Stress Fractures: Diagnosis, Treatment, and Prevention DEEPAK S

Total Page:16

File Type:pdf, Size:1020Kb

Stress Fractures: Diagnosis, Treatment, and Prevention DEEPAK S Stress Fractures: Diagnosis, Treatment, and Prevention DEEPAK S. PATEL, MD, Rush-Copley Family Medicine Residency, Aurora, Illinois MATT ROTH, MD, The Toledo Hospital Primary Care Sports Medicine Fellowship, Toledo, Ohio NEHA KAPIL, MD, Rush-Copley Family Medicine Residency, Aurora, Illinois Stress fractures are common injuries in athletes and military recruits. These injuries occur more commonly in lower extremities than in upper extremities. Stress fractures should be considered in patients who present with tenderness or edema after a recent increase in activity or repeated activity with limited rest. The differential diagnosis varies based on location, but commonly includes tendinopathy, compartment syndrome, and nerve or artery entrapment syndrome. Medial tibial stress syndrome (shin splints) can be distinguished from tibial stress fractures by diffuse tenderness along the length of the posteromedial tibial shaft and a lack of edema. When stress fracture is suspected, plain radiography should be obtained initially and, if negative, may be repeated after two to three weeks for greater accuracy. If an urgent diagnosis is needed, triple-phase bone scintigraphy or magnetic resonance imaging should be considered. Both modalities have a similar sensitivity, but magnetic resonance imaging has greater specificity. Treatment of stress frac- tures consists of activity modification, including the use of nonweight- bearing crutches if needed for pain relief. Analgesics are appropriate to relieve pain, and pneumatic bracing can be used to facilitate healing. After the pain is resolved and the examination shows improvement, patients may gradually increase their level of activity. Surgical consul- tation may be appropriate for patients with stress fractures in high-risk locations, nonunion, or recurrent stress fractures. Prevention of stress fractures has been studied in military personnel, but more research is needed in other populations. (Am Fam Physician. 2011;83(1):39-46. Copyright © 2011 American Academy of Family Physicians.) ILLUSTRATION BY DAVID KLEMM ▲ Patient information: tress fractures are common injuries who participate in sports involving throwing A handout on stress that begin with repetitive and exces- or other overhead motions.5 fractures, written by the authors of this article, is sive stress on the bone. This leads Persons who participate in repetitive, provided on page 47. to the acceleration of normal bone high-intensity training, such as athletes and S remodeling, the production of microfrac- military recruits, are at increased risk of tures (caused by insufficient time for the developing stress fractures.3-6 Recreational bone to repair), the creation of a bone stress runners who average more than 25 miles injury (i.e., stress reaction), and, eventually, per week are at increased risk of stress frac- a stress fracture.1,2 In contrast, pathological tures,4,7 as well as athletes who participate in (insufficiency) fractures occur under nor- track and field, basketball, soccer, or dance mal stress in bone weakened by a tumor, (Table 12-9).3,5 Women are at higher risk of infection, or osteoporosis.1,2 stress fracture than men,4 especially women The most common locations for stress frac- in the military,2 although there are conflict- tures are the tibia (23.6 percent), tarsal navic- ing data among female athletes.3,5 ular (17.6 percent), metatarsal (16.2 percent), Poor nutrition and lifestyle habits may fibula (15.5 percent), femur (6.6 percent), increase the risk of stress fracture. One pelvis (1.6 percent), and spine (0.6 percent).3,4 study found lower 25-hydroxyvitamin D Although less common, upper extrem- levels in Finnish male military recruits ity stress fractures can occur in persons with stress fractures.8 Women with the Downloaded from the American Family Physician Web site at www.aafp.org/afp. Copyright © 2010 American Academy of Family Physicians. For the private, noncommer- January cial1, 2011use of ◆one Volume individual 83, user Number of the Web 1 site. All other rights reserved.www.aafp.org/afp Contact [email protected] for copyright questionsAmerican and/or permission Family requests. Physician 39 Stress Fractures SORT: KEY RECOMMENDATIONS