
Pulmonary Pressure Assessment with the Total Artificial Heart
Author(s) -
David L. Joyce,
Margaret M. Redfield,
Sudhir S. Kushwaha,
Atta Behfar,
Barry A. Borlaug,
Richard C. Daly,
Gurpreet S. Sandhu,
Lyle D. Joyce
Publication year - 2018
Publication title -
asaio journal
Language(s) - English
Resource type - Journals
eISSN - 1538-943X
pISSN - 1058-2916
DOI - 10.1097/mat.0000000000000632
Subject(s) - medicine , pulmonary hypertension , artificial heart , pulmonary artery , cardiology , implant , ventricle , diastole , hemodynamics , blood pressure , vascular resistance , heart transplantation , transplantation , surgery
Reversal of pulmonary hypertension has been observed in patients during a bridge to transplant with a left ventricular assist device. Total artificial heart (TAH) implant prevents subsequent right heart catheterization. Consequently, controversy exists over whether the prosthetic right ventricle improves or exacerbates pulmonary hypertension. A pulmonary artery (PA) pressure monitor was placed in two patients undergoing TAH implant, as a bridge to transplant. One patient had pulmonary hypertension at implant; the other had normal pulmonary pressures. Daily measurements were taken of systolic, diastolic, and mean PA pressures throughout support. Patient 1 received successful transplant after TAH support of 91 days. Systolic/diastolic (mean) PA pressures steadily decreased from 55/39 (28) mm Hg at implant to 29/18 (7) mm Hg currently. Patient 2 received support for 101 days before death due to abdominal ischemic complications. Pulmonary arterial pressures stayed consistent throughout this period, from 26/17 (20) mm Hg at implant to 23/13 (17) mm Hg at the time of death. These findings suggest that an implantable PA pressure monitor may be useful in optimizing hemodynamics and planning appropriate timing of transplant with TAH support.