Left ventricular unloading using a percutaneous paracorporeal
left ventricular assist device – University Hospital Centre Zagreb experience

    Authors

    Abstract

    **Background**: Veno-arterial extracorporeal membrane oxygenation (VA-ECMO) is widely used in refractory cardiogenic shock and cardiac arrest but is characterized by increased left ventricular (LV) afterload and consequent development of pulmonary oedema (ECMO lungs). The ProtekSoloTM (LivaNova, IT) cannula is inserted via the right femoral vein to the left atrium, by a trans-septal puncture (under the guidance of transesophageal echocardiography and fluoroscopy). This bypasses the LV by draining blood from the left atrium to a paracorporeal pump (eg Rotaflow pump (Maquet, DE)) and returning it via a femoral artery cannula, thus providing direct unloading of LV. (1-3) We aimed to demonstrate our experience with the paracorporeal LV assist device using the ProtekSolo cannula and Rotaflow pump (PSp-LVAD). **Patients and Methods**: 7 adult patients underwent PSp-LVAD placement in UHC Zagreb from January to December 2020. We divided the patients in two groups: those who required PSp-LVAD to treat ECMO lungs (n=4) and those who received PSp-LVAD implantation prior to developing ECMO lungs (n=3). In addition to the description of the treated patients, we also assessed 30-day all-cause mortality. **Results**: The baseline characteristics of patients are shown in **Table 1**. All patients were male, mean age 56±9.3 years. 57.1% of patients underwent PSp-LVAD placement due to worsening of chronic heart failure and 42.9% due to acute coronary syndrome. Concurrent infection was present in 57.1% of patients. 71.4% were first on VA-ECMO support, of those 80% developed ECMO lungs. Laboratory tests (**Figure 1**) show improvement in kidney and liver function after PSp-LVAD placement. Outcomes are shown in **Table 2**; patients in prophylactic group have lower observed 30-day mortality rate (33% vs 75%) and longer VA-ECMO support duration due to lower mortality. Besides 2 patients who are still in active treatment, all others died during initial hospitalization due to infective complications, predominantly those that had a concurrent infection upon institution of the PSp-LVAD. ### TABLE 1: Baseline characteristics. | **N** | **7** | **N** | **7** | | --- | --- | --- | --- | | **Mean age (years)** | 56±9.3 | **Heart rate (beats/min)** | 90 (85-125) | | **Sex (male %)** | 7 (100%) | **Urinary output hourly (ml/h)** | 100 (15-180) | | **Mean BMI (kg/m2)** | 25.5±2.9 | **Laboratory values** | | | **Aetiology of cardiogenic shock** | | Lactate (mmol/L) | 2.1 (0.4-4.8) | | Worsening of chronic heart failure | 4 (57.1%) | BUN (mmol/L) | 11.5 (1.9-19.7) | | Acute coronary syndrome | 3 (42.9%) | Creatinine (umol/L) | 91 (61-133) | | **Duration of disease** | | AST (IU/L) | 193 (19-2132) | | Cardiomyopathy (years) | 8±5.3 | ALT (IU/L) | 75 (17-566) | | Acute coronary syndrome (days) | 5±6 | NTproBNP (ng/L) | 8118 (41-26245) | | **SAVE score** | -3 (-13, 6) | **Inotropic or vasopressor therapy before PSp-LVAD placement** | | | **VA-ECMO prior to PSp-LVAD** | 5 (71.4%) | Dobutamine | 4 (57.1%) | | **ECMO lungs** | 4 (57.1%) | Milrinone | 3 (42.9%) | | **Infection prior to VA-ECMO** | 4 (57.1%) | Levosimendan | 4 (57.1%) | | **Mean arterial pressure (mmHg)** | 76 (60-79) | Norepinephrine | 5 (71.4%) | [†] BMI: body mass index, SAVE: Survival After Veno-arterial Ecmo, VA-ECMO: veno-arterial extra corporeal membrane oxygenation, PSp-LVAD: Protek Solo paracorporeal left ventricular assist device, BUN: blood urea nitrogen, AST: aspartate transaminase, ALT alanine transaminase, NTproBNP: N-terminal prohormone of brain natriuretic peptide. FIGURE 1. Laboratory values before and after Protek Solo paracorporeal left ventricular assist device placement. BUN: blood urea nitrogen, NTproBNP: N-terminal prohormone of brain natriuretic peptide, AST: aspartate transaminase. ### TABLE 2: Outcomes. | | **ECMO lungs before PSp-LVAD (N=4)** | **No ECMO lungs before PSp-LVAD (N=3)** | | --- | --- | --- | | **30-day mortality** | 3 (75%) | 1 (33%) | | **Survival to decannulation** | 1 (25%) | 1 (33%) | | **Mean PSp-LVAD days** | 11±5 | 32.5±12 | | **VA-ECMO prior to PSp-LVAD** | 4 (100%) | 1 (33%) | | **Removal of oxygenator** | 2 (50%) | 3 (100%) | | **Durable LVAD implantation** | 0 (0%) | 1 (33%) | | **Complications** | | | | Infective | 4 (100%) | 1 (33%) | | Bleeding | 2 (50%) | 1 (33%) | [†] VA-ECMO: veno-arterial extra corporeal membrane oxygenation, PSp-LVAD: Protek Solo paracorporeal left ventricular assist device, LVAD: left ventricular assist device. **Conclusion**: Pulmonary edema (ECMO lungs) due to increased LV afterload is a major complication of VA-ECMO. Prophylactic LV unloading by PSp-LVAD seems associated with lower 30-days mortality.

