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1.
J Pediatr ; 245: 246-249, 2022 06.
Artículo en Inglés | MEDLINE | ID: mdl-35718377
2.
J Allergy Clin Immunol Pract ; 9(10): 3662-3671.e1, 2021 10.
Artículo en Inglés | MEDLINE | ID: mdl-34148858

RESUMEN

BACKGROUND: U.S. guidelines recommend that patients with severe asthma be referred to specialists (allergists/immunologists or pulmonologists) for systematic assessment or comanagement; however, contemporary, real-world data on the frequency and impact of specialist care among U.S. severe asthma patients are lacking. OBJECTIVES: To quantify the frequency of asthma specialist visits among U.S. patients with severe asthma, identify patient demographic and clinical characteristics associated with specialist visits and describe health outcomes following specialist care. METHODS: Severe asthma patients aged 6 years or older were identified between January 1, 2015, and December 31, 2017, in the IQVIA PharMetrics® Plus database of commercially insured individuals, based on Healthcare Effectiveness Data and Information Set (HEDIS) criteria and Global Initiative for Asthma (GINA) step 4 or 5 treatment regimens. The frequency of asthma specialist (allergist/immunologist or pulmonologist) visits was described over 2 years. Patient characteristics associated with having 1 or more specialist visits were analyzed using multivariate regressions. Asthma exacerbations and health care resource utilization before and after specialist visit were compared. RESULTS: Of 54,332 patients identified, 38.2% had 1 or more specialist visits over 2 years. Patient characteristics predictive of specialist visits were asthma exacerbation frequency, younger age, and allergy/respiratory comorbidity burden (all P < .001). Among patients with 1 or more specialist visits, a lower prevalence of asthma exacerbations and rescue inhaler use was observed following the first observed specialist visit. CONCLUSIONS: Specialist care was observed in fewer than half of U.S. patients with severe asthma and was least frequent among older adult patients and those with more nonrespiratory comorbidities. Increased specialist involvement in managing severe asthma may help improve care and patient outcomes.


Asunto(s)
Asma , Anciano , Asma/epidemiología , Asma/terapia , Bases de Datos Factuales , Atención a la Salud , Humanos , Nebulizadores y Vaporizadores , Aceptación de la Atención de Salud
3.
Braz J Med Biol Res ; 51(7): e7372, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29846410

RESUMEN

The effect of bisacodyl on the treatment of rats with slow transit constipation (STC) was studied. Forty-five female Wister rats were divided into control group, STC group, and STC bisacodyl group. The immunohistochemical method was used to determine interstitial cells of Cajal (ICC) and the expression of c-Kit protein. Body mass and the number of defecations were significantly decreased in the STC group compared with the control group on the 100th day after diphenoxylate administration, while dry weight of feces was significantly increased and the intestinal transit time was prolonged. There were significant differences in the number of defecations, dry weight of feces, and intestinal transit time among the three groups. The number of defecations was higher, dry weight of feces was lower, and intestinal transit time was shorter in the STC bisacodyl group compared to the STC group. In addition, ICC basement membrane dissolution occurred in the colon wall of the STC group. The connection between ICC and surrounding cells was destroyed, and the nucleus shrunken to different degrees. Moreover, c-Kit expression in the STC group was significantly lower than the control group. The connection between ICC and surrounding cells in the STC bisacodyl group was significantly stronger than the STC group, and the number of ICC and the expression of c-Kit were increased. Bisacodyl could reduce the severity of STC in rats by increasing the number of ICC and the expression of c-Kit.


Asunto(s)
Bisacodilo/uso terapéutico , Catárticos/uso terapéutico , Colon/metabolismo , Estreñimiento/tratamiento farmacológico , Tránsito Gastrointestinal/efectos de los fármacos , Células Intersticiales de Cajal/efectos de los fármacos , Proteínas Proto-Oncogénicas c-kit/metabolismo , Animales , Colon/efectos de los fármacos , Colon/patología , Estreñimiento/metabolismo , Estreñimiento/fisiopatología , Femenino , Tránsito Gastrointestinal/fisiología , Inmunohistoquímica , Células Intersticiales de Cajal/metabolismo , Células Intersticiales de Cajal/patología , Ratas , Ratas Wistar
4.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;51(7): e7372, 2018. tab, graf
Artículo en Inglés | LILACS | ID: biblio-951733

RESUMEN

The effect of bisacodyl on the treatment of rats with slow transit constipation (STC) was studied. Forty-five female Wister rats were divided into control group, STC group, and STC bisacodyl group. The immunohistochemical method was used to determine interstitial cells of Cajal (ICC) and the expression of c-Kit protein. Body mass and the number of defecations were significantly decreased in the STC group compared with the control group on the 100th day after diphenoxylate administration, while dry weight of feces was significantly increased and the intestinal transit time was prolonged. There were significant differences in the number of defecations, dry weight of feces, and intestinal transit time among the three groups. The number of defecations was higher, dry weight of feces was lower, and intestinal transit time was shorter in the STC bisacodyl group compared to the STC group. In addition, ICC basement membrane dissolution occurred in the colon wall of the STC group. The connection between ICC and surrounding cells was destroyed, and the nucleus shrunken to different degrees. Moreover, c-Kit expression in the STC group was significantly lower than the control group. The connection between ICC and surrounding cells in the STC bisacodyl group was significantly stronger than the STC group, and the number of ICC and the expression of c-Kit were increased. Bisacodyl could reduce the severity of STC in rats by increasing the number of ICC and the expression of c-Kit.


Asunto(s)
Animales , Femenino , Ratas , Bisacodilo/uso terapéutico , Tránsito Gastrointestinal/efectos de los fármacos , Catárticos/uso terapéutico , Colon/metabolismo , Proteínas Proto-Oncogénicas c-kit/metabolismo , Estreñimiento/tratamiento farmacológico , Células Intersticiales de Cajal/efectos de los fármacos , Tránsito Gastrointestinal/fisiología , Inmunohistoquímica , Ratas Wistar , Colon/efectos de los fármacos , Colon/patología , Estreñimiento/fisiopatología , Estreñimiento/metabolismo , Células Intersticiales de Cajal/metabolismo , Células Intersticiales de Cajal/patología
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