1.Pre-sensitive reaction in severe burn patients with white blood cell transfusion
Journal of Practical Medicine 2003;425(5):60-61
The pre-sensitive reaction state of 10 severe burn patients after transfusion of 1-3 units of neutrophile granulocyte was investigated. After 3 weeks, almost patients had < 20% positive reaction and only 1/10 of patients had 30% positive reaction. They had received 3 units of neutrophile granulocyte
Burns
;
Leukocyte Transfusion
;
patients
2.The change of peripheral white blood cell count and the transfusion of white blood cells for treating leucopenia in patients with burn sepsis
Journal of Practical Medicine 2003;425(5):63-66
101 patients with burn sepsis including 22 patients, having peripheral white blood cell count of < 3.109/l treated in the National Institute of Burn, had received 23 units of white blood cells in transfusion. Results showed a decrease of white blood cell count in 58.4% of burn sepsis patients, and an increase in 21.8%. The peripheral white blood cell count was related closely to the germ of sepsis, the state of infections shock and the mortality. The monitoring of white blood cell count has had good impact on early diagnosis and a prognostic significance. The transfusion of white blood cells increases the white blood cell count and promotes its restoration processes
Leukocytes
;
Leukocyte Transfusion
;
Burns
;
Sepsis
;
Therapeutics
3.Evaluation of two methods for counting residual white blood cells in thrombocytaphoresis concentrates.
Yong-Jun WANG ; Zhuo-Lan SHENG ; Jian XU ; Bo-Li HUANG ; Qing-Feng HU ; Wu-Wei FENG
Journal of Experimental Hematology 2006;14(3):614-616
To evaluate flow-cytometry and Nageotte method for counting residual WBC in thrombocytaphoresis concentrates, their accuracies were determined by dilution studies separately; the repeatability was determined by measuring the interassay coefficient of variation for 14 replicates of a sample with known leukocyte concentration. 102 samples of leukocyte-depleted thrombocytaphoresis concentrates were detected by the above mentioned two methods, and the results were compared each other. The results showed that no difference was observed between two methods over a range of leukocyte concentrations from 0.8 to 10 WBC/microl (P > 0.05). In conclusion, flow-cytometry and Nageotte methods can be used for quality control of WBC-reduced blood components.
Blood Component Transfusion
;
Evaluation Studies as Topic
;
Flow Cytometry
;
Humans
;
Leukocyte Count
;
methods
;
Leukocyte Reduction Procedures
;
methods
;
Plateletpheresis
4.Analysis of Granulocyte Transfusions in Patients with Infections and Neutropenia: A Single Center Experience.
Se Na LEE ; Youmi HU ; Hyeon Seok EOM ; Hyewon LEE ; Eunyoung LEE ; Sun Young KONG
Korean Journal of Blood Transfusion 2016;27(3):247-256
BACKGROUND: Granulocyte transfusion therapy has been used as supportive care for patients with prolonged neutropenia after intensive chemotherapy or peripheral blood stem cell transplantation (PBSCT). Here, we investigated clinical factors of granulocyte transfusion therapy for neutropenic patients with infection to evaluate its efficacy and safety. METHODS: A retrospective analysis of 25 neutropenic patients treated with 99 granulocyte collection and granulocyte transfusion therapy from October 2011 to April 2016 at the National Cancer Center was conducted. Two groups, a count recovery group with a cut off of >1,000/µL and a no recovery group were compared and symptoms related with granulocyte transfusion were analyzed. RESULTS: Granulocyte collection and transfusions were performed in 99 procedures. After granulocyte transfusion therapy, 21 patients (84%) showed count recovery, whereas 4 patients (16%) had no response. Significant differences in pre-absolute neutrophil count (29/µL vs. 0/µL, P=0.048), duration of neutropenia before granulocyte transfusion (11 days vs. 26 days, P=0.011), and total number of granulocyte transfusion (2 times vs. 11 times, P=0.049) were observed between groups. Temporary symptoms related granulocyte transfusion were observed in seven patients (28%); however, all patients showed clinical improvement. The median of the single transfusion volume was 220 mL (200 to 397 mL) and the mean total granulocyte content was 4.92×10¹⁰. CONCLUSION: Granulocyte transfusion therapy is safe and effective for patient with life threatening neutropenia and infection, also considerable for early onset trial for granulocyte transfusion.
