Symptom-triggered diagnosis in lung transplant recipients: does it underestimate the true venous thromboembolism burden and its consequences?
Letter to the Editor

Symptom-triggered diagnosis in lung transplant recipients: does it underestimate the true venous thromboembolism burden and its consequences?

Jia Wang1,2, Hai Guo1 ORCID logo

1Department of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China; 2Department of Thoracic Surgery, West China Tianfu Hospital, Sichuan University, Chengdu, China

Correspondence to: Hai Guo, MD. Department of Thoracic Surgery, West China Hospital, Sichuan University, No. 37 Guoxue Alley, Chengdu 610041, China. Email: Guohai@wchscu.cn.

Response to: Kim NT, Miyashita Y, Kaihou T, et al. Risk factors and perioperative complications associated with deep venous thrombosis and pulmonary embolism after lung transplantation. J Thorac Dis 2025;17:9342-56.



Submitted Dec 06, 2025. Accepted for publication Jan 21, 2026. Published online Feb 06, 2026.

doi: 10.21037/jtd-2025-1-2549


We read with great interest the insightful article by Kim et al. titled “Risk factors and perioperative complications associated with deep venous thrombosis and pulmonary embolism after lung transplantation” in a recent issue of the Journal of Thoracic Disease (1). The authors conducted a rigorous retrospective analysis of 399 lung transplant recipients, reporting a strikingly high incidence of postoperative deep vein thrombosis (DVT) of 53.6% (214/399 patients). Their data reveal a profoundly increased mortality in patients with DVT compared to those without (33.2% vs. 13.0%, P<0.001), accompanied by significantly higher rates of pulmonary embolism (PE) (22.4% vs. 5.4%), hemothorax/hematoma (50.5% vs. 29.7%), and prolonged hospitalization. Of paramount clinical importance, their multivariate Cox analysis within the DVT cohort demonstrated that mortality was driven by hemorrhagic complications [adjusted hazard ratio (HR) =2.24; 95% confidence interval (CI): 1.32–3.81] rather than by PE itself (adjusted HR =1.12; 95% CI: 0.62–1.99). This finding critically underscores the perilous equilibrium between thrombotic and bleeding risks in this population.

We commend the authors for their valuable contribution. However, the interpretation and generalizability of these pivotal results must be contextualized within a key methodological framework detailed in their paper. The authors state: “Duplex ultrasound or further imaging for DVT was performed only when patients developed clinical symptoms suggestive of venous thrombosis; no routine screening protocol was in place for asymptomatic patients” (1). This symptom-triggered diagnostic strategy is a standard yet potentially limiting approach, as it may systematically fail to detect a clinically silent reservoir of venous thromboembolism (VTE).


The rationale for this concern is twofold

High risk for asymptomatic VTE: post-lung transplant patients frequently experience prolonged immobilization, sedation, central venous catheterization, and a systemic inflammatory state—all factors that elevate thrombotic risk while masking classic symptoms (2,3). Studies in thoracic surgery and intensive care settings found that 7.5–12.1% of patients had DVT detected only through screening, with up to 79% of these being asymptomatic (4). In such high-acuity settings, studies have shown that routine screening uncovers a significant incidence of asymptomatic DVT that would otherwise go undiagnosed (5).


Implications for reported epidemiology and associations

The 53.6% DVT incidence, while remarkably high, may represent an underestimation of the true postoperative burden. This potential under-ascertainment could influence several of the study’s conclusions:

  • The identified risk factors for PE (lower extremity DVT, elevated preoperative platelet count) are robust for the symptomatic cohort but may not fully capture the risk profile of the overall VTE population.
  • The null association between PE and mortality (HR =1.12; P=0.72) is a crucial finding. One interpretation is that DVT is a marker of overall illness severity. An alternative, non-exclusive explanation is that some patients with undiagnosed (and thus untreated) DVT may have progressed to fatal PE (6), with their outcomes not being attributed to VTE in this analysis. This could bias the observed HR toward the null.

The authors rightly acknowledge this limitation in their discussion. Their work therefore not only highlights a major clinical challenge but also illuminates a significant evidence gap. To advance toward personalized, risk-adapted management, we must first accurately define the scope of the problem. We strongly concur with the need for prospective, multi-center studies that employ protocolized, serial postoperative VTE screening. Such research is essential to establish the true incidence of symptomatic and asymptomatic VTE, to validate risk stratification models in an unbiased cohort, and to provide the foundational evidence for trials assessing optimized prophylactic and therapeutic strategies. The substantial mortality burden associated with this complication, as clearly demonstrated by Kim et al. (1), calls for a more proactive diagnostic paradigm.


Acknowledgments

None.


Footnote

Provenance and Peer Review: This article was a standard submission to the journal. The article did not undergo external peer review.

Funding: None.

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at https://jtd.amegroups.com/article/view/10.21037/jtd-2025-1-2549/coif). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Kim NT, Miyashita Y, Kaihou T, et al. Risk factors and perioperative complications associated with deep venous thrombosis and pulmonary embolism after lung transplantation. J Thorac Dis 2025;17:9342-56. [Crossref] [PubMed]
  2. Zheng M, Yousef I, McEldrew J, et al. Incidence and Potentially Modifiable Risk Factors for Venous Thromboemblism Post Lung Transplant. The Journal of Heart and Lung Transplantation 2020;39:S316.
  3. Zheng M, Yousef I, Mamary AJ, et al. Venous thromboembolism in lung transplant recipients real world experience from a high volume center. J Heart Lung Transplant 2021;40:1145-52. [Crossref] [PubMed]
  4. De León LE, Bravo-Iñiguez CE, Fox S, et al. Routine surveillance for diagnosis of venous thromboembolism after pleurectomy for malignant pleural mesothelioma. J Thorac Cardiovasc Surg 2020;160:1064-73. [Crossref] [PubMed]
  5. Lim W, Le Gal G, Bates SM, et al. American Society of Hematology 2018 guidelines for management of venous thromboembolism: diagnosis of venous thromboembolism. Blood Adv 2018;2:3226-56. [Crossref] [PubMed]
  6. Liederman Z, Chan N, Bhagirath V. Current Challenges in Diagnosis of Venous Thromboembolism. J Clin Med 2020;9:3509. [Crossref] [PubMed]
Cite this article as: Wang J, Guo H. Symptom-triggered diagnosis in lung transplant recipients: does it underestimate the true venous thromboembolism burden and its consequences? J Thorac Dis 2026;18(2):176. doi: 10.21037/jtd-2025-1-2549

Download Citation