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Quantitative Assessment of Hypertrophic Obstructive Cardiomyopathy With Intraoperative Three-dimensional Transesophageal Echocardiography Under Provocative Dobutamine Stress Test

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University Health Network, Toronto

Status and phase

Not yet enrolling
Phase 4

Conditions

Hypertrophic Obstructive Cardiomyopathy

Treatments

Drug: Pre and post-CPB Drug: Dobutamine Hydrochloride
Drug: Post-CPB Drug: Dobutamine Hydrochloride

Study type

Interventional

Funder types

Other

Identifiers

NCT05025644
16-5412

Details and patient eligibility

About

The objectives of this study are to determine if the left ventricle outflow tract (LVOT) gradients may be reproduced with dobutamine (DBT) provocation test in obstructive HCM patients under general anesthesia and to analyze the change in anatomic LVOT area and pressure gradients (PG) before and after septal myectomy.

If the DBT stress test can reproduce preoperative gradients in HCM patients during septal myectomy surgery, surgeons will have the opportunity to assess the quality of the surgical procedure depending on the obtained gradients with DBT stress test after surgery when gradients can't be reproduced during general anesthesia after myectomy, and decide if further myectomy is required, saving a re-operation on the patient in the future.

Full description

Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiomyopathy. Echocardiography is the noninvasive method of choice for the evaluation of morphologic and functional abnormalities in HCM. It is of paramount importance to distinguish between obstructive or non-obstructive HCM, based on the presence or absence of left ventricle outflow tract (LVOT) gradient using continuous wave Doppler (CWD), under resting and/or provocable conditions. HCM can then be divided into three different subgroups. When the gradient at rest is ≥ 30 mmHg the HCM is considered obstructive (HOCM); when the gradient is <30 mmHg at rest but ≥ 30 mmHg with provocation, the HCM is considered latent obstructive, and finally, non-obstructive occurs when the gradient is < 30mmHg at rest or with provocation.

The gold standard technique to treat symptomatic HOCM is the surgical transaortic septal myectomy, when the resting gradient or the provocable gradient is ≥50 mmHg. Hemodynamic conditions may change and lead to worsening or improvement in LVOT obstruction during general anesthesia. LVOT gradients during surgery should be measured under reproducible conditions possibly mimicking preoperative hemodynamics.

Dobutamine is a well-known inotropic agent, capable to induce sub-aortic gradients in HOCM. The development of a dynamic LVOT gradient during this test is a pharmacological phenomenon with no clinical significance, not been associated with increased frequency of chest pain, shortness of breath or ischemic wall motion abnormalities, because obstruction resolves after termination of dobutamine (DBT) infusion.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. HOCM refractory to medical treatment with symptoms like syncope, angina or NYHA functional classes III and IV, with a resting gradient or provocable gradient equal or greater than 50 mmHg, requiring surgical intervention.
  2. Absence of other cardiac or systemic diseases capable of producing hypertrophy.
  3. Sinus rhythm.

Exclusion criteria

  1. Patient refusal.
  2. Patient unable to give consent.
  3. TEE contraindication.
  4. Different rhythm than sinus.
  5. Other systemic diseases capable of producing hypertrophy.
  6. Severe Aortic or coronary artery pathology.

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Preoperative Transesophageal Echocardiogram (TEE) PG under anesthesia <50mmHg (Group A)
Experimental group
Description:
* Pre-cardiopulmonary bypass (CPB) (pre-myectomy) echocardiographic parameters: PG under DBT stress test at 5, 10, 15 and 20 mcg/kg/min or until a PG ≥ 50mmHg is achieved, will be recorded. * Post-CPB (post-myectomy) echocardiographic parameters: PG at DBT peak dose (DBT-pd) will be recorded. If LVOT PG post myectomy are \>16 mmHg, the surgeon will be advised, for surgical management considerations.
Treatment:
Drug: Pre and post-CPB Drug: Dobutamine Hydrochloride
Preoperative PG under anesthesia ≥ 50mmHg (Group B)
Experimental group
Description:
* Pre-cardiopulmonary bypass (CPB) (pre-myectomy) echocardiographic parameters: PG without DBT stress test will be recorded. * Post-CPB (post-myectomy) echocardiographic parameters: PG at 5, 10, 15, 20 mcg/kg/min DBT stress test or until the postoperative provocable PG is \>16 mmHg will be recorded.
Treatment:
Drug: Post-CPB Drug: Dobutamine Hydrochloride

Trial contacts and locations

0

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Central trial contact

Jo Carroll; Azad Mashari, MD

Data sourced from clinicaltrials.gov

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