33 results match your criteria: "Department of Neurology and Danish Pain Research Center[Affiliation]"

Thyroid [I]MIBG uptake is proposed as a tool for differentiating between Parkinson's disease (PD) and diabetes mellitus (DM) on [I]MIBG scintigraphies since both patient groups show decreased cardiac uptake. One study compared thyroid [I]MIBG uptake in DM and PD patients and reported reduced [I]MIBG uptake only in the PD group. Here, we investigated thyroid [I]MIBG uptake in patients with PD and DM and found severely reduced thyroid [I]MIBG uptake in DM.

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Background: Complex regional pain syndrome (CRPS) is a debilitating pain condition often resistant to standard treatment modalities. In these cases, spinal cord stimulation (SCS) can be an option, but the effect on CRPS remains disputed. We aimed to assess the long-term effect of SCS on CRPS.

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Schwann cell p75 neurotrophin receptor modulates small fiber degeneration in diabetic neuropathy.

Glia

December 2020

Department of Biomedicine, Danish Research Institute of Translational Neuroscience-DANDRITE, Nordic-EMBL Partnership for Molecular Medicine, Aarhus University, Aarhus C, Denmark.

Diabetic neuropathy has an incidence as high as 50% of diabetic patients and is characterized by damage to neurons, Schwann cells and blood vessels within the peripheral nervous system. The low-affinity neurotrophin receptor p75 (p75 ), particularly expressed by the Schwann cells in the peripheral nerve, has previously been reported to play a role in developmental myelination and cell survival/death. Increased levels of p75 , in the endoneurium and plasma from diabetic patients and rodent models of disease, have been observed, proposing that this receptor might be involved in the pathogenesis of diabetic neuropathy.

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Complex regional pain syndrome (CRPS) can be a debilitating, persistent, and treatment-resistant pain condition. This report presents a case of severe CRPS affecting multiple limbs, resistant to standard treatment modalities. Treatment with spinal cord stimulation (SCS) had an initial good effect.

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Background And Purpose: Trigeminal neuralgia (TN) is an extremely painful condition which can be difficult to diagnose and treat. In Europe, TN patients are managed by many different specialities. Therefore, there is a great need for comprehensive European guidelines for the management of TN.

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Context: Clinical trials have demonstrated the efficacy and safety of the capsaicin 8% patch in patients with peripheral neuropathic pain (PNP); however, few studies have assessed this treatment in a clinical practice.

Objective: To determine whether treatment and re-treatment with the capsaicin 8% patch reduce PNP intensity in clinical practice.

Methods: Three non-interventional, observational studies were concurrently conducted in Denmark, Norway and Sweden.

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Pre-diabetes and diabetes are a global epidemic, and the associated neuropathic complications create a substantial burden on both the afflicted patients and society as a whole. Given the enormity of the problem and the lack of effective therapies, there is a pressing need to understand the mechanisms underlying diabetic neuropathy (DN). In this review, we present the structural components of the peripheral nervous system that underlie its susceptibility to metabolic insults and then discuss the pathways that contribute to peripheral nerve injury in DN.

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The Impact of Serum Drug Concentration on the Efficacy of Imipramine, Pregabalin, and their Combination in Painful Polyneuropathy.

Clin J Pain

December 2017

*Department of Neurology, Odense University Hospital §Clinical Pharmacology, Institute of Public Health, University of Southern Denmark, Odense Departments of †Neurology ‡Department of Neurology and Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark.

Objective: The aim of this study was to explore the serum concentration-effect relation for first-line drugs in neuropathic pain and to determine if efficacy could be increased.

Methods: Data from a randomized, placebo-controlled, cross-over trial on imipramine, pregabalin, and their combination in painful polyneuropathy were used. Treatment periods were of 4 weeks' duration, outcome was the weekly median of daily pain rated by a 0 to 10 numeric scale, and drug concentrations were determined by high-performance liquid chromatography.

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Who is healthy? Aspects to consider when including healthy volunteers in QST--based studies-a consensus statement by the EUROPAIN and NEUROPAIN consortia.

