4.7 Article

Pure Transvaginal Appendectomy Versus Traditional Laparoscopic Appendectomy for Acute Appendicitis A Prospective Cohort Study

Journal

ANNALS OF SURGERY
Volume 255, Issue 2, Pages 266-269

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/SLA.0b013e31823b2748

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Funding

  1. Covidien Corporation

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Objective: This report describes the first cohort study comparing pure transvaginal appendectomies (TVAs) to traditional 3-port laparoscopic appendectomies (LAs). Methods: Between August 2008 and August 2010, 42 patients were offered a pure TVA. Patients who did not wish to undergo a TVA underwent a LA and served as the control group. Demographic data, operative time, length of stay, patient controlled analgesia (PCA) 12-hour-morphine utilization, complications, return to normal activity, and return to work were recorded. Results: Eighteen of 40 enrolled patients underwent a pure TVA. Two patients refused to participate in this study. Mean age (TVA: 31.3 +/- 2.5 years vs. LA: 28.2 +/- 2.3 years, P = 0.36), mean body mass index (TVA: 23.7 +/- 1.2 kg/m(2) vs. LA: 23.6 +/- 0.7 kg/m(2), P = 0.96) mean operative time (TVA: 44.4 +/- 4.5 minutes vs. LA: 39.8 +/- 2.6 minutes, P = 0.38), and mean length of hospital stay (TVA: 1.1 +/- 0.1 days vs. LA: 1.2 +/- 0.1 days, P = 0.53) were not statistically significant. However, mean postoperative morphine-use (TVA: 8.7 +/- 2.0 mg vs. LA: 23.0 +/- 3.4 mg, P < 0.01), return to normal activity (TVA: 3.3 +/- 0.4 days vs. LA: 9.7 +/- 1.6 days, P < 0.01), and return to work (TVA: 5.4 +/- 1.1 days vs. LA: 10.7 +/- 1.5 days, P = 0.01) were statistically significant. One conversion in the TVA group to a LA was necessary because of inability to maintain adequate pneumoperitoneum. Four complications were observed: 1 intraabdominal abscess and 1 case of urinary retention in the TVA group; 1 early postoperative bowel obstruction and 1 case of urinary retention in the LA group. Conclusions: Pure TVA is a safe and well-tolerated procedure with significantly less pain and faster recovery compared to traditional LA. This study is registered with www.clinicaltrials.gov as NCT00806429.

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