Thromboembolic complications during and after hospitalization for COVID-19: Incidence, risk factors and thromboprophylaxis

Abstract

Introduction

The incidence of thromboembolism during COVID-19 and the use of thromboprophylaxis vary greatly between studies. Only a few studies have investigated the rate of thromboembolism post-discharge. This study determined the 90-day incidence of venous and arterial thromboembolic complications, risk factors for venous thromboembolic events and characterized the use of thromboprophylaxis during and after hospitalization.

Materials and methods

We retrospectively reviewed medical records for adult patients hospitalized for >24 h for COVID-19 before May 15, 2020, in ten Norwegian hospitals. We extracted data on demographics, thromboembolic complications, thromboembolic risk factors, and the use of thromboprophylaxis. Cox proportional hazards regression was used to determine risk factors for VTE.

Results

550 patients were included. The 90-day incidence of arterial and venous thromboembolism in hospitalized patients was 6.9% (95% CI: 5.1–9.3) overall and 13.8% in the ICU. Male sex (hazard ratio (HR) 7.44, 95% CI 1.73–32.02, p = 0.007) and previous VTE (HR 6.11, 95% CI: 1.74–21.39, p = 0.005) were associated with risk of VTE in multivariable analysis. Thromboprophylaxis was started in 334 patients (61%) with a median duration of 7 days (25th–75th percentile 3–13); in the VTE population 10/23 (43%) started thromboprophylaxis prior to diagnosis. After discharge 20/223 patients received extended thromboprophylaxis and 2/223 (0.7%, 95% CI: 0.3–1.9) had a thromboembolism.

Conclusions

The 90-day incidence of thromboembolism in COVID-19 patients was 7%, but <1% after discharge. Risk factors were male sex and previous VTE. Most patients received thromboprophylaxis during hospitalization, but only <10% after discharge.

1. Introduction

Coronavirus disease 2019 (COVID-19) predisposes to both arterial and venous thromboembolic complications, including venous thromboembolism (VTE), ischemic stroke and myocardial infarction (MI) [[1], [2], [3], [4]]. The rates of thrombotic complications are higher in acute COVID-19 than in non-COVID-19 acute respiratory distress syndrome (ARDS) [5].

Autopsy studies have demonstrated microvascular thrombi, excessive activation of neutrophils and platelets, as well as neutrophil-platelet aggregates in blood [6]. Further on, endothelial injury is evident from the direct invasion of endothelial cells by SARS-CoV-2, as well as from cytokines and various acute-phase reactants [7]. Elevated circulating prothrombotic factors contribute to a hypercoagulable state [7,8] and immobilization promotes stasis.

Few studies have systematically assessed risk factors for VTE in COVID-19 patients. General VTE risk assessment models might aid in identifying high risk patients, and the IMPROVE-DD score has been externally validated for COVID-19 patients [9,10]. Identified risk factors include active cancer, immobilization, previous VTE, ICU admission, advanced age and elevated D-dimer, amongst others.

The increased risk of VTE has prompted routine institution of thromboprophylaxis in hospitalized patients with COVID-19. However, despite the use of thromboprophylaxis, the incidence of VTE during acute COVID-19 ranges from 3% to 85% in published reports [11]. Variable incidence estimates are likely explained by variations in study design, populations, and assessment methods. Only a few studies have investigated the rate of thromboembolic complications after discharge and in ambulatory patients [12,13]. There is still a debate regarding the need for higher prophylactic dosage in this patient group [14], and whether thromboprophylaxis after hospital discharge is warranted [15].

The main aim of our study was to determine the 90-day incidence of arterial and venous thromboembolism. Secondary aims were to assess risk factors for VTE and describe the use of thromboprophylaxis.

2. Material and methods

2.1. Study design and population

This was a national multicenter retrospective cohort study in ten Norwegian hospitals comprising 550 patients hospitalized with COVID-19. We included subjects ≥18 years of age admitted for >24 h before May 15, 2020. Patients were identified through the hospital diagnosis registries at each hospital using the ICD-10 code for polymerase chain reaction (PCR) confirmed COVID-19 (U07.1).

