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1.
Laryngorhinootologie ; 89(10): 599-605, 2010 Oct.
Artigo em Alemão | MEDLINE | ID: mdl-20597040

RESUMO

OBJECTIVE: To evaluate which way of topical drug application would result in a better deposition pattern after FESS. MATERIAL AND METHODS: We compared the deposition pattern of a nasal steroid after application with a metered pump spray or inhalation using the Pari sinus device. Visualization was achieved via colouring using 1% Sodium-fluorescein solution. All patients had a well healed sinus system with an endoscopically wide open access after FESS. We looked for the deposition with Blue-light-endoscopy directly after application and after washing out using a nasal douche. Analysis was performed blinded by two independent experienced sinus surgeons via representative single shots. RESULTS: Data of 11 patients revealed, that deposition after metered pump spray application was superior than after inhalation for all localisations. By far most part of the drug was deposited in the anterior nasal cavity, followed by the head of the middle turbinate, ethmoid. Small amounts reached the maxillary sinus, the anterior wall of the sphenoid sinus, the olfactory cleft and the entrance to the frontal sinus. The frontal sinus itself was not reached in any case. Washing out led to a decrease of deposition intensity, in some cases to a better distribution into the maxillary and sphenoid sinus and frontal recess. CONCLUSIONS: Postoperative deposition of topical nasal steroids after FESS is insufficient. We need better methods and devices to optimize efficacy of topical treatment.


Assuntos
Corticosteroides/administração & dosagem , Inaladores Dosimetrados , Pólipos Nasais/cirurgia , Cuidados Pós-Operatórios , Pulsoterapia/instrumentação , Sinusite/cirurgia , Corticosteroides/farmacocinética , Aerossóis , Algoritmos , Disponibilidade Biológica , Doença Crônica , Endoscopia , Fluoresceína , Humanos , Pólipos Nasais/tratamento farmacológico , Sinusite/tratamento farmacológico , Gravação em Vídeo
2.
Nutr Metab Cardiovasc Dis ; 14(1): 20-5, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-15053160

RESUMO

BACKGROUND AND AIM: To assess the relationships between different diurnal triglyceride (TG) profiles (p) and the atherogenicity of the lipoprotein phenotype and adhesion molecule concentrations in patients with coronary artery disease (CAD). METHODS AND RESULTS: Repeated measurements of fasting TG and TGp were made in 29 CAD patients; fasting cholesterol levels (total-C, VLDL, LDL, HDL and small dense LDL) and soluble cell adhesion molecules (sCAM) (ICAM-1 and E-selectin) were measured once. Three different TGps were defined: fasting (137.0 +/- 60.7 mg/dL) and all other TG levels <200 mg/dL (LL; n=7); a fasting TG level <200 mg/dL (147.0 +/- 49.9 mg/dL) and maximum TG levels >200 mg/dL (LH; n=13); and both fasting (225.1+/-76.2 mg/dL) and maximum TG levels >200 mg/dL (HH; n=9). We then analysed the associations between the TGp types and the lipoprotein phenotype and CAMs. LL had significantly lower values than LH (p<0.05 for all parameters except sE-selectin) and HH (p<0.05 for all parameters) of VLDL (11.2 +/- 5.8, 18.8 +/- 9.4, 28.1 +/- 8.8 mg/dL), LDL-5 (11.6 +/- 3.3, 16.4 +/- 4.5, 22.1 +/-7.9 mg/dl) and LDL-6 (12.0 +/- 3.2, 17.0 +/- 5.7, 25.7 +/- 9.6 mg/dL), sICAM-1 (209.4 +/- 30.3, 267.5 +/- 60.6, 273.4 +/- 59.1 ng/dL) and sE-selectin (25.1 +/- 17.6, 35.5 +/- 11.5, 48.5 +/- 20.2 ng/dL). CONCLUSION: Although the differences in fasting TG levels between the LL and LH groups were not significantly different, LH had a more atherogenic lipoprotein phenotype and higher concentrations of adhesion molecules. TGp measurements seem to be suitable for identifying CAD patients with an unfavourable diurnal TG and atherosclerosis-prone lipoprotein metabolism.


Assuntos
Moléculas de Adesão Celular/sangue , Ritmo Circadiano/fisiologia , Doença da Artéria Coronariana/sangue , Hiperlipidemias/sangue , Triglicerídeos/sangue , Idoso , Glicemia/metabolismo , Colesterol/sangue , Doença da Artéria Coronariana/etiologia , Selectina E/sangue , Feminino , Humanos , Hiperlipidemias/complicações , Molécula 1 de Adesão Intercelular/sangue , Lipoproteínas HDL/sangue , Lipoproteínas LDL/sangue , Masculino , Pessoa de Meia-Idade , Fenótipo , Fatores de Risco
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