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Synergizing QUERI Research and Operations Analyses in Monitoring
and Improving the Population Health of Veterans with Diabetes
D. Aron, L. Pogach, E. Kerr and D. MillerWORKSHOP OBJECTIVES
• (1) address issues surrounding current diabetes quality measures and discuss alternatives and how they can be used in both research and clinical practice; and
• (2) describe two data sources: the Patient Care Services (PCS)-VSSC Diabetes Cube and Diabetes Epidemiological Cohort (DEPIC) and their potential use in operations and research.
Introduction and Context for Diabetes Quality Measurement
David C. Aron, MD, MS
Co-Clinical Coordinator, DM QUERIACOS/Education, Louis Stokes
Cleveland DVAMCProfessor of Medicine
Case Western Reserve University School of Medicine
QUERI WORKSHOP Agenda1. Context for performance
measurement2. Limitations of measurement3. Alternative means for cross
sectional measurement4. Cross sectional measures vs
Longitudinal Measures5. Individuals versus populations6. Sources of Data
How Do We Use Performance Measurement
Public Accountability (External)• External transparency• To compare healthcare plans or physicians
based upon a metric• To financially reward plans and physicians
Quality Improvement (Internal)• Internal to plan or practice• To guide population based improvement• Can be used for internal reimbursement
LowerMedical
loss ratio
Proftability
Offer better
products
↑MarketShare
PayersPayersSeekingSeekingValueValue
QI
↑SustainabilityQuality
Improved practice
Re-Assess
IdentifyGaps
Provider inProvider inbroadbroadsense-sense-
PDCA/QIPDCA/QI
GetInformation
MakeHealthcare
choices
Assess
Chooseamongplayers
InformedInformedConsumerConsumer
ChoiceChoice
MarketingMarketing
UtilizationUtilization(Macro-(Macro-Choice)Choice)
UtilizationUtilization(Micro-(Micro-Choice)Choice)
MarketingMarketing
Encourage Disease ManagementEncourage Disease Management
Inform product designInform product design
Research
Evidence
Reports
Measuresand
ReportsMeasures
NON-TRANSPARENT INFLUENCES ON MEASURES AND PUBLIC REPORTING OF
QUALITY DATA
Specialty Societies, Big Pharma, Disease Group Advocacy
Direct toConsumer
Advertising
Drug Detailing
Formulary Management
WHO RAN THE CAMPAIGN?
Who are the patient?Age Distribution of VA
Patients - 2005
0
0.5
1
1.5
2
2.5
3
3.5
4
20 30 40 50 60 70 80 90 100 AGE
%
14%14%
24%24%
40%40%
23%23%
WWIIKorea WarVietnam WarPost-Vietnam
Dramatic increase in proportion of younger patient recent years.
Pogach et al. AJMC March, 2007
5-year Mortality Rates in Veterans with Diabetes <65 Years with Co-morbidities
Evolving Evidence Base:Studies of Glycemic Control and Its
Relationship to CVD Outcomes
Study Acronym
Number of Participants
Follow-up
(years)
Intensive A1c Target
Standard A1c Target
Results
ACCORD 10,251 4 <6.0%
Achieved 6.4
7.0%-7.9% Achieved
7.5
higher mortality
in intensive
group
ADVANCE 11,140 ~4.5 ≤6.5% Achieved
6.4
Usual care
Achieved 7.0
No difference
VADT ~1700 5-7 ≤6.0% 8%-9% Difference not
significant
What populations do worse on glycemic control ?
• Longer duration of diabetes African Americans and White Hispanic
• <45 yrs worse than 45-54 than 55-64• Mental Health Conditions: Psychoses,
Substance Abuse and/or anxiety/PTSD disorders
• Lower socioeconomic-educational status (buying healthy food, diabetes numeracy?)
