Determination of the rate of reduction in platelet counts in recipients of hematopoietic stem and progenitor cell transplant: clinical implications for platelet transfusion therapy

Transfusion ◽  
1997 ◽  
Vol 37 (11-12) ◽  
pp. 1163-1168 ◽  
Author(s):  
ML Rosario ◽  
KI Kao
Hematology ◽  
2015 ◽  
Vol 2015 (1) ◽  
pp. 462-470 ◽  
Author(s):  
Ross M. Fasano ◽  
Cassandra D. Josephson

Abstract Despite the advances in platelet component preparation and transfusion support over the years, platelet products remain a limited resource due to their short (5 day) shelf life, and therefore their optimal use in the non-bleeding thrombocytopenic patient continue to draw much attention. There have been a number of national and international guidelines for platelet transfusion therapy in patients with hematologic diseases, some within the last 1-2 years that have incorporated key randomized controlled trials (RCTs) which address issues, such as the optimal platelet dose, the most appropriate threshold for prophylactic platelet transfusions, and whether prophylactic platelet transfusions are superior to therapeutic-only platelet transfusion practices for the prevention life-threatening bleeding in patients with hypoproliferative thrombocytopenia. This review highlights key RCTs and recent systematic reviews focused on optimal platelet transfusion therapy in adult and pediatric patients with hypoproliferative thrombocytopenia secondary to chemotherapy or hematopoietic stem cell transplant (HSCT), discuss how recent innovations in platelet component processing may affect transfusion efficiency, and introduce renewed concepts on adjuvant therapies to prevent bleeding in the hypoproliferative thrombocytopenic patient.


Blood ◽  
1997 ◽  
Vol 89 (8) ◽  
pp. 2679-2688 ◽  
Author(s):  
Francesco Bertolini ◽  
Manuela Battaglia ◽  
Paolo Pedrazzoli ◽  
Gian Antonio Da Prada ◽  
Annalisa Lanza ◽  
...  

Abstract We evaluated different culture conditions to obtain a lineage-selected proliferation of clonogenic megakaryocytic progenitors (MP). In low-density (LD) or CD34+ cell cultures, the best results were obtained in serum-free medium in the presence of megakaryocyte growth and development factor, stem cell factor, interleukin-3 (IL-3), IL-6, IL-11, FLT-ligand, and macrophage inflammatory protein-1α. In paired studies, expansion of LD cells was less effective than expansion of CD34+ cells, and pre-enrichment of CD34+ cells using negative depletion of lineage-positive cells produced significantly larger quantities of MP than pre-enrichment using positive selection. MP proliferation peaked on day 7 in culture, and an 8- ± 5-fold expansion of CD34+/CD61+ cells, a 17- ± 5-fold expansion of colony-forming units-megakaryocytes, and a 58- ± 14-fold expansion of the total number of CD61+ cells was obtained. In a feasibility clinical study, 10 cancer patients (8 with breast cancer and 2 with non-Hodgkin's lymphoma) undergoing autologous peripheral blood progenitor cell (PBPC) transplant received MP generated ex vivo (range, 1 to 21 × 105/kg CD61+ cells) together with unmanipulated PBPC. Eight patients received a single allogeneic platelet transfusion, whereas platelet transfusion support was not needed in 2 of the 4 patients receiving the highest doses of cultured MP. This result compares favorably with a retrospective control group of 14 patients, all requiring platelet transfusion support. Adverse reactions or bacterial contamination of cell cultures have not been observed. In conclusion, MP can be expanded ex vivo and safely administered to autologous transplant recipients. Further clinical trials will indicate the reinfusion schedule able to consistently abrogate the need for allogeneic platelet transfusion support in autologous transplantation.


Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 2116-2116
Author(s):  
Louis-Bassett Porter ◽  
Hanaa Shihadeh ◽  
Kim Dittus

