von Willebrand disease (VWD) is associated with significant morbidity as a result of excessive mucocutaneous bleeding. Early diagnosis and treatment are important to prevent and treat these symptoms. We systematically reviewed the accuracy of diagnostic tests using different cutoff values of von Willebrand factor antigen (VWF:Ag) and platelet-dependent von Willebrand factor (VWF) activity assays in the diagnosis of VWD. We searched Cochrane Central Register for Controlled Trials, MEDLINE, and Embase databases for eligible studies. We pooled estimates of sensitivity and specificity and reported patient-important outcomes when relevant. This review included 21 studies that evaluated VWD diagnosis. The results showed low certainty in the evidence for a net health benefit from reconsidering the diagnosis of VWD vs removing the disease diagnosis in patients with VWF levels that have normalized with age. For the diagnosis of type 1 VWD, VWF sequence variants were detected in 75% to 82% of patients with VWF:Ag < 0.30 IU/mL and in 44% to 60% of patients with VWF:Ag between 0.30 and 0.50 IU/mL. A sensitivity of 0.90 (95% confidence interval [CI], 0.83-0.94) and a specificity of 0.91 (95% CI, 0.76-0.97) were observed for a platelet-dependent VWF activity/VWF:Ag ratio < 0.7 in detecting type 2 VWD (moderate certainty in the test accuracy results). VWF:Ag and platelet-dependent activity are continuous variables that are associated with an increase in bleeding risk with decreasing levels. This systematic review shows that using a VWF activity/VWF:Ag ratio < 0.7 vs lower cutoff levels in patients with an abnormal initial VWD screen is more accurate for the diagnosis of type 2 VWD.

The reported prevalence of VWD is up to 1% in the general population based on epidemiologic studies1,2  with a symptomatic prevalence ∼0.1% at the level of primary care.3,4  The prevalence of VWD is ∼15% in women with heavy menstrual bleeding, making it the most common inherited bleeding disorder known in humans.5,6  VWD is caused by deficiency or dysfunction of VWF, a multimeric glycoprotein that binds platelets at sites of vascular injury and stabilizes circulating coagulation factor VIII (FVIII).7-10 

Patients with VWD can experience easy bruising, bleeding from the oral cavity, heavy menstrual bleeding, as well as bleeding after dental work, surgical procedures, and childbirth. Joint bleeding may also occur in more severe deficiency. These symptoms vary among patients with VWD, and the bleeding phenotype can fluctuate throughout the life of a patient with VWD, leading to the need for accurate diagnosis of VWD types and subtypes and individualized management plans.11,12  Different types and subtypes of VWD have been defined depending on the type of abnormality in VWF. A patient with partial quantitative deficiency in VWF would have type 1 VWD, whereas a patient with virtual absence of VWF would have type 3 VWD. Patients with type 2 VWD have qualitative abnormalities of VWF: type 2A is characterized by reduced or absent high molecular weight VWF, type 2B results from a gain of function in VWF that increases its affinity for platelets, type 2M is caused by reduced VWF interactions with platelets or collagen, and type 2N results from reduced binding of VWF to FVIII.2,5,10 

Multiple variables that affect VWF levels can make confirming a clear diagnosis of VWD difficult. For example, estrogen therapy or pregnancy will lead to an elevation in VWF, obscuring the diagnosis of hereditary VWD in some women. Additionally, mildly reduced VWF:Ag and platelet-dependent VWF activity levels do not always establish a diagnosis of VWD; conversely, low normal VWF:Ag and platelet-dependent VWF activity do not always exclude the diagnosis. This is related, in part, to the VWF:Ag assays, which have good precision and reproducibility; however, the platelet-dependent VWF activity assay has greater variability, resulting in the potential for misdiagnosis and/or misclassification.13 

Data show that 43% of previously diagnosed patients with partial quantitative deficiency have normalized VWF levels with age.14-17  However, data are not available to show that an increase in VWF is accompanied by improvement in symptoms. This results in the need for health care providers to carefully consider excluding or removing the diagnosis.

