Skip to main content

Advertisement

Rationale and design of a prospective, observational study for the QUantitative EStimation of Thrombus burden in patients with ST-Elevation Myocardial Infarction using micro-computed tomography: the QUEST-STEMI trial

Abstract

Background

Although the presence of thrombus in patients with ST-elevation myocardial infarction (STEMI) has been linked to adverse outcomes, routine thrombus aspiration has not been proven effective. A potential explanation is that these patients should be risk-stratified. Traditional clinical, laboratory and angiographic parameters used in clinical trials have been proven inadequate to classify patients. Aspirated thrombotic material characteristics might be an additional important parameter that has not yet been addressed. In this report, we aim to describe a methodological analysis of thrombus aspirated from coronary arteries during primary PCI using micro-Computed Τomography (micro-CT). These data will be combined with traditional factors to develop a risk-stratification system with high discriminative power for these patients.

Methods

Eighty-seven patients with STEMI undergoing thrombus aspiration in AHEPA University Hospital, Greece, will be enrolled in the study. The first patient was enrolled in June 2018. After being aspirated, thrombi are preserved in formalin and their volume and density are calculated with micro-CT. Micro-CT allows us to create 3D models of thrombi from a series of x-ray projection images. These models are further analyzed to find the volume and density of extracted thrombi and to assess potential differences in their structure. Association of these variables with clinical parameters and angiographic outcomes will be explored.

Discussion

QUEST-STEMI is-to our knowledge-the first study of volumetric coronary thrombus assessment by micro-CT. This method could be used in larger, clinically-oriented trials to help stratify patients with thrombus burden according to their risk for adverse outcomes.

Trial registration

QUEST-STEMI trial ClinicalTrials.gov number: NCT03429608 Date of registration: February 12, 2018. The study was prospectively registered (registered prior to enrollment of the first participant).

Peer Review reports

Background

Introduction

Acute myocardial infarction with ST-elevation (STEMI) remains one of the leading causes of mortality, despite the advances in pharmacological therapy and in mechanical reperfusion therapy. It is attributed to acute thrombotic occlusion of an epicardial coronary artery due to rupture of an atherosclerotic plaque leading to platelet aggregation and thrombus formation. According to guidelines, the preferred reperfusion strategy is primary PCI, as it further reduces mortality compared to fibrinolytic therapy [1]. However, despite improving outcomes over time, mortality among patients with STEMI undergoing primary PCI remains significant [2]. Interestingly, the presence of thrombus in patients suffering from acute coronary syndrome and undergoing PCI has been found to increase the incidence of Major Adverse Cardiac and Cerebrovascular events (MACCE) [3]. Apart from MACCE, high thrombus burden in patients with STEMI has been independently associated with stent thrombosis [4], distal embolization [5], no-reflow phenomenon [6], late incomplete stent apposition and late stent thrombosis [7].

Conceptually, based on the evidence, mechanical removal of thrombus, using thrombus aspiration catheters, should be beneficial for the patients. However, large randomized controlled trials of routine thrombus aspiration (such as TAPAS [8], TASTE [9], TOTAL [10] and INFUSE-AMI [11]) showed controversial results, providing in total no evidence of distinct benefits for thrombus aspiration, according to many recent meta-analyses [12,13,14,15], Moreover, the TOTAL trial showed an increase in risk of stroke for patients undergoing thrombus aspiration [16]. Thus, according to the current guidelines of the European Society of Cardiology (ESC), routine thrombus aspiration is not recommended in patients with STEMI [17].

Rationale for the study

A potential explanation for the controversial results of the randomized controlled trials could be that, in all these trials, thrombus aspiration was performed as a routine strategy in all patients presenting with STEMI, whereas these patients should be considered as a heterogeneous group and thus they should be risk-stratified. The need for patient-level risk stratification is also reflected in the recent guidelines of the ESC, according to which, although thrombus aspiration is not recommended as a routine strategy, it may be considered in certain patients [17]. However, no specification about the profile of patients, in whom thrombus aspiration should be undertaken, is provided, and performing thrombus aspiration is left at the discretion of the interventional cardiologist conducting the primary PCI. Presently, there is evidence suggesting that angiographically quantified thrombotic burden (as assessed using the classification by Gibson [18] and  by Sianos [19]) could potentially be one of the parameters affecting the clinical outcomes, as patients with large thrombus burden are at higher risk for future adverse outcomes [20]. Nonetheless, a subgroup analysis of the TOTAL trial, which assessed the benefit of thrombus aspiration in patients with high thrombus burden, showed that routine thrombus aspiration in this patient subgroup did not improve cardiovascular outcomes [21]. Hence, additional factors are required to stratify risk in patients with STEMI, since traditional clinical, laboratory and angiographic parameters used in clinical trials have been proven inadequate. Aspirated thrombotic material characteristics might be an additional important parameter that has not yet been addressed and might further provide evidence of patients that will benefit from thrombus removal.

