Department of Psychiatry and Behavioral Health, Greenwich Hospital, Greenwich, CT, United States of America.
Department of Psychiatry, Yale School of Medicine, New Haven, Connecticut, United States of America.
PLoS One. 2022 Jun 16;17(6):e0269772. doi: 10.1371/journal.pone.0269772. eCollection 2022.
Anxiety disorders, including panic disorder (PD), generalized anxiety disorder (GAD), social anxiety disorder (SAD), agoraphobia, and specific phobia, are among the most common psychiatric disorders. Although the traditional pharmacologic treatments for anxiety included barbiturates and then benzodiazepines, the introduction of tricyclic antidepressants, followed by the selective serotonin reuptake inhibitors (SSRIs), marked a tidal shift in the treatment of anxiety. Although not approved for treatment of anxiety disorders (with the exception of trifluoperazine) there is ongoing off-label, unapproved use of both first-generation "typical" antipsychotics (FGAs) and second-generation or "atypical" antipsychotics (SGAs) for anxiety. Although there have been systematic reviews and meta-analyses on the use of antipsychotics in anxiety disorders, most of these reviews focused on SGAs, primarily the use of quetiapine in GAD. Given that there is little known about the potential benefits and short-and long-term risks of using antipsychotics in anxiety, there is a need for an umbrella review of systematic reviews and meta-analyses of the use of both FGAs and SGAs in anxiety disorders. The specific aims of this study are as follows: (1) Evaluate the evidence of efficacy of FGAs and SGAs in anxiety disorders as an adjunctive treatment to SSRIs, serotonin norepinephrine reuptake inhibitors (SNRIs) and other non-antipsychotic medications; (2) Compare monotherapy with antipsychotics to first-line treatments for anxiety disorders in terms of effectiveness, risks, and side effects; and (3) Evaluate the short- and long-term risks and side effects of prescribing antipsychotics in anxiety disorders. The review is registered on PROSPERO (CRD42021237436). Since data extraction has not begun, there is not preliminary data to share.
焦虑障碍包括惊恐障碍(PD)、广泛性焦虑障碍(GAD)、社交焦虑障碍(SAD)、广场恐怖症和特定恐惧症,是最常见的精神障碍之一。虽然传统的焦虑症药物治疗包括巴比妥类药物和苯二氮䓬类药物,但三环类抗抑郁药的引入,随后是选择性 5-羟色胺再摄取抑制剂(SSRIs)的引入,标志着焦虑症治疗的重大转变。虽然没有批准用于治疗焦虑障碍(除了三氟拉嗪),但第一代“典型”抗精神病药(FGAs)和第二代或“非典型”抗精神病药(SGAs)仍在未经批准的情况下用于治疗焦虑症。尽管已经有关于抗精神病药在焦虑障碍中的使用的系统评价和荟萃分析,但这些综述大多集中在 SGAs 上,主要是在 GAD 中使用喹硫平。鉴于人们对使用抗精神病药治疗焦虑症的潜在益处和短期及长期风险知之甚少,因此需要对 FGAs 和 SGAs 在焦虑障碍中的使用进行系统评价和荟萃分析的综述。本研究的具体目的如下:(1)评估 FGAs 和 SGAs 作为 SSRIs、去甲肾上腺素和 5-羟色胺再摄取抑制剂(SNRIs)和其他非抗精神病药物的辅助治疗在焦虑障碍中的疗效证据;(2)比较抗精神病药物单药治疗与焦虑障碍一线治疗的疗效、风险和副作用;(3)评估在焦虑障碍中开处方抗精神病药的短期和长期风险和副作用。该综述已在 PROSPERO(CRD42021237436)上注册。由于数据提取尚未开始,目前没有初步数据可分享。