FOR PRACTICE Evidence Clinical recommendations rating References Comments Plain radiography should be the initial imaging modality to diagnose C 15 Consensus opinion stress fractures. Magnetic resonance imaging is preferred over bone scintigraphy for C 15 Consensus opinion the diagnosis of stress fractures because of greater specificity. Patients with tibial stress fracture may use a pneumatic compression A 20 Cochrane review device to reduce the time to resumption of full activity. Bone stimulators should not be used for the treatment of most stress B 24, 25 Good-quality randomized fractures. controlled trial Shock-absorbing orthotics and footwear modification may reduce B 20 Cochrane review lacking the occurrence of lower extremity stress injury. firm recommendation A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease- oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to http://www.aafp. org/afpsort.xml. female athlete triad (i.e., eating disorders, with limited rest.5-7,10 Pain is a common functional hypothalamic amenorrhea, and presenting symptom that can vary by loca- osteoporosis) are at higher risk of stress tion, such as knee pain with a proximal tibial fracture.9 A study of female military recruits injury, hip pain with a femoral neck injury, demonstrated an increased risk of stress or groin pain with a pelvic fracture.2,7 Spe- fracture with a history of smoking, exer- cifically, pain with ambulation is common cising less than three times per week, and (81 percent).10 On examination, patients usu- consuming more than 10 alcoholic drinks ally demonstrate focal tenderness (65.9 to per week before the start of basic training.6 100 percent) and edema (18 to 44 percent) at Additionally, 16.2 percent of white recruits the site of injury.4,10,11 who smoked and did not exercise developed Although the hop test (i.e., single leg hop- a stress fracture.6 ping that produces severe localized pain) is often used and cited in texts as a diagnostic Diagnosis test for lower extremity fractures, no recent Stress fracture should be suspected in per- literature was found to validate its accuracy. sons with a drastic recent increase in physi- In some studies, a positive hop test was an cal activity or repeated excessive activity inclusion criterion4 or a common finding (70 to 100 percent 7,11) in patients with pre- sumed stress fractures, but was also noted Table 1. Risk Factors for Stress in nearly one-half (45.6 percent) of patients Fracture with suspected medial tibial stress syn- drome (shin splints).12 Another diagnostic Consuming more than 10 alcoholic drinks measure used often, but with little support- per week ing evidence, is the tuning fork test (i.e., Excessive physical activity with limited rest applying a tuning fork to the fracture site to periods produce focal pain). One small study found Female athlete triad (eating disorders, that the tuning fork test had a sensitivity amenorrhea, osteoporosis) of 75 percent, a specificity of 67 percent, a Female sex positive predictive value of 77 percent, and Low levels of 25-hydroxyvitamin D a negative predictive value of 63 percent for Recreational running (more than 25 miles 13 per week) tibial stress fractures. Smoking Diagnosing stress fractures can be chal- Sudden increase in physical activity lenging and warrants consideration of the Track (running sports) differential diagnosis, based on location (Table 23,6,7,14). The differential diagnosis Information from references 2 through 9. may include tendinopathy, compartment syndrome, and nerve or artery entrapment 40 American Family Physician www.aafp.org/afp Volume 83, Number 1 ◆ January 1, 2011 Stress Fractures Table 2. Risk Factors, Signs and Symptoms, and Differential Diagnosis of Common Stress Fractures Differential Fracture type Risk factors Signs and symptoms diagnosis Comments Tibial Running, walking, Shin pain, focal tenderness Medial tibial stress Shin splints may cause pain along jumping, dancing, over anterior aspect of syndrome (shin the posteromedial border of the female athlete tibia, edema splints) distal tibia; no abnormalities will triad appear on radiography Metatarsal Running, walking, Foot or ankle pain, focal Plantar fasciitis, Plantar fasciitis may cause pain or dancing, marching tenderness, swelling metatarsalgia, tenderness along the fascia Morton neuroma Metatarsalgia may cause tenderness on