Time-to-onset analysis of amiodarone-associated thyroid dysfunction

被引:71
作者
Kinoshita, Sayoko [1 ]
Hosomi, Kouichi [2 ]
Yokoyama, Satoshi [2 ]
Takada, Mitsutaka [2 ]
机构
[1] Ebisu Pharm, Osaka, Japan
[2] Kindai Univ, Sch Pharm, Div Clin Drug Informat, 3-4-1 Kowaka, Higashiosaka, Osaka 5778502, Japan
关键词
adverse event; amiodarone; spontaneous reporting system; thyroid dysfunction; time-to-onset; LONG-TERM THERAPY; INDUCED THYROTOXICOSIS; RISK-FACTORS; INDUCED HYPOTHYROIDISM; CLINICAL EFFICACY; SIGNAL-DETECTION; DESETHYLAMIODARONE; ADULTS;
D O I
10.1111/jcpt.13024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
What is known and objective Amiodarone (AMD) treatment is associated with a number of significant adverse effects including thyroid dysfunction. However, the relationship between the development of thyroid dysfunction and the dosage and treatment duration of AMD remains unclear. The purpose of this study was to examine the onset profiles of amiodarone-associated thyroid dysfunction using a spontaneous adverse drug reaction (ADR) reporting database. Methods Data were obtained from the US Food and Drug Administration Adverse Event Reporting System (FAERS). For signal detection of spontaneous ADRs, the reporting odds ratio (ROR) and information component (IC) were calculated. Cumulative incidences of hyperthyroidism and hypothyroidism were assessed using the Kaplan-Meier method, and time-to-onset profiles were analysed using the Weibull shape parameter (WSP) test. Results and discussion The median time-to-onset of hyperthyroidism associated with AMD and other drugs was 720.0 (range: 225.5-1145.0) and 101.5 (range: 14.0-468.8) days, respectively. Patients treated with AMD showed a significantly longer time-to-onset of hyperthyroidism than those treated with other drugs (P < .001). The median time-to-onset of hypothyroidism associated with AMD and other drugs was 183.0 (range: 35.0-727.8) and 153.0 (range: 19.0-608.0) days, respectively. There was no significant difference in the time-to-onset of hypothyroidism between patients treated with AMD and those treated with other drugs (P = .13). For hyperthyroidism, the WSP test showed that AMD had a wear-out failure-type profile and other drugs had early failure-type profiles. For hypothyroidism, the WSP test showed that both AMD and other drugs had early failure-type profiles. What is new and conclusions Amiodarone-associated hyperthyroidism had a different onset profile than hyperthyroidism associated with other drugs. Because the time-to-onset of AMD-associated hyperthyroidism is widely distributed, sustained and continuous attention is required to detect and treat hyperthyroidism during AMD treatment. In contrast, AMD-associated hypothyroidism had an onset profile that was similar to that of other drugs, suggesting that attention should be focused on the earlier stages of treatment.
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页码:65 / 71
页数:7
相关论文
共 47 条
[1]  
Abe J, 2016, J PHARM HEALTH CARE, V2, DOI 10.1186/s40780-016-0048-5
[2]   Determinants and outcome of amiodarone-associated thyroid dysfunction [J].
Ahmed, Sheba ;
Van Gelder, Isabelle C. ;
Wiesfeld, Ans C. P. ;
Van Veldhuisen, Dirk J. ;
Links, Thera P. .
CLINICAL ENDOCRINOLOGY, 2011, 75 (03) :388-394
[3]  
Aleksic Zeljka, 2011, Med Pregl, V64, P533
[4]   Novel statistical tools for monitoring the safety of marketed drugs [J].
Almenoff, J. S. ;
Pattishall, E. N. ;
Gibbs, T. G. ;
DuMouchel, W. ;
Evans, S. J. W. ;
Yuen, N. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2007, 82 (02) :157-166
[5]   AMIODARONE AND THE THYROID [J].
ALVES, LE ;
ROSE, EP ;
CAHILL, TB .
ANNALS OF INTERNAL MEDICINE, 1985, 102 (03) :412-412
[6]   Quantitative signal detection using spontaneous ADR reporting [J].
Bate, A. ;
Evans, S. J. W. .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2009, 18 (06) :427-436
[7]   A Bayesian neural network method for adverse drug reaction signal generation [J].
Bate, A ;
Lindquist, M ;
Edwards, IR ;
Olsson, S ;
Orre, R ;
Lansner, A ;
De Freitas, RM .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 54 (04) :315-321
[8]   CYTOTOXIC EFFECTS OF AMIODARONE AND DESETHYLAMIODARONE ON HUMAN THYROCYTES [J].
BEDDOWS, SA ;
PAGE, SR ;
TAYLOR, AH ;
MCNERNEY, R ;
WHITLEY, GSJ ;
JOHNSTONE, AP ;
NUSSEY, SS .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (24) :4397-4403
[9]   Amiodarone and the thyroid: A 2012 update [J].
Bogazzi, F. ;
Tomisti, L. ;
Bartalena, L. ;
Aghini-Lombardi, F. ;
Martino, E. .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2012, 35 (03) :340-348
[10]   EFFECT OF LONG-TERM AMIODARONE THERAPY ON THYROID-HORMONE LEVELS AND THYROID-FUNCTION [J].
BOROWSKI, GD ;
GAROFANO, CD ;
ROSE, LI ;
SPIELMAN, SR ;
ROTMENSCH, HR ;
GREENSPAN, AM ;
HOROWITZ, LN .
AMERICAN JOURNAL OF MEDICINE, 1985, 78 (03) :443-450