303 results match your criteria: "Centre d'evaluation et de traitement de la douleur[Affiliation]"

[French guidelines for diagnosis and treatment of cluster headache (French Headache Society)].

Rev Neurol (Paris)

November 2014

Inserm/UdA, U1107, Neuro-Dol Clermont-Ferrand, faculté de médecine, BP 38, 28, place Henri-Dunant, 63001 Clermont-Ferrand, France; Département d'évaluation et de traitement de la douleur, hôpital Cimiez, bâtiment Mossa, 4, avenue Reine-Victoria, 06000 Nice, France.

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Rationale and design of a multicenter randomized clinical trial with memantine and dextromethorphan in ketamine-responder patients.

Contemp Clin Trials

July 2014

Clermont Université, Université d'Auvergne, Pharmacologie Fondamentale et Clinique de la Douleur, Laboratoire de Pharmacologie, Facultés de Médecine/Pharmacie, F-63000 Clermont-Ferrand, France; Inserm, U1107 Neuro-Dol, F-63001 Clermont-Ferrand, France.; CHU Clermont-Ferrand, Inserm CIC 1405, Centre de Pharmacologie Clinique, F-63003 Clermont-Ferrand, France.

The N-methyl-D-aspartate receptor plays an important role in central sensitization of neuropathic pain and N-methyl-D-aspartate receptor antagonists, such as ketamine, memantine and dextromethorphan may be used for persistent pain. However, ketamine cannot be repeated too often because of its adverse events. A drug relay would be helpful in the outpatient to postpone or even cancel the next ketamine infusion.

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Dexamethasone and peripheral nerve blocks: on the nerve or intravenous?

Br J Anaesth

September 2014

Service d'anesthésie, Hôpital Raymond Poincaré, Assistance Publique Hôpitaux de Paris, F-92380 Garches, France INSERM, U-987, Hôpital Ambroise Paré, Centre d'Evaluation et de Traitement de la Douleur, F-92100 Boulogne Billancourt, France Université Versailles Saint-Quentin, F-78035 Versailles, France

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Opioid-induced hyperalgesia in patients after surgery: a systematic review and a meta-analysis.

Br J Anaesth

June 2014

Service d'anesthésie, Hôpital Raymond Poincaré, Garches, Assistance Publique Hôpitaux de Paris, Garches F-92380, France INSERM, U-987, Hôpital Ambroise Paré, Centre d'Evaluation et de Traitement de la Douleur, Garches F-92100, France Université Versailles Saint-Quentin, Garches F-78035, France.

Background: Opioids can increase sensitivity to noxious stimuli and cause opioid-induced hyperalgesia. We performed a systematic review to evaluate the clinical consequences of intra-operative doses of opioid.

Methods: We identified randomized controlled trials which compared intra-operative opioid to lower doses or placebo in adult patients undergoing surgery from MEDLINE, EMBASE, LILAC, Cochrane, and hand searches of trial registries.

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Background And Aims: The French Pain Society published guidelines for neuropathic pain management in 2010. Our aim was to evaluate the compliance of GPs with these guidelines three years later.

Methods: We used "e" case vignette methodology for this non interventional study.

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rTMS in fibromyalgia: a randomized trial evaluating QoL and its brain metabolic substrate.

Neurology

April 2014

From EA 3279-Self-perceived Health Assessment Research Unit (L.B.), School of Medicine, La Timone University, Marseille; Centre d'Evaluation et de Traitement de la Douleur (A. Dousset, P.R., N.D., V.P., A. Donnet) and Service Central de Biophysique et Médecine Nucléaire (S.C., O.M., E.G.), APHM, Hôpital de la Timone, Marseille; CERIMED (S.C., O.M., E.G.) and Institut de Neurosciences de la Timone, CNRS UMR 7289 (S.K., E.G.), Aix-Marseille Université, Marseille, France.

Objective: This double-blind, randomized, placebo-controlled study investigated the impact of repetitive transcranial magnetic stimulation (rTMS) on quality of life (QoL) of patients with fibromyalgia, and its possible brain metabolic substrate.

Methods: Thirty-eight patients were randomly assigned to receive high-frequency rTMS (n = 19) or sham stimulation (n = 19), applied to left primary motor cortex in 14 sessions over 10 weeks. Primary clinical outcomes were QoL changes at the end of week 11, measured using the Fibromyalgia Impact Questionnaire (FIQ).

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[Management of chronic daily headache in migraine patients: medication overuse headache and chronic migraine. French guidelines (French Headache Society, French Private Neurologists Association, French Pain Society)].

