Palacios-Garrán Roberto, Llorca-Bofí Vicent, Arteaga-Henriquez Gara, Del Agua Enrique
Department of Psychiatry, Mental Health, and Addiction, GSS-Hospital Santa Maria, Lleida, Spain.
Department of Psychiatry, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Front Psychiatry. 2022 May 11;13:828088. doi: 10.3389/fpsyt.2022.828088. eCollection 2022.
Cariprazine's efficacy and safety have been previously tested in adult patients with acute mania associated with bipolar I disorder, but there is no available data in FEM. The objective of this study is to assess the efficacy and safety of cariprazine in combination with a mood stabilizer in treating FEM as well as to evaluate patients' adherence to the treatment.
FEM patients were recruited from the acute inpatient unit at Lleida University Hospital Santa Maria, between January and June 2021. Their symptoms were evaluated using the Young Mania Rating Scale (YMRS) and the Clinical Global Impressions-Severity (CGI-S) scale at admission and at discharge. Akathisia was assessed using the Barnes Akathisia Rating Scale. Patient adherence to medication treatment was assessed 30 days after discharge using the Morisky, Green and Levine Medication Adherence Scale. Socio-demographic and clinical information were further collected.
Eleven patients with FEM were involved, seven women and four men. Their mean age was 26.00+/-6.37 years. Mean hospitalization was 17.36+/-4.7 days. Cariprazine was combined with a mood stabilizer: lithium in seven patients and divalproex in four. Mean YMRS change from baseline was -24.55+/-7.5 and the mean CGI-S change from baseline was -2.55+/-0.82. Regarding adverse events, two (18.2%) patients presented with akathisia. At the 30-day treatment-adherence assessment, six (54.5%) patients were adherent and four (36.4%) had moderate adherence.
In this sample, cariprazine in combination with mood stabilizers proved to be safe and effective in the treatment of FEM with more than half the patients being adherent to treatment. Therefore, cariprazine add-on is a good choice for promoting the long-term adherence of patients, thus minimizing the risk of relapse and improving prognosis.
卡立普嗪的疗效和安全性此前已在患有双相I型障碍相关急性躁狂的成年患者中进行过测试,但在女性急性躁狂(FEM)患者中尚无可用数据。本研究的目的是评估卡立普嗪联合心境稳定剂治疗FEM的疗效和安全性,并评估患者对治疗的依从性。
2021年1月至6月期间,从莱里达大学圣玛丽亚医院的急性住院部招募FEM患者。在入院时和出院时使用青年躁狂评定量表(YMRS)和临床总体印象-严重程度(CGI-S)量表评估他们的症状。使用巴恩斯静坐不能评定量表评估静坐不能。出院30天后使用莫斯基、格林和莱文药物依从性量表评估患者对药物治疗的依从性。进一步收集社会人口统计学和临床信息。
纳入了11例FEM患者,7名女性和4名男性。他们的平均年龄为26.00±6.37岁。平均住院时间为17.36±4.7天。卡立普嗪与心境稳定剂联合使用:7例患者使用锂盐,4例患者使用丙戊酸。YMRS较基线的平均变化为-24.55±7.5,CGI-S较基线的平均变化为-2.55±0.82。关于不良事件,2例(18.2%)患者出现静坐不能。在30天治疗依从性评估中,6例(54.5%)患者依从,4例(36.4%)患者依从性中等。
在本样本中,卡立普嗪联合心境稳定剂被证明在治疗FEM方面安全有效,超过半数患者坚持治疗。因此,加用卡立普嗪是促进患者长期依从性的良好选择,从而将复发风险降至最低并改善预后。