Development of the 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria, Phase III‐D Report: Multicriteria Decision Analysis
Objective The 2023 American College of Rheumatology/EULAR antiphospholipid syndrome (APS) classification criteria development, which aimed to identify patients with high likelihood of APS for research, employed a four‐phase methodology. Phase I and II resulted in 27 proposed candidate criteria, whic...
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creator | Barbhaiya, Medha Zuily, Stephane Amigo, Mary‐Carmen Andrade, Danieli Avcin, Tadej Bertolaccini, Maria Laura Branch, D. Ware Costedoat‐Chalumeau, Nathalie Crowther, Mark Ramires de Jesus, Guilherme Devreese, Katrien M. J. Frances, Camille Garcia, David Gómez‐Puerta, Jose A. Guillemin, Francis Levine, Steven R. Levy, Roger A. Lockshin, Michael D. Ortel, Thomas L. Petri, Michelle Sanna, Giovanni Sciascia, Savino Seshan, Surya V. Tektonidou, Maria G. Wahl, Denis Willis, Rohan Yelnik, Cecile Hendry, Alison Naden, Ray Costenbader, Karen Erkan, Doruk Agmon‐Levin, Nancy Aguilar, Cassyanne Alba, Paula Alpan, Oral Ambrozic, Ales Andrade, Luis Appenzeller, Simone Berkun, Yackov Cabral, Antonio Canaud, Guillame Chen, Pojen Chighizola, Cecilia Cimaz, Rolando Cuadrado, Maria Jose Groot, Philip G. Moerloose, Philippe Derksen, Ronald Dörner, Thomas Fortin, Paul Giannakopoulos, Bill Gonzalez, Emilio B. Inanc, Murat Kenet, Gili Khamashta, Munther Kriegel, Martin Krilis, Steven Ladha, Danyal Manneville, Florian Massicotte, Patti McCarty, Gale Mikdashi, Jamal Myones, Barry Sammaritano, Lisa Signorelli, Flavio Soybilgic, Arzu Woller, Scott Zuo, Ray |
description | Objective
The 2023 American College of Rheumatology/EULAR antiphospholipid syndrome (APS) classification criteria development, which aimed to identify patients with high likelihood of APS for research, employed a four‐phase methodology. Phase I and II resulted in 27 proposed candidate criteria, which are organized into laboratory and clinical domains. Here, we summarize the last stage of phase III efforts, employing a consensus‐based multicriteria decision analysis (MCDA) to weigh candidate criteria and identify an APS classification threshold score.
Methods
We evaluated 192 unique, international real‐world patients referred for “suspected APS” with a wide range of APS manifestations. Using proposed candidate criteria, subcommittee members rank ordered 20 representative patients from highly unlikely to highly likely to have APS. During an in‐person meeting, the subcommittee refined definitions and participated in an MCDA exercise to identify relative weights of candidate criteria. Using consensus decisions and pairwise criteria comparisons, 1000Minds software assigned criteria weights, and we rank ordered 192 patients by their additive scores. A consensus‐based threshold score for APS classification was set.
Results
Premeeting evaluation of 20 representative patients demonstrated variability in APS assessment. MCDA resolved 81 pairwise decisions; relative weights identified domain item hierarchy. After assessing 192 patients by weights and additive scores, the Steering Committee reached consensus that APS classification should require separate clinical and laboratory scores, rather than a single‐aggregate score, to ensure high specificity.
Conclusion
Using MCDA, candidate criteria preliminary weights were determined. Unlike other disease classification systems using a single‐aggregate threshold score, separate clinical and laboratory domain thresholds were incorporated into the new APS classification criteria. |
doi_str_mv | 10.1002/acr.25415 |
format | Article |
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The 2023 American College of Rheumatology/EULAR antiphospholipid syndrome (APS) classification criteria development, which aimed to identify patients with high likelihood of APS for research, employed a four‐phase methodology. Phase I and II resulted in 27 proposed candidate criteria, which are organized into laboratory and clinical domains. Here, we summarize the last stage of phase III efforts, employing a consensus‐based multicriteria decision analysis (MCDA) to weigh candidate criteria and identify an APS classification threshold score.
