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Antibiotic prophylaxis is not protective in severe acute pancreatitis: a systematic review and meta-analysis Dr Mohammed Al-Shehri KFHU – Khobar General Surgery 2010
Definition It is an inflammatory disorder of previously normal  pancreas. Typically cause pain and interfere with the exocrine function of the gland.  Cause local, adjacent and remote organs involvement.
Severity ,[object Object]
 Best test
Can be done at 24 hrs, can be repeated
Ranson’s Criteria (1974!)
Needs to be done at 24 and 48 hrs
Balthazar’s (CT scan criteria)
Glascow
Single Markers of Severity,[object Object]
APACHE II http://www.sfar.org/scores2/apache22.html ≥ 8 is severe.
SINGLEMARKER’S
The American Journal of Surgery (May 2009) 197, 806-813 Review Antibiotic prophylaxis is not protective in severe acute pancreatitis: a systematic review and meta-analysis Nadim S. Jafri, M.D., M.Sc.a,b, Suhal S. Mahid, M.D., Ph.D.c, Spencer R. Idsteinc, Carlton A. Hornung, Ph.D., M.P.H.a,b, Susan Galandiuk, M.D.c,* aDivision of Internal Medicine, Department of Medicine, bDepartment of Epidemiology and Population Health, cPrice Institute of Surgical Research and the Section of Colorectal Surgery, Department of Surgery, University of Louisville, School of Medicine, Louisville, KY 40292, USA
Outline Background . Methods. Results. 4. Conclusion.
Background ,[object Object]
 may lead to life threatening conditions .
 SAP usually develops when part of the pancreas become  necrotic and many complications are associated with the presence of this dead pancreatic tissue.
It requires intensive and aggressive management.
International symposium on AP described SAP as being associated organ failure and/or local complications such as abscess  ,necrosis, or pseudocyst.,[object Object]
Cont…. at least 8 of APACHE II criteria. ,[object Object]
The disease process comprises 2 stage :the initial phase is characterized by SIRS that can lead to multi-organ failure and ultimately death. The later phase  compromises secondary bacterial infection of devitalized tissues primarily caused by gut organism. ,[object Object]
Sterile necrosis can be infected with gut bacteria in up to 70% .,[object Object]
Hypothesis.,[object Object]
Limited to the human studies without language restrictions.
Hand –searched  the references of review articles , evaluated symposia proceeding, poster presentations and abstracts from major gastrointestinal and surgical meetings. ,[object Object]
SAP was  diagnosed with contrast enhanced CT scan and any of the following : APACHE II, Imrie classification and increased C-reactive protein levels > 120 mg /Dl.
Necrosis by CT scan.
Prophylactic antibiotics were administered IV .
Defined length of  antibiotics treatment.
M and  M measured objectively .
If there were multiple publications of the same trail, only the most recent publication was considered for analysis. ,[object Object]
Non randomized studies. ,[object Object]
Each articles scrutinized to meet the criteria.
Data abstracted independently by each reviewer using a standardized data collection to increase the uniformity of data and to reduce the reporting bias.
In discrepancy , a consensus  decision was made with the help of the senior author.,[object Object]
first author, year of publication, institution, single/multicenter study, number of pt in the treatment and controlled arms, etiologies, length of follow up period, name of antibiotics , dose and timing of antibiotics administration, incidence of non pancreatic infection, incidence of surgery, incidence of mortality , method of data analysis and the method of diagnosing complications.    ,[object Object]
< 3 low study quality.
3 or more high quality,  used as part of the sensitivity analysis.,[object Object]
The effect measures estimated were relative risk (RR) for dichotomous data, which we report with 95% confidence intervals (CIs).
The RR indicates the risk of an individual who received prophylactic antibiotics developing a wound infection compared with the risk of an individual not receiving prophylactic antibiotics.
Relative risk reduction (RRR), absolute risk reduction (ARR), and number needed to treat (NNT) were calculated to assess if the relative risk was clinically important.,[object Object]
Cont…. PATIENTS AND ANTIBIOTCS TREATMENT ,[object Object]

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Antibiotic prophylaxis in sever Acute Panceriatitis

  • 1. Antibiotic prophylaxis is not protective in severe acute pancreatitis: a systematic review and meta-analysis Dr Mohammed Al-Shehri KFHU – Khobar General Surgery 2010
  • 2. Definition It is an inflammatory disorder of previously normal pancreas. Typically cause pain and interfere with the exocrine function of the gland. Cause local, adjacent and remote organs involvement.
  • 3.
  • 5. Can be done at 24 hrs, can be repeated
  • 7. Needs to be done at 24 and 48 hrs
  • 10.
  • 13.
