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1.
Transplant Proc ; 40(8): 2510-1, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18929782

ABSTRACT

BACKGROUND AND OBJECTIVE: The course of atrial septal defects (ASD) in children undergoing liver transplantation is poorly described. Our objective was to present our experience in living donor liver transplantation (LDLT) in children with type II ASD. PATIENTS AND METHODS: Between June 1994 and December 2006, 18/140 (12.8%) pediatric LDLT were diagnosed to have both type II ASD and end-stage liver disease. We reviewed the records of these patients. The median follow-up was 48.7 months. Data were analyzed using descriptive statistics. RESULTS: There were 8 male and 10 female patients whose overall mean age was 12 months. There were 15 biliary atresia and 3 neonatal hepatitis patients. The median Child score was 9. The mean Pediatric Model End-stage Liver Disease score was 14. There were 13 with small (< or =4 mm), 4 with medium (5 to 9 mm), and 1 large (>10 mm) ASD. Six small ASD closed spontaneously pretransplant. Seven small ASD closed posttransplant. The medium and large ASD persisted or increased in size posttransplant. Only one patient showed hemodynamically significant ASD based on cardiac echocardiography and catheterization. This patient underwent Amplatzer closure of the ASD at 10 months posttransplant. All patients are surviving with their original grafts to date. There were no perioperative cardiac or neurologic complications. CONCLUSION: This series demonstrated that LDLT can be safely performed in hemodynamically stable patients with small- to large-sized ASD. Small ASD may close pre- or posttransplant.


Subject(s)
Heart Septal Defects, Atrial/complications , Liver Failure/complications , Liver Failure/surgery , Liver Transplantation/physiology , Living Donors , Adolescent , Adult , Biliary Atresia/complications , Child , Female , Heart Septal Defects, Atrial/classification , Hemodynamics , Hepatitis/complications , Humans , Liver Transplantation/mortality , Male , Patient Selection , Retrospective Studies , Treatment Outcome
2.
Br J Anaesth ; 96(2): 262-5, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16361301

ABSTRACT

We report a case of a spinal-epidural haematoma occurring in a patient after a combined spinal-epidural anaesthetic. She had been taking clopidogrel and had received perioperative dalteparin for thromboprophylaxis. Despite adhering to standard guidelines concerning administration of low molecular weight heparin perioperatively and stopping the clopidogrel 7 days before the anaesthetic, the patient developed an epidural haematoma.


Subject(s)
Anesthesia, Epidural/adverse effects , Anesthesia, Spinal/adverse effects , Dalteparin/adverse effects , Hematoma, Epidural, Spinal/etiology , Ticlopidine/analogs & derivatives , Aged , Aged, 80 and over , Anticoagulants/adverse effects , Clopidogrel , Female , Hematoma, Epidural, Spinal/diagnosis , Humans , Magnetic Resonance Imaging , Platelet Aggregation Inhibitors/adverse effects , Ticlopidine/adverse effects
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