pemeriksaan elektrodiagnostik pada neuropati
Transcription
pemeriksaan elektrodiagnostik pada neuropati
PEMERIKSAAN ELEKTRODIAGNOSTIK PADA NEUROPATI HERIANTO DIVISI NEUROLOGI EKA HOSPITAL BSD Update on Diabetic Neuropathy - Nov. 4th 2013 PENDAHULUAN Px elektrodiagnostik (Edx) → gangguan neuromuskuler Edx rutin → - NCS - RNS - Late responses - Needle EMG Edx ↔ NCS + Needle EMG Tujuan px Edx: Lokalisasi dan tingkat keparahan kelainan saraf tepi Tipe saraf tepi yang terlibat Patofisiologi yang mendasari → degenerasi aksonal / demielinisasi Perjalanan waktu Pada umumnya tidak dapat menentukan etiologi secara pasti Anatomi • Susunan saraf tepi meliputi: – Saraf kranial • (kecuali n. optikus) – Radiks spinalis – dorsal root ganglia – peripheral nerve trunks and their terminal branches – Sistim saraf otonom Saraf Tepi Characteristics of the disease Nerve cell body: motor neuron disease (1) Motor neuron axon/neuromuscular junction: peripheral neuropathy (2&3) Muscle degeneration: myopathy (4) Pola distribusi neuropati Tipe-tipe saraf tepi Saraf motorik – dari medulla spinalis ke otot Saraf sensorik – dari reseptor sensorik menuju ke medula spinalis Small fiber (pain, temperature) Large fiber (vibration, position, balance) Saraf otonom – mengatur tekanan darah, keringat, fungsi kandung kemih, denyut jantung, peristaltik usus Mekanisme kerusakan saraf tepi PENENTUAN DERAJAT KERUSAKAN SARAF TEPI Edx membantu menentukan patomekanisme neuropati - demielinisasi, degenerasi aksonal atau tipe campuran. Demielinisasi → remielinisasi ›beberapa minggu Degenerasi aksonal (primer/sekunder) → prognosis lebih buruk Fase akut → secara klinis tidak dapat dibedakan antara degenerasi aksonal dengan demielinisasi • Neuromuscular Junction – Myasthenia Gravis – Lambert-Eaton – Myasthenic - Syphilis, SS paraneoplastic – Muscle Myelin Sheath Sensory Ganglionitis – Polymyositis - Guillain-Barré Syndrome - CIDP – Rhabdomyolysis - MCBN • Motor neuron Disease – ALS/WNV – Polio – West Nile Virus Axonal Neuropathy – Diabetes – Alcohol Symptoms Weakness Pain Burning Thick soles Walking on stones Tingling Imbalance Stimulation Simplified Model A nerve is a Chain of Polarized Membrane Segments (Myelin Action). Stimulation in one point generates a depolarization. - + - + - + - + - + - + Electrical Shock Mechanical Compression Magnetic Field + - + - + - + A nerve could be depolarized by: - - + Current Stimulation + + - + - + - + - + - + - + - + - + - + - + - NERVE Supramaximal Stimuli Min. 3 Times Sensory Threshold Depolarization + - + - + - + - + - + - + - + - + - + - - ORTHODROMIC + + NERVE ANTIDROMIC Once a nerve is depolarized at some point, a wave of depolarization passes in both directions from that point. Propagation - Refractory Period + + - + - + - + - + - - + - + + - + - + - + - NERVE Propagation by Successive Depolarization followed by Repolarization. Time before Repolarization is called the Refractory Period. Motor Latency Motor Response + - + + - + - + - + - + - + - + - + - + S MOTOR LATENCY in ms = Propagation Time from S to M - + - NERVE M NERVE CONDUCTION STUDIES (NCS) Nerve conduction study (NCS) : stimulation and recording of electrical activity individual peripheral nerves with sufficient accuracy, reproducibility, and standardization to determine normal values, characterize abnormal findings, and correlate neurophysiologic-pathologic features. These clinical studies are used to: Diagnose focal and generalized disorders of peripheral nerves Aid in the differentiation of primary nerve and muscle disorders (although NCS itself evaluates nerve and not muscle) Classify peripheral nerve conduction abnormalities due to axonal degeneration, demyelination, and conduction block Prognosticate regarding clinical course and efficacy of treatment Motor Conduction Median Nerve Latency Rec. 3.5 ms Wrist Stim. 1 8.2 ms Elbow Stim. 2 Diff.: 4.7 ms Distance mm: Recording: Surface Electrodes Stimulation: Handgrip or Bipolar 240 C.V.: 51 m/s Sensory Conduction Ulnaris Nerve AVERAGING Stimulation Latency