Observational longitudinal multicentre investigation of acute pancreatitis (GOULASH PLUS) follow-up of the GOULASH study, protocol /

Acute pancreatitis (AP) is an inflammatory condition that can lead to late consequences. Recurrent AP (RAP) develops in 20% of patients and chronic pancreatitis (CP) occurs in 7%-12.8%. However, we do not have sufficient information to establish an evidence-based statement to define early CP, or how...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Mikó Alexandra
Erőss Bálint Mihály
Sarlós Patrícia
Hegyi Péter, ifj
Márta Katalin
Pécsi Dániel
Vincze Áron
Bódis Beáta
Nemes Orsolya
Faluhelyi Nándor
Farkas Orsolya
Papp Róbert
Kelemen Dezső
Szentesi Andrea Ildikó
Hegyi Eszter
Papp Mária
Czakó László
Izbéki Ferenc
Gajdán László
Novák János
Sahin-Tóth Miklós
Lerch Markus M.
Neoptolemos John
Petersen Ole H.
Hegyi Péter
Dokumentumtípus: Cikk
Megjelent: 2019
Sorozat:BMJ OPEN 9 No. 8
doi:10.1136/bmjopen-2018-025500

mtmt:30789520
Online Access:http://publicatio.bibl.u-szeged.hu/16749
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245 1 0 |a Observational longitudinal multicentre investigation of acute pancreatitis (GOULASH PLUS)   |h [elektronikus dokumentum] :  |b follow-up of the GOULASH study, protocol /  |c  Mikó Alexandra 
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490 0 |a BMJ OPEN  |v 9 No. 8 
520 3 |a Acute pancreatitis (AP) is an inflammatory condition that can lead to late consequences. Recurrent AP (RAP) develops in 20% of patients and chronic pancreatitis (CP) occurs in 7%-12.8%. However, we do not have sufficient information to establish an evidence-based statement to define early CP, or how to prevent its development.The aim of this study was to understand the influencing factors and to determine which parameters should be measured or used as a biomarker to detect the early phase of CP.This is an observational prospective follow-up study of the GOULASH-trial (ISRTCN 63827758) in which (1) all severity of pancreatitis are included; (2) patients receive only therapeutic modalities which are accepted by the evidence based medicine (EBM) guideline; (3) whole blood, serum and plasma samples are stored in our biobank; and (4) large amount of variables are collected and kept in our electronic database including anamnestic data, physical examination, laboratory parameters, imaging, therapy and complications. Therefore, this fully characterised patient cohort are well suitable for this longitudinal follow-up study. Patients' selection: patients enrolled in the GOULASH study will be offered to join to the longitudinal study. The follow-up will be at 1, 2, 3, 4, 5 and 6 years after the episode of AP. Anamnestic data will be collected by questionnaires: (1) diet history questionnaire, (2) 36-Item Short-Form Health Survey, (3) physical activity questionnaire and (4) stress questionnaire. Genetic tests will be performed for the genes associated with CP. The exocrine and endocrine pancreatic, liver and kidney functions will be determined by laboratory tests, stool sample analyses and imaging. Cost-effectiveness will be analysed to examine the relationship between events of interest and health-related quality of life or to explore subgroup differences.This study will provide information about the risk and influencing factors leading to CP and identify the most useful measurable parameters.ISRCTN63396106. 
700 0 1 |a Erőss Bálint Mihály  |e aut 
700 0 1 |a Sarlós Patrícia  |e aut 
700 0 1 |a Hegyi Péter, ifj.  |e aut 
700 0 1 |a Márta Katalin  |e aut 
700 0 1 |a Pécsi Dániel  |e aut 
700 0 1 |a Vincze Áron  |e aut 
700 0 1 |a Bódis Beáta  |e aut 
700 0 1 |a Nemes Orsolya  |e aut 
700 0 1 |a Faluhelyi Nándor  |e aut 
700 0 1 |a Farkas Orsolya  |e aut 
700 0 1 |a Papp Róbert  |e aut 
700 0 1 |a Kelemen Dezső  |e aut 
700 0 1 |a Szentesi Andrea Ildikó  |e aut 
700 0 1 |a Hegyi Eszter  |e aut 
700 0 1 |a Papp Mária  |e aut 
700 0 1 |a Czakó László  |e aut 
700 0 1 |a Izbéki Ferenc  |e aut 
700 0 1 |a Gajdán László  |e aut 
700 0 1 |a Novák János  |e aut 
700 0 2 |a Sahin-Tóth Miklós  |e aut 
700 0 2 |a Lerch Markus M.  |e aut 
700 0 2 |a Neoptolemos John  |e aut 
700 0 2 |a Petersen Ole H.  |e aut 
700 0 2 |a Hegyi Péter  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/16749/1/30789520_Miko_BMJ_Open_2019.pdf  |z Dokumentum-elérés