metatarsal heads Morton neuroma may cause pain (with compression) between the third and fourth metatarsals Femoral or Running, walking, Groin pain, pain with Pathologic Urgent imaging is needed to identify sacral female athlete activity, pain with passive fracture, rectus underlying pathology triad, cycling hip range of movement femoris strain Localized tenderness and swelling (with sacral fracture only) Spondylolysis Soccer, gymnastics, Tenderness, extension- Lumbar sprain, Most commonly associated with volleyball, related pain during pathologic L4 and L5 vertebrae; confirm dancing, football, “stork” test (single-leg fracture diagnosis with scintigraphy with weightlifting hyperextension/rotation) single-photon emission computed tomography14 Information from references 3, 6, 7, and 14. Table
Recommended publications
  • Severe Septicaemia in a Patient with Polychondritis and Sweet's
    81 LETTERS Ann Rheum Dis: first published as 10.1136/ard.62.1.88 on 1 January 2003. Downloaded from Severe septicaemia in a patient with polychondritis and Sweet’s syndrome after initiation of treatment with infliximab F G Matzkies, B Manger, M Schmitt-Haendle, T Nagel, H-G Kraetsch, J R Kalden, H Schulze-Koops ............................................................................................................................. Ann Rheum Dis 2003;62:81–82 D Sweet first described an acute febrile neutrophilic dermatosis in 1964 characterised by acute onset, fever, Rleucocytosis, and erythematous plaques.1 Skin biopsy specimens show infiltrates consisting of mononuclear cells and neutrophils with leucocytoclasis, but without signs of vasculi- tis. Sweet’s syndrome is frequently associated with solid malig- nancies or haemoproliferative disorders, but associations with chronic autoimmune connective tissue disorders have also been reported.2 The aetiology of Sweet’s syndrome is unknown, but evidence suggests that an immunological reaction of unknown specificity is the underlying mechanism. CASE REPORT A 51 year old white man with relapsing polychondritis (first diagnosed in 1997) was admitted to our hospital in June 2001 with a five week history of general malaise, fever, recurrent arthritis, and complaints of morning stiffness. Besides Figure 1 autoimmune polychondritis, he had insulin dependent Manifestation of Sweet’s syndrome in a patient with relapsing polychondritis. diabetes mellitus that was diagnosed in 1989. On admission, he presented with multiple small to medium, sharply demarked, raised erythematous plaques on both fore- dose of glucocorticoids (80 mg) and a second application of http://ard.bmj.com/ arms and lower legs, multiple acne-like pustules on the face, infliximab (3 mg/kg body weight) were given.
    [Show full text]
  • Hypophosphatasia Could Explain Some Atypical Femur Fractures
    Hypophosphatasia Could Explain Some Atypical Femur Fractures What we know Hypophosphatasia (HPP) is a rare genetic disease that affects the development of bones and teeth in children (Whyte 1985). HPP is caused by the absence or reduced amount of an enzyme called tissue-nonspecific alkaline phosphatase (TAP), also called bone-specific alkaline phosphatase (BSAP). The absence of TAP raises the level of inorganic pyrophosphate (Pi), which prevents calcium and phosphate from creating strong, mineralized bone. Without TAP, bones can become weak. In its severe form, HPP is fatal and happens in 1/100,000 births. Because HPP is genetic, it can appear in adults as well. A recent study has identified a milder, more common form of HPP that occurs in 4 of 1000 adults (Dahir 2018). This form of HPP is usually seen in early middle aged adults who have low bone density and sometimes have stress fractures in the feet or thigh bone. Sometimes these patients lose their baby teeth early, but not always. HPP is diagnosed by measuring blood levels of TAP and vitamin B6. An elevated vitamin B6 level [serum pyridoxal 5-phosphate (PLP)] (Whyte 1985) in a patient with a TAP level ≤40 or in the low end of normal can be diagnosed with HPP. Almost half of the adult patients with HPP in the large study had TAP >40, but in the lower end of the normal range (Dahir 2018). The connection between hypophosphatasia and osteoporosis Some people who have stress fractures get a bone density test and are treated with an osteoporosis medicine if their bone density results are low.
