Assuntos
Phytoplasma , Solanum , Índia , Phytoplasma/genética , Folhas de Planta , RNA Ribossômico 16SRESUMO
Contact lens wear is generally safe and provides excellent vision. However, contact lens wear is often associated with the risk of developing ocular surface infection and inflammation, and in severe cases, the infection can result in loss of vision. Antimicrobial peptide-coated contact lenses have been made to help reduce the incidence of infection and inflammation. This paper reviews the research progress from conception, through the laboratory and preclinical tests to the latest information on clinical testing of an antimicrobial contact lens. We provide insights into the pathways followed and pitfalls that have been encountered. The journey has not always been linear or smooth, but has resulted in some of the first published clinical testing of antimicrobial peptide-coated contact lenses in humans. We hope this may help lead to the development and commercialisation of antimicrobial contact lenses in the future.
Assuntos
Anti-Infecciosos/farmacologia , Peptídeos Catiônicos Antimicrobianos/farmacologia , Infecções Bacterianas/prevenção & controle , Materiais Revestidos Biocompatíveis/farmacologia , Lentes de Contato/microbiologia , Ceratite/prevenção & controle , Micoses/prevenção & controle , Sequência de Aminoácidos , Animais , Infecções Bacterianas/etiologia , Infecções Bacterianas/microbiologia , Infecções Bacterianas/patologia , Ensaios Clínicos como Assunto , Lentes de Contato/efeitos adversos , Avaliação Pré-Clínica de Medicamentos , Humanos , Ceratite/etiologia , Ceratite/microbiologia , Ceratite/patologia , Testes de Sensibilidade Microbiana , Micoses/etiologia , Micoses/microbiologia , Micoses/patologia , Pseudomonas aeruginosa/efeitos dos fármacos , Pseudomonas aeruginosa/crescimento & desenvolvimento , Pseudomonas aeruginosa/patogenicidade , Coelhos , Serratia marcescens/efeitos dos fármacos , Serratia marcescens/crescimento & desenvolvimento , Serratia marcescens/patogenicidade , Staphylococcus aureus/efeitos dos fármacos , Staphylococcus aureus/crescimento & desenvolvimento , Staphylococcus aureus/patogenicidadeRESUMO
BACKGROUND: Data are scant on bone health in endocrinopathies from India. This study evaluated bone mineral density (BMD) loss in endocrinopathies [Graves' disease (GD), type 1 diabetes mellitus (T1DM), hypogonadotrophic hypogonadism (HypoH), hypergonadotropic hypogonadism (HyperH), hypopituitarism, primary hyperparathyroidism (PHPT)] as compared to age-related BMD loss [postmenopausal osteoporosis (PMO), andropause]. MATERIALS AND METHODS: Retrospective audit of records of patients >30 years age attending a bone clinic from August 2014 to January 2016 was done. RESULTS: Five-hundred and seven records were screened, out of which 420 (females:male = 294:126) were analyzed. A significantly higher occurrence of vitamin D deficiency and insufficiency was noted in T1DM (89.09%), HyperH (85%), and HypoH (79.59%) compared to age-related BMD loss (60.02%; P < 0.001). The occurrence of osteoporosis among females and males was 55.41% and 53.97%, respectively, and of osteopenia among females and males was 28.91% and 32.54%, respectively. In females, osteoporosis was significantly higher in T1DM (92%), HyperH (85%), and HypoH (59.26%) compared to PMO (49.34%; P < 0.001). Z score at LS, TF, NOF, and greater trochanter (GT) was consistently lowest in T1DM women. Among men, osteoporosis was significantly higher in T1DM (76.67%) and HypoH (54.55%) compared to andropause (45.45%; P = 0.001). Z score at LS, TF, NOF, GT, and TR was consistently lowest in T1DM men. In GD, the burden of osteoporosis was similar to PMO and andropause. BMD difference among the study groups was not significantly different after adjusting for body mass index (BMI) and vitamin D. CONCLUSION: Low bone mass is extremely common in endocrinopathies, warranting routine screening and intervention. Concomitant vitamin D deficiency compounds the problem. Calcium and vitamin D supplementations may improve bone health in this setting.
Assuntos
Envelhecimento , Densidade Óssea , Doença de Graves/complicações , Osteoporose/complicações , Deficiência de Vitamina D/complicações , Absorciometria de Fóton , Adulto , Fatores Etários , Idoso , Andropausa , Diabetes Mellitus Tipo 2/epidemiologia , Feminino , Doença de Graves/epidemiologia , Humanos , Índia , Masculino , Pessoa de Meia-Idade , Osteoporose/epidemiologia , Osteoporose/metabolismo , Ossos Pélvicos/metabolismo , Ossos Pélvicos/fisiopatologia , Pós-Menopausa , Prevalência , Estudos Retrospectivos , Índice de Gravidade de Doença , Deficiência de Vitamina D/epidemiologiaRESUMO
Although ciprofloxacin is one of the recommended drugs of choice for the treatment of gonorrhea, in vitro resistance to this drug has been observed in surveillance studies and case reports from many parts of the world, including Bangladesh. However, to our knowledge, there have been no prospective studies of the correlation between in vitro response to the drug and treatment outcome. Therefore, a prospective study of 217 female sex workers in Dhaka, Bangladesh, was conducted to examine the correlation between the in vitro response of Neisseria gonorrhoeae and the outcome of ciprofloxacin treatment. Overall, 37.8% of the gonococcal isolates recovered from female sex workers were resistant to ciprofloxacin, and there was a good correlation between in vitro resistance and treatment failure. These findings suggest that in vitro resistance to ciprofloxacin is predictive of clinical treatment failure in patients with gonorrhea.
