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CASE REPORT article

Front. Med., 23 January 2026

Sec. Intensive Care Medicine and Anesthesiology

Volume 12 - 2025 | https://doi.org/10.3389/fmed.2025.1688556

Veno-venous ECMO-assisted orthopedic stabilization for polytrauma with severe ARDS and refractory hypoxemia: a case report


Lin Liu&#x;Lin LiuKaiji Deng&#x;Kaiji DengHaifeng Tang
Haifeng Tang*Yanjun Wang
Yanjun Wang*
  • Department of Emergency, Honghui Hospital, Xi’an Jiaotong University, Xi’an, Shaanxi, China

This case report describes the successful integration of veno-venous extracorporeal membrane oxygenation (VV-ECMO) with physiologically optimized fracture fixation in a critically ill polytrauma patient who presented with life-threatening acute respiratory distress syndrome (ARDS). A 23-year-old male with bilateral femoral fractures, Gustilo IIIB open tibiofibular injury, left radius-ulna fractures, and refractory hypoxemia (PaO2/FiO2 40.5 mm Hg) underwent VV-ECMO initiation 1 h postinjury (total ECMO duration 144 h). Physiological optimization guided delayed surgical intervention on day 5, incorporating heparin-based anticoagulation and dynamic ECMO parameter modulation, resolving lactic acidosis (peak lactate 5.0 mmol/L on day 1 to 1.8 mmol/L preoperatively). The patient achieved successful decannulation by day 6 with satisfactory recovery at the 2-month follow-up [Short Musculoskeletal Function Assessment (SMFA) score 28.1, gait speed 1.2 m/s]. This case demonstrates the feasibility of a multidisciplinary protocol challenging traditional contraindications to surgery in severe ARDS patients and providing a replicable protocol for managing competing priorities of oxygenation and hemorrhage control.

Introduction

The management of polytrauma patients with concurrent acute respiratory failure and complex orthopedic injuries presents a critical clinical challenge (1). Acute hypoxemic respiratory failure with refractory hypoxemia requires advanced management strategies, including VV-ECMO, which is distinct from veno-arterial ECMO (VA-ECMO) in its indications and applications (2). Recent evidence supports the feasibility of orthopedic procedures during ECMO support, highlighting the importance of integrated management for fracture stabilization (3, 4). The strategic timing of orthopedic surgery in these critically ill patients remains a key consideration, balancing the benefits of early stabilization against the risks of bleeding and systemic inflammation. This case addresses the gap in managing polytrauma with severe ARDS through a multidisciplinary approach.

Case report

A 23-year-old male was transferred to our trauma center 9 h after a motor vehicle collision. Initial assessment revealed bilateral femoral shaft fractures, left Gustilo IIIB tibiofibular fractures, and ARDS with a PaO2/FiO2 ratio of 40.5 mm Hg (Figure 1). Chest imaging showed bilateral diffuse infiltrates consistent with ARDS Berlin criteria. Early surgical intervention was precluded by physiological barriers, including coagulopathy (INR 1.8, platelets 65 × 109/L), lactic acidosis (pH 7.18, lactate 5.0 mmol/L), and hemodynamic instability requiring vasopressor support (5). Persistent hypoxemia despite a lung-protective ventilation strategy (tidal volume 220 mL (3.1 mL/kg predicted body weight), PEEP 14 cm H2O, plateau pressure 26 cm H2O, driving pressure 12 cm H2O) with transpulmonary pressure monitoring necessitated VV-ECMO cannulation via the right femoral vein and right internal jugular vein at 1 h postadmission. The selection of PEEP at 14 cm H2O was guided by an individualized lung-protective strategy.

FIGURE 1
Five-panel image of different X-ray views. Panel A shows a lower leg with metal fixation. Panel B illustrates a hip and knee joint. Panel C depicts a forearm with a visible fracture. Panel D presents a side view of an arm with a broken bone. Panel E shows a knee joint and upper leg.