    [Show full text]
  • Osteomalacia and Osteoporosis D
    Postgrad. med.J. (August 1968) 44, 621-625. Postgrad Med J: first published as 10.1136/pgmj.44.514.621 on 1 August 1968. Downloaded from Osteomalacia and osteoporosis D. B. MORGAN Department of Clinical Investigation, University ofLeeds OSTEOMALACIA and osteoporosis are still some- in osteomalacia is an increase in the alkaline times confused because both diseases lead to a phosphatase activity in the blood (SAP); there deficiency of calcium which can be detected on may also be a low serum phosphorus or a low radiographs of the skeleton. serum calcium. This lack of calcium is the only feature Our experience with the biopsy of bone is that common to the two diseases which are in all a large excess of uncalcified bone tissue (osteoid), other ways easily distinguishable. which is the classic histological feature of osteo- malacia, is only found in patients with the other Osteomalacia typical features of the disease, in particular the Osteomalacia will be discussed first, because it clinical ones (Morgan et al., 1967a). Whether or is a clearly defined disease which can be cured. not more subtle histological techniques will detect Osteomalacia is the result of an imbalance be- earlier stages of the disease remains to be seen. tween the supply of and the demand for vitamin Bone pains, muscle weakness, Looser's zones, D. The the following description of disease is raised SAP and low serum phosphate are the Protected by copyright. based on our experience of twenty-two patients most reliable aids to the diagnosis of osteomalacia, with osteomalacia after gastrectomy; there is no and approximately in that order.
    [Show full text]
  • An Unusual Cause of Back Pain in Osteoporosis: Lessons from a Spinal Lesion
    Ann Rheum Dis 1999;58:327–331 327 MASTERCLASS Series editor: John Axford Ann Rheum Dis: first published as 10.1136/ard.58.6.327 on 1 June 1999. Downloaded from An unusual cause of back pain in osteoporosis: lessons from a spinal lesion S Venkatachalam, Elaine Dennison, Madeleine Sampson, Peter Hockey, MIDCawley, Cyrus Cooper Case report A 77 year old woman was admitted with a three month history of worsening back pain, malaise, and anorexia. On direct questioning, she reported that she had suVered from back pain for four years. The thoracolumbar radiograph four years earlier showed T6/7 vertebral collapse, mild scoliosis, and degenerative change of the lumbar spine (fig 1); but other investigations at that time including the eryth- rocyte sedimentation rate (ESR) and protein electophoresis were normal. Bone mineral density then was 0.914 g/cm2 (T score = −2.4) at the lumbar spine, 0.776 g/cm2 (T score = −1.8) at the right femoral neck and 0.738 g/cm2 (T score = −1.7) at the left femoral neck. She was given cyclical etidronate after this vertebral collapse as she had suVered a previous fragility fracture of the left wrist. On admission, she was afebrile, but general examination was remarkable for pallor, dental http://ard.bmj.com/ caries, and cellulitis of the left leg. A pansysto- lic murmur was heard at the cardiac apex on auscultation; there were no other signs of bac- terial endocarditis. She had kyphoscoliosis and there was diVuse tenderness of the thoraco- lumbar spine. Her neurological examination was unremarkable. on September 29, 2021 by guest.
    [Show full text]
  • Distinguishing Transient Osteoporosis of the Hip from Avascular Necrosis
    Original Article Article original Distinguishing transient osteoporosis of the hip from avascular necrosis Anita Balakrishnan, BMedSci;* Emil H. Schemitsch, MD;* Dawn Pearce, MD;† Michael D. McKee, MD* Introduction: To review the circumstances surrounding the misdiagnosis of transient osteoporosis of the hip (TOH) as avascular necrosis (AVN) and to increase physician awareness of the prevalence and diagnosis of this condition in young men, we reviewed a series of cases seen in the orthopedic unit at St. Michael’s Hospital, University of Toronto. Methods: We studied the charts of patients with TOH referred between 1998 and 2001 with a diagnosis of AVN for demographic data, risk factors, imaging results and outcomes. Results: Twelve hips in 10 young men (mean age 41 yr, range from 32–55 yr) were identified. Nine men underwent magnetic resonance imaging (MRI) before referral, which showed characteristic changes of TOH. All 10 patients were referred for surgical intervention for a diagnosis of AVN. The correct diagnosis was made after reviewing patients’ charts and the scans and was confirmed by spontaneous resolution of both symptoms and MRI findings an average of 5.5 months and 7.5 months, respectively, after consultation. Conclusions: Despite recent publications, the prevalence of TOH among young men is still overlooked and the distinctive MRI appearance still misinterpreted. Symptoms may be severe but resolve over time with reduced weight bearing. The absence of focal changes on MRI is highly suggestive of a transient lesion. A greater level of awareness of this condition is needed to differentiate TOH from AVN, avoiding unnecessary surgery and ensuring appropriate treatment.
