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  • 1
    Online Resource
    Online Resource
    Walter de Gruyter GmbH ; 2021
    In:  Romanian Journal of Internal Medicine Vol. 59, No. 3 ( 2021-09-01), p. 270-277
    In: Romanian Journal of Internal Medicine, Walter de Gruyter GmbH, Vol. 59, No. 3 ( 2021-09-01), p. 270-277
    Abstract: Ibrutinib is a novel drug used in haematological malignancies. Its use is associated with an increased risk of atrial fibrillation (AF), which, in turn, exposes patients to embolic risk, including stroke. Reducing this risk requires anticoagulant therapy which is a matter of concern in the context of the increased bleeding risk of patients with haematological malignancies. In this context the presence of thrombocytopenia related to haematological disorder, ibrutinib-anticoagulants and ibrutinib-platelets interactions contribute to the amplification of the problem. The correct assessment of the thrombosis vs. haemorrhage balance represents a significant challenge for the clinician. In this paper we discuss practical issues related to anticoagulation in patients treated with ibrutinib and incident AF.
    Type of Medium: Online Resource
    ISSN: 2501-062X
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2021
    detail.hit.zdb_id: 2683745-6
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  • 2
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2022
    In:  American Journal of Therapeutics Vol. 29, No. 1 ( 2022-01), p. e50-e55
    In: American Journal of Therapeutics, Ovid Technologies (Wolters Kluwer Health), Vol. 29, No. 1 ( 2022-01), p. e50-e55
    Abstract: Ibrutinib, a relatively new antineoplastic agent, has multiple cardiovascular effects that are still insufficiently known and evaluated, including subclinical myocardial damage. Study Question: The present study aims to assess the role of the myocardial strain, alone and in combination with cardiac biomarkers, in the early detection of ibrutinib-induced cardiotoxicity. Study Design: We included 31 outpatients with normal left ventricular ejection fraction (LVEF) on ibrutinib, in a tertiary University Hospital between 2019 and 2020, and evaluated them at inclusion and after 3 months. Measures and Outcomes: Data on myocardial strain, cardiac biomarkers [high-sensitive troponin T (hs TnT) and N-terminal probrain natriuretic peptide (NT-proBNP)], and ambulatory electrocardiographic monitoring were collected. Results: Myocardial deformation decreased significantly ( P 〈 0.001) at later evaluation and hs TnT and NT-proBNP increased significantly ( P = 0.019 and P = 0.03, respectively). The increase in hs TnT correlated with the increase in the left ventricle global longitudinal strain (LVGLS); in other words, it correlated with the decrease in myocardial deformation. No association was found between LVGLS increase and the increase in NT-proBNP. LVGLS modification was not significantly influenced by age, anemia, or arrhythmia burden quantified by 24-hour Holter monitoring ( P = 0.747, P = 0.072, respectively; P = 0.812). LVEF did not change significantly during follow-up. Conclusions: In patients on ibrutinib, evaluation of myocardial strain is useful in identifying early cardiac drug toxicity, surpassing the sensitivity and specificity limits of LVEF. In these patients, concomitant assessment of hs TnT increases the predictive power for subclinical myocardial involvement.
    Type of Medium: Online Resource
    ISSN: 1075-2765
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2022
    detail.hit.zdb_id: 2026900-6
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  • 3
    Online Resource
    Online Resource
    Elsevier BV ; 2019
    In:  IJC Heart & Vasculature Vol. 25 ( 2019-12), p. 100441-
    In: IJC Heart & Vasculature, Elsevier BV, Vol. 25 ( 2019-12), p. 100441-
    Type of Medium: Online Resource
    ISSN: 2352-9067
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2019
    detail.hit.zdb_id: 2818464-6
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