SlideShare une entreprise Scribd logo
1  sur  14
Télécharger pour lire hors ligne
1
Performance Measurement
Diagnosis and Treatment of Rheumatoid Arthritis: Review of the Performance Measures by the
Performance Measurement Committee of the American College of Physicians
Writing Committee
Amir Qaseem, MD, David Baker, MD, Robert Gluckman, MD, Catherine MacLean, MD, PhD,
Sarah West, MSN, RN
ACP Performance Measurement Committee Members*
David W. Baker, MD, MPH (Chair); J. Thomas Cross, MD, MPH; Andrew Dunn, MD, MPH; Mary
Ann Forciea, MD; Robert A. Gluckman, MD; Robert H. Hopkins, MD; Eve Kerr, MD; Kesavan
Kutty, MD; Ana Maria López, MD, MPH; Catherine MacLean, MD, PhD; Stephen D. Persell, MD,
MPH; and Terrence Shaneyfelt, MD
Corresponding author:
A. Qaseem
190 N. Independence Mall West
Philadelphia, PA 19106
Email aqaseem@acponline.org
* Individuals who served on the Performance Measurement Committee from initiation of the
project until its approval
2
Introduction
Rheumatoid arthritis (RA) is systemic polyarthritis, which disproportionately affects women. It
affects an estimated 1.5 million Americans over the age of 18 and accounts for as much as $8.6
billion in medical costs and an additional $2.7 billion in excess indirect and non-medical costs
annually (both in 2000 dollars) (1-2). Over the last decades, advances in therapies and
therapeutic approach have dramatically improved health outcomes with the achievement of
minimal disease activity or remission in 10-30% of treated patients (3-4). Although the
availability of such effective therapies and the opportunity to withhold or discontinue therapy
with minimal disease activity or remission warrant periodic assessment of disease activity, such
assessment is not routine (54% in 2012) and represents an opportunity for improvement in care
(5).
The ACP Performance Measurement Committee (PMC) reviewed performance measures
related to the management of rheumatoid arthritis (RA) to assess whether the measures are
evidence-based, methodologically sound, and clinically meaningful.
Methods
We performed a search to identify relevant performance measures from the National Quality
Forum (NQF), the American Medical Association-Physician Consortium for Performance
Improvement (AMA-PCPI), and National Quality Measures Clearinghouse (NQMC) websites.
The inclusion criteria were performance measures currently used in the Centers for Medicare
and Medicaid Services (CMS) Physician Quality Reporting System (PQRS) or currently used in
the CMS Electronic Record Incentive program. The PMC identified and reviewed 7 performance
measures.
Conclusion
3
Recommendation
ACP supports NQF 0054 for physicians managing Rheumatoid Arthritis (RA), with modifications:
“Disease-Modifying Anti-Rheumatic Drug (DMARD) Therapy for Rheumatoid Arthritis.”
Rationale
The current evidence supports the benefit of DMARD therapy in reducing the symptoms of RA
and decelerating the progression of joint damage (6). Furthermore, a wide range of DMARD
prescribing across health plans in the 2013 measurement year suggests a performance gap (7).
However, given the availability of highly effective therapies and a more aggressive therapeutic
approach than in previous decades, remission or minimal disease activity is now achievable for
a significant numbers of patients [10-30% (3-4)]. Therefore, DMARD therapy may be
appropriately withheld for a period of time (a “drug holiday”) or discontinued for such patients.
Hence, minimal disease activity or clinical remission should be included in the denominator
exclusions. This is a physician level measure and should only be applicable to physicians who
are managing and providing medical therapy for RA. Most often this will apply to
rheumatologists, but primary care physicians may also manage RA.
Measure Specifications
NQF 0054: Disease-Modifying Anti-Rheumatic Drug Therapy for Rheumatoid Arthritis
Status: NQF Endorsed, UPDATED November 10, 2014 (2015 PQRS #108)
Measure
Steward:
National Committee for Quality Assurance
Description: The percentage of patients 18 years and older by the end of the
measurement period, diagnosed with rheumatoid arthritis and who had at
least one ambulatory prescription for a disease-modifying anti-rheumatic
drug (DMARD)
Numerator
Statement:
Patients diagnosed with rheumatoid arthritis who were dispensed at least
one ambulatory prescription for a disease-modifying anti-rheumatic drug
(DMARD) during the measurement year.
Denominator
Statement:
All patients, ages 18 years and older by December 31 of the measurement
year who had two of the following with different dates of service on or
between January 1 and November 30 of the measurement year:
- Outpatient visit, with any diagnosis of rheumatoid arthritis
- Non-acute inpatient discharge, with any diagnosis of rheumatoid arthritis
Visit type need not be the same for the two visits
Exclusions: Exclude patients who have a diagnosis of HIV. Look for evidence of HIV
diagnosis as far back as possible in the patient’s history through the end of
the measurement year.
Exclude patients who have a diagnosis of pregnancy during the
measurement year.
Type of
Measure:
Process
Level of Analysis: Health Plan, Integrated Delivery System
4
Care Setting: Ambulatory Care: Clinician Office/Clinic
Data Source: Administrative claims, Electronic Clinical Data, Electronic Clinical Data:
Pharmacy
Recommendation
ACP supports NQF 2522 for physicians managing Rheumatoid Arthritis (RA): “Rheumatoid
Arthritis: Tuberculosis Screening.”
Rationale
Biologic Disease-Modifying Anti-Rheumatic (DMARD) therapy can reactivate latent tuberculosis,
leading to significant morbidity and even mortality (5, 8). Administrative data suggests that
over 1 in 4 individuals with RA receive biologic DMARDs (8). Over 1.3 million individuals in the
United States have RA (9-10); therefore this measure is expected to impact over 300,000
Americans with RA (9-10). This is a physician level measure and should only be applicable to
physicians who are managing and providing medical therapy for RA. Most often this will apply
to rheumatologists, but primary care physicians may also manage RA.
Measure Specifications
NQF 2522: Rheumatoid Arthritis: Tuberculosis Screening
Status: NQF Endorsed, Updated November 10, 2014 (2015 PQRS #176)
Measure
Steward:
American College of Rheumatology
Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid
arthritis who have documentation of a tuberculosis (TB) screening
performed within 12 months prior to receiving a first course of therapy
using a biologic disease-modifying anti-rheumatic drug (DMARD)
Numerator
Statement:
Any record of TB testing documented or performed (PPD, IFN-gamma
release assays, or other appropriate method) in the medical record in the
12 months preceding the biologic DMARD prescription
Denominator
Statement:
Patients 18 years and older with a diagnosis of rheumatoid arthritis who
are seen for at least one face-to-face encounter for RA who are newly
started on biologic therapy during the measurement period
Exclusions: None
Type of Measure: Process
Level of Analysis: Clinician: Individual
Care Setting: Ambulatory Care: Clinician Office/Clinic
Data Source: Electronic Clinical Data: Electronic Health Record
5
Recommendation
ACP supports 2523 for physicians managing Rheumatoid Arthritis (RA): “Rheumatoid Arthritis:
Assessment of Disease Activity.”
Rationale
