Venous or arterial thromboses after venoarterial extracorporeal membrane oxygenation support: Frequency and risk factors

https://doi.org/10.1016/j.healun.2020.12.007Get rights and content

BACKGROUND

Although venous thrombosis after venovenous–extracorporeal membrane oxygenation (ECMO) is well described, vascular complications occurring after venoarterial ECMO (VA-ECMO) removal have not yet been thoroughly described. Our aim was to evaluate the frequency of vascular (arterial and venous) complications after VA-ECMO removal and try to identify the risk factors associated with them.

METHODS

Retrospective analysis of data prospectively collected in 2 intensive care units was performed. Consecutive patients successfully weaned off VA-ECMO during year 1 were screened for cannula-associated deep vein thrombosis (CaDVT) or arterial complications (arterial thrombosis/stenosis) using Doppler ultrasonography.

RESULTS

From November 2018 to November 2019, a total of 107 patients with a median (interquartile range [IQR]) age of 54 (42–63) years and a median (IQR) ECMO support duration of 8 (2–5) days were successfully weaned off VA-ECMO and included. CaDVT occurred in 44 patients (41%), and arterial complications occurred in 15 (14%) (9 acute leg ischemia, 1 arteriovenous femoral fistula, and 5 late femoral stenosis). Multivariable analysis retained longer duration of ECMO support (odds ratio [OR]: 1.12 per day; 95% CI: 1.02–1.22) and infection occurring on ECMO (OR: 3.03; 95% CI: 1.14–8.03) as independent risk factors for CaDVT, whereas older age (OR: 0.97 per year; 95% CI: 0.94–0.99) and previous anti-coagulation use (OR: 0.21; 95% CI: 0.06–0.68) were protective factors for CaDVT. No risk factors for arterial complications were identified.

CONCLUSIONS

In patients requiring VA-ECMO support, vascular complications occurred frequently after its removal, especially CaDVT. Arterial complications, either early leg ischemia or late arterial stenosis, were observed less often. Strategies aimed at preventing CaDVT after VA-ECMO remain to be determined.

Section snippets

Patients

All consecutive patients who received VA-ECMO and were successfully weaned off it in 2 ICUs between November 2018 and November 2019 were included. Patients who had <48 hours of extracorporeal membrane oxygenation (ECMO) run, died on ECMO, or were not screened for cannula-related thrombosis were excluded. All the following information was collected prospectively: ICU admission Simplified Acute Physiology Score II and Sequential Organ-Failure Assessment score, local infectious complications

Patient characteristics

Between November 2018 and November 2019, a total of 107 patients were successfully weaned off ECMO, and all were included in the study. Their median age was 54 (42–63) years, and the median time on ECMO support was 8 (2–15) days. The main indications for ECMO were acute on chronic cardiac failure (35.5%) and post-cardiotomy care (31.8%). VAV-ECMO hook up was used for 5 patients. Their baseline characteristics, course on ECMO, and outcomes are reported in Table 1.

CaDVT and arterial complications

Among the 107 patients, 44 (41%)

Discussion

The results of this study showed that arterial thrombosis and CaDVT were frequent in VA-ECMO–treated patients, with the latter occurring in 41% of patients and being more frequent than the former. In addition, several risk factors for developing CaDVT in this population were identified, namely infection on ECMO support and longer duration of ECMO support, whereas older age and anti-coagulant therapy before ECMO support were protective factors. To the best of our knowledge, vascular

Conclusions

In conclusion, vascular complications after VA-ECMO removal are frequent. CaDVT was the most frequent and should be actively sought in every patient after VA-ECMO explantation, especially in patients with prolonged ECMO runs, or when an on-ECMO infection occurs. Arterial complications were less frequent and could occur early after ECMO withdrawal (acute ischemia) or later (arterial stenosis). Further studies are needed to evaluate the precise duration of anti-coagulation in patients with CaDVT.

Disclosure statement

C.E.L. reports personal fees from Merck Sharp and Dohme, Thermo Fischer Brahms, Biomérieux, Carmat, Bayer Healthcare, and Aerogen and grants from Bayer Healthcare, outside the scope of the submitted work. M.S. reports lecture fees from Maquet, Getinge, and Fresenius, outside the scope of the submitted work. The remaining authors have no conflicts of interest to disclose.

The authors thank Janet Jacobson for her help during the preparation of the manuscript.

Support for this study was provided

Author contributions

All authors participated in data collection and final manuscript preparation and agreed on the latest manuscript.

Concept and design: F.B., C.E.L.

Acquisition, analysis, or interpretation of data: F.B., C.E.L.

Drafting of the manuscript: F.B., C.E.L.

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