Max % Qs Topics Covered from Orthobullets in Study Plan General
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ICD-9CM Coding Achilles Bursitis Or Tendinitis 726.71 Adhesive
ICD-9CM CODING OF COMMON CHIROPRACTIC CONDITIONS CONDITION ICD-9CM coding Achilles bursitis or tendinitis 726.71 Adhesive capsulitis of shoulder 726 Anklyosing Spondylitis (spine only) 720 Anterior cruciate ligament (old disruption) 717.83 Bicipital tenosynovitis 726.12 Boutonniere deformity 736.21 Brachial neuritis or radiculitis 723.4 Bunion 727.1 Bursitis of knee 726.6 Calcaneal spur 726.73 Carpal tunnel syndrome 354 Cervical radiculitis 723.4 Cervical spondylosis with myelopathy 721.1 Cervical spondylosis without myelopathy 721 Cervicalgia 723.1 Chondromalacia of patella 717.7 Claw hand (acquired) 736.06 Claw toe (acquired) 735.5 Coccygodynia 724.79 Coxa plana 732.1 Coxa valga (acquired) 736.31 Coxa vara (acquired) 736.32 de Quervain's disease 727.04 Degeneration of cervical intervertebral disc 722.4 Degeneration of thoracic or lumbar intervertebral disc 722.5 Disc Degeneration (Cervical with myelopathy) 722.71 Disc Degeneration (Lumbar with myelopathy) 722.73 Disc Degeneration (Thoracic) 722.51 Disc Degeneration (Cervical) 722.4 Disc Degeneration (Lumbar) 722.52 Disc Degeneration (Thoracic with myelopathy) 722.72 Disc displacement without myelopathy (Thoracic) 722.11 Disc displacement of without myelopathy (Cervical ) 722 Disc displacement without myelopathy (Lumbar) 722.1 Dupuytren's contracture 728.6 Entrapment syndromes 354.0-355.9 Epicondylitis (Lateral) 726.32 Epicondylitis (Medial) 726.31 Flat foot-Pes planus (acquired) 734 Fracture (Lumbar) 805.4 Ganglion of tendon sheath 727.42 Genu recurvatum (acquired) 736.5 Genu valgum -
A Case Report on Charcot-Marie-Tooth Disease with a Novel Periaxin Gene Mutation
Open Access Case Report DOI: 10.7759/cureus.5111 A Case Report on Charcot-Marie-Tooth Disease with a Novel Periaxin Gene Mutation Sorabh Datta 1 , Saurabh Kataria 1 , Raghav Govindarajan 1 1. Neurology, University of Missouri, Columbia, USA Corresponding author: Sorabh Datta, [email protected] Abstract Charcot-Marie-Tooth (CMT) disease is one of the most common primary hereditary neuropathies causing peripheral neuropathies. More than 60 different gene mutations are causing this disease. The PRX gene codes for Periaxin proteins that are expressed by Schwann cells and are necessary for the formation and maintenance of myelination of peripheral nerves. Dejerine-Sottas neuropathy and Charcot-Marie-Tooth type 4F (CMT4F) are the two different clinical phenotypes observed in association with PRX gene mutation. This article describes a case of an elderly male with a novel mutation involving the PRX gene. Categories: Genetics, Internal Medicine, Neurology Keywords: neurology, sensorimotor neuropathy, congenital, gene expression, genetic mutation, protein, pes cavus, demyelinating diseases, charcot-marie-tooth, autosomal recessive disorder Introduction As per the Dyck classification in the year 1970, primary hereditary neuropathies are divided into hereditary motor sensory neuropathy (HMSN) and hereditary sensory autonomic neuropathy (HSAN) [1]. Charcot- Marie-Tooth (CMT) disease is a type of HMSN with an estimated prevalence of 1 in 2,500 [2]. CMT can follow autosomal recessive (ARCMT), X-linked recessive, and also an autosomal dominant pattern. CMT type 4 is a rapidly increasing ARCMT disease form in HMSN, although CMT type 1 and 2 still account for the most substantial proportion of the patient population [3]. CMT4F is a severe, demyelinating subtype of CMT type 4 and is characterized by childhood onset of slowly progressing weakness in the distal muscles associated with atrophy. -
ICD-9 to ICD-10 Mapping Tool Courtesy Of: the Paperwork Project
ICD-9 to ICD-10 Mapping Tool Courtesy of: The Paperwork Project Spinal Subluxation ICD-9 ICD-10 M99.00 Segmental and somatic dysfunction, Head region (occipito-cervical) 739.0 Segmental and somatic dysfunction, Head region (occipito-cervical) M99.10 Subluxation complex (vertebral), Head region M99.01 Segmental and somatic dysfunction, Cervical region 739.1 Segmental and somatic dysfunction, Cervical region M99.11 Subluxation complex (vertebral), Cervical region M99.02 Segmental and somatic dysfunction, Thoracic region 739.2 Segmental and somatic dysfunction, Thoracic region M99.12 Subluxation complex (vertebral), Thoracic region M99.03 Segmental and somatic dysfunction, Lumbar region 739.3 Segmental and somatic dysfunction, Lumbar region M99.13 Subluxation complex (vertebral), Lumbar region M99.04 Segmental and somatic dysfunction, Sacral region 739.4 Segmental and somatic dysfunction, Sacral region M99.14 Subluxation complex (vertebral), Sacral region M99.05 Segmental and somatic dysfunction, Sacroiliac, hip, pubic regions 739.5 Segmental and somatic dysfunction, Sacroiliac, hip, pubic regions M99.15 Subluxation complex (vertebral), Pelvic region 839.08 Closed dislocation, Multiple cervical vertebra (injury) S13.101_ Dislocation of unspecified cervical vertebra (injury) ** 839.20 Closed dislocation, Lumbar vertebra (injury) S33.101_ Dislocation of unspecified lumbar vertebra (injury) ** 839.21 Closed dislocation, Thoracic vertebra (injury) S23.101_ Dislocation of unspecified thoracic vertebra (injury) ** 839.42 Closed dislocation, Sacrum, -
