Lecture 58-Rheumatoid Arthritis and Osteoarthritis.Pdf
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Patellofemoral Pain Syndrome and Chondromalacia: the Effect of Ozone on Pain, Function and Quality of Life. a Non-Randomized Control-Trial
Central JSM Physical Medicine and Rehabilitation Bringing Excellence in Open Access Research Article *Corresponding author Marcos Edgar Fernández-Cuadros, Calle del Ánsar, 44, piso Segundo, CP 28047, Madrid, Spain, Tel: Patellofemoral Pain Syndrome 34-620314558; Email: [email protected]; Submitted: 23 November 2016 and Chondromalacia: The Effect Accepted: 05 December 2016 Published: 06 December 2016 of Ozone on Pain, Function Copyright © 2016 Fernández-Cuadros et al. and Quality of Life. A Non- OPEN ACCESS Keywords Randomized Control-Trial • Patellofemoral pain syndrome • Chondromalacia Marcos Edgar Fernández-Cuadros1,2*, Olga Susana Pérez-Moro1, • Pain and María Jesús Albaladejo-Florin1 • Ozone therapy • Quality of life 1Servicio de Rehabilitación, Hospital Universitario Santa Cristina, Spain 2de Rehabilitación, Fundación, Hospital General Santísima Trinidad, Spain Abstract Objectives: 1) To demonstrate the effectiveness of a treatment protocol with Ozone therapy on pain, function and quality of life in patients with Patellofemoral Pain Syndrome (PFPS) and Chondromalacia; and 2) to apply Ozone as a conservative treatment option with a demonstrable level of scientific evidence. Material and Methods: Prospective quasi-experimental before-after study (non-randomized control-trial) on 41 patients with PFPS and Chondromalacia grade 2 or more, who attended to Santa Cristina’s University Hospital, from January 2012 to November 2016 The protocol consisted of an intra articular infiltration of a medical mixture of Oxygen-Ozone (95% -5%) 20ml, at a 20ug / ml concentration, and a total number of 4 sessions (1 per week). Pain and quality of life were measured by Visual Analogical Scale (VAS) and Western Ontario and Mc Master Universities Index for Osteoarthritis (WOMAC) at the beginning / end of treatment. -
SODIUM HYALURONATE Policy Number: PHARMACY 059.37 T2 Effective Date: April 1, 2018
UnitedHealthcare® Oxford Clinical Policy SODIUM HYALURONATE Policy Number: PHARMACY 059.37 T2 Effective Date: April 1, 2018 Table of Contents Page Related Policies INSTRUCTIONS FOR USE .......................................... 1 Autologous Chondrocyte Transplantation in the CONDITIONS OF COVERAGE ...................................... 1 Knee BENEFIT CONSIDERATIONS ...................................... 2 Unicondylar Spacer Devices for Treatment of Pain COVERAGE RATIONALE ............................................. 2 or Disability APPLICABLE CODES ................................................. 4 DESCRIPTION OF SERVICES ...................................... 5 CLINICAL EVIDENCE ................................................. 5 U.S. FOOD AND DRUG ADMINISTRATION ................... 10 REFERENCES .......................................................... 12 POLICY HISTORY/REVISION INFORMATION ................ 14 INSTRUCTIONS FOR USE This Clinical Policy provides assistance in interpreting Oxford benefit plans. Unless otherwise stated, Oxford policies do not apply to Medicare Advantage members. Oxford reserves the right, in its sole discretion, to modify its policies as necessary. This Clinical Policy is provided for informational purposes. It does not constitute medical advice. The term Oxford includes Oxford Health Plans, LLC and all of its subsidiaries as appropriate for these policies. When deciding coverage, the member specific benefit plan document must be referenced. The terms of the member specific benefit plan document [e.g., -
Acute < 6 Weeks Subacute ~ 6 Weeks Chronic >
Pain Articular Non-articular Localized Generalized . Regional Pain Disorders . Myalgias without Weakness Soft Tissue Rheumatism (ex., fibromyalgia, polymyalgia (ex., soft tissue rheumatism rheumatica) tendonitis, tenosynovitis, bursitis, fasciitis) . Myalgia with Weakness (ex., Inflammatory muscle disease) Clinical Features of Arthritis Monoarthritis Oligoarthritis Polyarthritis (one joint) (two to five joints) (> five joints) Acute < 6 weeks Subacute ~ 6 weeks Chronic > 6 weeks Inflammatory Noninflammatory Differential Diagnosis of Arthritis Differential Diagnosis of Arthritis Acute Monarthritis Acute Polyarthritis Inflammatory Inflammatory . Infection . Viral - gonococcal (GC) - hepatitis - nonGC - parvovirus . Crystal deposition - HIV - gout . Rheumatic fever - calcium . GC - pyrophosphate dihydrate (CPPD) . CTD (connective tissue diseases) - hydroxylapatite (HA) - RA . Spondyloarthropathies - systemic lupus erythematosus (SLE) - reactive . Sarcoidosis - psoriatic . - inflammatory bowel disease (IBD) Spondyloarthropathies - reactive - Reiters . - psoriatic Early RA - IBD - Reiters Non-inflammatory . Subacute bacterial endocarditis (SBE) . Trauma . Hemophilia Non-inflammatory . Avascular Necrosis . Hypertrophic osteoarthropathy . Internal derangement Chronic Monarthritis Chronic Polyarthritis Inflammatory Inflammatory . Chronic Infection . Bony erosions - fungal, - RA/Juvenile rheumatoid arthritis (JRA ) - tuberculosis (TB) - Crystal deposition . Rheumatoid arthritis (RA) - Infection (15%) - Erosive OA (rare) Non-inflammatory - Spondyloarthropathies -
Axial Spondyloarthritis
Central JSM Arthritis Review Article *Corresponding author Mali Jurkowski, Department of Internal Medicine, Temple University Hospital, 3401 North Broad Street, Axial Spondyloarthritis: Clinical Philadelphia, PA 19140, USA Submitted: 07 December 2020 Features, Classification, and Accepted: 31 January 2021 Published: 03 February 2021 ISSN: 2475-9155 Treatment Copyright Mali Jurkowski1*, Stephanie Jeong1 and Lawrence H Brent2 © 2021 Jurkowski M, et al. 1Department of Internal Medicine, Temple University Hospital, USA OPEN ACCESS 2Section of Rheumatology, Department of Medicine, Lewis Katz School of Medicine at Temple University, USA Keywords ABBREVIATIONS • Spondyloarthritis • Ankylosing spondylitis HLA-B27: human leukocyte antigen-B27; SpA: • HLA-B27 spondyloarthritis; AS: ankylosing spondylitis; nr-axSpA: non- • Classification criteria radiographic axial spondyloarthritis; ReA: reactive arthritis; PsA: psoriatic arthritis; IBD-SpA: disease associated spondyloarthritis; ASAS: Assessment of of rheumatoid arthritis [6]. AS affects men more than women SpondyloArthritis international Society; NSAIDs:inflammatory nonsteroidal bowel 79.6%, whereas nr-axSpA affects men and women equally 72.4% CASPAR: [7], independent of HLA-B27. This article will discuss the clinical for Psoriatic Arthritis; DMARDs: disease modifying anti- and diagnostic features of SpA, compare the classification criteria, rheumaticanti-inflammatory drugs; CD:drugs; Crohn’s disease; ClassificationUC: ulcerative Criteriacolitis; and provide updates regarding treatment options, including the ESR: erythrocyte sedimentation rate; CRP: C-reactive protein; developmentCLINICAL FEATURESof biologics and targeted synthetic agents. TNFi: X-ray: plain radiography; MRI: magnetic resonance imaging; CT: computed Inflammatory back pain tomography;tumor US: necrosis ultrasonography; factor-α wb-MRI:inhibitors; ESSG: European Spondyloarthropathy Study Group; IL-17i: whole-body MRI; JAKi: PDE4i: Inflammatory back pain is the hallmark of SpA, present in 70- 80% of patients [8]. -
Charcot Arthropathy: Differential Diagnosis of Inflammatory Arthritis
CHARCOT ARTHROPATHY: DIFFERENTIAL DIAGNOSIS OF INFLAMMATORY ARTHRITIS CAMILA DA SILVA CENDON DURAN (USP-SP, SÃO PAULO, SP, Brasil), CARLA BALEEIRO RODRIGUES SILVA (USP-SP, SÃO PAULO, SP, Brasil), CARLO SCOGNAMIGLIO RENNER ARAUJO (USP-SP, SÃO PAULO, SP, Brasil), LUCAS BRANDÃO ARAUJO DA SILVA (USP-SP, SÃO PAULO, SP, Brasil), LUCIANA PARENTE COSTA SEGURO (USP-SP, SÃO PAULO, SP, Brasil), LISSIANE KARINE NORONHA GUEDES (USP-SP, SÃO PAULO, SP, Brasil), ROSA MARIA RODRIGUES PEREIRA (USP-SP, SÃO PAULO, SP, Brasil), EDUARDO FERREIRA BORBA NETO (USP-SP, SÃO PAULO, SP, Brasil) BACKGROUND Charcot-Marie-Tooth Disease (CMT) is the most common hereditary neuropathy, with an estimated prevalence of 40 cases per 100,000 individuals. CMT type 2, the most common subtype, is an axonal disorder, usually beginning during the second or third decade of life. Clinical features include distal weakness, muscle atrophy, reduced sensitivity, decreased deep tendon reflexes and deformity of the foot. It may lead to the development of Charcot arthropathy, with increased osteoclastic activity and joint destruction. Ultrasonography can show effusion, synovitis, high-grade doppler activity and bone irregularities, findings that can lead to a misdiagnosis of inflammatory arthritis. CASE REPORT Male, 27-year-old, reported a history of pain and warm swelling of the left ankle and midfoot, worsening after exercise and improving with rest, that started nine years ago and persisted for one year. During this period, he self-medicated with non-steroidal anti-inflammatory drugs. He denied associated symptoms such as ocular inflammation, skin lesions, diarrhea, urethritis or fever. Ten months ago, he began to present similar symptoms in right ankle and midfoot, after a 7-year asymptomatic period. -
