Remote noninvasive allograft rejection monitoring for heart transplant recipients: study protocol for the novel evaluation with home electrocardiogram and remote transmission (NEW HEART) study

<p>Abstract</p> <p>Background</p> <p>Acute allograft rejection is a major cause of early mortality in the first year after heart transplantation in adults. Although endomyocardial biopsy (EMB) is not a perfect "gold standard" for a correct diagnosis of acute a...

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Main Authors: Doering Lynn V, Hickey Kathleen, Pickham David, Chen Belinda, Drew Barbara J
Format: Article
Language:English
Published: BMC 2012-03-01
Series:BMC Cardiovascular Disorders
Subjects:
Online Access:http://www.biomedcentral.com/1471-2261/12/14
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author Doering Lynn V
Hickey Kathleen
Pickham David
Chen Belinda
Drew Barbara J
author_facet Doering Lynn V
Hickey Kathleen
Pickham David
Chen Belinda
Drew Barbara J
author_sort Doering Lynn V
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Acute allograft rejection is a major cause of early mortality in the first year after heart transplantation in adults. Although endomyocardial biopsy (EMB) is not a perfect "gold standard" for a correct diagnosis of acute allograft rejection, it is considered the best available test and thus, is the current standard practice. Unfortunately, EMB is an invasive and costly procedure that is not without risk. Recent evidence suggests that acute allograft rejection causes delays in ventricular repolarization and thereby increases the cellular action potential duration resulting in a longer QT interval on the electrocardiogram (ECG). No prospective study to date has investigated whether such increases in the QT interval could provide early detection of acute allograft rejection. Therefore, in the Novel Evaluation With Home Electrocardiogram And Remote Transmission (NEW HEART) study, we plan to investigate the potential benefit of daily home QT interval monitoring to predict acute allograft rejection.</p> <p>Methods/design</p> <p>The NEW HEART study is a prospective, double-blind, multi-center descriptive research study. A sample of 325 adult heart transplant recipients will be recruited within six weeks of transplant from three sites in the United States. Subjects will receive the HeartView™ ECG recorder and its companion Internet Transmitter, which will transmit the subject's ECG to a Core Laboratory. Subjects will be instructed to record and transmit an ECG recording daily for 6 months. An increase in the QT<sub>C </sub>interval from the previous day of at least 25 ms that persists for 3 consecutive days will be considered abnormal. The number and grade of acute allograft rejection episodes, as well as all-cause mortality, will be collected for one year following transplant surgery.</p> <p>Discussion</p> <p>This study will provide "real world" prospective data to determine the sensitivity and specificity of QT<sub>C </sub>as an early non invasive marker of cellular rejection in transplant recipients during the first post-transplant year. A non-invasive indicator of early allograft rejection in heart transplant recipients has the potential to limit the number and severity of rejection episodes by reducing the time and cost of rejection surveillance and by shortening the time to recognition of rejection.</p> <p>Trial Registration</p> <p>ClinicalTrials.gov: <a href="http://www.clinicaltrials.gov/ct2/show/NCT01365806">NCT01365806</a></p>
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spelling doaj.art-b1c7c4bb98c349dfb7c143503ea9ba8d2022-12-22T03:07:16ZengBMCBMC Cardiovascular Disorders1471-22612012-03-011211410.1186/1471-2261-12-14Remote noninvasive allograft rejection monitoring for heart transplant recipients: study protocol for the novel evaluation with home electrocardiogram and remote transmission (NEW HEART) studyDoering Lynn VHickey KathleenPickham DavidChen BelindaDrew Barbara J<p>Abstract</p> <p>Background</p> <p>Acute allograft rejection is a major cause of early mortality in the first year after heart transplantation in adults. Although endomyocardial biopsy (EMB) is not a perfect "gold standard" for a correct diagnosis of acute allograft rejection, it is considered the best available test and thus, is the current standard practice. Unfortunately, EMB is an invasive and costly procedure that is not without risk. Recent evidence suggests that acute allograft rejection causes delays in ventricular repolarization and thereby increases the cellular action potential duration resulting in a longer QT interval on the electrocardiogram (ECG). No prospective study to date has investigated whether such increases in the QT interval could provide early detection of acute allograft rejection. Therefore, in the Novel Evaluation With Home Electrocardiogram And Remote Transmission (NEW HEART) study, we plan to investigate the potential benefit of daily home QT interval monitoring to predict acute allograft rejection.</p> <p>Methods/design</p> <p>The NEW HEART study is a prospective, double-blind, multi-center descriptive research study. A sample of 325 adult heart transplant recipients will be recruited within six weeks of transplant from three sites in the United States. Subjects will receive the HeartView™ ECG recorder and its companion Internet Transmitter, which will transmit the subject's ECG to a Core Laboratory. Subjects will be instructed to record and transmit an ECG recording daily for 6 months. An increase in the QT<sub>C </sub>interval from the previous day of at least 25 ms that persists for 3 consecutive days will be considered abnormal. The number and grade of acute allograft rejection episodes, as well as all-cause mortality, will be collected for one year following transplant surgery.</p> <p>Discussion</p> <p>This study will provide "real world" prospective data to determine the sensitivity and specificity of QT<sub>C </sub>as an early non invasive marker of cellular rejection in transplant recipients during the first post-transplant year. A non-invasive indicator of early allograft rejection in heart transplant recipients has the potential to limit the number and severity of rejection episodes by reducing the time and cost of rejection surveillance and by shortening the time to recognition of rejection.</p> <p>Trial Registration</p> <p>ClinicalTrials.gov: <a href="http://www.clinicaltrials.gov/ct2/show/NCT01365806">NCT01365806</a></p>http://www.biomedcentral.com/1471-2261/12/14ECG monitoringQT intervalHeart transplantationAllograft rejection
spellingShingle Doering Lynn V
Hickey Kathleen
Pickham David
Chen Belinda
Drew Barbara J
Remote noninvasive allograft rejection monitoring for heart transplant recipients: study protocol for the novel evaluation with home electrocardiogram and remote transmission (NEW HEART) study
BMC Cardiovascular Disorders
ECG monitoring
QT interval
Heart transplantation
Allograft rejection
title Remote noninvasive allograft rejection monitoring for heart transplant recipients: study protocol for the novel evaluation with home electrocardiogram and remote transmission (NEW HEART) study
title_full Remote noninvasive allograft rejection monitoring for heart transplant recipients: study protocol for the novel evaluation with home electrocardiogram and remote transmission (NEW HEART) study
title_fullStr Remote noninvasive allograft rejection monitoring for heart transplant recipients: study protocol for the novel evaluation with home electrocardiogram and remote transmission (NEW HEART) study
title_full_unstemmed Remote noninvasive allograft rejection monitoring for heart transplant recipients: study protocol for the novel evaluation with home electrocardiogram and remote transmission (NEW HEART) study
title_short Remote noninvasive allograft rejection monitoring for heart transplant recipients: study protocol for the novel evaluation with home electrocardiogram and remote transmission (NEW HEART) study
title_sort remote noninvasive allograft rejection monitoring for heart transplant recipients study protocol for the novel evaluation with home electrocardiogram and remote transmission new heart study
topic ECG monitoring
QT interval
Heart transplantation
Allograft rejection
url http://www.biomedcentral.com/1471-2261/12/14
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