This documentation presents (1) a description of each of the Special Needs Plan (SNP) HEDIS measures that CMS collected for 427 SNP plan benefit packages (PBPs) for health care provided in calendar year 2013 to Medicare SNP beneficiaries and (2) the location of the rates associated with each SNP HEDIS measure within the HEDIS workbook (HEDIS2014_SNP.XLS). CMS took the description and additional information for each measure from HEDIS 2014 Volume 2: Technical Specifications. This release contains only those rates, percentages, or averages for each measure and not the numerator or denominator used to create those measures.
CMS requires that all managed care organizations undergo an audit on all HEDIS measures. The summary data file includes all submitted data following the audit.
The HEDIS measure descriptions reprinted here are done so with the permission of the National Committee for Quality Assurance (NCQA). HEDIS is a registered trademark of NCQA, and a copyright for HEDIS 2014 is held by the National Committee for Quality Assurance, 1100 13th Street, NW, Suite 1000, Washington, DC 20005. All rights reserved.
The reporting unit for SNP HEDIS is the PBP. Each Medicare Advantage contract must have at least one PBP; many contracts offer more than one. SNP PBPs limit enrollment to special needs individuals, i.e., those who are dual-eligible, institutionalized, or have one or more severe or disabling chronic conditions. In 2014, CMS collected data from 215 Medicare Advantage contracts for health care delivered by 427 SNP PBPs in 2013.
The "Service_Area" sheet in the SNP HEDIS workbook identifies the state(s) and counties where services are offered for that PBP.
The description and related information provided for each measure in this documentation are taken from the HEDIS 2014 Technical Specifications, which are the specific instructions for calculating HEDIS measures that NCQA provides to Medicare managed care plans. For each measure, the Technical Specifications detail the precise method for sampling (when appropriate), identification of the numerator and denominator, measure calculation, and any other important considerations specific to that measure. The Technical Specifications also contain general guidelines that apply to all measures, such as the use of medical records and when a plan should not report a measure because its eligible membership is too small. Some measures require more detailed specifications than others.
The HEDIS guidelines distinguish between three different types of missing values in the rate field: Not Applicable (NA), No Benefit (NB) and Not Reportable (NR). Health plans report NA when they: do not have a large enough population to calculate a representative rate (e.g., many measures require that rates be based on at least 30 members) or are not eligible for a measure (e.g., a health plan cannot calculate outpatient drug utilization if it does not offer an outpatient drug benefit; a health plan cannot calculate a measure requiring a year of continuous enrollment if its first enrollment began mid-way through the reporting year.) A value of NB is recorded when the health plan did not offer the health benefit required by the measure (e.g., Mental Health/Chemical Dependency). Health plans report NR when: they choose not to calculate and report a rate, or the health plans HEDIS Compliance Auditor determines that a rate is materially biased (applicable only to audited measures).
For measures reported as a percentage, material bias is defined as a deviation of more than five percentage points from the true rate. For other measures (e.g., procedures per 1,000 member years), material bias exists if the number of counted procedures deviates by more than ten percent from the true number of procedures.
Under the Privacy Act, CMS cannot publish or otherwise disclose the data in a form raising unacceptable possibilities that an individual could be identified (i.e., the data must not be beneficiary-specific and must be aggregated to a level where no data cells have 10 or fewer beneficiaries). To ensure that no beneficiary can be identified, CMS has chosen not to report certain measures, specifically enrollment by age category, and has suppressed an extremely small number of rates. CMS has replaced suppressed rates with an NA.' Please see the section on missing values above for an explanation of missing value designations.
CMS includes our record of enrollment as of December of the measurement year in the "GENERAL" sheet in the HEDIS workbook. The HEDIS reported value is adjusted for individuals with partial-year enrollment and reflects the entire contract's enrollment as well as the PBP enrollment.
We have included the Post Balanced Budget Amendment Naming of plan types as well as indicators if the contract offered a Special Needs benefit package or a Part D drug benefit in 2013. These values and others can be found on the sheet named "GENERAL". The full list of fields included on this sheet is described later in this document.
There is a separate sheet called "Service Area" in the SNP HEDIS workbook which contains the contract, state(s) and counties served by the PBPs reporting HEDIS. There is an additional field "EGHP" which indicates if the county is available only to beneficiaries in Employer Groups.
