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Circulation. 2006;114:1225

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(Circulation. 2006;114:1225.)
© 2006 American Heart Association, Inc.

Issue Highlights


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 


*    CLINICAL UTILITY AND SAFETY OF A PROTOCOL FOR NONCARDIAC AND CARDIAC MAGNETIC RESONANCE IMAGING OF PATIENTS WITH PERMANENT PACEMAKERS AND IMPLANTABLE CARDIOVERTER DEFIBRILLATORS AT 1.5 TESLA, by Nazarian et al.
 
and


*    STRATEGY FOR SAFE PERFORMANCE OF EXTRATHORACIC MAGNETIC RESONANCE IMAGING AT 1.5 TESLA IN THE PRESENCE OF CARDIAC PACEMAKERS IN NON–PACEMAKER-DEPENDENT PATIENTS: A PROSPECTIVE STUDY WITH 115 EXAMINATIONS, by Sommer et al.
 
Parallel with the evolution of clinically useful applications of magnetic resonance imaging (MRI), there is an increasing population of patients considered to have a contraindication to having an MRI study, i.e. those with internal devices such as pacemakers or implantable defibrillators. This issue is especially prevalent among patients with heart failure and LV dysfunction, based on the evidence for biventricular pacing as well as defibrillators. Small series have suggested that there may be some patients with devices who can safely undergo an MRI study. Two papers in this issue of Circulation advance the knowledge regarding this controversy, incorporating novel approaches. Sommer and colleagues report on 82 patients with pacemakers having nonthoracic MRI studies after prophylactic preprogramming of the pacemakers. This study assessed post-MRI pacemaker function, measured troponin levels as an indicator of thermal injury, and followed short-term outcomes to suggest that selected patients with devices, given specific pre-MRI programming, can safely undergo MRI. Nazarian and colleagues follow their recently published Circulation study assessing safety of selected devices for cardiac MRI in animal models by now reporting on 55 patients who had the same devices undergoing cardiac MRI, which was shown to be safe. The authors’ conclusions involve the relative safety given specific preimaging programming and the predefined device selectivity. These 2 studies together provide safety information on over 100 patients with devices having MRI studies. At what point can clinicians feel comfortable with the safety data? This question is addressed from a regulatory perspective in an accompanying editorial by . . . [Full Text of this Article]


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