在接受屈昔多巴治疗的神经源性直立性低血压人群中,对患者报告的 "好日子坏日子 "单项评估进行心理计量学验证。

Q2 Medicine Journal of market access & health policy Pub Date : 2022-01-10 eCollection Date: 2022-01-01 DOI:10.1080/20016689.2021.2010961
Clément François, Nicola Germain, Renata Majewska, Vanessa Taieb, L Arthur Hewitt, Steven Kymes
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引用次数: 0

摘要

背景:神经源性正张力性低血压(nOH)的症状包括头昏/眩晕、晕厥前、晕厥和跌倒,可导致功能受损和生活质量下降。由于静力性低血压症状的严重程度和发生频率时有时无,患者可能很难使用现有的结果测量方法准确量化症状对其日常生活的影响。我们开发了一种新的单项工具 "好日子坏日子",并对其在 nOH 患者中的心理测量有效性进行了评估:方法:采用一项为期 6 个月的前瞻性观察性队列研究的数据,研究对象为新开始接受屈昔多巴治疗的 nOH 患者。患者被要求量化过去7天中好的和坏的天数,并对其他经过验证的患者报告结果工具做出回答。对 "好日子和坏日子 "工具的并发效度、判别效度和稳定性进行了评估:共有 153 名患者参与分析(平均年龄为 62.3 [17]岁)。好日子数量的变化与其他患者报告结果的改善呈中度相关(rho 值范围为 -0.38 至 -0.61)。当对数据进行分类(症状严重程度低与症状严重程度高)检查时,症状严重程度低的亚组在1、3和6个月时的平均好天数更高(所有P均≤0.01):好日子坏日子工具在基线和随时间变化的情况下都有很好的区分度,有助于评估 nOH 症状对患者的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Psychometric validation of a patient-reported single-item assessment of 'Good Day Bad Day' in a neurogenic orthostatic hypotension population treated with droxidopa.

Background: Symptoms of neurogenic orthostatic hypotension (nOH), including lightheadedness/dizziness, presyncope, syncope, and falls, can lead to impaired functional ability and reduced quality of life. Because the severity and frequency of nOH symptoms fluctuate, it may be difficult for patients to accurately quantify the effect of symptoms on their daily lives using available outcome measures. A new single-item instrument, the 'Good Day Bad Day,' was developed, and its psychometric validity was assessed in patients with nOH.

Methods: Data from a 6-month, prospective, observational cohort study of patients with nOH who were newly initiating droxidopa treatment were used. Patients were asked to quantify the number of good and bad days in the previous 7 days and responded to other validated patient-reported outcomes instruments. The concurrent and discriminant validities and the stability of the Good Day Bad Day instrument were assessed.

Results: A total of 153 patients were included in the analysis (mean [SD] age, 62.3 [17] years). Change in the number of good days moderately correlated with improvements in other patient-reported outcomes (rho value range, -0.38 to -0.61). When data were examined categorically (low vs high symptom severity), the mean number of good days was higher in subgroups representing low symptom severity across measures at 1, 3, and 6 months (all P ≤ 0.01).

Conclusions: The Good Day Bad Day instrument provided good discrimination at baseline and over time and may aid in assessment of the effects of nOH symptoms on patients.

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