BMTCN REVIEW COURSE PRE-TRANSPLANT CARE

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BMTCN REVIEW COURSE PRE-TRANSPLANT CARE Jennifer Shamai MS, RN, AOCNS, BMTCN Professional Practice Leader Department of Clinical Practice And Professional Education Click How to edit the Master Experts Presentation Treat Hematologic Date Malignancies Las Vegas, NV March 11, 2016

DISCLOSURES No Disclosures

Objectives Discuss recipient and donor eligibility, evaluation, and management Review recipient, caregiver, and donor education Discuss the process of collecting and storing stem cells Note: the primary reference source for this course is Ezzone, S. (2013) Hematopoietic stem cell transplantation: a manual for nursing practice. Oncology Nursing Society, Pittsburgh, PA

Recipient Eligibility General considerations Extent of underlying disease Chemotherapy-sensitive disease Remission status Adequate organ function and performance status No life-threatening viral exposures or comorbidities Age Variations among transplant centers

Recipient Evaluation and Management Health history Physical examination Laboratory evaluation CBC, chem profile, electrolytes, LFTs, BUN, PTT, INR, GFR, ABO/Rh, pregnancy test Infectious disease testing: Hep B, Hep C, HIV, CMV, HSV Histocompatibility testing (HLA) Organ function testing: echocardiogram, pulmonary function tests, dental exam Disease evaluation Bone marrow aspirates and biopsies Lumbar puncture

Recipient Evaluation and Management Psychosocial assessment Financial issues Psychological well-being Family concerns Comprehension of procedure, risks, side effects, and complications Ability to comply with therapy Informed consent Pediatric considerations

Recipient Education HSCT is an intense and complicated process Based on complex concepts High levels of distress prior to HSCT Pre-transplant education topics Conditioning regimen Cell infusion Supportive medications Best practices Individualized and ongoing education with comprehension evaluation Utilize multimodal methods Teach-back http://www.teachbacktraining.org/

Caregiver Education Physical and psychosocial elements of process Role of the caregiver Demands of care Changing roles within the family Identification of key support people for activity delegation Group participation and support networks Discharge planning recipient and caregiver/family Pediatric considerations Child life specialists

Recipient and Caregiver Education Resources Blood and Marrow Transplant Information Network Books, monthly newsletters, and on-line support network http://www.bmtinfonet.org/ National Marrow Donor Program/Be The Match Registry Resources for patients and families https://bethematch.org/for-patients-and-families/ BMT Support Online Peer support, education, and awareness http://bmtsupport.org/

Donor Selection and Care Thorough clinical evaluation Complete medical history, physical examination, blood tests Psychosocial assessment Donor education Collection process Outcomes of collection and recipient Anonymity of donors for unrelated transplants Voluntary process with informed consent Other considerations Legal aspects pediatric donation, joint-custody Ethical aspects psychological effects, motive for donation, pressure to donate, discovery of unknown medical conditions

Unrelated Donors Majority of patients do not have HLA-compatible related donor (~70%) National and international registries provide unrelated donor options Process 1) Obtain the patient s HLA 2) Perform a preliminary search 3) Formal search is initiated 4) Donor work-up

National Marrow Donor Program Largest database of marrow, cord blood and stem cell donors Facilitate transport of unrelated products to the transplant center

Collection Process 1) Donor/recipient evaluated for collection 2) Transplant physician writes a collection and processing order Recipient and donor information Treatment plan Collection protocol mobilization, target dose Processing and cryopreservation method 3) Product is collected 4) Lab determines the number of cells collected CD34+ cells 5) Additional collections performed if necessary

Stem Cell Mobilization Stimulation of stem cells that originate in the bone marrow to move into the peripheral blood Number of circulating stem cells in the blood is lower than in the bone marrow Results in fewer apheresis collections and faster hematopoietic recovery after transplant Methods Chemotherapy Hematopoietic growth factors Chemokine antagonists

Stem Cell Mobilization Chemotherapy: cyclophosphamide, ICE, R-ICE Transient increase in circulating stem cells following standard chemotherapy Disadvantages: neutropenia, sepsis, failure to mobilize Colony stimulating factors: G-CSF, GM-CSF Reduce cytopenia and increase number of circulating progenitor cells Side effects: bone pain, arthralgia/myalgia, fever, malaise Chemokine antagonists: plerixafor (Mozobil ) Schedule: G-CSF up to 8 days, plerixafor on day 4 Side effects: GI symptoms, injection-site reactions, headache, fatigue, arthralgias, dizziness

Stem Cell Collection Bone Marrow Harvest HPCs harvested from the posterior iliac crests via multiple large-bore needle aspirations Collection procedure: Scheduled in the OR Multiple needle aspirations of bone marrow Side effects: post-procedural pain and anesthesia complications Harvested product is filtered and processed Assess: bleeding, drainage, hematoma development

Bone Marrow Harvest

Stem Cell Collection PBSC Apheresis Donors are connected to an apheresis machine via central or peripheral vascular access Blood is removed from the patient and passes through a cell separator Centrifuge separates blood components by cell density Stem cell layer is isolated, and remaining blood returned Dana-Farber/Harvard Cancer Center

PBSC Apheresis Procedure Outpatient 12-15 liters of blood 2-4 hours May need multiple collections Requires vascular access Advantages Outpatient procedure Option for those with a tumor in the marrow or had pelvic irradiation that caused marrow fibrosis

PBSC Apheresis Side effects and complications Hypocalcemia from citrate toxicity Hypovolemia Chilling Peripheral and central catheter complications Decreased platelets and/or hemoglobin Pediatric considerations Volume of blood processed must be based on the child s size (200-250 ml/kg) Pre-prime with irradiated RBCs if more than 10-15% of the child s total blood volume is needed for priming Typically not performed in children under 13 years of age

Stem Cell Collection Umbilical Cord Blood Stem cells collected at the time of childbirth from the umbilical cord and placenta Scheduled prior to delivery Cord blood center must have the ability to collect and arrange for storage of the product Frozen and stored after collection Donated to public cord blood bank Stored in private cord banks Ethical issues

Umbilical Cord Blood Collection Procedure Placenta and umbilical cord is removed from delivery room Cleanse and puncture the umbilical vein with a 16 or 17 gauge needle Blood is drained by gravity into a blood bag Products are counted, tested for infectious diseases, HLAtyped

Photographs courtesy of A. Scaradavou, NYBC Cord Blood Collection

Stem Cell Processing Blood and HLA typing Sterility and infectious disease testing Volume reduction Autologous stem cell purging Negative cell selection: removing tumor cells Positive cell selection: removing stem cells from the product Allogeneic processing ABO incompatibilities red cell or plasma-depletion T-cell depletion: remove enough T lymphocytes to minimize graft versus host disease (GVHD)

Cryopreservation Preserve stem cells and prevent cell damage during freezing or thawing Cryoprotectant dimethyl sulfoxide (DMSO) followed by controlled-rate freezing Storage in liquid nitrogen freezers Preparation, storage, and thawing performed by specialized technologists Adverse effects: infusion reactions