ms 2.6 Distance mm 155 Digit V CV m/s 60 Latency ms 3.1 Distance mm 175 Recording Digit IV CV m/s 56 Nerve Conduction Studies • • Prolonged latency and conduction velocity suggest pathology of the myelin sheath, which is most commonly affected in entrapment and demyelinating neuropathy. Reduced CMAP indicates a loss of axons, suggesting a more severe and longstanding compression or degeneration (axonal neuropathy). F-waves and H-reflex Useful for identifying proximal segmental demyelination Can only be done when motor amplitude is > 1 mV Extremely heightdependent ELECTROMYOGRAPHY (EMG) • The clinical study of the electrical activity muscle fibers individually and collectively. of • This electrical activity can be recorded via surface or needle electrodes. • The latter being used far more commonly in the clinical setting, and is evaluated during needle insertion, during periods of rest (spontaneous activity), and during periods of voluntary muscle contraction Needle Electromyography: Data Insertional Activity Spontaneous Activity Motor Unit Configuration Motor Unit Recruitment Interference Pattern EMG - Normal • Normal spontaneous activity - silent • Normal Motor Unit -3 phases • Normal firing of multiple units, filling screen EMG - Abnormal • Fibrillations - single muscle fibers contract • Polyphasic MUPs reorganization of motor units due to axon loss and reinnervation • Rapid firing of single, polyphasic MUPs indicates axon loss TAKE HOME MASSAGE HAL-HAL PENTING YANG PERLU DIPERHATIKAN DALAM PEMERIKSAAN EDX 1. 2. 3. NCS dan EMG merupakan kelanjutan dari pemeriksaan klinis Bila didapatkan hasil yang meragukan, selalu pikirkan kemungkinan adanya faktor teknis. Apabila kondisi pemeriksaan Edx meragukan, lakukan pemeriksaan ulang. 5. 6. 7. Temuan Edx harus dilaporkan dalam konteks gejala klinis yang menyertai dan diagnosis kerja dari klinisi yang merujuk pasien. Bila pertimbangan korelasi klinis-Edx meragukan, jangan membuat diagnosis yang berlebihan Selalu pikirkan tentang korelasi kliniselektrofisiologis → gejala klinis, NCS dan EMG LIMITATIONS • The limitations of EMG/NCS should be taken into account when interpreting the findings. – There is no reliable means of studying proximal sensory nerves. – NCS results can be normal in patients with small-fiber neuropathies – Lower extremity sensory responses can be absent in normal elderly patients. • EMG/NCS are not substitutes for a good clinical examination. When to order NCSs and EMG Mononeuropathy Mononeuropathy Multiplex Radiculopathy Plexopathy (Brachial or Lumbosacral) Anterior Horn Cell Disorders Diffuse neuropathies Cranial neuropathies Neuromuscular Junction Disorders Myopathy When Not to order NCSs and EMG Central Nervous System Disorders (Stroke, TIA, Encephalopathy, spinal cord injury) Multiple Sclerosis Total body fatigue, fibromyalgia Joint pain Unexplained weakness (without a neurologic consultation) Failed back, S/P multiple neck and low back surgeries TERIMA KASIH ATAS PERHATIANNYA !!! ASPEK TEKNIS PEMERIKSAAN ELEKTRODIAGNOSTIK MOTOR CONDUCTION STUDY Motor NCS Parameters Distal Latency Amplitude determined by conduction velocity of the nerve, neuromuscular junction & muscle determined by number of muscle fibers activated Proximal conduction velocity determined by conduction velocity of the fastest fibers SENSORY CONDUCTION STUDY Sensory NCS Parameters Onset and peak latencies Conduction velocity determined by velocity of a very few fast fibers Amplitude determined by the number of large sensory fibers activated LATE RESPONSE F- RESPONSE F-RESPONSE H-REFLEX H-REFLEX REPETITIVE NERVE STIMULATION (RNS) REPETITIVE NERVE STIMULATION (RNS) NEUROPHYSIOLOGY TRAINING PROGRAM EEG and EMG Workshop, Tan Tock Seng Hospital, Singapore, November 2009 Neurophysiology Training, Neurophysiology Clinic, Gasthuisberg University Hospital, Leuven – Belgium, 2011 Mayo Clinic EMG, EEG and Neurophysiology in Clinical Practice, Mayo School of Continuous Development Program, Jacksonville, Florida, USA, February 24 – March 2, 2013