Next Article in Journal
The Importance of Orthostatic Increase in Pulse Wave Velocity in the Diagnosis of Early Vascular Aging
Previous Article in Journal
Adenosquamous Carcinoma of the Lung: Survival, Radiologic Findings, PD-L1, and Driver Mutations
Previous Article in Special Issue
Homograft Aortic Root Replacement for Destructive Prosthetic Valve Endocarditis: Results in the Current Era
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Mechanical versus Biological Valve Prostheses for Infective Endocarditis Presenting with Stroke

1
Department of Cardiac Surgery, Medical University of Vienna, 1090 Vienna, Austria
2
Department of Emergency Medicine, Medical University of Vienna, 1090 Vienna, Austria
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2024, 13(19), 5712; https://doi.org/10.3390/jcm13195712
Submission received: 26 August 2024 / Revised: 8 September 2024 / Accepted: 24 September 2024 / Published: 25 September 2024
(This article belongs to the Special Issue Clinical Challenges in Endocarditis—2nd Edition)

Abstract

:
Objectives: This study aimed to compare the clinical outcomes of mechanical and biological valve prostheses in patients with infective endocarditis presenting with stroke. Methods: Ninety-five adults with infective endocarditis complicated by stroke at baseline who underwent aortic and/or mitral valve replacement were analyzed retrospectively. The primary outcome was a composite outcome of all-cause mortality, ischemic stroke, hemorrhagic stroke, and re-endocarditis. Secondary outcomes included the individual components of the composite outcome and modified Rankin scale deterioration during follow-up. Results: Among the study cohort, 34 patients (35.8%) received mechanical valve prostheses and 61 (64.2%) received biological valve prostheses. Implantation of a mechanical valve prosthesis seems to be associated with a decreased risk of attaining the composite outcome (adjusted HR 0.46, 95% CI 0.22–0.96, and p = 0.037). Analyses of the individual components of the composite outcome showed that implantation of a mechanical valve prosthesis might not be associated with an increased risk of ischemic stroke, hemorrhagic stroke, and all-cause mortality during the follow-up period. Further, the risk of re-endocarditis was significantly lower in recipients of a mechanical valve prosthesis (adjusted HR 0.15, 95% CI 0.06–0.77, p = 0.026). Notably, a trend toward decreased risk of modified Rankin scale deterioration throughout the follow-up period was observed in this group (adjusted odds ratio 0.22, 95% CI 0.05–1.02, p = 0.053). Conclusions: Implantation of mechanical valve prostheses in patients presenting with infective endocarditis complicated by stroke seems to be beneficial in terms of a reduced risk of experiencing a composite outcome. Analyses of larger cohorts are required to validate our findings.

1. Introduction

Infective endocarditis (IE) frequently presents as a stroke, with an incidence ranging from 20% to 40% [1,2]. As of now, no published data are available regarding long-term clinical outcomes after the implantation of mechanical or biological valve prostheses in patients presenting with IE complicated by stroke. Indeed, endocarditis guidelines are inconclusive regarding the precise indications of prosthesis selection and long-term outcomes in this subset of patients [3,4,5].
The potential downside of implanting a mechanical valve prosthesis in patients presenting with stroke might be stroke exacerbation related to mandatory anticoagulant therapy [6,7]. Conversely, anticoagulant therapy might provide protection against new stroke onsets during the follow-up period and potentially enhance long-term neurological outcomes [8,9,10,11].
The implantation of a biological valve prosthesis may mitigate concerns related to hemorrhagic conversion of the infracted cerebral tissue [4]. However, it is important to consider that younger patients still face the inherent risk of structural valve deterioration and the potential need for reoperation [12].
In the setting of IE, it is plausible that the implantation of a mechanical valve prosthesis, which involves using more artificial material within the infected and inflamed environment, might be associated with an increased risk of re-endocarditis.
We aimed to retrospectively analyze the clinical outcomes in recipients of mechanical versus biological valve prostheses for IE complicated by stroke.

2. Materials and Methods

2.1. Ethical Statement

The Ethics Committee of the Medical University Vienna (vote number 1210/2022; approval date: 5 April 2022) granted approval for this study, and the need for individual patient consent was waived.

2.2. Patients and Clinical Data

Patient screening was conducted by reviewing the regularly updated database of the Department of Cardiac Surgery, Medical University of Vienna, between January 2009 and December 2020. A total of 95 consecutive patients with IE complicated by ischemic or/and hemorrhagic stroke within 2 months prior to surgery were included in this retrospective study. The modified Duke criteria were used to diagnose IE [13]. Based on the Stroke Council of the American Heart Association/American Stroke Association, stroke was defined as an acute neurological impairment accompanied by positive findings on computed tomography and/or magnetic resonance imaging [14]. All patients underwent surgical aortic and/or mitral valve replacement with either mechanical or biological valve prostheses. Patients beyond 18 years of age, as well as those who underwent isolated mitral valve repair and implantation of a homograft, were excluded. Additionally, patients with missing preoperative neuroimaging confirmation of stroke as well as those with isolated meningoencephalitis, intracerebral abscess, infectious intracranial aneurysm, and encephalopathy were excluded. Patients were grouped based on the type of valve prosthesis implanted (mechanical vs. biological valve prostheses).

2.3. Study Outcomes

The primary study outcome was a composite outcome of all-cause mortality, ischemic stroke, hemorrhagic stroke, and re-endocarditis. Secondary study outcomes included individual components of the composite outcome and modified Rankin scale (mRS) deterioration during follow-up. Concerning long-term neurological impairment, the mRS was used to assess the degree of disability in activities of daily living [15]. The mRS score was evaluated at baseline and follow-up, with an mRS score of ≥ 4 denoting severe disability or death. The mRS deterioration was defined as the worsening of a neurological deficit compared to the degree of disability prior to surgery. Study outcomes were extracted retrospectively from patients’ medical records. Mortality data were obtained from the Austrian Federal Statistical Agency. The date of the last follow-up was 1 March 2022.

