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1.
Ann Hepatol ; 21: 100161, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-31836423

RESUMEN

In laparoscopic cholecystectomy (LC), the treatment of iatrogenic biliary tract injury has been given much attention. However, most accidental right hepatic artery (RHA) injuries are treated with simple clipping. The reason is that the RHA has difficulty in revascularization, and it is generally considered that RHA injury does not cause serious consequences. However, some studies suggest that some cases of RHA ligation can cause a series of pathological changes correlated to arterial ischemia, such as liver abscess, bile tumor, liver atrophy and anastomotic stenosis. Theoretically, RHA blood flow should be restored when possible, in order to avoid the complications of right hepatic ischemia. The present study involved two patients, including one male and one female patient. Both patients were admitted to the hospital with the diagnosis of chronic cholecystitis and gallbladder stone, and developed ischemia of the right half hepatic after accidental transection of the RHA. Both patients underwent continuous end-end anastomosis of the RHA with 6-0 Prolene suture. After the blood vessel anastomosis, the right half liver quickly recovered to its original bright red. No adverse complications were observed in follow-ups at three and six months after the operation. Laparoscopic repair of the RHA is technically feasible. Reconstruction of the RHA can prevent complications associated with right hepatic ischemia.


Asunto(s)
Colecistectomía/efectos adversos , Cálculos Biliares/cirugía , Arteria Hepática/lesiones , Complicaciones Intraoperatorias/cirugía , Laparoscopía/métodos , Procedimientos Quirúrgicos Vasculares/métodos , Lesiones del Sistema Vascular/etiología , Femenino , Arteria Hepática/cirugía , Humanos , Masculino , Persona de Mediana Edad , Lesiones del Sistema Vascular/diagnóstico , Lesiones del Sistema Vascular/cirugía
2.
Ann Clin Lab Sci ; 43(1): 64-9, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23462607

RESUMEN

PURPOSE: To evaluate the effects of different-time ischemic preconditioning (IPC) schemes on the ischemia-reperfusion (I/R) injury in moderate to severe hepatocirrhosis in rats and to identify the optimal time window of IPC. METHODS: A total of 90 male SD rats with moderate to severe hepatocirrhosis were randomly divided into 5 groups (IR group, 5-10 min-IPC group, 8-10 min-IPC group, 10-10 min-IPC group and 15-10 min-IPC group), in which the liver was preconditioned by IPC of various durations, and then subjected to I/R injury in the last four groups. Thirty-six normal (non-cirrhotic) SD rats were divided into 2 groups (IR group and 10-10 min-IPC group). Ischemia-reperfusion injury was induced by clamping of the portal triad for 30 min followed by reperfusion for 30 min. Hepatocellular viability was assessed by measuring the concentration of ALT and AST in serum. The concentration of NO in serum and those of MDA, MPO, and SOD in the liver tissue were also assessed at 1h, 4h, and 24h after the operation respectively. RESULTS: After 30-30min of I/R, the levels of ALT and AST were significantly elevated in the IR group and the groups under IPC, but the elevations were significantly lower in the 5-10 min-IPC group and the 8-10 min-IPC group, especially at 4h after I/R (P<0.05). The levels of MDA and MPO in liver tissue were lower in the 5-10 min-IPC and 8-10min-IPC groups than in the rest of the IPC groups and IR group in the cirrhotic rats, and the level of SOD was higher (P <0.05). The level of serum NO was significantly higher in the 5-10 min-IPC and 8-10min-IPC groups than in the rest of the cirrhotic groups (P <0.05). CONCLUSIONS: The 5-10 min through 8-10 min-IPC achieves the highest protective effect on the I/R injury of moderate to severe hepatocirrhosis. With the aggravation of liver cirrhosis, the pre-implementation time has been shortened. Thus, IPC of 5-10min may be effective for severe liver cirrhosis.


Asunto(s)
Precondicionamiento Isquémico , Cirrosis Hepática/complicaciones , Cirrosis Hepática/patología , Daño por Reperfusión/complicaciones , Daño por Reperfusión/patología , Alanina Transaminasa/sangre , Animales , Aspartato Aminotransferasas/sangre , Hígado/enzimología , Hígado/patología , Cirrosis Hepática/sangre , Cirrosis Hepática/enzimología , Masculino , Malondialdehído/metabolismo , Óxido Nítrico/sangre , Peroxidasa/metabolismo , Ratas , Ratas Sprague-Dawley , Daño por Reperfusión/sangre , Daño por Reperfusión/enzimología , Superóxido Dismutasa/metabolismo , Factores de Tiempo
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