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(1)

Using  Medicare  Part  D  Data  

Holly  M.  Holmes,  MD  

(2)

Objectives  

Understand  the  contents  of  the  Medicare  Part  

D  files  

Discuss  the  strengths  and  limitations  in  using  

(3)

Medicare  Part  D  –  what  is  it?  

Established  by  the  Medicare  Prescription  

Drug,  Improvement,  and  Modernization  Act  

of  2003  

Covers  prescription  medications  

Not  OTC,  not  supplements  

Available  to  all  43  million  Medicare  

beneficiaries  

(4)

PART  D  QUIZ  

True  or  False:  

Enrollment  in  Part  D  is  optional.  

True  or  False:  

Once  you  choose  a  Part  D  plan,  you  cannot  

switch.  

(5)

Part  D  enrollment  

60%  of  Medicare  beneficiaries  were  enrolled  

in  Part  D  in  2011  

Open  enrollment  for  2012:  10/15/11-­‐12/7/11  

6%  switch  every  year  (therefore  94%  do  not  

(6)

PART  D  QUIZ  

True  or  False:    

Medicare  Advantage  enrollees  who  have  Part  D  

coverage  are  enrolled  in  stand-­‐alone  Part  D  

(7)

Part  D  Enrollment  in  2010  

(8)

Part  D  Enrollment  in  2010  

Source:  ResDAC  

If  you  are  studying  A+B+D,  you  really  

only  have  37%  of  Medicare  

beneficiaries.    

And  since  ½  of  PDP  is  Low  Income  

Subsidy,  you  only  have  18%  of  

“middle-­‐class”-­‐ish  benes.  

If  you  want  to  study  all  of  the  Low  

Income  Subsidy  beneficiaries,  you  

need  both  PDP  and  MAPD.  

(9)

PART  D  QUIZ  

Part  D  plans  can  offer  different  

A.

Deductibles  

B.

Copays  

C.

Premiums  

D.

Gap  Coverage  

(10)

This  goes  to  0  by   2020  (fed  govt   picks  up  rest)  

Source:  Kaiser  Family  Foundation.  

These  are   determined   based  on   true  out-­‐of-­‐ pocket  cost   (TROOP)    

(11)

This  goes  to  0  by   2020  (fed  govt   picks  up  rest)  

Source:  Kaiser  Family  Foundation.  

These  are   determined   based  on   true  out-­‐of-­‐ pocket  cost   (TROOP)    

Beneficiary  Phase  Variable  

identifies  where  the  bene  

is  when  the  prescription  is  

filled.  

(12)

Part  D  QUIZ  

True  or  False:  

Part  D  data  for  Medicare  Advantage  (HMO)  

beneficiaries  is  available  to  researchers.  

(13)

What  types  of  Part  D  data  are  

available?  

Public  use  (landscape)  files  

Not  linkable  to  beneficiary-­‐level  files  

Beneficiary-­‐Level  Part  D  Data  

Final  Part  D  Rule  (5/28/2008):  keeps  sensitive  data  

encrypted  and  cost  data  aggregated  

(14)

What  types  of  Part  D  data  are  

available?  

Public  use  (landscape)  files  

Not  linkable  to  beneficiary-­‐level  files  

Beneficiary-­‐Level  Part  D  Data  

Final  Part  D  Rule  (5/28/2008):  keeps  sensitive  data  

encrypted  and  cost  data  aggregated  

Cannot  identify  prescriber,  pharmacy,  or  plan  

Part  D  files  are  linkable  to  A  +  B  only  

through  the  beneficiary  ID,  which  is  

encrypted  and  the  same  as  the  bene  

ID  from  A  +  B.  This  will  not  change  

until  the  Part  D  Rule  changes.    

(15)

Part  D  Denominator  File    

Called  the  Master  Beneficiary  Summary  File  

(MBSF)  

Contents    

Beneficiary  Summary  File  (BSF)    

Chronic  Conditions  (26)  

Cost  &  Utilization  –  annual  summary  

(16)

Part  D  Denominator  File    

Called  the  Master  Beneficiary  Summary  File  

(MBSF)  

Contents    

Beneficiary  Summary  File  (BSF)    

Chronic  Conditions  (26)  

Cost  &  Utilization  –  annual  summary  

Death  Information  

The  BSF  is  available  by  summer  of  year  

20xx+1.  

