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1 microbial stewardship enhanced antimicrobial de-escalation.
2 resistant Gram-negative bacteria followed by de-escalation.
3 h cohorts at the starting dose required dose de-escalation.
4 eltamivir in infants aged <2 years in an age-de-escalation, adaptive design with a targeted systemic
6 ty of axillary management, and any policy of de-escalation and avoidance of morbidity must not compro
10 re has been a shift to a procedural conflict de-escalation approach to addressing clinical questions
12 We aimed to examine the effects of treatment de-escalation as a prelude to complete cessation, not on
13 rt-course treatment regimens and the use of 'de-escalation' as a strategy for antibiotic prescribing.
16 terature to identify studies reporting after de-escalation (drug cessation or dose reduction) of anti
17 we analyzed findings from 69 studies (18 on de-escalation [drug cessation or dose reduction] of immu
19 It also has the potential to enable early de-escalation from broad-spectrum empirical antimicrobia
20 omodulator monotherapy, 8 on immunomodulator de-escalation from combination therapy, and 43 on de-esc
21 had a dose-limiting toxic effect in the dose de-escalation group receiving FOLFIRINOX plus PF-0413630
22 on-phase group (n=33) with those in the dose de-escalation group that received PF-04136309 at the rec
25 ysis the resulting theoretical definition of de-escalation in healthcare is "a collective term for a
26 olecular testing had the potential to enable de-escalation in number and/or spectrum of antimicrobial
27 late production; a trend toward evolutionary de-escalation in the numbers and diversity of glucosinol
28 py, we classified patients into four groups: de-escalation (interruption of an antimicrobial agent or
29 y purport to use, the antecedents that their de-escalation intervention is targeting, its key attribu
31 g a robust evidence-base for the efficacy of de-escalation is striking and must, at least in part, be
33 nsivists and infectious disease specialists, de-escalation may actually be possible in <50% of cases.
34 scalation than the control group (34%), with de-escalation occurring sooner in the BCID group (48 h;
35 most commonly reported environment in which de-escalation occurs, and nursing the disciplinary group
36 calation from combination therapy, and 43 on de-escalation of anti-TNF agents, including 3 during pre
37 e VAP so that appropriate discontinuation or de-escalation of antimicrobial therapy can be initiated
38 matic review and meta-analysis of studies of de-escalation of BMAs, and two randomized trials of BMAs
39 rminant of poor outcomes in this population, de-escalation of chemotherapy intensity might be feasibl
40 s change in antimicrobial prescriptions (ie, de-escalation of empirical antimicrobial therapy or comm
42 mucosal and pharyngeal-related DLT required de-escalation of gemcitabine dose in successive patient
44 -limiting myelosuppression persisted despite de-escalation of TOPO to 0.3 mg/m(2)/d and use of G-CSF.
46 of the 18 patients and was managed with dose de-escalation or discontinuation per standard of care.
48 from Gram stain to appropriate antimicrobial de-escalation or escalation was shortest in the rmPCR/AS
49 econdary outcomes were time to antimicrobial de-escalation or escalation, length of stay (LOS), morta
51 calation was shortest in the rmPCR/AS group (de-escalation: rmPCR/AS 21 hours, control 34 hours, rmPC
52 igned by using a traditional dose-escalation/de-escalation rule based on observed toxicities in the c
53 s are exploring the feasibility of treatment de-escalation strategies in patients with a negative int
56 under suboptimal conditions, an antigen dose de-escalation study was performed in the presence of eit
63 s to the implementation and effectiveness of de-escalation techniques in practice are not well unders
64 ntly conceptualised by staff as a feature of de-escalation techniques, yet, there was evidence of a l
66 2%) groups had higher rates of antimicrobial de-escalation than the control group (34%), with de-esca
69 he starting dose of 12 mg/m(2)/d resulted in de-escalation to 8 mg/m(2)/d and subsequent re-escalatio
70 was myelosuppressive, requiring several dose de-escalations to 2 mg/m(2), the dose suggested for phas
73 ulated radiation therapy, immunotherapy, and de-escalation trials, might allow for improved treatment
80 ssessment of antimicrobial therapy daily for de-escalation, when appropriate (1B); infection source c
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