Ultrasound Axillary Vein Access: Evaluation of Learning Curve for an Alternative Approach to Cardiac Device Implantation
- Conditions
- Venous AccessUltrasound Therapy; ComplicationsCardiac Device Implant
- Interventions
- Procedure: Ultrasound guided venous accessProcedure: Conventional technique
- Registration Number
- NCT04382430
- Lead Sponsor
- University of Kansas Medical Center
- Brief Summary
The purpose of this study is to determine the learning curve associated with Ultrasound (US) guided axillary vein access for cardiac device implantation based on length of procedure among operators of various levels of experience and to assess the 30-day complication rate for patients undergoing US guided device placement versus traditional implant methods.
- Detailed Description
Ultrasound (US) guided axillary vein access for device implantation is an uncommon approach to gain venous access for cardiac device implantation - an extremely common procedure. However, there has been a growing trend of utilizing this approach to obtain venous access for device implantation among operators. Axillary vein access was described back as far as 1997, when it was utilized for contrast guided venipuncture to access the axillary vein for device implantation. Literature has suggested that an axillary venous approach, with either a superficial landmark or radiographic contrast, has better long-term efficacy and lower lead complications than a conventional subclavian approach for patients that had permanent pacemaker implantation. There are a variety of ways to access the axillary vein including contrast venography to help localization, "blind puncture" (utilizing fluoroscopy to identify anatomical landmarks), and US. More recently, operators have begun to utilize US guidance for axillary vein access. Esmaiel has described that US guidance for axillary vein access could potentially improve the success rate of venous access and limit complications. Others, albeit few, have reported US guided access for cardiac device implantation has the ability to reduce complications, is faster to complete, and easier to learn. According to the Agency for Healthcare Research and Quality in the United States, US guided central venous catheter placement is one of the 11 patient safety practices that have the strongest evidence supporting its use in improving patient outcomes. Evidence supports US guidance being standard of care in central venous catheter placement and using US for axillary access as helpful in cardiac device implantation, but providers still utilize predominantly alternative approaches to obtain venous access via the subclavian vein, cephalic cutdown, extrathoracic axillary using fluoroscopy and thoracic axillary using fluoroscopy.
Currently, there is limited data describing outcomes, the efficiency of US guided axillary access for cardiac device implantation, and the learning curve associated with this technique. Data suggests that utilizing the US approach can improve outcomes, be more efficient, and be easier to learn. Investigators recently reported a high success (95%) and low complication rate with US guided axillary access in 187 patients. Despite this limited data, operators still largely use alternative approaches for venous access. In part, this may be due to the learning curve associated with US axillary venous access.
While there is data demonstrating the utility of US guided axillary access, there is little evidence showing the learning curve for operators associated with this technique. The aim of this project is to assess the learning curve of this technique among operators of various levels of experience.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
- Sign written Informed Consent Form.
- ≥18 years of age up to 90 years old.
- Eligible and referred for cardiac device implantation.
- BMI < 35.
- Unable to sign consent.
- Patient eligible for cardiac device upgrades/ extractions, subcutaneous implantable cardioverter defibrillators (SICD) & leadless devices.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description US Guided Axillary venous access Ultrasound guided venous access Physician/ provider will perform 2 unassisted \& 10 solo Ultrasound (US) guided venous access and pocket creation cardiac device implant. First 2 device implant will be done to educate physicians about ultrasound guided venous access. Subsequent subject will be randomized to 2:1 in ultrasound vs. conventional technique. Conventional technique Conventional technique Physician/ provider will perform 5 cardiac device implant using conventional technique for venous access and pocket creation.
- Primary Outcome Measures
Name Time Method Venous access time between US guided and conventional technique During procedure Assess changes in venous access and pocket creation time with progressive experience with US guided axillary venous access (learning curve).
Time spent for pocket creation between US guided venous access technique and conventional technique. During procedure Compare the pocket creation time with US guided axillary venous access versus conventional techniques.
Time spent to obtain venous access & pocket creation between experienced and inexperienced physicians. During procedure Compare venous access and pocket creation time amongst experienced and inexperienced physicians.
To assess 30 day post procedure complications 30 Day post procedure Assess 30-day complications between techniques.
Assess acute procedural success between two techniques. During procedure Compare overall procedural success whether device was successfully placed or not post procedure between US guided axillary venous access \& conventional technique. Success as Assigned- whether implant technique assigned was successful or whether had to switch to an alternative technique.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Kansas Medical Center
🇺🇸Kansas City, Kansas, United States