Drug Therapy
;
Granulocytes*
;
Humans
;
Leukocyte Transfusion
;
Neutropenia*
;
Neutrophils
;
Peripheral Blood Stem Cell Transplantation
;
Retrospective Studies
5.Three times spontaneous remission of severe aplastic anemia following granulocyte transfusion from related donors: a case report and literature review.
Bao-zhi FANG ; Guang-sheng HE ; Hai-xia ZHOU ; Hui-rong CHANG ; De-pei WU ; Ai-ning SUN ; Su-ning CHEN
Chinese Medical Sciences Journal 2013;28(1):58-60
Aplastic anemia (AA) is a bone marrow failure disease caused by abnormal activation of T lymphocytes, resulting in the apoptosis of hematopoietic cells and bone marrow failure. Currently, hematopoietic stem cell transplantation (HSCT), immunosuppressive - therapy (IST), and supportive care (e.g. transfusion adjuvant therapy, hematopoietic growth factors, and prevention of infection) are the main treatments of AA. Granulocyte transfusion has recently been accepted as an useful adjuvant therapy of HSCT and intensive IST. This article reported a severe AA patient who failed to respond to IST, but achieved spontaneous remission three times after granulocyte transfusions from related donors. Such cases have rarely been reported. Existence of human leukocyte antigen (HLA) cross between the patient and his relatives may influence the T cell-mediated immunity, which might explain this patient's recovery.
Adult
;
Anemia, Aplastic
;
immunology
;
physiopathology
;
therapy
;
Granulocytes
;
transplantation
;
Humans
;
Leukocyte Transfusion
;
Male
;
Remission, Spontaneous
6.Proposal of Evaluation Method for Leukoreduction Blood Filter and Evaluation of Domestic Filter.
Geon Sik SHIN ; Sung Hoon KIM ; Bohee KIM ; Kyeong Rak LEE ; Jae Won KANG ; Kwang HUH ; Juwon KIM ; Ki Jong RHEE ; Yoon Suk KIM
Korean Journal of Blood Transfusion 2017;28(3):256-263
BACKGROUND: A leukoreduction filter was recently developed in Korea to reduce various kinds of adverse transfusion reactions. The objective of this study was to propose a domestic evaluation system for leukoreduction filters and to apply this evaluation system to assess the newly developed leukoreduction filter. METHODS: We prepared packed red blood cells from 60 units of whole blood (400 mL) collected from 60 normal individuals and evaluated the efficacy of the newly developed filter (FINECELL, KOLON INDUSTRIES, Gumi, Korea) and a control filter (RCM1, Haemonetics, MA, USA). To verify the evaluation system, we assessed the filtration time, residual leukocyte count, RBC recovery, RBC hemolysis, hemoglobin concentration, and hematocrit using a control filter RCM1 and compared the results with those of an evaluation performed by the American Red Cross (ARC) in 2013. We then evaluated the efficacy of the test filter FINECELL using the methods established in this study and compared the results with those of the control filter RCM1. RESULTS: The results of the current study were similar to those of the ARC with the control filters. The test filters developed in Korea were not inferior to commonly used control filters regarding residual leukocyte count, RBC recovery, and RBC hemolysis at 35 days after filtration. All of the results in the evaluation satisfied the international standards. CONCLUSION: These results of this study showed that the efficacy of the newly developed domestic leukoreduction filter were satisfactory and will contribute to improvement of quality of blood components in Korea.
