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dc.contributor.authorHuang, W
dc.contributor.authorDe La Iglesia García, Daniel 
dc.contributor.authorBastón Rey, Iria 
dc.contributor.authorCALVIÑO SUAREZ, CRISTINA 
dc.contributor.authorLariño Noia, José 
dc.contributor.authorIglesias García, Julio 
dc.contributor.authorShi, N
dc.contributor.authorZhang, XY
dc.contributor.authorCai, WH
dc.contributor.authorDeng, LH
dc.contributor.authorMoore, D
dc.contributor.authorSingh, VK
dc.contributor.authorXia, Q
dc.contributor.authorWindsor, JA
dc.contributor.authorDomínguez Muñoz, Juan Enrique 
dc.contributor.authorSutton, R
dc.date.accessioned2022-02-02T08:18:20Z
dc.date.available2022-02-02T08:18:20Z
dc.date.issued2019
dc.identifier.issn0163-2116
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584228/pdf/10620_2019_Article_5568.pdfes
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16085
dc.description.abstractBACKGROUND/OBJECTIVES: The epidemiology of exocrine pancreatic insufficiency (EPI) after acute pancreatitis (AP) is uncertain. We sought to determine the prevalence, progression, etiology and pancreatic enzyme replacement therapy (PERT) requirements for EPI during follow-up of AP by systematic review and meta-analysis. METHODS: Scopus, Medline and Embase were searched for prospective observational studies or randomized clinical trials (RCTs) of PERT reporting EPI during the first admission (between the start of oral refeeding and before discharge) or follow-up (>/= 1 month of discharge) for AP in adults. EPI was diagnosed by direct and/or indirect laboratory exocrine pancreatic function tests. RESULTS: Quantitative data were analyzed from 370 patients studied during admission (10 studies) and 1795 patients during follow-up (39 studies). The pooled prevalence of EPI during admission was 62% (95% confidence interval: 39-82%), decreasing significantly during follow-up to 35% (27-43%; risk difference: - 0.34, - 0.53 to - 0.14). There was a two-fold increase in the prevalence of EPI with severe compared with mild AP, and it was higher in patients with pancreatic necrosis and those with an alcohol etiology. The prevalence decreased during recovery, but persisted in a third of patients. There was no statistically significant difference between EPI and new-onset pre-diabetes/diabetes (risk difference: 0.8, 0.7-1.1, P = 0.33) in studies reporting both. Sensitivity analysis showed fecal elastase-1 assay detected significantly fewer patients with EPI than other tests. CONCLUSIONS: The prevalence of EPI during admission and follow-up is substantial in patients with a first attack of AP. Unanswered questions remain about the way this is managed, and further RCTs are indicated.en
dc.language.isoenges
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subject.meshRisk Factors*
dc.subject.meshAdult*
dc.subject.meshMiddle Aged*
dc.subject.meshHumans*
dc.subject.meshTreatment Outcome*
dc.subject.meshEnzyme Replacement Therapy*
dc.subject.meshPancreatitis*
dc.subject.meshRandomized Controlled Trials as Topic*
dc.subject.meshExocrine Pancreatic Insufficiency*
dc.subject.meshAged*
dc.subject.meshPrevalence*
dc.titleExocrine Pancreatic Insufficiency Following Acute Pancreatitis: Systematic Review and Meta-Analysisen
dc.typeArtigoes
dc.identifier.doi10.1007/s10620-019-05568-9
dc.identifier.pmid31161524
dc.identifier.sophos35023
dc.issue.number7es
dc.journal.titleDIGESTIVE DISEASES AND SCIENCESes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Dixestivoes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)es
dc.page.initial3990es
dc.rights.accessRightsopenAccesses
dc.subject.decspancreatitis*
dc.subject.decsresultado del tratamiento*
dc.subject.decsanciano*
dc.subject.decsprevalencia*
dc.subject.decsfactores de riesgo*
dc.subject.decsmediana edad*
dc.subject.decshumanos*
dc.subject.decstratamiento de sustitución enzimática*
dc.subject.decsadulto*
dc.subject.decsensayos clínicos controlados aleatorizados como asunto*
dc.subject.decsinsuficiencia pancreática exocrina*
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtículo de Revisiónes
dc.typesophosArtículo de Revisiónes
dc.volume.number64es


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