2.4. Statistical Analysis

Continuous variables with non-normal distributions are described by the median and interquartile range (IQR) (25th and 75th percentiles). Total numbers and percentages were reported for categorical variables. Continuous variables with non-normal distributions were compared using the Mann-Whitney U test. Categorical variables were assessed using the chi-square test. The study employed a cohort design, utilizing individuals as the unit of analysis and the type of valve prosthesis (mechanical vs. biological) as the exposure variable. Within the study cohort, the age distribution displayed a bimodal pattern, with a pronounced decline observed at the age of 55. Based on the likelihood ratio test, no interaction was found for age. The multivariable Cox proportional hazards regression analysis was used to assess the effect of the prosthesis type on both the primary (composite outcome) and secondary study outcomes (individual components of the composite outcome). The effects were reported as an adjusted hazard ratio (HR) with a 95% confidence interval (CI). The co-variables that were likely to constitute common causes for the selection of valve prosthesis and each outcome were included in the multivariable models. The Kaplan-Meier curves were generated to visualize the cumulative probability of a composite outcome for both study groups. The multivariable logistic regression model was used to analyze the long-term neurological impairment during follow-up. A significance level of <0.05 was used to determine the statistical significance. Statistical analyses were performed using STATA 16.1 software (StataCorp LLC, College Station, TX, USA) and SPSS software 27.0 (IBM Corp, Armonk, NY, USA).

3. Results

  • Baseline characteristics
Among our study cohort, 34 patients (35.8%) received mechanical valve prostheses, whereas 61 patients (64.2%) received biological valve prostheses (Table 1). Recipients of mechanical valve prostheses were younger (median 47.4, IQR 41.6–56.7 vs. median 65.1, IQR 55.3–71.5; p < 0.001) and had a lower rate of hypertension (41.2% vs. 68.9%; p = 0.009) and diabetes mellitus (8.8% vs. 29.5%; p = 0.020). A higher rate of echocardiographic confirmed vegetation was observed in recipients of mechanical valve prostheses (100% vs. 85.3%; p = 0.019).
  • Detected pathogens in the blood culture
The species encountered in blood culture are summarized in Supplemental Table S1. For either prosthesis type, no significant difference was observed in the rates of pathogens in blood culture at baseline.
  • Neurological and radiological characteristics
Neuroimaging scans confirmed ischemic stroke as the predominant type of cerebral lesion in both study groups (Table 2). Only one patient presenting with pure hemorrhagic stroke at baseline received a mechanical valve prosthesis. The percentage of mixed lesions, comprising both ischemic and hemorrhagic stroke, was 17.7% and 13.1% in recipients of mechanical and biological valve prostheses, respectively. For either prosthesis type, no significant difference in the neurologic presentation at admission was observed. Time from stroke onset to surgery was similar between both groups. In terms of brain areas affected, middle cerebral artery involvement was similar in both groups. In contrast, recipients of mechanical valve prostheses had a significantly lower rate of cerebellar lesions (0% vs. 13.1%; p = 0.027).
  • Operative characteristics
The operative characteristics are provided in Table 3. Concerning urgency status, no differences were observed among the study groups. Aortic valve replacement (AVR), mitral valve replacement (MVR), and combined valve replacement were performed at similar rates. Regarding combined valve replacement, all patients received either mechanical or biological valve prostheses. Recipients of mechanical valve prostheses underwent aortic root enlargement more frequently (14.7% vs. 3.3%; p = 0.041). All other operative characteristics variables were comparable between study groups.
  • Postoperative in-hospital adverse events
For either prosthesis type, no significant difference was observed in the rates of postoperative in-hospital adverse events (Supplemental Table S2).
  • Antithrombotic therapy
Information regarding antithrombotic therapy, including anticoagulation and antiplatelet drugs, was collected upon discharge (Supplemental Table S3). Vitamin K antagonists were used more frequently in recipients of mechanical valve prostheses (35.3% vs. 8.2%; p ≤ 0.001). However, indirect thrombin inhibitors were used at a lower rate in this group (38.2% vs. 60.7%; p = 0.036). Regarding antiplatelet drugs, no difference was observed among the study groups. Long-term anticoagulation was typically switched to Vitamin K antagonists after discharge in patients with mechanical valves.
  • Primary study outcome—Composite outcome
A composite outcome was observed in 57 (60%) patients during the follow-up period. Multivariable Cox proportional hazards analysis showed a significantly lower risk of experiencing a composite outcome among recipients of mechanical valve prostheses (adjusted HR 0.46, 95% CI 0.22–0.96, p = 0.037) (Table 4). The Kaplan-Meier curves of both groups are depicted in Figure 1.
  • Secondary study outcomes
Analyses of individual components of the composite outcome showed that implantation of a mechanical valve prosthesis was not associated with an increased risk of ischemic stroke (adjusted HR 0.74, 95% CI 0.24–2.24, p = 0.590), hemorrhagic stroke (adjusted HR 0.31, 95% CI, 0.08–1.11; p = 0.073), and all-cause mortality (adjusted HR 0.48, 95% CI 0.21–1.09, p = 0.081) during the follow-up period (Table 5). Further, the risk of re-endocarditis was significantly lower in recipients of a mechanical valve prosthesis (adjusted HR 0.15, 95% CI 0.06–0.77, p = 0.026). Notably, a trend toward decreased risk of mRS deterioration throughout the follow-up period was observed in this group (adjusted odds ratio (OR) 0.22, 95% CI 0.05–1.02, p = 0.053) (Table 5).
  • Causes of death
The causes of death were comparable between study groups (Table 6).

