Within-subject biological variation of activated partial thromboplastin time, prothrombin time, fibrinogen, factor VIII and von Willebrand factor in pregnant women

被引:15
作者
Kristoffersen, Ann Helen [1 ,2 ]
Petersen, Per Hyltoft [2 ]
Bjorge, Line [3 ,4 ]
Roraas, Thomas [2 ]
Sandberg, Sverre [2 ,5 ,6 ]
机构
[1] Haukeland Hosp, Helse Bergen HF, Lab Clin Biochem, PB 1400, N-5021 Bergen, Norway
[2] Haraldsplass Deaconess Hosp, Norwegian Qual Improvement Lab Examinat Noklus, Bergen, Norway
[3] Univ Bergen, Ctr Canc Biomarkers CCBIO, Dept Clin Sci, Bergen, Norway
[4] Haukeland Hosp, Dept Gynecol & Obstet, Bergen, Norway
[5] Haukeland Hosp, Lab Clin Biochem, Bergen, Norway
[6] Univ Bergen, Dept Global Publ Hlth & Primary Care, Bergen, Norway
关键词
biological variation; blood coagulation tests; haemostasis; multiples of median; pregnancy; DISSEMINATED INTRAVASCULAR COAGULATION; REFERENCE CHANGE VALUES; MENSTRUAL BLOOD-LOSS; POSTPARTUM HEMORRHAGE; HEMOSTATIC CHANGES; REFERENCE INTERVALS; CLINICAL-CHEMISTRY; CRITICAL-APPRAISAL; PROTEIN-S; D-DIMER;
D O I
10.1515/cclm-2017-1220
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: During pregnancy, interpretation of results from coagulation parameters can be difficult as the physiological changes that occur may affect the biochemical parameters. The aim of this study was to describe the normal course of five coagulation parameters in healthy pregnancies, and to estimate the within-subject biological variation (CVI). Methods: Blood samples were obtained every 4th week during pregnancy and three samples after delivery in 20 healthy women and every 4th week during a 40-week period in 19 healthy non-pregnant women. Activated partial thromboplastin time (APTT), prothrombin time (PT), PT International Normalized Ratio (INR), fibrinogen, factor VIII clot (FVIII: C) and von Willebrand factor antigen (vWF: Ag) were analyzed. The physiological changes during pregnancy were compensated by transformation into multiples of the median (MoM) and it is natural logarithm (lnMoM) in order to establish a kind of steady state, and CVI was calculated from the standard deviation. Results: During pregnancy, APTT, PT and INR remained unchanged or decreased, depending upon the reagent used, while fibrinogen, FVIII: C and vWF: Ag increased gradually until delivery. The CVI in pregnancy were 2.2 and 3.0% for APTT, 2.3 and 2.6% for PT, 2.2 and 2.3% for INR, 7.2% for fibrinogen, 12.2% for FVIII: C and 11.3% for vWF: Ag, and corresponded with the CVI in non-pregnant women. Conclusions: Transformation of coagulation parameters in healthy pregnancies to MoM is a tool to establish a kind of steady state. Although there is a physiological change in these coagulation parameters during pregnancy, the CVI after lnMoM transformation was comparable with the CVI of non-pregnant women.
引用
收藏
页码:1297 / 1308
页数:12
相关论文
共 49 条
[1]   The Biological Variation Data Critical Appraisal Checklist: A Standard for Evaluating Studies on Biological Variation [J].
Aarsand, Aasne K. ;
Roraas, Thomas ;
Fernandez-Calle, Pilar ;
Ricos, Carmen ;
Diaz-Garzon, Jorge ;
Jonker, Niels ;
Perich, Carmen ;
Gonzalez-Lao, Elisabet ;
Carobene, Anna ;
Minchinela, Joana ;
Coskun, Abdurrahman ;
Simon, Margarita ;
Alvarez, Virtudes ;
Bartlett, William A. ;
Fernandez-Fernandez, Pilar ;
Boned, Beatriz ;
Braga, Federica ;
Corte, Zoraida ;
Aslan, Berna ;
Sandberg, Sverre .
CLINICAL CHEMISTRY, 2018, 64 (03) :501-514
[2]  
Altman D.G., 1994, Practical statistics for medical research
[3]  
[Anonymous], Desirable Specifications for Total Error, Imprecision, and Bias, derived from intraand inter-individual biologic variation
[4]  
[Anonymous], 1983, World Health Organization Technical Report Series, V687, P1
[5]   Biological Variation in Tests of Hemostasis (vol 34, pg 635, 2008) [J].
Banfi, Giuseppe ;
Del Fabbro, Massimo .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2009, 35 (01) :119-126
[6]   A checklist for critical appraisal of studies of biological variation [J].
Bartlett, William A. ;
Braga, Federica ;
Carobene, Anna ;
Coskun, Abdurrahman ;
Prusa, Richard ;
Fernandez-Calle, Pilar ;
Roraas, Thomas ;
Jonker, Neils ;
Sandberg, Sverre .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2015, 53 (06) :879-885
[7]  
Bliss CI., 1967, STAT BIOL STAT METHO, VI, P239
[8]   A diagnostic approach to mild bleeding disorders [J].
Boender, J. ;
Kruip, M. J. H. A. ;
Leebeek, F. W. G. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2016, 14 (08) :1507-1516
[9]   The responsiveness of different APTT reagents to mild factor VIII, IX and XI deficiencies [J].
Bowyer, A. ;
Kitchen, S. ;
Makris, M. .
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2011, 33 (02) :154-158
[10]   Haemostatic changes in pregnancy [J].
Bremme, KA .
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2003, 16 (02) :153-168