    Keywords

    cardiogenic shock, extracorporeal membrane oxygenation, ProtekSolo, left ventricular unloading

    DOI

    https://doi.org/10.15836/ccar2021.31

    Literature

    1. Russo JJ, Aleksova N, Pitcher I, Couture E, Parlow S, Faraz M, et al. Left Ventricular Unloading During Extracorporeal Membrane Oxygenation in Patients With Cardiogenic Shock. J Am Coll Cardiol. 2019 February 19;73(6):654–62. https://doi.org/10.1016/j.jacc.2018.10.085
    2. Meani P, Gelsomino S, Natour E, Johnson DM, Rocca HB, Pappalardo F, et al. Modalities and Effects of Left Ventricle Unloading on Extracorporeal Life support: a Review of the Current Literature. Eur J Heart Fail. 2017 May;19 Suppl 2:84–91. https://doi.org/10.1002/ejhf.850
    3. Na SJ, Yang JH, Yang JH, Sung K, Choi JO, Hahn JY, et al. Left heart decompression at venoarterial extracorporeal membrane oxygenation initiation in cardiogenic shock: prophylactic versus therapeutic strategy. J Thorac Dis. 2019 September;11(9):3746–56. https://doi.org/10.21037/jtd.2019.09.35
    Cardiologia Croatica
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    Left ventricular unloading using a percutaneous paracorporeal
left ventricular assist device – University Hospital Centre Zagreb experience

    Extended Abstract
    Issue1-2
    Published
    Pages31-32
    PDF via DOIhttps://doi.org/10.15836/ccar2021.31
    cardiogenic shock
    extracorporeal membrane oxygenation
    ProtekSolo
    left ventricular unloading

    Authors

    Dubravka Šipuš*ORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Ivo PlanincORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Boško SkorićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Vedran VelagićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Marijan PašalićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Hrvoje JurinORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Daniel LovrićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Jure SamardžićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Jana Ljubas MačekORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Hrvoje GašparovićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Bojan BiočinaORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Davor MiličićORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia
    Maja ČikešORCIDUniversity of Zagreb School of Medicine, Zagreb, Croatia

