Neuropathic (Charcot) Arthropathy

Total Page:16

File Type:pdf, Size:1020Kb

Neuropathic (Charcot) Arthropathy Neuropathic (Charcot) Arthropathy Disturbance in sensation leads to multiple microfractures o Pain sensation is intact from muscles and soft tissue Distribution and causes o Shoulders – syrinx, spinal tumor o Hips – tertiary syphilis, diabetes o Knees – tertiary syphilis (more bone production), diabetes (less bone production) o Feet – diabetes o Other causes . Amyloidosis . Congenital indifference to pain . Polio . Alcoholism X-ray findings o Sclerosis o Destruction of joint o Fragmentation o Soft tissue swelling from synovitis o Joint effusions o Osteophytosis o Disorganized and disrupted joint o No osteoporosis Marked sclerosis, fragmentation and joint destruction are the hallmarks of a neuropathic joint here cause by tabes DDX o Degenerative joint disease . Eventually neuropathic joint shows more sclerosis . More fragmentation in neuropathic . More destruction of bone in neuropathic o CPPD . Associated with chondrocalcinosis which a neuropathic joint is not Neuropathic (Charcot) Arthropathy General Considerations Most commonly caused by diabetes today Bilaterally is rare in foot Disturbance in sensation leads to multiple microfractures o Pain sensation is intact from muscles and soft tissue Distribution and causes o Shoulders – syringomyelia, spinal tumor o Elbows and wrists -- syringomyelia o Hips – tertiary syphilis, diabetes o Knees – tertiary syphilis (more bone production), diabetes (less bone production) o Feet – diabetes, congenital insensitivity to pain, chronic alcoholism o Other causes . Leprosy . Amyloidosis – knee and ankle . Congenital indifference to pain . Polio . Alcoholism Clinical Findings Signs of inflammation in acute phase Swelling is very common Pain can occur in 75% of cases but is usually less severe than would be expected on the basis of the radiologic findings Instability Loss of joint function May produce a mass at the joint because of swelling Imaging Findings Conventional radiography is usually sufficient to make the diagnosis Findings include: o Sclerosis from eburnation of subchondral bone o Destruction of joint o Fragmentation o Subluxation and dislocation o Soft tissue swelling from synovitis may be massive o Joint effusions o Osteophytosis o Disorganized and disrupted joint o No osteoporosis Differential Diagnosis Degenerative joint disease o Especially in early stages o Eventually neuropathic joint shows more sclerosis o More fragmentation in neuropathic o More destruction of bone in neuropathic Calcium Pyrophosphate Deposition Disease o Associated with chondrocalcinosis which a neuropathic joint is not o Also more fragmentation in neuropathic joint Osteomyelitis o MRI and nuclear medicine scans, including FDG-PET scans, may help in differentiation Treatment Usually non-operative Surgery if unstable, nonreducible fractures or dislocations Neuropathic arthropathy (Charcot joint) can be defined as bone and joint changes that occur secondary to loss of sensation and that accompany a variety of disorders. Charcot first described the relationship between loss of sensation and arthropathy in 1868. The radiographic changes of this condition include destruction of articular surfaces, opaque subchondral bones, joint debris, deformity, and dislocation (see the images below). Neuropathic arthropathy (Charcot joint) poses a special problem in imaging when it is associated with a soft-tissue infection.[1, 2, 3, 4, 5, 6, 7] Neuropathic arthropathy (Charcot joint). Neuropathic arthropathy of the shoulder in a patient with syringomyelia. Note the destruction of the articular surface, dislocation, and debris, which are pathognomonic for a neuropathic joint. Neuropathic arthropathy (Charcot joint). Osteolysis of the distal metatarsals and phalanges with tapering results in a pencil-like appearance in the late stage of diabetic neuropathy. Leprosy is one of many causes of neuropathic arthropathy (Charcot joint); joint manifestations of this disease include signs of Charcot disease, which advances despite treatment.