key: cord-0869520-8053dncu authors: Huette, Pierre; Abou Arab, Osama; Jounieaux, Vincent; Guilbart, Mathieu; Belhout, Mohamed; Haye, Guillaume; Dupont, Hervé; Beyls, Christophe; Mahjoub, Yazine title: Almitrine for COVID-19 critically ill patients – a vascular therapy for a pulmonary vascular disease: Three case reports date: 2021-05-16 journal: World J Clin Cases DOI: 10.12998/wjcc.v9.i14.3385 sha: 8d6baa8259388c5091e48a4159fcd50ebe729075 doc_id: 869520 cord_uid: 8053dncu BACKGROUND: Several reports with clinical, histological and imaging data have observed the involvement of lung vascular function to explain the severe hypoxemia in coronavirus disease 2019 (COVID-19) patients. It has been hypothesized that an increased pulmonary blood flow associated with an impairment of hypoxic pulmonary vasoconstriction is responsible for an intrapulmonary shunt. COVID-19 may lead to refractory hypoxemia (PaO(2)/FiO(2 )ratio below 100 mmHg) despite mechanical ventilation and prone positioning. We hypothesized that the use of a pulmonary vasoconstrictor may help decrease the shunt and thus enhance oxygenation. CASE SUMMARY: We report our experience with three patients with refractory hypoxemia treated with almitrine to enhance oxygenation. Low dose almitrine (Vectarion(®); Servier, Suresnes, France) was started at an infusion rate of 4 μg × kg/min on a central line. The PaO(2)/FiO(2 )ratio and total respiratory system compliance during almitrine infusion were measured. For the three patients, the PaO(2)/FiO(2 )ratio time-course showed a dramatic increase whereas total respiratory system compliance was unchanged. The three patients were discharged from the intensive care unit. The intensive care unit length of stay for patient 1, patient 2 and patient 3 was 30 d, 32 d and 31 d, respectively. Weaning from mechanical ventilation was performed 13 d, 18 d and 15 d after almitrine infusion for patient 1, 2 and 3, respectively. We found no deleterious effects on the right ventricular function, which was similar to previous studies on almitrine safety. CONCLUSION: Almitrine may be effective and safe to enhance oxygenation in coronavirus disease 2019 patients. Further controlled studies are required. Several reports with clinical, histological and imaging data in coronavirus disease 2019 (COVID-19) have observed that the involvement of lung vascular function may explain the severe hypoxemia [1] [2] [3] [4] [5] . It has been hypothesized that an increased pulmonary blood flow is responsible for an intrapulmonary shunt with a decrease of ventilation/perfusion ratio [2, 3] . Recently, three retrospective case series reported the use of almitrine, a pulmonary vasoconstrictor, in COVID-19 patients with inconsistent effects on oxygenation and outcome [6] [7] [8] . However, no data on key safety factors, such as right ventricular function or pulmonary artery pressure, were reported in these series. We report our experience with three patients with refractory hypoxemia treated with almitrine to enhance oxygenation. Complete hemodynamic assessment with transesophageal echocardiography and pulmonary artery catheter was performed. Patients were admitted at Amiens University hospital intensive care unit for severe acute respiratory distress syndrome (ARDS) related to COVID-19. Severe acute respiratory syndrome coronavirus-2 infection was confirmed by real-time reverse transcription polymerase chain reaction on a sample from nasopharyngeal swab. Patient condition deteriorated rapidly leading to mechanical ventilation and refractory hypoxemia despite medical management. Case 1: The patient was admitted to the hospital 7 d after onset of symptoms (dyspnea and headache). Initial treatment included lopinavir/ritonavir and high flow nasal oxygen for 2 d. Respiratory worsening lead to mechanical ventilation 2 d after hospital admission. Case 2: The patient was admitted to the hospital 11 d after onset of symptoms (dyspnea and cough). Initial treatment included lopinavir/ritonavir. Respiratory worsening required mechanical ventilation 5 d after intensive care unit (ICU) admission. The patient was admitted to the hospital 5 d after symptoms onset (anosmia, dyspnea and cough). He was admitted to the ICU because of respiratory worsening 