Approach to Polyarthritis for the Primary Care Physician
24 Osteopathic Family Physician (2018) 24 - 31 Osteopathic Family Physician | Volume 10, No. 5 | September / October, 2018 REVIEW ARTICLE Approach to Polyarthritis for the Primary Care Physician Arielle Freilich, DO, PGY2 & Helaine Larsen, DO Good Samaritan Hospital Medical Center, West Islip, New York KEYWORDS: Complaints of joint pain are commonly seen in clinical practice. Primary care physicians are frequently the frst practitioners to work up these complaints. Polyarthritis can be seen in a multitude of diseases. It Polyarthritis can be a challenging diagnostic process. In this article, we review the approach to diagnosing polyarthritis Synovitis joint pain in the primary care setting. Starting with history and physical, we outline the defning characteristics of various causes of arthralgia. We discuss the use of certain laboratory studies including Joint Pain sedimentation rate, antinuclear antibody, and rheumatoid factor. Aspiration of synovial fuid is often required for diagnosis, and we discuss the interpretation of possible results. Primary care physicians can Rheumatic Disease initiate the evaluation of polyarthralgia, and this article outlines a diagnostic approach. Rheumatology INTRODUCTION PATIENT HISTORY Polyarticular joint pain is a common complaint seen Although laboratory studies can shed much light on a possible diagnosis, a in primary care practices. The diferential diagnosis detailed history and physical examination remain crucial in the evaluation is extensive, thus making the diagnostic process of polyarticular symptoms. The vast diferential for polyarticular pain can difcult. A comprehensive history and physical exam be greatly narrowed using a thorough history. can help point towards the more likely etiology of the complaint. The physician must frst ensure that there are no symptoms pointing towards a more serious Emergencies diagnosis, which may require urgent management or During the initial evaluation, the physician must frst exclude any life- referral. -
Biological Treatment in Resistant Adult-Onset Still's Disease: a Single-Center, Retrospective Cohort Study
Arch Rheumatol 2021;36(x):i-viii doi: 10.46497/ArchRheumatol.2021.8669 ORIGINAL ARTICLE Biological treatment in resistant adult-onset Still’s disease: A single-center, retrospective cohort study Seda Çolak, Emre Tekgöz, Maghrur Mammadov, Muhammet Çınar, Sedat Yılmaz Department of Internal Medicine, Division of Rheumatology, Gülhane Training and Research Hospital, Ankara, Turkey ABSTRACT Objectives: The aim of this study was to assess the demographic and clinical characteristics of patients with adult-onset Still’s disease (AOSD) under biological treatment. Patients and methods: This retrospective cohort study included a total of 19 AOSD patients (13 males, 6 females; median age: 37 years; range, 28 to 52 years) who received biological drugs due to refractory disease between January 2008 and January 2020. The data of the patients were obtained from the patient files. The response to the treatment was evaluated based on clinical and laboratory assessments at third and sixth follow-up visits. Results: Interleukin (IL)-1 inhibitor was prescribed for 13 (68.4%) patients and IL-6 inhibitor prescribed for six (31.6%) patients. Seventeen (89.5%) patients experienced clinical remission. Conclusion: Biological drugs seem to be effective for AOSD patients who are resistant to conventional therapies. Due to the administration methods and the high costs of these drugs, however, tapering the treatment should be considered, after remission is achieved. Keywords: Adult-onset Still’s disease, anakinra, tocilizumab, treatment. Adult-onset Still’s disease (AOSD) is a rare diseases that may lead to similar clinical and systemic inflammatory disease with an unknown laboratory findings. etiology. The main clinical manifestations of It is well known that proinflammatory the disease are fever, maculopapular salmon- pink rash, arthralgia, and arthritis. -
