Research Project Poster MCrowe FINAL

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  • 7/29/2019 Research Project Poster MCrowe FINAL

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    Objective

    To determine the correlation between medication

    adherence to biologic therapy and patient-reported

    measures of disease activity, after the initiation of

    therapy in patients with RA, receiving care from this

    community-based specialty pharmacy.

    The Correlation Between Medication Adherence and Disease Activity in Adult Patients

    with Rheumatoid Arthritis Receiving Care at a Specialty PharmacyMichael W. Crowe1, Ho-Cheong S. Lee2, Heidi M. Michels1, Chris Y. Baek1, Mark S. Chaffee1

    1Diplomat Specialty Pharmacy, Grand Rapids, MI; 2Ferris State University, Grand Rapids, MI

    PatientsBackground

    Methods

    In patients with rheumatoid arthritis (RA),

    non-adherence to and non-persistence with disease

    modifying antirheumatic drugs (DMARDs) is prevalent

    (20-70%).1

    Low adherence results in poor health outcomes, improper

    assessment of efficacy, and increased healthcare costs. It

    also contributes to treatment failure, delayed disease

    recovery, accelerated disease progression, and the need

    for more aggressive treatment. Treatment failure rates

    are lower in patients with higher adherence.2-5

    Improved adherence has been demonstrated in patients

    with RA receiving:

    Satisfactory contact with healthcare professionals6

    Disease and treatment education6

    Pharmacist interventions, such as telephone calls, to

    discuss adherence or medication-related problems7

    Diplomat Specialty Pharmacy has previously established a

    drug therapy management program (DTM) for patients

    with RA.

    Eligibility Criteria

    1. Patient > 18 years of age diagnosed with RA

    2. Receive FDA-approved doses of either adalimumab or

    etanercept, for the treatment of RA, for > 12 months

    from this specialty pharmacy

    3. Competent (i.e. responsible for their own healthcare)

    4. No record of receiving previous biologic DMARD therapy

    within 4 weeks of enrollment into the DTM program

    5. Enrolled between June 1, 2008 and February 28, 2010

    6. No biologic-free periods lasting greater than 4 weeks

    7. At least 1 score available for each survey (HAQ-II, NRS)

    Exclusion Summary

    284 patients met eligibility criteria 1 through 5 above.

    87 were excluded for having a drug-free period > 4 weeks.

    107 were excluded for missing outcomes data.

    Patients Eligible for Evaluation

    Indicates patients that switched from adalimumab to

    etanercept (or vice versa), during their enrollment period

    Overall

    (n = 90)

    Adalimumab

    (n = 30)

    Etanercept

    (n = 54)

    Switched

    (n = 6)

    Mean Age

    (range)

    54

    (20-75)

    52

    (51-75)

    56

    (30-73)

    46

    (20-69)

    % Female 70% 60% 72% 100%

    Results

    Discussion Conclusions

    References

    1. Pascual-Ramos V, Contreras-YanezI, Villa AR, et al. Medicationpersistence over 2 yearsof follow-upin acohort of early rheuma

    arthritis patients: associatedfactorsandrelationshipwithdisease activity andwithdisability. Arthritis Res Ther. 2009;11(1):R26

    2. HaynesR, AcklooE, SahotaN, et al. Interventionsfor enhancingmedicationadherence.Cochrane Database Syst Rev 2008,Issue

    Art.No.:CD000011.

    3. Osterberg L, Blaschke T. Adherence tomedication.N Engl J Med. 2005;353:487-97.

    4. GrijalvaC, Chung C, Arbogast P, et al. Assessment of adherence toandpersistence ondisease-modifyingantirheumaticdrugs(D

    patientswithrheumatoidarthritis. MedCare.2007;45(10):S66-76.

    5. Fernandez-NebroA, IrigoyenMV, UrenaI, et al. Effectiveness, predictive response factors, andsafety of anti-tumor necrosisfac

    therapiesinanti-TNF-nave rheumatoidarthritis. J Rheumatol. 2007;34(12):2334.