Figure 1. Preoperative radiographic findings: (A) Fracture of the right fibula (proximal, non-displaced); fracture of the left tibia (distal third, displaced); (B) Fracture of the right femur (midshaft, significantly displaced); (C,D) Left radial and ulnar fractures (midshaft, both displaced); (E) Fracture of the left femur (proximal third, displaced).

Anticoagulation was initiated with unfractionated heparin infusion (18 U/kg/h), adjusted to maintain ACT for 180–200 s and anti-Xa at 0.3–0.7 IU/mL, with fibrinogen supplementation maintained at 2.8 g/L. Platelet count recovery (> 100 × 109/L) and fibrinogen levels (> 2.5 g/L) were confirmed prior to surgery. Physiological optimization by postinjury day 5 (pH 7.32, platelet count 112 × 109/L, fibrinogen 2.8 g/L) permitted closed reduction and external fixation of the bilateral femurs and left tibia. Intraoperative ECMO management included dynamic sweep gas adjustment from 4.3 L/min during dissection to 4.5 L/min during reduction, maintaining SvO2 > 75% throughout the 30-min procedure with minimal blood loss (50 mL) attributed to percutaneous fixation techniques (Figure 2). The patient was switched to prone position ventilation after surgery to promote sputum discharge (6). Successful decannulation occurred on day 6 following pulmonary recovery [PaO2/FiO2 320 mm Hg on pressure support ventilation (PSV 10 cm H2O, PEEP 8 cm H2O)]. Staged internal fixation was successfully completed by postoperative day 30 (Figure 3). At the 2-month follow-up evaluation, the patient demonstrated significant functional recovery, with independent ambulation at a gait speed of 1.2 m/s, Timed Up and Go test of 11 s, and hip flexion range of motion 0–115°. Additionally, the short Musculoskeletal Function Assessment (SMFA) score improved to 28.1, and C-reactive protein (CRP) normalized from 68 to 12 mg/L. The patient achieved independent ambulation without clinical signs of deep vein thrombosis (DVT).

FIGURE 2
X-ray images showcasing external fixation devices on the lower legs and hips. Panels A to C display the left leg and hip with fixation rods and screws in various angles. Panels D to F show the right leg and hip similarly fitted with external fixators. Each image highlights the alignment and placement of the orthopedic hardware.

Figure 2. Postoperative external fixation for patients: (A,B) External fixation of the left tibia; (C) Left femoral external fixation; (D,E) Right femoral external fixation; (F) Left femoral external fixation.

FIGURE 3
X-ray images labeled A to G display various views of bones with metal plates and screws. Each image shows different positions and angles of treated fractures, primarily focusing on long bones like the femur and tibia. Images highlight left (L) and right (R) orientations.

Figure 3. Postoperative internal fixation of patients: (A) Left tibial internal fixation; (B) Bilateral femoral internal fixation; (C) Right femoral internal fixation; (D) Left femoral internal fixation; (E) Left tibial internal fixation; (F,G) Left radial and ulnar internal fixation.

Discussion

This intervention redefines two critical paradigms in contemporary trauma care. First, it establishes the viability of orthopedic procedures under VV-ECMO support for patients with life-threatening ARDS (PaO2/FiO2 < 50 mm Hg), a population traditionally excluded from surgical candidacy. Our intraoperative ECMO protocol, featuring real-time sweep gas titration (4.3→4.5 L/min) to sustain cerebral oxygenation (SvO2 > 75%) during fracture manipulation, synthesizes cardiovascular (7) and transplant surgery (8) techniques into a novel trauma application. Second, this case resolves the historical dilemma between anticoagulation and surgical hemostasis through thrombin-targeted therapy.

In contrast to previous reports advocating heparin-free strategies (9, 10), we observed that controlled heparinization (18 U/kg/h) coupled with fibrinogen supplementation (> 2.5 g/L) achieved hemostasis without circuit thrombosis. Despite emerging evidence favoring direct thrombin inhibitors for thromboprophylaxis (1114), our heparin-based regimen (18 U/kg/h, ACT 180–200 s) with fibrinogen supplementation (> 2.5 g/L) achieved dual success: negligible intraoperative bleeding (50 mL) and circuit patency, aligning with ELSO guidelines for trauma-ECMO anticoagulation (15). This cost-efficacy advantage persists even when factoring in potential platelet transfusion requirements, as demonstrated in recent pharmacoeconomic analyses (12).

Recent evidence from a randomized controlled pilot study by Pintado et al. (16) demonstrated that, compared with conventional FiO2-guided approaches, compliance-guided PEEP in ARDS patients significantly increased the number of organ dysfunction-free days. This physiological optimization protocol aligns with our dynamic ECMO management, where maintaining a plateau pressure below 30 cm H2O while achieving optimal compliance proved critical for mitigating ventilator-induced lung injury in this polytrauma-ARDS scenario. The strategic delay to postinjury day 5 challenges conventional DCO (17), guided by a triad of physiological parameters: acid–base equilibrium restoration (pH 7.32), hemostatic recovery (platelets > 100 × 109/L), and pulmonary compliance improvement (ΔP 18 cm H2O). This “resuscitation window” concept gains biological plausibility from preclinical models showing that delayed fixation reduces secondary inflammatory cascades in thoracic trauma (18). The dual osteogenic mechanism of ECMO—sustaining tissue oxygenation (pO2 > 60 mm Hg) to prevent hypoxia-induced osteoblast dysfunction (19) and curtailing ventilator-induced IL-6 elevation (6 vs. 14 days) that impairs BMP-2 signaling (20)—likely contributed to accelerated functional recovery, as evidenced by independent ambulation (gait speed 1.2 m/s) and improved SMFA scores (28.1), indicating mild dysfunction.

Neurological protection constituted a cornerstone of our protocol, integrating multimodal monitoring (cerebral oximetry, MAP regulation) to mitigate ECMO-associated encephalopathy risks (21). The absence of neurological sequelae underscores the feasibility of real-time neuromonitoring in trauma-ECMO, although standardized protocols remain elusive. While single-center experience and survivor bias limit generalizability, this case provides a framework for multicenter validation using advanced biomarkers (thromboelastography) and cytokine profiling to optimize immunomodulatory strategies.

Conclusion

This case demonstrates that VV-ECMO can enable safe orthopedic stabilization in polytrauma patients with severe ARDS.

Data availability statement

The original contributions presented in this study are included in this article/supplementary material, further inquiries can be directed to the corresponding authors.

Ethics statement

The studies involving human participants were reviewed and approved by the Ethics Committee of Honghui Hospital, Xi’an Jiaotong University (No. 2025-KY-051-01). The participants provided their written informed consent to participate in this study. Written informed consent was obtained from the participant/patient(s) for the publication of this case report.

Author contributions

LL: Data curation, Formal analysis, Funding acquisition, Investigation, Writing – original draft. KD: Formal analysis, Investigation, Writing – original draft. HT: Funding acquisition, Writing – original draft, Writing – review & editing. YW: Data curation, Formal analysis, Writing – original draft.

Funding

The author(s) declare financial support was received for the research and/or publication of this article. This work was supported by Shanxi Natural Science Basic Research Program (2025JC-YBQN-1089), and Youth Talent Support Program of Xi’an Association for Science and Technology (0959202513182).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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The authors declare that no Generative AI was used in the creation of this manuscript.

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Keywords: ECMO, polytrauma, anticoagulation, ARDS, damage control orthopedics

Citation: Liu L, Deng K, Tang H and Wang Y (2026) Veno-venous ECMO-assisted orthopedic stabilization for polytrauma with severe ARDS and refractory hypoxemia: a case report. Front. Med. 12:1688556. doi: 10.3389/fmed.2025.1688556

Received: 22 August 2025; Accepted: 31 October 2025;
Published: 23 January 2026.

Edited by:

Peter Rosenberger, University of Tübingen, Germany

Reviewed by:

Javier Aquiles Hidalgo Acosta, University of Guayaquil, Ecuador
Eric Tretter, University of Texas Southwestern Medical Center, United States

Copyright © 2026 Liu, Deng, Tang and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Haifeng Tang, dGhmNTExQDEyNi5jb20=; Yanjun Wang, dGhvbWFzd3lqQDE2My5jb20=

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.