University of Florida, Fixel Institute for Neurological Diseases, Gainesville, FL, USA.
Center for Networked Biomedical Research in Neurodegenerative Diseases (CIBERNED), Carlos III Institute of Health, Madrid, Spain.
BMC Neurol. 2022 Jan 24;22(1):35. doi: 10.1186/s12883-022-02560-1.
The burden of Parkinson's disease (PD) worsens with disease progression. However, the lack of objective and uniform disease classification challenges our understanding of the incremental burden in patients with advanced Parkinson's disease (APD) and suboptimal medication control. The 5-2-1 criteria was proposed by clinical consensus to identify patients with advancing PD. Our objective was to evaluate the screening accuracy and incremental clinical burden, healthcare resource utilization (HCRU), and humanistic burden in PD patients meeting the 5-2-1 screening criteria.
Data were drawn from the Adelphi Parkinson's Disease Specific Program (DSP™), a multi-country point-in-time survey (2017-2020). People with PD who were naive to device-aided therapy and on oral PD therapy were included. Patients meeting the 5-2-1 screening criteria had one or more of the three clinical indicators of APD: (i) ≥5 doses of oral levodopa/day, OR (ii) "off" symptoms for ≥2 h of waking day, OR (iii) ≥1 h of troublesome dyskinesia. Clinician assessment of PD stage was used as the reference in this study. Clinical screening accuracy of the 5-2-1 criteria was assessed using area under the curve and multivariable logistic regression models. Incremental clinical, HCRU, and humanistic burden were assessed by known-group comparisons between 5 and 2-1-positive and negative patients.
From the analytic sample (n = 4714), 33% of patients met the 5-2-1 screening criteria. Among physician-classified APD patients, 78.6% were 5-2-1 positive. Concordance between clinician judgment and 5-2-1 screening criteria was > 75%. 5-2-1-positive patients were nearly 7-times more likely to be classified as APD by physician judgment. Compared with the 5-2-1-negative group, 5-2-1-positive patients had significantly higher clinical, HCRU, and humanistic burden across all measures. In particular, 5-2-1-positive patients had 3.8-times more falls, 3.6-times higher annual hospitalization rate, and 3.4-times greater dissatisfaction with PD treatment. 5-2-1-positive patients also had significantly lower quality of life and worse caregiver burden.
5-2-1 criteria demonstrated potential as a screening tool for identifying people with APD with considerable clinical, humanistic, and HCRU burden. The 5-2-1 screening criteria is an objective and reliable tool that may aid the timely identification and treatment optimization of patients inadequately controlled on oral PD medications.
帕金森病(PD)的负担随着疾病的进展而恶化。然而,缺乏客观和统一的疾病分类标准,使得我们难以理解晚期帕金森病(APD)患者的增量负担,以及药物控制不佳的情况。临床共识提出的 5-2-1 标准用于识别进展性 PD 患者。我们的目的是评估符合 5-2-1 筛选标准的 PD 患者的筛查准确性和增量临床负担、医疗资源利用(HCRU)和人文负担。
数据来自 Adelphi Parkinson's Disease Specific Program(DSP™),这是一项多国家时点调查(2017-2020 年)。纳入对设备辅助治疗和口服 PD 治疗均无经验的 PD 患者。符合 5-2-1 筛选标准的患者有 APD 的三个临床指标之一:(i)每天口服左旋多巴≥5 剂,或(ii)清醒日“关期”症状≥2 小时,或(iii)出现≥1 小时的麻烦性运动障碍。本研究中,临床医生评估的 PD 阶段作为参考。使用曲线下面积和多变量逻辑回归模型评估 5-2-1 标准的临床筛查准确性。通过已知组比较,评估 5-2-1 阳性和阴性患者之间的增量临床、HCRU 和人文负担。
在分析样本(n=4714)中,33%的患者符合 5-2-1 筛选标准。在医生分类的 APD 患者中,78.6%为 5-2-1 阳性。临床医生判断与 5-2-1 筛选标准的一致性>75%。与 5-2-1 阴性组相比,5-2-1 阳性患者更有可能被医生判断为 APD,约为 7 倍。与 5-2-1 阴性组相比,5-2-1 阳性患者在所有指标上的临床、HCRU 和人文负担都明显更高。特别是,5-2-1 阳性患者跌倒的风险增加了 3.8 倍,年住院率增加了 3.6 倍,对 PD 治疗的满意度降低了 3.4 倍。5-2-1 阳性患者的生活质量也明显下降,照顾者负担更重。
5-2-1 标准可作为识别 APD 患者的工具,具有相当的临床、人文和 HCRU 负担。5-2-1 筛选标准是一种客观可靠的工具,可能有助于及时识别和优化口服 PD 药物治疗控制不佳的患者。