Methods
We evaluated 192 unique, international real‐world patients referred for “suspected APS” with a wide range of APS manifestations. Using proposed candidate criteria, subcommittee members rank ordered 20 representative patients from highly unlikely to highly likely to have APS. During an in‐person meeting, the subcommittee refined definitions and participated in an MCDA exercise to identify relative weights of candidate criteria. Using consensus decisions and pairwise criteria comparisons, 1000Minds software assigned criteria weights, and we rank ordered 192 patients by their additive scores. A consensus‐based threshold score for APS classification was set.
Results
Premeeting evaluation of 20 representative patients demonstrated variability in APS assessment. MCDA resolved 81 pairwise decisions; relative weights identified domain item hierarchy. After assessing 192 patients by weights and additive scores, the Steering Committee reached consensus that APS classification should require separate clinical and laboratory scores, rather than a single‐aggregate score, to ensure high specificity.
Conclusion
Using MCDA, candidate criteria preliminary weights were determined. Unlike other disease classification systems using a single‐aggregate threshold score, separate clinical and laboratory domain thresholds were incorporated into the new APS classification criteria.</description><identifier>ISSN: 2151-464X</identifier><identifier>ISSN: 2151-4658</identifier><identifier>EISSN: 2151-4658</identifier><identifier>DOI: 10.1002/acr.25415</identifier><identifier>PMID: 39135467</identifier><language>eng</language><publisher>Boston, USA: Wiley Periodicals, Inc</publisher><subject>Adult ; Antiphospholipid syndrome ; Antiphospholipid Syndrome - classification ; Antiphospholipid Syndrome - diagnosis ; Autoimmune diseases ; Classification ; Classification systems ; Consensus ; Decades ; Decision Support Techniques ; Female ; Humans ; Male ; Middle Aged ; Rheumatology ; Rheumatology - standards</subject><ispartof>Arthritis care & research (2010), 2024-12, Vol.76 (12), p.1617-1625</ispartof><rights>2024 American College of Rheumatology</rights><rights>2024 American College of Rheumatology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2785-9c8ee15cb48b5a94272f8ed94bb949c6ae13721a6aa624f0d35f4a6ca97bb0bd3</cites><orcidid>0000-0003-1441-5373 ; 0000-0003-4260-5035 ; 0000-0002-8972-9388 ; 0000-0001-8177-702X ; 0000-0001-7216-677X ; 0000-0002-6670-7696 ; 0000-0002-6715-0180 ; 0000-0003-2238-0975 ; 0000-0003-1266-9441</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Facr.25415$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Facr.25415$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39135467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barbhaiya, Medha</creatorcontrib><creatorcontrib>Zuily, Stephane</creatorcontrib><creatorcontrib>Amigo, Mary‐Carmen</creatorcontrib><creatorcontrib>Andrade, Danieli</creatorcontrib><creatorcontrib>Avcin, Tadej</creatorcontrib><creatorcontrib>Bertolaccini, Maria Laura</creatorcontrib><creatorcontrib>Branch, D. Ware</creatorcontrib><creatorcontrib>Costedoat‐Chalumeau, Nathalie</creatorcontrib><creatorcontrib>Crowther, Mark</creatorcontrib><creatorcontrib>Ramires de Jesus, Guilherme</creatorcontrib><creatorcontrib>Devreese, Katrien M. J.</creatorcontrib><creatorcontrib>Frances, Camille</creatorcontrib><creatorcontrib>Garcia, David</creatorcontrib><creatorcontrib>Gómez‐Puerta, Jose A.</creatorcontrib><creatorcontrib>Guillemin, Francis</creatorcontrib><creatorcontrib>Levine, Steven R.