Expert consensus regarding standardization of sample preparation for clotting time assays
Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centri...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Ieko, Masahiro [verfasserIn] Komiyama, Yutaka [verfasserIn] Yamazaki, Satoshi [verfasserIn] Katagiri, Hisako [verfasserIn] Shimazu, Chisato [verfasserIn] Naito, Sumiyoshi [verfasserIn] Matsuda, Masato [verfasserIn] Yuki, Yoichi [verfasserIn] Miyata, Kazuyoshi [verfasserIn] Arai, Rika [verfasserIn] Kumano, Osamu [verfasserIn] Emmi, Mari [verfasserIn] Yoshida, Tatsuya [verfasserIn] Tanaka, Hideaki [verfasserIn] Okuhara, Toshihiko [verfasserIn] Yamashita, Tetsuji [verfasserIn] Sekine, Yasuji [verfasserIn] Homma, Masaru [verfasserIn] Kawai, Yohko [verfasserIn] Tohyama, Kaoru [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2020 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: International journal of hematology - Tokyo [u.a.] : Springer, 1995, 112(2020), 5 vom: 14. Sept., Seite 614-620 |
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| Übergeordnetes Werk: |
volume:112 ; year:2020 ; number:5 ; day:14 ; month:09 ; pages:614-620 |
| Links: |
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| DOI / URN: |
10.1007/s12185-020-02983-x |
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| Katalog-ID: |
SPR041410742 |
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| 245 | 1 | 0 | |a Expert consensus regarding standardization of sample preparation for clotting time assays |
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| 520 | |a Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. (4) After the plasma sample is prepared, it should be stored at room temperature and assayed within 4 h. | ||
| 650 | 4 | |a Clotting time assay |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Plasma sample |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Centrifugation condition |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Sample store condition |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Komiyama, Yutaka |e verfasserin |4 aut | |
| 700 | 1 | |a Yamazaki, Satoshi |e verfasserin |4 aut | |
| 700 | 1 | |a Katagiri, Hisako |e verfasserin |4 aut | |
| 700 | 1 | |a Shimazu, Chisato |e verfasserin |4 aut | |
| 700 | 1 | |a Naito, Sumiyoshi |e verfasserin |4 aut | |
| 700 | 1 | |a Matsuda, Masato |e verfasserin |4 aut | |
| 700 | 1 | |a Yuki, Yoichi |e verfasserin |4 aut | |
| 700 | 1 | |a Miyata, Kazuyoshi |e verfasserin |4 aut | |
| 700 | 1 | |a Arai, Rika |e verfasserin |4 aut | |
| 700 | 1 | |a Kumano, Osamu |e verfasserin |4 aut | |
| 700 | 1 | |a Emmi, Mari |e verfasserin |4 aut | |
| 700 | 1 | |a Yoshida, Tatsuya |e verfasserin |4 aut | |
| 700 | 1 | |a Tanaka, Hideaki |e verfasserin |4 aut | |
| 700 | 1 | |a Okuhara, Toshihiko |e verfasserin |4 aut | |
| 700 | 1 | |a Yamashita, Tetsuji |e verfasserin |4 aut | |
| 700 | 1 | |a Sekine, Yasuji |e verfasserin |4 aut | |
| 700 | 1 | |a Homma, Masaru |e verfasserin |4 aut | |
| 700 | 1 | |a Kawai, Yohko |e verfasserin |4 aut | |
| 700 | 1 | |a Tohyama, Kaoru |e verfasserin |4 aut | |
| 700 | 1 | |a Ieko, Masahiro |e verfasserin |4 aut | |
| 700 | 1 | |a Komiyama, Yutaka |e verfasserin |4 aut | |
| 700 | 1 | |a Yamazaki, Satoshi |e verfasserin |4 aut | |
| 700 | 1 | |a Katagiri, Hisako |e verfasserin |4 aut | |
| 700 | 1 | |a Shimazu, Chisato |e verfasserin |4 aut | |
| 700 | 1 | |a Naito, Sumiyoshi |e verfasserin |4 aut | |
| 700 | 1 | |a Matsuda, Masato |e verfasserin |4 aut | |
| 700 | 1 | |a Yuki, Yoichi |e verfasserin |4 aut | |
| 700 | 1 | |a Miyata, Kazuyoshi |e verfasserin |4 aut | |
| 700 | 1 | |a Arai, Rika |e verfasserin |4 aut | |
| 700 | 1 | |a Kumano, Osamu |e verfasserin |4 aut | |
| 700 | 1 | |a Emmi, Mari |e verfasserin |4 aut | |
| 700 | 1 | |a Yoshida, Tatsuya |e verfasserin |4 aut | |
| 700 | 1 | |a Tanaka, Hideaki |e verfasserin |4 aut | |
| 700 | 1 | |a Okuhara, Toshihiko |e verfasserin |4 aut | |
| 700 | 1 | |a Yamashita, Tetsuji |e verfasserin |4 aut | |
| 700 | 1 | |a Sekine, Yasuji |e verfasserin |4 aut | |
| 700 | 1 | |a Homma, Masaru |e verfasserin |4 aut | |
| 700 | 1 | |a Kawai, Yohko |e verfasserin |4 aut | |
| 700 | 1 | |a Tohyama, Kaoru |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t International journal of hematology |d Tokyo [u.a.] : Springer, 1995 |g 112(2020), 5 vom: 14. Sept., Seite 614-620 |w (DE-627)324615485 |w (DE-600)2028991-1 |x 1865-3774 |7 nnns |
