Study population
This is a retrospective cohort study of all patients diagnosed with COVID-19 infection who were admitted at Hospital Universitario Río Hortega Valladolid, Spain, from 18 March to 21 April 2020 and died during their hospitalization. The hospital ethics committee approved this study. Due to the nature of the retrospective chart review, waived the need for informed consent from individual patients.
Patients were included if they were diagnosed with confirmed COVID-19 and died during the study period. Patients were diagnosed according to World Health Organization guidance [13]. Laboratory confirmation for SARS-CoV-2 was defined as a positive result of real-time reverse transcriptase polymerase chain reaction (RT-PCR) assay of nasal and pharyngeal swabs or a positive serology test.
Data collection
A trained team of internal medicine physicians and specialist registrars reviewed and collected epidemiological, clinical and outcome data from electronic medical records. Patient confidentiality was protected by deidentification.
Every patient’s medical record was independently assessed by one of the researchers (MCS, MGM, PCM, IAJ, MRH, LHG, DVP, MCG, and MGF). The researchers were blinded to the outcome of interest during data collection. The assessment of the cause of death was done after they had gathered all the clinical information. When the cause of death was unclear, the medical record was assessed by a second researcher. Differences in opinion were resolved by discussion and consensus or by consulting one of the senior authors (LCG) if needed. Six patients’ cause of death should be assessed by a second researcher. All the patients whose cause of death was assessed as not caused directly by SARS-CoV-2 infection were double checked for the senior author. Three patients initially assigned to the death with SARS-CoV-2 infection group were finally switched to the death caused by SARS-CoV2 infection group after careful assessment of laboratory and imagen data.
Study outcomes and definitions
The primary outcome was the definition of the cause of death of the patients. As the secondary outcome, we assessed the development of ARDS, hyperinflammation response, sepsis or thromboembolic events.
Acute respiratory distress syndrome (ARDS) was identified according to the Berlin Definition [14]. All the following criteria were required:
-
1.
Onset respiratory symptoms must begin within 1 week of a known clinical insult, or the patient must have new or worsening symptoms during the past week.
-
2.
Chest imaging bilateral opacities must be present on a chest radiograph or computed tomographic (CT) scan. These opacities must not be fully explained by pleural effusions, lobar collapse, lung collapse or pulmonary nodules.
-
3.
Origin of pulmonary infiltrates the patient’s respiratory failure must not be fully explained by cardiac failure or fluid overload. ARDS can be diagnosed once cardiogenic pulmonary oedema and alternative causes of acute hypoxemic respiratory failure have been excluded.
-
4.
Oxygenation impairment: a moderate to severe impairment of oxygenation must be present, as defined by the ratio of arterial oxygen tension to fraction of inspired oxygen (PaO2/FiO2), or the ratio of oxygen saturation to FiO2 (SaO2/FiO2) when PaO2 is not available. The severity of the hypoxemia defines the severity of ARDS:
-
a.
mild: PaO2/FiO2 200–300 mmHg or SaO2/FiO2 237–317 mmHg;
-
b.
moderate: PaO2/FiO2 100–200 mmHg or SaO2/FiO2 155–237 mmHg;
-
c.
severe: PaO2/FiO2 ≤ 100 mmHg or SaO2/FiO2 < 155 mmHg.
Hyperinflammation response we considered a hyperinflammatory response present in the context of moderate to severe COVID-19 infection with a lymphocyte count of < 1000 × 109/mL, and one of the following laboratory parameters:
-
1.
serum ferritin > 1000 ng/mL;
-
2.
C-reactive protein > 150 mg/L;
-
3.
D-dimer > 800 μg/L;
-
4.
Interleukin 6 > 20 pg/mL.
Cause-specific death in individuals infected with SARS-CoV-2 we defined clinical criteria for assessing COVID-related causes of death. It was not possible to support the diagnosis of death by necropsies, as they were not available. Patients were divided in two groups according their cause of death.
Deaths caused by SARS-CoV-2 infection we considered that death was directly caused by SARS-CoV-2 infection complications when the patient developed
-
1.
ARDS or hyperinflammation response that led to their death;
-
2.
acute respiratory failure leading to death without meeting ARDS and hyperinflammation response criteria, and severe lung injury likely due to COVID-19 on X-ray or CT;
-
3.
acute respiratory failure or thrombotic events in the context of pulmonary embolism or other forms of venous thromboembolism that led to death;
-
4.
septic shock due to SARS-CoV-2 that led to their death.
Death with SARS-CoV-2 infection we considered that COVID-19 infection was a precipitating factor to decompensate other chronic or acute pathologies and death was unrelated to severe complications of SARS-CoV-2 infection when
-
1.
The patient developed acute respiratory failure caused by cardiogenic pulmonary oedema or other alternative causes of acute hypoxemic respiratory failure unrelated to COVID-19 that led to death. There were no lung injuries on X-ray or CT likely caused by COVID-19, or they were mild (only interstitial infiltrates of peripheral distribution, with neither alveolar infiltrates, nor consolidation, affecting less than 50% of lung in X-ray or CT scan: equivalent to Brixia score < 4 [15]).
-
2.
The patient developed multiorgan failure associated with frailty that led to death. Septic shock was excluded. There were no lung injuries on X-ray or CT likely caused by COVID-19, or they were mild to moderate (interstitial or interstitial and alveolar infiltrates with interstitial predominance, affecting less than 50% of lung in X-ray or CT scan; equivalent to Brixia score < 7).
-
3.
The patient's death was from any confirmed cause unrelated to COVID-19 complications, including septic shock due to another microorganism.
Patients’ grade of frailty was defined according Clinical Frailty Scale [16]. The grade of dependency was assessed using Barthel Index for activities of daily living [17].
Statistical analysis
The sample size was equal to the number of patients who died during the study period. Descriptive analysis of the continuous variables is expressed as the median and interquartile range (IQR). Categorical variables are presented as the number of patients (%) with 95% CI.
Differences in distributions of patient characteristics by outcome subgroup were reported using differences with 95% CIs. Categorical data were compared using the Chi square test or the Fisher exact test when needed. For crosstabs larger than 2 × 2 of 3 ordinal variables (age, performance in activities of daily living and clinical frailty scale), we used the linear-by-linear association test to assess for trends. Continuous data were compared using Student’s t test or the Mann–Whitney rank sum test with non-parametric variables. ORs adjusted by age are presented with 95% CIs for all the variables associated with the cause of death in univariate analysis. Adjustment by age was done using logistic regression.
All tests were two sided with statistical significance set at p < 0.05. All analyses were performed with SPSS, version 21.0 (IBM SPSS).