Timely Topics in Transplantation Webinar Series
Speaker: Matt Cooper, MD • Medstar Georgetown Transplant Institute
Moderator: Harini Chakkera, MD • Mayo Clinic Hospital
After participating in this webinar, the learner will be able to:
- Define the components of a successful living donor kidney program to evaluate an efficient number of FTE’s and assistant personnel as well as developing and cultivating a culture within that personnel to best support living donors, their support staff, and their needs.
- Appraise the current resource allocation of their current living donor program and analyze where investments might be best undertaken to begin process improvements.
- Evaluate current living donor program metrics beyond number of potential donors and number of organs transplanted to work towards a more critical evaluation of measuring success in personnel activities as well as patient safety and program quality.
Free to AST members: $25 fee is waived upon logging in during the checkout process.
What You'll Learn:
- Identify risk factors for non-adherence and tools to measure non-adherence
- Evaluate the traditional methods used to improve/monitor medication adherence
- Review today's mobile adherence technologies for improving/monitoring medication adherence
- Summarize tomorrow's technologies for improving/monitoring medication adherence
What You'll Learn:
- Identify risk factors for non-adherence and tools to measure non-adherence
- Evaluate the traditional methods used to improve/monitor medication adherence
- Review today's mobile adherence technologies for improving/monitoring medication adherence
- Summarize tomorrow's technologies for improving/monitoring medication adherence
Kimberly Brown, MD • Henry Ford Hospital
Tiffany Kaiser, PharmD • University of Cincinnati
Moderated by Josh Levitsky, MD • Northwestern Memorial Hospital
Free to AST members: $25 fee is waived upon logging in during the checkout process.
This webinar is designed to focus on emerging therapies for HCV in transplant patients with specific attention to drug-drug interactions and limitations in patients with renal disease.
After participating in this webinar, the learner will be able to:
- Define current strategies for HCV treatment in the post transplant recipient
- Describe the limitations of current drug therapy in patients with renal disease
- Explain relevant drug-drug interactions of antiviral therapies with transplant medications
This webinar is designed to focus on emerging therapies for HCV in transplant patients with specific attention to drug-drug interactions and limitations in patients with renal disease.
Objectives:
- Define current strategies for HCV treatment in the post transplant recipient
- Describe the limitations of current drug therapy in patients with renal disease
- Explain relevant drug-drug interactions of antiviral therapies with transplant medications
Free to AST members: $25 fee is waived upon logging in during the checkout process.
Were you unable to attend the IPITA World Congress in September or need a review of talks you might have missed? If so, attend this webinar for a meeting review, and get caught up on all of the highlights you need to know!
Dr. Peter Stock, IPITA 2013 Congress Chair, will provide a meeting summary highlighting the marked improvements in rates of insulin independence following both pancreastic islet and whole organ pancreas transplants for diabetes mellitus, as well as novel strategies for increasing the source of beta cells (stem cells/xenotransplants) and blocking the immune response.
Were you unable to attend the IPITA World Congress in September or need a review of talks you might have missed? If so, attend this webinar for a meeting review, and get caught up on all of the highlights you need to know!
Dr. Peter Stock, IPITA 2013 Congress Chair, will provide a meeting summary highlighting the marked improvements in rates of insulin independence following both pancreastic islet and whole organ pancreas transplants for diabetes mellitus, as well as novel strategies for increasing the source of beta cells (stem cells/xenotransplants) and blocking the immune response.
Atul Humar, MD • University Health Network-University of Toronto
Camille Kotton, MD • Massachusetts General Hospital
Raymund Razonable, MD • Mayo Clinic
Moderated by Shirish Huprikar, MD • Icahn School of Medicine at Mount Sinai
Read the Q&A that wasn't answered during webinar
Free to AST members: $25 fee is waived upon logging in during the checkout process.
Dr. Kotton will describe the importance of prevention, and the various methods of preventing CMV, including; universal prophylaxis, preemptive therapy, and a hybrid approach, along with the merits and downfalls of each approach. Dr. Razonable will review the current recommendations for the treatment of cytomegalovirus infection and disease in transplant recipients, and discuss antiviral drugs in the pipeline that may be useful for the treatment of drug-resistant infections. Dr. Humar will explain how measurements of host immune response to CMV can be used to predict the risk of CMV reactivation in different settings, and how prevention and treatment strategies might be refined with the use of immune monitoring tools.
After participating in this webinar, the learner will be able to:
- Discuss the importance of CMV prevention, along with the various approaches used for optimal prevention
- Explain the standard treatment for CMV infection and disease in transplant recipients and discuss novel antiviral drugs
- Describe the potential for using immune monitoring tools to refine and improve prevention and treatment strategies
Dr. Kotton will describe the importance of prevention, and the various methods of preventing CMV, including; universal prophylaxis, preemptive therapy, and a hybrid approach, along with the merits and downfalls of each approach. Dr. Razonable will review the current recommendations for the treatment of cytomegalovirus infection and disease in transplant recipients, and discuss antiviral drugs in the pipeline that may be useful for the treatment of drug-resistant infections. Dr. Humar will explain how measurements of host immune response to CMV can be used to predict the risk of CMV reactivation in different settings, and how prevention and treatment strategies might be refined with the use of immune monitoring tools.