[8] Neuropathic arthropathy related to diabetes, syphilis, leprosy, and connective tissue disorders is more common in the elderly population. Neuroarthropathy related to asymbolia, spina bifida, and spinal trauma is more common in young individuals. Sensory impairment associated with spina bifida and myelomeningocele is the most frequent cause of neuropathic arthropathy (Charcot joint) in childhood. Neuropathic arthropathy can be classified into hypertrophic and atrophic types. Hypertrophic changes predominate in the upper motor neuron lesions, and atrophic changes occur in peripheral nerve injuries. The early stage ofosteoarthritis simulates neuropathic arthropathy (Charcot joint), both radiologically and pathologically. Progressive joint effusion, fracture, fragmentation, and subluxation should raise the suspicion of neuroarthropathy. In the advanced stage, abnormal findings on radiographs include subchondral sclerosis, osteophytosis, subluxation, and soft-tissue swelling. Long-standing neuroarthropathy is characterized by disorganization of joints. The finding of considerable amounts of cartilaginous and osseous debris within the synovial membrane (termed detritic synovitis) should alert the pathologist that the changes may represent a neuropathic joint. Other causes of detritic synovitis include osteonecrosis, calcium pyrophosphate dihydrate crystal deposition disease, psoriatic arthritis, osteoarthritis, and osteolysis with detritic synovitis. Preferred examination Radiography may be the only imaging required for the diagnosis of neuropathic arthropathy (Charcot joint). In the appropriate clinical setting, a fairly accurate diagnosis can be achieved. The roles of ultrasonography and computed tomography (CT) scanning are limited; however, these 2 modalities can be helpful in identifying any local collection, and they can be used to guide aspiration cytology. The role of magnetic resonance imaging (MRI) and radionuclide scanning is to differentiate soft-tissue infection from osteomyelitis.[9, 10] Limitation of techniques Radiographic findings in the early stages of neuropathic arthropathy (Charcot joint) may simulate osteoarthritis. Radiographs may not demonstrate findings that help in diagnosing osteomyelitis in neuropathic joints, which is a common problem. The roles of ultrasonography and CT scanning are limited. Ultrasonography can be used to identify any local collection when infection occurs and to guide aspiration for cytologic analysis; however, it provides no further information regarding the integrity of underlying bone. Although CT scanning may be helpful in evaluating cortical destruction, sequestra, and intraosseous gas, these changes are not specific for neuropathic arthropathy. The role of MRI and radionuclide scanning is to differentiate soft-tissue infection from osteomyelitis. Bone marrow edema is nonspecific and has several causes; therefore, differentiating bone marrow edema from neuropathic arthropathy (Charcot joint) may not be possible on the basis of MRI findings alone. Similarly, enhanced bone activity on radionuclide scans is a nonspecific finding and may occur with several neoplastic, inflammatory, and degenerative processes. Differential diagnosis and other problems to be considered Calcium pyrophosphate deposition disease and primary osteoarthritis are in the differential diagnosis. In addition, in the early stage, neuropathic arthropathy (Charcot joint) can simulate osteoarthritis, and bone fragmentation and collapse are seen in osteonecrosis, posttraumatic osteoarthritis, intra- articular steroid injection, infection, and alkaptonuria. Baker et al reviewed neuropathic arthropathy in diabetics.