Physical Examination of the Knee: Meniscus, Cartilage, and Patellofemoral Conditions
Review Article Physical Examination of the Knee: Meniscus, Cartilage, and Patellofemoral Conditions Abstract Robert D. Bronstein, MD The knee is one of the most commonly injured joints in the body. Its Joseph C. Schaffer, MD superficial anatomy enables diagnosis of the injury through a thorough history and physical examination. Examination techniques for the knee described decades ago are still useful, as are more recently developed tests. Proper use of these techniques requires understanding of the anatomy and biomechanical principles of the knee as well as the pathophysiology of the injuries, including tears to the menisci and extensor mechanism, patellofemoral conditions, and osteochondritis dissecans. Nevertheless, the clinical validity and accuracy of the diagnostic tests vary. Advanced imaging studies may be useful adjuncts. ecause of its location and func- We have previously described the Btion, the knee is one of the most ligamentous examination.1 frequently injured joints in the body. Diagnosis of an injury General Examination requires a thorough knowledge of the anatomy and biomechanics of When a patient reports a knee injury, the joint. Many of the tests cur- the clinician should first obtain a rently used to help diagnose the good history. The location of the pain injured structures of the knee and any mechanical symptoms were developed before the avail- should be elicited, along with the ability of advanced imaging. How- mechanism of injury. From these From the Division of Sports Medicine, ever, several of these examinations descriptions, the structures that may Department of Orthopaedics, are as accurate or, in some cases, University of Rochester School of have been stressed or compressed can Medicine and Dentistry, Rochester, more accurate than state-of-the-art be determined and a differential NY. -
Pathophysiology of Anterior Knee Pain
1 Patellofemoral Online Education Pathophysiology of Anterior Knee Pain Vicente Sanchis-Alfonso, MD, PhD The original publication is available at www.springerlink.com INTRODUCTION Anterior knee pain, diagnosed as Patellofemoral Pain Syndrome (PFPS), is one of the most common musculoskeletal disorders [61]. It is of high socioeconomic relevance as it occurs most frequently in young and active patients. The rate is around 15-33% in active adult population and 21-45% of adolescents [36]. However, in spite of its high incidence and abundance of clinical and basic science research, its pathogenesis is still an enigma (“The Black Hole of Orthopaedics”). The numerous treatment regimes that exist for PFPS highlight the lack of knowledge regarding the etiology of pain. The present review synthesizes our research on pathophysiology [53-62] of anterior knee pain in the young patient. BACKGROUND: CHONDROMALACIA PATELLAE, PATELLOFEMORAL MALALIGMENT, TISSUE HOMEOSTASIS THEORY Until the end of the 1960’s anterior knee pain was attributed to chondromalacia patellae, a concept from the beginnings of the 20th century that, from a clinical point of view, is of no value, and ought to be abandoned, given that it has no diagnostic, therapeutic or prognostic implications. In fact, many authors have failed to find a connection between anterior knee pain and chondromalacia [52, 61]. Currently, however, there is growing evidence that a subgroup of patients with chondral lesions may have a component of their 2 pain related to that lesion due to the overload of the subchondral bone interface which is richly innervated. In the 1970’s anterior knee pain was related to the presence of patellofemoral malaligment (PFM) [14, 24, 26, 40]. -
Ambulatory Surgery Job
Ambulatory Surgery ICD-10-CM 2014: Reference Mapping Card ICD-9-CM ICD-10-CM ICD-9-CM ICD-10-CM 354.0 Carpal tunnel syndrome G56.00 Carpal tunnel 715.94 Osteoarthrosis hand M18.9 Osteoarthritis of first syndrome carpometacarpal joint 366.14 Post subcap senile H25.041 Posterior subcapsular 717.7 Chondromalacia patellae M22.41 Chondromalacia patellae cataract polar age-related right knee cataract, right eye M22.41 Chondromalacia patellae Posterior subcapsular left knee H25.042 polar age-related cataract, left eye 721.0 Cervical spondylosis M47.812 Spondylosis without Posterior subcapsular myelopathy or H25.043 polar age-related radiculopathy, cervical cataract, bilateral region eyes 721.3 Lumbosacral spondylosis M47.817 Spondylosis without Posterior subcapsular myelopathy or radiculopathy, Posterior subcapsular polar age-related cataract is only applicable lumbosacral region to adult patients age 15 - 124 years. 