4. Discussion

The main findings of the present study are as follows: (1) implantation of a mechanical valve prosthesis seems to be associated with a significantly lower risk of experiencing a composite outcome during the follow-up period; (2) implantation of a mechanical valve prosthesis was not associated with an increased risk of ischemic stroke, hemorrhagic stroke, or all-cause mortality during the follow-up period; (3) implantation of a mechanical valve prosthesis was associated with a significantly lower risk of re-endocarditis; and (4) a trend toward a lower risk of mRS deterioration during follow-up, which might be observed in recipients of mechanical valve prostheses.
To our knowledge, this is the first cohort study to compare the long-term clinical outcomes of recipients of mechanical versus biological valve prostheses for IE complicated by stroke.
The optimal timing of surgery after the onset of stroke is an important consideration in this clinical setting, involving a delicate balance between the potential neurological exacerbation and the risks associated with delaying the operation. The existing literature indicates that early surgery is advisable for patients with ischemic stroke, particularly in circumstances of high embolic risk, heart failure, and uncontrolled infection [16,17,18,19]. For individuals with hemorrhagic stroke, surgery within two weeks of stroke onset may offer benefits [20,21,22], while a few studies have indicated advantages in delaying surgery for more than one month [23]. In the present study, the time from stroke onset to surgery was not statistically significant between recipients of mechanical valve prostheses (median 13.5, IQR 3.4–29.4) and recipients of biological valve prostheses (median 10.0, IQR 5.8–17.7), and p = 0.470.
Implantation of mechanical valve prostheses in patients presenting with stroke at baseline remains a contentious issue due to the conceivable risk of stroke exacerbation attributed to anticoagulant therapy [6,7]. In contrast, mandatory anticoagulant therapy, along with the implantation of a mechanical valve prosthesis, might potentially provide protection against new-onset stroke during the follow-up period [8,10,11]. Our analysis suggests that the implantation of a mechanical valve prosthesis was not associated with an increased risk of ischemic stroke or hemorrhagic stroke during the follow-up period. Nevertheless, in elective clinical settings, several studies have reported that recipients of mechanical prostheses are at a higher risk of new-onset bleeding yet a lower risk of reoperation during the follow-up period compared to those of biological valve prostheses [24,25]. Offering a non-mechanical valve substitute might be beneficial in certain patient groups such as women of childbearing age, individuals engaged in physically demanding work, and those with a high likelihood of requiring extended mechanical circulatory support [3,26,27].
Indeed, the long-term neurological outcome is undoubtedly a crucial aspect to be considered in patients with stroke at baseline undergoing surgery for IE. According to the current analysis, recipients of mechanical valve prostheses exhibited a trend toward a lower risk of mRS deterioration during the follow-up period (adjusted OR 0.22, 95% CI 0.05–1.02, p = 0.053). Notably, patients treated with anticoagulant therapy may have long-term clinical benefits in terms of stroke prophylaxis and improved neurological recovery [8,9,28]. The literature reports complete neurological recovery (mRS = 0) in 70% of patients undergoing surgery for IE complicated by stroke (irrespective of the type of valve prosthesis) [19]. In a similar manner, Murai and associates documented complete neurological recovery in patients who underwent early surgery for IE [29]. Nevertheless, in the present study, the recipients of mechanical valve prostheses were younger and potentially had a higher neurological recovery potential.
Concerning mortality, numerous studies have examined the impact of hemorrhagic and ischemic strokes at baseline on postoperative mortality in patients undergoing surgery for IE, regardless of the type of valve prosthesis. However, these studies have yielded diverse findings. Several analyses have indicated increased mortality in patients undergoing surgery for IE complicated by stroke [19,29]. Conversely, a study by Diab and colleagues found that preoperative intracranial hemorrhage was not associated with increased in-hospital mortality [30]. Likewise, a large retrospective analysis by Said et al. concluded that stroke prior to surgery for IE was not associated with increased mortality [31]. Nevertheless, several analyses have investigated preferential types of valve prostheses in the context of IE and reported that implantation of a mechanical valve prosthesis was not associated with an increased risk of all-cause mortality [32,33], which is in line with our data.
The present study suggests a lower rate of experiencing a composite outcome in recipients of mechanical valve prostheses. This finding appears to be primarily driven by a significantly decreased risk of re-endocarditis among recipients of mechanical valve prostheses (Table 5). Notably, similar results have been reported in the literature, reinforcing the potential benefits of mechanical valve prostheses in terms of a lower risk of re-endocarditis [34,35,36,37,38].
Regarding the main indications for surgery, no significant differences in the rates of heart failure, uncontrolled infection, and high embolic risk were found between recipients of mechanical and biological valve prostheses. Pizzino et al. conducted a study analyzing the composite outcomes of all-cause mortality, hospitalizations, and relapses of IE among patients categorized by the primary indication for surgery. However, the findings revealed that patients presenting with heart failure and an elevated risk of embolism were independently associated with a higher risk of experiencing a composite outcome [39].
Nonetheless, it is essential to highlight the critical role of a multidisciplinary endocarditis team in evaluating the risk-benefit assessment for each patient and clinical situation [4]. Postoperative close monitoring of the coagulation profile is indispensable in this clinical setting [10].

