Keywords
centrifugation - automation - laboratory/instrumentation - laboratory/methods - laboratory/standards
- blood coagulation tests
Introduction
Total laboratory automation (TLA) is seen as an important strategy to tackle today's
challenges in laboratory medicine and related health care.[1]
[2]
[3]
[4]
[5]
[6] Integrating diverse analyzers of multiple specialities as well as preanalytic and
sorting modules to one track can replace many manual tasks and save labor.[4]
[5]
[7] TLA can save a relevant amount of long-term health care costs despite high initial
investments.[8] The efficiency can be improved by reducing the turnaround time (TAT) and increasing
the throughput.[9]
[10] Risky and laborious manual sample management can be avoided by algorithms identifying
samples and triggering rerun or reflex tests, thus improving accuracy of results.[4] Controlling all phases of the analytical process using software programs run centrally
enhances standardization, supports accreditation procedures, and improves quality
in general.[4] One important requirement for the integration of analyzers and specialities into
TLA is uniform and ideally rapid centrifugation schemes. This might prevent delay
of samples on the track and improve total TAT.
It is however uncertain whether rapid centrifugation schemes—used in clinical chemistry
as well as immunochemistry—can be applied in the hemostasis laboratory. Coagulation-based
assays are considered to be influenced by many preanalytic factors.[11] The residual platelet count after centrifugation is regarded as the most important
influencing factor[12] and the platelet count is subject to the centrifugal forces applied.[13] Mechanical stimulation is discussed as a contributing factor as well.[14] Some authors recommend avoiding centrifugal forces above 1,500 × g
[15] but others do not.[16]
[17] Several scientific societies in the United States (Clinical and Laboratory Standards
Institute [CLSI][18]), France (Groupe d'Etude sur l'Hémostase et la Thrombose[19]), and the United Kingdom (British Committee for Standards in Haematology[20]) as well as other authors[11] have released guidance documents and recommend centrifugation schemes that aim to
achieve a platelet count below 10 × 10^9/L using 1,500 × g for 10 to 15 minutes. Whether this can be accelerated using higher centrifugal forces
remains unclear. Limitations of previous investigations include (1) a limited number
of patients or samples, (2) a paucity of hemostasis tests studied, (3) a very limited
spectrum of test results covered (normal only), (4) nonstandard centrifugation schemes
as comparators, and (5) use of insensitive statistical measures.
With the present study, we aimed to comprehensively assess the accuracy of a rapid,
high-speed centrifugation scheme compared with an established and recommended centrifugation
scheme in a comprehensive set of hemostasis tests, covering a large spectrum of values,
and using meaningful statistical measures.
Methods
Study Design, Setting, and Population
This prospective cohort study was conducted in a university hospital (Inselspital,
Bern University Hospital, Bern, Switzerland) between October 2015 and March 2016.
We included consecutive patients from a variety of departments (cardiovascular surgery,
internal medicine, intensive care unit, and hemophilia outpatient unit). The inclusion
criterion was “suspected abnormal hemostasis laboratory test result” to obtain a sample
set covering a broad spectrum of results. Exclusion criteria were an age below 18
years and refused general consent. Patients were screened by treating physicians in
the respective departments. The protocol was approved by the local ethics committee
(Kantonale Ethikkommission Bern; March 18, 2014) and all patients signed the general
consent of the hospital.
Collection and Handling of Samples
An in-house protocol for blood drawing was implemented at our institution to ensure
adequate preanalytic conditions.[18] Plasma samples were collected after ethylenediaminetetraacetic acid (EDTA) and serum
samples to avoid contamination with residual heparin or tissue factor if blood was
accidentally obtained from a vascular access device or using a butterfly needle.[12]
[19]
[21] Venous blood was drawn into two plastic syringes of 4.5 mL containing 0.106 mol/L
trisodium citrate (Monovette, Sarstedt, Nümbrecht, Germany). Samples were transported
immediately to the central laboratory and the handling of both samples was identical.
