Edoxaban and Frailty in Senior Individuals

University of Padova180 enrolled

Overview

Edoxaban, has shown in clinical registration trials a significant reduction of major bleeding compared to warfarin, especially in elderly patients. Efficacy and safety of edoxaban will be assessed in a cohort of very elderly patients (≥80 years of age) with NVAF. A secondary analysis will correlate outcomes with frailty defined according to SHARE-FI (not-frail, pre-frail or frail).

Aim of the study To assess the efficacy and safety of edoxaban in a cohort of very elderly patients (≥80 years of age) with NVAF. Edoxaban has never been tested in elderly frail patients. In both sexes, there is a non-linear association between age and frailty. A secondary analysis according to frailty assessment (not-frail, pre-frail or frail) will be also performed. Study Design Observational prospective cohort study including patients of ≥80 years of age with a new diagnosis of NVAF. Edoxaban 60 mg (or 30 mg for patients with CrCL 15 - 50 mL/min or with body weight ≤ 60 kg) will be administered to all patients. All participants will be stratified according to frailty, as assessed by SHARE-FI score, to non-frail, pre-frail, and frail. Study Population Patients of both sexes, of ≥80 years of age with a new diagnosis of non-valvular atrial fibrillation and without contraindications to Edoxaban. Outcomes The following events will be included as outcomes: * arterial ischemic events (TIA or stroke documented a CT scan; documented systemic embolism) * major bleeding events (according to the ISTH definition) * clinically relevant non-major bleeding (CRNM), defined as bleeding that did not meet the definition of major bleeding, but considered clinically significant (including spontaneous gastrointestinal bleeding or rectal bleeding; macroscopic haematuria or urethral bleeding requiring medical attention; skin haematoma \>25 cm2; and gingival bleeding or spontaneous ear-nose-throat bleeding lasting ≥5 min) and/or resulted in discontinuation of study medication18. * death (divided into cardiovascular death, fatal bleeding and other causes of death). Follow up Follow-up visits will be performed at 3, 6, 12 and 24 months to assess adherence and compliance to therapy, evaluation of relevant blood test and clinical assessment. Temporary discontinuation of edoxaban for a planned surgical intervention will be allowed. Patients will be followed until the occurrence of a first outcome event, permanent discontinuation of edoxaban or the end of follow-up period, whichever comes first.

Study Type

OBSERVATIONAL

Enrollment

180

Conditions

Atrial Fibrillation

Eligibility

Sex: ALLMin age: 80 Years

Medical Language ↔ Plain English

Inclusion Criteria: * NVAF diagnosed in the past 30 days * Age at baseline of 80 years or older with indication for anticoagulation treatment with edoxaban Exclusion Criteria: * NVAF diagnosed more than 30 days prior to baseline visit * Other OAT, except for warfarin or LMWH, already started at the time of baseline visit * Patients with end stage renal disease (ESRD) (CrCL \< 15 mL/min) or on dialysis * Severe hepatic impairment (defined as Child-Pugh Class B or C or increase in transaminases more than three times the upper reference value of normality) or hepatic disease associated with coagulopathy * Elevated liver enzymes (ALT/AST \> 2 x ULN) or total bilirubin ≥ 1.5 x ULN at baseline * Recent (within 1 month) or persisting gastrointestinal ulceration * Active neoplasm * Known or suspected oesophageal varices * Arteriovenous malformations, vascular aneurysms or major intraspinal or intracerebral vascular abnormalities * Life expectancy \<1 year * Concomitant use of strong P-gp drugs which contraindicate edoxaban use12 (e.g. HIV protease inhibitors) * Clinically significant active bleeding or high risk of bleeding conditions such as: recent brain or spinal injury; recent brain, spinal or ophthalmic surgery; recent intracranial haemorrhage * Known contraindications or hypersensitivity to the active substance or to any of the excipients of Lixiana * Lack of acquisition of informed consent or refusal to participate by the subject or family representative

Locations (1)

Padua University Hospital

Padova, Italy

Outcomes

Primary Outcomes

Cumulative incidence of arterial ischemic events, major bleeding, and clinically relevant non-major bleeding

Cumulative incidence of arterial ischemic events (stroke/TIA and systemic embolism), major bleeding according to ISTH definition, and clinically relevant non-major bleeding (bleeding not meeting major bleeding criteria but considered clinically significant).

Time frame: Through study completion, an average of 24 months

Death

Divided into cardiovascular death, fatal bleeding and other causes of death

Time frame: Through study completion, an average of 24 months

Secondary Outcomes

Correlation of frailty, as measured with Survey of Health, Ageing and Retirement in Europe - Frailty Instrument, with the cumulative incidence of stroke/TIA, systemic embolism, major bleeding and clinically relevant non-major bleeding.

Patients will be divided into 3 groups according to frailty measured with Survey of Health, Ageing and Retirement in Europe - Frailty Instrument (SHARE-FI) which provides 3 patient categories (non-frail, pre-frail and frail). A score of \< 0.3151361243 defines non frail female patients; a score of 0.3151361243 to 2.1301121973 defines pre-frail female patients; a score of 2.1301121973 to 6 defines frail female patients. A score of \< 1.211878526 defines non frail male patients; a score of 1.211878526 to 3.0052612772 defines pre-frail male patients; a score of 3.0052612772 to 7 defines frail male patients. Further SHARE-FI score details and calculations are available at: https://sites.google.com/a/tcd.ie/share-frailty-instrument-calculators/. Outcome events will be compared among the three groups.

Time frame: 24 months

Death

All cause mortality

Time frame: Through study completion, an average of 24 months

Data from ClinicalTrials.gov

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