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Derivation and validation of the systemic lupus international collaborating clinics classification criteria for systemic lupus erythematosus

Date
2012
Author
Callen, Jeffrey P.
Sigler, Lisa
Jorizzo, Joseph L.
Lim, S. Sam
Franks, Andrew G.
Sturfelt, Gunnar
Ramsey-Goldman, Rosalind
Bae, Sang-Cheol
Hanly, John G.
Sanchez-Guerrero, Jorge
Clarke, Ann
Hameed, Suhail
Fang, Hong
Ngoc Pham, Ngoc Pham
Brey, Robin
Weisman, Michael H.
McGwin, Gerald
Magder, Laurence S.
Inanc, Murat
Steinsson, Kristjan
Nived, Ola
Wallace, Daniel J.
Isenberg, David
Bruce, Ian N.
Fortin, Paul R.
Merrill, Joan T.
Gordon, Caroline
Alarcon, Graciela S.
Orbai, Ana-Maria
Petri, Michelle
Rahman, Anisur
Kamen, Diane L.
Fessler, Barri J.
Aranow, Cynthia
Manzi, Susan
Urowitz, Murray
Gladman, Dafna
Kalunian, Kenneth
Costner, Melissa
Werth, Victoria P.
Zoma, Asad
Bernatsky, Sasha
Ruiz-Irastorza, Guillermo
Khamashta, Munther A.
Jacobsen, Soren
Buyon, Jill P.
Maddison, Peter
Dooley, Mary Anne
van vollenhoven, Ronald F.
Ginzler, Ellen
Stoll, Thomas
Peschken, Christine
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Abstract
Objective The Systemic Lupus International Collaborating Clinics (SLICC) group revised and validated the American College of Rheumatology (ACR) systemic lupus erythematosus (SLE) classification criteria in order to improve clinical relevance, meet stringent methodology requirements, and incorporate new knowledge regarding the immunology of SLE. Methods The classification criteria were derived from a set of 702 expert-rated patient scenarios. Recursive partitioning was used to derive an initial rule that was simplified and refined based on SLICC physician consensus. The SLICC group validated the classification criteria in a new validation sample of 690 new expert-rated patient scenarios. Results Seventeen criteria were identified. In the derivation set, the SLICC classification criteria resulted in fewer misclassifications compared with the current ACR classification criteria (49 versus 70; P = 0.0082) and had greater sensitivity (94% versus 86%; P < 0.0001) and equal specificity (92% versus 93%; P = 0.39). In the validation set, the SLICC classification criteria resulted in fewer misclassifications compared with the current ACR classification criteria (62 versus 74; P = 0.24) and had greater sensitivity (97% versus 83%; P < 0.0001) but lower specificity (84% versus 96%; P < 0.0001). Conclusion The new SLICC classification criteria performed well in a large set of patient scenarios rated by experts. According to the SLICC rule for the classification of SLE, the patient must satisfy at least 4 criteria, including at least one clinical criterion and one immunologic criterion OR the patient must have biopsy-proven lupus nephritis in the presence of antinuclear antibodies or antidouble-stranded DNA antibodies.
URI
http://hdl.handle.net/20.500.12627/41385
https://doi.org/10.1002/art.34473
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Creative Commons Lisansı

İstanbul Üniversitesi Akademik Arşiv Sistemi (ilgili içerikte aksi belirtilmediği sürece) Creative Commons Alıntı-GayriTicari-Türetilemez 4.0 Uluslararası Lisansı ile lisanslanmıştır.

DSpace software copyright © 2002-2016  DuraSpace
Contact Us | Send Feedback
Theme by 
Atmire NV