5. Study Strengths and Limitations

The findings of this study may provide valuable insights into this specific clinical setting and serve as a basis for future research. Our study has the inherent limitations of a retrospective single-center analysis. Most importantly, the size of our study cohort is small. Additionally, the time interval from stroke to surgery was heterogeneous and was defined within a 2 months timeframe. A detailed analysis of the extent of the infarcted area was not performed. The mRS scores at baseline were assessed retrospectively. The study groups differed in sample size and baseline characteristics such as hypertension and diabetes mellitus. Molecular analyses, including the examination of Cluster of Differentiation 93 gene dysregulation and its potential association with cardiovascular outcomes, have not been investigated [40]. Moreover, information regarding adherence to anticoagulant therapy at baseline and during the follow-up period was not available for the statistical analysis.

6. Conclusions

In conclusion, the implantation of mechanical valve prostheses in patients presenting with IE complicated by stroke might be beneficial in terms of a reduced the risk of experiencing the composite outcome and demonstrating similar risks of ischemic stroke, hemorrhagic stroke, and all-cause mortality during the follow-up period compared with biological valve prostheses. Further studies would be needed to validate our results.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/jcm13195712/s1, Table S1: Detected pathogens in the blood culture; Table S2: Postoperative in-hospital adverse events; Table S3: Antithrombotic therapy.

Author Contributions

Conceptualization, A.K. (Amila Kahrovic), P.A. and M.A.; methodology, A.K. (Amila Kahrovic), H.H. and P.W.; formal analysis, H.H. and P.A.; investigation, A.K. (Amila Kahrovic), A.A. and T.P.; data curation, A.K. (Amila Kahrovic), A.A. and S.L.; writing—original draft preparation, A.K. (Amila Kahrovic), A.A., S.L. and T.P.; writing—review and editing, M.A., A.K. (Alfred Kocher), G.L., H.H., P.W. and P.A.; supervision, M.A. and A.K. (Alfred Kocher), and G.L.; project administration, A.K. (Amila Kahrovic), and M.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Ethics Committee of the Medical University Vienna (protocol code 1210/2022, date of approval 5 April 2022).

Informed Consent Statement

Patient consent was waived because of the retrospective nature of this study.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors upon request.

Conflicts of Interest

M.A. has received institutional research funding (Edwards, Abbott, Medtronic, and LSI) and has served as a proctor/speaker/consultant (Edwards, Abbott, Medtronic, Zoll, Boston, and Abbvie). The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as potential conflicts of interest.

Abbreviations

AVRAortic valve replacement
CABGCoronary artery bypass grafting
CIConfidence interval
CPBCardiopulmonary bypass
ECMOExtracorporeal Membrane Oxygenation
Euro SCORE IIEuropean System for Cardiac Operative Risk Evaluation II
HRHazard ratio
IEInfective endocarditis
IQRInterquartile range
mRSmodified Rankin Scale
MVRMitral valve replacement
OROdds Ratio

