TY - JOUR
T1 - The value of procalcitonin at predicting the severity of acute pancreatitis and development of infected pancreatic necrosis
T2 - Systematic review
AU - Mofidi, Reza
AU - Suttie, Stuart A.
AU - Patil, Pradeep V.
AU - Ogston, Simon
AU - Parks, Rowan W.
N1 - MEDLINE® is the source for the MeSH terms of this document.
PY - 2009/7
Y1 - 2009/7
N2 - Background. Many studies have evaluated serum levels of procalcitonin (PCT) as a predictor in the development of severe acute pancreatitis (SAP) and infected pancreatic necrosis (H-W). This study assesses the value of PCT as a marker of development of SAP and IPN.Methods. Medline, Web of Science, the Cochrane clinical trials register, and international conference proceedings were searched systematically for prospective studies, which evaluated the usefulness of PCT as a marker of SAP and IPN. The sensitivity, specificity, and diagnostic odds ratios (DORs) were calculated for each study, and the study quality and heterogeneity among the studies were evaluated.Results. Twenty-four of 59 studies identified were included in data extraction. The sensitivity and specificity of PCT for development of SAP were 0.72 and 0.86, respectively (area under the curve [AUC] = 0.87; DOR = 14.9; 95% confidence interval [CI] = 5.6-39.8), albeit with a significant degree of heterogeneity Q = 28.56, P .01). The sensitivity and specificity of PCT for prediction of infected pancreatic necrosis were 0.80 and 0.91 (AUC = 0.91; DOR = 28.3; 95% CI = 13.8-58.3) with no significant heterogeneity Q = 7.83, P = .18). No significant heterogeneity was observed among the studies when only higher quality studies (AUC = 0.91; DOR = 30.7; 95% CI = 10. 7-87.8) or studies that used a cutoff PCT level >0.5 ng/mL (AUC = 0.88, 32.8; 95% CI = 10.1-106.6) were included.Conclusion. Serum measurements of PCT may be valuable in predicting the severity of acute pancreatitis and the risk of developing infected pancreatic necrosis. (Surgery 2009;146:72-81.)
AB - Background. Many studies have evaluated serum levels of procalcitonin (PCT) as a predictor in the development of severe acute pancreatitis (SAP) and infected pancreatic necrosis (H-W). This study assesses the value of PCT as a marker of development of SAP and IPN.Methods. Medline, Web of Science, the Cochrane clinical trials register, and international conference proceedings were searched systematically for prospective studies, which evaluated the usefulness of PCT as a marker of SAP and IPN. The sensitivity, specificity, and diagnostic odds ratios (DORs) were calculated for each study, and the study quality and heterogeneity among the studies were evaluated.Results. Twenty-four of 59 studies identified were included in data extraction. The sensitivity and specificity of PCT for development of SAP were 0.72 and 0.86, respectively (area under the curve [AUC] = 0.87; DOR = 14.9; 95% confidence interval [CI] = 5.6-39.8), albeit with a significant degree of heterogeneity Q = 28.56, P .01). The sensitivity and specificity of PCT for prediction of infected pancreatic necrosis were 0.80 and 0.91 (AUC = 0.91; DOR = 28.3; 95% CI = 13.8-58.3) with no significant heterogeneity Q = 7.83, P = .18). No significant heterogeneity was observed among the studies when only higher quality studies (AUC = 0.91; DOR = 30.7; 95% CI = 10. 7-87.8) or studies that used a cutoff PCT level >0.5 ng/mL (AUC = 0.88, 32.8; 95% CI = 10.1-106.6) were included.Conclusion. Serum measurements of PCT may be valuable in predicting the severity of acute pancreatitis and the risk of developing infected pancreatic necrosis. (Surgery 2009;146:72-81.)
KW - ACUTE NECROTIZING PANCREATITIS
KW - C-REACTIVE PROTEIN
KW - CONTROLLED CLINICAL-TRIAL
KW - SERUM PROCALCITONIN
KW - INFLAMMATORY RESPONSE
KW - DIAGNOSTIC RELEVANCE
KW - ANTIBIOTIC-TREATMENT
KW - METAANALYSIS
KW - DYSFUNCTION
KW - MULTICENTER
UR - http://www.scopus.com/inward/record.url?scp=67349213202&partnerID=8YFLogxK
U2 - 10.1016/j.surg.2009.02.013
DO - 10.1016/j.surg.2009.02.013
M3 - Review article
C2 - 19541012
SN - 0039-6060
VL - 146
SP - 72
EP - 81
JO - Surgery
JF - Surgery
IS - 1
ER -