  • 14. The American Journal of Surgery (May 2009) 197, 806-813 Review Antibiotic prophylaxis is not protective in severe acute pancreatitis: a systematic review and meta-analysis Nadim S. Jafri, M.D., M.Sc.a,b, Suhal S. Mahid, M.D., Ph.D.c, Spencer R. Idsteinc, Carlton A. Hornung, Ph.D., M.P.H.a,b, Susan Galandiuk, M.D.c,* aDivision of Internal Medicine, Department of Medicine, bDepartment of Epidemiology and Population Health, cPrice Institute of Surgical Research and the Section of Colorectal Surgery, Department of Surgery, University of Louisville, School of Medicine, Louisville, KY 40292, USA
  • 15. Outline Background . Methods. Results. 4. Conclusion.
  • 16.
  • 17. may lead to life threatening conditions .
  • 18. SAP usually develops when part of the pancreas become necrotic and many complications are associated with the presence of this dead pancreatic tissue.
  • 19. It requires intensive and aggressive management.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24.
  • 25. Limited to the human studies without language restrictions.
  • 26.
  • 27. SAP was diagnosed with contrast enhanced CT scan and any of the following : APACHE II, Imrie classification and increased C-reactive protein levels > 120 mg /Dl.
  • 29. Prophylactic antibiotics were administered IV .
  • 30. Defined length of antibiotics treatment.
  • 31. M and M measured objectively .
  • 32.
  • 33.
  • 34. Each articles scrutinized to meet the criteria.
  • 35. Data abstracted independently by each reviewer using a standardized data collection to increase the uniformity of data and to reduce the reporting bias.
  • 36.
  • 37.
  • 38. < 3 low study quality.
  • 39.
  • 40. The effect measures estimated were relative risk (RR) for dichotomous data, which we report with 95% confidence intervals (CIs).
  • 41. The RR indicates the risk of an individual who received prophylactic antibiotics developing a wound infection compared with the risk of an individual not receiving prophylactic antibiotics.
  • 42.
  • 43.
  • 44. A total of 253 pts were randomized to the antibiotic prophylaxis group and 249 were randomized to the placebo arm.
  • 45. Age ranged from 43 to 59 yrs.
  • 46. 60 % alcoholic , 24% biliary , and 20 % other causes.
  • 47. Duration of antibiotics treatment ranged from 5 to 21 days .
  • 48.
  • 49. Cont… Crude outcome rates are presented in Table 2. By using a fixed-effect model to evaluate mortality, antibiotic prophylaxis resulted in a RR of .76 (95% CI, .49 –1.16; I2 8.8%; indicating homogeneity among studies)
  • 51. Cont…. SENSITIVITY ANALYSIS Sensitivity analysis was conducted to determine whether infected necrosis, surgical interventions, nonpancreatic infections, class of antibiotic, or study quality (Jadad et al16 scale 3) had a significant effect on the strength and direction of the results.
  • 52.
  • 53.
  • 54.
  • 55. Cont… Surgicalinterventions. Four studies that used B–lactams and evaluated surgical intervention (n=305; antibiotics, 30 of 152; placebo, 29 of 153) found no beneficial effect. Nonpancreaticinfections. Four studies that used B-lactams and evaluated nonpancreatic infections (n = 305; antibiotics, 29 of 152; placebo, 53 of 153) found a beneficial effect.
  • 56.
  • 57. Cont… Surgicalintervention. All 5 studies evaluated surgical intervention in SAP (n 367; antibiotics, 35 of 182; placebo, 38 of 185) and found no benefit of prophylactic antibiotics (RR, .91; 95% CI, .61–1.38; I2 16.5). Nonpancreaticinfections. Four studies evaluated nonpancreatic infections in SAP (n 307; antibiotics, 35 of 152; placebo, 49 of 155) and found no benefit of prophylactic antibiotics.
  • 58. Funnel plot of high-quality studies (Jadad et al16 score 3). The vertical axis represents the line of no effect with the horizontal axis representing log of RR. The 95% CI is represented by the diagonal lines. The circles represent each study
  • 59. Meta-analysis of RCTs on prophylactic antibiotics versus placebo/no intervention on mortality.
  • 60. Conclusion The role of systemic antibiotics in the management of acute pancreatitis remains controversial. The development of complications such as infected pancreatic necrosis, abscesses, and infected pseudocysts, herald the development of a deteriorating disease process that is associated with considerable morbidity and mortality.
  • 61. Cont… The present meta-analysis does not support the use of prophylactic antibiotics to reduce the frequency of surgical intervention, infected necrosis, or mortality in patients with SAP. They may, however, be beneficial in protecting against the development of nonpancreatic infections. The mechanisms of which are not understood. This does need to be weighed against the significant adverse events associated with antibiotics, including increased bacterial resistance and fungal infections.
  • 62.
  • 63.
  • 64.
  • 65. Systemic review and meta-analysis until May 2008 was used.
  • 66. Systematic search of MEDLINE ,EMBASE and Cochrane central register of controlled trial used.
  • 67. Manually searched the references of original/ review articles and evaluated symposia proceedings, poster presentations, and abstracts from major gastrointestinal and surgical meetings.
  • 68.
  • 69. Results were subjected to sensitivity analysis to determine heterogeneity among studies.
  • 70. 502 patients from 8 studies.
  • 71.
  • 72. Thanks for your attention Dr. Mohammed Alshehri