The Nutrition and Food Web Archive Medical Terminology Book
The Nutrition and Food Web Archive Medical Terminology Book www.nafwa. -
Musculoskeletal Radiology.Pdf
MS 1 Acute osteomyelitis Acute osteomyelitis Plain radiographs reviewed Spine Other bones MRI Acute osteomyelitis Acute osteomyelitis diagnosed not diagnosed CT, MRI or Nuclear medicine Diagnosis Normal established scan Osteomyelitis Treatment excluded 144 MS 1 Acute osteomyelitis REMARKS 1 Plain radiograph 1.1 Regional radiographs should be the initial examination to determine whether there is any underlying pathological condition. 1.2 Typical findings of bone destruction and periosteal reaction may not appear until 10- 21 days after the onset of infection because 30-50% of bone density loss must occur before radiographs become abnormal. 1.3 Plain radiographs are unreliable to establish the diagnosis of osteomyelitis in patients with violated bone. 1.4 Plain radiographs of spine are not sensitive to detect vertebral osteomyelitis but findings of endplate destruction and progressive narrowing of adjacent disc space are highly suggestive of infection. 2 Nuclear medicine 2.1 Scans should be interpreted with contemporary radiographs. 2.2 Three-phase Technetium-99m methylene diphosphonate (Tc-99m-MDP) bone scan 2.2.1 Bone scan is more sensitive than plain radiography (up to 90% sensitivity). 2.2.2 Bone scan can be positive as early as 3 days after onset of disease (10-14 days earlier than plain radiograph). 2.3 Gallium scan 2.3.1 Gallium scan is helpful as conjunction with a bone scan. Combined gallium and bone scan studies has sensitivity of 81-90% and specificity of 69-100% 2.4 White blood cells (WBC) scan 2.4.1 This is sensitive and specific for bone infection and particularly useful in violated bone. -
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. -
Hughston Health Alert US POSTAGE PAID the Hughston Foundation, Inc
HughstonHughston HealthHealth AlertAlert 6262 Veterans Parkway, PO Box 9517, Columbus, GA 31908-9517 • www.hughston.com/hha VOLUME 26, NUMBER 4 - FALL 2014 Fig. 1. Knee Inside... anatomy and • Rotator Cuff Disease ACL injury. Extended (straight) knee • Bunions and Lesser Toe Deformities Femur • Tendon Injuries of the Hand (thighbone) Patella In Perspective: (kneecap) Anterior Cruciate Ligament Tears Medial In 1992, Dr. Jack C. Hughston (1917-2004), one of the meniscus world’s most respected authorities on knee ligament surgery, MCL LCL shared some of his thoughts regarding injuries to the ACL. (medial “You tore your anterior cruciate ligament.” On hearing (lateral collateral collateral your physician speak those words, you are filled with a sense ligament) of dread. You envision the end of your athletic life, even ligament) recreational sports. Today, a torn ACL (Fig. 1) has almost become a household Tibia word. Through friends, newspapers, television, sports Fibula (shinbone) magazines, and even our physicians, we are inundated with the hype that the knee joint will deteriorate and become arthritic if the ACL is not operated on as soon as possible. You have been convinced that to save your knee you must Flexed (bent) knee have an operation immediately to repair the ligament. Your surgery is scheduled for the following day. You are scared. Patella But there is an old truism in orthopaedic surgery that says, (kneecap) “no knee is so bad that it can’t be made worse by operating Articular Torn ACL on it.” cartilage (anterior For many years, torn ACLs were treated as an emergency PCL cruciate and were operated on immediately, even before the initial (posterior ligament) pain and swelling of the injury subsided. -
Hammer Toe Information Sheet
