Guest guest Posted June 30, 2011 Report Share Posted June 30, 2011 http://www.transplantation-proceedings.org/article/PIIS0041134511003198/abstract\ ?rss=yes TRANSPLANTATION PROCEEDINGS Volume 43, Issue 5, Pages 1780-1782 (June 2011) Safety of Ultra-Rapid Intravenous Infusion of Hepatitis B Immunoglobulin in Liver Transplant Recipients S. Hwangab, Y.D. Yua, G.C. Parka, Y.I. Choia, P.J. Parka, S.W. Junga, J.M. Namgoonga, S.Y. Yoona, H.S. Hab, J.J. Hongb, I.O. Kimb, M.K. Jeonb, J.E. Mab, S.Y. Choia, J.S. Yuna, D.H. Junga, G.W. Songa, T.Y. Haa, D.B. Moona, K.H. Kimya, C.S. Ahna, S.G. Leeab Abstract Purpose To evaluate the safety of institutional protocol for ultra-rapid hepatitis B immunoglobulin (HBIG) infusion (10,000 IU in 30 minutes) for hepatitis B virus prophylaxis in adult liver transplant recipients. Methods In this case-controlled study, prospectively recruited liver transplant recipients received ultra-rapid infusions of HBIG (10,000 units in 30 minutes) for 6 months. The historical control group consisted of patients who had received 1-hour HBIG infusions (conventional rapid infusion) for the precedent 6 months. Results We found that 1472 patients had received 5744 ultra-rapid HBIG infusions, whereas 1343 patients had received 5200 conventional rapid HBIG infusions. Adverse side-effects were observed after 7 (0.13%) and 9 (0.16%) infusions, respectively (P = .763). The number of infusions per month increased significantly, from 878 ± 34 before the introduction of ultra-rapid infusion to 957 ± 29 afterwards (P < .001), an increase of 10.5%. The maximal capacity of HBIG infusions per day in the outpatient clinic increased from 53 for conventional rapid infusion to 65 for ultra-rapid infusion, without expansion of the outpatient facility or equipment. Conclusions Nearly all adult liver recipients able to tolerate 1-hour infusions of HBIG can also tolerate ultra-rapid infusions well. Thus, it seems to be reasonable to perform ultra-rapid infusion protocol widely for patient convenience. a Division of Hepatobiliary Surgery and Liver Transplantation, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea b Organ Transplantation Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea Address reprint requests Shin Hwang, MD, Division of Hepatobiliary Surgery and Liver Transplantation, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, 138-736, Korea PII: S0041-1345(11)00319-8 doi:10.1016/j.transproceed.2011.02.013 © 2011 Elsevier Inc. All rights reserved. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 30, 2011 Report Share Posted June 30, 2011 http://www.transplantation-proceedings.org/article/PIIS0041134511003198/abstract\ ?rss=yes TRANSPLANTATION PROCEEDINGS Volume 43, Issue 5, Pages 1780-1782 (June 2011) Safety of Ultra-Rapid Intravenous Infusion of Hepatitis B Immunoglobulin in Liver Transplant Recipients S. Hwangab, Y.D. Yua, G.C. Parka, Y.I. Choia, P.J. Parka, S.W. Junga, J.M. Namgoonga, S.Y. Yoona, H.S. Hab, J.J. Hongb, I.O. Kimb, M.K. Jeonb, J.E. Mab, S.Y. Choia, J.S. Yuna, D.H. Junga, G.W. Songa, T.Y. Haa, D.B. Moona, K.H. Kimya, C.S. Ahna, S.G. Leeab Abstract Purpose To evaluate the safety of institutional protocol for ultra-rapid hepatitis B immunoglobulin (HBIG) infusion (10,000 IU in 30 minutes) for hepatitis B virus prophylaxis in adult liver transplant recipients. Methods In this case-controlled study, prospectively recruited liver transplant recipients received ultra-rapid infusions of HBIG (10,000 units in 30 minutes) for 6 months. The historical control group consisted of patients who had received 1-hour HBIG infusions (conventional rapid infusion) for the precedent 6 months. Results We found that 1472 patients had received 5744 ultra-rapid HBIG infusions, whereas 1343 patients had received 5200 conventional rapid HBIG infusions. Adverse side-effects were observed after 7 (0.13%) and 9 (0.16%) infusions, respectively (P = .763). The number of infusions per month increased significantly, from 878 ± 34 before the introduction of ultra-rapid infusion to 957 ± 29 afterwards (P < .001), an increase of 10.5%. The maximal capacity of HBIG infusions per day in the outpatient clinic increased from 53 for conventional rapid infusion to 65 for ultra-rapid infusion, without expansion of the outpatient facility or equipment. Conclusions Nearly all adult liver recipients able to tolerate 1-hour infusions of HBIG can also tolerate ultra-rapid infusions well. Thus, it seems to be reasonable to perform ultra-rapid infusion protocol widely for patient convenience. a Division of Hepatobiliary Surgery and Liver Transplantation, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea b Organ Transplantation Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea Address reprint requests Shin Hwang, MD, Division of Hepatobiliary Surgery and Liver Transplantation, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, 138-736, Korea PII: S0041-1345(11)00319-8 doi:10.1016/j.transproceed.2011.02.013 © 2011 Elsevier Inc. All rights reserved. Quote Link to comment Share on other sites More sharing options...
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