CX NEWS

Yesterday, for the first time, the Charing Cross International Symposium broadcast peripheral live cases that were directly linked to data presented the previous day on the theme of peripheral arterial controversies. The aim of the course was to provide delegates with opportunities to learn techniques to achieve the best results with the approaches discussed in the data.

Speaking from Bad Krozingen via satellite video, Thomas Zeller (Bad Krozingen, Germany), the director of the peripheral live cases course, said: “The live case transmissions are little bit different from what people are used to seeing at conferences. Our goal is not to educate or teach you about complex interventions; our goal is to provide you with context to data from recently published trials or even ongoing trials.” He explained that he would be the chief operator in the cases and would be assisted by Alijoscha Rastan, Elias Noory, and Ulrich Beschomer (all from Bad Krozingen, Germany).

The first case of the course was related to the 24-month ILLUMENATE data that were presented on Tuesday at CX by Stephan Duda (Berlin, Germany). It involved a patient who was enrolled in the ILLUMENATE Global Registry, which is evaluating Spectranetic’s Stellarex drug-coated balloon. Zeller explained that the patient appeared to have very mild disease of the distal superficial femoral artery. He added that they had purposely chosen a patient with a “relatively simple lesion” to remind the audience that “almost all of the data you can see so far regarding drug-eluting balloons are TASC A or B lesions”.

Zeller reported that he would be using an 8cm drug-coated balloon (with a 4cm balloon to predilate the vessel) because the rule for using drug-coated balloons should be the same as that for using stents in the coronary arteries: treat from a healthy segment into a healthy segment. He explained that the patient in this case had diffuse disease in proximal areas.

According to Zeller, another rule for using drug-coated balloons was not to put the balloon into the vessel until “everything was prepared”. He said: “Preparation means slashing off the guidewire; it is evacuating cracked air from inside the vessel so that you can see the exact actions of the balloon when it is inflated. If you wait until the balloon is inside the vessel to do the preparation, the balloon is already exposed to the bloodstream; the longer the balloon is exposed to the bloodstream, the more drug you will lose from the surface.”

The second case, in which the Silverhawk atherectomy device (Covidien-Medtronic) and a drug-coated balloon were used to treat a popliteal artery stenosis, was also related to data presented during the peripheral arterial controversies. Zeller commented that the rationale for using atherectomy in this patient was based on the results of the DEFINITIVE AR study, which indicated that directional atherectomy and anti-restenotic therapy (DAART) could be used to improve patency in long and severely calcified lesions: the Zeller himself presented the study’s 24-month results at CX on the peripheral day. However, he commented that the patient in the case was not the typical “DEFINITIVE AR” patient because her femoral artery was “free from disease”. “The popliteal artery, in particular the distal segment, is severely exposed to extra compression forces. Therefore, we usually try to avoid placing a stent in this artery. Thus, we used atherectomy before a drug-coated balloon in this particular patient to try to avoid the need for a stent,” Zeller explained.

Rotational atherectomy, with the Jetstream device (Boston Scientific), and a drug-coated balloon (Ranger, also Boston Scientific) were used, in the third case, to treat a calcified superficial femoral artery lesion. According to Noory, who gave the overview of the case, the first-in-man data for the Ranger device were not yet available but data from the preclinical studies were “promising”. The case sparked a discussion about when to use atherectomy and when to use rotational atherectomy, with Zeller commenting: “Rotational atherectomy is a pretty good tool for occlusions. Also small vessels, 4mm for example, also respond very well to the Jetstream system. If you have larger diameters, 5–6mm vessels, or bifurcations then I prefer to use atherectomy.”

The final case of the morning was supposed to involve the use of the TurboHawk (Covidien-Medtronic) and a drug-coated balloon for the treatment of a lesion in the common femoral artery. This related to the ongoing PESTO-CFA study, which is comparing percutaneous intervention with surgery for the management of common femoral artery lesions. However, Zeller had difficulties putting in the guidewire in the lesion and, after discussing the case with the audience, decided to proceed to putting in the drug-coated balloon without using atherectomy.

