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Arthritis & Rheumatism· 2013

Sistemik Skleroz İçin 2013 Sınıflandırma Kriterleri: Bir Amerikan Romatoloji Koleji/Avrupa Romatizma ve Artrit Ligi İşbirlikçi Girişimi

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

F.H.J. van den Hoogen, Dinesh Khanna, Jaap Fransen, Sindhu R. Johnson ve diğerleri

Kısa özet

ACR/EULAR tarafından Sistemik Skleroz (SSc) için yeni sınıflandırma kriterleri geliştirildi; bu kriterler, 1980 kriterlerine kıyasla duyarlılık ve özgüllükte önemli iyileşmeler sağlamaktadır.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Ana noktalar

  • Sistemik Skleroz (SSc) için yeni ACR/EULAR sınıflandırma kriterleri geliştirildi.
  • Metakarpofalangeal eklemlerin proksimalindeki cilt kalınlaşması yeterli bir kriterdir.
  • Sınıflandırmaya katkıda bulunan yedi ek madde (örn. parmak ucu lezyonları, İLL, Raynaud fenomeni) bulunmaktadır.
  • Yeni kriterler %91 duyarlılık ve %92 özgüllük elde etti.
  • 1980 ACR kriterleri %75 duyarlılık ve %72 özgüllüğe sahipti.

Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.

Özet (abstract)

OBJECTIVE: The 1980 American College of Rheumatology (ACR) classification criteria for systemic sclerosis (SSc) lack sensitivity for early SSc and limited cutaneous SSc. The present work, by a joint committee of the ACR and the European League Against Rheumatism (EULAR), was undertaken for the purpose of developing new classification criteria for SSc. METHODS: Using consensus methods, 23 candidate items were arranged in a multicriteria additive point system with a threshold to classify cases as SSc. The classification system was reduced by clustering items and simplifying weights. The system was tested by 1) determining specificity and sensitivity in SSc cases and controls with scleroderma-like disorders, and 2) validating against the combined view of a group of experts on a set of cases with or without SSc. RESULTS: It was determined that skin thickening of the fingers extending proximal to the metacarpophalangeal joints is sufficient for the patient to be classified as having SSc; if that is not present, 7 additive items apply, with varying weights for each: skin thickening of the fingers, fingertip lesions, telangiectasia, abnormal nailfold capillaries, interstitial lung disease or pulmonary arterial hypertension, Raynaud's phenomenon, and SSc-related autoantibodies. Sensitivity and specificity in the validation sample were, respectively, 0.91 and 0.92 for the new classification criteria and 0.75 and 0.72 for the 1980 ACR classification criteria. All selected cases were classified in accordance with consensus-based expert opinion. All cases classified as SSc according to the 1980 ACR criteria were classified as SSc with the new criteria, and several additional cases were now considered to be SSc. CONCLUSION: The ACR/EULAR classification criteria for SSc performed better than the 1980 ACR criteria for SSc and should allow for more patients to be classified correctly as having the disease.

Yazarların özeti; kaynağından alınmıştır. Arthritis & Rheumatism, 2013 · DOI ↗

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Pathology and Forensic MedicineMedicine