Literature DB >> 22793063

Adverse events in clinical islet transplantation: one institutional experience.

Morihito Takita1, Shinichi Matsumoto, Hirofumi Noguchi, Masayuki Shimoda, Tetsuya Ikemoto, Daisuke Chujo, Yoshiko Tamura, Greg S Olsen, Bashoo Naziruddin, Kerri Purcell, Nicholas Onaca, Marlon F Levy.   

Abstract

Islet transplantation is one of the most promising treatments for an unstable form of type 1 diabetes. However, islet transplantation still has some obstacles, such as low success rate of islet isolation, difficulty to obtain long-term insulin freedom, and adverse events related to transplant protocol. We describe the adverse events of current clinical islet transplantation at our institute in this report. Nine type 1 diabetic patients received 17 islet infusions from March 2005 to October 2008. The islet infusion procedure and immunosuppression regimen were based on a modified Edmonton protocol. Severe adverse events (SAEs) were defined as events that were more than grade 3 according to the Terminology Criteria for Adverse Events in Trials of Adult Pancreatic Islet Transplantation, version 4.1 (Collaborative Islet Transplant Registry, CITR). Sixteen events were reported as SAEs and among them 12 events were probably or definitely related to transplant protocols; all occurred within 1 year after infusion except for one. Five adverse events (31%) occurred within 10 days after transplantation and were related to infusion procedures. Seven events (44%) occurred after 50 days and were related to immunosuppressive therapy. SAEs related to the protocol included three events of elevated liver enzymes, two of hemorrhage into gall bladder or peritoneal cavity, two of neutropenia, two of infection, one of vomiting, one of diarrhea, and one of renal dysfunction. All events were grade 3, except for one case that was grade 4 of neutropenia. All SAEs resolved with no sequelae. Neoplasms and deaths were not observed in our study. The present study suggests need to improve both infusion procedure and immunosuppressive strategy from the view of preventing SAEs.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22793063     DOI: 10.3727/096368911X605466

Source DB:  PubMed          Journal:  Cell Transplant        ISSN: 0963-6897            Impact factor:   4.064


  5 in total

1.  One hundred human pancreatic islet isolations at Baylor Research Institute.

Authors:  Morihito Takita; Shinichi Matsumoto; Hirofumi Noguchi; Masayuki Shimoda; Daisuke Chujo; Koji Sugimoto; Takeshi Itoh; Jeffrey P Lamont; Luis F Lara; Nicholas Onaca; Bashoo Naziruddin; Goran B Klintmalm; Marlon F Levy
Journal:  Proc (Bayl Univ Med Cent)       Date:  2010-10

2.  Effect of a new drug releasing system on microencapsulated islet transplantation.

Authors:  Binjie Lu; Qingkun Gao; Rui Liu; Ming Ren; Yan Wu; Zaixing Jiang; Yi Zhou
Journal:  Int J Clin Exp Pathol       Date:  2015-10-01

Review 3.  Pancreas Islet Transplantation for Patients With Type 1 Diabetes Mellitus: A Clinical Evidence Review.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2015-09-01

4.  Clinical allogeneic and autologous islet cell transplantation: update.

Authors:  Shinichi Matsumoto
Journal:  Diabetes Metab J       Date:  2011-06-30       Impact factor: 5.376

5.  Long-term outcome of islet transplantation on insulin-dependent diabetes mellitus: An observational cohort study.

Authors:  Toshihiro Nakamura; Junji Fujikura; Takayuki Anazawa; Ryo Ito; Masahito Ogura; Hideaki Okajima; Shinji Uemoto; Nobuya Inagaki
Journal:  J Diabetes Investig       Date:  2019-09-17       Impact factor: 4.232

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.