PCI in Patients with Diabetes: Role of the Cre8 Drug-eluting Stent

Register or Login to View PDF Permissions
Permissions× For commercial reprint enquiries please contact Springer Healthcare:

For permissions and non-commercial reprint enquiries, please visit to start a request.

For author reprints, please email
Average (ratings)
No ratings
Your rating


Patients with diabetes have poor outcomes compared to the general patient population when undergoing percutaneous coronary intervention. The Cre8TM (Alvimedica) drug-eluting stent (DES) has unique features that may improve clinical outcomes in patients with diabetes. These include abluminal reservoir technology, a proprietary polymer-free drug-release system consisting of reservoirs on the stent’s outer surface that control and direct drug release exclusively towards the vessel wall, and the AmphilimusTM formulation, which enables enhanced drug tissue permeation, utilising fatty acid transport pathways. This is particularly advantageous in diabetic patients, since increased uptake of fatty acid occurs in diabetic cells. Furthermore, mTOR inhibitors (-limus drugs), which are utilised in DESs, are relatively ineffective in diabetic cells. Clinical efficacy and safety of the Cre8TM in patients with diabetes has been demonstrated in a number of clinical trials and real-world studies, and further studies are on-going.

Disclosure:The authors have no relevant disclosures to make.



Acknowledgements:The authors are grateful to the technical editing support provided by Katrina Mountfort of Medical Media Communications (Scientific) Ltd, which was funded by Alvimedica.

Correspondence Details:Katrina Mountfort, Medical Writer, Medical Media Communications (Scientific) Ltd, Unit F, First Floor, Bourne Park, Bourne End, SL8 5AS, UK. E:

Copyright Statement:

The copyright in this work belongs to Radcliffe Medical Media. Only articles clearly marked with the CC BY-NC logo are published with the Creative Commons by Attribution Licence. The CC BY-NC option was not available for Radcliffe journals before 1 January 2019. Articles marked ‘Open Access’ but not marked ‘CC BY-NC’ are made freely accessible at the time of publication but are subject to standard copyright law regarding reproduction and distribution. Permission is required for reuse of this content.

Percutaneous coronary intervention (PCI) and coronary artery bypass grafting (CABG) are established strategies for revascularisation in patients with coronary artery disease. While CABG was the standard of care for patients with multivessel disease, the introduction of baremetal stents (BMSs) and, later, drug-eluting stents (DESs) has led to an increased use of PCI in these more challenging cases. The latest generation of polymeric metallic DESs has shown improved efficacy and safety compared with BMSs and first-generation DESs, facilitating the treatment of more complex lesions.1 However, certain lesions and patient subsets remain difficult to treat. Patients with diabetes represent a particular challenge as they have rapidly progressing and more diffuse coronary artery disease, with lesions of longer length. They therefore continue to have worse outcomes following PCI compared with non-diabetic patients.2 In patients with diabetes and multivessel disease, CABG remains the preferred strategy but it is associated with a higher risk of peri-procedural stroke.3,4

Diabetes has reached epidemic proportions worldwide and its prevalence is rising. In 2015, 415 million adults had diabetes; nearly half (46.5%) of these remain undiagnosed.5 By 2040 this number is projected to rise to 642 million,5 representing a major health and economic burden. There is an urgent need to enhance procedural success and long-term clinical outcomes in the coronary revascularisation of patients with diabetes. In particular, there is a need for improved stent technology tailored to the needs of the diabetic population. This article describes the Cre8 DES, which has a novel design that may provide particular efficacy and safety advantages in patients with diabetes.

Introduction to the Cre8

The Cre8 has unique features that may specifically improve clinical outcomes in patients with diabetes. These include abluminal reservoir technology, which is a proprietary polymer-free drugrelease system consisting of reservoirs on the stent’s outer surface that control and direct drug release exclusively towards the vessel wall (see Figure 1). The reservoir’s design directly impacts on the drug dosage and release kinetics, allowing peak drug tissue concentration during the first days post-implantation, 50 % drug elution in approximately 18 days, 65–70 % elution within 30 days and complete drug elution within 90 days.6

The polymer-free system overcomes a major challenge of DES design. Polymer coatings have been routinely used to control drug release and optimise DES efficacy, but have also been implicated in late inflammatory reactions and delayed arterial healing after stenting.7 The Intracoronary Stenting and Angiographic Restenosis Investigators – Test Efficacy of Rapamycin-eluting Stents with Different Polymer Coating Strategies (ISAR-TEST-3) study found that failure to retard drug release results in suboptimal antirestenotic activity.8

A second design characteristic unique to the Cre8 is the Amphilimus formulation of the active antirestenotic drug. In this proprietary technology, sirolimus and a fatty acid are eluted together, allowing sustained drug elution, modulated drug bioavailability, a more homogeneous drug distribution and enhanced drug stability. Also important is the bioinducer surface, an integral ultra-thin (<0.3 μm) pure carbon coating that is covalently bonded to the thin CoCr platform (total thickness 70–80 μm). This is hypothesised to passivate stent–platelet interactions (since the bulk of the CoCr platform is sealed by the coating) and reduce the risk of thrombotic events. Other features of the Cre8™ include homogeneous stent design in lengths from 8 to 46 mm, excellent longitudinal stability on expansion, and two platinum markers at the stent ends.

Figure 1: Cre8™ Abluminal Reservoir Technology

Article image

Challenges of DES Use in Patients with Diabetes

The use of second-generation DESs in patients with diabetes has been associated with suboptimal outcomes. A pooled patient analysis of data from four randomised trials – the Clinical Evaluation of the XIENCE V Everolimus Eluting Coronary Stent System in the Treatment of Patients with de novo Native Coronary Artery Lesions (SPIRIT) II, SPIRIT III, SPIRIT IV trials, and the Second-Generation Everolimus-Eluting and Paclitaxel-Eluting Stents in Real-Life Practice (COMPARE) trial – found that, in the non-diabetic population (n=3,911), the use of an everolimus-eluting stent (EES) significantly reduced the endpoints of cardiac death or myocardial infarction (MI) at 1 year (4.3 versus 9.5 %; HR 0.44; 95 % CI [0.35–0.55]; p<0.001) compared with a paclitaxeleluting stent (PES). However, in the diabetic population (n=1,869), there was no difference between the two DESs (8 versus 7.8 %; HR 1.01; 95 % CI [0.72–1.42]; p=0.95). In addition, the incidences of death, MI and target-lesion revascularisation were all higher in diabetic than in non-diabetic patients.9 Furthermore, in the Randomized Comparison of Everolimus-Eluting Stent versus Sirolimus-Eluting Stent Implantation for De Novo Coronary Artery Disease in Patients with Diabetes Mellitus (ESSENCE-DIABETES), 300 patients with diabetes were randomised to receive either EES or sirolimus-eluting stents (a first-generation DES) for the treatment of coronary lesions. No difference in outcomes was seen between the two groups.10

Basic research has shed additional light on the reasons for the lack of benefit second-generation DESs have shown in patients with diabetes. The mammalian target of rapamycin (mTOR) inhibitors (-limus drugs) have been found to be less active in patients with diabetes compared with the general population. One reason is the direct resistance of vascular smooth muscle cells to mTOR inhibition.11,12 Dose-response curves show that a tenfold higher concentration of mTOR inhibitor is required in the diabetic cell to achieve similar inhibition to the non-diabetic cell.12 Another reason for the relative ineffectiveness of -limus drugs in diabetic patients is the effect of other hormones. BMI strongly correlates with diabetes riks: 90 % of patients with type 2 diabetes are overweight.13 Human obesity is associated with elevated levels of the hormone leptin, which has been found to promote vascular remodelling and neointimal growth in animal studies.14 Increased leptin levels cause a ninefold increase in the dose of sirolimus required for effective inhibition of neointimal formation.15 Moreover, leptin levels have been associated with in-stent restenosis.16,17

These data highlight the potential unmet need with regard to currentgeneration DES technology in patients with diabetes. Increasing total drug delivery to the vessel wall is one approach. This may be achieved by incorporation of an increased drug–polymer load, although this is likely to negatively impact overall vessel wall healing. Another possibility would be to use the same coating thickness with an increased drug:polymer ratio, but this would negatively affect the drug-release kinetics and make the polymer brittle. Placing the drug directly onto the bare metal would also be problematic in terms of control of drug release. An optimum approach might be to use standard drug–polymer loads combined with a formulation targeted to enhance uptake of drug at the cellular level.

The Amphilimus formulation of Cre8 is designed to take advantage of the key role of fatty acids in cellular metabolism in patients with diabetes. In the non-diabetic cell, fatty acid metabolism is responsible for 70 % of the generation of adenosine triphosphate, the remaining 30 % being produced by glucose oxidation. However, in the diabetic cell, membrane protein overexpression leads to higher binding and translocation of fatty acids, and as a result 100 % of adenosine triphosphate production results from fatty acid oxidation.18 In diabetic mouse models, a doubling of cardiac fatty acid uptake has been demonstrated.19 This technique of using fatty acids has been shown to enhance the transdermal delivery of other drugs.20

Clinical Evidence for Use of the Cre8

The first clinical study of the Cre8 was the International Randomized Comparison between DES Limus Carbostent and Taxus Drug-eluting Stents in the Treatment of de novo Coronary Lesions (NEXT) clinical study, which randomly allocated patients (n=323) to the Cre8 or a PES (TAXUS® Liberté®, Boston Scientific).21 The primary endpoint was 6-month angiographic in-stent late lumen loss (LLL). At 6 months, the Cre8 group had a 60 % reduction in in-stent LLL compared with the PES group (0.14 ± 0.36 mm versus 0.34 ± 0.40 mm; p<0.0001). This finding was even more pronounced in the subgroup of patients with diabetes (n=82), where a 72 % reduction in in-stent LLL was seen (0.12 ± 0.29 mm versus 0.43 ± 0.41 mm; p<0.0001). In terms of 3-year major adverse cardiac events (MACE), a 37 % reduction in target lesion revascularisation (TLR) was seen in the Cre8 versus the PES group (6.9 versus 10.9 %; p=0.2464) in the overall population and a 68 % reduction in the subgroup with diabetes (6.8 versus 21.2 %; p=0.888).21,22

These findings led to the initiation of a study enrolling patients more representative of those seen in routine clinical practice. The Prove Abluminal Reservoir Technology clinICal benefIt in all-comer PATiEnts (pARTicip8) study recruited ‘real world’ patients with ischaemic myocardial symptoms due to de novo lesions in native coronary arteries from across 30 European sites. The objective of this study was to evaluate the safety and efficacy of Cre8 in a group of patients comparable to the everyday clinical practice population, with a specific focus on subgroups with diabetes. The primary endpoint was a composite of cardiac death, target vessel MI and clinically-indicated TLR 6 months after the index procedure. Of those enrolled (n=1,186), 308 (25.8 %) had diabetes. At 1 year, the incidence of clinically-indicated TLR was 1 % in the overall population and 1.4 % in the diabetic subgroup. The LLL in the diabetic subgroup was 0.16 ± 0.13. Definite late stent thrombosis was detected in only 0.08 % of the patient population.22 By contrast, most other DESs have shown a significantly higher LLL in people with diabetes compared to those without.10,21,23,24

Figure 2: Incidence of Composite Endpoint, Cardiac Death, Target Vessel Myocardial Infarction (TV MI) and Clinically-indicated Target Lesion Revascularisation (Cl. Ind. TLR) at 12 Months in the INVESTIG8 Study

Article image

The next step in the Cre8 clinical development programme was the retrospective MultIceNtric and RetrospectiVe REgiStry in 'real world' paTients with polymer-free drug elutInG stent Cre8 (INVESTIG8) study. The primary endpoint was the incidence of a clinical composite endpoint (cardiac death/target vessel MI/clinically-driven TLR) at 12 months from the index procedure.25,26 Secondary endpoints comprised the incidence of a clinical composite endpoint (all deaths/all MI/any revascularisation) from the time of the index procedure to 12 months; and the incidence of stent thrombosis from the index procedure to 12 months, classified according to the Bleeding Academic Research Consortium definition (see Twelve-month followup data were available for 589 out of the 647 patients enrolled (91 %). Of these, 47.4 % had diabetes. Chronic total occlusions were present in 3.4 %, ostial lesions in 15.5 %, bifurcation in 17.8 % and de novo lesions in 93.8 % of participants. The composite endpoint occurred in 4.2 % of patients, and clinically-indicated target vessel revascularisation in 1.5 %. In a sub-analysis of non-diabetic versus diabetic patients, only the composite endpoint was higher in patients with diabetes (5.0 versus 3.5 %; p=0.4863), and this was due to the expected higher incidence of cardiac death and MI. However, the incidence of clinically-indicated TLR was not higher in the subgroup with diabetes (1.6 versus 1.4 %; p=1.000; see Figure 2).

The Randomized Comparison of Reservoir-Based Polymer-Free Amphilimus-Eluting Stent Versus Polymer-Based Everolimus-Eluting Stent in Diabetic Patients (RESERVOIR) clinical trial enrolled only patients with diabetes receiving glucose-lowering agents.27 The 112 participants were randomised either to Cre8 or an EES (XIENCE®, Abbott Vascular). The primary endpoint – mean neointimal hyperplasia volume obstruction – was 11.97 ± 5.94 % in the Cre8 group and 16.11 ± 18.18 % in the EES group (noninferiority p=0.0003; superiority p=0.22). Prespecified subgroup analysis showed consistent treatment effect in favour of the Cre8 arm across all subgroups. In terms of secondary endpoints, LLL in the Cre8 arm was 0.14 ± 0.24 mm compared with 0.24 ± 0.57 mm in the EES arm. The difference between the standard deviations is striking, and demonstrates the consistent performance of the Cre8 (see Figure 3). The minimal lumen diameter was also higher in the Cre8, both in-stent (2.38 ± 0.44 mm versus 2.19 ± 0.59 mm; p=0.07) and in segment (2.09 ± 0.59 mm versus 1.84 ± 0.61 mm; p=0.02).

Figure 3: The RESERVOIR Clinical Study Results for Late Lumen Loss at 9 Months

Article image

Finally, a matched analysis has been performed in which 187 consecutive patients treated with Cre8 between January 2011 and August 2013 in four Italian centres were propensity matched with 150 patients treated with new-generation EESs during the same period. The incidence of 1-year estimated MACE was numerically lower in Cre8 compared to the EESs, although the difference was not statistically significant (7.4 versus 10.2 %, respectively; p=0.261). The same was true of allcause mortality (1.3 % Cre8 versus 1.4 % EES; p=0.823), target vessel revascularisation (5.2 % Cre8 versus 8.8 % EES; p=0.169) and TLR (3 % Cre8 versus 7.4 % EES; p=0.108). Subgroup analysis showed that these differences were more pronounced in patients with diabetes, with a 50 % decrease in the incidence of MACE, although this was not statistically significant (10 % Cre8 versus 20 % EES; p=0.204). Of particular note, in patients with diabetes (Cre8, n = 42; EES, n = 41), 1-year TLR was 2.5 % in the Cre8 group versus 14.6 % in the EES group, which represented an 83 % reduction (p=0.05; see Figure 4).28

While a growing body of clinical and real-world data has provided support for the efficacy of the Cre8, studies have been underpowered to demonstrate statistical superiority over other DESs. To do so, a large clinical study is planned: the Clinical benefit in ‘all comers’ patients with DIABetes to prove Cre8 DES superior efficacy (DIAB8).29 In this study, all-comer patients with diabetes undergoing PCI will be randomised in a 1:1 ratio to the Cre8 or to an everolimus DES. The primary endpoint will be 12-month target lesion failure. Around 2,200 patients from 50 international sites will be recruited and clinical follow-up will be at 1 and 3 years.


In addition to these efficacy data, the Cre8 has demonstrated excellent safety. In the INVESTIG8 study, the incidence of definite stent thrombosis at 12 months was low in both non-diabetic and diabetic patients (0.3 % in each group). The ranDomizEd coMparisOn betweeN novel Cre8 DES and BMS to assess neoinTimal coveRAge by OCT Evaluation (Demonstr8) study was designed to assess whether strut coverage 3 months after implantation of the Cre8, once it becomes a BMS after complete drug-elution, was equivalent to a standard BMS.30 Patients (n=38) with ischaemic myocardial symptoms related to de novo lesions in native coronary arteries were randomised 1:1 to receive a Cre8 or a BMS (VISION®, Abbott Vascular). The primary endpoint of ratio of uncovered to total stent struts per cross section (RUTTS) score <30% occurred in 99.8% of Cre8 struts and in 99.6% of the BMS struts (p for noninferiority <0.001).

Figure 4: Target Lesion Revascularisation at 12 Months in Patients Treated with the Cre8™ versus XIENCE® Drug-&lt;br /&gt;&#10;eluting Stents: a Propensity-matched Analysis

Article image

The first results of a single centre registry study undertaken in Utrecht (U-Cre8) have recently been presented.31 This study involved 332 coronary lesions in 201 patients with diabetes and accrued data from 2012 to 2014. A retrospective analysis propensity-matched 99 patients receiving the Cre8 with 102 patients receiving a zotarolimus-eluting stent (ZES). The mean duration of dual antiplatelet therapy following PCI was 4.8 ± 3.4 months in the Cre8 group versus 5.9 ± 4.1 in the ZES group. Target-lesion failure occurred in six (6.1 %) patients in the Cre8 group compared to 11 (10.7 %) in the ZES group. These failures were attributable to TLR in three Cre8 patients (3.0 %) and seven ZES patients (6.9 %). End MACE-free survival was reported in 93 (93.9 %) Cre8 patients compared to 87 (85.2 %) of the ZES group at study end. It must be stressed, however, that these are preliminary data that still require independent adjudication.

The Prospective, Single Center, Open Label, Randomized Controlled, Two Arm Study Evaluating Safety and Efficacy of the Permanent Polymer Zotarolimus Eluting Stent Resolute Integrity Compared to the Polymer Free Amphilimus-Eluting Stent Cre8 (ReCre8) is currently recruiting participants. In this all-comer study, patients (n=1,530) with ischaemic myocardial symptoms are randomised to the Cre8 or the Resolute DES (Medtronic).32 The study is also investigating the use of dual antiplatelet therapy for 1 month in elective PCI. Clinical follow-up is at 1, 2 and 3 years, and the primary endpoint is MACE at 12 months.

Excellent safety and efficacy data have been reported in support of the Cre8, and results of the ReCre8 study are awaited.


Poorer outcomes following PCI reflect an unmet need in stent technology for patients with diabetes. The lower efficacy of DESs in these patients is largely due to reduced responsiveness of cells to -limus drugs. The Cre8 utilises a proprietary polymer-free drugrelease system consisting of reservoirs on the stent’s outer surface, maximising drug delivery without increasing the dose. The Amphilimus formulation enhances cellular drug uptake, particularly in diabetic cells. Finally, clinical trial and real-world data have demonstrated the superior performance of the Cre8 compared with other DESs in diabetic subgroups, as well as remarkable consistency in terms of LLL. These findings suggest that the Cre8 is a useful option in PCI in this challenging patient population. Data from on-going studies are eagerly anticipated.


  1. Byrne RA, Serruys PW, Baumbach A, et al. Report of a European Society of Cardiology-European Association of Percutaneous Cardiovascular Interventions task force on the evaluation of coronary stents in Europe: executive summary. Eur Heart J 2015;36:2608–20. 
    Crossref | PubMed
  2. Berry C, Tardif JC, Bourassa MG. Coronary heart disease in patients with diabetes: part II: recent advances in coronary revascularization. J Am Coll Cardiol 2007;49:643–56. 
    Crossref | PubMed
  3. Lim JY, Deo SV, Kim WS, et al. Drug-eluting stents versus coronary artery bypass grafting in diabetic patients with multi-vessel disease: a meta-analysis. Heart Lung Circ 2014;23:717–25. 
    Crossref | PubMed
  4. Tu B, Rich B, Labos C, et al. Coronary revascularization in diabetic patients: a systematic review and Bayesian network meta-analysis. Ann Intern Med 2014;161 :724–32.
    Crossref | PubMed
  5. International Diabetes Federation. IDF Diabetes Atlas. 7th ed. Brussels: International Diabetes Federation, 2015. Available at: (accessed 5 October 2016)
  6. Moretti C, Lolli V, Perona G, et al. Cre8 coronary stent: preclinical in vivo assessment of a new generation polymerfree DES with Amphilimus formulation. EuroIntervention 2012;7:1087–94. 
    Crossref | PubMed
  7. Mehilli J, Byrne RA, Wieczorek A, et al.; Intracoronary Stenting and Angiographic Restenosis Investigators – Test Efficacy of Rapamycin-eluting Stents with Different Polymer Coating Strategies (ISAR-TEST-3). Randomized trial of three rapamycin-eluting stents with different coating strategies for the reduction of coronary restenosis. Eur Heart J 2008;29:1975–82. 
    Crossref | PubMed
  8. Byrne RA, Kufner S, Tiroch K, et al.; ISAR-TEST-3 Investigators. Randomised trial of three rapamycin-eluting stents with different coating strategies for the reduction of coronary restenosis: 2-year follow-up results. Heart 2009;95:1489–94. 
    Crossref | PubMed
  9. Stone GW, Kedhi E, Kereiakes DJ, et al. Differential clinical responses to everolimus-eluting and paclitaxel-eluting coronary stents in patients with and without diabetes mellitus. Circulation 2011;124:893–900.
    Crossref | PubMed
  10. Kim WJ, Lee SW, Park SW, et al.; ESSENCE-DIABETES Study Investigators. Randomized comparison of everolimuseluting stent versus sirolimus-eluting stent implantation for de novo coronary artery disease in patients with diabetes mellitus (ESSENCE-DIABETES): results from the ESSENCE-DIABETES trial. Circulation 2011;124:886–92.
    Crossref | PubMed
  11. Woods TC. Dysregulation of the mammalian target of rapamycin and p27Kip1 promotes intimal hyperplasia in diabetes mellitus. Pharmaceuticals (Basel) 2013;6:716–27.
    Crossref | PubMed
  12. Lightell DJ, Jr., Woods TC. Relative resistance to mammalian target of rapamycin inhibition in vascular smooth muscle cells of diabetic donors. Ochsner J 2013;13:56–60. 
  13. Obesity Society. Your Weight and Diabetes. February 2015. Available at: (accessed 5 October 2016)
  14. Schafer K, Halle M, Goeschen C, et al. Leptin promotes vascular remodeling and neointimal growth in mice. Arterioscler Thromb Vasc Biol 2004;24:112–7.
    Crossref | PubMed
  15. Shan J, Nguyen TB, Totary-Jain H, et al. Leptin-enhanced neointimal hyperplasia is reduced by mTOR and PI3K inhibitors. Proc Natl Acad Sci U S A 2008;105:19006–11.
    Crossref | PubMed
  16. Piatti P, Di Mario C, Monti LD, et al. Association of insulin resistance, hyperleptinemia, and impaired nitric oxide release with in-stent restenosis in patients undergoing coronary stenting. Circulation 2003;108:2074–81. 
    Crossref | PubMed
  17. Shoukry A, El-Sherbieny I, Swelan E. Association of insulin resistance, insulin and leptin levels with coronary in-stent restenosis. Egyptian Heart J 2012;64:35–42.
  18. Glatz JF, Luiken JJ, Bonen A. Membrane fatty acid transporters as regulators of lipid metabolism: implications for metabolic disease. Physiol Rev 2010;90:367–417. 
    Crossref | PubMed
  19. Chabowski A, Gorski J, Glatz JF, et al. Protein-mediated fatty acid uptake in the heart. Curr Cardiol Rev 2008;4:12–21. 
    Crossref | PubMed
  20. Kim MJ, Doh HJ, Choi MK, et al. Skin permeation enhancement of diclofenac by fatty acids. Drug Deliv 2008;15:373–9. 
    Crossref | PubMed
  21. Carrie D, Berland J, Verheye S, et al. A multicenter randomized trial comparing amphilimus- with paclitaxel-eluting stents in de novo native coronary artery lesions. J Am Coll Cardiol 2012;59:1371–6. 
    Crossref | PubMed
  22. 22.Carrie D. Polymer-free Cre8TM DES: Design, current status and future directions. Presented at: TCT 2015 – Transcatherter Cardiovascular Therapeutics, San Francisco, CA, 11–15 October 2015.
  23. Park GM, Lee SW, Park SW, et al. Comparison of zotarolimuseluting stent versus sirolimus-eluting stent for de novo coronary artery disease in patients with diabetes mellitus from the ESSENCE-DIABETES II trial. Am J Cardiol 2013;112:1565–70. 
    Crossref | PubMed
  24. Grube E, Chevalier B, Guagliumi G, et al. The SPIRIT V diabetic study: a randomized clinical evaluation of the XIENCE V everolimus-eluting stent vs the TAXUS Liberte paclitaxeleluting stent in diabetic patients with de novo coronary artery lesions. Am Heart J 2012;163:867–75 e1. 
    Crossref | PubMed
  25. Sardella G. The latest available data on polymer-free DES technology in diabetic patients. Presented at: Euro PCR, Paris, France, 19-22 May 2015. Available at: (accessed 25 February 2016)
  26. Mountfort K. Patient-tailored drug-eluting stent choice – a solution for patients with diabetes. Interventional Cardiology Review 2015;10:158–61. 
  27. Romaguera R, Gomez-Hospital JA, Gomez-Lara J, et al. A Randomized Comparison of Reservoir-Based Polymer-Free Amphilimus-Eluting Stents Versus Everolimus-Eluting Stents With Durable Polymer in Patients With Diabetes Mellitus: The RESERVOIR Clinical Trial. JACC Cardiovasc Interv 2016;9:42–50. 
    Crossref | PubMed
  28. Panoulas VF, Latib A, Naim C, et al. Clinical outcomes of real-world patients treated with an amphilimus polymerfree stent versus new generation everolimus-eluting stents. Catheter Cardiovasc Interv 2015;86:1168–76. 
    Crossref | PubMed
  29. PCR Devices. DIAB8, 2016. Available at: Stents/Trials-FINDER/Diab8 (accessed 14 September 2016)
  30. Prati F, Romagnoli E, Valgimigli M, et al. Randomized comparison between 3-month Cre8 DES vs. 1-month Vision/Multilink8 BMS neointimal coverage assessed by OCT evaluation: the DEMONSTRATE study. Int J Cardiol 2014;176:904–9.
    Crossref | PubMed
  31. PCR Devices. U-Cre8, 2016. Available at: Stents/Trials-FINDER/U-Cre8 (accessed 14 September 2016)
  32. PCR Devices. ReCre8 (A Prospective, Single Center, Open Label, Randomized Controlled, Two Arm Study Evaluating Safety and Efficacy of the Permanent Polymer Zotarolimus Eluting Stent Resolute Integrity Compared to the Polymer Free Amphilimus Eluting Stent Cre8), 2016. Available at: (accessed 14 September 2016)