How to interpret and pursue a prolonged quick time orAPTT

被引:0
作者
Clauser, S. [1 ,2 ]
Calmette, L. [1 ]
机构
[1] Hop Ambroise Pare, AP HP, Serv Hematol Immunol Transfus, 9 Ave Charles De Gaulle, F-92104 Boulogne Billancourt, France
[2] Univ Versailles St Quentin En Yvelines, UFR Sci Sante Simone Veil, 2 Ave Source De la Bievre, F-78180 Montigny Le Bretonneux, France
来源
REVUE DE MEDECINE INTERNE | 2024年 / 45卷 / 09期
关键词
Quick time; APTT; Interpretation; Orientation; Tests; Hemostasis; RARE COAGULATION DISORDERS; ANTIPHOSPHOLIPID SYNDROME; LUPUS ANTICOAGULANT; BLEEDING DISORDER; LIVER-DISEASE; FACTOR-VII; CLASSIFICATION; DEFICIENCY; MANAGEMENT; HYPOPROTHROMBINEMIA;
D O I
10.1016/j.revmed.2024.05.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The standard hemostasis workup [quick time (QT), and activated partial thrombin time (APTT)] is very commonly prescribed but its interpretation is often difficult for practitioners who are not specialized in hemostasis. Here, we review the principles of the diagnostic approach to these tests. Only a very basic knowledge of the coagulation cascade is necessary to identify which clotting factor tests to prescribe and to interpret the results. Deficiency in several clotting factors suggests liver dysfunction, disseminated intravascular coagulation (DIC) or vitamin K deficiency. If a single factor is deficient, we review the different causes of acquired deficiencies and briefly discuss the characteristics of the different congenital defects, which generally require specialized management. Lupus anticoagulant is a common and generally benign cause of prolonged APTT to be aware of, which is not related to a hemorrhagic risk. A good knowledge of the diagnostic approach to abnormal QT or APTT generally allows the resolution of the most common situations. (c) 2024 The Author(s). Published by Elsevier Masson SAS on behalf of Socie<acute accent>te<acute accent> Nationale Franc,aise , aise de Me<acute accent>decine Interne (SNFMI). This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:549 / 558
页数:10
相关论文
共 51 条
  • [1] Rare bleeding disorder registry: Deficiencies of factors II, V, VII, X, XIII fibrinogen and dysfibrinogenemias
    Acharya, SS
    Coughlin, A
    DiMichele, DM
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (02) : 248 - 256
  • [2] Disseminated intravascular coagulation: epidemiology, biomarkers, and management
    Adelborg, Kasper
    Larsen, Julie B.
    Hvas, Anne-Mette
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2021, 192 (05) : 803 - 818
  • [3] French National Diagnostic and Care Protocol for antiphospholipid syndrome in adults and children
    Amoura, Z.
    Bader-Meunier, B.
    Sollier, C. Bal Dit
    Belot, A.
    Benhamou, Y.
    Bezanahary, H.
    Cohen, F.
    Costedoat-Chalumeau, N.
    Darnige, L.
    Drouet, L.
    Elefant, E.
    Harroche, A.
    Lambert, M.
    Martin, T.
    Martin-Toutain, I.
    Mathian, A.
    Mekinian, A.
    De Chambrun, M. Pineton
    de Pontual, L.
    Wahl, D.
    Yelnik, C.
    Zuilyr, S.
    Clouscard, J.
    Frere, C.
    Hachulla, E.
    Kone-Paut, I.
    Lasne, D.
    Lecompte, T.
    Le Guern, V.
    Zard, J. Ni
    Papo, T.
    Riviere, M.
    Schleinitz, N.
    Tossier, B.
