2020
DOI: 10.1007/s10047-020-01184-x
|View full text |Cite
|
Sign up to set email alerts
|

Aortic insufficiency associated with Impella that required surgical intervention upon implantation of the durable left ventricular assist device

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

1
14
0

Year Published

2020
2020
2023
2023

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 8 publications
(15 citation statements)
references
References 11 publications
1
14
0
Order By: Relevance
“…[8][9][10][11][12]16,17 For example, Oishi et al describe two cases of AI caused by Impella 5.0 devices for two patients supported for 91 and 98 days. 12 In both of these cases, patients underwent at least one Impella LVAD exchange procedure; although one patient developed AI only after the final device was removed, the other patient developed AI during Impella LVAD support. 12 Similarly, Chandola et al describe a case of severe AI development after leaflet damage during Impella 5.0 explantation.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…[8][9][10][11][12]16,17 For example, Oishi et al describe two cases of AI caused by Impella 5.0 devices for two patients supported for 91 and 98 days. 12 In both of these cases, patients underwent at least one Impella LVAD exchange procedure; although one patient developed AI only after the final device was removed, the other patient developed AI during Impella LVAD support. 12 Similarly, Chandola et al describe a case of severe AI development after leaflet damage during Impella 5.0 explantation.…”
Section: Discussionmentioning
confidence: 99%
“…Worsening AI is particularly problematic with the use of some types of mechanical circulatory support and requires valve procedures for durable LVAD implantation. 12,13 To our knowledge, no studies have been performed to assess how common valvular complications are among Impella 5.0 and Impella CP devices. This study seeks to clarify the relationship and incidence between Impella LVAD use and secondary AR and MR, with an emphasis on Impella 5.0 and Impella CP use.…”
mentioning
confidence: 99%
“…In another report, the severity of AI worsened in 14.7% of patients, which included 3.3% of patients with new severe AI within 24 hours of Impella device support [ 5 ]. Since AI during LVAD support would cause recirculation and decreases LVAD efficiency, surgical treatment would be considered if greater than mild AI had occurred in patients with LVADs [ 6 , 7 ]. Robertson et al.…”
Section: Discussionmentioning
confidence: 99%
“…1 However, device-related complications, including hemolysis, stroke, limb ischemia, vascular complications, and valve injury have been reported. 2 Although rare, iatrogenic aortic valve (AV) injury can be caused by device placement across the valve, 1 , 36 which is not evident until after it is removed. A few case reports have described iatrogenic AV injury due to the Impella device implantation, but none have clarified the mechanism of injury.…”
Section: Introductionmentioning
confidence: 99%