The  Part  D  denominator  part  of  the  

BSF  is  added  in  March  of  20xx+2.  

You  may  need  2  pieces  of  the  BSF.  

Demographic  information  known  to  

CMS  overwrites  all  demographic  

information  from  a  claim  or  Part  D  event  

in  the  MBSF.    

That  means  agreement  between  MBSF  

and  claims/PDE  unless  there  is  a  change.  

(17)

Part  D  Event  Files  

Bene_ID  

Drug  info:  from  NDC  linkage  with  First  Data  Bank  

Generic/brand  name  

Dosage  (strength  and  unit  of  measure,  eg  mg)  

Form  (tablet,  capsule,  cream,  spray,  patch)  

Claim  info:    

Quantity  dispensed  

Date  dispensed  

Days  supply  

(18)

Part  D  Event  Files  

Bene_ID  

Drug  info:  from  NDC  linkage  with  First  Data  Bank  

Generic/brand  name  

Dosage  (strength  and  unit  of  measure,  eg  mg)  

Form  (tablet,  capsule,  cream,  spray,  patch)  

Claim  info:    

Quantity  dispensed  

Date  dispensed  

Days  supply  

The  directions  on  the  prescription  are  

not  part  of  the  PDE  files.  Frequency  of  

dosing  can  be  calculated  by  quantity  

dispensed  /  days  supply.    

(19)

Dosing  Frequency  Example  

Drug

% of Claims with Dosing Frequency

<1/day

1-­‐<2/day

2-­‐<3/day

>3/day

Amlodipine

6.4

89.3

4.1

0.22

(20)

Part  D  Appended  Files  

Prescriber  

Encrypted  ID,  type,  specialty,  subspecialty,  and  state  

Plan  

Encrypted  ID,  benefits,  premiums,  tiers,  service  areas  

Pharmacy  

(21)

Part  D  Appended  Files  

Prescriber  

Encrypted  ID,  type,  specialty,  subspecialty,  and  state  

Plan  

Encrypted  ID,  benefits,  premiums,  tiers,  service  areas  

Pharmacy  

Encrypted  ID,  type  of  pharmacy,  state  

The  encrypted  ID  for  prescribers,  

plans,  and  pharmacies  does  not  

link  with  A  or  B  files  or  with  any  

other  beneficiary-­‐level  files.  

(22)

PART  D  QUIZ  

True  or  False:  

Medicare  beneficiaries  with  Medicaid  (dual  

eligibles)  continue  to  get  their  prescriptions  

through  Medicaid.  

(23)
(24)

Identifying  Low  Income  

Beneficiaries  

State  Buy-­‐In:  A  state  paid  for  the  beneficiary’s  Part  B  

coverage  through  Medicaid  or  a  savings  program  

Low  Income  Subsidy:  benes  with  help  paying  

premiums,  deductibles,  and/or  copay,  no  gap,  no  late  

enrollment  

Dual  Eligible  status:  traditional  Medicaid  and  other  

(25)

Identifying  Low  Income  

Beneficiaries  

State  Buy-­‐In:  A  state  paid  for  the  beneficiary’s  Part  B  

coverage  through  Medicaid  or  a  savings  program  

Low  Income  Subsidy:  benes  with  help  paying  

premiums,  deductibles,  and/or  copay,  no  gap,  no  late  

enrollment  

Dual  Eligible  status:  traditional  Medicaid  and  other  

Medicare  savings  programs  

How  to  identify:  

State  Buy-­‐In

:  State  buy-­‐in  variable  in  BSF  

LIS

:  Cost  share  group  variable  

Dual  Eligible

:  State  reported  dual  eligible  

(26)

PART  D  QUIZ  

What  is  the  minimum  number  of  Part  D  plans  a  

beneficiary  could  choose  from  for  2012?  

A.

5  

B.

15  

C.

25  

(27)

What  drugs  are  covered?  

No  OTCs  

Protected  Drugs:  

Immunosuppressant  

Antidepressant  

Antipsychotic  

Anticonvulsant  

Antiretroviral  

Antineoplastic  

(28)

What  drugs  are  covered?  

