Monday, October 31, 2016
Clinical prediction rules for prognosis and treatment prescription in neck pain: A systematic review
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Thursday, October 27, 2016
Are physiotherapists adhering to quality indicators for the management of knee osteoarthritis? An observational study
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Wednesday, October 26, 2016
Neuropsychology: Pain passed on by smell
Neuropsychology: Pain passed on by smell
Nature 538, 7626 (2016). doi:10.1038/538430c
Mice housed in the same room as one another can pass certain types of pain to each other through smell.Exposure to inflammatory molecules or withdrawal from drugs or alcohol can cause hyperalgesia, a painful hypersensitivity to touch, heat or chemical irritants. Andrey Ryabinin and
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An incidental finding
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An unusual cause of a mass in the groin
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Monday, October 24, 2016
Updating the definition of pain
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Spotlight on pain: optogenetic approaches for interrogating somatosensory circuits
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Mindfulness-based stress reduction and cognitive behavioral therapy for chronic low back pain: similar effects on mindfulness, catastrophizing, self-efficacy, and acceptance in a randomized controlled trial
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Opioid prescribing for patients with cancer in the last year of life: a longitudinal population cohort study
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Does degree of vulvar sensitivity predict vulvodynia characteristics and prognosis?
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National Trends in Direct Healthcare Expenditures Among Us Adults With Migraine: 2004-2013
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Evaluation of computed tomography in patients with atypical angina or chest pain clinically referred for invasive coronary angiography: randomised controlled trial
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Sunday, October 23, 2016
Threat and fear of pain induces attentional bias to pain words: An eye-tracking study
Abstract
Background
This study aimed to investigate the effects of fear of pain (FOP) and threat on attentional biases, using eye-tracking methods.
Method
One hundred and seven undergraduate students were randomized to receive threatening or reassuring information about the cold pressor task; and divided into high and low FOP groups. Participants completed the dot-probe task, while their eye movements were tracked.
Results
Results showed that those who received threatening information were less likely to have their first fixation on pain words, particularly affective pain words. Furthermore, under conditions of high threat, the high FOP group who did fixate on affective pain words, fixated more quickly than for sensory pain words, whereas the opposite was the case under low threat. In regression analyses, initial vigilance towards affective pain words was a significant predictor of reporting pain more quickly on the cold pressor.
Conclusions
Taken together, these results suggest that initial vigilance of affective pain stimuli predicts actual hypervigilance to an acute experimental pain task. However, under conditions of high threat, participants show evidence of avoidance of affective pain words, even though when they do fixate on these stimuli, the high FOP group does so more quickly. These results confirm that attentional processes, characterized by vigilance avoidance, appear important.
Significance
Interventions that change attention towards pain to reduce vigilance and subsequent avoidance may be indicated to improve pain outcomes.
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Saturday, October 22, 2016
Extinction of fear generalization: a comparison between fibromyalgia patients and healthy controls
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Functional characterization of at-level hypersensitivity in patients with spinal cord injury
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Thursday, October 20, 2016
Exploration of conditioned pain modulation effect on long-term potentiation-like pain amplification in humans
Abstract
Background
This study aimed to explore conditioned pain modulation (CPM) effect on long-term potentiation (LTP)-like pain amplification induced by cutaneous 10-Hz conditioning electrical stimulation (CES).
Methods
Conditioned pain modulation was induced by cold pressor conditioning stimulus (CPCS) (4 °C) which was applied immediately before CES in the active session. In the control session, water with a temperature of 32 °C was used. Twenty subjects participated in two sessions in a randomized crossover design with at least 1-week interval. Perceptual intensity ratings to single electrical stimulation (SES) at the conditioned skin site and to pinprick and light-stroking stimuli in the immediate vicinity of the CES electrodes were measured . Superficial blood flow (SBF), skin temperature (ST) and heat pain threshold (HPT) were measured covering both homotopic and heterotopic skin. The pain intensities during CES process were measured and short-form McGill Pain Questionnaire (SF-MPQ) was used for assessing CES pain experience.
Results
Cold pressor conditioning stimulus reduced pain perception increments to weak pinprick and light-stroking stimuli after 10-Hz CES compared with the control session. Moreover, CPCS resulted in lower pain intensity ratings during CES process but without affecting the SF-MPQ scores between two sessions. The SBF and ST increased after CES and then gradually declined but without differences between CPCS and control sessions. CPM did not affect HPT and pain intensity increments to SES.
Conclusions
The CPCS inhibited heterotopic perception amplification to weak mechanical stimuli after CES. The results indicate that endogenous descending inhibitory systems might play a role against development of non-nociceptive perception amplificatory states (e.g. allodynia).
Significance
Conditioned pain modulation (CPM) may play a role in inhibiting the pain amplificatory process at the central nervous system and prompting central desensitization. CPM has a special inhibition effect for the development of perception amplification to non-painful mechanical stimuli.
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When Less Is More: The indications for MIS Techniques and Separation Surgery in Metastatic Spine Disease
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Cognitive Interventions and Nutritional Supplements (The CINS Trial): A Randomized Controlled, Multicenter Trial Comparing a Brief Intervention With Additional Cognitive Behavioral Therapy, Seal Oil, and Soy Oil for Sick-Listed Low Back Pain Patients
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Can Patients With Low Back Pain Be Satisfied With Less Than Expected?
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Wednesday, October 19, 2016
Neuroscience: Why mole rats don't feel the heat
Neuroscience: Why mole rats don't feel the heat
Nature 538, 7625 (2016). doi:10.1038/538293c
A gene variant could explain why naked mole rats are impervious to certain types of pain that most mammals experience when exposed to heat.In the nervous system, a peptide called nerve growth factor (NGF) mediates hypersensitivity to pain caused by heat. Gary Lewin at
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A mass on the spine indicating Pott’s disease
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Tuesday, October 18, 2016
Quiet dissent: The attitudes, beliefs and behaviours of UK osteopaths who reject low back pain guidance – A qualitative study
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Authors’ reply to Hawkins
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