</creatorcontrib><creatorcontrib>Levy, Roger A.</creatorcontrib><creatorcontrib>Lockshin, Michael D.</creatorcontrib><creatorcontrib>Ortel, Thomas L.</creatorcontrib><creatorcontrib>Petri, Michelle</creatorcontrib><creatorcontrib>Sanna, Giovanni</creatorcontrib><creatorcontrib>Sciascia, Savino</creatorcontrib><creatorcontrib>Seshan, Surya V.</creatorcontrib><creatorcontrib>Tektonidou, Maria G.</creatorcontrib><creatorcontrib>Wahl, Denis</creatorcontrib><creatorcontrib>Willis, Rohan</creatorcontrib><creatorcontrib>Yelnik, Cecile</creatorcontrib><creatorcontrib>Hendry, Alison</creatorcontrib><creatorcontrib>Naden, Ray</creatorcontrib><creatorcontrib>Costenbader, Karen</creatorcontrib><creatorcontrib>Erkan, Doruk</creatorcontrib><creatorcontrib>Agmon‐Levin, Nancy</creatorcontrib><creatorcontrib>Aguilar, Cassyanne</creatorcontrib><creatorcontrib>Alba, Paula</creatorcontrib><creatorcontrib>Alpan, Oral</creatorcontrib><creatorcontrib>Ambrozic, Ales</creatorcontrib><creatorcontrib>Andrade, Luis</creatorcontrib><creatorcontrib>Appenzeller, Simone</creatorcontrib><creatorcontrib>Berkun, Yackov</creatorcontrib><creatorcontrib>Cabral, Antonio</creatorcontrib><creatorcontrib>Canaud, Guillame</creatorcontrib><creatorcontrib>Chen, Pojen</creatorcontrib><creatorcontrib>Chighizola, Cecilia</creatorcontrib><creatorcontrib>Cimaz, Rolando</creatorcontrib><creatorcontrib>Cuadrado, Maria Jose</creatorcontrib><creatorcontrib>Groot, Philip G.</creatorcontrib><creatorcontrib>Moerloose, Philippe</creatorcontrib><creatorcontrib>Derksen, Ronald</creatorcontrib><creatorcontrib>Dörner, Thomas</creatorcontrib><creatorcontrib>Fortin, Paul</creatorcontrib><creatorcontrib>Giannakopoulos, Bill</creatorcontrib><creatorcontrib>Gonzalez, Emilio B.</creatorcontrib><creatorcontrib>Inanc, Murat</creatorcontrib><creatorcontrib>Kenet, Gili</creatorcontrib><creatorcontrib>Khamashta, Munther</creatorcontrib><creatorcontrib>Kriegel, Martin</creatorcontrib><creatorcontrib>Krilis, Steven</creatorcontrib><creatorcontrib>Ladha, Danyal</creatorcontrib><creatorcontrib>Manneville, Florian</creatorcontrib><creatorcontrib>Massicotte, Patti</creatorcontrib><creatorcontrib>McCarty, Gale</creatorcontrib><creatorcontrib>Mikdashi, Jamal</creatorcontrib><creatorcontrib>Myones, Barry</creatorcontrib><creatorcontrib>Sammaritano, Lisa</creatorcontrib><creatorcontrib>Signorelli, Flavio</creatorcontrib><creatorcontrib>Soybilgic, Arzu</creatorcontrib><creatorcontrib>Woller, Scott</creatorcontrib><creatorcontrib>Zuo, Ray</creatorcontrib><creatorcontrib>ACR/EULAR APS Classification Criteria Collaborators</creatorcontrib><creatorcontrib>the ACR/EULAR APS Classification Criteria Collaborators</creatorcontrib><title>Development of the 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria, Phase III‐D Report: Multicriteria Decision Analysis</title><title>Arthritis care & research (2010)</title><addtitle>Arthritis Care Res (Hoboken)</addtitle><description>Objective
The 2023 American College of Rheumatology/EULAR antiphospholipid syndrome (APS) classification criteria development, which aimed to identify patients with high likelihood of APS for research, employed a four‐phase methodology. Phase I and II resulted in 27 proposed candidate criteria, which are organized into laboratory and clinical domains. Here, we summarize the last stage of phase III efforts, employing a consensus‐based multicriteria decision analysis (MCDA) to weigh candidate criteria and identify an APS classification threshold score.