In addition to variation in the diagnosis and management, there is limited awareness of the importance of VWD types and subtypes, as well as lack of consensus on diagnostic criteria.18  The aim of this systematic review was to determine the accuracy of different VWF diagnostic thresholds (ie, VWF cutoff values) for the diagnosis of VWD. Additionally, we assessed the potential benefits and harms from reconsidering the diagnosis of VWD vs simply removing the diagnostic label of VWD from patients with VWF levels that have normalized with age. The results were used to inform the recently published evidence-based recommendations for clinical practice guidelines on VWD, developed as a combined effort from the American Society of Hematology (ASH), the International Society on Thrombosis and Haemostasis (ISTH), the National Hemophilia Foundation, the World Federation of Hemophilia, and the University of Kansas Medical Center.19,20  The guidelines aim to inform all stakeholders on essential issues where there is variation or uncertainty in clinical practice, and they will support decision making in the context of patients’ values and preferences.

Search strategy and data sources

We searched MEDLINE, Embase, and the Cochrane Central Register of Controlled Trials from inception until August of 2019. We also manually searched the reference lists of relevant articles and existing reviews. Studies published in English were included in this review. We limited the search to studies reporting data on the accuracy of diagnostic tests. The complete search strategy is available in Supplement 1. The prespecified protocol for this review is registered with PROSPERO (CRD42020147977). This review is reported in accordance with Preferred Reporting Items for Systematic reviews and Meta-Analyses for diagnostic test accuracy guidelines.21 

Study selection

The eligibility criteria are discussed below.

Studies.

We included studies reporting data on diagnostic test accuracy (cohort studies, cross-sectional studies) for VWD.

Participants.

Participants included patients, of any age, presenting to inpatient or outpatient settings with suspected VWD.

Index tests for diagnosis.

The following tests were considered in eligible studies: VWF:Ag and platelet-dependent VWF activity (VWF ristocetin cofactor [VWF:RCo], VWF activity assays based on ristocetin-induced binding of VWF to a recombinant wild-type GPIb fragment, and VWF activity assays based on spontaneous binding of VWF to a gain-of-function mutant GPIb fragment). We did not exclude studies based on the timing of when the index test was conducted.

Reference standards.

If a reference diagnostic test was not conducted, we accepted clinical follow-up for symptoms alone as a reference standard.

Exclusion criteria.

Although studies reporting on patients with VWD, as well as other bleeding disorders, were eligible for inclusion, we excluded studies in which >80% of the study population included a different bleeding disorder. When possible, we extracted data separately for patients with VWD from these studies. We also excluded studies that did not provide sufficient data to determine test accuracy (sensitivity and specificity), abstracts, and studies with a sample size < 10 patients.

Screening and data extraction

Independent reviewers conducted title and abstract screening and full-text review in duplicate to identify eligible studies. Two reviewers completed data extraction independently and in duplicate, and data were verified by a third reviewer (M.A.K.). Disagreements were resolved by discussion to reach consensus, in consultation with 2 expert clinician scientists (N.T.C. and P.D.J.). We extracted data about general study characteristics (investigators, publication year, country, study design), diagnostic index test and reference standard, prevalence of VWD, and parameters to determine test accuracy (ie, sensitivity and specificity of the index test).

Risk of bias and certainty of evidence

We conducted the risk of bias assessment for diagnostic test accuracy studies using the Quality Assessment of Diagnostic Accuracy Studies 2 revised tool.22  We used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework to assess overall certainty by evaluating the evidence for each outcome on the following domains: risk of bias, imprecision, inconsistency, indirectness, and publication bias.23,24 

Data synthesis

When feasible, we combined the accuracy estimates from individual studies quantitatively (ie, pooled) for each test using Open Meta-Analyst. We conducted a bivariate analysis for pooling sensitivity and specificity for each of the test comparisons to account for variation within and between studies. Forest plots were created for each comparison. The Breslow-Day test was used to measure the percentage of total variation across studies due to heterogeneity (I2); however, the results did not influence our judgment about inconsistency because of the known methodological limitations of I2 in test accuracy reviews.25 

Diagnostic strategies for VWD are based on assessment of the pretest probability (PTP) for individual patients, which provides an estimate of the expected prevalence of VWD at a population level. We calculated the absolute differences in effects for each comparison as true positives, true negatives, false positives, and false negatives. Here, we present the results for the low-, intermediate-, and high-PTP groups.

Description of studies

The initial search retrieved 5693 nonduplicate studies, of which 669 were included for full-text review. Following full-text review, we identified 106 studies eligible for data abstraction, of which 21 answered the questions addressed in this systematic review.14-17,26-34  A list of excluded studies is provided in Supplement 3. Reasons for exclusion at full-text review were ineligible study design, study population, or diagnostic test; sample size < 10 patients; unacceptable reference standards; and/or not enough information to determine diagnostic test accuracy for VWD. Figure 1 summarizes the flow diagram of the included studies.

Figure 1.

Flow diagram for included studies. pts, patients.

Figure 1.

Flow diagram for included studies. pts, patients.

Close modal

Use of different VWF levels to diagnose type 1 VWD

Of the included studies, 9 reported on the cutoff values of VWF. Supplement 4 summarizes the general characteristics of the included studies, as well as the index and reference tests. The complete risk of bias assessment for individual studies is included in Supplement 5. There was very low certainty in the evidence supporting the use of different VWF levels to diagnose type 1 VWD and assessing the implications and consequences of using different levels.

Table 1 summarizes the evidence of using different VWF levels to diagnose type 1 VWD. The interactive summary of findings can be accessed using the following link: https://gdt.gradepro.org/presentations/#/isof/isof_c5b33e22-a646-4654-9f09-b820aff36c5c-1569520689536?_k=eump67.

Use of platelet-dependent VWF activity/VWF:Ag ratio to confirm type 2 VWD

Of the included studies, 6 reported on the VWF level in type 2 VWD. Table 2 summarizes the general characteristics of included studies, as well the index and reference standards. The complete risk of bias assessment for individual studies is included in Supplement 4. The certainty of the evidence for test accuracy is very low, which is due to the case-control design leading to serious population-selection bias. The studies do not compare the 2 tests cutoffs directly, and there is significant unexplained inconsistency.

Test accuracy of a platelet-dependent VWF activity assay/VWF:Ag ratio < 0.7 to confirm type 2 VWD was pooled from 5 cohort studies that included 204 participants. Studies used laboratory testing, including a platelet function analyzer (PFA), ristocetin-induced platelet aggregation (RIPA), VWF:Ag, FVIII activity, VWF collagen binding, and molecular diagnosis through DNA sequencing, as a reference standard for confirming type 2 VWD. The pooled estimates for sensitivity and specificity were 0.93 (95% CI, 0.87-0.98) and 0.82 (95% CI, 0.63-0.99), respectively (moderate certainty in the sensitivity results and very low certainty in the specificity results). Figure 2 shows the forest plot displaying the sensitivity and specificity from individual studies and the pooled estimates.

Figure 2.

Forest plots for sensitivity and specificity for individual studies and the pooled estimates for a ratio < 0.7.

Figure 2.

Forest plots for sensitivity and specificity for individual studies and the pooled estimates for a ratio < 0.7.

Close modal

Table 3 shows GRADE test accuracy evidence summary when using a platelet-dependent VWF activity assay/VWF:Ag ratio < 0.7 to diagnose type 1 VWD. The interactive summary of findings can be accessed using the following link: https://gdt.gradepro.org/presentations/#/isof/isof_2e5b5dac-94e0-4108-9ff3-effcce27648b-1606770452095?_k=r1ooaz.

We summarized the test accuracy using a platelet-dependent VWF activity assay/VWF:Ag ratio < 0.6 to confirm type 2 VWD from 3 cohort studies that included 184 participants. Studies used laboratory testing, including PFA, RIPA, VWF:Ag, FVIII:C, VWF:CB, and molecular diagnosis through DNA sequencing, as a reference standard for confirming type 2 VWD, with some studies also including a clinical historic diagnosis. The ranges for estimates for sensitivity and specificity were 0.68 to 0.97 and 0.87 to 0.88, respectively (very low certainty in the sensitivity results and low certainty in the specificity results). Figure 3 shows the forest plot displaying the sensitivity and specificity from individual studies.

Figure 3.

Forest plots for sensitivity and specificity for individual studies for a ratio < 0.6. FN, false negatives; FP, false positives; TN, true negatives; TP, true positives.

Figure 3.

Forest plots for sensitivity and specificity for individual studies for a ratio < 0.6. FN, false negatives; FP, false positives; TN, true negatives; TP, true positives.

Close modal

Table 4 shows the GRADE test accuracy evidence summary when using a platelet-dependent VWF activity assay/VWF:Ag ratio < 0.6 to diagnose type 1 VWD.

