A population-based survey of the epidemiology of symptom-defined gastroesophageal reflux disease: the Systematic Investigation of Gastrointestinal Diseases in China |
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Authors: | Jia He Xiuqiang Ma Yanfang Zhao Rui Wang Xiaoyan Yan Hong Yan Ping Yin Xiaoping Kang Jiqian Fang Yuantao Hao Qiang Li John Dent Joseph JY Sung Duowu Zou Mari-Ann Wallander Saga Johansson Wenbin Liu Zhaoshen Li |
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Affiliation: | 1. Department of Gastroenterology and Hepatology, University Hospital of Geneva, Rue Gabrielle-Perret-Gentil 4, Geneva, 1211, Switzerland 2. Division of Clinical Pharmacology and Toxicology, University Hospital Zurich, Ramistrasse 100, 8091, Zurich, Switzerland 3. Red Cross Blood Transfusion Service of Southern Switzerland, Via Tesserete 50, 6900, Lugano, Switzerland 4. General Medicine Outpatient Clinic, University Hospital of Geneva, Rue Gabrielle-Perret-Gentil 4, Geneva, 1211, Switzerland 5. Blood Transfusion Service, University Hospital of Geneva, Rue Gabrielle-Perret-Gentil 4, Geneva, 1211, Switzerland 6. Hepatology Service, Clinica Luganese, Via Moncucco 10, 6903, Lugano, Switzerland 7. Transplantation Unit, Department of Visceral Surgery, University Hospital of Geneva, Rue Gabrielle-Perret-Gentil 4, Geneva, 1211, Switzerland
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Abstract: | ![]()
Background Hepatitis B immune globulins (HBIG) in combination with nucleos(t)ide analogues (NA) are effectively used for the prevention of hepatitis B virus (HBV) recurrence after liver transplantation (LT). However, associated treatment costs for HBIG are exceedingly high. Methods Fresh frozen plasma obtained from blood donors with high anti-HBs levels (hyperimmune plasma, HIP) containing at least 4,500 IU anti-HBs was used as alternative treatment for HBV recurrence prophylaxis post-LT. Results Twenty-one HBV-related LT recipients received HIP starting at transplantation, followed by long-term combination treatment with NA. Mean follow-up time was 4.5 years (range 0.5-12.6) and each patient received on average 8.2 HIP per year (range 5.8-11.4). Anti-HBs terminal elimination kinetic after HIP administration was 20.6 days (range 13.8-30.9), which is comparable to values reported for commercial HBIG products. All 21 patients remained free of HBV recurrence during follow-up and no transfusion-transmitted infection or other serious complication was observed. Seven patients developed reversible mild transfusion reactions. The cost for one HIP unit was US$140; average yearly HBIG treatment cost was US$1,148 per patient, as compared to US$25,000-100,000 for treatment with commercial HBIG. Conclusion The results of this study suggest that the use of HIP may be a useful and economical approach for the prevention of HBV recurrence post-LT if used in combination with NA. Additional prospective controlled studies in larger populations are needed to confirm these results. |
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