Cargando…
Secondary systemic amyloidosis in inflammatory bowel disease: a nationwide analysis
BACKGROUND: Secondary systemic amyloidosis (SSA) is a rare but severe complication of inflammatory bowel disease (IBD). We aimed to evaluate the clinical characteristics, predictors of complications, and in-hospital mortality of patients with Crohn’s disease (CD) and Ulcerative colitis (UC) who deve...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hellenic Society of Gastroenterology
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566770/ https://www.ncbi.nlm.nih.gov/pubmed/28845105 http://dx.doi.org/10.20524/aog.2017.0168 |
_version_ | 1783258601601630208 |
---|---|
author | Sharma, Prabin Aguilar, Rodrigo Siddiqui, Omer Asif Nader, Mark Abi |
author_facet | Sharma, Prabin Aguilar, Rodrigo Siddiqui, Omer Asif Nader, Mark Abi |
author_sort | Sharma, Prabin |
collection | PubMed |
description | BACKGROUND: Secondary systemic amyloidosis (SSA) is a rare but severe complication of inflammatory bowel disease (IBD). We aimed to evaluate the clinical characteristics, predictors of complications, and in-hospital mortality of patients with Crohn’s disease (CD) and Ulcerative colitis (UC) who develop SSA. METHODS: Using the National Inpatient Sample, we identified patients hospitalized for IBD and SSA between 2004 and 2012. Using multivariate logistic regression, patients with CD were compared with those with UC regarding the presence or absence of SSA. IBD patients without SSA were matched in a 2:1 ratio with those with SSA using propensity matching. We analyzed the hospitalization trends of SSA in CD and UC patients using Pearson’s χ(2) test. Analyses were performed using SAS version 9.3. RESULTS: Among the 302,548 patients with CD and 174,057 patients with UC hospitalized between 2004 and 2012, we identified 47 (0.02%) and 36 (0.02%) cases of SSA, respectively. We noted rising annual hospitalization trends for both CD and UC patients with or without SSA. In-hospital mortality was significantly higher for both the UC+SSA group (16.7% vs. 2.1%, P<0.0001) and the CD+SSA group (6.4% vs. 1.0%, P=0.0001) before propensity matching. However, this difference was not seen for either UC+SSA (17.1% vs. 7.1%, P=0.11) or CD+SSA (6.8% vs. 2.3%, P=0.20) after matching. CONCLUSIONS: SSA rarely affects IBD patients, but when it does, it is associated with increased rates of infection, severe sepsis, and multi-organ system involvement. Despite this, SSA does not affect in-hospital mortality in IBD patients. Further studies are needed to explore this association. |
format | Online Article Text |
id | pubmed-5566770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hellenic Society of Gastroenterology |
record_format | MEDLINE/PubMed |
spelling | pubmed-55667702017-08-25 Secondary systemic amyloidosis in inflammatory bowel disease: a nationwide analysis Sharma, Prabin Aguilar, Rodrigo Siddiqui, Omer Asif Nader, Mark Abi Ann Gastroenterol Original Article BACKGROUND: Secondary systemic amyloidosis (SSA) is a rare but severe complication of inflammatory bowel disease (IBD). We aimed to evaluate the clinical characteristics, predictors of complications, and in-hospital mortality of patients with Crohn’s disease (CD) and Ulcerative colitis (UC) who develop SSA. METHODS: Using the National Inpatient Sample, we identified patients hospitalized for IBD and SSA between 2004 and 2012. Using multivariate logistic regression, patients with CD were compared with those with UC regarding the presence or absence of SSA. IBD patients without SSA were matched in a 2:1 ratio with those with SSA using propensity matching. We analyzed the hospitalization trends of SSA in CD and UC patients using Pearson’s χ(2) test. Analyses were performed using SAS version 9.3. RESULTS: Among the 302,548 patients with CD and 174,057 patients with UC hospitalized between 2004 and 2012, we identified 47 (0.02%) and 36 (0.02%) cases of SSA, respectively. We noted rising annual hospitalization trends for both CD and UC patients with or without SSA. In-hospital mortality was significantly higher for both the UC+SSA group (16.7% vs. 2.1%, P<0.0001) and the CD+SSA group (6.4% vs. 1.0%, P=0.0001) before propensity matching. However, this difference was not seen for either UC+SSA (17.1% vs. 7.1%, P=0.11) or CD+SSA (6.8% vs. 2.3%, P=0.20) after matching. CONCLUSIONS: SSA rarely affects IBD patients, but when it does, it is associated with increased rates of infection, severe sepsis, and multi-organ system involvement. Despite this, SSA does not affect in-hospital mortality in IBD patients. Further studies are needed to explore this association. Hellenic Society of Gastroenterology 2017 2017-06-14 /pmc/articles/PMC5566770/ /pubmed/28845105 http://dx.doi.org/10.20524/aog.2017.0168 Text en Copyright: © Hellenic Society of Gastroenterology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Sharma, Prabin Aguilar, Rodrigo Siddiqui, Omer Asif Nader, Mark Abi Secondary systemic amyloidosis in inflammatory bowel disease: a nationwide analysis |
title | Secondary systemic amyloidosis in inflammatory bowel disease: a nationwide analysis |
title_full | Secondary systemic amyloidosis in inflammatory bowel disease: a nationwide analysis |
title_fullStr | Secondary systemic amyloidosis in inflammatory bowel disease: a nationwide analysis |
title_full_unstemmed | Secondary systemic amyloidosis in inflammatory bowel disease: a nationwide analysis |
title_short | Secondary systemic amyloidosis in inflammatory bowel disease: a nationwide analysis |
title_sort | secondary systemic amyloidosis in inflammatory bowel disease: a nationwide analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5566770/ https://www.ncbi.nlm.nih.gov/pubmed/28845105 http://dx.doi.org/10.20524/aog.2017.0168 |
work_keys_str_mv | AT sharmaprabin secondarysystemicamyloidosisininflammatoryboweldiseaseanationwideanalysis AT aguilarrodrigo secondarysystemicamyloidosisininflammatoryboweldiseaseanationwideanalysis AT siddiquiomerasif secondarysystemicamyloidosisininflammatoryboweldiseaseanationwideanalysis AT nadermarkabi secondarysystemicamyloidosisininflammatoryboweldiseaseanationwideanalysis |