Chronic Chagas cardiomyopathy manifests late after Trypanosoma cruzi
infection, and it is still one of the major causes of end-stage heart failure in
Latin America.[1] Published
experiences[2,3] with heart transplantation for
chronic Chagas disease have shown the feasibility and efficacy of this therapy,
being the disease reactivation not a major concern when appropriately diagnosed and
timely treated.[4]Nevertheless, the need for some sort of mechanical circulatory support on the waiting
list has progressively increased, according to the International Society for Heart
and Lung Transplantation Registry annual report.[5] Since the experience with mechanical circulatory support in
Latin America is very limited, and biventricular systolic failure is common in
Chagas cardiomyopathy, many unanswered questions regarding modalities of support
need to be elucidated.This case report describes the successful implant of an axial flow left ventricular
assist device in a patient with end-stage heart failure with severe biventricular
failure secondary to Chagas cardiomyopathy.
Case Report
A 26-year-old male, with a history of long-standing heart failure had multiple
hospital admissions in the past year despite optimal medical management. The
diagnosis of end-stage heart failure due to Chagas cardiomyopathy was confirmed by
serology a while ago, and an implantable cardioverter defibrillator was used for
sudden death secondary prevention. Echocardiography revealed a severely dilated left
ventricle (end-diastolic diameter of 72 millimeters), with severely depressed
function (ejection fraction of 18%) and 4+ mitral regurgitation. The right ventricle
also exhibit severe dysfunction with 3+ tricuspid regurgitation, tricuspid annular
plane systolic excursion of 15, and right ventricular systolic pressure of 65 mmHg.
The patient has been followed up in a different city of ours by another cardiology
team. At this point, he has never been considered for heart transplantation.Nonetheless, the patient was admitted in the emergency room with cardiogenic shock,
in Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS)
level 2. He was initially managed with the use of two inotropes, intra-aortic
balloon pump and hemodialysis. No temporary or durable mechanical assist devices
were available at this hospital.A right heart catheterization revealed low cardiac output (cardiac index of 0.9
L/min/m2, with systolic pulmonary pressure of 70 mmHg, transpulmonary
gradient of 16 mmHg and pulmonary vascular resistance of 6 Wood units. Filling
pressures were elevated (central venous pressure and pulmonary wedge pressure of 30
mmHg).The patient was transferred to our hospital for heart transplantation assessment. At
admission, he had sudden hemodynamic instability that deteriorated into cardiac
arrest. Cardiopulmonary resuscitation measures were effective, but circulation was
maintained with escalating doses of vasopressors. A percutaneous venous arterial
extracorporeal life support (ECLS) (Maquet GetingeTM, Germany) through
the femoral vessels was inserted as a bridge to decision strategy. Hemodynamics
stabilized, vasopressors were discontinued, tissue perfusion indices normalized, and
the patient neurologic status was intact. He was extubated on the next day, renal
function normalized, an aggressive diuresis allowed a twelve-liter negative fluid
balance in the following five days (Figure
1).
Figure 1
Chest radiography after ECLS implantation.
Chest radiography after ECLS implantation.Eighteen days after ECLS initiation, the patient was submitted to an axial flow left
ventricular assist device (HeartMate II, Abbott LaboratoriesTM, Chicago,
IL) implantation with ECMO explant under median sternotomy with cardiopulmonary
bypass.Postoperatively (Figure 2), the patient had
mediastinal bleeding requiring surgical revision; coagulopathy and pericarditis. A
transient right ventricular dysfunction required a five-day administration of
intravenous inotropic support, aggressive diuresis and oral pulmonary vasodilators.
He was eventually discharged home on postoperative day 35 in fair condition,
requiring rehabilitation due to malnutrition and muscular weakness.
Figure 2
Chest radiography after left ventricular assist device implantation.
Chest radiography after left ventricular assist device implantation.Sixteen months later, he is in functional class I with unremarkable recovery except
for a single episode of hemolysis that was treated with intravenous heparin. Pump
has functioned well with no evidence of failure or thrombosis. Late right heart
failure was not an issue, and his exercise performance is excellent.
Echocardiography revealed mild tricuspid regurgitation and right ventricular
systolic pressure of 30 mmHg. At this point, the patient does not manifest interest
in being transplanted.
