Fluoroquinolones and Risk of Aortic Aneurysm or Dissection in Patients With Congenital Aortic Disease and Marfan Syndrome

Background: Fluoroquinolone use can be associated with an increased risk of aortic aneurysm (AA) or aortic dissection (AD). The US Food and Drug Administration recently warned against fluoroquinolone use for high-risk patients, such as those with Marfan syndrome. However, the association between flu...

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Veröffentlicht in:Circulation Journal 2023/08/25, Vol.87(9), pp.1164-1172
Hauptverfasser: Chen, Shao-Wei, Lin, Chia-Pin, Chan, Yi-Hsin, Wu, Victor Chien-Chia, Cheng, Yu-Ting, Tung, Ying-Chang, Hsiao, Fu-Chih, Chen, Dong-Yi, Hung, Kuo-Chun, Chou, An-Hsun, Chu, Pao-Hsien
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container_end_page 1172
container_issue 9
container_start_page 1164
container_title Circulation Journal
container_volume 87
creator Chen, Shao-Wei
Lin, Chia-Pin
Chan, Yi-Hsin
Wu, Victor Chien-Chia
Cheng, Yu-Ting
Tung, Ying-Chang
Hsiao, Fu-Chih
Chen, Dong-Yi
Hung, Kuo-Chun
Chou, An-Hsun
Chu, Pao-Hsien
description Background: Fluoroquinolone use can be associated with an increased risk of aortic aneurysm (AA) or aortic dissection (AD). The US Food and Drug Administration recently warned against fluoroquinolone use for high-risk patients, such as those with Marfan syndrome. However, the association between fluoroquinolone use and AA/AD risk was unknown in these high-risk patients and therefore it was studied in this work.Methods and Results: Data were collected from a national database between 2000 and 2017 for 550 patients with AA/AD and any congenital aortic disease (mean age 41.5 years; 415 with Marfan syndrome). A case cross-over study was conducted to compare the risk of aortic events (AA/AD) associated with fluoroquinolone and amoxicillin use between the hazard period (from −60 days to −1 day) and a randomly selected reference period (−180 to −121 days; −240 to −181 days; and –300 to –241 days). Compared to the reference period without fluoroquinolone use, fluoroquinolone use during the hazard period was not associated with a greater risk of AA/AD (1.09% vs. 1.09%; odds ratio [OR] 1.000; 95% confidence interval [CI] 0.32–3.10), AA (OR 0.67; 95% CI 0.11–3.99), or AD (OR 1.33; 95% CI 0.30–5.96) in patients with congenital aortic disease or Marfan syndrome. This lack of association was maintained in subgroup analysis, including Marfan syndrome or not, age (≤50 vs. >50 years) and sex.Conclusions: Fluoroquinolone use was not associated with an increased risk of AA/AD in patients with congenital aortic disease, including Marfan syndrome. More evidence is required for a fluoroquinolone pharmacovigilance plan in these patients.