Using validated disease activity assessments is a standard component of guideline-based care
and has been shown to improve patient outcomes including; functional status, health-related
quality of life, and radiographic disease progression (11). This is a physician level measure and
should only be applicable to physicians who are managing and providing medical therapy for
RA. Most often this will apply to rheumatologists, but primary care physicians may also manage
RA.
Measure Specifications
NQF 2523: Rheumatoid Arthritis: Assessment of Disease Activity
Status: NQF Endorsed, Updated November 10, 2014 (2015 PQRS #177)
Measure
Steward:
American College of Rheumatology
Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid
arthritis and >=50% of total number of outpatient RA encounters in the
measurement year with assessment of disease activity using a standardized
measure
Numerator
Statement:
Number of patients with >=50% of total number of outpatient RA
encounters in the measurement year with assessment of disease activity
using a standardized measure
Denominator
Statement:
Patients 18 years and older with a diagnosis of rheumatoid arthritis seen for
two or more face-to-face encounters for RA with the same clinician during
the measurement period
Exclusions: None
Type of
Measure:
Process
Level of Analysis: Clinician: Individual
Care Setting: Ambulatory Care: Clinician Office/Clinic
Data Source: Electronic Clinical Data: Electronic Health Record
6
Recommendation
ACP supports NQF 2524 for physicians managing Rheumatoid Arthritis (RA): “Rheumatoid
Arthritis: Functional Status Assessment.”
Rationale
ACP supports this measure because therapeutic treatment goals include preservation of
function and quality of life (13-14). Findings of a joint examination alone may not adequately
reflect disease activity and structural damage; therefore, periodic measurements of functional
status should be performed (12). Additionally, it is important to determine whether a decline in
function is the result of inflammation, mechanical damage, or both because treatment
approaches will differ accordingly (12). This is a physician level measure and should only be
applicable to physicians who are managing and providing medical therapy for RA. Most often
this will apply to rheumatologists, but primary care physicians may also manage RA.
Measure Specifications
NQF 2524: Rheumatoid Arthritis: Functional Status Assessment
Status: NQF Endorsed, Updated November 10, 2014 (2015 PQRS #178)
Measure
Steward:
American College of Rheumatology
Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid
arthritis for whom a functional status assessment was performed at least
once during the measurement period
Numerator
Statement:
Number of patients with functional status assessment documented once
during the measurement period. Functional status can be assessed using
one of a number of valid and reliable instruments available from the
medical literature
Denominator
Statement:
Patients age 18 and older with a diagnosis of rheumatoid arthritis seen for
two or more face-to-face encounters for RA with the same clinician during
the measurement period
Exclusions: None
Type of
Measure:
Process
Level of Analysis: Clinician: Individual
Care Setting: Ambulatory Care: Clinician Office/Clinic
Data Source: Electronic Clinical Data: Electronic Health Record
7
Recommendation
ACP supports NQF 2525 for physicians managing RA, with modifications: “Rheumatoid Arthritis
(RA): Disease Modifying Anti-Rheumatic Drug (DMARD) Therapy.”
Rationale
The current evidence supports the benefit of DMARD therapy in reducing the symptoms of RA
and decelerating the progression of joint damage (6). Furthermore, a wide range of DMARD
prescribing across health plans in the 2013 measurement year suggests a performance gap (9).
However, given the availability of highly effective therapies and a more aggressive therapeutic
approach than in previous decades, remission or minimal disease activity is now achievable for
a significant numbers of patients [10-30% (3-4]. Therefore, DMARD therapy may be
appropriately withheld for a period of time (a “drug holiday”) or discontinued for such patients
and minimal disease activity or clinical remission should be included in the denominator
exclusions. This is a physician level measure and should only be applicable to physicians who
are managing and providing medical therapy for RA. Most often this will apply to
rheumatologists, but primary care physicians may also manage RA.
Measure Specifications
NQF 2525: Rheumatoid Arthritis: Disease Modifying Anti-Rheumatic Drug (DMARD) Therapy
Status: NQF Endorsed, Updated November 10, 2014
Measure
Steward:
American College of Rheumatology
Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid
arthritis who are newly prescribed disease modifying anti-rheumatic drug
(DMARD) therapy within 12 months
Numerator
Statement:
Patient received a DMARD
Denominator
Statement:
Patient age 18 years and older with a diagnosis of rheumatoid arthritis seen
for two or more face-to-face encounters for RA with the same clinician
during the measurement period
Exclusions: Patients with a diagnosis of HIV; patients who are pregnant; or patients
with inactive Rheumatoid Arthritis
Type of
Measure:
Process
Level of Analysis: Clinician: Individual
Care Setting: Ambulatory Care: Clinician Office/Clinic
Data Source: Electronic Clinical Data: Electronic Health Record
8
Recommendation
ACP does not support PQRS 179 for physicians managing Rheumatoid Arthritis (RA):
“Assessment and Classification of Disease Prognosis.”
Rationale
ACP does not support this measure because there is no evidence supporting annual frequency
or describing appropriate frequency for assessment or classification of disease prognosis.
Additionally, it seems unnecessary to reassess prognosis annually if a poor prognosis has been
established based on factors that will not change such as high titer anti-citric citrullinated
peptide (anti-CCP) antibodies, rheumatoid factor (RF) or radiographic erosions.
Measure Specifications
PQRS 179: Assessment and Classification of Disease Prognosis
Status: Not NQF Endorsed
Measure
Steward:
American Medical Association - Physician Consortium for Performance
Improvement
Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid
arthritis (RA) who have an assessment and classification of disease
prognosis at least once within 12 months
Numerator
Statement:
Patients with at least one documented assessment and classification
(good/poor) of disease prognosis* utilizing clinical markers of poor
prognosis** within 12 months
*Poor prognosis: RA patients with features of poor prognosis have active
disease with high
tender and swollen joint counts, often have evidence of radiographic
erosions, elevated levels of
rheumatoid factor (RF) and or anti-cyclic citrullinated peptide (anti-CCP)
antibodies, and an
elevated erythrocyte sedimentation rate, and an elevated C-reactive
protein level.
** Prognostic classification should be based upon at a minimum the
following markers of poor
prognosis: functional limitation (e.g., HAQ Disability Index), extra-articular
disease (e.g. vasculitis,
Sjorgen’s syndrome, RA lung disease, rheumatoid nodules), RF positivity,
positive anti-CCP
antibodies (both characterized dichotomously, per CEP recommendation),
and/or bony erosions
by radiography
Denominator
Statement:
Patients 18 years and older with a diagnosis of Rheumatoid Arthritis (RA)
Exclusions: None
9
Type of
Measure:
Process
Care Setting: Ambulatory Care
Data Source: Administrative claims; Medical record; Electronic medical record;
Administrative claims supplemented by medical records; Registries;
Prospective data collection flow-sheet
Recommendation
ACP does not support PQRS 180: “Glucocorticoid Management.”
Rationale
Although we recognize the importance of managing the lowest effective dose of glucocorticoids
and using alternative therapies when possible, both the numerator and the denominator are
poorly specified. A cleaner measure would specify “patients with rheumatoid arthritis (RA) who
are on glucocorticoids” in the denominator statement. Additionally, the current American
College of Rheumatology clinical guidelines demonstrate the importance of assessing
glucocorticoid use, but only in patients who have specifically been prescribed glucocorticoid
therapy (15).
Measure Specifications
PQRS 180: Glucocorticoid Management
Status: Not NQF Endorsed
Measure
Steward:
American Medical Association - Physician Consortium for Performance
Improvement
Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid
arthritis (RA) who have been assessed for glucocorticoid use and, for those
on prolonged doses of prednisone > 10 mg daily (or equivalent) with
improvement or no change in disease activity, documentation of
glucocorticoid management plan within 12 months
Numerator
Statement:
Patients who have been assessed for glucocorticoid use at least once
within 12 months, and for those on prolonged doses* of prednisone > 10
mg qD (or equivalent**) with improvement or no change in disease
activity, documentation of a glucocorticoid management plan***
*Prolonged doses are doses >6 months in duration
**Prednisone equivalents can be determined using the following:
1 mg of prednisone = 1 mg of prednisolone; 5 mg of cortisone; 4 mg of
hydrocortisone; 0.8 mg of
triamcinolone; 0.8 mg of methylprednisolone; 0.15 mg of dexamethasone;
0.15 mg of betamethasone.
***Glucocorticoid management plan: documentation of attempt to taper
steroids OR
documentation of a new prescription for a non-glucocorticoid DMARD OR
10
increase in dose of
non-glucocorticoid DMARD dose for persistent RA disease activity at
current or reduced dose.
Denominator
Statement:
Patients 18 years and older with a diagnosis of rheumatoid arthritis (RA)
Exclusions: Documentation of medical reason(s) for not documenting glucocorticoid
dose (i.e., glucocorticoid prescription is for a medical condition other than
RA)
Type of
Measure:
Process
Care Setting: Ambulatory Care
Data Source: Administrative claims; Medical record; Electronic medical record;
Administrative claims supplemented by medical record; Registries;
Prospective data collection flow-sheet
Gaps in Performance Measurement — Opportunities to Promote High-Value Care
There is a need for performance measures that focus on the individualized care of patients with
RA including the appropriate discontinuation of DMARDs in patients who have achieved
remission or minimal disease activity.
11
References
1. Gabriel SE, Crowson CS, Campion ME, O'Fallon WM. Direct medical costs unique to
people with arthritis. JRheumatol. 1997;24(4):719-25.
2. Gabriel SE, Crowson CS, Campion ME, O'Fallon WM. Indirect and nonmedical costs
among people with rheumatoid arthritis and osteoarthritis compared with nonarthritic
controls. JRheumatol. 1997;24(1):43-8.
3. De Punder YM, Fransen J, Kievit W, Houtman PM, Visser H, van de Laar MA, van
Riel PL. The prevalence of clinical remission in RA patients treated with
anti-TNF: results from the Dutch Rheumatoid Arthritis Monitoring (DREAM)
registry. Rheumatology. 2012;51(9):1610-7.
4. Jayakumar K, Norton S, Dixey J, James D, Gough A, Williams P, Prouse P, Young
A; Early Rheumatoid Arthritis Study (ERAS). Sustained clinical remission in
rheumatoid arthritis: prevalence and prognostic factors in an inception cohort of
patients treated with conventional DMARDS. Rheumatology. 2012;51(1):169-75.
5. Grossman JM, Gordon R, Ranganath VK et al. American College of Rheumatology 2010
Recommendations for the prevention and treatment of glucocorticoid-induced
osteoporosis. Arthritis Care & Research. 2010;62(11):1515-1526.
6. Smolen JS et al. EULAR recommendations for the management of rheumatoid arthritis
with synthetic and biological disease-modifying antirheumatic drugs: 2013 update. Ann
Rheum Dis. Mar 2014;73(3):492–509.
7. National Committee for Quality Assurance (NCQA). HEDIS 2014: Healthcare
Effectiveness Data and Information Set. Vol. 1, narrative. Washington (DC): National
Committee for Quality Assurance (NCQA); 2013. various p.
8. Zhang J, Xie F, Delzell E et al. Trends in the use of biologic agents among rheumatoid
patients enrolled in the US Medicare Program. Arthritis Care & Research.
2013;65(11):1743-1751.
9. National Quality Forum. Prioritization of high-impact Medicare conditions and measure
gaps. Measure Prioritization Advisory Committee Report. 2010
12
10. Yazdany, Jinoos, Kazi, Salahuddin, Francisco, Melissa, Myslinski, Rachel. “Uptake of the
American College of Rheumatology’s Rheumatology Clinical Registry (RCR): Quality
Measure Summary Data”. Annual Scientific Meeting. American College of
Rheumatology. Reed Convention Center, Washington, DC. 27 October 2013. Conference
Presentation.
11. Scott DL, Symmons DP, Coulton, BL, Popert, AJ. Long-term outcome of treating
rheumatoid arthritis: Results after 20 Years. The Lancet. 1987;1(8542):1108-1111.
12. American College of Rheumatology Subcommittee on Rheumatoid Arthritis Guidelines.
Guidelines for the management of rheumatoid arthritis: 2002 Update. Arthritis Rheum.
2002 Feb;46(2):328-46.
13. Helmick CG, Felson DT, Lawrence RC et al. Estimates of the prevalence of arthritis and
other rheumatic conditions in the US. Part 1. Arthritis & Rheumatology. 2008;58(1):15-
25.
14. Harris ED. Clinical features of rheumatoid arthritis. In: Ruddy S, Harris ED, Sledge CB,
Kelley WN, eds. Kelley’s Textbook of rheumatology. 7th ed. Philadelphia: WB Saunders,
2005:1043–78.
15. American College of Rheumatology Subcommittee on Rheumatoid Arthritis Guidelines.
Guidelines for the management of rheumatoid arthritis: 2002 update. Arthritis Rheum.
2002;46:328–46.
13
Financial Statement: Financial support for the Performance Measurement Committee comes
exclusively from the ACP operating budget.
Conflicts of Interest: Any financial and nonfinancial conflicts of interest of the group members
were declared, discussed, and resolved. A record of conflicts of interest is kept for each PMC
meeting and conference call and can be viewed at:
http://www.acponline.org/running_practice/performance_measurement/pmc/conflicts_pmc.h
tm
APPROVED BY THE ACP BOARD OF REGENTS ON:
April 27, 2015
Members of the PMC:
Individuals who served on the Performance Measurement Committee from initiation of the
project until its approval:
David W. Baker, MD, MPH
J. Thomas Cross, Jr., MD, MPH
Andrew Dunn, MD, MPH
Mary Ann Forciea, MD
Robert A. Gluckman, MD
Robert H. Hopkins, MD
Kesavan Kutty, MD
Eve Askanas Kerr, MD, MPH
Ana María López, MD, MPH
Catherine MacLean, MD, PhD
Stephen D. Persell, MD, MPH
Terrence Shaneyfelt, MD, MPH
Requests and inquiries: Amir Qaseem, MD, PhD, MHA, FACP, American College of Physicians,
190. N Independence Mall West, Philadelphia, PA 19106: email, aqaseem@acponline.org
14