• Less social support
QUERI WORKSHOP 12-091. Context for performance
measurement2. Limitations of measurement3. Alternative means for cross
sectional measurement4. Cross sectional measures vs
Longitudinal Measures5. Individuals versus populations6. Sources of Data
Technical Elements of Performance Measurement
• Measurement uncertainty
• Population at risk
• Bias (differences in population)
• Effectiveness in practice
• Feasibility and cost of data collection
• Baseline status, patient safety, patient preferences
Facility Variation in Factors Impacting Glycemic Control (1999-2000) Maney et al, Diabetes Care, 2007
Factor Mean P10 P90
<55 yrs 19.8 14.2 25.6
11+yr duration 35.9 31.3 41.8
Not high school grad 30.7 18.9 44.2
Food insufficiency 13.9 9.3 19.5
MHS (SF36V) 43.8 41.2 46.2
BMI =>35 15.7 11.2 19.9
No exercise in past month 43.2 36.1 49.1
Risk adjustment 30% of best/worse change >2 decile ranks
Dominant conditions/Decreased life expectancy <65 years
Range 20.9-52.6; 20% of facilities change =>2 deciles
FY08 Performance Measures A1c
• A1c FACILITY VARIATION RANGE (730-2270, mean 1560 EPRP charts)– <7=46% [range 42-49 VISNS]– <8=72% [range 66-72 VISNS]– >9=16% [range 15-20 VISNS]
• LDL-C– <120 mg/dl=81%– <100 mg/dl=68%
– Based upon ~32K charts
Vijan, S. et. al. Ann Intern Med 1997;127:788-795
Age is Important:Lifetime Risk for Blindness Due to Diabetic Retinopathy*
Vijan, S. et. al. Ann Intern Med 1997;127:788-795
Lifetime Risks for End-Stage Renal Disease*
Benefits of Glycemic Risk Reduction (7.9% to 7.0%) over 10 yrs from the UKPDS
(Budenholzer et al, BMJ 1245, 2001)
Outcome OR
(95%CI)
P NNT Per PY
ARR/ 1000PY
Rate per 1000 PY - Intensive Control
Any DM Endpoint
0.88
(.79-.99)
0.02 196
(153-272)
5.1 40.9 46
MI 0.84
(.71-1.00)
0.052 370
(279-551)
2.7 14.7 17.4
Stroke ----- ---- --- ---- 5.6 5.0
Microvasc 0.75
(.6-.93)
0.01 357
(285-478)
2.8 8.6 11.4
Laser Treatment
0.71
(.58-.98)
0.003 323 3.1 7.9 11.0
Diabetes Mortality
0.90 NS ----- -- 10.4 11.5
Outcome NNT x 10 years
ARR per 1000 person years
Rate per 1000 person years
Intensive Control
Any DM Endpoint
6.1 16.5 50.9 67.4
MI -- ---- 18.6 23.5
Stroke 19.6 (15.9-25.7)
5.1 6.5 11.6
Microvascular 13.8 (11.4-17.8)
7.2 12.0 19.2
Diabetes Mortality
15.2 (12.2-20.1)
6.6 13.7 20.3
Benefits of Blood Pressure Reduction 154/87 to Benefits of Blood Pressure Reduction 154/87 to 144/82 over 8.5 yrs from the UKPDS144/82 over 8.5 yrs from the UKPDS
Cross Sectional “Good” Measure Options
• Case mix adjustments: What is not under plan control? – Socio-positioning– Age– Duration, Type 1 or 2, others
• Exclusions: – What to exclude? Life expectancy, health
risk, side-effects• How To Score
– Pass/Fail? “Partial” credit:– How to weight?
Curvilinear relationship between A1c and Microvascular Disease: Risk of retinopathy and by A1C level
DCCT Research Group NEJM 1993DCCT Research Group NEJM 1993
Stringent Dichotomous Outcome Measures
• Don’t target patients most likely to benefit– Ignore the heterogeneity of patient risk factors
• Don’t help providers do the “right” thing– Do not give “partial credit” for actions or
improvements that may yield considerable benefits • Don’t take into account patient preferences
– Could mandate care that is contrary to the wishes of a reasonable, well informed patient
• Could result in unintended consequences– Polypharmacy, hypoglycemia, worse outcomes
Aron & Pogach JCJQS 2007;33:636-643
QUERI WORKSHOP 12-091. Context for performance
measurement2. Limitations of measurement3. Alternative means for cross
sectional measurement4. Cross sectional measures vs
Longitudinal Measures5. Individuals versus populations6. Sources of Data
Implementing Linked Clinical Action Measures for Assessment and
Improvement
Eve A. Kerr, MD, MPH
PI, Ann Arbor VA Center
for Clinical Management Research
Research Coordinator, DM QUERI
Associate Professor of Internal Medicine
University of Michigan Health System
The Paradox of Performance Measurement
"Not everything that can be counted counts, and not everything that counts can be counted."
- Albert Einstein (1879-1955) From a sign hanging in Albert Einstein's office at Princeton.
How can we measure what counts?
What Makes a Good Quality Measure?AHRQ/NIDDK/VA Scientific Conference on Diabetes Quality Assessment
• Target patients most likely to benefit
• Help providers do the “right” thing
• Incorporate (or at least don’t ignore) patient preferences
• Avoid unintended consequences
• Acknowledge limitations of current data sources and resulting measures (and motivate collection and use of clinically detailed data)
http://www.ahrq.gov/QUAL/diabetescare/
Measuring Quality in Diabetes
Patients with diabetes who are 75 years or younger should have
A1c < 7%
BP < 130/80
Do stringent dichotomous outcomes measure what counts?