[11] Neuropathic diabetic arthropathy, particularly in the feet, is the leading cause of morbidity in diabetic patients. It has many mimics. Ulcers, sinus tracts, or an abscess with an adjacent region of abnormal signal intensity in bone marrow suggests osteomyelitis. Contrast-enhanced MRI allows differentiation of viable tissue from necrotic regions in diabetic foot infections, which require surgical debridement in addition to antibiotic therapy. Subtraction images are particularly useful for visualizing nonviable tissue. Dialysis-associated spondyloarthropathy occurs in diabetic patients with a long history of hemodialysis. Intervertebral disk space narrowing without T2 signal hyperintensity, extensive endplate erosions without endplate remodelling, and facet joint involvement are suggestive of spondyloarthropathy instead of infectious diskitis or degenerative disk disease. The clinical features of infective diskitis and spondyloarthropathy overlap, but knowledge of the patient's medical history, and recognition of imaging characteristics described above allows the radiologist to make a prompt and accurate diagnosis, leading to prompt appropriate treatment.[11] Special concerns The incidence of osteomyelitis is increased in patients with neuropathic joints, particularly in the foot. Hence, careful follow-up imaging is essential. CHARCOT’S FOOT Figure 1: X-ray of the feet showing Figure 2: Annotated x-ray of the feet Charcot's joint deformity. showing Charcot's joint deformity. (Click on image to enlarge) (Click on image to enlarge) A Charcot joint (neuropathic joint) is due to a progressive destructive joint disorder in patients with impaired pain sensation and proprioception. In contemporary medicine, particularly when involving the foot/ankle, this is due to longstanding diabetes. The 2 theories for the pathophysiology of this condition are the
Recommended publications
  • Charcot Ankle Neuroarthropathy Pathology, Diagnosis and Management: a Review of Literature
    MOJ Orthopedics & Rheumatology Charcot Ankle Neuroarthropathy Pathology, Diagnosis and Management: A Review of Literature Keywords: Ankle charcot Arthropathy; Ankle arthrodesis; Ankle external fxation arthrodesis; Total contact cast; Ankle Review Article neuroarthropathy Volume 6 Issue 2 - 2016 Key Points: Charcot ankle neuroarthropathy is a common hard to treat condition, early diagnosis and proper management is the key point of treatment. Non- surgical options are feasible in certain stages, but surgical intervention is required in advanced 1Orthopaedic surgery specialist, Nasser institute for research disease. and treatment, Egypt 2Foot and ankle surgery fellow, Schmerzklinik Basel, Introduction Switzerland 3Lecturer of Orthopaedic surgery, Ain Shams University, Egypt Charcot neuroarthropathy can be described as a non-infective, destructive process activated by an isolated or accumulative *Corresponding author: neuro-traumatic stimulus that manifests as dislocation, peri- Ahmed E Galhoum, Orthopedic articular fracture or both in patients rendered insensate by Department, Schmirzklinik, Basel, 11-15 Hirschgasslein, peripheral neuropathy [1]. 4010 Basel, Switzerland, Email: Received: October 01, 2016 | Published: November 03, The ankle has swelling, warmth, and erythema, and the 2016 The bones and joints develop fractures, ligamentous laxity, dislocations,syndrome may cartilage initially damage, be difficult bone to erosions, distinguish and from hypertrophic infection. repair [2]. The resulting bone and joint deformities may be is present in 22% to 53% of patients with Charcot Arthropathy [6,14,15]. or braces. Furthermore, ulceration may result from instability or bonyassociated prominence with instability and may and cause may chronic compromise or recurrent the fitting soft of tissueshoes Classification infection and osteomyelitis. Amputation may be required for Modified eichenholtz stages management of infection or instability [2].
