From the Department of Neurology (J.A.A.), and School of Public Heath (M.B.F.), Division of Biostatistics, University of Minnesota, Minneapolis; Department of Neurology (M.P., M.M.D.), University of Kansas Medical Center, Kansas City; Department of Neurology (S.A.-D.), Northwestern University, Chicago, IL; Department of Neurology (T.H.B.), Columbia University Medical Center, New York, NY; Neurology at Johns Creek (A.A.C.), LLC, Atlanta, GA; BriovaRx (T.W.), Lenexa, KS; Department of Neurology (J.T.K.), Ohio State University, Columbus; Department of Neurology (I.M.), Maastricht University Medical Centre+; Curaçao Medical Center (I.M.), Willemstad, the Netherlands; Department of Neurology (K.C.G.), St. Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA; and Department of Neurology (R.A.L.), Cedars-Sinai Medical Center, Los Angeles, CA.
Neurology. 2021 Apr 6;96(14):e1876-e1886. doi: 10.1212/WNL.0000000000011703. Epub 2021 Feb 16.
The objective of this study was to explore the extent of IV immunoglobulin (IVIG) treatment-related fluctuations (TRFs) by using home collection of daily grip strength in patients with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and to use that information to develop evidence-based treatment optimization strategies.
This prospective observational study included 25 patients with well-defined CIDP. Participants recorded grip strength daily for 6 months. Disability and gait metrics were collected weekly. Serum immunoglobulin G levels were obtained at peak, trough, and midcycle IVIG intervals. Day-to-day grip strength changes <10% were considered random. To identify patients with TRFs, 3-day averaged grip strength was calculated on each consecutive day after an IVIG infusion. TRFs were defined as ≥10% 3-day averaged grip strength difference compared to the pre-IVIG baseline.
Participants successfully recorded grip strength on all but 9% of recordable days. Twelve patients (48%) were classified as low/no fluctuaters and 13 (52%) as frequent fluctuaters. In the frequent fluctuating group, grip strength improved over 1 week and thereafter was relatively stable until the third week after infusion. Grip strength was significantly correlated with measures of disability.
Grip strength collection by patients at home is reliable, valid, and feasible. A change in grip strength by ≥10% is a useful, practical, and evidence-based approach that may be used to identify clinically meaningful TRFs. From these data, we propose a treatment optimization strategy for patients with CIDP on chronic IVIG that may be applied to routine clinic care during both face-to-face and virtual video or telephone patient encounters.
ClinicalTrials.gov Identifier: NCT02414490.
本研究旨在通过使用家庭每日握力采集来探索慢性炎症性脱髓鞘性多发性神经病(CIDP)患者中静脉注射免疫球蛋白(IVIG)治疗相关波动(TRFs)的程度,并利用这些信息制定基于证据的治疗优化策略。
本前瞻性观察性研究纳入了 25 例明确诊断为 CIDP 的患者。参与者记录了 6 个月的每日握力。每周收集残疾和步态指标。在 IVIG 高峰期、低谷期和中期采集血清免疫球蛋白 G 水平。每日握力变化 <10% 被认为是随机的。为了确定有 TRFs 的患者,在 IVIG 输注后连续每天计算 3 天平均握力。TRFs 定义为与 IVIG 前基线相比,3 天平均握力差异≥10%。
除了 9%的可记录天数外,参与者成功记录了所有握力数据。12 名患者(48%)被归类为低/无波动者,13 名患者(52%)为频繁波动者。在频繁波动组中,握力在 1 周内得到改善,此后直到输注后第 3 周相对稳定。握力与残疾测量指标显著相关。
患者在家中进行握力采集是可靠、有效且可行的。握力变化≥10%是一种有用、实用且基于证据的方法,可用于识别具有临床意义的 TRFs。根据这些数据,我们提出了一种针对慢性 IVIG 治疗的 CIDP 患者的治疗优化策略,可应用于面对面和虚拟视频或电话患者就诊期间的常规临床护理。
ClinicalTrials.gov 标识符:NCT02414490。