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Randomized open-label study of second-generation antipsychotics for the treatment of schizophrenia: 104-week final results of the JUMPs study assessing treatment discontinuation, remission, and social functioning.
Ishigooka, Jun; Nakagome, Kazuyuki; Ohmori, Tetsuro; Iwata, Nakao; Inada, Ken; Iga, Jun-Ichi; Kishi, Taro; Fujita, Kiyoshi; Kikuchi, Yuka; Shichijo, Toshiaki; Tabuse, Hideaki; Koretsune, Shotatsu; Terada, Hiroshi; Terada, Haruko; Kishimoto, Toshifumi; Tsutsumi, Yuichiro; Ohi, Kazutaka.
Afiliación
  • Ishigooka J; Department of Psychiatry, School of Medicine, Tokyo Women's Medical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan. ishigooka@i-cnsp.com.
  • Nakagome K; Present address: Institute of CNS Pharmacology, 4-26-11 Sendagaya, Shibuya-ku, Tokyo, 151-0051, Japan. ishigooka@i-cnsp.com.
  • Ohmori T; Department of Psychiatry, National Center of Neurology and Psychiatry, 4 Chome-1-1 Ogawahigashicho, Kodaira, Tokyo, 187-8551, Japan.
  • Iwata N; Department of Psychiatry, Tokushima University Graduate School of Biomedical Sciences, 3-18- 15, Kuramoto-cho, Tokushima, 770-8503, Japan.
  • Inada K; Department of Psychiatry, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Iga JI; Department of Psychiatry, School of Medicine, Tokyo Women's Medical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan.
  • Kishi T; Present address: Department of Psychiatry, Kitasato University School of Medicine, 1-15-1, Kitasato, Minami-ku, Sagamihara-shi, Kanagawa, 252-0374, Japan.
  • Fujita K; Department of Psychiatry, Tokushima University Graduate School of Biomedical Sciences, 3-18- 15, Kuramoto-cho, Tokushima, 770-8503, Japan.
  • Kikuchi Y; Present address: Department of Neuropsychiatry, Molecules and Function, Ehime University Graduate School of Medicine, Shitsukawa, Toon, Ehime, 791-0295, Japan.
  • Shichijo T; Department of Psychiatry, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.
  • Tabuse H; Okehazama Hospital Fujita Kokoro Care Center, Minamiyakata, Sakaecho Toyoake, Aichi, 470-1168, Japan.
  • Koretsune S; Department of Psychiatry, Akita University Hospital, Hasunuma-44-2 Hiroomote, Akita, 010- 0041, Japan.
  • Terada H; Present address: Heart-Care Clinic Omachi, 1-2-7 Omachi, Akita, 010-0921, Japan.
  • Terada H; Mental Clinic Minami, 4 Chome-3-2 Honcho, Iwatsuki Ward, Saitama, 339-0057, Japan.
  • Kishimoto T; Department of Psychiatry, Holy Cross Hospital, 2431-160 Kujiri, Izumi-cho, Toki-shi, Gifu, 509-5142, Japan.
  • Tsutsumi Y; Kokorono Clinic Narimasu, 3-3-15 Narimasu, Itabashi-ku, Tokyo, 175-0094, Japan.
  • Ohi K; Aoi Clinic, 679-1 Okitsunakacho, Shimizu Ward, Shizuoka, 424-0204, Japan.
BMC Psychiatry ; 24(1): 600, 2024 Sep 05.
Article en En | MEDLINE | ID: mdl-39237918
ABSTRACT

BACKGROUND:

We report the final results of treatment with aripiprazole, blonanserin, and paliperidone from the Japan Useful Medication Program for Schizophrenia (JUMPs), a 104-week naturalistic study.

METHODS:

JUMPs was an open-label, three-arm, randomized, parallel-group, 104-week study. Patients aged ≥ 20 years with schizophrenia requiring antipsychotic treatment or a switch from previous therapy were enrolled. The primary endpoint was treatment discontinuation rate over 104 weeks. Secondary endpoints included remission rate, Personal and Social Performance (PSP), safety, Positive and Negative Syndrome Scale (PANSS), and quality of life (QOL; EuroQol-5 dimension).

RESULTS:

In total, 251 patients received aripiprazole (n = 82), blonanserin (n = 85), or paliperidone (n = 84). Treatment discontinuation rates (aripiprazole, 80.5%; blonanserin, 81.2%; paliperidone, 71.4%) were not significantly different (p = 0.2385) among the treatment groups at 104 weeks; comparable outcomes were observed for endpoints, including remission (42.9%, 46.7%, and 45.8%), PANSS, and safety. In the overall cohort, while the improvement in the PSP total score at Week 104 was not significantly different from baseline, a significant improvement (p < 0.05) in QOL and total PANSS scores (including all subscales) was observed at Week 104 compared with baseline. Multivariable analysis identified a shorter disease duration and a higher chlorpromazine-equivalent antipsychotic dosage level (≥ 1000 mg) before switching to monotherapy as predictors of treatment discontinuation.

CONCLUSIONS:

The 104-week treatment outcomes were comparable between groups; the overall trend of improvement in remission rate, safety, and QOL suggests the importance of continued treatment. CLINICAL TRIAL REGISTRATION UMIN-Clinical Trials Registry UMIN000007942 (public release date 14/05/2012).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calidad de Vida / Esquizofrenia / Antipsicóticos / Palmitato de Paliperidona / Aripiprazol Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: BMC Psychiatry Asunto de la revista: PSIQUIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Calidad de Vida / Esquizofrenia / Antipsicóticos / Palmitato de Paliperidona / Aripiprazol Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: BMC Psychiatry Asunto de la revista: PSIQUIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido