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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Veröffentlicht in:Arthritis care & research (2010) 2024-12, Vol.76 (12), p.1617-1625
Hauptverfasser: 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
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container_title Arthritis care & research (2010)
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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
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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</creator><creatorcontrib>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 ; ACR/EULAR APS Classification Criteria Collaborators ; the ACR/EULAR APS Classification Criteria Collaborators</creatorcontrib><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><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 &amp; 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 &amp; 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. 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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. 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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 &amp; 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>
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identifier ISSN: 2151-464X
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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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