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Causes and timing of death in critically ill COVID-19 patients

Mortality rate of critically ill COVID-19 patients is high, especially in those requiring invasive mechanical ventilation. However, the causes and the timing of death of patients admitted to the ICU for SARS-CoV-2 pneumonia have been poorly reported [1, 2]. Whether patients mainly die from refractory respiratory failure directly due to SARS-CoV-2 pneumonia or from sepsis as reported in non-COVID-19 ARDS patients [3] is unknown. Moreover, the increased risk of pulmonary embolism extensively described among COVID-19 patients together with the SARS-CoV-2-associated myocardial injuries [4] may expose critically ill COVID-19 patients to death from a cardiac origin [5]. Additionally, the increased intensity of thromboprophylaxis commonly used to prevent thrombotic events might also promote fatal hemorrhagic events.

We therefore aimed to describe the main causes of death among critically ill COVID-19 patients admitted to our ICU, as well as to report the timing of each cause of death.

We retrospectively reviewed all deaths occurring in adult COVID-19 patients (RT-PCR positive for SARS-CoV-2) admitted to our ICU between March 6th, 2020 and January 18th, 2021 for acute respiratory failure related to SARS-CoV-2 pneumonia.

Causes of death were categorized in four subgroups: (1) refractory respiratory failure, (2) shock with multiorgan failure, (3) cardiac death including proven pulmonary embolism (proximal thrombus on CT-pulmonary angiography with acute cor pulmonale on echocardiography and vasopressor requirement) and unexpected cardiac arrest (neither prior oxygen desaturation nor circulatory failure) and (4) neurological death (ischemic/hemorrhagic stroke with brain herniation).

After exclusion of COVID-19 patients still hospitalized, 152 patients were analyzed. Among them, 73 (48%, 95% confidence interval 40–56%) died with a median delay of 14 [9–23] days after ICU admission. Characteristics of the patients dying in the ICU are detailed in the Table 1.

Table 1 Characteristics of 73 critically ill COVID-19 patients dying during ICU stay

Distribution of the main causes of death (panel a) and timing of each cause of death (panel b) are detailed in the Fig. 1. The leading cause of death was refractory respiratory failure which accounted for 45% of ICU deaths. Cardiac deaths (all occurring in intubated patients) included 4 pulmonary embolisms (intravenous thrombolysis, n = 3) and 9 unexpected cardiac arrests (asystole, n = 7; pulseless electrical activity, n = 2). Neurological deaths included hemorrhagic (n = 4) and ischemic (n = 1) strokes. Overall, 10 (14%) and 6 (8%) patients directly died from a thrombotic or hemorrhagic event, respectively.

Fig. 1
figure 1

a Distribution of each cause of death among 73 critically ill COVID-19 patients dying during the ICU stay (VAP ventilator-associated pneumonia). b Kaplan–Meier survival estimates following ICU admission and median delay [quartile 1–quartile 3] (in days) between ICU admission and death according to each cause of death. In both panels, deaths from refractory respiratory failure, shock with multi-organ failure, cardiac and neurologic causes figure in blue, red, orange and grey, respectively

None of the patients dying from shock with multi-organ failure or from cardiac death died after a withholding (all the patients with unexpected cardiac arrest underwent cardiopulmonary resuscitation) or withdrawal procedure while all patients dying from a neurological cause died after a withdrawal procedure. Among patients dying from refractory respiratory failure, 22 (66%) and 4 died after a withholding (tracheal intubation, n = 2; extracorporeal membrane oxygenation, n = 19; renal replacement therapy, n = 1) or withdrawal procedure, respectively.

As opposed to non-COVID19 ARDS patients [3, 6], we herein report that refractory respiratory failure was the leading cause of death among COVID-19 ARDS patients, consistent with a previous report [2]. Deaths by refractory respiratory failure occurred late in the ICU course, potentially as a result of pulmonary fibrosis induced by SARS-CoV-2 and prolonged mechanical ventilation, making futile the use of extracorporeal membrane oxygenation support.

Noteworthy, cardiac deaths related to pulmonary embolism or unexpected cardiac arrest accounted for 18% of the deaths and occurred early in the ICU course. Similarly, a large multicenter study reported that up to 14% of the critically ill COVID-19 patients experienced cardiac arrest, mainly due to pulseless electrical activity and asystole, as a possible manifestation of fulminant myocarditis or proximal pulmonary embolism [2, 5].

Even if our study suffers from several limitations including its monocenter retrospective design, the limited number of patients and the lack of control with non-COVID-19 patients, it provides an informative picture of the main causes of death of critically ill COVID-19 patients.

Availability of data and materials

The dataset used and analyzed for the current study is available from the corresponding author on reasonable request.

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Acknowledgements

We warmly acknowledge Dr. Jo-Anna Tirolien, Dr. Olivia Picq, Dr. Olivier Pajot, Dr. Hervé Mentec and all the residents who cared of the patients.

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Authors

Contributions

DC, GP and RC are responsible for the conception and design. All the authors took care of the patients. DC, MF and RC are responsible for data acquisition. All the authors were responsible for analysis and interpretation of data. All authors read, critically reviewed and approved the final manuscript. DC takes responsibility for the paper as a whole.

Corresponding author

Correspondence to Damien Contou.

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This study was conducted in accordance with the amended Declaration of Helsinki and was approved by the Institutional Review Board (CE 2021-008) of the French Intensive Care Society.

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The authors declare that they have no competing interests.

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Contou, D., Cally, R., Sarfati, F. et al. Causes and timing of death in critically ill COVID-19 patients. Crit Care 25, 79 (2021). https://doi.org/10.1186/s13054-021-03492-x

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