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Kidney Function Decline and Serious Adverse Drug Reactions in Patients With CKD
dc.rights.license | open | en_US |
hal.structure.identifier | CHU Amiens-Picardie | |
hal.structure.identifier | Mécanismes physiopathologiques et conséquences des calcifications cardiovasculaires - UR UPJV 7517 [MP3CV] | |
dc.contributor.author | LAVILLE, Solène | |
hal.structure.identifier | CHU Amiens-Picardie | |
hal.structure.identifier | Mécanismes physiopathologiques et conséquences des calcifications cardiovasculaires - UR UPJV 7517 [MP3CV] | |
dc.contributor.author | GRAS-CHAMPEL, Valérie | |
hal.structure.identifier | Université de Lille | |
hal.structure.identifier | Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille] | |
hal.structure.identifier | Centre de recherche en épidémiologie et santé des populations [CESP] | |
dc.contributor.author | HAMROUN, Aghilès | |
hal.structure.identifier | CHU Amiens-Picardie | |
dc.contributor.author | MORAGNY, Julien | |
hal.structure.identifier | Centre de recherche en épidémiologie et santé des populations [CESP] | |
dc.contributor.author | LAMBERT, Oriane | |
hal.structure.identifier | Centre de recherche en épidémiologie et santé des populations [CESP] | |
hal.structure.identifier | Université de Versailles Saint-Quentin-en-Yvelines [UVSQ] | |
dc.contributor.author | METZGER, Marie | |
hal.structure.identifier | Agence de la biomédecine [Saint-Denis la Plaine] | |
hal.structure.identifier | Centre de recherche en épidémiologie et santé des populations [CESP] | |
dc.contributor.author | JACQUELINET, Christian | |
hal.structure.identifier | Bioingénierie tissulaire [BIOTIS] | |
hal.structure.identifier | Centre Hospitalier Universitaire de Bordeaux [CHU Bordeaux] | |
dc.contributor.author | COMBE, Christian
ORCID: 0000-0002-0360-573X IDREF: 58708871 | |
hal.structure.identifier | Cardiovasculaire, métabolisme, diabétologie et nutrition [CarMeN] | |
hal.structure.identifier | Centre Hospitalier Lyon Sud [CHU - HCL] [CHLS] | |
dc.contributor.author | FOUQUE, Denis | |
hal.structure.identifier | Cardiovasculaire, métabolisme, diabétologie et nutrition [CarMeN] | |
dc.contributor.author | LAVILLE, Maurice | |
hal.structure.identifier | Centre Hospitalier Régional Universitaire de Nancy [CHRU Nancy] | |
hal.structure.identifier | Adaptation, mesure et évaluation en santé. Approches interdisciplinaires [APEMAC] | |
dc.contributor.author | FRIMAT, Luc | |
hal.structure.identifier | University of Michigan [Ann Arbor] | |
dc.contributor.author | ROBINSON, Bruce | |
hal.structure.identifier | Arbor Research Collaborative for Health | |
dc.contributor.author | BIEBER, Brian | |
hal.structure.identifier | Centre de recherche en épidémiologie et santé des populations [CESP] | |
dc.contributor.author | STENGEL, Bénédicte | |
hal.structure.identifier | Centre de recherche en épidémiologie et santé des populations [CESP] | |
dc.contributor.author | DE PINHO, Natalia Alencar | |
hal.structure.identifier | Centre de recherche en épidémiologie et santé des populations [CESP] | |
hal.structure.identifier | Hôpital Ambroise Paré [AP-HP] | |
dc.contributor.author | MASSY, Ziad | |
hal.structure.identifier | Mécanismes physiopathologiques et conséquences des calcifications cardiovasculaires - UR UPJV 7517 [MP3CV] | |
hal.structure.identifier | CHU Amiens-Picardie | |
hal.structure.identifier | Centre de recherche en épidémiologie et santé des populations [CESP] | |
hal.structure.identifier | Chronic Kidney Disease - Réseau Epidémiologie et Information en Néphrologie [CKD REIN] | |
dc.contributor.author | LIABEUF, Sophie | |
hal.structure.identifier | Centre d'investigation clinique [Nancy] [CIC] | |
hal.structure.identifier | Centre Hospitalier Régional Universitaire de Nancy [CHRU Nancy] | |
dc.contributor.author | AYAV, Carole | |
hal.structure.identifier | Adaptation, mesure et évaluation en santé. Approches interdisciplinaires [APEMAC] | |
dc.contributor.author | BRIANÇON, Serge | |
dc.contributor.author | CANNET, Dorothée | |