References

  1. Thuny, F.; Avierinos, J.-F.; Tribouilloy, C.; Giorgi, R.; Casalta, J.-P.; Milandre, L.; Brahim, A.; Nadji, G.; Riberi, A.; Collart, F.; et al. Impact of cerebrovascular complications on mortality and neurologic outcome during infective endocarditis: A prospective multicentre study. Eur. Heart J. 2007, 28, 1155–1161. [Google Scholar] [CrossRef] [PubMed]
  2. Barsic, B.; Dickerman, S.; Krajinovic, V.; Pappas, P.; Altclas, J.; Carosi, G.; Casabé, J.H.; Chu, V.H.; Delahaye, F.; Edathodu, J.; et al. Influence of the Timing of Cardiac Surgery on the Outcome of Patients with Infective Endocarditis and Stroke. Clin. Infect. Dis. 2013, 56, 209–217. [Google Scholar] [CrossRef] [PubMed]
  3. Delgado, V.; Marsan, N.A.; de Waha, S.; Bonaros, N.; Brida, M.; Burri, H.; Caselli, S.; Doenst, T.; Ederhy, S.; Erba, P.A.; et al. 2023 ESC Guidelines for the management of endocarditis. Eur. Heart J. 2023, 44, 3948–4042. [Google Scholar] [CrossRef] [PubMed]
  4. AATS Surgical Treatment of Infective Endocarditis Consensus Guidelines Writing Committee Chairs; Pettersson, G.B.; Coselli, J.S.; Hussain, S.T.; Griffin, B.; Blackstone, E.H.; Gordon, S.M.; LeMaire, S.A.; Woc-Colburn, L.E. 2016 The American Association for Thoracic Surgery (AATS) consensus guidelines: Surgical treatment of infective endocarditis: Executive summary. J. Thorac. Cardiovasc. Surg. 2017, 153, 1241–1258.e29. [Google Scholar] [CrossRef] [PubMed]
  5. Vahanian, A.; Beyersdorf, F.; Praz, F.; Milojevic, M.; Baldus, S.; Bauersachs, J.; Capodanno, D.; Conradi, L.; De Bonis, M.; De Paulis, R.; et al. 2021 ESC/EACTS Guidelines for the management of valvular heart disease: Developed by the Task Force for the management of valvular heart disease of the European Society of Cardiology (ESC) and the European Association for Cardio-Thoracic Surgery (EACTS). Eur. Heart J. 2021, 60, 727–800. [Google Scholar] [CrossRef]
  6. Klein, C.F.; Gørtz, S.; Wohlfahrt, J.; Munch, T.N.; Melbye, M.; Bundgaard, H.; Iversen, K.K. Long-term Risk of Hemorrhagic Stroke in Patients with Infective Endocarditis: A Danish Nationwide Cohort Study. Clin. Infect. Dis. 2019, 68, 668–675. [Google Scholar] [CrossRef]
  7. García-Cabrera, E.; Fernández-Hidalgo, N.; Almirante, B.; Ivanova-Georgieva, R.; Noureddine, M.; Plata, A.; Lomas, J.M.; Gálvez-Acebal, J.; Hidalgo-Tenorio, C.; Ruíz-Morales, J.; et al. Neurological complications of infective endocarditis: Risk factors, outcome, and impact of cardiac surgery: A multicenter observational study. Circulation 2013, 127, 2272–2284. [Google Scholar] [CrossRef]
  8. Friberg, L.; Rosenqvist, M.; Lip, G.Y. Net clinical benefit of warfarin in patients with atrial fibrillation: A report from the Swedish atrial fibrillation cohort study. Circulation 2012, 125, 2298–2307. [Google Scholar] [CrossRef]
  9. Xian, Y.; Wu, J.; O’brien, E.C.; Fonarow, G.C.; Olson, D.M.; Schwamm, L.H.; Bhatt, D.L.; E Smith, E.; E Suter, R.; Hannah, D.; et al. Real world effectiveness of warfarin among ischemic stroke patients with atrial fibrillation: Observational analysis from Patient-Centered Research into Outcomes Stroke Patients Prefer and Effectiveness Research (PROSPER) study. BMJ 2015, 351, h3786. [Google Scholar] [CrossRef]
  10. Kleindorfer, D.O.; Towfighi, A.; Chaturvedi, S.; Cockroft, K.M.; Gutierrez, J.; Lombardi-Hill, D.; Kamel, H.; Kernan, W.N.; Kittner, S.J.; Leira, E.C.; et al. 2021 Guideline for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack: A Guideline From the American Heart Association/American Stroke Association. Stroke 2021, 52, e364–e467. [Google Scholar] [CrossRef]
  11. Biffi, A.; Kuramatsu, J.B.; Leasure, A.; Kamel, H.; Kourkoulis, C.; Schwab, K.; Ayres, A.M.; Elm, J.; Gurol, M.E.; Greenberg, S.M.; et al. Oral Anticoagulation and Functional Outcome after Intracerebral Hemorrhage. Ann. Neurol. 2017, 82, 755–765. [Google Scholar] [CrossRef] [PubMed]
  12. Dvir, D.; Bourguignon, T.; Otto, C.M.; Hahn, R.T.; Rosenhek, R.; Webb, J.G.; Treede, H.; Sarano, M.E.; Feldman, T.; Wijeysundera, H.C.; et al. Standardized Definition of Structural Valve Degeneration for Surgical and Transcatheter Bioprosthetic Aortic Valves. Circulation 2018, 137, 388–399. [Google Scholar] [CrossRef] [PubMed]
  13. Li, J.S.; Sexton, D.J.; Mick, N.; Nettles, R.; Fowler, V.G., Jr.; Ryan, T.; Bashore, T.; Corey, G.R. Proposed modifications to the Duke criteria for the diagnosis of infective endocarditis. Clin. Infect. Dis. 2000, 30, 633–638. [Google Scholar] [CrossRef] [PubMed]
  14. Sacco, R.L.; Kasner, S.E.; Broderick, J.P.; Caplan, L.R.; Connors, J.J.; Culebras, A.; Elkind, M.S.; George, M.G.; Hamdan, A.D.; Higashida, R.T.; et al. An updated definition of stroke for the 21st century: A statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2013, 44, 2064–2089. [Google Scholar] [CrossRef] [PubMed]
