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1.
Int Forum Allergy Rhinol ; 4(11): 877-84, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25137523

RESUMEN

BACKGROUND: The endoscopically magnified operative field in functional endoscopic sinus surgery (FESS) makes even a small amount of bleeding a potentially significant hindrance. It is thought that irrigation with hot saline during surgery may improve surgical field of view by producing a hemostatic effect. Our objective was to assess the effectiveness of hot saline irrigation (HSI) compared to room temperature saline irrigation (RTSI) in the control of intraoperative bleeding during FESS. METHODS: Sixty-two chronic rhinosinusitis (CRS) patients undergoing FESS were randomized to 2 treatment arms in an equal ratio. Subjects received either HSI (49°C) or RTSI (18°C), 20 mL every 10 minutes, for the duration of FESS. The Boezaart endoscopic field of view grading system was the primary outcome measure. Boezaart score, heart rate, and mean arterial blood pressure (MABP) were recorded at 10-minute intervals between irrigations. RESULTS: Mean endoscopic surgical field of view (Boezaart score) did not significantly differ between the HSI and RTSI groups (1.5 ± 0.6 vs 1.3 ± 0.5; p = 0.23). However, when FESS was longer than 2 hours in duration, the Boezaart scores were significantly better in the HSI group (1.6 ± 0.6 vs 1.2 ± 0.4; p = 0.04). We found that blood loss per minute was significantly reduced (p = 0.02) in all cases in which HSI was used (2.3 ± 1.0) compared to RTSI (1.7 ± 1.1). Despite this, heart rate (p = 0.32) and MABP (p = 0.14) did not significantly differ between treatment groups. CONCLUSION: HSI may be beneficial in improving surgical field of view in FESS after 2 hours of operating time. A significant reduction in rate of blood loss may be attained with HSI.


Asunto(s)
Hemostáticos/administración & dosificación , Procedimientos Quírurgicos Nasales/métodos , Rinitis/cirugía , Sinusitis/cirugía , Cloruro de Sodio/administración & dosificación , Irrigación Terapéutica/métodos , Pérdida de Sangre Quirúrgica/prevención & control , Enfermedad Crónica , Método Doble Ciego , Endoscopía/métodos , Femenino , Hemostasis Quirúrgica/métodos , Humanos , Hipertermia Inducida/métodos , Masculino , Persona de Mediana Edad , Pólipos Nasales/cirugía , Resultado del Tratamiento
2.
Int Forum Allergy Rhinol ; 4(5): 397-402, 2014 May.
Artículo en Inglés | MEDLINE | ID: mdl-24449682

RESUMEN

BACKGROUND: Budesonide is a potent corticosteroid commonly prescribed for management of inflammation in chronic rhinosinusitis (CRS). The standard for prescribing budesonide is via impregnated nasal saline irrigation (INSI), although recently the mucosal atomization device (MAD) has emerged as a theoretically superior method of distributing medication into the sinuses. The MAD atomizes medication into small droplets and this is thought to enhance absorption and improve bioavailability. However, no studies have shown whether enhanced absorption and improved bioavailability of budesonide via MAD causes adrenal suppression. The objective of this study is to determine whether budesonide via MAD affects the hypothalamic-pituitary-adrenal (HPA) axis. METHODS: Twenty CRS patients were recruited from a tertiary rhinology clinic and randomized to take budesonide (1 mg) via MAD or via INSI twice a day for 60 days. The adrenocorticotropic hormone (ACTH) stimulation test and 22-item Sinonasal Outcomes Test (SNOT-22) questionnaire were administered on days 1, 30, and 60 of the study. Plasma budesonide and cortisol levels were simultaneously quantified using a high-performance liquid chromatography-tandem mass spectrometry technique. RESULTS: There was no indication of adrenal suppression in either group (n = 20) based on ACTH stimulation test results nor was there significant plasma budesonide levels detected in either group. Quality of life, as indicated by SNOT-22, did not differ between groups at 60 days (p = 0.404; 95% confidence interval [CI], -37.2 to 15.9), but SNOT-22 scores for patients using MAD did show statistically significant improvement at 60 days compared to baseline (p = 0.02). CONCLUSION: The MAD is likely a safe and effective method of delivering budesonide to the sinuses in the short term.


Asunto(s)
Antiinflamatorios/administración & dosificación , Budesonida/administración & dosificación , Rinitis/tratamiento farmacológico , Sinusitis/tratamiento farmacológico , Administración a través de la Mucosa , Antiinflamatorios/efectos adversos , Antiinflamatorios/farmacocinética , Budesonida/efectos adversos , Budesonida/farmacocinética , Canadá , Enfermedad Crónica , Femenino , Humanos , Hidrocortisona/metabolismo , Sistema Hipotálamo-Hipofisario/efectos de los fármacos , Masculino , Pólipos Nasales/complicaciones , Nebulizadores y Vaporizadores/estadística & datos numéricos , Sistema Hipófiso-Suprarrenal/efectos de los fármacos , Estudios Prospectivos , Calidad de Vida , Rinitis/complicaciones , Sinusitis/complicaciones , Factores de Tiempo , Resultado del Tratamiento
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