Do stringent dichotomous outcomes target patients most likely to benefit?
45 55 65 757 0.3% 0.1% 0.0% 0.0%
Hgb 9 2.6% 1.2% 0.5% 0.1%A1c 11 7.9% 4.4% 1.9% 0.5%
13 12.5% 7.9% 4.2% 1.5%
Lifetime Risk of Blindness due to Retinopathy
Vijan et al. Ann Int Med, 1997
Stringent Dichotomous Outcome Measures
• Don’t target patients most likely to benefit– Ignore the heterogeneity of patient risk factors
• Don’t help providers do the “right” thing– Do not give “partial credit” for actions or improvements that
may yield considerable benefits
• Don’t take into account patient preferences– Could mandate care that is contrary to the wishes of a
reasonable, well informed patient
• Could result in unintended consequences– Polypharmacy, hypoglycemia, worse outcomes
Tightly Linked Clinical Action Measures
• Identify high risk populations by diagnosis or by a poor intermediate outcome or other assessment of high risk
• Evaluate processes of care that are strongly associated with important outcomes for that population
• Intrinsically identify appropriate quality improvement responses within the measure that are under a health system’s control
- Kerr et al. Am J Manag Care 2001
Linked Clinical Action Measures:Adequate Quality for Hyperlipidemia Treatment
• Tightly Linked Clinical Action Measure– LDL <130 mg/dl; or
– LDL>= 130 mg/dl with appropriate clinical action:
1) were on a high dose statin; or 2) had statin started or dose increase within 6
months; or 3) repeat LDL <130 mg/dl within 6 months; or 4) had contraindications noted to statin
treatment
Percentage with Adequate Quality
Type of Measure Adequate Quality N (%)
Dichotomous Intermediate Outcome (LDL<130)
847/1154 (73%)
Tightly Linked Measure
(LDL<130 OR appropriate clinical action OR contraindication)
1006/1154 (87%)
Kerr et al. Medical Care 2003
Linked Clinical Action Measures
• Target patients most likely to benefit by :– accounting for patients’ risk factors and benefits of
intervention– Incorporating exceptions
• Help providers do the “right” thing– Intrinsically incorporate quality improvement response
• Can take into account patient preferences– Incorporate refusals or patient priorities
• Diminish but don’t eliminate potential for unintended consequences
Kerr et al. Am J Managed Care 2001
Measuring What Counts
• Focus on high risk populations and high benefit interventions
• Consider the costs, burden and safety of the treatments needed to achieve the goals
• Give at least partial credit for processes under providers’ control
• Insist on improvements in availability of clinically meaningful data
• Guard against unintended consequences
“Everything should be made as simple as possible, but not one bit simpler.”
– Albert Einstein (1879 - 1955)
ACCORD: More deaths in intensive vs standard glycemic control groups
National Heart, Lung, and Blood Institute. ACCORD telebriefing prepared remarks. February 6, 2008.
Standard glycemic control
Intensive glycemic control
Deaths, n 203 (11/1000/y) 257 (14/1000/y)
Do stringent dichotomous outcomes target patients most likely to benefit?
The Universe of Performance Measures
Sampled performancemeasures = SUBSET OFQUALITY(+ MORE NOISE)
Universeof possible performance measures= OVERALL QUALITY (+ SOME NOISE)
VA Compared to Community
0%
20%
40%
60%
80%
100%
Acute Care Chronic Care Preventive Care
VA Community
Asch et al. Annals of Internal Medicine, 2004
*
*
*P<0.01
Designing Clinically Meaningful Measures
• Tightly-Linked Clinical Action Measures
• Weighted or QALY-adjusted Measures
Weighted MeasuresDavid Aron and Len Pogach
• Differentially weighting measures in a composite can reflect the relative contributions of each measure to outcomes of interest
• Outcomes of interest may be defined specifically: e.g., cardiovascular events, mortality, or QALYs
• Certain measures can be weighted (or stratified) to reflect the importance of achieving the measure to different populations
kerr
ADA-NCQA Diabetes Physician Recognition “Weights and Measures”
Scored Measures Threshold Weight
(% of patients in sample) HbA1c Control <7.0% 40%
10.0 HbA1c Poor Control >9.0 % 15%
15.0 Blood Pressure Control >140/90 mm Hg 35% 15.0 Blood Pressure Control <130/80 mm Hg 25%
10.0 LDL Control >130 mg/dl 37% 10.0 LDL Control <100 mg/dl 36% 10.0 Eye Examination 60%
10.0 Foot Examination 80% 5.0 Nephropathy Assessment 80%
5.0 Smoking Status and Cessation Advice or Rx 80%
10.0
Total Points = 100.0 Points to Achieve Recognition = 75.0
What Are Quality Adjusted Life Years?