In the afternoon, cases were focused on situations in which “stents were unavoidable or beneficial” and “where stents are unavoidable or beneficial and in-stent restenosis treatment”. The devices used in these cases were the Zilver PTX (Cook Medical) with a new release system, the Supera (Abbott Vascular), the Supera with a provisional re-entry device, the Innova  stent (Boston Scientific), the SmartFlex (Cordis), a sirolimus-eluting balloon and the BioMimics stent (Biosensors), heparin-bonded contoured-edge Viabahn (Gore Medical), and Rotarex (Straub Medical) and IN.PACT Pacific (Medtronic). During Tuesday’s peripheral programme, there were talks reviewing the current controversies in peripheral stenting.

Giovanni Torsello (Münster, Germany), who chaired the morning session of the live cases course, said the live cases were a valuable educational tool because delegates not only wanted to hear about study data but also see “how they can make their strategies, their techniques better than before. This is why people attend live case courses.”

LINC@CX

LINC (Leipzig Interventional Course) once again held a live case session at CX, which this year focused on below-the-knee interventions. The cases included recanalisation of an infrapopliteal obstruction with a drug-coated balloon, retrograde transpedal recanalisation with 3F access system, and lesion-specific use of a drug-eluting stent and a drug-coated balloon for an infrapopliteal obstruction. Giancarlo Biamino (Mercogliano, Italy) told CX Daily News that live cases that “do not go according to plan” were just as educational as the ones that did because it gave delegates opportunities to see how operator can manage and rectify unexpected situations.

In traditional Charing Cross fashion, yesterday’s debates stirred much discussion in the Main Auditorium. Particularly stirring was the debate where the audience voted 70% against the motion that EVAR is not sensible for any abdominal aortic aneurysm with a neck length less than 10mm. Stephen Cheng (Hong Kong) spoke for the motion, while Jan Blankensteijn (Amsterdam, Netherlands) sounded-off against the motion.

Making his case, Cheng said that even with new devices, there are more early complications, more late complications, more (difficult) secondary interventions and more adjuncts associated with short-neck endovascular aneurysm repair.

On the other hand, his opponent maintained that in selected cases of infrarenal neck length <10mm, “Any of the current infra/transrenal devices can be used with or without endoanchors for enhancement,” adding that even if it comes with a moderately increased risk of type 1a endoleak, it “balances against downsides of F-EVAR, CHIMPS, or against open repair (if F-EVAR is not an option).”

Discussing the outcome of the debate and the audience’s strong position against the motion, Blankensteijn said, “I think that people understand that things are not absolute and clearly we know that staying inside IFU you get better results. I am not running around proposing to treat any less than 10mm neck with an infrarenal device, but the point is that judicious use of these devices outside IFU can produce better results and injudicious use outside the IFU is an instruction that the industry gives you, we need to think with these device what to do an there are several occasions it does not make sense or it may even be dangerous to use a fenestrated stent graft. Then I would suppose that an infrarenal device (for instance Gore Excluder) preserves all the options juxtarenally, so if this fails, you still have the option to use a fenestrated cuff or go higher up.”

The debate took place during a session on procedures for infrarenal abdominal aortic neck.

The answer lies in the neck

While presenting the morphology findings from the IMPROVE trial, Robert Hinchliffe, London, UK, drew attention to independent association between neck length and mortality. “Only aortic neck length is significantly associated (inversely) with 30-day mortality both for open repair (p<0.001) and overall (p=0.007). The shorter the neck, the higher the mortality after open repair (and EVAR). With long necks, the 30-day mortality from EVAR and open repair is similar (and this is consistent with the results of the AJAX and ECAR trials),” he said.

Therefore, added Hinchliffe, a short aneurysm neck was the commonest reason for a patient being unsuitable for conventional EVAR. The results also explain why observational studies, which cherry pick long-necked aneurysms for EVAR leaving all the short necked aneurysms for open repair, always show that mortality is lower after EVAR. “Such observational studies are comparing apples and oranges,” he said.

The morphology findings could also explain the worse outcomes in women as short aneurysm necks are especially common in women.

“In the future, new, widely available endovascular strategies for rupture in short necked aneurysms are needed and results following rupture should report juxta-renal and infra-renal aneurysms separately,” Hinchliffe said.

“Aneurysm morphology indicates whether a patient with ruptured abdominal aortic aneurysm is eligible for EVAR and may influence the outcome of both EVAR and open surgical repair,” he concluded.

Stick to the IFU

Timothy Resch, Malmö, Sweden, enforced the point that the outcome of EVAR is “excellent if we stick to the IFU and hostile sealing zone anatomy affects the outcome of EVAR negatively both in the short and long term regardless of the device that you use.”

Resch explained that 10—20% of EVAR patients have necks <15mm, and these short infrarenal necks are predictive of initial technical failure, with increased incidence of early and late type 1 endoleak and increased use of intraoperative adjunctive procedures, where the long-term outcome is impaired and endoleaks, migration and late rupture are common.

Referring to a contemporary meta-analysis of 12,000 patients treated with modern devices, 3,039 patients with hostile necks saw an increase in 30-day mortality, intraoperative adjuncts, 30-day migration and an increase in type 1 endoleak at 30 days and one year.

Further, in the ANCHOR registry, Resch noted, a regression and ROC analysis was used to try to find predictive factors for type 1a endoleak which showed that the diameter of the neck correlates with poor outcome, as does the anatomic neck length. “This actually provides some solid data for calculating the risk in the individual patient,” he said.

“So one option of course in these short juxta pararenal aneurysms is to seal higher above and use the fenestrated and incorporate the visceral arteries in your repair. Does that solve the problem of the proximal endoleaks? Again, it depends on how you use the graft,” Resch suggested.

Making a case from some of his own data and that of a study at the Cleveland Clinic, USA. “We found no cases with proximal type 1 endoleaks during long-term follow-up of these patients. So maybe this is the solution for everything—using it in the right context. In a larger series from the Cleveland Clinic analysing over 900 patients with fenestrated grafts, indeed there was a 2.8% incidence of late type 1a endoleak occurring in a steady fashion over time and almost half after a year post-operatively. Looking at the risk factor in that series, what they identified again was a poor sealing zone, just as you would in an infrarenal neck and more that 10% was diameter change and they also found that the sealing zone was much more unstable in the juxtarenal vs. more proximal aorta. So from the clinical perspective, we have learned from that and we now place more fenestrations on the graft to reach a healthy sealing zone, which in our series, combined with the series from Lille with 300 patients, resulted in a higher placement of the endograft than we initially did without affecting the operative mortality or the one-year outcome,” he reported.

The INNOVATION study found that the rate of freedom proximal type I endoleaks and the rate of freedom from reintervention in patients who underwent endovascular aortic aneurysm repair (EVAR) with the Incraft (Cordis) device was, respectively, 100% and 95%, at three years. In this interview, CX Daily News speaks to Giovanni Pratesi (Florence, Italy)—who presented the data at CX yesterday—about Incraft and the three-year results.

How does the Incraft stent graft differ from other EVAR devices?

It is a new-generation stent graft system with unique features that have been specifically designed to overcome the limitations of current stent grafts. For example, the ultra-low profile integrated delivery system (14F OD) offers excellent navigational opportunities in challenging access vessels. Additionally, the micrometric deployment system allows for accurate placement—either at proximal and distal attachment site. Bilateral in-situ length adjustment, up to 3cm, permits you to customise every implant on the single patient anatomy. Therefore, the Incraft system, according to the “few-fits-most” concept, is able to cover a large spectrum of anatomies with only 23 product codes, four main bodies and 19 iliac limbs.

What are the main results of the INNOVATION study at three years?

The three-year results of the INNOVATION study have confirmed the very promising one- and two-year outcomes of the study. These data show, at three years, the device is associated with 100% freedom from type Ia and III endoleaks, stent-graft migrations, and device- or procedure-related major adverse events. They also show that the rate of limb patency is 97.8%, with only one case of limb occlusion. Other findings from the three-year data indicate that there is a significant reduction in mean aortic aneurysm diameter, up to 15 mm, compared with two-year data, a freedom from sac increase of 95.6% and freedom from stent fractures of 97.7%. Core lab analysis has identified two cases of aneurysm sac enlargement—both associated with a persistent type II endoleak—and one case of stent fracture, but these events did not appear to have any clinical consequences.

What other data were included in your presentation?

