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Absence of Scleroderma pattern at nail fold capillaroscopy valuable in the exclusion of Scleroderma in unselected patients with Raynaud's Phenomenon
To report the predictive value of nail-fold capillaroscopy (NFC) patterns of vasculopathy for systemic sclerosis (Scleroderma; SSc) in an unselected cohort of patients with Raynaud's phenomenon (RP). Patients referred to a tertiary SSc clinic with RP were evaluated by light/video-NFC. Clinical...
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Published in: | BMC musculoskeletal disorders 2016-08, Vol.17 (1), p.342-342, Article 342 |
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description | To report the predictive value of nail-fold capillaroscopy (NFC) patterns of vasculopathy for systemic sclerosis (Scleroderma; SSc) in an unselected cohort of patients with Raynaud's phenomenon (RP).
Patients referred to a tertiary SSc clinic with RP were evaluated by light/video-NFC. Clinical diagnosis, details and serology were recorded. Primary RP was defined as RP with no features of connective tissue disease (CTD)/antibody. NFC patterns were determined: normal, non-specific, 'early', 'active' or 'late' SSc patterns. Fulfilment of the VEDOSS or 2013 ACR/EULAR criteria for SSc was determined following NFC assessment.
Three hundred forty-seven patients were referred: mean (SD) age 47 (15.2) years. On clinical review, 54 (16 %) did not have RP, 69 (20 %) had primary RP, 52 (15 %) had SSc and 172 (50 %) had secondary RP. NFC SSc pattern was detected in 80 (23 %) patients; 37/52 with SSc, 30/172 with secondary RP, 9/69 with primary RP and 4/54 with no RP. For identifying patients who met either the VEDOSS or 2013 ACR/EULAR criteria for SSc, detection of a SSc NFC pattern had a sensitivity of 71 %, specificity 95 %, positive predictive value 84 % and negative predictive value 90 %.
The absence of SSc NFC pattern in patients with RP or suspected CTD is very valuable in the exclusion of SSc. |
doi_str_mv | 10.1186/s12891-016-1206-5 |
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Patients referred to a tertiary SSc clinic with RP were evaluated by light/video-NFC. Clinical diagnosis, details and serology were recorded. Primary RP was defined as RP with no features of connective tissue disease (CTD)/antibody. NFC patterns were determined: normal, non-specific, 'early', 'active' or 'late' SSc patterns. Fulfilment of the VEDOSS or 2013 ACR/EULAR criteria for SSc was determined following NFC assessment.
Three hundred forty-seven patients were referred: mean (SD) age 47 (15.2) years. On clinical review, 54 (16 %) did not have RP, 69 (20 %) had primary RP, 52 (15 %) had SSc and 172 (50 %) had secondary RP. NFC SSc pattern was detected in 80 (23 %) patients; 37/52 with SSc, 30/172 with secondary RP, 9/69 with primary RP and 4/54 with no RP. For identifying patients who met either the VEDOSS or 2013 ACR/EULAR criteria for SSc, detection of a SSc NFC pattern had a sensitivity of 71 %, specificity 95 %, positive predictive value 84 % and negative predictive value 90 %.
The absence of SSc NFC pattern in patients with RP or suspected CTD is very valuable in the exclusion of SSc.</description><identifier>ISSN: 1471-2474</identifier><identifier>EISSN: 1471-2474</identifier><identifier>DOI: 10.1186/s12891-016-1206-5</identifier><identifier>PMID: 27526772</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adult ; Aged ; Antibodies ; Care and treatment ; Clinical trials ; Diagnosis ; Female ; Humans ; Male ; Microscopic Angioscopy ; Middle Aged ; Nails - diagnostic imaging ; Patient Selection ; Physiological aspects ; Predictive Value of Tests ; Raynaud Disease - diagnostic imaging ; Retrospective Studies ; Risk factors ; Scleroderma (Disease) ; Scleroderma, Systemic - diagnostic imaging ; Sensitivity and Specificity ; Systemic scleroderma ; Viral antibodies</subject><ispartof>BMC musculoskeletal disorders, 2016-08, Vol.17 (1), p.342-342, Article 342</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>The Author(s). 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-44cf4a749bab95109e26e4b25863aabfad1fc5b795eed3ab783e788619bcb9ac3</citedby><cites>FETCH-LOGICAL-c466t-44cf4a749bab95109e26e4b25863aabfad1fc5b795eed3ab783e788619bcb9ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986250/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986250/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,36990,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27526772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bissell, Lesley-Anne</creatorcontrib><creatorcontrib>Abignano, Giuseppina</creatorcontrib><creatorcontrib>Emery, Paul</creatorcontrib><creatorcontrib>Del Galdo, Francesco</creatorcontrib><creatorcontrib>Buch, Maya H</creatorcontrib><title>Absence of Scleroderma pattern at nail fold capillaroscopy valuable in the exclusion of Scleroderma in unselected patients with Raynaud's Phenomenon</title><title>BMC musculoskeletal disorders</title><addtitle>BMC Musculoskelet Disord</addtitle><description>To report the predictive value of nail-fold capillaroscopy (NFC) patterns of vasculopathy for systemic sclerosis (Scleroderma; SSc) in an unselected cohort of patients with Raynaud's phenomenon (RP).
