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1.
Dig Dis ; 41(6): 879-889, 2023.
Article in English | MEDLINE | ID: mdl-37611561

ABSTRACT

BACKGROUND: Crohn's disease (CD) is characterized by the development of complications over the course of the disease. It is crucial to identify predictive factors of disabling disease, in order to target patients for early intervention. We evaluated risk factors of disabling CD and developed a prognostic model. METHODS: In total, 511 CD patients were retrospectively analyzed. Univariate and multivariate logistic regression analyses were used to identify demographic, clinical, and biological risk factors. A predictive nomogram model was developed in a subgroup of patients with noncomplicated CD (inflammatory pattern and no perianal disease). RESULTS: The rate of disabling CD within 5 years after diagnosis was 74.6%. Disabling disease was associated with gender, location of disease, requirement of steroids for the first flare, and perianal lesions. In the subgroup of patients (310) with noncomplicated CD, the rate of disabling CD was 80%. In the multivariate analysis age at onset <40 years (OR = 3.46, 95% confidence interval [CI] = 1.52-7.90), extensive disease (L3/L4) (OR = 2.67, 95% CI = 1.18-6.06), smoking habit (OR = 2.09, 95% CI = 1.03-4.27), requirement of steroids at the first flare (OR = 2.20, 95% CI = 1.09-4.45), and albumin (OR = 0.59, 95% CI = 0.36-0.96) were associated with development of disabling disease. The developed predictive nomogram based on these factors presented good discrimination, with an area under the receiver operating characteristic curve of 0.723 (95% CI: 0.670-0.830). CONCLUSION: We identified predictive factors of disabling CD and developed an easy-to-use prognostic model that may be used in clinical practice to help identify patients at high risk and address treatment effectively.


Subject(s)
Crohn Disease , Humans , Adult , Crohn Disease/diagnosis , Crohn Disease/epidemiology , Crohn Disease/complications , Retrospective Studies , Clinical Decision Rules , Risk Factors , Steroids/therapeutic use , Decision Making
2.
Rev Esp Enferm Dig ; 111(7): 566-568, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31215214

ABSTRACT

Endoscopic ultrasound (EUS) guided drainage of pelvic collections is an alternative to percutaneous or surgical drainage. We present our experience using lumen-apposing metal stents (LAMS) for the drainage of postoperative pelvic abscesses.


Subject(s)
Abdominal Abscess/therapy , Drainage/instrumentation , Drainage/methods , Endosonography , Postoperative Complications/therapy , Stents , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged
4.
Rev Esp Enferm Dig ; 110(5): 271-273, 2018 05.
Article in English | MEDLINE | ID: mdl-29745718

ABSTRACT

Enrolling patients for epidemiologic studies represents a challenge for researchers. Those who use traditional approaches, including in-person interviews and telephone or mail surveys, obtain increasingly lower participations. In the study by Martín-Fernández et al., the authors obtained 44 responses via mail and forums, and then 376 responses in just five days via Facebook. Online social networks (OSN) provide a unique opportunity to obtain epidemiologic data with resource savings and presumably collecting higher-quality information. However, disadvantages include loss of anonimity, selection and sampling biases, social acceptance bias, behavior changes, and lack of representativity.


Subject(s)
Inflammatory Bowel Diseases , Internet , Social Networking , Consumer Health Information/methods , Epidemiologic Research Design , Health Promotion/methods , Humans , Inflammatory Bowel Diseases/diagnosis , Inflammatory Bowel Diseases/therapy , Information Dissemination/methods
5.
Helicobacter ; 22(5)2017 Oct.
Article in English | MEDLINE | ID: mdl-28771880

