Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]

<p>Abstract</p> <p>Background</p> <p>Infectious complications are the major cause of death in acute pancreatitis. Small bowel bacterial overgrowth and subsequent bacterial translocation are held responsible for the vast majority of these infections. Goal of this study i...

Full description

Bibliographic Details
Main Authors: Akkermans Louis MA, Nieuwenhuijs Vincent B, Buskens Erik, Timmerman Harro M, Besselink Marc GH, Gooszen Hein G
Format: Article
Language:English
Published: BMC 2004-09-01
Series:BMC Surgery
Online Access:http://www.biomedcentral.com/1471-2482/4/12
id doaj-b719981dc6044391b5a898db31264ec1
record_format Article
spelling doaj-b719981dc6044391b5a898db31264ec12020-11-24T21:17:52ZengBMCBMC Surgery1471-24822004-09-01411210.1186/1471-2482-4-12Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]Akkermans Louis MANieuwenhuijs Vincent BBuskens ErikTimmerman Harro MBesselink Marc GHGooszen Hein G<p>Abstract</p> <p>Background</p> <p>Infectious complications are the major cause of death in acute pancreatitis. Small bowel bacterial overgrowth and subsequent bacterial translocation are held responsible for the vast majority of these infections. Goal of this study is to determine whether selected probiotics are capable of preventing infectious complications without the disadvantages of antibiotic prophylaxis; antibiotic resistance and fungal overgrowth.</p> <p>Methods/design</p> <p>PROPATRIA is a double-blind, placebo-controlled randomised multicenter trial in which 200 patients will be randomly allocated to a multispecies probiotic preparation (Ecologic 641) or placebo. The study is performed in all 8 Dutch University Hospitals and 7 non-University hospitals. The study-product is administered twice daily through a nasojejunal tube for 28 days or until discharge. Patients eligible for randomisation are adult patients with a first onset of predicted severe acute pancreatitis: Imrie criteria 3 or more, CRP 150 mg/L or more, APACHE II score 8 or more. Exclusion criteria are post-ERCP pancreatitis, malignancy, infection/sepsis caused by a second disease, intra-operative diagnosis of pancreatitis and use of probiotics during the study. Administration of the study product is started within 72 hours after onset of abdominal pain. The primary endpoint is the total number of infectious complications. Secondary endpoints are mortality, necrosectomy, antibiotic resistance, hospital stay and adverse events. To demonstrate that probiotic prophylaxis reduces the proportion of patients with infectious complications from 50% to 30%, with alpha 0,05 and power 80%, a total sample size of 200 patients was calculated.</p> <p>Conclusion</p> <p>The PROPATRIA study is aimed to show a reduction in infectious complications due to early enteral use of multispecies probiotics in severe acute pancreatitis.</p> http://www.biomedcentral.com/1471-2482/4/12
collection DOAJ
language English
format Article
sources DOAJ
author Akkermans Louis MA
Nieuwenhuijs Vincent B
Buskens Erik
Timmerman Harro M
Besselink Marc GH
Gooszen Hein G
spellingShingle Akkermans Louis MA
Nieuwenhuijs Vincent B
Buskens Erik
Timmerman Harro M
Besselink Marc GH
Gooszen Hein G
Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]
BMC Surgery
author_facet Akkermans Louis MA
Nieuwenhuijs Vincent B
Buskens Erik
Timmerman Harro M
Besselink Marc GH
Gooszen Hein G
author_sort Akkermans Louis MA
title Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]
title_short Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]
title_full Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]
title_fullStr Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]
title_full_unstemmed Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]
title_sort probiotic prophylaxis in patients with predicted severe acute pancreatitis (propatria): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [isrctn38327949]
publisher BMC
series BMC Surgery
issn 1471-2482
publishDate 2004-09-01
description <p>Abstract</p> <p>Background</p> <p>Infectious complications are the major cause of death in acute pancreatitis. Small bowel bacterial overgrowth and subsequent bacterial translocation are held responsible for the vast majority of these infections. Goal of this study is to determine whether selected probiotics are capable of preventing infectious complications without the disadvantages of antibiotic prophylaxis; antibiotic resistance and fungal overgrowth.</p> <p>Methods/design</p> <p>PROPATRIA is a double-blind, placebo-controlled randomised multicenter trial in which 200 patients will be randomly allocated to a multispecies probiotic preparation (Ecologic 641) or placebo. The study is performed in all 8 Dutch University Hospitals and 7 non-University hospitals. The study-product is administered twice daily through a nasojejunal tube for 28 days or until discharge. Patients eligible for randomisation are adult patients with a first onset of predicted severe acute pancreatitis: Imrie criteria 3 or more, CRP 150 mg/L or more, APACHE II score 8 or more. Exclusion criteria are post-ERCP pancreatitis, malignancy, infection/sepsis caused by a second disease, intra-operative diagnosis of pancreatitis and use of probiotics during the study. Administration of the study product is started within 72 hours after onset of abdominal pain. The primary endpoint is the total number of infectious complications. Secondary endpoints are mortality, necrosectomy, antibiotic resistance, hospital stay and adverse events. To demonstrate that probiotic prophylaxis reduces the proportion of patients with infectious complications from 50% to 30%, with alpha 0,05 and power 80%, a total sample size of 200 patients was calculated.</p> <p>Conclusion</p> <p>The PROPATRIA study is aimed to show a reduction in infectious complications due to early enteral use of multispecies probiotics in severe acute pancreatitis.</p>
url http://www.biomedcentral.com/1471-2482/4/12
work_keys_str_mv AT akkermanslouisma probioticprophylaxisinpatientswithpredictedsevereacutepancreatitispropatriadesignandrationaleofadoubleblindplacebocontrolledrandomisedmulticentertrialisrctn38327949
AT nieuwenhuijsvincentb probioticprophylaxisinpatientswithpredictedsevereacutepancreatitispropatriadesignandrationaleofadoubleblindplacebocontrolledrandomisedmulticentertrialisrctn38327949
AT buskenserik probioticprophylaxisinpatientswithpredictedsevereacutepancreatitispropatriadesignandrationaleofadoubleblindplacebocontrolledrandomisedmulticentertrialisrctn38327949
AT timmermanharrom probioticprophylaxisinpatientswithpredictedsevereacutepancreatitispropatriadesignandrationaleofadoubleblindplacebocontrolledrandomisedmulticentertrialisrctn38327949
AT besselinkmarcgh probioticprophylaxisinpatientswithpredictedsevereacutepancreatitispropatriadesignandrationaleofadoubleblindplacebocontrolledrandomisedmulticentertrialisrctn38327949
AT gooszenheing probioticprophylaxisinpatientswithpredictedsevereacutepancreatitispropatriadesignandrationaleofadoubleblindplacebocontrolledrandomisedmulticentertrialisrctn38327949
_version_ 1726011691153489920