Early stage 2 palliation is crucial in patients with a right-ventricle-to-pulmonary-artery conduit

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Early stage 2 palliation is crucial in patients with a right-ventricle-to-pulmonary-artery conduit. / Rüffer, André; Arndt, Florian; Potapov, Sergej; Mir, Thomas S; Weil, Jochen; Cesnjevar, Robert A.

In: ANN THORAC SURG, Vol. 91, No. 3, 03.2011, p. 816-822.

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@article{6d23443db882498097decc4f033f1728,
title = "Early stage 2 palliation is crucial in patients with a right-ventricle-to-pulmonary-artery conduit",
abstract = "BACKGROUND: Improved survival after Norwood stage 1 palliation is giving more patients the opportunity to reach stage 2 palliation; thus, more patients are exposed to the risk of interstage death.METHODS: A single-center review of patients who underwent stage 1 palliation from January 1998 to December 2007 (n = 58) was performed. Pulmonary blood flow was established either by a modified Blalock-Taussig-shunt (mBTS, n = 33) or a right ventricle-to-pulmonary artery conduit (RVPAC, n = 25).RESULTS: Hospital, interstage, and 1-year survival was not significantly different between groups. However, Kaplan-Meier survival analysis reflected a significantly higher survival probability for RVPAC patients until the age of 120 days (RVAPC, 92% ± 5% [standard error of the mean]; 95% confidence interval, 82 to 100; mBTS, 63% ± 9%; 95% confidence interval, 48 to 82; p = 0.01). During a 1-year follow-up, all 11 nonsurvivors with mBTS died at an age younger than 120 days, including 2 patients with early stage 2 palliation. In contrast, besides 2 early deaths, all RVPAC patients (n = 5) showed later attrition at an age older than 120 days while awaiting stage 2 palliation. Interstage death occurred significantly later among RVPAC patients (RVPAC, 146 ± 60 days versus mBTS, 81 ± 23 days; p = 0.01). After stage 2 palliation, all patients with RVPAC survived, including 7 patients with surgery at an age younger than 120 days. All interstage and late deaths were related to compromising cardiac lesions with no statistical difference between groups.CONCLUSIONS: After Norwood stage 1 palliation, survival was improved with RVPAC for the first 4 months. However, a loss of the favorable primary outcome was present by delaying stage 2 palliation beyond the age of 120 days. Progressive volume load as a result of conduit regurgitation may play a crucial role for later attrition. Residual lesions should be addressed early to preserve cardiac function.",
keywords = "Blood Flow Velocity, Cardiac Catheterization, Female, Follow-Up Studies, Germany/epidemiology, Heart Ventricles/physiopathology, Humans, Hypoplastic Left Heart Syndrome/mortality, Infant, Male, Norwood Procedures/methods, Palliative Care/methods, Prognosis, Pulmonary Artery/physiopathology, Retrospective Studies, Survival Rate/trends, Time Factors",
author = "Andr{\'e} R{\"u}ffer and Florian Arndt and Sergej Potapov and Mir, {Thomas S} and Jochen Weil and Cesnjevar, {Robert A}",
note = "Copyright {\textcopyright} 2011 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.",
year = "2011",
month = mar,
doi = "10.1016/j.athoracsur.2010.10.040",
language = "English",
volume = "91",
pages = "816--822",
journal = "ANN THORAC SURG",
issn = "0003-4975",
publisher = "Elsevier USA",
number = "3",

}

RIS

TY - JOUR

T1 - Early stage 2 palliation is crucial in patients with a right-ventricle-to-pulmonary-artery conduit

