TY - JOUR
T1 - Clinical practice guideline for Sjögren’s syndrome 2017
AU - Sumida, Takayuki
AU - Azuma, Naoto
AU - Moriyama, Masafumi
AU - Takahashi, Hiroyuki
AU - Asashima, Hiromitsu
AU - Honda, Fumika
AU - Abe, Saori
AU - Ono, Yuko
AU - Hirota, Tomoya
AU - Hirata, Shintaro
AU - Tanaka, Yoshiya
AU - Shimizu, Toshimasa
AU - Nakamura, Hideki
AU - Kawakami, Atsushi
AU - Sano, Hajime
AU - Ogawa, Yoko
AU - Tsubota, Kazuo
AU - Ryo, Koufuchi
AU - Saito, Ichiro
AU - Tanaka, Akihiko
AU - Nakamura, Seiji
AU - Takamura, Etsuko
AU - Tanaka, Masao
AU - Suzuki, Katsuya
AU - Takeuchi, Tsutomu
AU - Yamakawa, Noriyuki
AU - Mimori, Tsuneyo
AU - Ohta, Akiko
AU - Nishiyama, Susumu
AU - Yoshihara, Toshio
AU - Suzuki, Yasunori
AU - Kawano, Mitsuhiro
AU - Tomiita, Minako
AU - Tsuboi, Hiroto
N1 - Funding Information:
Therefore, standardization of diagnosis and treatment of SS is needed for appropriate management and accurate certification of designated intractable disease. CPG based on recently available evidences should also contribute to standardization of clinical practices across the country. The treatment guideline by the SS Foundation of the United States of America (USA) [2] and the management guideline for SS by the British Society for Rheumatology (BSR) [3] were published recently. Moreover, the CPG committee for SS, organized by the Research Team for Autoimmune Diseases, the Research Program for Intractable Disease of MHLW, has developed ‘CPG for SS 2017’ [4] which has been officially approved by both the Japan College of Rheumatology (JCR) and the Japanese society for SS (JSSS), according to the procedure proposed by the Medical Information Network Distribution Service (Minds) [5].
Funding Information:
diseases are organized and supported by the Research Program for Intractable Disease of MHLW and the Practical Research Project for Rare/Intractable Diseases from Japan Agency for Medical Research and Development (AMED). The Research Program for Intractable Disease of MHLW provides support for epidemiological studies, establishes diagnostic and severity criteria, develops clinical practice guideline (CPG) based on clinical and therapeutic evidences, and distributes and revises these criteria and CPG. On the other hand, the Practical Research Project for Rare/ Intractable Diseases from AMED supports clinical research on gene therapy and clinical application of new therapies and medical devices, and provides financial support for physician-led clinical trials. Moreover, patients with designated intractable diseases can obtain medical expenses subsidy once they satisfy certain diagnostic and severity criteria.
Funding Information:
T. S. has received honoraria from Astellas, Chugai, and Mitsubishi Tanabe; research grants from Astellas, Bristol-Myers Squibb, Chugai, Mitsubishi Tanabe, and Ono. H. A. has received a research grant from Mitsubishi Tanabe. S. H. has received honoraria from AbbVie. Y. T. has received honoraria from AbbVie, Asahi Kasei, Astellas, Bristol-Myers Squibb, Chugai, Daiichi Sankyo, Eli Lilly, GlaxoSmithKline, Janssen, Mitsubishi Tanabe, Teijin Pharma, Sanofi, Pfizer, Takeda, and Y. L. Biologics; research grants from AbbVie, Astellas, Bristol-Myers Squibb, Chugai, Daiichi Sankyo, Eisai., Eli Lilly, Kowa, Limited, Kyowa Hakko Kirin, Mitsubishi Tanabe, MSD, Novartis, Pfizer, Sanofi, Shionogi, Taisho Toyama, and Takeda. A. K. has received honoraria from AbbVie, Astellas, AstraZeneca, Bristol-Myers Squibb, Kissei, Mitsubishi Tanabe, Ono., Pfizer, and Takeda; research grants from Actelion, Bristol-Myers Squibb, Daiichi Sankyo, Janssen, Ono, and Takeda. H. S. has honorariums from Astellas, Bristol-Myers Squibb, Chugai, Mitsubishi Tanabe and Pfizer; research grants from Astellas and Chugai. K. T. has received research grants from Alcon, JINS, Santen, Fuji Xerox, Kowa, Ophtecs, Otsuka, QD Laser, Rohto, Sucampo Pharma, Pfizer, Tsubota Laboratory and Wakasa Seikatsu. M. T. has received research grants from AbbVie and Astellas; has belonged to the Donated Fund Laboratory sponsored by Mitsubishi Tanabe, Chugai, Bristol-Myers Squibb and Eisai. K. S. has received honoraria from AbbVie, Astellas, Bristol-Myers Squibb, Chugai, Eisai, Fuji Film, Janssen, Kissei, Mitsubishi