Skip to main content

Incremental prognostic value of echocardiography of left ventricular remodeling and diastolic function in STICH trial



We sought to determine which echocardiographic markers of left ventricular (LV) remodeling and diastolic dysfunction can contribute as incremental and independent prognostic information in addition to current clinical risk markers of ischemic LV systolic dysfunction in the Surgical Treatment for Ischemic Heart Failure (STICH) trial.

Methods and results

The cohort consisted of 1511 of 2136 patients in STICH for whom baseline transmitral Doppler (E/A ratio) could be measured by an echocardiographic core laboratory blinded to treatment and outcomes, and prognostic value of echocardiographic variables was determined by a Cox regression model. E/A ratio was the most significant predictor of mortality amongst diastolic variables with lowest mortality for E/A closest 0.8, although mortality was consistently low for E/A 0.6 to 1.0. Mortality increased for E/A < 0.6 and > 1.0 up to approximately 2.3, beyond which there was no further increase in risk. Larger LV end-systolic volume index (LVESVI) and E/A < 0.6 and > 1.0 had incremental negative effects on mortality when added to a clinical multivariable model, where creatinine, LVESVI, age, and E/A ratio accounted for 74% of the prognostic information for predicting risk. LVESVI and E/A ratio were stronger predictors of prognosis than New York Heart Association functional class, anemia, diabetes, history of atrial fibrillation, and stroke.


Echocardiographic markers of advanced LV remodeling and diastolic dysfunction added incremental prognostic value to current clinical risk markers. LVESVI and E/A ratio outperformed other markers and should be considered as standard in assessing risks in ischemic heart failure. E/A closest to 0.8 was the most optimal filling pattern.

Peer Review reports


The Surgical Treatment for Ischemic Heart Failure (STICH) trial represents one of the largest cohorts of ischemic cardiomyopathy.

Diastolic dysfunction of advanced LV remodeling can contribute incremental prognostic value to current clinical markers of heart failure severity: these may have different effects on patients treated with CABG vs medical therapy, but does not impact outcomes differently in patients treated with CABG alone vs CABG+ SVR.

Inclusion of E/A ratio and LVESVI could enhance prognostic models for ischemic heart failure.

E/A ratio closest to 0.8 is the most optimal filling pattern in ischemic HFrEF.


Prognosis in heart failure with reduced ejection fraction (HFrEF) due to ischemic cardiomyopathy is affected by the severity of left ventricular (LV) remodeling as well as clinical co-morbidities including anemia and renal failure [1, 2]. Although many echocardiographic markers of LV remodeling, including LV size and geometry, functional mitral regurgitation (MR), diastolic dysfunction, and right ventricular (RV) dysfunction, are known to impact on mortality in HFrEF [3,4,5,6], only EF is included in most clinical HFrEF prognostic models [7, 8]. Whether the inclusion of diastolic filling parameters or other echocardiographic variables added to current clinical risk markers will have incremental prognostic value is not well defined. The Surgical Treatment for Ischemic Heart Failure (STICH) trial represents one of the largest cohorts of patients with HFrEF due to ischemic cardiomyopathy and is therefore an ideal population in which to determine the incremental prognostic value of echocardiographic markers of LV remodeling when combined with clinical risk markers. We hypothesized that diastolic filling parameters would remain the most prognostically significant marker amongst other markers in ischemic HFrEF.


Patient selection

The STICH study design has been described [9, 10]. Between July 2002 and May 2007, 2136 patients with ischemic HFrEF (LVEF ≤35%) amenable to coronary artery bypass grafting (CABG) were enrolled from 127 clinical centers in 26 countries. Patients were stratified into the Hypothesis 1 (H1; CABG vs. medical therapy) and Hypothesis 2 (H2; CABG vs. CABG + surgical ventricular reconstruction) cohorts. Eligibility for surgical ventricular reconstruction (SVR) was determined by the presence of dominant anterior/ apical dyskinesia; on this basis 1000 patients were enrolled into H2 [9, 11]. Only the 1511 patients from both cohorts with adequate baseline echocardiographic systolic, diastolic left ventricular (LV) function and RV function assessment within 90 days of randomization were included.

