The Effect of Levosimendan on Pulmonary Artery Pressure and Right Ventricular Function in the Perioperative Period in Patients With CTEPH After Pulmonary Thromboendarterectomy (LEVO-CTEPH)
The Effect of Levosimendan on Pulmonary Artery Pressure and Right Ventricular Function in the Perioperative Period in Patients With CTEPH After Pulmonary Thromboendarterectomy: a Single-center Pilot Prospective Randomized Placebo-controlled Double-blind Clinical Trial
A single-center pilot prospective randomized placebo-controlled double-blind clinical trial.
Study objective - to investigate the efficacy and safety of levosimendan in patients in the perioperative period following pulmonary endarterectomy for chronic thromboembolic pulmonary hypertension (CTEPH).
Research Objectives:
- To assess the impact of levosimendan administration on pulmonary artery pressure during the perioperative period in patients who have undergone pulmonary endarterectomy for CTEPH.
- To evaluate the effect of levosimendan administration on right ventricular function parameters during the perioperative period in patients after pulmonary endarterectomy for CTEPH.
- To determine the influence of levosimendan on the need for inotropic and vasopressor support (VIS) during the perioperative period in patients following pulmonary endarterectomy for CTEPH.
- To examine the effect of levosimendan on the clinical course and complications during the postoperative period in patients after pulmonary endarterectomy for CTEPH.
- To evaluate the cardioprotective effect of levosimendan in patients following pulmonary endarterectomy for CTEPH.
- To assess the impact of levosimendan on in-hospital mortality in patients after pulmonary endarterectomy for CTEPH.
Tutkimuksen yleiskatsaus
Tila
Tila
Ehdot
Ehdot
Interventio / Hoito
Interventio / Hoito
Yksityiskohtainen kuvaus
Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare and severe form of pulmonary hypertension resulting from thrombotic obstruction of the pulmonary arteries. It is typically a late complication of acute pulmonary embolism. The incidence of CTEPH has been reported to reach 13 cases per million population per year.
Organized thrombotic masses cause stenosis or obstruction of the pulmonary arteries, leading to increased pulmonary artery pressure and pulmonary vascular resistance. This results in redistribution of pulmonary blood flow, microangiopathy, and remodeling of small-caliber pulmonary vessels. Pulmonary endarterectomy (PEA) is the recommended standard of care for patients with CTEPH and can be curative. In experienced centers, mortality rates are less than 5%.
Residual pulmonary hypertension after PEA, defined as a mean pulmonary artery pressure ≥25 mmHg, occurs in 17-51% of patients. This complication is associated with residual thrombotic material in distal pulmonary arteries and small-vessel disease. Severe pulmonary hypertension causes right ventricular maladaptive remodeling and dysfunction, ultimately leading to right ventricular failure, which is the most important determinant of survival and quality of life. Residual pulmonary hypertension negatively affects long-term survival, with higher mortality associated with mean pulmonary artery pressure ≥36 mmHg and pulmonary vascular resistance ≥416 dyn·s·cm-⁵.
Currently, a multimodal approach to CTEPH is being considered. Surgery addresses the primary component by removing thrombotic masses, but pharmacotherapy is required for the microvascular component and persistently elevated pulmonary artery pressure. Targeted therapies are costly, and their benefit remains unclear. Clinical guidelines currently recommend only symptomatic therapy for patients with residual pulmonary hypertension and right ventricular failure after PEA, and no optimal treatment strategy has been defined for this complication in the early postoperative period.
Rationale for Levosimendan: Levosimendan has shown promising effects in pulmonary hypertension and right ventricular failure. Its mechanism of action involves opening ATP-dependent potassium channels in vascular smooth muscle cells, leading to vasodilation and reduction of both preload and afterload. Additionally, levosimendan binds to cardiac troponin C, increasing myofibril contractility. Previous studies have demonstrated that levosimendan reduces pulmonary artery pressure and pulmonary vascular resistance, improves right ventricular function (including increased TAPSE, ejection fraction, and cardiac output), and suppresses smooth muscle cell proliferation in pulmonary arteries. However, no studies to date have investigated the effect of levosimendan in patients with CTEPH undergoing pulmonary endarterectomy, and the drug has not previously been used in the perioperative management of this patient population.
Study objective is to evaluate the effect of levosimendan on pulmonary artery pressure and right ventricular function in patients undergoing pulmonary endarterectomy for CTEPH.
