Vertaling van "rate of treatment " (Nederlands → Frans) :

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.

Spontaneous cessation rate: 2.5% OR counselling only: 1.73 Incremental OR NRT gum (relative to counselling only): 1.63 Incremental OR NRT patch (relative to counselling only): 1.79 Incremental OR NRT spray (relative to counselling only): 2.35 Incremental OR NRT inhaler (relative to counselling only): 2.14 Incremental OR bupropion (relative to counselling only): 2.30 % of smokers still under treatment after the first month: 50% (range 40-60% in sensitivity analysis) % of smokers still under treatment after the second month: 20% (range 15-25% in sensitivity analysis) Lifetime relapse probability after one year of abstinence: 35% (range 10-50% in sensitivity analysis) Effect of smoking cessation on mortality derived from the results of the American Cancer Society Prevention Study II. The mortality rate for former smokers was projected by calculating a weighted average of the incremental differentials between mortality rates of neversmokers and smokers, weighted according to the duration of abstinence.
Spontaneous cessation rate: 2.5% OR counselling only: 1.73 Incremental OR NRT gum (relative to counselling only): 1.63 Incremental OR NRT patch (relative to counselling only): 1.79 Incremental OR NRT spray (relative to counselling only): 2.35 Incremental OR NRT inhaler (relative to counselling only): 2.14 Incremental OR Buproprion (relative to counselling only): 2.30 % of smokers still under treatment after the first month: 50% (range 40-60% in sensitivity analysis) % of smokers still under treatment after the second month: 20% (range 15-25% in sensitivity analysis) Lifetime relapse probability after one year of abstinence: 35% (range 10-50% in sensitivity analysis) Effect of smoking cessation on mortality derived from the results of the American Cancer Society Prevention Study II. The mortality rate for former smokers was projected by calculating a weighted average of the incremental differentials between mortality rates of neversmokers and smokers, weighted according to the duration of abstinence.

De secundaire eindpunten omvatten progressievrije overleving (progression-free survival, PFS), objectieve mate van respons (objective response rate, ORR), mate van klinisch voordeel, tijd tot het falen van de behandeling (time to treatment failure, TTF), en de ”quality adjusted survival”-meting.
Les critères secondaires étaient la survie sans progression (SSP), le taux de réponse objective (RO), le taux de bénéfice clinique, le temps jusqu'à échec thérapeutique (TET) et la survie ajustée selon la qualité de vie.

One Hundred Thousand Cases of Influenza With a Death Rate of One-Fortieth of That Officially Reported Under Conventional Medical Treatment Griep, lymfatische technieken, lymfe, arterial rule [ publicatie ] [ 1/09/2008 ]
One Hundred Thousand Cases of Influenza With a Death Rate of One-Fortieth of That Officially Reported Under Conventional Medical Treatment Grippe, lymfatic technique, lymph, arterial rule [ publication ] [ 1/09/2008 ]

Relapse rate was het aandeel proefpersonen met een niet-detecteerbaar HCV-RNA bij End of Treatment (EOT) en een detecteerbaar HCV-RNA bij End of Follow-up (EOF) bij proefpersonen die niet detecteerbaar waren bij EOT en bij wie gegevens over EOF niet ontbraken.
Le taux de rechute était la proportion de sujets présentant un taux d’ARN-VHC indétectable à la fin du traitement (FDT) et un taux d’ARN-VHC détectable à la fin du suivi (FDS) parmi les sujets ayant un taux indétectable à la fin du traitement (FDT) et sans données manquantes à la fin du suivi (FDS).

HCV Relapse rate was het aandeel proefpersonen met niet-detecteerbaar HCV-RNA bij End of Treatment (EOT) en detecteerbaar HCV-RNA bij End of Follow-up (EOF) bij proefpersonen die niet detecteerbaar waren bij EOT en bij wie gegevens over EOF niet ontbraken.
Le taux de rechute pour le VHC était la proportion de sujets présentant un taux d’ARN-VHC indétectable à la fin du traitement (FDT) et un taux d’ARN-VHC détectable à la fin du suivi (FDS) parmi les sujets ayant un taux indétectable à la fin du traitement (FDT) et sans données manquantes à la fin du suivi (FDS).

Tabel 6 Sustained Virologic Response (SVR)*, End of Treatment (EOT) en HCV Relapse Rates † bij niet eerder behandelde proefpersonen met co-infectie met hiv
Tableau 6 Réponse Virologique Prolongée (RVP)*, Fin De Traitement (FDT) et taux de rechute † du VHC chez les sujets préalablement non-traités et co-infectés par le VIH