Centrifugation Schemes
Both plasma samples were centrifuged within 15 minutes after arrival in the laboratory.
The established standard centrifugation scheme in our institution was 1,500 × g for 10 minutes (established after determining residual platelet count in 30 samples).[11]
[19]
[20] The high-speed centrifugation scheme was defined as 3,137 × g for 7 minutes (3,137 × g is the established speed in clinical chemistry at our institution and the time of
7 minutes was chosen after conducting a pilot study analyzing residual platelet concentration).
Z500 centrifuges were used (HERMLE Labortechnik GmbH, Wehingen, Germany), implemented
in a GLP laboratory track (GLP Systems GmbH, Hamburg, Germany). The centrifuges work
at 20°C using a brake. After centrifugation, samples were transferred into aliquots
and snap-frozen at –20°C. Samples were transferred to –80°C if not analyzed within
1 to 2 weeks. All hemostasis parameters were determined within 2 months following
centrifugation.
Determination of Laboratory Assays
Platelet count was analyzed using an automated hematology analyzer (Coulter Counter
LH750, Beckman-Coulter Inc., Nyon, Switzerland). Prothrombin time was measured using
Dade Innovin reagent (Siemens Healthcare Diagnostics Products GmbH, Marburg, Germany)
on a Sysmex CS 5100 analyzer (distributed by Siemens Healthcare Diagnostics Products
GmbH) and expressed as prothrombin ratio (PR, %). Activated partial thromboplastin
time (aPTT) was determined using Pathrombin SL (Siemens Healthcare Diagnostics Products
GmbH) on a Sysmex CS 5100. Thrombin time was determined using Thromboclotin reagent
(Siemens Healthcare Diagnostics Products GmbH) on a Sysmex CS 5100. D-dimers were
measured immunoturbidimetrically by Innovance D-Dimer (Siemens Healthcare Diagnostics
Products GmbH) on a Sysmex CS 5100. Functional antithrombin activity was determined
using INNOVANCE Antithrombin (Siemens Healthcare Diagnostics Products GmbH) on a Sysmex
CS 5100. Fibrinogen was assessed in plasma by the Clauss method using Dade Thrombin
Reagent (Siemens Healthcare Diagnostics Products GmbH) on a Sysmex CS 5100. Factor
(F)II, FV, FVII, and FX were measured by a one-stage coagulometric assay using Dade
Innovin and factor-deficient plasma (Siemens Healthcare Diagnostics Products GmbH)
on a Sysmex CS 5100. FVIII, FIX, and FXI were determined using a one-stage coagulometric
assay using Pathrombin SL and factor-deficient plasma on a Siemens BCS XP analyzer
(Siemens Healthcare Diagnostics Products GmbH). FXIII was analyzed chromatographically
using Berichrom Factor XIII test kit (Siemens Healthcare Diagnostics Products GmbH)
on a Siemens BCS XP. von Willebrand factor antigen (VWF:Ag) was determined using the
VWF Ag Testkit (Siemens Healthcare Diagnostics Products GmbH) and activity (VWF:GPIbM)
using Siemens Innovance VWF Ac (Siemens Healthcare Diagnostics Products GmbH). Chromogenic
anti-Xa activity for monitoring unfractionated heparin (UFH) as well as low molecular
weight heparin (LMWH) was determined using BIOPHEN Heparin LRT (HYPHEN BioMed, Neuville-sur-Oise,
France) on a Sysmex CS 5100.
To contextualize these measurements, we determined the within-run and day-to-day imprecision
in two samples (one with results in the normal range [n] and one with results in the
abnormal range [p]), 10 times each.