We summarized the test accuracy using a 0.5 platelet-dependent VWF activity/VWF:Ag ratio < 0.5 to confirm type 2 VWD from 3 cohort studies that included 95 participants. Studies used laboratory testing, including PFA, RIPA, VWF:Ag, FVIII:C, VWF:CB and molecular diagnosis through DNA sequencing, as a reference standard for confirming type 2 VWD, with some studies also including clinical historic diagnosis. The range for estimates for sensitivity was 0.58 to 0.79; specificity was assumed to be 1 with a ratio < 0.5 (low certainty in the sensitivity results). Figure 4 shows the forest plot displaying the sensitivity and specificity from individual studies.

Figure 4.

Forest plots for sensitivity and specificity for individual studies for a ratio < 0.5. FN, false negatives; FP, false positives; TN, true negatives; TP, true positives.

Figure 4.

Forest plots for sensitivity and specificity for individual studies for a ratio < 0.5. FN, false negatives; FP, false positives; TN, true negatives; TP, true positives.

Close modal

Table 5 shows GRADE test accuracy evidence summary when using a platelet-dependent VWF activity assay/VWF:Ag ratio < 0.5 to diagnose type 1 VWD.

Normalization of VWF levels with age

Of the included studies, 6 reported on VWF levels that normalize with age in type 1 VWD. The risk of bias due to confounding factors was high, because the studies did not adjust for comorbidities, with the exception of the one by Sanders et al26 ; more elderly patients reported ≥1 comorbidity, including diabetes, cancer, cardiovascular disease, and depression, compared with younger patients. Atiq et al35  showed that comorbidities are associated with higher levels of VWF and FVIII in type 1 VWD, which may explain the age-related increase in VWF and FVIII levels. The complete risk of bias assessment for individual studies is included in Supplement 4. Table 6 summarizes the evidence assessing normalization of VWF levels with age.

VWF level cutoffs in the diagnosis of type 1 VWD

This review presents pooled and summary estimates of test accuracy and patient-important outcomes for different VWF levels for VWD diagnosis and the reconsideration of the diagnosis in patients with VWF levels that have normalized with age. Sequence variants within VWF were identified more frequently in cases with lower VWF levels. The benefit of using a higher cutoff for type 1 VWD is to not miss the diagnosis in an affected patient especially in those with a bleeding phenotype. The benefit of using a lower cutoff is to avoid mistreating (or providing unnecessary treatment to) a patient who does not have type 1 VWD. Consequently, it is reasonable to use a VWF level of < 0.30 IU/mL regardless of bleeding phenotype, and in patients with abnormal bleeding, a VWF level of < 0.50 IU/mL to confirm the diagnosis of type 1 VWD. However, recommendations on whether to use a 0.30 IU/mL or 0.50 IU/mL level in the clinical practice will depend on multiple factors, including the patients’ values in regards to their diagnosis. Also, VWF antigen and platelet-dependent activity are continuous variables with an increase in bleeding risk with decreasing levels. However, the clinical phenotype is determined by more than the levels only.

VWF activity/VWF:Ag ratio in the diagnosis of type 2 VWD

With regard to the platelet-dependent VWF activity/VWF:Ag ratio for the diagnosis of type 2 VWD, the pooled estimates for sensitivity and specificity for a ratio < 0.7 were higher than for the ratio < 0.5 and the ratio < 0.6. More false negatives are expected when using a diagnostic threshold < 0.50 IU/mL. Therefore, it would be appropriate to use a higher cutoff of < 0.7 to confirm type 2 VWD (2A, 2B, or 2M) in patients with an abnormal initial VWD screen. Quality of life and inaccurate counseling are concerns for patients when they are mislabeled. Some pregnant women are denied epidural anesthesia because they are labeled as having type 2 VWD, but this is less of a problem for type 1 VWD. Of note, when treatment is available it supports not denying epidural anesthesia; however, the decision is more complex and should be based on informed shared decision making with informed discussions about benefits and harms. It is very important for clinicians and patients to understand the differences in treatment for the different types of VWD.