Recent advances in non-invasive imaging enable the quantification of parameters that so far have only been subjective to the individual viewer. Micro-CT is an emerging non-destructive technique of 3D imaging, which has a much finer resolution compared to conventional Computational Tomography [22]. Although it was initially used for skeletal imaging, the development of contrast agents, which increase the low inherent contrast of soft-tissues in X-ray absorption, has expanded applications for micro-CT to the imaging of soft-tissues [22]. This facilitates precise soft-tissue visualization and characterization and can provide useful information about the compositional and morphological properties of extracted thrombi.

The purpose of the study is to assess for the first time, through the application of innovative technologies, important features of extracted thrombi, including their volume, their shape, their micro-architecture and their density, which might be linked to certain clinical outcomes. This will contribute to the development of a more sophisticated risk-stratification model with high discriminative power combining: clinical and laboratory data, angiographic parameters and data regarding the characteristics of aspirated thrombi, which will be derived using micro-CT. This might facilitate a more personalized risk-based approach in treating patients with STEMI.

Methods/design of the study

Study design and population

QUEST-STEMI (ClinicalTrials.gov Identifier: NCT03429608) is an investigator-initiated, prospective, single-arm, non-interventional cohort trial involving patients with STEMI, who undergo primary PCI and thrombus aspiration within 12 h of symptoms onset.

The trial is conducted in accordance with the principles set by the declaration of Helsinki, the International Conference on Harmonization Guidelines for Good Clinical Practice and all applicable regulatory requirements. The study protocol has been approved by the Medical Ethics Committee of the Aristotle University of Thessaloniki and by the Scientific Committee of AHEPA University Hospital. Each subject provides written informed consent before participating in the study.

A total of 87 patients presenting to AHEPA University Hospital with STEMI, who undergo primary PCI and thrombus aspiration at the discretion of the treating physician, will be enrolled in the study. Detailed eligibility criteria are described in Table 1.

Table 1 Summary of inclusion and exclusion criteria for the QUEST STEMI study

The first patient was enrolled in QUEST-STEMI on 5 June 2018. As of December 2019, 70 patients have been enrolled. Completion of enrollment is anticipated in the first quarter of 2020. The results of the study are expected until the end of 2021.

Thrombus aspiration procedure

The pharmacological treatment of each patient prior to PCI is according to standard practices (unfractionated heparin (100 IU/kg) and a loading dose of aspirin (325 mg) and either ticagrelor (180 mg) or prasugrel (60 mg) or clopidogrel (600 mg)) [17]. Thrombus aspiration is performed by experienced interventional cardiologists according to standard practices, as previously described [8,9,10]. Briefly, after crossing the lesion with a wire, the thrombus aspiration catheter is advanced proximal to the lesion. Two different aspiration systems, which are available at our institution, are being used: the 6F STENTYS aspiration catheter and the 6F Thrombuster II catheter (Kaneka). The choice of the aspiration device is at the discretion of the Interventional Cardiologist. Manual suction begins before the catheter crosses the lesion. The thrombus aspiration catheter is passed through the thrombotic occlusion many times, so that at least 40 cc of blood and material are aspirated. In case blood backflow stops suddenly during the procedure, the device should be removed to check for the presence of thrombus obstructing the lumen. The solid material aspirate is captured in a filter basket provided by the manufacturer of the thrombus aspiration catheter.

The aspirated thrombi are preserved in 10% formalin solution and are analyzed using the micro-CT.

Micro-CT procedure

Staining

The samples are sent to the Biodiversity Laboratory of the Institute of Marine Biology, Biotechnology and Aquaculture (IMBBC) and are thoroughly washed with distilled water. Subsequently, they are subjected to dehydration procedures so that they are gradually stored in alcohol solution 70% (Metscher protocol) [23].

In order to achieve the best imaging of the thrombi, chemical factors which strengthen the contrast of tissues, such as phosphotungstic acid (PTA), are being used (Fig. 1a) to achieve best quality of the micro-CT tomographs [24]. This contrast factor is widely used in the Tomography because it binds to many proteins and to connective tissue.