    [Show full text]
  • Hematological Diseases and Osteoporosis
    International Journal of Molecular Sciences Review Hematological Diseases and Osteoporosis , Agostino Gaudio * y , Anastasia Xourafa, Rosario Rapisarda, Luca Zanoli , Salvatore Santo Signorelli and Pietro Castellino Department of Clinical and Experimental Medicine, University of Catania, 95123 Catania, Italy; [email protected] (A.X.); [email protected] (R.R.); [email protected] (L.Z.); [email protected] (S.S.S.); [email protected] (P.C.) * Correspondence: [email protected]; Tel.: +39-095-3781842; Fax: +39-095-378-2376 Current address: UO di Medicina Interna, Policlinico “G. Rodolico”, Via S. Sofia 78, 95123 Catania, Italy. y Received: 29 April 2020; Accepted: 14 May 2020; Published: 16 May 2020 Abstract: Secondary osteoporosis is a common clinical problem faced by bone specialists, with a higher frequency in men than in women. One of several causes of secondary osteoporosis is hematological disease. There are numerous hematological diseases that can have a deleterious impact on bone health. In the literature, there is an abundance of evidence of bone involvement in patients affected by multiple myeloma, systemic mastocytosis, thalassemia, and hemophilia; some skeletal disorders are also reported in sickle cell disease. Recently, monoclonal gammopathy of undetermined significance appears to increase fracture risk, predominantly in male subjects. The pathogenetic mechanisms responsible for these bone loss effects have not yet been completely clarified. Many soluble factors, in particular cytokines that regulate bone metabolism, appear to play an important role. An integrated approach to these hematological diseases, with the help of a bone specialist, could reduce the bone fracture rate and improve the quality of life of these patients.
    [Show full text]
  • Hypophosphatasia: Canadian Update on Diagnosis and Management
    Osteoporosis International (2019) 30:1713–1722 https://doi.org/10.1007/s00198-019-04921-y CONSENSUS STATEMENT Hypophosphatasia: Canadian update on diagnosis and management A.A. Khan1 & R. Josse2 & P. Kannu3 & J. Villeneuve4 & T. Paul5 & S. Van Uum6 & C.R. Greenberg7 Received: 17 September 2018 /Accepted: 27 February 2019 /Published online: 26 March 2019 # International Osteoporosis Foundation and National Osteoporosis Foundation 2019, corrected publication 2019 Abstract Summary Hypophosphatasia (HPP) is a rare inherited disorder of bone and mineral metabolism caused by loss of function mutations in the ALPL gene. The presentation in children and adults can be extremely variable and natural history is poorly understood particularly in adults. Careful patient evaluation is required with consideration of pharmacologic intervention in individuals meeting criteria for therapy. Introduction The purposes of this review are to present current evidence regarding the diagnosis and management of hypophosphatasia in children and adults and provide evidence-based recommendations for management. Method A MEDLINE, EMBASE, and Cochrane database search and literature review was completed. The following consensus recommendations were developed based on the highest level of evidence as well as expert opinion. Results Hypophosphatasia is a rare inherited disorder of bone and mineral metabolism due to loss of function mutations in the tissue non-specific alkaline phosphatase (ALPL) gene causing reductions in the activity of the tissue non-specific isoenzyme of alkaline phosphatase (TNSALP). Deficient levels of alkaline phosphatase result in elevation of inhibitors of mineralization of the skeleton and teeth, principally inorganic pyrophosphate. The impaired skeletal mineralization may result in elevations in serum calcium and phosphate. Clinical features include premature loss of teeth, metatarsal and subtrochanteric fractures as well as fragility fractures.