Fitter Feet For Life Hammer toe information sheet. (ref. A15) A hammer toe is a deformity of the first small toe joint with in toes. (proximal inter-phalangeal joint) This deformity can occur in the second, third, fourth or fifth (relatively rare) toes, causing it to be permanently bent, resembling a hammer. This abnormality can create pressure on the foot when wearing shoes and cause discomfort and problems walking. The joints themselves can be arthritic and painful. There is a choice of different procedures to straighten a hammer toe. This information sheet has been written to help you choose which procedure is best for you. Fig 1 Hammer toe . Fig 2 Arthrodesis with K wires . Fig 3. Smart toe implant An arthrodesis is a surgical procedure to treat hammer toes. The deformed joint is fully removed and the apposing bone ends fused together in a corrected position. The joint will no longer move. The joint closer to the end of the toe will still move. The joint where the toe joins the foot will also continue to move. 1 Fitter Feet For life. 34 North Street. London SW40HD 0207 627 4901 Fitter Feet For Life 1. K-Wire Arthrodesis. Traditionally hammer toe correction is performed by arthrodesis surgery using K-Wires. The procedure is successful in most cases and has been performed for many years. The deformed joint is removed and the bone ends are secured together with a K-wire which protrudes though the tip of the toe. The foot must be kept dry, dressed and the k-wire protected in a post operative shoe for six weeks after the operation. -
Disorders of the Thoracic Spine: Pathology and Treatment
Disorders of the thoracic spine: pathology and treatment CHAPTER CONTENTS • Extraspinal tumours involve the bony parts of the Disorders and their treatment e169 vertebrae. Benign tumours are usually located in the posterior parts (spinous and transverse processes), Tumours of the thoracic spine . e169 malignant tumours in the vertebral body. Extradural haematoma . e171 Spinal cord herniation . e173 Thoracic spinal canal stenosis . e173 Chest deformities . e173 Intraspinal tumours Fracture of a transverse process . e179 Spinal infections . e179 Thoracic neurofibroma Lateral recess stenosis . e180 Pathology Arthritis of the costovertebral and This benign tumour usually originates from the dorsal root and costotransverse joints . e180 arises from proliferating nerve fibres, fibroblasts and Schwann Arthritis of the thoracic facet joints . e181 cells. Sensory or motor fibres may be involved.1 Some confu- Paget’s disease . e181 sion exists about the terminology: various names, such as neu- rofibroma, neurinoma, neurilemmoma or schwannoma have been used. Some believe that all these terms cover the same type of tumour; others distinguish some slight histological dif- Disorders and their treatment ferences between them. Multiple tumours in nerve fibres and the subcutaneous tissues, often accompanied by patchy café Tumours of the thoracic spine au lait pigmentation, constitute the syndrome known as von Recklinghausen’s disease. Neuromas are the most common primary tumours of the Spinal neoplasms, both primary and secondary, are unusual spine accounting for approximately one-third of the cases. causes of thoracolumbar pain. However, because these lesions They are most often seen at the lower thoracic region and the are associated with high mortality, examiners must always be thoracolumbar junction.2 More than half of all these lesions are aware of the possibility of neoplastic diseases and must include intradural extramedullary (Fig 1), 25% are purely extradural, them in their differential diagnosis. -
2012 Meeting Program
Western Orthopaedic Association 76th Annual Meeting June 13–16, 2012 The Hilton Portland Portland, Oregon 2012 Meeting Program Chuck Freitag Executive Director, Data Trace Management Services, a Data Trace Company Cynthia Lichtefeld Director of Operations, Data Trace Management Services, a Data Trace Company WOA Central Office, Data Trace Management Services 110 West Road, Suite 227 Towson, MD 21204 Phone: 866-962-1388 Fax: 410-494-0515 Email: [email protected] Visit us on the World Wide Web @ www.woa-assn.org Please notify the WOA Central Office of any changes in your home or office address. This activity has been planned and implemented in accordance with the Essential Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Ortho- paedic Surgeons and the Western Orthopaedic Association. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians. The American Academy of Orthopaedic Surgeons designates this live activity for a maximum of 28.75 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Cover Design by Lauren Murphy. Copyright © 2012 by Data Trace Publishing Company, Towson, MD. All rights reserved. Western Orthopaedic Association 76th Annual Meeting Portland, Oregon 2012 President’s Message Dear Colleagues, elcome to Portland for the 76th Annual Meeting of the Western Orthopaedic Association. Jeanne and I are honored to welcome you to The City of Roses. We hope Wyou enjoy the diverse and educational academic program in combination with unique social activities planned for you and your family. -
CT Guided Core Needle Bone Biopsy for Non-Vertebral Osteomyelitis: Is It Necessary?