Fig. 1
figure1

Methodology of the QUEST-STEMI study. a Staining of thrombi with phosphotungstic acid (PTA); b Skyscan 1172 in the Institute of Marine Biology, Biotechnology and Aquaculture Heraklion, Greece; c Samples are placed in a specific vial which contains ethanol; d Samples are mounted on the specific head inside the micro-CT; e-f Representative samples of thrombi. The samples were stained using 0.3% PTA as a contrast agent and scanned using Skyscan 1172 at a voltage of 48 kV and 204μΑ without filtering for a full rotation of 360o. Images were acquired at a pixel size of 5.52 μm with a camera binning of 1 × 1. The projections were reconstructed with the use of the NRecon (Bruker, Kontich, Belgium) software; g Graphical abstract-overview of the methodology of the QUEST-STEMI study

Scanning

Thrombi are scanned by means of the micro-CT SkyScan 1172 in the Biodiversity lab of IMBBC (Fig. 1B). This system uses a tungsten source with energies ranging from 20 to 200 kV. It is equipped with an 11megapixel CCD camera (4000 × 2672 pixel) with a maximum analysis of < 0.8 μm/pixel.

After the staining of the clots with 0.3% PTA, every sample is placed in a specific vial which contains ethanol (Fig. 1C) and is mounted on the specific head inside the micro-CT (Fig. 1D). Subsequently, the principal parameters (e.g. voltage, magnification, resolution) are regulated to achieve the best imaging result. Scans are performed at a full rotation of 360°.

The scanning procedure results into a series of projection images arranged in the form of image stacks which, in turn, are reconstructed into sections (cross-section images) with the use of the NRecon (Bruker, Kontich, Belgium) software, which employs a modified Feldkamp’s back-projection algorithm. The resulting sections are combined to create the 3D models, which will be further analyzed to extract useful measurements for the shape characteristics of the thrombi, such as the volume and the relative density. All scans are reconstructed using the same range of attenuation coefficients (0–0.7) in order to obtain comparable results. Figure 1E-F shows two representative micro-CT images of extracted thrombi.

Imaging analysis

Shape analysis on the surface and internal structure of the three-dimensional representations of the clots will lead to the identification of important characteristics that will be used to estimate variability within samples and perform clustering for the substantial differences between thrombi. Those features would be ranging from measurements on the actual virtual models to analysis of parameter-values after the application of a parametric representation of the variability in tissue shape.

The calculation of the total clot volume is one of the intrinsic measurements arising from the 3D models and is performed using Amira software (VSG, Burlington USA).

Moreover, potential differences in clot internal and external structure (e.g. architecture of the various cell types) will be evaluated through the 3D models rendered from the image stacks.

The clot relative density is calculated with the CTAnalyser (CTAn, Bruker, Kontich, Belgium) software, using information from the variability and structure in the 3D gray scale values of the images.

Ιn-vitro produced thrombi, which are characterized by a known homogeneous composition, have also been scanned in order to identify the exact grey scale histogram values, which correspond to each type of tissue. These artificial clots have been constructed in vitro by mixing platelet enriched plasma and whole blood from healthy volunteers, as previously described [25]. In this way, samples consisting mainly of platelets (reminiscent of the “white thrombi”) and samples, which predominately consist of erythrocytes and which are expected to share the same properties with the naturally occurring “red thrombi”, have been formed. The mean values and standard deviations of densities have been determined from measured densities of eight samples for each type of thrombus and the cut-off Housefield Units of different tissue types in thrombi have been identified using threshold analysis. This enables tissue characterization by comparing the measured densities of extracted thrombi to the estimated densities of the homogeneous artificial thrombi. Thus, we are able to quantify the presence of different cell types (for instance erythrocytes and platelets) within a thrombus.

Analysis of the clots is performed by two independent researchers who are blinded to the clinical variables and the outcome of the patients.

Histopathologic examination of thrombi

At the end of the experiment, histological and immunohistochemical analysis of thrombus aspirates is performed to validate the findings of the micro-CT analysis. Thrombi are embedded in paraffin blocks and cut into 4–5 μm sections. Routine staining is performed with hematoxylin and eosin. Moreover, thrombi are stained for leukocyte subsets, markers of thrombosis, and neutrophil extracellular traps (NETs), as described [26]. The stained sections are evaluated by two experienced pathologists, who are blinded to patient information. In each case, the percentage of fibrin, erythrocyte, and platelet area in relation to the whole thrombus area is investigated and thrombi are classified into white, mixed, and red categories according to their fibrin and erythrocyte content, as previously reported [25]. Furthermore, thrombi are classified according to their age into three groups: recent thrombi (< 1 day), lytic thrombi (1–5 days), and organized thrombi (> 5 days) [27].

