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1.
Arq Gastroenterol ; 60(3): 309-314, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37792759

RESUMEN

WHAT IS ALREADY KNOWN: •The rate and severity of Clostridioides difficile infection (CDI) has increased throughout North America, the United Kingdom, and Europe. •Scattered evidence about the association of CDI with antidepressant medications use exists in the literature so far. What are the new findings: •The risk of Clostridioides difficile infection is higher in patients who are on mirtazapine, nortriptyline, or trazodone. •The prevalence rate of Clostridioides difficile infection in patients who were using antidepressant medications and the ones who did not, increased with age. Background - During the past decade, Clostridioides difficile infection (CDI) has become the most common cause of antibiotic-associated diarrhea. Several risk factors have been implicated. Scattered evidence about the association of CDI with antidepressant medications use exists in the literature so far. Therefore, we aim to investigate whether the risk of developing CDI is increased in hospitalized patients using antidepressant medications.Methods - Patients who were hospitalized were included in our cohort. We excluded individuals aged less than 18 years. A multivariate regression analysis was performed to calculate the risk of CDI accounting for potential confounders. Results - The risk of CDI in hospitalized patients was increased in individuals diagnosed with inflammatory bowel disease (OR: 4.44; 95%CI: 4.35-4.52), and in patients using clindamycin (OR: 1.55; 95%CI: 1.53-1.57), beta-lactam antibiotics (OR: 1.62; 95%CI: 1.60-1.64), PPI (OR: 3.27; 95%CI: 3.23-3.30), trazodone (OR: 1.31; 95%CI: 1.29-1.33), nortriptyline (OR: 1.25; 95%CI: 1.21-1.28), and mirtazapine (OR: 2.50; 95%CI: 2.46-2.54). After controlling for covariates, the risk of CDI was not increased in patients who were taking fluoxetine (OR: 0.94; 95%CI: 0.92-0.96). Conclusion - In contrary to fluoxetine; mirtazapine, nortriptyline, and trazodone were associated with increased risk of CDI in hospitalized patients.


Asunto(s)
Clostridioides difficile , Infecciones por Clostridium , Trazodona , Humanos , Mirtazapina/uso terapéutico , Trazodona/uso terapéutico , Nortriptilina/efectos adversos , Fluoxetina/uso terapéutico , Infecciones por Clostridium/inducido químicamente , Infecciones por Clostridium/epidemiología , Antidepresivos/efectos adversos , Hospitales
2.
Rev Paul Pediatr ; 41: e2022117, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-36921180

RESUMEN

OBJECTIVE: The aim of this study was to analyze and identify documented infections and possible risk factors for Clostridioides difficile infections in children with cancer. METHODS: This is a retrospective case-control study, carried out in a pediatric cancer hospital, covering the years 2016-2019. Matching was performed by age and underlying disease, and for each case, the number of controls varied from 1 to 3. Logistic regression models were used to assess risk factors. RESULTS: We analyzed 63 cases of documented infection by C. difficile and 125 controls. Diarrhea was present in all cases, accompanied by fever higher than 38°C in 52.4% of the patients. Mortality was similar among cases (n=4; 6.3%) and controls (n=6; 4.8%; p=0.7). In all, 71% of patients in the case group and 53% in the control group received broad-spectrum antibiotics prior to the infection. For previous use of vancomycin, the Odds Ratio for C. difficile infection was 5.4 (95% confidence interval [95%CI] 2.3-12.5); for meropenem, 4.41 (95%CI 2.1-9.2); and for cefepime, 2.6 (95%CI 1.3-5.1). For the antineoplastic agents, the Odds Ratio for carboplatin was 2.7 (95%CI 1.2-6.2), melphalan 9.04 (95%CI 1.9-42.3), busulfan 16.7 (95%CI 2.1-134.9), and asparaginase 8.97 (95%CI 1.9-42.9). CONCLUSIONS: C. difficile symptomatic infection in children with cancer was associated with previous hospitalization and the use of common antibiotics in cancer patients, such as vancomycin, meropenem, and cefepime, in the last 3 months. Chemotherapy drugs, such as carboplatin, melphalan, busulfan, and asparaginase, were also risk factors.


