Pancreatic exocrine insufficiency following acute pancreatitis: Systematic review and study level meta-analysis
This study systematically explores the prevalence of pancreatic exocrine insufficiency (PEI) after acute pancreatitis in different subgroups of etiology (biliary/alcoholic/other), disease severity and follow-up time ( 36 months after index admission). PubMed and EMBASE databases were searched, 32 st...
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Veröffentlicht in: | Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2018-04, Vol.18 (3), p.253-262 |
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container_title | Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] |
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creator | Hollemans, Robbert A. Hallensleben, Nora D.L. Mager, David J. Kelder, Johannes C. Besselink, Marc G. Bruno, Marco J. Verdonk, Robert C. van Santvoort, Hjalmar C. |
description | This study systematically explores the prevalence of pancreatic exocrine insufficiency (PEI) after acute pancreatitis in different subgroups of etiology (biliary/alcoholic/other), disease severity and follow-up time ( 36 months after index admission).
PubMed and EMBASE databases were searched, 32 studies were included in this study level meta-analysis.
In a total of 1495 patients with acute pancreatitis, tested at a mean of 36 months after index admission, the pooled prevalence of PEI was 27.1% (95%-confidence interval [CI]: 20.3%–35.1%). Patients from seven studies (n = 194) underwent direct tests with pooled prevalence of 41.7% [18.5%–69.2%]. Patients from 26 studies (n = 1305) underwent indirect tests with pooled prevalence of 24.4% [18.3%–31.8%]. In subgroup analyses on patients that underwent fecal elastase-1 tests, PEI occurred more often in alcoholic pancreatitis (22.7% [16.6%–30.1%]) than in biliary pancreatitis (10.2% [6.2%–16.4%]) or other etiology (13.4% [7.7%–22.4%]; P = 0.02). Pooled prevalence of PEI after mild and severe pancreatitis was 19.4% [8.6%–38.2%] and 33.4% [22.6%–46.3%] respectively in studies using fecal elaste-1 tests (P = 0.049). Similar results were seen in patients without (18.9% [9.3%–34.6%]) and with necrotizing pancreatitis (32.0% [18.2%–49.8%]; P = 0.053). Over time, the prevalence of PEI decreased in patients who underwent the fecal elastase-1 test and increased in patients who underwent the fecal fat analysis.
After acute pancreatitis, a quarter of all patients develop PEI during follow-up. Alcoholic etiology and severe and necrotizing pancreatitis are associated with higher risk of PEI. The prevalence of PEI may change as time of follow-up increases. |
doi_str_mv | 10.1016/j.pan.2018.02.009 |
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PubMed and EMBASE databases were searched, 32 studies were included in this study level meta-analysis.
In a total of 1495 patients with acute pancreatitis, tested at a mean of 36 months after index admission, the pooled prevalence of PEI was 27.1% (95%-confidence interval [CI]: 20.3%–35.1%). Patients from seven studies (n = 194) underwent direct tests with pooled prevalence of 41.7% [18.5%–69.2%]. Patients from 26 studies (n = 1305) underwent indirect tests with pooled prevalence of 24.4% [18.3%–31.8%]. In subgroup analyses on patients that underwent fecal elastase-1 tests, PEI occurred more often in alcoholic pancreatitis (22.7% [16.6%–30.1%]) than in biliary pancreatitis (10.2% [6.2%–16.4%]) or other etiology (13.4% [7.7%–22.4%]; P = 0.02). Pooled prevalence of PEI after mild and severe pancreatitis was 19.4% [8.6%–38.2%] and 33.4% [22.6%–46.3%] respectively in studies using fecal elaste-1 tests (P = 0.049). Similar results were seen in patients without (18.9% [9.3%–34.6%]) and with necrotizing pancreatitis (32.0% [18.2%–49.8%]; P = 0.053). Over time, the prevalence of PEI decreased in patients who underwent the fecal elastase-1 test and increased in patients who underwent the fecal fat analysis.