Erythrocytes
;
Filtration
;
Gyeongsangbuk-do
;
Hematocrit
;
Hemolysis
;
Korea
;
Leukocyte Count
;
Methods*
;
Red Cross
;
Transfusion Reaction
7.Long-Term Efficacy and Safety of Partial Splenic Embolization in Hepatocellular Carcinoma Patients with Thrombocytopenia Who Underwent Transarterial Chemoembolization
Nam Hee KIM ; Hong Joo KIM ; Yong Kyun CHO ; Hyun Pyo HONG ; Byung Ik KIM
Journal of Korean Medical Science 2019;34(30):e208-
BACKGROUND: Performing transarterial chemoembolization (TACE) is difficult with the occurrence of thrombocytopenia in cirrhotic patients with hepatocellular carcinoma (HCC). We aimed to evaluate the long-term efficacy and safety of partial splenic embolization (PSE) combined with TACE in patients with HCC with severe thrombocytopenia related to splenomegaly. METHODS: We conducted a case–control study consisting of 18 HCC patients with severe thrombocytopenia (< 50 × 109/L) who underwent PSE concurrently with TACE (PSE group) and 72 controls who underwent TACE alone (non-PSE group). RESULTS: Mean platelet counts at 1 month and 1, 3, and 5 years after concurrent PSE and TACE significantly increased compared with baseline (all P < 0.05), whereas the platelet count did not significantly increase after TACE alone. In addition, the platelet count at several time points after treatment in the PSE group was significantly higher than that in the non-PSE group, although the baseline platelet count in the PSE group was significantly lower than that in the non-PSE group. The platelet increase after PSE significantly reduced the need for platelet transfusions (P = 0.040) and enabled the subsequent TACE procedures in time (P = 0.046). The leukocyte counts and hemoglobin concentrations after concurrent PSE and TACE were also significantly increased, without deterioration of Child-Turcotte-Pugh score and unexpected side effects. CONCLUSION: PSE combined with TACE is effective in inducing and maintaining long-term thrombocytopenia improvement which reduces the need for the platelet transfusion and helps to perform initial and serial TACE, and is well-tolerated in patients with HCC and thrombocytopenia. PSE may be a promising treatment option for HCC patients with severe thrombocytopenia associated with splenomegaly who will undergo TACE.
Blood Platelets
;
Carcinoma, Hepatocellular
;
Humans
;
Leukocyte Count
;
Platelet Count
;
Platelet Transfusion
;
Splenomegaly
;
Thrombocytopenia
8.Short and long term efficacy of immunosuppressive therapy and survival in adult severe aplastic anemia.
Xiao-Rong MA ; Nan YANG ; Jin WANG ; Wang-Gang ZHANG ; Xing-Mei CAO ; Yin-Xia CHEN ; Ai-Li HE ; Jie LIU ; Jian-Li WANG ; Yan XU
Journal of Experimental Hematology 2015;23(2):471-476
OBJECTIVETo evaluate the short and long term therapeutic efficacy of the immunosuppressive therapy(IST) for adult severe aplastic anemia(SAA), and to analysis the relationship between the clinical factors(age, typing, lymphocyte percentage, reticulocyte percentage, neutrophil count) and the response to IST.
METHODSThe response rate of 39 patients received the IST between September 2009 and September 2013 in our hospital was assayed, the effective time in which all patients had hematologic response, and the survival rate at the first year were analyzed. The survival rates, the average amounts of the RBC and Plt transfusion per month in the first year were compared by using χ2 test between the IST group and the non-IST group; the multinomial logistic regression was used to analyze the relationship between the clinical factors and the response to IST.