722.52 Lumbar/lumbosacral disc M51.36 Other intervertebral disc 366.15 Cortical senile cataract H25.011 Cortical age-related degeneration degeneration, lumbar cataract, right region eye M51.37 Other intervertebral disc H25.012 Cortical age-related degeneration, cataract, left lumbosacral region eye 723.4 Brachial M54.12 Radiculopathy, cervical H25.013 Cortical age-related neuritis/radiculitis region cataract, bilateral M54.13 Radiculopathy, eyes cervicothoracic region 724.02 Spinal stenosis – lumbar, M48.06 Spinal stenosis, lumbar Cortical age-related cataract is only applicable to adult without neurogenic region patients age 15 -
Differential Diagnosis of Juvenile Idiopathic Arthritis
pISSN: 2093-940X, eISSN: 2233-4718 Journal of Rheumatic Diseases Vol. 24, No. 3, June, 2017 https://doi.org/10.4078/jrd.2017.24.3.131 Review Article Differential Diagnosis of Juvenile Idiopathic Arthritis Young Dae Kim1, Alan V Job2, Woojin Cho2,3 1Department of Pediatrics, Inje University Ilsan Paik Hospital, Inje University College of Medicine, Goyang, Korea, 2Department of Orthopaedic Surgery, Albert Einstein College of Medicine, 3Department of Orthopaedic Surgery, Montefiore Medical Center, New York, USA Juvenile idiopathic arthritis (JIA) is a broad spectrum of disease defined by the presence of arthritis of unknown etiology, lasting more than six weeks duration, and occurring in children less than 16 years of age. JIA encompasses several disease categories, each with distinct clinical manifestations, laboratory findings, genetic backgrounds, and pathogenesis. JIA is classified into sev- en subtypes by the International League of Associations for Rheumatology: systemic, oligoarticular, polyarticular with and with- out rheumatoid factor, enthesitis-related arthritis, psoriatic arthritis, and undifferentiated arthritis. Diagnosis of the precise sub- type is an important requirement for management and research. JIA is a common chronic rheumatic disease in children and is an important cause of acute and chronic disability. Arthritis or arthritis-like symptoms may be present in many other conditions. Therefore, it is important to consider differential diagnoses for JIA that include infections, other connective tissue diseases, and malignancies. Leukemia and septic arthritis are the most important diseases that can be mistaken for JIA. The aim of this review is to provide a summary of the subtypes and differential diagnoses of JIA. (J Rheum Dis 2017;24:131-137) Key Words. -
Functional Outcome Following Modified Elmslie–Trillat Procedure ⁎ D
The Knee 13 (2006) 464–468 www.elsevier.com/locate/knee Functional outcome following modified Elmslie–Trillat procedure ⁎ D. Karataglis , M.A. Green, D.J.A. Learmonth Royal Orthopaedic Hospital, Bristol Road South, Birmingham B31 2AP, UK Received 30 October 2005; received in revised form 20 August 2006; accepted 21 August 2006 Abstract The aim of this study was to evaluate the mid- and long-term outcome of the modified Elmslie–Trillat procedure, as well as to detect factors affecting it. Thirty-eight patients (44 procedures) with a mean age of 31 years were included in this study. The reason for operation was patellar instability in 10 cases, anterior knee pain with malalignment of the extensor mechanism in 15 cases and a combination of both in 19 cases. Patients were followed for an average of 40 months (range=18–130 months). The functional outcome was very satisfactory or satisfactory for 73% of patients. According to Cox's criteria it was excellent in 13 cases (30%), good in 18 (41%), fair in 7 (16%) and poor in the remaining 6 (13%). Patients scored an average of 3.5 (range=2–8) in their Tegner Activity Scale, while their score in Activities of Daily Living Scale of the Knee Outcome Survey ranged from 43 to 98 (average=76). Result analysis revealed a better functional outcome when the operation was performed for patellar instability, as well as in the absence of grade 3 or 4 chondral changes in the patellofemoral joint at the time of operation. Elmslie–Trillat procedure satisfactorily restores patellofemoral stability and offers a very good functional outcome, especially in the absence of significant chondral changes in the patellofemoral joint at the time of operation.