Statins: new American guidelines for prevention of cardiovascular disease
Paul M Ridker,Nancy R Cook
The Lancet - 30 November 2013 ( Vol. 382, Issue 9907, Pages 1762-1765 )
DOI: 10.1016/S0140-6736(13)62388-0
Publicado en Lancet: Estudio Trascend
- 5926 pacientes, 2954 recibieron 80 mgr de Telmisartan, 2972 placebo. Estudio aleatorizado, controlado.
- Analisis por intencion de tratar. Seguimiento entre 51 a 64 meses.
- Disminucion de la TA media: HR 0,92 (IC 95% 0.81-1.05). No significativo.
- Resultados de muerte cardiovascular, IAM, ACV: 0,87 (IC 95% 0.76-1.00). Significativo a p 0,05 pero no a 0,01.
- Hospitalizacion por eventos cardiovasculares: RR 0,92 (CI 95% 0.85-0.99). No significativo a p 0.01.
- Telmisartan fue bien tolerado en pacientes que no toleran IECAs. Aunque el medicamento no mostro diferencias significativas en los resultados primariso, los cuales incluyeron fallta cardica, y una modesta reduccion del riesgo de padecer una serie de eventos cardiovascularses mayores compuestos (muerte cardiovascular, IAM, ACV).
- Financiamiento: Boheringer Ingelheim.
Conclusion: para que sirve el telmisartan????
Publicado en Lancet: Estudio Trascend
- 5926 pacientes, 2954 recibieron 80 mgr de Telmisartan, 2972 placebo. Estudio aleatorizado, controlado.
- Analisis por intencion de tratar. Seguimiento entre 51 a 64 meses.
- Disminucion de la TA media: HR 0,92 (IC 95% 0.81-1.05). No significativo.
- Resultados de muerte cardiovascular, IAM, ACV: 0,87 (IC 95% 0.76-1.00). Significativo a p 0,05 pero no a 0,01.
- Hospitalizacion por eventos cardiovasculares: RR 0,92 (CI 95% 0.85-0.99). No significativo a p 0.01.
- Telmisartan fue bien tolerado en pacientes que no toleran IECAs. Aunque el medicamento no mostro diferencias significativas en los resultados primariso, los cuales incluyeron fallta cardica, y una modesta reduccion del riesgo de padecer una serie de eventos cardiovascularses mayores compuestos (muerte cardiovascular, IAM, ACV).
- Financiamiento: Boheringer Ingelheim.
Conclusion: para que sirve el telmisartan????
Publicado en Lancet: Estudio Trascend
- 5926 pacientes, 2954 recibieron 80 mgr de Telmisartan, 2972 placebo. Estudio aleatorizado, controlado.
- Analisis por intencion de tratar. Seguimiento entre 51 a 64 meses.
- Disminucion de la TA media: HR 0,92 (IC 95% 0.81-1.05). No significativo.
- Resultados de muerte cardiovascular, IAM, ACV: 0,87 (IC 95% 0.76-1.00). Significativo a p 0,05 pero no a 0,01.
- Hospitalizacion por eventos cardiovasculares: RR 0,92 (CI 95% 0.85-0.99). No significativo a p 0.01.
- Telmisartan fue bien tolerado en pacientes que no toleran IECAs. Aunque el medicamento no mostro diferencias significativas en los resultados primariso, los cuales incluyeron fallta cardica, y una modesta reduccion del riesgo de padecer una serie de eventos cardiovascularses mayores compuestos (muerte cardiovascular, IAM, ACV).
- Financiamiento: Boheringer Ingelheim.
Conclusion: para que sirve el telmisartan????
Prof Richard Beasley DSc
a
, Tadd Clayton MSc b, Prof Julian CraneMBBS c, Prof Erika von Mutius MD d, Prof Christopher KW Lai DM e, ProfStephen Montefort PhD f and Alistair Stewart BSc g, for the ISAAC Phase Three Study Group
‡Members listed at end of paper
Exposure to paracetamol during intrauterine life, childhood, and adult life may increase the risk of developing asthma. We studied 6–7-year-old children from Phase Three of the International Study of Asthma and Allergies in Childhood (ISAAC) programme to investigate the association between paracetamol consumption and asthma.
