Usefulness of cardiac resynchronization therapy in the management of Doxorubicin-induced cardiomyopathy

被引:24
|
作者
Ajijola, Olujimi A. [1 ]
Nandigam, K. Veena [1 ]
Chabner, Bruce A. [3 ]
Orencole, Mary [1 ]
Dec, G. William [2 ]
Ruskin, Jeremy N. [1 ]
Singh, Jagmeet P. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Cardiac Arrhythmia Serv, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Heart Failure Serv,Div Cardiol, Boston, MA USA
[3] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Div Oncol,Dept Med, Boston, MA USA
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2008年 / 101卷 / 09期
关键词
D O I
10.1016/j.amjcard.2007.12.037
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Doxorubicin is a widely used antineoplastic agent that may cause irreversible dilated cardiomyopathy. Doxorubicin-induced cardiomyopathy (DIC) can occur several years after exposure and carries a poor prognosis. Although cardiac resynchronization therapy (CRT) is a useful intervention in end-stage heart failure unresponsive to optimal medical therapies, its efficacy in DIC remains unknown. Four consecutive patients receiving CRT for DIC were evaluated before and after CRT. CRT resulted in improvements in the mean left ventricular ejection fraction at 1 month from 21 +/- 4.7% to 34 +/- 5% (p = 0.03) and at 6 months (to 46 +/- 7.5%, p = 0.01). CRT-induced reverse remodeling was observed, with a mean reduction in left ventricular internal diameter at end-diastole from 54.75 +/- 3.7 to 52.5 +/- 1.9 min at 1 month (p = 0.06) and further to 47 +/- 2.3 mm at 6 months (p = 0.03). All patients experienced reductions in heart failure symptoms and improvements in New York Heart Association functional class (p < 0.05). The impact of CRT was sustained over a follow-up of 18.5 +/- 3.5 months. In conclusion, this study suggests that patients with DIC, refractory to optimal pharmacologic therapy and meeting criteria for resynchronization device implantation, may achieve sustained benefit from CRT. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1371 / 1372
页数:2
相关论文
共 50 条
  • [31] Unexpected doxorubicin-induced cardiomyopathy in sisters
    Gayle, Arlene A.
    Sachidanandam, Kamakshi
    Kolesar, Jill
    Robins, H. Ian
    INTERNATIONAL CANCER CONFERENCE JOURNAL, 2012, 1 (01): : 15 - 18
  • [32] Myofilament changes in doxorubicin-induced cardiomyopathy
    Rodrigues, P.
    Barros, C.
    CARDIOVASCULAR RESEARCH, 2012, 93 : S106 - S106
  • [33] Mitochondrial Determinants of Doxorubicin-Induced Cardiomyopathy
    Wallace, Kendall B.
    Sardao, Vilma A.
    Oliveira, Paulo J.
    CIRCULATION RESEARCH, 2020, 126 (07) : 926 - 941
  • [34] Doxorubicin-induced cardiac mitochondrionopathy
    Wallace, KB
    PHARMACOLOGY & TOXICOLOGY, 2003, 93 (03): : 105 - 115
  • [35] DOXORUBICIN-INDUCED CARDIAC TOXICITY
    DOROSHOW, JH
    NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (12): : 843 - 845
  • [36] Left ventricular assist device as destination therapy in doxorubicin-induced cardiomyopathy
    Simsir, SA
    Lin, SS
    Blue, LJ
    Gockerman, JP
    Russell, SD
    Milano, CA
    ANNALS OF THORACIC SURGERY, 2005, 80 (02): : 717 - 719
  • [37] Response of doxorubicin-induced cardiomyopathy to the current management strategy of heart failure
    Tallaj, JA
    Franco, V
    Rayburn, BK
    Pinderski, L
    Benza, RL
    Pamboukian, S
    Foley, B
    Bourge, RC
    JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2005, 24 (12): : 2196 - 2201
  • [38] Treatment of Pacing-Induced Cardiomyopathy With Cardiac Resynchronization Therapy
    Faddis, Mitchell N.
    JACC-CLINICAL ELECTROPHYSIOLOGY, 2018, 4 (02) : 178 - 180
  • [39] Mitochondria and Doxorubicin-Induced Cardiomyopathy: A Complex Interplay
    Schirone, Leonardo
    D'Ambrosio, Luca
    Forte, Maurizio
    Genovese, Riccardo
    Schiavon, Sonia
    Spinosa, Giulia
    Iacovone, Giuliano
    Valenti, Valentina
    Frati, Giacomo
    Sciarretta, Sebastiano
    CELLS, 2022, 11 (13)
  • [40] Heart rate dynamics in doxorubicin-induced cardiomyopathy
    Loncar-Turukalo, T.
    Vasic, M.
    Tasic, T.
    Mijatovic, G.
    Glumac, S.
    Bajic, D.
    Japunzic-Zigon, N.
    PHYSIOLOGICAL MEASUREMENT, 2015, 36 (04) : 727 - 739