PATIENT FACT SHEET Sulfasalazine
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Inflammatory Bowel Disease Irritable Bowel Syndrome
Inflammatory Bowel Disease and Irritable Bowel Syndrome Similarities and Differences 2 www.ccfa.org IBD Help Center: 888.MY.GUT.PAIN 888.694.8872 Important Differences Between IBD and IBS Many diseases and conditions can affect the gastrointestinal (GI) tract, which is part of the digestive system and includes the esophagus, stomach, small intestine and large intestine. These diseases and conditions include inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS). IBD Help Center: 888.MY.GUT.PAIN 888.694.8872 www.ccfa.org 3 Inflammatory bowel diseases are a group of inflammatory conditions in which the body’s own immune system attacks parts of the digestive system. Inflammatory Bowel Disease Inflammatory bowel diseases are a group of inflamma- Causes tory conditions in which the body’s own immune system attacks parts of the digestive system. The two most com- The exact cause of IBD remains unknown. Researchers mon inflammatory bowel diseases are Crohn’s disease believe that a combination of four factors lead to IBD: a (CD) and ulcerative colitis (UC). IBD affects as many as 1.4 genetic component, an environmental trigger, an imbal- million Americans, most of whom are diagnosed before ance of intestinal bacteria and an inappropriate reaction age 35. There is no cure for IBD but there are treatments to from the immune system. Immune cells normally protect reduce and control the symptoms of the disease. the body from infection, but in people with IBD, the immune system mistakes harmless substances in the CD and UC cause chronic inflammation of the GI tract. CD intestine for foreign substances and launches an attack, can affect any part of the GI tract, but frequently affects the resulting in inflammation. -
Rheumatology?
WHAT IS RHEUMATOLOGY? diseases affect nearly 50 million Americans and can cause joint and organ destruction, severe pain, disability and even death. Inflammatory rheumatic diseases with arthritis cause more disability in America than heart disease, cancer or diabetes. How can a Rheumatologist help? Most rheumatologic conditions previously led to severe disability and even death in many patients. Evidence-based medical treatment of rheumatological disorders is currently helping patients with rheumatism lead a near-normal life. Medications such as Methotrexate and Tumor necrosis factor inhibitors have had a significant impact on patients with Rheumatoid Arthritis (RA), and today patients with RA can lead a pain free and productive life. Rheumatology facts by numbers: • Over 7 million American adults suffer from inflam- matory rheumatic diseases; 1.3 million adults have rheumatoid arthritis; and 161,000 to 322,000 adults have lupus. • 8.4 percent of women will develop a rheumatic dis- heumatology is a rapidly ease during their lifetime. Women are 2 to 3 times R evolving subspecialty in more likely to be diagnosed with RA, and 10 times internal medicine and more likely to develop lupus than men. pediatrics which includes the pathogenesis, diagnosis, and • 5 percent of men in the U.S. will develop a rheu- management of over 100 complex inflammatory and matic disease during their lifetime. connective tissue diseases. Rheumatologists care for a wide • Osteoporosis and low bone mass are currently esti- array of patients – from children to senior citizens, see mated to be a major public health threat for almost diseases like Rheumatoid Arthritis, Systemic Lupus 44 million U.S. -
2017 American College of Rheumatology/American Association
Arthritis Care & Research Vol. 69, No. 8, August 2017, pp 1111–1124 DOI 10.1002/acr.23274 VC 2017, American College of Rheumatology SPECIAL ARTICLE 2017 American College of Rheumatology/ American Association of Hip and Knee Surgeons Guideline for the Perioperative Management of Antirheumatic Medication in Patients With Rheumatic Diseases Undergoing Elective Total Hip or Total Knee Arthroplasty SUSAN M. GOODMAN,1 BRYAN SPRINGER,2 GORDON GUYATT,3 MATTHEW P. ABDEL,4 VINOD DASA,5 MICHAEL GEORGE,6 ORA GEWURZ-SINGER,7 JON T. GILES,8 BEVERLY JOHNSON,9 STEVE LEE,10 LISA A. MANDL,1 MICHAEL A. MONT,11 PETER SCULCO,1 SCOTT SPORER,12 LOUIS STRYKER,13 MARAT TURGUNBAEV,14 BARRY BRAUSE,1 