This protocol demonstrates the use of point-of-care ultrasound to guide peripheral veno-arterial extracorporeal membrane oxygenation cannulation through pre-procedural assessment, real-time procedural guidance, and post-cannulation verification.
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Method Article
This protocol demonstrates the use of point-of-care ultrasound to guide peripheral veno-arterial extracorporeal membrane oxygenation cannulation through pre-procedural assessment, real-time procedural guidance, and post-cannulation verification.
Point-of-care ultrasound (POCUS) has become an important imaging modality for guiding peripheral veno-arterial extracorporeal membrane oxygenation (VA-ECMO) cannulation. This protocol describes the integration of POCUS throughout the peripheral VA-ECMO cannulation workflow, including pre-procedural assessment, real-time procedural guidance, and post-cannulation verification. During the pre-procedural assessment, POCUS facilitates differentiation of arteries from veins, measurement of vessel diameter to estimate appropriate cannula size, and identification of vascular pathology, including plaques, thrombosis, and stenosis. During cannulation, combined out-of-plane and in-plane ultrasound techniques enable real-time visualization of the guidewire, confirmation of guidewire placement within the target vessel, and avoidance of posterior wall perforation or injury to adjacent structures. Following cannulation, POCUS is used to verify drainage cannula positioning at the inferior vena cava–right atrium junction and arterial return cannula positioning at the external or common iliac artery level, and to assess for complications such as cardiac tamponade, cannula malposition, and thrombosis. Compared with landmark-based or fluoroscopy-guided techniques, POCUS provides bedside imaging without ionizing radiation and supports continuous procedural guidance without interrupting resuscitation. This protocol provides a practical, evidence-based approach for ultrasound-guided peripheral VA-ECMO cannulation and focuses specifically on vascular access and cannulation rather than broader VA-ECMO management.
Veno-arterial extracorporeal membrane oxygenation (VA-ECMO) is used as salvage therapy for patients with severe cardiogenic shock, refractory cardiac arrest, and profound cardiopulmonary failure1,2. As the use of VA-ECMO has increased, the need for safe, rapid, and reliable cannulation techniques has also grown. Percutaneous cannulation using the Seldinger technique is commonly used for peripheral VA-ECMO because it avoids the morbidity associated with surgical cutdown and can be performed at the bedside3,4. This method is intended specifically for ultrasound-guided peripheral VA-ECMO cannulation and does not address the broader use of ultrasound in other ECMO configurations or in comprehensive post-cannulation hemodynamic management.
Peripheral VA-ECMO cannulation has traditionally been guided by anatomical landmarks or fluoroscopy. Landmark-based techniques carry risks of cannula misplacement and vascular complications5. Although fluoroscopy provides accurate imaging guidance, it may require transport to a catheterization suite, exposes patients and staff to ionizing radiation, and may involve the use of contrast agents with a risk of nephropathy6. Point-of-care ultrasound (POCUS) provides a noninvasive, repeatable, and portable alternative that can be used at the bedside without substantially interrupting ongoing resuscitation efforts7. Using phased-array, curvilinear, or linear transducers as appropriate, operators can assess target vessels, visualize the guidewire and cannula in real time, confirm positioning at the inferior vena cava (IVC)-right atrium junction or within the iliac arterial system, and evaluate for complications such as cannula malposition or thrombosis8. During low-flow states or ongoing cardiopulmonary resuscitation, pulsatility and compressibility may be less reliable for vessel discrimination; therefore, vessel morphology, wall characteristics, anatomical location, and guidewire position should also be considered.
The overall goal of this protocol is to describe the use of POCUS throughout peripheral VA-ECMO cannulation, including pre-procedural vascular assessment, real-time guidance during needle puncture and guidewire advancement, post-cannulation cannula-position verification, and complication assessment. The protocol is intended for centers performing or developing bedside femoral VA-ECMO cannulation and may be most appropriate when fluoroscopy is unavailable, impractical, or would delay resuscitation. The principal contribution of this protocol is the integration of point-of-care ultrasound throughout the entire peripheral VA-ECMO cannulation workflow, encompassing pre-procedural vascular assessment, real-time procedural guidance, and post-cannulation verification6. All practitioners completed the standardized training program for restricted medical technologies in Zhejiang Province and obtained the required certification before performing the procedure. Senior attending physicians supervised the procedures to ensure adherence to institutional protocols and procedural safety.
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This study was approved by the Ethics Committee of Sir Run Run Shaw Hospital, Zhejiang University School of Medicine (Approval No. 2026-2186). The inclusion criterion was any patient receiving VA-ECMO, and the exclusion criterion was refusal to undergo ultrasound examination. Written informed consent for publication of the case report and accompanying images was obtained from the legally authorized representative. Potential risks associated with this procedure include vascular injury, vessel rupture, cardiac tamponade, cardiac rupture, retroperitoneal hematoma, and other clinically relevant adverse events.
1. Safety Procedures
2. Probe Selection
3. Patient Positioning
4. Ultrasound-Guided Procedure for VA-ECMO Cannulation
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Our institution is a 2,000-bed tertiary-care hospital. Bedside peripheral VA-ECMO cannulation is performed by attending physicians in emergency medicine and critical care medicine, with an annual procedural volume of approximately 30–40 cases. Ultrasound-guided bedside cannulation is the standard first-line approach at our institution. The representative ultrasound images were acquired during peripheral VA-ECMO cannulation procedures performed by critical care physicians in the Emergency Intensive Care Unit (EICU) of Sir...
