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Practice Parameter and Literature Review of the Usefulness of ...

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<strong>Practice</strong> <strong>Parameter</strong>: Carpal Tunnel Syndromeelectrodiagnosis.96. Hansson S. The association between nerve conduction velocity <strong>and</strong><strong>the</strong> compound action potential amplitude during ischemic blocking.Electromyogr Clin Neurophysiol 1999;39:113-122. Criteria Met (3/6:1,3,4) Source: Medline Search. Abstract: Ischemia was produced byinflating a tourniquet around <strong>the</strong> upper arm in five healthy subjects.When antidromic median sensory NCV <strong>and</strong> SNAP amplitudes wererecorded from <strong>the</strong> third digit with stimulation at <strong>the</strong> elbow, wrist <strong>and</strong>palm, <strong>the</strong> amplitude <strong>and</strong> CV decreased in parallel. This sequence <strong>of</strong>changes duplicates <strong>the</strong> blocking <strong>of</strong> nerve conduction during wristflexion in healthy subjects <strong>and</strong> CTS patients described previously(Hansson 1995).97. Hansson S, Nilsson BY. Median sensory nerve conduction blockduring wrist flexion in <strong>the</strong> carpal tunnel syndrome. Electromyogr ClinNeurophysiol 1995;35:99-105. Criteria Met (5/6: 1,2,3,5,6) Source:Medline Search. Abstract: Prospective study <strong>of</strong> <strong>the</strong> effect <strong>of</strong>prolonged passive wrist flexion on median <strong>and</strong> ulnar sensoryamplitude <strong>and</strong> latency in 10 normal controls <strong>and</strong> 30 CTS patients witha clinical diagnosis <strong>of</strong> CTS <strong>of</strong> whom 10 had mild abnormalities <strong>of</strong>median sensory latency measurements: digit wrist CV 0.4 ms.During prolonged (up to 45 min) passive wrist flexion, <strong>the</strong> antidromicmedian (wrist to 2nd finger) <strong>and</strong> ulnar (wrist to 5th finger) SNAPwere recorded. The measurements were made every 2.5 min duringsustained passive wrist flexion for up to 45 min <strong>and</strong> <strong>the</strong> time (T50) for<strong>the</strong> amplitude to fall to 50% <strong>of</strong> <strong>the</strong> initial amplitude determined. Themedian sensory conduction (but not <strong>the</strong> ulnar) became partiallyblocked in all CTS patients <strong>and</strong> also in 8 out <strong>of</strong> 10 controls. Mediansensory nerve conduction returned to normal in all subjects 30seconds after release <strong>of</strong> flexion. At 10 minutes <strong>of</strong> wrist flexion, nosignificant increase <strong>of</strong> <strong>the</strong> median SNAP peak latency in normalsubjects (mean 0.01 ± 0.04 ms) <strong>and</strong> CTS patients (mean 0.24 ± 0.26ms) was noted. The time (T50) necessary to reach a 50% reduction inmedian SNAP amplitude in 8 out <strong>of</strong> 10 probable CTS patients <strong>and</strong> in14 out <strong>of</strong> possible 20 CTS patients was below <strong>the</strong> lowest recordedvalue in <strong>the</strong> control group (25 min). It was shown that ischemiacaused <strong>the</strong> block (reduction in median SNAP amplitude) bydemonstrating (1) that <strong>the</strong> reversal <strong>of</strong> a 70% block with release <strong>of</strong>wrist flexion was prevented by inflating a pneumatic cuff around <strong>the</strong>upper arm to above systolic pressure for 5 minutes before release <strong>of</strong>wrist flexion after which (2) <strong>the</strong> SNAP amplitude returned to normal30 seconds after deflating <strong>the</strong> cuff. Determination <strong>of</strong> T50 <strong>of</strong> <strong>the</strong>median nerve SNAP during wrist flexion has <strong>the</strong> potential to add to<strong>the</strong> sensitivity <strong>and</strong> specificity <strong>of</strong> <strong>the</strong> electrophysiological diagnosis <strong>of</strong>CTS.98. Harmon RL, Naylor AH. Sensory <strong>and</strong> mixed