    6. Viller F, GuilleminF, BrianconS, et al. Compliance todrugtreatment of patientswithrheumatoidarthritis:a3 year longitudina

    Rheumatol. 1999;26:2114-22.

    7. CliffordS, Barber N, Elliot R, et al. Patient-centeredadviceiseffective inimprovingadherence tomedicines. PharmWorldSci. 2

    8. Day D. Use of pharmacy claimsdatabasesto determineratesof medicationadherence.Adv Ther. 2003May-Jun;20(3):164-76.

    9. tenKlooster P, Taal E, vande Laar M.Rasch analysis of the DutchHealthAssessment Questionnaire Disability Indexandthe Hea

    Questionnaire II inpatientswithrheumatoidarthritis. Arthritis andRheum. 2008;59(12):172128.

    10.Wolfe F, MichaudK, PincusT. Development andvalidationof the HealthAssessment Questionnaire II:a revisedversionof the h

    assessment questionnaire.Arthritis andRheum. 2004;50(10):3296305.

    11.FerrazM, QuaresmaM, AquinoL, et al. Reliability of painscales inthe assessment of literate andilliterate patientswithrheum

    J Rheumatol. 1990;17(8):1022-24.

    12.MinnockP, KirwanJ, BresnihanB. Fatigue is areliable,sensitive andunique outcomemeasure inrheumatoidarthritis. Rheuma

    2009;48:1533-36.

    n Mean MPR [range] Mean HAQ-II Score [range] Mean Pain Score [range] Mean Fatigue Score [range]

    90 0.939 [0.687-1] 0.56 [0-2.2] 3.1 [0-10] 3.1 [0-10]

    6-Month Outcomes

    51

    12-Month Outcomes

    58

    Despite the burden of added time for the patient and

    elevated operational costs for the pharmacy, measures of

    disease activity at 6 or 12 months were collected by the

    pharmacy team for nearly half of the patients meeting the

    eligibility criteria.

    107 patients were excluded because either their records

    did not contain recorded outcomes or they were not

    recorded at the correct interval of 6 and 12 months.

    Patients levels of medication adherence met our

    expectations and are likely attributable to the steps built

    into the DTM program.

    Our findings for the correlation between medication

    adherence and HAQ-II scores is consistent with our

    expectation that a higher MPR would correlate with a

    lower HAQ-II score, however a correlation between

    adherence and pain and fatigue was not found.

    Study Limitations

    Single-center study

    Small sample size

    Limited availability of data

    Samples were not identical at 6 and 12 months

    An increase in MPR shows a slight correlation with a

    decrease in HAQ-II score, more so at 6 months than a

    A correlation for pain and fatigue with MPR was not

    demonstrated.

    Inconsistencies in data collection may warrant closer

    monitoring by pharmacy administrative staff, in orde

    achieve the full potential of this DTM program.

    These results provide some insights on the relations

    between RA drug therapy adherence and measures o

    disease activity. This not only offers community

    pharmacies opportunities to improve patient care, b

    also provides valuable data for this pharmacys

    assessment of its current DTM program.

    Drug Therapy Management Program

    Patients receiving biologic therapy from this specialty pharmacy are enrolled into an RA DTM program, which includes

    disease-specific education, training, and monitoring aimed to optimize medication adherence.

    The Modified Health Assessment Questionnaire (HAQ-II) and numerical rating scales (NRS) for pain and fatigue are

    administered at baseline and every six months thereafter.

    Measured Outcomes

    The correlation between the MPR and the patient-reported measures of disease activity are determined.

    Adherence

    Defined as medication possessionratio (MPR) and based onpharmacy refill record

    Calculated using StandardizedTherapy Adherence Research Tool(START,Pfizer)8

    HAQ-II

    10-item questionnaire with higherscores (ranging 0-3) indicatinggreater disability9

    Reliable and validated in assessingthe physical function of patientswith RA10

    NRS for Pain and Fatigue

    11-point (0-10) numerical scaleswith higher scores indicatingworse symptoms

    Each have demonstratedreliability in assessing pain and

    fatigue in patients with RA