Echocardiography Core lab analysis

Echocardiographic data for STICH was prospectively acquired using a standardized protocol and a comprehensive list of baseline measurements including the number of patients feasible measurements was reported [4]. MR and RV systolic function were graded qualitatively; quantitative measurements were not prospectively acquired [3]. RV function was assessed prospectively by visual interpretation and categorized as normal, mild, moderate, or severe dysfunction. The appreciation of the overall mechanical function of the RV was mainly based on the extent of RV free wall segmental motion, wall thickening, RV cavity size, and subjective assessment of RV area change (normal> 50%, mild 30–50%, moderate 20–30%, and severe < 20% from diastole to systole). RV assessment was derived from the parasternal long-axis, apical 4-chamber, and subcostal views. This assessment was based on visual assessment by an experienced Echocardiography Core Laboratory physician [12, 13]. The severity of MR was primarily determined by the physician’s visual assessment of width, depth, and area of mitral regurgitation jet. In addition, effective regurgitant orifice (ERO) was determined using the PISA (proximal isovelocity surface area) method, as previously described whenever possible.

The Mayo Clinic Echocardiography Core Laboratory (Rochester, MN) analyzed echocardiographic data in a blinded fashion without knowledge of clinical or laboratory data and quality assurance methods have been described [3, 14, 15]. Patients in atrial fibrillation or who had undergone previous mitral valve surgery were excluded from diastolic function analysis.

Eleven echocardiographic variables were selected for analysis based on prior data: E and A velocity, E/A ratio, deceleration time, mitral annular e’ velocity, E/e’ ratio, LVEF, LV end-systolic volume index (LVESVI), LV end-diastolic volume index (LVEDVI), sphericity index, RV systolic function, severity of MR, and left atrial volume index (area-length method) [3,4,5,6, 16,17,18]. Estimated RV systolic pressure was measurable in only 449 of 2136 patients and was excluded from analysis [3].

Statistical analysis

Data were summarized using the mean and standard deviation or the median with 25th and 75th percentiles for continuous variables and frequencies and percentages for categorical variables. The distribution of continuous variables amongst groups was compared by the non-parametric Kruskal-Wallis test, and categorical variables with conventional chi-square statistics.

The relationship of each variable to mortality was assessed with the Cox regression model [19]. Linearity or non-linearity of the relationship with respect to the log hazard ratio was assessed using restricted cubic spline functions within the framework of the Cox model [20]. The strength of these relationships was characterized using chi-square statistics obtained from the modeling process. Both univariable and multivariable modeling were performed. Relative risks were expressed as hazard ratios with associated 95% confidence intervals and were generated from the Cox model. Due to missing data from suboptimal echo images 25 datasets were created and combined using multiple imputation and analyses performed for both the original and imputed datasets [21].

The multivariable model included clinical prognostic markers: age, creatinine, hemoglobin, history of stroke, history of atrial fibrillation, diabetes, NYHA functional class, and treatment (medical vs. surgical therapy, with surgical therapy including CABG or CABG + SVR), as well as the STICH risk at randomization (RAR) index [1, 2, 7, 10, 11, 22, 23]. All analyses were performed using SAS statistical software, version 9.4 (SAS Institute Inc., Cary, NC).


Study population

We reported baseline demographics and clinical data of the 2136 patients in STICH [3, 11, 23]. Baseline echocardiography was performed within 90 days of randomization and prior to initiating study treatment in 2009 (94% of 2136) patients, of which 498 (24.7% of 2009) were excluded due to technically inadequate E/A ratio measurement or absent A wave due to atrial fibrillation, the remaining 1511 patients comprised our cohort. The primary outcome was the rate of death from any cause. There were 604 deaths over a median follow-up of 56 months. Median age was 60 years (25th percentile; 54, 75th percentile; 68) and 84.6% were male. The median E/A ratio was 1.0 (25th percentile; 0.67, 75th percentile; 1.67) with no difference between the H1 and H2 populations with respect to the distribution of this variable [3]. At least moderate MR (≥grade 2) was present in 24.1% (344 of 1426 patients in whom MR was characterized) in the cohort, at least moderate MR was also present in 29.4% (p = 0.033 between groups) in the 498 patients excluded due to absent E/A ratio (118 of 402).

Median values for the eleven echocardiographic variables are shown (Table 1). By study design, E/A ratio was the most complete dataset, whereas E/e’ ratio had the most missing values.