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POCUS has emerged as an indispensable imaging modality throughout the entire workflow of peripheral VA-ECMO cannulation. Our protocol details a systematic approach encompassing pre-procedural vessel assessment, real-time intra-procedural guidance, and post-cannulation verification. Pre-procedural vascular assessment begins with selection of the optimal puncture site, followed by POCUS evaluation to differentiate the artery from the vein. Measurement of the vessel diameter to estimate the maximum cannula size (French [Fr]...
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This article utilized artificial intelligence (AI) assisted services for language polishing.
Z.Z. received funding from the Prevention and Control of Emerging and Major Infectious Diseases–National Science and Technology Major Project (No. 2025ZD01902500 and No. 2025ZD01902501); the China National Key Research and Development Program (No. 2023YFC3603104); the National Natural Science Foundation of China (No. 82472243 and No. 82272180); the Fundamental Research Funds for the Central Universities (No. 226-2025-00024); the Huadong Medicine Joint Funds of the Zhejiang Provincial Natural Science Foundation of China (No. LHDMD24H150001); the Key Research and Development Project of Zhejiang Province (No. 2024C03240); a collaborative scientific project co-established by the Science and Technology Department of the National Administration of Traditional Chinese Medicine and the Zhejiang Provincial Administration of Traditional Chinese Medicine (No. GZY-ZJ-KJ-24082); the General Health Science and Technology Program of Zhejiang Province (No. 2024KY1099); the Project of Zhejiang University Longquan Innovation Center (No. ZJDXLQCXZCJBGS2024016); the Beijing Natural Science Foundation (No. 7252298); the Wu Jieping Medical Foundation Special Research Grant (No. 320.6750.2024-23-07); and the Zhejiang Provincial Science and Technology Program for Disease Control and Prevention (No. 2026JKZ042).
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| Name | Company | Catalog Number | Comments |
|---|---|---|---|
| Curvilinear ultrasound transducer (2.5–5.0 MHz) | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 120-018844-00 | Specification: C5-1s |
| Curvilinear ultrasound transducer (2.5–5.0 MHz) | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 120-018844-00 | Specification: C5-1s |
| Guidewire | Terumo Corporation | 20153032566 | Specification: RF*GA35153M |
| Guidewire | Terumo Corporation | 20153032566 | Specification: RF*GA35153M |
| High-frequency linear ultrasound transducer (5.0–10.0 MHz) | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 120-018844-00 | Specification: L12-4s |
| High-frequency linear ultrasound transducer (5.0–10.0 MHz) | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 120-018844-00 | Specification: L12-4s |
| Latex-free gloves | ARMEDICOM (M) SDN. BHD. | 20190299 | Alternative to nitrile gloves for safety procedures |
| Latex-free gloves | ARMEDICOM (M) SDN. BHD. | 20190299 | Alternative to nitrile gloves for safety procedures |
| Nitrile gloves | Shandong Blue Sail Innovation Co., Ltd. | 20160003 | Required for safety procedures |
| Nitrile gloves | Shandong Blue Sail Innovation Co., Ltd. | 20160003 | Required for safety procedures |
| Peripheral extracorporeal membrane oxygenation cannula and puncture accessories | Maquet Cardiopulmonary GmbH | 20183101652 | Specification: BE-PAL1723 |
| Peripheral extracorporeal membrane oxygenation cannula and puncture accessories | Maquet Cardiopulmonary GmbH | 20183101652 | Specification: BE-PAL1723 |
| Phased-array ultrasound transducer (1.0–5.0 MHz) | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 120-018844-00 | Specification: SP5-1S |
| Phased-array ultrasound transducer (1.0–5.0 MHz) | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 120-018844-00 | Specification: SP5-1S |
| Scalpel | Hangzhou Huawei Pharmaceutical Co., Ltd. | 20152020713 | Used to make a 0.5-cm skin incision |
| Scalpel | Hangzhou Huawei Pharmaceutical Co., Ltd. | 20152020713 | Used to make a 0.5-cm skin incision |
| Sterile dressing | Shaoxing Fuqing Health Products Co., Ltd. | 20172140349 | Used to protect the cannulation site |
| Sterile dressing | Shaoxing Fuqing Health Products Co., Ltd. | 20172140349 | Used to protect the cannulation site |
| Suture material | Ethicon, LLC | XJ8720.O31 | Used to secure the cannula |
| Suture material | Ethicon, LLC | XJ8720.O31 | Used to secure the cannula |
| Ultrasound gel | Hangzhou Kaipule Medical Devices Co., Ltd. | 20150031 | Specification: KL-250 Type II |
| Ultrasound gel | Hangzhou Kaipule Medical Devices Co., Ltd. | 20150031 | Specification: KL-250 Type II |
| Ultrasound imaging system | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 20193061691 | Specification: M9 |
| Ultrasound imaging system | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 20193061691 | Specification: M9 |
| Vascular sheath | Terumo Corporation | 20193031784 | Specification: RS*A60K10SQ |
| Vascular sheath | Terumo Corporation | 20193031784 | Specification: RS*A60K10SQ |
| Vessel dilator set | Maquet Cardiopulmonary GmbH | 20183101652 | Used for sequential tissue and vessel dilation |
| Vessel dilator set | Maquet Cardiopulmonary GmbH | 20183101652 | Used for sequential tissue and vessel dilation |
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