Postoperative Antibacterial Prophylaxis for the Prevention of Infectious Complications Associated With Tube Thoracostomy in Patients Undergoing Elective General Thoracic Surgery A Double-blind, Placebo-Controlled, Randomized Trial

被引:29
作者
Oxman, David A. [1 ,5 ]
Issa, Nicolas C. [1 ]
Marty, Francisco M. [1 ]
Patel, Alka [3 ]
Panizales, Christia Z. [2 ]
Johnson, Nathaniel N. [2 ]
Licona, J. Humberto [1 ]
McKenna, Shannon S. [4 ]
Frendl, Gyorgy [4 ]
Mentzer, Steven J. [2 ]
Jaklitsch, Michael T. [2 ]
Bueno, Raphael [2 ]
Colson, Yolonda [2 ]
Swanson, Scott J. [2 ]
Sugarbaker, David J. [2 ]
Baden, Lindsey R. [1 ]
机构
[1] Brigham & Womens Hosp, Div Infect Dis, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Div Thorac Surg, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Pharm, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Anesthesiol, Boston, MA 02115 USA
[5] Thomas Jefferson Univ Hosp, Div Pulm & Crit Care, Philadelphia, PA 19107 USA
关键词
SURGICAL SITE INFECTION; ANTIBIOTIC-PROPHYLAXIS; PULMONARY SURGERY; RISK; EXPERIENCE; CEFUROXIME; GUIDELINE; RESECTION;
D O I
10.1001/jamasurg.2013.1372
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: To determine whether extended postoperative antibacterial prophylaxis for patients undergoing elective thoracic surgery with tube thoracostomy reduces the risk of infectious complications compared with preoperative prophylaxis only. Design: Prospective, randomized, double-blind, placebo-controlled trial. Setting: Brigham and Women's Hospital, an 800-bed tertiary care teaching hospital in Boston, Massachusetts. Participants: A total of 251 adult patients undergoing elective thoracic surgery requiring tube thoracostomy between April 2008 and April 2011. Interventions: Patients received preoperative antibacterial prophylaxis with cefazolin sodium (or other drug if the patient was allergic to cefazolin). Postoperatively, patients were randomly assigned (at a 1:1 ratio) using a computer-generated randomization sequence to receive extended antibacterial prophylaxis (n = 125) or placebo (n = 126) for 48 hours or until all thoracostomy tubes were removed, whichever came first. Main Outcome Measures: The combined occurrence of surgical site infection, empyema, pneumonia, and Clostridium difficile colitis by postoperative day 28. Results: A total of 245 patients were included in the modified intention-to-treat analysis (121 in the intervention group and 124 in the placebo group). Thirteen patients (10.7%) in the intervention group and 8 patients (6.5%) in the placebo group had a primary end point (risk difference, -4.3% [95% CI, -11.3% to 2.7%]; P = .26). Six patients (5.0%) in the intervention group and 5 patients (4.0%) in the placebo group developed surgical site infections (risk difference, -0.93% [95% CI, -6.1% to 4.3%]; P = .77). Seven patients (5.8%) in the intervention group and 3 patients (2.4%) in the placebo group developed pneumonia (risk difference, -3.4% [95% CI, -8.3% to 1.6%]; P = .21). One patient in the intervention group developed empyema. No patients experienced C difficile colitis. Conclusions: Extended postoperative antibacterial prophylaxis for patients undergoing elective thoracic surgery requiring tube thoracostomy did not reduce the number of infectious complications compared with preoperative prophylaxis only.
引用
收藏
页码:440 / 446
页数:7
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