You are in: eMedicine Specialties > Emergency Medicine > RHEUMATOLOGY Sjogren SyndromeArticle Last Updated: Nov 30, 2006AUTHOR AND EDITOR INFORMATIONAuthor: Darren Phelan, MD, Medical Director, Department of Emergency Medicine, Sierra Nevada Memorial Hospital Editors: Daniel J Dire, MD, FACEP, FAAP, FAAEM, Clinical Associate Professor, Department of Emergency Medicine, University of Texas-Houston; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Gino A Farina, MD, Program Director, Associate Professor of Clinical Emergency Medicine, Department of Emergency Medicine, Long Island Jewish Medical Center, Albert Einstein College of Medicine; John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center; Charles V Pollack, Jr, MD, MA, FACEP, Professor, Department of Emergency Medicine, University of Pennsylvania College of Medicine; Chairman, Department of Emergency Medicine, Pennsylvania Hospital Author and Editor Disclosure Synonyms and related keywords: Sjögren syndrome, Sjögren's syndrome, Sjogren's syndrome, sicca complex, Gougerot-Sjögren disease, sicca syndrome, Sjögren disease, Sjögren's disease, xerostomia, dry mouth, xerophthalmia, dry eyes, lymphocytic infiltration of the exocrine glands, autoimmune disorder, exocrine gland dysfunction, systemic lupus erythematosus, SLE, rheumatoid arthritis, scleroderma, systemic sclerosis, cryoglobulinemia, polyarteritis nodosa, rheumatologic disorder INTRODUCTIONBackgroundSjögren syndrome is a chronic autoimmune disorder characterized by xerostomia (dry mouth), xerophthalmia (dry eyes), and lymphocytic infiltration of the exocrine glands. This triad is also known as the sicca complex. Sjögren syndrome displays a wide spectrum of severity and can go undiagnosed for several months to years. The Swedish physician Henrik Sjögren first described the syndrome in 1933. PathophysiologySjögren syndrome can occur as a primary disease of exocrine gland dysfunction or in association with several other autoimmune diseases (eg, systemic lupus erythematosus [SLE], rheumatoid arthritis, scleroderma, systemic sclerosis, cryoglobulinemia, polyarteritis nodosa). These primary and secondary types occur with similar frequency, but the sicca complex seems to cause more severe symptoms in the primary form. Virtually all organs may be involved. The disease commonly affects the eyes, mouth, parotid gland, lungs, kidneys, skin, and nervous system. FrequencyUnited StatesSjögren syndrome is estimated to be the second most common rheumatologic disorder, behind only SLE. InternationalComparative studies between different ethnic groups have suggested that Sjögren syndrome is a homogeneous disease that occurs worldwide with similar prevalence and affects 1-2 million people. Mortality/Morbidity
SexThe female-to-male ratio is 9:1. AgePeak incidence occurs in the fourth and fifth decades of life. CLINICALHistoryOnset is insidious, and symptoms may be mild.
PhysicalThe disease may be mild or hard to detect clinically.
DIFFERENTIALSAnxiety Arthritis, Rheumatoid Candidiasis Conjunctivitis Corneal Abrasion Corneal Ulceration and Ulcerative Keratitis Gingivitis HIV Infection and AIDS Multiple Sclerosis Mumps Myopathies Systemic Lupus Erythematosus
|
| Drug Name | Artificial tears (Celluvisc, Murine, Refresh) |
|---|---|
| Description | Contain equivalent of 0.9% NaCl and are used to maintain ocular tonicity. Act to stabilize and thicken precorneal tear film and prolong tear film breakup time, which occurs with dry eye states. |
| Adult Dose | 1-2 gtt tid/qid prn |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| Pregnancy | A - Safe in pregnancy |
| Precautions | Hyperemia, photophobia, stickiness of eyelashes, ocular discomfort, or irritation may occur |
Use of sugarless chewing gums and salivary substitutes assists in management of oral symptoms.
| Drug Name | Pilocarpine (Salagen) |
|---|---|
| Description | This may increase salivary and lacrimal flow rates in some patients but should not be administered in the ED. MD may wish to write prescription for patient to take home. |
| Adult Dose | 5 mg PO qd; improvement evident following 6 wk of treatment |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; acute inflammatory disease of anterior chamber |
| Interactions | May be ineffective when used concomitantly with nonsteroidal anti-inflammatory agents |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in acute cardiac failure, peptic ulcer, hyperthyroidism, GI spasm, bronchial asthma, Parkinson disease, recent MI, urinary tract obstruction, and hypertension or hypotension |
These agents increase activity of exocrine glands, including salivary glands.
| Drug Name | Cevimeline (Evoxac) |
|---|---|
| Description | Binds to cholinergic (muscarinic) receptors, causing increase in secretion of salivary glands. |
| Adult Dose | 30 mg PO tid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; narrow-angle glaucoma; acute iritis; uncontrolled asthma |
| Interactions | May have additive effects when used with other cholinergic agents; concurrent use with beta-blockers may cause potential for cardiac conduction disturbances; CYP2D6 inhibitors (eg, fluoxetine, amiodarone, quinidine, ritonavir, paroxetine) or CYP3A3/4 (eg, itraconazole, diltiazem, ketoconazole, verapamil) may increase toxicity; anticholinergic agents (eg, phenothiazines, TCAs, atropine) may decrease effects of cevimeline |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in cardiovascular disease, controlled asthma, COPD, or chronic bronchitis; may induce smooth muscle spasms and precipitate cholangitis, biliary obstruction, cholecystitis, or urethral reflux in patients with history of biliary stones or nephrolithiasis |
These agents are used with varying degrees of success for glomerulonephritis, interstitial pneumonitis, and pseudolymphoma. They do not appear to aid in the oral or ocular manifestations.
| Drug Name | Hydroxychloroquine (Plaquenil) |
|---|---|
| Description | May be useful in treating arthralgias and skin symptoms, but it has not been shown to affect salivary or lacrimal gland function. Patients with evidence of marked immune dysregulation may benefit from prophylactic therapy with hydroxychloroquine to prevent progression to extraglandular sites. Hydroxychloroquine sulfate 200 mg is equivalent to 155 mg hydroxychloroquine base and 250 mg chloroquine phosphate. |
| Adult Dose | 200 mg PO qd |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; psoriasis; retinal and visual field changes attributable to 4-aminoquinolones |
| Interactions | Serum levels increase with cimetidine; magnesium trisilicate may decrease absorption |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Caution in hepatic disease, G-6-PD deficiency, psoriasis, and porphyria; not recommended for long term in children; perform periodic (6 mo) ophthalmologic examinations; test periodically for muscle weakness |
Article Last Updated: Nov 30, 2006