Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Evaluation of left ventricular diastolic function in patients operated for aortic stenosis

  • Henrik Hultkvist ,

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Validation, Visualization, Writing – original draft, Writing – review & editing

    henrik.hultkvist@regionostergotland.se

    Affiliation Department of Cardiothoracic and Vascular Surgery, Heart Centre, Linköping University Hospital, Linköping, Sweden

  • Eva Nylander,

    Roles Methodology, Software, Validation, Writing – review & editing

    Affiliation Department of Clinical Physiology and Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden

  • Éva Tamás,

    Roles Software, Validation, Writing – review & editing

    Affiliation Department of Cardiothoracic and Vascular Surgery, Heart Centre, Linköping University Hospital, Linköping, Sweden

  • Rolf Svedjeholm,

    Roles Conceptualization, Funding acquisition, Methodology, Project administration, Supervision, Validation, Writing – review & editing

    Affiliation Department of Cardiothoracic and Vascular Surgery, Heart Centre, Linköping University Hospital, Linköping, Sweden

  • Jan Engvall,

    Roles Software, Validation, Writing – review & editing

    Affiliations Department of Clinical Physiology and Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden, Center for Medical Image Science and Visualization (CMIV), Linköping University, Linköping, Sweden

  • Jonas Holm,

    Roles Writing – review & editing

    Affiliation Department of Cardiothoracic and Vascular Surgery, Heart Centre, Linköping University Hospital, Linköping, Sweden

  • Eva Maret,

    Roles Software, Validation

    Affiliation Department of Clinical Physiology, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden

  • Farkas Vánky

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Supervision, Validation, Visualization, Writing – review & editing

    Affiliation Department of Cardiothoracic and Vascular Surgery, Heart Centre, Linköping University Hospital, Linköping, Sweden

Abstract

Background

Left ventricular diastolic dysfunction is common in patients with aortic valve stenosis (AS) and reportedly affects prognosis after surgical aortic valve replacement (SAVR). Here we investigated whether and how diastolic function (assessed following the most recent guidelines) was affected by SAVR, and whether preoperative diastolic function affected postoperative outcome. We also examined whether long-term mortality was associated with preoperative NT-proBNP and postoperative heart failure (PHF).

Methods

We performed a prospective observational study of 273 patients with AS who underwent AVR with or without concomitant coronary artery bypass surgery. Of these patients, 247 were eligible for assessment of left ventricular (LV) filling pressure. Preoperatively and at the 6-month postoperative follow-up, we measured N-terminal pro-B type natriuretic peptide (NT-proBNP) in serum and assessed diastolic function with Doppler echocardiography. PHF was diagnosed using prespecified criteria. Multivariable logistic regression was performed to explore variables associated with high LV filling pressure. Cox regression was performed to explore variables associated with mortality, accounting for timeto-event.

Results

At the time of surgery, 22% (n = 54) of patients had diastolic dysfunction expressed as high LV filling pressure. Of these 54 patients, 27 (50%) showed postoperative diastolic function improvement. Among the 193 patients with preoperative low LV filling pressure, 24 (12%) showed postoperative diastolic function deterioration. Increased long-term mortality was associated with PHF and high preoperative NT-proBNP, but not with preoperative or postoperative diastolic dysfunction. Cox regression revealed the following independent risk factors for long-term mortality: diabetes, renal dysfunction, preoperative NT-proBNP>960 ng/L, age, and male gender.

Conclusions

Surgery for aortic stenosis improved diastolic function in patients with high LV filling pressure in 50% of the patients. Our results could not confirm the previously suggested role of diastolic dysfunction as a marker for poor long-term survival after SAVR. Our findings showed that both PHF and high preoperative NT-proBNP were associated with long-term mortality.

Introduction

Hemodynamically significant aortic valve stenosis (AS) results in concentric left ventricular (LV) hypertrophy caused by efforts to maintain normal wall tension. LV hypertrophy affects LV diastolic function and is often accompanied by increased diffuse interstitial fibrosis in advanced AS [1]. The diastole can be divided into three phases: relaxation with rapid ventricle filling, diastasis, and end-diastole with atrial contraction. Initial LV filling is mainly influenced by relaxation, which is an active calcium-dependent process, while LV filling towards the end of diastole relies more on LV compliance. Early milder diastolic dysfunction is often characterized by abnormal relaxation, but normal filling pressure (at least at rest), while more severe diastolic dysfunction involves reduced compliance, resulting in high LV filling pressure.

