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1.
United European Gastroenterol J ; 12(3): 286-298, 2024 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-38376888

RESUMEN

BACKGROUND: Delayed cholecystectomy in patients with symptomatic gallstone disease is associated with recurrence. Limited data on the recurrence patterns and the factors that determine them are available. OBJECTIVE: We aimed to determine the pattern of relapse in each symptomatic gallstone disease (acute pancreatitis, cholecystitis, cholangitis, symptomatic choledocholithiasis, and biliary colic) and determine the associated factors. METHODS: RELAPSTONE was an international multicenter retrospective cohort study. Patients (n = 3016) from 18 tertiary centers who suffered a first episode of symptomatic gallstone disease from 2018 to 2020 and had not undergone cholecystectomy during admission were included. The main outcome was relapse-free survival. Kaplan-Meier curves were used in the bivariate analysis. Multivariable Cox regression models were used to identify prognostic factors associated with relapses. RESULTS: Mean age was 76.6 [IQR: 59.7-84.1], and 51% were male. The median follow-up was 5.3 months [IQR 2.1-12.4]. Relapse-free survival was 0.79 (95% CI: 0.77-0.80) at 3 months, 0.71 (95% CI: 0.69-0.73) at 6 months, and 0.63 (95% CI: 0.61-0.65) at 12 months. In multivariable analysis, older age (HR = 0.57; 95% CI: 0.49-0.66), sphincterotomy (HR = 0.58, 95% CI: 0.49-0.68) and higher leukocyte count (HR = 0.79; 95% CI: 0.70-0.90) were independently associated with lower risk of relapse, whereas higher levels of alanine aminotransferase (HR = 1.22; 95% CI: 1.02-1.46) and multiple cholelithiasis (HR = 1.19, 95% CI: 1.05-1.34) were associated with higher relapse rates. CONCLUSION: The relapse rate is high and different in each symptomatic gallstone disease. Our independent predictors could be useful for prioritizing patients on the waiting list for cholecystectomies.


Asunto(s)
Coledocolitiasis , Pancreatitis , Humanos , Masculino , Anciano , Femenino , Estudios Retrospectivos , Enfermedad Aguda , Pancreatitis/etiología , Factores de Riesgo , Coledocolitiasis/diagnóstico , Coledocolitiasis/epidemiología , Coledocolitiasis/cirugía , Recurrencia
3.
Gastroenterol Hepatol ; 44(10): 671-679, 2021 Dec.
Artículo en Inglés, Español | MEDLINE | ID: mdl-33248178

RESUMEN

OBJECTIVE: To study the epidemiological and clinical characteristics, and response to treatment in patients with microscopic colitis. PATIENTS AND METHOD: Epidemiological, clinical, blood test and endoscopic data were retrospectively collected from 113 patients with microscopic colitis. Response to treatment was analyzed in 104 of them. Efficacy and relapse after treatment with budesonide were assessed using survival curves (Kaplan-Meier). RESULTS: 78% of the patients were women, with a mean age of 65 ± 16 years. In smokers, the mean age was 10 years younger. 48% of them had some concomitant autoimmune disease; 60% suffered a single outbreak of the disease. The clinical presentation was similar in both subtypes, although patients with collagenous colitis had a chronic course more frequently (48% vs. 29%, p = 0.047). The remission rate with budesonide was 93% (95% CI 82-98). The cumulative incidence of relapse, after a median follow-up of 21 months, was 39% (95% CI 26-54%): 19% at one year, 32% at two years, and 46% at three years of follow-up. There were no differences in clinical response to budesonide based on smoking habit or microscopic colitis subtype. CONCLUSIONS: Microscopic colitis is more frequent in elderly women. Smoking was associated with earlier onset of the disease, although it did not influence the clinical course or response to treatment. The majority (> 90%) of patients treated with budesonide achieved remission, although nearly half subsequently relapsed.