Assuntos
Anti-Infecciosos/uso terapêutico , Ciprofloxacina/uso terapêutico , Gonorreia/tratamento farmacológico , Neisseria gonorrhoeae/efeitos dos fármacos , Adulto , Anti-Infecciosos/farmacologia , Bangladesh , Ciprofloxacina/farmacologia , Resistência Microbiana a Medicamentos , Feminino , Humanos , Testes de Sensibilidade Microbiana , Neisseria gonorrhoeae/genética , Polimorfismo de Fragmento de Restrição , Estudos Prospectivos , Trabalho Sexual , Falha de TratamentoRESUMO
UNLABELLED: In a randomized controlled clinical trial, the efficacy of a low-sodium low-glucose oral rehydration solution (ORS) and a low-sodium rice-based ORS was compared with standard WHO glucose ORS in the treatment of severe cholera in children aged 2-10y. In total, 120 children were evaluated for the study, of whom 58 patients were positive for Vibrio cholerae and were included in the study. Of these 58 cases, 19 received rice-based hypo-osmolar ORS, 20 received WHO-ORS and 19 received glucose-based hypo-osmolar ORS. The clinical characteristics (age, preadmission duration of diarrhoea, frequency of stool before admission, incidence of vomiting, body weight and volume of initial fluid requirement) were comparable in the three treatment groups. All patients received tetracycline in a dose of 50 mg/kg/d of body weight in 4 divided doses for 3 d. CONCLUSIONS: Patients who received rice-based hypo-osmolar ORS had subsequently reduced (p < 0.05) stool output, ORS consumption and diarrhoea duration than the patients who received either WHO-ORS or glucose-based hypo-osmolar ORS.
Assuntos
Cólera/terapia , Hidratação/métodos , Oryza/uso terapêutico , Fitoterapia , Criança , Pré-Escolar , Feminino , Glucose/uso terapêutico , Humanos , Masculino , Concentração Osmolar , Tetraciclina/administração & dosagem , Tetraciclina/uso terapêutico , Vibrio cholerae/isolamento & purificação , Organização Mundial da SaúdeRESUMO
BACKGROUND: Recent animal experiments and clinical trials have shown that both osmolarity and rice as the organic components are important factors for net intestinal absorption of an oral rehydration salt solution. METHODS: In a controlled clinical trial 123 male adult patients with severe cholera, after initial rehydration with intravenous Ringer's lactate solution, were randomly assigned to receive one of the four oral rehydration salt solutions: WHO ORS, ORS containing 70 mmol/l Na+ and 16.2 g/l glucose, rice ORS containing 50 g/l rice and 90 mmol/l Na+, and rice ORS containing 50 g/l rice and 70 mmol/l Na+. All patients received 300 mg of doxycycline as a single dose. RESULTS: Patients who received rice-low-sodium ORS subsequently had lower (P < 0.05) stool output, ORS consumption, and diarrhoea duration than the other three ORS groups. CONCLUSIONS: We conclude that rice-based low-sodium ORS is superior for treating adult cholera.
Assuntos
Cólera/tratamento farmacológico , Glucose/administração & dosagem , Mucosa Intestinal/metabolismo , Intestino Delgado/metabolismo , Oryza/química , Soluções para Reidratação/administração & dosagem , Adulto , Canais de Cloreto/antagonistas & inibidores , Canais de Cloreto/efeitos dos fármacos , Cloretos/metabolismo , Cólera/sangue , AMP Cíclico/fisiologia , Diarreia/tratamento farmacológico , Doxiciclina/uso terapêutico , Humanos , Mucosa Intestinal/citologia , Mucosa Intestinal/efeitos dos fármacos , Intestino Delgado/citologia , Intestino Delgado/efeitos dos fármacos , Masculino , Análise Multivariada , Extratos Vegetais/administração & dosagem , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/farmacologia , Análise de Regressão , Soluções para Reidratação/análise , Soluções para Reidratação/farmacologia , Sódio/sangue , Resultado do Tratamento , Vibrio cholerae/efeitos dos fármacos , Vibrio cholerae/isolamento & purificaçãoRESUMO
Efficacy and safety of glycine fortified oral rehydration solution (ORS) was compared with a standard ORS (WHO formula) in a randomized clinical trial in children aged between 4 months and 5 yr with moderate degree of dehydration owing to acute watery diarrhoea. No significant differences (P greater than 0.05) were observed in diarrhoeal stool output, duration of diarrhoea and intake of ORS between the study and control groups respectively. Thus glycine fortified ORS does not have any additional advantage over standard ORS. Moreover, two children developed hypernatraemia after receiving glycine fortified ORS in contrast to the control group. It is therefore suggested that glycine supplemented ORS should not be prescribed for the treatment of diarrhoeal dehydration in children.