1 2013 Classification Criteria for Systemic Sclerosis An American College of Rheumatology/European League Against Rheumatism Collaborative Initiative van.

Slides:



Advertisements
Similar presentations
SYSTEMIC LUPUS ERYTHEMATOSUS (SLE)
Advertisements

Hemodynamic Disorders, Thrombosis & Shock
Scleroderma Nicole Bundy, MD, MPH Assistant Professor Division of Rheumatology and Immunology
CHEST X-RAY FINDINGS: Left-to-Right Shunt
Pulmonary Oedema.
Virginia Steen, MD Professor of Medicine
ACR – EULAR Classification Criteria for Systemic Sclerosis May 25, 2013 Sindhu Johnson MD PhD.
CREST J. Ryan Altman, MD AM REPORT 9 December 2009.
ACR/EULAR Classification Criteria for Systemic Sclerosis (SSc, Scleroderma) © 2013 ACR / EULAR.
Vascular Diseases of Lungs. Pulmonary Hypertension It is the increase in blood pressure in pulmonary arteries, veins and capillaries. It leads to shortness.
Chronic pulmonary heart disease. Chronic pulmonary Heart disease resulting from a lung (pulmonary) disorder. A complication of lung disorders where the.
Scleroderma derived from greek and means hard skin
Skin lesions.
Pathology of Pulmonary Hypertension Wolter J. Mooi Department of Pathology, VUmc Amsterdam
Raynaud’s Disease.
Part 1.  Cause Thrombus (blood clot) Embolism Trauma Crush injuries.
General Examination for CVS Physical signs: These are the manifestations that the doctor finds during examination. Certain abnormalities in the general.
Raynaud’s Disease or Raynaud’s Phenomenon
Copyright ©2000 BMJ Publishing Group Ltd. Stratton, I. M et al. BMJ 2000; 321:
Mosby items and derived items © 2006, 2003, 1999, 1995, 1991, 1987 by Mosby, Inc. an affiliate of Elsevier Inc. Slide 1 PHAR 741 Peripheral Vascular System.
SCLERODERMA DEFINATION :-
Scleroderma (Systemic Sclerosis)
"On-line Atlas" of Dermatology and Rheumatology Cutaneous Manifestations of Rheumatic Diseases
Nursing Management: Arthritis and Connective Tissue Diseases
1 Benign Nephrosclerosis Definition: renal changes in benign hypertension It is always associated with hyaline arteriolosclerosis. mild benign nephrosclerosis.
Author: Cumurciuc Mihai Co-author:Silvia Ioana Morar Coordinator: Dr. Parvu Mirela.
Classification of sclerodermas Localized sclerodermas Morhpea Linear scleroderma.
Pathophysiology BMS 243 Vascular Diseases Lecture IV Dr. Aya M. Serry
Undifferentiated Connective Tissue Disease (What is the relationship between UCTD and SLE?) R. John Looney, MD Stephen and Elise Rosenfeld Distinguished.
CLINICAL MANIFESTATION OF SYSTEMIC SCLEROSIS
+ Raynaud’s Phenomenon By: Alison Cunliffe. + What is Raynaud’s Disease Condition resulting in a series of discolorations of the fingers and/or toes after.
Systemic Sclerosis (Scleroderma)
SCLERODERMA Gentleman’s Review Daniel Martingano OMSII.
Diffuse connective tissue diseases. Modern pictures are of clinic, diagnostics. Доц. Н.З.Ярема.
Basic Head to Toe Assessment Part 4 Including:
General examination Whether patient is conscious, Oriented to place/person/time, His built, nourishment, Dehydrated, depressed, distress, Anxious,
2013 Classification Criteria for Systemic Sclerosis An American College of Rheumatology/European League Against Rheumatism Collaborative Initiative An.
Introduction to collagen-vascular diseases. Definition: Rheumatologic (or Rheumatic) Disease: diseases characterized by pain and inflammation in joints.
CVC LUNG, LIVER AND SPLEEN
Scleroderma Lab Data and Diagnosis Iraj Salehi-Abari MD., Internist
Scleroderma Raynaud’s phenomenon Iraj Salehi-Abari MD., Internist
Dr. Ashwin Kulkarni M.S.Ramaiah Medicial College Bangalore India
Systemic Sclerosis (Scleroderma)
Systemic sclerosis.
Scleroderma.
III. Endocrine Pancreas Diabetes Mellitus
Scleroderma (Systemic Sclerosis)
Fig 1: Skin thickening and sclerodactyly Fig 2: Digital tip ulcers
Systemic Sclerosis (Scleroderma)
Systemic Lupus Erythematosis
Systemic Sclerosis Criteria.
Research Project: The outcome of African American patients with scleroderma in relationship to autoantibody, genetics and socioeconomic status Donna Swistowski,
Scleroderma Description: Scleroderma (Sclero= hardening, Derma=skin) is a chronic autoimmune disorder characterized by the hardening of the skin, shrinking.
by Dr. Ammar Tlib Al-yassiri
Pulmonary Function Testing in Interstitial Pulmonary Disease
Autoimmune diseases Ali Al Khader, M.D. Faculty of Medicine
Systemic Sclerosis (Scleroderma) AND MIXED CONNECTIVE TISSUE DISORDES ( MCTD ) By Dr. Zahoor.
Volume 108, Issue 6, Pages (December 1995)
Nails Protective coverings at the ends of fingers and toes
Prevention and Treatment of Athletic Injuries
Chest X-ray interpretation
Systemic sclerosis (SSc; also known as scleroderma) is a complex connective tissue disease (CTD) of unknown etiology. It is characterized by fibrotic.
Salman Waheeduddin MD Rheumatology, Aurora Health Care.
Atelectasis, acute respiratory distress syndrome & pulmonary edema
Autoimmune diseases Ali Al Khader, M.D. Faculty of Medicine
Summary of Information Seen on Musculoskeletal Examination
Volume 140, Issue 4, Pages (October 2011)
High-resolution computed tomography scan of a 59-year-old female patient with undifferentiated connective tissue disease, showing patterns of nonspecific.
Khalid AlHabib Professor of Cardiac Sciences Cardiology Consultant
Presentation transcript:

Classification Criteria for Systemic Sclerosis An American College of Rheumatology/European League Against Rheumatism Collaborative Initiative van den Hoogen F, Khanna D et al. Arthritis Rheum 2013, 65: The criteria on the next slide are applicable to any patient considered for inclusion in an SSc study. The criteria are not applicable to patients with skin thickening sparing the fingers or to patients who have a scleroderma-like disorder that better explains their manifestations (e.g., nephrogenic sclerosing fibrosis, generalized morphea, eosinophilic fasciitis, scleredema diabeticorum, scleromyxedema, erythromyalgia, porphyria, lichen sclerosis, graft-versus-host disease, diabetic cheiroarthropathy). The total score is determined by adding the maximum weight (score) in each category. Patients with a total score of 9 are classified as having definite SSc.

Classification Criteria for Systemic Sclerosis ItemSub-item(s)Weight/ Score Skin thickening of the fingers of both hands extending proximal to the metacarpophalangeal joints (sufficient criterion) –9 Skin thickening of the fingers (only count the higher score)Puffy fingers Sclerodactyly of the fingers (distal to the metacarpo- phalangeal joints but proximal to the proximal interphalangeal joints) 2424 Fingertip lesions (only count the higher score)Digital tip ulcers Fingertip pitting scars 2323 Telangiectasia –2 Abnormal nailfold capillaries –2 Pulmonary arterial hypertension and/or interstitial lung disease (maximum score is 2) Pulmonary arterial hypertension Interstitial lung disease 2222 Raynaud‘s phenomenon –3 SSc-related autoantibodies (anticentromere, anti- topoisomerase I [anti-Scl-70], anti-RNA polymerase III) (maximum score is 3) Anticentromere Anti-topoisomerase I Anti-RNA polymerase III 3 For definitions of items/sub-items see next slide

3 Definition of items/sub-items ItemDefinition Skin thickeningSkin thickening or hardening not due to scarring after injury, trauma, etc. Puffy fingersSwollen digits — a diffuse, usually nonpitting increase in soft tissue mass of the digits extending beyond the normal confines of the joint capsule. Normal digits are tapered distally with the tissues following the contours of the digital bone and joint structures. Swelling of the digits obliterates these contours. Not due to other causes such as inflammatory dactylitis. Fingertip ulcers or pitting scarsFingertip ulcers or pitting scars Ulcers or scars distal to or at the proximal interphalangeal joint not thought to be due to trauma. Digital pitting scars are depressed areas at digital tips as a result of ischemia, rather than trauma or exogenous causes. TelangiectasiaTelangiectasia Telangiectasiae are visible macular dilated superficial blood vessels, which collapse upon pressure and fill slowly when pressure is released. Telangiectasiae in a scleroderma-like pattern are round and well demarcated and found on hands, lips, inside of the mouth, and/or are large mat-like telangiectasiae. Distinguishable from rapidly filling spider angiomas with central arteriole and fromdilated superficial vessels. Abnormal nailfold capillary pattern consistent with systemic sclerosis Enlarged capillaries and/or capillary loss with or without pericapillary hemorrhages at the nailfold. May also be seen on the cuticle. Pulmonary arterial hypertensionPulmonary arterial hypertension Pulmonary arterial hypertension diagnosed by right-sided heart catheterization according to standard definitions. Interstitial lung diseasePulmonary fibrosis seen on high-resolution computed tomography or chest radiography, most pronounced in the basilar portions of the lungs, or occurrence of “Velcro” crackles on auscultation, not due to another cause such as congestive heart failure. Raynaud‘s phenomenonSelf-reported or reported by a physician, with at least a 2-phase color change in finger(s) and often toe(s) consisting of pallor, cyanosis, and/or reactive hyperemia in response to cold exposure or emotion; usually one phase is pallor. SSc-related autoantibodiesAnticentromere antibody or centromere pattern seen on antinuclear antibody testing, anti– topoisomerase I antibody (also known as anti–Scl-70 antibody), or anti–RNA polymerase III antibody. Positive according to local laboratory standards.