| Echo parameter | Study | Study design/setting | N | Measured outcome | Results |
---|---|---|---|---|---|---|
Left ventricle | Â | Â | Â | Â | Â | Â |
Systolic | EF | Sevilla Berrios et al. (2014) [33] | Meta-analysis | 585 | To evaluate the significance of reduced LVEF in patients with severe sepsis and septic shock. Primary outcome was association between depressed LVEF and 30-day mortality | Depressed LVEF had a sensitivity of 52% (95% CI 29–73%) and specificity of 63% (95% CI 53–71%) for mortality and was therefore not a sensitive nor specific predictor of mortality |
Huang et al. (2013) [32] | Meta-analysis | 762 | To evaluate the association of both reduced LVEF and increased LV dimensions with mortality in patients with severe sepsis and septic shock | No significant difference in LVEF and LV dimensions in survivors vs non-survivors | ||
Jardin et al. (1999) [24] | Single-center prospective cohort study | 90 | To evaluate changes in LV function, including LVEF and LV volumes, during volume resuscitation in patients with septic shock | LVEF was depressed in all patients. LV parameters were additionally unaffected by fluid loading | ||
Parker et al. (1984) [1] | Single-center prospective cohort study | 20 | To evaluate cardiac function in septic shock | 10/20 patients (50%) had depressed LVEF (< 0.40). Mean LVEF was lower among survivors (LVEF 0.32 ± 0.04) when compared to non-survivors. Mean ESV and EDV were increased in survivors | ||
GLS | Boissier et al. (2017) [17] | Single-center prospective cohort study/ICU | 132 | To evaluate the role of GLS, LVEF, and TDI in patients with septic shock. Primary outcome was the role of loading conditions on evaluation of cardiac contractility | GLS was impaired in a majority of the patients (> 70%); however, feasibility was limited (< 50%) | |
Chang et al. (2015) [39] | Multi-center prospective cohort study/ICU | 111 | To evaluate LV function, as well as the prognostic value of GLS, in septic patients. Primary outcome was both ICU and hospital mortality | GLS is an independent prognostic indicator of ICU mortality. Patients with GLS ≥ − 13% had higher ICU mortality rates (HR 4.34; p < 0.001) | ||
De Geer et al. (2015) [43] | Single-center prospective cohort study/ICU | 50 | To evaluate GLS in patients with septic shock. Primary outcomes were mortality at 30 and 90Â days | GLPS did not correlate between survivors and non-survivors and therefore could not be used to predict mortality | ||
Innocenti et al. (2016) [41] | Single-center prospective cohort study/ED observation unit | 147 | To evaluate LVEF and GLS in septic patients. Primary outcome was all-cause mortality at 7Â days | LVEF is not an independent indicator of prognosis | ||
Kalam et al. (2014) [37] | Meta-analysis | 5721 | To assess if GLS is a more accurate predictor of cardiovascular outcome compared to LVEF. Primary outcome was all-cause mortality. Secondary outcome was composite endpoint including cardiac death, malignant arrhythmia, and hospitalization | GLS is a better predictor of adverse outcomes (HR 0.50; p < 0.002) and mortality (HR 1.62; p = 0.009) than LVEF (HR 0.81; p = 0.572) | ||
Ng et al. (2016) [38] | Case–control study/ICU | 62 | To evaluate the role of GLS in the diagnosis of SMD. Primary outcome was to compare GLS values in patients with septic shock compared to patients with only sepsis | There was a significant difference in GLS values (− 14.5 vs –18.3%, p < 0.001) between patients with septic shock and sepsis. LVEF was not statistically significant between patients with septic shock and patients with sepsis | ||
Orde et al. (2014) [42] | Single-center prospective cohort study/ICU | 60 | To evaluate GLS in patients with severe sepsis or septic shock. Primary outcomes were mortality at 30Â days and 6Â months | No difference in mortality for LV GLS or GLS rate in survivors compared with non-survivors at 30Â days or 6Â months | ||
Palmieri et al. (2015) [40] | Single-center prospective cohort study/ED observation unit | 115 | To evaluate LV EF and peak GLS in patients with sepsis and septic shock. Primary outcome was death by any cause at 28 days from hospitalization | Abnormal GLS correlates significantly with mortality rate at 28 days. GLS values close to 0 demonstrated a higher mortality (HR 1.16%; p = 0.05). | ||
Zaky et al. (2016) [44] | Single-center prospective cohort study/ICU | 54 | To evaluate LVLS in patients with sepsis or septic shock. Primary outcomes were mechanical ventilation, ICU and hospital length of stay, and in-hospital mortality | Global LVLS was not associated with rates of mechanical ventilation, ICU or hospital length of stay, or in-hospital mortality | ||
Systolic mitral annular velocity (S′) | Chang et al. (2015) [39] | Multi-center prospective cohort study/ICU | 111 | To evaluate LV function, as well as the prognostic value of GLS, in septic patients. Primary outcome was both ICU and hospital mortality | There was no statistically significant difference in S′ between ICU non-survivors compared to survivors (11.0 ± 4.3 vs 11.4 ± 4.0; p < 0.66) | |
