1954
|
Sign up to set email alerts
Detachment of Retina With Use of Diisopropyl Fluorophosphate (Fluropryl) in Treatment of Glaucoma
Search citation statements
Order By: Relevance
Paper Sections
Select...
19
2
0
0
Citation Types
0
4
0
0
Year Published
Range
1953
19532025
2025Publication Types
Select...
13
4
1
1
Relationship
0
19
Authors
Journals
Cited by 19 publications
(4 citation statements)
References 0 publications
0
4
0
0
Order By: Relevance
Abstract
Smart CitationsHow this paper cites the one you are viewing
“…Lipophilic drugs can cross the blood-brain barrier, resulting in neurological adverse effects such as depression, decreased libido, lethargy, and irritability. This is most frequently reported with β-blockers, followed by α-agonists (2.7-19.9%) and direct-acting parasympathomimetics like pilocarpine and carbachol [12,26,[38][39][40][41][173][174][175][176]. Furthermore, drugs that modulate the sympathetic or parasympathetic nervous systems, or affect blood osmolarity, may increase the risk of cardiovascular complications.…”
Section: Discussion
mentioning
confidence: 99%
“…Due to the lipophilicity of most β-blockers, they readily cross the blood-brain barrier, capable of inducing neurological symptoms [172]. These neurological adverse events include depression, decreased libido, anxiety, nausea, lethargy, emotional lability or irritability, and anorexia [26,[173][174][175][176]. It is important to note that most of these events were associated with timolol maleate, the earliest topical β-blocker approved for use.…”
Section: Beta (β)-Blockers
mentioning
confidence: 99%
Abstract
Smart CitationsHow this paper cites the one you are viewing
“…Lipophilic drugs can cross the blood-brain barrier, resulting in neurological adverse effects such as depression, decreased libido, lethargy, and irritability. This is most frequently reported with β-blockers, followed by α-agonists (2.7-19.9%) and direct-acting parasympathomimetics like pilocarpine and carbachol [12,26,[38][39][40][41][173][174][175][176]. Furthermore, drugs that modulate the sympathetic or parasympathetic nervous systems, or affect blood osmolarity, may increase the risk of cardiovascular complications.…”
Section: Discussion
mentioning
confidence: 99%
“…Due to the lipophilicity of most β-blockers, they readily cross the blood-brain barrier, capable of inducing neurological symptoms [172]. These neurological adverse events include depression, decreased libido, anxiety, nausea, lethargy, emotional lability or irritability, and anorexia [26,[173][174][175][176]. It is important to note that most of these events were associated with timolol maleate, the earliest topical β-blocker approved for use.…”
Section: Beta (β)-Blockers
mentioning
confidence: 99%
Abstract
Smart CitationsHow this paper cites the one you are viewing
“…Lipophilic drugs can cross the blood-brain barrier, resulting in neurological adverse effects such as depression, decreased libido, lethargy, and irritability. This is most frequently reported with β-blockers, α agonists, and direct-acting parasympathomimetics like pilocarpine and carbachol [9,61,[76][77][78][159][160][161][162]164]. Furthermore, drugs that modulate the sympathetic or parasympathetic nervous systems, or affect blood osmolarity, may increase the risk of cardiovascular complications.…”
Section: Discussion
mentioning
confidence: 99%
“…Due to the lipophilicity of most β-blockers, they readily cross the blood-brain barrier, capable of inducing neurological symptoms [158]. These neurological adverse events include depression, decreased libido, anxiety, nausea, lethargy, emotional lability or irritability, and anorexia [61,[159][160][161][162]. Most of these events have been associated with timolol maleate, the earliest topical β-blocker approved for use.…”
Section: βEta (β) Blockers
mentioning
confidence: 99%
Abstract
Smart CitationsHow this paper cites the one you are viewing
