RETRACTED: Peritonitis from Perforated Peptic Ulcer and Immune Response (Retracted article. See vol. 32, pg. 95, 2019)

被引:22
作者
Schietroma, Mario [1 ]
Piccione, Federica [1 ]
Carlei, Francesco [1 ]
Sista, Federico [1 ]
Cecilia, Emanuela Marina [1 ]
Amicucci, Gianfranco [1 ]
机构
[1] Univ Aquila, Dept Surg, Coppito, Italy
关键词
peritonitis; peptic ulcer; immune response; laparoscopy; bacterial translocation; open treatment; LAPAROSCOPIC REPAIR; ANIMAL-MODEL; APPENDECTOMY; ENDOTOXEMIA; LAPAROTOMY; STRESS;
D O I
10.3109/08941939.2012.762073
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Elevated intra-abdominal pressure during the laparoscopy may promote bacteremia, endotoxemia, and systemic inflammatory response. In patients with generalized peritonitis from perforated peptic ulcer (PPU), we sought to compare acute phase response, immunologic status, and bacterial translocation from laparoscopic and open approach. Study Design: From July 2005 to September 2011, 115 consecutive patients underwent peptic ulcer repair for PPU: 58 cases laparoscopic peptic ulcer repair (LR) and 57 cases open peptic ulcer repair (OR). Bacteremia, endotoxemia, white blood cells population, human leukocyte antigen-DR (HLA-DR), neutrophil-elastase, interleukin-1 and 6 (IL-1 and IL-6), and C-reactive protein (CRP) were investigated. Results: Patients characteristics and grade of peritoneal contamination were similar in the two groups. One hour after intervention, bacteremia was significantly higher in the "open" group than in the laparoscopic group (p < .001). A significantly higher concentration of systemic endotoxin was detected intraoperatively in the "open" group of patients in comparison to the laparoscopic group (p < .0001). Laparotomy caused a significant increase in neutrophil concentration, neutrophil-elastase, IL-1 and IL-6, CRP, and decrease of HLA-DR. We recorded six cases (10.3%) of intra-abdominal abscess in the "open" group and one (1.7%) in laparoscopic group (p < .001). Conclusions: OR, in case of peritonitis after PPU, increased the incidence of bacteremia, endotoxemia, and systemic inflammation compared with LR. Early enhanced postoperative systemic inflammation may cause lower transient immunologic defense after laparotomy (decrease of HLA-DR), leading to enhanced sepsis in these patients.
引用
收藏
页码:294 / 304
页数:11
相关论文
共 42 条
[1]   Laparoscopic appendectomy for complicated appendicitis - An evaluation of postoperative factors [J].
Ball, CG ;
Kortbeek, JB ;
Kirkpatrick, AW ;
Mitchell, P .
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES, 2004, 18 (06) :969-973
[2]   Laparoscopic correction of perforated peptic ulcer: first choice? A review of literature [J].
Bertleff, Marietta J. O. E. ;
Lange, Johan F. .
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES, 2010, 24 (06) :1231-1239
[3]   Randomized Clinical Trial of Laparoscopic Versus Open Repair of the Perforated Peptic Ulcer: The LAMA Trial [J].
Bertleff, Marietta J. O. E. ;
Halm, Jens A. ;
Bemelman, Willem A. ;
van der Ham, Arie C. ;
van der Harst, Erwin ;
Oei, Hok I. ;
Smulders, J. F. ;
Steyerberg, E. W. ;
Lange, Johan F. .
WORLD JOURNAL OF SURGERY, 2009, 33 (07) :1368-1373
[4]   Comparison Between Open and Laparoscopic Repair of Perforated Peptic Ulcer Disease [J].
Bhogal, Ricky H. ;
Athwal, Ruvinder ;
Durkin, Damien ;
Deakin, Mark ;
Cheruvu, Chandra N. V. .
WORLD JOURNAL OF SURGERY, 2008, 32 (11) :2371-2374
[5]   PREDICTION OF OUTCOME USING THE MANNHEIM PERITONITIS INDEX IN 2003 PATIENTS [J].
BILLING, A ;
FROHLICH, D ;
SCHILDBERG, FW ;
FUGGER, R ;
SCHULZ, F ;
DAU, H ;
THIEDE, A ;
KRENZIEN, J ;
VONBERGMANN, E ;
VANLAARHOVEN, CJHM ;
LABUS, HN ;
WACHA, H ;
NITSCHE, D .
BRITISH JOURNAL OF SURGERY, 1994, 81 (02) :209-213
[6]  
BORREGAARD N, 1988, EUR J HAEMATOL, V41, P401
[7]  
Busic Z, 2010, COLLEGIUM ANTROPOL, V34, P279
[8]   Stress response to laparoscopic surgery - A review [J].
Buunen, M ;
Gholghesaei, M ;
Veldkamp, R ;
Meijer, DW ;
Bonjer, HJ ;
Bouvy, ND .
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES, 2004, 18 (07) :1022-1028
[9]  
Carlei F, 1999, WORLD J SURG, V23, P18, DOI 10.1007/s002689900559
[10]   MULTIPLE ORGAN FAILURE - PATHOPHYSIOLOGY AND POTENTIAL FUTURE THERAPY [J].
DEITCH, EA .
ANNALS OF SURGERY, 1992, 216 (02) :117-134