AU - Rüffer, André

AU - Arndt, Florian

AU - Potapov, Sergej

AU - Mir, Thomas S

AU - Weil, Jochen

AU - Cesnjevar, Robert A

N1 - Copyright © 2011 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

PY - 2011/3

Y1 - 2011/3

N2 - BACKGROUND: Improved survival after Norwood stage 1 palliation is giving more patients the opportunity to reach stage 2 palliation; thus, more patients are exposed to the risk of interstage death.METHODS: A single-center review of patients who underwent stage 1 palliation from January 1998 to December 2007 (n = 58) was performed. Pulmonary blood flow was established either by a modified Blalock-Taussig-shunt (mBTS, n = 33) or a right ventricle-to-pulmonary artery conduit (RVPAC, n = 25).RESULTS: Hospital, interstage, and 1-year survival was not significantly different between groups. However, Kaplan-Meier survival analysis reflected a significantly higher survival probability for RVPAC patients until the age of 120 days (RVAPC, 92% ± 5% [standard error of the mean]; 95% confidence interval, 82 to 100; mBTS, 63% ± 9%; 95% confidence interval, 48 to 82; p = 0.01). During a 1-year follow-up, all 11 nonsurvivors with mBTS died at an age younger than 120 days, including 2 patients with early stage 2 palliation. In contrast, besides 2 early deaths, all RVPAC patients (n = 5) showed later attrition at an age older than 120 days while awaiting stage 2 palliation. Interstage death occurred significantly later among RVPAC patients (RVPAC, 146 ± 60 days versus mBTS, 81 ± 23 days; p = 0.01). After stage 2 palliation, all patients with RVPAC survived, including 7 patients with surgery at an age younger than 120 days. All interstage and late deaths were related to compromising cardiac lesions with no statistical difference between groups.CONCLUSIONS: After Norwood stage 1 palliation, survival was improved with RVPAC for the first 4 months. However, a loss of the favorable primary outcome was present by delaying stage 2 palliation beyond the age of 120 days. Progressive volume load as a result of conduit regurgitation may play a crucial role for later attrition. Residual lesions should be addressed early to preserve cardiac function.

AB - BACKGROUND: Improved survival after Norwood stage 1 palliation is giving more patients the opportunity to reach stage 2 palliation; thus, more patients are exposed to the risk of interstage death.METHODS: A single-center review of patients who underwent stage 1 palliation from January 1998 to December 2007 (n = 58) was performed. Pulmonary blood flow was established either by a modified Blalock-Taussig-shunt (mBTS, n = 33) or a right ventricle-to-pulmonary artery conduit (RVPAC, n = 25).RESULTS: Hospital, interstage, and 1-year survival was not significantly different between groups. However, Kaplan-Meier survival analysis reflected a significantly higher survival probability for RVPAC patients until the age of 120 days (RVAPC, 92% ± 5% [standard error of the mean]; 95% confidence interval, 82 to 100; mBTS, 63% ± 9%; 95% confidence interval, 48 to 82; p = 0.01). During a 1-year follow-up, all 11 nonsurvivors with mBTS died at an age younger than 120 days, including 2 patients with early stage 2 palliation. In contrast, besides 2 early deaths, all RVPAC patients (n = 5) showed later attrition at an age older than 120 days while awaiting stage 2 palliation. Interstage death occurred significantly later among RVPAC patients (RVPAC, 146 ± 60 days versus mBTS, 81 ± 23 days; p = 0.01). After stage 2 palliation, all patients with RVPAC survived, including 7 patients with surgery at an age younger than 120 days. All interstage and late deaths were related to compromising cardiac lesions with no statistical difference between groups.CONCLUSIONS: After Norwood stage 1 palliation, survival was improved with RVPAC for the first 4 months. However, a loss of the favorable primary outcome was present by delaying stage 2 palliation beyond the age of 120 days. Progressive volume load as a result of conduit regurgitation may play a crucial role for later attrition. Residual lesions should be addressed early to preserve cardiac function.

KW - Blood Flow Velocity

KW - Cardiac Catheterization

KW - Female

KW - Follow-Up Studies

KW - Germany/epidemiology

KW - Heart Ventricles/physiopathology

KW - Humans

KW - Hypoplastic Left Heart Syndrome/mortality

KW - Infant

KW - Male

KW - Norwood Procedures/methods

KW - Palliative Care/methods

KW - Prognosis

KW - Pulmonary Artery/physiopathology

KW - Retrospective Studies

KW - Survival Rate/trends

KW - Time Factors

U2 - 10.1016/j.athoracsur.2010.10.040

DO - 10.1016/j.athoracsur.2010.10.040

M3 - SCORING: Journal article

C2 - 21353005

VL - 91

SP - 816

EP - 822

JO - ANN THORAC SURG

JF - ANN THORAC SURG

SN - 0003-4975

IS - 3

ER -