Endpoints- endpoint adjudication-patient follow-up

The study primarily aims to develop a methodology for the quantitative and qualitative assessment of aspirated thrombi, using micro-CT. Hence, important characteristics of thrombi, including their volume (in mm3) and their density (in Housefield units), will be measured. At a second level, correlation of these variables with clinical parameters, angiographic data and electrocardiographic data will be conducted. In particular, any association between the extracted thrombus volume and density with factors from patients’ medical history (e.g smoking, diabetes mellitus) will be explored. Moreover, potential correlation of the volume of aspirated thrombus burden, as assessed using the micro-CT and the angiographic classification of thrombus burden according to Sianos [19], will be examined. Furthermore, association of thrombus volume and thrombus density with electrocardiographic and angiographic outcomes suggestive of poor patient prognosis will be explored; in particular: ST-segment resolution (complete (> 70%), partial (30–70%), or absent (< 30%)) [28], post-procedural Thrombolysis in Myocardial Infarction(TIMI) flow and distal embolization. All patients will be followed-up (through telephone contacts on a quarterly basis) for 12 months for any MACCE (acute myocardial infarction, stent thrombosis, target lesion revascularization, cardiac death, cerebrovascular death, or stroke). Electrocardiographic and angiographic outcomes and MACCE will be evaluated based on pre-specified definitions by two experienced interventional cardiologists, who will be blinded to the findings of the micro-CT analysis. Detailed primary and secondary endpoints are described in Table 2.

Table 2 Primary and secondary endpoints for the QUEST STEMI study

Statistical considerations

Sample size estimation

Sample size estimation was performed using the G*Power tool [29]. The primary endpoint of the study is to develop a methodology for the quantitative and qualitative assessment of aspirated thrombi, using micro-CT. Thus, sample size estimation was based on a secondary endpoint of the study and in particular, on parameters affecting the volume of extracted thrombi. For the F-test, of the multivariate regression model using ten predictors for high thrombus burden and assuming power of 0.9, significance level of 0.05 and effect size of 0.3 (based on a preliminary analysis on the first 25 patients), the required number of subjects is 79. This initial sample size will be increased by 10%, because of the possibility that some patients might be lost to follow-up. Hence, we aim for a total sample size of 87 patients.

Statistical analysis

Continuous data will be presented as mean ± SD., whereas categorical variables will be displayed as counts. Normally distributed data will be analyzed using parametrical tests, such as Student t-test and for non-normally distributed data nonparametric Mann-Whitney test will be utilized. Categorical variables will be compared using chi-square test.

Intra- and interobserver variability of the measurements of the volume and the density of aspirated thrombi will be calculated to assess the reliability and the reproducibility of the proposed methodology. For this reason, a Bland–Altman analysis will be performed and the intraclass correlation coefficient (ICC) will be determined [30]. Regarding, qualitative variables Cohen’s k-coefficient will be calculated [31].

Univariate and multivariate linear and logistic regression analyses will be used to determine independent predictors of high thrombus burden and of adverse clinical outcomes. Receiver operating characteristic (ROC) curve analysis -and the derived area under the curve (AUC)- will be constructed to determine the optimal cut-off value for high and low thrombus burden. Cox regression analyses will be performed to identify independent predictors of MACCE. Kaplan-Meier survival will be calculated to evaluate the MACCE-free survival at 1 year follow-up, with the difference between different patient sub-groups analyzed by the log-rank test. Patients that are lost to follow-up will be censored at their last study encounter. Missing data in the multivariate model will be replaced by means of multiple imputation, using chained equations. To verify the stability of the results, complementary sensitivity analysis will be performed under various missing-data models. Statistical analysis will be performed using programming language R.

An overview of the design and the methodology of the QUEST-STEMI study is presented in Fig. 1 G.

Discussion

In this study we aim to develop a methodology for the quantitative and qualitative assessment of extracted thrombi in patients presenting with STEMI and undergoing thrombus aspiration during primary PCI. Our goal is to quantify characteristics that so far have only been subjective to the individual viewer, such as the thrombus volume and the thrombus fine structure, and to investigate the predictive value of these characteristics.

