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Cardiac resynchronization therapy improves the uptake of MIBI-99mTc and cardiac function

Abstracts

This case shows the improvement promoted by cardiac resynchronization therapy (CRT) on myocardial perfusion and left ventricular (LV) performance assessed by gated myocardial perfusion scintigraphy. The patient had idiopathic dilated cardiomyopathy, left bundle branch block and severe heart failure despite optimized medical treatment. After CRT, clinical improvement, QRS reduction and improvement of previously hypoperfused anterior and septal walls were observed. There was also decrease in LV end-diastolic and systolic volumes and increase in LV ejection fraction.

Myocardial perfusion; ventricular function; left ventricular function; dilated cardiomyopathy


Este caso mostra a melhora proporcionada pela terapia de ressincronização cardíaca (TRC) sobre a perfusão miocárdica e o desempenho do ventrículo esquerdo (VE) avaliados pela cintilografia de perfusão miocárdica com MIBI-99mTc sincronizada ao eletrocardiograma. Paciente portadora de miocardiopatia dilatada idiopática, bloqueio de ramo esquerdo e insuficiência cardíaca refratária ao tratamento medicamentoso otimizado. Após TRC, foi observada melhora clínica, redução da duração do QRS e melhora na perfusão das paredes anterior e ântero-septal que se encontravam previamente hipoperfundidas. Houve também redução dos volumes diastólico e sistólico finais e aumento da fração de ejeção do VE.

Perfusão miocárdica; função ventricular esquerda; bloqueio de ramo esquerdo; cardiomiopatia dilatada


CASE REPORT

Instituto do Coração (InCor) - Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP), São Paulo - SP - Brazil

Mailing Address

ABSTRACT

This case shows the improvement promoted by cardiac resynchronization therapy (CRT) on myocardial perfusion and left ventricular (LV) performance assessed by gated myocardial perfusion scintigraphy. The patient had idiopathic dilated cardiomyopathy, left bundle branch block and severe heart failure despite optimized medical treatment. After CRT, clinical improvement, QRS reduction and improvement of previously hypoperfused anterior and septal walls were observed. There was also decrease in LV end-diastolic and systolic volumes and increase in LV ejection fraction.

Key words: Myocardial perfusion; ventricular function, left ventricular function and dilated cardiomyopathy.

Introduction

In recent years, the cardiac resynchronization therapy (CRT) has been considered an important adjunct therapy in heart failure (HF) refractory to optimized drug treatment and it has shown to be beneficial to many patients. In most patients with dilated myocardiopathy, the increase of the QRS complex duration at the electrocardiogram (ECG) presents as a left bundle branch block (LBBB)1,2 . This is not only a marker of disease progression, but it can also lead to ventricular dyssynchrony3,4.

Several studies have demonstrated the benefits of CRT on cardiovascular hemodynamics; however, little has been described on its effects on myocardial perfusion. In this case report, the behavior of myocardial perfusion and left ventricle (LV) function was evaluated by myocardial perfusion scintigraphy (MPS) with MIBI-99mTc at rest and after pharmacological stress with dipyridamole, gated to ECG (GS) pre- and three months after CRT.

Case Report

A 64-year-old female patient, who presented idiopathic dilated cardiomyopathy and functional class III HF according to the New York Heart Association, despite optimized drug therapy for HF and LBBB at the ECG, was submitted to atrial-biventricular pacemaker implant. Pre-CRT, MPS images showed persistent low uptake of MIBI-99mTc, of moderate to severe degree, in the anterior and anteroseptal walls of the LV, Figure 1. At GS, the end-diastolic volume (EDV) was 257 mL; the end-systolic volume (ESV) was 186 mL; the LV ejection fraction (LVEF) at rest was 27%, Figure 1. Three months after the CRT, the patient presented Functional Class I, QRS duration decreased from 180 to 120 ms (Figure 2) and MPS showed a significant improvement in perfusion of the anterior and anteroseptal walls of the LV, Figure 1. At GS, a decrease in EDV to 150 mL and ESV to 86 mL was observed as well as LVEF at rest increase to 43%, Figure 1.



Discussion

The present case shows, through MPS images gated to ECG, the benefits provided by the CRT on myocardial perfusion and cardiac performance, with important LV reverse remodeling. The MPS is a valuable tool for the non-invasive evaluation of relative myocardial perfusion and of the regional and global LV function, when the images are gated to ECG. The physiological basis for the redistribution of the coronary blood flow after the change in the pattern of electrical activation of the LV is partially understood. Many patients with LBBB present areas of myocardial hypoperfusion, mainly in the septal wall, which are not related to obstructive coronary disease5,6. The myocardial perfusion is a predominantly diastolic process. The cardiac dyssynchrony reduces diastole, prolonging the stress time during the cardiac cycle, decreasing the LV filling time6. This last phenomenon is even more prominent in patients with dilated cardiomyopathy7. Additionally, the myocardial blood flow supply can be interrupted at the asynchronous contraction, as in some regions the contraction starts or is continued at the diastole, when most of the coronary blood flow is occurring. However, this might not be the only explanation, since the delayed activated regions, which are still contracting in early diastole, have their blood flow increased8.

The degree of perfusion for a ventricular wall can be the reflex of its workload. The asynchronous activation leads to the decrease in the contractile force in the early activated myocardial regions and increase in the delayed activated ones5,6. It is speculated that the abnormal relation between regional contraction/relaxation in patients with ventricular dyssynchrony causes abnormalities in wall stress with an altered local distribution of blood flow due to a metabolic adaptation of the flow to the regional differences in the workload5. The endothelial dysfunction with impairment of the coronary flow reserve can be another mechanism involved in the flow alteration caused by the electromechanical cardiac dyssynchrony6.

The decrease in myocardial blood flow reserve in HF, regardless of its cause, can generate intermittent periods of ischemia, leading to a chronic LV dysfunction, which is associated with a poor prognosis9. Thus, the perfusion improvement, especially in the anterior and septal walls of the LV through CRT can induce the recovery of the function and improve the prognosis10.

However, in spite of the results observed in the present clinical case and the previously reported studies in the literature, more evidence is needed to confirm whether the modifications triggered by the CRT in the uptake of MIBI-99mTc are in fact associated with a significant increase in LVEF and decrease in the LV remodeling, which occur in many patients submitted to this therapy.

Potential Conflict of Interest

No potential conflict of interest relevant to this article was reported.

Sources of Funding

This study was partially funded by FAPESP.

Study Association

This article is part of the thesis of doctoral submitted by Simone Cristina Soares Brandão, from Instituto do Coração (INCOR) do Hospital das Clínicas da USP.

REFERENCES

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  • Cardiac resynchronization therapy improves the uptake of MIBI-99mTc and cardiac function

    Simone Cristina Soares Brandão; Maria Clementina Giorgi; Silvana D'Orio Nishioka; Martino Martinelli Filho; José Soares Jr.; José Cláudio Meneghetti
  • Publication Dates

    • Publication in this collection
      01 Oct 2008
    • Date of issue
      Sept 2008

    History

    • Accepted
      26 Dec 2007
    • Received
      07 Dec 2007
    • Reviewed
      26 Dec 2007
    Sociedade Brasileira de Cardiologia - SBC Avenida Marechal Câmara, 160, sala: 330, Centro, CEP: 20020-907, (21) 3478-2700 - Rio de Janeiro - RJ - Brazil, Fax: +55 21 3478-2770 - São Paulo - SP - Brazil
    E-mail: revista@cardiol.br