Statistical Analysis
Median (interquartile range, IQR) and numbers (percentages) were used for descriptive
purposes. To analyze concordance between the two centrifugation schemes, we determined
the Spearman's rank correlation coefficient as well as the coverage probability (CP
π). The CP π outlines agreement with several advantages compared with more traditional
measures: the computation is simple, discordant measurements can be identified rapidly,
the interpretation is intuitive, and it can be applied to continuous as well as categorical
data in a broad spectrum of observers and populations.[22] The CP π can be interpreted as the proportion of observations falling within the
paired absolute difference κ, a priori defined as acceptable (the tolerable total
deviation index, TDI). In our study, we defined a TDI of 0.15 as acceptable. The tolerable
CP π was assumed at 0.9. Bland–Altman difference plots for determination of bias as
well as lower and higher limits of agreement were additionally created. Coefficients
of variation were calculated for within-run and day-to-day imprecision. Analyses were
restricted to observations in a meaningful range: PR, 0 to 110%; international normalized
ratio (INR), 0.9 to 5.0; thrombin time, 10 to 70 seconds; aPTT, 15 to 100 seconds;
fibrinogen, 0 to 6.0 g/L; D-dimer, 0 to 2,000 µg/L; antithrombin, 0 to 120%; FII,
FV, FVII, FX: 0 to 120%; FVIII, FIX, FXI, FXIII: 0 to 200%; and VWF:GPIbM and VWF:Ag:
0 to 200%. In addition, LMWH measurements below 0.1 U/mL and D-dimer below 400 U/mL
were censored for CP measurements. The Stata 14.1 statistics software package (StataCorp.
2015; Stata Statistical Software: Release 14.2, StataCorp LP, College Station, Texas,
United States) as well as R (R Development Core Team [2008]; R: A language and environment
for statistical computing; R Foundation for Statistical Computing, Vienna, Austria;
ISBN 3–900051–07–0, http://www.R-project.org) were used for statistical analyses. Figures were created using Prism 6 (GraphPad
Software, Inc., La Jolla, California, United States).
Results
Patients
Samples from 198 patients were analyzed, the flow is illustrated in [Fig. 1]. Seventy-four patients were recruited from hematology outpatient unit (37%), 51
patients from intensive care unit (26%), 48 patients from general internal medicine
(24%), and 25 patients from the surgery department (13%). The median age of the patients
was 56.0 years (range: 19.7–94.4) and 47.5% were female (n = 94). The number of observations per test is shown in [Table 1]. The range of values is reported in [Table 1], the distribution is illustrated in scatterplots ([Supplementary Figs. S1]–[S3], available in the online version).
Fig. 1 Sample flow.
Table 1
Concordance results of routine hemostasis measurements obtained with a rapid, high-speed
