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Published on: January 3, 2011
NeuroQuick--a novel bedside test for small fiber neuropathy?
Ida S Haussleiter1, Helmut Richter, Andrea Scherens
1Neurologische Universitätsklinik, Berufsgenossenschaftliche Universitätsklinik Bergmannsheil, Ruhr-Universität Bochum, Germany. ida@haussleiter.de
The NeuroQuick device is not a suitable bedside screening tool for cold hypaesthesia in neuropathic pain patients. It shows high specificity but low sensitivity, failing to reliably detect small fiber dysfunction.
Area of Science:
- Neurology
- Medical Devices
- Pain Management
Background:
- Small fiber neuropathy diagnosis lacks an appropriate bedside test.
- Cold hypaesthesia is an early symptom of small fiber neuropathy.
- The NeuroQuick (NQ) device was proposed for quantitative assessment of cold perception.
Purpose of the Study:
- To compare the NeuroQuick (NQ) device with quantitative sensory testing (QST).
- To evaluate NQ's performance in patients with chronic painful dysesthesia.
- To assess NQ's accuracy in detecting pathological cold detection thresholds (CDT).
Main Methods:
- Forty-one patients with chronic painful dysesthesia were enrolled.
- Quantitative sensory testing (QST) was performed per German network protocol.
- The NeuroQuick device was used for bedside quantitative cold thermal perception testing.
Main Results:
- The NeuroQuick showed 7.4% false positives and 50% false negatives for cold hypaesthesia.
- NQ demonstrated 92.6% specificity but only 50% sensitivity.
- Positive and negative predictive values for NQ were 78%.
Conclusions:
- The NeuroQuick is inadequate as a screening device for cold hypaesthesia in neuropathic pain.
- The device exhibits high specificity but insufficient sensitivity for small fiber dysfunction.
- A reliable screening tool requires both high sensitivity and specificity.
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