Contenu connexe

Tendances

Clinical trails overview
 Clinical trails overview Clinical trails overview
Clinical trails overviewshashi sinha
 
Effect of rosuvastatin on rheumatoid arthritis clinical disease activity inde...
Effect of rosuvastatin on rheumatoid arthritis clinical disease activity inde...Effect of rosuvastatin on rheumatoid arthritis clinical disease activity inde...
Effect of rosuvastatin on rheumatoid arthritis clinical disease activity inde...Alexander Decker
 
Dia Care-2001-Clark-1079-86 (1)
Dia Care-2001-Clark-1079-86 (1)Dia Care-2001-Clark-1079-86 (1)
Dia Care-2001-Clark-1079-86 (1)Denise Burgh, MBA
 
Characteristics of efficacy evidence supporting approval of supplemental indi...
Characteristics of efficacy evidence supporting approval of supplemental indi...Characteristics of efficacy evidence supporting approval of supplemental indi...
Characteristics of efficacy evidence supporting approval of supplemental indi...Sandeepkumar Balabbigari, PharmD, RPh
 
Antimicrobial Stewardship and Applications to Common Infections
Antimicrobial Stewardship and Applications to Common InfectionsAntimicrobial Stewardship and Applications to Common Infections
Antimicrobial Stewardship and Applications to Common InfectionsPASaskatchewan
 
Osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, a...
Osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, a...Osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, a...
Osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, a...OARSI
 
Breakthrough Therapy Designation- Spring 2014 Reg. Intelligence
Breakthrough Therapy Designation- Spring 2014 Reg. IntelligenceBreakthrough Therapy Designation- Spring 2014 Reg. Intelligence
Breakthrough Therapy Designation- Spring 2014 Reg. IntelligenceCharles Kemmerer
 
Medication_NonAdherenceX
Medication_NonAdherenceXMedication_NonAdherenceX
Medication_NonAdherenceXDavid Donohue
 
InappMedsClinicalToolsSlideShare
InappMedsClinicalToolsSlideShareInappMedsClinicalToolsSlideShare
InappMedsClinicalToolsSlideSharehedavidson
 
Understanding the Accelerated Pathway
Understanding the Accelerated PathwayUnderstanding the Accelerated Pathway
Understanding the Accelerated PathwayOARSI
 
Breakthrough Designation Opportunities Challenges AAPS 2014
Breakthrough Designation Opportunities Challenges AAPS 2014Breakthrough Designation Opportunities Challenges AAPS 2014
Breakthrough Designation Opportunities Challenges AAPS 2014Ajaz Hussain
 
Burry et al-2012-pediatric_blood_&_cancer
Burry et al-2012-pediatric_blood_&_cancerBurry et al-2012-pediatric_blood_&_cancer
Burry et al-2012-pediatric_blood_&_cancerisabelerazochaves
 
Effect of Behavioral Intervention on Reducing Symptom Severity during First C...
Effect of Behavioral Intervention on Reducing Symptom Severity during First C...Effect of Behavioral Intervention on Reducing Symptom Severity during First C...
Effect of Behavioral Intervention on Reducing Symptom Severity during First C...iosrjce
 
BioTech Medical Solutions - Pain RD short 8.5x11
BioTech Medical Solutions - Pain RD short 8.5x11BioTech Medical Solutions - Pain RD short 8.5x11
BioTech Medical Solutions - Pain RD short 8.5x11William Tillman
 
Opioid Analgesia Use After Ambulatory Surgery: Mismatch Between Quantities Pr...
Opioid Analgesia Use After Ambulatory Surgery: Mismatch Between Quantities Pr...Opioid Analgesia Use After Ambulatory Surgery: Mismatch Between Quantities Pr...
Opioid Analgesia Use After Ambulatory Surgery: Mismatch Between Quantities Pr...BU School of Medicine
 

Tendances (20)

Clinical trails overview
 Clinical trails overview Clinical trails overview
Clinical trails overview
 
Effect of rosuvastatin on rheumatoid arthritis clinical disease activity inde...
Effect of rosuvastatin on rheumatoid arthritis clinical disease activity inde...Effect of rosuvastatin on rheumatoid arthritis clinical disease activity inde...
Effect of rosuvastatin on rheumatoid arthritis clinical disease activity inde...
 
Dia Care-2001-Clark-1079-86 (1)
Dia Care-2001-Clark-1079-86 (1)Dia Care-2001-Clark-1079-86 (1)
Dia Care-2001-Clark-1079-86 (1)
 
Characteristics of efficacy evidence supporting approval of supplemental indi...
Characteristics of efficacy evidence supporting approval of supplemental indi...Characteristics of efficacy evidence supporting approval of supplemental indi...
Characteristics of efficacy evidence supporting approval of supplemental indi...
 
Antimicrobial Stewardship and Applications to Common Infections
Antimicrobial Stewardship and Applications to Common InfectionsAntimicrobial Stewardship and Applications to Common Infections
Antimicrobial Stewardship and Applications to Common Infections
 
Osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, a...
Osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, a...Osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, a...
Osteoarthritis: Structural Endpoints for the Development of Drugs, Devices, a...
 
Breakthrough Therapy Designation- Spring 2014 Reg. Intelligence
Breakthrough Therapy Designation- Spring 2014 Reg. IntelligenceBreakthrough Therapy Designation- Spring 2014 Reg. Intelligence
Breakthrough Therapy Designation- Spring 2014 Reg. Intelligence
 
Medication_NonAdherenceX
Medication_NonAdherenceXMedication_NonAdherenceX
Medication_NonAdherenceX
 
InappMedsClinicalToolsSlideShare
InappMedsClinicalToolsSlideShareInappMedsClinicalToolsSlideShare
InappMedsClinicalToolsSlideShare
 
Understanding the Accelerated Pathway
Understanding the Accelerated PathwayUnderstanding the Accelerated Pathway
Understanding the Accelerated Pathway
 
2019 beerscriteria jags
2019 beerscriteria jags2019 beerscriteria jags
2019 beerscriteria jags
 
Criteria for screening
Criteria for screeningCriteria for screening
Criteria for screening
 
Breakthrough Designation Opportunities Challenges AAPS 2014
Breakthrough Designation Opportunities Challenges AAPS 2014Breakthrough Designation Opportunities Challenges AAPS 2014
Breakthrough Designation Opportunities Challenges AAPS 2014
 
Burry et al-2012-pediatric_blood_&_cancer
Burry et al-2012-pediatric_blood_&_cancerBurry et al-2012-pediatric_blood_&_cancer
Burry et al-2012-pediatric_blood_&_cancer
 
Adverse drug reaction causality assessment
Adverse drug reaction causality assessmentAdverse drug reaction causality assessment
Adverse drug reaction causality assessment
 
mohammed aiyaz
mohammed aiyazmohammed aiyaz
mohammed aiyaz
 
Effect of Behavioral Intervention on Reducing Symptom Severity during First C...
Effect of Behavioral Intervention on Reducing Symptom Severity during First C...Effect of Behavioral Intervention on Reducing Symptom Severity during First C...
Effect of Behavioral Intervention on Reducing Symptom Severity during First C...
 
Beer's list 2015 update
Beer's list 2015 updateBeer's list 2015 update
Beer's list 2015 update
 
BioTech Medical Solutions - Pain RD short 8.5x11
BioTech Medical Solutions - Pain RD short 8.5x11BioTech Medical Solutions - Pain RD short 8.5x11
BioTech Medical Solutions - Pain RD short 8.5x11
 
Opioid Analgesia Use After Ambulatory Surgery: Mismatch Between Quantities Pr...
Opioid Analgesia Use After Ambulatory Surgery: Mismatch Between Quantities Pr...Opioid Analgesia Use After Ambulatory Surgery: Mismatch Between Quantities Pr...
Opioid Analgesia Use After Ambulatory Surgery: Mismatch Between Quantities Pr...
 

