Phase 3b Multicenter, Prospective, Open-label Trial to Evaluate the Effects of a Digital Medicine System on Inpatient Psychiatric Hospitalization Rates for Adults With Schizophrenia.

Elan A Cohen, T. Skubiak, Dusica Hadzi Boskovic, Keinya Norman, Jonathan Knights, H. Fang, Antonia K Coppin-Renz, T. Peters-Strickland, J. Lindenmayer, J. C. Reuteman-Fowler
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Abstract

Objective: Inpatient psychiatric admissions drive the financial burden of schizophrenia, and medication adherence remains challenging. We assessed whether aripiprazole tablets with sensor (AS; system includes ingestible event-marker sensor, wearable sensor patches, and smartphone application) could reduce psychiatric hospitalizations compared with oral standard-of-care (SOC) antipsychotics. Methods: This phase 3b, mirror-image clinical trial was conducted from April 29, 2019-August 11, 2020, in adults with schizophrenia with ≥ 1 hospitalization in the previous 48 months who had been prescribed oral SOC for the preceding 6 months (retrospective phase). All participants used AS for at least 3 months and up to 6 months. Primary endpoint was the inpatient psychiatric hospitalization rate in the modified intent-to-treat (mITT; n = 113) population during prospective months 1-3 versus retrospective phase. Proportion of days covered by medication was the secondary endpoint. Safety endpoints included adverse events related to the medication or patch and suicidality. Results: AS significantly reduced hospitalizations during prospective months 1-3 (-9.7%) and months 1-6 (-21.3% [P ≤ .001 for all comparisons]) in the mITT population versus the corresponding retrospective phase. AS use improved confirmed medication ingestion by 26.5 percentage points in prospective months 1-3 (P ≤ .001) and reduced PANSS scores. Patches were well-tolerated, and no participant reported changes in suicide risk. Conclusions: Compared with oral SOC, AS reduced inpatient psychiatric hospitalization rates for adults with mild-to-moderate schizophrenia. The AS system may aid medication ingestion and is associated with improvements in symptoms, potentially reducing acute-care needs among patients with schizophrenia. Trial Registration: ClinicalTrials.gov identifier: NCT03892889.
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3b期多中心、前瞻性、开放标签试验评估数字医疗系统对成年精神分裂症患者住院率的影响
目的:精神科住院患者增加了精神分裂症的经济负担,并且药物依从性仍然具有挑战性。我们评估了阿立哌唑片是否具有传感器(AS);系统包括可摄取的事件标记传感器、可穿戴传感器贴片和智能手机应用程序)与口服标准护理(SOC)抗精神病药物相比,可以减少精神病住院。方法:该3b期镜像临床试验于2019年4月29日至2020年8月11日在过去48个月内住院≥1次且在过去6个月内服用口服SOC的精神分裂症成人患者中进行(回顾性试验)。所有参与者使用AS至少3个月,最多6个月。主要终点是改良治疗意向(mITT;N = 113)人群在未来1-3个月与回顾性阶段。用药天数的比例是次要终点。安全性终点包括与药物或贴片相关的不良事件和自杀倾向。结果:AS显著减少了预期1-3个月(-9.7%)和1-6个月(-21.3%)的住院率[P≤。0.001[所有比较])在mITT人群中与相应的回顾性阶段。使用AS可使预期1-3个月的确诊药物摄入提高26.5个百分点(P≤0.001),并降低PANSS评分。贴片耐受性良好,没有参与者报告自杀风险发生变化。结论:与口服SOC相比,AS降低了轻中度精神分裂症成人患者的住院率。AS系统可能有助于药物摄入,并与症状改善有关,可能减少精神分裂症患者的急性护理需求。试验注册:ClinicalTrials.gov标识符:NCT03892889。
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Emerging Perspectives in Addiction Psychiatry. Emerging Therapies for Attention-Deficit/Hyperactivity Disorder Charles Bowden, MD, 1938-2022. In Memoriam: Jan Fawcett, MD, 1934-2022. The Relationship Between Mental Pain, Suicide Risk, and Childhood Traumatic Experiences: Results From a Multicenter Study.
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