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Liu, Chiu, Suresh, Patel, Bains, Shear, Ruditsky, Henry, Dubin, Sahai, Prakash, Amin, Bivona, Jauregui, Koh, Ludwig, and Cavanaugh: Thoracolumbar spine surgery in the post-pandemic era: a national retrospective analysis of thrombotic complications, vaccination status, and prior hospitalization with COVID-19

Abstract

Study Design

Retrospective cohort study.

Purpose

To compare thrombotic complication rates in thoracolumbar spine surgery patients before and after the coronavirus disease 2019 (COVID-19) pandemic.

Overview of Literature

Thrombotic complications are a major cause of postoperative morbidity and mortality in spine surgery. Both COVID-19 infection and vaccination have been linked to hypercoagulability. However, data on pre- versus post-pandemic thrombotic risk in spine surgery are limited, and the influence of infection severity or vaccination status has not been examined.

Methods

Adult patients (≥18 years) undergoing primary thoracolumbar decompression with or without fusion were identified, excluding trauma and neoplastic cases. Patients were divided into “pre-COVID” and “post-COVID” cohorts. Outcomes included 90-day rates of postoperative deep venous thrombosis (DVT), pulmonary embolism (PE), myocardial infarction (MI), and cerebrovascular accident (CVA). Cohorts were compared using Pearson’s chi-square tests, and multivariable regression adjusted for demographics and comorbidities.

Results

A total of 784,498 patients were included. Post-COVID, rates of DVT (1.4% vs. 1.3%; risk ratio [RR], 1.11; p<0.001), PE (0.9% vs. 0.8%; RR, 1.14; p<0.001, and CVA (0.8% vs. 0.7%; RR, 1.17; p<0.001) were higher. Multivariable analysis demonstrated a 7% increase in odds of VTE post-COVID (odds ratios [OR], 1.07; p=0.002). Unvaccinated patients had a 6% higher odds of VTE (OR, 1.06; p=0.006), whereas vaccinated patients showed a nonsignificant increase (OR, 1.16; p=0.109). Patients with prior COVID-19 hospitalization had approximately double the odds of VTE (OR, 2.03; p=0.011).

Conclusions

Thrombotic complications modestly increased after the COVID-19 pandemic. Vaccination status showed no clear association, while prior hospitalization for COVID-19 was the strongest predictor of postoperative thrombotic risk.

Introduction

Thrombotic complications are a feared cause of morbidity and mortality following thoracolumbar spine surgery. Venous thromboembolism (VTE), manifesting primarily as deep venous thrombosis (DVT) or pulmonary embolism (PE), is the most commonly reported complication [1,2]. Although overall uncommon, the incidence of VTE varies widely across studies. Reported rates of DVT following thoracolumbar procedures range between 0.3% and 31%, while PE rates range between 0.2% and 37.5% [3]. Postoperative VTEs are associated with significant morbidity, increased mortality, prolonged hospitalization, and up to a threefold increase in healthcare costs [46]. Cerebrovascular accident (CVA), another potential thrombotic complication, accounts for approximately 10% of in-hospital mortality following thoracolumbar procedures [7].
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease 2019 (COVID-19) has been strongly associated with a hypercoagulable state [8,9]. Both VTE and CVA are known complications of COVID-19 [10]. Emerging evidence suggests that hypercoagulability may persist long after severe infection, with the phenomenon of “long COVID” garnering increasing attention [11,12]. In addition, case reports have documented thromboembolic events after vaccination [13]. According to the Centers for Disease Control and Prevention, seroprevalence data indicate that approximately 97% of the US population has either been infected by SARS-CoV-2 or vaccinated against it [14]. However, whether this widespread exposure has impacted baseline coagulability is not well understood.
Some evidence suggests that a history of severe COVID-19, such as COVID-19 requiring hospitalization, is more strongly associated with a persistent prothrombotic state [11]. At the height of the pandemic, high infection rates resulted in mass hospitalizations worldwide. In the United States, the cumulative hospitalization rate between May 2020 and April 2021 was 1,093 per 100,000 individuals [15]. Rates varied by age, ranging from approximately 0.4% in individuals younger than 40 to 9.2% in those older than 60 [16]. As vaccines became available, mounting evidence showed that vaccination reduces the incidence of severe infection and mortality [16,17]. Nevertheless, as of May 2023, an estimated 19% of the US population remained unvaccinated, 31% had not completed the primary series, and 83% had not received an updated booster [18].
Numerous studies have examined differences in healthcare delivery and outcomes before and after the COVID-19 pandemic [19]. However, there is a paucity of data on thrombotic complications following spine surgery in the post-pandemic era. Further, no studies have evaluated the potential influence of non-vaccinated status or a history of severe infection. The present study aimed to compare the rates of VTE and CVA after thoracolumbar spine surgery in the post-COVID era with those observed pre-COVID. Importantly, not all patients in the post-COVID cohort had a history of infection with COVID-19; rather, this group represents a surgical population potentially affected by environmental, immunologic, and systemic changes in the wake of the pandemic. Subgroup analyses were conducted to isolate the effect of vaccination status and prior COVID-19 hospitalization. We hypothesized that thrombotic complication rates would be higher in the post-COVID cohort.