Similaire à PMC Measure Review RA v8FINAL Website

Predicting Patient Adherence: Why and How
Predicting Patient Adherence: Why and HowPredicting Patient Adherence: Why and How
Predicting Patient Adherence: Why and HowCognizant
 
Surrogate Endpoints: Are drug review processes flexible enough to expedite pa...
Surrogate Endpoints: Are drug review processes flexible enough to expedite pa...Surrogate Endpoints: Are drug review processes flexible enough to expedite pa...
Surrogate Endpoints: Are drug review processes flexible enough to expedite pa...CanCertainty
 
Hbp Stategy Hypertension Management Initiative Feb07
Hbp Stategy Hypertension Management Initiative Feb07Hbp Stategy Hypertension Management Initiative Feb07
Hbp Stategy Hypertension Management Initiative Feb07primary
 
How to Define Effective and Efficient Real World Trials
How to Define Effective and Efficient Real World TrialsHow to Define Effective and Efficient Real World Trials
How to Define Effective and Efficient Real World TrialsTodd Berner MD
 
How to design effective and efficient real world trials TB Evidence 2014 10.2...
How to design effective and efficient real world trials TB Evidence 2014 10.2...How to design effective and efficient real world trials TB Evidence 2014 10.2...
How to design effective and efficient real world trials TB Evidence 2014 10.2...Todd Berner MD
 
Measuring & Monitoring Clinical Quality Measures Using Practice Fusion
Measuring & Monitoring Clinical Quality Measures Using Practice FusionMeasuring & Monitoring Clinical Quality Measures Using Practice Fusion
Measuring & Monitoring Clinical Quality Measures Using Practice FusionPractice Fusion
 
The Design of Accountable Care Organizations
The Design of Accountable Care OrganizationsThe Design of Accountable Care Organizations
The Design of Accountable Care OrganizationsCJ Fulton
 
Electronic Medical Records: From Clinical Decision Support to Precision Medicine
Electronic Medical Records: From Clinical Decision Support to Precision MedicineElectronic Medical Records: From Clinical Decision Support to Precision Medicine
Electronic Medical Records: From Clinical Decision Support to Precision MedicineKent State University
 
Podium Presentation Midwest Social and Administrative Conference,Chicago,2008
Podium Presentation Midwest Social and Administrative Conference,Chicago,2008Podium Presentation Midwest Social and Administrative Conference,Chicago,2008
Podium Presentation Midwest Social and Administrative Conference,Chicago,2008aramasa3
 
New Clinical Quality Measures and PQRS EHR Reporting
New Clinical Quality Measures and PQRS EHR ReportingNew Clinical Quality Measures and PQRS EHR Reporting
New Clinical Quality Measures and PQRS EHR ReportingPractice Fusion
 
AJMC-02-15-Pande-e80
AJMC-02-15-Pande-e80AJMC-02-15-Pande-e80
AJMC-02-15-Pande-e80Julie Donahue
 
BUSINESS83www.AHDBonline.com l American Health & Drug Ben.docx
BUSINESS83www.AHDBonline.com  l American Health & Drug Ben.docxBUSINESS83www.AHDBonline.com  l American Health & Drug Ben.docx
BUSINESS83www.AHDBonline.com l American Health & Drug Ben.docxjasoninnes20
 
Ebm talk-general-mar99-ppt95
Ebm talk-general-mar99-ppt95Ebm talk-general-mar99-ppt95
Ebm talk-general-mar99-ppt95rubenroa
 
Applying the Surviving Sepsis Campaign Guidelines to Clinical Practice
Applying the Surviving Sepsis Campaign Guidelines to Clinical PracticeApplying the Surviving Sepsis Campaign Guidelines to Clinical Practice
Applying the Surviving Sepsis Campaign Guidelines to Clinical PracticeInternational Fluid Academy
 
Prescription Audit PPT.pptx
Prescription Audit PPT.pptxPrescription Audit PPT.pptx
Prescription Audit PPT.pptxkoushikMazumder6
 
Measurement and Modeling Issues with Adherence to Pharmacotherapy
Measurement and Modeling Issues with Adherence to PharmacotherapyMeasurement and Modeling Issues with Adherence to Pharmacotherapy
Measurement and Modeling Issues with Adherence to PharmacotherapyM. Christopher Roebuck
 

Similaire à PMC Measure Review RA v8FINAL Website (20)

presentation.pptx
presentation.pptxpresentation.pptx
presentation.pptx
 
2015 Vivette Escueta enbrel pharmacoepidemiological study protocol - AAPS p...
2015   Vivette Escueta enbrel pharmacoepidemiological study protocol - AAPS p...2015   Vivette Escueta enbrel pharmacoepidemiological study protocol - AAPS p...
2015 Vivette Escueta enbrel pharmacoepidemiological study protocol - AAPS p...
 
Predicting Patient Adherence: Why and How
Predicting Patient Adherence: Why and HowPredicting Patient Adherence: Why and How
Predicting Patient Adherence: Why and How
 
Surrogate Endpoints: Are drug review processes flexible enough to expedite pa...
Surrogate Endpoints: Are drug review processes flexible enough to expedite pa...Surrogate Endpoints: Are drug review processes flexible enough to expedite pa...
Surrogate Endpoints: Are drug review processes flexible enough to expedite pa...
 
Hbp Stategy Hypertension Management Initiative Feb07
Hbp Stategy Hypertension Management Initiative Feb07Hbp Stategy Hypertension Management Initiative Feb07
Hbp Stategy Hypertension Management Initiative Feb07
 
How to Define Effective and Efficient Real World Trials
How to Define Effective and Efficient Real World TrialsHow to Define Effective and Efficient Real World Trials
How to Define Effective and Efficient Real World Trials
 
How to design effective and efficient real world trials TB Evidence 2014 10.2...
How to design effective and efficient real world trials TB Evidence 2014 10.2...How to design effective and efficient real world trials TB Evidence 2014 10.2...
How to design effective and efficient real world trials TB Evidence 2014 10.2...
 
Measuring & Monitoring Clinical Quality Measures Using Practice Fusion
Measuring & Monitoring Clinical Quality Measures Using Practice FusionMeasuring & Monitoring Clinical Quality Measures Using Practice Fusion
Measuring & Monitoring Clinical Quality Measures Using Practice Fusion
 
The Design of Accountable Care Organizations
The Design of Accountable Care OrganizationsThe Design of Accountable Care Organizations
The Design of Accountable Care Organizations
 
Electronic Medical Records: From Clinical Decision Support to Precision Medicine
Electronic Medical Records: From Clinical Decision Support to Precision MedicineElectronic Medical Records: From Clinical Decision Support to Precision Medicine
Electronic Medical Records: From Clinical Decision Support to Precision Medicine
 
Hepatitis C Drugs - Evidence to Demonstrate Effectiveness & Value
Hepatitis C Drugs - Evidence to Demonstrate Effectiveness & ValueHepatitis C Drugs - Evidence to Demonstrate Effectiveness & Value
Hepatitis C Drugs - Evidence to Demonstrate Effectiveness & Value
 
Podium Presentation Midwest Social and Administrative Conference,Chicago,2008
Podium Presentation Midwest Social and Administrative Conference,Chicago,2008Podium Presentation Midwest Social and Administrative Conference,Chicago,2008
Podium Presentation Midwest Social and Administrative Conference,Chicago,2008
 
New Clinical Quality Measures and PQRS EHR Reporting
New Clinical Quality Measures and PQRS EHR ReportingNew Clinical Quality Measures and PQRS EHR Reporting
New Clinical Quality Measures and PQRS EHR Reporting
 
RA Nice G
RA  Nice GRA  Nice G
RA Nice G
 
AJMC-02-15-Pande-e80
AJMC-02-15-Pande-e80AJMC-02-15-Pande-e80
AJMC-02-15-Pande-e80
 
BUSINESS83www.AHDBonline.com l American Health & Drug Ben.docx
BUSINESS83www.AHDBonline.com  l American Health & Drug Ben.docxBUSINESS83www.AHDBonline.com  l American Health & Drug Ben.docx
BUSINESS83www.AHDBonline.com l American Health & Drug Ben.docx
 
Ebm talk-general-mar99-ppt95
Ebm talk-general-mar99-ppt95Ebm talk-general-mar99-ppt95
Ebm talk-general-mar99-ppt95
 
Applying the Surviving Sepsis Campaign Guidelines to Clinical Practice
Applying the Surviving Sepsis Campaign Guidelines to Clinical PracticeApplying the Surviving Sepsis Campaign Guidelines to Clinical Practice
Applying the Surviving Sepsis Campaign Guidelines to Clinical Practice
 
Prescription Audit PPT.pptx
Prescription Audit PPT.pptxPrescription Audit PPT.pptx
Prescription Audit PPT.pptx
 
Measurement and Modeling Issues with Adherence to Pharmacotherapy
Measurement and Modeling Issues with Adherence to PharmacotherapyMeasurement and Modeling Issues with Adherence to Pharmacotherapy
Measurement and Modeling Issues with Adherence to Pharmacotherapy
 