  15. Banks, J.L.; Marotta, C.A. Outcomes validity and reliability of the modified Rankin scale: Implications for stroke clinical trials: A literature review and synthesis. Stroke 2007, 38, 1091–1096. [Google Scholar] [CrossRef]
  16. Sorabella, R.A.; Han, S.M.; Grbic, M.; Wu, Y.S.; Takyama, H.; Kurlansky, P.; Borger, M.A.; Argenziano, M.; Gordon, R.; George, I. Early Operation for Endocarditis Complicated by Preoperative Cerebral Emboli Is Not Associated With Worsened Outcomes. Ann. Thorac. Surg. 2015, 100, 501–508. [Google Scholar] [CrossRef]
  17. Samura, T.; Yoshioka, D.; Toda, K.; Sakaniwa, R.; Yokoyama, J.; Suzuki, K.; Miyagawa, S.; Yoshikawa, Y.; Hata, H.; Takano, H.; et al. Emergency valve surgery improves clinical results in patients with infective endocarditis complicated with acute cerebral infarction: Analysis using propensity score matching. Eur. J. Cardiothorac. Surg. 2019, 56, 942–949. [Google Scholar] [CrossRef]
  18. Bonaros, N.; Czerny, M.; Pfausler, B.; Müller, S.; Bartel, T.; Thielmann, M.; Shehada, S.-E.; Folliguet, T.; Obadia, J.-F.; Holfeld, J.; et al. Infective endocarditis and neurologic events: Indications and timing for surgical interventions. Eur. Heart J. Suppl. 2020, 22, M19–M25. [Google Scholar] [CrossRef]
  19. Ruttmann, E.; Abfalterer, H.; Wagner, J.; Grimm, M.; Müller, L.; Bates, K.; Ulmer, H.; Bonaros, N. Endocarditis-related stroke is not a contraindication for early cardiac surgery: An investigation among 440 patients with left-sided endocarditis. Eur. J. Cardiothorac. Surg. 2020, 58, 1161–1167. [Google Scholar] [CrossRef]
  20. Murai, R.; Kaji, S.; Kitai, T.; Kim, K.; Ota, M.; Koyama, T.; Furukawa, Y. The Clinical Significance of Cerebral Microbleeds in Infective Endocarditis Patients. Semin. Thorac. Cardiovasc. Surg. 2019, 31, 51–58. [Google Scholar] [CrossRef]
  21. Kume, Y.; Fujita, T.; Fukushima, S.; Shimahara, Y.; Matsumoto, Y.; Yamashita, K.; Kawamoto, N.; Kobayashi, J. Intracranial mycotic aneurysm is associated with cerebral bleeding post-valve surgery for infective endocarditis. Interact. Cardiovasc. Thorac. Surg. 2018, 27, 635–641. [Google Scholar] [CrossRef] [PubMed]
  22. Salaun, E.; Touil, A.; Hubert, S.; Casalta, J.-P.; Gouriet, F.; Robinet-Borgomano, E.; Doche, E.; Laksiri, N.; Rey, C.; Lavoute, C.; et al. Intracranial haemorrhage in infective endocarditis. Arch. Cardiovasc. Dis. 2018, 111, 712–721. [Google Scholar] [CrossRef] [PubMed]
  23. Okita, Y.; Minakata, K.; Yasuno, S.; Uozumi, R.; Sato, T.; Ueshima, K.; Konishi, H.; Morita, N.; Harada, M.; Kobayashi, J.; et al. Optimal timing of surgery for active infective endocarditis with cerebral complications: A Japanese multicentre study. Eur. J. Cardiothorac. Surg. 2016, 50, 374–382. [Google Scholar] [CrossRef] [PubMed]
  24. Goldstone, A.B.; Chiu, P.; Baiocchi, M.; Lingala, B.; Patrick, W.L.; Fischbein, M.P.; Woo, Y.J. Mechanical or Biologic Prostheses for Aortic-Valve and Mitral-Valve Replacement. N. Engl. J. Med. 2017, 377, 1847–1857. [Google Scholar] [CrossRef] [PubMed]
  25. Glaser, N.; Jackson, V.; Holzmann, M.J.; Franco-Cereceda, A.; Sartipy, U. Aortic valve replacement with mechanical vs. biological prostheses in patients aged 50–69 years. Eur. Heart J. 2016, 37, 2658–2667. [Google Scholar] [CrossRef]
  26. Cannegieter, S.C.; Rosendaal, F.R.; Briët, E. Thromboembolic and bleeding complications in patients with mechanical heart valve prostheses. Circulation 1994, 89, 635–641. [Google Scholar] [CrossRef]
  27. Chan, W.S.; Anand, S.; Ginsberg, J.S. Anticoagulation of pregnant women with mechanical heart valves: A systematic review of the literature. Arch. Intern. Med. 2000, 160, 191–196. [Google Scholar] [CrossRef]
  28. Kernan, W.N.; Ovbiagele, B.; Black, H.R.; Bravata, D.M.; Chimowitz, M.I.; Ezekowitz, M.D.; Fang, M.C.; Fisher, M.; Furie, K.L.; Heck, D.V.; et al. Guidelines for the prevention of stroke in patients with stroke and transient ischemic attack: A guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 2014, 45, 2160–2236. [Google Scholar] [CrossRef]
  29. Murai, R.; Funakoshi, S.; Kaji, S.; Kitai, T.; Kim, K.; Koyama, T.; Furukawa, Y. Outcomes of early surgery for infective endocarditis with moderate cerebral complications. J. Thorac. Cardiovasc. Surg. 2017, 153, 831–840.e8. [Google Scholar] [CrossRef]
  30. Diab, M.; Musleh, R.; Lehmann, T.; Sponholz, C.; Pletz, M.W.; Franz, M.; Schulze, P.C.; Witte, O.W.; Kirchhof, K.; Doenst, T.; et al. Risk of postoperative neurological exacerbation in patients with infective endocarditis and intracranial haemorrhage. Eur. J. Cardiothorac. Surg. 2021, 59, 426–433. [Google Scholar] [CrossRef]
  31. Said, S.M.; Abdelsattar, Z.M.; Schaff, H.V.; Greason, K.L.; Daly, R.C.; Pochettino, A.; Joyce, L.D.; Dearani, J.A. Outcomes of surgery for infective endocarditis: A single-centre experience of 801 patients. Eur. J. Cardiothorac. Surg. 2018, 53, 435–439. [Google Scholar] [CrossRef] [PubMed]
