key: cord-0691854-30p7hnc0
authors: Natanov, Ruslan; Wiesner, Olaf; Haverich, Axel; Kühn, Christian
title: Mechanical circulatory support in coronavirus disease-2019-positive patients with severe respiratory failure
date: 2021-04-05
journal: Interact Cardiovasc Thorac Surg
DOI: 10.1093/icvts/ivab087
sha: 1cae4fa10bed204ee3be463595468c2f2a7e0f47
doc_id: 691854
cord_uid: 30p7hnc0

OBJECTIVES: Treatment of severe acute respiratory distress syndrome (ARDS) induced by severe acute respiratory syndrome coronavirus 2 has been heavily debated. Our goal was to describe our findings in patients with severe ARDS due to severe coronavirus disease 2019 (sCOVID-19) treated with venovenous extracorporeal membrane oxygenation (vv-ECMO). METHODS: We retrospectively examined all patients treated with vv-ECMO for severe ARDS due to acute respiratory syndrome coronavirus 2. RESULTS: In total, 13 patients were treated with vv-ECMO in our medical centre. The mean patient age was 48.1 years. Most patients were obese (69%) and male (85%). All patients were mechanically ventilated before ECMO. The mean time from intubation to proning was 16.6 h; the time from start of prone therapy to vv-ECMO implantation was 155.1 h. The mean total ECMO run time was 358 h. Significant reduction of positive end-expiratory pressure (P = 0.02), peak pressure (P = 0.001) and minute volume (P = 0.03) could be achieved after implantation of vv-ECMO. All patients showed an inflammatory response. Overall mortality was 30.7%: 1 patient died of mesenteric ischaemia; 3 patients died of multiple organ failure. A worse prognosis was seen in patients with highly elevated concentrations of interleukin-6. CONCLUSIONS: The use of vv-ECMO in patients with sCOVID-19-induced ARDS is safe and associated with improved respiratory ventilation settings. The rate of immune system involvement plays a pivotal role in the development and outcome of sCOVID-19.

Treatment of acute respiratory distress syndrome (ARDS) and respiratory failure due to severe coronavirus disease-19 (sCOVID- 19) have been heavily discussed in the past few months. Conservative therapy such as noninvasive ventilation has been proposed for mild forms of COVID-19. Patients with mild COVID-19 usually present with dyspnoea, coughing and fever. Severe COVID-19 may, however, lead to respiratory failure with rapid development of ARDS, hypoxaemia and death. For this patient population, invasive ventilation, high positive end-expiratory pressure (PEEP) and prone positioning have been proposed as the therapy of choice [1] . Despite the early start of aggressive therapy, patients admitted to the intensive care unit (ICU) with sCOVID-19 are prone to high mortality rates [2, 3] . As an ultima ratio, the use of venovenous extracorporeal membrane oxygenation (vv-ECMO) was proposed for the critically ill [4] [5] [6] . Although previous experience in patients with severe ARDS showed beneficial results for patients on ECMO therapy, early reporting on vv-ECMO use in sCOVID-19 showed devastatingly high mortality rates. Due to the high complication and mortality rates, the use of vv-ECMO in sCOVID-19 patients was initially discouraged [7] . Recent data, however, showed improvement in survival rates of patients with sCOVID-19 treated with ECMO. Survival rates of patients with sCOVID-19 treated with ECMO compared to those of patients with severe ARDS of other causes showed similar results [8, 9] . These results suggest the possibility of vv-ECMO implementation during severe COVID-19-induced ARDS. Because there are limited data on the use and efficacy of vv-ECMO in this population, our goal was to present our findings on the treatment with vv-ECMO of patients with sCOVID-19.

This retrospective study was performed in our tertiary medical facility. The ethics committee at our institution (Hannover Medical School, Hannover, Germany) waived the need for patient consent for this study. All data were retrieved by retrospective review of patient records.

This retrospective study was done using medical records of patients treated with vv-ECMO for severe COVID-19 at our medical centre. All patients >18 years were included. COVID-19 was confirmed using polymerase chain reaction analysis of tracheal swabs. All patients were sedated using propofol/sufentanil; inhalation anaesthetics (isofuran) were delivered as per house standard. All patients were intubated and mechanically ventilated before the implementation of mechanical circulatory support. Implementation of vv-ECMO was considered when patients met the criteria outlined in the Extracorporeal Life Support Organization guidelines [10] . In brief, patients were evaluated for vv-ECMO when the Horowitz index was <80 mmHg for > 6 h or <50 mmHg > 3 h due to severe respiratory failure under lungprotective ventilation. The Horowitz index was determined as the PaO2=FiO2 ratio mmHg ð Þ ¼ Partial pressure of oxygen PaO2 ðmmHgÞ Fraction of inspired oxygen FiO2 ð%Þ . Furthermore, prolonged hypercapnic acidosis (pH< 7.25 due to PaCO2 > 60 mmHg for >6 h) was also considered an inclusion criterion for vv-ECMO evaluation.