Materials and Methods

Study design and data source

This retrospective cohort study was deemed exempt from full Institutional Review Board review, and informed consent was therefore not required. Data were obtained from the Mariner dataset of the PearlDiver Patient Records Database (PearlDiver Technologies, Colorado Springs, CO, USA). The Mariner dataset aggregates medical and prescription data sourced from commercial, Medicare, Medicaid, and cash payers. At the time of data extraction, insurance claims data were available from January 2010 to October 2021, representing over 157 million patients across the United States. The dataset enables longitudinal tracking through unique patient identifiers, minimizing loss to follow-up due to changes in insurance status. Patients were identified using international Current Procedural Terminology (CPT) codes, International Classification of Diseases (ICD) codes, or drug codes available through the database querying language. Because patient identification relied on code-based queries, a broad spectrum of thoracolumbar procedures was included. This heterogeneity ensured adequate sample size and national representativeness, but limits procedure-specific risk evaluation.

Inclusion/exclusion criteria

Patients undergoing primary decompression with or without fusion of the thoracolumbar spine were identified using CPT codes (Appendix 1). Procedures included laminectomy, hemilaminectomy, partial facetectomy, foraminotomy, discectomy, microdiscectomy, transpedicular decompression, endoscopic decompression, partial or complete vertebral corpectomy, posterolateral fusion, and interbody fusion. Only adults aged ≥18 years were included. Eligible cases required a first instance of surgery (primary procedure) and ≥90 days of active follow-up. Patients with indications for fracture or spinal malignancy, as determined by CPT and ICD codes on the day of the procedure (Appendix 1), were excluded. Accordingly, the final cohort consisted primarily of elective procedures.

Experimental and control cohorts

Patients were divided into “pre-COVID” and “post-COVID” cohorts, using March 2020 as the cutoff, when the United States declared COVID-19 a national emergency [20]. Before March 1, 2020, fewer than 70 confirmed cases had been reported in the United States [21]. The pre-COVID cohort comprised patients who underwent surgery within the preceding 5 calendar years before this cutoff point, from January 2015 to February 2020. The post-COVID cohort included all patients who underwent surgery in March 2020 or thereafter. Thus, the overall analysis was conducted from January 2015 through October 2021. Demographic variables collected included age, biological sex, and the Charlson comorbidity index (CCI). Coagulopathy was defined using ICD codes for coagulation and bleeding disorders (Appendix 1) and encompassed both hypo- and hypercoagulable conditions documented in the patient’s history. Additional preoperative comorbidities recorded included coagulopathy, diabetes, chronic kidney disease (CKD), morbid obesity, and perioperative (intra- or postoperative) blood transfusion (Appendix 1). These variables have previously been shown to increase the risk of VTE after spine surgery [2224] and were categorized as “high-risk” comorbidities in this analysis.