Rev Neurol (Paris)

March 2014

Inserm/UdA, U1107, Neuro-Dol Clermont-Ferrand, faculté de médecine, BP 38, 28, place Henri-Dunant, 63001 Clermont-Ferrand, France; Centre d'évaluation et de traitement de la douleur, hôpital de la Timone, boulevard Jean-Moulin, 264, rue Saint-Pierre, 13385 Marseille, France. Electronic address:

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Sensory profiles of patients with neuropathic pain based on the neuropathic pain symptoms and signs.

Pain

February 2014

Autonomic and Peripheral Nerve Laboratory, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, USA Division of Neurological Pain Research and Therapy, Department of Neurology, Christian-Albrechts University, Kiel, Germany INSERM U987, Centre d'Evaluation et de Traitement de la Douleur, Hôpital Ambroise Paré, Boulogne-Billancourt F-92100, France Université Versailles-Saint-Quentin, Versailles F-78035, France Department of Statistics and Biostatistics, Rutgers University, New Brunswick, NJ, USA Pfizer Inc, New York, NY, USA.

This manuscript aimed to characterize the clinical profile of various neuropathic pain (NeP) disorders and to identify whether patterns of sensory symptoms/signs exist, based on baseline responses on the Neuropathic Pain Symptom Inventory (NPSI) questionnaire and the quantitative sensory testing (QST). These post hoc analyses were based on data from 4 randomized, double-blind, placebo-controlled clinical studies of pregabalin (150-600mg/day) in patients with NeP syndromes: central poststroke pain, posttraumatic peripheral pain, painful HIV neuropathy, and painful diabetic peripheral neuropathy. The NPSI questionnaire includes 10 different pain symptom descriptors.

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[Opioid therapy for chronic noncancer pain: retrospective analysis of patients hospitalized for withdrawal].

Therapie

May 2014

Département de Pharmacologie médicale et Toxicologie, Centre d'Addictovigilance, Hôpital Lapeyronie, CHRU Montpellier, UM1, Montpellier, France.

Objective: The prescription of opioids for the treatment of chronic non-cancer pain (CNCP) is not recommended for all of them, and can expose the patients to a benefit/risk ratio unfavorable. The objective of this study was to evaluate the management of patients hospitalized at the centre for evaluation and treatment of pain for opioid withdrawal, their outcome during hospitalization.

Method: This is a retrospective descriptive study.

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[Management of chronic pain in the future].

Rev Prat

June 2013

Inserm U987, centre d'évaluation et de traitement de la douleur, hôpital Ambroise-Paré, AP-HP, 92100 Boulogne-Billancourt, France.

The major development of experimental and clinical pain research over the last two decades should result in the development of new treatment strategies. In the future, the management of chronic pain should rely both on new molecules targetting specific pathophysiological mechanisms and new non pharmacological approaches, such as non invasive transcranial magnetic stimulation, acting on endogenous pain modulatory systems. The variety of new treatment options should allow a more efficacious management of chronic pain, taylored to each patient's profile.

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[Pharmacological treatment of neuropathic pain in primary care].

Rev Prat

June 2013

Inserm U987, centre d'évaluation et de traitement de la douleur, hôpital Ambroise-Paré, AP-HP, 92100 Boulogne-Billancourt, France.

Neuropathic pain is difficult to treat. First line treatment includes tricyclic antidepressants (notably amitriptyline), mixed serotonin and norepinephrine reuptake inhibitors (duloxetine for diabetic peripheral neuropathic pain), antiepileptics (gabapentin and pregabalin) and topical agents (lidocaine plasters for postherpetic neuralgia). These drugs can be subsequently associated in case of partial response to monotherapy.

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Relieving pain in rheumatology patients: repetitive transcranial magnetic stimulation (rTMS), a developing approach.

Joint Bone Spine

January 2014

Service de Médecine Interne et Centre d'Evaluation et de Traitement de la Douleur, INSERM U 987, Université Paris Descartes, Hôtel Dieu, Paris, France.

Transcranial magnetic stimulation (TMS) is a non-invasive method for activating specific areas of the brain. There are two variants, repetitive TMS (rTMS) and direct TMS. Rapid changes in an electrical current induce a magnetic field, which in turn induces an electrical current in a nearby conductor.

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Value of quantitative sensory testing in neurological and pain disorders: NeuPSIG consensus.