Myocardial pump function was monitored using transthoracic echocardiography throughout the patient's stay in the ICU.

Patients meeting vv-ECMO criteria due to respiratory failure were taken off mechanical circulatory support. While the patient was in the ICU, guidewires were placed percutaneously in the common femoral vein and jugular vein. Prior to cannulation, a bolus of 5000 IE unfractionated heparin was given intravenously. Subsequently, a continuous intravenous heparin infusion was given, and the infusion rate was adjusted according to the activated clotting time. The activated clotting time goal was set at 160-180 s according to the ECMO standard at our medical centre. Venous blood was drained via Seldinge rs technique into the femoral vein using a 55-cm long HLS cannula with BIOLINE coating (Maquet, Rastatt, Germany), size 21, 23 or 25 Fr, depending on the patient's weight and size. The optimal position for the outflow cannula was the entrance of the inferior vena cava to the right atrium. The position of the cannula was optimized using an ultrasound examination. A similar technique was used for the inflow cannula, a 15-cm long HLS cannula coated with BIOLINE, size 13, 15 or 17 Fr, which was placed in the jugular vein. In 1 patient, the inflow cannula was placed in the contralateral femoral vein. After successful cannulation, the cannulas were connected to our mobile ECMO system, the CardioHelp pump (Maquet), and to an HLS Set Advanced oxygenator (Maquet). The patient was weaned from vv-ECMO as soon as pulmonary function was restored. Ventilation parameters such as FiO2, peak pressure, PEEP and driving pressure were used to determine the reduction of vv-ECMO support. Implementation of ECMO removal occurred after pulmonary gas exchange was sufficiently restored: spontaneous breathing, Horowitz index > _150 mmHg, PEEP < _15 mbar and tidal volumes > _4-6 ml/kg of predicted body weight. After weaning, the percutaneously placed cannulas were extracted using 0/0 skin sutures.

Between January and August 2020, a total of 13 patients (11 male; 85%) presented to our tertiary centre with sCOVID-19 in need of ECMO therapy. The mean patient age was 48.1 (range 19-71) years. Patient characteristics are presented in Table 1 .

Medical therapy consisted of fluid substitution and antibiotic treatment using predominantly ß-lactam antibiotics. Furthermore, antiviral treatment was initiated using remdesivir. Although elevated levels of interleukin 6 were measured, no clear signs of a cytokine storm were seen. Therefore, we did not use cytokine filters. All patients were treated with a dilative tracheostomy in the ICU ward.

As previously noted, transthoracic echocardiography was used to determine myocardial dysfunction. No significant myocardial dysfunction was noted during the in-hospital stays. Furthermore, there were no signs of right ventricular strain indicating pulmonary embolisms.

Prone therapy was used in 12 (92%) patients prior to vv-ECMO. Proning was done 3 times for 12 h and was repeated when needed. All patients were treated with vv-ECMO; classical cannulation was done in 12 (92%) patients as previously described. One of the externally cannulated patients was cannulated via both femoral veins.

After initiation of ECMO therapy, mechanical ventilation pressures were significantly reduced, allowing for lung-protective ventilation ( Table 2) . Patients treated with prone positioning continued to do so after the initiation of ECMO. Management of the vv-ECMO was based on the clinical presentation: Patients were maintained with a mild negative fluid balance; vv-ECMO blood flow was kept at 4-5 l/min. There were no complications due to prone ventilation in patients on vv-ECMO treatment. As previously stated, patient anticoagulation was done using heparin. Clinical parameters for coagulation monitoring are shown in Table 3 . Due to deteriorating oxygenator function over time, an ECMO system exchange was needed in 3 patients. There were no signs of thrombotic material in the oxygenator upon macroscopic examination. There were no clear signs of hypercoagulability when a system exchange was done on day 9 in 1 patient; the second patient's system was changed on day 8 and the third patient's system, on day 11. Of the 3 patients in need of an ECMO system exchange, 1 died of multiorgan failure.

During ECMO therapy, complications were noted in 6 (46%) patients. Five (38%) patients had renal failure with the need for renal replacement therapy. Gastrointestinal complications occurred in 1 patient; mesenteric necrosis due to occlusion of the mesenteric vasculature was determined post-mortem. Pulmonary complications were seen in 3 (23%) patients: 2 patients developed pulmonary haemorrhages and 1 patient developed a pneumothorax on the contralateral side of the cannulation. Although there were no cerebral complications due to bleeding or ischaemia in our population, all surviving patients developed severe postanaesthesia delirium. The mean ECMO runtime was 358 h (72-1224 h). Three patients were cannulated at another hospital and transferred to our medical centre. Weaning from ECMO was possible for 9 (69%) patients; 4 patients (31%) died while on ECMO. As stated previously, 1 patient died of mesenteric ischaemia. The other 3 patients died of multiple organ failure. With the exception of the patient with mesenteric ischaemia, relatives of the remaining non-surviving patients did not allow post-mortem examinations. Criteria for vv-ECMO weaning included improved pulmonary gas exchange function. After ECMO removal, all patients were breathing spontaneously with PEEP <15 mmHg, Horowitz >150 mmHg and tidal volumes >4-6 ml/kg predicted body weight.