ANTONIA F. CHEN,15 JEREMY GILILLAND,16 MARK GOODMAN,17 ARLENE HURLEY-ROSENBLATT,18 KYRIAKOS KIROU,1 ELENA LOSINA,19 RONALD MacKENZIE,1 KALEB MICHAUD,20 TED MIKULS,21 LINDA RUSSELL,1 22 14 23 17 ALEXANDER SAH, AMY S. MILLER, JASVINDER A. SINGH, AND ADOLPH YATES Guidelines and recommendations developed and/or endorsed by the American College of Rheumatology (ACR) are intended to provide guidance for particular patterns of practice and not to dictate the care of a particular patient. The ACR considers adherence to the recommendations within this guideline to be volun- tary, with the ultimate determination regarding their application to be made by the physician in light of each patient’s individual circumstances. Guidelines and recommendations are intended to promote benefi- cial or desirable outcomes but cannot guarantee any specific outcome. Guidelines and recommendations developed and endorsed by the ACR are subject to periodic revision as warranted by the evolution of medi- cal knowledge, technology, and practice. -
Rheuma.Stamp Line&Box
Arthritis Mutilans: A Report from the GRAPPA 2012 Annual Meeting Vinod Chandran, Dafna D. Gladman, Philip S. Helliwell, and Björn Gudbjörnsson ABSTRACT. Arthritis mutilans is often described as the most severe form of psoriatic arthritis. However, a widely agreed on definition of the disease has not been developed. At the 2012 annual meeting of the Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA), members hoped to agree on a definition of arthritis mutilans and thus facilitate clinical and molecular epidemiological research into the disease. Members discussed the clinical features of arthritis mutilans and defini- tions used by researchers to date; reviewed data from the ClASsification for Psoriatic ARthritis study, the Nordic psoriatic arthritis mutilans study, and the results of a premeeting survey; and participated in breakout group discussions. Through this exercise, GRAPPA members developed a broad consensus on the features of arthritis mutilans, which will help us develop a GRAPPA-endorsed definition of arthritis mutilans. (J Rheumatol 2013;40:1419–22; doi:10.3899/ jrheum.130453) Key Indexing Terms: OSTEOLYSIS ANKYLOSIS PENCIL-IN-CUP SUBLUXATION FLAIL JOINT ARTHRITIS MUTILANS Psoriatic arthritis (PsA) is an inflammatory musculoskeletal gists as a severe destructive form of PsA, a precise disease specifically associated with psoriasis. Moll and definition has not yet been universally accepted. The earliest Wright defined PsA as “psoriasis associated with inflam- definition of arthritis mutilans was provided -
Prediction of Premature Termination Codon Suppressing Compounds for Treatment of Duchenne Muscular Dystrophy Using Machine Learning
Prediction of Premature Termination Codon Suppressing Compounds for Treatment of Duchenne Muscular Dystrophy using Machine Learning Kate Wang et al. Supplemental Table S1. Drugs selected by Pharmacophore-based, ML-based and DL- based search in the FDA-approved drugs database Pharmacophore WEKA TF 1-Palmitoyl-2-oleoyl-sn-glycero-3- 5-O-phosphono-alpha-D- (phospho-rac-(1-glycerol)) ribofuranosyl diphosphate Acarbose Amikacin Acetylcarnitine Acetarsol Arbutamine Acetylcholine Adenosine Aldehydo-N-Acetyl-D- Benserazide Acyclovir Glucosamine Bisoprolol Adefovir dipivoxil Alendronic acid Brivudine Alfentanil Alginic acid Cefamandole Alitretinoin alpha-Arbutin Cefdinir Azithromycin Amikacin Cefixime Balsalazide Amiloride Cefonicid Bethanechol Arbutin Ceforanide Bicalutamide Ascorbic acid calcium salt Cefotetan Calcium glubionate Auranofin Ceftibuten Cangrelor Azacitidine Ceftolozane Capecitabine Benserazide Cerivastatin Carbamoylcholine Besifloxacin Chlortetracycline Carisoprodol beta-L-fructofuranose Cilastatin Chlorobutanol Bictegravir Citicoline Cidofovir Bismuth subgallate Cladribine Clodronic acid Bleomycin Clarithromycin Colistimethate Bortezomib Clindamycin Cyclandelate Bromotheophylline Clofarabine Dexpanthenol Calcium threonate Cromoglicic acid Edoxudine Capecitabine Demeclocycline Elbasvir Capreomycin Diaminopropanol tetraacetic acid Erdosteine Carbidopa Diazolidinylurea Ethchlorvynol Carbocisteine Dibekacin Ethinamate Carboplatin Dinoprostone Famotidine Cefotetan Dipyridamole Fidaxomicin Chlormerodrin Doripenem Flavin adenine dinucleotide -
Rheumatology Connections