Opintotyyppi
Opintotyyppi
Ilmoittautuminen (Arvioitu)
Ilmoittautuminen
Vaihe
Vaihe
- Ei sovellettavissa
Yhteystiedot ja paikat
Opiskeluyhteys
Opiskeluyhteys
- Nimi: Gleb Moroz, PhD
- Puhelinnumero: +79833177148
- Sähköposti: g_moroz@meshalkin.ru
Opiskelupaikat
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-
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Novosibirsk, Venäjä, 630055
- Rekrytointi
- Meshalkin Research Institute of Pathology of Circulation
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Osallistumiskriteerit
Kelpoisuusvaatimukset
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
Inclusion Criteria:
- Voluntary signed informed consent to participate in the study
- Scheduled for pulmonary thromboendarterectomy surgery
- Aged ≥18 years
Exclusion Criteria :
- Patient refusal
- Language barrier preventing understanding of the study
- Severe renal failture (creatinine clearance <30 mL/min)
- Severe hepatic insufficiency (Child-Pugh score >9 points)
- Participation in other clinical trials
- History of allergic reaction to levosimendan, Soluvit, or any of their components
- Use of levosimendan within 30 days prior to screening
Discontinuation Criteria (or Withdrawal Criteria):
- Need for extracorporeal membrane oxygenation (ECMO) support during the perioperative period
- Pulmonary hemorrhage during the perioperative period
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Yksittäinen
Aseiden lukumäärä
Aseet ja interventiot
Osallistujaryhmä / ArmOsallistujaryhmä / Arm |
Interventio / HoitoInterventio / Hoito |
|---|---|
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Kokeellinen: Levosimendan
A levosimendan infusion after induction of anesthesia. |
Infusion of levosimendan will be initiated after the induction of anesthesia, discontinued at the onset of patient cooling, and resumed at the time of rewarming at 34°C. The drug will be administered using an infusion pump as a continuous infusion at a rate of 0.1 mcg/kg/min. The duration of the drug infusion will be up to 48 hours. Preoperative management will be conducted according to the patients' primary and concomitant diseases. |
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Placebo Comparator: "Soluvit"
A placebo infusion after induction of anesthesia. |
Patients in the placebo group will receive an equivalent amount of a colored solution of Soluvit.Soluvit (ATC B05XC; a yellow vitamin mixture indistinguishable from the investigational drug, levosimendan). Preoperative management will be conducted according to the patients' primary and concomitant diseases. |
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Mean pulmonary artery pressure (mPAP)
Aikaikkuna: 24 hours at the end of surgery
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Mean pulmonary artery pressure (mPAP) measured 24 hours after the end of surgery |
24 hours at the end of surgery
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Toissijaiset tulostoimenpiteet
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Pulmonary Vascular Resistance (PVR)
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
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Pulmonary vascular resistance |
• before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
|
Pulmonary Artery Pulsatility Index (PAPI)
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
Pulmonary artery pulsatility index. PAPi = (PASP - PADP) / RAP (PASP - PADP): Pulmonary Artery Pulse Pressure. This is the difference between the pressure in the pulmonary artery when the heart contracts (systolic) and relaxes (diastolic). RAP: Right Atrial Pressure. |
• before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
|
Pulmonary Artery Pressure (PAP)
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
Pulmonary artery pressure |
• before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
|
Arterial Blood Pressure (ABP)
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
Arterial blood pressure |
• before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
|
Central Venous Pressure (CVP)
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
Central venous pressure |
• before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
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Cardiac Index (CI)
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
Cardiac index |
• before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
|
Systemic Vascular Resistance (SVR)
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
Systemic vascular resistance |
• before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
|
Right Ventricular Stroke Work Index (RVSWI)
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
Right ventricular stroke work index |
• before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
|
Pulmonary Capillary Wedge Pressure (PAWP)
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
Pulmonary capillary wedge pressure |
• before skin incision • at the end of surgery • 4 hours after of surgery • 24 hours after of surgery • 48 hours after of surgery • 72 hours after of surgery