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10.1007/s12185-020-02983-x doi (DE-627)SPR041410742 (SPR)s12185-020-02983-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.86 bkl Ieko, Masahiro verfasserin aut Expert consensus regarding standardization of sample preparation for clotting time assays 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. (4) After the plasma sample is prepared, it should be stored at room temperature and assayed within 4 h. Clotting time assay (dpeaa)DE-He213 Plasma sample (dpeaa)DE-He213 Centrifugation condition (dpeaa)DE-He213 Sample store condition (dpeaa)DE-He213 Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Ieko, Masahiro verfasserin aut Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Enthalten in International journal of hematology Tokyo [u.a.] : Springer, 1995 112(2020), 5 vom: 14. Sept., Seite 614-620 (DE-627)324615485 (DE-600)2028991-1 1865-3774 nnns volume:112 year:2020 number:5 day:14 month:09 pages:614-620 https://dx.doi.org/10.1007/s12185-020-02983-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.86 ASE AR 112 2020 5 14 09 614-620 |
| spelling |
10.1007/s12185-020-02983-x doi (DE-627)SPR041410742 (SPR)s12185-020-02983-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.86 bkl Ieko, Masahiro verfasserin aut Expert consensus regarding standardization of sample preparation for clotting time assays 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. (4) After the plasma sample is prepared, it should be stored at room temperature and assayed within 4 h. Clotting time assay (dpeaa)DE-He213 Plasma sample (dpeaa)DE-He213 Centrifugation condition (dpeaa)DE-He213 Sample store condition (dpeaa)DE-He213 Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Ieko, Masahiro verfasserin aut Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Enthalten in International journal of hematology Tokyo [u.a.] : Springer, 1995 112(2020), 5 vom: 14. Sept., Seite 614-620 (DE-627)324615485 (DE-600)2028991-1 1865-3774 nnns volume:112 year:2020 number:5 day:14 month:09 pages:614-620 https://dx.doi.org/10.1007/s12185-020-02983-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.86 ASE AR 112 2020 5 14 09 614-620 |
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10.1007/s12185-020-02983-x doi (DE-627)SPR041410742 (SPR)s12185-020-02983-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.86 bkl Ieko, Masahiro verfasserin aut Expert consensus regarding standardization of sample preparation for clotting time assays 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. (4) After the plasma sample is prepared, it should be stored at room temperature and assayed within 4 h. Clotting time assay (dpeaa)DE-He213 Plasma sample (dpeaa)DE-He213 Centrifugation condition (dpeaa)DE-He213 Sample store condition (dpeaa)DE-He213 Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Ieko, Masahiro verfasserin aut Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Enthalten in International journal of hematology Tokyo [u.a.] : Springer, 1995 112(2020), 5 vom: 14. Sept., Seite 614-620 (DE-627)324615485 (DE-600)2028991-1 1865-3774 nnns volume:112 year:2020 number:5 day:14 month:09 pages:614-620 https://dx.doi.org/10.1007/s12185-020-02983-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.86 ASE AR 112 2020 5 14 09 614-620 |
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10.1007/s12185-020-02983-x doi (DE-627)SPR041410742 (SPR)s12185-020-02983-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.86 bkl Ieko, Masahiro verfasserin aut Expert consensus regarding standardization of sample preparation for clotting time assays 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. (4) After the plasma sample is prepared, it should be stored at room temperature and assayed within 4 h. Clotting time assay (dpeaa)DE-He213 Plasma sample (dpeaa)DE-He213 Centrifugation condition (dpeaa)DE-He213 Sample store condition (dpeaa)DE-He213 Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Ieko, Masahiro verfasserin aut Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Enthalten in International journal of hematology Tokyo [u.a.] : Springer, 1995 112(2020), 5 vom: 14. Sept., Seite 614-620 (DE-627)324615485 (DE-600)2028991-1 1865-3774 nnns volume:112 year:2020 number:5 day:14 month:09 pages:614-620 https://dx.doi.org/10.1007/s12185-020-02983-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.86 ASE AR 112 2020 5 14 09 614-620 |
