TY - JOUR
T1 - Current status of shared decision making for rheumatoid arthritis treatment in Japan
T2 - a web-based survey on physicians and patients
AU - Tsuboi, Hiroto
AU - Kaneko, Yuko
AU - Ikeda, Kei
AU - Aranishi, Toshihiko
AU - Cai, Zhihong
AU - Ishizuka, Tomoko
N1 - Funding Information:
The authors would like to thank all patients and physicians for participating in this study, which helps us understand the current status of SDM in RA clinical practice in Japan. We are also grateful to the members of Social Survey Research Information Co., Ltd.; Tomoyuki Kusaka for the study design; Kohei Mizui for conducting the survey and the statistical analysis; Chie Kikutake for conducting the statistical analysis, supporting the interpretation of study results and drafting; and Sachiko Funabashi for the study design, supporting the interpretation of study results and drafting. Additional writing and editorial assistance were provided by Rebecca Lew, PhD, CMPP, and Jeanne Claypoole of ProScribe–Envision Pharma Group, funded by Eli Lilly Japan K.K.
Funding Information:
Hiroto Tsuboi has received speaking fees and/or honoraria from Eli Lilly Japan K.K. Yuko Kaneko has received grants or speaking fees from AbbVie GK, Astellas Pharma Inc., AYUMI Pharmaceutical Corporation, Bristol Myers Squibb K.K., Chugai Pharmaceutical Co., Ltd., Eisai Co., Ltd., Eli Lilly Japan K.K., Janssen Pharmaceutical K.K., Kissei Pharmaceutical Co., Ltd., Kyowa Kirin Co., Ltd., Novartis Pharma K.K., Pfizer Japan Inc., Sanofi K.K., Takeda Pharmaceutical Company Limited, Mitsubishi Tanabe Pharma Corporation, and UCB Japan Co. Ltd. Kei Ikeda has received speaking fee from Eli Lilly Japan K.K., AbbVie GK, Novartis Pharma K.K., Mitsubishi Tanabe Pharma Corporation, and Asahi Kasei Pharma Corporation and has received research grants from Mitsubishi Tanabe Pharma Corporation. Toshihiko Aranishi, Zhihong Cai, and Tomoko Ishizuka are full-time employees of Eli Lilly Japan K.K. and minor stockholders of Eli Lilly and Company. Toshihiko Aranishi is a stockholder of Chugai Pharmaceutical Co., Ltd.
Publisher Copyright:
© 2022 Eli Lilly Japan K.K. Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Objective: To assess the current status of shared decision making (SDM) in rheumatoid arthritis (RA) clinical practice in Japan from the perspectives of physicians and patients. Methods: A web-based survey was conducted to recruit patients with RA who were prescribed, for the first time, a conventional synthetic disease-modifying antirheumatic drug (csDMARD) or a biological drug/Janus kinase (JAK) inhibitor, and physicians who prescribed these treatments to patients with RA. The SDM Questionnaire-Physician version (SDM-Q-Doc) and the 9-item SDM Questionnaire (SDM-Q-9) were used to assess the SDM levels of physicians and patients, respectively. The scale ranged from 0 to 100, and higher scores indicated better SDM status. Results: The responses from 107 physicians who treat patients with RA, 107 patients prescribed a csDMARD, and 110 patients prescribed a biological drug/JAK inhibitor were collected. The mean SDM score for SDM-Q-Doc was 74.5 when physicians decided to prescribe a csDMARD and 77.2 when they decided to prescribe a biological drug/JAK inhibitor. However, the mean SDM score for SDM-Q-9 was 62.3 when patients were prescribed csDMARDs and 72.6 when they were prescribed biological drugs/JAK inhibitors. Conclusions: The results showed differences in SDM level between patients and physicians and, from the patient perspective, between treatment types.
AB - Objective: To assess the current status of shared decision making (SDM) in rheumatoid arthritis (RA) clinical practice in Japan from the perspectives of physicians and patients. Methods: A web-based survey was conducted to recruit patients with RA who were prescribed, for the first time, a conventional synthetic disease-modifying antirheumatic drug (csDMARD) or a biological drug/Janus kinase (JAK) inhibitor, and physicians who prescribed these treatments to patients with RA. The SDM Questionnaire-Physician version (SDM-Q-Doc) and the 9-item SDM Questionnaire (SDM-Q-9) were used to assess the SDM levels of physicians and patients, respectively. The scale ranged from 0 to 100, and higher scores indicated better SDM status. Results: The responses from 107 physicians who treat patients with RA, 107 patients prescribed a csDMARD, and 110 patients prescribed a biological drug/JAK inhibitor were collected. The mean SDM score for SDM-Q-Doc was 74.5 when physicians decided to prescribe a csDMARD and 77.2 when they decided to prescribe a biological drug/JAK inhibitor. However, the mean SDM score for SDM-Q-9 was 62.3 when patients were prescribed csDMARDs and 72.6 when they were prescribed biological drugs/JAK inhibitors. Conclusions: The results showed differences in SDM level between patients and physicians and, from the patient perspective, between treatment types.
KW - Janus kinase (JAK) inhibitor
KW - Rheumatoid arthritis
KW - SDM-Q-9
KW - biological drugs
KW - shared decision making
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U2 - 10.1080/03007995.2022.2050108
DO - 10.1080/03007995.2022.2050108
M3 - Article
C2 - 35260022
AN - SCOPUS:85127214172
SN - 0300-7995
VL - 38
SP - 853
EP - 861
JO - Current Medical Research and Opinion
JF - Current Medical Research and Opinion
IS - 5
ER -