nerve action potentialtemporal dispersion in median neuropathy at <strong>the</strong> wrist. Am J PhysMed Rehabil 1999;78:213-215. Criteria Met (1/6: 6) Source: MedlineSearch. Abstract: Retrospective study to determine <strong>the</strong> usefulness <strong>of</strong>measuring SNAP <strong>and</strong> mixed nerve AP temporal dispersion todiagnose CTS demonstrated that increased median mixed nerve APtemporal dispersion may occur in association with peak latencyprolongation in CTS. However, <strong>the</strong> small magnitude <strong>of</strong> <strong>the</strong> increasemakes <strong>the</strong> clinical usefulness <strong>of</strong> this observation unclear.99. Healy C, Watson JD, Longstaff A, Campbell MJ. Magnetic resonanceimaging <strong>of</strong> <strong>the</strong> carpal tunnel. J H<strong>and</strong> Surg Br 1990;15:243-248.Criteria Met (3/6: 1,2,3) Source: Medline Search.100. Herrick RT, Herrick SK. Thermography in <strong>the</strong> detection <strong>of</strong> carpaltunnel syndrome <strong>and</strong> o<strong>the</strong>r compressive neuropathies. J H<strong>and</strong> SurgAm 1987;12:943-949. Criteria Met (1/6: 1) Source: Medline Search.101. *Holmgren H, Rabow L. Internal neurolysis or ligament division onlyin carpal tunnel syndrome. II. A 3 year follow-up with an evaluation<strong>of</strong> various neurophysiological parameters for diagnosis. ActaNeurochir (Wien) 1987;87:44-47. Criteria Met (2/6: 1,2) Source:Medline Search.102. *Holmgren-Larsson H, Leszniewski W, Linden U, Rabow L,Thorling J. Internal neurolysis or ligament division only in carpaltunnel syndrome—results <strong>of</strong> a r<strong>and</strong>omized study. Act Neurochir(Wien) 1985;74:118-121. Criteria Met (0/6) Source: Holmgren, 1987.103. *Homan MM, Franzblau A, Werner RA, Albers JW, Armstrong TJ,Bromberg MB. Agreement between symptom surveys, physicalexamination procedures <strong>and</strong> electrodiagnostic findings for <strong>the</strong> carpaltunnel syndrome. Sc<strong>and</strong> J Work Environ Health 1999;25:115-124.Background Reference. Source: Medline Search. Abstract: The goal<strong>of</strong> this study was to evaluate <strong>the</strong> concordance between various clinicalscreening procedures for carpal tunnel syndrome. The subjectpopulation consisted <strong>of</strong> 824 workers from 6 facilities. The proceduresevaluated included bilateral median sensory nerve conduction testing,physical examinations, <strong>and</strong> symptom surveys, including h<strong>and</strong>diagrams. The agreement between <strong>the</strong> outcomes <strong>of</strong> variouscombinations <strong>of</strong> <strong>the</strong>se procedures was assessed by determining <strong>the</strong>kappa coefficient. There was relatively poor overlap between <strong>the</strong>reported symptoms, <strong>the</strong> physical examination findings, <strong>and</strong> <strong>the</strong>electrodiagnostic results consistent with carpal tunnel syndrome.Overall, only 23 out <strong>of</strong> 449 subjects (5%) with at least 1 positivefinding met all 3 criteria (symptoms, physical examination findings,<strong>and</strong> electrophysiological results consistent with carpal tunnelsyndrome) for <strong>the</strong> dominant h<strong>and</strong>. The screening procedures showedpoor or no agreement with kappa values ranging between 0.00 <strong>and</strong>0.18 for all <strong>the</strong> case definitions evaluated for carpal tunnel syndrome.The poor overlap between <strong>the</strong> various screening procedures warnsagainst <strong>the</strong> use <strong>of</strong> electrodiagnostic findings alone without <strong>the</strong>symptom presentation being considered. The results <strong>of</strong> this study alsopoint to a need for <strong>the</strong> fur<strong>the</strong>r development <strong>and</strong> evaluation <strong>of</strong> methodsfor detecting carpal tunnel syndrome.104. Hughes ACR. An evaluation <strong>of</strong> 2 electrodiagnostic