Inflammatory Bowel Diseases Clinical Trial
Official title:
A Prospective Study on the Incidence and Risk Factors Related to Infection in Patients With Inflammatory Bowel Disease
The purpose of this study is to determine the incidence and risk factors related to Infection in patients with Inflammatory Bowel Disease (IBD)
IBD could lead to an increased risk of infections, particularly related to immunosuppressive
therapy. The true effect of having IBD in the development of infections has not been studied
in depth since the cohort studies are scarce and the results of studies with different
approaches are contradictory.
The limited time period of former studies may not be enough to assess infectious
complications that may occur in a long term period.
Moreover, certain polymorphisms demonstrated to confer a higher risk of opportunistic
infections under immunosuppressive conditions, for instance HIV, patients with cystic
fibrosis and Candida' infections. For this reason, it seems reasonable to think that genetic
factors might play a role in the risk of opportunistic infections in IBD.
The hypothesis of this study is that patients with IBD have an increased risk of infection by
immunosuppressive treatment.
TYPE OF STUDY Prospective cohort study that evaluates the effect of immunosuppression and
other clinical factors in the onset of infection in IBD
STUDY DESIGN PATIENTS & METHODS This study is aimed to all incidental patients diagnosed with
Crohn's disease and ulcerative colitis included in the ENEIDA database.
METHODS An infection would be considered as relevant when: 1) requires hospital admission, 2)
leads to death or endangers the patient's life (ICU admission, presence of hemodynamic
instability, sepsis, tracheal intubation, vasoactive drug requirement), 3) must be treated
with specific antibiotics (antibacterials, antivirals, antifungals) 4) affects recurrently
(herpes virus, papilloma virus, etc). 5) requires change/withdrawal of immunosuppressive or
biological treatment.
The appearance of relevant infection will be prospectively evaluated, performing a
subanalysis at 3 and 5 years using ENEIDA platform. ENEIDA is a database from a Spanish
national study in IBD on genetic and environmental determinants run under GETECCU (Grupo
Español de Trabajo en Enfermedad de Crohn y Colitis Ulcerosa) supervision. This database
basically comprises: demographic characteristics, type of IBD, immunosuppressant treatment,
biological treatment or surgery)
At the time of inclusion the following variables should be available (and are mandatory):
demographic characteristics, type of IBD, date of diagnosis, phenotypic characteristics of
the disease, history of serious infections, information on received treatments particularly
the exposure to immunosuppressants, biological treatment or surgery and whether an infection
has occurred as a complication of the three treatment groups. It should also be collected the
following serologic details: hepatitis type B virus C, HIV, tuberculosis (TB), varicella
zoster status.
At the time of registration a blood sample (10cc) will be drawn and sent to a biobank to
analyze the DNA for genetic research.
STUDY ANALYSIS Sample calculation
The main objective of this study is to determine the percentage of infections in IBD and the
related risk factors for the development of infections in patients with IBD. Given that the
reported prevalence of infection varies between 6 and 10%the formula for estimating endless
samples, establishing:
- Security level of the confidence interval at 95%
- Expected value for the worst case scenario of 6% (prevalence of infection)
- Precision of 1.5%
- The minimum sample number is set to 963, and assuming a loss rate of 20%
With these assumptions, the total number of patients to be included is 1204 patients.
The statistical analysis will be in three steps: (1) independent clinical factors analysis,
(2) genetic factors infection-related analysis and (3) clinical and genetic factors
infection- related analysis.
Baseline and follow up data will be compared among patients who develop infection and those
who do not. Quantitative variables will be contrast by T-student and Mann-Whitney test.
Qualitative variable will be contrast by X2 or Fisher test. Logistic regression will be
conducted to analyze independent associations between variables and Kaplan-Meier test to
calculate survival curves.
An analysis of Cox proportional hazards will be conducted to assess the effect of exposure to
independent predictors of the risk of significant infection or mortality.
Finally the intensity of the significant associations will be measured by calculating the OR,
HR and confidence interval of 95%.
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