Asunto(s)
Clostridioides difficile , Infecciones por Clostridium , Infección Hospitalaria , Neoplasias , Humanos , Niño , Estudios de Casos y Controles , Estudios Retrospectivos , Vancomicina , Cefepima/uso terapéutico , Meropenem , Busulfano/uso terapéutico , Melfalán/uso terapéutico , Asparaginasa/uso terapéutico , Instituciones Oncológicas , Carboplatino/uso terapéutico , Infección Hospitalaria/epidemiología , Infección Hospitalaria/inducido químicamente , Infección Hospitalaria/tratamiento farmacológico , Antibacterianos/uso terapéutico , Infecciones por Clostridium/epidemiología , Infecciones por Clostridium/inducido químicamente , Infecciones por Clostridium/tratamiento farmacológico , Neoplasias/complicaciones , Factores de Riesgo
3.
J Pediatr ; 165(5): 979-84.e1, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25112692

RESUMEN

OBJECTIVE: Multiple studies have confirmed associations between acid suppression medication and Clostridium difficile infections (CDIs) in adults. Therefore, we sought to evaluate an association between acid suppression medications and CDI in children. STUDY DESIGN: A retrospective self-controlled case series was performed utilizing billing records from the TRICARE Management Activity military health system database. Children ages 2-18 years from October 1, 2001 to July 31, 2013, who had an outpatient or inpatient record of CDI diagnosis were included. The relative incidences (RIs) of CDI or recurrent CDI were calculated comparing time periods prescribed and not prescribed proton pump inhibitors (PPIs) or histamine-2 receptor antagonists (H2RAs). RESULTS: There were 2531 cases of CDI among 2437 patients, and 1190 (48.8%) were prescribed acid suppression medications. CDI were more likely to occur during periods when patients were prescribed a PPI (RI 2.36; 95% CI 2.22-2.52), H2RA (RI 1.95; 95% CI 1.63-2.34), or during periods while prescribed both simultaneously (RI 2.40; 95% CI 1.90-3.04). There were 265 (10.4%) cases that were classified as recurrent among 217 (8.9%) patients. Recurrent CDI also was found to be more likely during prescription periods of PPI (RI 1.74; 95% CI 1.51-2.00) and H2RA (RI 2.63; 95% CI 1.89-3.66). CONCLUSIONS: Acid suppression medications are associated with an increased risk of CDI and recurrent CDI. Judicious use of acid suppression medication should be considered, especially among those at highest risk for CDI.


Asunto(s)
Antiácidos/efectos adversos , Clostridioides difficile , Infecciones por Clostridium/inducido químicamente , Enfermedades Gastrointestinales/inducido químicamente , Antagonistas de los Receptores H2 de la Histamina/efectos adversos , Inhibidores de la Bomba de Protones/efectos adversos , Adolescente , Niño , Preescolar , Infecciones por Clostridium/epidemiología , Infecciones por Clostridium/microbiología , Femenino , Enfermedades Gastrointestinales/epidemiología , Enfermedades Gastrointestinales/microbiología , Humanos , Incidencia , Masculino , Estudios Retrospectivos , Factores de Riesgo
6.
Travel Med Infect Dis ; 9(5): 243-5, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21767993

RESUMEN

Malaria chemoprophylaxis with doxycycline is commonly used in the United Kingdom and in many other countries. It is considered to be associated with an increased risk of Clostridium difficile associated diarrhea (CDAD). We describe a case of diarrhea and a positive stool assay for C. difficile in a returning traveler, and review available literature. The commonly held concept of an association between doxycycline chemoprophylaxis and CDAD is not supported by available data.


Asunto(s)
Antimaláricos/efectos adversos , Clostridioides difficile/aislamiento & purificación , Infecciones por Clostridium/inducido químicamente , Infecciones por Clostridium/parasitología , Doxiciclina/efectos adversos , Malaria/microbiología , Adulto , Albendazol/uso terapéutico , Profilaxis Antibiótica , Antimaláricos/uso terapéutico , Brasil , Chile , Enfermedad Crónica , Doxiciclina/uso terapéutico , Femenino , Humanos , Malaria/tratamiento farmacológico , Malaria/prevención & control , Viaje
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