PMC Measure Review RA v8FINAL Website

  • 1. 1 Performance Measurement Diagnosis and Treatment of Rheumatoid Arthritis: Review of the Performance Measures by the Performance Measurement Committee of the American College of Physicians Writing Committee Amir Qaseem, MD, David Baker, MD, Robert Gluckman, MD, Catherine MacLean, MD, PhD, Sarah West, MSN, RN ACP Performance Measurement Committee Members* David W. Baker, MD, MPH (Chair); J. Thomas Cross, MD, MPH; Andrew Dunn, MD, MPH; Mary Ann Forciea, MD; Robert A. Gluckman, MD; Robert H. Hopkins, MD; Eve Kerr, MD; Kesavan Kutty, MD; Ana Maria López, MD, MPH; Catherine MacLean, MD, PhD; Stephen D. Persell, MD, MPH; and Terrence Shaneyfelt, MD Corresponding author: A. Qaseem 190 N. Independence Mall West Philadelphia, PA 19106 Email aqaseem@acponline.org * Individuals who served on the Performance Measurement Committee from initiation of the project until its approval
  • 2. 2 Introduction Rheumatoid arthritis (RA) is systemic polyarthritis, which disproportionately affects women. It affects an estimated 1.5 million Americans over the age of 18 and accounts for as much as $8.6 billion in medical costs and an additional $2.7 billion in excess indirect and non-medical costs annually (both in 2000 dollars) (1-2). Over the last decades, advances in therapies and therapeutic approach have dramatically improved health outcomes with the achievement of minimal disease activity or remission in 10-30% of treated patients (3-4). Although the availability of such effective therapies and the opportunity to withhold or discontinue therapy with minimal disease activity or remission warrant periodic assessment of disease activity, such assessment is not routine (54% in 2012) and represents an opportunity for improvement in care (5). The ACP Performance Measurement Committee (PMC) reviewed performance measures related to the management of rheumatoid arthritis (RA) to assess whether the measures are evidence-based, methodologically sound, and clinically meaningful. Methods We performed a search to identify relevant performance measures from the National Quality Forum (NQF), the American Medical Association-Physician Consortium for Performance Improvement (AMA-PCPI), and National Quality Measures Clearinghouse (NQMC) websites. The inclusion criteria were performance measures currently used in the Centers for Medicare and Medicaid Services (CMS) Physician Quality Reporting System (PQRS) or currently used in the CMS Electronic Record Incentive program. The PMC identified and reviewed 7 performance measures. Conclusion
  • 3. 3 Recommendation ACP supports NQF 0054 for physicians managing Rheumatoid Arthritis (RA), with modifications: “Disease-Modifying Anti-Rheumatic Drug (DMARD) Therapy for Rheumatoid Arthritis.” Rationale The current evidence supports the benefit of DMARD therapy in reducing the symptoms of RA and decelerating the progression of joint damage (6). Furthermore, a wide range of DMARD prescribing across health plans in the 2013 measurement year suggests a performance gap (7). However, given the availability of highly effective therapies and a more aggressive therapeutic approach than in previous decades, remission or minimal disease activity is now achievable for a significant numbers of patients [10-30% (3-4)]. Therefore, DMARD therapy may be appropriately withheld for a period of time (a “drug holiday”) or discontinued for such patients. Hence, minimal disease activity or clinical remission should be included in the denominator exclusions. This is a physician level measure and should only be applicable to physicians who are managing and providing medical therapy for RA. Most often this will apply to rheumatologists, but primary care physicians may also manage RA. Measure Specifications NQF 0054: Disease-Modifying Anti-Rheumatic Drug Therapy for Rheumatoid Arthritis Status: NQF Endorsed, UPDATED November 10, 2014 (2015 PQRS #108) Measure Steward: National Committee for Quality Assurance Description: The percentage of patients 18 years and older by the end of the measurement period, diagnosed with rheumatoid arthritis and who had at least one ambulatory prescription for a disease-modifying anti-rheumatic drug (DMARD) Numerator Statement: Patients diagnosed with rheumatoid arthritis who were dispensed at least one ambulatory prescription for a disease-modifying anti-rheumatic drug (DMARD) during the measurement year. Denominator Statement: All patients, ages 18 years and older by December 31 of the measurement year who had two of the following with different dates of service on or between January 1 and November 30 of the measurement year: - Outpatient visit, with any diagnosis of rheumatoid arthritis - Non-acute inpatient discharge, with any diagnosis of rheumatoid arthritis Visit type need not be the same for the two visits Exclusions: Exclude patients who have a diagnosis of HIV. Look for evidence of HIV diagnosis as far back as possible in the patient’s history through the end of the measurement year. Exclude patients who have a diagnosis of pregnancy during the measurement year. Type of Measure: Process Level of Analysis: Health Plan, Integrated Delivery System
  • 4. 4 Care Setting: Ambulatory Care: Clinician Office/Clinic Data Source: Administrative claims, Electronic Clinical Data, Electronic Clinical Data: Pharmacy Recommendation ACP supports NQF 2522 for physicians managing Rheumatoid Arthritis (RA): “Rheumatoid Arthritis: Tuberculosis Screening.” Rationale Biologic Disease-Modifying Anti-Rheumatic (DMARD) therapy can reactivate latent tuberculosis, leading to significant morbidity and even mortality (5, 8). Administrative data suggests that over 1 in 4 individuals with RA receive biologic DMARDs (8). Over 1.3 million individuals in the United States have RA (9-10); therefore this measure is expected to impact over 300,000 Americans with RA (9-10). This is a physician level measure and should only be applicable to physicians who are managing and providing medical therapy for RA. Most often this will apply to rheumatologists, but primary care physicians may also manage RA. Measure Specifications NQF 2522: Rheumatoid Arthritis: Tuberculosis Screening Status: NQF Endorsed, Updated November 10, 2014 (2015 PQRS #176) Measure Steward: American College of Rheumatology Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid arthritis who have documentation of a tuberculosis (TB) screening performed within 12 months prior to receiving a first course of therapy using a biologic disease-modifying anti-rheumatic drug (DMARD) Numerator Statement: Any record of TB testing documented or performed (PPD, IFN-gamma release assays, or other appropriate method) in the medical record in the 12 months preceding the biologic DMARD prescription Denominator Statement: Patients 18 years and older with a diagnosis of rheumatoid arthritis who are seen for at least one face-to-face encounter for RA who are newly started on biologic therapy during the measurement period Exclusions: None Type of Measure: Process Level of Analysis: Clinician: Individual Care Setting: Ambulatory Care: Clinician Office/Clinic Data Source: Electronic Clinical Data: Electronic Health Record
  • 5. 5 Recommendation ACP supports 2523 for physicians managing Rheumatoid Arthritis (RA): “Rheumatoid Arthritis: Assessment of Disease Activity.” Rationale Using validated disease activity assessments is a standard component of guideline-based care and has been shown to improve patient outcomes including; functional status, health-related quality of life, and radiographic disease progression (11). This is a physician level measure and should only be applicable to physicians who are managing and providing medical therapy for RA. Most often this will apply to rheumatologists, but primary care physicians may also manage RA. Measure Specifications NQF 2523: Rheumatoid Arthritis: Assessment of Disease Activity Status: NQF Endorsed, Updated November 10, 2014 (2015 PQRS #177) Measure Steward: American College of Rheumatology Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid arthritis and >=50% of total number of outpatient RA encounters in the measurement year with assessment of disease activity using a standardized measure Numerator Statement: Number of patients with >=50% of total number of outpatient RA encounters in the measurement year with assessment of disease activity using a standardized measure Denominator Statement: Patients 18 years and older with a diagnosis of rheumatoid arthritis seen for two or more face-to-face encounters for RA with the same clinician during the measurement period Exclusions: None Type of Measure: Process Level of Analysis: Clinician: Individual Care Setting: Ambulatory Care: Clinician Office/Clinic Data Source: Electronic Clinical Data: Electronic Health Record
  • 6. 6 Recommendation ACP supports NQF 2524 for physicians managing Rheumatoid Arthritis (RA): “Rheumatoid Arthritis: Functional Status Assessment.” Rationale ACP supports this measure because therapeutic treatment goals include preservation of function and quality of life (13-14). Findings of a joint examination alone may not adequately reflect disease activity and structural damage; therefore, periodic measurements of functional status should be performed (12). Additionally, it is important to determine whether a decline in function is the result of inflammation, mechanical damage, or both because treatment approaches will differ accordingly (12). This is a physician level measure and should only be applicable to physicians who are managing and providing medical therapy for RA. Most often this will apply to rheumatologists, but primary care physicians may also manage RA. Measure Specifications NQF 2524: Rheumatoid Arthritis: Functional Status Assessment Status: NQF Endorsed, Updated November 10, 2014 (2015 PQRS #178) Measure Steward: American College of Rheumatology Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid arthritis for whom a functional status assessment was performed at least once during the measurement period Numerator Statement: Number of patients with functional status assessment documented once during the measurement period. Functional status can be assessed using one of a number of valid and reliable instruments available from the medical literature Denominator Statement: Patients age 18 and older with a diagnosis of rheumatoid arthritis seen for two or more face-to-face encounters for RA with the same clinician during the measurement period Exclusions: None Type of Measure: Process Level of Analysis: Clinician: Individual Care Setting: Ambulatory Care: Clinician Office/Clinic Data Source: Electronic Clinical Data: Electronic Health Record