No  OTCs  

Protected  Drugs:  

Immunosuppressant  

Antidepressant  

Antipsychotic  

Anticonvulsant  

Antiretroviral  

Antineoplastic  

Benzodiazepines  and  

barbiturates  are  not  covered  

under  Medicare  Part  D,  but  they  

may  be  covered  by  some  states’  

LIS  programs  

(29)
(30)
(31)
(32)

Medication-­‐Centered  Research  

Ideas  with  Part  D  

• 

Polypharmacy  

Overutilization  

Use  of  inappropriate  medications  

• 

Suboptimal  prescribing  

Drug  interactions  

Underutilization  

• 

Adherence  

(33)

Medication  Adherence

 

1.

Determine  predictors  of  adherence  in  

Medicare  Part  D  beneficiaries  with  

hypertension.  

2.

Quan<fy  the  extent  to  which  con<nuity  of  

care  with  a  provider  affects  adherence.  

3.

Es<mate  the  amount  of  nonadherence  

(34)

Methods  

Study  Popula<on  

• 

Medicare  claims  and  Part  D  event  files  for  5%  sample  of  

Medicare  beneficiaries  

• 

66  and  older  on  January  1,  2007  

• 

Coverage    

24  months  A  and  B  without  HMO  2006-­‐2007  

12  months  Part  D  in  2007  

(35)

Methods  

Stable  an<hypertensive  users  

Uncomplicated  Hypertension  (401.xx)  

PDE  files  for  an<hypertensive  medica<on  in  2006  and  2007  

Mul<ple  med  classes,  categorized  as  BP  meds  by  JNC7  

No  dose  changes  

(36)

Medication Possession Ratio: (MPR)

# days supply dispensed between 1st and last fill date

# days between 1st and last fill date

Exclude days supply on last fill date

Measure  of  adherence:  MPR  

Medica'ons  

Thiazides   Beta  blockers  

Calcium  channel  blockers   ACEIs/ARBs  

Vasodilators   Clonidine   Renin  inhibitors  

Alpha  blockers  

Potassium  sparing  diure<cs   Loop  diure<cs  

(37)

Measures  

Medica<on  Possession  Ra<o  (MPR)  

–  Sum  of  days  supply  between  1st  and  last  fill  /  total  days  between  1st  and  last  fill  

Main  outcome  =  %  adherent  

–  Adherent  =  average  MPR  80%  or  greater  

Possible  predictors  

–  Demographics  

–  Socioeconomic  status  

–  Comorbidity    

–  Medica<on  use  

(38)

Age  66  on  1/1/07   n=382939  

24  months  of  Part  A  and  B   n=319359  

Part  D  events  for  blood  pressure   medica<ons  

n=276443  

Uncomplicated  HTN   n=236158  

Medicare  beneficiaries  with  HTN   n=471190   1,698684  benes  without   hypertension     88,251  younger  than  66   on  1/1/07   63,580  with  HMO   14,900  no  BP  meds   27,810  with  <2  claims   206  with  dose  change  

Medicare  enrollees  with  PDE  files  in   2006  –  2007    n=2,169,874   38,125  comp.  HTN   2160  with  MPR  >1.43   Uncomplicated  HTN   N=168522   Study  Popula<on   N=168522   56,651  hospitalized  2007   9,550  in  nursing  home   324  in  Territories  or   unknown  

(39)

Table  1.  Characteristics  of  Study  Population  

(n=168,522)  

Variable Category Total                        

(Column  %) Percent  Adherent

AGE  GROUP 66-­‐69 36468  (21.6%) 78.9% 70-­‐74 42178  (25%) 79.3% 75-­‐79 37936  (22.5%) 79.7% 80-­‐84 28488  (16.9%) 79.2% 85+ 23452  (13.9%) 80.5% SEX Female 116942  (69.4%) 79.4% Male 51580  (30.6%) 79.6% RACE/ETHNICITY Non-­‐Hispanic  white 137981  (81.9%) 81.5% Black 14249  (8.5%) 67.8% Hispanic 9656  (5.7%) 69.3% Amer.  Indian/Alaskan 563  (0.3%) 67.7% Asian/pacific  island 4950  (2.9%) 78.4% Other 882  (0.5%) 74.7% Unknown 241  (0.1%) 80.1%

(40)

Table  1.  Characteris'cs  of  Study  Popula'on  (n=168,522)  