Outcomes of interest

The primary outcome was the change in the incidence rate of postoperative VTE within 90 days of surgery from the pre-COVID to the post-COVID period. VTE was defined as the occurrence of either DVT or PE, identified using ICD-9 and ICD-10 diagnosis codes (Supplement 1). Secondary outcomes included the 90-day incidence of postoperative acute myocardial infarction (MI) and CVA.

Subgroup analysis

Subgroup analyses were performed to evaluate VTE incidence within the pre- and post-COVID cohorts, stratified by demographic characteristics, comorbid risk factors, vaccination status, and prior COVID-related hospitalization. Vaccination status was determined using drug codes corresponding to the Pfizer, Moderna, and Johnson & Johnson vaccines. A history of COVID-related hospitalization was defined as an inpatient admission with a primary diagnosis of COVID-19 (ICD-10 code U07.1).

Data reporting and statistical analysis

Demographics and baseline characteristics were summarized as frequencies and percentages. Outcomes of interest were reported as the number of patients, incidence rates (percentages), and risk ratios (RRs) relative to the pre-COVID incidence rate. Univariate analysis was conducted using Pearson’s chi-square test. Multivariate logistic regression was conducted to adjust for age, biological sex, CCI, and high-risk comorbidities (coagulopathy, diabetes mellitus, CKD, morbid obesity, and perioperative blood transfusion). Odds ratios (ORs) from the multivariate models were reported relative to pre-COVID odds. Statistical significance was defined as p<0.05. All analyses were conducted in R (R Foundation for Statistical Computing, Vienna, Austria), using software provided within the PearlDiver Database.

Results

Patient population and baseline characteristics

A total of 784,498 patients met the inclusion criteria. Of these, 50% were male and 50% were female. The pre-COVID cohort comprised 637,614 patients, while the post-COVID cohort comprised 146,884 patients. Compared with the pre-COVID cohort, the post-COVID cohort had a greater proportion of patients aged ≥80 years (6% vs. 2%) and a higher proportion of patients with a CCI of 1 or 2 (53% vs. 50%) or >3 (35% vs. 30%). The post-COVID cohort also had a slightly higher prevalence of high-risk comorbidities (50% vs. 44%), including coagulopathy, diabetes, CKD, and morbid obesity (Table 1). Vaccinated and unvaccinated patients had comparable demographic and comorbidity profiles. Patients with a previous history of COVID-19-related hospitalization tended to be older (11% aged >80) and carried greater comorbidity burdens (75% with CCI≥3 and 83% with high-risk comorbidities for VTE) than the general post-COVID cohort (Table 1).

Univariate analysis

The incidence of VTE was higher in the post-COVID cohort compared with the pre-COVID cohort (2.0% vs. 1.8%; RR, 1.12; p<0.001). Rates of DVT (1.4% vs. 1.3%; RR, 1.11; p<0.001), PE (0.9% vs. 0.8%; RR, 1.14; p<0.001), and CVA (0.8% vs. 0.7%; RR, 1.17; p<0.001) were also significantly higher post-COVID (Table 2, Fig. 1). Comorbidities associated with increased post-COVID VTE incidence were coagulopathy (RR, 1.13; p=0.018) and diabetes (RR, 1.08; p=0.012) (Table 3). Both vaccinated and unvaccinated patients demonstrated higher complication rates compared with pre-COVID. Vaccinated patients had a higher risk of VTE (RR, 1.30; p=0.004), PE (RR, 1.34; p=0.033), and CVA (RR, 1.34; p=0.040) compared to pre-COVID. Unvaccinated patients were at significantly increased risk of all complications compared to pre-COVID (p<0.001 for all). The subgroup at highest risk of thrombotic complications comprised patients with a history of COVID-19–related hospitalization, who had significantly higher rates of VTE (5.7%; RR, 3.17; p<0.001), DVT (3.6%; RR, 2.87; p=0.002), PE (2.8%; RR, 3.58; p=0.001, and CVA (2.8%; RR, 3.99; p<0.001) (Table 2, Fig. 2).

Multivariate analysis

After adjusting for confounders, the post-COVID cohort had a 7% higher odds of VTE compared with the pre-COVID cohort (OR, 1.07; p=0.002). There was a 6% increase in the odds of VTE in unvaccinated patients (OR, 1.06; p=0.006). Patients with a history of COVID-19–related hospitalization had approximately double the odds of VTE (OR, 2.03; p=0.011). Vaccinated patients also demonstrated higher odds of VTE compared with pre-COVID levels (OR, 1.16), but this did not reach statistical significance (Table 4).

Discussion

In this large retrospective cohort study, patients undergoing thoracolumbar spine surgery in the post-COVID era demonstrated an increased risk of thrombotic complications compared with pre-COVID rates. Notably, unvaccinated patients and those with a history of COVID-19–related hospitalization were at the highest risk.
Our results are consistent with prior studies examining thrombotic risk in surgical patients during the COVID-19 era. In a large cohort of orthopedic procedures, including lumbar fusion, Johnson et al. [24] reported increased VTE risk among patients diagnosed with COVID-19 within 90 days of surgery. Similarly, Chehrassan et al. [25], in a single-center study from Iran, observed higher rates of DVT, PE, and MI in the post-COVID era. Using the American College of Surgeons National Surgical Quality Improvement Program database, Song et al. [18] demonstrated that patients undergoing spine surgery in 2020 experienced longer hospital stays and higher rates of DVT, pneumonia, and sepsis. However, their analysis was limited to the early pandemic, before vaccines became widely available and infection rates began to decline.
Although vaccination protects against severe SARS-CoV-2 infection, thrombotic complications have also been reported following vaccination [26]. In our cohort, the odds of VTE were increased regardless of vaccination status, although statistical significance was reached only in non-vaccinated patients. Demographic factors are unlikely to account for this difference, as unvaccinated and vaccinated groups were comparable in age, sex, and comorbidities, and these variables were adjusted for in multivariable analysis. However, interpretation is limited by the relatively small number of vaccinated patients in our dataset and the inability to determine whether vaccinated individuals may have had unrecognized prior infection with SARS-CoV-2. Thus, the clinical relevance of vaccination status to postoperative outcomes remains uncertain. If immunization does play a role, additional investigation is warranted to clarify the underlying mechanisms. For example, Macanu et al. [27] reported that complications after elective bariatric surgery increased only when COVID-19 was diagnosed postoperatively, not preoperatively. Further research in spine surgery should evaluate whether vaccination mitigates the risk of postoperative complications by reducing susceptibility to nosocomial COVID-19 infection, which remains an independent concern.
Existing literature suggests that COVID-19–induced hypercoagulability may be driven by systemic inflammation and cytokine storm, particularly in severe infections [28]. Hospitalization can therefore serve as a proxy for illness severity [29]. In the present study, patients with a history of COVID-19–related hospitalization had more than double the odds of postoperative VTE, even after adjusting for demographic variables and comorbidities. This finding is consistent with prior reports. For example, the Association of Anaesthetists of Great Britain and Ireland recommends that patients with prior moderate-to-severe COVID-19 be managed as a distinct high-risk category for elective surgery [30]. The American Society of Anesthesiologists similarly advises incorporating the severity of prior infection, ongoing symptoms, and vaccination status into perioperative risk assessment [30]. Our results support these recommendations and add evidence that previously hospitalized patients represent a particularly high-risk group for thrombotic complications. Collectively, these findings reinforce the importance of integrating COVID-19 history, vaccination status, and infection severity into preoperative risk stratification for thoracolumbar spine surgery.
This study has several limitations. First, the use of a large administrative database provided a substantial sample size and statistical power, but also increased the likelihood of detecting minor differences that may be statistically significant yet clinically modest. However, the database was uniquely suited for this research, as our goal was to evaluate national-scale trends. Nonetheless, both effect size and statistical significance should be considered when interpreting the findings. Second, patients were identified using ICD and CPT codes, which were designed for billing rather than research. While coding inaccuracies are possible, the complications and procedures evaluated are common and therefore less prone to coding errors compared with niche procedures or rare diagnoses. Inclusion of patients from diverse payer types reduces selection bias related to insurance status. Lastly, this study encompassed a heterogeneous group of thoracolumbar procedures varying in invasiveness, ranging from discectomy to interbody fusion. Although this allowed for a broad capture of thoracolumbar surgeries, we were unable to stratify risk by specific procedure type or instrumentation due to limitations of the database. Future studies with more granular data may address procedure-specific risks. Furthermore, the PearlDiver database lacks physiologic or laboratory data (e.g., thrombocytosis, D-dimer levels) or clinical mobility status (e.g., bed rest), which are established contributors to thrombotic risk. This limits the ability to control for these important covariates. Despite these limitations, our cohort’s composition helped achieve this study’s goals, which were to establish broad changes in thrombotic complications in the post-COVID era. Future research should incorporate EMR-linked databases with laboratory values, medication data, and mobility measures. Prospective studies may help identify persistent biomarkers of hypercoagulability in patients with prior COVID-19 undergoing elective spine surgery.

Conclusions

Thrombotic complications appear to be increased among patients undergoing thoracolumbar spine surgery in the post-COVID era. A history of COVID-19–related hospitalization was the strongest predictor of risk, while the influence of preoperative vaccination remains uncertain and warrants further investigation.

Key Points

  • Increased thrombotic risk post-coronavirus disease 2019 (COVID-19): Thoracolumbar spine surgery patients in the post-COVID era experienced higher rates of thrombotic complications compared with pre-pandemic rates.

  • Prior severe COVID-19 infection is a major risk factor: A history of COVID-19–related hospitaliza-tion more than doubled the odds of postoperative venous thromboembolism (VTE), even after ad-justing for comorbidities.

  • Vaccination status impact unclear: Both vacci-nated and unvaccinated patients showed increased thrombotic risks compared with pre-COVID, but the increase was statistically significant only in un-vaccinated patients.

  • Comorbidities matter: Coagulopathy and diabetes were independently associated with higher VTE incidence in the post-COVID population.

  • Implications for preoperative risk stratification: Patients with prior severe COVID-19 should be considered high-risk in the perioperative period, reinforcing the need for tailored preoperative eval-uation and thromboprophylaxis strategies.

Notes

Conflict of Interest

The following conflicts of interest and funding sources have been declared by the authors below. For the remaining authors, no potential conflict of interest relevant to this article was reported. BS: Maryland Orthopaedic Association: board or committee member. JJ: Children: editorial or governing board. DC: Alphatec Spine: paid consultant, stock or stock options. EK: Alphatec Spine: stock or stock options. SL: AAOS: board or committee member; Alphatec Spine: IP royalties, stock or stock Options; American Board of Orthopaedic Surgery Inc.: board or committee member; American Orthopaedic Association: board or committee member; AO Spine North America Spine Fellowship Support: research support; ASIP, ISD: stock or stock options; Atlas Spine: IP royalties; Baxter: research support; Cervical Spine Research Society: board or committee member; Contemporary Spine Surgery: editorial or governing board; DePuy, A Johnson & Johnson Company: IP royalties; LSRS: board or committee member; MDC: stock or stock options; Nuvasive: IP royalties, paid consultant, paid presenter or speaker, stock or stock options; OMEGA: research support; Smiss: board or committee member; Stryker: IP royalties; and The Spine Journal: editorial or governing board.