  • 7. 7 Recommendation ACP supports NQF 2525 for physicians managing RA, with modifications: “Rheumatoid Arthritis (RA): Disease Modifying Anti-Rheumatic Drug (DMARD) Therapy.” Rationale The current evidence supports the benefit of DMARD therapy in reducing the symptoms of RA and decelerating the progression of joint damage (6). Furthermore, a wide range of DMARD prescribing across health plans in the 2013 measurement year suggests a performance gap (9). However, given the availability of highly effective therapies and a more aggressive therapeutic approach than in previous decades, remission or minimal disease activity is now achievable for a significant numbers of patients [10-30% (3-4]. Therefore, DMARD therapy may be appropriately withheld for a period of time (a “drug holiday”) or discontinued for such patients and minimal disease activity or clinical remission should be included in the denominator exclusions. This is a physician level measure and should only be applicable to physicians who are managing and providing medical therapy for RA. Most often this will apply to rheumatologists, but primary care physicians may also manage RA. Measure Specifications NQF 2525: Rheumatoid Arthritis: Disease Modifying Anti-Rheumatic Drug (DMARD) Therapy Status: NQF Endorsed, Updated November 10, 2014 Measure Steward: American College of Rheumatology Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid arthritis who are newly prescribed disease modifying anti-rheumatic drug (DMARD) therapy within 12 months Numerator Statement: Patient received a DMARD Denominator Statement: Patient age 18 years and older with a diagnosis of rheumatoid arthritis seen for two or more face-to-face encounters for RA with the same clinician during the measurement period Exclusions: Patients with a diagnosis of HIV; patients who are pregnant; or patients with inactive Rheumatoid Arthritis Type of Measure: Process Level of Analysis: Clinician: Individual Care Setting: Ambulatory Care: Clinician Office/Clinic Data Source: Electronic Clinical Data: Electronic Health Record
  • 8. 8 Recommendation ACP does not support PQRS 179 for physicians managing Rheumatoid Arthritis (RA): “Assessment and Classification of Disease Prognosis.” Rationale ACP does not support this measure because there is no evidence supporting annual frequency or describing appropriate frequency for assessment or classification of disease prognosis. Additionally, it seems unnecessary to reassess prognosis annually if a poor prognosis has been established based on factors that will not change such as high titer anti-citric citrullinated peptide (anti-CCP) antibodies, rheumatoid factor (RF) or radiographic erosions. Measure Specifications PQRS 179: Assessment and Classification of Disease Prognosis Status: Not NQF Endorsed Measure Steward: American Medical Association - Physician Consortium for Performance Improvement Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid arthritis (RA) who have an assessment and classification of disease prognosis at least once within 12 months Numerator Statement: Patients with at least one documented assessment and classification (good/poor) of disease prognosis* utilizing clinical markers of poor prognosis** within 12 months *Poor prognosis: RA patients with features of poor prognosis have active disease with high tender and swollen joint counts, often have evidence of radiographic erosions, elevated levels of rheumatoid factor (RF) and or anti-cyclic citrullinated peptide (anti-CCP) antibodies, and an elevated erythrocyte sedimentation rate, and an elevated C-reactive protein level. ** Prognostic classification should be based upon at a minimum the following markers of poor prognosis: functional limitation (e.g., HAQ Disability Index), extra-articular disease (e.g. vasculitis, Sjorgen’s syndrome, RA lung disease, rheumatoid nodules), RF positivity, positive anti-CCP antibodies (both characterized dichotomously, per CEP recommendation), and/or bony erosions by radiography Denominator Statement: Patients 18 years and older with a diagnosis of Rheumatoid Arthritis (RA) Exclusions: None
  • 9. 9 Type of Measure: Process Care Setting: Ambulatory Care Data Source: Administrative claims; Medical record; Electronic medical record; Administrative claims supplemented by medical records; Registries; Prospective data collection flow-sheet Recommendation ACP does not support PQRS 180: “Glucocorticoid Management.” Rationale Although we recognize the importance of managing the lowest effective dose of glucocorticoids and using alternative therapies when possible, both the numerator and the denominator are poorly specified. A cleaner measure would specify “patients with rheumatoid arthritis (RA) who are on glucocorticoids” in the denominator statement. Additionally, the current American College of Rheumatology clinical guidelines demonstrate the importance of assessing glucocorticoid use, but only in patients who have specifically been prescribed glucocorticoid therapy (15). Measure Specifications PQRS 180: Glucocorticoid Management Status: Not NQF Endorsed Measure Steward: American Medical Association - Physician Consortium for Performance Improvement Description: Percentage of patients 18 years and older with a diagnosis of rheumatoid arthritis (RA) who have been assessed for glucocorticoid use and, for those on prolonged doses of prednisone > 10 mg daily (or equivalent) with improvement or no change in disease activity, documentation of glucocorticoid management plan within 12 months Numerator Statement: Patients who have been assessed for glucocorticoid use at least once within 12 months, and for those on prolonged doses* of prednisone > 10 mg qD (or equivalent**) with improvement or no change in disease activity, documentation of a glucocorticoid management plan*** *Prolonged doses are doses >6 months in duration **Prednisone equivalents can be determined using the following: 1 mg of prednisone = 1 mg of prednisolone; 5 mg of cortisone; 4 mg of hydrocortisone; 0.8 mg of triamcinolone; 0.8 mg of methylprednisolone; 0.15 mg of dexamethasone; 0.15 mg of betamethasone. ***Glucocorticoid management plan: documentation of attempt to taper steroids OR documentation of a new prescription for a non-glucocorticoid DMARD OR
  • 10. 10 increase in dose of non-glucocorticoid DMARD dose for persistent RA disease activity at current or reduced dose. Denominator Statement: Patients 18 years and older with a diagnosis of rheumatoid arthritis (RA) Exclusions: Documentation of medical reason(s) for not documenting glucocorticoid dose (i.e., glucocorticoid prescription is for a medical condition other than RA) Type of Measure: Process Care Setting: Ambulatory Care Data Source: Administrative claims; Medical record; Electronic medical record; Administrative claims supplemented by medical record; Registries; Prospective data collection flow-sheet Gaps in Performance Measurement — Opportunities to Promote High-Value Care There is a need for performance measures that focus on the individualized care of patients with RA including the appropriate discontinuation of DMARDs in patients who have achieved remission or minimal disease activity.
  • 11. 11 References 1. Gabriel SE, Crowson CS, Campion ME, O'Fallon WM. Direct medical costs unique to people with arthritis. JRheumatol. 1997;24(4):719-25. 2. Gabriel SE, Crowson CS, Campion ME, O'Fallon WM. Indirect and nonmedical costs among people with rheumatoid arthritis and osteoarthritis compared with nonarthritic controls. JRheumatol. 1997;24(1):43-8. 3. De Punder YM, Fransen J, Kievit W, Houtman PM, Visser H, van de Laar MA, van Riel PL. The prevalence of clinical remission in RA patients treated with anti-TNF: results from the Dutch Rheumatoid Arthritis Monitoring (DREAM) registry. Rheumatology. 2012;51(9):1610-7. 4. Jayakumar K, Norton S, Dixey J, James D, Gough A, Williams P, Prouse P, Young A; Early Rheumatoid Arthritis Study (ERAS). Sustained clinical remission in rheumatoid arthritis: prevalence and prognostic factors in an inception cohort of patients treated with conventional DMARDS. Rheumatology. 2012;51(1):169-75. 5. Grossman JM, Gordon R, Ranganath VK et al. American College of Rheumatology 2010 Recommendations for the prevention and treatment of glucocorticoid-induced osteoporosis. Arthritis Care & Research. 2010;62(11):1515-1526. 6. Smolen JS et al. EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2013 update. Ann Rheum Dis. Mar 2014;73(3):492–509. 7. National Committee for Quality Assurance (NCQA). HEDIS 2014: Healthcare Effectiveness Data and Information Set. Vol. 1, narrative. Washington (DC): National Committee for Quality Assurance (NCQA); 2013. various p. 8. Zhang J, Xie F, Delzell E et al. Trends in the use of biologic agents among rheumatoid patients enrolled in the US Medicare Program. Arthritis Care & Research. 2013;65(11):1743-1751. 9. National Quality Forum. Prioritization of high-impact Medicare conditions and measure gaps. Measure Prioritization Advisory Committee Report. 2010
  • 12. 12 10. Yazdany, Jinoos, Kazi, Salahuddin, Francisco, Melissa, Myslinski, Rachel. “Uptake of the American College of Rheumatology’s Rheumatology Clinical Registry (RCR): Quality Measure Summary Data”. Annual Scientific Meeting. American College of Rheumatology. Reed Convention Center, Washington, DC. 27 October 2013. Conference Presentation. 11. Scott DL, Symmons DP, Coulton, BL, Popert, AJ. Long-term outcome of treating rheumatoid arthritis: Results after 20 Years. The Lancet. 1987;1(8542):1108-1111. 12. American College of Rheumatology Subcommittee on Rheumatoid Arthritis Guidelines. Guidelines for the management of rheumatoid arthritis: 2002 Update. Arthritis Rheum. 2002 Feb;46(2):328-46. 13. Helmick CG, Felson DT, Lawrence RC et al. Estimates of the prevalence of arthritis and other rheumatic conditions in the US. Part 1. Arthritis & Rheumatology. 2008;58(1):15- 25. 14. Harris ED. Clinical features of rheumatoid arthritis. In: Ruddy S, Harris ED, Sledge CB, Kelley WN, eds. Kelley’s Textbook of rheumatology. 7th ed. Philadelphia: WB Saunders, 2005:1043–78. 15. American College of Rheumatology Subcommittee on Rheumatoid Arthritis Guidelines. Guidelines for the management of rheumatoid arthritis: 2002 update. Arthritis Rheum. 2002;46:328–46.
  • 13. 13 Financial Statement: Financial support for the Performance Measurement Committee comes exclusively from the ACP operating budget. Conflicts of Interest: Any financial and nonfinancial conflicts of interest of the group members were declared, discussed, and resolved. A record of conflicts of interest is kept for each PMC meeting and conference call and can be viewed at: http://www.acponline.org/running_practice/performance_measurement/pmc/conflicts_pmc.h tm APPROVED BY THE ACP BOARD OF REGENTS ON: April 27, 2015 Members of the PMC: Individuals who served on the Performance Measurement Committee from initiation of the project until its approval: David W. Baker, MD, MPH J. Thomas Cross, Jr., MD, MPH Andrew Dunn, MD, MPH Mary Ann Forciea, MD Robert A. Gluckman, MD Robert H. Hopkins, MD Kesavan Kutty, MD Eve Askanas Kerr, MD, MPH Ana María López, MD, MPH Catherine MacLean, MD, PhD Stephen D. Persell, MD, MPH Terrence Shaneyfelt, MD, MPH Requests and inquiries: Amir Qaseem, MD, PhD, MHA, FACP, American College of Physicians, 190. N Independence Mall West, Philadelphia, PA 19106: email, aqaseem@acponline.org
  • 14. 14