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1.
J Pediatr ; 228: 155-163.e1, 2021 01.
Artículo en Inglés | MEDLINE | ID: mdl-32918920

RESUMEN

OBJECTIVE: To analyze the findings of both multichannel intraluminal impedance with pH (MII-pH) and endoscopy/histopathology in children with esophageal atresia at age 1 year, according to current recommendations for the evaluation of gastroesophageal reflux disease (GERD) in esophageal atresia. STUDY DESIGN: We retrospectively reviewed both MII-pH and endoscopy/histopathology performed in 1-year-old children with esophageal atresia who were followed up in accordance with international recommendations. Demographic data and clinical characteristics were also reviewed to investigate factors associated with abnormal GERD investigations. RESULTS: In our study cohort of 48 children with esophageal atresia, microscopic esophagitis was found in 33 (69%) and pathological esophageal acid exposure on MII-pH was detected in 12 (25%). Among baseline variables, only the presence of long-gap esophageal atresia was associated with abnormal MII-pH. Distal baseline impedance was significantly lower in patients with microscopic esophagitis, and it showed a very good diagnostic performance in predicting histological changes. CONCLUSIONS: Histological esophagitis is highly prevalent at 1 year after esophageal atresia repair, but our results do not support a definitive causative role of acid-induced GERD. Instead, they support the hypothesis that chronic stasis in the dysmotile esophagus might lead to histological changes. MII-pH may be a helpful tool in selecting patients who need closer endoscopic surveillance and/or benefit from acid suppression.


Asunto(s)
Atresia Esofágica/cirugía , Esofagoplastia/efectos adversos , Esófago/fisiopatología , Reflujo Gastroesofágico/diagnóstico , Complicaciones Posoperatorias , Adolescente , Niño , Impedancia Eléctrica , Endoscopía Gastrointestinal , Monitorización del pH Esofágico/métodos , Esófago/metabolismo , Femenino , Estudios de Seguimiento , Reflujo Gastroesofágico/etiología , Reflujo Gastroesofágico/fisiopatología , Humanos , Masculino , Manometría , Estudios Retrospectivos , Factores de Tiempo
2.
Int J Rheum Dis ; 21(11): 2019-2027, 2018 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-29611343

RESUMEN

OBJECTIVE: To study the prevalence and the associated factors of work disability (WD) in systemic lupus erythematosus (SLE) patients. METHODS: A sample of 419 SLE patients from an observational cross-sectional multicenter study was included. Sociodemographic features, disease characteristics, comorbidities, quality of life, unhealthy behaviors, and work-related factors were measured in a standardized interview. Work disability was defined by patient self-report of not being able to work because of SLE. To identify variables associated with work disability, two different multivariate regression models using a stepwise backward method were performed. RESULTS: Prevalence of WD due to SLE was 24.3%. Eighty-nine percent were female and 51% were Caucasians. Mean disease duration was 8.9 ± 7.2 years, and median System Lupus International Collaborating Clinics/American College of Rheumatology damage index SLICC-SDI was 1.5 (range 0-17). In stepwise multivariate logistic regression, living below the poverty line (odds ratio [OR] = 4.65), less than 12 years of education (OR = 2.84), Mestizo ethnicity (OR = 1.94) and SLICC-SDI (OR = 1.25) were predictors of WD. A second model was performed including patient-derived measures; in this model sedentary lifestyle (OR = 2.69) and lower emotional health domain score of the Lupus Quality of Life (LupusQoL) questionnaire (OR = 1.03) were found to be associated to WD and a higher score in LupusQoL physical health domain (OR = 0.93) was protective. CONCLUSION: The prevalence of WD in Argentinian SLE patients was 24.3%. WD was associated with ethnic (Mestizo), socioeconomic (poverty) and disease-related factors. Patient-related outcomes such us sedentary lifestyle and poor emotional quality of life were also associated with WD.