These novel imaging parameters, combined with clinical and laboratory data, will enable the in-depth exploration of the complex cellular interactions in the STEMI setting and will potentially improve patient risk stratification. This might facilitate the development of a personalized approach in treating patients with STEMI.

Furthermore, the 2018 ESC / EACTS Guidelines on myocardial revascularization strongly support future trials of improved thrombus aspiration technologies in patients with high risk [17]. However, previous studies evaluating newly developed strategies for thrombus aspiration have failed to quantify the volume of thrombi retrieved [32]. Due to its high accuracy for the quantification of the volume of the extracted thrombotic material, this methodology will potentially enable the assessment of different thrombus aspiration technologies based on their ability for thrombus removal.

Micro-CT has often been used in medical studies [33, 34] and has been proven to accurately visualize and quantify venous thrombi in experimental models [35]. Nonetheless, this is-to our knowledge-the first study of volumetric coronary thrombus assessment by micro-CT. In the TOTAL-OCT study, a sub-study of the TOTAL trial, Optical Coherence Tomography (OCT) was used to quantify thrombus in vivo prior to stent implantation after restoration of TIMI 2–3 flow to the culprit vessel [36]. The study showed that measurement of pre-stent thrombus burden by OCT in patients suffering from STEMI is feasible and repeatable [36]. However, although intravascular OCT has a tremendous potential of helping us to visualize and manage thrombus in STEMI patients, this method has certain limitations: First, it cannot provide clear images in the thrombus-occluded vessel due to significant signal attenuation caused by erythrocytes [37]. Moreover, its shallow penetration depth (1.0 to 1.5 mm in a blood-free environment) might limit its ability to visualize the full size of a large clot [37]. Last, OCT cannot distinguish between mural thrombi and plaques [38]. On the other hand, micro-CT imaging provides the opportunity to use chemical factors which strengthen the contrast of tissues. This will facilitate an improved image quality of thrombi and will enable more accurate tissue characterization, as potential differences in clot internal and external structure, such as architecture of the various cell types, can be better visualized. Thus, OCT and micro-CT represent two complementary research pathways, which can both provide valuable information for the quantitative and qualitative characteristics of thrombi and for risk-stratification of patients with STEMI.

There are certain limitations to this study. First, the study is restricted to patients with STEMI who undergo thrombus aspiration at the discretion of the interventional cardiologist performing the primary PCI. Thus, the study population is not necessarily representative of the whole spectrum of STEMI patients. Moreover, additional imaging (OCT) will not be used to quantify residual thrombus, as this technology is not routinely available in our catheterization laboratory. Furthermore, it is possible that formalin fixation might influence the actual size of aspirated thrombi. This formalin-induced shrinkage effect might result in underestimating the actual dimensions of thrombi. Nonetheless, this will affect the size of all samples, as they are all subjected to the same fixation procedures. Last, the present study is a pilot study with small sample size, and it is not powered to show correlation between imaging variables and hard clinical endpoints.

In conclusion, we propose a novel methodological approach for the assessment of aspirated thrombotic material from coronary arteries using micro-CT, offering new perspectives for future research. This method could be used in larger, clinically-oriented trials to help stratify patients with thrombus burden according to their risk for adverse outcomes.

Availability of data and materials

Data are available from Georgios Sianos (e-mail: gsianos@auth.gr) upon reasonable request and with permission of AHEPA University Hospital.

Abbreviations

ECG:

Electrocardiogram

ESC:

European society of cardiology

IMBBC:

Institute of Marine Biology, biotechnology and aquaculture

MACCE:

Major adverse cardiac and cerebrovascular events

Micro-CT:

Micro-computed tomography

NETs:

Neutrophil extracellular traps

OCT:

Optical coherence tomography

PCI:

Percutaneous coronary intervention

PTA:

Phosphotungstic acid

STEMI:

Myocardial infarction with ST-elevation

References

  1. 1.

    Keeley EC, Boura JA, Grines CL. Primary angioplasty versus intravenous thrombolytic therapy for acute myocardial infarction: a quantitative review of 23 randomised trials. Lancet. 2003;361(9351):13–20.

  2. 2.

    Andrikopoulos G, Terentes-Printzios D, Tzeis S, Vlachopoulos C, Varounis C, Nikas N, et al. Epidemiological characteristics, management and early outcomes of acute coronary syndromes in Greece: the PHAETHON study. Hell J Cardiol. 2016;57(3):157–66.