centrifugation scheme in comparison to a traditional scheme
|
Parameter
|
Obs.
|
Results
|
Correlation coefficient
|
Coverage probability π[a]
|
Bland–Altman difference plot
|
Analytical variability[b]
|
|
|
|
r
s
|
|
Bias
|
LLA
|
HLA
|
Within-run imprecision
|
Day-to-day imprecision
|
|
Numbers
|
Median (range)
|
(95% CI)
|
(95% CI)
|
(95% CI)
|
|
|
(CV in %)
|
(CV in %)
|
|
PR (%)
|
125
|
78.5
(6.6, 107.8)
|
0.99
(0.98, 0.99)
|
0.99
(0.84, 1.00)
|
0.2
(–0.3, 0.7)
|
–5.6
|
6.0
|
0.6 (n)
0.8 (p)
|
4.0 (n)
2.2 (p)
|
|
INR
|
146
|
1.04
(0.9, 3.5)
|
0.99
(0.99, 0.99)
|
1.00
(0.96, 1.00)
|
0.0
(–0.0, 0.0)
|
–0.2
|
0.2
|
0.7 (n)
0.9 (p)
|
4.2 (n)
2.4 (p)
|
|
Thrombin time (s)
|
105
|
16.5
(13.2, 57.3)
|
0.97
(0.95, 0.98)
|
1.00
(1.00, 1.00)
|
–0.1
(–0.3, 0.0)
|
–1.6
|
1.4
|
2.0 (n)
2.9 (p)
|
2.2 (n)
2.6 (p)
|
|
aPTT (s)
|
119
|
34.9
(22.0, 96.0)
|
0.99
(0.99, 0.99)
|
1.00
(1.00, 1.00)
|
0.0
(–0.2, 0.2)
|
–2.1
|
2.1
|
0.6 (n)
1.1 (p)
|
1.8 (n)
6.7 (p)
|
|
Fibrinogen (g/L)
|
125
|
2.3
(0.0, 5.8)
|
0.98
(0.97, 0.99)
|
0.96
(0.91, 0.99)
|
–0.0
(–0.0, 0.0)
|
–0.3
|
0.3
|
1.2 (n)
1.1 (p)
|
3.2 (n)
6.0 (p)
|
|
D-dimer (µg/L)
|
34
|
395
(17, 1970)
|
0.99
(0.99, 1.00)
|
1.00
(0.99, 1.00)
|
13.4
(3.5, 23.4)
|
–43.4
|
70.3
|
12.0 (n)
2.0 (p)
|
3.0 (n)
2.0 (p)
|
|
Antithrombin (%)
|
31
|
76.6
(40.4, 108.5)
|
0.99
(0.99, 1.00)
|
1.00
(0.99, 1.00)
|
0.2
(–0.7, 1.1)
|
–4.7
|
5.1
|
1.3 (n)
2.8 (p)
|
1.1 (n)
2.2 (p)
|
|
Anti-Xa activity
(UFH; U/mL)
|
30
|
0.10
(0.01, 0.92)
|
0.99
(0.98, 1.00)
|
0.94
(0.86, 0.99)
|
0.00
(–0.01, 0.01)
|
–0.03
|
0.03
|
2.1 (p)
|
3.8 (p)
|
|
Anti-Xa activity (LMWH; U/mL)
|
27
|
0.06
(0.00, 0.51)
|
0.99
(0.97, 0.99)
|
0.93
(0.77, 1.00)
|
0.00
(–0.01, 0.01)
|
–0.03
|
0.03
|
1.7 (p)
|
5.9 (p)
|
|
Factor II (%)
|
69
|
84.0
(16.0, 119.0)
|
0.97
(0.96, 0.98)
|
0.95
(0.81, 1.00)
|
0.6
(–0.6, 1.8)
|
–9.2
|
10.4
|
1.4 (n)
1.9 (p)
|
1.8 (n)
6.9 (p)
|
|
Factor V (%)
|
64
|
85.0
(0.0, 120.0)
|
0.92
(0.86, 0.95)
|
0.41
(0.20, 0.65)
|
–1.6
(–4.3, 1.1)
|
–23.3
|
20.2
|
2.2 (n)
2.4 (p)
|
4.1 (n)
5.2 (p)
|
|
Factor VII (%)
|
64
|
65.3
(15.0, 120.0)
|
0.95
(0.92, 0.97)
|
0.57
(0.36, 0.84)
|
–1.1
(–3.2, 0.9)
|
–17.5
|
15.3
|
1.6 (n)
3.4 (p)
|
2.9 (n)
3.3 (p)
|
|
Factor X (%)
|
67
|
75.1
(5.0, 118.8)
|
0.95
(0.91, 0.97)
|
0.60
(0.46, 0.74)
|
–0.4
(–2.4, 1.7)
|
–17.2
|
16.5
|
1.9 (n)
1.4 (p)
|
3.0 (n)
5.6 (p)
|
|
Factor VIII (%)
|
55
|
79.5
(0.3, 198.0)
|
0.96
(0.93, 0.98)
|
0.30
(0.21, 0.38)
|
–17.5
(–22.3, –12.7)
|
–53.0
|
17.9
|
2.8 (n)
2.3 (p)
|
5.5 (n)
4.0 (p)
|
|
Factor IX (%)
|
37
|
104.0
(15.0, 138.0)
|
0.84
(0.70, 0.91)
|
0.79
(0.61, 0.90)
|
–0.9
(–4.5, 2.7)
|
–22.5
|
20.7
|
1.9 (n)
2.1 (p)
|
3.3 (n)
6.2 (p)
|
|
Factor XI (%)
|
35
|
96.0
(47.0, 163.0)
|
0.79
(0.61, 0.89)
|
0.80
(0.68, 0.90)
|
–1.3
(–4.8, 2.2)
|
–21.6
|
19.0
|
3.1 (n)
1.8 (p)
|
2.6 (n)
7.3 (p)
|
|
Factor XIII (%)