Methods
We evaluated 192 unique, international real‐world patients referred for “suspected APS” with a wide range of APS manifestations. Using proposed candidate criteria, subcommittee members rank ordered 20 representative patients from highly unlikely to highly likely to have APS. During an in‐person meeting, the subcommittee refined definitions and participated in an MCDA exercise to identify relative weights of candidate criteria. Using consensus decisions and pairwise criteria comparisons, 1000Minds software assigned criteria weights, and we rank ordered 192 patients by their additive scores. A consensus‐based threshold score for APS classification was set.
Results
Premeeting evaluation of 20 representative patients demonstrated variability in APS assessment. MCDA resolved 81 pairwise decisions; relative weights identified domain item hierarchy. After assessing 192 patients by weights and additive scores, the Steering Committee reached consensus that APS classification should require separate clinical and laboratory scores, rather than a single‐aggregate score, to ensure high specificity.
Conclusion
Using MCDA, candidate criteria preliminary weights were determined. Unlike other disease classification systems using a single‐aggregate threshold score, separate clinical and laboratory domain thresholds were incorporated into the new APS classification criteria.</description><subject>Adult</subject><subject>Antiphospholipid syndrome</subject><subject>Antiphospholipid Syndrome - classification</subject><subject>Antiphospholipid Syndrome - diagnosis</subject><subject>Autoimmune diseases</subject><subject>Classification</subject><subject>Classification systems</subject><subject>Consensus</subject><subject>Decades</subject><subject>Decision Support Techniques</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Rheumatology</subject><subject>Rheumatology - standards</subject><issn>2151-464X</issn><issn>2151-4658</issn><issn>2151-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10U-L1DAYBvAiiruse_ALSMCLgrOTv23irXRWHRhRRhe8lTR9y2RJm27SKnPb8578jH4Ss864B8FASA6_9-GFJ8ueE3xBMKZLbcIFFZyIR9kpJYIseC7k44c__3aSncd4jdNhVEqmnmYnTBEmeF6cZncr-A7Ojz0ME_IdmnaAKKYMldV2eXm1KbeoHCY77nxM19nRtujLfmiD7wFVTsdoO2v0ZP2AqmAnCFa_QZ93OgJar9e_bn-u0BZGH6a36OPsJmuOCK3A2Hg_Vg7a7aONz7InnXYRzo_vWXb17vJr9WGx-fR-XZWbhaGFFAtlJAARpuGyEVpxWtBOQqt40yiuTK6BsIISnWudU97hlomO69xoVTQNblp2lr065I7B38wQp7q30YBzegA_x5phRVmeF0Ik-vIfeu3nkPZNijCmlKRMJvX6oEzwMQbo6jHYXod9TXB931GdOqr_dJTsi2Pi3PTQPsi_jSSwPIAf1sH-_0l1KugQ-Rvx2Jtc</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Barbhaiya, Medha</creator><creator>Zuily, Stephane</creator><creator>Amigo, Mary‐Carmen</creator><creator>Andrade, Danieli</creator><creator>Avcin, Tadej</creator><creator>Bertolaccini, Maria Laura</creator><creator>Branch, D. Ware</creator><creator>Costedoat‐Chalumeau, Nathalie</creator><creator>Crowther, Mark</creator><creator>Ramires de Jesus, Guilherme</creator><creator>Devreese, Katrien M. 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Ware ; Costedoat‐Chalumeau, Nathalie ; Crowther, Mark ; Ramires de Jesus, Guilherme ; Devreese, Katrien M. J. ; Frances, Camille ; Garcia, David ; Gómez‐Puerta, Jose A. ; Guillemin, Francis ; Levine, Steven R. ; Levy, Roger A. ; Lockshin, Michael D. ; Ortel, Thomas L. ; Petri, Michelle ; Sanna, Giovanni ; Sciascia, Savino ; Seshan, Surya V. ; Tektonidou, Maria G. ; Wahl, Denis ; Willis, Rohan ; Yelnik, Cecile ; Hendry, Alison ; Naden, Ray ; Costenbader, Karen ; Erkan, Doruk ; Agmon‐Levin, Nancy ; Aguilar, Cassyanne ; Alba, Paula ; Alpan, Oral ; Ambrozic, Ales ; Andrade, Luis ; Appenzeller, Simone ; Berkun, Yackov ; Cabral, Antonio ; Canaud, Guillame ; Chen, Pojen ; Chighizola, Cecilia ; Cimaz, Rolando ; Cuadrado, Maria Jose ; Groot, Philip G. ; Moerloose, Philippe ; Derksen, Ronald ; Dörner, Thomas ; Fortin, Paul ; Giannakopoulos, Bill ; Gonzalez, Emilio B. ; Inanc, Murat ; Kenet, Gili ; Khamashta, Munther ; Kriegel, Martin ; Krilis, Steven ; Ladha, Danyal ; Manneville, Florian ; Massicotte, Patti ; McCarty, Gale ; Mikdashi, Jamal ; Myones, Barry ; Sammaritano, Lisa ; Signorelli, Flavio ; Soybilgic, Arzu ; Woller, Scott ; Zuo, Ray</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2785-9c8ee15cb48b5a94272f8ed94bb949c6ae13721a6aa624f0d35f4a6ca97bb0bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Antiphospholipid syndrome</topic><topic>Antiphospholipid Syndrome - classification</topic><topic>Antiphospholipid Syndrome - diagnosis</topic><topic>Autoimmune diseases</topic><topic>Classification</topic><topic>Classification systems</topic><topic>Consensus</topic><topic>Decades</topic><topic>Decision Support Techniques</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Rheumatology</topic><topic>Rheumatology - standards</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbhaiya, Medha</creatorcontrib><creatorcontrib>Zuily, Stephane</creatorcontrib><creatorcontrib>Amigo, Mary‐Carmen</creatorcontrib><creatorcontrib>Andrade, Danieli</creatorcontrib><creatorcontrib>Avcin, Tadej</creatorcontrib><creatorcontrib>Bertolaccini, Maria Laura</creatorcontrib><creatorcontrib>Branch, D. Ware</creatorcontrib><creatorcontrib>Costedoat‐Chalumeau, Nathalie</creatorcontrib><creatorcontrib>Crowther, Mark</creatorcontrib><creatorcontrib>Ramires de Jesus, Guilherme</creatorcontrib><creatorcontrib>Devreese, Katrien M. J.</creatorcontrib><creatorcontrib>Frances, Camille</creatorcontrib><creatorcontrib>Garcia, David</creatorcontrib><creatorcontrib>Gómez‐Puerta, Jose A.</creatorcontrib><creatorcontrib>Guillemin, Francis</creatorcontrib><creatorcontrib>Levine, Steven R.</creatorcontrib><creatorcontrib>Levy, Roger A.</creatorcontrib><creatorcontrib>Lockshin, Michael D.</creatorcontrib><creatorcontrib>Ortel, Thomas L.</creatorcontrib><creatorcontrib>Petri, Michelle</creatorcontrib><creatorcontrib>Sanna, Giovanni</creatorcontrib><creatorcontrib>Sciascia, Savino</creatorcontrib><creatorcontrib>Seshan, Surya V.</creatorcontrib><creatorcontrib>Tektonidou, Maria G.</creatorcontrib><creatorcontrib>Wahl, Denis</creatorcontrib><creatorcontrib>Willis, Rohan</creatorcontrib><creatorcontrib>Yelnik, Cecile</creatorcontrib><creatorcontrib>Hendry, Alison</creatorcontrib><creatorcontrib>Naden, Ray</creatorcontrib><creatorcontrib>Costenbader, Karen</creatorcontrib><creatorcontrib>Erkan, Doruk</creatorcontrib><creatorcontrib>Agmon‐Levin, Nancy</creatorcontrib><creatorcontrib>Aguilar, Cassyanne</creatorcontrib><creatorcontrib>Alba, Paula</creatorcontrib><creatorcontrib>Alpan, Oral</creatorcontrib><creatorcontrib>Ambrozic, Ales</creatorcontrib><creatorcontrib>Andrade, Luis</creatorcontrib><creatorcontrib>Appenzeller, Simone</creatorcontrib><creatorcontrib>Berkun, Yackov</creatorcontrib><creatorcontrib>Cabral, Antonio</creatorcontrib><creatorcontrib>Canaud, Guillame</creatorcontrib><creatorcontrib>Chen, Pojen</creatorcontrib><creatorcontrib>Chighizola, Cecilia</creatorcontrib><creatorcontrib>Cimaz, Rolando</creatorcontrib><creatorcontrib>Cuadrado, Maria Jose</creatorcontrib><creatorcontrib>Groot, Philip G.