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Kelly Patrick, MS, CTBS

Kelly Patrick, MS, CTBS

Recovery Partner Director

Community Blood Center DBA Solvita (Dayton)

Kelly Patrick has 21 years of tissue banking experience, working the last 18 years for Solvita (formerly Community Tissue Services).  She has worked as a Tissue Processing Technician, Production Planning Manager, Quality Systems Specialist, and Recovery Partner Director.  Kelly has been a Certified Tissue Banking Specialist (CTBS) since 2005, and earned her MS in Regulatory Science in 2019 from Johns Hopkins University.  Kelly also serves on AATB's Quality Council and Certification Committee, and has presented in-person and virtually on various tissue banking topics for AATB, FDA, and several Solvita customers and Recovery Partners over the last 15 years.

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  • Contains 3 Component(s), Includes Credits

    In this webinar we will delve into an overview of Hepatitis B panel testing (core, surface antigen and surface antibody), the move from manual to automated testing, and practical application of FDA guidelines. In addition, best practices for the blood sample draw and test preparation to limit false positives will be discussed.

  • Contains 3 Component(s), Includes Credits

    In this webinar we will delve into an overview of Hepatitis B panel testing (core, surface antigen and surface antibody), the move from manual to automated testing, and practical application of FDA guidelines. In addition, best practices for the blood sample draw and test preparation to limit false positives will be discussed.

  • Contains 4 Component(s), Includes Credits

    This presentation will dive into the Allograft Planning process. The allograft planning team reviews donor information from eligible donors and decides which grafts should be produced in order to maximize and optimize the gifts of tissue donation. The planning process considers current and forecasted distribution needs, as well as each donor’s unique attributes, such as age, height, weight, medical history, number and types of tissue recovered, etc. The 3 primary objectives of this presentation are to: 1) Summarize the allograft planning process (i.e., the steps that occur between tissue recovery and tissue processing) 2) Recognize the different processing and distribution options for each recovered tissue (ex. frozen vs. freeze dried grafts, aseptic vs. irradiated grafts, etc.) 3) Understand the factors that can affect how and why recovered tissues are transformed into different types of final grafts (ex. bone density, authorization restrictions, etc.) This presentation is geared more towards M/S tissue planning that takes place several weeks to months after recovery, and after an MD has determined that the donor is eligible for transplantation. The reason for this is that skin, cartilage, and some fresh M/S tissue has to be processed within several days of recovery and can’t really be “planned” in the same way that traditional M/S tissue is planned. I will discuss a wide array of donor attributes that can affect graft production, including but not limited to: • Authorization restrictions (ex. not for international use) • Medication history (ex. warfarin) • Medical history findings (ex. knee replacement or previous surgeries) • Lifestyle (ex. sedentary vs. active) • Weight-bearing vs. non-weight-bearing grafts (ex. tri-cortical blocks vs. bone powder) The entire presentation is geared towards optimizing tissue donations by planning the types of grafts that are best suited for each donor’s attributes. This is done to both honor the donor’s wishes of helping as many people as possible, as well as to meet each organization’s distribution needs. Planning is also a very important step because it prevents processing teams from over-producing or making grafts that may end up expiring before they can be transplanted because there is no current demand.

  • Contains 4 Component(s), Includes Credits

    This presentation will dive into the Allograft Planning process. The allograft planning team reviews donor information from eligible donors and decides which grafts should be produced in order to maximize and optimize the gifts of tissue donation. The planning process considers current and forecasted distribution needs, as well as each donor’s unique attributes, such as age, height, weight, medical history, number and types of tissue recovered, etc. The 3 primary objectives of this presentation are to: 1) Summarize the allograft planning process (i.e., the steps that occur between tissue recovery and tissue processing) 2) Recognize the different processing and distribution options for each recovered tissue (ex. frozen vs. freeze dried grafts, aseptic vs. irradiated grafts, etc.) 3) Understand the factors that can affect how and why recovered tissues are transformed into different types of final grafts (ex. bone density, authorization restrictions, etc.) This presentation is geared more towards M/S tissue planning that takes place several weeks to months after recovery, and after an MD has determined that the donor is eligible for transplantation. The reason for this is that skin, cartilage, and some fresh M/S tissue has to be processed within several days of recovery and can’t really be “planned” in the same way that traditional M/S tissue is planned. I will discuss a wide array of donor attributes that can affect graft production, including but not limited to: • Authorization restrictions (ex. not for international use) • Medication history (ex. warfarin) • Medical history findings (ex. knee replacement or previous surgeries) • Lifestyle (ex. sedentary vs. active) • Weight-bearing vs. non-weight-bearing grafts (ex. tri-cortical blocks vs. bone powder) The entire presentation is geared towards optimizing tissue donations by planning the types of grafts that are best suited for each donor’s attributes. This is done to both honor the donor’s wishes of helping as many people as possible, as well as to meet each organization’s distribution needs. Planning is also a very important step because it prevents processing teams from over-producing or making grafts that may end up expiring before they can be transplanted because there is no current demand.