Traduction de «no significant » (Néerlandais → Français) :

TERMINOLOGIE

dood of significant letsel van patiënt of personeelslid als gevolg van fysieke aanval (vb. geweldpleging) die zich voordoet binnen of op terrein van gezondheidszorgfaciliteit
mort ou blessure importante d'un patient ou d'un membre du personnel résultant d'une agression physique (c.-à-d. coups et blessures) qui se produit dans ou sur le terrain d'un établissement de soins de santé

significant | belangrijk
signifiant | significatif

TRADUCTIONS EN CONTEXTE

Door het includeren van één nieuwe studie is het verschil tussen varenicline en nicotinevervangende therapie voor rookstop op 6 maanden niet langer significant (relatief risico van 1,13; 95%-betrouwbaarheidsinterval 0,94 tot 1,35) [ Cahill K.: Cochrane Database Syst Rev 2011; 3 Art. No.: CD005353].
Suite à l’inclusion d’une nouvelle étude, la différence entre la varénicline et le traitement de substitution nicotinique n’est plus significative en ce qui concerne le sevrage tabagique après 6 mois (risque relatif de 1,13; intervalle de confiance à 95% 0,94-1,35) [ Cahill K.: Cochrane Database Syst Rev 2011; 3 Art. No.: CD005353].

Tabel 1. Survival, pregnancy and delivery rates after single embryo transfer of human blastocysts vitrified with either the Cryotop or the CryoTip method. Cryotop (open) Cryotip (gesloten) Survived/vitrified rate (%) 221/227 (97) 82/88 (93) Pregnancy/transfer rate (%) 131/221 (59) 42/82 (51) Delivery/transfer rate (%) 113/221 (51) 39/82 (48) No significant differences between corresponding values were found.
Tableau 1. Survival, pregnancy and delivery rates after single embryo transfer of human blastocysts vitrified with either the Cryotop or the CryoTip method Cryotop TM (ouvert) Cryotip TM (fermé) Survived/vitrified rate (%) 221/227 (97) 82/88 (93) Pregnancy/transfer rate (%) 131/221 (59) 42/82 (51) Delivery/transfer rate (%) 113/221 (51) 39/82 (48)

Cushing's disease is a debilitating hormonal disorder for which there are currently no approved medicines. In another Phase III study, Onbrez Breezhaler was shown to be significantly better in the treatment of chronic obstructive pulmonary disease (COPD) than salmeterol, one of the current mainstays of treatment.
Dans une autre étude de phase III, Onbrez Breezhaler s’est montré bien meilleur pour traiter la broncho-pneumopathie chronique obstructive (BPCO) que salmétérol, l’un des principaux traitements courants.

The absolute probability of not smoking at 6 to 12 months was greater in trials which provided high-intensity additional support, rather than low-intensity, particularly with nicotine gum, although this was of no significance.
The absolute probability of not smoking at 6 to 12 months was greater in trials which provided high-intensity additional support, rather than lowintensity, particularly with nicotine gum, although this was of no significance.

In the first scenario, there is no significant difference between the respondents with regard to the choice of the place where the information is given (inside or outside the existing decision-making organs) according their current/past membership (or not) of the INAMI – RIZIV organs.
Only 26% would choose to inform the patient outside the existing organs, and with a stronger preference on informing after the decision is taken. In the first scenario, there is no significant difference between the respondents with regard to the choice of the place where the information is given (inside or outside the existing decision-making organs) according their current/past membership (or not) of the INAMI – RIZIV organs.

FTY720 (fingolimod), a novel oral development therapy for multiple sclerosis, showed continued low relapse rates after four years in patients with relapsing-remitting MS in an open-label Phase II extension study. The data, presented at the American Academy of Neurology (AAN) meeting in April, also showed no significant change in the safety profile from three to four years.
FTY720 (fingolimode), nouveau traitement par voie orale de la sclérose en plaques (SEP), a continué de montrer de faibles taux de rechute après quatre ans de traitement de patients souffrant de la forme cyclique (poussées/rémissions) de la SEP, selon les résultats d’un essai ouvert étendu de phase II. Les résultats présentés au congrès de l’American Academy of Neurology, qui a eu lieu en avril, ont également montré que le profil d’innocuité n’avait pas changé en passant de trois à quatre ans.