Pain

September 2013

Department of Neurology, University of Wisconsin-Madison, Madison, WI, USA CRI Lifetree Research, Salt Lake City, UT, USA INSERM U-987, Centre d'Evaluation et de Traitement de la Douleur, Hôpital Ambroise Paré, APHP, Boulogne-Billancourt, France Université Versailles Saint-Quentin, France Division of Neurological Pain Research and Therapy, Department of Neurology, Universitatsklinikum Schleswig-Holstein, Kiel, Germany Dental Public Health Sciences, University of Washington, Seattle, WA, USA Mayo Clinic, 200 First Street SW, Rochester, MN, USA Department of Anesthesiology, Harvard Medical School, Brigham & Women's Hospital, Chestnut Hill, MA, USA Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA Center for Neurosensory Disorders, University of North Carolina, CB No. 7280, 3330 Thurston Bldg, Chapel Hill, NC, USA Department of Neurosurgery, Helsinki University Central Hospital, Helsinki, Finland Clinical Pain Research, Department of Molecular Medicine and Surgery, Karolinska Institutet, 17176 Stockholm, Sweden Clinic of Physical and Rehabilitation Medicine, Brugmann University Hospital, 4 place Van Gehuchten, B-1020 Brussels, Belgium Institute of Neuroscience, 52, Avenue E. Mounier, B-1200 Brussels, Belgium Université Catholique de Louvain, Leuven, Belgium Department of Neurology, Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil GmbH, Ruhr-University Bochum, Germany Danish Pain Research Center and Department of Neurology, Aarhus University Hospital, Aarhus, Denmark Department of Pain Medicine, Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil GmbH Bochum, Ruhr University Bochum, Germany Center for Pain Evaluation and Treatment, University Neurological Hospital, Lyon, France Imperial College London, UK Chelsea and Westminster Hospital London, UK Department of Palliative Medicine, Rheinische Friedrich-Wilhelms University, Bonn, Germany Department of Neurology, MC Mutual, Barcelona, Spain Neuroscience Technologies, Barcelona, Spain Neuroscience Technologies, London, UK Department of Neurology, Technische Universität München, Munich, Germany Chair of Neurophysiology, Center for Biomedicine and Medical Technology Mannheim, Heidelberg University, Heidelberg, Germany Department of Neuroscience and Rehabilitation, S. Anna University Hospital of Ferrara, Ferrara, Italy University of Minnesota, 425 Delaware St SE, MMC 295, Minneapolis, MN, USA Department of Anesthesiology, University of California-San Diego, La Jolla, CA, USA Department of Family Medicine and Department of Anesthesia, McGill University, Montreal, Quebec, Canada Department of Neurology, Rambam Health Care Campus, Haifa, Israel Institute for Clinical Diabetology, German Diabetes Center at Heinrich Heine University, Leibniz Center for Diabetes Research and Department of Metabolic Diseases, University Hospital, Düsseldorf, Germany.

Quantitative sensory testing (QST) is a psychophysical method used to quantify somatosensory function in response to controlled stimuli in healthy subjects and patients. Although QST shares similarities with the quantitative assessment of hearing or vision, which is extensively used in clinical practice and research, it has not gained a large acceptance among clinicians for many reasons, and in significant part because of the lack of information about standards for performing QST, its potential utility, and interpretation of results. A consensus meeting was convened by the Neuropathic Pain Special Interest Group of the International Association for the Study of Pain (NeuPSIG) to formulate recommendations for conducting QST in clinical practice and research.

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Duloxetine and pregabalin: high-dose monotherapy or their combination? The "COMBO-DN study"--a multinational, randomized, double-blind, parallel-group study in patients with diabetic peripheral neuropathic pain.

Pain

December 2013

University of Sheffield, Royal Hallamshire Hospital, Sheffield, UK Regional Medical Affairs, Lilly Deutschland GmbH, Bad Homburg, Germany Unidad de Neurología, Clínica Creu Blanca, Barcelona, Spain Global Statistical Sciences, Lilly Deutschland GmbH, Bad Homburg, Germany Neurologische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität, München, Germany INSERM U987 Centre d'Evaluation et de Traitement de la Douleur, Hôpital Ambroise Paré, Boulogne Billancourt, France Sapienza University, Department of Neurology & Psychiatry, Roma, Italy Lilly Research Laboratories, Indianapolis, IN, USA Zentrum für Anästhesiologie, Intensivmedizin, Schmerztherapie & Palliativmedizin, Benedictus Krankenhaus, Tutzing & Klinik für Anästhesiologie, Technische Universität München, Germany.

