001     276749
005     20250216000800.0
024 7 _ |a 10.1186/s12916-025-03919-0
|2 doi
024 7 _ |a pmid:39920723
|2 pmid
024 7 _ |a pmc:PMC11806691
|2 pmc
024 7 _ |a altmetric:173996823
|2 altmetric
037 _ _ |a DZNE-2025-00307
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Wicherski, Julia
|0 P:(DE-2719)9000812
|b 0
|u dzne
245 _ _ |a High risk for life-threatening adverse events of fluoroquinolones in young adults: a large German population-based cohort study.
260 _ _ |a London
|c 2025
|b BioMed Central
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1739454336_21758
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Fluoroquinolone antibiotics have a high potential for serious adverse drug reactions, but real-world evidence in European patient cohorts is lacking. Therefore, we aim to examine the association between fluoroquinolone exposure and potentially life-threatening adverse events stratified by age and gender in Germany.We conducted an administrative cohort study using the active comparator new user design with a risk window up to 365 days between January 2013 and December 2019. Population-based longitudinal data from one of the largest German statutory health insurances were used. Episodes of newly dispensed fluoroquinolones (ciprofloxacin, levofloxacin, ofloxacin, moxifloxacin, norfloxacin, and enoxacin) were compared to other antibiotics (amoxicillin, amoxicillin clavulanic acid, azithromycin, cefuroxime, cephalexin, clindamycin, sulfamethoxazole-trimethoprim, and doxycycline). Endpoints were defined by incident diagnoses of aortic aneurysm/dissection, cardiac arrhythmia, hepatotoxicity, and all-cause mortality. Adjusted hazard ratios were estimated from piece-wise exponential additive mixed models with smooth non-linear effects for person-time and age and adjusted for comorbidities, year and quarter at index.The cohorts comprised 15,139,840; 11,760,159; 11,027,175; and 15,305,757 antibiotic episodes. Patients during fluoroquinolone episodes were older (59 versus 51 years) and more often female (58% versus 54%). We counted 46,502; 446,727; 19,125; and 474,411 incident endpoints. Relative risk for all-cause mortality and hepatotoxicity was high for < 40-year- and 40-69-year-old females (aHR = 1.77, 95% CI 1.55-2.03 and aHR = 1.42, 95% CI 1.32-1.53), respectively. For aortic aneurysm/dissection a nominally increased relative risk for < 40-year-old females was found (aHR = 1.42, 95% CI 0.96-2.11), although 95% CI indicates that a small relative risk reduction is also supported by the data. Relative risk for cardiac arrhythmia was increased for men aged < 40 years (aHR = 1.14, 95% CI 1.08-1.20). High relative risks for each endpoint were also identified depending on choice of active comparator, and risks increased with higher defined daily doses and shorter follow-up.This study contributes real-world evidence to endpoint-specific differences of risks in patient subgroups which need to be considered to improve fluoroquinolone drug safety.
536 _ _ |a 354 - Disease Prevention and Healthy Aging (POF4-354)
|0 G:(DE-HGF)POF4-354
|c POF4-354
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: pub.dzne.de
650 _ 7 |a Adverse drug reactions
|2 Other
650 _ 7 |a Antibiotics
|2 Other
650 _ 7 |a Cohort study
|2 Other
650 _ 7 |a Fluoroquinolones
|2 Other
650 _ 7 |a Real-world evidence
|2 Other
650 _ 7 |a Fluoroquinolones
|2 NLM Chemicals
650 _ 7 |a Anti-Bacterial Agents
|2 NLM Chemicals
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Germany: epidemiology
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Fluoroquinolones: adverse effects
|2 MeSH
650 _ 2 |a Adult