• Trade off between quality and length of life• QALY for a given intervention is the
average number of years of life gained by the intervention, multiplied by a judgment of quality of life in those years, summed over a lifetime
• Can address summary benefits and harms• Can address issues of life expectancy at
time of intervention
QALY Model
• Trade off between quality and length of life• QALYs are the most important and broadly
used method for evaluating health quality.
• Panel on Cost Effectiveness in Health and Medicine (Gold et al. 1996): Medical CE studies should incorporate morbidity and mortality consequences into a single measure using QALYs.
s
Time in state s Quality of life in sQALYs
The Case for QALYs to Assess Quality
• A1c reduction improves QOL by reducing complications, which differ in their impact upon QALYs
• Prioritization of public health measures requires an assessment of the impact of an intervention (ARR)
• The relationship of A1c to absolute reduction of complications is log-linear over a wide A1c range and is a function of life expectancy
Problems with QALYs
• Numerous studies have demonstrated that the correlation between one’s current health and the time-tradeoff or standard gamble utility for that health state is at best modest. (Tsevat 2000)
• Maximum endurable time: Subjects can tolerate no more than a particular time in an undesirable health state, beyond which each additional increment of time decreases overall utility. Miyamoto et al (1998)
• Such behavior cannot be accommodated within the QALY model.
QALY model and Extrinsic Goals
• In the QALY model, quality of health is given weight proportional to health duration; It follows that the QALY model cannot directly account for extrinsic goals, whose importance is by definition independent of duration– an author might want to complete a book;– many individuals seek to have children and
raise families.
Additional Considerations (QALYs)
• Equity considerations– interventions for young preferred to interventions for
old• Young have more life years remaining
– life extensions for healthy preferred to life extensions to less-healthy
• Healthy have a higher quality than chronically ill
CE Ratios (Cost/QALY)
Age Intensive GlycCntr
Intensive BloodPr Cntr
CholesterolReduction
35-44 $18,309 -$5,407 $79,473
45-54 $37,086 -$2,534 $52,544
55-64 $71,816 -$949 $43,331
65-74 $154,376 -$468 $40,471
75-84 $401,883 -$188 $51,459
All $41,384 -$1,959 $51,889
CDC, JAMA 2002
• Compares loss in QALY with expected QALY– The higher the proportion– The higher the need for equity compensation
Proportional short fall
Prop. Short Fall = 25% Prop. Short Fall = 50% Prop. Short Fall = 60%
QALY lostQALY gain
t
QoL
Prop. Short Fall = 50%
Now
Comparison of Weighted Performance Measurement and Dichotomous Thresholds for Glycemic Control (Pogach, Rajan, Aron, Diabetes Care, February 2006):
• 141 VA Centers• Thresholds <7%, <8%, or QALYsS• Incremental lifetime QALYs gained are
based on assumptions:– Linear relationship between QALY and
A1C between 7.0 and 7.9%– Lifetime QALYs range by age from 0 to
0.648– Maintaining A1c over lifetime– No adjustment for comorbid conditions
Weighted Measures• Gives “partial credit” to
achieved A1c levels ranging from 7.0 – 7.9%
• Differential credit based on potential for Quality Life Years Saved (QALYS) in different age groups of moving from 7.9 - 7.0%
• A1c values ≥7.9% (or not performed) received zero credit; A1c values <7% received full credit
*Pogach, Rajan, Aron. Diabetes Care, 2006.
Top and bottom decile ranking using <7% or QALY weighted
measure
Advantages of Weighted A1c Measure
• Assesses progress toward achieving thresholds, rather than whether the targets were completely met
• Motivates movement toward target even if target cannot be fully achieved
• Takes differential benefit of decreasing A1c by age into account
• Can be easily calculated using A1c data currently collected
kerr
Disadvantages of Weighted Measures
• Need underlying QALY information
• “Credit” given for a narrow range of A1c levels and not for intensity or modification of treatments
• Maximal QALYs calculations are based only on age strata
kerr
Use of Continuous Weighted Measures and Exclusion Criteria Can Address Possible
Unintended Consequences of <7% Measure for Public Reporting
• Avoids selection of marginal A1cs closest to 7% which may decrease
• Adverse Selection biases• Incorporation of Patient Preferences into
target setting • Use of additional medications without
consideration of actual benefit • Adverse events from additional
medications
QUERI WORKSHOP 12-091. Context for performance
measurement2. Limitations of measurement3. Alternative means for cross
sectional measurement4. Cross sectional measures vs
Longitudinal Measures5. Individuals versus populations6. Sources of Data
Diabetes Epidemiology Cohorts:A Resource for Quality Measures
Donald R. Miller
Monitoring and Improving the Population Health of Veterans with Diabetes:
Cross-sectional vs. Longitudinal Measures
DEpiC and affiliated projects are maintained by over 30 people across U.S.
