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Effects of Pancreatic Enzyme Replacement Therapy on Body Weight and Nutritional Assessments After Pancreatoduodenectomy in a Randomized Trial

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dc.contributor.authorKim H.-
dc.contributor.authorYoon Y.-S.-
dc.contributor.authorHan Y.-
dc.contributor.authorKwon W.-
dc.contributor.authorKim S.-W.-
dc.contributor.authorHan H.-S.-
dc.contributor.authorYoon D.-S.-
dc.contributor.authorPark J.S.-
dc.contributor.authorPark S.-J.-
dc.contributor.authorHan S.-S.-
dc.contributor.authorLee S.E.-
dc.contributor.authorChoi S.H.-
dc.contributor.authorHan I.W.-
dc.contributor.authorKim E.-
dc.contributor.authorJang J.-Y.-
dc.date.available2020-04-16T07:20:22Z-
dc.date.issued2020-04-
dc.identifier.issn1542-3565-
dc.identifier.issn1542-7714-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/38498-
dc.description.abstractBackground & Aims: We studied the effects of pancreatic enzyme replacement therapy (PERT) on body weight, nutritional status, and quality of life (QoL) in patients with pancreatic exocrine insufficiency after pancreatoduodenectomy. Methods: We performed a randomized, double-blind trial of 304 patients who underwent pancreatoduodenectomy at 7 tertiary referral hospitals in South Korea. Patients with fecal levels of elastase of 200 μg/g or less, before and after surgery, were assigned randomly to groups that received PERT (a single capsule of 40,000 IU pancreatin, Norzyme (40,000 IU, Pankreatan; Nordmark Arzneimittel GmbH & Co, Uetersen, Germany), 3 times each day during meals for 3 months; n = 151) or placebo (n = 153). Protocol completion was defined as taking more than two thirds of the total dose without taking other digestive enzymes; the protocol was completed by 71 patients in the PERT group and 93 patients in the placebo group. Patients underwent a physical examination, oral glucose tolerance tests, and blood tests at baseline and at month 3 of the study period. The primary end point was change in body weight. Secondary end points were changes in bowel habits, nutritional parameters, and QoL. Results: In the per-protocol analysis, 3 months after the study began, patients in the PERT group gained a mean of 1.09 kg in weight and patients in the placebo group lost a mean of 2.28 kg (difference between groups, 3.37 kg; P < .001). However, no difference in body weight was observed between groups in the intent-to-treat analysis. Three months after the study began, the mean serum levels of prealbumin increased by 10.9 mg/dL in the PERT group and increased by 7.8 mg/dL in the placebo group (P = .002). Poor compliance to PERT was a significant risk factor for weight loss (P < .001). There was no significant difference in QoL scores between groups. Conclusions: In the intent-to-treat analysis of data from a randomized trial, we found no significant effect of PERT on mean body weights of patients with pancreatic exocrine insufficiency after pancreatoduodenectomy. However, with active education and monitoring, PERT could increase body weight and nutritional parameters. ClinicalTrials.gov no: NCT02127021. © 2020 AGA Institute-
dc.language영어-
dc.language.isoENG-
dc.publisherW.B. Saunders-
dc.titleEffects of Pancreatic Enzyme Replacement Therapy on Body Weight and Nutritional Assessments After Pancreatoduodenectomy in a Randomized Trial-
dc.typeArticle-
dc.identifier.doi10.1016/j.cgh.2019.08.061-
dc.identifier.bibliographicCitationClinical Gastroenterology and Hepatology, v.18, no.4, pp 926 - 934.e4-
dc.description.isOpenAccessN-
dc.identifier.wosid000520865700031-
dc.identifier.scopusid2-s2.0-85081671657-
dc.citation.endPage934.e4-
dc.citation.number4-
dc.citation.startPage926-
dc.citation.titleClinical Gastroenterology and Hepatology-
dc.citation.volume18-
dc.identifier.urlhttps://www.cghjournal.org/article/S1542-3565(19)30990-5/fulltext-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorDigestion-
dc.subject.keywordAuthorPancreas-
dc.subject.keywordAuthorPancreatectomy-
dc.subject.keywordAuthorPEI-
dc.subject.keywordPlusDOUBLE-BLIND-
dc.subject.keywordPlusEXOCRINE INSUFFICIENCY-
dc.subject.keywordPlusPATIENT OUTCOMES-
dc.subject.keywordPlusCLINICAL-TRIAL-
dc.subject.keywordPlusSURGERY-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusCREON-
dc.subject.keywordPlusDIAGNOSIS-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordPlusMMS-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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