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Abstract Number: 1913

Expectations RA Patients Have For Their Treatment – A Comparison Of Clinical Results For Biologic and Disease-Modifying Anti-Rheumatic Drug Treated Patients Using Multiple Medical Cohorts

Tsukasa Matsubara1,2, Hiroaki Matsuno2, Tomomaro Izumihara2, Yuichi Takahashi2, Akira Sagawa2, Motohiro Oribe2, Eisuke Shono2, Kensuke Kume2, Masanori Adachi2, Yuichi Nishioka2, Nobumasa Miyake2, Keisuke Hashimoto2, Toshikaki Miyamoto2, Shigeto Kiyokawa2, Tomohiko Yoshida2, Syoichi Kondo2, Yoshiki Shiohira2, Takanori Azuma2, Yukio Sato2, Masaaki Yoshida2, Kenji Mannami2, Akihiko Nakamura2, Yasuhiko Hirabarashi2, Keiko Funahashi3 and James E. Middleton4, 1Department of Orthopedics, Matsubara Mayflower Hospital, Kato, Japan, 2Japanese Clinician's Biologic Research Group, Kobe, Japan, 3Department of Clinical Research, Matsubara Mayflower Hospital, Kato, Japan, 4Research Institute of Joint Diseases, Kobe, Japan

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Biologic drugs, DMARDs, Patient questionnaires, quality of care and quality of life

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Session Information

Title: Health Services Research, Quality Measures and Quality of Care - Innovations in Health Care Delivery

Session Type: Abstract Submissions (ACR)

Background/Purpose: Treat to Target (T2T) primary principal – “The treatment of rheumatoid arthritis must be based on a shared decision between patient and rheumatologist”. Japan uses T2T, but its impact on patients is not yet clear. To better understand T2T implementation, a large scale survey was conducted using a multi-cohort study.

Methods: A survey was given to 4489 RA outpatients in multiple facilities in Japan; contents included; age, gender, medical history, and comments on; 1) things to know before administration, 2) expectations of medication, 3) disappointment with medication, 4) anxiety switching medication 5) biologics experience, 6) goals for treatment, 7) satisfaction level, 8) questions and expectation of doctors, 9) treatment fees, 10) impression of biologics, 11) injections, 12) desires for the future. For further analysis the total results from respondents were divided into 2 groups; Biologics (BG), 1728 patients, and DMARDs Group (DG), 2264 patients.

Results: Eighty-two point five percent of the respondents were female and 27% had disease duration of 10-20 years. Usage; DG 80% BG, 35%. For ‘expectations of medication’, 35% responded with ‘assured improvement of the condition’ while 22% responded ‘reduced destruction or deformation of joints’; no difference between groups. In BG more patients (22%) hoped for long-lasting efficacy than in DG (14%). ‘Experience of disappointment’ was 22% in total, but the rate of BG was twice that of DG; reason for disappointment for BG was lack of efficacy, however, for DG it was adverse events. The reason for ‘anxiety when switching’ was mainly ‘adverse events’ and ‘efficacy’ in both groups, but ‘diminishing efficacy’ showed a higher rate in BG, related with the reason for disappointment. In both groups the ‘goals for treatment’ was mostly ‘the improvement of QOL’ and ‘reduced destruction/deformation of joints’, but ‘reduced destruction/deformation of joints’ for BG were 1.5 times that of DG. BG wanted more information about future treatment. In DG, 70% were willing to spend up to ¥10,000 a month, as opposed to 30% in BG, suggesting BG understood the cost of biologics. For injections, many in both groups, responded ‘troublesome’ or ‘frightening’, but the image was higher for self-injection, especially in DG, but, half the respondents in BG chose ‘convenient’.

Conclusion: Expectations for medication in terms of assured improvement of conditions and prevention for joint destruction, were confirmed with results of a single-institution study 2 years ago. But, rate of ‘long-lasting efficacy of drugs’ was higher in BG this time. Data indicated BG showed these tendencies after secondary failure, which was also suggested in both studies. The patients in BG, due to knowledge of prevention of joint destruction, have higher treatment goals than DG. The comparison between 2 groups indicated once patients experience high efficacy, they can tolerate self-injection and higher fees. We should be aware that what Japanese RA patients are expecting is assured improvement of condition including prevention from joint destruction and long-lasting efficacy. Our study indicates steady implementation of T2T while patients are receiving good education, clearly understanding 3 standards for remission of RA.


Disclosure:

T. Matsubara,

Bristol-Myers K.K., Chugai Pharmaceutical Co., Ltd., Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma Corporation, Santen Pharmaceutical Co., Ltd.,

5;

H. Matsuno,

Bristol-Myers K.K., Chugai Pharmaceutical Co., Ltd., Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma Corporation, Santen Pharmaceutical Co., Ltd.,

5;

T. Izumihara,
None;

Y. Takahashi,
None;

A. Sagawa,
None;

M. Oribe,
None;

E. Shono,
None;

K. Kume,
None;

M. Adachi,
None;

Y. Nishioka,
None;

N. Miyake,
None;

K. Hashimoto,
None;

T. Miyamoto,
None;

S. Kiyokawa,
None;

T. Yoshida,
None;

S. Kondo,
None;

Y. Shiohira,
None;

T. Azuma,
None;

Y. Sato,
None;

M. Yoshida,
None;

K. Mannami,
None;

A. Nakamura,
None;

Y. Hirabarashi,
None;

K. Funahashi,

Bristol-Myers K.K., Chugai Pharmaceutical Co., Ltd., Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma Corporation, Santen Pharmaceutical Co., Ltd.,

5;

J. E. Middleton,
None.

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All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

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