Patients' and professionals' views on managing fibromyalgia.
暂无分享,去创建一个
E. Briones-Vozmediano | Erica Briones-Vozmediano | Carmen Vives-Cases | Elena Ronda-Pérez | Diana Gil-González | E. Ronda-Pérez | C. Vives‐Cases | D. Gil‐González
[1] A. Norberg,et al. Men living with fibromyalgia-type pain: experiences as patients in the Swedish health care system. , 2002, Journal of advanced nursing.
[2] Sue Ziebland,et al. Analysing qualitative data , 2000, BMJ : British Medical Journal.
[3] Dianna T Kenny,et al. Constructions of chronic pain in doctor-patient relationships: bridging the communication chasm. , 2004, Patient education and counseling.
[4] V. Extremera,et al. [Frequent users and difficult patients: how do they feel about their treatment by doctors?]. , 2006, Anales del sistema sanitario de Navarra.
[5] R. Epstein,et al. Physicians’ Responses to Patients’ Medically Unexplained Symptoms , 2006, Psychosomatic medicine.
[6] J. Wild,et al. Interdisziplinäre Gruppentherapie für die Fibromyalgie , 1998, Zeitschrift für Rheumatologie.
[7] F. Angst,et al. Clinical effectiveness of an interdisciplinary pain management programme compared with standard inpatient rehabilitation in chronic pain: a naturalistic, prospective controlled cohort study. , 2009, Journal of rehabilitation medicine.
[8] A. Cuesta,et al. Investigación cualitativa sobre la conceptualización de la hiperfrecuentación por parte del personal médico de atención primaria , 2009 .
[9] H. Sprott,et al. Multidisciplinary treatment for chronic pain: a systematic review of interventions and outcomes. , 2008, Rheumatology.
[10] M. Fernández,et al. Problemas y soluciones en la atención sanitaria de enfermedades crónicas. Un estudio cualitativo con pacientes y médicos , 2006 .
[11] J. Brown,et al. Experience of fibromyalgia. Qualitative study. , 2000, Canadian family physician Medecin de famille canadien.
[12] Kirsti Malterud,et al. Identity and coping experiences in Chronic Fatigue Syndrome: a synthesis of qualitative studies. , 2007, Patient education and counseling.
[13] L. Carmona,et al. The burden of musculoskeletal diseases in the general population of Spain: results from a national survey , 2001, Annals of the rheumatic diseases.
[14] L. Arnold,et al. Fibromyalgia syndrome: practical strategies for improving diagnosis and patient outcomes. , 2010, The American journal of medicine.
[15] A. Norberg,et al. Struggling for Dignity: The Meaning of Women’s Experiences of Living with Fibromyalgia , 1999, Qualitative health research.
[16] K. Rodham,et al. A qualitative exploration of carers' and 'patients' experiences of fibromyalgia: one illness, different perspectives. , 2010, Musculoskeletal care.
[17] T. Houle,et al. Multidisciplinary and interdisciplinary management of chronic pain. , 2006, Physical medicine and rehabilitation clinics of North America.
[18] S. Peters,et al. Patients' perceptions of medical explanations for somatisation disorders: qualitative analysis , 1999, BMJ.
[19] L. Hallberg,et al. Coping with fibromyalgia. A qualitative study. , 2000, Scandinavian journal of caring sciences.
[20] S. Ziebland,et al. Analysing qualitative data , 2000, BMJ : British Medical Journal.
[21] J. Bullington,et al. A phenomenological study of fibromyalgia. Patient perspectives. , 1999, Scandinavian journal of primary health care.
[22] B MilesMatthew,et al. Qualitative Data Analysis , 2009, Approaches and Processes of Social Science Research.
[23] W. Müller,et al. [Interdisciplinary group therapy for fibromyalgia]. , 1998, Zeitschrift fur Rheumatologie.
[24] J. Schaefer,et al. Collaborative Management of Chronic Illness , 1997, Annals of Internal Medicine.
[25] K. Barker. Listening to Lyrica: contested illnesses and pharmaceutical determinism. , 2011, Social science & medicine.
[26] J. Recla,et al. New and emerging therapeutic agents for the treatment of fibromyalgia: an update , 2010, Journal of pain research.
[27] P. Mease,et al. Fibromyalgia syndrome: review of clinical presentation, pathogenesis, outcome measures, and treatment. , 2005, The Journal of rheumatology. Supplement.
[28] G. Glaeske,et al. Fibromyalgia syndrome: prevalence, pharmacological and non-pharmacological interventions in outpatient health care. An analysis of statutory health insurance data. , 2011, Joint, bone, spine : revue du rhumatisme.
[29] D. Turk,et al. Guidelines on the management of fibromyalgia syndrome – A systematic review , 2010, European journal of pain.
[30] K. Malterud,et al. The fibromyalgia diagnosis – hardly helpful for the patients? , 2007, Scandinavian journal of primary health care.
