Division of Biobehavioral Nursing and Health Informatics, Department of Nursing, University of Washington, Seattle, WA, USA.
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA, USA.
BMC Pulm Med. 2024 Jul 24;24(1):360. doi: 10.1186/s12890-024-03148-w.
Pulmonary exacerbations (PExs) in people with cystic fibrosis (PwCF) are associated with increased healthcare costs, decreased quality of life and the risk for permanent decline in lung function. Symptom burden, the continuous physiological and emotional symptoms on an individual related to their disease, may be a useful tool for monitoring PwCF during a PEx, and identifying individuals at high risk for permanent decline in lung function. The purpose of this study was to investigate if the degree of symptom burden severity, measured by the Cystic Fibrosis Respiratory Symptom Diary (CFRSD)- Chronic Respiratory Infection Symptom Scale (CRISS), at the onset of a PEx can predict failure to return to baseline lung function by the end of treatment.
A secondary analysis of a longitudinal, observational study (N = 56) was conducted. Data was collected at four time points: year-prior-to-enrollment annual appointment, termed "baseline", day 1 of PEx diagnosis, termed "Visit 1", day 10-21 of PEx diagnosis, termed "Visit 2" and two-weeks post-hospitalization, termed "Visit 3". A linear regression model was performed to analyze the research question.
A regression model predicted that recovery of lung function decreased by 0.2 points for every increase in CRISS points, indicating that participants with a CRISS score greater than 48.3 were at 14% greater risk of not recovering to baseline lung function by Visit 2, than people with lower scores.
Monitoring CRISS scores in PwCF is an efficient, reliable, non-invasive way to determine a person's status at the beginning of a PEx. The results presented in this paper support the usefulness of studying symptoms in the context of PEx in PwCF.
囊性纤维化(CF)患者的肺部恶化(PEx)与医疗保健费用增加、生活质量下降以及肺功能永久性下降的风险有关。症状负担是指个体与其疾病相关的持续生理和情绪症状,可能是监测 PEx 期间 CF 患者的有用工具,并可识别出肺功能永久性下降风险较高的个体。本研究旨在探讨 PEx 发作时症状负担严重程度(通过囊性纤维化呼吸症状日记(CFRSD)-慢性呼吸道感染症状量表(CRISS)测量)是否可以预测治疗结束时无法恢复到基线肺功能。
对一项纵向观察性研究(N=56)进行了二次分析。数据在四个时间点收集:入组前一年的年度预约,称为“基线”,PEx 诊断的第 1 天,称为“就诊 1”,PEx 诊断的第 10-21 天,称为“就诊 2”和住院后两周,称为“就诊 3”。进行线性回归模型分析以回答研究问题。
回归模型表明,CRISS 评分每增加 1 分,肺功能恢复就会降低 0.2 分,这表明 CRISS 评分大于 48.3 的患者在就诊 2 时恢复到基线肺功能的风险比得分较低的患者高 14%。
监测 CF 患者的 CRISS 评分是一种有效、可靠、非侵入性的方法,可以确定 PEx 开始时患者的状况。本文介绍的结果支持在 CF 患者的 PEx 背景下研究症状的有用性。