    [J]. REVUE DE MEDECINE INTERNE, 2023, 44 (09): : 495 - 520
  • [4] Influence of factor XII deficiency on activated partial thromboplastin time (aPTT) in critically ill patients
    Bachler, Mirjam
    Niederwanger, Christian
    Hell, Tobias
    Hoefer, Judith
    Gerstmeyr, Dominic
    Schenk, Bettina
    Treml, Benedikt
    Fries, Dietmar
    [J]. JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 2019, 48 (03) : 466 - 474
  • [5] Prospective validation of the International Society of Thrombosis and Haemostasis scoring system for disseminated intravascular coagulation
    Bakhtiari, K
    Meijers, JCM
    de Jonge, E
    Levi, M
    [J]. CRITICAL CARE MEDICINE, 2004, 32 (12) : 2416 - 2421
  • [6] 2023 ACR/EULAR Antiphospholipid Syndrome Classification Criteria
    Barbhaiya, Medha
    Zuily, Stephane
    Naden, Ray
    Hendry, Alison
    Manneville, Florian
    Amigo, Mary-Carmen
    Amoura, Zahir
    Andrade, Danieli
    Andreoli, Laura
    Artim-Esen, Bahar
    Atsumi, Tatsuya
    Avcin, Tadej
    Belmont, Michael H.
    Bertolaccini, Maria Laura
    Branch, D. Ware
    Carvalheiras, Graziela
    Casini, Alessandro
    Cervera, Ricard
    Cohen, Hannah
    Costedoat-Chalumeau, Nathalie
    Crowther, Mark
    de Jesus, Guilherme
    Delluc, Aurelien
    Desai, Sheetal
    De Sancho, Maria
    Devreese, Katrien M.
    Diz-Kucukkaya, Reyhan
    Duarte-Garcia, Ali
    Frances, Camille
    Garcia, David
    Gris, Jean-Christophe
    Jordan, Natasha
    Leaf, Rebecca K.
    Kello, Nina
    Knight, Jason S.
    Laskin, Carl
    Lee, Alfred, I
    Legault, Kimberly
    Levine, Steve R.
    Levy, Roger A.
    Limper, Maarten
    Lockshin, Michael D.
    Mayer-Pickel, Karoline
    Musial, Jack
    Meroni, Pier Luigi
    Orsolini, Giovanni
    Ortel, Thomas L.
    Pengo, Vittorio
    Petri, Michelle
    Pons-Estel, Guillermo
    [J]. ARTHRITIS & RHEUMATOLOGY, 2023, 75 (10) : 1687 - 1702
  • [7] Haemophilia in France: Modelisation of the Clinical Pathway for Patients
    Beny, Karen
    du Sartz de Vigneulles, Benjamin
    Carrouel, Florence
    Bourgeois, Denis
    Gay, Valerie
    Negrier, Claude
    Dussart, Claude
    [J]. INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2022, 19 (02)
  • [8] Haemophilia
    Berntorp, Erik
    Fischer, Kathelijn
    Hart, Daniel P.
    Mancuso, Maria Elisa
    Stephensen, David
    Shapiro, Amy D.
    Blanchette, Victor
    [J]. NATURE REVIEWS DISEASE PRIMERS, 2021, 7 (01)
  • [9] ORTHOTOPIC LIVER-TRANSPLANTATION IN FULMINANT AND SUBFULMINANT HEPATITIS - THE PAUL-BROUSSE EXPERIENCE
    BISMUTH, H
    SAMUEL, D
    CASTAING, D
    ADAM, R
    SALIBA, F
    JOHANN, M
    AZOULAY, D
    DUCOT, B
    CHICHE, L
    [J]. ANNALS OF SURGERY, 1995, 222 (02) : 109 - 119
  • [10] Acquired von Willebrand syndrome: A case series of nine patients and literature review
    Boissier, E.
    Darnige, L.
    Dougados, J.
    Arlet, J. -B.
    Dupeux, S.
    Georgin-Lavialle, S.
    Caron, C.
    Tapon-Bretaudiere, J.
    Pouchot, J.
    Ranque, B.
    [J]. REVUE DE MEDECINE INTERNE, 2014, 35 (03): : 154 - 159