Asunto(s)
Colitis Microscópica , Adulto , Anciano , Antiinflamatorios/uso terapéutico , Budesonida/uso terapéutico , Colitis Colagenosa/complicaciones , Colitis Colagenosa/tratamiento farmacológico , Colitis Colagenosa/epidemiología , Colitis Colagenosa/mortalidad , Colitis Linfocítica/complicaciones , Colitis Linfocítica/tratamiento farmacológico , Colitis Linfocítica/epidemiología , Colitis Linfocítica/mortalidad , Colitis Microscópica/complicaciones , Colitis Microscópica/tratamiento farmacológico , Colitis Microscópica/epidemiología , Colitis Microscópica/mortalidad , Colonoscopía , Ex-Fumadores , Femenino , Humanos , Incidencia , Estimación de Kaplan-Meier , Masculino , Persona de Mediana Edad , Recurrencia , Estudios Retrospectivos , Fumadores , Fumar/efectos adversos , Resultado del Tratamiento
4.
Rev Esp Enferm Dig ; 112(1): 53-58, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31880163

RESUMEN

Microscopic colitis is a common cause of chronic watery diarrhea with a great impact on patient quality of life. Microscopic colitis includes two histological subtypes: collagenous colitis and lymphocytic colitis. Due to the increasing incidence and awareness of this disease over the last decades, several international guidelines have been recently published. However, there is still significant heterogeneity in the management of these patients, and treatments without solid scientific evidence support are often used in clinical practice. This article reviews the therapeutic role of budesonide in microscopic colitis and summarizes the current evidence regarding other treatments available for this disease, especially for the management of refractory patients. Finally, an updated treatment algorithm is proposed.


Asunto(s)
Antiinflamatorios/uso terapéutico , Budesonida/uso terapéutico , Colitis Colagenosa/tratamiento farmacológico , Colitis Linfocítica/tratamiento farmacológico , Corticoesteroides/uso terapéutico , Antiinflamatorios/efectos adversos , Antiinflamatorios/metabolismo , Antidiarreicos/uso terapéutico , Antimetabolitos/uso terapéutico , Azatioprina/uso terapéutico , Productos Biológicos/efectos adversos , Productos Biológicos/uso terapéutico , Budesonida/efectos adversos , Budesonida/metabolismo , Colitis Colagenosa/patología , Colitis Linfocítica/patología , Colitis Microscópica/tratamiento farmacológico , Colitis Microscópica/patología , Diarrea/etiología , Humanos , Loperamida/uso terapéutico , Síndromes de Malabsorción/tratamiento farmacológico , Mesalamina/uso terapéutico , Metotrexato/uso terapéutico , Prednisolona/uso terapéutico , Calidad de Vida , Ensayos Clínicos Controlados Aleatorios como Asunto , Recurrencia , Inducción de Remisión , Factores de Tiempo
5.
Sci Rep ; 9(1): 9264, 2019 06 25.
Artículo en Inglés | MEDLINE | ID: mdl-31239457

RESUMEN

Current HCV genotyping methods may have some limitations in detecting mixed infections. We aimed to determine the accuracy of genotyping and the detection of mixed-genotype infections using the Abbott-RealTime HCV Genotype II assay (Abbott-RT-PCR) in comparison with a Roche-Next Generation Sequencing assay (Roche-NGS). Plasma samples collected from 139 HCV-infected patients tested with Abbott-RT-PCR, 114 with single genotype (GT) and 25 with mixed GTs were genotyped using Roche-NGS. Roche-NGS confirmed all single GTs obtained with Abbott-RT-PCR. One case of Abbott GT 4 was found as GT 1a using Roche-NGS. Genotype 5 was confirmed using Roche-NGS in 75% cases (3 out of 4 cases). Twenty-five patients were identified as having mixed HCVinfections using Abbott-RT-PCR. The concordance between Abbott-RT-PCR and Roche-NGS was 76% (19 out of 25 cases). Three mixed-GT infections identified with the Abbott assay (two (1b + 4); one (1a + 3)) were reported as pure 1b using Roche-NGS. Very divergent results were found for the other three samples. When compared to Roche-NGS, Abbott-RT-PCR has performed excellently for the determination of patients infected with single GTs. For patients that are categorized as having a mixed infection using Abbott-RT-PCR, we recommend an NGS assay as a confirmation test.


Asunto(s)
Hepacivirus/clasificación , Hepacivirus/genética , Hepatitis C/diagnóstico , Secuenciación de Nucleótidos de Alto Rendimiento/métodos , Proteínas no Estructurales Virales/genética , Adulto , Anciano , Anciano de 80 o más Años , Estudios de Cohortes , Femenino , Genotipo , Técnicas de Genotipaje , Hepacivirus/aislamiento & purificación , Hepatitis C/virología , Humanos , Masculino , Persona de Mediana Edad , Reacción en Cadena en Tiempo Real de la Polimerasa
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