Table 1 Baseline Echo Variablesa

Univariable modeling of prognostic variables with the original dataset

Each of the eleven variables, when considered without imputation, was associated with all- cause mortality. LVESVI had a strong relationship with mortality (χ2 = 57.5, p < 0.001) even with a large number of missing values (350 patients), as did EF (χ2 = 43.5, p < 0.001) and E/A ratio (χ2 = 41.1, p < 0.001). However, due to the degree and variation of missing data, a meaningful comparison of the strength of the relationship of each variable to mortality required the use of imputation.

Mortality increased with increasing LVESVI and decreasing EF in a non-linear fashion. For example, mortality was lowest for LVESVI < 65 cc/m2 with minimal increase in risk up to a LVESVI of 65 cc/m2. Beyond this, mortality increased linearly with increasing LVESVI. Similarly, there was modest effect on mortality with decreasing EF down to 30%. For EF ≤30%, mortality increased in a linear fashion as EF decreased.

E/A ratio had a u-shaped relationship with mortality (Fig. 1). Mortality was higher for small (E/A < 0.6) and large (> 1.0) values than intermediate (0.6–1.0) values, and was lowest for E/A ≈ 0.8. However, the higher mortality for E/A < 0.6 was not significantly different from mortality with E/A 0.6–1.0 (HR 1.16, 95% CI 0.88–1.53, p = 0.28). In contrast, mortality was highest for large E/A ratios (> 1.0 up to approximately 2.3, beyond which there was no further increase in risk) compared to E/A < 0.6 (HR 1.35, 95% CI 1.04–1.75, p = 0.02) and E/A 0.6–1.0 (HR 1.58, 95% CI 1.30–1.92, p < 0.001).

Fig. 1

Five year all-cause mortality for the combined cohort (Hypothesis 1 and 2) with increasing E/A ratio in the non-imputed (original) dataset; dotted lines indicate 95% confidence interval. Mortality risk was higher in patients with low (< 0.6) and high (> 1.0) E/A ratio and lowest for those with intermediate E/A ratio (0.6–1.0)

Of the 1511 patients, 273 had E/A ratio ≤ 0.6, 1010 had E/A > 0.6–2.3 (n = 622 with E/A 0.6–1.0), and 228 had E/A > 2.3. Differences in baseline characteristics for each E/A group are shown (Table 2). The E/A ratio > 2.3 group had worse renal function, lower EF, larger LVESVI, more spherical LV, worse RV function, lower systolic blood pressure, higher heart rate and RAR mortality index compared to the other groups. The E/A ≤ 0.6 and E/A > 0.6–2.3 groups were similar, except that those with E/A ≤ 0.6 were older, and more often female. Cardiac index was similar across the three groups.

Table 2 Baseline Characteristics by E/A Ratio

Univariable modeling of prognostic variables with imputed datasets

Univariable modeling using the combined 25 imputed datasets are shown (Table 3). LVEDVI was excluded due to its high correlation with LVESVI (r = 0.96). E/A ratio was a significant predictor of all-cause mortality (χ2 41.1, p < 0.001). Only LVEF (χ2 43.1, p < 0.001; HR 0.94, 95% CI 0.93–0.96) and LVESVI (χ2 41.1, p < 0.001; HR 1.11, 95% CI 1.07–1.14) were more significant predictors of mortality than E/A ratio.

Table 3 Univariable Model for All-Cause Mortality Cased on 25 Imputed Datasets

Multivariable modeling of prognostic variables with imputed datasets

Multivariable models in which each echocardiographic variable was considered together with the eight clinical variables are shown in Table 4. Each echocardiographic variable provided incremental prognostic value to the combined set of eight clinical variables. E/A ratio was the third most significant echo variable (χ2 = 29.1, p < 0.001), following LVESVI (χ2 = 44.3, p < 0.001) and LVEF (χ2 = 31.9, p < 0.001).

Table 4 Incremental Prognostic Effect of Echo Variables after Adjusting for Clinical Co-variablesa

The combined clinical and echocardiographic multivariable mortality model is shown in Table 5. Creatinine (χ2 = 30.0, p < 0.001; HR 3.21 95% CI 2.11–4.86), LVESVI (χ2 = 27.3, p < 0.001; HR 1.09 95% CI 1.06–1.13), age, and E/A ratio (χ2 = 12.4, p < 0.001) combined accounted for 74% of the prognostic information for predicting risk. Increasing E/A ratio (χ2 = 12.4, p < 0.001) was the 5th most important variable after age and treatment strategy (MED vs CABG or CABG +SVR).