CMS has calculated and included a weighted national average for all of the Effectiveness of Care (EOC) measures. These rates are reported on a separate sheet called "National Rates" in the SNP HEDIS workbook. The rate for each of the EOC measures was calculated using the following formula:
((En1/TotE)*Sn1)+((En2/TotE)*Sn2)+ +((Enx/TotE)*Snx)=National Enrollment Weighted Average Score
Where: TotE
= Total enrollment for all PBPs with a valid numeric rate in the measure
En1 = Enrollment in the first PBP with a valid numeric rate
Sn1 = Reported rate for the first PBP with a valid numeric rate
Enx = Enrollment in the last PBP with a valid numeric rate
Snx = Reported rate for the last PBP with a valid numeric rate
DESCRIPTION - 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.
1 - The percentage of discharges for which the member received follow-up within 30 days of discharge
2 - The percentage discharges for which the member received follow-up within 7 days of discharge
(HEDIS 2014, Volume 2: Technical Specification, Pg. 181)
EOC010-0011 Rate - 7 Days
EOC010-0012 Rate - 30 Days
EOC010-0021 Upper Confidence Interval - 7 Days
EOC010-0022 Upper Confidence Interval - 30 Days
EOC010-0031 Lower Confidence Interval - 7 Days
EOC010-0032 Lower Confidence Interval - 30 Days
DESCRIPTION - The percentage of members 18 years of age and older who were diagnosed with a new episode of major depression and treated with antidepressant medication, and who remained on an antidepressant medication treatment. Two rates are reported.
Effective Acute Phase Treatment. The percentage of newly diagnosed and treated members who remained on an antidepressant medication for at least 84 days (12 weeks).
Effective Continuation Phase Treatment. The percentage of newly diagnosed and treated members who remained on an antidepressant medication for at least 180 days (6 months).
(HEDIS 2014, Volume 2: Technical Specifications, Pg. 172)
EOC030-0010 Rate - Effect.Continuation Phase Treat.
EOC030-0020 Lower Confidence Interval - Effect.Continuation Phase Treat.
EOC030-0030 Upper Confidence Interval - Effect.Continuation Phase Treat.
EOC030-0040 Rate - Effect.Acute Phase Treatment
EOC030-0050 Lower Confidence Interval - Effect.Acute Phase Treatment
EOC030-0060 Upper Confidence Interval - Effect.Acute Phase Treatment
DESCRIPTION - The percentage of members 1885 years of age who had a diagnosis of hypertension (HTN) and whose BP was adequately controlled (<140/90) during the measurement year. Use the Hybrid Method for this measure. (HEDIS 2014, Volume 2: Technical Specification, Pg. 134)
EOC035-0100 Rate - Total
EOC035-0110 Lower Confidence Interval tot
EOC035-0120 Upper Confidence Interval tot
DESCRIPTION - The percentage of members 5075 years of age who had appropriate screening for colorectal cancer. (HEDIS 2014, Volume 2: Technical Specification, Pg. 85)
EOC040-0010 Reported Rate
EOC040-0020 Lower Confidence Interval
EOC040-0030 Upper Confidence Interval
DESCRIPTION - 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. (HEDIS 2014, Volume 2: Technical Specification, Pg. 164)
EOC045-0010 Reported rate
EOC045-0020 Lower Confidence Interval
EOC045-0030 Upper Confidence Interval
DESCRIPTION - The percentage of Medicare members 65 years and older who received a glaucoma eye exam by an eye care professional for early identification of glaucomatous conditions. (HEDIS 2014, Volume 2: Technical Specification, Pg. 91)
EOC050-0010 Reported Rate
EOC050-0020 Lower Confidence Interval
EOC050-0030 Upper Confidence Interval
DESCRIPTION - 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 AMI and who received persistent beta-blocker treatment for six months after discharge. (HEDIS 2014, Volume 2: Technical Specification, Pg. 139)
EOC055-0010 Reported rate
EOC055-0020 Lower Confidence Interval
EOC055-0030 Upper Confidence Interval
DESCRIPTION
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.