  3. 3.

    Singh M, Berger PB, Ting HH, Rihal CS, Wilson SH, Lennon RJ, et al. Influence of coronary thrombus on outcome of percutaneous coronary angioplasty in the current era (the Mayo Clinic experience). Am J Cardiol. 2001;88(10):1091–6.

  4. 4.

    Sianos G, Papafaklis MI, Daemen J, Vaina S, van Mieghem CA, van Domburg RT, et al. Angiographic stent thrombosis after routine use of drug-eluting stents in ST-segment elevation myocardial infarction. The importance of Thrombus burden. J Am Coll Cardiol. 2007;50(7):573–83.

  5. 5.

    Henriques JPS, Zijlstra F, Ottervanger JP, De Boer MJ, Van’T Hof AWJ, Hoorntje JCA, et al. Incidence and clinical significance of distal embolization during primary angioplasty for acute myocardial infarction. Eur Heart J. 2002;23(14):1112–7.

  6. 6.

    Iijima R, Shinji H, Ikeda N, Itaya H, Makino K, Funatsu A, et al. Comparison of coronary arterial finding by intravascular ultrasound in patients with “transient no-reflow” versus “reflow” during percutaneous coronary intervention in acute coronary syndrome. Am J Cardiol. 2006 Jan;97(1):29–33.

  7. 7.

    Hong M-K, Mintz GS, Lee CW, Park D-W, Park K-M, Lee B-K, et al. Late stent malapposition after drug-eluting stent implantation: an intravascular ultrasound analysis with long-term follow-up. Circulation. 2006;113(3):414–9.

  8. 8.

    Vlaar PJ, Svilaas T, van der Horst IC, Diercks GFH, Fokkema ML, de Smet BJGL, et al. Cardiac death and reinfarction after 1 year in the Thrombus Aspiration during Percutaneous coronary intervention in Acute myocardial infarction Study (TAPAS): a 1-year follow-up study. Lancet (London, England). 2008;371(9628):1915–20.

  9. 9.

    Frobert O, Lagerqvist B, Olivecrona GK, Omerovic E, Gudnason T, Maeng M, et al. Thrombus aspiration during ST-segment elevation myocardial infarction. N Engl J Med. 2013;369(17):1587–97.

  10. 10.

    Jolly SS, Cairns JA, Yusuf S, Meeks B, Pogue J, Rokoss MJ, et al. Randomized trial of primary PCI with or without routine manual thrombectomy. N Engl J Med. 2015;372(15):1389–98.

  11. 11.

    Stone GW, Maehara A, Witzenbichler B, Godlewski J, Parise H, Dambrink J-HE, et al. Intracoronary abciximab and aspiration thrombectomy in patients with large anterior myocardial infarction: the INFUSE-AMI randomized trial. JAMA. 2012;307(17):1817–26.

  12. 12.

    Elgendy IY, Huo T, Bhatt DL, Bavry AA. Is aspiration Thrombectomy beneficial in patients undergoing primary percutaneous coronary intervention? Meta-analysis of randomized trials. Circ Cardiovasc Interv. 2015;8(7):e002258.

  13. 13.

    Mancini JG, Filion KB, Windle SB, Habib B, Eisenberg MJ. Meta-analysis of the long-term effect of routine aspiration Thrombectomy in patients undergoing primary percutaneous coronary intervention. Am J Cardiol. 2016;118(1):23–31.

  14. 14.

    Jolly SS, James S, Džavík V, Cairns JA, Mahmoud KD, Zijlstra F, et al. Thrombus Aspiration in ST-Segment-Elevation Myocardial Infarction: An Individual Patient Meta-Analysis: Thrombectomy Trialists Collaboration. Circulation. 2017;135(2):143–52. https://www.ahajournals.org/doi/full/10.1161/CIRCULATIONAHA.116.025371?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%3dpubmed.

  15. 15.

    Marmagkiolis K, Hakeem A, Cilingiroglu M, Feldman DN, Charitakis K. Efficacy and safety of routine aspiration thrombectomy during primary PCI for ST-segment elevation myocardial infarction: a meta-analysis of large randomized controlled trials. Hell J Cardiol. 2018;59(3):168–73 Available from: https://doi.org/10.1016/j.hjc.2017.09.003.

  16. 16.