Table 5 Multivariable Mortality Model

Interaction with treatment strategy

Hypothesis 1 (MED vs. CABG)

Of the 1511 patients included in this analysis, 845 were enrolled in H1 (60 were enrolled in both H1 and H2) [9, 23]. Only E/A ratio had a significant treatment interaction (p = 0.033). While the medical treatment arm displayed a u-shaped relationship with mortality (Fig. 2a), in the CABG arm, mortality increased in a more linear fashion as E/A increased. Compared to the medical arm, mortality was lower for CABG with smaller E/A ratio ≤ 0.6 (HR 0.64 95% CI 0.36, 1.14, p = 0.13) and higher E/A ratio > 1.4 (HR 0.78, 95% CI 0.54, 1.12, p = 0.17), although this difference was not statistically significant. Mortality risk was similar for CABG and medical therapy when E/A ratio approached 0.8 (HR 1.05, 95% CI 0.75, 1.47, p = 0.79).

Fig. 2

Five-year all-cause mortality by treatment. a Hypothesis 1: CABG vs. Medical Therapy. Medical treatment arm is shown in red; shaded area indicates 95% confidence interval. CABG arm is shown in blue; shaded area indicates 95% confidence interval. b Hypothesis 2: CABG vs. CABG + SVR. CABG + SVR arm is shown in red; shaded area indicates 95% confidence interval. CABG arm is shown in blue; shaded area indicates 95% confidence interval

Hypothesis 2 (CABG vs. CABG +SVR)

The remaining 726 patients in our study cohort had sufficient anterior and apical dyskinesia to be eligible for SVR and were enrolled in H2 [9, 11]. In H2, only RV dysfunction (p = 0.038) had a significant treatment interaction. With normal RV function (680 patients), there was no difference in mortality with CABG versus CABG +SVR. With mild RV dysfunction (100 patients), there was a trend towards increased mortality with CABG+SVR versus CABG alone (HR 1.47 95% CI 0.71–3.04, p = 0.301). However, with moderate or severe RV dysfunction (76 patients), mortality was significantly higher with CABG +SVR compared to CABG alone (HR 3.05 95% CI 1.29–7.22, p = 0.008). LVESVI, EF, MR severity, and E/A ratio did not have a significant treatment interaction in H2. E/A ratio exhibited a u-shaped relationship with mortality for CABG and CABG + SVR without any significant difference in mortality between the two groups (Fig. 2b).


We observed that baseline echocardiographic markers of LV remodeling can contribute as incremental prognostic values to current clinical risk markers in ischemic HFrEF. Diastolic dysfunction was a stronger predictor of mortality than NYHA functional class, anemia, diabetes, history of atrial fibrillation and stroke. When combined with advancing renal dysfunction and elderly age, larger LVESVI and worsening diastolic dysfunction accounted for 74% of the prognostic information in predicting risk of death. Mortality of those with less advanced diastolic dysfunction may be lower when treated with surgical revascularization compared to medical therapy. We did not observe a treatment interaction with E/A ratio for CABG vs. CABG + SVR.

The degree of LV remodeling in HFrEF is variable and reflects differences in hemodynamics, cardiac structure, and geometry [3, 5, 6, 18, 24]. For example, while the STICH cohort all had EF ≤ 35%, diastolic function varied widely, with mild diastolic dysfunction in one-third and severe diastolic dysfunction in only one-fifth [3]. RV function was normal in most of the cohort (75.5% of 1838 patients with baseline RV function assessment) but < 5% had severe RV dysfunction [3]. MR severity and LV volumes also varied [3]. Progression of RV and diastolic dysfunction, functional MR, and LV enlargement suggests more advanced cardiac remodeling. Consistent with previous studies [5, 6], we observed that each of these was associated with increased mortality risk and could explain differences in mortality amongst HFrEF patients with similar EF. Decreased EF was associated with mortality risk with univariable modeling but not when other echo variables were included in multivariable analysis, supporting the notion that these markers of LV remodeling provide prognostic information beyond EF alone.