|
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Ejection fraction
Aikaikkuna: • before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
Ejection fraction (EF) of both the right and left ventricles (LVEF and RVEF) |
• before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
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Right Ventricular End-Diastolic Volume (RVEDV)
Aikaikkuna: • before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
Right ventricular end diastolic volume |
• before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
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Right Ventricular systolic pressure (RVSP)
Aikaikkuna: • before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
Right ventricular systolic pressure |
• before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
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Fractional area change (FAC) of the right ventricle
Aikaikkuna: • before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
Fractional area change (FAC) of the right ventricle |
• before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
|
Tricuspid annular plane systolic excursion (TAPSE)
Aikaikkuna: • before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
Tricuspid annular plane systolic excursion |
• before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
|
Right ventricular free-wall longitudinal strain (RV FW LS)
Aikaikkuna: • before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
Right ventricular free-wall longitudinal strain |
• before skin incision • at the end of surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
|
Quantitative troponin I level
Aikaikkuna: • before skin incision• 24 hours after the end of surgery• 48 hours after surgery
|
Quantitative concentration of troponin I |
• before skin incision• 24 hours after the end of surgery• 48 hours after surgery
|
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Vasoactive Inotropic Support
Aikaikkuna: • before skin incision • at the end of surgery • 4 hours after surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
In the perioperative period, the Vasoactive-Inotropic Score (VIS) will be calculated using the following formula: VIS = dobutamine (mcg/kg/min) + dopamine (mcg/kg/min) + (100 × epinephrine (mcg/kg/min) + (100 × norepinephrine (mcg/kg/min)) + (10 × milrinone (mcg/kg/min)) |
• before skin incision • at the end of surgery • 4 hours after surgery • 24 hours after surgery • 48 hours after surgery • 72 hours after surgery
|
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Residual Pulmonary Hypertension
Aikaikkuna: From the end of surgery up to 72 hours postoperatively
|
Number of participants with residual pulmonary hypertension, defined as postoperative mean pulmonary artery pressure (mPAP) > 25 mm Hg, measured by right heart catheterization in the postoperative period (up to 72 hours after surgery). |
From the end of surgery up to 72 hours postoperatively
|
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Incidence of reperfusion pulmonary edema
Aikaikkuna: From the end of surgery up to 72 hours postoperatively
|
Number of participants who develop pulmonary edema within 24 hours following pulmonary endarterectomy (PEA), confirmed by chest X-ray or chest CT and clinical criteria (including dyspnea, hypoxemia, and bilateral infiltrates), characterized by the presence of frothy secretions in the endotracheal tube (ETT), asymmetric opacities on chest X-ray, and an oxygenation index (PaO₂/FiO₂) < 300 mm Hg in the early postoperative period (up to 72 hours) |
From the end of surgery up to 72 hours postoperatively
|
|
Incidence of cardiac arrhythmias
Aikaikkuna: 30 days
|
Proportion of participants who develop any new-onset cardiac arrhythmia (including atrial fibrillation/flutter, ventricular tachycardia) during the study period, as documented by 12-lead ECG or continuous cardiac monitoring. |
30 days
|
|
Cardiovascular events: myocardial infarction or stroke
Aikaikkuna: 30 days
|
Number of participants with cardiovascular events, defined as myocardial infarction (MI) or stroke (cerebrovascular accident, CVA), occurring during the postoperative period.Myocardial infarction is defined according to the Fourth Universal Definition of Myocardial Infarction (elevated cardiac troponin with at least one of the following: ischemic symptoms, new ischemic ECG changes, or imaging evidence of new loss of viable myocardium). Stroke is defined as an acute episode of focal or global neurological dysfunction caused by infarction or hemorrhage in the brain, spinal cord, or retina, confirmed by neuroimaging (CT or MRI). |
30 days
|
|
Respiratory Complications: Pneumothorax
Aikaikkuna: 30 days
|
Number of participants with postoperative pneumothorax, defined as the presence of air in the pleural cavity, confirmed by chest X-ray or chest CT, occurring during the postoperative period. |
30 days
|
|
Neurological Complications: Seizures
Aikaikkuna: From enrollment to the end of treatment at 30 days
|
