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1.
Endoscopy ; 44(5): 536-8, 2012 May.
Article in English | MEDLINE | ID: mdl-22370701

ABSTRACT

In the present study we prospectively evaluated the safety and efficacy of temporary fully covered, self-expandable metal stents (fcSEMS) to treat biliary strictures (n = 9), leaks (n = 9), and combined lesions (n = 1) occurring after liver transplantation, when standard endoscopic attempts had failed. Placement of fcSEMS and their removal in scheduled patients were successful and without complications. Resolution of the biliary lesion was confirmed in 15 of 19 patients (79 %). Treatment was not successful in two patients and not evaluable in 2 other patients. Complications occurred in 9 /19 patients (47 %): stent migration in 6, stent occlusion in 1, and de novo stricture after successful treatment of a biliary leak in 2. After a median follow-up of 12 months, one recurrent anastomotic stricture was noted. Temporary placement of fcSEMS in biliary strictures and leaks after liver transplantation provides satisfactory results even in patients who have undergone multiple previous conventional endoscopic attempts, and offers an alternative approach to surgical intervention.


Subject(s)
Cholestasis/surgery , Liver Transplantation/adverse effects , Sphincterotomy, Endoscopic , Stents , Adult , Aged , Anastomosis, Surgical/adverse effects , Cholestasis/etiology , Cholestasis/therapy , Coated Materials, Biocompatible , Device Removal , Female , Humans , Male , Metals , Middle Aged , Treatment Failure
2.
Transplant Proc ; 42(7): 2634-41, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20832559

ABSTRACT

BACKGROUND: Cytomegalovirus (CMV) infection and related disease is a feared complication after liver transplantation. Antiviral prophylaxis is recommended in clinical practice guidelines depending on the CMV status of both donor and recipient as well as the individual risk profile. METHODS: We retrospectively analyzed 211 liver transplant recipients with respect to the incidence of CMV infection after transplantation, the influence of donor and recipient CMV status, and the effect of antiviral prophylaxis. In addition, the underlying liver disease and immunosuppressive regimen were compared with the incidence of CMV infection. Patients were divided into 4 groups according to CMV donor/recipient (D/R) profile: group A (D-/R-) 28 patients (13.3%), group B (D-/R+) 64 patients (30.3%), group C (D+/R+) 79 patients (37.4%), and group D (D+/R-) 40 patients (19.0%). RESULTS: CMV infection was observed in 17.9%, 29.7%, 24.1%, and 22.5% of the patients, respectively, with no significant difference in infection rates between the groups. CMV infection occurred in 5 patients (17.9%) in the presumed low-risk profile (group A), despite an antiviral prophylaxis in 4 out of these 5 patients. In contrast, CMV infection occurred in only 9/40 patients (22.5%) in the presumed high-risk profile (group D). The most frequent infection rates were found in groups B and C (R+ groups). After successful treatment of CMV infection, no recurrence was detected. Underlying liver disease or immunosuppressive protocol had no influence on CMV infection. CONCLUSION: Approximately one fourth of patients will acquire CMV infection after liver transplantation independent of donor/recipient status. Surprisingly, antiviral prophylaxis does not seem to be sufficient to reduce this proportion of patients, either in presumed high-risk or in presumed low-risk situations.


Subject(s)
Antiviral Agents/therapeutic use , Cytomegalovirus Infections/epidemiology , Cytomegalovirus Infections/prevention & control , Liver Transplantation/adverse effects , Adult , Antigens, Viral/analysis , Cytomegalovirus/genetics , Cytomegalovirus Infections/drug therapy , DNA, Viral/genetics , DNA, Viral/isolation & purification , Drug Therapy, Combination , Female , Gene Amplification , Humans , Immunosuppressive Agents/therapeutic use , Incidence , Liver Diseases/classification , Liver Diseases/surgery , Male , Middle Aged , Phosphoproteins/analysis , Polymerase Chain Reaction/methods , Risk Assessment , Tissue Donors , Viral Matrix Proteins/analysis
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