TY - JOUR
T1 - Does RV lead positioning provide additional benefit to cardiac resynchronization therapy in patients with advanced heart failure?
AU - Shimano, Masayuki
AU - Inden, Yasuya
AU - Yoshida, Yukihiko
AU - Tsuji, Yukiomi
AU - Tsuboi, Naoya
AU - Okada, Taro
AU - Yamada, Takumi
AU - Murakami, Yoshimasa
AU - Takada, Yasunobu
AU - Hirayama, Haruo
AU - Murohara, Toyoaki
PY - 2006/10
Y1 - 2006/10
N2 - Background and Objectives: The left ventricular (LV) stimulation site is currently recommended to position the lead at the lateral wall. However, little is known as to whether right ventricular (RV) lead positioning is also important for cardiac resynchronization therapy. This study compared the acute hemodynamic response to biventricular pacing (BiV) at two different RV stimulation sites: RV high septum (RVHS) and RV apex (RVA). Methods and Results: Using micro-manometer-tipped catheter, LV pressure was measured during BiV pacing at RV (RVA or RVHS) and LV free wall in 33 patients. Changes in LV dP/dtmax and dP/dtmin from baseline were compared between RVA and RVHS. BiV pacing increased dP/dtmax by 30.3 ± 1.2% in RVHS and by 33.3 ± 1.7% in RVA (P = n.s.), and decreased dP/dt min by 11.4 ± 0.7% in RVHS and by 13.0 ± 1.0% in RVA (P = n.s.). To explore the optimal combination of RV and LV stimulation sites, we assessed separately the role of RV positioning with LV pacing at anterolateral (AL), lateral (LAT), or posterolateral (PL) segment. When the LV was paced at AL or LAT, the increase in dP/dtmax with RVHS pacing was smaller than that with RVA pacing (AL: 12.2 ± 2.2% vs 19.3 ± 2.1%, P < 0.05; LAT: 22.0 ± 2.7% vs 28.5 ± 2.2%, P < 0.05). There was no difference in dP/dtmin between RVHS- and RVA pacing in individual LV segments. Conclusions: RVHS stimulation has no overall advantage as an alternative stimulation site for RVA during BiV pacing. RVHS was equivalent with RVA in combination with the PL LV site, while RVA was superior to RVHS in combination with AL or LAT LV site.
AB - Background and Objectives: The left ventricular (LV) stimulation site is currently recommended to position the lead at the lateral wall. However, little is known as to whether right ventricular (RV) lead positioning is also important for cardiac resynchronization therapy. This study compared the acute hemodynamic response to biventricular pacing (BiV) at two different RV stimulation sites: RV high septum (RVHS) and RV apex (RVA). Methods and Results: Using micro-manometer-tipped catheter, LV pressure was measured during BiV pacing at RV (RVA or RVHS) and LV free wall in 33 patients. Changes in LV dP/dtmax and dP/dtmin from baseline were compared between RVA and RVHS. BiV pacing increased dP/dtmax by 30.3 ± 1.2% in RVHS and by 33.3 ± 1.7% in RVA (P = n.s.), and decreased dP/dt min by 11.4 ± 0.7% in RVHS and by 13.0 ± 1.0% in RVA (P = n.s.). To explore the optimal combination of RV and LV stimulation sites, we assessed separately the role of RV positioning with LV pacing at anterolateral (AL), lateral (LAT), or posterolateral (PL) segment. When the LV was paced at AL or LAT, the increase in dP/dtmax with RVHS pacing was smaller than that with RVA pacing (AL: 12.2 ± 2.2% vs 19.3 ± 2.1%, P < 0.05; LAT: 22.0 ± 2.7% vs 28.5 ± 2.2%, P < 0.05). There was no difference in dP/dtmin between RVHS- and RVA pacing in individual LV segments. Conclusions: RVHS stimulation has no overall advantage as an alternative stimulation site for RVA during BiV pacing. RVHS was equivalent with RVA in combination with the PL LV site, while RVA was superior to RVHS in combination with AL or LAT LV site.
KW - Congestive heart failure
KW - Hemodynamics
KW - Pacing
UR - http://www.scopus.com/inward/record.url?scp=33750088427&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33750088427&partnerID=8YFLogxK
U2 - 10.1111/j.1540-8159.2006.00500.x
DO - 10.1111/j.1540-8159.2006.00500.x
M3 - Article
C2 - 17038138
AN - SCOPUS:33750088427
SN - 0147-8389
VL - 29
SP - 1069
EP - 1074
JO - PACE - Pacing and Clinical Electrophysiology
JF - PACE - Pacing and Clinical Electrophysiology
IS - 10
ER -