2014
DOI: 10.1016/j.purol.2014.06.003
|View full text |Cite
|
Sign up to set email alerts
|

Traitement anticholinergique de l’hyperactivité vésicale de la personne âgée et ses impacts sur la cognition. Revue de la littérature

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
8
0

Year Published

2016
2016
2020
2020

Publication Types

Select...
5
3

Relationship

0
8

Authors

Journals

citations
Cited by 23 publications
(8 citation statements)
references
References 32 publications
0
8
0
Order By: Relevance
“…As a result of its prolonged release formulation and its 7–9-hr half-life, fesoterodine can be taken daily as a single dose without the risk of accumulation of the active ingredient 18. Finally, fesoterodine has a very low risk of crossing the blood-brain barrier19 and has no significant effect on cognitive function, which has been confirmed in clinical trials 10,20,21…”
Section: Second Casementioning
confidence: 78%
“…As a result of its prolonged release formulation and its 7–9-hr half-life, fesoterodine can be taken daily as a single dose without the risk of accumulation of the active ingredient 18. Finally, fesoterodine has a very low risk of crossing the blood-brain barrier19 and has no significant effect on cognitive function, which has been confirmed in clinical trials 10,20,21…”
Section: Second Casementioning
confidence: 78%
“…Trospium and fesoterodine were reported to have significantly lower CNS penetration than other anticholinergic agents in an in vitro study [55]. The relatively high molecular weight and low lipophilicity of fesoterodine, hydrophilic trospium, and the active metabolite of fesoterodine, 5-hydroxymethyl tolterodine, suggest that only very small amounts may cross the BBB [55,66,67]. A study also reported the effects of taking fesoterodine for 12 weeks in older patients with urge incontinence and revealed no deterioration in cognitive function when subjects were assessed by the mean Mini-Mental Status Examination (MMSE) [68].…”
Section: Anticholinergicsmentioning
confidence: 99%
“…Antimuscarinic agents cross the BBB via passive diffusion according to their lipophilicity and molecular weight. 34 38 Some antimuscarinics are removed from the brain via an active transport mechanism facilitated by Pgp, which limits the levels of drugs in the brain. The BBB can be impaired by different causes, including aging, medication, or systemic diseases (inflammatory; neurodegenerative diseases, such as Alzheimer’s, Parkinson’s disease, and multiple sclerosis; vascular conditions; neoplasia; brain edema; meningitis; and trauma).…”
Section: Dealing With Oab In Patients At Risk Of Cognitive Impairmentmentioning
confidence: 99%
“…It has the highest molecular weight of the antimuscarinics and low lipophilicity ( Table 1 ); moreover, the active moiety of fesoterodine, 5-HMT, is pumped out of the brain by Pgp, an efflux transporter. 7 , 33 , 38 , 40 – 42 Trospium is a quaternary amine and a hydrophilic molecule that does not cross the BBB.…”
Section: Dealing With Oab In Patients At Risk Of Cognitive Impairmentmentioning
confidence: 99%
See 1 more Smart Citation