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Electrically guided versus imaging-guided implant of the left ventricular lead in cardiac resynchronization therapy: a study protocol for a double-blinded randomized controlled clinical trial (ElectroCRT)

Abstract

Background

Cardiac resynchronization therapy (CRT) is an established treatment in patients with heart failure and prolonged QRS duration where a biventricular pacemaker is implanted to achieve faster activation and more synchronous contraction of the left ventricle (LV). Despite the convincing effect of CRT, 30–40% of patients do not respond. Among the most important correctable causes of non-response to CRT is non-optimal LV lead position.

Methods

We will enroll 122 patients in this patient-blinded and assessor-blinded, randomized, clinical trial aiming to investigate if implanting the LV lead guided by electrical mapping towards the latest LV activation as compared with imaging-guided implantation, causes an excess increase in left ventricular (LV) ejection fraction (LVEF). The patients are randomly assigned to either the intervention group: preceded by cardiac computed tomography of the cardiac venous anatomy, the LV lead is placed according to the latest LV activation in the coronary sinus (CS) branches identified by systematic electrical mapping of the CS at implantation and post-implant optimization of the interventricular pacing delay; or patients are assigned to the control group: placement of the LV lead guided by cardiac imaging. The LV lead is targeted towards the latest mechanical LV activation as identified by echocardiography and outside myocardial scar as identified by myocardial perfusion (MP) imaging. The primary endpoint is change in LVEF at 6-month follow up (6MFU) as compared with baseline measured by two-dimensional echocardiography. Secondary endpoints include relative percentage reduction in LV end-systolic volume, all-cause mortality, hospitalization for heart failure, and a clinical combined endpoint of response to CRT at 6MFU defined as the patient being alive, not hospitalized for heart failure, and experiencing improvement in NYHA functional class or/and > 10% increase in 6-minute walk test.

Discussion

We assume an absolute increase in LVEF of 12% in the intervention group versus 8% in the control group. If an excess increase in LVEF can be achieved by LV lead implantation guided by electrical mapping, this study supports the conduct of larger trials investigating the impact of this strategy for LV-lead implantation on clinical outcomes in patients treated with CRT.

Trial registration

ClinicalTrials.gov, NCT02346097. Registered on 12 January 2015.

Patients were enrolled between 16 February 2015 and 13 December 2017.

Peer Review reports

Background

Cardiac resynchronization therapy (CRT) improves survival, symptoms, and left ventricular (LV) function in patients with medical refractory heart failure and prolonged QRS duration [1,2,3,4]. Nevertheless, 30–40% of the patients experience no clinical benefit and the associated risk of complications is non-negligible [5,6,7].

Potentially correctable causes of non-response to CRT are LV lead positioning and device programming [7, 8]. Guidelines recommend positioning of the LV lead in non-scarred, non-apical, and postero-lateral myocardial segments with late electrical activation [1]. Recent randomized controlled trials have demonstrated improved response to CRT when applying an imaging-guided LV lead placement strategy targeting the latest mechanically activated, non-scarred, myocardial segment, compared with standard care [9,10,11]. However, imaging-guided strategies are time-consuming, costly, and difficult to align with fluoroscopic imaging during device implantation.

An alternative approach for individualized LV lead placement is to target the myocardial region with the latest electrical activation; a strategy with the advantage of electrical measurements being immediately available during the implant procedure. Retrospective studies have documented an association between pacing the LV in a region with late electrical activation and improved outcome after CRT [12, 13]. However, these studies did not perform systematic electrical activation mapping or evaluate the influence of myocardial scar tissue.

Recently, electrical resynchronization with narrowing of the QRS width during CRT has been associated with better outcome [14]. Furthermore, programming of the interventricular pacing delay (VVd) to achieve the shortest QRS duration is suggested to increase CRT response [15, 16]. Whether the outcome of CRT is improved when combining electrically guided LV lead placement and optimizing the VVd to achieve the shortest QRS duration is unknown.

To clarify the potential value of an electrically guided strategy for optimizing CRT response, we designed a prospective, double-blinded, randomized trial comparing an electrically guided CRT strategy with an imaging-guided approach. We hypothesize that an electrically guided CRT strategy improves CRT response by optimal electrical resynchronization targeting LV lead placement towards the region with the latest electrical activation combined with VVd optimization to achieve the narrowest biventricular paced QRS. The aim of the present study is to investigate if this strategy of optimal electrical resynchronization causes an excess improvement in LV ejection fraction (LVEF) as compared with an imaging-guided strategy positioning the LV lead according to the latest mechanically activated non-scarred myocardial segment.

Methods

Study design

The Electrically versus Imaging-guided Implant of the Left Ventricular Lead in Cardiac Resynchronization Therapy Study (ElectroCRT) is a prospective, patient-blinded and assessor-blinded, single-center, randomized, controlled trial. Study participants are allocated 1:1 to either the intervention group or the control group as follows:

  1. 1.

    Intervention group (electrically guided) including pre-implant cardiac computed tomography (CT) to visualize cardiac venous anatomy, procedural electrical activation mapping of all available coronary sinus (CS) branches, placement of the LV lead to pace the site of latest electrical activation, and procedural VVd optimization to achieve the shortest possible QRS duration.

  2. 2.