I specifically addressed endograft durability and anatomical preservation in my analysis of the Innovation study. Data from core lab analysis have confirmed the excellent stent graft stability that has already been observed during follow-up. A median proximal migration of 2mm was observed at three-year compared with the one-month computed tomography (CT) scan. The same result was achieved in terms of distal migration with a median change of 1.1mm and 2mm on the right and left side respectively, compared with the one-month CT scan.

Aortic neck diameter, neck angulation and iliac artery diameter, compared with one-month CT scan, were analysed at three years to review endograft influence on anatomic changes during follow-up. The observed 1mm proximal neck dilatation and 2mm iliac artery dilatation, combined with the 0.6 degree changes for infrarenal neck angulation and 2.4 degree for suprarenal neck angulation, confirmed the excellent stent graft conformability to the preoperative anatomy.

What were the main take-home messages from your presentation?

These data confirm the very promising earlier outcomes of Incraft stent graft system and add new evidence regarding its effectiveness in terms of anatomy preservation with a 100% freedom from both proximal aortic neck and iliac dilatation, and from proximal supra- and infrarenal aortic neck angulation changes.

Yesterday saw the beginning of the two-day CX Venous Workshop, in which delegates can enjoy expert demonstrations of a selection of the most interesting and important phlebological technologies currently in use. Now in its seventh year, the event continues to attract more and more delegates to its plethora of new and established technologies, and this year occupied its largest space ever on the Upper Level of the Gallery. The first day of the workshop largely focused on varicose vein treatment and superficial venous issues.

Ian Franklin (Imperial College, London, UK) is leading the workshop over both days, and has done since it first featured at the Charing Cross Symposium seven years ago. He explained, “I think it is important to provide a combination of the big plenary sessions in the hall and smaller interactive workshops like this one—not all techniques and discussions lend themselves the plenary environment. By providing these training stations and this small-group one-to-one teaching format, it means that people can interact in a much more informal, personal level.”

Over its seven years the workshop has grown and changed, keeping pace with the changing face of the vascular field. “The needs have changed,” Franklin commented. “When we first started doing this it was an office-based varicose vein course. Now it is far more than that. We have found that quite a lot of the techniques that people were hungry to learn at the beginning are ‘old hat’ now, so each year we offer new things. Now people are hungry to learn deep vein stenting, intravascular ultrasound, non-thermal techniques for treating veins, and so on. This year we have some completely new things that people will not have seen before.”

Given the quality of the Charing Cross faculty, such one-to-one interaction presents an exciting educational opportunity. “All of our faculty are well-known names and enthusiasts in their field. You can interact with them much better if you talk to them face-to-face rather than if they are up on a podium and you are down in the audience and asking the questions through a microphone. This way you can ask things you might not be able to go into in a lecture theatre.” Franklin added that these face-to-face interactions combine with practical experience, and delegates can “hold the kit in their hands, practice on the simulator and talk through tips and tricks with someone who has done it a lot before—you cannot do that in a lecture theatre.”

The workshop’s layout with multiple training stations also means that delegates can be efficient with their time, heading straight for those stations dealing with subjects they are unfamiliar with. “They do not have to sit through things they already know about, so they can make very efficient use of their time,” Franklin said.

The workshop features both established and new technology. One of the busiest stations yesterday was that of a well-established technology—foam sclerotherapy.  Simon Ashley (Plymouth, UK), was one of the trainers at the station. He spoke to CX Daily News during the workshop, and explained, “Personally it is the first time that I have been involved as a trainer, but I know that it has been running for a number of years and has grown increasingly popular—that is why so much space has been devoted to it.” As to why the station was so busy, Ashley noted that foam sclerotherapy “is a walk-in walk-out treatment that only takes about 20 minutes and there is no down time or restriction of activities afterwards. It is also very attractive for NHS and private practice because it is undoubtedly the most cost-effective treatment.”

In keeping with the Charing Cross Symposium’s passion for innovation, there was also a selection of new techniques and products on show. The Biolas station, exhibiting the company’s non-thermal ablation VariClose vein sealing system, was kept busy throughout the day by curious delegates. The company are attending their first ever Charing Cross Symposium, and chief medical officer, Yunus Çakiroĝlu, told CX Daily News “We are new this year, so I think a lot of people are wondering about our products and our company—they want to find out who we are and what we have at our station. The meeting is very exciting, and the workshop is a great way for the delegates to understand new technology.”

