Department of Psychiatry, Case Western Reserve University, 10524 Euclid Ave., Cleveland, OH 44106, USA.
Psychiatr Serv. 2012 Feb 1;63(2):176-8. doi: 10.1176/appi.ps.201100133.
A three-month prospective trial of a psychosocial intervention--customized adherence enhancement (CAE)--was conducted with 43 medication-nonadherent individuals with bipolar disorder.
CAE modules were administered as indicated by a screen that identifies reasons for nonadherence. The primary outcome was change in adherence to mood-stabilizing medications as measured by the Tablet Routines Questionnaire and pill counts. Secondary outcomes included change in symptoms, measured by the Hamilton Rating Scale for Depression (HAM-D), Young Mania Rating Scale (YMRS), and Brief Psychiatric Rating Scale (BPRS).
Participants completed 76% of sessions. Dropout at three months was 13 (30%). Adherence improved from a baseline mean±SD of 34%±27% of tablets missed in the past month to only 10%±15% (p<.001). BPRS, HAM-D, andYMRS scores all indicated significant improvement at three-month follow-up (p<.05).
Although conclusions must be tempered by the uncontrolled design, CAE appeared to be well accepted and was associated with improvements in adherence, symptoms, and functioning.
对 43 名患有双相情感障碍且药物治疗不依从的患者进行了为期三个月的前瞻性试验,以评估一种心理社会干预措施——定制依从增强(CAE)。
根据识别不依从原因的筛查结果,为患者提供 CAE 模块。主要结局指标是通过 Tablet Routines Questionnaire 和药丸计数来衡量的情绪稳定剂药物的依从性变化。次要结局指标包括症状的变化,通过汉密尔顿抑郁量表(HAM-D)、Young 躁狂评定量表(YMRS)和简明精神病评定量表(BPRS)进行测量。
参与者完成了 76%的疗程。三个月时的辍学率为 13(30%)。依从性从基线时过去一个月漏服药物的平均±SD 34%±27%提高到仅 10%±15%(p<.001)。BPRS、HAM-D 和 YMRS 评分在三个月随访时均表明有显著改善(p<.05)。
尽管结论必须受到非控制设计的限制,但 CAE 似乎被很好地接受,并与依从性、症状和功能的改善相关。