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1.
Heliyon ; 9(4): e15379, 2023 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-37064466

RESUMO

Background and aims: COVID-19 has disrupted the patient workflow in all healthcare settings. Procedures such as bronchoscopy and spirometry require additional pre-procedure screening for SARS-CoV-2. However, there is uncertainty regarding the utility of this universal pre-procedure screening. The State of Qatar has a robust contact tracing system in place in the form of the mobile application 'Ehteraz.' This study assesses the utility of various pre-procedural screening measures in asymptomatic patients and generate recommendations for any potential improvement in the workflow. Methods: This is a cross-sectional study of asymptomatic patients who had SARS-CoV-2 RT-PCR screening performed before bronchoscopy or lung function testing scheduled on an elective basis. Descriptive statistics were used to summarize and determine the sample characteristics. The rate of the positive PCR test result was subsequently calculated. Results: Two patients (0.34%) tested positive for COVID-19 on their pre-procedural screen. Four patients (0.68%) had an inconclusive result. Conclusion: The positivity rate of SARS-CoV-2 RT-PCR is extremely low in asymptomatic individuals screened before bronchoscopy and spirometry. The authors recommend pre-procedural symptom and electronic application-based contact screening instead of universal pre-procedural SARS-CoV-2 RT-PCR for screening asymptomatic individuals.

2.
Indian J Thorac Cardiovasc Surg ; 37(1): 27-37, 2021 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-33442205

RESUMO

PURPOSE: Ticagrelor combined with aspirin had shown better saphenous vein graft patency than aspirin with clopidogrel after off-pump coronary artery bypass grafting. However, the safety of this drug in regard to bleeding complications remains unknown. The aim of our study was to assess the bleeding complications of dual antiplatelet therapy with aspirin and ticagrelor compared with aspirin and clopidogrel within the first 3 months after off-pump surgery. METHODS: Three hundred eighty-two consecutive patients who were prescribed aspirin with ticagrelor (ticagrelor group) were compared with 660 patients who received aspirin and clopidogrel (clopidogrel group). After propensity matching, 144 patients in each group were compared for bleeding events and major adverse cardiac and cerebral events. Major bleeding was defined as composite outcome of re-exploration for bleeding, any fatal bleeding, intracranial bleeding, and any bleeding requiring hospitalization. RESULTS: Patients in the ticagrelor group had more incidence of re-exploration for bleeding (p = 0.042), pericardial effusion requiring drainage (p = 0.007), readmissions (p < 0.01), gastrointestinal bleeding (p = 0.01), and major bleeding (5.8% vs. 2.1%, p < 0.01, OR 2.8 (1.43-5.58)). After propensity analysis, gastrointestinal bleed (p = 0.024), major bleeding (7.6% vs.1.4%, p < 0.001, OR 5.8 (1.28-26.97)), length of ICU stay (p = 0.039), and readmissions (p = 0.003, OR 11.83 (1.51-92.86)) were more in the ticagrelor group. Major adverse cardiac and cerebral events were similar between the groups. CONCLUSION: Dual antiplatelet therapy with aspirin and ticagrelor increased gastrointestinal bleeding events, major bleeding events, and readmission rates compared with aspirin and clopidogrel after off-pump coronary artery bypass grafting.

3.
Pharm Dev Technol ; 22(3): 418-425, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-27499352

RESUMO

Evaluate the effects of nonionic surfactants Brij 58 and Tween 40 with different structures but similar hydrophilic lipophilic balances (HLBs) on theophylline (TH)-loaded ethylcellulose (EC) microspheres. Microspheres were formulated using ratios of the surfactants with matching HLB values but different chemical-structures at temperatures (22/35 °C) by hydrophobic solvent-emulsion evaporation. Particle size, GMD, drug loading, encapsulation efficiency and dissolution were evaluated. Drug release was determined using the zero- and first-order, Higuchi and Hixson-Crowell models. EC microspheres prepared with surfactant Brij 58 showed discrete, free-flowing spherical particles, solid interiors and increased particle smoothness as temperature increased; those prepared with Tween 40 appeared porous with coarser surface morphology as temperature increased; both were CHLB (Combined HLB) dependent. Dissolution obeyed the Higuchi model drug release for both microspheres prepared with Tween 40 and Brij 58 except for those prepared with Brij 58 at 35 °C, which presented as zero order. The results were ascribed to the different chemical structure of Brij 58 versus Tween 40 and preparation temperature. Surfactant chemical structure is an unreported processing parameter shown here to be important in microsphere formulation. Brij 58 possesses properties unique to its chemical structure that influence pharmaceutical and molecular biopharmaceutical research.