Pain

November 2015

Division of Neurological Pain Research and Therapy, Department of Neurology, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Germany Department of Neurology, BG University Hospital Bergmannsheil GmbH, Ruhr-University Bochum, Bochum, Germany Department of Pain Medicine, BG University Hospital Bergmannsheil GmbH, Ruhr-University Bochum, Bochum, Germany INSERM U-987, Centre d'Evaluation et de Traitement de la Douleur, CHU Ambroise Paré, Boulogne-Billancourt, France Université Versailles-Saint-Quentin, Versailles, France Department Neurology and Psychiatry, Sapienza University, Roma, Italy Department of Neurology and Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark Department of Neurosurgery, Helsinki University Central Hospital, Helsinki, Finland Etera Mutual Pension Insurance Company, Helsinki, Finland Department of Pain Management and Research, Oslo University Hospital, Oslo, Norway Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden Department of Anaesthesiology, Critical Care Medicine, Pain Therapy & Palliative Care, Pain Center Lake Starnberg, Benedictus Hospital, Tutzing, Germany Neuroscience Discovery Research, Eli Lilly and Company, Indianapolis, IN, USA Pain Research, Department of Surgery and Cancer, Imperial College, London, United Kingdom H. Lundbeck A/S, Copenhagen, Denmark Department of Physiology and Pharmacology, Karolinska Institute, Stockholm, Sweden Department of Neurology, Odense University Hospital, Odense, Denmark Neuroscience Technologies, Barcelona, Spain Department of Neurology, Klinikum rechts der Isar, Technische Universität München, Munich, Germany Chair of Neurophysiology, Center of Biomedicine and Medical Technology Mannheim CBTM, Medical Faculty Mannheim, Heidelberg University, Germany (T. Mainka is now with the Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany).

Clinical and human experimental pain studies often include so-called "healthy" controls in investigations of sensory abnormalities, using quantitative sensory testing (QST) as an outcome measure. However, the criteria for what is considered "healthy" vary among the different studies and between study centers and investigators, partly explaining the high variability of the results. Therefore, several aspects should be considered during inclusion of healthy volunteers in QST-based trials to have homogenous groups of healthy controls with less variability between human experimental studies, so that results are less likely to be false negative or false positive because of subject-related factors.

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The aim of this investigation was to examine the prevalence of and factors associated with chronic pain in the pelvic area or lower extremities after rectal cancer treatment and its impact on quality of life (QoL). This is a population-based cross-sectional study of chronic pain and QoL in patients treated for rectal cancer from 2001 to 2007. A modified version of the Brief Descriptive Danish Pain Questionnaire and the European Organization for Research and Treatment of Cancer QLQ-C30 questionnaire were mailed to 1713 Danish patients.

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Neuropathic pain: principles of diagnosis and treatment.

Mayo Clin Proc

April 2015

Department of Neurology and Danish Pain Research Center, Aarhus University Hospital, Aarhus C, Denmark.

Neuropathic pain is caused by disease or injury of the nervous system and includes various chronic conditions that, together, affect up to 8% of the population. A substantial body of neuropathic pain research points to several important contributory mechanisms including aberrant ectopic activity in nociceptive nerves, peripheral and central sensitization, impaired inhibitory modulation, and pathological activation of microglia. Clinical evaluation of neuropathic pain requires a thorough history and physical examination to identify characteristic signs and symptoms.

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Imipramine and pregabalin combination for painful polyneuropathy: a randomized controlled trial.

Pain

May 2015

Department of Neurology, Odense University Hospital, Odense, Denmark Department of Neurology, Aalborg University Hospital, Aalborg, Denmark Department of Neurology and Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark Department of Clinical Pharmacology, Institute of Public Health, University of Southern Denmark, Odense, Denmark.

Monotherapy with first-line drugs for neuropathic pain often fails to provide sufficient pain relief or has unacceptable side effects because of the need for high doses. The aim of this trial was to test whether the combination of imipramine and pregabalin in moderate doses would relieve pain more effectively than monotherapy with either of the drugs. This was a randomized, double-blind, placebo-controlled, crossover, multicenter trial consisting of four 5-week treatment periods in patients with painful polyneuropathy.

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A new definition of neuropathic pain.

Pain

October 2011

Department of Neurology and Danish Pain Research Center, Aarhus University Hospital, Norrebrogade 44, Building 1A, DK-8000 Aarhus C, Denmark Sektion für Neurologische Schmerzforschung und -therapie, Klinik für Neurologie, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Kiel, Germany Department of Neurosurgery, Helsinki University Central Hospital, Helsinki, Finland Department of Anaesthesiology, Pain Clinic, Helsinki University, Helsinki, Finland Department of Neurological Surgery, University of Washington, Seattle, WA, USA Pain Research Group, Imperial College London, Chelsea and Westminster Hospital Campus, London, UK Chair of Neurophysiology, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

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Pain following thoracotomy: is it neuropathic?

Pain

January 2011

Department of Neurology and Danish Pain Research Center, Aarhus University Hospital, Norrebrogade 44, Building 1A, DK-8000 Aarhus C, Denmark Tel.: +45 8949 3380; fax: +45 8949 3269 Section of Surgical Pathophysiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.

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The evidence for pharmacological treatment of neuropathic pain.

Pain

September 2010

Department of Neurology and Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark Department of Neurology, Odense University Hospital, Odense, Denmark.