(HEDIS 2014, Volume 2: Technical Specification, Pg. 211)
EOC070-0010 Rate - one prescription
EOC070-0020 Lower Confidence Interval - one prescription
EOC070-0030 Upper Confidence Interval - one prescription
EOC070-0040 Rate - at least 2 prescriptions
EOC070-0050 Lower Confidence Interval - at least 2 prescriptions
EOC070-0060 Upper Confidence Interval - at least 2 prescriptions
DESCRIPTION - The percentage of members 18 years of age and older who received at least 180 treatment days 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)
(HEDIS 2014, Volume 2: Technical Specification, Pg. 198)
EOC075-0010 Reported rate - ACE inhibitors or ARBs
EOC075-0020 Lower Confidence Interval - ACE inhibitors or ARBs
EOC075-0030 Upper Confidence Interval - ACE inhibitors or ARBs
EOC075-0040 Reported rate - Digoxin
EOC075-0050 Lower Confidence Interval - Digoxin
EOC075-0060 Upper Confidence Interval - Digoxin
EOC075-0070 Reported rate - Diuretics
EOC075-0080 Lower Confidence Interval - Diuretics
EOC075-0090 Upper Confidence Interval - Diuretics
EOC075-0100 Reported rate - Anticonvulsants
EOC075-0110 Lower Confidence Interval - Anticonvulsants
EOC075-0120 Upper Confidence Interval - Anticonvulsants
EOC075-0160 Rate - Total
EOC075-0170 Lower Confidence Interval - Total
EOC075-0180 Upper Confidence Interval - Total
DESCRIPTION - The percentage of members 40 years of age and older with a new diagnosis of COPD or newly active COPD, who received appropriate spirometry testing to confirm the diagnosis. (HEDIS 2014, Volume 2: Technical Specification, Pg. 112)
EOC080-0010 Reported rate
EOC080-0020 Lower Confidence Interval
EOC080-0030 Upper Confidence Interval
DESCRIPTION - 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
CRF 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)
Members with more than one disease or condition may appear in the measure multiple times (i.e., in each indicator for which they qualify). A lower rate represents better performance for all three rates.
(HEDIS 2014, Volume 2: Technical Specification, Pg. 206)
EOC090-0010 Rate - DDI Falls + Tricyclic Antidepress or Antipsych
EOC090-0020 Lower Confidence Interval - DDI Falls + Tricyclic Antidepress or Antipsych
EOC090-0030 Upper Confidence Interval - DDI Falls + Tricyclic Antidepress or Antipsych
EOC090-0040 Rate - DDI Dementia + Tricyclic Antidepress or Anticholl
EOC090-0050 Lower Confidence Interval - DDI Dementia + Tricyclic Antidepress or Anticholl
EOC090-0060 Upper Confidence Interval - DDI Dementia + Tricyclic Antidepress or Anticholl
EOC090-0070 Rate - DDI Chronic Renal Failure + Non Asp NSAIDs or Cox-2
EOC090-0080 Lower Confidence Interval - DDI Chronic Renal Failure + Non Asp NSAIDs or Cox-2
EOC090-0090 Upper Confidence Interval - DDI Chronic Renal Failure + Non Asp NSAIDs or Cox-2
EOC090-0100 Rate - Total
EOC090-0110 Lower Confidence Interval - Total
EOC090-0120 Upper Confidence Interval - Total
DESCRIPTION - The percentage of COPD exacerbations for members 40 years of age and older who had an acute inpatient discharge or ED encounter on or between January 1November 30 of the measurement year and who were dispensed appropriate medications. Two rates are reported.
1. Dispensed a systemic corticosteroid within 14 days of the event
2. Dispensed a bronchodilator within 30 days of the event
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.
(HEDIS 2014, Volume 2: Technical Specification, Pg. 114)
EOC105-0010 Reported rate - Systemic corticosteroid
EOC105-0020 Lower 95% confidence interval - Systemic corticosteroid
EOC105-0030 Upper 95% confidence interval - Systemic corticosteroid
EOC105-0040 Reported rate - Bronchodilator
EOC105-0050 Lower 95% confidence interval - Bronchodilator
EOC105-0060 Upper 95% confidence interval - Bronchodilator
DESCRIPTION - The percentage of adults 66 years and older who had each of the following during the measurement year.
Advance care planning
Medication review
Functional status assessment
Pain screening
(HEDIS 2014, Volume 2: Technical Specification, Pg. 93)
EOC115-0010 Reported Rate - Advance Care Planning
EOC115-0020 Lower Confidence Interval - Advance Care Planning
EOC115-0030 Upper Confidence Interval - Advance Care Planning
EOC115-0040 Reported Rate - Medication Review
EOC115-0050 Lower Confidence Interval - Medication Review
EOC115-0060 Upper Confidence Interval - Medication Review
EOC115-0070 Reported Rate - Functional Status Assessment
EOC115-0080 Lower Confidence Interval - Functional Status Assessment
EOC115-0090 Upper Confidence Interval - Functional Status Assessment
EOC115-0100 Reported Rate - Pain Assessment
EOC115-0110 Lower Confidence Interval - Pain Assessment
EOC115-0120 Upper Confidence Interval - Pain Assessment
DESCRIPTION - The percentage of discharges from January 1 - December 1 of the measurement year for members 66 years of age and older for whom medications were reconciled on or within 30 days of discharge.