Discussion
The present report illustrates that, in patients with Chagas cardiomyopathy with
severe biventricular failure, a left ventricular assist device (and not necessarily
a biventricular support) may be considered as a modality of mechanical circulatory
support as a bridge to candidacy or transplantation. Frequent pathologic findings
that need to be observed are apical aneurysms, mural thrombi, very thin ventricular
walls and complex ventricular arrhythmias refractory to ablation. Destination
therapy, in theory, is a possible alternative for those patients that do not present
with late right heart failure, which is a possible natural manifestation of the
disease.Since published data is very limited and the experience with mechanical circulatory
support in Latin America is scarce, there are no consensus regarding the best
strategy. Moreira et al were the first to report the use of paracorporeal devices in
Chagas cardiomyopathy, with inconsistent results.[6] More recently, Kransdorf et al[7] reported the United States experience on 11 heart
transplants for Chagas cardiomyopathy. Three out of 11 patients (27%) had mechanical
circulatory support in place at the time of transplant (two patients had
paracorporeal devices in biventricular configuration and one patient had a HeartMate
II device). Ruzza et al[8] described
the successful support with a total artificial heart prior to heart transplantation.
They argue that this approach is justifiable because it allows treatment of
extracardiac Chagas disease, and it potentially reduces the infectious burden of the
causative organism that may make progress the disease on a heart supported with a
device.This particular case presented cardiogenic shock, fluid overloaded, with a recent
cardiac arrest that required the use of venous arterial ECLS. It was very difficult
to determine whether the pulmonary hypertension was severe enough to contraindicate
the heart transplantation. Therefore, a bridge to candidacy strategy seemed
reasonable in this regard. After six months of support, it proved to be effective in
reducing the pulmonary vascular resistance making the patient eligible for heart
transplantation.
Authors: E A Bocchi; G Bellotti; A O Mocelin; D Uip; F Bacal; M L Higuchi; V Amato-Neto; A Fiorelli; N A Stolf; A D Jatene; F Pileggi Journal: Ann Thorac Surg Date: 1996-06 Impact factor: 4.330
Authors: A Ruzza; L S C Czer; M De Robertis; D Luthringer; J Moriguchi; J Kobashigawa; A Trento; F Arabia Journal: Transplant Proc Date: 2016 Jan-Feb Impact factor: 1.066
Authors: Lars H Lund; Leah B Edwards; Anne I Dipchand; Samuel Goldfarb; Anna Y Kucheryavaya; Bronwyn J Levvey; Bruno Meiser; Joseph W Rossano; Roger D Yusen; Josef Stehlik Journal: J Heart Lung Transplant Date: 2016-08-21 Impact factor: 10.247
Authors: Luiz Felipe P Moreira; João Galantier; Anderson Benício; Adolfo A Leirner; Idágene A Cestari; Noedir A G Stolf Journal: Artif Organs Date: 2007-04 Impact factor: 3.094
Authors: Sílvia V Campos; Tânia Mara V Strabelli; Vicente Amato Neto; Christiano P Silva; Fernando Bacal; Edimar A Bocchi; Noedir Antônio G Stolf Journal: J Heart Lung Transplant Date: 2008-04-24 Impact factor: 10.247
Authors: E P Kransdorf; L S C Czer; D J Luthringer; J K Patel; S P Montgomery; A Velleca; J Mirocha; P C Zakowski; R Zabner; C R Gaultier; Y Qvarnstrom; T Benedict; F Steurer; E Bosserman; C D Paddock; M Rafiei; J A Kobashigawa Journal: Am J Transplant Date: 2013-10-28 Impact factor: 8.086
Authors: Savio Cardoso; Clerio Francisco de Azevedo Filho; Fábio Fernandes; Barbara Ianni; Jorge Andion Torreão; Mateus Diniz Marques; Luiz Francisco Rodrigues de Ávila; Raul Santos Filho; Charles Mady; Roberto Kalil-Filho; José Antônio Franchine Ramires; Marcio Sommer Bittencourt; Carlos E Rochitte Journal: Arq Bras Cardiol Date: 2020-12 Impact factor: 2.000