    Jolly SS, Cairns JA, Yusuf S, Meeks B, Gao P, Hart RG, et al. Stroke in the TOTAL trial: a randomized trial of routine thrombectomy vs. percutaneous coronary intervention alone in ST elevation myocardial infarction. Eur Heart J. 2015;36(35):2364–72.

  17. 17.

    Neumann FJ, Sousa-Uva M, Ahlsson A, Alfonso F, Banning AP, Benedetto U, et al. 2018 ESC / EACTS guidelines on myocardial revascularization the task force on myocardial revascularization of the European Society of Cardiology ( ESC ) and European association for. Eur Heart J. 2019;40:87–165.

  18. 18.

    Gibson CM, De Lemos JA, Murphy SA, Marble SJ, McCabe CH, Cannon CP, et al. Combination therapy with abciximab reduces angiographically evident thrombus in acute myocardial infarction a TIMI 14 substudy. Circulation. 2001;103(21):2550–4.

  19. 19.

    Sianos G, Papafaklis MI, Serruys PW. Angiographic thrombus burden classification in patients with ST-segment elevation myocardial infarction treated with percutaneous coronary intervention. J Invasive Cardiol. 2010;22(10 Suppl B):6B–14B.

  20. 20.

    Napodano M, Dariol G, Al Mamary AH, Marra MP, Tarantini G, D’Amico G, et al. Thrombus burden and myocardial damage during primary percutaneous coronary intervention. Am J Cardiol. 2014;113(9):1449–56.

  21. 21.

    Jolly SS, Cairns JA, Lavi S, Cantor WJ, Bernat I, Cheema AN, et al. Thrombus aspiration in patients with high Thrombus burden in the TOTAL trial. J Am Coll Cardiol. 2018;72(14):1589–96.

  22. 22.

    Campbell GM, Sophocleous A. Quantitative analysis of bone and soft tissue by micro-computed tomography: applications to ex vivo and in vivo studies. Bonekey Rep. 2014;3(June):1–12 Available from: https://doi.org/10.1038/bonekey.2014.59.

  23. 23.

    Metscher BD. Micro CT for comparative morphology: Simple staining methods allow high-contrast 3D imaging of diverse non-mineralized animal tissues. BMC Physiol. 2009;9(11). https://doi.org/10.1186/1472-6793-9-11.

  24. 24.

    Pauwels E, Van Loo D, Cornillie P, Brabant L, Van Hoorebeke L. An exploratory study of contrast agents for soft tissue visualization by means of high resolution X-ray computed tomography imaging. J Microsc. 2013;250(1):21–31.

  25. 25.

    Kirchhof K, Welzel T, Mecke C, Zoubaa S, Sartor K. Differentiation of white, mixed, and red thrombi: value of CT in estimation of the prognosis of thrombolysis - phantom study. Radiology. 2003;228(1):126–30.

  26. 26.

    Mangold A, Alias S, Scherz T, Hofbauer T, Jakowitsch J, Panzenböck A, et al. Coronary neutrophil extracellular trap burden and deoxyribonuclease activity in ST-elevation acute coronary syndrome are predictors of ST-segment resolution and infarct size. Circ Res. 2015;116(7):1182–92.

  27. 27.

    Rittersma SZH, van der Wal AC, Koch KT, Piek JJ, Henriques JPS, Mulder KJ, et al. Plaque instability frequently occurs days or weeks before occlusive coronary thrombosis: a pathological thrombectomy study in primary percutaneous coronary intervention. Circulation. 2005;111(9):1160–5.

  28. 28.

    Harkness JR, Sabatine MS, Braunwald E, Morrow DA, Sloan S, Wiviott SD, et al. Extent of ST-segment resolution after fibrinolysis adds improved risk stratification to clinical risk score for ST-segment elevation myocardial infarction. Am Heart J. 2010;159(1):55–62.

  29. 29.

    Faul F, Erdfelder E, Buchner A, Lang A-G. Statistical power analyses using G*power 3.1: tests for correlation and regression analyses. Behav Res Methods. 2009;41(4):1149–60.

  30. 30.

    Popovic ZB, Thomas JD. Assessing observer variability: a user’s guide. Cardiovasc Diagn Ther. 2017;7(3):317–24.

  31. 31.

    McHugh ML. Interrater reliability: the kappa statistic. Biochem Med. 2012;22(3):276–82 Available from: https://www.ncbi.nlm.nih.gov/pubmed/23092060.

  32. 32.

    Farooq V, Serruys PW, Mustafa AHS, Mamas MA, Malik N, Alhous HA, et al. Forward and back aspiration during ST-elevation myocardial infarction: a feasibility study. EuroIntervention J Eur Collab with Work Gr Interv Cardiol Eur Soc Cardiol. 2016;11(14):e1639–48.

  33. 33.

    Degenhardt K, Wright AC, Horng D, Padmanabhan A, Epstein JA. Rapid 3D phenotyping of cardiovascular development in mouse embryos by micro-CT with iodine staining. Circ Cardiovasc Imaging. 2010;3(3):314–22.

  34. 34.

    Munce NR, Strauss BH, Qi X, Weisbrod MJ, Anderson KJ, Leung G, et al. Intravascular and extravascular microvessel formation in chronic total occlusions a micro-CT imaging study. JACC Cardiovasc Imaging. 2010;3(8):797–805.

  35. 35.

    Grover SP, Saha P, Jenkins J, Mukkavilli A, Lyons OT, Patel AS, et al. Quantification of experimental venous thrombus resolution by longitudinal nanogold-enhanced micro-computed tomography. Thromb Res. 2015;136(6):1285–90 Available from: https://doi.org/10.1016/j.thromres.2015.10.006.

  36. 36.

    Kajander OA, Koistinen LS, Eskola M, Huhtala H, Bhindi R, Niemelä K, et al. Feasibility and repeatability of optical coherence tomography measurements of pre-stent thrombus burden in patients with STEMI treated with primary PCI. Eur Heart J. 2014;16(1):96–107.

  37. 37.

    Kume T, Akasaka T, Kawamoto T, Ogasawara Y, Watanabe N, Toyota E, et al. Assessment of coronary arterial thrombus by optical coherence tomography. Am J Cardiol. 2006;97(12):1713–7.

  38. 38.

    Yamaguchi T, Kubo T, Ino Y, Matsuo Y, Shiono Y, Yamano T, et al. Optical coherence tomography assessment of efficacy of thrombus aspiration in patients undergoing a primary percutaneous coronary intervention for acute ST-elevation myocardial infarction. Coron Artery Dis. 2015;26(7):567–72.

Download references

Acknowledgements

The authors gratefully acknowledge the valuable contribution of Professor Stavros Hadjimiltiades for his support for the recruitment of patients and for his outstanding insights at every stage of the design and conduct of the research. This paper and the research behind it would not have been possible without the exceptional support of Senior Researcher Christos Arvanitidis, Mrs. Kleoniki Keklikoglou and Professor James S Michaelson, who contributed significantly to the development of the micro-CT protocol. We also thank Dr. Fotis Girtovitis for his invaluable assistance in constructing the artificial thrombi.

Funding

This project is implemented through the Operational Program “Human Resources Development, Education and Lifelong Learning” and is co-financed by the European Union (European Social Fund) and Greek national funds (MIS 5004707). The funder had no role in the design or conduct of the study; preparation, review or approval of the manuscript; and decision to submit the manuscript for publication.

Author information

EK, NK, GS1 and GS2 developed the concept, the trial protocol and wrote the manuscript. EC contributed to the development of the micro-CT protocol and performed the scanning of the thrombi. All authors have read and approved the final manuscript (GS1 refers to Georgios Sofidis and GS2 refers to Georgios Sianos).

Correspondence to Georgios Sianos.

Ethics declarations

Ethics approval and consent to participate

The study protocol has been approved by the Medical Ethics Committee of the Aristotle University of Thessaloniki (reference number 373/05-07-2017), by the Scientific Committee of AHEPA University Hospital (reference number 38/25-01-2018) and by the Directory Board of AHEPA University Hospital (reference number 07/01-03-2018). Each subject provides written informed consent before participating in the study.

Consent for publication

Written informed consent for publication was obtained by patients, whose images (intracoronary thrombi-coronary angiography) were used.

Competing interests

The authors declare that they have no competing interests.

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 distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Karagiannidis, E., Konstantinidis, N.V., Sofidis, G. et al. Rationale and design of a prospective, observational study for the QUantitative EStimation of Thrombus burden in patients with ST-Elevation Myocardial Infarction using micro-computed tomography: the QUEST-STEMI trial. BMC Cardiovasc Disord 20, 125 (2020). https://doi.org/10.1186/s12872-020-01393-5

Download citation

Keywords

  • Thrombus
  • Thrombus aspiration
  • Micro-computed tomography
  • ST-elevation myocardial infarction
  • Interventional cardiology