(HEDIS 2014, Volume 2: Technical Specification, Pg. 203)
EOC120-0010 Reported Rate
EOC120-0020 Lower Confidence Interval
EOC120-0030 Upper Confidence Interval
DESCRIPTION - 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. Report each product separately as of December 31 of the measurement year.
(HEDIS 2014, Volume 2: Technical Specification, Pg. 379)
PDI801-0010 Family Medicine Board Cert Pct
PDI801-0030 Oth Specialists Board Cert Pct
PDI801-0050 Geriatricians Board Cert Pct
PDI801-0060 Internal Medicine Board Cert Pct
PDI801-0070 OB/GYN Provs Board Cert Pct
PDI801-0080 Pediatrician Board Cert Pct
DESCRIPTION - For members 18 years of age and older, the number of acute inpatient stays during the measurement year that were followed by an acute readmission for any diagnosis within 30 days and the predicted probability of an acute readmission. Data are reported in the following categories:
1. Count of Index Hospital Stays (IHS) (denominator)
2. Count of 30-Day Readmissions (numerator)
3. Average Adjusted Probability of Readmission
(HEDIS 2014, Volume 2: Technical Specification, Pg. 314)
UOS524-0010 Count of Index Stays (Denominator) Total 65-74 Num
UOS524-0020 Count of 30-Day readmissions (Numerator) Total 65-74 Num
UOS524-0025 Observed Readmission (Num/Den) Total 65-74
UOS524-0030 Average Adjusted Probability Total 65-74 Num
UOS524-0035 Total Variance Total 65-74
UOS524-0040 Count of Index Stays (Denominator) Total 75-84 Num
UOS524-0050 Count of 30-Day readmissions (Numerator) Total 75-84 Num
UOS524-0055 Observed Readmission (Num/Den) Total 75-84
UOS524-0060 Average Adjusted Probability Total 75-84 Num
UOS524-0065 Total Variance Total 75-84
UOS524-0070 Count of Index Stays (Denominator) Total 85+ Num
UOS524-0080 Count of 30-Day readmissions (Numerator) Total 85+ Num
UOS524-0085 Observed Readmission (Num/Den) Total 85+
UOS524-0090 Average Adjusted Probability Total 85+ Num
UOS524-0095 Total Variance Total 85+
UOS524-0100 Count of Index Stays (Denominator) Total Total Num
UOS524-0110 Count of 30-Day readmissions (Numerator) Total Num
UOS524-0120 Observed Readmission (Num/Den) Total Total
UOS524-0130 Average Adjusted Probability Total Total Num
UOS524-0140 Total Variance Total Total
UOS524-0150 Observed-to-Expected Ratio
UOS524-0160 Lower Confidence Interval
UOS524-0170 Upper Confidence Interval
UOS524-0510 Count of Index Stays (Denominator) Total 18-44 Num
UOS524-0520 Count of 30-Day readmissions (Numerator) Total 18-44 Num
UOS524-0525 Observed Readmission (Num/Den) Total 18-44
UOS524-0530 Average Adjusted Probability Total 18-44 Num
UOS524-0535 Total Variance Total 18-44
UOS524-0540 Count of Index Stays (Denominator) Total 45-54 Num
UOS524-0550 Count of 30-Day readmissions (Numerator) Total 45-54 Num
UOS524-0555 Observed Readmission (Num/Den) Total 45-54
UOS524-0560 Average Adjusted Probability Total 45-54 Num
UOS524-0565 Total Variance Total 45-54
UOS524-0570 Count of Index Stays (Denominator) Total 55-64 Num
UOS524-0580 Count of 30-Day readmissions (Numerator) Total 55-64 Num
UOS524-0585 Observed Readmission (Num/Den) Total 55-64
UOS524-0590 Average Adjusted Probability Total 55-64 Num
UOS524-0595 Total Variance Total 55-64
UOS524-0600 Count of Index Stays (Denominator) Total Total
UOS524-0610 Count of 30-Day readmissions (Numerator) Total
UOS524-0620 Average Adjusted Probability Total Total
UOS524-0630 Observed Readmission (Num/Den) Total Total
UOS524-0640 Total Variance Total Total
UOS524-0650 Observed-to-Expected Ratio
UOS524-0660 Lower Confidence Interval
UOS524-0670 Upper Confidence Interval