Variable   Category   Total                  

(Column  %)   Percent  Adherent  

DIVISION  

East  North  Central   27970  (16.6%)   82%  

East  South  Central     13688  (8.1%)   77.3%  

Middle  Atlantic   20407  (12.1%)   80.4%  

Mountain   7189  (4.3%)   78.2%  

New  England   10079  (6%)   83%  

Pacific   17964  (10.7%)   76.7%  

South  Atlantic   35746  (21.2%)   78%  

West  North  Central   17192  (10.2%)   84.2%  

West  South  Central   18287  (10.9%)   75.6%  

LOW-­‐INCOME   SUBSIDY   No   127781  (75.8%)   80.5%   Yes   40741  (24.2%)   76.1%   MEDIAN  INCOME   IN  CENSUS  TRACT   0    -­‐      31,000   36229  (22.1%)   76.1%   31,000-­‐38,000   42412  (25.9%)   79.8%   38,000-­‐49,000   42033  (25.7%)   80.6%   49,000+   43187  (26.4%)   81%   %  IN  CENSUS   TRACT  WITH  <12   YEARS   EDUCATION   0  -­‐    12.2   41473  (25.3%)   81.7%   12.2-­‐18.6   40877  (24.9%)   81.6%   18.6-­‐27.1   40786  (24.9%)   79.5%   27.1+   40712  (24.8%)   75.2%  

(41)

Table  1.  Characteristics  of  Study  Population  (n=168,522)  

Variable   Category   Total                  

(Column  %)   Percent  Adherent  

DEPRESSION   No   155027  (92%)   79.6%   Yes   13495  (8%)   78.2%   DEMENTIA   No   160071  (95%)   79.5%   Yes   8451  (5%)   79%   NUMBER  OF   ELIXHAUSER S   CONDITIONS   0-­‐1  comorbidity   74943  (44.5%)   80.4%   2-­‐3  comorbidity   62119  (36.9%)   79.3%   4+  comorbidity   31460  (18.7%)   77.6%   IN  COVERAGE  GAP   IN  2007   NoYes     108046  (64.1%)60476  (35.9%)     83.5%77.2%    

NUMBER  OF  MEDS   8.9  (+/-­‐4.8)  

(42)

Logistic  Regression  Model  for  Adherence  

(n=168,522)    

Characteristic   Odds  Ratio  (95%  CI)  

Low  Income  Subsidy   1.14  (1.10-­‐1.18)  

%  in  Census  Tract  <12  yrs  Education   (>18.6%  vs.  0-­‐18.6%)  

0.93  (0.90-­‐0.95)  

Depression               0.94  (0.90-­‐0.99)  

Comorbidity  (0-­‐1  conditions  as  reference)  

       2  to  3  conditions   0.93  (0.90-­‐0.95)  

       4  or  more  conditions   0.85  (0.82-­‐0.88)  

Number  of  Medications   0.97  (0.97-­‐0.98)  

In  the  Coverage  Gap  in  2007   1.65  (1.60-­‐1.70)  

Total  Copay  ($1000  incr.)     1.23  (1.20-­‐1.25)  

(43)

0   0.1   0.2   0.3   0.4   0.5   0.6   0.7   0.8   0.9   1   1   8   15   22   29   36   43    50 57   64   71   78   85   92   99   10 6   11 3   12 0   12 7   13 4   14 1   14 8   155   162   169   176   183   190   197   20 4   21 1   21 8   22 5   23 2   23 9   246   253   26 0   26 7   27 4   281   288   295   302   Percent  of  Population  in  HRR  with  ≥80%  Adherence  

Regional  Differences  in  Adherence  

% ADHERENT

0.757

0.793

0.836

(44)

Regional  Differences  

Model  with  HRR  (mull):  ICC  =  1.8%  

Model  with  HRR  level  variables:  ICC  =  1.4%    

Medicare  enrollees  in  HRR  

Total  Part  B  expenditure  

Primary  Care  Physicians  in  HRR  

Model  with  Pa<ent  level  variables:  ICC  =  1.0%  

(45)

Conclusions  

Significant  differences  in  an<hypertensive  

medica<on  adherence  among  different  racial/

ethnic  groups  and  in  persons  with  higher  

levels  of  comorbidity.  

Differences  by  region,  medica<on  use,  number  

(46)
(47)
(48)
(49)

Medication-­‐Centered  Research  

Ideas  with  Part  D  

• 

Polypharmacy  

Overutilization  

Use  of  inappropriate  medications  

• 

Suboptimal  prescribing  

Drug  interactions  

Underutilization  

• 

Adherence  

(50)

Inappropriate  Medication  Use

1. 

