Polymyalgia rheumatica (PMR) is a common inflammatory rheumatic disease with little known about its etiology or incidence. Frequently found in older adult women, this disease can be debilitating, painful, and dangerous. Diagnosing PMR can be elusive due to lack of specific laboratory tests, and treatment with use of long-term glucocorticoids can be difficult due to side effects. The following article describes the pathophysiology, diagnosis, signs and symptoms, and treatment of PMR, as well as implications for home healthcare.
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http://dx.doi.org/10.1097/NHH.0000000000000199 | DOI Listing |
Praxis (Bern 1994)
July 2020
Klinik für Rheumatologie, Universitätsspital Zürich, Zürich.
Polymyalgia rheumatica and Giant Cell Arteritis - Update on Diagnosis and Therapy Polymyalgia rheumatica (PMR) is an inflammatory syndrome which often co-incides with giant cell arteritis (GCA). Due to unspecific symptoms and a plethora of possible alternative diagnoses, PMR often represents a diagnostic challenge. The use of ultrasound, but also other imaging methods has improved and accelerated the time to diagnosis in PMR and GCA, so that complications such as blindness can be reduced.
View Article and Find Full Text PDFHome Healthc Now
March 2015
Diana R. Mager, DNP, RN-BC, is an Assistant Professor, Fairfield University School of Nursing, Fairfield, Connecticut, and a Home Care Nurse and Consultant, Visiting Nurse and Hospice of Fairfield County, Norwalk, Connecticut.
Polymyalgia rheumatica (PMR) is a common inflammatory rheumatic disease with little known about its etiology or incidence. Frequently found in older adult women, this disease can be debilitating, painful, and dangerous. Diagnosing PMR can be elusive due to lack of specific laboratory tests, and treatment with use of long-term glucocorticoids can be difficult due to side effects.
View Article and Find Full Text PDFAnn Vasc Surg
October 2013
Department of Vascular Surgery, Mid Essex Hospitals Services NHS Trust, Broomfield Hospital, Essex, UK.
Background: The aim of this study is to describe a case of ruptured cryptogenic mycotic abdominal aortic aneurysm by Salmonella enteritidis (SE) and present a comprehensive review of the literature.
Methods: A 66-year-old man with a past medical history of coronary artery bypass graft (CABG) and polymylagia rheumatica (PMR) presented with a 2-day history of right-flank-to-groin pain and fever. He was found to have tenderness on the right of the umbilical region and laboratory data showed leukocytosis, raised C-reactive protein, and a significant drop in hemoglobin level as compared with his first visit 17 days earlier, with no hemodynamic instability.
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