RESULTSThe response rates of the 39 SAA patients at the first month, the third month, the sixth month and the first year were 29.73%, 70.27%, 75.68%, 86.49%, respectively. The median effective time of hematologic response in all patients had was 61.5 d(10 d-344 d). The survival rate of the IST group was 92.31%, which was much higher than that of the non-IST group (P<0.05). The average amounts of the RBC and Plt transfusion per month at the first year in the IST group were 1.04(0.13-2.78)×400 ml and 1.38(0.17-5.10)×200 ml, respectively, which were much lower than those in the non-IST group (P<0.01). Among the five clinical factors, the age, lymphocyte percentage and neutrophil count related to the response of IST (P<0.05).
CONCLUSIONThe response rate of the 39 SAA patients received IST is 86.49% at the first year, and their long term survival is better than that of non-IST group. The age, lymphocyte percentage and neutrophil count relate to the response of IST.
Adult ; Anemia, Aplastic ; Blood Transfusion ; Cyclosporine ; Humans ; Immunosuppressive Agents ; Leukocyte Count ; Logistic Models ; Neutrophils ; Reticulocytes ; Survival Rate
9.Intravenous Immunoglobulin Treatment in Women with Unexplained Recurrent Spontaneous Abortion.
Myung Shin SHIN ; Nak Yon KIM ; Chung Hoon KIM ; Byung Moon KANG ; Yoon Seok CHANG ; Jung Eun MOK
Korean Journal of Obstetrics and Gynecology 1997;40(4):740-746
This study was undertaken to verify a specific effect of intravenous immunoglobulin treatment on the outcome of pregnancy in the patients with a history of unexplained recurrent spontaneous abortion. Five patients with a history of unexplained recurrent spontaneous abortion were treated with intravenous immunoglobulin during their following pregnancy, as soon as pregnancy was confirmed. When pregnancy was confirmed, women were started with 10 gm of immunoglobulin intravenously which was repeated every 2 weeks and four to six times. One of them experienced termination of pregnancy due to blighted ovum syndrome at 9th weeks of gestation and four patients delivered live births at term. Two of them had experienced cesarean section because of breech presentation and placenta previa respectively, rest of them delivered vaginally without problem. There were no adverse reaction in the study patients. These results imply that intravenous immunoglobulin could be effective on the patients with a history of unexplained recurrent spontaneous abortion, and could be applied to them as an alternative method of allogenic leukocyte transfusion.
Abortion, Spontaneous*
;
Breech Presentation
;
Cesarean Section
;
Female
;
Humans
;
Immunoglobulins*
;
Leukocyte Transfusion
;
Live Birth
;
Ovum
;
Placenta Previa
;
Pregnancy
10.Intravenous Immunoglobulin Treatment in Women with Unexplained Recurrent Spontaneous Abortion.
Myung Shin SHIN ; Nak Yon KIM ; Chung Hoon KIM ; Byung Moon KANG ; Yoon Seok CHANG ; Jung Eun MOK
Korean Journal of Obstetrics and Gynecology 1997;40(4):740-746
This study was undertaken to verify a specific effect of intravenous immunoglobulin treatment on the outcome of pregnancy in the patients with a history of unexplained recurrent spontaneous abortion. Five patients with a history of unexplained recurrent spontaneous abortion were treated with intravenous immunoglobulin during their following pregnancy, as soon as pregnancy was confirmed. When pregnancy was confirmed, women were started with 10 gm of immunoglobulin intravenously which was repeated every 2 weeks and four to six times. One of them experienced termination of pregnancy due to blighted ovum syndrome at 9th weeks of gestation and four patients delivered live births at term. Two of them had experienced cesarean section because of breech presentation and placenta previa respectively, rest of them delivered vaginally without problem. There were no adverse reaction in the study patients. These results imply that intravenous immunoglobulin could be effective on the patients with a history of unexplained recurrent spontaneous abortion, and could be applied to them as an alternative method of allogenic leukocyte transfusion.
Abortion, Spontaneous*
;
Breech Presentation
;
Cesarean Section
;
Female
;
Humans
;
Immunoglobulins*
;
Leukocyte Transfusion
;
Live Birth
;
Ovum
;
Placenta Previa
;
Pregnancy