    Control group (imaging-guided) including pre-implant cardiac CT to visualize cardiac venous anatomy, speckle-tracking echocardiography to identify the LV myocardial segment with the latest mechanical activation, and myocardial perfusion (MP) imaging (82Rubidium positron emission tomography (Rb-PET)) to localize the LV myocardial scar. The LV lead is targeted towards the CS branch closest to the latest mechanically activated non-scarred segment and simultaneous biventricular stimulation is applied [17].

One day prior to implantation, all patients undergo identical pre-implant clinical evaluation and imaging acquisition after providing written informed consent. Patients are followed for 6 months. The study course is illustrated in Figs. 1 and 2.

Fig. 1
figure 1

Consort diagram of the study course. 6MWT, 6-minute walk test; AV, atrioventricular; CRT, cardiac resynchronization therapy; CT, computed tomography; LV, left ventricular; LVEF, left ventricular ejection fraction; MLHFQ, Minnesota Living with Heart Failure Questionnaire; MP, myocardial perfusion; NYHA, New York Heart Association; QoL, quality of life; VVd, interventricular pacing delay

Fig. 2
figure 2

Control group: pre-implant imaging obtained to guide implantation of the left ventricular (LV) lead. a Echocardiographic LV short-axis view of the basal (left) and mid-LV imaging plane (right) each divided into six anatomical segments. Numbers indicate time to peak radial strain in milliseconds (ms). b Baseline cardiac computed tomography (CT) images in three-dimensional 3D reconstruction illustrating cardiac venous anatomy. Posterior (left) and lateral (right) view of LV. c Baseline cardiac CT image in the mid-LV multiplanar reformatted short-axis view illustrating cardiac venous anatomy. d Rubidium positron emission tomography (Rb-PET) myocardial perfusion (MP) imaging, LV 17-segment bulls-eye plot. Numbers indicate percentage of tracer-uptake; < 50% is considered as transmural scar tissue. AIV, anterior interventricular vein; Ant, anterior; Ant-Sept, antero-septal; CS, coronary sinus; Inf, inferior; LAD, left anterior descending artery; Lat, lateral; LMA, left marginal artery (circumflex artery branch); LMV, left marginal vein; MCV, middle cardiac vein; PDA, posterior descending artery (right coronary artery branch); PLA, posterolateral artery; Post, posterior; PV, posterior vein; RCA, right coronary artery; RV, right ventricle; Sept, septal

Study population

Patients are recruited at a tertiary referral center (Department of Cardiology, Aarhus University Hospital, Denmark). Consecutive patients referred to CRT-pacemaker (CRT-P) or CRT-defibrillator (CRT-D) and meeting the inclusion and exclusion criteria are eligible for study participation (Table 1).

Table 1 Inclusion and exclusion criteria

Ethical considerations

The trial will be conducted according to the principles of the Helsinki Declaration II [18] and the protocol has been written in accordance with the Standard Protocol Items: Recommendation For Interventional Trials (SPIRIT) checklist (Additional file 1). The trial has been registered at ClinicalTrials.gov (identifier NCT02346097), 12 January 2015. Patients were enrolled between 16 February 2015 and 13 December 2017. The study protocol has been approved by The Central Denmark Region Committees on Health Research Ethics and by the Danish Data Protection Agency. Both implantation strategies have previously been used in clinical settings and are not known to be associated with excess risks.

Baseline functional and clinical evaluation

Functional capacity and quality of life (QoL) are assessed by New York Heart Association (NYHA) classification [19], six-minute walk test (6MWT) [20], and Minnesota Living with Heart Failure Questionnaire (MLHFQ) using the official Danish version [21, 22].

Echocardiography

Echocardiography is performed at baseline and 6-month follow up (6MFU) using a 3.5-MHz transducer and a commercially available system (Vivid E9, GE, Horten, Norway). Electrocardiogram (ECG)-triggered, two-dimensional (2D), tissue Doppler images (TDI), and color Doppler images are obtained during breath hold. A frame rate of 50–80 frames per second is intended. Echocardiographic images are stored in cine-loop format and analyzed offline (EchoPac BT201, GE, Horten, Norway). All measurements are averaged over three cycles. Simpson’s bi-plane method is applied to assess LV volumes and LVEF [23].

The latest mechanically activated myocardial segment is determined by speckle-tracking radial strain analysis in the LV short-axis view in the basal and mid-LV imaging plane. According to the standardized LV segmentation [24], the LV short axis (SAX) is divided into six myocardial segments. Time from QRS onset to peak radial strain is measured in the basal and mid-LV segments (Fig. 3a). LV mechanical dyssynchrony is determined as the time delay between peak radial strain in the mid-LV antero-septal and the posterior segment [17]. Where radial strain analysis is not applicable in the LV SAX view (TDI), time-to-peak longitudinal strain analysis performed in the mid-LV segments in the A4Ch, A2ch and long-axis views are applied to identify the latest activated myocardial segment [25]. Echocardiograms will be analyzed by two observers, and interobserver and intraobserver variability will be reported.

Fig. 3
figure 3

Intervention group: electrical mapping. The local electrical activation delay is measured as time in milliseconds (ms) from QRS onset in the surface 12-lead electrocardiogram (ECG) to the maximum voltage change over time recorded in the local LV electrogram (EGM), reflecting the near-field activation of the myocardium according to the LV lead (QLV interval). The figure shows three examples of QLV measurements with the LV lead in a basal, mid, and apical position, exhibiting the longest QLV interval in the apical position. For simplicity, only the surface leads V2 and V6 and the local LV EGM (Pace 1–2) are shown

Assessment of cardiac venous anatomy and LV lead position by cardiac CT

A contrast enhanced (Optiray 350 mg/ml, Covidien, Ireland) high-pitch spiral CT scan (Siemens SOMATOM Definition Flash or Siemens SOMATOM Force, Siemens, Forchheim, Germany) is performed for pre-implant assessment of cardiac venous anatomy. Sublingual nitroglycerin is administered prior to the scan. Data are acquired with 80–140 kV tube voltage. The scans are performed ECG-gated with full pulsing only in diastole (65–80% of the RR interval), and during breath-hold. The time-tracking technique is applied to determine contrast filling in the LV cavity (20 ml for the test bolus and 50 ml for the scan). Two successive high-pitch spiral scans are performed at 15 and 19 s after peak contrast filling of the LV cavity.

The scan with the best CS visualization is used for study purposes. Images are reconstructed iteratively (Siemens SOMATOM Force) or with filtered back-projection (Siemens SOMATOM Flash). Image analysis is performed in Syngo.via, using the InSpace application (Siemens, Forchheim, Germany) for evaluation of multi-planar and three-dimensional (3D) images, respectively (Fig. 3b and c). Contrast enhanced (40 ml) high-pitch ECG-gated CT using the same scan protocol is performed the day after implantation to determine final LV lead position. Cardiac CT will not be performed in the minority of patients with depressed renal function with estimated glomerular filtration rate (eGFR) < 35 ml/min/1.73 m2., thyrotoxicosis or in the case of former severe reactions to the contrast medium.

Localization of the myocardial scar

Pre-implant ECG-gated Rb-PET is performed in all patients using a commercially available scanner (GE Healthcare, Buckinghamshire, UK). Briefly, intravenous injection of 1150 MBq rubidium is directly followed by a 7-min list mode scan of the heart. List mode data are subsequently re-binned into 27 dynamic frames (12 × 5, 6 × 10, 4 × 20, 4 × 40, and 1 × 60 s) and one static frame (2.5–7 min following initiation of the scan). Resting MP values are calculated from dynamic Rb PET/CT images and normalized for differences in rate pressure product (RPP) using an assumed population average value of 10,000 divided by the RPP. Data are analyzed using the commercially available automatic program Quantitative PET (Cedar-Sinai Medical Center, Los Angeles, CA, USA). Static data are displayed in polar map format and analyzed using the 17-segment model (Fig. 3d) [24]. Segments with a tracer uptake < 50% are considered as transmural scar tissue, those between 50 and 75% as non-transmural scar tissue, and those ≥ 75% are considered viable myocardium [26].

Randomization and blinding procedures

After baseline clinical evaluation and pre-implant imaging, patients are allocated either to the intervention or the control group. Study data are recorded in a web-based case record form (CRF) with logging of all data entries. The CRF is also used for randomization using computerized permuted blocks of different sizes. Randomization is stratified according to ischemic or non-ischemic heart failure etiology. An external data manager is responsible for the CRF and has programmed a computerized random-number generator.

Patients and physicians responsible for enrollment, baseline and follow-up clinical evaluation, including imaging acquisition, are blinded to the allocated treatment. Information about randomization is available only to the physician performing the implant. Data related to the device implantation, post-implant device-tests, and optimization are collected and entered into the CRF by the physicians performing the implantation and the dedicated research nurses, to ensure blinding of the investigator collecting clinical and imaging data. Information on the randomization code will be available when all patients have completed the 6MFU and all statistical analyses have been performed.

The applied strategies for cardiac resynchronization therapy

Intervention group: prior to implantation fluoroscopic venography is co-registered to the CT venography to ensure visualization of all available CS branches. During the implantation procedure, systematic electrical activation mapping of all available epicardial veins is performed using the LV electrode and/or a specialized mapping guidewire (Visionwire®, Biotronik, Berlin, Germany). Simultaneous local LV electrograms (EGM) and 12-lead surface ECGs are acquired (CardioLab IT, GE Healthcare). The local electrical activation delay is measured as the time interval from QRS onset in the surface ECG to the maximum voltage change over time recorded in the EGM, reflecting the near-field activation of the myocardium according to the LV lead (QLV interval) [12] (Fig. 4). The QLV interval is measured in the basal, mid and apical region of each CS branch. A quadripolar LV electrode will be used as first choice in all patients. The LV electrode is implanted at the site exhibiting the longest QLV interval (and thereby the latest local electrical activation) with acceptable pacing threshold and no diaphragmatic stimulation.

Fig. 4
figure 4

SPIRIT figure of the ElectroCRT study protocol. ECG, electrocardiogram; NYHA, New York Heart Association; MLHFQ, Minnesota Living with Heart Failure Questionnaire; 6MWT, 6-minute walk test; Rb-PET MP, rubidium positron emission tomography myocardial perfusion imaging; CT, computed tomography; VV, interventricular; AV, atrioventricular; LV, left ventricular; LVEF, left ventricular ejection fraction; LVESV, left ventricular end-systolic volume, CRT, cardiac resynchronization therapy; 6MFU, 6-month follow up; QoL, quality of life; Nt Pro-BNP, N-terminal prohormone of brain natriuretic peptide, LVEDV, left ventricular end-diastolic volume

Immediately after the implantation, the VVd settings are programmed by the physician performing the implantation, to obtain the narrowest QRS width. This is performed by measuring QRS width as the maximal QRS duration in any lead in the 12-lead ECG recorded at five different VVd settings: (1) right ventricle (RV) stimulation 20 ms prior to LV stimulation, (2) simultaneous biventricular pacing, (3) LV stimulation 20 ms prior to RV stimulation, (4) LV stimulation 40 ms prior to RV stimulation, and (5) LV stimulation 60 ms prior to RV stimulation.

Control group: prior to implantation the fluoroscopic venography is co-registered to the CT venography to visualize available CS branches. After combining information from echocardiography, Rb-PET, and cardiac CT, the LV electrode is targeted towards the CS branch closest to the latest mechanically activated non-scarred myocardial segment. Basal and mid-LV segments of the CS tributaries are prioritized separately according to the relation with basal and mid-LV segmental mechanical activation delay. CT images of cardiac venous anatomy are available to the physician performing the implantation in a 2D short-axis view and in 3D volume-rendered reconstructions. The CS tributary closest to the optimal LV pacing site is labeled as first priority for LV lead placement. Tributaries closest to the second, third, or fourth latest activated segment with viable myocardium are chosen as the second, third, or fourth priority [17].

In the imaging group, the VVd is programmed to simultaneous biventricular stimulation. In both treatment groups, atrioventricular (AV) optimization is performed the day after implantation using the iterative method ensuring maximal separation of the E-wave and A-wave without termination of the A-wave [27].

Endpoints

The primary endpoint is absolute change in left ventricular ejection fraction (LVEF) from baseline to 6MFU measured by 2D echocardiography. Secondary outcomes include relative percentage reduction in LV end-systolic volume (LVESV) and a combined clinical outcome measure of response to CRT at 6MFU defined as the patient being alive, not hospitalized for heart failure, and experiencing an improvement in NYHA functional class or/and > 10% increase in 6MWT [17]. Hospitalization for heart failure is defined as admission to hospital for more than 24 h with symptoms of congestive heart failure and need for intensified drug treatment for heart failure. Other secondary outcome measures include:

  • All-cause mortality.

  • Hospitalization for heart failure.

  • Implantation procedure time.

  • Procedural radiation exposure.

  • Device-related complications.

  • Indices of dyssynchrony and association between dyssynchrony, LV lead placement, and response to CRT.

  • Changes in QoL, NYHA functional class, 6MWT, N-terminal prohormone of brain natriuretic peptide (Nt Pro-BNP), QRS duration, LV end-diastolic volume (LVEDV), LVESV, LVEF, mechanical dyssynchrony, and LV lead parameters (pacing threshold, sensing value, impedance).

Sample size

We hypothesize that the intervention group strategy will result in an excess increase in LVEF of 4% compared with the strategy used in the control group, where an 8% increase in LVEF is expected [9]. To identify this absolute increase in LVEF of 12% in the intervention group and to achieve statistical power of 80%, the study will need a sample size of 98 patients, given a standard deviation (SD) of 7% in both groups, and a two-sided alpha value of 0.05. To achieve statistical power of 80% for the secondary endpoint of relative reduction in LVESV a sample size of 116 patients is needed, when assuming a 33% reduction in the control group and a 45% reduction in the intervention group (expected SD of 23% in both groups and given a two-sided alpha value of 0.05%). To achieve statistical power of > 80% with a margin of non-inferiority of 20% for the secondary endpoint of clinical response to CRT (assuming a 75% clinical response rate in the control group) we will need a sample size of 116 patients (given a two-sided alpha value of 0.05%). Taking into consideration expected loss to follow up in approximately 5% of patients, 122 patients are included.

Statistical analysis

All analyses will be conducted according to the intention-to-treat principle and will be performed before breaking the randomization code. Baseline characteristics are presented and compared clinically. Primary and secondary endpoints will be analyzed using linear regression for continuous variables and logistic regression for binary outcome measures, including heart failure etiology as a variable in the model. Multivariate regression analysis will be reported for absolute change in LVEF including baseline LVEF, heart failure etiology, sex, and baseline QRS width as covariates. Predictors of missing outcome values will be identified by comparing baseline characteristics and will be included in a multivariate regression model for sensitivity analysis. Intraclass correlation coefficients are computed to assess intraobserver and interobserver agreement for the echocardiographic parameters included in the primary endpoint: LVEF, LVEDV, LVESV assessed for 20 echocardiograms. A two-sided P value < 0.05 is considered significant.

Discussion

Electrically guided CRT strategy

Positioning of the LV lead according to the latest activated myocardial segment has been shown to be an important determinant of response to CRT. In this current study, the strategy is to target the myocardial region with the latest electrical activation. The advantage of this approach is that the electrical data obtained from mapping are readily available during the implant procedure without the need for alignment of imaging modalities to target a specific myocardial segment. Several observational studies indicate that a LV lead location in regions with late electrical activation is associated with improved clinical outcome and reverse remodeling [12, 13, 28]. No randomized studies have evaluated the impact of systematic electrical mapping of available CS branches to target the segment with the latest electrical activation. In addition, post-implant device programming in the VVd producing the shortest biventricular paced QRS duration will be applied to optimize the electrical resynchronization suggested to increase the response to CRT [16]. The impact of this combined electrical CRT optimization strategy has not previously been evaluated.

Imaging-guided LV lead placement

Randomized studies have demonstrated that targeting LV lead placement towards the latest mechanically activated non-scarred myocardial area as assessed by speckle-tracking echocardiography strain analysis improves clinical outcome and LV reverse remodeling compared with a routine anatomical approach targeting the non-apical posterolateral region [9, 11]. Similar findings have been observed using a multimodality imaging-guided approach combining speckle-tracking echocardiography, MP imaging, and cardiac CT to target the cardiac vein closest to the latest contracting non-scarred myocardial region [10, 17]. However, echocardiographic measurement of the myocardial mechanical activation pattern may be difficult to align with fluoroscopic imaging during the implant procedure [29] and may have substantial degree of interobserver variability [30]. Furthermore, pre-implant imaging is costly and time consuming.

Due to the superior outcome associated with the imaging-guided approach as compared with conventional LV lead placement [9,10,11], we applied the imaging-guided approach as our control group strategy. This was done to evaluate the potential benefit of the simpler electrically guided CRT optimization strategy not limited by the need for pre-implant imaging and alignment of imaging modalities.

Methods used in the ElectroCRT study

The extent of myocardial scar tissue is inversely related to the response to CRT [31] and placement of the LV lead in a myocardial region with scar tissue is associated with poor CRT outcome [32]. Rb-PET is well-established for visualizing regions [26, 33] and distribution of myocardial scar [34], but it has lower spatial resolution than cardiac magnetic resonance (MR). However, we chose to assess scar with MP imaging, as a substantial proportion of our patients are not eligible for cardiac MR due to an indwelling device. Myocardial scar as detected by MP imaging is not considered in the electrically guided intervention group when implanting the LV lead, to ensure complete separation of the electrically and imaging-guided strategy.

Pre-implant cardiac CT is applied to assess CS anatomy as potentially available CS tributaries may be missed during fluoroscopic balloon occlusive angiography and to ease planning implantation of the LV lead. Post-implant cardiac CT is performed to determine the final LV pacing site because fluoroscopy has been shown to be inaccurate and poorly reproducible for this purpose [35].

Choice of endpoint

Considering the complex design, this trial would be difficult to conduct as a multi-center study, and therefore it does not have statistical power to investigate differences between groups in “harder” endpoints such as survival or hospitalization due to heart failure. We chose LVEF as the primary endpoint, because it is a commonly used and universally understood echocardiographic measure of LV systolic function, which furthermore is a good predictor of survival in patients with CRT [36]. Accordingly, the findings in this study may generate hypotheses to be tested in future larger-scale, multi-center, randomized studies.

Limitations of the ElectroCRT study

We acknowledge the inherent limitations of a single-center study design. Nevertheless, the double-blinded, randomized, controlled trial design for comparing two advanced strategies for CRT optimization is the strongest research instrument to investigate a difference in outcome caused by these interventions.

We do not merge the applied imaging modalities and the procedural fluoroscopy in the control group. However, we use the standard myocardial segmentation [24] to ease an approximated alignment of the echocardiography, MP imaging, 2D and 3D cardiac CT reconstructions of cardiac venous anatomy and procedural fluoroscopy [10].

The introduction of cardiac CT and Rb-PET prior to CRT will increase the patient’s cumulative radiation exposure. Several approaches to minimize radiation dose are applied in this study, including the use of iterative reconstruction algorithms, application of prospectively triggered high-pitch CT scans, individual settings of tube voltage and current, and the use of Rb-PET for MP imaging, respectively. Furthermore, the utility and potential benefits of participating in this study are expected to equalize the risks of exposure to ionizing radiation, possible adverse effects, and inconvenience to the patients.

Perspective

No randomized trial has investigated the effect of a CRT implant-strategy targeting optimal electrical resynchronization achieved by guiding LV lead placement to the myocardial region with the latest electrical activation combined with post-implant VVd optimization for narrowing the paced QRS width. If an excess increase in LVEF is achieved by LV lead implantation guided by systematic electrical mapping followed by VVd optimization for narrowing paced QRS, this study supports the conduct of larger, multicenter, randomized clinical trials investigating the impact of electrically guided LV lead implantation on clinical outcomes in patients treated with CRT.

Trial status

Patients were enrolled between 16 February 2015 and 13 December 2017. The current protocol article was submitted to Trials before all patients were enrolled and before analyzing any data and breaking the randomization code.

Abbreviations

2D:

Two-dimensional

3D:

Three-dimensional

6MFU:

Six-month follow-up

6MWT:

Six-minute walk test

AIV:

Anterior interventricular vein

Ant:

Anterior

Ant-Sept:

Antero-septal

AV:

Atrioventricular

CABG:

Coronary artery bypass Graft

CRF:

Case record form

CRT:

Cardiac resynchronization therapy

CRT-D:

Cardiac resynchronization therapy defibrillator

CRT-P:

Cardiac resynchronization therapy pacemaker

CS:

Coronary sinus

CT:

Computed tomography

ECG:

Electrocardiogram

eGFR:

Estimated glomerular filtration Rate

EGM:

Electrogram

Inf:

Inferior

LAD:

Left anterior descending artery

Lat:

Lateral

LBBB:

Left bundle branch block

LMA:

Left marginal artery (circumflex artery branch)

LMV:

Left marginal vein

LVEDV:

Left ventricular end-diastolic volume

LVEF:

Left ventricular ejection fraction

LVESV:

Left ventricular end-systolic volume

MBq:

Mega Becquerel

MCV:

Middle cardiac vein

mHz:

Megahertz

ml:

Milliliters

MLHFQ:

Minnesota Living with Heart Failure Questionnaire

MP:

Myocardial perfusion

MR:

Magnetic resonance

ms:

Milliseconds

Nt Pro-BNP:

N-terminal prohormone of brain natriuretic peptide

NYHA:

New York Heart Association

OMT:

Optimal medical treatment

PDA:

Posterior descending artery (right coronary artery branch)

PLA:

Posterolateral artery

Post:

Posterior

PV:

Posterior vein

QLV interval:

The interval from onset of the QRS on the surface 12-lead ECG to the maximum voltage change over time recorded in the EGM, reflecting the near-field activation of the myocardium according to the LV lead

QoL:

Quality of life

Rb-PET:

82Rubidium positron emission tomography

RCA:

Right coronary artery

RV:

Right ventricle/right ventricular

SAX:

Short axis view

Sept:

Septal

SPIRIT:

Standard Protocol Items: Recommendation For Interventional Trials

TDI:

Tissue Doppler Images

VVd:

Interventricular pacing delay

References

  1. Abraham WT, Fisher WG, Smith AL, Delurgio DB, Leon AR, Loh E, et al. Cardiac resynchronization in chronic heart failure. N Engl J Med. 2002;346(24):1845–53.

    Article  Google Scholar 

  2. Bristow MR, Saxon LA, Boehmer J, Krueger S, Kass DA, De Marco T, et al. Cardiac-resynchronization therapy with or without an implantable defibrillator in advanced chronic heart failure. N Engl J Med. 2004;350(21):2140–50.

    Article  CAS  Google Scholar 

  3. Cleland JG, Daubert JC, Erdmann E, Freemantle N, Gras D, Kappenberger L, et al. The effect of cardiac resynchronization on morbidity and mortality in heart failure. N Engl J Med. 2005;352(15):1539–49.

    Article  CAS  Google Scholar 

  4. European Society of Cardiology (ESC), European Heart Rhythm Association (EHRA), Brignole M, Auricchio A, Baron-Esquivias G, Bordachar P, et al. ESC guidelines on cardiac pacing and cardiac resynchronization therapy: the task force on cardiac pacing and resynchronization therapy of the European Society of Cardiology (ESC). Developed in collaboration with the European Heart Rhythm Association (EHRA). Europace. 2013;15(8):1070–118.

    Article  Google Scholar 

  5. Kirkfeldt RE, Johansen JB, Nohr EA, Jorgensen OD, Nielsen JC. Complications after cardiac implantable electronic device implantations: an analysis of a complete, nationwide cohort in Denmark. Eur Heart J. 2014;17(18):1186–94.

    Article  Google Scholar 

  6. Kronborg MB, Mortensen PT, Kirkfeldt RE, Nielsen JC. Very long term follow-up of cardiac resynchronization therapy: clinical outcome and predictors of mortality. Eur J Heart Fail. 2008;10(8):796–801.

    Article  Google Scholar 

  7. Yu CM, Sanderson JE, Gorcsan J 3rd. Echocardiography, dyssynchrony, and the response to cardiac resynchronization therapy. Eur Heart J. 2010;31(19):2326–37.

    Article  Google Scholar 

  8. Mullens W, Grimm RA, Verga T, Dresing T, Starling RC, Wilkoff BL, et al. Insights from a cardiac resynchronization optimization clinic as part of a heart failure disease management program. J Am Coll Cardiol. 2009;53(9):765–73.

    Article  Google Scholar 

  9. Khan FZ, Virdee MS, Palmer CR, Pugh PJ, O'Halloran D, Elsik M, et al. Targeted left ventricular lead placement to guide cardiac resynchronization therapy: the TARGET study: a randomized, controlled trial. J Am Coll Cardiol. 2012;59(17):1509–18.

    Article  Google Scholar 

  10. Sommer A, Kronborg MB, Norgaard BL, Poulsen SH, Bouchelouche K, Bottcher M, et al. Multimodality imaging-guided left ventricular lead placement in cardiac resynchronization therapy: a randomized controlled trial. Eur J Heart Fail. 2016;18(11):1365–74.

    Article  Google Scholar 

  11. Saba S, Marek J, Schwartzman D, Jain S, Adelstein E, White P, et al. Echocardiography-guided left ventricular lead placement for cardiac resynchronization therapy: results of the Speckle Tracking Assisted Resynchronization Therapy for Electrode Region trial. Circ Heart Fail. 2013;6(3):427–34.

    Article  CAS  Google Scholar 

  12. Gold MR, Birgersdotter-Green U, Singh JP, Ellenbogen KA, Yu Y, Meyer TE, et al. The relationship between ventricular electrical delay and left ventricular remodelling with cardiac resynchronization therapy. Eur Heart J. 2011;32(20):2516–24.

    Article  Google Scholar 

  13. Kandala J, Upadhyay GA, Altman RK, Parks KA, Orencole M, Mela T, et al. QRS morphology, left ventricular lead location, and clinical outcome in patients receiving cardiac resynchronization therapy. Eur Heart J. 2013;34(29):2252–62.