The regional ethics committee approved the study (Helse Sør-Øst, approval no. 138629, 2020). An opt-out consent process was granted based on the distribution of study information to all participants, and consent exemption was approved for deceased patients.

2.1.1. Medical record review

Investigators in the respective hospitals reviewed medical records, extracting the following data [1]: demographics including age, sex, weight and height, comorbidity, smoking status, previous arterial or venous thrombosis [2], clinical biochemical data [3], type, dosage and duration of anticoagulation during and after hospitalization [4], time and duration of admission to the intensive care unit (ICU) [5], use and duration of invasive mechanical ventilation and [6] study outcomes within 90 days of hospital admission. Thrombotic complications were ischemic stroke, myocardial infarction (MI), pulmonary embolism (PE), or deep vein thrombosis (DVT). Ischemic stroke and VTEs were radiologically confirmed, while MIs were diagnosed based on a rise and fall in cardiac biomarkers together with clinical symptoms, typical changes in an electrocardiogram or during percutaneous coronary intervention. Data on the following comorbidities were recorded to calculate Charlson Comorbidity Index score [16]: previous myocardial infarction, congestive heart failure, peripheral vascular disease, cerebrovascular accident or transient ischemic attack, connective tissue disease, dementia, chronic obstructive pulmonary disease, peptic ulcer disease, liver disease, diabetes, hemiplegia, kidney disease, solid tumor, leukemia, lymphoma, acquired immunodeficiency syndrome and immune thrombocytopenia.

2.2. Statistical analysis

Descriptive statistics and thromboembolic complications are presented with the mean and standard deviation (SD), median (25th–75th percentile) or absolute number (%). Groups were compared using Mann-Whitney U test or t-test for continuous data and Fisher's exact or chi-square test for categorical variables.

We calculated the incidence rates for arterial and venous thromboembolism and thromboprophylaxis practice and estimated 95% confidence intervals using the Wilson method. The cumulative incidence of VTE for males and females was presented using a Kaplan Meier curve.

We used Cox proportional hazards regression to determine risk factors for VTE during 90 days after admission to hospital for COVID-19 infection. We used time to VTE as the dependent variable and estimated hazard ratios (HR) with 95% confidence intervals. Observations were censored at 90 days. We checked the proportional hazards assumption using log-minus-log plots and a test of non-zero slope of Schoenfeld residuals and found the assumption to be acceptable.

We performed univariate analysis using age, sex (male or female), a history of previous VTE (yes or no), body mass index (BMI) ≥ 30 kg/m² (yes or no), D-dimer ≥ 75 percentile (1.4 mg/L) fibrinogen equivalent units (FEU) at admission to hospital (yes or no), C-reactive protein (CRP) > 75th percentile (129 mg/L) at admission to hospital (yes or no) and Charlson comorbidity index (0–2 or >2) as independent variables. In the analysis that included D-dimer as a predictor, we excluded VTE events during the first 2 days after admission, as an elevated D-dimer could be considered the first sign of a VTE.

Because of a limited number of VTE events prior to the analysis, we initially chose four independent variables (age, sex, previous VTE and BMI) for inclusion in a multivariable analysis. As a rule of thumb, a minimum of five to ten events per independent variable is recommended [17]. There were too few arterial events to conduct meaningful analysis on potential risk factors.

We used Stata software version 17.0 (StataCorp, College Station, TX, USA) for all analyses, choosing a significance level of p < 0.05 in two-sided tests.

3. Results

We included and reviewed medical records of 550 patients who were admitted for COVID-19 during the study period. Of these, 61 patients (11%) had died during hospitalization. Mean age was 61.5 years (SD 16.4), and 345 (52%) were males. The majority (64.7%) of patients had a Charlson Comorbidity Index ≥3 (range: 0–11). The median (25th to 75th percentile) length of stay in the hospital was 7 days [[4], [5], [6], [7], [8], [9], [10], [11], [12]] overall. In total, 130 patients (23%) were admitted to the ICU, with a median length of stay in the ICU of 13 days [[6], [7], [8], [9], [10], [11], [12], [13], [14], [15], [16], [17], [18], [19], [20]] (Table 1 ). There was a difference in sex, BMI, inflammatory biomarkers, such as CRP and D-dimer levels, length of stay, ICU admission rate and need of mechanical ventilation between the VTE and non-VTE group (all p<0.05) (Table 1).

Table 1.

Descriptive statistics, presented as number (%) or median (25th-75th percentile unless otherwise stated.

	Total	VTE	Non-VTE	P**
Patients, n	550	23	527
Age (years), mean (SD)	61.5 (16.4)	60.2 (14)	61.5 (17)	0.65
Sex, males	345 (52)	21 (91)	324 (62)	0.003
Body mass index, kg/m2, mean (SD)	28.0 (5.6)	31.0 (5.2)	27.8 (5.6)	0.008
Current smokers	13 (4)	0	13 (4)	0.571
Former smokers	165 (35)	8 (38)	157 (35.3)	0.818
Diabetes mellitus type 2	101 (18)	2 (18)	99 (18)	0.281
Chronic obstructive lung disease	28 (5)	0	28 (5)	0.622
Chronic kidney disease moderate/severe*	21 (4)	0	21 (4)	1
Previous venous thromboembolism	21 (4)	3 (13)	18 (3)	0.052
Charlson comorbidity index	3 (2-5)	3 (2-4)	3 (2-5)	0.604
0–2	194 (35)	6 (26)	188 (35)
≥3	356 (64)	17 (73)	339 (64)
Laboratory values at admission
D-dimer (mg/L FEU), n = 366	0.8 (0.4–1.4)	2.6 (0.9–4.1)	0.7 (0.4–1.3)	< 0.001
C-reactive protein (mg/L)	60 (25–129)	115 (70–186)	60 (24–128)	0.002
Creatinine (μmol/L)	81.5 (67–100)	83 (76–102)	81 (66–100)	0.098
Laboratory values, highest
D-dimer (mg/L FEU)	1.3 (0.7–3.1)	4.1 (4.1–19.2)	1.2 (0.6–2.8)	< 0.001
C-reactive protein (mg/L)	130 (55–235)	268 (146–340)	128 (52–224)	< 0.001
Creatinine (μmol/L)	86 (68–111)	88 (77–145)	85 (68–110)	0.445
Days from positive PCR to admission	0 (0–3)	0 (0–5)	0 (0–3)	0.469
Days hospitalized	7 (4-12)	11 (7-27)	7 (4-12)	0.001
Intensive care unit	130 (23)	13 (56)	117 (22)	< 0.001
Days	13 (6-20)	18 (13-20)	12 (6-20)	0.189
Thromboprophylaxis	118 (91)	13 (100)	105 (90)	0.227
Invasive mechanical ventilation	96 (17)	12 (52)	84 (16)	< 0.001
Days	13 (9-20)	15 (12-21)	13 (9-20)	0.541
Deceased	61 (11)	2 (9)	59 (11)	0.709
Thromboprophylaxis initiated in hospital	334 (61)	10 (43)***	324 (61)	0.009
Duration of thromboprophylaxis, days	7 (3-13)	5 (2-20)	7 (3-13)	0.005

PCR = polymerase chain reaction; VTE = venous thromboembolism; * (creatinine >0.27 mmol/L).

**Bold font indicate significance *** Initiated minimum 2 days prior to VTE diagnosis.

In total, 38 out of 550 patients (6.9%, 95% CI: 5.1–9.3) had an arterial thromboembolic event (ATE) or VTE within 90 days of admission (Table 2 ). In the ICU 18/130 patients (13.8%, 95% CI: 8.9–20.8) had a thromboembolic event. The cumulative incidence of VTE was higher in male and female patients with COVID-19 with an increased incidence of VTE among male than in female patients (Fig. 1 ).

Table 2.

