Angioseal VIP® vs. StarClose SE® closure devices: a comparative analysis in non-cardiological procedures

التفاصيل البيبلوغرافية
العنوان: Angioseal VIP® vs. StarClose SE® closure devices: a comparative analysis in non-cardiological procedures
المؤلفون: Carlo Cirelli, Mario Corona, Fabrizio Fanelli, Alessandro Cannavale, Alessandro d’Adamo, Filippo Maria Salvatori, Pierleone Lucatelli, Carlo Catalano
المصدر: The Journal of cardiovascular surgery. 58(1)
سنة النشر: 2013
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Time Factors, medicine.medical_treatment, Hemorrhage, Femoral artery, Punctures, 030204 cardiovascular system & hematology, 03 medical and health sciences, Pseudoaneurysm, Young Adult, 0302 clinical medicine, Hematoma, Recurrence, Risk Factors, Angioplasty, medicine.artery, medicine, Deep Femoral Artery, Humans, Vascular closure device, Embolization, Aged, Retrospective Studies, Aged, 80 and over, business.industry, Hemostatic Techniques, Endovascular Procedures, General Medicine, Equipment Design, Middle Aged, medicine.disease, Surgery, Femoral Artery, Treatment Outcome, Hemostasis, 030211 gastroenterology & hepatology, Equipment Failure, Female, Cardiology and Cardiovascular Medicine, business, Vascular Closure Devices
الوصف: Background The aim of this paper was to compare the use of two different commercially available vascular closure devices (VCD), Angioseal VIP® (St. Jude Medical, St. Paul, MN, USA) and StarClose SE (Abbott Laboratories, Abbott Park, IL, USA). Methods From January 2010 to January 2012, 347 patient underwent retrograde femoral arterial puncture for different interventional procedures (angioplasty, stenting, embolization for bleeding, fibrinolysis for ischemia and chemoembolization). Hemostasis was achieved by deployment of an Angioseal VIP® (N.=184) or StarClose SE® (N.=163). In 94 cases, the retrograde femoral access was bilateral and managed with two StarClose SE devices (N.=53) or an Angioseal VIP® plus a StarClose SE® (N.=41). Results Technical success was obtained in 95.1% (330/347) of patients. Overall time to hemostasis (TTH) and time to ambulation (TTA) were 5,5±1,5 min (range 3-8 min) and 6±2.5 hr (range 2-9 hours) respectively. No statistical significative difference (P>0.05) were appreciable between to groups for both TTH and TTA: Angioseal VIP® TTH was 5.3±1.4 min and StarClose SE® TTH was 5.6±1.6 min; Angioseal VIP® TTA was 5.9±1.8 hr and StarClose SE® TTA was 6.1±1.9 hr. VAS scores result underline a mild difference between two devices. Angioseal VIP® patients experience a mild to moderate pain within the first 3 minutes from the deployment. Whereas StarClose SE® patients still experience pain at 5 minutes from deployment. The device failure rate was 4.9% (17 cases) and included 13 minor complications and 4 major complications. Minor complications (3.75%) occurred during the initial phase and consisted in recurrent wound bleeding (N.=5 StarClose SE®; N.=4 Angioseal VIP®) treated with manual compression, and hematoma (N.=2 StarClose SE®; N.=2 Angioseal VIP®) that solved spontaneously. The 4 major complications (1,15%) were: 1 Angioseal-related common femoral artery (CFA) obstruction treated with surgical bypass from the CFA to the superficial femoral artery; 1 Angioseal-related CFA dissection solved with surgery; 1 Angioseal-related embolization of the deep femoral artery partially treated with localized fibrinolysis; 1 StarClose-related pseudoaneurysm treated with manual compression. Conclusions Both Angioseal VIP® and StarClose SE® systems can be considered safe and effective in providing hemostasis following a variety of interventional vascular procedures.
تدمد: 1827-191X
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f23854b2cb95c68fe9bf100590c5162fTest
https://pubmed.ncbi.nlm.nih.gov/24309473Test
رقم الانضمام: edsair.doi.dedup.....f23854b2cb95c68fe9bf100590c5162f
قاعدة البيانات: OpenAIRE