This multicentre, double-blind, parallel-group study in diabetic peripheral neuropathic pain addressed whether, in patients not responding to standard doses of duloxetine or pregabalin, combining both medications is superior to increasing each drug to its maximum recommended dose. For initial 8-week therapy, either 60 mg/day duloxetine (groups 1, 2) or 300 mg/day pregabalin (groups 3, 4) was given. Thereafter, in the 8-week combination/high-dose therapy period, only nonresponders received 120 mg/day duloxetine (group 1), a combination of 60 mg/day duloxetine and 300 mg/day pregabalin (groups 2, 3), or 600 mg/day pregabalin (group 4).

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A randomized, double-blind, placebo-controlled trial of a chemokine receptor 2 (CCR2) antagonist in posttraumatic neuralgia.

Pain

May 2013

AstraZeneca R&D Södertälje, SE-151 85 Södertälje, Sweden INSERM U987, Centre d'Evaluation et de Traitement de la Douleur, Hôpital Ambroise Paré, Boulogne-Billancourt F-92100, France Université Versailles-Saint-Quentin, Versailles F-78035, France Department of Neurology, Aarhus University Hospital, Aalborg Sygehus DK-9100, Denmark MAC UK Neuroscience, 4 Lumsdale Road, Cobra Court, Trafford Park, Manchester M32 0UT, UK Department of Palliative Care and Palliative Medicine, Medical University of Silesia, 40-752 Katowice, Poland Department of Neurology, I.M. Sechenov Moscow Medical Academy, Trubeckaya Street 8, Building 2, 119992 Moscow, Russian Federation.

We evaluated the analgesic efficacy, safety and tolerability of a novel chemokine receptor 2 (CCR2) antagonist, AZD2423, in posttraumatic neuralgia. This was a double-blind, randomized, parallel-group, multicentre study. One hundred thirty-three patients with posttraumatic neuralgia were equally randomized to 28days' oral administration of 20mg AZD2423, 150mg AZD2423 or placebo.

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[Nursing expertise in transcutaneous neurostimulation].

Rev Infirm

January 2013

Centre d'évaluation et de traitement de la douleur, pôle accueil-urgences-imagerie, Hôpital Avicenne, AP-HP, Bobigny, France.

Transcutaneous neurostimulation is a non-drug based method of analgesia, prescribed by a pain specialist in a pain assessment and treatment centre. The tests are carried out by a nurse specialised in the treatment of pain. They require specialist nursing expertise in a therapeutic education approach in collaboration with a doctor.

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Invasive stimulation therapies for the treatment of refractory pain.

Discov Med

October 2012

Centre d'Evaluation et de Traitement de la Douleur, Centre Fédératif Douleur-Soins de Support-Ethique Clinique, Centre Hospitalier Universitaire, Nantes, France.

Invasive neurostimulation therapies may be proposed to patients with neuropathic pain refractory to conventional medical management, in order to improve pain relief, functional capacity, and quality of life. In this review, the respective mechanisms of action and efficacy of peripheral nerve stimulation (PNS), nerve root stimulation (NRS), spinal cord stimulation (SCS), deep brain stimulation (DBS), and motor cortex stimulation (MCS) are discussed. PNS appears to be useful in various refractory neuropathic pain indications (as long as there is some preservation of sensation in the painful area), such as intractable chronic headache, pelvic and perineal pain, and low back pain, but evidence for its efficacy is not strongly conclusive, and large-scale randomized controlled studies are necessary to confirm the efficacy in the long term.

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Non-invasive stimulation therapies for the treatment of refractory pain.

Discov Med

July 2012

Centre d'Evaluation et de Traitement de la Douleur, Centre Fédératif Douleur-Soins de Support-Ethique Clinique, Centre Hospitalier Universitaire, Nantes, France.

Drug-refractory pain is an indication for neurostimulation therapy, which can be either non-invasive [mainly transcutaneous electrical nerve stimulation (TENS), repetitive Transcranial Magnetic Stimulation (rTMS), and transcranial direct current stimulation (tDCS)] or invasive which requires the intervention of a surgeon to implant electrodes and a pulse generator [peripheral nerve stimulation (PNS), nerve root stimulation (NRS), spinal cord stimulation (SCS), deep brain stimulation (DBS), and motor cortex stimulation (MCS)]. In this review, the respective mechanisms of action and efficacy of TENS, rTMS, and tDCS are discussed. The advantages of TENS include non-invasiveness and ease to use, so that the technique can be operated by the patient.

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Risk factors predictive of chronic postsurgical neuropathic pain: the value of the iliac crest bone harvest model.