Diastolic dysfunction is reportedly common after aortic valve replacement (AVR), and is associated with mortality [2, 3]. It has also been proposed that diastolic dysfunction may lead to heart failure many years after surgery [2, 4]. Conflicting data have been reported regarding whether surgical AVR (SAVR) actually improves diastolic function [5].

Echocardiography is frequently used to evaluate diastolic function. Upon the development of blood flow Doppler, this method became more convenient and widely used.

The later introduction of tissue Doppler and other modalities brought additional options for diastolic function characterization [6]. Different generations of guidelines all recommend the use of combinations of parameters for the characterization of diastolic function. The most recent guidelines were published in 2016 by the European Association of Cardiovascular Imaging (EACVI) and the American Society of Echocardiography [7].

B-type natriuretic peptide (BNP) is an endogenous hormone that counteracts some symptoms of heart failure—affecting diuresis and vasodilation, having anti-hypertrophy and anti-fibrosis properties, and exerting inhibitory effects on the sympathetic nervous system and renin-angiotensin-aldosterone system [2]. The amino-terminal fragment of BNP’s prohormone, NT-proBNP, is released into circulation from myocytes in response to myocyte stretch, increased wall tension, and ischemia [3, 4], and is a well-established biomarker of heart failure [5]. We previously described the dynamics of NT-proBNP in aortic valve surgery, and its association with 1-year mortality [8]. The clinical manifestation of postoperative cardiac dysfunction, defined as postoperative heart failure (PHF), is also associated with poor outcome after AVR [9, 10].

In the present study, we aimed to examine how surgery for aortic stenosis impacted LV diastolic function, using an adapted version of the most recent guidelines. We further evaluated how outcome after aortic valve surgery for AS was impacted by pre- and postoperative high LV filling pressure, NT-proBNP level, and PHF. Our hypotheses were that diastolic LV function improves after surgery for AS, and that pre- and postoperative high LV filling pressures negatively impact post-SAVR outcome, alone or in combination with elevated NT-proBNP and PHF.

Methods

This prospective longitudinal observation study included 273 patients scheduled for aortic valve surgery due to aortic stenosis between June 2008 and January 2013. Patients were recruited from the south-east region of Sweden, and surgery was performed at Linköping University Hospital—the only tertiary care hospital performing open heart surgery, which serves a population of over one million people. Exclusion criteria were emergency operations, active endocarditis, double-valve procedures, and inability to provide written informed consent. Patients with coronary artery disease or undergoing ascending aorta replacement without circulatory arrest were not excluded.

The main protocol included obtaining blood samples for NT-proBNP measurement and performing a detailed echocardiographic evaluation of diastolic LV function before surgery and at 6 months post-surgery. Clinical data were prospectively registered in our clinical database (Carath; Fujitsu, Tokyo, Japan) and mortality records were retrieved from the Swedish Civil registry.

Definitions

The clinical manifestation of low cardiac output syndrome (LCOS) with post-cardiotomy cardiogenic shock was evident at weaning from cardio-pulmonary bypass (CPB) or during the early hours after surgery. We also included cases not fulfilling criteria for cardiogenic shock and defined postoperative heart failure (PHF) as a hemodynamic state at which cardiac output does not meet systemic demand without supportive measures, other than correction of volume or vascular resistance. This hemodynamic state was assessed using previously reported mixed venous oxygen criteria [11]. Supportive measures and treatment comprised the use of an intra-aortic balloon pump or ventricular assist device, or infusion of one or more inotropes for over 30 minutes at the following dosages: epinephrine, ≥0.05–0.3 μg/kg body weight per minute; milrinone, ≥0.375 μg/kg body weight per minute; dopamine, ≥4 μg/kg body weight per minute; dobutamine, ≥4 μg/kg body weight per minute; and levosimendan 0.1 (0.05–0.2)μg/kg body weight in 24 hours. Perioperative myocardial infarction (PMI) was defined as a sustained elevation of troponin T to ≥2000 ng/L on or after the third postoperative day [12].