Investigate the utility of Medicare Part D data to

describe prescriber-level variation in medication use

2. 

Evaluate the variation in PIM use in Medicare Part D

beneficiaries at the prescriber level, controlling for

patient characteristics associated with getting a PIM

(51)

Design and Methods

100% Texas Medicare claims and Part D event files for 2007

and 2008

Enrollees 66 and older in 2008 with 12 months of A, B, and D,

without HMO in 2008

Prescribers who were physicians, with 10 or more beneficiaries

per prescriber

PIMs defined according to Beers 2003 list

List of medications/drug classes only (did not include

drug-disease combinations)

(52)

Design and Methods

Variables   Data  Source  

Patient   Age,  sex,  race/ethnicity,  state  buy-­‐in   PDE  denominator  

Comorbidities  (Elixhauser s  Index)   2007  carrier  file  and  MEDPAR  

Hospitalization  in  2007   MEDPAR  

PIM    in  2008  according  to  Beers  list   PDE  files  

Prescriber   Credentials,  specialty   PDE  Prescriber  Characteristics  

File    

Analysis  Plan  

Patient  and  prescriber  characteristics  associated  with  PIM  use  by  

patients  

Bivariate  

Multivariable  model  for  patient  factors      

Multilevel  model  for  prescriber,  controlling  for  patient  level  

(53)

Texas  Medicare  Part  D  

Beneficiaries  Age  66  in  2008  

N  =  2,261,766  

12  months  of  A,  B,  and  D  coverage  

and  no  HMO  all  of  2008  

N  =  760,703  

Had  Part  D  claims  for  any  drug  in  

2008  

N  =  716,930  

10  or  more  beneficiaries  per  

physician  prescriber  

N  =  677580  (24,561  MD/DO)  

(54)

Results: Number of Beneficiaries Per

Prescriber

Distribution of BID_PCT_PROVIDER & CLM_PCT_PROVIDER

0 4 8 12 16 20 24 28 32 36 40 44 48 52 56 60 64 68 72 76 80 84 88 0 1 2 3 4 5 6 7 8 9 Pe rc en t BID_PCT_PROVIDER

Number  of  beneficiaries  per  prescriber  

Pe

rc

en

t  o

f  p

re

sc

rib

er

s  

(55)

Results: Prevalence of PIM Use

Overall, 216,364 (31.9%) of 677,580

Texas Part D beneficiaries who filled

prescriptions received a PIM in 2008

85% of the 24,561 prescribers prescribed

(56)

Table 1: Characteristics of 677,580 Beneficiaries

PIM use increased with increasing age, and differed

between sexes and categories of race/ethnicity

Characteristic   Category   Number   %  Getting  a  PIM  

Age   66-­‐69   157,530   29.6   70-­‐74   171,984   30.9   75-­‐79   142,225   32.7   80-­‐84   107,999   33.8   85+   97,842   34.4   Sex   Female   441,657   35.0   Male   235,923   26.2   Race/Ethnicity   White     465,680   32.2   Black   52,611   34.2   Hispanic   139,223   31.3   Asian   16,797   22.9   Other   3,269   28.3   PIM  –   poten<ally   inappropriate   medica<on  

(57)

Table 1 (cont’d): Characteristics of 677,580 Beneficiaries

Characteristic   Number   %  Getting  a  PIM  

State  Buy-­‐in  in  2008   YES   206,113   35.0  

NO   471,467   30.6  

Hospitalization  in  2007   143,741   41.5  

Comorbidities   Heart  Failure   108,703   42.5  

Uncomplicated  DM   213,993   35.9   Complicated  DM   81,271   40.3   Hypertension   523,380   34.2   Pulmonary  Disease   150,589   38.5   PVD   133,021   39.7   Depression   70,283   42.4   Cancer   72,654   32.7   Psychoses     43,211   40.1   Neurologic  Disorder   91,586   37.7  

Total  Number  of  Medication  Claims  

(SD)   39.2  (+/-­‐  32.0)   52.2  (+/-­‐  35.9)   PIM  –   poten<ally   inappropriate   medica<on   DM  –  Diabetes   mellitus   PVD  –   peripheral   vascular  disease  

(58)