Incidence of thromboembolic complications 30- and 90-days after admission to hospital, presented as number of events and incidence rates with 95% confidence intervals (CI).

(n = 550)	30 days		90 days
	No. of events	Incidence % (95% CI)	No. of events	Incidence % (95% CI)
ATE or VTE	344	6.2 (1.0–8.5)	38	6.9 (5.1–9.3)
In-hospital	32	5.8 (4.2–8.1)	34	6.2 (4.5–8.5)
Intensive care unit, n = 130	13	10.0 (5.9–16.4)	18	13.8 (8.9–20.8)
Post discharge*	2	0.4 (0.0–1.3)	4	0.7 (0.3–2.1)
Venous thrombosis	20	3.6 (2.4–5.5)	23	4.2 (2.8–6.2)
Only deep vein thrombosis	2	0.4 (0.0–1.3)	2	0.4 (0.0–1.3)
Pulmonary embolism**	17	3.1 (1.8–4.9)	20	3.6 (2.2–5.6)
Catheter-related VTE	1	0.2 (0.0–1.0)	1	0.2 (0.0–1.0)
Arterial thrombosis	14	2.5 (2.0–4.0)	15	2.7 (1.7–4.5)
Myocardial infarction	10	1.8 (1.0–3.3)	11	2.0 (1.0–3.6)
Ischemic stroke	4	0.7 (0.2–1.9)	4	0.7 (0.2–1.9)

ATE = arterial thromboembolic event; VTE = venous thromboembolic event; * 2 pulmonary embolisms, 1 myocardial infarction and 1 ischemic stroke. **10 central and 13 peripheral pulmonary embolisms*** 1 ST-elevation myocardial infarction, the rest non-ST-elevation myocardial infarction.

Fig. 1.

Kaplan Meier plot of the cumulative incidence of venous thromboembolic events (VTE) during and after hospitalization for males and females.

A VTE occurred in 23 patients (4.2%, 95% CI: 2.8–6.2), 20/23 (87%) were pulmonary embolisms, of which 10 were central (pulmonary trunk or main pulmonary arteries) and 13 were peripheral (segmental or subsegmental pulmonary arteries). Among those diagnosed with a VTE 13/23 (56%) had been treated in the ICU compared to 22% in the non-VTE group. Four thromboembolic events were diagnosed after discharge, giving a post-discharge 90-day incidence rate of 0.7% (95% CI: 0.3–1.9) with a median time from discharge to thromboembolic event of 17 days (25th–75th percentile 3.5–34 days).

ATE occurred in 15 patients (2.7%, 95% CI: 1.7–4.5) within 90 days of admission to hospital, of which 11 were MI and 4 ischemic strokes. Among the patients with MIs, 10/11 (91%) were non-ST-elevation myocardial infarctions, 4/11 (36%) were admitted to the ICU and 1 occurred after discharge from hospital. Only 1/4 (25%) patients with ischemic stroke were admitted to the ICU and 1 occurred after discharge from hospital.

Thromboprophylaxis was initiated in 334/550 patients (61%, 95% CI: 56.6–64.7); dosages are shown in Table 3 . The median duration of the thromboprophylaxis was 7 days (25th–75th percentile 3–13 days). Dosages were frequently changed depending on fluctuations in clinical and biochemical parameters. Of the patients admitted in the hospital wards 214/420 (51%) received thromboprophylaxis and 6 (2.7%) of those developed VTE, whereas of those admitted in the ICU 118/130 (91%) received thromboprophylaxis and 13 (11%) of these developed a VTE. In a subgroup of 223 patients with data on discharge medications, 20/223 (9%) were discharged with thromboprophylaxis initiated during the hospital stay. Further on, 15/223 (6.7%) were discharge with newly initiated anticoagulation due to other causes such as treatment of established VTE, atrial fibrillation or unknown/unspecified in the remaining. Low-molecular-weight heparin (LMWH) was most often prescribed (71.4%).

Table 3.

