To the Editor:
The severe acute respiratory syndrome coronavirus-2–related disease, coronavirus-2019 (COVID-19), mainly is characterized by respiratory manifestations, with approximately 15% to 30% of patients developing acute respiratory distress syndrome (ARDS).1 The World Health Organization guidelines recommend to proceed to venovenous extracorporeal membrane oxygenation (ECMO) for eligible patients with COVID-19–related ARDS only in centers with “sufficient case volume to ensure clinical expertise.”2 The Amiens ECMO center received many calls from several hospitals in the region about refractory ARDS secondary to COVID-19 during the first weeks after COVID-19 was declared a pandemic. The decision was made rapidly to set up a mobile ECMO team in order to start on-site ECMO treatment.
Start of the Outbreak in Picardy
Located in the north of France, the Picardy region has a population of 1.925 million inhabitants living in a 19,399-km territory. A network of 29 general hospitals is located in this regional territory, with 128 intensive care unit (ICU) beds. The only ICU in Picardy with the ability to manage ECMO is the cardiac thoracic vascular and respiratory unit of Amiens University Medical Centre. The unit has performed about 60 ECMO treatments every year for more than 10 years (one-third of those have been venovenous ECMO treatments).
The COVID-19 outbreak occurred in Picardy at the end of February 2020, resulting in a rapid need for ICU beds. Calls from peripheral centers for ECMO services increased rapidly. In 1 month (March 2020), 676 patients were admitted to the region's hospitals for COVID-19–related disease. Among those patients, 156 required ICU admission (admission rate: 23.1%).3
Setting up the Mobile ECMO Team
Clustering infected patients requiring ECMO within an expert center was necessary to ensure adequate care and resource management. A unique phone number was publicized to all ICUs of the region to centralize the request for ECMO services. An on-call ECMO team member was able to give advice and evaluate the need for ECMO. All ECMO team members were educated on the management and eligibility criteria for ECMO initiation. The mobile ECMO team was composed of a specialized intensivist, thoracic surgeon, and trained perfusion nurse. A roster was started in order to make the team available 24 hours a day, 7 days a week. The decision to initiate ECMO treatment was always a multiconsultant decision. The ECMO team was able to reach any hospital in the region in less than 45 minutes (by road or by air, depending on the weather). On arrival to the site, the ECMO team decided whether to perform conventional ventilation or to initiate ECMO on site and transfer the patient on ECMO support. Patients on ECMO were admitted to a specialized ICU with trained staff. The Cardiohelp (Getinge, Gothenburg, Sweden) ECMO device was used for each transport because of its compact and light (10 kg) design.
Number of Calls and Patient Characteristics
During March 2020, 22 calls were received at our ECMO center. The ECMO team initiated 8 venovenous ECMO treatments on site and transferred 3 patients on conventional ventilation. For all patients, the drainage cannula (size 25 F) was inserted in the right femoral vein and the return cannula (size 19 F) was inserted in the right jugular vein. Heparin treatment was started after the procedure with continuous perfusion of unfractionated heparin for an anti-XA level target of 0.2 to 0.4 UI/mL. Despite this treatment, cannula thrombosis occurred in 2 patients, leading to procedure failure and death for both patients. This probably was due to the high inflammatory state that increases the risk of thrombosis, as suggested in some reports.4 The ECMO team was not available 3 times due to simultaneous calls. Only 1 ECMO treatment was initiated during a night shift. Four patients (50%) were discharged from the ICU. Characteristics, outcomes, and complications of the patients are detailed in Table 1 . The role of ECMO in COVID-19–related ARDS still is unclear. To date, only limited case series are available. Our report is in accordance with previous reports on limited cases series of COVID-19 patients on ECMO support. Li et al. reported a similar rate of 50% of weaning for 8 patients on ECMO.5 Jacobs et al., in a larger case series of 32 COVID-19 patients on ECMO, had a weaning rate of 16% (5 of 32), but the majority of their ECMO treatments still were ongoing at the time of publication.6 In contrast to other case series, we performed only venovenous ECMO therapies because all treated patients were hemodynamically stable without acute ventricular dysfunction.7
Table 1.