6 d after hospital admission. After 5 d with high flow nasal oxygen, respiratory worsening required mechanical ventilation. After 2 d of mechanical ventilation, the patient developed severe ARDS. The patients' medical histories is presented in Table 1 . The first patient was a 57-yearold female with a medical history of smoking and hypertension. The second patient was a 56-year-old female with a medical history of dyslipidemia and obesity (body mass index (BMI) = 39 kg/m 2 ). The third patient was a 53-year-old male with a history of obesity (BMI = 40 kg/m 2 ) and rheumatoid arthritis treated with steroids. The patients had no personal or family history. Case 1: Prior to almitrine infusion, the plateau pressure was 28 cmH 2 O and positive end expiratory pressure (PEEP) at 14 cmH 2 O. Baseline pulmonary compliance was 32 mL/cmH 2 O. Pulmonary artery catheter showed pulmonary vascular resistance at 5.9 Wood units and pulmonary artery occlusion pressure of 7 mmHg. Cardiac index (CI) was 2.6 L/min/m 2 . Right ventricular (RV) fractional area change (FAC) was 45%. Speckle tracking based right ventricular two-dimensional strain was performed (Table 1 and Figure 1 ). Prior to almitrine infusion, the plateau pressure was 27 cmH 2 O and PEEP at 14 cmH 2 O. Baseline pulmonary compliance was 33 mL/cmH 2 O. Pulmonary artery catheter showed pulmonary vascular resistance at 4.1 Wood units and pulmonary artery occlusion pressure of 9 mmHg. CI was 2.9 L/min/m 2 . RV FAC was 42%. Prior to almitrine infusion, the plateau pressure was 29 cmH 2 O and PEEP at 15 cmH 2 O. Baseline pulmonary compliance was 31 mL/cmH 2 O. Pulmonary artery catheter showed pulmonary vascular resistance at 3.3 Wood units and pulmonary artery occlusion pressure of 11 mmHg. CI was 2.9 L/min/m 2 . RV FAC was 58%. Case 1: Prior to almitrine infusion, the PaO 2 /FiO 2 ratio was 77 mmHg. Arterial blood gas sample showed PaCO 2 of 46.2 mmHg, pH at 7.4 and lactate at 1.8 mmol/L. Laboratory investigations revealed lymphopenia at 550/mm 3 and high C reactive protein level at 65 mg/L. Prior to almitrine infusion, the PaO 2 /FiO 2 ratio was 91 mmHg. Arterial blood gas sample showed PaCO 2 of 39.5 mmHg, pH at 7.4 and lactate at 1.9 mmol/L. Laboratory investigations revealed lymphopenia at 370/mm 3 and high C reactive protein level at 95 mg/L. Prior to almitrine infusion, the PaO 2 /FiO 2 ratio was 95 mmHg. Arterial blood gas sample showed PaCO 2 of 49 mmHg, pH at 7.3 and lactate at 1.4 mmol/L. Laboratory investigations did not reveal any other specificities. Case 1: Chest computed tomography (CT) angiography showed ground-glass opacity with crazy paving and severe lobar involvement (> 75%). There was no pulmonary embolism. Case 2: Chest CT angiography showed ground-glass opacity with crazy paving and moderate lobar involvement (50%-75%). There was no pulmonary embolism. Chest CT angiography showed ground-glass opacity with bilateral crazy paving, consolidation and limited lobar involvement (25%). There was no pulmonary embolism. All three patients were admitted to the ICU for severe ARDS according to the Berlin definition with a PaO 2 /FiO 2 ratio < 150. They were treated with protective ventilation (low tidal volume 6-7 mL/kg, PEEP for plateau pressure ≤ 30 cmH 2 O), neuromuscular blocking agents and inhaled nitric oxide (at 10 ppm). Despite medical management they presented persistent severe hypoxemia. The local institutional review board waived the need for written informed consent; data storage was authorized by national licensing authority (CNIL PI2020_843_0026). Patients and/or next of kin were informed of the study. We prospectively collected data from three consecutive patients with COVID-19 and severe ARDS who received almitrine infusion. Low dose of almitrine (Vectarion ® ; Servier, Suresnes, France) was started at an infusion rate of 4 μg × kg × min -1 on a central line. The effect of almitrine infusion on respiratory parameters (blood gases, PaO 2 /FiO 2 ratio, total respiratory system compliance) was evaluated. Pulmonary artery pressure (PAP), cardiac output and pulmonary vascular resistance (PVR) were monitored via a pulmonary artery catheter. RV FAC, RV global longitudinal strain and tricuspid longitudinal annular displacement were