Assuntos
Celulose/análogos & derivados , Portadores de Fármacos/química , Composição de Medicamentos/métodos , Tensoativos/química , Teofilina/administração & dosagem , Celulose/química , Cetomacrogol/química , Liberação Controlada de Fármacos , Microscopia Eletrônica de Varredura , Microesferas , Tamanho da Partícula , Polissorbatos/química , Solubilidade , Propriedades de Superfície
4.
J Environ Health Sci Eng ; 12(1): 26, 2014 Jan 10.
Artigo em Inglês | MEDLINE | ID: mdl-24410999

RESUMO

BACKGROUND: The main objective of the study was the assessment of the prevalence and the identification of species of human gastrointestinal parasites as an indicator of the pollution of the seashore of Gaza City. METHODS: The investigation was conducted by analysis of the parasitic contamination of seawater along the study area. A total of 52 samples of seawater were analyzed during the summer period; from June to October 2011. The study area was divided into six zones (A, B, C, D, E and F) according to specific criteria such as the presence of the wastewater discharge points and other geographical characteristics. RESULTS: The results show that about 48% of the seawater samples from the shoreline region of Gaza City were contaminated with parasites. Zones A, B and D (mouth of Wadi Gaza, Al Sheikh Ejleen discharge and Al Shalehat discharge points respectively) have the highest level of parasitic contamination, while, zones C and E (From Al-Baydar restaurant to Khalel Alwazer Mosque and the basin of the Gaza marina respectively) had a lower level of contamination and zone F (From the northern part of the Gaza marina to the Intelligence Building) was uncontaminated. The parasitic species found were: Ascaris lumbricoides, Giardia lamblia, Strongyloides stercoralis, Hymenolepis nana, Entamoeba histolytica/dispar and Cryptosporidium parvum. CONCLUSIONS: The present study revealed a high level of contamination with parasites at most of the points which were investigated along the Gaza City coast line.

5.
Pharm Dev Technol ; 18(5): 1213-9, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-21991996

RESUMO

Altering the combined hydrophilic-lipophilic balance (CHLB), by varying the ratio of dual surfactants, on formulation parameters and in vitro drug release of ethyl cellulose microspheres was examined. Theophylline, a xanthine bronchodilator was used to model controlled release owing to its narrow therapeutic index. Microspheres were prepared using different ratios of dual surfactant in an emulsion-solvent evaporation process. Drug loading, encapsulation efficiency, particle size distribution, and geometric mean diameters were evaluated. Drug release was evaluated using several kinetic models including zero and first order, Higuchi square root, and Hixson-Crowell. Microspheres presented as mostly spherical particles and diffusional drug release was affected by microsphere construction. For this novel, dual surfactant system the microsphere matrix is a hydrophobic polymer and the release rate may be modulated with variation in ratio of dual surfactants. Dissolution data followed the Higuchi model and supports the formation of a monolithic microsphere matrix that releases theophylline by Fickian diffusion. Dual surfactants for preparation of microspheres are an inadequately studied research area that offers another means to modulate particle size and drug release. For the current study microspheres prepared with surfactant ratios of Span 65: Tween 40 between 3:1 and 2:1 provided the best control of size and drug release.


Assuntos
Celulose/análogos & derivados , Tensoativos/química , Teofilina/química , Celulose/química , Química Farmacêutica/métodos , Composição de Medicamentos/métodos , Emulsões/química , Interações Hidrofóbicas e Hidrofílicas , Microesferas , Tamanho da Partícula , Polímeros/química , Solventes/química
6.
Pharm Dev Technol ; 17(1): 48-54, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-20858066

