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      KCI등재 SCIE SCOPUS

      혈소판농축액 보관 시 교반 중단 및 백혈구의 제거가 혈소판의 품질에 미치는 영향 = Effect of Interrupted Agitation and Removal of Leukocyte on Platelet Quality during theStorage of Platelet Concentrates

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      https://www.riss.kr/link?id=A101631249

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      다국어 초록 (Multilingual Abstract)

      Background : This study aimed to analyze the influence of the interruption of agitation and removal
      of leukocytes on platelet concentrates (PCs), and determine the maximum amount of time the agitation
      could be interrupted without impairing PCs’ effectiveness during the storage period.
      Methods : Four ABO-identical random donor platelets agitated for 24 hr were pooled, and divided
      into 4 units, and 2 units of them were leukoreduced. Then 52 pooled units were categorized into 4
      groups, non-leukoreduced continuous agitation (Non-LRCA), non-leukoreduced interrupted agitation
      (Non-LRIA), leukoreduced continuous agitation (LRCA), and leukoreduced interrupted agitation
      (LRIA), and preserved for 6 days (total 7 days). Mean platelet volume (MPV), pH, HCO3
      -, pO2, pCO2,
      CD62P, CD61, glucose, lactate, ammonia and free fatty acid were measured during the period.
      Results : Starting from the Day 4, the pH and HCO3
      - of Non-LRIA group begun to decrease while
      the amount of lactate production, glucose consumption, and MPV increased compared to the Non-
      LRCA group (P<0.01). An increase in pO2 level was observed in the interrupted agitation groups
      as the storage period prolonged (P<0.01). The pH levels of all the units in the agitation groups remained
      higher than 6.4 up to Day 7, while those of the non-leukoreduction group did so only up to Day
      2, but those of leukoreduction in the interrupted agitation groups did so up to Day 4.
      Conclusions : The interruption of agitation reduced the platelet’s capacity to utilize oxygen, increasing
      lactate amount and reducing pH level. However, the in vitro parameters of the Non-LRIA and
      Non-LRCA groups on Day 2 were similar to each other and the pH level remained at 6.4 or higher,
      making one day of agitation interruption possible after 24 hr of agitation. With leukocytes removed,
      the effective agitation interruption period may become longer. (Korean J Lab Med 2008;28:221-9)
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      Background : This study aimed to analyze the influence of the interruption of agitation and removal of leukocytes on platelet concentrates (PCs), and determine the maximum amount of time the agitation could be interrupted without impairing PCs’ effe...

      Background : This study aimed to analyze the influence of the interruption of agitation and removal
      of leukocytes on platelet concentrates (PCs), and determine the maximum amount of time the agitation
      could be interrupted without impairing PCs’ effectiveness during the storage period.
      Methods : Four ABO-identical random donor platelets agitated for 24 hr were pooled, and divided
      into 4 units, and 2 units of them were leukoreduced. Then 52 pooled units were categorized into 4
      groups, non-leukoreduced continuous agitation (Non-LRCA), non-leukoreduced interrupted agitation
      (Non-LRIA), leukoreduced continuous agitation (LRCA), and leukoreduced interrupted agitation
      (LRIA), and preserved for 6 days (total 7 days). Mean platelet volume (MPV), pH, HCO3
      -, pO2, pCO2,
      CD62P, CD61, glucose, lactate, ammonia and free fatty acid were measured during the period.
      Results : Starting from the Day 4, the pH and HCO3
      - of Non-LRIA group begun to decrease while
      the amount of lactate production, glucose consumption, and MPV increased compared to the Non-
      LRCA group (P<0.01). An increase in pO2 level was observed in the interrupted agitation groups
      as the storage period prolonged (P<0.01). The pH levels of all the units in the agitation groups remained
      higher than 6.4 up to Day 7, while those of the non-leukoreduction group did so only up to Day
      2, but those of leukoreduction in the interrupted agitation groups did so up to Day 4.
      Conclusions : The interruption of agitation reduced the platelet’s capacity to utilize oxygen, increasing
      lactate amount and reducing pH level. However, the in vitro parameters of the Non-LRIA and
      Non-LRCA groups on Day 2 were similar to each other and the pH level remained at 6.4 or higher,
      making one day of agitation interruption possible after 24 hr of agitation. With leukocytes removed,
      the effective agitation interruption period may become longer. (Korean J Lab Med 2008;28:221-9)

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      참고문헌 (Reference)

      1 Moroff G, "The maintenance of platelet properties upon limited discontinuation of agitation during storage" 30 : 427-430, 1990

      2 Hunter S, "The effect of interruption of agitation on platelet quality during storage for transfusion" 41 : 809-814, 2001

      3 Wallvik J, "The effect of different agitation modes on platelet metabolism, thromboxane formation, and alphagranular release during platelet storage" 639-643, 1990