The workshop will continue today with a focus on acute deep vein thrombosis interventions, intravenous ultrasound and deep venous stenting, but still including ablation technologies for superficial veins. The stations open for delegates to visit will include: thermal (laser), thermal (radiofrequency ablation), non-thermal, practical training stations, valves, vascular ultrasound training simulator, venous malformations, pelvic venous imaging, pelvic vein embolisation, acute deep vein thrombosis, caval filters, follow-up protocols, air plethysmography, intravascular ultrasound and deep vein stenting.

Franklin expects the Upper Gallery to be just as busy as it was yesterday thanks to the planning of this year’s programme. He said, “We have made an effort to separate the days this year, with Wednesday focusing more on superficial techniques. On Thursday we are going to have a big focus on deep vein stenting, deep vein thrombosis treatments, pelvic vein embolisation and intravascular ultrasound. These are all quite new for us and should attract a new group, so I expect it to be busy tomorrow as well.”

According to Janet Powell, Imperial College London, UK, the highest risk factors for rupture of abdominal aortic aneurysms (AAA) are female gender, smoking, increasing age and mean arterial pressure, but there are still few useful indicators of how to manage screen-detected aneurysms to stop them enlarging. Powell put forward this view during yesterday’s Abdominal Aortic Controversies Main Programme which explored epidemiology, indications and medical management of abdominal aortic aneurysms.

In trying to work out what makes aneurysms grow, Powell said that mostly the “mundane” cardiovascular risk factors have been looked at—alcohol, diet, obesity, smoking, medicines taken, exercise taken.

Turning to the existing and ongoing randomised trials that provide evidence for growth factors, Powell pointed out three trials already completed and without a positive result—AAA:STOP, PHAST and AORTA.

“Even in 2015, it is quite difficult to find information about trials because some trials still remain unregistered. Large epidemiological studies have mainly shown us about the risks for developing aneurysms, but the focus has been on baseline risk factors, not aneurysm progression,” she said.

Powell referred to RESCAN, a large international project primarily with the purpose of looking at optimal surveillance intervals for small aortic aneurysms, which was an individual patient data meta-analysis of small aneurysms, their growth and rupture in more than 15,000 persons.

“As we all know, growth rate increases with aortic diameter—just 1.34mm a year for the smallest aneurysms and 3.63mm when it comes to 5cm aneurysms—with exactly the same growth rate between men and women,” she pointed out.

When it comes to smoking, Powell maintained that the data are remarkably consistent that it increases aneurysm growth rate but that the effect is modest. Similarly, the effect of diabetes to slow or reduce the aneurysm growth rate is very consistent, but small.

“So we identified out of the available baseline data we had only two factors in these 15,000 patients that influenced growth rate and both effects were relatively modest—smoking increases, diabetes decreases. Cholesterol, blood pressure, statins, anti-hypertensive drugs and aspirin had no effect, and the year of enrolment [1985–2008] had absolutely no effect either. Disappointing,” Powell stated.

Rupture rates

Even though rupture of small aneurysms is not common, findings were more informative. RESCAN showed that the smallest of aneurysms take eight or more years before the risk of rupture is anything substantive, but as the diameter increases, so does the risk of rupture. But even for a 5cm aneurysm, it is more than year before risk of rupture exceeds 1%.

Powell pointed to some strong associations with factors that increase rupture rates. “Most notable, the fact that in women, there is fourfold increase in rupture rates vs. men. With smokers there is a twofold increase, with a far bigger effect on rupture than on growth. Mean arterial pressure increases growth rate, as does age. The older you are, the more likely your aneurysm is to rupture for any given diameter. So we cannot have any of this ageism, we need to treat aneurysms in older people too,” Powell maintained.

In the EVAR 2 trial, and subsequently reproduced in other papers, Powell observed that aortic neck length was associated with rupture and the shape of the aneurysm might have mattered, and a long neck was associated with relative protection from aneurysm rupture.

“Where are we in 2015? For rupture, there are some strong factors increasing risk: female gender, smoking (which we can do something about), increasing age, higher mean arterial pressures (we could have more effective blood pressure control), and the fact that a long aneurysm neck could just be protective. However, for growth, the effects that we have identified are modest: smoking, which increases it, and diabetes, which is protective,” Powell said.