Randomized, double-blind, placebo-controlled trials on neuropathic pain treatment are accumulating, so an updated review of the available evidence is needed. Studies were identified using MEDLINE and EMBASE searches. Numbers needed to treat (NNT) and numbers needed to harm (NNH) values were used to compare the efficacy and safety of different treatments for a number of neuropathic pain conditions.

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Pharmacology and treatment of neuropathic pains.

Curr Opin Neurol

October 2009

Department of Neurology and Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark.

Purpose Of Review: This review briefly discusses the definition and clinical presentation of neuropathic pain and highlights recent advances in the treatment of neuropathic pain.

Recent Findings: Recent publications have confirmed the efficacy of tricyclic antidepressants, gabapentin, pregabalin, opioids, and tramadol for various neuropathic pain conditions. Selective serotonin noradrenaline reuptake inhibitors have been found to reduce pain in painful neuropathy.

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Fabry disease is an X-linked inherited lysosomal disorder with dysfunction of the lysosomal enzyme alpha-galactosidase A causing accumulation of glycolipids in multiple organs including the nervous system. Pain and somatosensory disturbances are prominent manifestations of this disease. Until recently disease manifestations in female carriers of Fabry disease have been questioned.

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Management of neuropathic pain.

Curr Opin Support Palliat Care

August 2007

Department of Neurology and Danish Pain Research Center, Aarhus University, Aarhus, Denmark.

Purpose Of Review: Neuropathic pain is a chronic pain condition arising from injury or disease of the peripheral or central nervous system with a substantial impact on quality of life. This brief review focuses on the increasing evidence for effective treatments and discusses an evidence-based algorithm for treating neuropathic pain conditions.

Recent Findings: Randomized controlled trials have consistently shown efficacy of tricyclic antidepressants, gabapentin/pregabalin, opioids, tramadol, and serotonin and noradrenaline-reuptake inhibitors for the treatment of various neuropathic pain conditions, lidocaine patches for postherpetic neuralgia and cannabinoids for pain in multiple sclerosis.

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Background: Surgical removal of third molars may carry a risk of developing persistent orofacial pain, and central sensitization appears to play an important role in the transition from acute to chronic pain.

Aim: The aim of this study was to investigate sensitization (primarily central sensitization) after orofacial trauma using quantitative sensory testing (QST).

Methods: A total of 32 healthy men (16 patients and 16 age-matched control subjects) underwent a battery of quantitative tests adapted to the trigeminal area at baseline and 2, 7, and 30 days following surgical removal of a lower impacted third molar.

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A PET activation study of brush-evoked allodynia in patients with nerve injury pain.

Pain

January 2006

Department of Neurology and Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark CFIN, Aarhus University and Aarhus University Hospital, Aarhus, Denmark PET unit and Department of Surgical Pathophysiology, Rigshospitalet, Copenhagen, Denmark Department of Oral Maxillofacial Surgery, Aarhus University Hospital, Aarhus, Denmark Department of Clinical Oral Physiology, Royal Dental College, Aarhus, Denmark.

Acute experimental brush-evoked allodynia induces a cortical activation pattern that differs from that typically seen during experimental nociceptive pain. In this study, we used positron emission tomography to measure changes in regional cerebral blood flow (rCBF) in patients with clinical allodynia. Nine patients with peripheral nerve injury were scanned during rest, brush-evoked allodynia, and brushing of normal contralateral skin.

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Background: Neuropathic pain in spinal cord injury is a common challenging therapeutic condition. The current study examines the analgesic effect of the sodium channel blocker lidocaine on neuropathic pain in patients with spinal cord injury and the predictive role of concomitant evoked pain on pain relief with lidocaine.

Methods: Twenty-four spinal cord injury patients with neuropathic pain at or below the level of injury were randomized and completed a double-blind crossover trial of 5 mg/kg lidocaine and placebo infused over 30 min.

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Background: In chronic pain, increased activity from intact or damaged peripheral nerve endings results in an enhanced response in central pain transmission systems, a mechanism known as central sensitization. Central sensitization can also be invoked in human experimental models. Therefore, these models may be useful to characterize novel analgesics in humans.

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Aim: Do distraction from- or attention to sural nerve stimulation affect pain, heart rate variability, and a spinal withdrawal reflex?

Material And Methods: In 26 male volunteers, electrical stimulation at the distal cutaneous receptive field of the sural nerve elicited pain and a nociceptive withdrawal reflex. Intensity of pain was rated on a numeric rating scale. Electromyographic reflex responses were measured from biceps femoris muscle.

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Neuronal hyperexcitability is a key finding in patients with neuropathic pain. Contributing to hyperexcitability may be decreased activity in the endogenous pain inhibitory systems. The present study aimed at recruiting descending inhibition, by the use of painful heterotopic stimulation (HTS), in 16 patients with peripheral chronic neuropathic pain and associated brush-evoked allodynia.

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