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10.1007/s12185-020-02983-x doi (DE-627)SPR041410742 (SPR)s12185-020-02983-x-e DE-627 ger DE-627 rakwb eng 610 ASE 44.86 bkl Ieko, Masahiro verfasserin aut Expert consensus regarding standardization of sample preparation for clotting time assays 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. (4) After the plasma sample is prepared, it should be stored at room temperature and assayed within 4 h. Clotting time assay (dpeaa)DE-He213 Plasma sample (dpeaa)DE-He213 Centrifugation condition (dpeaa)DE-He213 Sample store condition (dpeaa)DE-He213 Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Ieko, Masahiro verfasserin aut Komiyama, Yutaka verfasserin aut Yamazaki, Satoshi verfasserin aut Katagiri, Hisako verfasserin aut Shimazu, Chisato verfasserin aut Naito, Sumiyoshi verfasserin aut Matsuda, Masato verfasserin aut Yuki, Yoichi verfasserin aut Miyata, Kazuyoshi verfasserin aut Arai, Rika verfasserin aut Kumano, Osamu verfasserin aut Emmi, Mari verfasserin aut Yoshida, Tatsuya verfasserin aut Tanaka, Hideaki verfasserin aut Okuhara, Toshihiko verfasserin aut Yamashita, Tetsuji verfasserin aut Sekine, Yasuji verfasserin aut Homma, Masaru verfasserin aut Kawai, Yohko verfasserin aut Tohyama, Kaoru verfasserin aut Enthalten in International journal of hematology Tokyo [u.a.] : Springer, 1995 112(2020), 5 vom: 14. Sept., Seite 614-620 (DE-627)324615485 (DE-600)2028991-1 1865-3774 nnns volume:112 year:2020 number:5 day:14 month:09 pages:614-620 https://dx.doi.org/10.1007/s12185-020-02983-x lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.86 ASE AR 112 2020 5 14 09 614-620 |
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International journal of hematology |
| authorswithroles_txt_mv |
Ieko, Masahiro @@aut@@ Komiyama, Yutaka @@aut@@ Yamazaki, Satoshi @@aut@@ Katagiri, Hisako @@aut@@ Shimazu, Chisato @@aut@@ Naito, Sumiyoshi @@aut@@ Matsuda, Masato @@aut@@ Yuki, Yoichi @@aut@@ Miyata, Kazuyoshi @@aut@@ Arai, Rika @@aut@@ Kumano, Osamu @@aut@@ Emmi, Mari @@aut@@ Yoshida, Tatsuya @@aut@@ Tanaka, Hideaki @@aut@@ Okuhara, Toshihiko @@aut@@ Yamashita, Tetsuji @@aut@@ Sekine, Yasuji @@aut@@ Homma, Masaru @@aut@@ Kawai, Yohko @@aut@@ Tohyama, Kaoru @@aut@@ |
| publishDateDaySort_date |
2020-09-14T00:00:00Z |
| hierarchy_top_id |
324615485 |
| dewey-sort |
3610 |
| id |
SPR041410742 |
| language_de |
englisch |
| fullrecord |
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The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. 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610 ASE 44.86 bkl Expert consensus regarding standardization of sample preparation for clotting time assays Clotting time assay (dpeaa)DE-He213 Plasma sample (dpeaa)DE-He213 Centrifugation condition (dpeaa)DE-He213 Sample store condition (dpeaa)DE-He213 |
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Ieko, Masahiro Komiyama, Yutaka Yamazaki, Satoshi Katagiri, Hisako Shimazu, Chisato Naito, Sumiyoshi Matsuda, Masato Yuki, Yoichi Miyata, Kazuyoshi Arai, Rika Kumano, Osamu Emmi, Mari Yoshida, Tatsuya Tanaka, Hideaki Okuhara, Toshihiko Yamashita, Tetsuji Sekine, Yasuji Homma, Masaru Kawai, Yohko Tohyama, Kaoru |
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expert consensus regarding standardization of sample preparation for clotting time assays |
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Expert consensus regarding standardization of sample preparation for clotting time assays |
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Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. (4) After the plasma sample is prepared, it should be stored at room temperature and assayed within 4 h. |
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Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. (4) After the plasma sample is prepared, it should be stored at room temperature and assayed within 4 h. |
| abstract_unstemmed |
Abstract Accurate clotting time assay results are vital, as the test is employed to indicate the amount of oral anticoagulant to be prescribed, while it is also used for screening the hemorrhagic and thrombotic diseases. The procedure chosen for preparation of a patient blood sample including centrifugation can contribute to significant differences in the results obtained. Thus, for the purpose of proposing a standardized method to appropriately prepare blood samples prior to assay, the Japanese Society of Laboratory Hematology organized the Working Group for Standardization of Sample Preparation for Clotting Time Assays (WG). Following reviews of previously announced guidelines and original experimental results, consensus was obtained by the WG, with the main findings as follows. (1) The recommended anticoagulant in the blood collection tube is sodium citrate solution at 0.105–0.109 M (3.13–3.2%). (2) Whole blood samples should be stored at room temperature (18–25 ˚C) within 1 h of collection from the patient. (3) For plasma preparation, centrifugation at 1500 × g should be performed for at least 15 min or at 2000 × g for at least 10 min at room temperature. (4) After the plasma sample is prepared, it should be stored at room temperature and assayed within 4 h. |
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