Zimmerman Mark, Holst Carolina Guzman, Clark Heather L, Multach Matthew, Walsh Emily, Rosenstein Lia K, Gazarian Douglas
Department of Psychiatry, Rhode Island Hospital, Providence, RI, USA.
Department of Psychiatry and Human Behavior, Brown Medical School, Rhode Island Hospital, 146 West River Street, Providence, RI, 02904, USA.
CNS Drugs. 2016 Dec;30(12):1209-1218. doi: 10.1007/s40263-016-0381-0.
Concerns about the generalizability of pharmacotherapy efficacy trials to "real-world" patients have been raised for more than 40 years. Almost all of this literature has focused on treatment studies of major depressive disorder (MDD).
The aim of the study was to review the psychiatric inclusion and exclusion criteria used in placebo-controlled trials that assessed the efficacy of medications for bipolar depression (bipolar disorder efficacy trials [BDETs]) and compare the criteria used in BDETs with those used in efficacy trials of antidepressants to treat MDD (antidepressant efficacy trials [AETs]).
We searched the MEDLINE, Embase, and PsycINFO databases for articles published from January 1995 through December 2014. We identified 170 placebo-controlled AETs and 22 BDETs published during these 20 years. Two of the authors independently reviewed each article and completed a pre-specified information extraction form listing the psychiatric inclusion and exclusion criteria used in the study.
Six inclusion/exclusion criteria were used in at least half of the BDETs: minimum severity on a depression symptom severity scale, significant suicidal ideation, diagnosis of alcohol or drug use disorder, presence of a comorbid nondepressive, nonsubstance use Axis I disorder, current episode of depression being too long, and absence of current manic symptoms. BDETs were significantly less likely than AETs to exclude patients with a history of psychotic features/disorders, borderline personality disorder, and post-traumatic stress disorder and more likely to exclude individuals who scored too low on the first item of the Hamilton Depression Rating Scale. Nearly two-thirds of the BDETs placed an upper limit on the duration of the current depressive episode, three times higher than the rate in the AETs. There was no difference on other variables between the AETs and BDETs.
Similar to treatment studies of nonbipolar MDD, the treatment studies of bipolar depression frequently excluded patients with comorbid psychiatric and substance use disorders and insufficient severity of depressive symptoms as rated on standardized scales. These findings indicate that concerns about the generalizability of data from trials of recently approved medications for the treatment of bipolar depression are as relevant as the concerns that have been raised about studies of antidepressants for nonbipolar depression.
40多年来,人们一直对药物治疗疗效试验结果能否推广至“现实世界”患者存在担忧。几乎所有此类文献都聚焦于重度抑郁症(MDD)的治疗研究。
本研究旨在回顾安慰剂对照试验中用于评估双相抑郁症药物疗效的精神科纳入和排除标准(双相障碍疗效试验[BDETs]),并将BDETs中使用的标准与抗抑郁药治疗MDD疗效试验(抗抑郁药疗效试验[AETs])中使用的标准进行比较。
我们检索了MEDLINE、Embase和PsycINFO数据库,查找1995年1月至2014年12月发表的文章。我们确定了这20年间发表的170项安慰剂对照AETs和22项BDETs。两位作者独立审阅每篇文章,并填写一份预先指定的信息提取表,列出研究中使用的精神科纳入和排除标准。
至少一半的BDETs使用了6项纳入/排除标准:抑郁症状严重程度量表上的最低严重程度、显著的自杀意念、酒精或药物使用障碍的诊断、存在共病的非抑郁性、非物质使用的轴I障碍、当前抑郁发作时间过长以及目前无躁狂症状。与AETs相比,BDETs排除有精神病性特征/障碍、边缘性人格障碍和创伤后应激障碍病史患者的可能性显著更低,而排除汉密尔顿抑郁量表第一项得分过低个体的可能性更高。近三分之二的BDETs对当前抑郁发作的持续时间设置了上限,这一比例是AETs的三倍。AETs和BDETs在其他变量上没有差异。
与非双相MDD的治疗研究类似双相抑郁症的治疗研究经常排除有共病精神科和物质使用障碍以及标准化量表评定的抑郁症状严重程度不足的患者。这些发现表明,对近期获批用于治疗双相抑郁症药物试验数据可推广性的担忧,与对非双相抑郁症抗抑郁药研究提出的担忧同样相关。