doi_str_mv 10.1253/circj.CJ-22-0682
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The US Food and Drug Administration recently warned against fluoroquinolone use for high-risk patients, such as those with Marfan syndrome. However, the association between fluoroquinolone use and AA/AD risk was unknown in these high-risk patients and therefore it was studied in this work.Methods and Results: Data were collected from a national database between 2000 and 2017 for 550 patients with AA/AD and any congenital aortic disease (mean age 41.5 years; 415 with Marfan syndrome). A case cross-over study was conducted to compare the risk of aortic events (AA/AD) associated with fluoroquinolone and amoxicillin use between the hazard period (from −60 days to −1 day) and a randomly selected reference period (−180 to −121 days; −240 to −181 days; and –300 to –241 days). Compared to the reference period without fluoroquinolone use, fluoroquinolone use during the hazard period was not associated with a greater risk of AA/AD (1.09% vs. 1.09%; odds ratio [OR] 1.000; 95% confidence interval [CI] 0.32–3.10), AA (OR 0.67; 95% CI 0.11–3.99), or AD (OR 1.33; 95% CI 0.30–5.96) in patients with congenital aortic disease or Marfan syndrome. This lack of association was maintained in subgroup analysis, including Marfan syndrome or not, age (≤50 vs. &gt;50 years) and sex.Conclusions: Fluoroquinolone use was not associated with an increased risk of AA/AD in patients with congenital aortic disease, including Marfan syndrome. More evidence is required for a fluoroquinolone pharmacovigilance plan in these patients.</description><identifier>ISSN: 1346-9843</identifier><identifier>ISSN: 1347-4820</identifier><identifier>EISSN: 1347-4820</identifier><identifier>DOI: 10.1253/circj.CJ-22-0682</identifier><identifier>PMID: 36823078</identifier><language>eng</language><publisher>Japan: The Japanese Circulation Society</publisher><subject>Adult ; Aortic aneurysm ; Aortic Aneurysm - chemically induced ; Aortic Aneurysm - epidemiology ; Aortic dissection ; Aortic Dissection - chemically induced ; Aortic Dissection - epidemiology ; Congenital aortic disease ; Cross-Over Studies ; Fluoroquinolones ; Fluoroquinolones - adverse effects ; Humans ; Marfan syndrome ; Marfan Syndrome - complications</subject><ispartof>Circulation Journal, 2023/08/25, Vol.87(9), pp.1164-1172</ispartof><rights>2023, THE JAPANESE CIRCULATION SOCIETY</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-8dce12046885606fd237590280a88fe69a9c4424a073cd907abab0d9a6ff3df43</citedby><cites>FETCH-LOGICAL-c470t-8dce12046885606fd237590280a88fe69a9c4424a073cd907abab0d9a6ff3df43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1881,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36823078$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Shao-Wei</creatorcontrib><creatorcontrib>Lin, Chia-Pin</creatorcontrib><creatorcontrib>Chan, Yi-Hsin</creatorcontrib><creatorcontrib>Wu, Victor Chien-Chia</creatorcontrib><creatorcontrib>Cheng, Yu-Ting</creatorcontrib><creatorcontrib>Tung, Ying-Chang</creatorcontrib><creatorcontrib>Hsiao, Fu-Chih</creatorcontrib><creatorcontrib>Chen, Dong-Yi</creatorcontrib><creatorcontrib>Hung, Kuo-Chun</creatorcontrib><creatorcontrib>Chou, An-Hsun</creatorcontrib><creatorcontrib>Chu, Pao-Hsien</creatorcontrib><title>Fluoroquinolones and Risk of Aortic Aneurysm or Dissection in Patients With Congenital Aortic Disease and Marfan Syndrome</title><title>Circulation Journal</title><addtitle>Circ J</addtitle><description>Background: Fluoroquinolone use can be associated with an increased risk of aortic aneurysm (AA) or aortic dissection (AD). The US Food and Drug Administration recently warned against fluoroquinolone use for high-risk patients, such as those with Marfan syndrome. However, the association between fluoroquinolone use and AA/AD risk was unknown in these high-risk patients and therefore it was