플러스100%마이너스

  • 화면크기
통합검색

한의약융합데이터센터


근거중심한의약 DB

Home > 한의약융합데이터센터 > 근거중심한의약 DB
Title

뇌졸중 후 우울증에 대한 천왕보심단의 유효성 및 안전성 연구 : 무작위 배정, 이중맹검, 비열등성 연구.

Authors

이일석, 김문수, 이상관.

Journal

대한한방내과학회지.

Year

2014

Vol (Issue)

35(2)

Page

145-156.

doi

PMID

Url

MeSH

Keywords

Tianwangbuxin-dan; Fluoxetine; poststroke depression; Beck’s depression inventory; Hamilton depression rating scale

한글 키워드

천왕보심단; 플루옥세틴; 뇌졸중 후 우울증; 벡 우울 척도; 해밀턴 우울평가 척도

KMCRIC
Summary & Commentary

KMCRIC 비평 보기 +

Korean Study

Y

Abstract

Objectives : The aim of this study was to compare Tianwangbuxin-dan to Fluoxetine for antidepressive efficacy and safety in poststroke depression (PSD).

Methods : A randomized, double blinded, non-inferiority trial was conducted. 113 PSD patients were recruited from a stroke center. Except for the 25 excluded patients, 88 PSD patients were randomly given either Tianwangbuxin-dan 1100 ㎎ or Fluoxetine 20 ㎎ per a day for 16 weeks. PSD was evaluated using Beck’s depression inventory (BDI) and Hamilton depression rating scale (HDRS) and followed every fourth week. Repeated measure analysis of variance (ANOVA) was used to compare and contrast the depression scores of the two groups and to compare them among the evaluation times, at the beginning, 4th, 8th, 12th and 16th weeks. In addition, independent t-tests were used to find the difference between two groups at every evaluation time.

Results : Finally, 88 PSD patients were included in the study, 63 PSD patients completed the procedure and 25 PSD patients were dropped out by the incompliance or withdrawal of consent. Tianwangbuxin-dan (or Fluoxetine) improved the depression of stroke patients and the efficacy of Tianwangbuxin-dan was not inferior to that of Fluoxetine. In addition, there was no significant side effect in two groups.

Conclusions : This study showed that antidepressive efficacy and safety of Tianwangbuxin-dan in PSD patients.

국문초록

Language

한국어

첨부파일