Amongst markers of advanced LV remodeling, diastolic dysfunction may be more important prognostic marker than abnormal LV geometry. We previously demonstrated that increased LVESVI and sphericity index influences poor survival following CABG or CABG+SVR [4, 25], but in our current analysis, diastolic function outperformed sphericity index. Whereas previous HFrEF studies have identified deceleration time, E/e’ ratio or diastolic function grade as prognostic diastolic function variables [5, 6], we found that E/A ratio was the most robust indicator in HFrEF due to ischemic etiology. E/A ratio is the most easily obtainable diastolic function parameter and is recommended by the American Society of Echocardiography and European Association of Cardiovascular Imaging joint guidelines as the first parameter to grade diastolic function and estimate LV filling pressure [15]. Since it reflects transmitral gradient and captures dynamic changes in LV filling pressure, E/A can discriminate HFrEF with optimized hemodynamics from decompensated HF. In contrast, the mitral annulus early diastolic velocity (e’) reflects the status of myocardial relaxation [17], and is reduced in almost all HFrEF patients, resulting in increased E/e’ ratio. Therefore, E/A ratio is a better prognostic parameter than E/e’ ratio.

While our data do not replace the diastolic function grading recommended by the ASE and EACVI [15], they do have implications for the optimal diastolic filling pattern in HFrEF due to ischemic etiology. We found that mortality risk was higher in patients with low (< 0.6) and high (> 1.0) E/A ratio and lowest for those with intermediate E/A ratio (0.6–1.0). Similar findings were observed in the Strong Heart Study, a population based cohort of middle aged to elderly Native Americans [26]. While higher mortality is expected in HFrEF patients with E/A > 1.0 suggesting advanced diastolic dysfunction [6], an impaired relaxation pattern (E/A < 0.6) is usually considered to be an optimal diastolic filling pattern. One explanation could be that poor outcomes with E/A < 0.6 reflected hemodynamic compromise, but cardiac output and systolic blood pressure were similar to patients with E/A 0.6–2.3. Another possibility is that intravascular volume depletion due to diuresis or other mechanisms contributes to lower than ideal preload in those with E/A ratio < 0.6.

E/A ratio ≥ 2.0 is a restrictive diastolic filling pattern usually portending the worst prognosis [6], but surprisingly, we observed that E/A ratio > 2.3 was associated with minimal further increased mortality risk. However, this group also had lower systolic blood pressure, hemoglobin, and EF, larger LVESVI, and worse renal function, and perhaps when E/A ratio is severely elevated these factors had a greater effect on mortality.

Restrictive diastolic filling has been shown to be associated with reduced myocardial viability and poor survival after CABG [27]. We also observed increasing mortality with CABG as E/A ratio increased up to 2.3, but mortality trended higher in this group in the medical treatment arm compared to CABG, with similar trends for E/A ratio < 0.6. In contrast, mortality in both treatment groups was lowest when E/A closest 0.8, further emphasizing that this is the optimal filling pattern in ischemic HFrEF and that treatment, such as diuresis, should be tailored to avoid E/A < 0.6 or > 1.0. Whether those with E/A < 0.6 or > 1.0 will have better survival with medical therapy or CABG is less certain, as the differences in mortality were not statistically significant.

We did not find treatment interactions with E/A ratio in H2 (CABG versus CABG + SVR), although moderate to severe RV dysfunction predicted worse survival with SVR, consistent with our recent report [12]. In H2, RV dysfunction was also associated with increased E/A ratio, advanced HF, and lower cardiac index [12], suggesting more advanced LV remodeling. We also previously demonstrated that smaller LVESVI and more preserved EF, both markers of less advanced LV remodeling, could identify a subgroup of STICH patients more likely to benefit from SVR [4]. Together, these data suggest that echocardiographic variables could identify patients with less advanced remodeling more likely to benefit from SVR that could not be determined by risk stratification based on clinical characteristics or EF alone [22].

