The Effect of CRT on the Frank Starling Mechanism
Study Details
Study Description
Brief Summary
The investigators are examining a scientific principle called the Frank Starling Mechanism and how it relates to Cardiac Resynchronisation Therapy (CRT), a form of pacemaker therapy used in the treatment of heart failure.
The Frank Starling Mechanism is an established biological principle. The law states that the stroke volume of the heart increases in response to an increase in the volume of blood in the ventricles, before contraction, when all other factors remain constant. In other words, the law states that the more blood enters the heart, the more blood is pumped out of the heart with any given beat.
There is some evidence that in some patients with chronic heart conditions, the Frank Starling Mechanism is LESS EFFECTIVE, meaning that the heart is less able to cope with a reduction in heart pumping function over time. There is also evidence that treatment with CRT may IMPROVE the Frank Starling Mechanism - evidence for this has been shown in dog and mice hearts, however, has never been shown in humans.
The investigators aim to conduct a study where subjects undergo an ultrasound scan of the heart (echocardiogram) whilst the participants pacemaker settings are temporarily changed. This allows the investigators to measure the pumping function of the heart as more blood enters the heart. The investigators will perform this test on 20 participants before and after CRT, as well as 20 participants who have pacemakers, but no heart failure. This study aims to test 3 hypotheses.
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In participants with pacemakers, a REDUCED Frank Starling Mechanism predicts which participants go on to develop heart failure.
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Treatment with CRT IMPROVES the Frank Starling Mechanism in participants with pacemakers and heart failure.
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The degree of improvement of the Frank Starling Mechanism after treatment with CRT predicts which participants will respond to this treatment.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
The primary research investigation in this study is a non-invasive test of the Frank Starling mechanism, which involves performing a transthoracic echocardiogram (ultrasound scan of the heart) whilst temporarily changing pacemaker settings to mimic conditions such as faster heart rates or increased blood flow to the heart. Measurements taken from the echocardiogram during these changes in pacemaker settings will be used to determine the effectiveness of the heart's Starling Mechanism. This test will last between 20-40 minutes. No special preparation is needed and participants will be able to go home immediately afterwards. Pacemaker settings will be returned to normal once the test is completed.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: CRT Group CRT group: We will include patients with symptomatic heart failure (LV ejection fraction <35% on TTE, NYHA II-IV) and an RV pacing percentage of >40%, thus meeting ESC Criteria for CRT upgrade. |
Other: Test Of The Frank Starling Mechanism - Adjustment Of Av Delay And Measurement Of Pre-load -Control
(Control Group): One test of the Starling mechanism Visit 1: Sign consent form, doctor assessment, electrocardiogram (ECG), Starling Test. If patients are in this category, this will be their only research visit
|
| Active Comparator: Control Group Control group: patients with an existing dual chamber pacemaker and with preserved ejection fraction |
Other: Other: Test Of The Frank Starling Mechanism - Adjustment Of Av Delay And Measurement Of Pre-load -CRT
(CRT Group): Two tests of the Starling mechanisms Visit 1: Sign consent form, assessment by doctor, electrocardiogram (ECG), Test of the Starling mechanism Visit 2: CRT upgrade procedure - your Cardiologist will explain this procedure to you. Visit 3: CRT pacing check at 6 weeks post-procedure Visit 4: Assessment by doctor, ECG, Echocardiogram, Test of the Starling mechanism at 6 months post-procedure.
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Outcome Measures
Primary Outcome Measures
- Difference in starling mechanism [Prior to pacing test (starling mechanism test) and after six months]
1. Difference in maximum change in stroke volume (SV) in millilitres with AV delay modification "Starling mechanics" pre-CRT versus post-CRT (difference between lowest and highest SV).
Secondary Outcome Measures
- Left ventricular end-systolic volume (ml) [Prior to pacing test (starling mechanism test) and after six months]
Difference in left ventricular end-systolic volume in millimetres recorded on echocardiogram
- Left ventricular ejection fraction (%) [Prior to pacing test (starling mechanism test) and after six months]
Difference in Left ventricular ejection fraction in percent measured on echocardiogram
- Quality of life with heart failure symptoms [Prior to pacing test (starling mechanism test) and after six months]
Quality of life in heart failure assessed by Minnesota Living with Heart Failure Questionnaire
- Heart failure symptoms [Prior to pacing test (starling mechanism test) and after six months]
New York Heart Association ( NYHA) class - breathlessness on different levels of exercise - from walking on the flat (NYHA 2) up to limited by breathlessness on little movement (NYHA 4)
- Packer's clinical composite score [Prior to pacing test (starling mechanism test) and at six months]
Difference in patient outcome measured by the clinical composite score - the score ranges from improved to unchanged or worsened
- Difference in baseline Starling mechanics between CRT group and control group [Prior to pacing test (starling mechanism test) and at six months]
Difference in stroke volume in millilitres during the pacing test (starling mechanism test) between the CRT and control group
Eligibility Criteria
Criteria
Inclusion Criteria:
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• Ability to provide informed consent to participate and willing to comply with the clinical investigation plan and follow-up schedule.
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Existing dual chamber pacemaker or ICD including atrial lead and RV lead.
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RV pacing percentage >40%.
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CRT group - Severe left ventricular systolic impairment (LVEF≤35%). Clinical symptoms of heart failure despite optimum medical therapy (NYHA class II-IV).
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Control group - LVEF >50%.
Exclusion Criteria:
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• Previous treated with CRT (existing LV lead/His-Bundle lead/Left Bundle Branch Area lead).
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Persistent atrial fibrillation
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Female participants who are pregnant, lactating or planning pregnancy during the course of the study.
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Participation in other studies with active treatment / investigational arm
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Guy's and St Thomas' NHS Trust | London | United Kingdom | SE1 7EH |
Sponsors and Collaborators
- Guy's and St Thomas' NHS Foundation Trust
- King's College London
Investigators
- Principal Investigator: Christopher Aldo Rinaldi/Professor, MD, FHRS, Guy's and St Thomas' NHS Trust
- Principal Investigator: Steven Niederer/Professor, PhD, King's College London
Study Documents (Full-Text)
None provided.More Information
Publications
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