All ECMO-weaned patients were transferred to a respiratory weaning centre for further recovery; no patients were readmitted due to respiratory failure. Follow-up computer tomography examinations of the surviving patients showed no signs of pulmonary emboli. Compared to the patients who survived, the patients who did not survive showed no significant difference in time from intubation to prone positioning. Also, no significant difference was seen in time from proning to ECMO implantation or from time from presentation to ECMO implantation. However, concentrations of interleukin-6 were significantly higher in the non-surviving population prior to ECMO implantation (P = 0.005) ( Table 4 ). Other inflammatory parameters, such as C-reactive protein and procalcitonin, did not significantly differ between surviving and non-surviving population prior to ECMO implantation. During the ECMO treatment, a significantly worse Horowitz index was seen in the non-surviving population (P < 0.001). Furthermore, non-surviving patients needed significantly more norepinephrine support (P = 0.009), had higher procalcitonin concentrations (P = 0.012) and had more haemolysis because lactate dehydrogenase levels were significantly higher (P = 0.015). Interestingly, interleukin-6 concentrations were similar during ECMO treatment in both groups.

We have presented our results for patients on vv-ECMO due to sCOVID-19-induced ARDS and severe respiratory failure. To date, there is no adequate curative option for patients with severe respiratory impairment. Thus, guidelines for the management of moderate-to-severe respiratory impairment due to COVID-19 infection have been proposed [11] . These guidelines recommend the use of vv-ECMO in patients in whom conservative therapeutic options have failed. Our study showed a population with severe COVID-19 and respiratory failure in need of vv-ECMO support. Our population showed no complications during cannulation for vv-ECMO. Furthermore, prone ventilation in patients on vv-ECMO could be done without problems. These findings are consistent with findings reported elsewhere [11] [12] [13] . During the vv-ECMO runs, several complications were noted. Renal insufficiency with the need for dialysis was the most frequent complication in our population. Although most authors reported renal failure during vv-ECMO, a comparison is difficult due to the relatively small population sizes provided in the literature [8, [14] [15] [16] . Furthermore, other complications such as bleeding and thrombosis have been described [9] . Although all our patients showed signs of severe delirium, no patients had cerebral bleeding or ischaemia, which was in contrast to a series of 10 patients described by Usman et al. [15] in which 4 patients developed cerebral haemorrhage during ECMO therapy. This finding may, however, be attributed to the relatively high rate of anticoagulation with unfractionated heparin. Although the development of delirium during sCOVID-19 has been described, few data are available on the effect of ECMO in this patient population [17, 18] . To our knowledge, propofol is the sedative of choice in these patients. After vv-ECMO initiation, a significant reduction in mechanical ventilator support was possible. Interestingly, acute inflammation seems to play a pivotal role in the development and outcome of sCOVID-19-induced ARDS. We saw a clearly elevated interleukin 6 concentration in the non-surviving population. This finding is in accordance with the reports in the literature on cytokine expression during sCOVID-19-induced ARDS. Previous data confirmed worse outcomes in patients with elevated interleukin 6 concentrations [19, 20] . After being weaned from vv-ECMO, all patients were transferred to a respiratory weaning centre for further recovery. Although the role of vv-ECMO in severe ARDS is debated, post hoc Bayesian analysis of the EOLIA (Extracorporeal Membrane Oxygenation for Severe Acute Respiratory Distress Syndrome) study showed a favourable outcome in the vv-ECMO group [21] . In sCOVID-19-induced severe ARDS, to date, it is too early to determine the protective role of an early vv-ECMO implant on the development of late secondary pulmonary damage. Furthermore, determining the effects of ECMO will be difficult because many centres lack the manpower and resources needed for this therapy. Significantly higher inflammatory cytokine expression prior to ECMO implantation was associated with worse outcome. Furthermore, a worse Horowitz index, a higher demand for norepinephrine and higher concentrations of procalcitonin and lactate dehydrogenase could be measured in non-surviving patients during ECMO. All data are shown as mean (SEM). The Horowitz index is defined as PaO2/FiO2 ratio in mmHg. CRP: C-reactive protein; IL-6: Interleukin 6; ECMO: extracorporeal membrane oxygenation; LDH: lactate dehydrogenase; PaO2/FiO2: arterial oxygen partial pressure/fractional inspired oxygen.

Our findings show that the implementation of vv-ECMO in patients with moderate to severe ARDS caused by sCOVID-19 infection is safe and associated with improved respiratory ventilation settings. Furthermore, immune system activation seems to play a pivotal role in the development and outcome of sCOVID-19-induced ARDS.

This work was not supported by external funds.

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Conflict of interest: none declared. 

Interactive CardioVascular and Thoracic Surgery thanks Davide Pacini, Jarle Vaage and the other, anonymous reviewer(s) for their contribution to the peer review process of this article.