Patient-reported outcomes and daily activity assessed with a digital wearable device in patients with paroxysmal nocturnal hemoglobinuria treated with ravulizumab: REVEAL, a prospective, observational study.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-08-09 DOI:10.1186/s12955-024-02279-2
Elizabeth A Griffiths, Jae S Min, Wei-Nchih Lee, Jeffrey C Yu, Yogesh Patel, Karl-Johan Myren, David Dingli
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Abstract

Background: Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, chronic blood disorder. Symptoms such as fatigue can have a substantial impact on patients' physical activity levels, sleep, quality of life, and work productivity. Ravulizumab treatment can reduce thrombosis risk, improve survival and quality of life, and reduce fatigue in PNH, but information is limited on how it impacts sleep and physical activity. Here, data on resting heart rate, daily physical activity, and sleep in ravulizumab-treated patients with PNH were passively collected via a digital wearable activity-tracking device and patient-reported outcome (PRO) data were collected via weekly surveys in the same cohort.

Methods: REVEAL was a 32-week prospective observational cohort study in individuals with PNH receiving ravulizumab in the USA. A wrist-worn Fitbit™ collected data on resting heart rate, daily step count, and sleep duration from eligible patients. Patients also completed the following electronic weekly surveys: Functional Assessment of Chronic Illness Therapy (FACIT) - Fatigue, Patient-Reported Outcomes Measurement Information System (PROMIS) Global Physical Health, PROMIS Global Mental Health, PROMIS Sleep-Related Impairment and Sleep Disturbance, and Work Productivity and Activity Impairment Questionnaire - Specific Health Problem (WPAI-SHP). Data collected from the activity trackers and surveys were compared against US general population values reported in the literature.

Results: Twenty-eight ravulizumab-treated patients were included (median age: 34 years; 54% female). PRO scores were within US general population normative values, including FACIT-Fatigue (40.0), PROMIS Global Physical Health (51.0), Global Mental Health (51.0), Sleep-Related Impairment (50.0), and Sleep Disturbance (49.0). Similarly, mean resting heart rate (67 bpm), daily step count (7476), and sleep duration (7.7 h) were within the range of US general population values. Daily step count was positively correlated with PROMIS Global Physical and Mental Health scores.

Conclusions: This was the first study to use digital monitoring technology to collect data on physical activity and sleep in patients with PNH. The findings indicate that ravulizumab treatment enables patients with PNH to achieve activity levels (heart rate, sleep duration, step count) and quality of life that are comparable to those of the US general population. A weak positive correlation was identified between patient-reported physical and mental health and daily physical activity levels.

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使用数字可穿戴设备评估接受雷珠单抗治疗的阵发性夜间血红蛋白尿患者的患者报告结果和日常活动:REVEAL,一项前瞻性观察研究。
背景:阵发性夜间血红蛋白尿症(PNH)是一种罕见的慢性血液疾病:阵发性夜间血红蛋白尿症(PNH)是一种罕见的慢性血液疾病。疲劳等症状会严重影响患者的体力活动水平、睡眠、生活质量和工作效率。雷珠单抗治疗可降低血栓形成风险、提高存活率和生活质量,并减轻 PNH 患者的疲劳,但有关它如何影响睡眠和体力活动的信息却很有限。在此,我们通过数字可穿戴活动追踪设备被动收集了接受雷珠单抗治疗的PNH患者的静息心率、日常体力活动和睡眠数据,并通过每周调查收集了同一队列的患者报告结果(PRO)数据:REVEAL是一项为期32周的前瞻性观察性队列研究,研究对象是在美国接受雷珠单抗治疗的PNH患者。腕戴式 Fitbit™ 收集了符合条件的患者的静息心率、每日步数和睡眠时间等数据。患者还完成了以下每周电子调查:慢性疾病治疗功能评估 (FACIT) - 疲劳、患者报告结果测量信息系统 (PROMIS) 全球身体健康、PROMIS 全球心理健康、PROMIS 睡眠相关损害和睡眠干扰,以及工作效率和活动损害问卷 - 特定健康问题 (WPAI-SHP)。从活动追踪器和调查中收集的数据与文献中报道的美国普通人群数值进行了比较:纳入了28名接受过雷武利珠单抗治疗的患者(中位年龄:34岁;54%为女性)。PRO评分符合美国普通人群标准值,包括FACIT-疲劳(40.0)、PROMIS全球身体健康(51.0)、全球心理健康(51.0)、睡眠相关损害(50.0)和睡眠障碍(49.0)。同样,平均静息心率(67 bpm)、每日步数(7476 步)和睡眠时间(7.7 小时)也在美国普通人群的范围之内。每日步数与 PROMIS 全球身心健康评分呈正相关:这是第一项使用数字监测技术收集 PNH 患者体力活动和睡眠数据的研究。研究结果表明,雷珠单抗治疗可使 PNH 患者达到与美国普通人群相当的活动水平(心率、睡眠时间、步数)和生活质量。患者报告的身心健康与日常体育活动水平之间存在微弱的正相关性。
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