IN THIS ISSUE Uncommon Manifestations of SLE 3 | PACNS or RCVS? 6 | Psychosocial Burden of PsA 9 Advances in IL-6 Biology 10 | AHCT for Systemic Sclerosis 12 | PET in Large Vessel Vasculitis 14 Rheumatology Connections An Update for Physicians | Summer 2018 112236_CCFBCH_18RHE1077_ACG.indd 1 7/10/18 2:06 PM Dear Colleagues, Welcome to another issue of Rheumatology Con- From the Chair of Rheumatic nections. I think you’ll find our title perfectly apt as and Immunologic Diseases you browse these articles, full of connections to an array of other specialties, to our patients and to our clinical, scientific and educational missions. Dr. Chatterjee’s collaboration with the Department of Medical Oncology and Hematology for treating severe systemic sclerosis is but one example of the relevance of our field across disciplines (p. 12). Cleveland Clinic’s Rheumatology This issue also features a study of psychosocial fac- Program is ranked among the top tors in psoriatic arthritis co-authored by Dr. Husni 2 in the nation in U.S. News & and a colleague in the Neurological Institute (p. 9). World Report’s “America’s Best Our connections to neurology become even clearer Hospitals” survey. as Drs. Calabrese and Hajj-Ali offer guidance on distinguishing between a neurological condition and the more fatal, less common rheumatologic one that it mimics (p. 6). Rheumatology Connections, published by We are always searching for ways to transcend Cleveland Clinic’s Department of Rheumatic disciplinary boundaries to provide better patient care. Our multidisciplinary style of caring for patients was and Immunologic Diseases, provides information critical in a case co-authored with a colleague in pathology and Drs. -
Stems for Nonproprietary Drug Names
USAN STEM LIST STEM DEFINITION EXAMPLES -abine (see -arabine, -citabine) -ac anti-inflammatory agents (acetic acid derivatives) bromfenac dexpemedolac -acetam (see -racetam) -adol or analgesics (mixed opiate receptor agonists/ tazadolene -adol- antagonists) spiradolene levonantradol -adox antibacterials (quinoline dioxide derivatives) carbadox -afenone antiarrhythmics (propafenone derivatives) alprafenone diprafenonex -afil PDE5 inhibitors tadalafil -aj- antiarrhythmics (ajmaline derivatives) lorajmine -aldrate antacid aluminum salts magaldrate -algron alpha1 - and alpha2 - adrenoreceptor agonists dabuzalgron -alol combined alpha and beta blockers labetalol medroxalol -amidis antimyloidotics tafamidis -amivir (see -vir) -ampa ionotropic non-NMDA glutamate receptors (AMPA and/or KA receptors) subgroup: -ampanel antagonists becampanel -ampator modulators forampator -anib angiogenesis inhibitors pegaptanib cediranib 1 subgroup: -siranib siRNA bevasiranib -andr- androgens nandrolone -anserin serotonin 5-HT2 receptor antagonists altanserin tropanserin adatanserin -antel anthelmintics (undefined group) carbantel subgroup: -quantel 2-deoxoparaherquamide A derivatives derquantel -antrone antineoplastics; anthraquinone derivatives pixantrone -apsel P-selectin antagonists torapsel -arabine antineoplastics (arabinofuranosyl derivatives) fazarabine fludarabine aril-, -aril, -aril- antiviral (arildone derivatives) pleconaril arildone fosarilate -arit antirheumatics (lobenzarit type) lobenzarit clobuzarit -arol anticoagulants (dicumarol type) dicumarol -
Rheumatology Certification Exam Blueprint
Rheumatology Certification Examination Blueprint Purpose of the exam The exam is designed to evaluate the knowledge, diagnostic reasoning, and clinical judgment skills expected of the certified rheumatologist in the broad domain of the discipline. The ability to make appropriate diagnostic and management decisions that have important consequences for patients will be assessed. The exam may require recognition of common as well as rare clinical problems for which patients may consult a certified rheumatologist. Exam content Exam content is determined by a pre-established blueprint, or table of specifications. The blueprint is developed by ABIM and is reviewed annually and updated as needed for currency. Trainees, training program directors, and certified practitioners in the discipline are surveyed periodically to provide feedback and inform the blueprinting process. The primary medical content categories of the blueprint are shown below, with the percentage