A National Registry of Diabetes since 1998A National Registry of Diabetes since 1998
A Resource for Studying Diabetes in the VAA Resource for Studying Diabetes in the VA
DEpiC - DEpiC - Diabetes Epidemiology Cohorts,Diabetes Epidemiology Cohorts,VA EpidemiologyVA Epidemiology
Donald R. Miller – Epidemiologist - Bedford VA, Boston UniversityLeonard Pogach – Endocrinologist - East Orange VA, UMDNJB. Graeme Ficnke – Internal Medicine - Bedford VA, Boston UniversityMonika Safford – Internal Medicine – Birmingham VA, U. Alabama Susan Frayne – Internal Medicine – Palo Alto VA, Stanford Univ. Cindy Christianson - Statistician - Bedford VA, Boston UniversityChin-lin Tseng - Statistician - East Orange VA, UMDNJAnn Hendricks – Health Economist - Boston VA, Boston UniversityYujing Shen – Health Economist - East Orange VA, Rutgers UniversityMangala Rajan – Program Analyst - East Orange VA, UMDNJQing Shao – Program Analyst - Bedford VAXi Chen - Program Analyst – Boston University
Applications for DEpiC
Distribution of people and diseases Epidemiology
Monitoring processes of care Quality assessment
Measuring outcomes of care Quality improvement
Risk adjustment Costs of treatment
Medication safety & effectiveness Evidence basedBroad collaboration; over 20 funded
projects
DEpiCDiabetes Epidemiology Cohorts
Other data links: - Vital signs - Health care costs - Disease Registries
VA National Patient Care
Databases
VA PharmacyPrescriptions
Laboratory Test Results
VA National Health Surveys
Medicare ClaimsCMS
Mortality Records
• Define explicitly, evaluate rigorously.
• Working definition of 2 or more diabetes diagnostic codes over a 24 month period or prescribed diabetes medication in the year + other restrictions and conditions.– Specificity of 98.3%– Positive predictive value of 93.4%
• Fixed cohorts + linked longitudinal data; or dynamic cohort analysis
Who Has Diabetes?
Diabetes Prevalence and Incidence in VA FY98-FY05
0%
5%
10%
15%
20%
25%
FY98 FY99 FY00 FY01 FY02 FY03 FY04 FY05
Incident New to VA Prevalent
2.8% 1.9% 1.7% 2.0% 2.2% 2.0% 2.6%
2.9% 3.1% 2.6% 2.0% 1.0% 1.1%
16.6% 18.1%19.3%
20.9%22.0% 22.9% 23.1%
23.7%*499,243 → → → → 117% increase → → → → 1,082,678
* projected
0
2000
4000
6000
8000
10000
12000
14000
16000
180002
.3
3.4
4.1
4.8
5.5
6.2
6.9
7.6
8.3 9
9.7
10
.4
11
.1
11
.8
12
.5
13
.2
13
.9
14
.6
15
.3 16
16
.7
17
.4
>9.5 - 81,386 (14.0%)
>8.0 - 117,401 (30.6%)
Hemoglobin A1c in VA 2000 - Maximum ValuesTotal number of diabetic patients: 654,677 Total # of tests: 1,061,350Total # of patients with tests: 579,891
>7.0 – 54%
Intermediate Outcome of Diabetes Care
Hemoglobin A1c Trends in VA
What are the trends and what do they mean?
Is better treatment progressively improving glucose control?
Are there differences by race, comorbidities, or other population groups?
Can these be used in quality monitoring to improve care?