|2 MeSH
650 _ 2 |a Middle Aged
|2 MeSH
650 _ 2 |a Anti-Bacterial Agents: adverse effects
|2 MeSH
650 _ 2 |a Aged
|2 MeSH
650 _ 2 |a Cohort Studies
|2 MeSH
650 _ 2 |a Young Adult
|2 MeSH
650 _ 2 |a Arrhythmias, Cardiac: chemically induced
|2 MeSH
650 _ 2 |a Arrhythmias, Cardiac: epidemiology
|2 MeSH
650 _ 2 |a Aortic Dissection: epidemiology
|2 MeSH
650 _ 2 |a Aortic Dissection: chemically induced
|2 MeSH
650 _ 2 |a Chemical and Drug Induced Liver Injury: epidemiology
|2 MeSH
650 _ 2 |a Chemical and Drug Induced Liver Injury: etiology
|2 MeSH
650 _ 2 |a Adolescent
|2 MeSH
650 _ 2 |a Drug-Related Side Effects and Adverse Reactions: epidemiology
|2 MeSH
650 _ 2 |a Age Factors
|2 MeSH
650 _ 2 |a Risk Factors
|2 MeSH
700 1 _ |a Peltner, Jonas
|0 P:(DE-2719)9002192
|b 1
|u dzne
700 1 _ |a Becker, Cornelia
|0 P:(DE-2719)9000482
|b 2
|u dzne
700 1 _ |a Schüssel, Katrin
|b 3
700 1 _ |a Brückner, Gabriela
|b 4
700 1 _ |a Schlotmann, Andreas
|b 5
700 1 _ |a Schröder, Helmut
|b 6
700 1 _ |a Kern, Winfried V
|b 7
700 1 _ |a Haenisch, Britta
|0 P:(DE-2719)2810511
|b 8
|e Last author
|u dzne
773 _ _ |a 10.1186/s12916-025-03919-0
|g Vol. 23, no. 1, p. 76
|0 PERI:(DE-600)2131669-7
|n 1
|p 76
|t BMC medicine
|v 23
|y 2025
|x 1741-7015
856 4 _ |u https://pub.dzne.de/record/276749/files/DZNE-2025-00307%20SUP.docx
856 4 _ |y OpenAccess
|u https://pub.dzne.de/record/276749/files/DZNE-2025-00307.pdf
856 4 _ |u https://pub.dzne.de/record/276749/files/DZNE-2025-00307%20SUP.doc
856 4 _ |u https://pub.dzne.de/record/276749/files/DZNE-2025-00307%20SUP.odt
856 4 _ |u https://pub.dzne.de/record/276749/files/DZNE-2025-00307%20SUP.pdf
856 4 _ |y OpenAccess
|x pdfa
|u https://pub.dzne.de/record/276749/files/DZNE-2025-00307.pdf?subformat=pdfa
909 C O |o oai:pub.dzne.de:276749
|p openaire
|p open_access
|p VDB
|p driver
|p dnbdelivery
910 1 _ |a External Institute
|0 I:(DE-HGF)0
|k Extern
|b 0
|6 P:(DE-2719)9000812
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 1
|6 P:(DE-2719)9002192
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 8
|6 P:(DE-2719)2810511
913 1 _ |a DE-HGF
|b Gesundheit
|l Neurodegenerative Diseases
|1 G:(DE-HGF)POF4-350
|0 G:(DE-HGF)POF4-354
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Disease Prevention and Healthy Aging
|x 0
914 1 _ |y 2025
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0600
|2 StatID
|b Ebsco Academic Search
|d 2024-12-05
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b BMC MED : 2022
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0501
|2 StatID
|b DOAJ Seal
|d 2024-04-10T15:34:47Z
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0500
|2 StatID
|b DOAJ
|d 2024-04-10T15:34:47Z
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2024-12-05
915 _ _ |a Fees
|0 StatID:(DE-HGF)0700
|2 StatID
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2024-12-05
915 _ _ |a Creative Commons Attribution CC BY 4.0
|0 LIC:(DE-HGF)CCBY4
|2 HGFVOC
915 _ _ |a OpenAccess
|0 StatID:(DE-HGF)0510
|2 StatID
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b ASC
|d 2024-12-05
915 _ _ |a Article Processing Charges
|0 StatID:(DE-HGF)0561
|2 StatID
|d 2024-12-05
915 _ _ |a IF >= 5
|0 StatID:(DE-HGF)9905
|2 StatID
|b BMC MED : 2022
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1110
|2 StatID
|b Current Contents - Clinical Medicine
|d 2024-12-05
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2024-12-05
920 1 _ |0 I:(DE-2719)1013010
|k AG Hänisch
|l Pharmacoepidemiology
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a UNRESTRICTED
980 _ _ |a I:(DE-2719)1013010
980 1 _ |a FullTexts


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21