| Literature DB >> 33452763 |
Nima Moghaddam1, Sean van Diepen2, Derek So3, Patrick R Lawler4,5,6, Christopher B Fordyce1.
Abstract
Cardiogenic shock (CS) portends high morbidity and mortality in the contemporary era. Despite advances in temporary mechanical circulatory supports (MCS), their routine use in CS to improve outcomes has not been established. Delays in diagnosis and timely delivery of care, disparities in accessing adjunct therapies such revascularization or MCS, and lack of a systematic approach to care of CS contribute to the poor outcomes observed in CS patients. There is growing interest for developing a standardized multidisciplinary team-based approach in the management of CS. Recent prospective studies have shown feasibility of CS teams in improving survival across a spectrum of CS presentations. Herein, we will review the rationale for CS teams focusing on evidence supporting its use in streamlining care, optimizing revascularization strategies, and patient identification and MCS selection. The proposed structure and flow of CS teams will be outlined. An in-depth analysis of four recent studies demonstrating improved outcomes with CS teams is presented. Finally, we will explore potential implementation hurdles and future directions in refining and widespread implementation of dedicated cross-specialty CS teams. © 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.Entities:
Keywords: Cardiogenic shock; Cardiogenic shock centres; Cardiogenic shock teams
Mesh:
Year: 2021 PMID: 33452763 PMCID: PMC8006679 DOI: 10.1002/ehf2.13180
Source DB: PubMed Journal: ESC Heart Fail ISSN: 2055-5822
Studies to date using dedicated cardiogenic shock teams and protocols
| Study | Number of patients | Quality Measures/Goals | Intervention(s) | Outcome(s) |
|---|---|---|---|---|
|
National Cardiogenic Shock Initiative
Prospective single‐arm study |
Total: 171 All patients with AMI‐CS *No control group |
1. MCS use pre‐PCI 2. Shock onset to device <90 min 3. Establish TIMI 3 Flow 4. Complete revascularization 5. Maintain CPO > 0.6 W 6. Maintain PAPi >0.9 7. Routine RHC use |
PCI: 171 of 171 patients MCS [Impella 2.5, CP, or RP]: 169 of 171 pts • 74% pre‐PCI • 7.1% during PCI • 18.9% post‐PCI RHC: 154 of 171 pts |
MCS pre‐PCI: 74% RHC usage: 92% Maintain CPO > 0.6 W: 62% Door to support time: 85 ± 63 min Survival to discharge: 72% |
|
Inova Heart and Vascular Institute Cardiogenic Shock Initiative
Prospective, pre‐intervention and post‐intervention study |
Total: 204 AMI‐CS: 81 ADHF‐CS: 122 *Control group not presented |
1. Rapid CS identification 2. Early MCS (LV and RV) 3. RHC: Thresholds at 24 h: i. Lactate <3 ii. CPO >0.6 W iii. PAPi >1.0 4. Minimize inotropes/vasopressors 5. Cardiac recovery |
PCI: 82 of 204 patients MCS: 135 of 204 pts • 35.3% IABP • 44.9% Impella only • 6.4% VA‐ECMO only • 13.5% Impella + VA‐ECMO RHC: 167 of 204 patients |
30 day survival: • Pre‐shock team implementation: 47% • After 1 year of shock team implementation: 58% • After 2 years of shock team implementation: 77% ( |
|
Utah Cardiac Recovery shock team
Prospective, pre‐intervention and post‐intervention study |
Total: 244
AMI‐CS:
Non‐AMI CS:
|
If STEMI: 1. Central arterial access for LVEDP measurement 2. Consideration for MCS and simultaneous angiogram‐PCI 3. Urgent RHC If not STEMI: 1. Urgent RHC 2. Consideration for MCS 3. Possible LHC as needed |
MCS: 123 of 123 in shock team (vs. control) • 30.2% IABP (vs. 62.8%) • 33.3% Impella (vs. 9.9%) • 8.9% VA‐ECMO (vs. 5%) • 27.6% combination of devices (vs.. 22.3%)
|
Shock to support time: 19 ± 5 (vs. 25 ± 8 h, Mean length of MCS support: 121 ± 13 (vs. 104 ± 16 h, In‐hospital survival: 61% (vs. 47.9%; 30 day all‐cause mortality HR 0.61 [95% CI, 0.41–0.93] |
|
University of Ottawa Heart Institute code shock team
Retrospective, CPO, MCS, PAPi, RHC pre‐intervention and post‐intervention study |
Total: 100
AMI‐CS:
Non‐AMI CS:
|
1. Confirmation of CS 2. Resuscitation 3. Medical optimization 4. Temporary MCS evaluation 5. Heart transplant, LVAD evaluation |
Revascularization: 12 of 100 patients—all AMI‐CS (75% PCI, 8% CABG, 17% both) MCS: 29 of 64 in shock team (vs. 10 of 36 in control) • 34% IABP (vs. 40%) • 28% Impella (vs. 10%) • 7% VA‐ECMO (vs. 10%) • 14% combination (vs. 11%)
RHC: 50 of 100 patients |
Temporary MCS use: 45% (vs. 28%, In‐hospital survival: 69% (vs. 61%; 30 day survival: 72% (vs. 69%; Long‐term survival: 67% (vs. 42%; Cumulative survival: HR 0.53 [95% CI 0.28–0.99] |
AMI, acute myocardial infarction; CABG, coronary artery bypass graft; CI, confidence interval; CPO, cardiac power output; CS, cardiogenic shock; HR, hazard ratio; IABP, intra‐aortic balloon pump; LVAD, left ventricular assist device; MCS, mechanical circulatory support; NS, not significant; PAPi, pulmonary artery pulsatility index; PCI, primary coronary intervention; RHC, right heart catheterization; VA‐ECMO, venoarterial extracorporeal membrane oxygenation.
Figure 1Survival outcomes pre‐shock and post‐shock team/protocol implementation in the (A) National Cardiogenic Shock Initiative, (B) INOVA Heart and Vascular Institute Shock Team Protocol, (C) Utah Cardiac Recovery shock team, and (D) University of Ottawa Heart Institute Code shock team. *Data from the IMPRESS in Severe Shock Trial. **No baseline institutional survival outcomes or controls reported in the National Cardiogenic Shock Initiative.