Echocardiography

Echocardiographic examination was performed by experienced technicians on the day before surgery and at the 6-month postoperative follow-up. Preoperative examination was conducted using Vivid V7 and E9 ultrasound systems (GE Ultrasound, Horten, Norway). For postoperative examination, some patients were additionally examined using Philips or Siemens systems. All echocardiograms were evaluated and double-checked by three senior experienced physicians.

Standard 2-dimensional and Doppler echocardiography and measurements were performed in accordance with guidelines [7, 13]. We evaluated diastolic function using a guideline-based automated decision algorithm (https://liu.se/en/research/left-ventricularhttps://liu.se/en/research/left-ventricular-diastolic-function-decision-supportdiastolic-function-decision-support), which accounted for age-adjusted normal ranges [14]. Briefly, the evaluation was primarily based on mitral E/A ratio, pulmonary venous systolic and diastolic flow velocities, E/eʹ (mean of septal and lateral eʹ) and left atrial size (left atrial end systolic area in the 4-chamber view, indexed to BSA; LAAi). If a patient had contradictory or otherwise unclassifiable measurements, an individualized evaluation was performed with consideration of mitral flow deceleration time, isovolumetric relaxation time, and tricuspid regurgitation velocity. General instructions regarding the applicability of diastolic function criteria described in the guidelines were adhered to, i.e., diastolic function was not evaluated in patients with atrial fibrillation, neither in patients with significant mitral annular calcification nor in cases of insufficient quality of the registrations.

Left ventricular diastolic function (LVDF) was classified into four categories (normal or Grade I–III dysfunction) according to guidelines. Normal and Grade I dysfunction are considered to be associated with low LV filling pressure, and Grade II and III dysfunction with high LV filling pressure. All data were digitally stored using EchoPAC version BT 11 (GE Healthcare, Horton, Norway). Patients with atrial fibrillation at echocardiographic evaluation were excluded from analysis of diastolic function. For each case, systolic LV function was semiquantitatively evaluated by two observers, using a 4-degree scale (normal, mildly abnormal, moderately abnormal, and severely abnormal), corresponding to the EF categories recommended by Lang et al. [13].

NT-proBNP

Blood samples for plasma NT-proBNP analysis were obtained on the day before surgery and at the 6-month follow-up. Samples were collected in lithium heparin tubes and analyzed within 3 hours. Plasma levels of NT-proBNP were measured using an electro-chemo luminescence immunoassay with a Roche Elecsys 2010 automated device (Roche Diagnostics, Basel, Switzerland). The results were blinded prior to data analyses. Analyses were performed in one core laboratory. The assay had an effective measurement range of 5–35 000 ng/L, and inter-assay variability or coefficient of variation (CV) was <4% for all intervals.

Clinical management

All patients underwent surgery via full sternotomy and involving standard use of cardiopulmonary bypass with normal or moderate hypothermia and aortic occlusion. Diluted blood cardioplegia (one part blood and four parts crystalloid cardioplegia, supplemented with procaine hydrochloride) was used with an antegrade or combined antegrade and retrograde delivery system (Plegisol™, Abbot, IL, USA).

Statistics

Continuous data are presented as median with interquartile range (IQR), and categorical variables as number and percentage (%). For between-group comparisons, the Mann-Whitney U test was used for continuous data, and the X2 test and Fisher’s exact test for dichotomous data. Pairwise comparisons were performed using the Wilcoxon matched pairs signed rank sum test. Multivariable logistic regression was applied to explore variables associated with high filling pressure, and Cox regression was used to explore variables associated with mortality, accounting for time-to-event. Variables were selected a priori, accounting for confounders as described by Stralen et al. [15]. Variables were tested in the final model if P<0.1. The finite number of terms in the final model was parsimoniously chosen according to the limited number of events. We performed receiver operating characteristic (ROC) analyses to evaluate the discrimination of preoperative NT-proBNP on 5-year mortality, and Youden’s index was used to determine the best cut-off point (NT-proBNP>960 ng/L) with regards to specificity and sensitivity. Survival curves were calculated using the Kaplan-Meier method, and the log-rank test was performed to investigate between-group differences in survival times. Statistical analyses were performed using NCSS 12 Statistical Software, 2018 (NCSS, LLC. Kaysville, Utah, USA, ncss.com/software/ncss) and Statistica v.13.2 (StatSoft, Tulsa, Oklahoma, USA).

