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Title: SNP Training Topic 2: SNP Subset of HEDIS Measures


1
SNP Training Topic 2 SNP Subset of HEDIS
Measures
  • March 18, 19, 20, 25 26, 2008

2
Overview
  • Describe the SNP evaluation project NCQA is
    executing on behalf of CMS
  • Review the SNP HEDIS reporting requirements
  • Which measures do SNPs have to report?
  • Who has to report?
  • Overview of individual measures
  • Descriptions
  • Eligible population
  • Numerator criteria

3
Introduction to SNP EvaluationBrett
KayDirector, SNP Assessment
4
Goal for SNP Evaluation Program
  • Robust and comprehensive assessment strategy
  • Applies to all SNPs
  • Responsive to the special in SNP
  • Can be implemented soon

5
Three-Year Strategy
6
Project Time Line Phase 1
  • March 14 - Release final SP measures
  • April 15 - Release ISS Data Collection Tool
  • S P Measures
  • April 25 - Release IDSS Data Collection Tool
  • HEDIS Measures
  • June 30 - HEDIS submissions and SP measures
    submissions due to NCQA
  • Sept 30 - NCQA delivers SNP Assessment Report to
    CMS

7
Training Education
  • Five training topic areas, focus is on content
    and data submission
  • Introduction to NCQA HEDIS
  • SNP Subset of HEDIS Measures
  • Interactive Data Submission System (IDSS)
  • Structure Process Measures
  • Interactive Survey System (ISS)

8
Additional Resources
  • NCQA SNP Web page www.ncqa.org/snp.aspx
  • FAQs (HEDIS)
  • Training descriptions schedule
  • SP measures
  • NCQA Policy Clarification Support (PCS)
  • http//app04.ncqa.org/pcs/web/asp/TIL_Client
  • Login.asp
  • HEDIS Audit information
  • http//www.ncqa.org/tabid/204/Default.aspx

9
NCQA Policy Clarification Support (PCS)
  • Web address
  • http//app04.ncqa.org/pcs/web/asp/TIL_ClientLogin
    .asp
  • Link from SNP Web page
  • www.ncqa.org/snp.aspx

10
PCS (contd)
  • Under Standard Categories/HEDIS Domain, select
    one of the following options
  • SNP General Reporting Guidance
  • SNP HEDIS
  • SNP Structure Process Measures
  • Menu options under Standard/Measures
  • If SNP General Reporting Guidance was
    selected
  • Not Applicable

11
PCS (contd)
  • Menu options under Standard/Measures
  • If SNP HEDIS was selected
  • (COL) Colorectal Cancer Screening
  • (GSO) Glaucoma Screening in Older Adults
  • (SPR) Use of Spirometry Testing in the Assessment
    and Diagnosis of COPD
  • (PCE) Pharmacotherapy of COPD Exacerbation
  • (CBP) Controlling High Blood Pressure
  • (PBH) Persistence of Beta Blocker Treatment After
    a Heart Attack
  • (OMW) Osteoporosis Management in Older Women
  • (AMM) Antidepressant Medication Management
  • (FUH) Follow-Up After Hospitalization for Mental
    Illness
  • (MPM) Annual Monitoring for Patients on
    Persistent Medications
  • (DDE) Potentially Harmful Drug-Disease
    Interactions
  • (DAE) Use of High Risk Medication in the Elderly
  • (BCR) Board Certification
  • Other

12
PCS (contd)
  • Menu options under Standard/Measures
  • If SNP Structure Process was selected
  • SNP 1 Complex Case Management
  • SNP 2 Improving Member Satisfaction
  • SNP 3 Clinical Quality Improvements
  • Other

13
Contacts
  • Brett KayDirector, SNP Assessment202-955-1722k
    ay_at_ncqa.orgCasandra MonroeAssistant Director,
    SNP Assessment202-955-5136monroe_at_ncqa.org

14
SNP HEDIS Reporting Requirements Mary
BramanDirector, Licensure Certification.
15
SNP HEDIS Reporting Requirements
  • Required Measures
  • (COL) Colorectal Cancer Screening
  • (GSO) Glaucoma Screening in Older Adults
  • (SPR) Use of Spirometry Testing in the
    Assessment and Diagnosis of COPD
  • (PCE) Pharmacotherapy of COPD Exacerbation
  • (CBP) Controlling High Blood Pressure
  • (PBH) Persistence of Beta Blocker Treatment
    After a Heart Attack
  • (OMW) Osteoporosis Management in Older Women
  • (AMM) Antidepressant Medication Management
  • (FUH) Follow-Up After Hospitalization for Mental
    Illness
  • (MPM) Annual Monitoring for Patients on
    Persistent Medications
  • (DDE) Potentially Harmful Drug-Disease
    Interactions
  • (DAE) Use of High Risk Medication in the Elderly
  • (BCR) Board Certification
  • SNP benefit packages under PPO Contracts do not
    have to report these measures because these
    measures rely on medical record review.
  • This first-year measure is optional for all MA
    reporting, including the SNP benefit packages.