Table 2: PIM Use According to Number of

Prescribers

73% of beneficiaries had >1 prescriber for all prescriptions

PIM use increased considerably with increased numbers of

unique prescribers

Number  of  Unique  

Prescribers   Beneficiaries  Number  of   %  of  Beneficiaries  Getting  a  PIM  

1   182,884   19.2  

2   178,487   26.6  

3   130,779   34.1  

(59)

Table 3: Prescriber Characteristics and PIM Use

• 

14.4% of all beneficiaries who got a prescription

from an MD got a PIM from that MD

Characteristic  of  Prescriber  

Number  of  

Prescriptions  

%  of  Beneficiaries  

Getting  PIMs  

Credentials   MD  

1,753,953  

14.4  

DO  

133,790  

18.5  

Specialty  

Gen.  Internal  

Medicine  

355,262  

19.0  

Family  Medicine  

438,185  

19.3  

General  Practice  

20,730  

19.7  

Internal  Medicine  

Specialty  

364,597  

8.0  

Geriatrics   30,767   18.7  

Gynecology  

27,021  

11.4  

(60)

Table 4: 10 Most Commonly Prescribed PIMs

PIM  Name  

Beneficiaries  

Number  of  

Propoxyphene  

83,415  

Nitrofurantoin  

37,908  

Clonidine  

28,496  

Cyclobenzaprine  

27,893  

Amitriptyline  

19,390  

Doxazosin  

11,941  

Amiodarone  

10,906  

Dicyclomine  

9753  

Carisoprodol  

8475  

Methocarbamol  

7958  

(61)

Table 5: Multivariable Model for Odds of PIM Use

Characteristic   Odds  Ratio   95%  CI  

Age   66-­‐69   1.0   Ref   70-­‐74   1.0   0.98-­‐1.01   75-­‐79   0.99   0.97-­‐1.01   80-­‐84   0.98   0.96-­‐1.00   85+   0.97   0.95-­‐0.99   Gender   Female     1.37   1.35-­‐1.38   Male   1.0   Ref  

State  Buy-­‐in   Yes   1.11   1.09-­‐1.12  

No   1.0     Ref  

Race/Ethnicity   White   1.0   Ref  

Black   1.04   1.02-­‐1.07  

Hispanic   0.94   0.92-­‐0.95  

Asian   0.74   0.71-­‐0.77  

(62)

Table 5 (cont’d): Multivariable Model for Odds of PIM Use

Adjusted for other patient factors, sex and hospitalization were still

significant, and most comorbidities were not statistically or clinically

significant predictors of getting a PIM.

Characteristic   Odds  Ratio   95%  CI  

Hospitalization  in  2007   1.11   1.10-­‐1.13   Heart  Failure   0.98   0.96-­‐0.99   Uncomplicated  DM   0.92   0.91-­‐0.94   Complicated  DM   0.96   0.94-­‐0.98   Hypertension   0.93   0.92-­‐0.95   Pulmonary  Disease   1.03   1.02-­‐1.05   PVD   1.05   1.03-­‐1.06   Depression   1.08   1.06-­‐1.10   Cancer   0.97   0.95-­‐0.99   Psychoses     0.84   0.82-­‐0.86   Neurologic  Disorder   0.85   0.84-­‐0.87  

(63)

Table 5 (cont’d): Multivariable Model for Odds of PIM Use

Increasing number of unique prescribers remained a strong

independent predictor of PIM use in the multivariable model for

patient factors.

Number  of  Unique  

Prescribers   Odds  Ratio   95%  CI  

1   1.0   Ref  

2   1.42   1.40-­‐1.44  

3   1.90   1.87-­‐1.94  

(64)

!

Results: Adjusted % of Beneficiaries on PIMs Across All Prescribers

Ad ju st ed  %  o f  b en efi ci ar ie s   ge in g   a   PIM   Prescribers  (N=10747)   1113  (10.4%)   607  (5.7%)   10th  percen'le  =  13.4%       90th  percen'le  =  30.0%   mean  =  21.1%  

(65)

Opportunities  Provided  by  Part  D  Data

Link  with  other  data  sources  

MCBS  data  

SEER,  Texas  Cancer  Registry  

– 

Medicare  A  and  B  

(66)

Using  MAPD  Data  

Risk  adjustment  

is  still  possible  

with  Rx-­‐Risk  

(67)

What  can  you  do  with  Part  D  Data?  

Toxicities  

Cost    

Policy  

Access  

Disparities  

(68)

Questions?  

[email protected]  

References

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