Classification Criteria for Sjögren’s Syndrome
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Revised international classification criteria for Sjögren’s syndrome- Ocular symptoms: a positive response to at least one of the following questions:
- Have you had daily, persistent, troublesome dry eyes for more than 3 months?
- Do you have a recurrent sensation of sand or gravel in the eyes?
- Do you use tear substitutes more than 3 times a day?
- Oral symptoms: a positive response to at least one of the following questions:
- Have you had a daily feeling of dry mouth for more than 3 months?
- Have you had recurrently or persistently swollen salivary glands as an adult?
- Do you frequently drink liquids to aid in swallowing dry food?
- Ocular signs—that is, objective evidence of ocular involvement defined as a positive result for at least one of the following two tests:
- Schirmer’s I test, performed without anaesthesia (<5 mm in 5 minutes)
- Rose bengal score or other ocular dye score (>4 according to van Bijsterveld’s scoring system)
- Histopathology: In minor salivary glands (obtained through normal-appearing mucosa) focal lymphocytic sialoadenitis, evaluated by an expert histopathologist, with a focus score >1, defined as a number of lymphocytic foci (which are adjacent to normal-appearing mucous acini and contain more than 50 lymphocytes) per 4 mm² of glandular tissue
- Salivary gland involvement: objective evidence of salivary gland involvement defined by a positive result for at least one of the following diagnostic tests:
- Unstimulated whole salivary flow (<1.5 ml in 15 minutes)
- Parotid sialography showing the presence of diffuse sialectasias (punctate, cavitary or destructive pattern), without evidence of obstruction in the major ducts
- Salivary scintigraphy showing delayed uptake, reduced concentration and/or delayed excretion of tracer
- Autoantibodies: presence in the serum of the following autoantibodies:
- Antibodies to Ro(SSA) or La(SSB) antigens, or both
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Revised rules for classification#
For primary Sjögren's SyndromeIn patients without any potentially associated disease, primary SS may be defined as follows:
- The presence of any 4 of the 6 items is indicative of primary SS, as long as either item IV (Histopathology) or VI (Serology) is positive.
- The presence of any 3 of the 4 objective criteria items (that is, items III, IV, V, VI).
- The classification tree procedure represents a valid alternative method for classification, although it should be more properly used in clinical-epidemiological survey.
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For secondary Sjögren's SyndromeIn patients with a potentially associated disease (for instance, another well-defined connective tissue disease), the presence of item I or item II plus any 2 from among items III, IV, and V may be considered as indicative of secondary SS
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Exclusion criteria:- Past head and neck radiation treatment
- Hepatitis C infection
- Acquired immunodeficiency disease (AIDS)
- Pre-existing lymphoma
- Sarcoidosis
- Graft versus host disease
- Use of anticholinergic drugs (since a time shorter than 4-fold the half-life of the drug)
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Related Pages- Medical Disorders
- Oral Health Care Considerations
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References/Websites- References
- Shiboski CH, et al. 2016 American College of Rheumatology/European League against rheumatism classification criteria for primary Sjögren's syndrome. Arthritis Rheumatol. 2017 Jan;69(1):35-45.
- Vitali C, et al. Classification criteria for Sjögren’s syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann Rheum Dis. 2002 Jun;61(6):554-8.
- Websites