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  • Ju, Shuai  (2)
  • Luo, Jianjun  (2)
  • 2020-2024  (2)
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  • 2020-2024  (2)
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  • 1
    In: Acta Radiologica, SAGE Publications, Vol. 64, No. 2 ( 2023-02), p. 868-873
    Kurzfassung: Portal vein puncture (PVP) is a critical step during transjugular intrahepatic portosystemic shunt (TIPS) and correlates to several complications. Techniques guiding PVP are needed. Purpose To evaluate the safety, feasibility, and efficiency of digital subtraction angiography (DSA) overlay reference during TIPS creation and compare it with transhepatic portal vein (THPV) guiding. Material and Methods The clinical records of 185 patients at three medical centers who underwent TIPS placement were reviewed. Portal vein access was guided by THPV guiding in 120 cases and DSA overlay reference in 60 cases. The number of punctures, portal vein entry time, procedural adverse events, technical and hemodynamic success rate were analyzed to compare the safety, feasibility, and efficiency of the two methods. Results The median numbers of punctures in group 1 and group 2 were 2 (1–4) and 2 (1–5), respectively ( P = 0.094). There was no statistical difference between two groups in needle passes. The median portal vein entry time of group 1 was 12 min (8–16 min) and 13 min (8–16 min) in group 2. No significant difference was found in the PVP time ( P = 0.802). Arterioportal fistula formation occurred in 15 patients in group 1; two patients in group 2 had hepatic artery injury. The patients in group 2 had lower rates of procedural adverse events ( P = 0.047). Median dose area product of G1 was lower than G2 statistically ( P 〈 0.001). There was no significant difference in total fluoroscopy time ( P = 0.856). Conclusion DSA overlay reference has lower procedural adverse events rates compared with THPV guiding TIPS. It seems to be a safe and effective method for guiding PVP.
    Materialart: Online-Ressource
    ISSN: 0284-1851 , 1600-0455
    RVK:
    Sprache: Englisch
    Verlag: SAGE Publications
    Publikationsdatum: 2023
    ZDB Id: 2024579-8
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2021
    In:  European Journal of Gastroenterology & Hepatology Vol. 33, No. 8 ( 2021-08), p. 1110-1116
    In: European Journal of Gastroenterology & Hepatology, Ovid Technologies (Wolters Kluwer Health), Vol. 33, No. 8 ( 2021-08), p. 1110-1116
    Kurzfassung: Hepatic encephalopathy after transjugular intrahepatic portosystemic shunt (TIPS) remains an unsolved problem; therefore, this study aimed to compare the efficacy of shunting different portal vein branch during TIPS with 8 mm covered stent for preventing gastroesophageal variceal rebleeding in cirrhotic patients. Methods Between November 2015 and December 2018, the medical records of consecutive cirrhotic patients who received TIPS with an 8 mm covered stent for preventing gastroesophageal variceal rebleeding were analyzed retrospectively. Shunting the left and right branches of the portal vein was performed in 58 (group A) and 104 patients (group B), respectively. Afterwards, 54 patients in each group were produced by the PSM method. The incidence of overt hepatic encephalopathy (OHE), shunt patency, variceal rebleeding and survival were compared between two groups by using Kaplan–Meier analysis and log-rank test. Results The median follow-up time was 37 months (range 0.3–50 months). The 6-,12- and 24-months cumulative OHE free rates in groups A and B were 92.5, 86.2, 83.6% and 74.1, 70.2, 67.6%, respectively ( P  = 0.042; hazard ratio = 0.469; 95% CI, 0.223–0.988). Two (3.7%) and eight (14.8%) patients experienced severe OHE in groups A and B, respectively ( P  = 0.042). There were no significant differences between the two groups in terms of shunt patency, variceal rebleeding and survival. Conclusion Shunting the left portal vein branch during TIPS with an 8 mm covered stent for preventing gastroesophageal variceal rebleeding in cirrhotic patients might decrease the occurrence of OHE significantly. The prospective trial is needed to further provide evidence of this results in future.
    Materialart: Online-Ressource
    ISSN: 0954-691X
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2021
    ZDB Id: 2030291-5
    Standort Signatur Einschränkungen Verfügbarkeit
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