CT Guided Core Needle Bone Biopsy for Non-Vertebral Osteomyelitis: is it Necessary? Cameron Smith DO, Gregory Bradley DO, Donald von Borstel DO Oklahoma State University Medical Center, Department of Radiology Disclosure statement . None of the authors have conflicts of interest or relevant financial relationships to disclose. Target audience . Seasoned and training musculoskeletal radiologists. Physicians involved in the care of osteomyelitis patients. Introduction . Osteomyelitis is inflammation of the bone marrow which results from infection. It can progress to osteonecrosis, bone destruction, and septic arthritis. Osteomyelitis is an important cause of permanent disability worldwide. Bimodal age distribution with incidence peaking in children under 5-years-old and adults over 50-years-old. Introduction . Etiology: . Hematogenous spread . Predominant etiology of infection in children. Less common in adults, however usually leads to vertebral osteomyelitis when it occurs. Contiguous spread . Infection originating from soft tissues and joints. Usually coincides with vascular insufficiency, such as patients with diabetes mellitus or peripheral vascular disease. Most commonly the lower extremities. Direct inoculation . Direct seeding of organism into the bone usually from open fractures, surgery, or puncture wounds. Introduction . Imaging diagnosis . Radiography . Low sensitivity and specificity for detecting acute osteomyelitis. Approximately 80% of patients within 1-2 weeks of infection have normal radiograph. Bone marrow edema is the earliest pathological feature and NOT well visualized on radiography. Useful as first-line imaging to exclude other differentials (i.e. fracture) and to assess progression from priors. Nuclear Medicine . Sensitivity of a 3-phase bisphosphonate-linked technetium bone scan is greater than that of radiography for early osteomyelitis. Diagnostic sensitivity of approximately 50-85%. -
Clinical Features, Diagnostic and Therapeutic Approaches to Haematogenous Vertebral Osteomyelitis AL
European Review for Medical and Pharmacological Sciences 2005; 9: 53-66 Clinical features, diagnostic and therapeutic approaches to haematogenous vertebral osteomyelitis AL. GASBARRINI, E. BERTOLDI, M. MAZZETTI*, L. FINI***, S. TERZI, F. GONELLA, L. MIRABILE, G. BARBANTI BRÒDANO, A. FURNO**, A. GASBARRINI***, S. BORIANI* Department of Orthopaedics and Traumatology, Maggiore Hospital “C.A. Pizzardi” - Bologna (Italy) *Department of infections disease, Maggiore Hospital “C.A. Pizzardi” - Bologna (Italy) **Nuclear Medicine, Maggiore Hospital “C.A. Pizzardi” - Bologna (Italy) ***Internal Medicine, Catholic University - Rome (Italy) Abstract. – This article review the clinical Chronic ostemyelitis may require surgery in features and the diagnostic approach to case of a development of biomechanical insta- haematogenous vertebral osteomyelitis in order bility and/or a vertebral collapse with progres- to optimise treatment strategies and follow-up sive deformity. assessment. Haematogenous spread is consid- ered to be the most important route: the lumbar spine is the most common site of involvement Key words: for pyogenic infection and the thoracic spine for Vertebral osteomyelitis, Spondylodiscitis, Pyogenic os- tuberculosis infection. The risk factors for devel- teomyelitis, Skeletal tuberculosis. oping haematogenous vertebral osteomyelitis are different among old people, adults and chil- dren: the literature reports that the incidence seems to be increasing in older patients. The Introduction source of infection in the elderly has been relat- ed to the use of intravenous access devices and Haematogenous vertebral osteomyelitis the asymptomatic urinary infections. In young (HVO) is a relatively rare disorder which ac- patients the increase has been correlated with counts for 2-4% of all cases of infectious bone the growing number of intravenous drug 1 abusers, with endocarditis and with immigrants disease .