Author Contributions

Conceptualization: DLC, SCL, EYK, JJJ. Methodology: DLC, EYK, SCL, SL, AKC, RIS. Data curation: SL, AKC, RIS, HeP, AR, LH, AS, HaP, IA, LJB, BS, SB. Formal analysis: SL, AKC, RIS, AS, JAD, DLC. Visualization: SL, AKC, RIS, BS, AR, LH. Project administration: DLC, SCL, EYK, JJJ. Writing (original draft): SL, AKC, RIS. Writing (review and editing): HeP, SB, BS, AR, LH, JAD, AS, HaP, IA, LJB, JJJ, EYK, SCL, DLC. Final approval of the manuscript: all authors.

Fig. 1
Relative change in rate of venous thromboembolisms (VTEs) over time. PE, pulmonary embolism; DVT, deep venous thrombosis.
asj-2025-0245f1.jpg
Fig. 2
Relative risk ratios of 90-day thrombotic complications compared to pre-coronavirus disease 2019 (COVID-19) levels, by risk factor. VTE, venous thromboembolism; DVT, deep venous thrombosis; PE, pulmonary embolism; CVA, cerebrovascular accident.
asj-2025-0245f2.jpg
Table 1
Baseline characteristics
Characteristic Pre-COVID: total Post-COVID: total Vaccinated for COVID-19 Not vaccinated or unknown History of COVID-19 admission
Total 637,614 146,884 5,475 141,409 247
Age 18–<65 yr 391,262 (61) 86,028 (59) 2,641 (48) 83,387 (59) 113 (46)
Age 65–<80 yr 256,200 (40) 58,109 (40) 2,651 (48) 55,458 (39) 125 (51)
Age ≥80 yr 15,284 (2) 9,281 (6) 480 (9) 8,801 (6) 28 (11)
Male sex 321,155 (50) 72,064 (49) 2,509 (46) 69,555 (49) 121 (49)
Female sex 316,459 (50) 74,820 (51) 2,966 (54) 71,854 (51) 126 (51)
CCI 0 129,802 (20) 18,493 (13) 655 (12) 17,839 (13) 3 (1)
CCI 1–2 315,929 (50) 77,139 (53) 2,745 (50) 74,394 (53) 58 (23)
CCI ≥3 191,883 (30) 51,252 (35) 2,075 (38) 49,177 (35) 186 (75)
Coagulopathy 31,184 (5) 9,679 (7) 417 (8) 9,262 (7) 57 (23)
Diabetes 221,185 (35) 53,781 (37) 2,241 (41) 51,540 (36) 156 (63)
Chronic kidney disease 56,907 (9) 18,027 (12) 790 (14) 17,237 (12) 80 (32)
Morbid obesity 73,056 (11) 24,926 (17) 1,019 (19) 23,907 (17) 103 (42)
Any high-risk comorbidity 281,313 (44) 73,218 (50) 2,952 (54) 70,266 (50) 206 (83)
Perioperative blood transfusion 5,463 (1) 1,417 (1) 61 (1) 1,356 (1) 12 (5)

Values are presented as number of patients or number of patients (%).

COVID-19, coronavirus disease 2019; CCI, Charlson comorbidity index.

Table 2
Ninety-day thrombotic complications, stratified by vaccination status and history of hospitalization for COVID-19
Variable Pre-COVID Post-COVID Risk ratioa) p-valueb)
Total
 VTE 11,418 (1.79) 2,936 (2.00) 1.12 <0.001
 DVT 8,084 (1.27) 2,065 (1.41) 1.11 <0.001
 PE 5,053 (0.79) 1,328 (0.9) 1.14 <0.001
 CVA 4,508 (0.71) 1,226 (0.83) 1.17 <0.001
Vaccinated preoperatively
 VTE - 127 (2.32) 1.3 0.004
 DVT - 85 (1.55) 1.22 0.07
 PE - 58 (1.06) 1.34 0.033
 CVA - 52 (0.95) 1.34 0.04
Not vaccinated preoperatively
 VTE - 2,809 (1.99) 1.11 <0.001
 DVT - 1,980 (1.4) 1.1 <0.001
 PE - 1,270 (0.9) 1.14 <0.001
 CVA - 1,174 (0.83) 1.17 <0.001
History of COVID-19 admission
 VTE - 14 (5.67) 3.17 <0.001
 DVT - 9 (3.64) 2.87 0.002
 PE - 7 (2.83) 3.58 0.001
 CVA - 7 (2.83) 3.99 <0.001

Values are presented as number of patients (incidence %). Statistically significant results are marked in bold.