    [Show full text]
  • ICD-10 Code Descriptions
    ICD-10 Code Descriptions TYPE 1 DIABETES MELLITUS WITH... (E10) TYPE 2 DIABETES MELLITUS WITH... (E11) E10.10 Ketoacidosis without coma E11.00 Hyperosmolarity w/o nonket hyprgly-hypros coma (NKHHC) E10.11 Ketoacidosis with coma Hyperosmolarity without nonketotic hyperglycemic- E11.00 E10.21 Diabetic nephropathy hyperosmolar coma (NKHHC) E10.22 Diabetic chronic kidney disease E11.01 Hyperosmolarity with coma E10.29 Other diabetic kidney complication E11.21 Diabetic nephropathy E10.311 Unspecified diabetic retinopathy with macular edema E11.22 Diabetic chronic kidney disease E11.29 Other diabetic kidney complication E10.319 Unspecified diabetic retinopathy without macular edema E11.311 Unspecified diabetic retinopathy with macular edema Mild nonproliferative diabetic retinopathy without macular E10.329 edema E11.319 Unspecified diabetic retinopathy without macular edema Moderate nonproliferative diabetic retinopathy with E11.321 Mild nonproliferative diabetic retinopathy with macular edema E10.331 macular edema Mild nonproliferative diabetic retinopathy without macular E11.329 edema Moderate nonproliferative diabetic retinopathy without E10.339 Moderate nonproliferative diabetic retinopathy with macular macular edema E11.331 edema Mellitus with severe nonproliferative diabetic retinopathy E10.341 Moderate nonproliferative diabetic retinopathy without macular with macular edema E11.339 edema Severe nonproliferative diabetic retinopathy without E10.349 Severe nonproliferative diabetic retinopathy with macular macular edema E11.341 edema E10.351
    [Show full text]
  • Outcome After Protected Full Weightbearing Treatment in an Orthopedic Device in Diabetic Neuropathic Arthropathy
    Renner et al. BMC Musculoskeletal Disorders (2016) 17:504 DOI 10.1186/s12891-016-1357-4 RESEARCH ARTICLE Open Access Outcome after protected full weightbearing treatment in an orthopedic device in diabetic neuropathic arthropathy (Charcot arthropathy): a comparison of unilaterally and bilaterally affected patients Niklas Renner1*, Stephan Hermann Wirth2, Georg Osterhoff3, Thomas Böni2 and Martin Berli2 Abstract Background: Charcot neuropathic arthropathy (CN) is a chronic, progressive, destructive, non-infectious process that most frequently affects the bone architecture of the foot in patients with sensory neuropathy. We evaluated the outcome of protected weightbearing treatment of CN in unilaterally and bilaterally affected patients and secondarily compared outcomes in protected versus unprotected weightbearing treatment. Methods: Patient records and radiographs from 2002 to 2012 were retrospectively analyzed. Patients with Type 1 or Type 2 diabetes with peripheral neuropathy were included. Exclusion criteria included immunosuppressive or osteoactive medication and the presence of bone tumors. Ninety patients (101 ft), mean age 60.7 ± 10.6 years at first diagnosis of CN, were identified. Protected weightbearing treatment was achieved by total contact cast or custom-made orthosis. Ulcer, infection, CN recurrence, and amputation rates were recorded. Mean follow-up was 48 (range 1–208) months. Results: Per the Eichenholtz classification, 9 ft were prodromal, 61 in stage 1 (development), 21 in stage 2 (coalescence) and 10 in stage 3 (reconstruction). Duration of protected weightbearing was 20 ± 21 weeks and 22 ± 29 weeks in patients with unilateral and bilateral CN, respectively. In bilaterally affected patients, new ulcers developed in 9/22 (41%) feet. In unilaterally affected patients, new ulcers developed in 5/66 (8%) protected weightbearing feet and 4/13 (31%) unprotected, full weightbearing feet (p = 0.036).
    [Show full text]
  • Pathogenesis and Potential Relative Risk Factors of Diabetic Neuropathic
    Zhao et al. Journal of Orthopaedic Surgery and Research (2017) 12:142 DOI 10.1186/s13018-017-0634-8 REVIEW Open Access Pathogenesis and potential relative risk factors of diabetic neuropathic osteoarthropathy Hong-Mou Zhao1, Jia-Yu Diao2, Xiao-Jun Liang1, Feng Zhang3* and Ding-Jun Hao4* Abstract Diabetic neuropathic osteoarthropathy (DNOAP) is an uncommon, but with considerable morbidity and mortality rates, complication of diabetes. The real pathogenesis is still unclear. The two popular theories are the neuro-vascular theory and neuro-traumatic theory. Most theories and pathways focused on the uncontrolled inflammations that resulted in the final common pathway, receptor activator of nuclear factor κβ ligand (RANKL)/osteoprotegerin (OPG) axis, for the decreased bone density in DNOAP with an osteoclast and osteoblast imbalance. However, the RANKL/OPG pathway does not explain all the changes, other pathways and factors also play roles. A lot of DNOAP potential relative risk factors were evaluated and reported in the literature, including age, gender, weight, duration and type of diabetes, bone mineral density, peripheral neuropathy and arterial disease, trauma history, and some others. However, most of them are still in debates. Future studies focus on the pathogenesis of DNOAP are still needed, especially for the genetic factors. And, the relationship between DNOAP and those potential relative risk factors are still need to further clarify. Keywords: Charcot foot, Diabetic neuropathic osteoarthropathy, Pathogenesis, Risk factor, Receptor activator of nuclear factor κβ ligand (RANKL) Background DNOAP is a devastating complication for diabetes, Musgrave firstly reported neuropathic joint changes as a culminating in bone destruction and involving joints and complication of venereal disease in 1703 [1].