    *Correspondence email: dubravka.sipus@gmail.com

    Abstract

    **Background**: Veno-arterial extracorporeal membrane oxygenation (VA-ECMO) is widely used in refractory cardiogenic shock and cardiac arrest but is characterized by increased left ventricular (LV) afterload and consequent development of pulmonary oedema (ECMO lungs). The ProtekSoloTM (LivaNova, IT) cannula is inserted via the right femoral vein to the left atrium, by a trans-septal puncture (under the guidance of transesophageal echocardiography and fluoroscopy). This bypasses the LV by draining blood from the left atrium to a paracorporeal pump (eg Rotaflow pump (Maquet, DE)) and returning it via a femoral artery cannula, thus providing direct unloading of LV. (1-3) We aimed to demonstrate our experience with the paracorporeal LV assist device using the ProtekSolo cannula and Rotaflow pump (PSp-LVAD). **Patients and Methods**: 7 adult patients underwent PSp-LVAD placement in UHC Zagreb from January to December 2020. We divided the patients in two groups: those who required PSp-LVAD to treat ECMO lungs (n=4) and those who received PSp-LVAD implantation prior to developing ECMO lungs (n=3). In addition to the description of the treated patients, we also assessed 30-day all-cause mortality. **Results**: The baseline characteristics of patients are shown in **Table 1**. All patients were male, mean age 56±9.3 years. 57.1% of patients underwent PSp-LVAD placement due to worsening of chronic heart failure and 42.9% due to acute coronary syndrome. Concurrent infection was present in 57.1% of patients. 71.4% were first on VA-ECMO support, of those 80% developed ECMO lungs. Laboratory tests (**Figure 1**) show improvement in kidney and liver function after PSp-LVAD placement. Outcomes are shown in **Table 2**; patients in prophylactic group have lower observed 30-day mortality rate (33% vs 75%) and longer VA-ECMO support duration due to lower mortality. Besides 2 patients who are still in active treatment, all others died during initial hospitalization due to infective complications, predominantly those that had a concurrent infection upon institution of the PSp-LVAD. ### TABLE 1: Baseline characteristics. | **N** | **7** | **N** | **7** | | --- | --- | --- | --- | | **Mean age (years)** | 56±9.3 | **Heart rate (beats/min)** | 90 (85-125) | | **Sex (male %)** | 7 (100%) | **Urinary output hourly (ml/h)** | 100 (15-180) | | **Mean BMI (kg/m2)** | 25.5±2.9 | **Laboratory values** | | | **Aetiology of cardiogenic shock** | | Lactate (mmol/L) | 2.1 (0.4-4.8) | | Worsening of chronic heart failure | 4 (57.1%) | BUN (mmol/L) | 11.5 (1.9-19.7) | | Acute coronary syndrome | 3 (42.9%) | Creatinine (umol/L) | 91 (61-133) | | **Duration of disease** | | AST (IU/L) | 193 (19-2132) | | Cardiomyopathy (years) | 8±5.3 | ALT (IU/L) | 75 (17-566) | | Acute coronary syndrome (days) | 5±6 | NTproBNP (ng/L) | 8118 (41-26245) | | **SAVE score** | -3 (-13, 6) | **Inotropic or vasopressor therapy before PSp-LVAD placement** | | | **VA-ECMO prior to PSp-LVAD** | 5 (71.4%) | Dobutamine | 4 (57.1%) | | **ECMO lungs** | 4 (57.1%) | Milrinone | 3 (42.9%) | | **Infection prior to VA-ECMO** | 4 (57.1%) | Levosimendan | 4 (57.1%) | | **Mean arterial pressure (mmHg)** | 76 (60-79) | Norepinephrine | 5 (71.4%) | [†] BMI: body mass index, SAVE: Survival After Veno-arterial Ecmo, VA-ECMO: veno-arterial extra corporeal membrane oxygenation, PSp-LVAD: Protek Solo paracorporeal left ventricular assist device, BUN: blood urea nitrogen, AST: aspartate transaminase, ALT alanine transaminase, NTproBNP: N-terminal prohormone of brain natriuretic peptide. FIGURE 1. Laboratory values before and after Protek Solo paracorporeal left ventricular assist device placement. BUN: blood urea nitrogen, NTproBNP: N-terminal prohormone of brain natriuretic peptide, AST: aspartate transaminase. ### TABLE 2: Outcomes. | | **ECMO lungs before PSp-LVAD (N=4)** | **No ECMO lungs before PSp-LVAD (N=3)** | | --- | --- | --- | | **30-day mortality** | 3 (75%) | 1 (33%) | | **Survival to decannulation** | 1 (25%) | 1 (33%) | | **Mean PSp-LVAD days** | 11±5 | 32.5±12 | | **VA-ECMO prior to PSp-LVAD** | 4 (100%) | 1 (33%) | | **Removal of oxygenator** | 2 (50%) | 3 (100%) | | **Durable LVAD implantation** | 0 (0%) | 1 (33%) | | **Complications** | | | | Infective | 4 (100%) | 1 (33%) | | Bleeding | 2 (50%) | 1 (33%) | [†] VA-ECMO: veno-arterial extra corporeal membrane oxygenation, PSp-LVAD: Protek Solo paracorporeal left ventricular assist device, LVAD: left ventricular assist device. **Conclusion**: Pulmonary edema (ECMO lungs) due to increased LV afterload is a major complication of VA-ECMO. Prophylactic LV unloading by PSp-LVAD seems associated with lower 30-days mortality.

    Literature

    1. 1.
      Russo JJ, Aleksova N, Pitcher I, Couture E, Parlow S, Faraz M, et al. Left Ventricular Unloading During Extracorporeal Membrane Oxygenation in Patients With Cardiogenic Shock. J Am Coll Cardiol. 2019 February 19;73(6):654–62.DOI
    2. 2.
      Meani P, Gelsomino S, Natour E, Johnson DM, Rocca HB, Pappalardo F, et al. Modalities and Effects of Left Ventricle Unloading on Extracorporeal Life support: a Review of the Current Literature. Eur J Heart Fail. 2017 May;19 Suppl 2:84–91.DOI
    3. 3.
      Na SJ, Yang JH, Yang JH, Sung K, Choi JO, Hahn JY, et al. Left heart decompression at venoarterial extracorporeal membrane oxygenation initiation in cardiogenic shock: prophylactic versus therapeutic strategy. J Thorac Dis. 2019 September;11(9):3746–56.DOI