assigned to each for a typical exam: Medical Content Category % of Exam Basic and Clinical Sciences 7% Crystal-induced Arthropathies 5% Infections and Related Arthritides 6% Metabolic Bone Disease 5.5% Osteoarthritis and Related Disorders 5% Rheumatoid Arthritis 13% Seronegative Spondyloarthropathies 6.5% Other Rheumatic and Connective Tissue Disorders (ORCT) 16.5 % Lupus Erythematosus 9% Nonarticular and Regional Musculoskeletal Disorders 7% Nonrheumatic Systemic Disorders 9% Vasculitides 8.5% Miscellaneous Topics 2% 100% Exam questions in the content areas above may also address clinical topics in geriatrics, pediatrics, pharmacology and topics in general internal medicine that are important to the practice of rheumatology. Exam format The exam is composed of multiple-choice questions with a single best answer, predominantly describing clinical scenarios. -
Sulfasalazine (Azulfidine)
Sulfasalazine (Azulfidine) Description Sulfasalazine (Azulfidine), used to treat pain and swelling in arthritis, belongs to a class of drugs called sulfa drugs. It is a combination of salicylate (the main ingredient in aspirin) and a sulfa antibiotic. Sulfasalazine is also known as a disease modifying antirheumatic drug (DMARD) because it not only decreases the pain and swelling of arthritis, but also may prevent damage to joints. In addition, it may reduce the risk of long term loss of function. Uses Sulfasalazine was first used over 70 years ago to treat rheumatoid arthritis which, at one time, was thought to be caused by a bacterial infection. Sulfasalazine was designed as a combination of an aspirin- like anti-inflammatory medicine with a sulfa containing antibiotic. While a bacterial infectious cause for rheumatoid arthritis is longer believed to be true, sulfasalazine continues to be useful for treating for mild to moderate symptoms, or may be given with other drugs for more severe symptoms of rheumatoid arthritis. It is also used for other conditions, including juvenile idiopathic arthritis (also called juvenile rheumatoid arthritis), ankylosing spondylitis, psoriatic arthritis, and ulcerative colitis. How it works Sulfasalazine treats swelling, pain, and stiffness in arthritis. However, it is not entirely clear how this medication works for rheumatoid arthritis. Dosing Sulfasalazine comes in a 500 milligram tablet, and should be taken with food and a full glass of water to prevent stomach upset. The medication is often started at low doses to treat rheumatoid arthritis, typically one to two tablets a day, to prevent side effects. After the first week, the dose may be increased slowly to the usual 2 tablets (1 gram) taken twice a day. -
Use of Diagnostic Imaging in Rheumatology Practice
AMERICAN COLLEGE OF RHEUMATOLOGY POSITION STATEMENT SUBJECT: Use of diagnostic imaging in rheumatology practice PRESENTED BY: Committee on Rheumatologic Care FOR DISTRIBUTION TO: Members of the American College of Rheumatology Medical Societies Members of Congress Health Care Organizations/Third Party Carriers Managed Care Entities POSITION: 1. The American College of Rheumatology supports the ordering, performance and/or interpretation of imaging studies of the musculoskeletal system as an integral part of the rheumatology practice. A rheumatologist’s unique training in the clinical diagnosis and management of rheumatic diseases, as well as demonstrated abilities and competence in diagnostic imaging, combine to increase the relevance of imaging studies performed or interpreted by a rheumatologist which can be better tailored to an individual patient’s problem(s). 2. The ACR further supports the propriety of the assessment and collection of appropriate fees for these services. The ACR supports reimbursement by Medicare and other insurers for the performance and interpretation of musculoskeletal imaging studies and bone mineral density measurements by rheumatologists. BACKGROUND: Rheumatologists routinely evaluate, diagnose and manage patients with arthritis, systemic rheumatic, autoimmune, autoinflammatory syndromes, osteoporosis and metabolic bone disease as well as other disorders of connective tissues, muscles, bones and joints. Diagnostic and interventional imaging of the musculoskeletal system provide rheumatologists with information critical to the diagnosis, evaluation of damage, and progression or halting of progression of arthritic diseases (1-3). Specifically regarding conventional radiographs, rheumatologists, unlike radiologists, have the ability to assess erosive changes in the context of other disease activity measures and clinically relevant information, allowing for more robust treatment decision-making (4). -
