REFERRAL AND DIAGNOSTIC TRENDS IN PEDIATRIC ELECTROMYOGRAPHY IN THE MOLECULAR ERA

被引:13
作者
Karakis, Ioannis [1 ,2 ,3 ]
Liew, Wendy [1 ]
Darras, Basil T. [1 ]
Jones, H. Royden [1 ,2 ]
Kang, Peter B. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Neurol, Boston Childrens Hosp, Boston, MA 02115 USA
[2] Lahey Clin Fdn, Dept Neurol, Burlington, MA USA
[3] Emory Univ, Sch Med, Dept Neurol, Atlanta, GA 30322 USA
关键词
clinical neurophysiology; EMG; pediatric EMG; pediatric neuromuscular disorders; practice of electromyography; MUSCLE BIOPSY; NEUROMUSCULAR DISORDERS; NERVE-CONDUCTION; DISEASE; POLYNEUROPATHIES; MONONEUROPATHY; ULTRASOUND; MYASTHENIA; ACCURACY; SPECTRUM;
D O I
10.1002/mus.24152
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Major advances in genetic analysis and neuroimaging have modified the traditional diagnostic approach for neuromuscular disorders. The purpose of this study was to investigate the role of electromyography (EMG) in the molecular era. Methods: We retrospectively surveyed reports of all EMG studies performed at Boston Children's Hospital from 2001 through 2011. Data were collected on study numbers, patient ages, referring provider subspecialty, study indication, electrophysiological diagnosis, and study utility. Results: A total of 2100 studies were performed. The volume increased from similar to 160 to similar to 250 studies/year. There was a trend toward studying older children. Neurologists, including neuromuscular specialists, constituted the major referral pool, whereas referrals from orthopedics increased steadily. Polyneuropathies followed by mononeuropathies were the most common indications and diagnoses. Fifty-seven percent of studies were normal. EMG provided meaningful information in 94% of cases. Conclusion: EMG continues to play a cardinal role in the diagnosis of pediatric neuromuscular disorders, although its practice paradigm is evolving.
引用
收藏
页码:244 / 249
页数:6
相关论文
共 57 条
[1]   A Practical Approach to Molecular Diagnostic Testing in Neuromuscular Diseases [J].
Arnold, W. David ;
Flanigan, Kevin M. .
PHYSICAL MEDICINE AND REHABILITATION CLINICS OF NORTH AMERICA, 2012, 23 (03) :589-+
[2]  
Bady B, 1983, Rev Electroencephalogr Neurophysiol Clin, V13, P282, DOI 10.1016/S0370-4475(83)80039-2
[3]   DIAGNOSTIC ACCURACY OF CLINICAL DATA, QUANTITATIVE ELECTROMYOGRAPHY AND HISTOCHEMISTRY IN NEUROMUSCULAR DISEASE - STUDY OF 105 CASES [J].
BLACK, JT ;
BHATT, GP ;
DEJESUS, PV ;
SCHOTLAND, DL ;
ROWLAND, LP .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1974, 21 (JAN) :59-70
[4]   A COMPARISON OF HISTOLOGIC AND ELECTROMYOGRAPHIC FINDINGS IN VARIOUS NEUROMUSCULAR DISORDERS [J].
BRUSA, A ;
SACCO, G ;
MORETTI, G ;
LOEB, C .
NEUROLOGY, 1963, 13 (08) :630-&
[5]   THE DIAGNOSTIC YIELD OF QUANTIFIED ELECTROMYOGRAPHY AND QUANTIFIED MUSCLE BIOPSY IN NEUROMUSCULAR DISORDERS [J].
BUCHTHAL, F ;
KAMIENIECKA, Z .
MUSCLE & NERVE, 1982, 5 (04) :265-280
[6]   Multifocal slowing of nerve conduction in metachromatic leukodystrophy [J].
Cameron, CL ;
Kang, PB ;
Burns, TM ;
Darras, BT ;
Jones, HR .
MUSCLE & NERVE, 2004, 29 (04) :531-536
[7]  
Cetin E., 2009, Annals of Physical and Rehabilitation Medicine, V52, P546, DOI 10.1016/j.rehab.2009.06.004
[8]   A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3 [J].
Chew, Sheena ;
Balasubramanian, Ravikumar ;
Chan, Wai-Man ;
Kang, Peter B. ;
Andrews, Caroline ;
Webb, Bryn D. ;
MacKinnon, Sarah E. ;
Oystreck, Darren T. ;
Rankin, Jessica ;
Crawford, Thomas O. ;
Geraghty, Michael ;
Pomeroy, Scott L. ;
Crowley, William F., Jr. ;
Jabs, Ethylin Wang ;
Hunter, David G. ;
Grant, Patricia E. ;
Engle, Elizabeth C. .
BRAIN, 2013, 136 :522-535
[9]   JUVENILE MYASTHENIA GRAVIS [J].
Chiang, Laura M. ;
Darras, Basil T. ;
Kang, Peter B. .
MUSCLE & NERVE, 2009, 39 (04) :423-431
[10]   CLINICAL ELECTROPHYSIOLOGY OF INFANTILE BOTULISM [J].
CORNBLATH, DR ;
SLADKY, JT ;
SUMNER, AJ .
MUSCLE & NERVE, 1983, 6 (06) :448-452