Risk Factors of Acute Pancreatitis in Oral Double Balloon Enteroscopy
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
27638962
DOI
10.14712/18059694.2016.95
PII: 18059694.2016.95
Knihovny.cz E-resources
- Keywords
- Acute pancreatitis, Deep enteroscopy, Device assisted endoscopy, Double balloon enteroscopy, Hyperamylasemia, Small intestinal disorders,
- MeSH
- Acute Disease MeSH
- alpha 1-Antitrypsin blood MeSH
- Amylases blood urine MeSH
- Biomarkers blood urine MeSH
- C-Reactive Protein metabolism MeSH
- Double-Balloon Enteroscopy adverse effects MeSH
- E-Selectin blood MeSH
- Hyperamylasemia blood etiology MeSH
- Calcitonin blood MeSH
- Cathepsins blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Lipase blood MeSH
- Malondialdehyde blood MeSH
- Pancreatitis blood etiology MeSH
- Risk Factors MeSH
- Case-Control Studies MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- alpha 1-Antitrypsin MeSH
- Amylases MeSH
- Biomarkers MeSH
- C-Reactive Protein MeSH
- E-Selectin MeSH
- Calcitonin MeSH
- Cathepsins MeSH
- Lipase MeSH
- Malondialdehyde MeSH
- SERPINA1 protein, human MeSH Browser
Double balloon enteroscopy (DBE) was introduced 15 years ago. The complications of diagnostic DBE are rare, acute pancreatitis is most redoubtable one (incidence about 0.3%). Hyperamylasemia after DBE seems to be a rather common condition respectively. The most probable cause seems to be a mechanical straining of the pancreas. We tried to identify patients in a higher risk of acute pancreatitis after DBE. We investigated several laboratory markers before and after DBE (serum cathepsin B, lactoferrin, E-selectin, SPINK 1, procalcitonin, S100 proteins, alfa-1-antitrypsin, hs-CRP, malondialdehyde, serum and urine amylase and serum lipase). Serum amylase and lipase rose significantly with the maximum 4 hours after DBE. Serum cathepsin and procalcitonin decreased significantly 4 hours after DBE compared to healthy controls and patients values before DBE. Either serum amylase or lipase 4 hours after DBE did not correlate with any markers before DBE. There was a trend for an association between the number of push-and-pull cycles and procalcitonin and urine amylase 4 hours after DBE; between procalcitonin and alfa-1-antitrypsin, cathepsin and hs-CRP; and between E-selectin and malondialdehyde 4 hours after DBE. We found no laboratory markers determinative in advance those patients in a higher risk of acute pancreatitis after DBE.
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