Fujita Masaya, Ishizuka Takuya
Juntendo Iji Zasshi. 2023 Sep 29;69(5):370-377. doi: 10.14789/jmj.JMJ22-0024-OA. eCollection 2023.
Alongside non-pharmacological intervention, pharmacotherapy particularly with atypical antipsychotics is assumed to be effective for behavioral and psychological symptoms of dementia (BPSD).
This retrospective study investigated the effectiveness and safety of pharmacotherapy including antipsychotics in outpatients or inpatients with BPSD.
Of all Alzheimer-type dementia (AD) patients with BPSD initiating treatment between March and August 2011, a total of 102 patients available for 12-month follow-up comprised the subjects in this chart review. Of these, 68 (66.7%) continued treatment in the ambulatory or inpatient setting, with their MMSE scores improved from 17.3 ± 3.6 at baseline to 18.3 ± 3.53, 17.9 ± 3.80 and 17.0 ± 4.14 after 3, 6 and 12 months, respectively. In contrast, their NPI scores were significantly different from 11.7 ± 11.2 at baseline to 4.86 ± 5.40, 3.56 ± 4.65 and 2.27 ± 3.77 after 3, 6 and 12 months, respectively. Of the 36 inpatients available for follow-up, 27 (75%) on concurrent antipsychotics (chlorpromazine [CP] equivalent, 162.2 mg) at baseline remained on concurrent antipsychotics (CP equivalent, 212.5 mg) after 12 months, while, of the 66 outpatients available for follow-up, 13 (19.7%) on concurrent antipsychotics (CP equivalent, 93.4 mg) at baseline remained on concurrent antipsychotics (CP equivalent, 113.0 mg) after 12 months.
Study results confirmed the effectiveness and safety of the study treatment in Japanese AD patients with BPSD for up to 12 months. How best to incorporate antipsychotics into the treatment of BPSD in clinical settings lies in the hands of us Japanese clinicians.
除了非药物干预外,药物治疗尤其是使用非典型抗精神病药物被认为对痴呆的行为和心理症状(BPSD)有效。
这项回顾性研究调查了药物治疗(包括抗精神病药物)对BPSD门诊或住院患者的有效性和安全性。
在2011年3月至8月间开始治疗的所有患有BPSD的阿尔茨海默病型痴呆(AD)患者中,共有102例可进行12个月随访的患者纳入了本次图表回顾研究。其中,68例(66.7%)在门诊或住院环境中继续接受治疗,其简易精神状态检查表(MMSE)评分从基线时的17.3±3.6分别提高到3个月后的18.3±3.53、6个月后的17.9±3.80和12个月后的17.0±4.14。相比之下,他们的神经精神症状问卷(NPI)评分从基线时的11.7±11.2分别显著变化到3个月后的4.86±5.40、6个月后的3.56±4.65和12个月后的2.27±3.77。在36例可进行随访的住院患者中,27例(75%)在基线时同时使用抗精神病药物(氯丙嗪[CP]等效剂量,162.2毫克),12个月后仍继续使用抗精神病药物(CP等效剂量,212.5毫克),而在66例可进行随访的门诊患者中,13例(19.7%)在基线时同时使用抗精神病药物(CP等效剂量,93.4毫克),12个月后仍继续使用抗精神病药物(CP等效剂量,113.0毫克)。
研究结果证实了该研究治疗方法在日本患有BPSD的AD患者中长达12个月的有效性和安全性。如何在临床环境中最佳地将抗精神病药物纳入BPSD的治疗,掌握在我们日本临床医生手中。