Pain

July 2012

Service d'Anesthésie Réanimation Chirurgicale, Hôpital Raymond Poincaré, Assistance Publique Hôpitaux de Paris, 104 Boulevard Raymond Poincaré, F-92380 Garches, France INSERM, U-987, Hôpital Ambroise Paré, Centre d'Evaluation et de Traitement de la Douleur, Boulogne Billancourt F-92100, France Service de chirurgie orthopédique et traumatologique, Hôpital Raymond Poincaré, Assistance Publique Hôpitaux de Paris, 104 Boulevard Raymond Poincaré, F-92380 Garches, France Université Versailles Saint-Quentin, 55 Avenue de Paris, Versailles F-78035, France.

Nerve lesions and secondary hyperalgesia may both be present after surgery, and their relative contributions to chronic postsurgical neuropathic pain (CPSNP) remain unclear. This prospective study explored the roles of these factors in the development of CPSNP after iliac crest bone harvest. CPSNP was defined as pain in the area of hypoesthesia, with a positive Douleur neuropathique 4 questionnaire (DN4) score 3 months after iliac crest bone harvest.

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Pain management in heroin and cocaine users.

Joint Bone Spine

October 2012

Inserm U 987, Centre d'Évaluation et de Traitement de la Douleur, Université Paris Pierre-et-Marie-Curie, Hôpital Saint-Antoine, 184 rue du Faubourg-Saint-Antoine, 75012 Paris, France.

Drug addicts often seek medical help for pain. Numerous fears and beliefs may hinder the recognition, evaluation, and management of pain in addicts. Nevertheless, the same fundamental principles apply to these patients as to other patients in terms of pain evaluation, analgesic selection, and dosage adjustment.

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Do clinicians adhere to treatment recommendations for neuropathic pain?

Pain

April 2012

Department of Neurology and Psychiatry, Sapienza University, Viale Università 30, Rome I-00185, Italy Inserm U 987 and Centre d'Evaluation et de Traitement de la Douleur, Hôpital Ambroise Paré, 9 Avenue Charles de Gaulle, Boulogne-Billancourt F-92100, France.

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Herpes zoster is due to the reactivation of the virus causing varicella, called varicella-zoster virus. It affects peripheral nerves and causes painful skin and nerve lesions. This pain may last for months, or years after the initial lesions have resolved: post-herpetic neuralgia is the most frequent complication.

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Patient perspective on herpes zoster and its complications: an observational prospective study in patients aged over 50 years in general practice.

Pain

February 2012

INSERM U987, Centre d'Evaluation et de Traitement de la Douleur, Hôpital Ambroise Paré, Boulogne-Billancourt F-92100, France Université Versailles-Saint-Quentin, Versailles, F-78035, France AP-HP, Département de la Recherche Clinique et du Développement, Hôpital Saint-Louis, Paris, France Université Paris-Diderot, France Service des Maladies Infectieuses, Centre Hospitalier de la Région d'Annecy, Pringy, France Université Versailles Saint Quentin en Yvelines, Versailles, France Assistance Publique Hôpitaux de Paris, Paris, France Service de Médecine Interne, Hôpital Ambroise Paré, Boulogne-Billancourt, France Faculté de Médecine, Université Paris Descartes, Paris, France INSERM CIC BT505, Assistance Publique Hôpitaux de Paris, CIC de Vaccinologie Cochin Pasteur, Groupe Hospitalier, Broca-Cochin-Hôtel-Dieu, Paris, France Service d'Anesthésie-Réanimation B, Hôpital Saint-Eloi, CHU de Montpellier, Montpellier, France Service de Maladies Infectieuses et Tropicales, CHU de Nancy, Hôpitaux de Brabois, Vandoeuvre les Nancy, France Infectiologie et maladies tropicales, Centre Hospitalier de Chambéry, Chambéry, France Service de Maladies Infectieuses et Tropicales, CHU de Reims, Hôpital Robert Debré, Reims, France.

Understanding the effect of herpes zoster and zoster-related pain should inform care to improve health-related quality of life in elderly patients. A 12-month, longitudinal, prospective, multicenter observational study conducted in primary care in France enrolled patients aged ≥ 50 years with acute eruptive herpes zoster. Patient-reported zoster-related pain was assessed by validated questionnaires (Douleur Neuropathique en 4 Questions [DN4], Zoster Brief Pain Inventory [ZBPI], and Neuropathic Pain Symptom Inventory [NPSI]) on days 0 and 15, and at months 1, 3, 6, 9, and 12.

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