Background Interventions for venous thromboembolism (VTE) prophylaxis and primary antimicrobial prophylaxis for chemotherapy-induced neutropenia and hematopoietic stem cell transplant (HSCT) recipients have resulted in reduced rates of VTE and infection. Appropriate prevention of thrombosis and infection requires a day-to-day evaluation in hospitalized hematology patients experiencing changing chemotherapy regimens and fluctuating neutrophil or platelet counts. Inappropriate use of anticoagulants in patients with thrombocytopenia may result in iatrogenic bleeding. Methods To evaluate appropriate antimicrobial and anticoagulant prophylaxis, a retrospective extraction of electronic medical records of hematology inpatients meeting eligibility criteria from 06/2017 - 06/2018 was completed. Appropriate use was determined by the University of Vermont Medical Center's internal protocols, which are derived from the current standard of care. Anti-viral prophylaxis (AVP) is required for any hospital day for patients undergoing HSCT and was within 180 days of transplant, or having a diagnosis of acute myeloid leukemia (AML) or acute lymphocytic leukemia (ALL), while on induction, consolidation, or maintenance chemotherapy, or was receiving specific therapy (e.g., Hyper-CVAD, CODOX-M, R-DA-EPOCH, VD-PACE, bendamustine, alemtuzumab (stopping when CD4 count >200), proteosome inhibitors, or Daratumumab). Anti-pneumocystis prophylaxis (APP) is required for any hospital day for patients diagnosed with ALL (on induction, consolidation, or maintenance chemotherapy, or therapies listed above), receiving high dose steroids (prednisone >20 mg/day or dexamethasone >4 mg/day for 30 or more days), purine analogs (e.g., fludarabine, clofarabine) or undergoing HSCT (after platelet engraftment). Antimicrobial prophylaxis was considered inappropriate when the above conditions were met but the patient was not provided the appropriate therapy during an inpatient day and did not have a documented contraindication. Anticoagulant prophylaxis (ACP) was considered inappropriate when an anticoagulant was provided on a hospital day when platelets were less than 50 K/cmm. Days where the patient missed a dose at admission or discharge were excluded. Results We evaluated a total of 221 patient visit records comprised of 142 unique patients. In total, on 189 (10.9%) of 1,734 total inpatient days evaluated, appropriate antimicrobial prophylaxis was not provided (Table 1). Regarding AVP, 15 (6.8%) patients missed at least one day, a total of 69 (4.0%) days. 11 (5.0%) patients missed at least one day of APP, a total of 120 (6.9%) days. Regarding ACP, there are 1,961 platelet count observations which included 219 visits from 140 unique patients (Table 2). Of these observations, 603 (30.8%) had platelet counts below 50 K/cmm. ACP was not held 18 times (3.0%) when platelet levels fell below 50 K/cmm. 51 patients (36.4%) had their platelets drop below 50 K/cmm at some point during their visit(s) of which 7 (13.7%) did not have ACP withheld. Conclusions and Discussion The results identify areas of improvement regarding antimicrobial prophylaxis. Antimicrobial prophylaxis is often not systematically evaluated on inpatient services and as such may not be consistently evaluated by clinicians rotating on the hematology service. Conversely, guidelines for withholding anticoagulant prophylaxis were more closely followed. This is likely due to the focus in recent years on anticoagulation prophylaxis and the near universal knowledge of bleeding risk when provided at low platelet levels. Inappropriate antithrombotic prophylaxis was most frequently noted at platelets of just below 50 K/cmm (i.e., 47-49 K/cmm) and immediately discontinued for following doses as platelet values declined. A potential intervention is the use of a daily checklist that can evaluate the use of these therapies. Disclosures No relevant conflicts of interest to declare.


Blood ◽  
1998 ◽  
Vol 91 (9) ◽  
pp. 3509-3517 ◽  
Author(s):  
Steven H. Bernstein ◽  
Auayporn P. Nademanee ◽  
Julie M. Vose ◽  
Guido Tricot ◽  
Joseph W. Fay ◽  
...  

An observational study was conducted at 18 transplant centers in the United States and Canada to characterize the platelet recovery of patients receiving myeloablative therapy and stem cell transplantation and to determine the clinical variables influencing recovery, determine platelet utilization and cost, and incidence of hemorrhagic events. The study included 789 evaluable patients transplanted in 1995. Clinical, laboratory, and outcome data were obtained from the medical records. Variables associated with accelerated recovery in multivariate models included (1) higher CD34 count; (2) higher platelet count at the start of myeloablative therapy; (3) graft from an HLA-identical sibling donor; and (4) prior stem cell transplant. Variables associated with delayed recovery were (1) prior radiation therapy; (2) posttransplant fever; (3) hepatic veno-occlusive disease; and (4) use of posttransplant growth factors. Disease type also influenced recovery. Recipients of peripheral blood stem cells (PBSC) had faster recovery and fewer platelet transfusion days than recipients of bone marrow (BM). The estimated average 60-day platelet transfusion cost per patient was $4,000 for autologous PBSC and $11,000 for allogeneic BM transplants. It was found that 11% of all patients had a significant hemorrhagic event during the first 60 days posttransplant, contributing to death in 2% of patients. In conclusion, clinical variables influencing platelet recovery should be considered in the design and interpretation of clinical strategies to accelerate recovery. Enhancing platelet recovery is not likely to have a significant impact on 60-day mortality but could significantly decrease health care costs and potentially improve patient quality of life.