|
20
|
110.5
(15.1, 162.0)
|
0.96
(0.89, 0.98)
|
0.96
(0.82, 0.99)
|
–2.5
(–5.9, 1.0)
|
–17.0
|
12.1
|
3.2 (n)
2.0 (p)
|
5.6 (n)
3.8 (p)
|
|
VWF:Ag (%)
|
25
|
87.0
(12.0, 191.3)
|
0.99
(0.97, 0.99)
|
0.96
(0.83, 0.99)
|
–1.2
(–2.9, 0.5)
|
–9.4
|
7.0
|
1.7 (n)
2.4 (p)
|
1.9 (n)
4.1 (p)
|
|
VWF:GPIbM (%)
|
27
|
84.0
(7.0, 178.9)
|
0.98
(0.95, 0.99)
|
0.76
(0.59, 0.89)
|
–3.8
(–6.6, –1.0)
|
–18.1
|
10.4
|
1.7 (n)
1.6 (p)
|
2.2 (n)
2.7 (p)
|
Abbreviations: aPTT, activated partial thromboplastin time; CV, coefficient of variation;
HLA, higher limit of agreement; INR, international normalized ratio; LLA, lower limit
of agreement; LMWH, low molecular weight heparin; Obs., observations; PR, prothrombin
ratio; r
s, Spearman's rank correlation coefficient; UFH, unfractionated heparin; VWF:Ag, von
Willebrand factor antigen; VWF:GPIbM, von Willebrand factor functional activity as
measured using the spontaneous binding of VWF to a gain-of-function mutant GPIb fragment.
a Based on an accepted total deviation index of 0.15.
b Obtained in two samples, one with results in the normal range [n] and one with results
in the abnormal range [p], 10 times each.
Platelet count
The median platelet count in plasma after centrifugation with 3,137 × g for 7 minutes was 8 × 10^9/L (IQR: 4–12 × 10^9/L; n = 30). Platelet count was 6 × 10^9/L (IQR: 3–9; n = 30) in samples centrifuged at 1,500 × g for 10 minutes.
Concordance between Centrifugation Schemes
All results are reported in detail in [Table 1]. Scattergrams of PR, aPTT, fibrinogen, and D-dimer are shown as an example in [Fig. 2]. Scattergrams and Bland–Altman difference plots for all tests are shown in [Supplementary Figs. S1]–[S3] (available in the online version). [Fig. 3] summarizes the accuracy of all tests and contrasts r
s to CP estimates.
Fig. 2 Concordance of routine hemostasis measurements obtained with a rapid, high-speed
centrifugation scheme in comparison to a traditional scheme. Scattergrams of prothombin
ratio (PR, %), activated partial thromboplastin time (aPTT, seconds), fibrinogen (Clauss
method; g/L), and D-dimer (µg/L) are shown as an example, all other results are shown
in the [Supplementary Material]. Spearman's rank correlation coefficient (r
s) is reported.
Fig. 3 Accuracy of routine hemostasis measurements obtained with a rapid, high-speed centrifugation
scheme. Spearman's rank correlation coefficient (r
s) is contrasted to the coverage probability (CP π) at a given acceptable total deviation index κ of 0.15. The acceptable r
s was set at 0.95, and the acceptable CP π at 0.9. aPTT, activated partial thromboplastin time; INR, international normalized
ratio; LMWH, low molecular weight heparin; PR, prothrombin ratio; UFH, unfractionated
heparin; VWF:Ag, von Willebrand factor antigen; VWF:GPIbM, von Willebrand factor activity.