RESUMO

The current investigation reports skin permeation of three novel mutual prodrugs (MP) which couple n-acetyl-glucosamine with an NSAID, either ketoprofen or ibuprofen. They were evaluated for transdermal permeation using shed snakeskin, and to our knowledge represent the first MPs synthesized for this purpose, although they also could be used for subcutaneous delivery. MPs are defined as two active drug compounds usually connected by an ester linkage. Glucosamine administration has been linked to damaged cartilage repair, and pain relief in joints afflicted with osteoarthritis. NSAIDs are commonly used orally in transdermal creams or gels for joint pain relief. Two novel compounds we report (MP1 and MP2) covalently link ibuprofen and ketoprofen directly to the amide nitrogen of n-acetyl-glucosamine (NAG); the other compound (MP3) covalently links ibuprofen to the amide nitrogen, using a short chain acetyl linker. Permeability studies show that the ketoprofen mutual prodrug (MP2) permeates shed snakeskin more than three times greater than either ibuprofen derivative, while ethanol markedly increases the permeation for all three. The ketoprofen mutual prodrug appears the most likely candidate for transdermal administration; all three mutual prodrugs may be candidates for subcutaneous injection.


Assuntos
Acetilglucosamina/farmacocinética , Anti-Inflamatórios não Esteroides/farmacocinética , Acetilglucosamina/administração & dosagem , Acetilglucosamina/química , Administração Cutânea , Animais , Anti-Inflamatórios não Esteroides/administração & dosagem , Anti-Inflamatórios não Esteroides/química , Permeabilidade da Membrana Celular , Combinação de Medicamentos , Etanol/farmacologia , Hidrólise , Ibuprofeno/administração & dosagem , Ibuprofeno/farmacocinética , Técnicas In Vitro , Indicadores e Reagentes , Cetoprofeno/administração & dosagem , Cetoprofeno/farmacocinética , Cinética , Pró-Fármacos , Absorção Cutânea , Serpentes , Solubilidade , Solventes
7.
Am J Orthod Dentofacial Orthop ; 137(2): 266-73, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-20152685

RESUMO

The introduction of 3-dimensional (3D) volumetric technology and the massive amount of information that can be obtained from it compels the introduction of new methods and new technology for orthodontic diagnosis and treatment planning. In this article, methods and tools are introduced for managing 3D images of orthodontic patients. These tools enable the creation of a virtual model and automatic localization of landmarks on the 3D volumes. They allow the user to isolate a targeted region such as the mandible or the maxilla, manipulate it, and then reattach it to the 3D model. For an integrated protocol, these procedures are followed by registration of the 3D volumes to evaluate the amount of work accomplished. This paves the way for the prospective treatment analysis approach, analysis of the end result, subtraction analysis, and treatment analysis.


Assuntos
Cefalometria/métodos , Arco Dental/anatomia & histologia , Imageamento Tridimensional/métodos , Modelos Dentários , Radiografia Dentária Digital/métodos , Simulação por Computador , Arco Dental/diagnóstico por imagem , Humanos , Mandíbula/anatomia & histologia , Mandíbula/diagnóstico por imagem , Maxila/anatomia & histologia , Maxila/diagnóstico por imagem , Tamanho do Órgão , Tomografia Computadorizada por Raios X
8.
Pharm Dev Technol ; 14(1): 9-17, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-18785078

RESUMO

Theophylline controlled release capsules (THEO-24 CR) were used as a model system to evaluate accelerated dissolution tests for process and quality control and formulation development of controlled release formulations. Dissolution test acceleration was provided by increasing temperature, pH, flow rate, or adding surfactant. Electron microscope studies on the theophylline microspheres subsequent to each experiment showed that at pH values of 6.6 and 7.6 the microspheres remained intact, but at pH 8.6 they showed deterioration. As temperature was increased from 37-57 degrees C, no change in microsphere integrity was noted. Increased flow rate also showed no detrimental effect on integrity. The effect of increased temperature was determined to be the statistically significant variable.


Assuntos
Microesferas , Soluções Tampão , Cápsulas/química , Preparações de Ação Retardada , Concentração de Íons de Hidrogênio , Microscopia Eletrônica de Varredura , Farmacopeias como Assunto , Dodecilsulfato de Sódio/química , Espectrofotometria Ultravioleta , Tecnologia Farmacêutica , Temperatura , Teofilina/química , Teofilina/metabolismo , Teofilina/normas , Fatores de Tempo
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