Autores: Torres Machorro Adriana, Guerrero Hernández Manuel, Anaya Ayala Javier E, Torre Delgadillo Aldo, Laparra Escareño Hugo, Cuen Ojeda Cesar, Garcia Alva Ramón, Hinojosa Becerril Carlos Arturo
Introduction. Endovascular therapy represents a less invasive alternative to open surgery for reconstruction of the portal vein (PV) and the spleno-mesenteric venous confluence to treat Portal hypertension. The objective of this study is to determine if the Model for End-Stage Liver Disease (MELD) score is a useful method to evaluate the risk of morbidity and mortality during endovascular approaches. Material and methods. Patients that underwent endovascular reconstruction of the PV or spleno-mesenteric confluence were identified retrospectively. Data were collected from November 2011 to August 2016. The MELD score was calculated using international normalized ratio, serum billirubin and creatinine. Patients were grouped into moderate (<15) and high (> 15) MELD. Associations of the MELD score on the postprocedural morbidity, mortality and vessels patency were assessed by two-sided Fisher's exact test. Results. Seventeen patients were identified; MELD score distribution was: < 15 in 10 patients (59%) and > 15 in 7 (41%). Even distribution of severe PV thrombosis was treated in both groups, performing predominately jugular access in the high MELD score group (OR 0.10; 95%; CI 0.014-0.89; p = 0.052) in contrast to a percutaneous transhepatic access in the moderate MELD score group. Analysis comparing moderate and high MELD scores was not able to demonstrate differences in mortality, morbidity or patency rates. Conclusion. MELD score did not prove to be a useful method to evaluate risk of morbidity and mortality; however a high score should not contraindicate endovascular approaches. In our experience a high technical success, good patency rates and low complication rates were observed.
Palabras clave: Portal vein thrombosis portal hypertension endovascular treatment.
2017-12-13 | 458 visitas | Evalua este artículo 0 valoraciones
Vol. 16 Núm.6. Noviembre-Diciembre 2017 Pags. 950-958 Ann Hepatol 2017; 16(6)