Questions
All
Mean <7% <8%
2000 7.7 54% 76%
2001 7.5 59% 80%
2002 7.4 59% 81%
2003 7.3 60% 83%
Cross Sectional Trends in A1c Measures
All Prevalent, since 98
Mean <7% <8% Mean <7% <8%
2000 7.7 54% 76% 7.9 47% 72%
2001 7.5 59% 80% 7.8 50% 75%
2002 7.4 59% 81% 7.8 49% 75%
2003 7.3 60% 83% 7.7 50% 76%
Cross Sectional Trends in A1c Measures
All Prevalent, since 98 Recent-onset
Mean <7% <8% Mean <7% <8% Mean <7% <8%
2000 7.7 54% 76% 7.9 47% 72% 7.0 76% 89%
2001 7.5 59% 80% 7.8 50% 75% 7.0 78% 91%
2002 7.4 59% 81% 7.8 49% 75% 7.0 75% 90%
2003 7.3 60% 83% 7.7 50% 76% 6.9 75% 90%
Cross Sectional Trends in A1c Measures
Adherence in meeting threshold measures in overall diabetes population is dependent upon diabetes “duration”
27%
32%
36%
39%
Longitudinal HbA1c Trends in VA FY99-05
Methods
• 13 million measures from 1.2 million patients
• Growth curve model: longitudinal linear regression with random effects (slopes and intercepts) for individuals nested within facility and year
• Adjustment for age, sex, race, facility, seasonality
Trends in HbA1c in VA FY2000-2004
HbA1c declines steadily by nearly 0.5% over 5 years
FY2000 2001 2002 2003 2004
N= 1,351,551 patients with 9,400,875 A1c values
6.6
6.8
7.0
7.2
7.4
7.6
7.8
8.0
8.2
Mean annual decline of 0.09% per year
Mean HbA1c by month
7
7.1
7.2
7.3
7.4
7.5
7.6
7.7
7.8
7.9
O N D J F MA M J J A S O N D J F MA M J J A S O N D J F MA M J J A S O N D J F MA M J J A S
Average A1c is highest in late winterAverage A1c is highest in late winter
Average A1c is lowest in late summerAverage A1c is lowest in late summer
Seasonality of HbA1c in VA - FY1999-2003
Monthly mean HbA1c
6.8
7
7.2
7.4
7.6
7.8
8
1999 2000 2001 2002 2003
Average HbA1c by Year FY1999-2003
ALL diabetes patients -0.09% per year
HighestHighest
LowestLowest
Substantial within year variation.Industry measures last a1c in year but
clinicians treat last value.
6.6
6.8
7.0
7.2
7.4
7.6
7.8
8.0
8.2O
ct
De
c
Fe
b
Ap
r
Jun
Au
g
Oct
De
c
Fe
b
Ap
r
Jun
Au
g
Oct
De
c
Fe
b
Ap
r
Jun
Au
g
Oct
De
c
Fe
b
Ap
r
Jun
Au
g
Oct
De
c
Fe
b
Ap
r
Jun
Au
g
Trends in HbA1c by Subgroup in VA FY2000-2004
Prevalent panel surviving:Prevalent panel surviving: -0.06% per year -0.06% per year
IncidentIncident:: -0.01% per year -0.01% per year
Prevalent panel diedPrevalent panel died:: -0.14% per year -0.14% per year
Prevalent new to VAPrevalent new to VA:: -0.12% per year -0.12% per year
Lower HbA1c level and little trend with incident diabetes.
Steepest trend if prevalent and near death or new to VA
FY2000 2001 2002 2003 2004
N= 1,351,551 patients with 9,400,875 A1c values
6.6
6.8
7.0
7.2
7.4
7.6
7.8
8.0
8.2
Oct
Jan
Apr
Jul
Oct
Jan
Apr
Jul
Oct
Jan
Apr
Jul
Oct
Jan
Apr
Jul
Oct
Jan
Apr
Jul
Trends in HbA1c in VA FY2000-2004in National Panel of 248,768 patients
FY2000 2001 2002 2003 2004
Prevalent panel surviving:Prevalent panel surviving: -0.06% per year -0.06% per year
7.3
7.4
7.5
7.6
7.7
7.8
7.9
8.0
8.1
FY2000 2001 2002 2003 2004
Sicker patients have lower HbA1c and flatter trends
Without co-morbidities
With stroke, CVD, recent cancer, liver failure, COPD
Trends in HbA1c by Month by Co-morbidity inNational Panel of VA Diabetes Patients FY2000-2004
-0.06%
-0.03%
A1c %
Mean Monthly A1C for Veteran Clinic Users By Age Category
7
7.2
7.4
7.6
7.8
8
8.2
8.4
8.6
8.8
Oct-98
Nov-98
Dec-98
Jan-99
Feb-99
Mar-99
Apr-99
May-99
Jun-99
Jul-99
Aug-99
Sep-99
Oct-99
Nov-99
Dec-99
Jan-00
Feb-00
Mar-00
Apr-00
May-00
Jun-00
Jul-00
Aug-00
Sep-00
Month Year
Mea
n A
1C %
Age <55 Age 55 - 65 Age 65 - 75 Age 75 + Total
Additionally, a regression model that adjusts for clustering (patient and facility) and seasonal effects was used to confirm thedownward linear trend in monthly A1c values overall (-0.013, p=<.0001) and minimal differences in this trend by each age category (p=.492)HbA1c declines steadily with age
Chart Title
7.3
7.4
7.5
7.6
7.7
7.8
7.9
8.0
8.1
White, non-Hispanic
FY2000 2001 2002 2003 2004
A1c %
Trends in HbA1c by Month by Race/Ethnicity inNational Panel of VA Diabetes Patients FY2000-2004
