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Abstracts 4. Gemeinsamer Jahreskongress der ... - SWISS KNIFE

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swissknife spezial 06 12.06.2006 13:39 Uhr Seite 49<br />

(p=0.003), and 36% vs 25% in younger patients, respectively (p=0.025). In none of these<br />

analyses the method of revascularization, i.e. open surgical versus endovascular procedure,<br />

was associated with outcome.<br />

Conclusion: Revascularization significantly improves the prognosis of CLI at any age.<br />

Attempts to re-establish a sufficient circulation are therefore mandatory even in patients of 80<br />

years or ol<strong>der</strong>. However, no significant differences were found with respect to the choice of<br />

method of revascularization in this series for this age group.<br />

30.03<br />

P. Tozzi 1 , E. Borghi 2 , B. Perrin 3 , G. Siniscalchi 4 , E. Haesler 5 , D. Hayoz 5 , L.K. von Segesser 6<br />

1 Chirurgie Cardiovasculaire, CHUV, 1011 Lausanne/CH, 2 Engineering, Idee & Sviluppo, Bologna/IT,<br />

3 Cardiovascular Surgery, CHUV, Lausanne/CH, 4 Chirurgie Cardiovasculaire, CHUV,<br />

1011 Lausanne/CH, 5 Angiologie, CHUV, Lausanne/CH, 6 Chirurgie Cardiovasculaire, CHUV,<br />

1011 Lausanne/CH<br />

Edge-to-edge vascular repair: a new technique to improve long term anastomosis patency<br />

rate<br />

Objective: The suture technique described more than 100 years ago by Carrel still provides<br />

the best long term results in terms of anastomosis patency, with respect to other suture and<br />

sutureless techniques. Several sutureless anastomosis devices have been designed to facilitate<br />

the surgeon’s work but, almost in all cases, they have failed to reproduce the same long<br />

term results. The Vascular Join (VJ) is a sutureless vascular anastomosis device that has<br />

been designed and developed in our institution to facilitate the anastomosis construction and<br />

eventually improve its patency rate. We designed an animal study to assess its reliability and<br />

long-term efficacy and we report the preliminary results.<br />

Methods: Device description: VJ allows the construction of end-to-end and end-to-side anastomoses.<br />

It consists of two metallic crowns fixed to the extremity of the two conduits so that vessel<br />

edges are joined layer by layer. There is no foreign material exposed to blood. Animal<br />

model: in adult sheep, 45 to 55 kg, equipped with femoral arterial line, both carotid arteries<br />

were prepared and severed. After injection of heparin 100 U/kg, end-to-end anastomoses<br />

were performed using the VJ device on one side and the classical running suture technique<br />

with 6-0 prolene on the other side. Carotid blood flow was measured with Medistim probe.<br />

Animal received aspirin 100 mg/day and were followed-up with Duplex-scan every 3 months<br />

and sacrificed after 12 months. Hystopathological analysis was carried out.<br />

Results: Sixteen animals were enrolled and all survived the procedure. A total of 16 sutureless<br />

anastomeses were successfully completed in less than 2 minutes versus 6±3 min for running<br />

suture. Mean post operative carotid flow was 180±46 ml/min on the sutureless side and<br />

163±36 ml/min in the control side. Duplex showed the occlusion at 3 months of 3 controls<br />

and one sutureless anastomosis. 2 controls and 1 sutureless had stenosis >50% at 12<br />

months. Histology showed very thin layer of myointimal hyperplasia (50±10 mm) in the sutureless<br />

group versus 300±27 mm in the control. No significant inflammatory reaction was<br />

detected.<br />

Conclusion: VJ provides edge-to-edge vascular repair that can be consi<strong>der</strong>ed the most physiological<br />

way to restore vessel continuity. For the first time, in an animal study with long term<br />

follow up, an anastomotic device provided better results than suture technique. Clinical trial is<br />

about to start to validate these results.<br />

30.04<br />

H. Probst 1 , F. Huot 2 , S. Déglise 3 , C. Haller 4 , L. Mazzolai 5 , F. Saucy 1 , F. Bosman 6 , J. Corpataux 7<br />

1 Service De Chirurgie Thoracique et Vasculaire, Centre Hospitalier Universitaire Vaudois, 1011<br />

Lausanne/CH, 2 Bioengineering, MachineVision, 1011 Lausanne/CH, 3 1012 Lausanne/CH,<br />

4 Thoracic and Vascular Surgery, CHUV, 1011 Lausanne/CH, 5 Service D'angiologie, Centre Hospitalier<br />

Universitaire Vaudois, 1011 Lausanne/CH, 6 Institut De Pathologie, Centre Hospitalier<br />