</creatorcontrib><creatorcontrib>Moerloose, Philippe</creatorcontrib><creatorcontrib>Derksen, Ronald</creatorcontrib><creatorcontrib>Dörner, Thomas</creatorcontrib><creatorcontrib>Fortin, Paul</creatorcontrib><creatorcontrib>Giannakopoulos, Bill</creatorcontrib><creatorcontrib>Gonzalez, Emilio B.</creatorcontrib><creatorcontrib>Inanc, Murat</creatorcontrib><creatorcontrib>Kenet, Gili</creatorcontrib><creatorcontrib>Khamashta, Munther</creatorcontrib><creatorcontrib>Kriegel, Martin</creatorcontrib><creatorcontrib>Krilis, Steven</creatorcontrib><creatorcontrib>Ladha, Danyal</creatorcontrib><creatorcontrib>Manneville, Florian</creatorcontrib><creatorcontrib>Massicotte, Patti</creatorcontrib><creatorcontrib>McCarty, Gale</creatorcontrib><creatorcontrib>Mikdashi, Jamal</creatorcontrib><creatorcontrib>Myones, Barry</creatorcontrib><creatorcontrib>Sammaritano, Lisa</creatorcontrib><creatorcontrib>Signorelli, Flavio</creatorcontrib><creatorcontrib>Soybilgic, Arzu</creatorcontrib><creatorcontrib>Woller, Scott</creatorcontrib><creatorcontrib>Zuo, Ray</creatorcontrib><creatorcontrib>ACR/EULAR APS Classification Criteria Collaborators</creatorcontrib><creatorcontrib>the ACR/EULAR APS Classification Criteria Collaborators</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis care & research (2010)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barbhaiya, Medha</au><au>Zuily, Stephane</au><au>Amigo, Mary‐Carmen</au><au>Andrade, Danieli</au><au>Avcin, Tadej</au><au>Bertolaccini, Maria Laura</au><au>Branch, D. Ware</au><au>Costedoat‐Chalumeau, Nathalie</au><au>Crowther, Mark</au><au>Ramires de Jesus, Guilherme</au><au>Devreese, Katrien M. J.</au><au>Frances, Camille</au><au>Garcia, David</au><au>Gómez‐Puerta, Jose A.</au><au>Guillemin, Francis</au><au>Levine, Steven R.</au><au>Levy, Roger A.</au><au>Lockshin, Michael D.</au><au>Ortel, Thomas L.</au><au>Petri, Michelle</au><au>Sanna, Giovanni</au><au>Sciascia, Savino</au><au>Seshan, Surya V.</au><au>Tektonidou, Maria G.</au><au>Wahl, Denis</au><au>Willis, Rohan</au><au>Yelnik, Cecile</au><au>Hendry, Alison</au><au>Naden, Ray</au><au>Costenbader, Karen</au><au>Erkan, Doruk</au><au>Agmon‐Levin, Nancy</au><au>Aguilar, Cassyanne</au><au>Alba, Paula</au><au>Alpan, Oral</au><au>Ambrozic, Ales</au><au>Andrade, Luis</au><au>Appenzeller, Simone</au><au>Berkun, Yackov</au><au>Cabral, Antonio</au><au>Canaud, Guillame</au><au>Chen, Pojen</au><au>Chighizola, Cecilia</au><au>Cimaz, Rolando</au><au>Cuadrado, Maria Jose</au><au>Groot, Philip G.</au><au>Moerloose, Philippe</au><au>Derksen, Ronald</au><au>Dörner, Thomas</au><au>Fortin, Paul</au><au>Giannakopoulos, Bill</au><au>Gonzalez, Emilio B.</au><au>Inanc, Murat</au><au>Kenet, Gili</au><au>Khamashta, Munther</au><au>Kriegel, Martin</au><au>Krilis, Steven</au><au>Ladha, Danyal</au><au>Manneville, Florian</au><au>Massicotte, Patti</au><au>McCarty, Gale</au><au>Mikdashi, Jamal</au><au>Myones, Barry</au><au>Sammaritano, Lisa</au><au>Signorelli, Flavio</au><au>Soybilgic, Arzu</au><au>Woller, Scott</au><au>Zuo, Ray</au><aucorp>ACR/EULAR APS Classification Criteria Collaborators</aucorp><aucorp>the ACR/EULAR APS Classification Criteria Collaborators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of the 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria, Phase III‐D Report: Multicriteria Decision Analysis</atitle><jtitle>Arthritis care & research (2010)</jtitle><addtitle>Arthritis Care Res (Hoboken)</addtitle><date>2024-12</date><risdate>2024</risdate><volume>76</volume><issue>12</issue><spage>1617</spage><epage>1625</epage><pages>1617-1625</pages><issn>2151-464X</issn><issn>2151-4658</issn><eissn>2151-4658</eissn><abstract>Objective