Anticoagulation pattern during and after hospitalization, presented as number (%) with 95% confidence intervals (CI), unless otherwise specified.

Variables	n = 550	%, 95% CI
Anticoagulation initiated during hospitalization	341	62 (57.9–66.0)
Low-molecular-weight heparin	334	61 (56.6–64.7)
Intermediate-therapeutic intensity*	71	22 (17.2–26.0)
Prophylactic intensity	249	77 (72.0–81.1)
Direct oral anticoagulation	22	7 (4.3–9.)
Duration, days, median (25th-75th percentile)	7 (3-13)
Discharged with newly initiated anticoagulation**	35	16 (11.5–21.1)
Indication***
Venous thromboembolism	9	26 (14.2–42.1)
Atrial fibrillation	2	6 (1.6–18.6)
Thromboprophylaxis	20	57 (40.9–72.0)
Unknown/other	4	11 (4.5–26.0)
Duration***
Unknown	10	29
≤10 days	10	29
≥2 weeks <3 months	5	14
3 months	5	14
Indefinite	5	14
Type***
Low-molecular-weight heparin	25	71
Direct oral anticoagulation	10	28

*Intermediate intensity refers to standard prophylactic dose twice daily (enoxaparin 40 mg bd or dalteparin 5000 mg bd),**n = 223, ***n = 35.

The cumulative incidence of VTE was higher in male than in female patients (Fig. 1). In univariate proportional hazard regression analysis, male sex (HR 6.13, 95% CI: 1.44–26.20, p = 0.014) and previous venous thromboembolism (HR 4.58, 95% CI: 1.35–15.55, p = 0.015) were associated with risk of VTE (Table 4 ). In further multivariable analysis, male sex (HR 7.44, 95% CI: 1.74–32.02, p = 0.007) and history of previous VTE (HR 6.11, 95% CI: 1.74–21.39, p = 0.005) were associated with risk of VTE.

Table 4.

Univariate and multivariable analysis of risk factors of venous thromboembolism, presented as hazard ratios with 95% confidence intervals (CI) and p-values.

Variable	Univariate****			Multivariable*****
	Hazard ratio	95% CI	P	Hazard ratio	95% CI	P
Age, per years	0.99	0.97–1.0	0.70	0.99	0.97–1.03	0.998
Sex, males	6.13	1.44–26.20	0.014	7.44	1.73–32.02	0.007
Previous venous thromboembolism	4.58	1.35–15.55	0.015	6.11	1.74–21.39	0.005
Body mass index ≥30 kg/m2 *	1.87	0.79–4.43	0.155	2.33	0.95–5.71	0.065
Charlson comorbidity index >2	1.30	0.53–3.14	0.57
D-dimer ≥ 75th percentile (1.4 mg/L FEU) **	2.89	0.77–10.69	0.116
C-reactive protein >75th percentile (129mg/L)***	2.04	0.86–4.82	0.106

*n = 407; ** At admission to hospital; n = 359, events the first two days of hospitalization are excluded.

***n = 542, at admission to hospital; ****n=23; *****n = 407, number of events = 23.

4. Discussion

There are three main findings in this study; First, the 90-day incidence of thromboembolic events during hospitalization was about 7% in a population where 62% already had received thromboprophylaxis, mainly standard prophylactic intensity. Second, the rate of thrombotic events after discharge was very low (0.7%), despite subgroup analysis revealing that less than 10% had further prophylactic anticoagulation upon discharge from hospital. Third, male sex and a history of previous VTE were associated with an increased risk of VTE.

Early reports indicated very high rates of VTE up to 85% in patients admitted for COVID-19, even in patients receiving standard thromboprophylaxis, which led to suggestions of the possible need for higher prophylactic dosage [4,11,18]. Some recent studies indicate a lower incidence of thromboembolic complications than earlier studies, but reports still show a large variation [[19], [20], [21], [22], [23], [24], [25]]. In a recent meta-analysis of more than 30.000 patients, the overall incidence of VTE during hospitalization was 12.8%; 24.1% in patients admitted to the ICU, and 7.7% in non-ICU patients [20], not considering distal deep vein thrombosis (DVT). A study of 399 patients admitted for COVID-19 reported ATE (MI and stroke) in 15/399 patients (3.8%) and VTE in 51/399 patients (12.8%) [26].