procedures inpatients with symptoms <strong>of</strong> a carpal tunnel syndrome.Electroencephalogr Clin Neurophysiol 1977;43:140. Criteria Met(0/6) (abstract only) Source: AAEM Consultant 1993.105. *Imai T, Matsumoto H, Minami R. Asymptomatic ulnar neuropathyin carpal syndrome. Arch Phys Med Rehabil 1990;71:992-994.Criteria Met (3/6: 1,3,5) Source: Medline Search.106. Imaoka H, Yorifuji S, Takahashi M, Nakamura Y, Kitaguchi M, TaruiS. Improved inching method for <strong>the</strong> diagnosis <strong>and</strong> prognosis <strong>of</strong> carpaltunnel syndrome. Muscle Nerve 1992;15:318-324. Criteria Met (5/6:2,3,4,5,6) Source: Medline Search. Abstract: A modified sensory“inching” method for <strong>the</strong> electrodiagnosis <strong>of</strong> CTS is described. Themedian nerve as stimulated at <strong>the</strong> cubital segment with 8 channelrecording electrodes placed at 15 mm intervals along <strong>the</strong> mediannerve from a point 3 cm proximal to <strong>the</strong> distal wrist crease up to <strong>the</strong>middle finder. Eight consecutive SNAP were recorded <strong>and</strong> <strong>the</strong>negative peak latency measured. Each latency (ms) was plottedagainst distance (mm). The results were a linear relationship (1) fromchannel 1 to 8 in 32 normal subjects <strong>and</strong> (2) from channel 1 to at leastchannel 4 in CTS patients. In 73 <strong>of</strong> 84 (87%) limbs <strong>of</strong> CTS patients,<strong>the</strong>re was a conductive abnormality in <strong>the</strong> distal recordings asdetermined by discontinuous changes in <strong>the</strong> SNAP latency (greaterthan 0.6 ms) or amplitude (absence <strong>of</strong> response). The results suggestthat this method provides high sensitivity <strong>and</strong> specificity for <strong>the</strong>diagnosis <strong>of</strong> CTS. A prospective study with comparison to currenttechniques would help determine whe<strong>the</strong>r or not <strong>the</strong> technique hasadvantages over current recommended techniques.107. Iyer V, Fenichel GM. Normal median nerve proximal latency incarpal tunnel syndrome: a clue to coexisting Martin-Gruberanastomosis. J Neurol Neurosurg Psychiatry 1976;39:449-452.Background Reference. Source: AAEM Consultant 1993.108. Jablecki CK, Andary MT, Di Benedetto M, Horowitz SH, Marino RJ,Rosenbaum RB, Shields RW, Stevens JC, Williams FH. AmericanAssociation <strong>of</strong> Electrodiagnostic Medicine. Guidelines for outcomestudies in electrodiagnostic medicine. Muscle Nerve 1996;19:1626-1635. Source: AAEM 2000 CTS Task Force member.109. Jablecki CK, Andary MT, So YT, Wilkins DE, Williams FH.<strong>Literature</strong> review <strong>of</strong> <strong>the</strong> usefulness <strong>of</strong> nerve conduction studies <strong>and</strong>electromyography for <strong>the</strong> evaluation <strong>of</strong> patients with carpal tunnelsyndrome. Muscle Nerve 1993;16:1392-1444. Background Reference.Source: AAEM 2000 CTS Task Force member.110. Jackson D, Clifford JC. Electrodiagnosis <strong>of</strong> mild carpal tunnelsyndrome. Arch Phys Med Rehabil 1989;70:199-204. Criteria Met(6/6: 1,2,3,4,5,6) Source: Medline Search. Abstract: This studyevaluated <strong>the</strong> following techniques: (a) median nerve stimulation in<strong>the</strong> palm <strong>and</strong> recording proximal at <strong>the</strong> wrist (8 cm), (b) sensorylatency difference between median <strong>and</strong> radial stimulation at <strong>the</strong> wrist<strong>and</strong> recording on <strong>the</strong> thumb (10 cm), (c) medial-ulnar sensory latencydifference with stimulation at <strong>the</strong> wrist <strong>and</strong> recording on <strong>the</strong> ringfinger (14 cm), (d) median-ulnar sensory latency difference withstimulation in <strong>the</strong> palm <strong>and</strong> recording at <strong>the</strong> wrist (8 cm), <strong>and</strong> (e)Muscle & Nerve Supplement X 2002 S965

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