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A comparison of standard and high-dose regimens for the initiation of amiodarone therapy

dc.contributor.authorSummitt, Jonien_US
dc.contributor.authorMorady, Freden_US
dc.contributor.authorKadish, Alan H.en_US
dc.date.accessioned2006-04-10T15:08:19Z
dc.date.available2006-04-10T15:08:19Z
dc.date.issued1992-08en_US
dc.identifier.citationSummitt, Joni, Morady, Fred, Kadish, Alan (1992/08)."A comparison of standard and high-dose regimens for the initiation of amiodarone therapy." American Heart Journal 124(2): 366-373. <http://hdl.handle.net/2027.42/29927>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6W9H-4BT89N9-97/2/29921c859006d4066d9490b323856fd9en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29927
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1636580&dopt=citationen_US
dc.description.abstractThe effects of two regimens for the initiation of amiodarone therapy were compared in 92 patients with inducible sustained ventricular tachycardia (VT) at baseline electrophysiologic testing. Two groups of 46 patients each received a total of 16.8 gm of oral amiodarone before follow-up electrophysiologic testing. Group A (standard dose) received 1200 mg/day for 14 days, and group B (high dose) received 2400 mg/day for 7 days. Amiodarone suppressed the induction of sustained VT in six subjects (13%) in group A versus 10 (22%) in group B (p = NS). In subjects who continued to have inducible VT after amiodarone loading, the mean increase in cycle length of induced VT was similar in group A ([Delta] = 85 +/- 73 msec) and group B ([Delta] = 78 +/- 59 sec). The mean increase in sinus cycle length, AH and HV intervals, paced QRS duration, and ventricular refractory periods was also not significantly different between the two groups. Side effects developed in 10 (22%) patients in group B but were serious only in one, and one patient required a reduction in dosage. Thus compared to the 14-day standard-dose regimen, the 7-day high-dose regimen was well tolerated and had similar effects on VT inducibility and electrophysiologic variables. Its use may significantly shorten the duration of hospitalization in patients with life-threatening inducible VT who are undergoing loading with amiodarone on an inpatient basis.en_US
dc.format.extent1368421 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleA comparison of standard and high-dose regimens for the initiation of amiodarone therapyen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich, USAen_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich, USAen_US
dc.contributor.affiliationumDivision of Cardiology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Mich, USAen_US
dc.identifier.pmid1636580en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29927/1/0000284.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-8703(92)90599-Qen_US
dc.identifier.sourceAmerican Heart Journalen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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