  32. Nguyen, D.T.; Delahaye, F.; Obadia, J.-F.; Duval, X.; Selton-Suty, C.; Carteaux, J.-P.; Hoen, B.; Alla, F.; for the AEPEI Study Group. Aortic valve replacement for active infective endocarditis: 5-year survival comparison of bioprostheses, homografts and mechanical prostheses. Eur. J. Cardiothorac. Surg. 2010, 37, 1025–1032. [Google Scholar] [CrossRef] [PubMed]
  33. Musci, M.; Hübler, M.; Amiri, A.; Stein, J.; Kosky, S.; Meyer, R.; Weng, Y.; Hetzer, R. Surgical treatment for active infective prosthetic valve endocarditis: 22-year single-centre experience. Eur. J. Cardiothorac. Surg. 2010, 38, 528–538. [Google Scholar] [CrossRef] [PubMed]
  34. Kahrovic, A.; Angleitner, P.; Herkner, H.; Kocher, A.; Ehrlich, M.; Laufer, G.; Andreas, M. Mechanical versus biological valve prostheses for left-sided infective endocarditis. Eur. J. Cardiothorac. Surg. 2022, 62, ezac056. [Google Scholar] [CrossRef]
  35. Anantha-Narayanan, M.; Reddy, Y.N.V.; Sundaram, V.; Murad, M.H.; Erwin, P.J.; Baddour, L.M.; Schaff, H.V.; A Nishimura, R. Endocarditis risk with bioprosthetic and mechanical valves: Systematic review and meta-analysis. Heart 2020, 106, 1413–1419. [Google Scholar] [CrossRef]
  36. Tao, E.; Wan, L.; Wang, W.; Luo, Y.; Zeng, J.; Wu, X. The prognosis of infective endocarditis treated with biological valves versus mechanical valves: A meta-analysis. PLoS ONE 2017, 12, e0174519. [Google Scholar] [CrossRef]
  37. Lee, H.-A.; Wu, V.C.-C.; Chan, Y.-S.; Cheng, Y.-T.; Lee, J.-K.; Chu, P.-H.; Chen, S.-W. Infective endocarditis after surgical aortic or mitral valve replacement: A nationwide population-based study. J. Thorac. Cardiovasc. Surg. 2023, 166, 1056–1068.e7. [Google Scholar] [CrossRef]
  38. Østergaard, L.; Valeur, N.; Ihlemann, N.; Smerup, M.H.; Bundgaard, H.; Gislason, G.; Torp-Pedersen, C.; Bruun, N.E.; Køber, L.; Fosbøl, E.L. Incidence and factors associated with infective endocarditis in patients undergoing left-sided heart valve replacement. Eur. Heart J. 2018, 39, 2668–2675. [Google Scholar] [CrossRef]
  39. Pizzino, F.; Paradossi, U.; Trimarchi, G.; Benedetti, G.; Marchi, F.; Chiappino, S.; Conti, M.; Di Bella, G.; Murzi, M.; Di Sibio, S.; et al. Clinical Features and Patient Outcomes in Infective Endocarditis with Surgical Indication: A Single-Centre Experience. J. Cardiovasc. Dev. Dis. 2024, 11, 138. [Google Scholar] [CrossRef]
  40. Piani, F.; Tossetta, G.; Cara-Fuentes, G.; Agnoletti, D.; Marzioni, D.; Borghi, C. Diagnostic and Prognostic Role of CD93 in Cardiovascular Disease: A Systematic Review. Biomolecules 2023, 13, 910. [Google Scholar] [CrossRef]
Figure 1. Kaplan-Meier curves show the probability of experiencing a composite outcome in recipients of mechanical versus biological valve prostheses.
Figure 1. Kaplan-Meier curves show the probability of experiencing a composite outcome in recipients of mechanical versus biological valve prostheses.
Jcm 13 05712 g001
Table 1. Baseline characteristics.
Table 1. Baseline characteristics.
VariablesMechanical
n = 34
(35.8%)
Biological
n = 61
(64.2%)
p-Value
Age (years) (25th–75th interval)47.4 (41.6–56.7)65.1 (55.3–71.5)<0.001
Age > 55 years (%)10 (29.4)45 (73.8)<0.001
Female (%) 10 (29.4)20 (32.8)0.734
EuroSCORE II (25th–75th interval)7.5 (2.4–18.1)10.3 (5.2–24.6)0.073
Ejection fraction > 60% (%)27 (79.4)49 (80.3)0.915
Atrial fibrillation (%) 10 (29.4)14 (23.0)0.487
Hypertension (%)14 (41.2)42 (68.9)0.009
Diabetes mellitus (%)3 (8.8)18 (29.5)0.020
Dialysis (%)2 (5.9)7 (11.5)0.372
Prosthetic valve endocarditis (%)6 (17.7)14 (23.0)0.543
Positive blood culture (%)32 (94.1)59 (96.7)0.545
Laboratory data (25th–75th interval)
  C-reactive protein (mg/dL)6.0 (2.9–9.0)6.7 (3.8–14.1)0.244
  White blood cell count (G/L)8.5 (6.7–12.4)9.0 (7.1–12.7)0.650
  Lactate value (mmol/L)1.0 (0.7–1.5)1.0 (0.8–1.3)0.941
Positive echocardiography findings
  Vegetation (%)34 (100)52 (85.3)0.019
  Annular abscess (%)8 (23.5)17 (27.9)0.645
  Pseudoaneurysm (%)2 (5.9)1 (1.6)0.257
  Fistula (%)1 (2.9)1 (1.6)0.672
Peripheral embolism (%)16 (47.1)37 (60.7)0.201
Main indication for surgery
  Heart failure (%)14 (41.2)16 (26.2)0.133
  Uncontrolled infection (%)10 (29.4)23 (37.7)0.416
  High embolic risk (%)10 (29.4)22 (36.1)0.511
Preoperative antibiotic treatment (d) (25th–75th interval)14.0 (6.6–24.8)10.3 (6.4–22.4)0.342
Boldface denotes statistical significance (p < 0.05). Euro SCORE II: European System for Cardiac Operative Risk Evaluation II.
Table 2. Neurological and radiological characteristics.
Table 2. Neurological and radiological characteristics.
VariablesMechanical
n = 34
(35.8%)
Biological
n = 61
(64.2%)
p-Value
Stroke prior to surgery
  Ischemic (%)27 (79.4)49 (80.3)0.915
  Hemorrhagic (%)1 (2.9)4 (6.6)0.449
  Mixed lesion (%)6 (17.7)8 (13.1)0.550
Time from stroke to surgery (d)
(25th–75th interval)
13.5 (3.4–29.4)10.0 (5.8–17.7)0.470
Neurologic presentation at admission