Ethics

This study was approved by The Regional Ethics Review Board (M 198–07, T 126–08, 2012/422-32), and patients were included only after providing written informed consent, in accordance with the World Medical Association’s Helsinki declaration on ethical principles for medical research.

Results

A complete echocardiographic evaluation with regards to diastolic function was possible in 247 of 273 patients. Patients were divided into two groups based on preoperative diastolic function: patients with signs of low LV filling pressure (n = 193/247; 78%), and those fulfilling criteria for high LV filling pressure (n = 54/247; 22%). Patients with high LV filling pressure were significantly older, presented with higher EuroSCORE II, and presented with more comorbidities. Table 1 shows patients’ baseline characteristics and preoperative data, and Table 2 summarizes the perioperative data and adverse events.

Diastolic LV function

Of the 54 patients with preoperative high LV filling pressure, 27 (50%) improved and showed postoperative low LV filling pressure. Among the 193 patients with preoperative low LV filling pressure, 24 (12%) deteriorated and exhibited postoperative high LV filling pressure (P<0.001) (Fig 1). Table 3 presents the data regarding patients who changed from preoperative low LV filling pressure to postoperative high LV filling pressure (n = 24), and those patients who maintained low LV filling pressure (n = 153). Compared to patients who maintained low LV filling pressure, those who showed diastolic function deterioration at the 6-month postoperative follow-up (n = 24) had a significantly longer time on ECC (120 min [88–132 min] vs. 94 min [91–112 min]; P = 0.02) and longer cross-clamp time (90 min [64–100 min] vs. 68 min [60–82 min]; P = 0.02), and more commonly underwent concomitant CABG procedure (10 (42%) vs. 35 (23%); P = 0.049) (Table 3). Table 4 presents the patients who showed improved diastolic function (n = 27) compared to those who maintained high LV filling pressure (n = 19) postoperatively.

thumbnail
Fig 1. Diastolic function categorized as low or high left ventricle (LV) filling pressure before surgery and 6 months after surgical aortic valve replacement (SAVR), along with the corresponding levels of NT-proBNP (ng/L).

https://doi.org/10.1371/journal.pone.0263824.g001

thumbnail
Table 3. Data from patients with preoperative low filling pressurea.

https://doi.org/10.1371/journal.pone.0263824.t003

thumbnail
Table 4. Data regarding patients with preoperative high filling pressurea.

https://doi.org/10.1371/journal.pone.0263824.t004

In a multivariable analysis, only preoperative NT-proBNP of >960 ng/L emerged as an independent predictor of preoperative high LV filling pressure (OR, 6.4; 95% CI: 3.3–12.4; P<0.001). The tested variables included age, sex, body mass index (BMI), creatinine clearance, diabetes on insulin or oral treatment, hypertension, and LV mass index. Table 5 shows the variables tested for association with high LV filling pressure at the 6-month postoperative follow-up. Preoperative high LV filling pressure and aortic cross-clamp time emerged as independent predictors (Table 5).

thumbnail
Table 5. Logistic regression, univariable and multivariable analyses of postoperative high LV filling pressure.

https://doi.org/10.1371/journal.pone.0263824.t005

NT-proBNP and diastolic function

In both pre- and postoperative evaluations, higher NT-proBNP was significantly associated with high LV filling pressure compared with low LV filling pressure (Tables 1 and 2). Between preoperative measurement and 6-month follow-up, NT-proBNP was significantly reduced among patients with preoperative low LV filling pressure (320 ng/L [170–760 ng/L] vs. 270 ng/L [150–490 ng/L]; P = 0.04) and patients with preoperative high LV filling pressure (1100 ng/L [510–2800 ng/L] vs. 760 ng/L [380–1080 ng/L]; P<0.001) (Fig 1). Both preoperatively and postoperatively, we found a weak but significant correlation between high LV filling pressure and NT-proBNP, with the Spearman’s rank correlation coefficient between these variables being 0.32 (P<0.001) preoperatively, and 0.29 (P<0.001) postoperatively.

