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2.
Semin Arthritis Rheum ; 57: 152101, 2022 12.
Article in English | MEDLINE | ID: mdl-36183478

ABSTRACT

OBJECTIVES: To develop evidence-based expert recommendations for non-pharmacological treatments for pain, fatigue, sleep problems, and depression in fibromyalgia. METHODS: An international, multidisciplinary Delphi exercise was conducted. Authors of EULAR and the Canadian Fibromyalgia Guidelines Group, members of the American Pain Society and clinicians with expertise in fibromyalgia were invited. Participants were asked to select non-pharmacological interventions that could be offered for specific fibromyalgia symptoms and to classify them as either core or adjunctive treatments. An evidence summary was provided to aid the decision making. Items receiving >70% votes were accepted, those receiving <30% votes were rejected and those obtaining 30-70% votes were recirculated for up to two additional rounds. RESULTS: Seventeen experts participated (Europe (n = 10), North America (n = 6), and Israel (n = 1)) in the Delphi exercise and completed all three rounds. Aerobic exercise, education, sleep hygiene and cognitive behavioural therapy were recommended as core treatments for all symptoms. Mind-body exercises were recommended as core interventions for pain, fatigue and sleep problems. Mindfulness was voted core treatment for depression, and adjunctive treatment for other symptoms. Other interventions, namely music, relaxation, hot bath, and local heat were voted as adjunctive treatments, varying between symptoms. CONCLUSIONS: This study provided evidence-based expert consensus recommendations on non-pharmacological treatments for fibromyalgia that may be used to individualise treatments in clinical practice targeting the diverse symptoms associated with fibromyalgia.


Subject(s)
Fibromyalgia , Sleep Wake Disorders , Humans , Fibromyalgia/therapy , Consensus , Delphi Technique , Canada , Fatigue/etiology , Fatigue/therapy , Pain
3.
J Am Board Fam Med ; 34(4): 838-848, 2021.
Article in English | MEDLINE | ID: mdl-34312277

ABSTRACT

Hypermobility spectrum disorders (HSDs) encompass an array of connective tissue disorders characterized by joint instability and chronic pain. Fatigue and other systemic symptoms that affect daily functioning may occur, as well. Accurate data on incidence and prevalence of HSDs is hampered by lack of awareness of these conditions and the wide heterogeneity of their clinical presentation. Identifying which type of HSD is present is important in guiding appropriate care. In particular, making the diagnosis of hypermobile Ehlers-Danlos syndrome (hEDS) is important, as individuals with hEDS may be at risk for more significant multisystem involvement. Diagnostic criteria for hEDS include measures of joint hypermobility, skin and other connective tissue findings, and lack of evidence of a different type of Ehlers-Danlos syndrome. Beyond accurate diagnosis, HSDs pose many challenges for primary care providers, as ongoing patient education, patient empowerment, and coordination of a multidisciplinary treatment team are integral to proper care. This article describes the incidence and prevalence, pathophysiology, diagnosis, and management of HSDs, including clinical cases exemplifying how joint hypermobility might present within a primary care setting.


Subject(s)
Joint Instability/congenital , Primary Health Care , Diagnosis, Differential , Humans , Joint Instability/diagnosis
6.
Anesth Analg ; 99(5): 1478-1485, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15502052

ABSTRACT

We have demonstrated that subjects with complex regional pain syndrome (CRPS) have asymmetric venous pool plasma concentrations of norepinephrine (NE) when affected and unaffected limbs are compared, with most demonstrating decreased NE levels in the affected limb. This pilot study explored whether systemic venous plasma catecholamine levels in CRPS subjects with sympathetically maintained pain (SMP) differ from those found in healthy volunteers. We also explored whether catecholamine levels were correlated with scores on psychometric measures of depression, anxiety, and personality. Venous blood samples from 33 CRPS/SMP patients (from unaffected limbs) and 30 healthy control subjects were assayed for plasma NE and epinephrine (E) concentrations. Plasma NE levels were significantly higher in the CRPS group (P < 0.001). Statistical comparisons of E levels across groups did not achieve significance (P < 0.06), although 52% of CRPS/SMP patients had E levels exceeding the 95% confidence interval based on control data. Significant positive correlations were found between E levels and scores on the Beck Depression Inventory and Scales 1, 3, and 6 on the Minnesota Multiphasic Personality Inventory-2 (all P < 0.05). This preliminary work suggests that increased NE and E levels in CRPS/SMP patients may result from the pain of CRPS, consequent affective distress, or both. Alternatively, our findings could reflect premorbid adrenergic hyperactivity caused by affective, endocrine, or other pathology, which might predispose these individuals to develop the syndrome. Definitive studies are needed to examine these hypotheses in detail.


Subject(s)
Catecholamines/blood , Complex Regional Pain Syndromes/blood , Complex Regional Pain Syndromes/psychology , Adult , Aging/metabolism , Anxiety/diagnosis , Anxiety/psychology , Chromatography, High Pressure Liquid , Complex Regional Pain Syndromes/therapy , Depression/diagnosis , Depression/psychology , Electrochemistry , Epinephrine/blood , Female , Humans , Male , Neuropsychological Tests , Norepinephrine/blood , Pain Measurement , Pilot Projects , Psychiatric Status Rating Scales , Psychometrics
7.
Curr Pain Headache Rep ; 7(6): 433-42, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14604502

ABSTRACT

Myofascial pain syndrome (MPS) and fibromyalgia (FM) are complex conditions and pose significant challenges to clinicians and patients. This chapter explores available treatments for MPS and FM in the context of pathophysiology, clinical evidence, and experimental support. This information may prove to be helpful in designing individualized treatment for patients with these complex syndromes. New treatments should be critically and carefully evaluated as they appear.


Subject(s)
Fibromyalgia/therapy , Myofascial Pain Syndromes/therapy , Animals , Fibromyalgia/drug therapy , Fibromyalgia/psychology , Humans , Myofascial Pain Syndromes/drug therapy , Myofascial Pain Syndromes/psychology
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