TY - JOUR
T1 - Noninvasive monitoring of serial changes in pulmonary vascular resistance and acute vasodilator testing using cardiac magnetic resonance
AU - García-Álvarez, Ana
AU - Fernández-Friera, Leticia
AU - García-Ruiz, José Manuel
AU - Nuño-Ayala, Mario
AU - Pereda, Daniel
AU - Fernández-Jiménez, Rodrigo
AU - Guzmán, Gabriela
AU - Sanchez-Quintana, Damián
AU - Alberich-Bayarri, Angel
AU - Pastor-Escuredo, David
AU - Sanz-Rosa, David
AU - García-Prieto, Jaime
AU - Gonzalez-Mirelis, Jesús G.
AU - Pizarro, Gonzalo
AU - Jimenez-Borreguero, Luis Jesús
AU - Fuster, Valentín
AU - Sanz, Javier
AU - Ibáñez, Borja
N1 - Funding Information:
This work has been partially funded by the competitive grant “CNIC-Translational 01-2009” (to Dr. Ibáñez), by the Fondo de Investigacion Sanitaria-FIS PI10/02268 (to Dr. Ibáñez), and by the grant “Basic research project from the Spanish Heart Foundation 2012” (to Dr. García-Álvarez). Drs. García-Álvarez and García-Ruiz have been supported by a CNIC-Cardiojoven Fellowship, Madrid, Spain. Drs. Mirelis and Guzmán are supported by a CNIC-CardioImage Fellowship, Madrid, Spain. Dr. Alberich-Bayarri is supported by the CENIT Project 2009-2012 “CEN-20091044” , Madrid, Spain. Dr. Sanz-Rosa is supported by a CNIC Postdoctoral fellowship, Madrid, Spain. Dr. Pastor-Escuredo is supported by TEC2010-21619-C04-03. All authors have reported that they have no relationships relevant to the contents of this paper to disclose.
PY - 2013/10/22
Y1 - 2013/10/22
N2 - Objectives The study sought to evaluate the ability of cardiac magnetic resonance (CMR) to monitor acute and long-term changes in pulmonary vascular resistance (PVR) noninvasively. Background PVR monitoring during the follow-up of patients with pulmonary hypertension (PH) and the response to vasodilator testing require invasive right heart catheterization. Methods An experimental study in pigs was designed to evaluate the ability of CMR to monitor: 1) an acute increase in PVR generated by acute pulmonary embolization (n = 10); 2) serial changes in PVR in chronic PH (n = 22); and 3) changes in PVR during vasodilator testing in chronic PH (n = 10). CMR studies were performed with simultaneous hemodynamic assessment using a CMR-compatible Swan-Ganz catheter. Average flow velocity in the main pulmonary artery (PA) was quantified with phase contrast imaging. Pearson correlation and mixed model analysis were used to correlate changes in PVR with changes in CMR-quantified PA velocity. Additionally, PVR was estimated from CMR data (PA velocity and right ventricular ejection fraction) using a formula previously validated. Results Changes in PA velocity strongly and inversely correlated with acute increases in PVR induced by pulmonary embolization (r = -0.92), serial PVR fluctuations in chronic PH (r = -0.89), and acute reductions during vasodilator testing (r = -0.89, p ≤ 0.01 for all). CMR-estimated PVR showed adequate agreement with invasive PVR (mean bias -1.1 Wood units,; 95% confidence interval: -5.9 to 3.7) and changes in both indices correlated strongly (r = 0.86, p < 0.01). Conclusions CMR allows for noninvasive monitoring of acute and chronic changes in PVR in PH. This capability may be valuable in the evaluation and follow-up of patients with PH.
AB - Objectives The study sought to evaluate the ability of cardiac magnetic resonance (CMR) to monitor acute and long-term changes in pulmonary vascular resistance (PVR) noninvasively. Background PVR monitoring during the follow-up of patients with pulmonary hypertension (PH) and the response to vasodilator testing require invasive right heart catheterization. Methods An experimental study in pigs was designed to evaluate the ability of CMR to monitor: 1) an acute increase in PVR generated by acute pulmonary embolization (n = 10); 2) serial changes in PVR in chronic PH (n = 22); and 3) changes in PVR during vasodilator testing in chronic PH (n = 10). CMR studies were performed with simultaneous hemodynamic assessment using a CMR-compatible Swan-Ganz catheter. Average flow velocity in the main pulmonary artery (PA) was quantified with phase contrast imaging. Pearson correlation and mixed model analysis were used to correlate changes in PVR with changes in CMR-quantified PA velocity. Additionally, PVR was estimated from CMR data (PA velocity and right ventricular ejection fraction) using a formula previously validated. Results Changes in PA velocity strongly and inversely correlated with acute increases in PVR induced by pulmonary embolization (r = -0.92), serial PVR fluctuations in chronic PH (r = -0.89), and acute reductions during vasodilator testing (r = -0.89, p ≤ 0.01 for all). CMR-estimated PVR showed adequate agreement with invasive PVR (mean bias -1.1 Wood units,; 95% confidence interval: -5.9 to 3.7) and changes in both indices correlated strongly (r = 0.86, p < 0.01). Conclusions CMR allows for noninvasive monitoring of acute and chronic changes in PVR in PH. This capability may be valuable in the evaluation and follow-up of patients with PH.
KW - magnetic resonance
KW - monitoring
KW - pulmonary hypertension
KW - pulmonary vascular resistance
KW - vasodilator testing
UR - http://www.scopus.com/inward/record.url?scp=84886049143&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2013.07.037
DO - 10.1016/j.jacc.2013.07.037
M3 - Article
C2 - 23954344
AN - SCOPUS:84886049143
SN - 0735-1097
VL - 62
SP - 1621
EP - 1631
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 17
ER -