We hypothesize that in patients with chronic heart failure, the responsiveness of the vascular system is permanently altered due to chronic endogenous adrenergic stimulation, resulting in down regulation and/or desensitization of vascular a1-…
ID
Bron
Verkorte titel
Aandoening
Heart failure
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
- Change in SVR after phenylephrine administration
Achtergrond van het onderzoek
Vasoplegia is a state defined by hypotension, a high cardiac index and the continuous need of vasopressors. It occurs in 5-25% of the patients undergoing cardiac surgery on cardiopulmonary bypass (CPB) and is associated with an increased morbidity and mortality. Vasoplegia is a result of activation of several vasodilator pathways, inactivation of vasoconstrictor pathways and the resistance to vasopressors, but the precise aetiology remains unclear. Important risk factors for the development of vasoplegia after cardiac surgery are a left ventricular ejection fraction <30%, CPB and CPB duration.
Doel van het onderzoek
We hypothesize that in patients with chronic heart failure, the responsiveness of the vascular system is
permanently altered due to chronic endogenous adrenergic stimulation, resulting in down regulation and/or
desensitization of vascular a1-adrenoreceptors. The vascular system of patients with heart failure is easily pushed out
of balance by the systemic inflammatory reaction caused by the CPB and surgical trauma, making these patients more
prone for developing vasoplegia. Also activation of inducible nitric oxide synthase, activation of adenosine triphosphate
dependent potassium channels and deficiency of arginine vasopressin may play an important role.
Onderzoeksopzet
The phenylephrine challenge will be performed:
1. Before induction, before start medication (dobutamine, milrinone, noradrenalin)
2. Before induction, after start medication
3. After induction
4. After CPB, before emergence
5. On day 1 postoperative
The vasodilation test will be performed at the beginning of the surgery after placement of the arterial catheter and 1 day post-operatively.
The biopsy (pericardial fat) will be collected at the beginning of the surgery and at from the same area as the surgical incision.
In phase 2 of the study (VASOR part 2) only a biopsy will be collected.
Onderzoeksproduct en/of interventie
- Phenylephrine challenge
- Vasodilation test;
- Pericardial fat biopsy.
Algemeen / deelnemers
Marieke E. van Vessem
Leids Universitair Medisch Centrum Postbus 9600
Leiden 2300 RC
The Netherlands
071 5297623
m.e.van_vessem@lumc.nl
Wetenschappers
Marieke E. van Vessem
Leids Universitair Medisch Centrum Postbus 9600
Leiden 2300 RC
The Netherlands
071 5297623
m.e.van_vessem@lumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Group 1:
- Diagnosed with heart failure in line with the European Society of Cardiology (ESC) guidelines (McMurray et al., 2012);
- LVEF <35%.
- Undergoing cardiac surgery on CPB.
Group 2:
- Not diagnosed with heart failure;
- LVEF >50%.
- Undergoing cardiac surgery on CPB.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Age <18 years;
- Incapacitated adults;
- Emergency operation;
- Patients in need of moderate of high dosages of intravenous inotropic support (>4 gamma dobutamine or dopamine), vasopression and/or mechanical support;
- Patients with aortic have insufficiency > grade 1;
- Patients using a daily dosage of nitroglycerine or isosorbide denigrate;
- Patients using alpha blockers.
Opzet
Deelname
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In overige registers
Register | ID |
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NTR-new | NL5520 |
NTR-old | NTR5647 |
CCMO | NL51125.058.14 |
OMON | NL-OMON55621 |