After acute pancreatitis, a quarter of all patients develop PEI during follow-up. Alcoholic etiology and severe and necrotizing pancreatitis are associated with higher risk of PEI. The prevalence of PEI may change as time of follow-up increases.</description><identifier>ISSN: 1424-3903</identifier><identifier>EISSN: 1424-3911</identifier><identifier>DOI: 10.1016/j.pan.2018.02.009</identifier><identifier>PMID: 29482892</identifier><language>eng</language><publisher>Switzerland: Elsevier B.V</publisher><subject>Acute Disease ; Acute pancreatitis ; Alcoholism - complications ; Classification ; Elastase ; Enzymes ; Etiology ; Exocrine insufficiency ; Exocrine Pancreatic Insufficiency - etiology ; Feces ; Follow-up ; Follow-Up Studies ; Gangrene ; Humans ; Meta-analysis ; Pancreas ; Pancreatitis ; Pancreatitis - complications ; Pancreatitis - etiology ; Pancreatitis, Acute Necrotizing - complications ; Prevalence ; Studies ; Systematic review</subject><ispartof>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2018-04, Vol.18 (3), p.253-262</ispartof><rights>2018 IAP and EPC</rights><rights>Copyright © 2018 IAP and EPC. Published by Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Limited Apr 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-a15dd318bb214fced89c53f459e9869db03fc519591dc56aa3a3b4013aa60a4d3</citedby><cites>FETCH-LOGICAL-c381t-a15dd318bb214fced89c53f459e9869db03fc519591dc56aa3a3b4013aa60a4d3</cites><orcidid>0000-0002-2760-2867</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29482892$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hollemans, Robbert A.</creatorcontrib><creatorcontrib>Hallensleben, Nora D.L.</creatorcontrib><creatorcontrib>Mager, David J.</creatorcontrib><creatorcontrib>Kelder, Johannes C.</creatorcontrib><creatorcontrib>Besselink, Marc G.</creatorcontrib><creatorcontrib>Bruno, Marco J.</creatorcontrib><creatorcontrib>Verdonk, Robert C.</creatorcontrib><creatorcontrib>van Santvoort, Hjalmar C.</creatorcontrib><creatorcontrib>for the Dutch Pancreatitis Study Group</creatorcontrib><creatorcontrib>Dutch Pancreatitis Study Group</creatorcontrib><title>Pancreatic exocrine insufficiency following acute pancreatitis: Systematic review and study level meta-analysis</title><title>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]</title><addtitle>Pancreatology</addtitle><description>This study systematically explores the prevalence of pancreatic exocrine insufficiency (PEI) after acute pancreatitis in different subgroups of etiology (biliary/alcoholic/other), disease severity and follow-up time (<12, 12–36 and > 36 months after index admission).
PubMed and EMBASE databases were searched, 32 studies were included in this study level meta-analysis.
In a total of 1495 patients with acute pancreatitis, tested at a mean of 36 months after index admission, the pooled prevalence of PEI was 27.1% (95%-confidence interval [CI]: 20.3%–35.1%). Patients from seven studies (n = 194) underwent direct tests with pooled prevalence of 41.7% [18.5%–69.2%]. Patients from 26 studies (n = 1305) underwent indirect tests with pooled prevalence of 24.4% [18.3%–31.8%]. In subgroup analyses on patients that underwent fecal elastase-1 tests, PEI occurred more often in alcoholic pancreatitis (22.7% [16.6%–30.1%]) than in biliary pancreatitis (10.2% [6.2%–16.4%]) or other etiology (13.4% [7.7%–22.4%]; P = 0.02). Pooled prevalence of PEI after mild and severe pancreatitis was 19.4% [8.6%–38.2%] and 33.4% [22.6%–46.3%] respectively in studies using fecal elaste-1 tests (P = 0.049). Similar results were seen in patients without (18.9% [9.3%–34.6%]) and with necrotizing pancreatitis (32.0% [18.2%–49.8%]; P = 0.053). Over time, the prevalence of PEI decreased in patients who underwent the fecal elastase-1 test and increased in patients who underwent the fecal fat analysis.
