Quantitative Sensory Testing (QST) - Does assessing ... - TI Pharma
Quantitative Sensory Testing (QST) - Does assessing ... - TI Pharma
Quantitative Sensory Testing (QST) - Does assessing ... - TI Pharma
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5. <strong>QST</strong> in patients with tendinopathy<br />
are adequate (Visentini et al 1998; Zwerver et al 2009).<br />
Healthy control athletes were recruited from local sports clubs and through<br />
advertisements on websites. Inclusion criteria for participation of this study were a<br />
VISA-P score had to be above 90. All subjects were asked neither to take analgesics<br />
24h before participation in the study nor to take part in sport activities on the day<br />
of the study. Subjects with diseases or conditions associated with possible altered<br />
somatosensory function, such as a knee surgery, diabetes, fibromyalgia or neurological<br />
diseases were excluded. All participants signed an informed consent prior to their<br />
inclusion <strong>QST</strong> testing was approved by the Medical Ethical Commission (Stichting<br />
Beoordeling Ethiek Bio-Medisch Onderzoek Assen, The Netherlands).<br />
2.2. <strong>Quantitative</strong> <strong>Sensory</strong> <strong>Testing</strong><br />
<strong>QST</strong> entails the measurement of the subjects’ responses to standardized thermal and<br />
mechanical stimuli. <strong>QST</strong> is used to determine detection, disappearances and pain<br />
thresholds. The German Research Network on Neuropathic Pain – DFNS has developed<br />
a standardized <strong>QST</strong> protocol. This protocol consists of 7 different tests that measure<br />
13 parameters, including various types of mechanical and thermal detection and pain<br />
thresholds for the hand, foot and face (Rolke et al 2006a). <strong>QST</strong> was performed by<br />
two research nurses, who had undergone a comprehensive training at the DNFS in<br />
Germany. All tests were performed in the same research facility. Thermal <strong>QST</strong> tests<br />
were performed using the Medoc Pathway System (Medoc, Israel) and consisted of<br />
threshold assessments for warm and cold detection (WDT, CDT) and heat pain and<br />
cold pain (HPT, CPT). Thermal measurements were obtained with ramped stimuli (1<br />
˚C/s) that were terminated when the subject pressed a button. Minimal and maximal<br />
temperatures were 0 and 50 ˚C. The baseline temperature was 32 ˚C. In addition, subjects<br />
were asked about paradoxical heat sensations (PHS) during the thermal sensory limen<br />
(TSL) procedure of alternating warm and cold stimuli.<br />
Mechanical <strong>QST</strong> tests consisted of seven different parameters. The mechanical<br />
detection threshold (MDT) was determined with a standardized set of modified von<br />
Frey filaments (Optihair2-Set, Marstock Nervtest, Germany). The mechanical pain<br />
threshold (MPT) was measured using a set of seven pinprick devices with fixed stimulus<br />
intensities that exerted forces of 8, 16, 32, 64, 128, 256, and 512 mN. Mechanical pain<br />
sensitivity (MPS) was assessed using the same set of seven weighted pinprick stimuli<br />
to obtain a stimulus–response function for pinprick-evoked pain. Dynamic mechanical<br />
allodynia (DMA) was assessed as part of the test above, using a set of three light tactile<br />
stimulators as dynamic innocuous stimuli: cotton wisp, cotton wool tip fixed to an<br />
elastic strip and a standardized brush (SENSElab No.5 Somedic, Sweden). Vibration<br />
disappearance threshold (VDT) was performed with a Rydel–Seiffer graded tuning<br />
fork (64 Hz, 8/8 scale) that was placed on the patellar tendon; the vibration is graded<br />
from 0 to 8 (max). The wind up ratio (WUR) test was assessed with a pinprick intensity