The 2023 American College of Rheumatology/EULAR antiphospholipid syndrome (APS) classification criteria development, which aimed to identify patients with high likelihood of APS for research, employed a four‐phase methodology. Phase I and II resulted in 27 proposed candidate criteria, which are organized into laboratory and clinical domains. Here, we summarize the last stage of phase III efforts, employing a consensus‐based multicriteria decision analysis (MCDA) to weigh candidate criteria and identify an APS classification threshold score.
Methods
We evaluated 192 unique, international real‐world patients referred for “suspected APS” with a wide range of APS manifestations. Using proposed candidate criteria, subcommittee members rank ordered 20 representative patients from highly unlikely to highly likely to have APS. During an in‐person meeting, the subcommittee refined definitions and participated in an MCDA exercise to identify relative weights of candidate criteria. Using consensus decisions and pairwise criteria comparisons, 1000Minds software assigned criteria weights, and we rank ordered 192 patients by their additive scores. A consensus‐based threshold score for APS classification was set.
Results
Premeeting evaluation of 20 representative patients demonstrated variability in APS assessment. MCDA resolved 81 pairwise decisions; relative weights identified domain item hierarchy. After assessing 192 patients by weights and additive scores, the Steering Committee reached consensus that APS classification should require separate clinical and laboratory scores, rather than a single‐aggregate score, to ensure high specificity.
Conclusion
Using MCDA, candidate criteria preliminary weights were determined. Unlike other disease classification systems using a single‐aggregate threshold score, separate clinical and laboratory domain thresholds were incorporated into the new APS classification criteria.</abstract><cop>Boston, USA</cop><pub>Wiley Periodicals, Inc</pub><pmid>39135467</pmid><doi>10.1002/acr.25415</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1441-5373</orcidid><orcidid>https://orcid.org/0000-0003-4260-5035</orcidid><orcidid>https://orcid.org/0000-0002-8972-9388</orcidid><orcidid>https://orcid.org/0000-0001-8177-702X</orcidid><orcidid>https://orcid.org/0000-0001-7216-677X</orcidid><orcidid>https://orcid.org/0000-0002-6670-7696</orcidid><orcidid>https://orcid.org/0000-0002-6715-0180</orcidid><orcidid>https://orcid.org/0000-0003-2238-0975</orcidid><orcidid>https://orcid.org/0000-0003-1266-9441</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2151-464X |
ispartof | Arthritis care & research (2010), 2024-12, Vol.76 (12), p.1617-1625 |
issn | 2151-464X 2151-4658 2151-4658 |
language | eng |
recordid | cdi_proquest_miscellaneous_3092366755 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Adult Antiphospholipid syndrome Antiphospholipid Syndrome - classification Antiphospholipid Syndrome - diagnosis Autoimmune diseases Classification Classification systems Consensus Decades Decision Support Techniques Female Humans Male Middle Aged Rheumatology Rheumatology - standards |
title | Development of the 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria, Phase III‐D Report: Multicriteria Decision Analysis |
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