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Survival of Patients With Primary Prophylactic ICD Indication

Survival of Patients With Primary Prophylactic ICD Indication, Provided With Intensified Care After 1st ICD Therapy

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00619593
Acronym
SPIRIT-ICD
Enrollment
504
Registered
2008-02-21
Start date
2008-02-29
Completion date
2014-07-31
Last updated
2015-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Prevention, Sudden Cardiac Death, Tachycardia, Ventricular

Keywords

Heart failure, Ventricular Fibrillation, Sudden cardiac death, Hospitalization due to heart failure, Implantable cardioverter-defibrillator, Risk of 1st heart failure hospitalization

Brief summary

The MADIT-II trial has shown that patients with severely reduced left ventricular ejection fraction (LVEF) post myocardial infarction benefit from the implantable cardioverter-defibrillator (ICD). However, retrospective analyses of the MADIT-II data have revealed a significantly increased morbidity and mortality in patients with appropriate ICD therapy: Appropriate ICD therapy is associated with 3.3-fold increased all-cause mortality, and the risk of a first heart failure hospitalization is 90% higher after 1st appropriate ICD therapy. Hence, the 1st appropriate therapy might indicate the necessity and utility of further clinical diagnostics and therapy in these patients. This trial is designed to (i) improve the knowledge of the group characteristics of patients suffering from 1st appropriate ICD therapy, (ii) but moreover to take additional therapeutic steps to reduce the mortality of this patient population.

Detailed description

The MADIT-II trial has shown that patients with severely reduced left ventricular ejection fraction (LVEF) post myocardial infarction benefit from the implantable cardioverter-defibrillator (ICD). However, retrospective analyses of the MADIT-II data have revealed a significantly increased morbidity and mortality in patients with appropriate ICD therapy: Appropriate ICD therapy is associated with 3.3-fold increased all-cause mortality, and the risk of a first heart failure hospitalization is 90% higher after 1st appropriate ICD therapy. Hence, the 1st appropriate therapy might indicate the necessity and utility of further clinical diagnostics and therapy in these patients. This trial is designed to (i) improve the knowledge of the group characteristics of patients suffering from 1st appropriate ICD therapy, (ii) but moreover to take additional therapeutic steps to reduce the mortality of this patient population. After standard ICD implantation procedure, the following steps are performed at the pre-discharge follow-up: * Programming: VR-T: VVI 40 ppm, Onset 20%, Stability 20 ms * DR-T: DDD 50-60 ppm, activation of IRSplus and SMART * HF-T: DDD-BiV 50-60 ppm, achieve at least 85% biventricular resynchronisation, activation of SMART * All devices: VT zone as therapy zone, VF zone. Programming recommendations for VT/VF zones to standardize treatment: * VF zone: 200-250 bpm/ 300-240 ms, ATPoneshot ON * VT1 zone: 167-200 bpm/ 360-300 ms, ATP ON * VT2 zone: 120-167 bpm/ 500-360 ms, ATP ON * Activation of Home Monitoring (HM) and online registration for HM service Standard Follow-up: Timing and scope of follow-up in patients without episodes is to the physician's own discretion and should follow the standard clinical routine. Follow-up after 1st appropriate ICD therapy: Immediately after having received the 1st appropriate ICD therapy, the patients have to be called to the clinic for intensified clinical diagnostics and, if necessary or useful, intensified therapy. Standard ICD follow-up has to be started within 72 hours after 1st appropriate ICD therapy. * ICD interrogation * General health status (weight, BP, NYHA) * Laboratory tests (hemoglobin, Nt-proBNP, creatinine, GDF-15) * Echocardiography (LVEF, LVEDD, mitral regurgitation) * Non-invasive ischemia evaluation * Coronary angiography (if indicated by ischemia evaluation) * Upgrade to CRT, if indicated * Ventricular ablation (if indicated: VT storm, slow VT, bundle branch reentry) * 24 hrs ECG Holter (Heart rate variability) * Further treatment (if applicable) * Changes in ICD settings, or medication * Adverse events / adverse device effects Final follow-up visit: For patients without appropriate ICD therapy, the final follow-up shall be performed 12 months after enrolment. For patients with appropriate ICD therapy, the final follow-up shall be performed 12 months after 1st appropriate ICD therapy. The final follow-up visit comprises: * ICD interrogation * General health status (weight, BP, NYHA) * Echocardiography (LVEF, LVEDD, mitral regurgitation) * Laboratory tests (hemoglobin, Nt-proBNP, creatinine, GDF-15) * 24 hrs ECG Holter (Heart rate variability) * Further treatment (if applicable) * Changes in ICD settings, or medication * Adverse events / adverse device effects

Interventions

OTHERIntensified diagnostic and treatment measures following 1st appropriate ICD therapy

* Assessment of general health status (weight, BP, NYHA) * Laboratory tests (hemoglobin, Nt-proBNP, creatinine, GDF-15) * Echocardiography (LVEF, LVEDD, mitral regurgitation) * Non-invasive ischemia evaluation * Coronary angiography (if indicated by ischemia evaluation) * Upgrade to CRT, if indicated * Ventricular ablation (if indicated: VT storm, slow VT, bundle branch reentry) * 24 hrs ECG Holter (Heart rate variability) * Further treatment (if applicable) * Changes in ICD settings, or medication

OTHERStandard follow-up

Standard follow-up in patients without appropriate ICD therapy

Sponsors

Biotronik SE & Co. KG
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Indication for ICD implantation according to MADIT-II: * Myocardial infarction 30 days or more before implantation * LVEF of 30% or less within 3 months before implantation * Angiography within the preceding 12 months * The patient is willing and able to comply with the clinical investigation plan and has provided written informed consent

Exclusion criteria

* Patients with contraindication for ICD implantation * Conventional ICD indication (i.e. other than MADIT-II) * Myocardial infarction within the past 30 days * Coronary revascularisation within the preceding 3 months (i.e., if revascularization has been performed wait at least 3 months until enrolment, given that no appropriate/ inappropriate ICD therapy has occured) * NYHA functional class IV * Unexplained syncope within 3 years * Advanced cerebrovascular disease * Life expectancy very probably below 12 months * Pregnant or breast-feeding women * Age \< 18 years * Patients who are already enrolled in another study (therapy/intervention phase)

Design outcomes

Primary

MeasureTime frame
Mortality12 months

Secondary

MeasureTime frame
Sudden cardiac death12 months
Non-sudden cardiac death12 months
Risk of 1st heart failure hospitalization12 months
No. of VT Storms (> 3 VT/24h)12 months
No. of delivered ICD therapies12 months

Countries

Austria, Czechia, Germany, Hungary, Israel, Latvia, New Zealand, Poland, Slovakia, Spain, Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026