    [Show full text]
  • Endocrine, Nutritional and Metabolic Diseases (E00-E89)
    Endocrine, Nutritional and Metabolic Diseases (E00-E89) Presented by Lawrence Santi, DPM, FASPS November 20, 2014 1 APMA Resources ICD-10 Webinars • Register for upcoming webinars • View archived recordings • Download PDF versions of each presentation • www.apma.org/icd10 APMA’s Coding Resource Center • The single best podiatric online coding resource • www.apmacodingrc.org Questions? Contact APMA’s Health Policy & Practice Department [email protected] 2 ICD-10-CM Resources www.apma.org/icd10 3 APMA Coding Resource Center www.apmacodingrc.org 4 GUIDELINES AND INSTRUCTIONS FOR CHAPTER 4 (E00-E89) 5 Endocrine, Nutritional & Metabolic Diseases (E00-E89) • Excludes1: Transitory endocrine and metabolic disorders specific to newborn (P70-P74). These codes cannot be reported together with other codes in this chapter since the two conditions cannot occur together. 6 Endocrine, Nutritional & Metabolic Diseases (E00-E89) This chapter contains the following blocks: • E00-E07 Disorders of thyroid gland • E08-E13 Diabetes mellitus • E15-E16 Other disorders of glucose regulation and pancreatic internal secretion • E20-E35 Disorders of other endocrine glands • E36 Intraoperative complications of endocrine system 7 Endocrine, Nutritional & Metabolic Diseases (E00-E89) • E40-E46 Malnutrition • E50-E64 Other nutritional deficiencies • E65-E68 Overweight, obesity and other hyperalimentation • E70-E88 Metabolic disorders • E89 Postprocedural endocrine and metabolic complications and disorders, not elsewhere classified 8 E10 Type 1 Diabetes Mellitus Includes: • brittle diabetes (mellitus) • diabetes (mellitus) due to autoimmune process • diabetes (mellitus) due to immune mediated pancreatic islet beta-cell destruction • idiopathic diabetes (mellitus) • juvenile onset diabetes (mellitus) • ketosis-prone diabetes (mellitus) 9 E10 Type 1 Diabetes Mellitus Excludes 1: This means the following codes cannot be reported together with other codes in this chapter since the two conditions cannot occur together.