Weng et al. (2012) [49] | Single-center prospective cohort study/ICU | 61 | To evaluate the prognostic significance of several TDI variables, including systolic mitral annular velocity, S′, in patients with septic shock. Primary outcome was all-cause mortality | Non-survivors had a higher S′ when compared to survivors (11.0 vs 7.8 cm/s; p < 0.0001). Patients with S′ > 9 cm/s had a higher mortality rate (75 versus 17%; p < 0.0001). S′ > 9 cm/s had SN 75% and SP 86% to predict 90-day mortality | ||
Weng et al. (2013) [50] | Single-center prospective cohort study/ICU | 51 | To evaluate LV longitudinal systolic dysfunction and LV intraventricular systolic asynchrony assessed by TDI in patients with septic shock and normal LVEF. Primary outcome was all-cause mortality at 28Â days | Normal EF, LV longitudinal systolic dysfunction and LV systolic asynchrony assessed by TDI within 24Â h of onset of septic shock were associated with improved mortality at 28Â days | ||
MAPSE | Zhang et al. (2017) [65] | Case-control study/ICU | 45 | To evaluate LVEF, MAPSE, Sa, and TAPSE in patients with septic shock. Primary outcome was sepsis | MAPSE values were significantly lower in septic patients when compared to non-septic patients (p ≤ 0.001) | |
MPI | Nizamuddin et al. (2017) [78] | Single-center prospective cohort study/ICU | 47 | To assess if changes in LV MPI were associated with higher 90-day mortality in patients with severe sepsis. Primary outcome was all-cause mortality | Decline in MPI over the initial 24-h study period was associated with higher mortality at 90 days (p = 0.04) | |
Diastolic | e’ and E/e’ | Brown et al. (2012) [52] | Single-center prospective cohort study/ICU | 78 | To evaluate whether severity of diastolic dysfunction predicts mortality in patients with severe sepsis or septic shock. Primary outcome was mortality at 28 days | Grade I diastolic dysfunction was associated with increased mortality; grades II/III were not associated with increased mortality |
Landesberg et al. (2012) [54] | Single-center prospective cohort study/ICU | 262 | To evaluate the association between diastolic dysfunction and mortality in severe sepsis and septic shock. Primary outcomes were in-hospital mortality and overall mortality at 6 months to 2 years | Decreased septal e’ or increased septal E/e’ were the strongest independent predictors of mortality (HR 0.76, p ≤ 0.001 and HR 1.08, p ≤ 0.001, respectively) | ||
Rolando et al. (2015) [57] | Single-center prospective cohort study/ICU | 53 | To evaluate the prognostic significance of myocardial dysfunction, including E/e’ ratio, in patients with severe sepsis and septic shock. Primary outcome was hospital mortality | E/e’ is an independent predictor of hospitality mortality (OR = 1.36; p = 0.02). An E/e’ > 11 had a sensitivity of 50% and specificity of 94% for predicting ICU mortality | ||
Sanfilippo et al. (2017) [59] | Meta-analysis | 1507 | To evaluate the association of e’ and E/e’ with mortality in patients with severe sepsis or septic shock | A significant association was found between mortality and both a lower e’ (SC 0.33; 95% CI 0.05, 0.62; p = 0.02) and higher E/e’ (SC 0.33; 95% CI – 0.57, − 0.10; p = 0.006) in patients with severe sepsis and/or septic shock. There was high overall heterogeneity in both e’ and E/e’ analysis | ||
Sturgess et al. (2010) [56] | Single-center prospective cohort study/ICU | 21 | To evaluate the prognostic significance of TDI and cardiac biomarkers in septic shock. Primary outcome was hospital mortality | E/e’ is an independent predictor of hospital survival and is a better prognosticator than cardiac biomarkers. E/e’ was greater in non-survivors than survivors (15.32 ± 2.74 vs 9.05 ± 2.75, respectively; p = 0.0002) | ||
Lanspa et al. (2016) [60] | Single-center prospective cohort study/ICU | 167 | To compare the feasibility and prognostic significance of a simplified definition of diastolic dysfunction (using e’ and E/e’) with 2009 ASE guidelines. Primary outcome was 28-day mortality | Simplified definition had better feasibility (87 vs 35%); similar clinical outcomes between groups suggesting limited utility of LAVI and DT in this setting | ||
Right ventricle | Â | Â | Â | Â | Â | Â |
Systolic | TAPSE | Gajanana et al. (2015) [64] | Single-center prospective cohort study/ICU | 120 | To evaluate the prognostic value of TAPSE in patients with critical illness | A reduced TAPSE measurement (< 2.4 cm) was correlated with increased in-hospital mortality (χ(2) = 4.6, P = 0.03) and a longer length of hospital stay |
TAPSE TDI RV FAC | Vallabhajosyula et al. (2017) [67] | Single-center retrospective cohort study/ICU | 388 | To evaluate the prognostic significance RV dysfunction in patients with severe sepsis and septic shock. Primary outcome was 1-year survival | Isolated RV dysfunction is an independent predictor of 1-year survival (HR 1.6; p = 0.002). Combined RV/LV dysfunction was not an independent predictor of 1-year survival (HR 0.9; p = 0.52) |