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Chronic verapamil therapy in pediatrie and young adult patients with hypertrophic cardiomyopathy

dc.contributor.authorSpicer, Robert L.en_US
dc.contributor.authorRocchini, Albert P.en_US
dc.contributor.authorCrowley, Dennis C.en_US
dc.contributor.authorRosenthal, Amnonen_US
dc.date.accessioned2006-04-07T18:27:40Z
dc.date.available2006-04-07T18:27:40Z
dc.date.issued1984-06-01en_US
dc.identifier.citationSpicer, Robert L., Rocchini, Albert P., Crowley, Dennis C., Rosenthal, Amnon (1984/06/01)."Chronic verapamil therapy in pediatrie and young adult patients with hypertrophic cardiomyopathy." The American Journal of Cardiology 53(11): 1614-1619. <http://hdl.handle.net/2027.42/24807>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T10-4BW0V81-2YS/2/4a1948951de1806669d5a4941d2508e7en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/24807
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6539561&dopt=citationen_US
dc.description.abstractOral verapamil, 5.2 +/- 1.1 mg/kg/day (range 2.8 to 7), was administered to 13 pediatric patients with hypertrophic Cardiomyopathy for 13 +/- 6 months (range 2 to 20). The patients had significant symptomatic improvement on verapamil therapy. Murmur intensity diminished in 6 patients during therapy and left ventricular (LV) electromotive forces on the electrocardiogram diminished in 4, increased in 5 and did not change in 4. Exercise endurance increased from 8.4 +/- 3.9 to 10.9 +/- 2.8 minutes (p &lt; 0.01). Seven patients had ST-segment depression (0.38 +/- 0.28 mV) before verapamil therapy, which improved after verapamil therapy in 5 (0.24 +/- 0.17 mV, p &lt; 0.02). Of 4 patients with exercise-induced ventricular ectopic activity, 3 had diminution or abolishment of ectopy following verapamil. By echocardiography, the patients had an increase in LV end-diastolic dimension from 3.4 +/- 0.7 to 3.9 +/- 0.8 cm (p &lt; 0.01), with no significant change in shortening fraction (46.1 +/- 8.0% vs 44.6 +/- 8.0%). When adjusted for body size and age there was a significant decrease in LV septal thickness (from 106 +/- 70 to 45 +/- 52% of predicted normal values, p &lt; 0.05) and LV posterior wall thickness (from 40 +/- 45 to 5 +/- 26% of predicted normal values p = 0.05) after verapamil. Isovolumic relaxation time decreased from 69 +/- 26 to 42 +/- 19 ms after verapamil (p &lt; 0.01). Systolic anterior motion of the anterior mitral leaflet disappeared in 5 of 8 patients and midsystolic closure of the aortic valve was no longer present in 4 of 8. Chronic oral verapamil appears to be an effective form of therapy for pediatric patients with hypertrophic Cardiomyopathy.en_US
dc.format.extent847638 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleChronic verapamil therapy in pediatrie and young adult patients with hypertrophic cardiomyopathyen_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.affiliationumDepartment of Pediatrics and the Clinical Research Center, University of Michigan Medical Center, Ann Arbor, Michigan, USA; Division of Pediatric Cardiology, C. S. Mott Children's Hospital, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumDivision of Pediatric Cardiology, C. S. Mott Children's Hospital, Ann Arbor, Michigan, USA; Department of Pediatrics and the Clinical Research Center, University of Michigan Medical Center, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumDepartment of Pediatrics and the Clinical Research Center, University of Michigan Medical Center, Ann Arbor, Michigan, USA; Division of Pediatric Cardiology, C. S. Mott Children's Hospital, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumDepartment of Pediatrics and the Clinical Research Center, University of Michigan Medical Center, Ann Arbor, Michigan, USA; Division of Pediatric Cardiology, C. S. Mott Children's Hospital, Ann Arbor, Michigan, USA.en_US
dc.identifier.pmid6539561en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/24807/1/0000233.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-9149(84)90589-7en_US
dc.identifier.sourceThe American Journal of Cardiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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