Our findings are in the lower end of previously reported rates of VTE, but similar to reported rates of ATE [19,26]. Previously reported VTE rates for hospitalized patients with COVID-19 may be overestimated due to selected high-risk populations, reports from ICU populations, routine use of chest CT, or intensive case findings by screening asymptomatic patients for VTE. This may have influenced the rates both in solitary studies and in meta-analyses. Several factors may have affected our VTE rate estimate and contributed to the low incidence of VTE. For instance, our study included patients hospitalized in the early days of the pandemic, when awareness of thromboembolic complications was limited.

In this early period, restrictions based on institutional infection control measures may have led to conservative use of radiological imaging. Because the incidence of COVID-19 infection in Norway has been lower than in other areas of Europe, and hospital capacity has not been overwhelmed, the threshold for admission may have been lower than in some other countries [27]. Lastly, only a small subset of fatal COVID-19 cases were autopsied, and the presence of unrecognized VTE and ATE in these patients cannot be excluded [28].

A large proportion of the patients that developed VTE had thromboprophylaxis at the time of diagnosis, however, the majority only received standard prophylactic intensity. It is possible that selected patients may benefit from higher intensity anticoagulation, although this could not be assessed in the present study. As our data did not include assessment of bleeding complications, we cannot conclude on the net benefit on mortality and morbidity. Whether the incidence of VTE in COVID-19 differs from that of other viral and bacterial pneumonia remains uncertain.

In our study, thromboprophylaxis was initiated in about 2 of 3 patients during hospitalization. At the start of the pandemic, there was no national or local guidelines of thromboprophylaxis for patients with COVID-19. However, currently a standard prophylactic dosing is recommended in hospital wards and mainly intermediate dosing (standard dose x 2) for patients in the ICU in Norway. Many hospitals have used the Padua score for thromboprophylaxis on COVID-19 patients. Current international guidelines are based on expert opinions and very low certainty of evidence, which may explain the diversity in recommendations [15,29,30]. A minimum of prophylactic intensity anticoagulation (40 mg enoxaparin or 5000IE dalteparin) is recommended for most patients after careful assessment of bleeding risk. Published evidence suggests no benefit of intermediate intensity (standard intensity bd) over standard intensity thromboprophylaxis [31], however, therapeutic intensity (1 mg/kg enoxaparin qd or 200IU/kg dalteparin qd) seems to be beneficial in non-critically ill patients [[32], [33], [34]].

We found that only 0.7% of patients had an ATE or VTE after hospital discharge, which is in line with previous reports of 0.2–2.5% [13,35,36]. Less than 10% of patients in the present study were discharged with continued prophylaxis. This practice is still heterogenous in Norway, as only some of the participating hospitals have guidelines recommending post-discharge thromboprophylaxis with low dose direct oral anticoagulation (DOAC) for 1–4 weeks to patients treated in the ICU with a complicated course of illness. Large randomized controlled trials (RCTs) investigating the impact of thromboprophylaxis after discharge and in an ambulatory setting are currently ongoing; one of these is the ACTIV-4C trial (NCT04650087), part of the Accelerating COVID-19 Therapeutic Interventions and Vaccines initiative coordinating research on COVID-19, which aims to determine whether extended thromboprophylaxis after hospitalization reduces risk of thromboembolism and mortality following discharge from the hospital [37]. Meanwhile, The American College of Chest Physicians (CHEST) guidelines recommend against thromboprophylaxis after hospital discharge with exceptions like a history of previous VTE or active cancer [15]. International Society of Thrombosis and Haemostasis (ISTH) guidelines recommend considering post-discharge thromboprophylaxis for all high-risk patients, including advanced age, ICU stay, D-dimer > 2 times ULN or IMPROVE VTE score of more than 4 [15,30]. Bleeding risk must also be taken into consideration.

In our study, male sex and a history of previous thrombosis were associated with time to VTE in multivariable analysis, consistent with results from previous studies [38,39]. In univariate analysis, D-dimer ≥ 75 percentile (1.4 mg/L FEU) was also associated with risk of VTE. However, because all patients did not have D-dimer measured at the time of admission, the possibility of an existing thrombosis at the time of admission, and the possible impact of inflammation on D-dimer values during COVID-19, we chose not to include D-dimer in the multivariable analysis. Further on, we chose to dichotomize D-dimer because different laboratories report different upper and lower limits, which makes a continuous variable problematic. Some studies have also indicated that biomarkers like D-dimer and CRP have a high predictive value for VTE [40], as well as clinical factors like severity of COVID-19, ICU admission, active malignancy and male sex [38,41]. The literature on age and association with VTE during COVID-19 is inconsistent, as both advanced age and young age may be associated with a higher incidence of VTE [9,39,42,43].

Risk assessment models (RAM), e.g., IMPROVE-DD, Padua or Caprini, can assist in the identification of COVID-19 patients at high risk for VTE [9,10,44]. Despite male sex being a prominent risk factor for VTE during COVID-19 in several studies, including the current study, sex is not included in any of these risk models [41,43,45]. The male predominance described among critically ill and ICU-admitted COVID-19 patients probably explains the increased risk of VTE among males during acute COVID-19 infection [38,39]. Further studies and external validation of prediction models are required to determine the optimal risk stratification scheme for this patient population. Male sex could be considered as a risk factor in future risk models for VTE during COVID-19.

The present study has some limitations. The study period was from the early days of the pandemic; thus, it does not take into account the increased awareness around thromboembolic complications and thromboprophylaxis, mutations of the virus and the effect of vaccines. Norwegian hospitals have not been overwhelmed during the pandemic; consequently, the population admitted to hospitals in Norway might differ from that of other countries. The hospitals included in this study received more than 50% of admitted COVID-19 patients in Norway, which supports generalization to a setting without severely constrained hospital capacity. In our opinion, the retrospective study design is not a major limitation, as the same patients are likely to have been included if the study was prospective. However, it is possible that some patients are missed due to insufficient ICD-10 coding or misclassification at the time of discharge. Further on, the number of thromboembolic events were few, which limits the multivariable analysis. We did not include variables describing the severity of the infection, which could have been interesting to assess potential associations with risk of VTE.

We found male sex to be a distinct risk factor of VTE during COVID-19, which could be considered a risk factor in future risk assessment models. Higher intensity thromboprophylaxis might be warranted in certain high-risk patients. Still, results from large RCTs, including both benefits of thromboprophylaxis and risk of bleeding, are needed to recommend specific dosage for different subpopulations.

5. Conclusion

The incidence of thrombotic complications in patients hospitalized for COVID-19 was lower in this study compared to many other early studies. However, many patients were diagnosed with VTEs despite receiving standard thromboprophylaxis. Male sex and previous thrombosis were associated with increased risk of VTE, emphasizing the need for thorough consideration of thromboprophylaxis in these patients.

Authors contributions

All authors have contributed to drafting, revision and approval of the manuscript. BT and KS analyzed the data.

Ethics approval

The study has approval from the Norwegian Regional Ethics committee (REK).

Funding

Funding was provided by a grant from Helse Sør-Øst (grant nr 2021008)

Declaration of competing interest

The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Waleed Ghanima reports fees for participation in Advisory board from Amgen, Novartis, Pfizer, Principia Biopharma Inc- a Sanofi Company, Sanofi, SOBI, Griffols, UCB, Argenx. Lecture honoraria from Amgen, Novartis, Pfizer, Bristol Myers Squibb, SOBI, Griffols, Sanofi. Research grants from Bayer, and BMS/Pfizer.

Galina Tsykunova reports lecture honoraria from Amgen, Janssen, Ablynx, Sanofi and Sobi. Research grants from Janssen.