Hitoshi Iida1, Junichi Iga2, Naomi Hasegawa3, Yuka Yasuda4, Tomoya Yamamoto5, Kenichiro Miura3, Junya Matsumoto3, Atsunobu Murata3, Kazuyoshi Ogasawara6, Hisashi Yamada7, Hikaru Hori8, Kayo Ichihashi9, Naoki Hashimoto10, Kazutaka Ohi11, Norio Yasui-Furukori12, Takashi Tsuboi13, Toshinori Nakamura14, Masahide Usami15, Ryuji Furihata16, Yoshikazu Takaesu13, Kunihiro Iwamoto17, Nobuhiro Sugiyama18, Taishiro Kishimoto19, Naohisa Tsujino20, Hiroki Yamada21, Akitoyo Hishimoto22, Kiyotaka Nemoto23, Kiyokazu Atake8, Hiroyuki Muraoka24, Eiichi Katsumoto25, Satoru Oishi26, Takahiko Inagaki27, Fumiaki Ito28, Yayoi Imamura13, Mikio Kido29, Tatsuya Nagasawa30, Shusuke Numata31, Shinichiro Ochi2, Masaaki Iwata32, Hidenaga Yamamori3, Junichi Fujita22, Toshiaki Onitsuka33, Satoshi Yamamura34, Manabu Makinodan35, Michiko Fujimoto36, Yoichiro Takayanagi37, Kenji Takezawa38, Hiroshi Komatsu28, Kentaro Fukumoto39, Shinichiro Tamai40, Hirotaka Yamagata41, Chika Kubota42, Tadasu Horai43, Ken Inada24, Koichiro Watanabe13, Hiroaki Kawasaki1, Ryota Hashimoto3. 1. Department of Psychiatry, Faculty of Medicine, Fukuoka University, Fukuoka, Japan. 2. Department of Neuropsychiatry, Molecules and Function, Ehime University Graduate School of Medicine, Ehime, Japan. 3. Department of Pathology of Mental Diseases, National Institute of Mental Health, National Center of Neurology and Psychiatry, Tokyo, Japan. 4. Medical Corporation Foster, Osaka, Japan. 5. Department of Pharmacy, Osaka University Hospital, Osaka, Japan. 6. Center for Postgraduate Clinical Training and Career Development, Nagoya University Hospital, Aichi, Japan. 7. Department of Neuropsychiatry, Hyogo College of Medicine, Hyogo, Japan. 8. Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Fukuoka, Japan. 9. Deaprtment of Neuropsychiatry, University of Tokyo Hospital, Tokyo, Japan. 10. Department of Psychiatry, Hokkaido University Graduate School of Medicine, Hokkaido, Japan. 11. Department of Psychiatry and Psychotherapy, Gifu University Graduate School of Medicine, Gifu, Japan. 12. Department of Psychiatry, Dokkyo Medical University School of Medicine, Tochigi, Japan. 13. Department of Neuropsychiatry, Kyorin University School of Medicine, Tokyo, Japan. 14. Department of Psychiatry, Shinshu University School of Medicine, Nagano, Japan. 15. Department of Child and Adolescent Psychiatry, Kohnodai Hospital, National Center for Global Health and Medicine, Chiba, Japan. 16. Department of Psychiatry, Nihon University School of Medicine, Tokyo, Japan. 17. Department of Psychiatry, Nagoya University Graduate School of Medicine, Aichi, Japan. 18. Department of Applied Occupational Therapy, Shinshu University School of Health Sciences, Nagano, Japan. 19. Department of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan. 20. Department of Neuropsychiatry, School of Medicine, Faculty of Medicine, Toho University, Tokyo, Japan. 21. Department of Psychiatry, Showa University Northern Yokohama Hospital, Kanagawa, Japan. 22. Department of Psychiatry, Yokohama City University Graduate School of Medicine, Kanagawa, Japan. 23. Department of Psychiatry, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan. 24. Department of Psychiatry, Tokyo Women's Medical University, Tokyo, Japan. 25. Katsumoto Mental Clinic, Osaka, Japan. 26. Department of Psychiatry, Kitasato University School of Medicine, Kanagawa, Japan. 27. Adolescent Mental Health Service, Biwako Hospital, Shiga, Japan. 28. Department of Psychiatry, Tohoku University Hospital, Miyagi, Japan. 29. Department of Neuropsychiatry, University of Toyama Graduate School of Medicine and Pharmaceutical Sciences, Toyama, Japan. 30. Department of Neuropsychiatry, Kanazawa Medical University, Ishikawa, Japan. 