Patients referred to a tertiary SSc clinic with RP were evaluated by light/video-NFC. Clinical diagnosis, details and serology were recorded. Primary RP was defined as RP with no features of connective tissue disease (CTD)/antibody. NFC patterns were determined: normal, non-specific, 'early', 'active' or 'late' SSc patterns. Fulfilment of the VEDOSS or 2013 ACR/EULAR criteria for SSc was determined following NFC assessment.
Three hundred forty-seven patients were referred: mean (SD) age 47 (15.2) years. On clinical review, 54 (16 %) did not have RP, 69 (20 %) had primary RP, 52 (15 %) had SSc and 172 (50 %) had secondary RP. NFC SSc pattern was detected in 80 (23 %) patients; 37/52 with SSc, 30/172 with secondary RP, 9/69 with primary RP and 4/54 with no RP. For identifying patients who met either the VEDOSS or 2013 ACR/EULAR criteria for SSc, detection of a SSc NFC pattern had a sensitivity of 71 %, specificity 95 %, positive predictive value 84 % and negative predictive value 90 %.
The absence of SSc NFC pattern in patients with RP or suspected CTD is very valuable in the exclusion of SSc.</description><subject>Adult</subject><subject>Aged</subject><subject>Antibodies</subject><subject>Care and treatment</subject><subject>Clinical trials</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Microscopic Angioscopy</subject><subject>Middle Aged</subject><subject>Nails - diagnostic imaging</subject><subject>Patient Selection</subject><subject>Physiological aspects</subject><subject>Predictive Value of Tests</subject><subject>Raynaud Disease - diagnostic imaging</subject><subject>Retrospective Studies</subject><subject>Risk factors</subject><subject>Scleroderma (Disease)</subject><subject>Scleroderma, Systemic - diagnostic imaging</subject><subject>Sensitivity and Specificity</subject><subject>Systemic scleroderma</subject><subject>Viral antibodies</subject><issn>1471-2474</issn><issn>1471-2474</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNptUl1rFTEUXESxtfoDfJGAD_Zl6yabTTYvwqVYFQqKH8_hJHu2N5JN1k22ev-HP9hcbi2tSAg55MwMc5Kpque0OaO0F68TZb2idUNFTVkj6u5BdUy5pDXjkj-8Ux9VT1L63jRU9q16XB0x2TEhJTuufm9MwmCRxJF8sR6XOOAyAZkhZ1wCgUwCOE_G6AdiYXbewxKTjfOOXINfwXgkLpC8RYK_rF-Ti-FfsdJfQ0KPNuOwl3YYciI_Xd6Sz7ALsA6vEvm0xRCnssPT6tEIPuGzm_Ok-nbx9uv5-_ry47sP55vL2nIhcs25HTlIrgwY1dFGIRPIDet60QKYEQY62s5I1SEOLZgyPMq-F1QZaxTY9qR6c9CdVzPhYIurBbyeFzfBstMRnL7fCW6rr-K15qoXrGuKwOmNwBJ_rJiynlyyWN4oYFyTpj1lnFMlVYG-PECvwKN2YYxF0e7hesOLJSV72hbU2X9QZQ04ORsDjq7c3yPQA8GWX0kLjrfuaaP3IdGHkOgSEr0Pie4K58XdsW8Zf1PR_gG7-bvC</recordid><startdate>20160815</startdate><enddate>20160815</enddate><creator>Bissell, Lesley-Anne</creator><creator>Abignano, Giuseppina</creator><creator>Emery, Paul</creator><creator>Del Galdo, Francesco</creator><creator>Buch, Maya H</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160815</creationdate><title>Absence of Scleroderma pattern at nail fold capillaroscopy valuable in the exclusion of Scleroderma in unselected patients with Raynaud's Phenomenon</title><author>Bissell, Lesley-Anne ; Abignano, Giuseppina ; Emery, Paul ; Del Galdo, Francesco ; Buch, Maya H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-44cf4a749bab95109e26e4b25863aabfad1fc5b795eed3ab783e788619bcb9ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antibodies</topic><topic>Care and treatment</topic><topic>Clinical trials</topic><topic>Diagnosis</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Microscopic Angioscopy</topic><topic>Middle Aged</topic><topic>Nails - diagnostic imaging</topic><topic>Patient