She re-stressed that both of those growth effects are modest, adding that, “unfortunately this leaves us in a position that as yet we have few useful indicators of how to manage screen-detected aneurysms to stop them enlarging other than the old classic that was used for intermittent claudication—stop smoking and possibly keep walking.”

Results from the 12-month data of the randomised controlled IMPROVE trial, presented for the first time at CX 2015 (28 April–1May, London, UK), show that an endovascular strategy is cost-effective when compared to open repair in the treatment of ruptured abdominal aortic aneurysms. The one-year data also revealed that the endovascular strategy conferred no survival benefit over open repair, except a trend towards benefitting women. It also showed that the endovascular strategy enabled more patients to be discharged from hospital to home, and significantly faster than with open repair. Patients also have an excellent quality of life with endovascular strategy, if they survive the rupture, delegates heard.

Twelve-month outcomes from the individual patient data meta-analysis of three randomised controlled trials of ruptured aneurysms [ie the Dutch AJAX trial, the French ECAR trial and the UK IMPROVE trial] also showed a trend towards survival benefit for endovascular aneurysm repair (EVAR), but this was not statistically significant. A CX audience poll in the session revealed that nearly 80% agreed that the 12-month results of the IMPROVE trial encouraged them to perform EVAR more often.

Janet Powell, Imperial College, London, UK, presented the latest data from the IMPROVE (Immediate management of the patient with rupture: Open vs. endovascular repair) trial that reported one-year outcomes following either a strategy of endovascular repair first or open repair of ruptured abdominal aortic aneurysm. The results demonstrate no survival benefit for the endovascular strategy for ruptured aneurysm at one year. However, an endovascular-first strategy for the management of ruptured aneurysms does offer patients faster discharge with better quality of life and it is also cost-effective. Both these factors are necessary for patient and clinical decision-making, delegates heard. These data were published in April in the European Heart Journal (EHJ).

IMPROVE, a pragmatic, multicentre (29 UK and one Canada) trial randomised 613 patients with a clinical diagnosis of ruptured aneurysm, 316 patients to an endovascular-first strategy (if aortic morphology was suitable and open repair if not) and 297 to open repair. Powell also drew attention to the fact that at baseline, the characteristics of the two groups were similar with almost three-quarters in each group being men. “The aneurysms in this trial were also very large with average diameters in each group being over 8cm,” she said. The principal one-year outcome was mortality and secondary outcomes were reinterventions, hospital discharge, health-related quality-of-life, costs, quality-adjusted-life-years and cost-effectiveness.

At CX 2015, Powell noted that the trial was designed to answer the question of what to do with a patient who presents to the emergency room with a diagnosis of ruptured abdominal aortic aneurysm. “What we had anticipated was that using an endovascular strategy, wherever it was morphologically feasible, we could reduce 30-day operative mortality from 47% in the open repair group to 33% where endovascular repair was used extensively,” she said.

Powell added: “At one year, all-cause mortality was 41.1% for the endovascular strategy group and 45.1% for the open repair group (p=0.325) with similar reintervention rates in each.  A subgroup analysis showed a stronger benefit for the endovascular strategy in women versus men. The endovascular strategy group and open repair groups had average total hospital stays of 17 and 26 days, respectively.

The 30-day mortality results, the primary outcome, previously published in British Medical Journal (BMJ) in 2014, also found no difference in 30-day mortality between the endovascular strategy group and the open repair group and subgroup analysis showed a strong benefit for the endovascular strategy in women compared with men.

Pooled individual patient data outcomes

Ron Balm presented the 12-month outcomes meta-analysis from the individual patient data from the three randomised controlled trials of ruptured aneurysms; the Dutch AJAX trial (Annals of Surgery 2013), the French ECAR trial (EJVES 2015) and the UK IMPROVE trial.

“These were all trials that were performed on patients with a clinical suspicion of ruptured aneurysm. In the AJAX trial the 30-day mortality in both groups was approximately 25%, in ECAR it was 22% and in IMPROVE, which had a slightly different study design, it was 35% in each group (BMJ 2014), but all failed to demonstrate the benefit of EVAR in the emergent setting. “The results were hampered by the fact that open repair performed so much better than we expected,” Balm noted.