COVID-19, coronavirus disease 2019; VTE, venous thromboembolism; DVT, deep venous thrombosis; PE, pulmonary embolism; CVA, cerebrovascular accident.

a) Risk ratio relative to the pre-COVID cohort, defined as a having a risk ratio equal to 1.00 for each outcome.

b) By Pearson’s chi-square test.

Table 3
Ninety-day VTEs, pre- versus post-COVID, stratified by demographic characteristics
Characteristic Pre-COVID Post-COVID Risk ratioa) p-valueb)
Total patients 637,614 146,884
Total VTEs 11,418 (1.79) 2,936 (2) 1.12 <0.001
Age 18–<65 yr 391,262 (1.52) 86,028 (1.72) 1.13 <0.001
Age 65–<80 yr 256,200 (2.19) 58,109 (2.39) 1.09 0.004
Age ≥80 yr 15,284 (2.58) 9,281 (2.78) 1.08 0.378
Male sex 321,155 (1.9) 72,064 (2.09) 1.1 <0.001
Female sex 316,032 (1.68) 74,662 (1.92) 1.14 <0.001
CCI 0 129,377 (1.07) 18,335 (1.13) 1.06 0.479
CCI 1–2 315,929 (1.45) 77,139 (1.54) 1.07 0.053
CCI ≥3 191,883 (2.84) 51,252 (3) 1.06 0.057
Coagulopathy 31,184 (4.5) 9,679 (5.08) 1.13 0.018
Diabetes 221,185 (2.21) 53,781 (2.39) 1.08 0.012
Chronic kidney disease 56,907 (3.1) 18,027 (3.35) 1.08 0.094
Morbid obesity 73,056 (2.86) 24,926 (2.96) 1.03 0.428
Any high-risk comorbidity 281,313 (2.36) 73,218 (2.53) 1.08 0.005
Perioperative blood transfusion 5,463 (7.49) 1,417 (8.05) 1.07 0.515

Values are presented as number of patients (VTE incidence %). Statistically significant results are marked in bold.

VTE, venous thromboembolism; COVID-19, coronavirus disease 2019; CCI, Charlson comorbidity index.

a) Relative to the pre-COVID cohort, which is defined as a having a risk ratio equal to 1.00 for each outcome.

b) By Pearson’s chi-square test.

Table 4
Multivariable analysis of the odds of post-COVID VTE compared to pre-COVID levels, adjusted for confoundersa)
Variable Total post-COVID Vaccinated for COVID-19 Not vaccinated or unknown History of COVID-19 admission




ORb) p-valuec) OR p-value OR p-value OR p-value
Total VTE 1.07 0.002 1.16 0.109 1.06 0.006 2.03 0.011

Deep venous thrombosis 1.06 0.014 1.1 0.407 1.06 0.021 1.81 0.082

Pulmonary embolism 1.08 0.009 1.19 0.198 1.08 0.018 2.24 0.037

Cerebrovascular accident 1.13 <0.001 1.12 0.431 1.12 <0.001 2.03 0.068

Statistically significant results are marked in bold.

COVID-19, coronavirus disease 2019; VTE, venous thromboembolism; OR, odds ratio.

a) Adjusted for age, sex, Charlson comorbidity index greater than 3, high risk comorbidities (coagulopathy, diabetes mellitus, chronic kidney disease, morbid obesity), and perioperative blood transfusion.

b) OR relative to the pre-COVID cohort, defined as a having a risk ratio equal to 1.00 for each outcome.

c) By Pearson’s chi-square test.

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Appendices

Appendix 1. Codes used for patient identification

asj-2025-0245-Appendix-1.pdf
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