Sajatovic Martha, Ng-Mak Daisy, Solem Caitlyn T, Lin Fang-Ju, Rajagopalan Krithika, Loebel Antony
Case Western Reserve University School of Medicine and University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
Sunovion Pharmaceuticals Inc., Global Health Economics & Health Outcomes Research, 84 Waterford Drive, Marlborough, MA 01752, USA.
Ther Adv Psychopharmacol. 2016 Dec;6(6):355-368. doi: 10.1177/2045125316672135. Epub 2016 Oct 13.
The aim of this study was to describe dosing patterns and medication adherence among bipolar patients who initiated lurasidone in a real-world setting.
Adult bipolar patients who initiated lurasidone between 1 November 2010 and 31 December 2012 (index period) with 6-month pre- and post-index continuous enrollment were identified from the IMS RWD Adjudicated Claims US database. Patients were grouped by starting lurasidone daily dose: 20 mg (7.1%), 40 mg (62.2%), 60-80 mg (28.7%), and 120-160 mg (2.1%). Patient characteristics were compared across doses using Cochran-Armitage trend tests. Multivariable ordinal logistic regression assessed the association between initial lurasidone dose and patient characteristics. Medication adherence was measured using medication possession ratio (MPR).
Of 1114 adult bipolar patients (mean age 40.6 years, 70.6% female), 90% initiated lurasidone at 40 mg or 80 mg/day (mean 51.9 mg/day). Of these, 16.2% initiated lurasidone as monotherapy. Mean lurasidone maintenance dose was 55.2 mg/day and mean MPR was 0.53 [standard deviation (SD) = 0.34] over the 6-month follow up. Substance use, hyperglycemia, obesity, and prior antipsychotic use were associated with higher initial lurasidone doses ( < 0.05). Odds of a 20 mg/day increase in initial lurasidone dose was 1.6-times higher for patients with substance use [95% confidence interval (CI): 1.16-2.24], 2.6-times higher with hyperglycemia problems (95% CI: 1.15-5.83), 1.7-times higher with obesity (95% CI: 1.05-2.60), and 1.3 (95% CI: 1.01-1.78) and 1.8-times higher (95% CI: 1.17-2.86) with prior use of second- and first-generation antipsychotics, respectively.
This real-world analysis of bipolar patients indicated that 40 mg or 80 mg/day were the most common starting doses of lurasidone. A majority of patients used concomitant psychiatric medications (polypharmacy). Higher doses of lurasidone were prescribed to patients with comorbidities or prior antipsychotic use. Adherence to lurasidone was comparable to or better than antipsychotic adherence reported in bipolar disorder literature.
本研究旨在描述在现实环境中开始使用鲁拉西酮的双相情感障碍患者的给药模式和药物依从性。
从IMS RWD美国裁决索赔数据库中识别出在2010年11月1日至2012年12月31日(索引期)开始使用鲁拉西酮且在索引前后连续登记6个月的成年双相情感障碍患者。患者按鲁拉西酮起始日剂量分组:20毫克(7.1%)、40毫克(62.2%)、60 - 80毫克(28.7%)和120 - 160毫克(2.1%)。使用 Cochr an - Armitage趋势检验比较不同剂量组的患者特征。多变量有序逻辑回归评估初始鲁拉西酮剂量与患者特征之间的关联。使用药物持有率(MPR)测量药物依从性。
在1114例成年双相情感障碍患者(平均年龄40.6岁,70.6%为女性)中,9