2016
DOI: 10.1016/j.jpeds.2016.04.013
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Both Exocrine Pancreatic Insufficiency and Signs of Pancreatic Inflammation Are Prevalent in Children with Complicated Severe Acute Malnutrition: An Observational Study

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Cited by 24 publications
(42 citation statements)
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“…Diarrhea in SAM is multifactorial; infectious causes and intestinal inflammation as well as impaired digestion of fat and protein related to exocrine pancreas and hepatobiliary dysfunction likely impact the overall nutrient absorptive capacity, and these pathways would not be directly ameliorated by our intervention [12,35,36]. Most cases of diarrhea were osmotic in nature rather than secretory, suggesting that bacterial infections such as enterotoxin-producing Escherichia coli or rotavirus were likely not contributing substantially to the diarrhea at day 3.…”
Section: Discussionmentioning
confidence: 99%
“…Diarrhea in SAM is multifactorial; infectious causes and intestinal inflammation as well as impaired digestion of fat and protein related to exocrine pancreas and hepatobiliary dysfunction likely impact the overall nutrient absorptive capacity, and these pathways would not be directly ameliorated by our intervention [12,35,36]. Most cases of diarrhea were osmotic in nature rather than secretory, suggesting that bacterial infections such as enterotoxin-producing Escherichia coli or rotavirus were likely not contributing substantially to the diarrhea at day 3.…”
Section: Discussionmentioning
confidence: 99%
“…There can be false positive results if the test is performed on a watery stool specimen; therefore, all FE-1 testing should be performed on a formed or semi-formed stool specimen. Individuals with severe malnutrition may also have false positive FE-1 [31], although in the case of a patient with CF the PI is the likely cause of the malnutrition. In non-CF patients, testing should be repeated after nutritional repletion.…”
Section: Indirect Testsmentioning
confidence: 99%
“…Current management strategies are 'blanket approaches' that disregard the different presentations of SAM and their associated clinical risk [4]. In general, edematous SAM is linked to higher morbidity and mortality [4,9], but the prevalence of underlying pathologies such as Human Immunodeficiency Virus (HIV) has changed the risk profiles associated with the different SAM phenotypes. Recent studies have shown children with non-edematous SAM to be more vulnerable in certain contexts (e.g., children with HIV and severe wasting have the highest mortality risk) [10,11].…”
Section: Introductionmentioning
confidence: 99%