All echocardiographic variables in our model conferred incremental mortality risk to clinical data but the combination of increased creatinine, elderly age, larger LVESVI, and abnormal E/A ratio, had the most influence on all-cause mortality. At present, the most commonly applied HF prognostic models, such as the Seattle Heart Failure Model and the Heart Failure Survival Score, synthesize clinical data and EF to estimate prognosis but do not include other echocardiographic markers [7, 8], and models that have proposed the addition of echocardiographic markers are not widely applied [28]. Our data are not only consistent with previous studies demonstrating the prognostic importance of advanced diastolic dysfunction and LV enlargement, but show that these are more powerful predictors than many other clinical markers. Our data argue for inclusion of diastolic dysfunction and LV enlargement markers in future prognostic models and decision aids to determine optimal treatment strategy in ischemic HFrEF.


Our analysis has limitations. First, excluding 498 patients without measureable E/A ratio may have introduced bias by excluding 118 patients with > moderate MR. Second, in the small number (7.8%; 111 of 1511) of patients with > moderate MR included, E/A ratio could reflect the severity of MR rather than diastolic function. Third, the results presented are based on LV diastolic function subgroup analyses of the overall study population. The perils of subgroup analysis are well documented, and thus cautious interpretation is required. Fourth, multiple imputation was required to create complete datasets due to additional missing echocardiographic data. However, this technique is a well-established method which permitted inclusion of all 1511 patients with E/A ratio and strengthened our analysis. Fifth, the sphericity index is an important index in decisions for a role in the for surgical ventricular reconstruction. However this was evaluated in 935 patients who made up only 62% of our study population.. Sixth, RV systolic pressure was not included in the model because of a large number (> 80%) of missing data. Finally, our analysis of clinical risk markers for HF was limited to data prospectively collected during the STICH trial and did not include functional studies (peak VO2) or biomarkers.


Diastolic dysfunction and echocardiographic markers of advanced LV remodeling can contribute incremental prognostic value to current clinical markers of HF severity. Inclusion of E/A ratio and LVESVI could enhance prognostic models for ischemic HF and influence treatment strategy. E/A ratio closest to 0.8 is the most optimal filling pattern in ischemic HFrEF and treatments which affect preload, such as diuresis, should be adjusted to maintain E/A > 0.6 and < 1.0.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.



Surgical Treatment for Ischemic Heart Failure


Left ventricle


Heart failure with reduced ejection fraction


Right ventricle


Mitral regurgitation


Left ventricular end-diastolic volume index


Left ventricular end-systolic volume index


Coronary artery bypass grafting


Surgical ventricular revascularization


Risk randomization index


  1. 1.

    Lin G, Gersh BJ, Greene EL, Redfield MM, Hayes DL, Brady PA. Renal function and mortality following cardiac resynchronization therapy. Eur Heart J. 2011;32(2):184–90.

    Article  Google Scholar 

  2. 2.

    Al-Ahmad A, Rand WM, Manjunath G, Konstam MA, Salem DN, Levey AS, et al. Reduced kidney function and anemia as risk factors for mortality in patients with left ventricular dysfunction. J Am Coll Cardiol. 2001;38(4):955–62.

    CAS  Article  Google Scholar 

  3. 3.

    Oh JK, Pellikka PA, Panza JA, Biernat J, Attisano T, Manahan BG, et al. Core lab analysis of baseline echocardiographic studies in the STICH trial and recommendation for use of echocardiography in future clinical trials. J Am Soc Echocardiogr. 2012;25(3):327–36.

    Article  Google Scholar 

  4. 4.

    Oh JK, Velazquez EJ, Menicanti L, Pohost GM, Bonow RO, Lin G, et al. Influence of baseline left ventricular function on the clinical outcome of surgical ventricular reconstruction in patients with ischaemic cardiomyopathy. Eur Heart J. 2013;34(1):39–47.

    Article  Google Scholar 

  5. 5.

    Grayburn PA, Appleton CP, DeMaria AN, Greenberg B, Lowes B, Oh J, et al. Echocardiographic predictors of morbidity and mortality in patients with advanced heart failure: the Beta-blocker evaluation of survival trial (BEST). J Am Coll Cardiol. 2005;45(7):1064–71.

    Article  Google Scholar 

  6. 6.

    Pinamonti B, Zecchin M, Di Lenarda A, Gregori D, Sinagra G, Camerini F. Persistence of restrictive left ventricular filling pattern in dilated cardiomyopathy: an ominous prognostic sign. J Am Coll Cardiol. 1997;29(3):604–12.