31. Department of Psychiatry, Institute of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan. 32. Department of Neuropsychiatry, Faculty of Medicine, Tottori University, Tottori, Japan. 33. Department of Neuropsychiatry, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. 34. Suzuka Kosei Hospital, Mie, Japan. 35. Department of Psychiatry, Nara Medical University School of Medicine, Nara, Japan. 36. Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan. 37. Department of Neuropsychiatry, University of Toyama School of Medicine, Toyama, Japan. 38. Medical Corporation Matsuzaki Hospital, Toyohashi Mental Care Center, Aichi, Japan. 39. Department of Neuropsychiatry, Iwate Medical University, Iwate, Japan. 40. Department of Neuropsychiatry, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan. 41. Division of Neuropsychiatry, Department of Neuroscience, Yamaguchi University School of Medicine, Yamaguchi, Japan. 42. Department of Psychiatry, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan. 43. Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.
According to past analyses of prescription and treatment patterns for major depressive disorder (MDD), the majority of MDDpatients in Japan have not been treated according to the recommended guidelines.
In this context, the Japanese Society of Mood Disorders published the ‘Treatment Guidelines for Major Depressive Disorders’ (GL) in 2012, and the ‘Effectiveness of Guidelines for Dissemination and Education in Psychiatric Treatment (EGUIDE)’ project was launched in 2016, which aimed to standardize medical practice using quality indicators (QI) as indices for the quality of medical practice.
,The present study was a cross‐sectional, retrospective study conducted in a total of 84 institutions (36 university hospitals, 23 national/public hospitals, and 25 private hospitals). According to the recommendations of the GL, a total of eight QI (Table S1) were evaluated based on the survey of the treatments and prescriptions at discharge for patients with MDD during the first year (2016–2018) in the participating hospitals. The data were collected by the EGUIDE project members. In this survey, we recorded all types and dosages of psychotropic drugs, including antidepressants, antipsychotics, mood stabilizers, and benzodiazepines. The use of modified electroconvulsive therapy (mECT) and cognitive behavioral therapy were also recorded. The ethics committees of the National Center of Neurology and Psychiatry and each participating university/hospital/clinic approved the entire study protocol. Written informed consent was obtained from all participants (psychiatrists who treated the inpatients). The treated inpatients could see the purpose and procedures of the study on websites and could refuse to participate freely (opt‐out).This survey involved a sample of 1283 patients who had been diagnosed with MDD at discharge (Table S2). Values of each QI in all subjects and in each hospital are presented in Table S3. In this study, only 60.2% of patients received antidepressant monotherapy, with a large institutional difference from less than 20% to 100% (Fig. 1). A previous report already confirmed that antidepressant polypharmacy prevailed in Japan,
while this is the first report showing a large institutional difference. The proportion of patients who received no prescription of anxiolytics or hypnotics was only 25.1%, which is consistent with the study showing long‐term benzodiazepine use despite the recent clinical guidelines in Japan.
Although combination therapy with antidepressants and benzodiazepines may be more effective than therapy with antidepressants alone in the early phase, these effects may not be maintained in the acute or continuous phase.