16
General Reporting Requirements
  • Who reports and what is the level of reporting?
  • Every SNP benefit package (identified by the CMS
    Plan ID)
  • Effective date of January 1, 2007
  • Enrollment 11 members as of January 1, 2007

For each SNP benefit package, the MA plan must
report the HEDIS and Structure Process measures
17
Reporting Structure
  • Question What are the HEDIS reporting
    requirements for MA plans and SNP benefit
    packages?
  • Response See the chart below for details about
    the reporting requirements.

Organizations with SNP benefit packages that
have an enrollment of lt11 as of January 1, 2007
do not report HEDIS measures.
18
Audit Requirement
  • Question Does every submission require an
    audit? 
  • Response Yes, every SNP benefit package level
    submission must undergo a HEDIS Compliance Audit.

19
Patient-Level Detail File
  • Question Does CMS require a Patient Level Detail
    File for each SNP benefit package submission?
  • Response No, the plan does not need to create a
    separate patient-level file for each SNP
    submission. However, the patient-level data
    submitted for the larger Contract-level must
    include all MA members, including members
    enrolled in its SNP benefit packages. (See the
    Reporting Structure Chart above.)

20
Medicare Specifications
  • Question Does the SNP submission use
    Medicare specifications for the measures? 
  • Response Yes, for the 13 required measures, use
    the specifications in Volume 2, HEDIS
    Specifications.

21
Continuous Enrollment
  • Question How is continuous enrollment calculated
    for the SNP benefit packages?
  • Response Calculate continuous enrollment for SNP
    members according to the standard HEDIS
    requirement for Medicare products. Report members
    in the SNP they are enrolled in at the end of the
    continuous enrollment period. For measures with
    no continuous enrollment requirement, report
    members in the SNP they were in at the time of
    service.

22
Medicare Advantage
  • Question If an MA plan has a SNP benefit
    package, does it report the members in the
    Medicare Contract submission AND the SNP
    submission?
  • Response Yes, SNP members will be reported in
    two submissions the full Medicare submission at
    the Contract-level and the SNP benefit package in
    which they receive benefits.

23
Dual-Eligible SNP
  • Question For Dual-Eligible SNP benefit packages,
    is a member reported to NCQA in the Medicare,
    Medicaid, and SNP submissions?
  • Response Yes, in all three. All HEDIS
    guidelines about dual eligible members still
    apply, and these members are also included in the
    SNP-specific submission.

24
SNP- only Plan
  • Question If a Medicare Advantage organization,
    which offers only SNP benefit packages, meets the
    HEDIS reporting threshold at the Contract level
    (1,000 members as of July 1, 2007), does it
    report all HEDIS measures required for
    Contract-level reporting or only the 13 SNP
    measures?
  • Response A Medicare Advantage, SNP-only
    organization that meets the regular Medicare
    Advantage HEDIS reporting requirements must
    report all HEDIS MA measures and the subset of
    SNP measures for each benefit package.

25
Medicare Advantage Hybrid Method
  • Question If an MA plan uses the hybrid method to
    report any measure, must they draw a separate
    sample for the SNP benefit packages?
  • Response Yes, every submission is treated
    separately for example, if a plan reports
    Colorectal Cancer Screening for the full MA plan
    population and a SNP benefit package, two
    distinct samples must be drawn.

26
Medicare Advantage Hybrid Method
  • Question If an MA plan draws a sample for the
    Controlling High Blood Pressure measure for the
    MA population and a separate sample for the same
    measure for the SNP benefit package, what does
    the plan do with the overlapping members?
  • Response If there are SNP members in the sample
    for the full MA plan (main sample), the plan may
    use them for the SNP sample. For example, the
    main sample of 411 has 5 SNP members. The SNP
    sample has 250. Randomly select 5 members from
    the SNP sample and replace them with 5 SNP
    members in the main sample. The 5 SNP members
    are evaluated in both samples. All SNP members in
    the main sample must be used for the SNP sample,
    and the auditor must approve the process.