    [Show full text]
  • Mineralization of Bones in Osteoporosis and Osteomalacia Walaa Fikry Elbossaty*
    Review Article iMedPub Journals Annals of Clinical and Laboratory Research 2017 www.imedpub.com Vol.5 No.4:201 ISSN 2386-5180 DOI: 10.21767/2386-5180.1000201 Mineralization of Bones in Osteoporosis and Osteomalacia Walaa Fikry Elbossaty* Department of Chemistry, Biochemistry Division, Faculty of Science, Damietta University, Damietta, Egypt *Corresponding author: Walaa Fikry Elbossaty, Department of Chemistry, Biochemistry Division, Faculty of Science, Damietta University, Damietta, Egypt, Tel: + 020573761683; E-mail: [email protected] Received: September 01, 2017; Accepted: November 20, 2017; Published: November 27, 2017 Citation: Elbossaty WF (2017) Mineralization of Bones in Osteoporosis and Osteomalacia. Ann Clin Lab Res Vol.5: No.4: 201. more well-known than osteomalacia [2]. Abstract Literature Review All vital process in human life as walking, jumping, working, and enjoy with good life apply healthy bone. The normal bone formation required significant amount of some minerals as calcium and phosphorous, also vitamin D which play important role in movement of calcium in to bone which responsible for bone healthy. There are different causes include life style, genetics, hormonal, and insufficient amount take from calcium and vitamin D which responsible for defect in bone formation process, and appear abnormal bone structure. The most bone diseases are osteoporosis, and osteomalacia in this work we discuss the definition, causes sign, diagnosis, pathophysiology, and treatment of both osteoporosis, and osteomalacia. Keywords: Osteoporosis; Vitamin D; Osteomalacia; Figure 1 Structure of bone Calcium Osteoporosis Introduction Definition of osteoporosis: Osteoporosis is a bone disease which characterized by low bone mass as result of body loses Bone too much bone and makes too little bone.
    [Show full text]
  • Adult Hypophosphatasia : a Disease Where the Clinical Complications Could Be Avoided by Careful Evaluation of Patients
    This is a repository copy of Adult Hypophosphatasia : a disease where the clinical complications could be avoided by careful evaluation of patients. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/154612/ Version: Accepted Version Proceedings Paper: Schini, M. orcid.org/0000-0003-2204-2095 and Eastell, R. orcid.org/0000-0002-0323-3366 (2018) Adult Hypophosphatasia : a disease where the clinical complications could be avoided by careful evaluation of patients. In: Osteoporosis International. Osteoporosis Conference 2018, 02-04 Dec 2018, Birmingham, UK. Springer , pp. 632-633. https://doi.org/10.1007/s00198-018-4738-8 This is a post-peer-review, pre-copyedit version of an abstract published in Osteoporosis International. The final authenticated version is available online at: https://doi.org/10.1007/s00198-018-4738-8 Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ ADULT HYPOPHOSPHATASIA: A DISEASE WHERE THE CLINICAL COMPLICATIONS COULD BE AVOIDED BY CAREFUL EVALUATION OF PATIENTS Background: Hypophosphatasia (HPP) is a rare disease that has to be excluded before starting treatment for osteoporosis; HPP patients are more prone to develop atypical femur fractures (AFF) from bisphosphonates.