Diagnosis in patients with VWD whose VWF levels normalize with age

For patients with VWF levels that normalize with age, this should trigger repeat evaluation of the bleeding phenotype and consideration of other bleeding disorders, particularly if other hemostatic testing (ie, platelet function testing) was not performed previously. The degree of normalization may influence the decision about how to manage minor procedures (ie, expectantly or pretreat). It is important to note that some treatments for VWD (ie, tranexamic acid) are also effective for other bleeding disorders. If the diagnosis is removed, there is a fear of undertreatment, particularly if the patient has had prior issues with major bleeding.

This review has several strengths. The comprehensive and systematic approach used to identify studies makes it unlikely that relevant ones were missed. Also, we assessed the certainty of evidence using the GRADE framework and identified sources of bias.

We note a few limitations of this comprehensive systematic review. The pooled sensitivity and specificity estimates of the tests from this review only apply when the test is performed alone; however, they can be used to model various diagnostic strategies to inform clinical decision making. Ultimately, the diagnostic tests will be used in a strategic approach based on clinical PTP and with consideration of availability, cost, and patient and provider values and preferences.

This comprehensive systematic review synthesizes and evaluates the accuracy of VWF levels in the diagnosis of VWD. Estimates of sensitivity and specificity from this review were used to inform evidence-based recommendations for a clinical practice guideline. For clinical decision making, the prevalence of PTP for VWD in a population, together with the sensitivity and specificity estimates, should influence how patients are managed.

The systematic review team acknowledges Jenny Castano; members of ASH, ISTH, the National Hemophilia Foundation, and the World Federation of Hemophilia; and the VWD disease diagnosis guidelines panel members for assistance and administrative support.

This systematic review was conducted to support the development of the ASH 2020 guidelines for diagnosis and management of VWD. The entire guideline development process was funded by ASH. Some researchers received salary or grant support and others participated to fulfill requirements of an academic degree or program or volunteered their time through the Outcomes and Implementation Research Unit at the University of Kansas Medical Center.

Contribution: R.A.M., M.A.K., R.B.-P. and N.H. design the study, selected the included studies, extracted data, performed statistical analyses, and interpreted results; O.A., O.D., A.E.A., S.T., B.M., A.D., and A.Q. selected the included studies and extracted data; M.A.K. and R.A.M. wrote the manuscript; and N.G., C.M., B.A., J.E., S.M., R.R.M., J.S.O.D., N.S., R.S., R.B.-P., P.D.J., N.T.C., and V.F. interpreted the results and critically revised the manuscript; and all authors approved the final version of the manuscript.

Conflict-of-interest disclosure: The authors were members of the diagnosis guideline panel, the systematic review team, or both. R.A.M. has received research funding from CSL Behring, Bayer, and Takeda.

The current affiliation for A.D. is East and North Hertfordshire NHS Trust, Lister Hospital, Stevenage, United Kingdom.

Correspondence: Reem A. Mustafa, Division of Nephrology and Hypertension, Department of Medicine, University of Kansas Medical Center, 3901 Rainbow Blvd, MS3002, Kansas City, KS 66160; e-mail: rmustafa@kumc.edu.