Universitaire Vaudois, 1011 Lausanne/CH, 7 Vascular and Thoracic Surgery, CHUV, 1011<br />

Lausanne/CH<br />

Comparative assessment of continuous and pulsatile ex-vivo perfusion of human saphenous<br />

vein after 14 days<br />

Objective: Vessel wall trauma induces vascular remodeling, as intimal hyperplasia (IH) and<br />

subse-quent thrombotic occlusions, compromising vascular reconstructions. Plasminogen<br />

activator system might precociously induce a prothrombotic state in the vein graft associated<br />

with stenosis development. Ex-vivo perfusion of human vessel segments is a well-suited setting<br />

to assess venous segments regarding vessel wall remodeling and fibrinolytic alterations.<br />

Methods: The ex-vivo vein support system (EVVSS) consists of an incubator containing a perfusion<br />

chamber and a gearing pump. This setting allows to perfuse vessel segments with a<br />

continous flow un<strong>der</strong> low shear stress conditions. This perfusion system modified to produce<br />

pulsatile flow by an arbitrary waveform generator controlled by computer is un<strong>der</strong> high shear<br />

stress conditions. Both systems maintain a constant perfusate temperature (37°C±0.l°C),<br />

pCO2 (35-45mmHg), pO2 (90-110mmHg) and pH (7.41±0.05). Human saphenous vein<br />

segments are perfused in both settings un<strong>der</strong> constant conditions (pressure, flow, shear<br />

stress) during 14 days. We performed computer-assisted histomorphometry, immunohistochemistry<br />

(CD 31, CD 34, Factor VIII, MIB 1, alpha-actin) and expression of fibrinolytic factor<br />

(t-PA, u-PA and PAI-l by Northern blot) before and after perfusion on each segment.<br />

Results: Nine human saphenous vein segments were perfused for 14 days, with respect of<br />

their morphological integrity. Histomorphometry revealed significant IH development in the<br />

continuous perfusion system after 14 days. No IH development was observed in the pulsatile<br />

system. Expression of CD31, CD34 and alpha actin was demonstrated in all segments after<br />

culture and perfusion indicating muscular and endothelial integrity in both groups. We observed<br />

an upregulation of PAI-1 in both settings after 14 days.<br />

Conclusion: Vessel wall integrity is maintained in the ex-vivo continuous and pulsatile flow<br />

perfusion. The continuous flow is a valid setting for the assessment of IH un<strong>der</strong> standardized<br />

conditions. The pulsatile flow conditions inhibits IH development un<strong>der</strong> high shear stress conditions.<br />

30.05<br />

A. Assadian, C. Senekowitsch, G.W. Hagmüller<br />

I. Chirurgie, Wilhelminenspital Vienna, A-1160 Vienna/AT<br />

Prevalence of patients continuing to smoke after vascular interventions<br />

Objective: Smoking is one of the most important risk factors for the development and progression<br />

of atherosclerosis. Smoking cessation presents an obligatory element in the manage-<br />

ment of vascular patients and also in patients scheduled for vascular interventions. The aim<br />

of this study was to assess the prevalence of patients smoking before and after vascular surgical<br />

procedures and to evaluate the requirements for inpatient smoking cessation programs<br />

and nicotine replacement therapy.<br />

Methods: 500 patients admitted for vascular interventions were included in this prospective<br />

study. Smoking status was evaluated as well as measurements of exhaled breath CO;<br />

patients had to answer a standardized Fagerström questionnaire on admission and after surgery<br />

to identify current smokers and to quantify nicotine dependency, respectively.<br />

Results: of 500 patients included, only 70 (14%) never had smoked, 243 (49 %) had quit<br />

smoking before admission and 161 (32%) were current smokers. of the current smokers 64<br />

(40%) did not smoke during hospitalization. 97 (60%) current smokers continued to smoke<br />

in hospital. of these patients, 78 patients (80%) were male and 19 female; the mean age was<br />

61 ± 4 years (range 40 84 years). 4 patients had surgery of infra-renal aortic aneurysm, 40<br />

patients had carotid endarterectomy and 53 patients had PAD. There was no difference between<br />

abstinent patients and continuing smokers concerning previous cigarette consumption<br />

or Fagerström score, a predictor for long term smoking behavior. Patients with carotid artery<br />

stenosis were significantly more abstinent while hospitalized (P=0.006). Patients with PAD,<br />

however, were more likely to continue smoking as inpatients (P=0.004). 65% of continuing<br />

smokers stated that they would stop smoking in hospital if counseling and nicotine replacement<br />

therapy would be provided. Regarding their predominant location of atherosclerosis,<br />

patients with PAD were less willing to quit smoking while hospitalized compared to patients<br />

with carotid stenosis (53% vs 88%, respectively; P < 0.001).<br />

Conclusion: A substantial fraction of patients admitted for vascular surgery are smokers.<br />