monitored via transesophageal echocardiography. Data were collected before and 1 h, 2 h and 12 h after almitrine infusion start. Case 1: Almitrine infusion was started after 2 d of mechanical ventilation and sustained for 3 d. Case 2: Almitrine was started at day 6 after ICU admission (5 d with high flow oxygen and 1 d under mechanical ventilation). Almitrine infusion was given for 3 d. The PaO 2 /FiO 2 ratio and total respiratory system compliance during almitrine infusion are presented in Figure 1 and Time-course of pulmonary artery catheter parameters and echocardiographic parameters during almitrine infusion are presented in Figure 1 . PAP and PVR remained unchanged during almitrine infusion. Regarding RV function, RV FAC and RV global longitudinal strain remained unchanged for patient 1 and patient 2 and improved for patient 3. Tricuspid longitudinal annular displacement remained unchanged for the three patients. None of the patients needed extracorporeal membrane oxygenation therapy. Liver function test remained unchanged. In this report, we found that almitrine infusion enhanced oxygenation of patients with severe COVID-19 related ARDS without any change in PAP and RV function. At baseline, the patients showed an increased PAP without pulmonary embolism and left ventricular dysfunction (normal pulmonary artery occlusion pressures and CI). Hence, we cannot discard the occurrence of at least a certain level of hypoxic pulmonary vasoconstriction that has been suggested by some authors [3] . In our patients, almitrine led to increased oxygenation without any changes in ventilatory parameters or right-side circulation. Hence, almitrine improved the ventilation/perfusion ratio by decreasing pulmonary flow. The lack of increase in PVR with almitrine is not in favor of an increase in hypoxic pulmonary vasoconstriction as encountered in typical ARDS. Recently, Ackermann et al [4] observed that the pulmonary histological pattern that distinguishes COVID-19 infected lungs from influenzae infected lung is the amount of new vessel growth in the COVID-19 lung. Moreover, Lang et al[1] studied lung perfusion by dual-energy chest CT scan for COVID-19 patients and found an increased perfusion of the lungs especially proximal to lung opacities. Increase of pulmonary vessels number is probably responsible of an intrapulmonary shunt with an increased ventilation/perfusion mismatch. Almitrine acts as a selective pulmonary vessel vasoconstrictor that is able to decrease and redistribute pulmonary blood flow from shunt areas to pulmonary units with normal ventilation/pulmonary flow ratios [9] . We believe that the improvement in oxygenation with almitrine for our patients was related to a decrease in intrapulmonary shunt in both aerated and non-aerated lung regions [2] . Inhaled nitric oxide is a selective pulmonary vasodilator, and intravenously administered almitrine is a selective pulmonary vasoconstrictor. The resulting effects of combining almitrine and inhaled nitric oxide are likely related to the respective vascular effect of each drug on aerated and non-aerated lung compartments and explain why additive respiratory effects were observed. Previous studies confirmed that when reinforcing hypoxic pulmonary vasoconstriction by small doses of almitrine, the nitric oxide-induced increase in arterial oxygenation can be markedly enhanced [10, 11] . The major risk with short term use of almitrine is the increase of RV afterload by excessive vasoconstriction. Hence, we evaluated RV function with very sensitive and reproducible parameters: RV global longitudinal strain and tricuspid longitudinal annular displacement [12, 13] . We found no deleterious effects on RV function, which was similar to previous studies on almitrine safety [14] . Recently, Barthélémy et al [6] tested almitrine for COVID-19 patients, but crucial data on RV function was not reported. Despite a small sample size, almitrine seems to be effective and safe to enhance oxygenation for COVID-19 critically ill patients. Further controlled studies are required. Hypoxaemia related to COVID-19: vascular and perfusion abnormalities on dual-energy CT Severe Covid-19 disease: rather AVDS than ARDS? 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