Patients with heart artery stenting can reduce risk of future heart attacks with additional heart artery stenting in other untreated arteries


Research has shown that patients who have had emergency heart attack treatment with heart artery stenting – and have significant narrowings in their other untreated arteries – can benefit from additional stenting to help prevent future heart attacks.

A stent is a tiny mesh tube that is inserted into affected, or clogged, arteries and expands to keep them open, reducing the chance of further heart attacks by allowing the blood to flow more freely around the heart.

The results of the COMPLETE study, presented at the European Society of Cardiology meeting in Paris in September 2019 and simultaneously published in the New England Journal of Medicine, showed that patients who underwent routine additional stenting had a lower risk of further heart attacks or heart-related death, compared to those who had just usual tablet treatment for managing the untreated narrowings (7.8 per cent versus 10.5 per cent over five years).

They also had less than one-fifth the risk of needing further emergency treatment for their heart arteries in the future.

As part of the international clinical trial of over 4000 patients, additional analysis of the study has been presented at the Transcatheter Cardiovascular Therapeutics (TCT 2019) meeting in San Francisco (Saturday 28 September 2019), looking at whether timing of the second stenting procedure – either during the same hospital admission or as a later outpatient procedure -was important in achieving the beneficial effects.

Similar benefits were seen regardless of whether the second procedure was performed as an in-patient or within six weeks as an outpatient.

Over 700 UK patients took part in the UK investigations led by Rob Storey, Professor of Cardiology at the University of Sheffield and Academic Director and Honorary Consultant Cardiologist in the Cardiology and Cardiothoracic Surgery Directorate at Sheffield Teaching Hospitals NHS Foundation Trust.

Professor Storey, who was also a member of the executive team running the study, said: “We have made huge strides in the treatment of heart attack over the last 20 years with the development of new drugs and new stents continuously improving the effectiveness of heart artery stenting.

For example, in Sheffield we have led the way in the development of ticagrelor, which has markedly reduced the risk of stent blockage and further heart attack, and this is now a standard treatment for heart attack around the world.”

One of the questions that had remained unanswered until now was whether or not patients with significant narrowings elsewhere in their main heart arteries benefit from additional routine stenting of these narrowings immediately after they have had emergency treatment to open a blocked heart artery.

“The COMPLETE study answers this question emphatically, showing that further stenting should be the standard treatment for these patients whenever feasible,” Professor Storey added.

“The results of our additional analysis shows that the dominant UK practice of bringing patients back as an outpatient for their second procedure was just as beneficial as performing the second procedure in hospital at the time of the initial hospital admission, since the benefits accrued over many years.

“So this strategy fits very well with UK best practice, since patients can return within a month or so for an outpatient stenting procedure and still receive the same benefit compared to staying in hospital as an inpatient longer after their heart attack for the second procedure.

This marks another milestone in the relentless progress towards improving the long-term outlook of heart attack patients.”

Next-generation drug-eluting stents (DES) reduce in-stent restenosis and stent thrombosis risks when accompanied by appropriate dual antiplatelet therapy (DAPT)1. Still, concern persists over toxicities of locally eluted drug and inflammation induced by polymer coatings2,3. It remains important to consider whether evolution in stent design can improve performance, potentially obviating the need for drug/polymer coatings.

Surface wettability alters thrombotic and inflammatory interactions. In vitro evidence suggests that hydrophilicity reduces platelet adhesion and improves endothelialisation46, yet contemporary stents are mildly hydrophilic at best (Figure 1A)4. Though phosphorylcho-line-coated stent surfaces are considered “hydrophilic”, a water contact angle of ~85° indicates their amphiphilic nature4,7 (90° is typically considered the transition between hydrophobic and hydrophilic surfaces). Many factors restrict DES polymer hydrophilicity, such as swelling of hydrophilic polymers in aqueous environments, too rapid drug release in the absence of hydrophobic constituents, and emerging concerns over polymeric embolisation3,5,8,9.

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Figure 1.
In vitro impact of stent ultra-hydrophilic surface treatment on cellular response. A) Water contact angles for common DES polymers4 and bare metal CoCr, without (BMS) or with ultra-hydrophilic treatment (UHS). B) In vitro response of BMS and UHS stents (SEM images). Left: stents after 2 hrs incubation with heparinised human blood, showing platelet adhesion (green) on BMS and neutrophil adhesion (blue) on UHS stents (images artificially colouredfor improved cell visibility). Right: after 72 hrs of endothelial cell proliferation, showing confluent cell coverage on both BMS and UHS stents.

We here consider an ultra-hydrophilic surface (UHS) treatment that activates metallic surfaces6, achieving a contact angle of 10°. This is far less than commercial DES polymers or stainless steel and cobalt-chromium (CoCr) bare metal surfaces (Figure 1A). When compared with untreated bare metal, UHS show promising results in vitro, dictated by alterations in surface chemistry and native oxide layer which tune blood protein absorption and cell adhesion (Figure 1B)6,10. This study extends the implications of ultra-hydrophilicity in vivo and in the context of next-generation stents. FDA-approved sec-ond-generation DES and bare metal stents (BMS) were compared with matched UHS-treated stents in A) porcine coronary models to assess intimai hyperplasia and late thrombosis; and B) a rabbit iliac model to assess early healing and subacute thrombosis (Figure 2).

More information: Shamir R. Mehta et al, Complete Revascularization with Multivessel PCI for Myocardial Infarction, New England Journal of Medicine (2019). DOI: 10.1056/NEJMoa1907775

Journal information: New England Journal of Medicine
Provided by University of Sheffield


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