    [Show full text]
  • Diabetic Neuropathic Arthropathy
    Review DIABETIC NEUROPATHIC ARTHROPATHY Ram Singh * Ashish Bhalla ** Atul Sachdev * S. S. Lehl * ABSTRACT nails along with proper selection of accommodative shoe wear (1). Table 1 shows the relationship Diabetic neuropathic arthropathy (Charcot's foot) is between duration of diabetes and the development being increasingly encountered in diabetic patients of neuropathic joint complications, as described by following their prolonged survival. It remains the Forgacs, in a study of 372 cases (4). On an average, foremost predisposing factor for foot amputation in over a two year period, the process can result in a diabetics. Other conditions associated with severely deformed foot, which is highly prone to Charcot's foot such as syphilis and syringomyelia ulcers, infection, and subsequent amputation (5). are rarely encountered. Early diagnosis, staging, Table 2 describes the commonly involved joints in preventive measures and the availability and utility diabetic neuroarthropathy (4). of newer imaging techniques is discussed. Conservative and early corrective surgical Tablel: Duration of Diabetes in Diabetic management techniques for stablization of this Osteoarthropathy (4). condition and prevention of amputation are emphasized. Duration of diabetes (years) Number of reported cases (%) 0-5 27(9.4) 6-10 50(7.5) KEY WORDS: Diabetic neuropathic arthropathy; 11-20 153(53.5) Charcot's foot; Staging; Imaging techniques; >21 56(19.6) Management. Total 286(100) INTRODUCTION Table 2: Localization of Diabetic Osteoarthropathy (4). Neuropathic arthropathy is a chronic, progressive Joints Number of reported cases (%) degenerative disorder affecting one or more Ankle 38 (10.2) Tarsus 81 (21.8) peripheral or vertebral articulations, which develops Tarsometatarsal joints 102 (27.4) as the result of a disturbance in the normal sensory Metatarsophalangeal joints 117 (31.5) (pain or proprioceptive) innervations of joints (1).
    [Show full text]
  • The Charcot Foot in Diabetes
    Reviews/Commentaries/ADA Statements CONSENSUS REPORT The Charcot Foot in Diabetes 1 8 LEE C. ROGERS, DPM ALEXANDRA JIRKOVSKA, MD associated with this condition is midfoot 2 4 ROBERT G. FRYKBERG, DPM, MPH EDWARD JUDE, MD “ ” 3 9 collapse, described as a rocker-bottom DAVID G. ARMSTRONG, DPM, PHD STEPHAN MORBACH, MD 4 10 foot (Fig. 1), although the condition ap- ANDREW J.M. BOULTON, MD WILLIAM B. MORRISON, MD 5 11 pears in other joints and with other pre- MICHAEL EDMONDS, MD MICHAEL PINZUR, MD 6 12 sentations. Pain or discomfort may be a GEORGES HA VAN, MD DARIO PITOCCO, MD 6 13 AGNES HARTEMANN, MD LEE SANDERS, DPM feature of this disorder at the active 7 14 FRANCES GAME, MD DANE K. WUKICH, MD (acute) stage, but the level of pain may 7 15 fi WILLIAM JEFFCOATE, MD LUIGI UCCIOLI, MD be signi cantly diminished when com- pared with individuals with normal sen- sation and equivalent degrees of injury. The diabetic Charcot foot syndrome is a serious and potentially limb-threatening lower-extremity The set of signs and symptoms that complication of diabetes. First described in 1883, this enigmatic condition continues to chal- occur together with CN qualifies this lenge even the most experienced practitioners. Now considered an inflammatory syndrome, the condition as a syndrome, the “Charcot diabetic Charcot foot is characterized by varying degrees of bone and joint disorganization foot syndrome.” secondary to underlying neuropathy, trauma, and perturbations of bone metabolism. An in- ternational task force of experts was convened by the American Diabetes Association and the Definition and classification American Podiatric Medical Association in January 2011 to summarize available evidence on the pathophysiology, natural history, presentations, and treatment recommendations for this entity.
    [Show full text]
  • DIABETES.Pdf
    The Diabetic Patient and Chronic Kidney Disease A Guide to Clinical Practice All rights are reserved by the author and publisher, including the rights of reprinting, reproduction in any form and translation. No part of this book may be reproduced, stored in a retrieval system or transmitted, in any form or by means, electronic, mechanical, photocopying, recording, or otherwise, without the prior written permission of the publisher. First edition: September 2011 European Dialysis and Transplant Nurses Association/ European Renal Care Association (EDTNA/ERCA) Pilatusstrase 35, Postfach 3052, 6002 Luzern, Switzerland www.edtnaerca.org ISBN: 978-84-615-0906-5 D.L.: M-20964-2011 Layout, Binding and Printing: Imprenta Tomás Hermanos Río Manzanares, 42-44 · E28970 Humanes de Madrid Madrid - Spain www.tomashermanos.com 5 Acknowledgements The Diabetic Patient and Chronic Kidney Disease 6 Acknowledgements This book was an initiative of EDTNA/ERCA with the intention to follow the series of books: “Guide to Clinical Practice”. The idea is to cover all areas of renal care to offer guides for integrated care for all patients with renal disease. This book has been divided into two different parts. The fi rst one focused on scientifi c content with the collaboration of experts in Diabetes and Diabetic Nephropathy. The second section concentrates on clinical practice. It has not been easy to compile all the information/input received regarding the important and major disease of Diabetes and its interaction with Chronic Kidney Disease. For that reason, the EDTNA/ERCA would like to recognize all those who contributed to the consolidation of this publication.