As part of Phase Three of ISAAC, parents or guardians of children aged 6–7 years completed written questionnaires about symptoms of asthma, rhinoconjunctivitis, and eczema, and several risk factors, including the use of paracetamol for fever in the child's first year of life and the frequency of paracetamol use in the past 12 months. The primary outcome variable was the odds ratio (OR) of asthma symptoms in these children associated with the use of paracetamol for fever in the first year of life, as calculated by logistic regression.
205 487 children aged 6–7 years from 73 centres in 31 countries were included in the analysis. In the multivariate analyses, use of paracetamol for fever in the first year of life was associated with an increased risk of asthma symptoms when aged 6–7 years (OR 1·46 [95% CI 1·36–1·56]). Current use of paracetamol was associated with a dose-dependent increased risk of asthma symptoms (1·61 [1·46–1·77] and 3·23 [2·91–3·60] for medium and high use vs no use, respectively). Use of paracetamol was similarly associated with the risk of severe asthma symptoms, with population-attributable risks between 22% and 38%. Paracetamol use, both in the first year of life and in children aged 6–7 years, was also associated with an increased risk of symptoms of rhinoconjunctivitis and eczema.
Use of paracetamol in the first year of life and in later childhood, is associated with risk of asthma, rhinoconjunctivitis, and eczema at age 6 to 7 years. We suggest that exposure to paracetamol might be a risk factor for the development of asthma in childhood.
The BUPA Foundation, the Health Research Council of New Zealand, the Asthma and Respiratory Foundation of New Zealand, the Hawke's Bay Medical Research Foundation, the Waikato Medical Research Foundation, Glaxo Wellcome New Zealand, the New Zealand Lottery Board, Astra Zeneca New Zealand, and Glaxo Wellcome International Medical Affairs.
Correspondence to: Prof Richard Beasley, Medical Research Institute of New Zealand, PO Box 10055, Wellington 6143, New Zealand
Prof Richard Beasley DSc
a
, Tadd Clayton MSc b, Prof Julian CraneMBBS c, Prof Erika von Mutius MD d, Prof Christopher KW Lai DM e, ProfStephen Montefort PhD f and Alistair Stewart BSc g, for the ISAAC Phase Three Study Group
‡Members listed at end of paper
Exposure to paracetamol during intrauterine life, childhood, and adult life may increase the risk of developing asthma. We studied 6–7-year-old children from Phase Three of the International Study of Asthma and Allergies in Childhood (ISAAC) programme to investigate the association between paracetamol consumption and asthma.
As part of Phase Three of ISAAC, parents or guardians of children aged 6–7 years completed written questionnaires about symptoms of asthma, rhinoconjunctivitis, and eczema, and several risk factors, including the use of paracetamol for fever in the child's first year of life and the frequency of paracetamol use in the past 12 months. The primary outcome variable was the odds ratio (OR) of asthma symptoms in these children associated with the use of paracetamol for fever in the first year of life, as calculated by logistic regression.
205 487 children aged 6–7 years from 73 centres in 31 countries were included in the analysis. In the multivariate analyses, use of paracetamol for fever in the first year of life was associated with an increased risk of asthma symptoms when aged 6–7 years (OR 1·46 [95% CI 1·36–1·56]). Current use of paracetamol was associated with a dose-dependent increased risk of asthma symptoms (1·61 [1·46–1·77] and 3·23 [2·91–3·60] for medium and high use vs no use, respectively). Use of paracetamol was similarly associated with the risk of severe asthma symptoms, with population-attributable risks between 22% and 38%. Paracetamol use, both in the first year of life and in children aged 6–7 years, was also associated with an increased risk of symptoms of rhinoconjunctivitis and eczema.
Use of paracetamol in the first year of life and in later childhood, is associated with risk of asthma, rhinoconjunctivitis, and eczema at age 6 to 7 years. We suggest that exposure to paracetamol might be a risk factor for the development of asthma in childhood.
The BUPA Foundation, the Health Research Council of New Zealand, the Asthma and Respiratory Foundation of New Zealand, the Hawke's Bay Medical Research Foundation, the Waikato Medical Research Foundation, Glaxo Wellcome New Zealand, the New Zealand Lottery Board, Astra Zeneca New Zealand, and Glaxo Wellcome International Medical Affairs.
Correspondence to: Prof Richard Beasley, Medical Research Institute of New Zealand, PO Box 10055, Wellington 6143, New Zealand