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Role of Nuclear Imaging in The Evaluvation of Non Coronary
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                                                           Artery Disease



              performed  to differentiate ischemic  cardiomyopathy  Frais  et al. demonstrated utility of phase
              from non-ischemic cardiomyopathy. Absence of per-  analysis of gated ERNA in assessment of
              fusion defect in stress  and  rest  studies in a patient
              with cardiomyopathy reliably ruled out possibilities of   cardiac  mechanical  dyssynchrony [2].  The
              coronary artery  disease  as a cause of heart failure.   phase  image  analysis  is  based  on the first
              However false negative results may happen in a case  Fourier  harmonic  fit of the blood pool  time
              of balanced ischemia where presence of triple vessel  vs. radioactive curve to measure the magni-
              disease  mask  the difference  between perfusion  of   tude and sequence of ventricular contraction
              different segments and falsely considered as normal
              studies.  However  careful evaluation  of studies  will   in each pixel of the image. A phase angle is
              reveal  presence  of transient ischemic  dilatation  and   assigned between 0º-360º depending on the
              stress induced dysfunction in these cases. With ad-  relative time delay from the R-wave  to the
              vent of PET perfusion radiotracer such as 13N-Ammo-  start of the cardiac  cycle for each  pixel.  A
              nia and 82- Rubidium this problem can be completely   phase histogram is constructed correspond-
              solved  since PET tracers give  actual  assessment of
              myocardial  blood  flow  (coronary flow  reserve)  to in-  ing to the sequence of ventricular contration
              dividual segments.
                                                                 during cardiac cycle. Mean & Standard devi-
              Determining the therapeutic options                ation (SD) of phase histogram is calculated
              The therapeutic decision for patients with cardiomy-  for each ventricle separately. Intraventricular
              opathy is  crucial. The  determination of  left  venricu-  dyssynchrony is measured by Standard de-
              lar ejection fraction  (LVEF) to its exact  value  is im-  viation  of the  mean  phase angle (SD  mPA)
              portant for decision regarding performing a surgical   for  left ventricle  (LV)  &  right  ventricle (RV)
              procedure  or  managing the patients conservatively.   and interventricular dyssynchrony  (IVD) is
              ERNA, commonly known as MUGA study (Multigated
              acquisition) being the most reliable and reproducible   calculated  as the  difference between LV
              methodology to determine the LVEF with minimal in-  and RV mean phase angles (LV-RVmPA), in
              ter-observer  variation, is  the method of  choice. Due  milliseconds (ms) and/or degree (°). Mukher-
              to its reliability and repeatability it is also performed   jee  et al. in their study of 32 patients with
              frequently to assess LVEF during follow up.
                                                                 non-ischemic  cardiomyopathy noted  that
              Identifying candidates suitable for device therapy  both intra left  ventricular dyssynchrony

              Implantable cardiac defibrillator (ICD) and cardiac re-  (ILVD) and IVD were  significantly larger  in
              synchronization therapy (CRT) are exciting treatment   responders vs. non responders. Reciever op-
              options for patients with drug refractory HF [1]. How-  erating curve (ROC)  curve analysis showed
              ever despite selecting the patient according the con-
              ventional criteria, approximately one third of patients   an  optimal  sensitivity of 95%  and  specific-
              who receive CRT will not have an improvement in LV   ity  of  80%  at cut-off value of  30° for  ILVD
              function or symptoms and are called nonresponders.  & an optimal sensitivity of 81% & specificity
              It has been suggested that ‘lack of a correctable form   of  80%  at  cut-off  value  of  23˚  for  IVD  for
              of mechanical dyssynchrony’ may be the prime rea-  prediction of response to CRT. However, on
              son behind  the  lack of response to CRT.  Therefore,
              assessment of cardiac mechanical dyssynchrony has   multivariate analysis, ILVD was found to be
              gained  considerable  attention  in recent years  with   most important independent predictor  for
              the aim to distinguish CRT responders from non-re-  response to CRT [3].
              sponders with a high degree of accuracy.
                                                                 Quantitative  softwares  for  assessment  of
              In recent  years,  many studies  have been published   cardiac  dyssynchrony on GMPS are  com-
              demonstrating role of nuclear imaging techniques in
              predicting  response  to CRT. Most of these studies   mercially  available providing  objective pa-
              are performed using ERNA and GMPS. Limited stud-   rameters  for assessment of intraventricular
              ies have also demonstrated the role of GBPS, gated  dyssynchrony [4]. The two parameters com-
              myocardial PET and myocardial autonomic  imaging   monly used to assess  cardiac  dyssynchro-
              in prediction of response to CRT.                  ny on GMPS are Phase Standard Deviation



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