Systemic Sclerosis Criteria Calculator

The calculator determines if patients are eligible for inclusion in a systemic sclerosis study.

Patients that score a total of 9 or more are classified as having systemic sclerosis.

Skin thickening of the fingers
Only count the higher score
Fingertip lesions
Only count the higher score
Pulmonary arterial hypertension and/or interstitial lung disease
Maximum Score is 2
SSc-related autoantibodies
Maximum Score is 3

The calculator’s criteria are not applicable to patients having a systemic sclerosis-like disorder that better explains their manifestations such as any of the following:

  • nephrogenic sclerosing fibrosis
  • scleredema diabeticorum
  • scleromyxedema
  • erythromylagia
  • porphyria
  • lichen sclerosis
  • graft versus host disease
  • diabetic chierarthropathy

Patients with skin thickening sparing the fingers are also not classified as having systemic sclerosis.

Definitions of Terms

Definitions of items/sub-items in the American College of Rheumatology/European League Against Rheumatism criteria for the classification of systemic sclerosis (SSc):

Skin thickening: Skin thickening or hardening not due to scarring after injury, trauma, etc.

Puffy fingers: Swollen 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 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.

Telangiectasia: 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 from dilated 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 hypertension: Pulmonary arterial hypertension diagnosed by right-sided heart catheterization according to standard definitions.

Interstitial lung disease: Pulmonary 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 phenomenon: Self-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 autoantibodies: Anticentromere 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.