The pooled inpatient data was subjected to two different analyses; the first was an analysis as randomised including all patients and the second contained only those patients with proven rupture and a restricted cohort from the IMPROVE trial who were anatomically suitable for EVAR.

“The 30-day survival data showed no significant benefit for endovascular repair. A subgroup analysis of age, sex and Hardman disability index showed that age and Hardman index had no influence on the main results, but female sex was identified as benefitting from endovascular repair. The time to discharge alive from primary admission was also significantly better for patients undergoing EVAR when compared to those undergoing open repair. We also looked at the influence of neck diameter, neck length and neck angulation. Longer neck lengths resulted in better survival for all patients,” Balm said.

In the pooled results of all patients, the three-month mortality rate included only those patients who were fit for endovascular repair, which reduces the patients in the IMPROVE trial. There seems a benefit for endovascular repair but this is statistically not significant, he said.

Summarising the survival results of all pooled patients to one year, Balm said, there is an advantage for EVAR, but this is statistically not significant. 

These findings led Balm to conclude that the early data from the pooled inpatient data meta-analysis did not suggest that there was any survival benefit for EVAR. “At one year, the small survival advantage of EVAR is not significant. Yet, although endovascular repair does not offer a significant survival advantage, endovascular repair should be used more widely. Open repair must remain available for those unsuitable for conventional EVAR,” Balm maintained.

Are patients with ruptured aneurysms being turned down too often?

A small majority of voters, 57%, did not agree with the motion “Too many patients with ruptured aneuryms are denied intervention” in an interesting debate on the topic.

Matt Thompson, London, UK, speaking for the motion, based his arguments on the data from Karthikesalingam et al (The Lancet, 2014), which used UK Hospital Episode Statistics (HES) data and US Nationwide Inpatient Sample (NIS) data to show that in-hospital survival from ruptured abdominal aortic aneurysm, intervention rates, and uptake of endovascular repair are lower in England than in the USA.

Thompson stated that 68% of patients in the UK receive no treatment for rupture. “There is a huge variation in the proportion of patients being offered therapy for ruptured abdominal aortic aneurysm at the regional and international level. Non-interventional treatment is universally fatal,” he said.

Thompson argued that apart from identifying the optimal management strategy for patients with ruptured aneurysms, more emphasis should be placed on treatment rates. “We must do better than refuse treatment to around 60% patients,” he said.

Peter Lamont, Bristol, UK, who persuaded the delegates that ruptured aneurysm patients were not being denied interventional treatment too often, contested the data presented by Thompson because with the HES data it made the assumption that the diagnostic code for ruptured abdominal aortic aneurysm without an operative code for the condition was a turndown. He also pointed out that a 2005 coding audit had found up to 23% HES codes to be incorrect. Further, NIS data misses 80% of patients, noted Lamont.

“Numerous direct audits in 2010 and after in the UK show consistent turndown rates of around 20% by vascular surgeons,” he said.

Lamont pointed to a Vascular Society members audit in 2011 that revealed a turndown rate of 24% and also showed that the average age of patients was 83. “Of these, 24% declined intervention, 14% had dementia and 21% had terminal malignancy/severe chronic disease,” he added.

Lamont concluded by saying that the service reconfiguration in the UK guarantees that vascular surgeons are now on call 24/7 for ruptured abdominal aortic aneurysm. “When comparing like for like, the turndown rates in the UK are similar to those in the USA,” Lamont said.

In the ensuing discussion, Powell made the point that twice as many women than men are turned down for treatment when they present with ruptured aneurysm and asked for a response on why this might be the case. “We did not formally address that in the IMPROVE trial, but there are several observational cohorts to suggest that adopting a more minimally invasive approach would lead to a reduction in turndown rates in these patients,” added Thompson.

Thompson explained the criteria for palliation; patients in whom intervention is completely futile, such as those with advanced malignancy or dementia, who have no quality of life are suitable candidates for palliation. “There are patients in whom it is cruel to intervene as they do not want their life prolonged,” agreed Lamont.

Frank Veith, New York, USA, made the point that the way to decrease the turn down rate for ruptured aneurysms was to embrace endovascular repair.