administration FAQs
  • When reporting infusion times, does the infusion
    time start when the drug/substance is being mixed
    or when the actual infusion starts?
  • The infusion time begins when the infusion
    starts. Infusion time reflects the time the
    drug/substance is actually being administered.

57
Drug Administration FAQs
  • Can we bill separately for starting an IV or
    accessing a port when providing drug
    administration services?
  • Starting an IV or accessing an IV or port are
    considered integral to the drug administration
    service and are therefore not separately
    reportable. In addition, use of local
    anesthesia, flushing at the conclusion of
    infusion, and standard tubing, syringes and
    supplies associated with infusions are considered
    to be included in the service.

58
Drug Administration FAQs
  • Is there a CPT code for flushing a port?
  • Yes. CPT code 96523 is for the irrigation of an
    implanted venous access device. Under Medicare
    rules, 96523 is payable only if it is the only
    physician fee schedule service provided on a date
    of service. This code should not be reported
    when an injection or infusion occurs on the same
    date of service.

59
And Last But Not Least Part D
  • Medicare prescription drug benefit began 1/1/06
  • Initial enrollment period continues through
    5/15/06
  • Prescription drug plans (PDPs) are available in
    all states
  • Premiums vary depending on the plan selected
  • Beneficiaries can choose
  • A stand-alone PDP which adds a drug benefit to
    traditional Medicare, or
  • A Medicare Advantage prescription drug plan or
    other Medicare health plan with prescription drug
    coverage

60
Part D
  • Part D does not affect coverage of Part B drugs
    drugs covered under Part B will remain covered as
    Part B drugs
  • Prescription drug plans must provide coverage
    under the cancer drugs/antineoplastic category
    but not all drugs will be covered
  • Prescription drug plans must have an exception
    process in place for formularies
  • You may need to advocate for coverage for
    particular drugs for your patients
  • Direct patient questions to 1-800-MEDICARE

61
ASCO Resources
  • Oncology Demonstration Project
  • FAQs
  • Complete list of G-codes
  • Documentation templates
  • Impact assessment tool
  • Complete listing of ASCO and NCCN guidelines
  • ASCO guidelines synopsis of recommendations
  • All available at www.asco.org/2006Demo

62
ASCO Resources
  • FAQs on drug administration codes and other
    changes in the 2006 physician fee schedule
  • http//www.asco.org/asco/downloads/FAQs_for_2006_D
    rug_Administration_122705.pdf
  • For drug administration coding information
  • Practical Tips for the Practicing Oncologist
    3rd Edition and Supplement for 2005
  • Available online at www.asco.org/practicaltips

63
ASCO Resources
  • Ask a Coding Question
  • Call 703-299-1054 or
  • Email practice_at_asco.org
  • Journal of Oncology Practice
  • Available by subscription and online at
    www.jopasco.org

64
Practice Guidelines
  • ASCO clinical practice guidelines
  • www.asco.org/guidelines
  • NCCN practice guidelines
  • www.nccn.org

65
CMS Resources
  • Oncology Demonstration Project
  • Guidance on data reporting for participating
    physicians
  • http//www.asco.org/asco/downloads/Medlearn_Articl
    e_Demo_Documentation_and_Reporting.pdf
  • Guidance on billing and coding
  • http//www.asco.org/asco/downloads/Medlearn_Articl
    e_Demo_Billing_and_Coding.pdf
  • Carrier instructions
  • http//www.cms.hhs.gov/transmittals/downloads/r36d
    emo.pdf
  • HCPCS code updates
  • http//www.cms.hhs.gov/HCPCSReleaseCodeSets/02_HCP
    CS_Quarterly_Update.aspTopOfPage
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