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Tytuł pozycji:

A single-institution retrospective study of causes of prolonged prothrombin time and activated partial thromboplastin time in the outpatient setting.

Tytuł:
A single-institution retrospective study of causes of prolonged prothrombin time and activated partial thromboplastin time in the outpatient setting.
Autorzy:
Hazim AZ; Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Ruan GJ; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.
Khodadadi RB; Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota, USA.
Slusser JP; Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota, USA.
Marshall AL; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Pruthi RK; Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Źródło:
International journal of laboratory hematology [Int J Lab Hematol] 2022 Feb; Vol. 44 (1), pp. 209-215. Date of Electronic Publication: 2021 Oct 05.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: Oxford : Blackwell Scientific Publications, c2007-
MeSH Terms:
Ambulatory Care Facilities*
Partial Thromboplastin Time*/methods
Partial Thromboplastin Time*/standards
Prothrombin Time*/methods
Prothrombin Time*/standards
Blood Coagulation Disorders/*blood
Blood Coagulation Disorders/*diagnosis
Adult ; Aged ; Blood Coagulation Disorders/etiology ; Blood Coagulation Tests/methods ; Blood Coagulation Tests/standards ; Clinical Decision-Making ; Disease Management ; Female ; Humans ; Male ; Middle Aged ; Outpatients ; Reference Values ; Retrospective Studies
References:
Kamal AH, Tefferi A, Pruthi RK. How to interpret and pursue an abnormal prothrombin time, activated partial thromboplastin time, and bleeding time in adults. Mayo Clin Proc. 2007;82:864-873.
Thiruvenkatarajan V, Pruett A, Adhikary SD. Coagulation testing in the perioperative period. Indian J Anaesth. 2014;58:565-572.
van Veen JJ, Spahn DR, Makris M. Routine preoperative coagulation tests: an outdated practice? Br J Anaesth. 2011;106:1-3.
Kitchens CS. Prolonged activated partial thromboplastin time of unknown etiology: a prospective study of 100 consecutive cases referred for consultation. Am J Hematol. 1988;27:38-45.
Chng WJ, Sum C, Kuperan P. Causes of isolated prolonged activated partial thromboplastin time in an acute care general hospital. Singapore Med J. 2005;46:450-456.
Rodeghiero F, Tosetto A, Abshire T, et al. ISTH/SSC joint VWF and Perinatal/Pediatric Hemostasis Subcommittees Working Group. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders. J Thromb Haemost. 2010;8(9):2063-2065. https://doi.org/10.1111/j.1538-7836.2010.03975.x.
Verbruggen B, Novakova I, Wessels H, Boezeman J, van den Berg M, Mauser-Bunschoten E. The Nijmegen modification of the Bethesda assay for factor VIII: C inhibitors: improved specificity and reliability. Thromb Haemost. 1995;73:247-251.
Barnes GD, Lucas E, Alexander GC, Goldberger ZD. National trends in ambulatory oral anticoagulant use. Am J Med. 2015;128(12):1300-1305.e2.
Herrmann FH, Wulff K, Auerswald G, et al. Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene. Haemophilia. 2009;15:267-280.
Liu J, Li F, Shu K, et al. The analysis of false prolongation of the activated partial thromboplastin time (activator: silica): Interference of C-reactive protein. J Clin Lab Anal. 2018;32(8):e22571. https://doi.org/10.1002/jcla.22571.
Contributed Indexing:
Keywords: Congenital factor deficiency; acquired factor deficiency; anticoagulation; liver disease; vitamin K deficiency
Entry Date(s):
Date Created: 20211006 Date Completed: 20220204 Latest Revision: 20220204
Update Code:
20240104
DOI:
10.1111/ijlh.13727
PMID:
34612006
Czasopismo naukowe
Introduction: An algorithmic approach, termed the prolonged clot time profile (PROCT), consisting of initial screening with prothrombin time (PT) and activated partial thromboplastin time (aPTT), reflexive mixing studies if indicated, and follow-up assays depending on initial testing results, offers an efficient approach to delineate the etiology of a prolonged PT/aPTT. Herein, we present the outcomes of the PROCT in the outpatient setting.
Methods: In this retrospective study, we reviewed medical records of consecutive outpatients who had prolonged PT and/or aPTT noted in the routine coagulation laboratory and who had PROCT ordered in our institutional Special Coagulation Laboratory between 2010 and 2017.
Results: One hundred and six patients, median age 55 years (IQR 30-67), met our study criteria. Twenty-nine patients had normal PT/aPTT, while 77 had persistent abnormalities and underwent reflexive testing. A prolonged PT, aPTT, or PT and aPTT was noted in 27 (35%), 27 (35%), and 23 (30%) respectively. Forty-nine (64%) had an acquired condition, 17 (22%) had a congenital condition, 7 (9%) had unclear etiology, and 4 (5%) were the result of laboratory artifact. The most common known cause of an isolated prolonged PT in our study was vitamin K deficiency in 8 (10%), the most common cause of an isolated prolonged aPTT was lupus anticoagulant in 4 (5%), and the most common cause of prolonged PT and aPTT was liver disease in 11 (14%).
Conclusion: Prolonged PT/aPTT have a wide range of causes, including artifactual prolongation or abnormalities in secondary hemostasis due to both inherited and acquired conditions.
(© 2021 John Wiley & Sons Ltd.)
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