Traduction de «young g interventions for treating » (Néerlandais → Français) :

J Pediatr Gastroenterol Nutr 2004; 39:448-64 Farmacotherapeutisch Kompas via www.cvzkompassen.nl/fk/ Jewell DJ en Young G. Interventions for treating constipation in pregnancy.
J Pediatr Gastroenterol Nutr 2004; 39: 448-64 Farmacotherapeutisch Kompas via www.cvzkompassen.nl/fk/ Jewell DJ et Young G. Interventions for treating constipation in pregnancy.

Odds ratio of NRT versus control: 1.67 Odds ratio of bupropion versus control: 2.1 Odds ratio of NRT+bupropion versus control: 2.65 From these Odds Ratios and information on the control 12-month quit rate in the comparator intervention (0.04 for brief advice and 0.10 for counselling), the 12-month quit rate of treatment is calculated: treated quit rate for brief advice+NRT: 0.0650 treated quit rate for brief advice+bupropion: 0.0805 treated quit rate for brief advice+bupropion+NRT: 0.0994 treated quit rate for counselling+NRT: 0.1565 treated quit rate for counselling+bupropion: 0.1892 treated quit rate for counselling+bupropion+NRT: 0.2275 spontaneous cessation rate: 0.01. lifetime relapse rate: 40% (range 30-50%). number of LYG per quitter: 2 (range 1-3). number of QALYs gained per quitter: 2.7 (range 1.35-4.05) not reported The table gives an overview of the assumptions with respect to costs and effects (quit rates) in the average scenario.
Odds ratio of NRT versus control: 1.67 Odds ratio of Buproprion versus control: 2.1 Odds ratio of NRT+Buproprion versus control: 2.65 From these Odds Ratios and information on the control 12-month quit rate in the comparator intervention (0.04 for brief advice and 0.10 for counselling), the 12-month quit rate of treatment is calculated: treated quit rate for brief advice+NRT: 0.0650 treated quit rate for brief advice+Buproprion: 0.0805 treated quit rate for brief advice+Buproprion+NRT: 0.0994 treated quit rate for counselling+NRT: 0.1565 treated quit rate for counselling+Buproprion: 0.1892 treated quit rate for counselling+Buproprion+NRT: 0.2275 spontaneous cessation rate: 0.01. lifetime relapse rate: 40% (range 30-50%). number of LYG per quitter: 2 (range 1-3). number of QALYs gained per quitter: 2.7 (range 1.35-4.05) not reported The table gives an overview of the assumptions with respect to costs and effects (quit rates) in the average scenario.

Pharmaceuticals Ilaris (canakinumab, ACZ885), a human antibody targeting IL-1 beta, was launched in the US and Switzerland in August 2009 as a new therapy to treat children as young as age four and adults with CAPS (Cryopyrin-Associated Periodic Syndrome), a rare life-long and potentially fatal auto-inflammatory disease.
Pharmaceuticals Ilaris (canakinumab, ACZ885), un anticorps humain ciblant IL-1 bêta, a été lancé en août aux Etats-Unis et en Suisse comme nouveau traitement chez les enfants de plus de quatre ans et les adultes atteints des syndromes périodiques associés à la cryopyrine (CAPS), une maladie auto-inflammatoire sévère durant toute la vie et potentiellement mortelle.

Ilaris (canakinumab, formerly ACZ885), a human antibody targeting IL-1 beta, received US regulatory approval in June as a new therapy to treat children as young as four years old and adults with CAPS (Cryopyrin-Associated Periodic Syndromes), a group of serious life-long auto-inflammatory diseases.
Ilaris (canakinumab, anciennement ACZ885), un anticorps humain ciblant IL-1 bêta, a été autorisé en juin aux Etats-Unis comme nouveau traitement chez les enfants de plus de quatre ans et les adultes atteints des syndromes périodiques associés à la cryopyrine (CAPS), un groupe de maladies auto-inflammatoires sévères durant toute la vie.