Gillick Bernadette T, Krach Linda E, Feyma Tim, Rich Tonya L, Moberg Kelli, Menk Jeremiah, Cassidy Jessica, Kimberley Teresa, Carey James R
Department of Physical Medicine and Rehabilitation, University of Minnesota Medical School, Minneapolis, MN.
Department of Physical Medicine and Rehabilitation, University of Minnesota Medical School, Minneapolis, MN; Gillette Children's Specialty Healthcare, St Paul, MN.
Arch Phys Med Rehabil. 2015 Apr;96(4 Suppl):S104-13. doi: 10.1016/j.apmr.2014.09.012. Epub 2014 Oct 2.
To investigate the safety of combining a 6-Hz primed low-frequency repetitive transcranial magnetic stimulation (rTMS) intervention in the contralesional hemisphere with a modified constraint-induced movement therapy (mCIMT) program in children with congenital hemiparesis.
Phase 1 randomized, double-blinded, placebo-controlled pretest/posttest trial.
University academic facility and pediatric specialty hospital.
Subjects (N = 19; age range, 8-17 y) with congenital hemiparesis caused by ischemic stroke or periventricular leukomalacia. No subject withdrew because of adverse events. All subjects included completed the study.
Subjects were randomized to 1 of 2 groups: either real rTMS plus mCIMT (n = 10) or sham rTMS plus mCIMT (n = 9).
Adverse events, physician assessment, ipsilateral hand function, stereognosis, cognitive function, subject report of symptoms assessment, and subject questionnaire.
No major adverse events occurred. Minor adverse events were found in both groups. The most common events were headaches (real: 50%, sham: 89%; P = .14) and cast irritation (real: 30%, sham: 44%; P = .65). No differences between groups in secondary cognitive and unaffected hand motor measures were found.
Primed rTMS can be used safely with mCIMT in congenital hemiparesis. We provide new information on the use of rTMS in combination with mCIMT in children. These findings could be useful in research and future clinical applications in advancing function in congenital hemiparesis.
探讨在先天性偏瘫患儿中,将对侧半球6赫兹启动的低频重复经颅磁刺激(rTMS)干预与改良的强制性使用运动疗法(mCIMT)方案相结合的安全性。
1期随机、双盲、安慰剂对照的预测试/后测试试验。
大学学术机构和儿科专科医院。
由缺血性中风或脑室周围白质软化症引起的先天性偏瘫受试者(N = 19;年龄范围8 - 17岁)。没有受试者因不良事件退出。所有纳入的受试者均完成了研究。
受试者被随机分为2组中的1组:真正的rTMS加mCIMT(n = 10)或假rTMS加mCIMT(n = 9)。
不良事件、医生评估、患侧手功能、实体觉、认知功能、受试者症状报告评估和受试者问卷。
未发生重大不良事件。两组均发现轻微不良事件。最常见的事件是头痛(真正的:50%,假的:89%;P = 0.14)和石膏刺激(真正的:30%,假的:44%;P = 0.65)。在次要认知和未受影响的手部运动测量方面,两组之间未发现差异。
启动的rTMS与mCIMT联合用于先天性偏瘫是安全的。我们提供了关于rTMS与mCIMT联合用于儿童的新信息。这些发现可能对先天性偏瘫功能改善的研究和未来临床应用有用。