    CAS  Article  Google Scholar 

  7. 7.

    Levy WC, Mozaffarian D, Linker DT, Sutradhar SC, Anker SD, Cropp AB, et al. The Seattle heart failure model: prediction of survival in heart failure. Circulation. 2006;113(11):1424–33.

    Article  Google Scholar 

  8. 8.

    Aaronson KD, Schwartz JS, Chen T-M, Wong K-L, Goin JE, Mancini DM. Development and prospective validation of a clinical index to predict survival in ambulatory patients referred for cardiac transplant evaluation. Circulation. 1997;95(12):2660–7.

    CAS  Article  Google Scholar 

  9. 9.

    Velazquez EJ, Lee KL, O’Connor CM, Oh JK, Bonow RO, Pohost GM, et al. The rationale and design of the surgical treatment for ischemic heart failure (STICH) trial. J Thorac Cardiovasc Surg. 2007;134(6):1540–7.e4.

    Article  Google Scholar 

  10. 10.

    Jones RH, White H, Velazquez EJ, Shaw LK, Pietrobon R, Panza JA, et al. STICH (surgical treatment for ischemic heart failure) trial enrollment. J Am Coll Cardiol. 2010;56(6):490–8.

    Article  Google Scholar 

  11. 11.

    Jones RH, Velazquez EJ, Michler RE, Sopko G, Oh JK, O'Connor CM, et al. Coronary bypass surgery with or without surgical ventricular reconstruction. N Engl J Med. 2009;360(17):1705–17.

    CAS  Article  Google Scholar 

  12. 12.

    Kukulski T, She L, Racine N, Gradinac S, Panza JA, Velazquez EJ, et al. Implication of right ventricular dysfunction on long-term outcome in patients with ischemic cardiomyopathy undergoing coronary artery bypass grafting with or without surgical ventricular reconstruction. J Thorac Cardiovasc Surg. 2015;149(5):1312–21.

    Article  Google Scholar 

  13. 13.

    Anavekar NS, Gerson D, Skali H, Kwong RY, Kent Yucel E, Solomon SD. Two-dimensional assessment of right ventricular function: an echocardiographic–MRI correlative study. Echocardiography. 2007;24(5):452–6.

    Article  Google Scholar 

  14. 14.

    Lang RM, Bierig M, Devereux RB, Flachskampf FA, Foster E, Pellikka PA, et al. Recommendations for chamber quantification: a report from the American Society of Echocardiography's guidelines and standards committee and the chamber quantification writing group, developed in conjunction with the European Association of Echocardiography, a branch of the European Society of Cardiology. J Am Soc Echocardiogr. 2005;18(12):1440–63 Epub 2005/12/27.

    Article  Google Scholar 

  15. 15.

    Nagueh SF, Smiseth OA, Appleton CP, Byrd BF, Dokainish H, Edvardsen T, et al. Recommendations for the evaluation of left ventricular diastolic function by echocardiography: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. Eur J Echocardiogr. 2016;17(12):1321–60.

    Google Scholar 

  16. 16.

    Di Donato M, Castelvecchio S, Brankovic J, Santambrogio C, Montericcio V, Menicanti L. Effectiveness of surgical ventricular restoration in patients with dilated ischemic cardiomyopathy and unrepaired mild mitral regurgitation. J Thorac Cardiovasc Surg. 2007;134(6):1548–53.

    Article  Google Scholar 

  17. 17.

    Ommen SR, Nishimura R, Appleton CP, Miller FA Jr, Oh JK, Redfield MM, et al. Clinical utility of Doppler echocardiography and tissue Doppler imaging in the estimation of left ventricular filling pressures: a comparative simultaneous Doppler- catheterization study. Circulation. 2000;102(15):1788–94.

    CAS  Article  Google Scholar 

  18. 18.

    White HD, Norris RM, Brown MA, Brandt PW, Whitlock RM, Wild CJ. Left ventricular end-systolic volume as the major determinant of survival after recovery from myocardial infarction. Circulation. 1987;76(1):44–51.

    CAS  Article  Google Scholar 

  19. 19.

    Cox DR. Regression models and life-tables. J Royal Statist Soc B. 1972;34(2):187–220.

    Google Scholar 

  20. 20.