    Article  Google Scholar 

  14. Kronborg MB, Nielsen JC, Mortensen PT. Electrocardiographic patterns and long-term clinical outcome in cardiac resynchronization therapy. Europace. 2010;12(2):216–22.

    Article  Google Scholar 

  15. Tamborero D, Vidal B, Tolosana JM, Sitges M, Berruezo A, Silva E, et al. Electrocardiographic versus echocardiographic optimization of the interventricular pacing delay in patients undergoing cardiac resynchronization therapy. J Cardiovasc Electrophysiol. 2011;22(10):1129–34.

    Article  Google Scholar 

  16. Tamborero D, Mont L, Sitges M, Silva E, Berruezo A, Vidal B, et al. Optimization of the interventricular delay in cardiac resynchronization therapy using the QRS width. Am J Cardiol. 2009;104(10):1407–12.

    Article  Google Scholar 

  17. Sommer A, Kronborg MB, Poulsen SH, Bottcher M, Norgaard BL, Bouchelouche K, et al. Empiric versus imaging guided left ventricular lead placement in cardiac resynchronization therapy (ImagingCRT): study protocol for a randomized controlled trial. Trials. 2013;14:113–6215–14-113.

    Article  Google Scholar 

  18. WMA: Declaration of Helsinki - ethical principles for medical research involving human subjects. https://www.wma.net/policies-post/wma-declaration-of-helsinki-ethical-principles-for-medical-research-involving-human-subjects/.

  19. The Criteria Committee of the New York Heart Association. Nomenclature and criteria for diagnosis and diseases of the heart and great vessels. Boston: Little Brown; 1964.

    Google Scholar 

  20. ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories. ATS statement: guidelines for the six-minute walk test. Am J Respir Crit Care Med. 2002;166(1):111–7.

    Article  Google Scholar 

  21. Rector TS, Tschumperlin LK, Kubo SH, Bank AJ, Francis GS, McDonald KM, et al. Use of the Living With Heart Failure questionnaire to ascertain patients' perspectives on improvement in quality of life versus risk of drug-induced death. J Card Fail. 1995;1(3):201–6.

    Article  CAS  Google Scholar 

  22. Rector TS, Anand IS, Cohn JN. Relationships between clinical assessments and patients’ perceptions of the effects of heart failure on their quality of life. J Card Fail. 2006;12(2):87–92.

    Article  Google Scholar 

  23. Schiller NB, Shah PM, Crawford M, DeMaria A, Devereux R, Feigenbaum H, et al. Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms. J Am Soc Echocardiogr. 1989;2(5):358–67.

    Article  CAS  Google Scholar 

  24. Cerqueira MD, Weissman NJ, Dilsizian V, Jacobs AK, Kaul S, Laskey WK, et al. Standardized myocardial segmentation and nomenclature for tomographic imaging of the heart. A statement for healthcare professionals from the Cardiac Imaging Committee of the Council on Clinical Cardiology of the American Heart Association. Circulation. 2002;105(4):539–42.

    Article  Google Scholar 

  25. Murphy RT, Sigurdsson G, Mulamalla S, Agler D, Popovic ZB, Starling RC, et al. Tissue synchronization imaging and optimal left ventricular pacing site in cardiac resynchronization therapy. Am J Cardiol. 2006;97(11):1615–21.

    Article  Google Scholar 

  26. vom Dahl J, Muzik O, Wolfe ER Jr, Allman C, Hutchins G, Schwaiger M. Myocardial rubidium-82 tissue kinetics assessed by dynamic positron emission tomography as a marker of myocardial cell membrane integrity and viability. Circulation. 1996;93(2):238–45.

    Article  CAS  Google Scholar 

  27. Gorcsan J 3rd, Abraham T, Agler DA, Bax JJ, Derumeaux G, Grimm RA, et al. Echocardiography for cardiac resynchronization therapy: recommendations for performance and reporting–a report from the American Society of Echocardiography Dyssynchrony Writing Group endorsed by the Heart Rhythm Society. J Am Soc Echocardiogr. 2008;21(3):191–213.

    Article  Google Scholar 

  28. Liang Y, Yu H, Zhou W, Xu G, Sun YI, Liu R, et al. Left ventricular lead placement targeted at the latest activated site guided by electrophysiological mapping in coronary sinus branches improves response to cardiac resynchronization therapy. J Cardiovasc Electrophysiol. 2015;26(12):1333–9.

    Article  Google Scholar 

  29. Behar JM, Claridge S, Jackson T, Sieniewicz B, Porter B, Webb J, et al. The role of multi modality imaging in selecting patients and guiding lead placement for the delivery of cardiac resynchronization therapy. Expert Rev Cardiovasc Ther. 2017;15(2):93–107.

    Article  CAS  Google Scholar 

  30. Chung ES, Leon AR, Tavazzi L, Sun JP, Nihoyannopoulos P, Merlino J, et al. Results of the Predictors of Response to CRT (PROSPECT) trial. Circulation. 2008;117(20):2608–16.

    Article  Google Scholar 

  31. Ypenburg C, Schalij MJ, Bleeker GB, Steendijk P, Boersma E, Dibbets-Schneider P, et al. Impact of viability and scar tissue on response to cardiac resynchronization therapy in ischaemic heart failure patients. Eur Heart J. 2007;28(1):33–41.