LV systolic function and LV mass

Most patients with preoperative low LV filling pressure exhibited normal left ventricular systolic function, corresponding to an ejection fraction (EF) of >52% (n = 174; 90%). On the other hand, the proportion of patients with normal systolic function was significantly lower among patients with preoperative high LV filling pressure (n = 34; 63%; P<0.001). Preoperatively, the LV mass index (LVMI) tended to be higher in patients with preoperative high LV filling pressure compared to those with preoperative low LV filling pressure, although this difference did not reach significance (Table 1).

At the 6-month follow-up, LV mass had decreased significantly in both groups: from 125 g/m2 [101–146 g/m2] to 96 g/m2 [83–109 g/m2] (P<0.001) in the low LV filling pressure group, and from 137 g/m2 [109–172 g/m2] to 109 g/m2 [89–129 g/m2] (P<0.001) in the high LV filling pressure group. On the other hand, the LVMI at the 6-month follow-up was significantly higher in patients with preoperatively high LV filling pressure compared to those with preoperative low LV filling pressure (Table 2). LV mass index regression was similar between both groups (Table 2).

Mortality

Within the whole cohort, 30-day mortality was 1.1% (n = 3), 1-year mortality was 3.7% (n = 10), and 5-year mortality was 14% (n = 39). The median follow-up was 7.1 years (minimum, 4.1 years; maximum, 9.1 years), with a total of 63 deaths (23%). Long-term mortality did not significantly differ in relation to preoperative or postoperative LV filling pressure (Fig 2). ROC analysis revealed that a preoperative NT-proBNP of >960 ng/L was the best cut-off value for predicting all-cause 5-year mortality, with an area under the curve (AUC) of 0.7 (95% CI, 0.6–0.8; P<0.001). Fig 2 (panels C and D) shows the KaplanMeier plots of cumulative long-term survival according to PHF and NT-proBNP>960 ng/L. The final Cox regression analysis showed that long-term mortality was associated with diabetes with insulin or oral treatment, preoperative NT-proBNP>960 ng/L, renal dysfunction, and age, whereas female sex appeared to be protective (Table 6).

thumbnail
Fig 2.

Kaplan-Meier survival curves categorized according to diastolic function before surgery (A), diastolic function at the 6-month postoperative follow-up (B), presence of PHF (C), and preoperative NT-proBNP above or below 960 ng/L (D).

https://doi.org/10.1371/journal.pone.0263824.g002

thumbnail
Table 6. Cox regression mortality, univariable and multivariable analyses.

https://doi.org/10.1371/journal.pone.0263824.t006

Discussion

The main findings of our present study were that a large proportion of patients with preoperative high LV filling pressures had normalized LV filling pressure at their 6-month postoperative follow-up. Despite this normalization, the overall proportion of patients with high LV filling pressure remained almost the same before and after surgery due to the LV deterioration in 12% (n = 24) of the patients with preoperative low LV filling pressure.

Notably, neither preoperative nor postoperative high LV filling pressure had a statistically significant effect on long-term survival. On the other hand, poor long-term survival was associated with both high preoperative NT-proBNP and PHF.

Preoperative high LV filling pressure was associated with PHF and longer ICU stay.

Both preoperative and postoperative high LV filling pressure were characterized by higher NT-proBNP levels, although both groups showed significantly decreased NT-proBNP at follow-up. Patients who changed from preoperative low LV filling pressure to postoperative high LV filling pressure group exhibited longer aortic cross-clamp times and cardiopulmonary bypass times, and a greater proportion had concomitant CABG procedures. These findings may suggest a higher degree of intraoperative ischemic injury, potentially leading to postoperative deterioration of diastolic function. This explanation is supported by the higher levels of CK-MB in this patient group, and is in line with previous research [16, 17].

We could not detect any impact of medication on the changes in LV filling pressures from preoperative state to postoperative state at six months, but a larger proportion of patients were on beta blockers in the cohort with high LV filling pressures preoperatively.

