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1.
Ann Allergy Asthma Immunol ; 108(6): 435-8, 2012 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-22626597

RESUMEN

BACKGROUND: Ectodermal dysplasia (ED) syndromes are a diverse group of disorders that affect multiple ectodermally derived tissues. Small studies and case reports suggest an increase in atopy and primary immunodeficiencies (PIDs) among patients with ED syndromes. OBJECTIVE: To determine the prevalence of clinical symptoms suggestive of atopy or immunodeficiency among a large cohort of children with ED syndromes. METHODS: A 9-page questionnaire was mailed to families who were members of the National Foundation for Ectodermal Dysplasias. The surveys were completed by parents of children younger than 18 years with a diagnosis of an ED syndrome or carrier state. Portions of the questionnaire were adapted from previously validated questionnaires developed by the International Study of Asthma and Allergies in Childhood (ISAAC). RESULTS: We received 347 completed questionnaires (41%). When compared with the 13- to 14-year-old children surveyed by ISAAC, we found both all-aged and age-matched children with ED syndromes, respectively, had significantly higher rates of asthma (32.2% and 37.2% vs 16.4%), rhinitis symptoms (76.1% and 78.3% vs 38.9%), and eczema (58.9% and 48.9% vs 8.2%). The prevalence of physician-diagnosed food allergies (20.7%) and PIDs (6.1%) in these ED patients also exceeded known rates in the general pediatric population. CONCLUSION: This large-scale, retrospective study demonstrates a greater reported prevalence of symptoms suggestive of atopic disorders and PIDs among children with ED syndromes than the general pediatric population. A combination of genetic and environmental factors in ED syndromes may contribute to breaches of skin and mucosal barriers, permitting enhanced transmission and sensitization to irritants, allergens, and pathogens.


Asunto(s)
Displasia Ectodérmica/epidemiología , Hipersensibilidad Inmediata/epidemiología , Síndromes de Inmunodeficiencia/epidemiología , Adolescente , Alérgenos/inmunología , Asma/complicaciones , Asma/epidemiología , Asma/inmunología , Niño , Preescolar , Estudios de Cohortes , Dermatitis Atópica/complicaciones , Dermatitis Atópica/epidemiología , Dermatitis Atópica/inmunología , Displasia Ectodérmica/complicaciones , Displasia Ectodérmica/inmunología , Eccema/complicaciones , Eccema/epidemiología , Eccema/inmunología , Femenino , Hipersensibilidad a los Alimentos/complicaciones , Hipersensibilidad a los Alimentos/epidemiología , Hipersensibilidad a los Alimentos/inmunología , Humanos , Hipersensibilidad Inmediata/complicaciones , Hipersensibilidad Inmediata/inmunología , Síndromes de Inmunodeficiencia/complicaciones , Síndromes de Inmunodeficiencia/inmunología , Masculino , Membrana Mucosa/inmunología , Prevalencia , Estudios Retrospectivos , Rinitis/complicaciones , Rinitis/epidemiología , Rinitis/inmunología , Piel/inmunología , Encuestas y Cuestionarios , Estados Unidos/epidemiología
2.
Biomed Instrum Technol ; 46(3): 230-7, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22591538

RESUMEN

It is commonly accepted that terminally sterilized healthcare products are rarely the source of a hospital-acquired infection (HAI). The vast majority of HAIs arise from human-borne contamination from the workforce, the clinical environment, less-than-aseptic handling techniques, and the patients themselves. Nonetheless, the requirement for a maximal sterility assurance level (SAL) of a terminally sterilized product has remained at 10(-6), which is the probability of one in one million that a single viable microorganism will be on a product after sterilization. This paper presents a probabilistic model that predicts choosing an SAL greater than 10(-6) (e.g. 10(-5) or 10(-4), and in some examples even 10(-3) or 10(-2)) does not have a statistically significant impact on the incidence of surgical site infections (SSIs). The use of a greater SAL might allow new, potentially life-saving products that cannot withstand sterilization to achieve a 10(-6) SAL to be terminally sterilized instead of being aseptically manufactured.


Asunto(s)
Infecciones Bacterianas/epidemiología , Infecciones Bacterianas/prevención & control , Infección Hospitalaria/epidemiología , Infección Hospitalaria/prevención & control , Equipos y Suministros/microbiología , Esterilización/estadística & datos numéricos , Infección de la Herida Quirúrgica/epidemiología , Simulación por Computador , Humanos , Modelos Estadísticos , Prevalencia , Medición de Riesgo , Factores de Riesgo , Infección de la Herida Quirúrgica/prevención & control , Estados Unidos/epidemiología
3.
J Heart Lung Transplant ; 25(5): 518-22, 2006 May.
Artículo en Inglés | MEDLINE | ID: mdl-16678029

RESUMEN

BACKGROUND: Calcineurin inhibitors such as cyclosporine are effective in preventing rejection in recipients of solid organ transplants. Unfortunately, the prolonged use of calcineurin inhibitors may result in progressive renal injury. METHODS: We studied the renal function of 15 pediatric heart transplant recipients who were taking calcineurin inhibitors. Their renal function was studied before and after rapamycin was introduced to their immunosuppression regimen. With the introduction of rapamycin, the patients were given a lower dose of calcineurin inhibitors, and the calcineurin inhibitor was discontinued in 5 patients. RESULTS: Renal function improved significantly in the patients by 30 days after these changes in the calcineurin inhibitor dose were instituted. Mean levels of blood urea nitrogen and mean serum creatinine decreased, and mean creatinine clearance increased. Pre-rapamycin, the patients' mean level of blood urea nitrogen was 27.1 +/- 12.4 mg/dl and post-rapamycin they decreased to 18.6 +/- 11.1 mg/dl (p = 0.014). Similarly, creatinine decreased from 1.0 +/- 0.5 mg/dl to 0.8 +/- 0.3 mg/dl (p = 0.019). Their creatinine clearance increased from 88 +/- 28 ml/min/1.73 mol/liter2 to 105 +/- 27 ml/min/1.73 mol/liter2 (p = 0.008). The patients' lipid levels did not change after they were prescribed rapamycin. Biopsy-negative rejection developed in 2 patients. CONCLUSIONS: The introduction of rapamycin to the immunosuppressive regimen of patients taking calcineurin inhibitors, with a concomitant reduction of the calcineurin inhibitor dose, may improve renal function within 30 days, without a significant increase in rejection.


Asunto(s)
Inhibidores de la Calcineurina , Ciclosporina/administración & dosificación , Trasplante de Corazón , Inmunosupresores/uso terapéutico , Riñón/efectos de los fármacos , Sirolimus/uso terapéutico , Tacrolimus/administración & dosificación , Nitrógeno de la Urea Sanguínea , Niño , Preescolar , Creatinina/sangre , Ciclosporina/uso terapéutico , Quimioterapia Combinada , Femenino , Trasplante de Corazón/inmunología , Humanos , Inmunosupresores/administración & dosificación , Inmunosupresores/farmacología , Lactante , Pruebas de Función Renal , Masculino , Recuento de Plaquetas , Estudios Retrospectivos , Sirolimus/farmacología , Tacrolimus/uso terapéutico
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