More than half of these continue to smoke in the hospital, an environment where smoking is<br />

prohibited by law. Counseling, nicotine replacement therapy as well as smoking cessation<br />

programs for vascular surgical inpatients is urgently needed.<br />

30.06<br />

S. Déglise 1 , C. Haller 2 , H. Probst 3 , S.D. Qanadli 4 , J. Corpataux 3<br />

1 1012 Lausanne/CH, 2 Thoracic and Vascular Surgery, CHUV, 1011 Lausanne/CH, 3 Vascular<br />

and Thoracic Surgery, CHUV, 1011 Lausanne/CH, 4 Radiology, CHUV, 1011 Lausanne/CH<br />

Is the use of the great saphenous vein a suitable alternative for arteriovenous fistulas creation<br />

in the upper limb?<br />

Objective: Failure or non-maturation of arteriovenous fistulas for haemodialysis access<br />

remains relatively frequent although preoperative assessment of forearm superficial venous<br />

system has been developped. Moreover, increasing the prevalence of arteriovenous fistula<br />

over synthetic graft is critical for decreasing the morbidity of these patients. Therfeore, the<br />

great saphenous vein could be an alternative when no suitable veins exist on the arm.<br />

Methods: Between August 2000 and September 2003, 12 patients un<strong>der</strong>went arteriovenous<br />

fistulas creation on the forearm for haemodialysis access. They were 10 men and 2 women<br />

with a mean age of 58 years (range 35-80). In all these patients but 2, one or more arteriovenous<br />

fistula had been previously created and failed. Data were reviewed to analyze the evolution<br />

of these fistulas in terms of blood flow, stenosis or patency rates.<br />

Results: The technical success was 92% (11/12) because in one patient, the fistula was<br />

rapidly oc-cluded leading to the use of a dialysis catheter. The mean blood flow measured in<br />

the 11 matured fistulas was 836 ml/min. In 5 patients, 12 stenoses occurred during the follow-up,<br />

the first stenosis appearing on average after 10 months. Seven (58%) of them were<br />

succesfully treated by angioplasty. Two surgical revisions were also necessary and in the 3<br />

remaining cases, a new prostethic fistula was created. Moreover, 2 occluded fistulas were<br />

successfully treated by surgical thrombectomy and one dilated fistula justifyied its surgical replacement.<br />

One patient with an occluded fistula died due to gastrointestinal sepsis. Overall<br />

primary, assisted primary and secondary patency rates were 33%, 42% and 50% respectively.<br />

Conclusion: The use of a saphenous vein for arteriovenous fistulas creation on the forearm<br />

seems to show low patency rates and high frequency of complications especially stenosis.<br />

Therefore, this procedure should be kept in reserve only for very specific conditions as presence<br />

of infection.<br />

30.07<br />

H.O. Savolainen 1 , J. Schmidli 2 , F. Dick 3 , I. Bau mgartner 2 , M. Mohaupt 4<br />

1 Vascular Surgery, Swiss Cardiovascular Center, 3010 Bern/CH, 2 Swiss Cardiovascular<br />

Centre, Uni-versity Hospital, Bern/CH, 3 Swiss Cardiovascular Centre, University Hospital, 3010<br />

Bern/CH, 4 Departement of Nephrology, University Hospital, Bern/CH<br />

Determinants of hemodialysis access survival<br />

Objective: Vascular access patency is vital for patients requiring hemodialysis. Various factors<br />

interfere with access patency. This analysis is projected to validate potential risk factors<br />

and benefits including unintended impact of co-medication.<br />

Methods: Hemodialysis access procedures between January 1999 and December 2001<br />

were retro-spectively analysed. Clinical data and concomitant medication were retrieved from<br />

files as were surgical data following a standardized data capture sheet. Minimal required follow-up<br />

with functioning access was 2 years.<br />

Results: During the observation period, 244 vascular accesses were created (60.7% male<br />

patients, 36.1% pre-emptive) with 102 remaining primarily patent. Censored (death, transplantation,<br />

access termination) primary (PP) and secondary patency (SP) was 5<strong>4.</strong>6% and<br />

71.7%, respectively, at 540 days. Patency of permanent cuffed catheters was lowest due to<br />

censoring events. Diabetes mellitus reduced PP (p

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