Asunto(s)
Absentismo , Evaluación de la Discapacidad , Indígenas Sudamericanos , Lupus Eritematoso Sistémico/etnología , Ausencia por Enfermedad , Determinantes Sociales de la Salud , Factores Socioeconómicos , Adulto , Argentina/epidemiología , Estudios Transversales , Emociones , Femenino , Estado de Salud , Humanos , Lupus Eritematoso Sistémico/diagnóstico , Lupus Eritematoso Sistémico/psicología , Lupus Eritematoso Sistémico/terapia , Masculino , Salud Mental , Persona de Mediana Edad , Pobreza , Prevalencia , Calidad de Vida , Factores de Riesgo , Conducta Sedentaria , Adulto Joven
3.
Bone ; 50(1): 9-13, 2012 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21920487

RESUMEN

Yerba Mate (Ilex paraguariensis) tea consumption is higher in Argentina and other South American countries than those of coffee or tea (Camellia sinensis). The effects of Yerba Mate on bone health have not previously been explored. From a program for osteoporosis prevention and treatment, postmenopausal women who drank at least 1 L of Yerba Mate tea daily during 4 or more years (n=146) were identified, and matched by age and time since menopause with an equal number of women who did not drink Yerba Mate tea. Their bone mineral density (BMD) was measured by dual-energy X-ray absorptiometry (DXA) at the lumbar spine and femoral neck. Yerba Mate drinkers had a 9.7% higher lumbar spine BMD (0.952 g/cm(2) versus 0.858 g/cm(2): p<0.0001) and a 6.2% higher femoral neck BMD (0.817 g/cm(2) versus 0.776 g/cm(2); p=0.0002). In multiple regression analysis, Yerba Mate drinking was the only factor, other than body mass index, which showed a positive correlation with BMD at both the lumbar spine (p<0.0001) and the femoral neck (p=0.0028). Results suggest a protective effect of chronic Yerba Mate consumption on bone.


Asunto(s)
Densidad Ósea/efectos de los fármacos , Ilex paraguariensis/química , Osteoporosis Posmenopáusica/terapia , Fitoterapia , Preparaciones de Plantas/farmacología , Preparaciones de Plantas/uso terapéutico , Té/química , Absorciometría de Fotón/métodos , Índice de Masa Corporal , Estudios Transversales , Femenino , Cuello Femoral/anatomía & histología , Humanos , Vértebras Lumbares/anatomía & histología , Osteoporosis Posmenopáusica/prevención & control , Estudios Retrospectivos
4.
J Pediatr ; 158(6): 973-6, 2011 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-21238988

RESUMEN

OBJECTIVES: To describe the prevalence and pathogenesis of symptomatic vocal cord paresis/paralysis (VCP) in patients treated for esophageal atresia (EA), tracheo-esophageal fistula (TEF) or both. STUDY DESIGN: Retrospective study of all patients treated for EA/TEF in our center (1995 to 2009). Patients with and without symptomatic VCP were compared for gestational age, birth weight, associated anomalies, referrals, long-gap EA (> 3 cm or 3 vertebral bodies), cervical esophagostomy, anastomotic leakage, length of ventilation, and major cardiac surgery. Prevalence or median (IQR) is reported. RESULTS: Of 174 patients, 7 (4%) had symptomatic VCP. Prevalence of referrals (5/7 versus 21/167; P = .0009), long gap (5/7 versus 41/167; P = .0146), previous cervical esophagostomy (5/7 versus 7/167; P < .0001), and anastomotic leakage (3/7 versus 10/167; P = .0097) was higher, and ventilation longer (8.5 days [7.0 to 15.5] versus 6.0 days (5.0 to 7.0); P = .0072) in patients with VCP. CONCLUSIONS: In infants treated for EA/TEF, VCP should be ruled out in case of persistent respiratory morbidity or, when present, cautiously monitored. Surgical risk factors should be actively controlled. Further studies are needed to define the prevalence of acquired and congenital VCP in patients with EA/TEF.


Asunto(s)
Atresia Esofágica/complicaciones , Atresia Esofágica/cirugía , Parálisis/etiología , Fístula Traqueoesofágica/complicaciones , Fístula Traqueoesofágica/cirugía , Parálisis de los Pliegues Vocales/etiología , Fuga Anastomótica , Estudios de Cohortes , Edad Gestacional , Humanos , Lactante , Recién Nacido , Parálisis/diagnóstico , Prevalencia , Estudios Retrospectivos , Factores de Riesgo , Resultado del Tratamiento , Parálisis de los Pliegues Vocales/diagnóstico , Pliegues Vocales/patología
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