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1.
Diabetes Obes Metab ; 23(3): 854-860, 2021 03.
Artigo em Inglês | MEDLINE | ID: mdl-33289297

RESUMO

Sotagliflozin, a dual sodium-glucose co-transporter (SGLT)1/SGLT2 inhibitor, is currently approved in Europe as an adjunct to optimal insulin therapy in adults with type 1 diabetes (T1D) and a body mass index (BMI) ≥ 27 kg/m2 . In this post hoc analysis, efficacy at 24 weeks and safety at 52 weeks from pooled phase 3 clinical trials were evaluated in patients with baseline BMI ≥ 27 kg/m2 . Sotagliflozin 200 mg and 400 mg added to insulin reduced glycated haemoglobin level and increased time in range assessed by continuous glucose monitoring versus placebo and also reduced body weight and systolic blood pressure. Differences in efficacy endpoints between sotagliflozin and placebo tended to be greater among patients with BMI ≥ 27 kg/m2 compared to those with baseline BMI < 27 kg/m2 . Consistent with published results for the entire population, fewer severe hypoglycaemia and documented hypoglycaemia ≤3.1 mmol/L events and a higher incidence of diabetic ketoacidosis occurred with sotagliflozin versus placebo in patients with BMI ≥ 27 kg/m2 . Sotagliflozin as an adjunct to optimized insulin therapy in overweight/obese patients with T1D addressed some unmet needs and may help achieve optimal glycaemic control, mitigating weight gain without increasing hypoglycaemia risk in this high-risk population.


Assuntos
Diabetes Mellitus Tipo 1 , Inibidores do Transportador 2 de Sódio-Glicose , Adulto , Glicemia , Automonitorização da Glicemia , Índice de Massa Corporal , Diabetes Mellitus Tipo 1/tratamento farmacológico , Diabetes Mellitus Tipo 1/epidemiologia , Método Duplo-Cego , Quimioterapia Combinada , Europa (Continente) , Hemoglobinas Glicadas/análise , Glicosídeos , Humanos , Hipoglicemiantes/efeitos adversos , Insulina/uso terapêutico , Sódio , Inibidores do Transportador 2 de Sódio-Glicose/efeitos adversos
4.
J Orthod ; 34(2): 128-36; discussion 111-2, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17545300

RESUMO

OBJECTIVE: To compare the clinical failure rates of bonded first molar tubes with those of cemented bands during fixed appliance therapy. DESIGN: Prospective randomized controlled clinical trial. SETTING: Two UK hospital orthodontic clinics, February 2001-December 2004. PARTICIPANTS: Hospital waiting list patients needing fixed appliances (n = 110). METHOD: Patients were randomly allocated to two groups. Experimental group patients (n = 55) received single first molar tubes (n = 181) bonded with a no-mix chemically cured composite (Rely-A-Bond) after a 30-second etch. Control group patients (n = 55) were treated with bands (n = 186) cemented with Intact glass ionomer cement (GIC). First-time failures were recorded together with the time of failure. All patients were followed to the end or discontinuation of treatment. RESULTS: First-time failures: bands = 18.8%; bonds = 33.7 %. Bonded tubes were more likely to fail [RR 2.4; 95% CI (1.4, 4.1)] compared with bands. Experimental group patients also had more bracket failures (P = 0.009), when analysed at patient level. CONCLUSION: First molar tubes bonded with Rely-A-Bond composite showed a significantly higher first-time failure rate than bands cemented with Intact GIC.


Assuntos
Colagem Dentária , Dente Molar , Aparelhos Ortodônticos , Braquetes Ortodônticos , Condicionamento Ácido do Dente , Adolescente , Adulto , Cimentação , Criança , Falha de Equipamento , Feminino , Seguimentos , Cimentos de Ionômeros de Vidro/química , Humanos , Masculino , Desenho de Aparelho Ortodôntico , Fios Ortodônticos , Estudos Prospectivos , Cimentos de Resina/química
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