    Harrell FE. Regression modeling strategies: with applicaitons to linear models, logistic regression, and survival analysis. New York: Springer-Verlag; 2001.

    Google Scholar 

  21. 21.

    Rubin DB. Multiple imputation for nonresponse in surveys: John Wiley & Sons; 2004.

    Google Scholar 

  22. 22.

    Zembala M, Michler RE, Rynkiewicz A, Huynh T, She L, Lubiszewska B, et al. Clinical characteristics of patients undergoing surgical ventricular reconstruction by choice and by randomization. J Am Coll Cardiol. 2010;56(6):499–507.

    Article  Google Scholar 

  23. 23.

    Velazquez EJ, Lee KL, Deja MA, Jain A, Sopko G, Marchenko A, et al. Coronary-artery bypass surgery in patients with left ventricular dysfunction. N Engl J Med. 2011;364(17):1607–16.

    CAS  Article  Google Scholar 

  24. 24.

    St John Sutton M, Pfeffer MA, Plappert T, Rouleau JL, Moyé LA, Dagenais GR, et al. Quantitative two-dimensional echocardiographic measurements are major predictors of adverse cardiovascular events after acute myocardial infarction. The protective effects of captopril. Circulation. 1994;89(1):68–75.

    CAS  Article  Google Scholar 

  25. 25.

    Choi J-O, Daly RC, Lin G, Lahr BD, Wiste HJ, Beaver TM, et al. Impact of surgical ventricular reconstruction on sphericity index in patients with ischaemic cardiomyopathy: follow-up from the STICH trial. Eur J Heart Fail. 2015;17(4):453–63.

    Article  Google Scholar 

  26. 26.

    Bella JN, Palmieri V, Roman MJ, Liu JE, Welty TK, Lee ET, et al. Mitral ratio of peak early to late diastolic filling velocity as a predictor of mortality in middle-aged and elderly adults: the strong heart study. Circulation. 2002;105(16):1928–33.

    Article  Google Scholar 

  27. 27.

    Yong Y, Nagueh SF, Shimoni S, Shan K, He Z-X, Reardon MJ, et al. Deceleration time in ischemic cardiomyopathy: relation to echocardiographic and Scintigraphic indices of myocardial viability and functional recovery after revascularization. Circulation. 2001;103(9):1232–7.

    CAS  Article  Google Scholar 

  28. 28.

    Senni M, Parrella P, De Maria R, Cottini C, Böhm M, Ponikowski P, et al. Predicting heart failure outcome from cardiac and comorbid conditions: the 3C-HF score. Int J Cardiol. 2013;163(2):206–11.

    Article  Google Scholar 

Download references




This work was supported by the National Institutes of Health, Heart, Lung, and Blood Institute grants (U01HL69015, U01HL69013, and U01HL69010) ( #NCT00023595; NCT00023595). The views expressed in this manuscript do not necessarily reflect those of the NIH or NHLBI.

Author information




G conceived of and designed the study. P, K, P, M, W, M and G made substantial contributions to conception and design. G, K and JK contributed to data interpretation and revision of the manuscript. L, C, T and V analyzed data and contributed to discussion of the results. JK, G and K collected and analyzed the data, searched for articles, analyzed the data and made substantial contribution to revision of the manuscript. K collected, managed and analyzed the data, searched for articles, drafted the figures, and drafted the first manuscript. The authors read and approved the final manuscript.

Corresponding author

Correspondence to Grace Lin.

Ethics declarations

Ethics approval and consent to participate

It is approved by each hospital’s IRB. Informed consent to participate in the study were obtained from participants.

Consent for publication

All authors read and approved the final manuscript.

Competing interests

Paul Grayburn: Consultant for Tendyne and Abbott Vascular; Grant support from Abbot Vascular and Medtronic; Echo core lab contract for ValTech Cardio, Guided Delivery Systems, and Tendyne David Prior; Consultant for Actelion, Astra-Zeneca and Servier. There are no other relationships with industry to disclose.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Kim, K., She, L., Lee, K.L. et al. Incremental prognostic value of echocardiography of left ventricular remodeling and diastolic function in STICH trial. Cardiovasc Ultrasound 18, 17 (2020).

Download citation


  • Heart failure
  • Diastolic dysfunction.
  • Ischemic cardiomyopathy