2018
DOI: 10.1111/pace.13342
|View full text |Cite
|
Sign up to set email alerts
|

Propofol for implantable cardioverter defibrillator implantation in patients with Brugada syndrome

Abstract: ICD implantation without significant ECG changes or adverse outcomes is feasible under propofol sedation in patients with Brugada syndrome. However, because of significant hemodynamic changes and respiratory compromise, close monitoring and meticulous propofol dose titration is warranted.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
7
0

Year Published

2018
2018
2022
2022

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 8 publications
(7 citation statements)
references
References 21 publications
0
7
0
Order By: Relevance
“…12 Recent studies have found lower incidence of ventricular arrhythmias following administration of a single dose of propofol in an unselected cohort as well as adults with BrS. [13][14][15][16][17] Interestingly, a bolus dose of propofol has been shown to attenuate BrS-associated arrhythmogenic risk in high-risk adults with BrS patients in a recent study. 18 In contrast to adults in these studies [13][14][15][16][17][18] who did not have clinically significant symptoms following propofol administration (mean dose 2.2-3.3 mg/kg), those with propofol infusion syndrome were administered a higher dose of propofol (4.5-7.3 mg/kg/hour).…”
Section: Discussionmentioning
confidence: 97%
See 2 more Smart Citations
“…12 Recent studies have found lower incidence of ventricular arrhythmias following administration of a single dose of propofol in an unselected cohort as well as adults with BrS. [13][14][15][16][17] Interestingly, a bolus dose of propofol has been shown to attenuate BrS-associated arrhythmogenic risk in high-risk adults with BrS patients in a recent study. 18 In contrast to adults in these studies [13][14][15][16][17][18] who did not have clinically significant symptoms following propofol administration (mean dose 2.2-3.3 mg/kg), those with propofol infusion syndrome were administered a higher dose of propofol (4.5-7.3 mg/kg/hour).…”
Section: Discussionmentioning
confidence: 97%
“…[13][14][15][16][17] Interestingly, a bolus dose of propofol has been shown to attenuate BrS-associated arrhythmogenic risk in high-risk adults with BrS patients in a recent study. 18 In contrast to adults in these studies [13][14][15][16][17][18] who did not have clinically significant symptoms following propofol administration (mean dose 2.2-3.3 mg/kg), those with propofol infusion syndrome were administered a higher dose of propofol (4.5-7.3 mg/kg/hour). 8 EKG changes in patients with BrS phenocopy due to propofol infusion syndrome have been shown to normalise as early as 24 hours after withdrawal of propofol, and provocative testing with sodium channel blockers typically does not reveal an underlying predisposition to BrS.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…It has been suggested that propofol should be avoided in patients with BrS due to its arrhythmogenic potential ( 4 ). However, it has been safely used for sedation during the implantation of an ICD ( 24 ). In our case, low-dose propofol was successfully used when the patient became a little restless halfway through surgery.…”
Section: Discussionmentioning
confidence: 99%
“…2 It remains unclear whether propofol and/or one of its metabolites is responsible for the reported adverse cardiac electrical effects. Moreover, cardiac electrical abnormalities have persisted well beyond the expected duration of effect for propofol, 3,4 and complete elimination period for several other drugs 5 suggesting permanent disruption of relevant ion channels or downstream proteins could underlie this observation.…”
Section: Utkarsh Kohlimentioning
confidence: 98%