[31] C. Chew‐Graham,et al. Medically unexplained symptoms and the problem of power in the primary care consultation: a qualitative study. , 2002, Family practice.
[32] Anna-Liisa Närvänen,et al. Patient Power and Control: A Study of Women with Uncertain Illness Trajectories , 2004, Qualitative health research.
[33] R. Fitzpatrick,et al. Qualitative methods for assessing health care. , 1994, Quality in health care : QHC.
[34] C. Chew‐Graham,et al. Practice Nurses' views of their role in the management of Chronic Fatigue Syndrome/Myalagic Encephalitis: a qualitative study , 2009, BMC nursing.
[35] Deborah Bambini,et al. Death of a Lifestyle: The Effects of Social Support and Healthcare Support on the Quality of Life of Persons With Fibromyalgia and/or Chronic Fatigue Syndrome , 2004, Orthopedic nursing.
[36] A. Arillo,et al. Pacientes hiperfrecuentadores y difíciles: ¿cómo se sienten tratados por sus médicos? , 2006 .
[37] A. Finset,et al. How do patients with rheumatic disease experience their relationship with their doctors? A qualitative study of experiences of stress and support in the doctor-patient relationship. , 2004, Patient education and counseling.
[38] J. Sim,et al. Systematic Review of Randomized Controlled Trials of Nonpharmacological Interventions for Fibromyalgia , 2002, The Clinical journal of pain.
[39] M. J. Escudero-Carretero,et al. [Fibromyalgia: Patient perception on their disease and health system. Qualitative research study]. , 2010, Reumatologia clinica.
[40] A. Fernández,et al. Evidencias en fibromialgia , 2007 .
[41] J. Brown,et al. Experience of fibromyalgia , 2000 .
[42] L. Arnold. Strategies for managing fibromyalgia. , 2009, The American journal of medicine.
[43] W. Häuser,et al. Ziele der Leitlinie zur Diagnostik und Therapie des Fibromyalgiesyndroms , 2008, Der Schmerz.
[44] Julius Sim,et al. Illness experience in fibromyalgia syndrome: a metasynthesis of qualitative studies. , 2008, Social science & medicine.
[45] J. Bullington,et al. Doctors' attitudes to fibromyalgia: a phenomenological study , 1998, Scandinavian journal of social medicine.
[46] Valorie A. Crooks,et al. Understanding, embracing, rejecting: Women's negotiations of disability constructions and categorizations after becoming chronically ill. , 2008, Social science & medicine.
[47] D. LaChapelle,et al. The meaning and process of pain acceptance. Perceptions of women living with arthritis and fibromyalgia. , 2008, Pain research & management.
[48] R. Mellins,et al. Physician‐patient partnership in managing chronic illness , 1995, Academic medicine : journal of the Association of American Medical Colleges.
[49] A. Michael Huberman,et al. An expanded sourcebook qualitative data analysis , 1994 .
[50] W. Brückle,et al. Fibromyalgiesyndrom – die neue Leitlinie , 2009, Zeitschrift für Rheumatologie.
[51] K. Malterud,et al. Part process analysis: a qualitative method for studying provider—patient interaction , 2003, Scandinavian journal of public health.
[52] J. Branco,et al. Prevalence of fibromyalgia: a survey in five European countries. , 2010, Seminars in arthritis and rheumatism.
[53] Anna-Liisa Närvänen,et al. Women’s Experiences of Stigma in Relation to Chronic Fatigue Syndrome and Fibromyalgia , 2002, Qualitative health research.
[54] Anna-Liisa Närvänen,et al. Ideal versus reality: physicians perspectives on patients with chronic fatigue syndrome (CFS) and fibromyalgia. , 2003, Social science & medicine.
[55] C. Jillings,et al. Individuals’ Descriptions of Living With Fibromyalgia , 2006, Clinical nursing research.
[56] C. Björkelund,et al. To be a helpless helpoholic – GPs’ experiences of women patients with non-specific muscular pain , 2004, Scandinavian journal of primary health care.
[57] A. Gibofsky. American College of Rheumatology. , 2002, Journal of the Medical Association of Georgia.
[58] P. Tugwell,et al. The American College of Rheumatology 1990 Criteria for the Classification of Fibromyalgia. Report of the Multicenter Criteria Committee. , 1990, Arthritis and rheumatism.
[59] F. Wolfe. The relation between tender points and fibromyalgia symptom variables: evidence that fibromyalgia is not a discrete disorder in the clinic , 1997, Annals of the rheumatic diseases.
[60] E. Choy,et al. Patients' experiences of living with and receiving treatment for fibromyalgia syndrome: a qualitative study , 2009, BMC musculoskeletal disorders.
[61] C. Mcnulty,et al. Chronic Fatigue Syndrome: a survey of GPs' attitudes and knowledge. , 2005, Family practice.
[62] M. B. Risør. Illness explanations among patients with medically unexplained symptoms: different idioms for different contexts , 2009, Health.