Background: Open chest cardiac massage (OCCM) is a commonly performed procedure after traumatic cardiac arrest (TCA). OCCM has been reported to be superior to closed chest compressions (CCC) in animal models and in non-traumatic cardiac arrest. The purpose of this study is to prospectively compare OCCM versus CCC in traumatic cardiac arrest using end-tidal carbon dioxide (ETCO2), the gold standard for determining the effectiveness of chest compressions and detection of return of spontaneous circulation (ROSC), as the surrogate for cardiac output and marker for adequacy of resuscitation. Methods: This prospective observational study enrolled patients over a nine-month period directly presenting to a Level 1 trauma center after TCA. Continuous high-resolution ETCO2 measurements were collected every six seconds for periods of CCC and OCCM, respectively. Patients receiving CCC-only were compared to patients receiving CCC followed by OCCM. Student t-tests were used to compare ETCO2 within and between groups. Results: Thirty-three patients were enrolled (16 OCCM, 17 CCC-only). Mean time of CCC prior to OCCM was sixty-six seconds. Within the OCCM group, final, peak, mean, and median ETCO2 levels significantly increased when comparing the initial CCC period to the OCCM interval. Using a time-matched comparison, significant increases were observed in final and peak but not mean and median values when comparing the first minute of CCC to the remaining time in the CCC-only group. However, when periods of OCCM were compared to equivalent periods of CCC-only, there were no differences in the initial, final, peak, mean, or median ETCO2 values. Correspondingly, no difference in rates of ROSC was observed between groups (OCCM 23.5% vs CCC 38.9%, p=0.53). Conclusions: Although we could not control for confounders, we found no significant improvement in ETCO2 or ROSC with OCCM. With newer endovascular techniques for aortic occlusion, thoracotomy solely for performing OCCM provides no benefit over CCC. Level of Evidence: Level III, therapeutic (C) 2016 Lippincott Williams & Wilkins, Inc.
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