Πέμπτη 19 Μαΐου 2016

Emergent non-image guided REBOA catheter placement: A cadaver-based study.

Background: Emergent REBOA(Resuscitative Endovascular Balloon Occlusion of the Aorta) insertion for critically injured patients in hemorrhagic shock is performed blindly with fluoroscopic imaging confirmation. The aim of this study was to determine a reliable method for initial REBOA catheter insertion with balloon deployment between the left subclavian artery takeoff and celiac trunk. Methods: Human cadaver study. External surface (sternal notch, mid-sternum, xiphoid) and intravascular (left subclavian artery(LSA), celiac trunk(CT)) landmarks were measured from standardized left and right common femoral artery puncture sites. The landing zone (LZ, distance between LSA and CT) and margins of safety (distance from distal balloon edge to LSA and proximal balloon edge to CT) were calculated using intravascular landmarks. The probability of balloon deployment in the LZ using external landmarks was compared in univariate analysis using Fisher's exact test. Results: 10 cadavers were analyzed (7 male, mean BMI 19.4 kg/m2). Mean intravascular distances from femoral puncture sites to the LSA and CT were 54.8cm (SD 1.9) and 32.9cm (SD 1.9). The mean LZ was 21.8cm (SD 3.8). Mean surface distances from femoral puncture sites to the xiphoid, mid-sternum and sternal notch were 31.8cm (SD 3.9), 41.8cm (SD 3.3) and 51.8cm (SD 3.2). Inserting the catheter to a distance approximated by surface distance from the femoral puncture site to mid-sternum resulted in a 100% likelihood balloon deployment in the LZ for both sides. This was superior to the xiphoid and sternal notch (left site p=0.005, right site p=0.036, mean of both sites p=0.083). Using the mid-sternum landmark, the mean margin of safety to the LSA and CT was 10.7cm (SD 4.3) and 3.1cm (SD 3.4). Conclusion: Using the mid-sternum landmark for REBOA balloon placement, the likelihood of balloon deployment in the LZ was 100% with an acceptable margin of safety Level of Evidence: III, diagnostic test (C) 2016 Lippincott Williams & Wilkins, Inc.

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