After acute pancreatitis, a quarter of all patients develop PEI during follow-up. Alcoholic etiology and severe and necrotizing pancreatitis are associated with higher risk of PEI. The prevalence of PEI may change as time of follow-up increases.</description><subject>Acute Disease</subject><subject>Acute pancreatitis</subject><subject>Alcoholism - complications</subject><subject>Classification</subject><subject>Elastase</subject><subject>Enzymes</subject><subject>Etiology</subject><subject>Exocrine insufficiency</subject><subject>Exocrine Pancreatic Insufficiency - etiology</subject><subject>Feces</subject><subject>Follow-up</subject><subject>Follow-Up Studies</subject><subject>Gangrene</subject><subject>Humans</subject><subject>Meta-analysis</subject><subject>Pancreas</subject><subject>Pancreatitis</subject><subject>Pancreatitis - complications</subject><subject>Pancreatitis - etiology</subject><subject>Pancreatitis, Acute Necrotizing - complications</subject><subject>Prevalence</subject><subject>Studies</subject><subject>Systematic review</subject><issn>1424-3903</issn><issn>1424-3911</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1u1TAQRi0Eoj_wAN0gS6wTPHYS7HZVVYUiVQIJWFsTe1L5Kje5tZ22eXvc3rZLVjOL73yaOYydgKhBQPdlU-9wqqUAXQtZC2HesENoZFMpA_D2dRfqgB2ltBFCSgDznh1I02ipjTxk8y-cXCTMwXF6mF0ME_EwpWUYggs0uZUP8zjO92G64eiWTHz3QuSQTvnvNWXaPvGR7gLdc5w8T3nxKx_pjka-pYwVTjiuKaQP7N2AY6KPz_OY_f12-efiqrr--f3Hxfl15ZSGXCG03ivQfS-hGRx5bVyrhqY1ZHRnfC_U4FowrQHv2g5RoeobAQqxE9h4dcw-73t3cb5dKGW7mZdYjki2-DL6q-i0KinYp1ycU4o02F0MW4yrBWEfFduNLe8-ItoKaYviwnx6bl76LflX4sVpCZztA1T-K0aiTU8myYdILls_h__U_wMWcI6h</recordid><startdate>201804</startdate><enddate>201804</enddate><creator>Hollemans, Robbert A.</creator><creator>Hallensleben, Nora D.L.</creator><creator>Mager, David J.</creator><creator>Kelder, Johannes C.</creator><creator>Besselink, Marc G.</creator><creator>Bruno, Marco J.</creator><creator>Verdonk, Robert C.</creator><creator>van Santvoort, Hjalmar C.</creator><general>Elsevier B.V</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><orcidid>https://orcid.org/0000-0002-2760-2867</orcidid></search><sort><creationdate>201804</creationdate><title>Pancreatic exocrine insufficiency following acute pancreatitis: Systematic review and study level meta-analysis</title><author>Hollemans, Robbert A. ; Hallensleben, Nora D.L. ; Mager, David J. ; Kelder, Johannes C. ; Besselink, Marc G. ; Bruno, Marco J. ; Verdonk, Robert C. ; van Santvoort, Hjalmar C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-a15dd318bb214fced89c53f459e9869db03fc519591dc56aa3a3b4013aa60a4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acute Disease</topic><topic>Acute pancreatitis</topic><topic>Alcoholism - complications</topic><topic>Classification</topic><topic>Elastase</topic><topic>Enzymes</topic><topic>Etiology</topic><topic>Exocrine insufficiency</topic><topic>Exocrine Pancreatic Insufficiency - etiology</topic><topic>Feces</topic><topic>Follow-up</topic><topic>Follow-Up Studies</topic><topic>Gangrene</topic><topic>Humans</topic><topic>Meta-analysis</topic><topic>Pancreas</topic><topic>Pancreatitis</topic><topic>Pancreatitis - complications</topic><topic>Pancreatitis - etiology</topic><topic>Pancreatitis, Acute Necrotizing - complications</topic><topic>Prevalence</topic><topic>Studies</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hollemans, Robbert A.</creatorcontrib><creatorcontrib>Hallensleben, Nora D.L.</creatorcontrib><creatorcontrib>Mager, David J.</creatorcontrib><creatorcontrib>Kelder, Johannes C.</creatorcontrib><creatorcontrib>Besselink, Marc G.</creatorcontrib><creatorcontrib>Bruno, Marco J.