Left ventricular diastolic function and NT-proBNP

Non-invasive evaluation of diastolic function is complex and must be based on several echocardiographic parameters. The American Society of Echocardiography (ASE) and the European Association of Cardiovascular Imaging (EACVI) recently provided updated recommendations to standardize diastolic function assessment [7]. Although the authors of these recommendations mention the age dependency of diastolic function parameters, this is not accounted for in their classification algorithms. Therefore, we have included age-adjusted reference values in a guideline-based decision support previously published by our group [14].

The relationship between NT-proBNP and diastolic function has been extensively studied [1822]. In line with prior findings, we also identified an association between diastolic function and NT-proBNP. After adjustment for common confounders, high preoperative NTproBNP was the sole predictor for preoperative high LV filling pressure.

One interesting and, to our knowledge, novel finding was that among patients with preoperative high LV filling pressure, those who exhibited improvement at the 6-month follow-up showed significantly higher levels of preoperative NT-proBNP and a higher LVmass index compared to patients who remained in the high LV filling pressure group, although both groups showed similar proportions of left ventricular hypertrophy. The group without improvement also exhibited significantly higher proportions of patients with diabetes mellitus and with postoperative atrial fibrillation.

Knowledge about the connection between AS, DM, NT-proBNP, and progression to fibrosis is currently expanding [23, 24]. Our present findings might suggest that patients without improvement at 6 months postoperatively had a more fixed diastolic dysfunction due to fibrosis; however, this possibility was not investigated in our study. Hypothetically, this could explain the difference in NT-proBNP levels, assuming that a more fibrotic LV releases less NT-proBNP than an LV wall containing more cardiac muscle cells and a lower proportion of fibrosis. On the other hand, a study of a community-based cohort recently reported that elevated NT-proBNP levels are associated with diffuse myocardial fibrosis [25]. However, in AS patients, myocardial fibrosis predominantly takes the form of diffuse interstitial fibrosis early in the disease process and might progress to replacement fibrosis with scarring and myocyte loss at end-stage heart failure [24].

Mortality and postoperative heart failure

The present results confirm our previous observations that PHF is associated with poor long-term survival, although it may initially appear benign [26]. Based on our previous study, we proposed that an episode of PHF may unmask a myocardial factor responsible for the delayed consequences. Since our previous study included adjustment for systolic function, it was reasonable to suggest that diastolic dysfunction might be involved [10]. The presently identified association between preoperative NT-proBNP and poor long-term survival, and our Cox regression model, support the assumption that an underlying myocardial factor is responsible. However, the current results do not clearly identify diastolic dysfunction as the culprit, since high LV filling pressure was not associated with increased mortality. Notably, this does not exclude that diastolic dysfunction due to fibrosis may be important for long-term outcome since the utilized methodology cannot discriminate between high diastolic LV pressure caused by hypertrophy versus fibrosis.

The literature includes conflicting data regarding the role of diastolic function for prognosis after AVR for AS [27, 28]. As mentioned earlier, different generations of guidelines have recommended different ways of classifying diastolic function. It has also been demonstrated that even when authors refer to the use of a certain classification, they may still apply different priorities and modes of action that influence the results [29]. There can also be differences in referral patterns, such that in some cohorts, the average patient might be considered for surgery at a later point in the disease process, and thus be in a more advanced state in terms of heart dysfunction. Other factors to consider are the differences in cohort sizes and outcome measures [30]. The missing link could be the degree of fibrosis. Future studies are needed to clarify the coupling between degree of fibrosis, improvement in diastolic function, and outcome after SAVR.

Although our present study population was relatively large, one major limitation was the low number of events. Missing data and excluded patients due to atrial fibrillation or MAC (Mitral annular calcification) contributed to this limitation. We were ultimately able to evaluate time-to-event in 52 of our 247 patients, and thus we must consider the possibility of a type II error. However, it is apparent that variables other than diastolic dysfunction were of greater importance in predicting outcome. Another limitation of our study is that when addressing long-term mortality, we did not differentiate between cardiac mortality and mortality due to other causes.

To conclude, our key points are SAVR improved diastolic function in patients with aortic stenosis and high LV filling pressure in 50% of the patients. Our results could not confirm the previously suggested role of diastolic dysfunction as a marker for poor long-term survival after SAVR. Our results indicate that both high preoperative NT-proBNP levels and an episode of postoperative heart failure after SAVR were associated with impaired long-term survival, in agreement with previous studies.

