2021
DOI: 10.1253/circrep.cr-21-0016
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Impella Support as a Bridge to Surgery for Severe Mitral Regurgitation With Cardiogenic Shock

Abstract: Background: Cardiogenic shock due to acute severe mitral regurgitation is characterized by multiple organ failure and acute pulmonary edema, leading to a high risk of mortality. Methods and Results: We report on a patient with acute, severe mitral regurgitation complicated by cardiogenic shock, refractory to both inotrope treatment and intra-aortic balloon pump support. The patient was successfully bridged to surgery with an Impella CP, a percutaneous left ventricular a… Show more

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Cited by 6 publications
(6 citation statements)
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“…Baseline hemodynamics in patients with trace/mild FMR were not significantly different from patients with moderate and moderate-tosevere/severe FMR. At 24 hours post-Impella implant, there was a significant decrease in CVP (12 [8-14] to 9 [7][8][9][10][11], p ¼ 0.012), a significant decrease in pulmonary artery diastolic pressure (PADP; 25 [19][20][21][22][23][24][25][26][27] to 18 [14-21], p ¼ 0.002) and pulmonary capillary wedge pressure (22 [16][17][18][19][20][21][22][23][24][25][26] to 17 [10][11][12][13][14][15][16][17][18][19][20], p ¼ 0.008), a significant drop in systemic vascular resistance (1541 [1225-1914] to 960 [864-1183], p 0.001), a significant decrease in serum lactate levels (1.9 [1.2-2.7] to 1.3 [1-1.7], p ¼ 0.046), and a significant decrease in vasoactive-inotrope score (VIS; 12 [7][8][9][10][11][12][13][14][15][16][17][18]…”
Section: Resultsmentioning
confidence: 99%
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“…Baseline hemodynamics in patients with trace/mild FMR were not significantly different from patients with moderate and moderate-tosevere/severe FMR. At 24 hours post-Impella implant, there was a significant decrease in CVP (12 [8-14] to 9 [7][8][9][10][11], p ¼ 0.012), a significant decrease in pulmonary artery diastolic pressure (PADP; 25 [19][20][21][22][23][24][25][26][27] to 18 [14-21], p ¼ 0.002) and pulmonary capillary wedge pressure (22 [16][17][18][19][20][21][22][23][24][25][26] to 17 [10][11][12][13][14][15][16][17][18][19][20], p ¼ 0.008), a significant drop in systemic vascular resistance (1541 [1225-1914] to 960 [864-1183], p 0.001), a significant decrease in serum lactate levels (1.9 [1.2-2.7] to 1.3 [1-1.7], p ¼ 0.046), and a significant decrease in vasoactive-inotrope score (VIS; 12 [7][8][9][10][11][12][13][14][15][16][17][18]…”
Section: Resultsmentioning
confidence: 99%
“…This study also found that neither baseline nor residual MR affected survival at 24 months post-LVAD implant. 13 The Impella 5.5 can provide flows comparable to durable LVADs, but only small case series have examined the use of Impella in the setting of CS with concomitant severe MR. 9,10 In our small, retrospective cohort, we make 3 important observations: (1) the Impella 5.5 did not appear to acutely (within 24 hours) ameliorate moderate or greater FMR; (2) Impella 5.5 did provide significant left ventricular unloading as evidenced by a reduction in intracardiac filling pressures and lactate clearance as well as a significant decrease in systemic vascular resistance and vasoactive-inotrope score (Table 1); and (3) a significant proportion of patients in our cohort (42%) experienced NHR on Impella 5.5 support, regardless of baseline/residual FMR severity (Figure 1). These observations were made across the entire cohort, regardless of baseline severity of FMR.…”
Section: Discussionmentioning
confidence: 99%
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“…The IABP provides a rescue strategy for afterload reduction when haemodynamic instability limits the use of vasodilators [ 43 ]. VA ECMO and Impella devices are emerging alternatives to provide temporary mechanical support as a bridge to surgical intervention in acute MR [ 44 , 45 ].
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Section: Mr In Critical Illnessmentioning
confidence: 99%
“…1 In the United States, the use of Impella devices is increasing for multiple indications. 2,3 An LV thrombus is a contraindication for inserting any Impella device. 4 However, thrombus formation can occur after Impella support is initiated by a combination of profound impairment of LV contractility, a poor flow state at the time of Impella 5.5 insertion, turbulent flow in the LV, or the thrombogenic nature of the device.…”
Section: Introductionmentioning
confidence: 99%