Prevalence and Impact of Reported Drug Allergies Among Rheumatology Patients
diagnostics Article Prevalence and Impact of Reported Drug Allergies among Rheumatology Patients Shirley Chiu Wai Chan , Winnie Wan Yin Yeung, Jane Chi Yan Wong, Ernest Sing Hong Chui, Matthew Shing Him Lee, Ho Yin Chung, Tommy Tsang Cheung, Chak Sing Lau and Philip Hei Li * Division of Rheumatology and Clinical Immunology, Department of Medicine, The University of Hong Kong, Queen Mary Hospital, Pokfulam, Hong Kong; [email protected] (S.C.W.C.); [email protected] (W.W.Y.Y.); [email protected] (J.C.Y.W.); [email protected] (E.S.H.C.); [email protected] (M.S.H.L.); [email protected] (H.Y.C.); [email protected] (T.T.C.); [email protected] (C.S.L.) * Correspondence: [email protected]; Tel.: +852-2255-3348 Received: 28 October 2020; Accepted: 7 November 2020; Published: 9 November 2020 Abstract: Background: Drug allergies (DA) are immunologically mediated adverse drug reactions and their manifestations depend on a variety of drug- and patient-specific factors. The dysregulated immune system underpinning rheumatological diseases may also lead to an increase in hypersensitivity reactions, including DA. The higher prevalence of reported DA, especially anti-microbials, also restricts the medication repertoire for these already immunocompromised patients. However, few studies have examined the prevalence and impact of reported DA in this group of patients. Methods: Patients with a diagnosis of rheumatoid arthritis (RA), spondyloarthritis (SpA), or systemic lupus erythematosus (SLE) were recruited from the rheumatology clinics in a tertiary referral hospital between 2018 and 2019. Prevalence and clinical outcomes of reported DA among different rheumatological diseases were calculated and compared to a cohort of hospitalized non-rheumatology patients within the same period. -
What a Rheumatologists Needs to Know About Nephrology
What a Rheumatologists needs to know about Nephrology Dr Louise Moist University of Western Ontario Louise/[email protected] May 2014 Disclosures • Advisory board Amgen, Leo Pharma, Roche Learning Objectives • Update in recent trends in nephrology pertinent to the rheumatologists in: • Proteinuria/eGFR • Lupus nephritis • Gout in CKD • Pain control in CKD • Drugs in CKD 3 Kidney Disease 101 Damage Function – Microalbuminuria is – Measure Cr a marker of – Interpret with age, vascular/ sex, weight endothelial damage – eGFR – Microalbuminuria – If abnormal consider is a risk factor CVD other kidney function and CKD – Lytes, Ca, Phos, Hb,acid base, clearance (urea) Proteinuria predicts progression to ESRD > than Creatinine 100x > risk of Dialysis Rate per 1,000 Patient Years Patient per 1,000 Rate Hemmelgarn et.al. JAMA. 2010;303(5):423-429 Proteinuria predicts death >creatinine Almost 10X > risk Rate per 1,000 Patient Years Patient per 1,000 Rate Hemmelgarn et.al. JAMA. 2010;303(5):423-429 KEY POINT When you see this... High albumin to creatinine ratio Or proteinuria on dip stick Think this... HIGH CVD RISK GFR(mL/min/1.73m2) > 90 60-89 30-59 15-29 <15 Stage 1 2 3 4 5 Kidney Severe Failure Moderate GFR Kidney GFR damage Kidney with mild Description damage GFR with normal or GFR Endstage Kidney Disease (ESKD) = Dialysis or Transplantation Stages of CKD GFR Hypertension* Hemoglobin < 12.0 g/dL Unable to walk 1/4 mile Serum albumin < 3.5 g/dL Serum calcium < 8.5 mg/dL Serum phosphorus > 4.5 mg/dL 90 80 70 60 50 40 30 20 10 Proportion of population (%) of population Proportion 0 15-29 30-59 60-89 90+ Estimated GFR (ml/min/1.73 m2) *>140/90 or antihypertensive medication p-trend < 0.001 for each abnormality Abnormalities in Uremia “Uremia” & the Uremic Toxin Membrane permeability & Intracellular Ca2+ integrity PTH (9000 daltons) Protein catabolism Soft tissue calcification Alters/mitochondrial pathways/ ATP generation abN phospholipid turnover Brain Platelets Glucose Pancreas Myocardium intolerance When you see this..