Number of participants with postoperative seizures, defined as a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain. Diagnosis is based on clinical assessment and, when available, confirmed by electroencephalography (EEG). |
From enrollment to the end of treatment at 30 days
|
|
Renal complications: acute kidney injury (AKI) according to KDIGO criteria
Aikaikkuna: 30 days
|
Number of participants with postoperative acute kidney injury (AKI), defined and staged according to the Kidney Disease: Improving Global Outcomes (KDIGO) criteria, occurring during the early postoperative period (up to 48 hours after surgery). AKI is defined as any of the following: increase in serum creatinine by ≥ 0.3 mg/dL (≥ 26.5 μmol/L) within 48 hours; or increase in serum creatinine to ≥ 1.5 times baseline, which is known or presumed to have occurred within the prior 7 days; or urine output < 0.5 mL/kg/hour for 6 hours. AKI is staged as follows: Stage 1 (serum creatinine 1.5-1.9 times baseline or ≥ 0.3 mg/dL increase, or urine output < 0.5 mL/kg/hour for 6-12 hours), Stage 2 (serum creatinine 2.0-2.9 times baseline, or urine output < 0.5 mL/kg/hour for ≥ 12 hours), and Stage 3 (serum creatinine ≥ 3.0 times baseline, or increase to ≥ 4.0 mg/dL, or initiation of renal replacement therapy, or urine output < 0.3 mL/kg/hour for ≥ 24 hours, or anuria for ≥ 12 hours). |
30 days
|
|
Renal replacement therapy (RRT)
Aikaikkuna: From enrollment to the end of treatment at 30 days
|
Number of participants who require renal replacement therapy (RRT) in the early postoperative period |
From enrollment to the end of treatment at 30 days
|
|
Use of inhaled nitric oxide (NO) and/or iloprost
Aikaikkuna: 30 days
|
Number of participants requiring administration of inhaled nitric oxide (NO) and/or inhaled iloprost in the postoperative period. for the management of residual pulmonary hypertension or right ventricular dysfunction. This includes administration as monotherapy or in combination |
30 days
|
|
Blood transfusion
Aikaikkuna: 30 days
|
Number of participants requiring perioperative blood transfusion, including packed red blood cells (PRBCs), fresh frozen plasma (FFP), platelet concentrates, or cryoprecipitate, in the postoperative period. Transfusion requirements will be recorded as the number of participants receiving any transfusion. |
30 days
|
|
Inotropic/vasopressor support
Aikaikkuna: From the end of surgery up to 72 hours postoperatively
|
Number of participants requiring postoperative inotropic and/or vasopressor support in the early postoperative period |
From the end of surgery up to 72 hours postoperatively
|
|
Duration of mechanical ventilation (MV)
Aikaikkuna: 30 days
|
Total duration of invasive mechanical ventilation (MV) measured in hours (or days) from the time of intubation in the operating room or ICU until successful extubation. This includes the total time on the ventilator, both in the operating room and in the ICU, and includes any episodes of reintubation. |
30 days
|
|
Duration of ICU stay
Aikaikkuna: 90 days
|
Total length of stay in the intensive care unit (ICU) measured in days from the time of admission to the ICU after surgery until discharge from the ICU to the general ward. |
90 days
|
|
Duration of hospital stay
Aikaikkuna: 90 days
|
Total length of hospital stay measured in days |
90 days
|
|
In-hospital mortality
Aikaikkuna: 90 days
|
yes/no |
90 days
|
Yhteistyökumppanit ja tutkijat
Sponsori
Sponsori
Julkaisuja ja hyödyllisiä linkkejä
Yleiset julkaisut
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- Delcroix M, Lang I, Pepke-Zaba J, Jansa P, D'Armini AM, Snijder R, Bresser P, Torbicki A, Mellemkjaer S, Lewczuk J, Simkova I, Barbera JA, de Perrot M, Hoeper MM, Gaine S, Speich R, Gomez-Sanchez MA, Kovacs G, Jais X, Ambroz D, Treacy C, Morsolini M, Jenkins D, Lindner J, Dartevelle P, Mayer E, Simonneau G. Long-Term Outcome of Patients With Chronic Thromboembolic Pulmonary Hypertension: Results From an International Prospective Registry. Circulation. 2016 Mar 1;133(9):859-71. doi: 10.1161/CIRCULATIONAHA.115.016522. Epub 2016 Jan 29.
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Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Opiskelun aloitus
Ensisijainen valmistuminen (Arvioitu)
Ensisijainen valmistuminen
Opintojen valmistuminen (Arvioitu)
Opintojen valmistuminen
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Ensimmäinen Lähetetty
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin päivitys julkaistu
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Avainsanat
Muita asiaankuuluvia MeSH-ehtoja
Muut tutkimustunnusnumerot
Muut tutkimustunnusnumerot
- 323
Yksittäisten osallistujien tietojen suunnitelma (IPD)
Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?
IPD-suunnitelman kuvaus
Data sharing is not planned as this is a single-center study and institutional regulations do not permit sharing of individual patient data.
Lääke- ja laitetiedot, tutkimusasiakirjat
Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta
Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta
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