Standardized to combined age & sex distribution
FY2000 yearly Δ FY2004
White, non-Hispanic 7.60 -0.06 7.32
70.2% 152,352
Whites similar to overall
7.3
7.4
7.5
7.6
7.7
7.8
7.9
8.0
8.1
Oct J an
Apr J ul
Oct J an
Apr J ul
Oct J an
Apr J ul
Oct J an
Apr J ul
Oct J an
Apr J ul
White, non-Hispanic
African American
FY2000 2001 2002 2003 2004
A1c %
Standardized to combined age & sex distribution
FY2000 yearly Δ FY2004African American 7.89 -0.08 7.48
White, non-Hispanic 7.60 -0.06 7.32
20.1% 43,641
70.2% 152,352
Trends in HbA1c by Month by Race/Ethnicity inNational Panel of VA Diabetes Patients FY2000-2004
AA have higher A1c but steeper decline & less difference in 2004
7.3
7.4
7.5
7.6
7.7
7.8
7.9
8.0
8.1
Oct J an
Apr J ul
Oct J an
Apr J ul
Oct J an
Apr J ul
Oct J an
Apr J ul
Oct J an
Apr J ul
White, non-Hispanic
Hispanic, non-White
FY2000 2001 2002 2003 2004
A1c %
Standardized to combined age & sex distribution
FY2000 yearly Δ FY2004African American 7.89 -0.08 7.48
Hispanic, White 7.81 -0.03 7.68White, non-Hispanic 7.60 -0.06 7.32
8.6% 18,716
70.2% 152,352
African American20.1% 43,641
Trends in HbA1c by Month by Race/Ethnicity inNational Panel of VA Diabetes Patients FY2000-2004
Hispanics are intermediate but less steep decline & highest in 2004
7.3
7.4
7.5
7.6
7.7
7.8
7.9
8.0
8.1
Oct J an
Apr J ul
Oct J an
Apr J ul
Oct J an
Apr J ul
Oct J an
Apr J ul
Oct J an
Apr J ul
FY2000 yearly Δ FY2004African American 7.89 -0.08 7.48Pacific Isl./Asian 7.82 -0.08 7.40Native American 7.82 -0.08 7.40Hispanic, White 7.81 -0.03 7.68White, nonhispanic 7.60 -0.06 7.32
White, non-Hispanic
Native American
Pacific Isl./Asian
Hispanic, non-White
African American
FY2000 2001 2002 2003 2004
A1c %
Standardized to combined age & sex distribution
0.7% 1,426
0.5% 1,030 8.6% 18,716
20.1% 43,641
70.2% 152,352
Trends in HbA1c by Month by Race/Ethnicity inNational Panel of VA Diabetes Patients FY2000-2004
Other racial groups just below AA but similar trends
Longitudinal HbA1c Trends in VA FY99-04
Mean HbA1c decreased (0.06% per year) and proportion below target levels increased (53.8%→60.4% -- <7%).
This may be due in part to better treatment of diabetes but there are other factors to consider, including:
• Incident versus prevalent diabetes
• Medical, psychiatric, and social conditions that contraindicate intensification of glucose control
• Seasonality and age modification
Trends varied by race, age, and comorbidity.
Can VA Longitudinal HbA1c Trends be used for Quality Monitoring?
Yes, but methodologic issues must be addressed?
Standardize data collection and data quality
Develop method for more rapid analysis – currently computationally demanding
Better understanding of external sources of variation
How to interpret and use in improving quality of care
QUERI WORKSHOP 12-091. Context for performance
measurement2. Limitations of measurement3. Alternative means for cross
sectional measurement4. Cross sectional measures vs
Longitudinal Measures5. Individuals versus populations6. Sources of Data
Two options: Interventions for Everybody or Targeted
A moderate intervention for all patients with DM (1 point improvement in A1c)
Vs.
An intensive intervention for the 20% at the highest risk (2 point improvement in A1c)
# of Treatment Years Needed to Prevent 1 Yr of Blindness
(Vijan Ann Intern Med 1997)
A1c 9% 7%
Pt Age (Pt Years)
45 yrs 40
65 yrs 180
# of Treatment Years Needed to Prevent 1 Yr of Blindness (Estimates if BP controlled)
A1c 8% 7%
Pt Age (Pt Years)
45 yrs > 400
65 yrs > 6000
Possible Action Steps• Identify sub-populations of veterans not doing
well (especially <65, MHCs)• >9% applies to all; <8% to many; <7% to some• Focus on shared care (mental health-primary
care)• Insulin initiation and management teams (NPs,
Pharm Ds) with “graduation”• Use of telehealth for patients who may not
have access during the day • Identify “innovative practices” by comparing
like facilities with like facilities.