27
Small Denominators
  • Question How are small denominators handled?
  • Response To understand the performance of the
    entire SNP program, it is important that SNPs
    report a measure even when there are fewer than
    30 members in the measures denominator.
  • Each SNP benefit package must collect data and
    report the required measures according to the
    specifications regardless of the denominator
    size.
  • In the SNP Performance Report we produce for CMS,
    NCQA will include SNP-specific performance rates
    for only measures that have denominators of 30 or
    more members.
  • Measures with fewer than 30 members in the
    denominator will be used for aggregated
    program-level reporting only.
  • NCQAs Interactive Data Submission System (IDSS)
    will not calculate a rate for measures where the
    denominator is fewer than 30, but NCQA will use
    the reported measure numerators and denominators
    for aggregated reporting.

28
For Support
  • Question How do I contact NCQA with a question
    about the SNP HEDIS reporting requirements or a
    specific HEDIS measure?
  • Response You can get help at any of these Web
    site links
  • NCQA SNP Webpage www.ncqa.org/snp.aspx
  • FAQs (HEDIS)
  • Training descriptions schedule
  • Final HEDIS and SP measures
  • NCQA Policy Clarification Support (PCS)
  • http//app04.ncqa.org/pcs/web/asp/TIL_ClientLogi
    n.asp
  • HEDIS Audit information
  • http//www.ncqa.org/tabid/204/Default.aspx

29
Aisha T. Pittman, MPH
  • Overview of SNP Subset of HEDIS Measures

30
HEDIS Measures for SNPs
  • Selected in collaboration with SNP Technical
    Panel
  • Excluded measures with upper age limit below 75
  • Excluded measures focusing on management of one
    chronic condition
  • Collected by SNP benefit package, regardless of
    size
  • Will be reported in aggregate

31
HEDIS Measures FY 08
SNP benefit packages under PPO Contracts do not
have to report these measures because these
measures rely on medical record review. This
first-year measure is optional for all MA
reporting, including the SNP benefit packages.
32
HEDIS General Guidelines
  • HEDIS 2008, Volume 2 Technical Specifications
  • General Guidelines for Data Collection and
    Reporting (p. 11) apply to SNP reporting

33
Components of HEDIS Measures
  • Measure Description
  • Explains what the rate is capturing
  • Definitions
  • Intake Period- time period to identify eligible
    episodes
  • Episode Date- date of event or service
  • Index Episode Start Date (IESD)- the earliest
    episode date during the intake period
  • Eligible Population
  • The total population that meet the measure
    specifications -also referred to as the
    denominator
  • Exclusions can be applied to the denominator if
    applicable

34
Components of HEDIS Measures
  • Rate
  • The rate is the numerator/eligible population
  • The numerator is comprised of those people who
    received the treatment or service indicated in
    the measure
  • Data Collection Methodology
  • There are three possible methods
  • Administrative
  • Medical Record or Hybrid
  • Survey

35
Eligible Population
  • Product lines
  • Commercial, Medicare, Medicaid
  • Ages
  • Continuous enrollment
  • The time period during which a member must be
    continuously enrolled in the plan
  • Allowable gap
  • Gaps allowed during the continuous enrollment
    period
  • Anchor date
  • Enrollment date criteria for the eligible
    population
  • Benefit
  • The type of benefits the member must have to be
    included in the measure
  • Event/diagnosis

36
Colorectal Cancer Screening (COL)
  • The percentage of members 50 80 years of age
    who had appropriate screening for colorectal
    cancer
  • Eligible Population
  • Members 51-80 years as of 12/31 of the
    measurement year
  • Continuously enrolled during the measurement year
    and the year prior
  • No more than one 45 day gap in enrollment during
    each year of continuous enrollment
  • Exclude members with diagnosis of colorectal
    cancer or total colectomy

37
Colorectal Cancer Screening (COL)
  • Numerator Criteria
  • One or more appropriate screenings defined by any
    one of the following criteria
  • Fecal occult blood test (FOBT) during the
    measurement year
  • Flexible sigmoidoscopy during the measurement
    year or the four years prior to the measurement
    year
  • Double contrast barium enema (DCBE) or air
    contrast barium enema during the measurement year
    or the four years prior to the measurement year
  • Colonoscopy during the measurement year or the
    nine years prior to the measurement year
  • This measure can be collected using the hybrid
    method