References

  1. 1. Lorell BH, Carabello BA. Left ventricular hypertrophy: pathogenesis, detection, and prognosis. Circulation. 2000;102(4):470–9. pmid:10908222
  2. 2. Lamb HJ, Beyerbacht HP, de Roos A, van der Laarse A, Vliegen HW, Leujes F, et al. Left ventricular remodeling early after aortic valve replacement: differential effects on diastolic function in aortic valve stenosis and aortic regurgitation. Journal of the American College of Cardiology. 2002;40(12):2182–8. pmid:12505232
  3. 3. Lund O, Flo C, Jensen FT, Emmertsen K, Nielsen TT, Rasmussen BS, et al. Left ventricular systolic and diastolic function in aortic stenosis. Prognostic value after valve replacement and underlying mechanisms. European heart journal. 1997;18(12):1977–87. pmid:9447328
  4. 4. Licker M, Cikirikcioglu M, Inan C, Cartier V, Kalangos A, Theologou T, et al. Preoperative diastolic function predicts the onset of left ventricular dysfunction following aortic valve replacement in high-risk patients with aortic stenosis. Critical care (London, England). 2010;14(3): R101. pmid:20525242
  5. 5. Gjertsson P, Caidahl K, Bech-Hanssen O. Left ventricular diastolic dysfunction late after aortic valve replacement in patients with aortic stenosis. The American journal of cardiology. 2005;96(5):722–7. pmid:16125503
  6. 6. Badiani S, van Zalen J, Treibel TA, Bhattacharyya S, Moon JC, Lloyd G. Aortic Stenosis, a Left Ventricular Disease: Insights from Advanced Imaging. Current cardiology reports. 2016;18(8):80. pmid:27384950
  7. 7. Nagueh SF, Smiseth OA, Appleton CP, Byrd BF 3rd, 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 Heart J Cardiovasc Imaging. 2016;17(12):1321–60. pmid:27422899
  8. 8. Hultkvist H, Holm J, Svedjeholm R, Vanky F. Rise and fall of NT-proBNP in aortic valve intervention. Open heart. 2018;5(1): e000739. pmid:29632678
  9. 9. Maganti MD, Rao V, Borger MA, Ivanov J, David TE. Predictors of low cardiac output syndrome after isolated aortic valve surgery. Circulation. 2005;112(9 Suppl):I448–52. pmid:16159861
  10. 10. Hultkvist H, Vanky F, Svedjeholm R. The combined impact of postoperative heart failure and EuroSCORE on long-term outcome after surgery for aortic stenosis. The Journal of heart valve disease. 2011;20(6):633–8. pmid:22655493
  11. 11. Vidlund M, Hakanson E, Friberg O, Juhl-Andersen S, Holm J, Vanky F, et al. GLUTAMICS—a randomized clinical trial on glutamate infusion in 861 patients undergoing surgery for acute coronary syndrome. The Journal of thoracic and cardiovascular surgery. 2012;144(4):922–30.e7. pmid:22721612
  12. 12. Dahlin LG, Kagedal B, Nylander E, Olin C, Rutberg H, Svedjeholm R. Unspecific elevation of plasma troponin-T and CK-MB after coronary surgery. Scandinavian cardiovascular journal: SCJ. 2003;37(5):283–7. pmid:14534070
  13. 13. Lang RM, Badano LP, Mor-Avi V, Afilalo J, Armstrong A, Ernande L, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015;28(1):1–39.e14. pmid:25559473
  14. 14. Tamas E, Nylander E. Decision support for assessment of left ventricular diastolic function. Physiological reports. 2018;6(16): e13815. pmid:30125045
  15. 15. van Stralen KJ, Dekker FW, Zoccali C, Jager KJ. Confounding. Nephron Clinical practice. 2010;116(2):c143–7. pmid:20516714
  16. 16. Fan J, Ma J, Xia N, Sun L, Li B, Liu H. Clinical Value of Combined Detection of CK-MB, MYO, cTnI and Plasma NT-proBNP in Diagnosis of Acute Myocardial Infarction. Clinical laboratory. 2017;63(3):427–33. pmid:28271683