</creatorcontrib><creatorcontrib>Verdonk, Robert C.</creatorcontrib><creatorcontrib>van Santvoort, Hjalmar C.</creatorcontrib><creatorcontrib>for the Dutch Pancreatitis Study Group</creatorcontrib><creatorcontrib>Dutch Pancreatitis Study Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hollemans, Robbert A.</au><au>Hallensleben, Nora D.L.</au><au>Mager, David J.</au><au>Kelder, Johannes C.</au><au>Besselink, Marc G.</au><au>Bruno, Marco J.</au><au>Verdonk, Robert C.</au><au>van Santvoort, Hjalmar C.</au><aucorp>for the Dutch Pancreatitis Study Group</aucorp><aucorp>Dutch Pancreatitis Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pancreatic exocrine insufficiency following acute pancreatitis: Systematic review and study level meta-analysis</atitle><jtitle>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]</jtitle><addtitle>Pancreatology</addtitle><date>2018-04</date><risdate>2018</risdate><volume>18</volume><issue>3</issue><spage>253</spage><epage>262</epage><pages>253-262</pages><issn>1424-3903</issn><eissn>1424-3911</eissn><abstract>This study systematically explores the prevalence of pancreatic exocrine insufficiency (PEI) after acute pancreatitis in different subgroups of etiology (biliary/alcoholic/other), disease severity and follow-up time (<12, 12–36 and > 36 months after index admission).
PubMed and EMBASE databases were searched, 32 studies were included in this study level meta-analysis.
In a total of 1495 patients with acute pancreatitis, tested at a mean of 36 months after index admission, the pooled prevalence of PEI was 27.1% (95%-confidence interval [CI]: 20.3%–35.1%). Patients from seven studies (n = 194) underwent direct tests with pooled prevalence of 41.7% [18.5%–69.2%]. Patients from 26 studies (n = 1305) underwent indirect tests with pooled prevalence of 24.4% [18.3%–31.8%]. In subgroup analyses on patients that underwent fecal elastase-1 tests, PEI occurred more often in alcoholic pancreatitis (22.7% [16.6%–30.1%]) than in biliary pancreatitis (10.2% [6.2%–16.4%]) or other etiology (13.4% [7.7%–22.4%]; P = 0.02). Pooled prevalence of PEI after mild and severe pancreatitis was 19.4% [8.6%–38.2%] and 33.4% [22.6%–46.3%] respectively in studies using fecal elaste-1 tests (P = 0.049). Similar results were seen in patients without (18.9% [9.3%–34.6%]) and with necrotizing pancreatitis (32.0% [18.2%–49.8%]; P = 0.053). Over time, the prevalence of PEI decreased in patients who underwent the fecal elastase-1 test and increased in patients who underwent the fecal fat analysis.
After acute pancreatitis, a quarter of all patients develop PEI during follow-up. Alcoholic etiology and severe and necrotizing pancreatitis are associated with higher risk of PEI. The prevalence of PEI may change as time of follow-up increases.</abstract><cop>Switzerland</cop><pub>Elsevier B.V</pub><pmid>29482892</pmid><doi>10.1016/j.pan.2018.02.009</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2760-2867</orcidid></addata></record> |
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subjects | Acute Disease Acute pancreatitis Alcoholism - complications Classification Elastase Enzymes Etiology Exocrine insufficiency Exocrine Pancreatic Insufficiency - etiology Feces Follow-up Follow-Up Studies Gangrene Humans Meta-analysis Pancreas Pancreatitis Pancreatitis - complications Pancreatitis - etiology Pancreatitis, Acute Necrotizing - complications Prevalence Studies Systematic review |
title | Pancreatic exocrine insufficiency following acute pancreatitis: Systematic review and study level meta-analysis |
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