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Evaluation of Percutaneous Mechanical Thrombectomy via the AngioJet System Combined with Catheter-Directed Thrombolysis for the Treatment of Symptomatic Lower Extremity Deep Venous Thrombosis.
Yin, Shi-Wu; Guo, Li-Wen; Bian, Lu; Xiang, Ting-Miao; Pan, Sheng-Quan.
Afiliação
  • Yin SW; Department of Intervention and Vascular Surgery, The Second People's Hospital of Hefei, Anhui Hefei, China. Electronic address: 15256202893@163.com.
  • Guo LW; Department of Intervention Therapy, Zhejiang Cancer Hospital, Zhejiang Hangzhou, China.
  • Bian L; Department of Intervention and Vascular Surgery, The Second People's Hospital of Hefei, Anhui Hefei, China.
  • Xiang TM; Department of Intervention and Vascular Surgery, The Second People's Hospital of Hefei, Anhui Hefei, China.
  • Pan SQ; Department of Intervention and Vascular Surgery, The Second People's Hospital of Hefei, Anhui Hefei, China.
Ann Vasc Surg ; 65: 66-71, 2020 May.
Article em En | MEDLINE | ID: mdl-31751599
ABSTRACT

BACKGROUND:

Current methods of treating lower extremity deep venous thrombosis (LEDVT), such as catheter-directed thrombolysis (CDT) alone, or percutaneous mechanical thrombectomy (PMT) alone, are accompanied by unacceptably high risks of complications. This preliminary retrospective study evaluated the efficacy of CDT combined with PMT (via the AngioJet system), relative to CDT alone, in treating LEDVT.

METHODS:

Forty-two patients (43 limbs) with symptomatic deep venous thrombosis received either CDT alone (n = 12) or PMT combined with CDT (PMT + CDT) from May 2012 to December 2016. The groups were compared for clinical outcomes and demographics, LEDVT risk factors, and dosages of urokinase. Thrombus removal, by venographic evidence, was classified as grades I (<50%), II (50 to 99%), or III (>99%).

RESULTS:

In the CDT (PMT + CDT) cohorts, grades I, II, and III thrombus removal was achieved by 8% (3%), 17% (10%), and 75% (87%) of patients, respectively. The urokinase dosage and hospitalization required by the CDT group (5.29 ± 0.45 million IU, 20.4 ± 4.6 days) were significantly greater than those required by the PMT + CDT group (4.08 ± 1.15 million IU, 16.0 ± 6.0 days; P = 0.001, 0.039). The clinical outcomes of the 2 groups were similar.

CONCLUSION:

Combined PMT and CDT was effective and safe for LEDVT clinical therapy, and hospital stay, urokinase dosage, and complications were less compared with patients who received CDT only.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ativador de Plasminogênio Tipo Uroquinase / Terapia Trombolítica / Trombectomia / Trombose Venosa / Extremidade Inferior / Fibrinolíticos Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Vasc Surg Assunto da revista: ANGIOLOGIA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ativador de Plasminogênio Tipo Uroquinase / Terapia Trombolítica / Trombectomia / Trombose Venosa / Extremidade Inferior / Fibrinolíticos Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Vasc Surg Assunto da revista: ANGIOLOGIA Ano de publicação: 2020 Tipo de documento: Article