38
Glaucoma Screening in Older Adults (GSO)
  • The percentage of Medicare members 65 years and
    older who received a glaucoma eye exam
  • Eligible Population
  • Members 65 years as of 12/31 of the measurement
    year
  • Continuously enrolled during the measurement year
    and year prior
  • No more than one 45 day gap in enrollment during
    each year of continuous enrollment
  • Exclude members with prior diagnosis of glaucoma
    or glaucoma suspect

39
Glaucoma Screening in Older Adults (GSO)
  • Numerator criteria
  • One or more eye exams for glaucoma by an eye care
    professional during the measurement year or the
    year prior

40
Use of Spirometry Testing in the Assessment and
Diagnosis of COPD (SPR)
  • The percentage of members 40 years of age and
    older with a new diagnosis or newly active
    chronic obstructive pulmonary disease (COPD) who
    received appropriate spirometry testing to
    confirm the diagnosis
  • Eligible Population
  • Members 42 years or older as of 12/31 of the
    measurement year
  • Continuously enrolled two years prior to IESD
    through 180 days after IESD
  • No more than one 45-day gap in enrollment in each
    12-month period before IESD or 6-month period
    after IESD

41
Use of Spirometry Testing in the Assessment and
Diagnosis of COPD (SPR)
  • Steps to Identify Eligible Population
  • Identify all members with diagnosis of COPD
    during intake period
  • Test for negative diagnosis history, exclude
    members with prior diagnosis of COPD
  • Calculate continuous enrollment
  • Numerator criteria
  • At least one claim/encounter with spirometry in
    the two years before to 180 days after the IESD

42
Pharmacotherapy of COPD Exacerbation (PCE)
  • The percentage of COPD exacerbations for members
    40 years of age and older who had an acute
    inpatient discharge or ED encounter between
    January 1December 1 of the measurement year and
    who were dispensed appropriate medications. Two
    rates are reported.
  • Dispensed a systemic corticosteroid within 14
    days of the event
  • Dispensed a bronchodilator within 30 days of the
    event
  • First-year measure, optional measure for SNP
    reporting

43
Pharmacotherapy of COPD Exacerbation (PCE)
  • Eligible Population
  • Members 40 years or older as of 12/1 of the
    measurement year
  • Continuously enrolled Episode Date through 30
    days after Episode date, no allowable gaps
  • A COPD exacerbation indicated by acute inpatient
    discharge or ED encounter
  • Note The eligible population for this measure is
    based on acute inpatient discharges and ED
    visits, not on members. It is possible for the
    denominator to include multiple events for the
    same individual
  • Steps indicated to identify eligible population
  • Numerator Criteria
  • Rate 1 Prescription for systematic
    corticosteroid on or 14 days after Episode Date
  • Rate 2 Prescription for bronchodilator on or 30
    days after Episode Date

44
Controlling High Blood Pressure (CBP)
  • The percentage of members 1885 years of age who
    had a diagnosis of hypertension (HTN) and whose
    blood pressure (BP) was adequately controlled
    (lt140/90) during the measurement year
  • Note The hybrid method must be used for this
    measure
  • Eligible population
  • Members 18-85 years as of 12/31 of the
    measurement year
  • No more than one 45-day gap in enrollment during
    the measurement year
  • At least one outpatient encounter with a
    diagnosis of hypertension in the first six months
    of the measurement year
  • Note Hypertensive diagnosis must be confirmed in
    the medical record on or before June 30 of the
    measurement year
  • Exclude members with ESRD, who are pregnant or
    were admitted to a non-acute inpatient setting
    (institutionalized)

45
Controlling High Blood Pressure (CBP)
  • Numerator criteria
  • Representative BP is adequately controlled
  • Adequate control- representative systolic BPlt
    140mmHg and representative diastolic BP lt90mmHg
  • Representative BP- the most recent BP during the
    measurement year after the hypertension diagnosis
  • If there are multiple BPs on the same date use
    the lowest systolic and lowest diastolic
  • If no BP is recorded assume the member is not
    controlled

46
Persistence of Beta Blocker Treatment After Heart
Attack (PBH)
  • The percentage of members 18 years of age and
    older during the measurement year who were
    hospitalized and discharged alive from July 1 of
    the year prior to the measurement year to June 30
    of the measurement year with a diagnosis of acute
    myocardial infarction (AMI) and who received
    persistent beta-blocker treatment for six months
    after discharge