Cases |
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---|---|---|---|---|---|---|---|---|
Variables | Case 1 | Case 2 | Case 3 | Case 4 | Case 5 | Case 6 | Case 7 | Case 8 |
Age (y) | 63 | 41 | 59 | 67 | 55 | 62 | 64 | 46 |
BMI (kg/m²) | 29 | 27 | 49 | 30 | 22 | 38 | 29 | 29 |
Smoking | No | Yes | No | No | No | No | No | No |
Hypertension | No | Yes | No | No | No | Yes | No | Yes |
Diabetes | No | Yes | No | No | No | Yes | No | No |
NSAIDs/corticoids/ID | No | Yes | No | Yes | Yes | No | Yes | No |
SOFA | 4 | 16 | 13 | 11 | 8 | 9 | 14 | 11 |
SAPS II | 36 | 70 | 51 | 76 | 38 | 64 | 65 | 60 |
Vasopressors (µg/kg/min) | 0 | 0.4 | 0 | 0 | 0 | 0.2 | 0 | 0 |
Tidal volume (mL/kg) | 5.8 | 4.2 | 6.4 | 6.1 | 4.8 | 5.6 | 6.5 | 4.5 |
Respiratory frequency | 30 | 32 | 30 | 30 | 30 | 30 | 31 | 35 |
PEEP (cmH2O) | 10 | 12 | 10 | 10 | 10 | 14 | 12 | 16 |
Driving pressure (cmH2O) | 15 | 9 | 20 | 17 | 20 | 12 | 15 | 14 |
Compliance (mL/cmH2O) | 23 | 30 | 28 | 26 | 18 | 33 | 30 | 23 |
PaO2/FiO2 | 51 | 67 | 52 | 57 | 69 | 73 | 95 | 87 |
ARDS Berlin grade | 3 | 3 | 3 | 3 | 3 | 3 | 3 | 3 |
Number of days of mechanical ventilation | 3 | 4 | 1 | 1 | 9 | 4 | 7 | 3 |
Number of prone positions before ECMO procedure | 2 | 2 | 1 | 1 | 3 | 3 | 3 | 1 |
Chest CT scan | ||||||||
Ground-glass opacities | N/A | N/A | Diffuse | Diffuse | Diffuse | Diffuse | Diffuse | Diffuse |
Consolidations | N/A | N/A | Diffuse | Diffuse | Posterior | Diffuse | Posterior | Posterior |
Crazy paving | N/A | N/A | No | No | Yes | Yes | No | No |
Degree of extension | N/A | N/A | >75% | >75% | >50% | >50% | >50% | >50% |
Lymphocyte count (per mm3) | 400 | 400 | 900 | 400 | 700 | 500 | 12,300* | 200 |
Fibrinogen (g/L) | 6.9 | 3.7 | 6.9 | 6 | 5.7 | >9 | 4.9 | 5 |
CRP (mg/L) | 177 | 194 | 325 | 295 | 360 | 480 | 219 | 301 |
Outcome at 28 d | ||||||||
Discharged from ICU | No | Yes | No | Yes | Yes | No | No | Yes |
In ICU weaned from ECMO | No | No | Yes | No | No | No | No | No |
Remained on ECMO | No | No | No | No | No | No | Yes | No |
Died in ICU | Yes | No | No | No | No | Yes | No | No |
ECMO support duration (d) | 26 | 10 | 17 | 8 | 22 | 26 | 28 | 14 |
Complications during ECMO | ||||||||
Thrombosis | No | No | No | No | No | No | No | No |
Bleeding | No | No | No | No | No | Yes | No | Yes |
Cannula infection | No | No | Yes | No | No | No | No | No |
Need for membrane change | No | No | No | No | Yes | Yes | Yes | No |
Abbreviations: ARDS, acute respiratory distress syndrome; BMI, body mass index; CRP, xxx, CT, computed tomography; ECMO, extracorporeal membrane oxygenation; FiO2, fraction of inspired oxygen; ICU, intensive care unit; ID, immunodepression NSAIDs, nonsteroidal anti-inflammatory drugs; PaO2, partial pressure of oxygen; PEEP, positive end-expiratory pressure; SAPS II, Simplified Acute Physiology Score; SOFA, Sequential Organ Failure Assessment.
Patient with chronic lymphoid leukemia.
To conclude, the setup of a mobile ECMO team within an experienced ECMO center is feasible and may help in the treatment of COVID-19 patients. To date, there are only limited case series regarding ECMO for COVID-19 patients, and larger studies are mandatory to draw any conclusion. However, sharing the experience among ECMO expert centers is necessary to improve our practice.
Conflict of Interest
None.
References
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