1.
Rodeghiero
F
,
Castaman
G
,
Dini
E
.
Epidemiological investigation of the prevalence of von Willebrand’s disease
.
Blood.
1987
;
69
(
2
):
454
-
459
.
2.
Werner
EJ
,
Broxson
EH
,
Tucker
EL
,
Giroux
DS
,
Shults
J
,
Abshire
TC
.
Prevalence of von Willebrand disease in children: a multiethnic study
.
J Pediatr.
1993
;
123
(
6
):
893
-
898
.
3.
Bowman
M
,
Hopman
WM
,
Rapson
D
,
Lillicrap
D
,
James
P
.
The prevalence of symptomatic von Willebrand disease in primary care practice
.
J Thromb Haemost.
2010
;
8
(
1
):
213
-
216
.
4.
Bowman
M
,
Hopman
WM
,
Rapson
D
,
Lillicrap
D
,
Silva
M
,
James
P
.
A prospective evaluation of the prevalence of symptomatic von Willebrand disease (VWD) in a pediatric primary care population
.
Pediatr Blood Cancer.
2010
;
55
(
1
):
171
-
173
.
5.
James
AH
.
Obstetric management of adolescents with bleeding disorders
.
J Pediatr Adolesc Gynecol.
2010
;
23
(
6 suppl
):
S31
-
S37
.
6.
Shankar
M
,
Lee
CA
,
Sabin
CA
,
Economides
DL
,
Kadir
RA
.
von Willebrand disease in women with menorrhagia: a systematic review
.
BJOG.
2004
;
111
(
7
):
734
-
740
.
7.
Fujimura
Y
,
Titani
K
,
Holland
LZ
, et al
.
von Willebrand factor. A reduced and alkylated 52/48-kDa fragment beginning at amino acid residue 449 contains the domain interacting with platelet glycoprotein Ib
.
J Biol Chem.
1986
;
261
(
1
):
381
-
385
.
8.
National Heart, Lung, and Blood Institute
. The diagnosis, evaluation, and management of von willebrand disease. https://www.nhlbi.nih.gov/health-topics/diagnosis-evaluation-and-management-of-von-willebrand-disease
9.
L
eebeek
FW
,
Eikenboom
JC
.
von Willebrand’s disease
.
N Engl J Med.
2016
;
375
(
21
):
2067
-
2080
.
10.
Sadler
JE
,
Budde
U
,
Eikenboom
JC
, et al;
Working Party on von Willebrand Disease Classification
.
Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor
.
J Thromb Haemost.
2006
;
4
(
10
):
2103
-
2114
.
11.
American Society of Hematology. ASH to Collaborate on Clinical Practice Guidelines on Diagnosis, Management of von Willebrand Disease, Accessed 19 January 2019, https://www.hematology.org/newsroom/press-releases/2018/ash-collaborate-clinical-practiceguidelines
12.
de Wee
EM
,
Mauser-Bunschoten
EP
,
Van Der Bom
JG
, et al;
Win Study Group
.
Health-related quality of life among adult patients with moderate and severe von Willebrand disease
.
J Thromb Haemost.
2010
;
8
(
7
):
1492
-
1499
.
13.
Bucciarelli
P
,
Siboni
SM
,
Stufano
F
, et al
.
Predictors of von Willebrand disease diagnosis in individuals with borderline von Willebrand factor plasma levels
.
J Thromb Haemost.
2015
;
13
(
2
):
228
-
236
.
14.
Borghi
M
,
Guglielmini
G
,
Mezzasoma
AM
, et al
.
Increase of von Willebrand factor with aging in type 1 von Willebrand disease: fact or fiction?
Haematologica.
2017
;
102
(
11
):
e431
-
e433
.
15.
Nummi
V
,
Lassila
R
,
Joutsi-Korhonen
L
,
Armstrong
E
,
Szanto
T
.
Comprehensive re-evaluation of historical von Willebrand disease diagnosis in association with whole blood platelet aggregation and function
.
Int J Lab Hematol.
2018
;
40
(
3
):
304
-
311
.
16.
Rydz
N
,
Grabell
J
,
Lillicrap
D
,
James
PD
.
Changes in von Willebrand factor level and von Willebrand activity with age in type 1 von Willebrand disease
.
Haemophilia.
2015
;
21
(
5
):
636
-
641
.
17.
Abou-Ismail
MY
,
Ogunbayo
GO
,
Secic
M
,
Kouides
PA
.
Outgrowing the laboratory diagnosis of type 1 von Willebrand disease: a two decade study
.
Am J Hematol.
2018
;
93
(
2
):
232
-
237
.
18.
Kalot
MA
,
Al-Khatib
M
,
Connell
NT
, et al;
VWD working group
.
An international survey to inform priorities for new guidelines on von Willebrand disease
.
Haemophilia.
2020
;
26
(
1
):
106
-
116
.
19.
Connell
NT
,
Flood
VH
,
Brignardello-Petersen
R
, et al
.
ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease
.
Blood Adv.
2021
;
5
(
1
):
301
-
325
.
20.
James
PD
,
Connell
NT