47
Persistence of Beta Blocker Treatment After Heart
Attack (PBH)
  • Eligible population
  • Members 18 and older as of 12/31 of the
    measurement year
  • Continuously enrolled from discharge to 180 days
    after discharge
  • Discharged alive from an acute inpatient setting
    with an AMI
  • Exclude members with a contraindication to
    beta-blocker therapy or transferred to a nonacute
    care facility (institutionalized)
  • Numerator Criteria
  • A 180-day course of treatment of beta blockers
  • Persistence of treatment must be at least 75 or
    135 days
  • If members were on beta blockers prior to
    admission, take into account those prescriptions
    in determining adherence

48
Osteoporosis Management in Women Who Had a
Fracture (OMW)
  • The percentage of women 67 years of age and older
    who suffered a fracture and who had either a bone
    mineral density (BMD) test or prescription for a
    drug to treat or prevent osteoporosis in the six
    months after the fracture

49
Osteoporosis Management in Women Who Had a
Fracture (OMW)
  • Eligible population
  • Women 67 years and older as of 12/31 of the
    measurement year
  • Continuously enrolled 12 months prior to through
    6 months after IESD
  • No more than one 45-day gap in enrollment during
    continuous enrollment period
  • Evidence of a fracture
  • Steps to identify eligible population
  • Numerator Criteria
  • A BMD test on the IESD or in the 180 day period
    after the IESD
  • A BMD test during the inpatient stay for the
    fracture
  • A dispensed prescription to treat osteoporosis

50
Antidepressant Medication Management (AMM)
  • The following components of this measure assess
    different facets of the successful
    pharmacological management of major depression.
  • Optimal Practitioner Contacts for Medication
    Management Percent of members with at least
    three follow-up contacts within 12 weeks of
    diagnosis
  • Effective Acute Phase Treatment percent of
    members who remained on an antidepressant drug
    during the 84 days/12 weeks following diagnosis
  • Effective Continuation Phase Treatment percent
    of members who remained on an antidepressant drug
    for at least 180 days/6 months

51
Antidepressant Medication Management (AMM)
  • Eligible Population
  • Members 18 years and older as of 4/30 of
    measurement year
  • Continuously enrolled 120 days prior to IESD
    through 245 days after IESD
  • Diagnosis of a new episode of major depressive
    disorder during the intake period
  • No more than one 45-day gap in enrollment
  • Steps to identify eligible population
  • Numerator criteria
  • Optimal practitioner contacts three face-to-face
    visits with a practitioner or two face-to-face
    visits and one telephone visit within 84 days
  • Effective acute phase members who fulfilled a
    sufficient number of separate prescription/refills
    of antidepressant medication to have continuous
    treatment for 84 days
  • Effective continuation phase a 180-day treatment
    with antidepressant medication

52
Follow-Up After Hospitalization for Mental
Illness (FUH)
  • The percentage of discharges for members 6 years
    of age and older who were hospitalized for
    treatment of selected mental health disorders and
    who had an outpatient visit, an intensive
    outpatient encounter or partial hospitalization
    with a mental health practitioner. Two rates are
    reported.
  • The percentage of members who received follow-up
    within 30 days of discharge
  • The percentage of members who received follow-up
    within 7 days of discharge

53
Follow-Up After Hospitalization for Mental
Illness (FUH)
  • Eligible Population
  • Members 6 years and older as of discharge date
  • Continuously enrolled from discharge date through
    30 days after discharge
  • No gaps in enrollment allowed
  • Discharged alive from an acute inpatient setting
    with a principal mental health diagnosis
  • Note The denominator is based on discharges, not
    members
  • Exclude members transferred directly to a
    nonacute facility for a non-mental health
    principal diagnosis (institutionalized)
  • Numerator Criteria
  • 30 day follow-up an outpatient visit, intensive
    outpatient encounter or partial hospitalization
    with a mental health practitioner within 30 days
    of discharge
  • 7 day follow-up an outpatient visit, intensive
    outpatient encounter or partial hospitalization
    with a mental health practitioner within 7 days
    of discharge

54
Annual Monitoring for Patients on Persistent
Medications (MPM)
  • The percentage of members 18 years of age and
    older who received at least a 180-days supply of
    ambulatory medication therapy for a select
    therapeutic agent during the measurement year and
    at least one therapeutic monitoring event for the
    therapeutic agent in the measurement year. For
    each product line, report each of the four rates
    separately and as a total rate.
  • Annual monitoring for members on angiotensin
    converting enzyme (ACE) inhibitors or angiotensin
    receptor blockers (ARB)
  • Annual monitoring for members on digoxin
  • Annual monitoring for members on diuretics
  • Annual monitoring for members on anticonvulsants
  • Total rate (the sum of the four numerators
    divided by the sum of the four denominators)