With regard to the routine parameters PT, INR, thrombin time, and aPTT, correlation (r
s) was clearly above 0.95 and CP π above 0.9 ([Table 1]). Bias and limits of agreement of the Bland–Altman difference plot were close to
zero. Accordingly, coefficient of variation (CV) was below 5% with regard to within-run
and day-to-day imprecision (day-to-day imprecision of the abnormal sample: 6.7%).
Similar results were observed with regard to fibrinogen, D-dimer, and antithrombin activity measurements: r
s was above 0.95, CP π above 0.9, and Bland–Altman estimates close to zero. CV was
below 5% (except within-run imprecision of the normal D-dimer sample: 12.0%).
Anti-Xa activity measurements (UFH and LMWH) resulted in r
s above 0.95 and a CP π above 0.9 as well. Bland–Altman estimates were close to zero
and CV was below 5% (except day-to-day imprecision of LMWH-measurements: 5.9%).
Correlation (r
s) was above 0.95 and CP π above 0.9 for VWF:Ag but not for VWF:GPIbM (0.76; 95% confidence interval: 0.59–0.89). Accordingly, the lower limit of agreement
was –18.1, and the higher limit of agreement was 10 for VWF:GPIbM. Within-run as well as day-to-day imprecision was below 5%.
A borderline r
s was observed for FV (92%), FVII (95%), and FX (95%), the CP π was clearly below 0.9 (see [Table 1]). Accordingly, the agreement interval of the Bland–Altman plot was wide. With regard
to FII, r
s was 0.97 and CP π 0.95. Within-run as well as day-to-day imprecision was low (CV < 5%
for FVII, and < 10% for FII, FV, and FX).
In the case of FVIII, r
s was 0.96 but CP π was 0.30; r
s was below 0.95 and CP π below 0.9 in the case of FIX as well as FXI. The agreement interval of the Bland–Altman plot was wide ([Table 1]). Within-run as well as day-to-day imprecision was below 10%.
With regard to FXIII, r
s was 0.96 and CP π 0.96; CV was below 10%.
Discussion
In the present study, we tested the accuracy of measurements obtained with rapid,
high-speed centrifugation scheme studying a large spectrum of hemostasis tests and
covering the full range of values obtained in clinical practice. CP π identified more
assays with nonconcordant results than Spearman's correlation coefficient. Whereas
an appropriate concordance between measurements were observed for all routine parameters,
relevant discrepancies were observed with regard to most single-factor determinations
as well as VWF:GPIbM.
Our observations and data reported here are in line with the limited data published
to date on this topic. Lippi et al compared samples obtained in 15 healthy volunteers
and centrifuged with 3,000 × g versus 1,500 × g. Significant differences were found with regard to FVIII and IX, but not for PT,
aPTT, or fibrinogen.[13] Several routine tests (fibrinogen, INR, aPTT, D-dimer) as well as single factors
have also been studied (1,500 × g for 5 minutes vs. 3,000 × g for 7 minutes) in a limited number of patients with mostly normal test results and
a correlation coefficient of all routine tests as well as most factors studies was
above 0.9.[23] Suchsland et al have compared PT, aPTT, FVIII, and protein S in one versus two runs
of 3,280 × g for 5 minutes. The outcome of that work reported a correlation coefficient above
0.9 for all but protein S.[24] Boissier et al[17] compared a centrifugal spin protocol of 4,500 × g for 2 minutes to a 2,200 × g for 15 minutes protocol in 200 patients in the following assays PT, INR, aPTT, fibrinogen,
thrombin time, FII, FV, antithrombin, and anti-Xa activity.[17] These authors concluded that the agreement was adequate. We have also essentially
repeated the Boissier centrifugation protocols in samples of patients treated with
direct oral anticoagulations and measurements of anti-Xa activity, and we have arrived
at similar conclusions.[16] In another study, PT, aPTT, and INR measurements were compared in platelet-poor
plasma and platelet-rich plasma of 100 samples, and again found to be similar.[21]
Strengths and Limitations/Implications
In contrast to previous studies, we have studied a broad range of hemostasis tests
covering the full spectrum of test results in a large number of patients recruited
in clinical practice. In addition, an established centrifugation scheme was used,
and sensitive statistical measures were applied. Thus, our results are meaningful
and are applicable to routine clinical practice. Our study nevertheless has several
limitations. First, lupus anticoagulant and other tests used in clinical practice
were not studied, and our results can therefore not be extrapolated to these tests.