    [Show full text]
  • International Classification of Diseases-10 Coding for Diabetes Joy Dugan and Jay Shubrook
    PRACTICAL POINTERS International Classification of Diseases-10 Coding for Diabetes Joy Dugan and Jay Shubrook ore than 29 million Ameri- new codes and did not include a way cans have diabetes. The Cen- to designate laterality. The ICD-10 Mters for Disease Control and system has 68,000 codes that are Prevention predict that the prevalence three to seven digits each and has the of diabetes will increase from 9% to capacity to expand. >30% in the next 35 years. (1) More In general, ICD-10 codes can be than 21 million offices medical visits/ up to seven characters long and are year are scheduled for diabetes. (2) A designed as follows: XXX.XXX.X total of one in five dollars spent on (category.anatomic site/severity.exten- health care in the United States (and sion). The first set of digits before one in three dollars spent through the first decimal point describes the Medicare) are spent on people with general disease or category. The next diabetes. (3) With this in mind, prop- three digits after the first decimal er and accurate coding for diabetes is point describe the etiology, anatom- a necessity. ical site, severity, or clinical detail. The International Classification Finally, some conditions will have a of Diseases 10th Revision—Clinical Modification (ICD-10) is designed second decimal point, followed by a to accurately classify and categorize final digit that may define an initial or all illnesses and diseases seen in the subsequent encounter, the laterality of U.S. health care setting. (4) The cod- a condition, or the number of weeks’ ing system was updated in October gestation (in the case of pregnancy).
    [Show full text]
  • Neuropathic Arthropathy of the Glenohumeral Joint As the Presenting Symptom of a Cervical Syrinx
    Neuropathic Arthropathy of the Glenohumeral Joint as the presenting symptom of a Cervical Syrinx: 1Nicole S. Belkin, MD A Case Report 2George Hung, BS 3Gabriel E Lewullis, MD Introduction the patient reported worsening left shoulder 1 University of Pennsylvania, Neuropathic arthropathy, also known as discomfort that started while shoveling snow. Department of Orthopeadic Surgery, Charcot’s joint disease, is an extreme form of Left arm weakness, acromioclavicular joint Philadelphia, PA non-inflammatory osteoarthritis caused by tenderness and limited range of motion were 2 Perelman School of Medicine at the disturbed sensory innervation and is typically noted. Radiographs demonstrated advanced AC University of Pennsylvania, asymmetric. Classically, neuropathic arthropathy joint arthrosis as well as a chronic-appearing Philadelphia, PA is found in older male patients with an unstable, deformity of the humeral head (Figure 1). 3 BayHealth Orthopedics, painless, and swollen joint.1 Radiographic An MRI revealed a large glenohumeral joint Dover, DE manifestations of neuropathic arthropathy may effusion, posterior humeral head dislocation, include advanced destructive changes in the humeral head deformity with bone marrow joint, scattered “chunks” of bone embedded edema, and chronic rotator cuff tear (Figure 2). in fibrous tissue, joint distension by fluid, and Despite immobilization, the patient’s discomfort heterotopic ossification.2 Diabetes is the most worsened and he developed significant swelling common overall cause and typically affects the about the shoulder. Multiple aspirations yielded foot and ankle joints.3 In the upper extremity, bloody fluid. Analysis of this fluid revealed no the most common cause of neuropathic signs of infection, no malignant cells, and trace arthropathy is syringomyelia, accounting for 80% amounts of extracellular monosodium urate of cases.4 Syringomyelia leads to myelopathy crystals.
