J Psychiatr Pract. 2020 Sep;26(5):360-366. doi: 10.1097/PRA.0000000000000493.
The goal of this survey study was to assess specific aspects of lithium therapy for bipolar disorder, including psychiatrists' prescribing practices, understanding of therapeutic drug monitoring, and concerns and perspectives regarding lithium therapy.
A 14-item survey was electronically distributed to 225 staff psychiatrists at 8 academic hospitals.
The survey was completed by 85 psychiatrists (38% of the 225 psychiatrists to whom the survey was distributed), with between 81 and 85 respondents completing the different items. When asked about the agents with which they initiated therapy, 49 (61%) reported initiating therapy with an atypical antipsychotic and 34 (42%) reported starting with lithium therapy in 50% or more of patients newly diagnosed with bipolar disorder. When prescribing lithium, most of the respondents (n=68, 82%) reported that they used once daily dosing, and 67 respondents (79%) indicated that they ordered lithium blood levels 12 hours postdose. When interpreting lithium levels, 46 respondents (55%) reported "always" changing a clinically stable patient's lithium dose when the level was above the therapeutic range, compared with 4 (5%) who reported always changing the dose when the level was below the therapeutic range. When asked about their concerns regarding lithium therapy, more than half of the respondents reported that they were especially concerned about toxicity, organ dysfunction, and other adverse effects, as well as therapeutic drug monitoring.
Shifts in prescribing practices, inconsistent interpretation of lithium levels, and concerns about safety and therapeutic drug monitoring highlight the need for evidence-informed guidelines reflective of current practice.
本调查研究旨在评估双相情感障碍锂治疗的具体方面,包括精神科医生的处方实践、对治疗药物监测的理解,以及对锂治疗的关注和看法。
对 8 家学术医院的 225 名在职精神科医生进行了 14 项调查。
共有 85 名精神科医生(占向 225 名精神科医生分发问卷的 38%)完成了调查,有 81 至 85 名受访者完成了不同的项目。在问及他们开始治疗的药物时,49 名(61%)报告说他们开始使用非典型抗精神病药物治疗,34 名(42%)报告说他们在 50%或更多新诊断为双相情感障碍的患者中开始锂治疗。在开锂药时,大多数受访者(n=68,82%)报告说他们使用每日一次的剂量,67 名受访者(79%)表示他们在给药后 12 小时测定锂血药浓度。在解释锂水平时,46 名受访者(55%)报告说,当水平高于治疗范围时,他们“总是”改变临床稳定患者的锂剂量,而 4 名受访者(5%)报告说,当水平低于治疗范围时,他们总是改变剂量。在问及他们对锂治疗的担忧时,超过一半的受访者表示,他们特别担心毒性、器官功能障碍和其他不良反应,以及治疗药物监测。
处方实践的转变、对锂水平的不一致解释,以及对安全性和治疗药物监测的关注,突出表明需要制定反映当前实践的基于证据的指南。