The Zucker Hillside Hospital, 75-59 263rd St, Glen Oaks, NY 11004.
Departments of Psychiatry and of Molecular Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York, USA.
J Clin Psychiatry. 2019 Apr 23;80(3):18m12546. doi: 10.4088/JCP.18m12546.
To document the acceptability of treatment with long-acting injectable (LAI) antipsychotic medication to early-phase schizophrenia patients as demonstrated by enrollment in a cluster-randomized LAI clinical trial.
Eligible patients aged 18-35 years with a DSM-5 diagnosis of schizophrenia and less than 5 years of lifetime antipsychotic use were recruited between December 2014 and December 2016. Training for LAI antipsychotic site staff included education regarding the role of nonadherence in relapse/hospitalization and the rationale for LAI antipsychotic use with early-psychosis patients, training in shared decision-making and communication strategies, review of frequently asked questions about LAI antipsychotics, and role-playing to develop skills and solutions to overcoming LAI antipsychotic logistical barriers. Study prescribers also received training on prescribing guidelines.
At the 19 US outpatient clinics randomized to provide LAI antipsychotic treatment, 576 potential participants were identified who met inclusion criteria based on a screening interview. Of these, 83 (14.4%) declined participation because they would not consider LAI antipsychotic treatment and 165 (28.6%) declined for other reasons, resulting in 328 providing written study consent. The first post-consent visit included detailed evaluations to confirm inclusion/exclusion criteria. Thirty-nine participants who consented did not complete this evaluation and 55 were found to not meet criteria, resulting in a final sample of 234 participants. Two hundred thirteen (91.0%) accepted at least one LAI antipsychotic injection during their first 3 months of study participation.
Large numbers of early-phase patients with schizophrenia were willing to participate in an LAI antipsychotic trial and by inference in non-study LAI antipsychotic treatment. LAI antipsychotic-focused staff training has the potential to substantially enhance the use of LAI antipsychotics.
ClinicalTrials.gov identifier: NCT02360319.
通过参与一项长效注射(LAI)抗精神病药物的聚类随机临床试验,记录早期精神分裂症患者对 LAI 治疗的可接受性。
2014 年 12 月至 2016 年 12 月期间,招募符合 DSM-5 精神分裂症诊断标准、年龄在 18-35 岁、使用抗精神病药物不到 5 年的患者。对 LAI 抗精神病药物网站工作人员进行培训,内容包括不遵医嘱与复发/住院之间的关系,以及对早期精神病患者使用 LAI 抗精神病药物的基本原理、共同决策和沟通策略的培训、对 LAI 抗精神病药物常见问题的回顾、角色扮演以发展克服 LAI 抗精神病药物后勤障碍的技能和解决方案。研究处方医生也接受了处方指南的培训。
在 19 家接受随机提供 LAI 抗精神病治疗的美国门诊诊所中,根据筛选访谈确定了 576 名符合纳入标准的潜在参与者。其中,83 人(14.4%)因不愿意考虑 LAI 抗精神病治疗而拒绝参与,165 人(28.6%)因其他原因拒绝参与,最终有 328 人提供书面研究同意书。首次同意后就诊包括详细评估以确认纳入/排除标准。有 39 名同意者未完成此评估,55 名不符合标准,最终样本为 234 名参与者。213 名(91.0%)在研究参与的前 3 个月内至少接受了一次 LAI 抗精神病药物注射。
大量早期精神分裂症患者愿意参与 LAI 抗精神病药物试验,并且推断他们也愿意接受非研究 LAI 抗精神病药物治疗。LAI 抗精神病药物为重点的工作人员培训有可能极大地增加 LAI 抗精神病药物的使用。
ClinicalTrials.gov 标识符:NCT02360319。