Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/75951
DC FieldValueLanguage
dc.contributor.authorRabellino, Martinen_US
dc.contributor.authorZander, Tobiasen_US
dc.contributor.authorBaldi, Sebastianen_US
dc.contributor.authorNielsen, Luis Garciaen_US
dc.contributor.authorAragon-Sanchez, F. Javieren_US
dc.contributor.authorZerolo, Ignacioen_US
dc.contributor.authorLlorens, Rafaelen_US
dc.contributor.authorMaynar Moliner, Manuelen_US
dc.date.accessioned2020-11-25T11:21:38Z-
dc.date.available2020-11-25T11:21:38Z-
dc.date.issued2009en_US
dc.identifier.issn1522-1946en_US
dc.identifier.otherWoS-
dc.identifier.urihttp://hdl.handle.net/10553/75951-
dc.description.abstractObjective: To demonstrate the technical success and clinical follow-up after endovascular treatment of femoropopliteal segment TASC II C and D lesions. Methods: From July 2002 to February 2007, 234 limbs in 190 patients with femoropopliteal segment TASC II C (n = 112) and D (n = 122) lesions were treated. Endovascular treatment consisted of PTA, fibrinolysis and PTA, subintimal recanalization and PTA, and finally stent graft. Patients were clinically evaluated at 30 days, 3, 6 month, and at 1 year in the outpatient setting with clinical examination and ankle-brachial indices (ABI). In the case of stent placement, additional ultrasound evaluation was performed at 12, 24, and 48 month. Results: 49.5% of procedures were performed on patients with lifestyle-limiting claudication (IC) and 50.5% were performed for critical limb ischemia (CLI). Technical success, defined as successful recanalization and treatment of the occluded vessel, was achieved in 97% of cases. Periprocedural mortality was 3.15% and all deaths occurred in the CLI group. A follow-up 13 +/- 6 months and was achieved in 76%. During the follow-up, clinical outcome for IC group and clinical CLI group was asymptomatic 72% vs. 29.8%, symptomatic with clinical improvement 22% vs. 33.7%, and major amputation 3% vs. 23.3%. Conclusion: The majority of claudicating patients with femoropopliteal TASC II C and D lesions will benefit from the endovascular treatment. Patient presenting CLI have a worse outcome, nevertheless the endovascular treatment can delay amputation, preserving the native vessel and does not impede surgical bypass if needed. For this reason, we consider that endovascular treatment may be the first choice treatment even in femoropopliteal TASC II C and D lesions.en_US
dc.languageengen_US
dc.relation.ispartofCatheterization and Cardiovascular Interventionsen_US
dc.sourceCatheterization And Cardiovascular Interventions [ISSN 1522-1946], v. 73 (5), p. 701-705, (Abril 2009)en_US
dc.subject320501 Cardiologíaen_US
dc.subject.otherPeripheral Arterial-Diseaseen_US
dc.subject.otherSuperficial Femoral-Arteryen_US
dc.subject.otherOcclusive Diseaseen_US
dc.subject.otherNational-Healthen_US
dc.subject.otherStent-Graftsen_US
dc.subject.otherBypassen_US
dc.subject.otherPrevalenceen_US
dc.subject.otherVeinen_US
dc.subject.otherPolytetrafluoroethyleneen_US
dc.subject.otherAngioplastyen_US
dc.titleClinical follow-up in endovascular treatment for TASC C-D lesions in femoro-popliteal segmenten_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/ccd.21971en_US
dc.identifier.isi000264737000025-
dc.identifier.eissn1522-726X-
dc.description.lastpage705en_US
dc.identifier.issue5-
dc.description.firstpage701en_US
dc.relation.volume73en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid1236857-
dc.contributor.daisngid94228-
dc.contributor.daisngid1496829-
dc.contributor.daisngid5655425-
dc.contributor.daisngid693544-
dc.contributor.daisngid3875761-
dc.contributor.daisngid28135379-
dc.contributor.daisngid30319800-
dc.description.numberofpages5en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Rabellino, M-
dc.contributor.wosstandardWOS:Zander, T-
dc.contributor.wosstandardWOS:Baldi, S-
dc.contributor.wosstandardWOS:Nielsen, LG-
dc.contributor.wosstandardWOS:Aragon-Sanchez, FJ-
dc.contributor.wosstandardWOS:Zerolo, I-
dc.contributor.wosstandardWOS:Llorens, R-
dc.contributor.wosstandardWOS:Maynar, M-
dc.date.coverdateAbril 2009en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr2,363
dc.description.jcrqQ2
dc.description.scieSCIE
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptGIR IUIBS: Tecnología Médica y Audiovisual-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0001-6307-5040-
crisitem.author.orcid0000-0001-9154-0712-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameAragón Sanchez,Javier-
crisitem.author.fullNameMaynar Moliner,Manuel-
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