    [Show full text]
  • Relapsing Polychondritis
    Disclosure statement Relapsing Collaborative research agreement with Polychondritis Novo Nordisk Jane Hoyt Buckner, MD Benaroya Research Institute Virginia Mason Medical Center Seattle WA 11/6/2011 Jane Hoyt Buckner 1 Topics of Discussion What is RP? Relapsing Polychondritis is an inflammatory disease of the hyaline cartilage Spectrum of disease in RP Hallmarks of the disease- inflammation of cartilage Diagnosis involving: Pathogenic mechanisms of disease • Auricular • Management Nasal • Costochondral Case Studies • Respiratory Tract • Joints Lahmer et al Autoimmunity Reviews (2010) 540–546 What is RP? Beyond Chrondritis Diagnostic Criteria Inflammation of structural component of end Clinical Manifestations organs: McAdam’s Criteria Bilateral auriclar chondritis require: 3 clinical Nonerosive, seronegative inflammatory polyarthritis manifestations, Nasal chondritis • Ocular with biopsy Ocular inflammation • Vasculopathy confirmation unless the Respiratory tract chondritis • Vasculitis diagnosis is Cochlear and /or vestibular dysfunction • Nephritis clinically obvious. Pathology • Encephalitis Cartilage biopsy with histologic findings compatible with relapsing polychondritis. Ref. Medicine 55:193, 1976 Lahmer et al Autoimmunity Reviews (2010) 540–546 Relapsing Polychondritis 1 Epidemiology Auricular Chondritis Frequency in the population Over 550 cases reported Inflammation of the external ear is the most common manifestation of 3.5 cases/million (Rochester, Minnesota) RP Age 83% of patients mean at onset 40-50 Erythema, tenderness and swelling Ranging from 16-90 present for days-weeks Gender Sparing of the ear lobe is typically F:M=1:1 found BRI RP registry Thickening and or drooping of ear 14 patients/3 million King County lobe may result from a flare of RP. 178 patients participating from the United States. Auricular Chondritis Clinical Manifestations Audiovestibular Symptoms: Differential diagnosis • Cellulitis .
    [Show full text]
  • Who Scientific Group on the Assessment of Osteoporosis at Primary Health Care Level
    WHO SCIENTIFIC GROUP ON THE ASSESSMENT OF OSTEOPOROSIS AT PRIMARY HEALTH CARE LEVEL Summary Meeting Report Brussels, Belgium, 5-7 May 2004 1 © World Health Organization 2007 All rights reserved. Publications of the World Health Organization can be obtained from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected] ). Requests for permission to reproduce or translate WHO publications – whether for sale or for noncommercial distribution – should be addressed to WHO Press, at the above address (fax: +41 22 791 4806; e- mail: [email protected] ). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. All reasonable precautions have been taken by the World Health Organization to verify the information contained in this publication. However, the published material is being distributed without warranty of any kind, either expressed or implied. The responsibility for the interpretation and use of the material lies with the reader.
    [Show full text]
  • Prevalence of Osteoporosis and Osteopenia Diagnosed Using Quantitative CT in 296 Consecutive Lumbar Fusion Patients
    NEUROSURGICAL FOCUS Neurosurg Focus 49 (2):E5, 2020 Prevalence of osteoporosis and osteopenia diagnosed using quantitative CT in 296 consecutive lumbar fusion patients Brandon B. Carlson, MD, MPH,1 Stephan N. Salzmann, MD,2 Toshiyuki Shirahata, MD, PhD,2 Courtney Ortiz Miller, BA,2 John A. Carrino, MD, MPH,3 Jingyan Yang, MHS, DrPH,2,4 Marie-Jacqueline Reisener, MD,2 Andrew A. Sama, MD,2 Frank P. Cammisa, MD,2 Federico P. Girardi, MD,2 and Alexander P. Hughes, MD2 1Marc A. Asher, MD, Comprehensive Spine Center, University of Kansas Medical Center, Kansas City, Kansas; 2Spine Care Institute and 3Department of Radiology and Imaging, Hospital for Special Surgery, New York; and 4Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York OBJECTIVE Osteoporosis is a metabolic bone disease that increases the risk for fragility fractures. Screening and diagnosis can be achieved by measuring bone mineral density (BMD) using quantitative CT tomography (QCT) in the lumbar spine. QCT-derived BMD measurements can be used to diagnose osteopenia or osteoporosis based on Ameri- can College of Radiology (ACR) thresholds. Many reports exist regarding the disease prevalence in asymptomatic and disease-specific populations; however, osteoporosis/osteopenia prevalence rates in lumbar spine fusion patients without fracture have not been reported. The purpose of this study was to define osteoporosis and osteopenia prevalence in lumbar fusion patients using QCT. METHODS A retrospective review of prospective data was performed. All patients undergoing lumbar fusion surgery who had preoperative fine-cut CT scans were eligible. QCT-derived BMD measurements were performed at L1 and L2.
    [Show full text]