,
Ameer
B
, et al
.
ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease
.
Blood Adv.
2021
;
5
(
1
):
280
-
300
.
21.
Moher
D
,
Liberati
A
,
Tetzlaff
J
,
Altman
DG
;
PRISMA Group
.
Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement
.
Ann Intern Med.
2009
;
151
(
4
):
264
-
269, W64
.
22.
Whiting
PF
,
Rutjes
AWS
,
Westwood
ME
, et al;
QUADAS-2 Group
.
QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies
.
Ann Intern Med.
2011
;
155
(
8
):
529
-
536
.
23.
Schünemann
HJ
,
Oxman
AD
,
Brozek
J
, et al;
GRADE Working Group
.
Grading quality of evidence and strength of recommendations for diagnostic tests and strategies [published correction appears in BMJ. 2008;336(7654)]
.
BMJ.
2008
;
336
(
7653
):
1106
-
1110
.
24.
Schünemann
HJ
,
Oxman
AD
,
Brozek
J
, et al
.
GRADE: assessing the quality of evidence for diagnostic recommendations
.
ACP J Club.
2008
;
149
(
6
):
2
.
25.
Macaskill
P
,
Gatsonis
C
,
Deeks
J
,
Harbord
R
,
Takwoingi
Y
. Cochrane handbook for systematic reviews of diagnostic test accuracy. Version 09 0 London: The Cochrane Collaboration.
2010
.
26.
S
anders
YV
,
Giezenaar
MA
,
Laros-van Gorkom
BA
, et al;
WiN study group
.
von Willebrand disease and aging: an evolving phenotype
.
J Thromb Haemost.
2014
;
12
(
7
):
1066
-
1075
.
27.
Lavin
M
,
Aguila
S
,
Schneppenheim
S
, et al
.
Novel insights into the clinical phenotype and pathophysiology underlying low VWF levels
.
Blood.
2017
;
130
(
21
):
2344
-
2353
.
28.
Goettl
UN
,
Caliebe
D
,
Kowalski
D
,
Maria
S
,
Limperger
VE
,
Kenet
G
.
Reclassification of pre-diagnosed von Willebrand disease in the eldery: a hospital-based cohort study
.
Blood.
2017
;
130
(
suppl 1
):
3685
.
29.
Adcock
DM
,
Bethel
M
,
Valcour
A
.
Diagnosing von Willebrand disease: a large reference laboratory’s perspective
.
Semin Thromb Hemost.
2006
;
32
(
5
):
472
-
479
.
30.
Caron
C
,
Hilbert
L
,
Vanhoorelbeke
K
,
Deckmyn
H
,
Goudemand
J
,
Mazurier
C
.
Measurement of von Willebrand factor binding to a recombinant fragment of glycoprotein Ibalpha in an enzyme-linked immunosorbent assay-based method: performances in patients with type 2B von Willebrand disease
.
Br J Haematol.
2006
;
133
(
6
):
655
-
663
.
31.
James
PD
,
Notley
C
,
Hegadorn
C
, et al;
Association of Hemophilia Clinic Directors of Canada
.
Challenges in defining type 2M von Willebrand disease: results from a Canadian cohort study
.
J Thromb Haemost.
2007
;
5
(
9
):
1914
-
1922
.
32.
Chen
D
,
Tange
JI
,
Meyers
BJ
,
Pruthi
RK
,
Nichols
WL
,
Heit
JA
.
Validation of an automated latex particle-enhanced immunoturbidimetric von Willebrand factor activity assay
.
J Thromb Haemost.
2011
;
9
(
10
):
1993
-
2002
.
33.
de Maistre
E
,
Volot
F
,
Mourey
G
, et al
.
Performance of two new automated assays for measuring von Willebrand activity: HemosIL AcuStar and Innovance
.
Thromb Haemost.
2014
;
112
(
4
):
825
-
830
.
34.
Vangenechten
I
,
Mayger
K
,
Smejkal
P
, et al
.
A comparative analysis of different automated von Willebrand factor glycoprotein Ib-binding activity assays in well typed von Willebrand disease patients
.
J Thromb Haemost.
2018
;
16
(
7
):
1268
-
1277
.
35.
Atiq F, Meijer K, Eikenboom J, et al. WiN study group. Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand disease. Br J Haematol. 2018 Jul;182(1):93-105. Epub 2018 May 16. PMID: 29767844; PMCID: PMC6032952.
36.
Flood VH, Christopherson, P. A., Gill JC, Friedman KD, Haberichter SL, et al. Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States. Blood. 2016;
127
(
20
):
2481
2488
.
37.
Tosetto A, Rodeghiero, F, Castaman G, Bernardi M, Bertoncello K, et al. Impact of plasma von Willebrand factor levels in the diagnosis of type 1 von Willebrand disease: Results from a multicenter European study (MCMDM-1VWD). J Thromb Haemost. 2007;
5
(
4
):
715
721
.

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