  17. 17. Staub D, Jonas N, Zellweger MJ, Nusbaumer C, Wild D, Pfisterer ME, et al. Use of N-terminal pro-B-type natriuretic peptide to detect myocardial ischemia. The American journal of medicine. 2005;118(11):1287. pmid:16271916
  18. 18. Mannacio V, Antignano A, De Amicis V, Di Tommaso L, Giordano R, Iannelli G, et al. B-type natriuretic peptide as a biochemical marker of left ventricular diastolic function: assessment in asymptomatic patients 1 year after valve replacement for aortic stenosis. Interactive cardiovascular and thoracic surgery. 2013;17(2):371–7. pmid:23656924
  19. 19. Boer BP, Vieira ML, Sampaio RO, Abensur H, Oliveira AG, Fernandes JR, et al. Correlation to NT-ProBNP and remodeling after cardiac surgery. Arquivos brasileiros de cardiologia. 2013;100(5):469–75. pmid:23579620
  20. 20. Cemri M, Arslan U, Kocaman SA, Cengel A. Relationship between N-terminal pro-B type natriuretic peptide and extensive echocardiographic parameters in mild to moderate aortic stenosis. Journal of postgraduate medicine. 2008;54(1):12–6. pmid:18296798
  21. 21. Grewal J, McKelvie R, Lonn E, Tait P, Carlsson J, Gianni M, et al. BNP and NT-proBNP predict echocardiographic severity of diastolic dysfunction. European journal of heart failure. 2008;10(3):252–9. pmid:18331967
  22. 22. Gumauskiene B, Krivickiene A, Jonkaitiene R, Vaskelyte JJ, Siudikas A, Ereminiene E. Impact of Left Ventricular Diastolic Dysfunction and Biomarkers on Pulmonary Hypertension in Patients with Severe Aortic Stenosis. Medicina (Kaunas, Lithuania). 2018;54(4). pmid:30344294
  23. 23. Russo I, Frangogiannis NG. Diabetes-associated cardiac fibrosis: Cellular effectors, molecular mechanisms and therapeutic opportunities. Journal of molecular and cellular cardiology. 2016; 90:84–93. pmid:26705059
  24. 24. Chin CW, Djohan AH, Lang CC. The role of cardiac biochemical markers in aortic stenosis. Biomarkers: biochemical indicators of exposure, response, and susceptibility to chemicals. 2016;21(4):316–27. pmid:26900722
  25. 25. Liu CY, Heckbert SR, Lai S, Ambale-Venkatesh B, Ostovaneh MR, McClelland RL, et al. Association of Elevated NT-proBNP With Myocardial Fibrosis in the Multi-Ethnic Study of Atherosclerosis (MESA). Journal of the American College of Cardiology. 2017;70(25):3102–9. pmid:29268924
  26. 26. Vanky FB, Hakanson E, Svedjeholm R. Long-term consequences of postoperative heart failure after surgery for aortic stenosis compared with coronary surgery. The Annals of thoracic surgery. 2007;83(6):2036–43. pmid:17532392
  27. 27. Metkus TS, Suarez-Pierre A, Crawford TC, Lawton JS, Goeddel L, Dodd OJ, et al. Diastolic dysfunction is common and predicts outcome after cardiac surgery. Journal of cardiothoracic surgery. 2018;13(1):67. pmid:29903030
  28. 28. Nakagawa D, Suwa M, Ito T, Kono T, Kitaura Y. Postoperative outcome in aortic stenosis with diastolic heart failure compared to one with depressed systolic function. International heart journal. 2007;48(1):79–86. pmid:17379981
  29. 29. Selmeryd J, Henriksen E, Leppert J, Hedberg P. Interstudy heterogeneity of definitions of diastolic dysfunction severely affects reported prevalence. Eur Heart J Cardiovasc Imaging. 2016;17(8):892–9. pmid:26374880
  30. 30. Kaw R, Hernandez AV, Pasupuleti V, Deshpande A, Nagarajan V, Bueno H, et al. Effect of diastolic dysfunction on postoperative outcomes after cardiovascular surgery: A systematic review and meta-analysis. The Journal of thoracic and cardiovascular surgery. 2016;152(4):1142–53. pmid:27364601