      4 Brecher ME, "Technical manual" American Association of Blood Banks 189-199, 2005

      5 Nieuwenhuis HK, "Studies with a monoclonal antibody against activated platelets: evidence that a secreted 53,000-molecular weight lysosome-like granule protein is exposed on the surface of activated platelets in the circulation" 70 : 838-845, 1987

      6 Murphy S, "Storage of platelet concentrates at 22 degrees C" 35 : 549-557, 1970

      7 Rinder HM, "Progressive platelet activation with storage: evidence for shortened survival of activated platelets after transfusion" 31 : 409-414, 1991

      8 Slichter SJ, "Preparation and storage of platelet concentrates. II. Storage variables influencing platelet viability and function" 34 : 403-419, 1976

      9 Murphy S, "Platelet storage at 22 degrees C: role of gas transport across plastic containers in maintenance of viability" 46 : 209-218, 1975

      10 Holme S, "Platelet storage at 22 degrees C for transfusion: interrelationship of platelet density and size, medium pH, and viability after in vivo infusion" 101 : 161-174, 198

      1 Moroff G, "The maintenance of platelet properties upon limited discontinuation of agitation during storage" 30 : 427-430, 1990

      2 Hunter S, "The effect of interruption of agitation on platelet quality during storage for transfusion" 41 : 809-814, 2001

      3 Wallvik J, "The effect of different agitation modes on platelet metabolism, thromboxane formation, and alphagranular release during platelet storage" 639-643, 1990

      4 Brecher ME, "Technical manual" American Association of Blood Banks 189-199, 2005

      5 Nieuwenhuis HK, "Studies with a monoclonal antibody against activated platelets: evidence that a secreted 53,000-molecular weight lysosome-like granule protein is exposed on the surface of activated platelets in the circulation" 70 : 838-845, 1987

      6 Murphy S, "Storage of platelet concentrates at 22 degrees C" 35 : 549-557, 1970

      7 Rinder HM, "Progressive platelet activation with storage: evidence for shortened survival of activated platelets after transfusion" 31 : 409-414, 1991

      8 Slichter SJ, "Preparation and storage of platelet concentrates. II. Storage variables influencing platelet viability and function" 34 : 403-419, 1976

      9 Murphy S, "Platelet storage at 22 degrees C: role of gas transport across plastic containers in maintenance of viability" 46 : 209-218, 1975

      10 Holme S, "Platelet storage at 22 degrees C for transfusion: interrelationship of platelet density and size, medium pH, and viability after in vivo infusion" 101 : 161-174, 198

      11 Kakaiya RM, "Platelet preservation in large containers" 46 : 111-118, 1984

      12 Kilkson H, "Platelet metabolism during storage of platelet concentrates at 22 degrees C" 406-414, 1984

      13 Cesar J, "Plasma free fatty acid metabolism during storage of platelet concentrates for transfusion" 27 : 434-437, 1987

      14 Fijnheer R, "Monitoring of platelet morphology during storage of platelet concentrates" 29 : 36-40, 1989

      15 van der Meer PF, "Interruption of agitation of platelet concentrates:effects on in vitro parameters" 227-234, 2005

      16 Kutlay S, "Influence of storage time on activation of platelets collected with CS 3000 Plus and Cobe Spec tra using platelet storage containers" 6 : 82-85, 2002

      17 de Wildt-Eggen J, "Improvement of platelet storage conditions by using new polyolefin containers" 37 : 476-481, 1997

      18 "Guide to the preparation use and quality assurance of blood components. Recommendation No. R(95)15. 12th ed. Strasbourg: Council of Europe, 2006:121-31"

      19 Simon TL, "Extension of platelet concentrate storage" 23 : 207-212, 1983

      20 Snyder EL, "Extended storage of platelets in a new plastic container. II. In vivo response to infusion of platelets stored for 5 day" 25 : 209-214, 1985

      21 Holme S, "Evaluation of a new, more oxygen- permeable, polyvinylchloride container" 29 : 159-164, 198

      22 Fijhneer R, "Detection of platelet activation with monoclonal antibodies and flow cytometry. Changes during platelet storage" 30 : 20-25, 1990

      23 Hagberg IA, "Apheresisinduced platelet activation: comparison of three types of cell separators" 40 : 182-192, 2000

      24 Kunicki TJ, "A study of variables affecting the quality of platelets stored at“ room temperature”" 15 : 414-421, 1975

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
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      2012-05-21 학술지명변경 한글명 : The Korean Journal of Laboratory Medicine -> Annals of Laboratory Medicine
      외국어명 : The Korean Journal of Laboratory Medicine -> Annals of Laboratory Medicine
      KCI등재
      2011-01-01 평가 학술지 분리 (기타) KCI등재
      2010-06-29 학술지명변경 한글명 : 대한진단검사의학회지 -> The Korean Journal of Laboratory Medicine KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.51 0.18 1.15
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.91 0.81 0.458 0.08
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