Objectives:
- Discuss the importance of CMV prevention, along with the various approaches used for optimal prevention
- Explain the standard treatment for CMV infection and disease in transplant recipients and discuss novel antiviral drugs
- Describe the potential for using immune monitoring tools to refine and improve prevention and treatment strategies
Free to AST members: $25 fee is waived upon logging in during the checkout process.
What You'll Learn:
- Appreciate highlights of updated ID COP Guidelines published in 2013
- Appraise novel additions to ID COP Guidelines published in 2013
- Review Updated International Consensus Guidelines on the Management of Cytomegalovirus in Solid-Organ Transplantation
Click here to download additional questions that were answered offline by Dr. Camille Kotton.
Peter Heeger, MD • Icahn School of Medicine at Mount Sinai
Moderated by Leonardo Riella, MD, PhD • Brigham and Women's Hospital
Free to AST members: $25 fee is waived upon logging in during the checkout process.
The goal of this webinar is to describe the available data on pre- and post-transplant immune monitoring and how incorporating specific tests may help us diagnose, predict, and better treat our transplant recipients.
After participating in this webinar, the learner will be able to:
- Summarize the current most promising and best tested urine and peripheral blood, molecular, and cellular assays available for risk assessment following transplantation
- Detail the utility, pitfalls and limitations of currently available assays
- Propose future directions and trial designs required to develop and validate immune monitoring tools for clinical use
The goal of this webinar is to describe the available data on pre- and post-transplant immune monitoring and how incorporating specific tests may help us diagnose, predict, and better treat our transplant recipients.
Objectives:
- Summarize the current most promising and best tested urine and peripheral blood, molecular, and cellular assays available for risk assessment following transplantation
- Detail the utility, pitfalls and limitations of currently available assays
- Propose future directions and trial designs required to develop and validate immune monitoring tools for clinical use
Free to AST members: $25 fee is waived upon logging in during the checkout process.
What You'll Learn:
- Summarize the major features of the 2013 Banff Conference on Allograft Pathology, held from August 19-23 in Comandatuba, Brazil
- Review the findings of the current Banff Working Groups that were presented at the conference
- Present the newly revised Banff Classification for antibody-mediated rejection in renal allografts, including the rationale for the revisions and the process involved in reaching a consensus on these
- Introduce the three new Banff Working Groups that have been formed as a result of presentations and discussions at the conference
Click here to download additional questions that were answered offline by Dr. Mark Haas.
Norah Terrault MD, MPH • University of California, San Francisco
Moderated by Robert Brown, MD, MPH • Columbia University Medical Center
Free to AST members: $25 fee is waived upon logging in during the checkout process.
The diagnosis of chronic hepatitis C has been considered a relative or absolute contraindication for non-liver transplantation in the past, due to concerns of liver disease progression post-transplantation and a lack of safe and effective therapies. The recent availability of interferon-free, all-oral, antiviral drug combinations to treat of chronic hepatitis C provides an opportunity to revise management algorithms to optimize the care of non-liver transplant candidates and recipients.
After participating in this webinar, the learner will be able to:
- Describe the components of the new HCV all-oral combinations, the role of ribavirin, and anticipated rates of HCV eradication with treatment
- Summarize the safety data of new HCV therapies as it pertains to non-liver transplant candidates and recipients, including key drug-drug interactions (HCV antivirals and immunosuppressive drugs)
- Evaluate the pros and cons of HCV treatment pre versus post-transplantation, including considerations related to use of anti-HCV positive donors
The diagnosis of chronic hepatitis C has been considered a relative or absolute contraindication for non-liver transplantation in the past, due to concerns of liver disease progression post-transplantation and a lack of safe and effective therapies. The recent availability of interferon-free, all-oral, antiviral drug combinations to treat of chronic hepatitis C provides an opportunity to revise management algorithms to optimize the care of non-liver transplant candidates and recipients.
Objectives:
- Describe the components of the new HCV all-oral combinations, the role of ribavirin, and anticipated rates of HCV eradication with treatment
- Summarize the safety data of new HCV therapies as it pertains to non-liver transplant candidates and recipients, including key drug-drug interactions (HCV antivirals and immunosuppressive drugs)
- Evaluate the pros and cons of HCV treatment pre versus post-transplantation, including considerations related to use of anti-HCV positive donors
Speaker: Daniel Brennan, MD • Washington University School of Medicine
Moderator: Robert Brown, MD • Weill Cornell Medical College
Optimal immunosuppression in organ transplantation is a balance between under immunosuppression, which is associated with graft rejection, and over immunosuppression, which is associated with infection and malignancy. Initial immunosuppression is designed to strike this balance. But how should one adjust immunosuppression when this balance is perturbed and there is an acute infectious complication or malignancy?
After participating in this webinar, the learner will be able to:
- Identify risks for development of acute infectious complications and malignancy in renal transplant recipients.
- Design rational immunosuppression strategies to manage acute infectious complications in renal transplant recipients.
- Design rational immunosuppression strategies to manage malignancy in renal transplant recipients.