Tanabe, Pfizer, Shionogi and Takeda; research grants from Bristol-Myers Squibb, Daiichi Sankyo, Eisai and Kissei; consulting fees from AbbVie and Pfizer. T. T. has received honoraria from AbbVie, Astellas, Chugai, Daiichi Sankyo, Mitsubishi Tanabe and Pfizer; received research grants from AbbVie, Asahikasei Pharma, Astellas, Ayumi Pharmaceutical, Bristol-Myers Squibb, Chugai, Daiichi Sankyo, Eisai, Mitsubishi Tanabe, Nipponkayaku, Pfizer, Taisyo Toyama, Takeda, and Teijin Pharma; consulting fees from AbbVie, Astellas, Astra Zeneca, Chugai, Eli Lilly, Janssen, Mitsubishi Tanabe, Nipponkayaku, Novartis, and Taiho. T. M. has received honoraria from Mitsubishi Tanabe, Astellas and Chugai; received research grants from Mitsubishi Tanabe, Astellas and Daiichi Sankyo. H. T. has received honoraria from Bristol-Myers Squibb. The other authors have no conflicts of interest.
Publisher Copyright:
© 2018 Japan College of Rheumatology. Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2018/5/4
Y1 - 2018/5/4
N2 - Objectives: The objective of this study is to develop clinical practice guideline (CPG) for Sjögren’s syndrome (SS) based on recently available clinical and therapeutic evidences. Methods: The CPG committee for SS was organized by the Research Team for Autoimmune Diseases, Research Program for Intractable Disease of the Ministry of Health, Labor and Welfare (MHLW), Japan. The committee completed a systematic review of evidences for several clinical questions and developed CPG for SS 2017 according to the procedure proposed by the Medical Information Network Distribution Service (Minds). The recommendations and their strength were checked by the modified Delphi method. The CPG for SS 2017 has been officially approved by both Japan College of Rheumatology and the Japanese Society for SS. Results: The CPG committee set 38 clinical questions for clinical symptoms, signs, treatment, and management of SS in pediatric, adult and pregnant patients, using the PICO (P: patients, problem, population, I: interventions, C: comparisons, controls, comparators, O: outcomes) format. A summary of evidence, development of recommendation, recommendation, and strength for these 38 clinical questions are presented in the CPG. Conclusion: The CPG for SS 2017 should contribute to improvement and standardization of diagnosis and treatment of SS.
AB - Objectives: The objective of this study is to develop clinical practice guideline (CPG) for Sjögren’s syndrome (SS) based on recently available clinical and therapeutic evidences. Methods: The CPG committee for SS was organized by the Research Team for Autoimmune Diseases, Research Program for Intractable Disease of the Ministry of Health, Labor and Welfare (MHLW), Japan. The committee completed a systematic review of evidences for several clinical questions and developed CPG for SS 2017 according to the procedure proposed by the Medical Information Network Distribution Service (Minds). The recommendations and their strength were checked by the modified Delphi method. The CPG for SS 2017 has been officially approved by both Japan College of Rheumatology and the Japanese Society for SS. Results: The CPG committee set 38 clinical questions for clinical symptoms, signs, treatment, and management of SS in pediatric, adult and pregnant patients, using the PICO (P: patients, problem, population, I: interventions, C: comparisons, controls, comparators, O: outcomes) format. A summary of evidence, development of recommendation, recommendation, and strength for these 38 clinical questions are presented in the CPG. Conclusion: The CPG for SS 2017 should contribute to improvement and standardization of diagnosis and treatment of SS.
KW - Medical Information Network Distribution Service (Minds)
KW - Sjögren’s syndrome
KW - clinical practice guideline
KW - clinical question
KW - systematic review
UR - http://www.scopus.com/inward/record.url?scp=85043701298&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85043701298&partnerID=8YFLogxK
U2 - 10.1080/14397595.2018.1438093
DO - 10.1080/14397595.2018.1438093
M3 - Review article
C2 - 29409370
AN - SCOPUS:85043701298
SN - 1439-7595
VL - 28
SP - 383
EP - 408
JO - Modern rheumatology
JF - Modern rheumatology
IS - 3
ER -