Second, even though our routine centrifugation scheme (1,500 × g for 10 minutes), which was used as comparator, was tested according to the CLSI guidelines,
most institutions are known to use a 15-minute scheme instead. We cannot fully exclude
that this might have affected our results. Third, only one centrifuge was tested,
and we have not excluded that different results might have been obtained using alternative
centrifuges. Thus, future investigations will seek to confirm our results in various
settings using different centrifuges as well. Forth, citrated samples were collected
after EDTA samples and we cannot fully exclude that residual EDTA might have influenced
the results. We believe that the risk of a bias is low because the tubes were applied
to the centrifugation schemes randomly and previous studies did not demonstrate a
relevant difference of standard coagulation test results.[25] Fifth, for reasons of practicability not all pairs of samples were analyzed within
the 2-week interval recommended by current guidelines but were transferred to a –80°C
freezer after several days and analyzed within 2 months. However, all pairs were handled
identically, and we do not think that this might have introduced any bias. In addition,
it might be argued that double centrifugation decreases preanalytical influences in
case of freezing. However, aiming to compare two different (single) centrifugation
schemes we did not apply double centrifugation for the purpose of this study. We do
not believe that this might have introduced any bias. Seventh, plasma pathologically
enriched with soluble fibrin might entrap VWF/FVIII by its complexes and technically
diminish these levels under low temperature conditions. The risk of a systematic bias
is low however, because both pairs of samples were treated identically.
We believe that our results add sufficient data on previous studies to justify rapid
centrifugation for routine hemostasis tests (PT, thrombin time, aPTT, fibrinogen,
D-dimer, antithrombin, and anti-Xa activity). Traditional centrifugation schemes shall
be used for all other tests. The problem of sample identification can be solved by
means of different adhesive labels (“routine” vs. “specialized hemostasis”) or by
means of laboratory automation procedures as done in our institution (samples with
certain tests requested will be put out of the laboratory track for “manual centrifugation”).
Conclusion
We tested the accuracy of measurements obtained with a rapid, high-speed centrifugation
scheme studying a large spectrum of hemostasis tests and covering the full spectrum
of values obtained in clinical practice. The new agreement measure CP π identified
more assays with nonconcordant results than Spearman's correlation coefficient. A
clinically appropriate concordance between measurements was observed for all routine
parameters, but relevant discrepancies were observed with regard to most single-factor
determinations as well as von Willebrand activity. We believe that our results add
sufficient data on previous studies to justify rapid centrifugation for routine hemostasis
tests (PT, thrombin time, aPTT, fibrinogen, D-dimer, antithrombin, and anti-Xa activity).
A traditional centrifugation scheme shall be used for all other tests.
What is known about this topic?
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Short and uniform centrifugation schemes contribute significantly to successful laboratory
automation.
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To date, it is unclear if this is applicable to the hemostasis laboratory.
What does this paper add?
-
We assessed a rapid, high-speed centrifugation scheme in a large set of hemostasis
tests, covering the full spectrum of values obtained in clinical practice, and using
meaningful statistical measures.
-
We demonstrated that high-speed centrifugation is applicable to the majority of routine
hemostasis parameters.
-
The coverage probability was more sensitive than Spearman's rank correlation to detect
disagreement among centrifugation schemes.