    Article  Google Scholar 

  32. Delgado V, van Bommel RJ, Bertini M, Borleffs CJ, Marsan NA, Arnold CT, et al. Relative merits of left ventricular dyssynchrony, left ventricular lead position, and myocardial scar to predict long-term survival of ischemic heart failure patients undergoing cardiac resynchronization therapy. Circulation. 2011 Jan 4;123(1):70–8.

    Article  Google Scholar 

  33. Anagnostopoulos C, Georgakopoulos A, Pianou N, Nekolla SG. Assessment of myocardial perfusion and viability by positron emission tomography. Int J Cardiol. 2013;167(5):1737–49.

    Article  Google Scholar 

  34. Qayyum AA, Hasbak P, Larsson HB, Christensen TE, Ghotbi AA, Mathiasen AB, et al. Quantification of myocardial perfusion using cardiac magnetic resonance imaging correlates significantly to rubidium-82 positron emission tomography in patients with severe coronary artery disease: a preliminary study. Eur J Radiol. 2014;83(7):1120–8.

    Article  Google Scholar 

  35. Sommer A, Kronborg MB, Norgaard BL, Gerdes C, Mortensen PT, Nielsen JC. Left and right ventricular lead positions are imprecisely determined by fluoroscopy in cardiac resynchronization therapy: a comparison with cardiac computed tomography. Europace. 2014;30(9):1334–41.

    Article  Google Scholar 

  36. Solomon SD, Foster E, Bourgoun M, Shah A, Viloria E, Brown MW, et al. Effect of cardiac resynchronization therapy on reverse remodeling and relation to outcome: multicenter automatic defibrillator implantation trial: cardiac resynchronization therapy. Circulation. 2010;122(10):985–92.

    Article  Google Scholar 

  37. Strauss DG, Selvester RH, Wagner GS. Defining left bundle branch block in the era of cardiac resynchronization therapy. Am J Cardiol. 2011;107:927–34.

    Article  Google Scholar 

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Acknowledgements

The authors would like to thank the physicians Henrik Kjærulf Jensen, Jens Kristensen, and Jens Christian Gerdes who contributed by implantation of the CRTs; Kirsten Andersen, Sonja Runge, and Rita Møhl for their work and expertise on pacemaker programming; Heidi Grønhøi and Henriette Holmberg for study coordination, and the Department of Nuclear Medicine, Aarhus University Hospital, for conducting the MP imaging.

Funding

The study is supported by unrestricted grants from the Danish Heart Foundation (grant number 14-R97-A5149–22865 and 15-R99-A5878–22937) and the Health Research Fund of the Central Denmark Region for the salary of the primary investigator. Half of the MP images are funded by Department of Nuclear Medicine, Aarhus University Hospital, Aarhus, Denmark. The protocol for this study has not been influenced in any way by the sponsors.

Availability of data and materials

The full protocol for the study will be available from the corresponding author. Datasets generated and/or analyzed during the current study will not be publicly available due to data privacy. However, data will be available from the corresponding author on reasonable request. The primary investigator and coauthors will have access to the final dataset for 10 years after enrollment of all patients. Thereafter, the material will be destroyed, according to the rules from The Central Denmark Region Committees on Health Research Ethics and by the Danish Data Protection Agency. Requiring a request on the written informed consent at enrollment, trial participants will be informed about the study outcome, when the trial has come to an end. Results from the trial will be published in peer-reviewed international journals and positive, negative, and inconclusive results will be published.

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Authors and Affiliations

Authors

Contributions

CS contributed to conception and design of the study, conducted data acquisition, and drafted the manuscript. AS contributed to conception and design of the study, conducted data acquisition, and was involved in drafting and revising the manuscript. MBK contributed to conception and design of the study, conducted data acquisition, and was involved in drafting and revising the manuscript. JMJ contributed to data acquisition and was involved in drafting and revising the manuscript. KB contributed to data acquisition and was involved in drafting and revising the manuscript. JCO contributed to conception and design of the study, conducted data acquisition, and was involved in drafting and revising the manuscript. All authors have read and approved the final version of the manuscript.

Corresponding author

Correspondence to Charlotte Stephansen.

Ethics declarations

Ethics approval and consent to participate

The study protocol has been approved by The Central Denmark Region Committees on Health Research Ethics (case number 1–10–72-230-14) (Additional file 1) and by the Danish Data Protection Agency (case number 1–16–02-622-14). All patients give informed written consent prior to enrolment in the study.

Consent for publication

Not applicable as images were anonymized.

Competing interests

CS has attended a conference supported by St Jude Medical. JCO is supported by a grant from the Novo Nordisk Foundation (NNF16OC0018658). MBK has received a speaker’s fee from Biotronik. The other authors have no competing interests.

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Additional file

Additional file 1:

SPIRIT checklist of the ElectroCRT study protocol. (PDF 174 kb)

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Stephansen, C., Sommer, A., Kronborg, M.B. et al. Electrically guided versus imaging-guided implant of the left ventricular lead in cardiac resynchronization therapy: a study protocol for a double-blinded randomized controlled clinical trial (ElectroCRT). Trials 19, 600 (2018). https://doi.org/10.1186/s13063-018-2930-y

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