September 16, 1977, in Zurich Germany, Andreas Grunzig performed the first balloon angioplasty in a coronary artery on Andreas Bachman. Grunzig used the first known balloon, a DG 20-30. This method of treating a coronary artery was effective 10 to 20 years after Bachman performed this first procedure. Follow-up studies revealed excellent vessel patency. Unfortunately, this is not the typical result for most patients receiving balloon angioplasty as the Achilles heel of balloon angioplasty is a 5% to 10% acute vessel closure after the procedure. Balloon angioplasty creates vessel dissection at the edges of plaques, and these are nidus points for thrombus and subsequent occlusion. This problem with balloon angioplasty led to the development of bare metal coronary stents that could act as scaffolds to uphold and outwardly compress the vascular epithelial bed. These original stents were thick stainless steel devices with poor radial force. They were effective in solving the mechanical problem of acute vessel closure from balloon angioplasty but introduced a new problem, stent thrombosis. Stent thrombosis caused by these new devices was remedied with dual antiplatelet therapy. As time passed, a new problem with the bare metal stents became evident, and this was in-stent stenosis. Bare metal stents have a restenosis rate anywhere between 20% to 50%. The pathology for this occurrence is neo-intimal hyperplasia due to inflammation and injury to the intima and media of the vessel. Given this response of the vessel to the bare metal stent, the next step in the development of intracoronary stents was to develop a stent that would limit or minimize this neo-intimal hyperplastic response. The development of first-generation, drug-eluting stents ensued. Drug-eluting stents are composed of 3 components: the metal base, a polymer to control the release of the antiproliferative medication, and antiproliferative medications. The first generation of drug-eluting stents was made of stainless steel with a closed-cell design. These first generation stents were relatively thick in diameter making them difficult to maneuver through significantly diseased and calcified vessels. The first drugs utilized with these stents were paclitaxel and sirolimus. Sirolimus is an analog of rapamycin an mTOR inhibitor, and paclitaxel targets tubulin in mitotic cells and inhibits the spindle apparatus during cell division.
In the TAXUS study, the use of first-generation, drug-eluting stents (when compared to bare metal stents) reduced the rate of target vessel revascularization by 50% over a 5-year period. The problems with first-generation, drug-eluting stents were in the very late stent thrombosis events. Accordingly, long-term evaluation of those patients in the TAXUS study noted in an increase in myocardial infarction rates over the period of 5 years due to this very late stent thrombosis event. This was suspected to be due in part to the polymer of drug delivery of these first-generation stents but also as up to 60% of the surface area of the first-generation, drug-eluting stents deployed never fully endothelialized. The drug and polymer combination within these first stents was powerful enough to stop neointimal hyperplasia but also powerful to the point of arresting endothelialization of the vessel where the stent was deployed, hence the very late stent thrombosis events. 
Second-generation, drug-eluting stents sought to remedy the problems of first-generation, drug-eluting stents. This next generation of stents was developed with thinner strut thickness therapy allowing for faster healing and endothelialization of the coronaries with less inflammation and injury to the media. Instead of stainless steel metal base, second-generation, drug-eluting stents are made of cobalt-chromium thereby making them more malleable and deliverable. The polymers within the second-generation stents were fluorinated polymers making them biocompatible with thromboresistant properties. The drugs utilized to inhibit neointimal hyperplasia in these stents were everolimus and zotarolimus. In the SPIRIT II, III, IV, and Compare trials, head-to-head comparison of everolimus-eluting stents as compared to paclitaxel-eluting stents were shown to significantly reduce major adverse cardiovascular event rates (MACE) defined as cardiac death, myocardial infarction, and ischemic target vessel revascularization over a period of 24 months by 30% to 40%. In these trials, the second-generation, drug-eluting stents reduced very late stent thrombosis by about 70%.
3rd generation stents that are currently still being developed make the stent struts thinner and have either bioabsorbable polymers, no polymer at all, and some eliminate the stent with a scaffold that degrades over time. In the BIOFlOW V trial, a thin strut 60-micron, bioabsorbable, third-generation, drug-eluting stent was compared to a current drug-eluting stent with stent struts of 82 microns and durable fluoropolymer. There was a significant reduction of target lesion failure and event rates in the thinner strut group likely secondary to the lower profile of the thinner stent. A meta-analysis performed by Bangalore and Stone comparing ultra-thin, less than 70-micron stents to thicker strut second-generation stents showed a trend toward better outcomes in the thinner stent group driven by less target lesion failure and less stent thrombosis. In a meta-analysis by Palmerini comparing bioabsorbable polymer-based, drug-eluting stents to durable, polymer, drug-eluting stents, there was a small trend toward lower cardiac death and myocardial infarction when compared to bare metal stents. Furthermore, there was less target vessel revascularization when compared to bare metal stents, but they did not show any significant benefit over the current durable, polymer, drug-eluting stents currently deployed. In the EVOLVE II trial comparing a bioabsorbable stent to a durable, polymer, drug-eluting stent after 36 months, there was no significant difference between the 2 stents in terms of target lesion failure.
Another possible evolving front in third-generation stents is polymer-free, drug-coated stents. These are 120-micron-thick, stainless steel stents with microstructured surfaces that hold the antiproliferative drug in an abluminal surface structure. These polymer-free stents offer possible shorter, dual, antiplatelet duration and also do away with possible issues of non-uniformity of drug elution from the polymer coating. This one stent in particular releases biolimus that is 10-times more lipophilic than sirolimus, everolimus, and zotarolimus, allowing it to stay in the surface layers of the cells and self-elute over time. In the Leaders Free trial, the drug-coated stent significantly decreased in target lesion failure as compared to a bare-metal stent, as well as lowered myocardial infarction and cardiac death; although, stent thrombosis rates were about the same. The stent thrombosis rates are likely attributable to the large stent structure of this stent (120-micron) and newer version of this product with more malleable thinner struts will be forthcoming. Another concept for the future is thin strut drug filled stents with an outer cobalt alloy layer, middle tantalum layer and inner layer core material removed becoming a lumen filled with an antiproliferative medication. This concept was tested in the RevElution trial and showed less in-stent late loss over 9 months.
During deployment of an intracoronary stent, the vessel anatomy in which the stent is deployed is of utmost importance. The stent is sized to the maximal diameter of the distal aspect of the vessel where it will be placed. If the vessel appears significantly calcified, a further assessment with intracoronary imaging with ultrasound or optical coherence tomography may need to be performed to better assess plaque morphology and the possible need to perform rotational, orbital, or laser atherectomy. Another consideration when deploying a stent is possible side-branch impingement and plaque shift during the procedure.
Placement of an intracoronary stent is indicated after successful balloon angioplasty of a significant lesion. It has been well documented that balloon angioplasty causes significant epithelial damage, including small edge dissections of intracoronary plaque, and these dissections ultimately can lead to acute vessel thrombosis. Balloon angioplasty without stent placement, although successful, has significantly elevated restenosis rates approaching 50%. When comparing balloon angioplasty to the placement of bare-metal or drug-eluting stents, all stents groups display significantly lower long-term, target vessel failure, and future revascularization is needed.
Contraindications to intracoronary stent placement tend to be due to systemic conditions that place patients at prohibitive risk to receive the necessary medications that are needed to be given during the procedure or after a stent has been deployed. Contraindications to the procedure are an inability to consume anti-platelet medications, significant anemia, and significant thrombocytopenia. Another contraindication, or relative contraindication, to the procedure is sepsis with active bacteremia and significant renal dysfunction and any significant comorbid condition where the possible harm of the procedure outweighs the possible benefit.
During preparation, to place an intracoronary stent, a 6F or larger guiding catheter must be utilized to engage the coronary ostia. Anticoagulation in the form of heparin, enoxaparin, or bivalirudin may be given to obtain an anticoagulation time greater than 250 seconds. Next, a coronary wire is utilized to provide a rail to be able to deliver balloons and stents to the lesions being treated. Once at the appropriate site in the vessel the stent delivery balloon is insufflated to high atmospheric pressures via an insufflator device that is manually inflated by the technician or the head operator.
During any intervention in placing an intracoronary stent, the team should consist of the primary operator who is the interventional cardiologist, a technician assisting with any necessary equipment, and a circulating nurse in the room responsible for any intravenous (IV) medications that may need to be given.
Prior to deploying an intracoronary stent, the vessel is appropriately prepared with balloon angioplasty prior to stent placement. Balloon angioplasty is utilized to assess if the lesion will expand and also to further determine lesion length. If the vessel is significantly calcified, the stent may not be amenable to maneuvering to the lesion in question. Rotational or orbital atherectomy may need to be performed to remodel the vessel architecture to facilitate stent delivery and deployment.
To deploy the intracoronary sent while observing the coronary artery via fluoroscopic guidance, the sent is advanced over the coronary wire and placed into position covering the lesion in question with the goal of landing the sent proximally and distally within a healthy portion of the vessel. Again, this technique can be facilitated with intravascular ultrasound or optical coherence tomography to assess better lesion length and type of lesion morphology being treated. Once the appropriate size and length stent has been positioned under constant fluoroscopic guidance, the insufflator device is connected to the stent delivery balloon catheter and is insufflated to high atmospheric pressures to deploy the stent. After the stent is deployed, further intravascular imaging may be performed to confirm adequate stent expansion and rule out any significant edge dissections.
As with balloon angioplasty, when placing an intracoronary stent, there can be vessel can perforation and dissection, and in some cases, the placed stent can acutely occlude after the procedure has been completed. Another complication is stent embolization off of its delivery balloon. If this occurs, it can be either inflated/deployed where it lies or recovered with a snare.
Despite the advances and progress that have been made with drug-eluting, coronary stents, there continues to be a need for further improvement to minimized early and late inflammatory and hypersensitivity reactions to the drug or the polymer. Improvements still need to be made with the drug-releasing polymer as irregularities within the polymer result in inconsistent drug delivery and can also serve as a nidus for possible thrombus formation within the stent. Further improvements in the structure and metal base continue to be developed due to ongoing issues with possible stent fracture and longitudinal deformation that can occur over time in up to 2% to 5% of stents, particularly in the right coronary artery. Also, issues with permanent metallic implants placed in the coronary vessel over time cause vessel straightening and loss of cyclic strain, loss of vasomotion, and adaptive vascular remodeling, and need to be addressed and improved. Lastly, neoatherosclerosis has been seen to develop in second-generation stents where a thin layer of neointimal hyperplasia has developed and begins to adapt and develop lipid accumulation with lipid-rich phenotypes similar to diseased native vessels. These are all areas for future improvement with third-generation stents as well.
|||State of the art: coronary artery stents - past, present and future., Stefanini GG,Byrne RA,Windecker S,Kastrati A,, EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology, 2017 Aug 25 [PubMed PMID: 28844032]|
|||Balloon Angioplasty - The Legacy of Andreas Grüntzig, M.D. (1939-1985)., Barton M,Grüntzig J,Husmann M,Rösch J,, Frontiers in cardiovascular medicine, 2014 [PubMed PMID: 26664865]|
|||[Pioneers of invasive cardiovascular medicine--Charles Theodore Dotter and colleagues: short historical review]., Kostić J,Beleslin B,Nedeljković M,Ostojić M,, Srpski arhiv za celokupno lekarstvo, 2014 Jan-Feb [PubMed PMID: 24684046]|
|||The History of Coronary Stenting., Tan C,Schatz RA,, Interventional cardiology clinics, 2016 Jul [PubMed PMID: 28582026]|
|||Stent thrombosis rates the first year and beyond with new- and old-generation drug-eluting stents compared to bare metal stents., Varenhorst C,Lindholm M,Sarno G,Olivecrona G,Jensen U,Nilsson J,Carlsson J,James S,Lagerqvist B,, Clinical research in cardiology : official journal of the German Cardiac Society, 2018 Apr 17 [PubMed PMID: 29667015]|
|||Kereiakes DJ,Cannon LA,Dauber I,Ball M,Bertolet B,Foster M,Nersesov AY,Underwood PL,Allocco DJ,Dawkins KD, Long-term follow-up of the platinum chromium TAXUS Element (ION) stent: The PERSEUS Workhorse and Small Vessel trial five-year results. Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography [PubMed PMID: 25678402]|
|||Stent thrombosis: insights on outcomes, predictors and impact of dual antiplatelet therapy interruption from the SPIRIT II, SPIRIT III, SPIRIT IV and COMPARE trials., Kedhi E,Stone GW,Kereiakes DJ,Serruys PW,Parise H,Fahy M,Simonton CA,Sudhir K,Sood P,Smits PC,, EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology, 2012 Sep [PubMed PMID: 22995087]|
|||One-year clinical outcomes of patients treated with everolimus-eluting bioresorbable vascular scaffolds versus everolimus-eluting metallic stents: a propensity score comparison of patients enrolled in the ABSORB EXTEND and SPIRIT trials., de Ribamar Costa J Jr,Abizaid A,Bartorelli AL,Whitbourn R,Jepson N,Perin M,Steinwender C,Stuteville M,Ediebah D,Sudhir K,Serruys PW,, EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology, 2016 Nov 20 [PubMed PMID: 27866134]|
|||Rationale of a novel study design for the BIOFLOW V study, a prospective, randomized multicenter study to assess the safety and efficacy of the Orsiro sirolimus-eluting coronary stent system using a Bayesian approach., Doros G,Massaro JM,Kandzari DE,Waksman R,Koolen JJ,Cutlip DE,Mauri L,, American heart journal, 2017 Nov [PubMed PMID: 29129253]|
|||Ultrathin, bioresorbable polymer sirolimus-eluting stents versus thin, durable polymer everolimus-eluting stents in patients undergoing coronary revascularisation (BIOFLOW V): a randomised trial., Kandzari DE,Mauri L,Koolen JJ,Massaro JM,Doros G,Garcia-Garcia HM,Bennett J,Roguin A,Gharib EG,Cutlip DE,Waksman R,, Lancet (London, England), 2017 Oct 21 [PubMed PMID: 28851504]|
|||Safety and efficacy of a bioabsorbable polymer-coated, everolimus-eluting coronary stent in patients with diabetes: the EVOLVE II diabetes substudy., Kereiakes DJ,Meredith IT,Masotti M,Carrié D,Moreno R,Erglis A,Mehta SR,Elhadad S,Berland J,Stein B,Airaksinen J,Jobe RL,Reitman A,Janssens L,Christen T,Dawkins KD,Windecker S,, EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology, 2017 Mar 20 [PubMed PMID: 27840326]|
|||Efficacy and safety of a novel bioabsorbable polymer-coated, everolimus-eluting coronary stent: the EVOLVE II Randomized Trial., Kereiakes DJ,Meredith IT,Windecker S,Lee Jobe R,Mehta SR,Sarembock IJ,Feldman RL,Stein B,Dubois C,Grady T,Saito S,Kimura T,Christen T,Allocco DJ,Dawkins KD,, Circulation. Cardiovascular interventions, 2015 Apr [PubMed PMID: 25855680]|
|||First Approval of Improved Medical Device Conditional on Use-Result Survey in Japan - Regulatory Review of Polymer-Free Drug-Coated BioFreedom Coronary Stent., Konishi A,Ho M,Shirai Y,Shirato H,, Circulation journal : official journal of the Japanese Circulation Society, 2018 Mar 21 [PubMed PMID: 29563353]|
|||Polymer-free Biolimus A9-coated stents in the treatment of de novo coronary lesions with short DAPT: 9-month angiographic and clinical follow-up of the prospective, multicenter BioFreedom USA clinical trial., Waksman R,Piegari GN,Kabour A,Cannon L,Wang J,Adams G,Solankhi N,Smeglin A,Kereiakes DJ,Leiboff R,Spad MA,Torguson R,Chandra N,Bastian R,DeGroot J,Kayo MW,Stoll HP,Garcia-Garcia HM,, Cardiovascular revascularization medicine : including molecular interventions, 2017 Oct - Nov [PubMed PMID: 28923692]|
|||2-Year Outcomes of High Bleeding Risk Patients After Polymer-Free Drug-Coated Stents., Garot P,Morice MC,Tresukosol D,Pocock SJ,Meredith IT,Abizaid A,Carrié D,Naber C,Iñiguez A,Talwar S,Menown IBA,Christiansen EH,Gregson J,Copt S,Hovasse T,Lurz P,Maillard L,Krackhardt F,Ong P,Byrne J,Redwood S,Windhövel U,Greene S,Stoll HP,Urban P,, Journal of the American College of Cardiology, 2017 Jan 17 [PubMed PMID: 27806919]|
|||Effectiveness and safety of the ABSORB bioresorbable vascular scaffold for the treatment of coronary artery disease: systematic review and meta-analysis of randomized clinical trials., Pavasini R,Serenelli M,Gallo F,Bugani G,Geraci S,Vicinelli P,Campo G,, Journal of thoracic disease, 2017 Aug [PubMed PMID: 28894594]|
|||Long-term outcomes of bioresorbable vascular scaffold in ST-elevation myocardial infarction., de Hemptinne Q,Picard F,Ly HQ,Ibrahim R,Asgar AW,de Guise P,Doucet S,Dorval JF,Marquis-Gravel G,Levi M,L-L'allier P,Tanguay JF,, Acta cardiologica, 2017 Sep 28 [PubMed PMID: 28954592]|
|||First-in-Human Evaluation of a Novel Polymer-Free Drug-Filled Stent: Angiographic, IVUS, OCT, and Clinical Outcomes From the RevElution Study., Worthley SG,Abizaid A,Kirtane AJ,Simon DI,Windecker S,Brar S,Meredith IT,Shetty S,Sinhal A,Almonacid AP,Chamié D,Maehara A,Stone GW,, JACC. Cardiovascular interventions, 2017 Jan 23 [PubMed PMID: 28104208]|
|||State of the art: coronary angiography., Collet C,Grundeken MJ,Asano T,Onuma Y,Wijns W,Serruys PW,, EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology, 2017 Aug 25 [PubMed PMID: 28844026]|
|||Shlofmitz E,Shlofmitz R,Lee MS, Orbital Atherectomy: A Comprehensive Review. Interventional cardiology clinics. 2019 Apr; [PubMed PMID: 30832940]|
|||Allen DW,Kaul P, Atherectomy and Specialty Balloons in Percutaneous Coronary Intervention. Current treatment options in cardiovascular medicine. 2019 Mar 4; [PubMed PMID: 30830449]|