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BASIS-32 英国修订版的初步验证。

Preliminary validation of a UK-modified version of the BASIS-32.

出版信息

Int J Psychiatry Clin Pract. 2001;5(1):41-8. doi: 10.1080/136515001300225187.

DOI:10.1080/136515001300225187
PMID:24936997
Abstract

INTRODUCTION

The authors examined the reliability and validity of a UK-modified version of the Behavioral and Symptom Identification Scale (BASIS-32).

METHOD

Data from two samples of patients from acute psychiatric inpatient settings were used in the analyses ( n =303, n =92). The factor structure of the scale differed from that of the original BASIS-32.

RESULTS

Five factors emerged: (i) depression and anxiety, (ii) lability, (iii) psychosis, (iv) substance misuse and (v) functioning. The full scale of the modified BASIS demonstrated high internal consistency (Cronbach's alpha=0.93). Internal consistency for the subscales ranged from 0.86 to 0.45. The depression and anxiety subscale discriminated patients with a diagnosis of unipolar depression from those with other diagnoses (median score=3.11 (Inter quartile range (IQR)=2.67,3.33) versus median score=2.44 (1.67,3.11), P < 0.001). The substance misuse subscale discriminated patients with a diagnosis of alcohol or opiate dependence from those with other diagnoses (median score=2.33 (2, 3) versus median score=1.33 (0.67, 2), P < 0.001). However, the psychosis subscale did not differentiate patients with a psychotic illness from those with a nonpsychotic diagnosis (median score=1.4 (0.6,2.4) versus median score=1.2, (0.6,2), P = 0.16).

CONCLUSION

The total scale appeared to be at least as good as the Brief Symptom Inventory (BSI) in its responsiveness to change. The effect size for the BASIS=1.17 versus 0.91 for the BSI. Convergent validity was partially demonstrated between the modified BASIS and the BSI. ( Int J Psych Clin Pract 2001; 5:41-48).

摘要

介绍

作者研究了英国版行为和症状识别量表(BASIS-32)的可靠性和有效性。

方法

分析使用了来自急性精神病住院患者的两个样本的数据(n=303,n=92)。该量表的因子结构与原始 BASIS-32 不同。

结果

出现了五个因素:(i)抑郁和焦虑,(ii)不稳定性,(iii)精神病,(iv)物质滥用和(v)功能。修改后的 BASIS 全量表具有较高的内部一致性(Cronbach's alpha=0.93)。子量表的内部一致性范围为 0.86 至 0.45。抑郁和焦虑子量表可区分单相抑郁诊断与其他诊断的患者(中位数分数=3.11(四分位距(IQR)=2.67,3.33)与中位数分数=2.44(1.67,3.11),P <0.001)。物质滥用子量表可区分酒精或阿片类药物依赖诊断与其他诊断的患者(中位数分数=2.33(2,3)与中位数分数=1.33(0.67,2),P <0.001)。然而,精神病子量表并不能区分精神病患者与非精神病诊断的患者(中位数分数=1.4(0.6,2.4)与中位数分数=1.2(0.6,2),P=0.16)。

结论

在对变化的反应性方面,总量表似乎至少与简明症状量表(BSI)一样好。BASIS 的效应量为 1.17,BSI 为 0.91。修改后的 BASIS 与 BSI 之间显示出部分的收敛效度。(Int J Psych Clin Pract 2001; 5:41-48)。

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