Huang Ting-Ying, Wei Yu-Jung, Moyo Patience, Harris Ilene, Lucas Judith A, Simoni-Wastila Linda
Department of Pharmaceutical Health Services Research, School of Pharmacy, University of Maryland, Baltimore, Maryland.
IMPAQ International, LLC, Columbia, Maryland.
J Am Geriatr Soc. 2015 Sep;63(9):1757-65. doi: 10.1111/jgs.13606. Epub 2015 Aug 27.
To assess changes in behavioral symptoms associated with Alzheimer's disease and related dementias (ADRDs) after antipsychotic (AP) or antidepressant (AD) treatment and to estimate the effect of treatment response on mortality risk.
Retrospective cohort study using 2006-2009 Medicare administrative and prescription drug claims data linked to Minimum Data Set 2.0.
Long-stay (≥101 days) nursing home residents.
Continuously enrolled fee-for-service Medicare beneficiaries who had ADRDs, initiated (no use in prior 6 months) AP (n = 2,035) or AD (n = 1,661) treatment during or after one or more behavioral symptoms (verbally abusive, physically abusive, socially inappropriate or disruptive behavior) presented, and had reassessment of behavioral symptoms after 3 consecutive months of the initiated treatment.
Behavioral symptom change was measured according to score (range 0-9, based on number and frequency of symptoms) change between baseline and reassessment (improved, <0; unchanged, 0; worsened, >0). Survival analyses were conducted on time to death after reassessment, comparing residents whose symptoms improved with those whose symptoms remained unchanged or worsened.
APs and ADs were comparable in treatment effectiveness, as evidenced by more than 85% of the behavioral symptom episodes in each cohort improving or remaining stable. Mortality risk was lower in both cohorts (AP: adjusted hazard ratio (aHRAP ) = 0.93, 95% confidence interval (CI) = 0.81-1.07; AD: aHRAD = 0.82, 95% CI = 0.70-0.97) for residents whose symptoms improved than for those whose symptoms unchanged or worsened.
ADs may be reasonable pharmacological alternatives to APs in clinical management of ADRD-related behavioral symptoms. Initial treatment response may alter medication-associated mortality risk. Further study is needed to confirm findings using other data and behavioral symptom-specific instruments.
评估抗精神病药物(AP)或抗抑郁药物(AD)治疗后与阿尔茨海默病及相关痴呆症(ADRDs)相关的行为症状变化,并估计治疗反应对死亡风险的影响。
回顾性队列研究,使用2006 - 2009年医疗保险行政和处方药索赔数据,并与最低数据集2.0相链接。
长期居住(≥101天)的养老院居民。
连续登记的按服务收费的医疗保险受益人,他们患有ADRDs,在出现一种或多种行为症状(言语辱骂、身体虐待、社交不当或破坏性行为)期间或之后开始(过去6个月未使用)AP治疗(n = 2035)或AD治疗(n = 1661),并在开始治疗连续3个月后对行为症状进行重新评估。
行为症状变化根据基线和重新评估之间的评分变化(范围0 - 9,基于症状的数量和频率)来衡量(改善,<0; 不变,0; 恶化,>0)。对重新评估后的死亡时间进行生存分析,比较症状改善的居民与症状未改变或恶化的居民。
AP和AD在治疗效果上具有可比性,每个队列中超过85%的行为症状发作得到改善或保持稳定。症状改善的居民在两个队列中的死亡风险均低于症状未改变或恶化的居民(AP:调整后风险比(aHRAP)= 0.93,95%置信区间(CI)= 0.81 - 1.07;AD:aHRAD = 0.82,95% CI = 0.70 - 0.97)。
在ADRD相关行为症状的临床管理中,AD可能是AP合理的药理学替代药物。初始治疗反应可能会改变药物相关的死亡风险。需要进一步研究使用其他数据和行为症状特异性工具来证实这些发现。