“…Lipophilic drugs can cross the blood-brain barrier, resulting in neurological adverse effects such as depression, decreased libido, lethargy, and irritability. This is most frequently reported with β-blockers, followed by α-agonists (2.7-19.9%) and direct-acting parasympathomimetics like pilocarpine and carbachol [12,26,[38][39][40][41][173][174][175][176]. Furthermore, drugs that modulate the sympathetic or parasympathetic nervous systems, or affect blood osmolarity, may increase the risk of cardiovascular complications.…”
Section: Discussion
mentioning
confidence: 99%
“…Due to the lipophilicity of most β-blockers, they readily cross the blood-brain barrier, capable of inducing neurological symptoms [172]. These neurological adverse events include depression, decreased libido, anxiety, nausea, lethargy, emotional lability or irritability, and anorexia [26,[173][174][175][176]. It is important to note that most of these events were associated with timolol maleate, the earliest topical β-blocker approved for use.…”
Section: Beta (β)-Blockers
mentioning
confidence: 99%
Abstract
Smart CitationsHow this paper cites the one you are viewing
“…Lipophilic drugs can cross the blood-brain barrier, resulting in neurological adverse effects such as depression, decreased libido, lethargy, and irritability. This is most frequently reported with β-blockers, α agonists, and direct-acting parasympathomimetics like pilocarpine and carbachol [9,61,[76][77][78][159][160][161][162]164]. Furthermore, drugs that modulate the sympathetic or parasympathetic nervous systems, or affect blood osmolarity, may increase the risk of cardiovascular complications.…”
Section: Discussion
mentioning
confidence: 99%
“…Due to the lipophilicity of most β-blockers, they readily cross the blood-brain barrier, capable of inducing neurological symptoms [158]. These neurological adverse events include depression, decreased libido, anxiety, nausea, lethargy, emotional lability or irritability, and anorexia [61,[159][160][161][162]. Most of these events have been associated with timolol maleate, the earliest topical β-blocker approved for use.…”
Section: βEta (β) Blockers
mentioning
confidence: 99%
Abstract
Smart CitationsHow this paper cites the one you are viewing
“…Lipophilic drugs can cross the blood-brain barrier, resulting in neurological adverse effects such as depression, decreased libido, lethargy, and irritability. This is most frequently reported with β-blockers, followed by α-agonists (2.7-19.9%) and direct-acting parasympathomimetics like pilocarpine and carbachol [12,26,[38][39][40][41][173][174][175][176]. Furthermore, drugs that modulate the sympathetic or parasympathetic nervous systems, or affect blood osmolarity, may increase the risk of cardiovascular complications.…”
Section: Discussion
mentioning
confidence: 99%
“…Due to the lipophilicity of most β-blockers, they readily cross the blood-brain barrier, capable of inducing neurological symptoms [172]. These neurological adverse events include depression, decreased libido, anxiety, nausea, lethargy, emotional lability or irritability, and anorexia [26,[173][174][175][176]. It is important to note that most of these events were associated with timolol maleate, the earliest topical β-blocker approved for use.…”
Section: Beta (β)-Blockers
mentioning
confidence: 99%
Abstract
Smart CitationsHow this paper cites the one you are viewing
“…Lipophilic drugs can cross the blood-brain barrier, resulting in neurological adverse effects such as depression, decreased libido, lethargy, and irritability. This is most frequently reported with β-blockers, α agonists, and direct-acting parasympathomimetics like pilocarpine and carbachol [9,61,[76][77][78][159][160][161][162]164]. Furthermore, drugs that modulate the sympathetic or parasympathetic nervous systems, or affect blood osmolarity, may increase the risk of cardiovascular complications.…”
Section: Discussion
mentioning
confidence: 99%
“…Due to the lipophilicity of most β-blockers, they readily cross the blood-brain barrier, capable of inducing neurological symptoms [158]. These neurological adverse events include depression, decreased libido, anxiety, nausea, lethargy, emotional lability or irritability, and anorexia [61,[159][160][161][162]. Most of these events have been associated with timolol maleate, the earliest topical β-blocker approved for use.…”
Section: βEta (β) Blockers
mentioning
confidence: 99%