studied in this work.Methods and Results: Data were collected from a national database between 2000 and 2017 for 550 patients with AA/AD and any congenital aortic disease (mean age 41.5 years; 415 with Marfan syndrome). A case cross-over study was conducted to compare the risk of aortic events (AA/AD) associated with fluoroquinolone and amoxicillin use between the hazard period (from −60 days to −1 day) and a randomly selected reference period (−180 to −121 days; −240 to −181 days; and –300 to –241 days). Compared to the reference period without fluoroquinolone use, fluoroquinolone use during the hazard period was not associated with a greater risk of AA/AD (1.09% vs. 1.09%; odds ratio [OR] 1.000; 95% confidence interval [CI] 0.32–3.10), AA (OR 0.67; 95% CI 0.11–3.99), or AD (OR 1.33; 95% CI 0.30–5.96) in patients with congenital aortic disease or Marfan syndrome. This lack of association was maintained in subgroup analysis, including Marfan syndrome or not, age (≤50 vs. &gt;50 years) and sex.Conclusions: Fluoroquinolone use was not associated with an increased risk of AA/AD in patients with congenital aortic disease, including Marfan syndrome. More evidence is required for a fluoroquinolone pharmacovigilance plan in these patients.</description><subject>Adult</subject><subject>Aortic aneurysm</subject><subject>Aortic Aneurysm - chemically induced</subject><subject>Aortic Aneurysm - epidemiology</subject><subject>Aortic dissection</subject><subject>Aortic Dissection - chemically induced</subject><subject>Aortic Dissection - epidemiology</subject><subject>Congenital aortic disease</subject><subject>Cross-Over Studies</subject><subject>Fluoroquinolones</subject><subject>Fluoroquinolones - adverse effects</subject><subject>Humans</subject><subject>Marfan syndrome</subject><subject>Marfan Syndrome - complications</subject><issn>1346-9843</issn><issn>1347-4820</issn><issn>1347-4820</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkL9v3CAcR1HVqEnT7p0qxi5OMWAD48nNpY1SpeoPdUQc_pJwtSEBPNx_X_vukizA8D5P4iH0oSYXNW3YZ-uT3V501xWlFWklfYXOasZFxSUlr_fvtlKSs1P0NuctIVSRRr1Bp2xmGRHyDO3WwxRTfJx8iEMMkLEJPf7p8z8cHV7FVLzFqwBT2uURx4S_-JzBFh8D9gH_MMVDKBn_9eUedzHcQfDFDE_LmQaTYS_9bpIzAf_ahT7FEd6hE2eGDO-P9zn6s7783X2tbm6vvnWrm8pyQUolews1JbyVsmlJ63rKRKMIlcRI6aBVRlnOKTdEMNsrIszGbEivTOsc6x1n5-jTwfuwfBNy0aPPFobBBIhT1lRIMqcQDZtRckBtijkncPoh-dGkna6JXoLrfXDdXWtK9RJ8nnw82qfNCP3z4KnwDKwPwDYXcwfPgFn6DHA0SqHVcryYX4B7kzQE9h-IBZfE</recordid><startdate>20230825</startdate><enddate>20230825</enddate><creator>Chen, Shao-Wei</creator><creator>Lin, Chia-Pin</creator><creator>Chan, Yi-Hsin</creator><creator>Wu, Victor Chien-Chia</creator><creator>Cheng, Yu-Ting</creator><creator>Tung, Ying-Chang</creator><creator>Hsiao, Fu-Chih</creator><creator>Chen, Dong-Yi</creator><creator>Hung, Kuo-Chun</creator><creator>Chou, An-Hsun</creator><creator>Chu, Pao-Hsien</creator><general>The Japanese Circulation Society</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></search><sort><creationdate>20230825</creationdate><title>Fluoroquinolones and Risk of Aortic Aneurysm or Dissection in Patients With Congenital Aortic Disease and Marfan Syndrome</title><author>Chen, Shao-Wei ; Lin, Chia-Pin ; Chan, Yi-Hsin ; Wu, Victor Chien-Chia ; Cheng, Yu-Ting ; Tung, Ying-Chang ; Hsiao, Fu-Chih ; Chen, Dong-Yi ; Hung, Kuo-Chun ; Chou, An-Hsun ; Chu, Pao-Hsien</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-8dce12046885606fd237590280a88fe69a9c4424a073cd907abab0d9a6ff3df43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adult</topic><topic>Aortic aneurysm</topic><topic>Aortic Aneurysm - chemically induced</topic><topic>Aortic Aneurysm - epidemiology</topic><topic>Aortic dissection</topic><topic>Aortic Dissection - chemically induced</topic><topic>Aortic Dissection - epidemiology</topic><topic>Congenital aortic disease</topic><topic>Cross-Over Studies</topic><topic>Fluoroquinolones</topic><topic>Fluoroquinolones - adverse effects</topic><topic>Humans</topic><topic>Marfan syndrome</topic><topic>Marfan Syndrome - complications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Shao-Wei</creatorcontrib><creatorcontrib>Lin, Chia-Pin</creatorcontrib><creatorcontrib>Chan, Yi-Hsin</creatorcontrib><creatorcontrib>Wu, Victor Chien-Chia</creatorcontrib><creatorcontrib>Cheng, Yu-Ting</creatorcontrib><creatorcontrib>Tung, Ying-Chang</creatorcontrib><creatorcontrib>Hsiao, Fu-Chih</creatorcontrib><creatorcontrib>Chen, Dong-Yi</creatorcontrib><creatorcontrib>Hung, Kuo-Chun</creatorcontrib><creatorcontrib>Chou, An-Hsun</creatorcontrib><creatorcontrib>Chu, Pao-Hsien</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><jtitle>Circulation Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Shao-Wei</au><au>Lin, Chia-Pin</au><au>Chan, Yi-Hsin</au><au>Wu, Victor Chien-Chia</au><au>Cheng, Yu-Ting</au><au>Tung, Ying-Chang</au><au>Hsiao, Fu-Chih</au><au>Chen, Dong-Yi</au><au>Hung, Kuo-Chun</au><au>Chou, An-Hsun</au><au>Chu, Pao-Hsien</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluoroquinolones and Risk of Aortic Aneurysm or Dissection in Patients With Congenital Aortic Disease and Marfan Syndrome</atitle><jtitle>Circulation Journal</jtitle><addtitle>Circ J</addtitle><date>2023-08-25</date><risdate>2023</risdate><volume>87</volume><issue>9</issue><spage>1164</spage><epage>1172</epage><pages>1164-1172</pages><artnum>CJ-22-0682</artnum><issn>1346-9843</issn><issn>1347-4820</issn><eissn>1347-4820</eissn><abstract>Background: Fluoroquinolone use can be associated with an increased risk of aortic aneurysm (AA) or aortic dissection (AD). The US Food and Drug Administration recently warned against fluoroquinolone use for high-risk patients, such as those with Marfan syndrome. However, the association between fluoroquinolone use and AA/AD risk was unknown in these high-risk patients and therefore it was studied in this work.Methods and Results: Data were collected from a national database between 2000 and 2017 for 550 patients with AA/AD and any congenital aortic disease (mean age 41.5 years; 415 with Marfan syndrome). A case cross-over study was conducted to compare the risk of aortic events (AA/AD) associated with fluoroquinolone and amoxicillin use between the hazard period (from −60 days to −1 day) and a randomly selected reference period (−180 to −121 days; −240 to −181 days; and –300 to –241 days). Compared to the reference period without fluoroquinolone use, fluoroquinolone use during the hazard period was not associated with a greater risk of AA/AD (1.09% vs. 1.09%; odds ratio [OR] 1.000; 95% confidence interval [CI] 0.32–3.10), AA (OR 0.67; 95% CI 0.11–3.99), or AD (OR 1.33; 95% CI 0.30–5.96) in patients with congenital aortic disease or Marfan syndrome. This lack of association was maintained in subgroup analysis, including Marfan syndrome or not, age (≤50 vs. &gt;50 years) and sex.Conclusions: Fluoroquinolone use was not associated with an increased risk of AA/AD in patients with congenital aortic disease, including Marfan syndrome. More evidence is required for a fluoroquinolone pharmacovigilance plan in these patients.</abstract><cop>Japan</cop><pub>The Japanese Circulation Society</pub><pmid>36823078</pmid><doi>10.1253/circj.CJ-22-0682</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source J-STAGE Free; MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Adult
Aortic aneurysm
Aortic Aneurysm - chemically induced
Aortic Aneurysm - epidemiology
Aortic dissection
Aortic Dissection - chemically induced
Aortic Dissection - epidemiology
Congenital aortic disease
Cross-Over Studies
Fluoroquinolones
Fluoroquinolones - adverse effects
Humans
Marfan syndrome
Marfan Syndrome - complications
title Fluoroquinolones and Risk of Aortic Aneurysm or Dissection in Patients With Congenital Aortic Disease and Marfan Syndrome
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