QUERI WORKSHOP 12-091. Context for performance
measurement2. Limitations of measurement3. Alternative means for cross
sectional measurement4. Cross sectional measures vs
Longitudinal Measures5. Individuals versus populations6. Sources of Data
DiabetesDiabetesCare ManagementCare Management
Data MartData Mart
Diabetes ResearchDiabetes ResearchData MartData Mart
DataDataWarehouseWarehouse
Health DataHealth DataRepositoryRepository
SourceSourceSystemsSystems
AcquireAcquire Populate Populate Create Create Access Access Data Data Warehouse Warehouse Data Marts Data Marts Information Information
11 33 44
Common Query, Reporting, Common Query, Reporting, Analysis, & Data Mining ToolsAnalysis, & Data Mining Tools
22
VHA Corporate Data Warehouse ArchitectureUnder Development
Clinical Care Management Site
Research site
Updated continuously
DiabetesDiabetesCare ManagementCare Management
Data MartData Mart
Diabetes ResearchDiabetes ResearchData MartData Mart
DataDataWarehouseWarehouse
AdministrativeAdministrative(DSS, PBM, etc.)(DSS, PBM, etc.)
OtherOther(Medicare, DoD)(Medicare, DoD)
VSSC Diabetes Cube - History
• Developed in 2005-2006.
• Definitions per evidence available at that time.
• As additional data (example: Vital Signs) are sent to/stored in HDR, additional “Hierarchies” can be added.
• ProClarity software used.
--------Facilities ------
----
----
Pat
ien
ts--
----
-
--Tim
e--
A Patient atA Facility on
A Date
What’s a Cube?
Multi-Dimensional Store of Data
What can a Cube Do?
• Organizes and optimizes data
• Efficient and fast querying
• Aggregated or detailed data
• Numerical analysis
• Graphical interface
• Easy to use
Hierarchies
• Diabetes Definitions– Definite DM– Possible Unrecognized
DM– Possible Pre-Diabetes
• Admin/Demographic– Employee– Fee Patient– Location, Preferred
Location
• Admin/Demog, Contd– Age (ranges)– OEF-OIF– SC status– PCP Assigned– Priority Status– FY– Home County– (Race: not reliable)
Hierarchies
• Lab Values (ranges)– A1C– Urine Alb/Cr Ratio– Total Cholesterol– HDL Cholesterol– LDL Cholesterol– Creatinine
• Complications (Y/N)– Retinopathy– ESRD– Amputations– Foot Ulcers– IHD– Stroke
Hierarchies
• Glycemice Rx’s (Y/N)– Insulins, any– Glargine– SU’s– Biguanides– TZD’s– Exenatide– AGI’s– Metaglitinide
• CV Rx’s (Y/N)– ACEI’s– ARB’s– Statins– Thiazides
Hierarchies
• Comorbidities (codes)– PTSD– Serious Mental Illness– Substance Abuse– Tobacco Use Disorder
• Costs– Overall Pharmacy $– Diabetes Pharmacy $– Inpatient/Outpatient
costs per encounter, per patient, etc.
Point Prevalence of possible pre-diabetes, possible
unrecognized diabetes and definite diabetes
With ProClarity, we can sort patients by any combinations) of hierarchies.
View of A1c control in patients on insulin versus no insulin (no
evaluation oral agents)
View of A1c control on insulin versus no insulin for patients on
metformin and sulfonylurea therapy
View of A1c control on insulin versus no insulin for patients on
metformin, sulfonylurea and TZD therapy
Example: Costs
A1C’s for Hi/Lo Cost VISNs
Diabetes TZD Cost view – TZD RX cost compared to Diabetes RX cost
TZD Study effectiveness ViewA1C changes within 8 months
After first TZD dose
37% have an increase or no change In the A1C value
Example: A1C by Site
VISN Service Support Center developmental database
Diabetes Data MartLatest Results of Critical Labs
Access via VSSC Site:http://klfmenu.med.va.gov/
Summary: Where Future Research is Relevant
• Defining exclusion criteria – establishing the proper denominator
• Developing linked and weighted measures
• Defining risk adjustment
• Evaluation of outlier status
• Evaluation of unit of measurement (provider vs clinic vs facility)
• Time Frame