Thus, long‐term benzodiazepine use is not recommended in the GL due to the potential side‐effects. The QI values for each hospital type are presented in Table S4. QI‐1 was significantly higher in university hospitals than in national/public hospitals, while QI‐3, QI‐4, QI‐5, and QI‐6 were significantly higher in university hospitals than in private hospitals. Possible explanations for institutional differences include different instructions from senior psychiatrists regarding prescribing and treatment. Many psychiatry residents included in this study were affiliated with university hospitals and they generally follow the GL rather than prescribing traditions introduced by senior psychiatrists. As regional differences in treatment patterns have been previously reported,
,
comparisons of QI values between eastern and western Japan are shown in Table S5. There was a significantly higher proportion of patients receiving mECT in eastern Japan (17.6%) compared to that in western Japan (8.4%). Although a compositional difference in hospital type between eastern and western Japan (university: 46.9% vs 37.1%; national/public: 34.7% vs 17.1%; private 18.4% vs 45.7%; χ2‐test P = 0.019) may affect the difference, the difference in the proportion of patients undergoing mECT may stem from different attitudes towards mECT in these regions. The low proportion of patients undergoing mECT treatment in private hospitals (3%) may be because most private hospitals do not have the facilities for mECT. The low proportion of patients undergoing cognitive behavioral therapy in all hospitals (1%) may reflect the low level of provision of cognitive behavioral therapy despite its coverage by Japanese health insurance.
Fig. 1
Proportion of patients with major depressive disorder (MDD) receiving antidepressant monotherapy (quality indicator‐1) in 84 hospitals. There is a large difference in the proportion of patients receiving antidepressant monotherapy among the hospitals, ranging from less than 20% to 100%.
Proportion of patients with major depressive disorder (MDD) receiving antidepressant monotherapy (quality indicator‐1) in 84 hospitals. There is a large difference in the proportion of patients receiving antidepressant monotherapy among the hospitals, ranging from less than 20% to 100%.This study has several limitations. First, we did not assess depressive symptoms using rating scales. Second, this study may have a selection bias because these 84 hospitals may not reflect the treatment and prescription patterns of all hospitals in Japan. The ratio of antidepressant monotherapy may be affected by not only hospital type but also the patient's background, such as refractory episodes, and the difference in positioning and role of the hospital in the community.In accordance with the GL, we should strive to reduce antidepressant polypharmacy and long‐term use of benzodiazepines in the treatment of MDD in Japan. Based on this baseline survey, we plan to report changes brought by the GL education program. In the future, proper diagnosis and treatment following dissemination of and adherence to the GL will provide suitable circumstances for high‐quality research of MDD.
,
,
Disclosure statement
The authors declare that they have no conflicts of interest related to this article.Table S1 The eight quality indicators (QI) used in the present study.Click here for additional data file.Table S2 Demographic data of patients with major depressive disorder (MDD).Click here for additional data file.Table S3 Quality indicator (QI) values for patients with major depressive disorder (MDD) in the first year of participation. The QI of each patient (n = 1283) is presented. The QI for each hospital (n = 84) was also calculated and is presented as the mean ± SD and the median with interquartile range (IQR).Click here for additional data file.Table S4 Quality indicator (QI) values for each hospital type in the first year of participation. The QI of five subgroups of the 84 hospitals divided by hospital type (university hospital, national/public hospitals, and private hospitals) are presented as the means ± SD. QI values in each group were compared with the Kruskal–Wallis test followed by the post‐hoc test (Dunn test). The significance level was set at two‐tailed P < 6.25 × 10−3 because the Bonferroni method was applied. The significance level of the post‐hoc test was set at P < 1.7 × 10−2. Significant P‐values are boldfaced and underlined.Click here for additional data file.Table S5 Quality indicator (QI) values of eastern Japan and western Japan in the first year of participation. The QI of five subgroups of the 84 hospitals divided by region (eastern Japan, western Japan) are presented as the means ± SD. QI values in each group were compared with the Mann–Whitney U‐test. The significance level was set at two‐tailed P < 6.25 × 10−3 as the Bonferroni method was applied. Significant P‐values are boldfaced and underlined. There was a significant compositional difference in hospital type between eastern and western Japan (university: 46.9% vs 37.1%; national/public: 34.7% vs 17.1%; private: 18.4% vs 45.7%; χ2‐test P = 0.019.Click here for additional data file.