    [Show full text]
  • EASD2020 Finalprogramme.Pdf
    56TH ANNUAL MEETING OF THE EUROPEAN ASSOCIATION FOR THE STUDY OF DIABETES Content Page EASD . 4 Morgagni Prize . 10 General Information . 12 EASD Community Plaza . 15 Programme at a Glance . 20 EASD e-Learning . 28 European Diabetes Forum (EUDF) . 29 EFSD Mentorship Programme . 30 Tuesday, 22 September . 32 Claude Bernard Lecture . 32 Poster Event A . 41 Poster Event B . 42 Camillo Golgi Lecture . 50 Albert Renold Lecture . 52 Wednesday, 23 September . 54 Poster Event C . 64 Poster Event D . 65 Diabetes Prize for Excellence Lecture . 72 Thursday, 24 September . 77 Rising Star Symposium . 80 Poster Event E . 90 Poster Event F . 91 Minkowski Lecture . 98 Friday, 25 September . 102 Posters . 119 Index of Presenting Authors . 230 Index of Symposium Speakers . 242 European Foundation for the Study of Diabetes (EFSD) . 244 Symposia on the occasion of the 56th EASD Annual Meeting . 248 Industry Symposia and Meet the Expert Sessions on the occasion of the 56th EASD Annual Meeting (organised by INTERPLAN) . 263 57th EASD Annual Meeting . 310 DEAR MEMBERS AND GUESTS, It is my great honour and pleasure to welcome you to the 56th Annual Meeting of the European Association for the Study of Diabetes, which will take place – due to the severe global impact of the COVID-19 pandemic – as an innovative Virtual Meeting from 21 to 25 September 2020. EASD We have developed a virtual experience using the latest technology to connect the global diabetes community, share ground-breaking diabetes science and research, and to provide educational opportunities that
    [Show full text]
  • OCTOBER 2019 Mrx Pipeline a View Into Upcoming Specialty and Traditional Drugs TABLE of CONTENTS
    OCTOBER 2019 MRx Pipeline A view into upcoming specialty and traditional drugs TABLE OF CONTENTS EDITORIAL STAFF Introduction Maryam Tabatabai, PharmD Editor in Chief Senior Director, Drug Information Pipeline Deep Dive Carole Kerzic, RPh Executive Editor Drug Information Pharmacist Keep on Your Radar Consultant Panel Michelle Booth, PharmD Director, Medical Pharmacy Strategy Becky Borgert, PharmD, BCOP Pipeline Drug List Director, Clinical Oncology Product Development Lara Frick, PharmD, BCPS, BCPP Drug Information Pharmacist Glossary Robert Greer, RPh, BCOP Senior Director, Clinical Strategy and Programs Sam Leo, PharmD Director, Clinical Strategy and Innovation, Specialty Troy Phelps Senior Director, COAR - Analytics Nothing herein is or shall be construed as a promise or representation regarding past or future events and Magellan Rx Management expressly disclaims any and all liability relating to the use of or reliance on the information contained in this presentation. The information contained in this publication is intended for educational purposes only and should not be considered clinical, financial, or legal advice. By receipt of this publication, each recipient agrees that the information contained herein will be kept confidential and that the information will not be photocopied, reproduced, distributed to, or disclosed to others at any time without the prior written consent of Magellan Rx Management. 1 | magellanrx.com INTRODUCTION Welcome to the MRx Pipeline. In its third year of publication, this quarterly report offers clinical insights and competitive intelligence on anticipated drugs in development. Our universal forecast addresses trends applicable across market segments. Traditional and specialty drugs, agents under the pharmacy and medical benefits, new molecular entities, pertinent new and expanded indications for existing medications, and biosimilars are profiled in the report.
    [Show full text]