ABSTRACT

BACKGROUND: Helicobacter pylori antibiotic resistance is an increasing problem worldwide. Pylera® may be an option as salvage therapy. AIM: To assess the effectiveness, safety, and tolerance of Pylera® as a third-line in clinical practice. MATERIALS AND METHODS: This was a multicenter, observational, prospective database study in four Spanish hospitals. Consecutive H. pylori-infected individuals treated with Pylera® and a proton-pump inhibitor (PPI) were invited to participate if they had failed to respond to PPI-clarithromycin-amoxicillin as first-line and to levofloxacin-amoxicillin-PPI as second-line therapy. Eradication was tested 4-8 weeks after Pylera® using a C13 -urea breath test. Treatment-related adverse effects (TRAEs) were assessed through a questionnaire and by reviewing databases. A questionnaire on patient satisfaction was completed in the last visit. RESULTS: Of 103 subjects fulfilling the selection criteria, 101 were included in the intention-to-treat (ITT) analysis and 97 in the per-protocol (PP) analysis. A 10 day course was prescribed in all patients. Esomeprazole 40 mg b.i.d. was the most used PPI regimen (ITT=94.1%). Ninety-seven individuals (ITT=96.04%) completed more than 90% of the treatment. Overall eradication rates were ITT=80.2% (95% confidence interval [CI]: 72.3%-88.1%) and PP=84.4% (95% CI: 76.8%-91.8%). One or more TRAEs were experienced by 67.3% (95% CI: 57.7%-75.7%), all mild or moderate. TRAEs and the number of pills were the main complaints. CONCLUSION: In an area of high antibiotic resistance to H. pylori, 10-day Pylera® plus double-dose PPI emerged as an alternative as third-line therapy, although not achieving optimal eradication rates. TRAEs were common but were neither severe nor did they condition compliance.


Subject(s)
Anti-Infective Agents/administration & dosage , Bismuth/administration & dosage , Helicobacter Infections/drug therapy , Helicobacter pylori/isolation & purification , Salvage Therapy/methods , Adult , Aged , Aged, 80 and over , Breath Tests , Drug Therapy, Combination/methods , Female , Hospitals , Humans , Male , Middle Aged , Patient Satisfaction , Prospective Studies , Proton Pump Inhibitors/administration & dosage , Spain , Surveys and Questionnaires , Treatment Outcome , Urea/analysis , Young Adult
6.
Rev Esp Enferm Dig ; 108(4): 207-24, 2016 Apr.
Article in English | MEDLINE | ID: mdl-27034082

ABSTRACT

INTRODUCTION: In the last few years a significant number of papers have related the use of proton-pump inhibitors (PPIs) to potential serious adverse effects that have resulted in social unrest. OBJECTIVE: The goal of this paper was to provide a literature review for the development of an institutional position statement by Sociedad Española de Patología Digestiva (SEPD) regarding the safety of long-term PPI use. MATERIAL AND METHODS: A comprehensive review of the literature was performed to draw conclusions based on a critical assessment of the following: a) current PPI indications; b) vitamin B12 deficiency and neurological disorders; c) magnesium deficiency; d) bone fractures; e) enteric infection and pneumonia; f) interactions with thienopyridine derivatives; e) complications in cirrhotic patients. RESULTS: Current PPI indications have remained unchanged for years now, and are well established. A general screening of vitamin B12 levels is not recommended for all patients on a PPI; however, it does seem necessary that magnesium levels be measured at therapy onset, and then monitored in subjects on other drugs that may induce hypomagnesemia. A higher risk for bone fractures is present, even though causality cannot be concluded for this association. The association between PPIs and infection with Clostridium difficile is mild to moderate, and the risk for pneumonia is low. In patients with cardiovascular risk receiving thienopyridines derivatives it is prudent to adequately consider gastrointestinal and cardiovascular risks, given the absence of definitive evidence regardin potential drug-drug interactions; if gastrointestinal risk is found to be moderate or high, effective prevention should be in place with a PPI. PPIs should be cautiously indicated in patients with decompensated cirrhosis. CONCLUSIONS: PPIs are safe drugs whose benefits outweigh their potential side effects both short-term and long-term, provided their indication, dosage, and duration are appropriate.


Subject(s)
Proton Pump Inhibitors/adverse effects , Drug Interactions , Evidence-Based Medicine , Fractures, Bone/epidemiology , Fractures, Bone/etiology , Humans , Infections/epidemiology , Liver Cirrhosis/complications , Magnesium Deficiency/chemically induced , Magnesium Deficiency/epidemiology , Nervous System Diseases/chemically induced , Nervous System Diseases/epidemiology , Proton Pump Inhibitors/administration & dosage , Proton Pump Inhibitors/therapeutic use
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