Author(s):  
Canan Eren ◽  
Serpil Çeçen

Platelet transfusion is used to prevent bleeding in patients with thrombocytopenia or platelet dysfunction. Purpose of investigating demographic characteristics of eligible volunteers as platelet donors and of demonstrating the association of platelet counts with blood groups as well as other factors. We used data of individuals who referred to a blood center in our hospital. Age, body weight, body mass index (BMI), and gender were determined, and than hemogram values such as leukocyte, hemoglobin, hematocrit, and platelet and ABO blood types of those individuals were identified. A statistically significant difference determined for height, body weight, and BMI in both genders. Although BMI was lower in the group of platelet count ≤ 250, it was higher in a group of platelet count > 250. Furthermore, platelet count was more moderate in blood group O Rh-positive but, no significant difference was group O Rh-negative. Platelet count was higher in other Rh-positive blood groups than Rh negatives. BMI is vital in apheresis donors, and individuals with higher BMI values may prefer in case of double dose or more apheresis need. The determination of platelet counts in Rh positives is more elevated than Rh negatives.


Blood ◽  
2011 ◽  
Vol 117 (3) ◽  
pp. 1014-1020 ◽  
Author(s):  
Laurence Corash ◽  
Jin Sying Lin ◽  
Claire D. Sherman ◽  
Joseph Eiden

Abstract Acute lung injury (ALI) during hematopoietic stem cell transplant (HSCT) is associated with substantial morbidity; however, the frequency of ALI in HSCT patients is poorly characterized. Platelets are postulated to play a critical role in the pathogenesis of ALI. Using a transfusion trial of pathogen inactivated platelet components (PC-Test) compared with conventional PC (Reference) populated with HSCT patients, data were reviewed by an adjudication panel to determine the frequency of ALI overall, by treatment groups, and key outcomes: PC exposure, ventilator-free days, and mortality. The diagnosis of ALI was based on American European Consensus Criteria. Of 645 patients who received PC over 28 days, 100 (15.5%) had clinically serious pulmonary adverse events, and 35 (5.4%) met criteria for ALI. Days of platelet support and number of platelet transfusions for patients with ALI were not significantly different from patients without ALI (P > .05). Mortality was greater for patients with ALI (57%) than those without (17%, P < .001) but not significantly different between treatment groups. For patients with ALI, the distributions of time to onset of mechanical ventilation were significantly different (P = .04). Patients supported with Reference PC were more likely to be ventilated sooner than patients receiving Test PC.


Blood ◽  
2021 ◽  
Author(s):  
Tomoyuki Tanaka ◽  
Kiyomi Morita ◽  
Feng Wang ◽  
Sanam Loghavi ◽  
Ken Furudate ◽  
...  

While clonal hematopoiesis (CH) can precede the development of acute myeloid leukemia (AML), it can also persist after achieving remission. Long-term clonal dynamics and clinical implications of persistent CH are not well understood. Here, we studied the prevalence, dynamics and clinical implications of post-remission CH in 164 AML patients who attained complete remission after induction chemotherapies. Post-remission CH was identified in 79 (49%) patients. Post-remission CH persisted long-term in 91% of the trackable patients despite treatment with various types of consolidation and maintenance therapies. Post-remission CH was eradicated in 20 out of 21 (95%) patients who underwent allogeneic stem cell transplant. While patients with post-remission CH as a group had comparable hematopoiesis with those without it, patients with persistent TET2 mutations showed significant neutropenia long-term. Post-remission CH had little impact on relapse risk, non-relapse mortality, and incidence of atherosclerotic cardiovascular disease, although the clinical impact of post-CR CH was heterogeneous among different mutations. These data suggest that while residual clonal hematopoietic stem cells (HSCs) are generally resistant to consolidation and maintenance therapies, they retain the ability to maintain normal hematopoiesis and have little impact on clinical outcomes, although larger study is needed to dissect the gene-specific heterogeneity.


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