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1.
J Small Anim Pract ; 64(4): 255-264, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-36316285

RESUMO

OBJECTIVES: To assess treatment satisfaction and owner preference for two delivery devices (VetPen, MSD Animal Health, and U40 insulin syringes) and the effect on glycaemic control in diabetic dogs treated with porcine insulin zinc suspension. MATERIALS AND METHODS: Randomised prospective cross-over study with two arms, each of 8 weeks. Twenty client-owned diabetic dogs on insulin treatment by U40 syringe were enrolled. Dogs were randomly assigned to receive insulin by syringe or pen injector for 2 months, followed by 2 months of the other injection method. Treatment satisfaction and owners' insulin delivery device preference were assessed using a questionnaire. Glycaemic control was assessed using a clinical score, serum fructosamine and glycated haemoglobin (HbA1c%) at the time of the enrolment (T0) and the end of each arm of treatment (T2 and T4). RESULTS: Treatment satisfaction differed for the two types of the delivery device when the order that each device was used was taken into consideration. Owners who used the syringe first did not have a significant preference for an injection device. In contrast, owners who used the pen injector first expressed a significant preference for VetPen compared to syringes. No significant differences in the number of dogs of Groups 1 and 2 with good and poor glycaemic control at T2 and T4 were detected. CLINICAL SIGNIFICANCE: Overall treatment satisfaction and preference for the two delivery methods were similar. However, VetPen was preferred by owners who were randomised to use this device first. Glycaemic control did not appear to be affected by the insulin delivery device used.


Assuntos
Diabetes Mellitus , Doenças do Cão , Cães , Animais , Controle Glicêmico/veterinária , Estudos Cross-Over , Estudos Prospectivos , Diabetes Mellitus/tratamento farmacológico , Diabetes Mellitus/veterinária , Insulina/uso terapêutico , Seringas , Doenças do Cão/tratamento farmacológico
2.
Minerva Ginecol ; 55(6): 483-92, 2003 Dec.
Artigo em Inglês, Italiano | MEDLINE | ID: mdl-14676737

RESUMO

AIM: The authors have evaluated the real efficacy of using hydrogen peroxide for previously treated recurrent bacterial vaginosis that is resistant to other forms of treatment. METHODS: The study included 58 women aged between 18 and 42 years old. Vaginal irrigations with 30 ml of hydrogen peroxide (3%) were prescribed in the evening for a week. The follow-up was carried out 3 months after the end of treatment. RESULTS: The results clearly show that the use of hydrogen peroxide in vagina can eliminate the main symptoms of bacterial vaginosis, and in particular the malodorous leucoxanthorrhea in 89% of cases at 3 months after the end of treatment, a result that is comparable to that obtained using metronidazole or clindamycin as a vaginal cream. Moreover, hydrogen peroxide facilitates the restoration of normal vaginal bacterial flora (represented by H202-producing lactobacillus) in 100% of cases and normal acid pH (pH<4.5) in 98% of cases; it also fosters the disappearance of clue cells from vaginal smears and anaerobic pathogenic flora from vaginal secretions in 100% of cases. The amine test became negative in 97.8% of cases. All results underwent statistical analysis and were found to be statistically significant. CONCLUSION: Hydrogen peroxide represents a valid alternative to conventional treatments for recurrent bacterial vaginosis, and associates the absence of collateral effects with low costs, excellent tolerability and real therapeutic efficacy.


Assuntos
Anti-Infecciosos Locais/uso terapêutico , Peróxido de Hidrogênio/uso terapêutico , Vaginose Bacteriana/tratamento farmacológico , Adolescente , Adulto , Anti-Infecciosos Locais/administração & dosagem , Feminino , Humanos , Peróxido de Hidrogênio/administração & dosagem , Lactobacillus acidophilus/isolamento & purificação , Recidiva , Vagina/microbiologia , Vaginose Bacteriana/microbiologia
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