dc.contributor.author | COMBE, Christian
ORCID: 0000-0002-0360-573X IDREF: 58708871 | |
dc.contributor.author | FOUQUE, Denis | |
dc.contributor.author | FRIMAT, Luc | |
dc.contributor.author | HERPE, Yves-Edouard | |
dc.contributor.author | JACQUELINET, Christian | |
dc.contributor.author | PASCAL, Christophe | |
dc.contributor.author | ROBINSON, Bruce | |
dc.contributor.author | LANGE, Céline | |
dc.contributor.author | LEGRAND, Karine | |
dc.contributor.author | METZGER, Marie | |
dc.contributor.author | SPEYER, Elodie | |
dc.date.accessioned | 2024-04-19T08:57:11Z | |
dc.date.available | 2024-04-19T08:57:11Z | |
dc.date.issued | 2023-11 | |
dc.identifier.issn | 0272-6386 | en_US |
dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/199242 | |
dc.description.abstractEn | Rationale & ObjectiveAdverse drug reactions (ADRs) are common in patients with chronic kidney disease (CKD). The impact of kidney function decline on serious ADR risk has been poorly investigated. We sought to comprehensively describe ADRs and assess the relationship between eGFR and serious ADR risk.Study DesignProspective cohort study.Setting & Participants3,033 participants in French Chronic Kidney Disease-Renal Epidemiology and Information Network (CKD-REIN) cohort study, a nationwide sample of nephrology outpatients with moderate-to-advanced CKD.PredictorsDemographic and biological data (including eGFR), medication prescriptions.OutcomesADRs (preventable or not) were prospectively identified from hospital discharge reports, medical records, and patient interviews. Expert pharmacologists used validated tools to adjudicate ADRs.Analytical ApproachRestricted cubic splines in fully adjusted cause-specific Cox proportional hazard models were used to evaluate the relationship between eGFR and the risk of serious ADRs (overall and by subtype).ResultsDuring a median follow-up period of 4.7 years, 360 patients experienced 488 serious ADRs. Kidney and urinary disorders (n=170) and hemorrhages (n=170) accounted for 70% of serious ADRs. The most common medications classes were antithrombotics and renin-angiotensin system inhibitors. The majority of those serious ADRs were associated with hospitalization (n=467), with 32 directly or indirectly associated with death, and 22 associated with life-threatening event. More than 27% of the 488 serious ADRs were preventable or potentially preventable. The eGFR is a major risk factor for serious ADRs. Risk of AKI was 2.2% higher and risk of bleeding ADRs were 8% higher for each 1 mL/min/1.73m2 lower baseline eGFR.LimitationsThe results cannot be extrapolated to patients who are not being followed up by a nephrologist.ConclusionsADRs constitute a major cause of hospitalization in CKD patients for whom lower eGFR level is a major risk factor. | |
dc.language.iso | EN | en_US |
dc.subject.en | Pharmacoepidemiology | |
dc.subject.en | bleeding | |
dc.subject.en | acute kidney injury | |
dc.subject.en | chronic kidney disease | |
dc.subject.en | adverse drug reaction | |
dc.title.en | Kidney Function Decline and Serious Adverse Drug Reactions in Patients With CKD | |
dc.type | Article de revue | en_US |
dc.identifier.doi | 10.1053/j.ajkd.2023.09.012 | en_US |
dc.subject.hal | Sciences du Vivant [q-bio]/Médecine humaine et pathologie | en_US |
bordeaux.journal | American Journal of Kidney Diseases | en_US |
bordeaux.hal.laboratories | Bioingénierie Tissulaire (BioTis) - U1026 | en_US |
bordeaux.institution | Université de Bordeaux | en_US |
bordeaux.institution | CNRS | en_US |
bordeaux.institution | INSERM | en_US |
bordeaux.institution | CHU de Bordeaux | en_US |
bordeaux.institution | Institut Bergonié | en_US |
bordeaux.peerReviewed | oui | en_US |
bordeaux.inpress | non | en_US |
bordeaux.import.source | hal | |
hal.identifier | hal-04288693 | |
hal.version | 1 | |
hal.popular | non | en_US |
hal.audience | Internationale | en_US |
hal.export | false | |
workflow.import.source | hal | |
dc.rights.cc | Pas de Licence CC | en_US |
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