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A Review of the Sapporo and Revised Sapporo Criteria for the Classification of Antiphospholipid Syndrome. Where Do the Revised Sapporo Criteria Add Value?
RAJA S. BOBBA, SINDHU R. JOHNSON, and AILEEN M. DAVIS
ABSTRACT. Methods. A computer search for articles describing use of the Sapporo and the revised Sapporo criteria was performed. Item generation, item reduction, sensibility, validity, and reliability of the criteria were evaluated. Results. The Sapporo criteria set has incremental face and content validity over its predecessors. However, through separation of anti-ß2-glycoprotein I antibodies as a sub-item, the specification of a wider time interval between serologic testing, the specification of a time interval between serology and clinical manifestations, and specification of definitions for clinical manifestations and laboratory titer thresholds, the revised Sapporo criteria set has incremental face and content validity over the Sapporo criteria. The complexity of the criteria, diagnostic tests, and immunologic tests limits their feasibility. The reliability of each criterion is unknown. The discriminative capacity of the Sapporo criteria is good, with sensitivity, specificity, and positive and negative predictive values of 0.71, 0.98, 0.95, and 0.88, respectively, compared to patients with systemic lupus erythematosus. The discriminative capacity of the revised Sapporo criteria is unknown. Conclusion. The revised Sapporo criteria set has incremental face and content validity compared its predecessors. Reliability testing of each criterion is needed before these criteria can be confidently used in multicenter APS trials. Discriminatory testing of the revised Sapporo criteria is required. (First Release June 1 2007; J Rheumatol 2007;34:1522-7) Key Indexing Terms:
ANTIPHOSPHOLIPID SYNDROME From the Division of Rheumatology, McMaster University, Hamilton, Ontario; Division of Rheumatology, Toronto Western Hospital, University Health Network, Toronto, Ontario; Department of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario; and Toronto Western Research Institute, Toronto, Ontario, Canada. Dr. Johnson is the recipient of an Abbott Scholar Award for Rheumatology Research and Research Fellowship Award from the Canadian Arthritis Network. Dr. Davis was supported as a Canadian Institutes of Health Research Scholar at the time of this work. R.S. Bobba, MS, MSc, Division of Rheumatology, McMaster University, Department of Health Policy, Management and Evaluation, University of Toronto; S.R. Johnson, MD, FRCPC, Division of Rheumatology, Toronto Western Hospital, University Health Network, Department of Health Policy, Management and Evaluation, University of Toronto; A.M. Davis, BScPT, MSc, PhD, Department of Health Policy, Management and Evaluation, Senior Scientist, Department of Health Care and Outcomes Research, Toronto Western Research Institute, University of Toronto. Address reprint requests to Dr. A.M. Davis, Department of Outcomes and Population Health, Toronto Western Research Institute, 399 Bathurst Street, MP11-322, Toronto, Ontario M5T 2S8, Canada. E-mail: adavis@uhnresearch.ca Accepted for publication March 22, 2007. |