Selection</topic><topic>Physiological aspects</topic><topic>Predictive Value of Tests</topic><topic>Raynaud Disease - diagnostic imaging</topic><topic>Retrospective Studies</topic><topic>Risk factors</topic><topic>Scleroderma (Disease)</topic><topic>Scleroderma, Systemic - diagnostic imaging</topic><topic>Sensitivity and Specificity</topic><topic>Systemic scleroderma</topic><topic>Viral antibodies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bissell, Lesley-Anne</creatorcontrib><creatorcontrib>Abignano, Giuseppina</creatorcontrib><creatorcontrib>Emery, Paul</creatorcontrib><creatorcontrib>Del Galdo, Francesco</creatorcontrib><creatorcontrib>Buch, Maya H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC musculoskeletal disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bissell, Lesley-Anne</au><au>Abignano, Giuseppina</au><au>Emery, Paul</au><au>Del Galdo, Francesco</au><au>Buch, Maya H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Absence of Scleroderma pattern at nail fold capillaroscopy valuable in the exclusion of Scleroderma in unselected patients with Raynaud's Phenomenon</atitle><jtitle>BMC musculoskeletal disorders</jtitle><addtitle>BMC Musculoskelet Disord</addtitle><date>2016-08-15</date><risdate>2016</risdate><volume>17</volume><issue>1</issue><spage>342</spage><epage>342</epage><pages>342-342</pages><artnum>342</artnum><issn>1471-2474</issn><eissn>1471-2474</eissn><abstract>To report the predictive value of nail-fold capillaroscopy (NFC) patterns of vasculopathy for systemic sclerosis (Scleroderma; SSc) in an unselected cohort of patients with Raynaud's phenomenon (RP).
Patients referred to a tertiary SSc clinic with RP were evaluated by light/video-NFC. Clinical diagnosis, details and serology were recorded. Primary RP was defined as RP with no features of connective tissue disease (CTD)/antibody. NFC patterns were determined: normal, non-specific, 'early', 'active' or 'late' SSc patterns. Fulfilment of the VEDOSS or 2013 ACR/EULAR criteria for SSc was determined following NFC assessment.
Three hundred forty-seven patients were referred: mean (SD) age 47 (15.2) years. On clinical review, 54 (16 %) did not have RP, 69 (20 %) had primary RP, 52 (15 %) had SSc and 172 (50 %) had secondary RP. NFC SSc pattern was detected in 80 (23 %) patients; 37/52 with SSc, 30/172 with secondary RP, 9/69 with primary RP and 4/54 with no RP. For identifying patients who met either the VEDOSS or 2013 ACR/EULAR criteria for SSc, detection of a SSc NFC pattern had a sensitivity of 71 %, specificity 95 %, positive predictive value 84 % and negative predictive value 90 %.
The absence of SSc NFC pattern in patients with RP or suspected CTD is very valuable in the exclusion of SSc.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>27526772</pmid><doi>10.1186/s12891-016-1206-5</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antibodies Care and treatment Clinical trials Diagnosis Female Humans Male Microscopic Angioscopy Middle Aged Nails - diagnostic imaging Patient Selection Physiological aspects Predictive Value of Tests Raynaud Disease - diagnostic imaging Retrospective Studies Risk factors Scleroderma (Disease) Scleroderma, Systemic - diagnostic imaging Sensitivity and Specificity Systemic scleroderma Viral antibodies |
title | Absence of Scleroderma pattern at nail fold capillaroscopy valuable in the exclusion of Scleroderma in unselected patients with Raynaud's Phenomenon |
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