  mRS score ≥ 4 (%)16 (47.1)29 (47.5)0.964
  Motor control impairment (%)14 (41.2)28 (45.9)0.657
  Impaired consciousness (%)4 (11.8)17 (27.9)0.070
  Asymptomatic (%)7 (20.6)6 (9.8)0.144
Brain area affected
  Middle cerebral artery (%)11 (32.4)13 (21.3)0.235
  Multiple site (%)12 (35.3)20 (32.8)0.804
  Frontoparietal (%)7 (20.6)12 (19.7)0.915
  Temporal (%)3 (8.8)5 (8.2)0.916
  Occipital (%)4 (11.8)7 (11.5)0.966
  Cerebellum (%)0 (0.0)8 (13.1)0.027
  Brain Stem (%)2 (5.9)1 (1.6)0.257
  Basal ganglia (%)1 (2.9)9 (14.8)0.072
Boldface denotes statistical significance (p < 0.05). mRS: modified Rankin scale.
Table 3. Operative characteristics.
Table 3. Operative characteristics.
VariablesMechanical
n = 34
(35.8%)
Biological
n = 61
(64.2%)
p-Value
Urgency status
  Urgent (%)28 (82.4)46 (75.4)0.434
  Emergent (%)6 (17.6)13 (21.3)0.669
  Salvage (%)0 (0.0)2 (3.3)0.056
AVR (%)12 (35.3)25 (41.0)0.586
MVR (%)18 (52.9)26 (42.6)0.334
Combined AVR and MVR (%)4 (11.8)10 (16.4)0.542
Right side involvement (%)2 (5.9)3 (4.9)0.840
CABG (%)3 (8.8)12 (19.7)0.164
Annular abscess exclusion (%)6 (17.6)18 (29.5)0.202
Commando procedure (%)2 (5.9)0 (0.0)0.056
Ventricular septal defect closure (%)1 (2.9)1 (1.6)0.672
Aortic root enlargement (%)5 (14.7)2 (3.3)0.041
Aortic root replacement (%)4 (11.8)2 (3.3)0.103
CPB time (min) (25th–75th interval)148 (95–221)145 (108–192)0.951
Cross-clamp time (min) (25th–75th interval)103 (63–164)103 (71–129)0.816
Boldface denotes statistical significance (p < 0.05). AVR: aortic valve replacement; CABG: coronary artery bypass grafting; CPB: cardiopulmonary bypass; MVR: mitral valve replacement.
Table 4. Primary study outcome—Composite outcome.
Table 4. Primary study outcome—Composite outcome.
VariablesHR95% CIp-Value
Mechanical valve prosthesis a0.460.22–0.960.037
  Age > 55 years0.420.19–0.940.035
  EuroSCORE II (log-transformed)1.491.07–2.060.017
  Time from stroke to surgery (days)0.980.96–1.000.078
  Atrial fibrillation1.740.88–3.460.112
  Intravenous drug abuse0.990.40–2.430.984
  Prosthetic valve endocarditis0.820.40–1.670.579
  Annular abscess1.320.69–2.520.398
  Cross-clamp time (min)1.001.00–1.010.417
a Effects presented as HR using multivariable Cox proportional hazards regression analysis. Boldface denotes statistical significance (p < 0.05). CI: confidence interval; EuroSCORE II: European System for Cardiac Operative Risk Evaluation II; HR: hazard ratio.
Table 5. Secondary study outcomes.
Table 5. Secondary study outcomes.
VariablesMultivariable Relative Effectsp-Value
Ischemic stroke a
  Mechanical valve prosthesis0.74 (0.24–2.24)0.590
Hemorrhagic stroke a
  Mechanical valve prosthesis0.31 (0.08–1.11)0.073
Re-endocarditis a
  Mechanical valve prosthesis0.15 (0.06–0.77)0.026
All-cause mortality a
  Mechanical valve prosthesis0.48 (0.21–1.09)0.081
mRS deterioration during follow-up b
  Mechanical valve prosthesis0.22 (0.05–1.02)0.053
a Effects presented as HR and 95% CI using multivariable Cox proportional hazards regression analysis. b Effects presented as OR and 95% CI using multivariable logistic regression analysis. Co-variables for these analyses were age > 55 years, EuroSCORE II (log-transformed), time from stroke to surgery (days), atrial fibrillation, intravenous drug abuse, prosthetic valve endocarditis, annular abscess, and cross-clamp time (min). Boldface denotes statistical significance (p < 0.05). CI: confidence interval; mRS: modified Rankin scale.
Table 6. Causes of death.
Table 6. Causes of death.
VariablesMechanical
n = 34
(35.8%)
Biological
n = 61
(64.2%)
p-Value
Cardiac (%)4 (11.8)7 (11.5)0.966
Infection (%)3 (8.8)10 (16.4)0.303
Multi-organ failure (%)2 (5.9)3 (4.9)0.840
Neurological (%)1 (2.9)4 (6.6)0.449
Cancer (%)0 (0.0)3 (4.9)0.286
Other (%)1 (2.9)3 (4.9)0.647
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Kahrovic, A.; Angleitner, P.; Herkner, H.; Werner, P.; Andreeva, A.; Poschner, T.; Laengle, S.; Kocher, A.; Laufer, G.; Andreas, M. Mechanical versus Biological Valve Prostheses for Infective Endocarditis Presenting with Stroke. J. Clin. Med. 2024, 13, 5712. https://doi.org/10.3390/jcm13195712

AMA Style

Kahrovic A, Angleitner P, Herkner H, Werner P, Andreeva A, Poschner T, Laengle S, Kocher A, Laufer G, Andreas M. Mechanical versus Biological Valve Prostheses for Infective Endocarditis Presenting with Stroke. Journal of Clinical Medicine. 2024; 13(19):5712. https://doi.org/10.3390/jcm13195712

Chicago/Turabian Style

Kahrovic, Amila, Philipp Angleitner, Harald Herkner, Paul Werner, Alexandra Andreeva, Thomas Poschner, Severin Laengle, Alfred Kocher, Guenther Laufer, and Martin Andreas. 2024. "Mechanical versus Biological Valve Prostheses for Infective Endocarditis Presenting with Stroke" Journal of Clinical Medicine 13, no. 19: 5712. https://doi.org/10.3390/jcm13195712

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop