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Equipamentos para pesquisa

Autorização ANVISA nº K6L5L3M48211

   : : QUEM SOMOS
 
   : : PRODUTOS
    •  EEG  
    •  EEG Ambulatorial
    •  Vídeo EEG
    •  Sleep PSG
    •  PSG Ambulatorial
    •  EMG / PE
    •  IOM
    •  Digitimer D185
    •  NeuroScan
    •  TSA-II
    •  VSA-3000
    •  Patway
    •  ThermalStim
    •  Estimuladores
    •  Holter de ECG
    •  Sleep Ambulatory
   : : COMPUMEDICS
    •  Somnea
    •  Somté
    •  Somté PSG
    •  Safiro
    •  Siesta
    •  E Serie EEG
    •  E Serie PSG
    •  Neuvo EEG LTM
   : : NEUROSCAN
    •  EEG/PE Research
    •  ESI
    •  MAGLINK
    •  Nuamps
    •  SCAN 4.3 e 4.4
    •  SCAN Nuamps Ex
    •  Stim
    •  Stim2
    •  SynAmps
    •  SynAmps2
    •  ToolBox
    •  Curry 5.0
    •  Curry 6
    •  Source 2.0
   : : PASTAS PARA
     ELETROENCEFALOGRIA
     E POLISSONOGRAFIA
    •  Pasta Condutiva
    •  Pasta Condutiva
     e Adesiva
    •  Pasta Abrasiva
     Escarificante
    •  Gel Condutivo
   : : SENSORES SONO
     Conserto e
     Reforma de
     Sensores para
     Polissonografia
    •  Faixa de Esforço
     Respiratório
     Torácico / Abdominal
    •  Sensor de Fluxo
     Buconasal - Termistor
    •  Sensor de Fluxo
     Buconasal - Termopar
    •  Transdutor de Fluxo
     Aéreo e Ronco para
     Cânula
    •  Sensor de Ronco
     Microfone
    •  Sensor de Ronco
     Piezoelétrico
    •  Sensor de Movimento
     de Pernas
    •  Sensor de Posição
    •  Eletrodos para EEG
     Copa Dourada 10 mm  
     Pino Touchproof
    •  Eletrodos para EEG
     Copa Dourada 10 mm  
     Pino Banana 2 mm
    •  Eletrodos para EEG
     Copa Dourada 10 mm  
     Pino Banana 4 mm
     Eletrodos para EEG
     Copa de Chumbo 
     Pino Touchproof
     Eletrodos para EEG
     Copa de Chumbo 
     Pino Banana 2mm
     Eletrodos para EEG
     Copa de Chumbo 
     Pino Banana 4mm
    : : SENSOR DE
      OXÍMETRO SPO2
    •  Clip de Dedo
    •  Clip de Orelha
    •  Flexi-Site Infantil
    : : ESTIMULADOR
    •  Digitimer D185
    : : MEDOC
    •  TSA II
     Neuro Sensory Analyzer
    •  TSA II - Accessories
    •  VSA-3000 - Vibratory
   
 Sensory Analyzer
    •  PATHWAY
    •  PATHWAY
     Model CHPS
    •  PATHWAY
     Model CHEPS 
     Accessories
    •  Pathway Model ATS
    •  Pathway Model ATS
     Accessories
    : : RIMED
     Doppler TCD
     Digi-Lite
    •  Doppler Transcraniano
     DTC Digi-Lite IP
     Carotid Image
     Ultrasound Color
    : : NEUROLINKS
    •  Eletromiografia
    •  Estimuladores
    •  Epilepsia
    •  Sono
    •  Sleep Glossary
    •  Diabetes
    •  Dor Crônica
    •  Hanseníase
    : : OUTROS LINKS
    •  Biolink
    •  Biolink1
    •  Biolink2
    •  Biolink3
    •  Biolink4
    •  Biolink5
    •  Biolink6
    •  Biolink7
    •  Biolink8
    •  Biolink9
    •  Biolink9
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
   
Medical Background
There are numerous disorders of the peripheral and central nervous system that lead to chronic pain states (see below). The pathophysiology of nerve injury in chronic pain can be highly complex and can therefore lead to unpredictable response to treatment courses. Patient history, physical and various standard tools have historically been used to evaluate the nociceptive system, often lacking sensivity and with inherent examiner bias. Imaging tools represent the most commonly used diagnostic tools, although these represent a picture of anatomy, not a measure of nerve function and can be associated with a significant number of false-positives. EMG and nerve conduction testing do not evaluate small-caliber, pain-mediating C and A-delta fibers.

Quantitative Sensory Testing (QST)
Quantitative Sensory Testing (QST) enables the user to evaluate specific components of the nociceptive system, including pain-mediating unmyelinated C-fibers that can be extremely useful to the practicing pain physician. The TSA-II NeuroSensory Analyzer allows investigation of the coexistence of pain with both central and peripheral nervous system abnormalities, to include permitting diagnosis of neuropathic pain syndromes. "In the clinical setting, quantitative sensory testing is becoming a clinical standard for evaluation of certain chronic pain conditions" (Stojanovic et al; Current Review of Pain, 1998).

Nerve Fibers
Nerves consist of fibers of variable diameter with the thicker fibers having a faster conduction velocity. Three types of fibers are generally recognized in the sensory subclass of nerve fibers, with small-caliber, pain-mediating fibers representing roughly 70% of the peripheral nerve system:

A-beta fibers, the largest fibers, mediate the sensations of touch and mild pressure, as well as the sensation of position of joints and vibration, at a conduction velocity above 30 m/sec.

A-delta fibers, smaller than A-beta fibers, mediate the sensation of cold and the first components of the sensation of pain, at a conduction velocity between 2 and 30 m/sec.

C fibers, the slowest and smallest, mediate the sensation of warmth and the main component of the sensation of pain, at a conduction velocity less than 2 m/sec. In addition, C fibers subserve most of the autonomic peripheral functions.
Small-caliber fibers (i.e., A-delta & C-fibers) constitute 70% of the peripheral nerve system, with C and A-delta fibers responsible for pain transmission. Several disease processes afflict the peripheral nerves, some of which affect the entire spectrum of fibers, while others are selective. These include metabolic diseases such as diabetes mellitius and uremia, chronic alcohol abuse, local compression of a peripheral nerve such as carpal tunnel syndrome and nerve injuries related to occupational injury, automobile accidents, etc. Traditionally, the clinical assessment of neural dysfunction consists of a clinical bedside examination and nerve conduction velocity, as well as muscle electrical activity (EMG), sampling solely large (and fast) peripheral nerve fibers.