Feeding and Pancreatic Rest in Acute Pancreatitis
Feeding and Pancreatic Rest in Acute Pancreatitis
批准号:
7927723
负责人:
DAVID Clement WHITCOMB
金额:
$27.5万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-01 至 2012-12-31
关键词:
AcuteAdult Respiratory Distress SyndromeAdverse effectsAmino AcidsBloodBlood CirculationBypassCatabolismCessation of lifeClinical TrialsCollectionComplexCritical IllnessDevelopmentDietDiseaseDistalEarly treatmentEatingEndoscopyEnteralEnteral FeedingEnteral NutritionEventExpenditureFailureFecesFeeding MethodsFigs - dietaryFunctional disorderGastric EmptyingGoalsHealedHospital CostsHospital MortalityHospitalizationHospitalsIncidenceInfectionInflammatoryInflammatory ResponseInterruptionIntestinesIntravenous FeedingLengthLigamentsLiquid substanceMaintenanceMeasuresMetabolicMethodsMolecular BiologyMorbidity - disease rateMulticenter StudiesMultiple Organ FailureNauseaNausea and VomitingNecrosisNutrientNutritionalNutritional RequirementsNutritional SupportOrgan failureOutcomePancreasPancreatitisParenteral NutritionPatientsPeptide YYPeptidesPopulationProcessProspective StudiesProtein DeficiencyProteinsRandomizedRecommendationRecruitment ActivityResearch PersonnelResolutionRestRiskSeriesSeveritiesStomachSupportive careSystemTechniquesTestingTimeTrypsinogenTubeVertebral columnacute pancreatitiscomparative trialcostcytokinefeedinghealingimprovedindexinginjuredjejunummeetingsmortalitynasogastric feedingnitrogen balancenutritionprematureprogramsprospectivesepticservice utilizationtube feeding
中文摘要
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英文摘要
Severe acute pancreatitis (SAP) is a disease of high (20-30%) mortality associated with prolonged
hospitalization and excessive costs. Despite the major advances in our understanding of the
pathophysiology of the disease, treatment remains supportive. The backbone of management is nutritional
support as metabolic expenditure is excessively high and patients cannot eat for extended lengths of time .
Because of concern that stimulation of the injured pancreas would exacerbate the disease process which is
characterized by the premature activation of trypsinogen within the pancreas, the cornerstone of
management has been pancreatic rest with intravenous feeding (TPN) which avoids pancreatic stimulation.
However, the infective and metabolic complications of TPN have been shown to outweigh its benefits, and
several prospective randomized comparative trials have demonstrated that patient outcome is better even
with post-pyloric enteral feeding, which is stimulatory. Furthermore, 2 recent studies have collaborated
studies in other populations of critically ill patients, showing that nasogastric (NG) feeding with a semielemental
diet is as effective as post-pyloric feeding with the same dietary formula and does not increase the
risk of aspiration despite the known impairmrnt of gastric emptying. This led to the recommendation that NG
feeding should be used preferentially as it does not require expertize to start and to do. The concern remains
that the mortality rate was not improved, raising the question whether NG feeding was better than no
feeding. However, no feeding is not an option in SAP as unopposed protein catabolism would result in lifethreatening
protein deficiency within 2 weeks. Exploratory studies of ours have suggested that feeding could
be optimized by the placement of specialized double-lumen feeding tubes in the mid-jejunum (40cm past the
ligament of Treitz) by transnasal endsocopic techniques to bypass the compressed upper Gl tract, to avoid
pancreatic stimulation, and to stimulate the ileal brake - which experimentally has been shown to suppress
acute pancreatitis. In the proposed study, we therefore plan to test the hypothesis that in comparison to
simple NG feeding, skilled placement of DJ feeding tube systems hastens the resolution of disease because
it is more effective in providing nutrition and does not exacerbate the disease process, thus leading to
reduced morbidity, mortality and hospital costs. To recruit sufficient patients (n=114) to satisfy our statistical
power calculations in a reasonable time period (5 years), we have formed a consortium with 8 leading
national centers to conduct a multicenter clinical trial to achieve our goal.
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资助金额:$1.5万
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财政年份:2015
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依托单位:
Consortium for the Study of Pancreatitis: Pittsburgh Clinical Center
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批准号:9044100
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资助金额:$38.0万
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财政年份:2015
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依托单位:
Consortium for the Study of Pancreatitis: Pittsburgh Clinical Center
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批准号:9352325
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项目类别:
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资助金额:$40.82万
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财政年份:2015
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负责人:DAVID Clement WHITCOMB
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依托单位:
Consortium for the study of chronic pancreatitis, diabetes and pancreatic cancer – Pittsburgh Clinical Center
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批准号:9987091
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项目类别:
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资助金额:$11.27万
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财政年份:2015
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负责人:DAVID Clement WHITCOMB
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依托单位:
Evaluation of Pain in Chronic Pancreatitis using the NAPS2 cohorts
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批准号:8876665
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项目类别:
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资助金额:$14.91万
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财政年份:2014
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负责人:DAVID Clement WHITCOMB
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依托单位:
Evaluation of Pain in Chronic Pancreatitis using the NAPS2 cohorts
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批准号:8638624
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项目类别:
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资助金额:$26.3万
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财政年份:2014
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负责人:DAVID Clement WHITCOMB
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依托单位:
PancreasFest 2014: Risks and Mechanisms of Pancreatitis and Pancreatic Diabetes
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财政年份:2014
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依托单位:
PancreasFest 2013: Risk, Progression & Therapeutic Advances in Acute Pancreatitis
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资助金额:$1.5万
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财政年份:2013
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依托单位:
Pancreasfest 2012 Pancreatic Cancer: Risk, Early Detection, Diagnosis & Treatment
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资助金额:$1.5万
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财政年份:2012
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负责人:DAVID Clement WHITCOMB
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依托单位:
PancreasFest 2010: Defining & Classifying Disease to Enhance Research & Care
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批准号:7916139
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项目类别:
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资助金额:$1.8万
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财政年份:2010
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-
依托单位:
NAPS2 Continuation - Genome-Wide Association Study of Pancreatitis
-
批准号:7929157
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项目类别:
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资助金额:$9.89万
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依托单位:
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项目类别:
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财政年份:2009
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负责人:DAVID Clement WHITCOMB
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依托单位:
Feeding and Pancreatic Rest in Acute Pancreatitis
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批准号:7807924
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项目类别:
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资助金额:$105.81万
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财政年份:2007
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依托单位:
Feeding and Pancreatic Rest in Acute Pancreatitis
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批准号:8217184
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项目类别:
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资助金额:$106.36万
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依托单位:
Feeding and Pancreatic Rest in Acute Pancreatitis
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批准号:7318137
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资助金额:$119.18万
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财政年份:2007
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依托单位:
Feeding and Pancreatic Rest in Acute Pancreatitis
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批准号:8033823
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资助金额:$108.53万
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负责人:DAVID Clement WHITCOMB
-
依托单位:
海外基金