55
Annual Monitoring for Patients on Persistent
Medications (MPM)
  • Eligible Population
  • Members 18 year and older as of 12/31 of the
    measurement year
  • Continuously enrolled during the measurement year
  • No more than one 45-day gap in enrollment during
    each year of enrollment
  • 180-days supply of an ambulatory medication of
    interest
  • Note Members with more than one persistent
    medication can appear in the measure multiple
    times (i.e., in each indicator for which they
    qualify)
  • Note Members may switch therapies with any
    medication listed during the measurement year and
    have the days supply for each of those
    medications count towards the 180-days supply
  • Exclude members with an inpatient stay in the
    measurement year
  • Numerator Criteria
  • ACEI/ARBs, Digoxin, Diuretics at least one serum
    potassium and either a serum creatinine or blood
    urea nitrogen therapeutic monitoring test
  • Anticonvulsants at least one drug serum
    concentration level monitoring test for the
    described drug

56
Potentially Harmful Drug-Disease Interactions in
the Elderly (DDE)
  • The percentage of Medicare members 65 years of
    age and older who have evidence of an underlying
    disease, condition or health concern and who were
    dispensed an ambulatory prescription for a
    contraindicated medication, concurrent with or
    after the diagnosis
  • Report each of the three rates separately and as
    a total rate
  • A history of falls and a prescription for
    tricyclic antidepressants, antipsychotics or
    sleep agents
  • Dementia and a prescription for tricyclic
    antidepressants or anticholinergic agents
  • Chronic renal failure and prescription for
    nonaspirin NSAIDs or Cox-2 Selective NSAIDs
  • Total rate (the sum of the three numerators
    divided by the sum of the three denominators)
  • For all three rates, a lower rate represents
    better performance

57
Potentially Harmful Drug-Disease Interactions in
the Elderly (DDE)
  • Eligible population
  • Members 67 years and older as of 12/31 of the
    measurement year
  • Continuously enrolled the measurement year and
    the year prior
  • No more than one 45-day gap in enrollment during
    each year of continuous enrollment
  • At least one disease or condition or procedure in
    the measurement year or the year prior
  • Note Members with more than one disease or
    condition can appear in the measure multiple
    times (i.e., in each indicator for which they
    qualify)
  • Numerator criteria
  • History of falls dispensed a tricyclic
    antidepressant
  • Dementia dispensed a tricyclic antidepressant
  • Chronic renal failure dispensed an NSAID or
    cox-2 selective NSAID

58
Use of High Risk Medications in the Elderly (DAE)
  • The percentage of Medicare members 65 years of
    age and older who received at least one high risk
    medication
  • The percentage of Medicare members 65 years of
    age and older who received at least two different
    high risk medications
  • For both rates, a lower rate represents better
    performance

59
Use of High Risk Medications in the Elderly (DAE)
  • Eligible population
  • Members 67 years and older as of 12/31 of the
    measurement year
  • Continuously enrolled during the measurement year
  • No more than on 45-day gap in enrollment
  • Numerator Criteria
  • Rate 1 At least one high risk medication
    dispensed
  • Rate 2 At least two high risk medications
    dispensed

60
Board Certification (BCR)
  • The percentage of the following physicians whose
    board certification is active as of December 31
    of the measurement year.
  • Family medicine physicians
  • Internal medicine physicians
  • Pediatricians
  • OB/GYN physicians
  • Geriatricians
  • Other physician specialists
  • Board certification refers to the various
    specialty certification programs of the American
    Board of Medical Specialties and the American
    Osteopathic Association.

61
Future HEDIS Measures for SNPs
  • HEDIS 2009 Measures
  • Care for Older Adults
  • Functional Status Assessment
  • Advance Care Planning
  • Annual Medication Review
  • Pain Screening
  • Medication Reconciliation after Hospitalization
  • Public Comment closed on March 14
  • Currently analyzing the comments

62
Additional Resources
  • NCQA SNP Website
  • www.ncqa.org/snp.aspx
  • FAQs (HEDIS)
  • Training descriptions schedule
  • Final HEDIS and SP measures (March 14)
  • NCQA Policy Clarification Support (PCS)
  • http//app04.ncqa.org/pcs/web/asp/TIL_ClientLogin.
    asp
  • HEDIS Audit information
  • http//www.ncqa.org/tabid/204/Default.aspx
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