Prospective evaluation of the clinical utility of quantitative bleeding severity assessment in patients referred for hemostatic evaluation

被引:108
作者
Tosetto, A. [1 ]
Castaman, G. [1 ]
Plug, I. [1 ,2 ]
Rodeghiero, F.
Eikenboom, J. [3 ]
机构
[1] S Bortolo Hosp, Dept Hematol, I-36100 Vicenza, Italy
[2] Leiden Univ, Med Ctr, Dept Clin Epidemiol, Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Thrombosis & Hemostasis, Leiden, Netherlands
关键词
blood coagulation disorders; diagnosis; epidemiology; VON-WILLEBRAND-DISEASE; QUESTIONNAIRE; DISORDERS; DIAGNOSIS; PREVALENCE; SYMPTOMS; SCORE; POWER;
D O I
10.1111/j.1538-7836.2011.04265.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Quantitative bleeding assessment tools (BATs) have been used to describe the severity of the bleeding phenotype in patients with von Willebrand disease. Objectives: To evaluate the clinical usefulness of a BAT for the diagnosis of mild bleeding disorders (MBDs) in previously undiagnosed patients. Methods: We prospectively assessed 215 patients who were consecutively referred for evaluation of bleeding symptoms (n = 71), abnormal laboratory clotting test results (n = 105) or family investigation (n = 39) at two second-level centers. The bleeding history was assessed by a young investigator who administered the BAT instrument, and also by a senior physician who independently evaluated the patient and made the final diagnoses. Sensitivity, specificity, negative predictive value (NPV) and positive predictive value (PPV) were computed for a predefined bleeding score (BS) cut-off (BS of > 3). Receiver operating characteristic curves were used to establish a diagnostic prediction rule. Results: Assuming the prevalence of MBD in the general population to be similar to 1%, a normal BS (< 3) had a very high NPV (99.2%). The PPVs in patients referred for hemostatic or family evaluation at second-level clinics were estimated to be 71.0% and 77.5% (assuming MDB prevalences of 20% and 50%, respectively, in these settings). Measurement of BS in addition to activated partial thromboplastin time significantly increased the diagnostic efficiency of the BAT instrument (NPV of 99.6%). Conclusions: BAT use improves the evaluation of patients with suspected MBD, and we propose its use in a clinical prediction guide based on BAT and activated partial thromboplastin time for the exclusion of patients with suspected MBD in a low-prevalence setting.
引用
收藏
页码:1143 / 1148
页数:6
相关论文
共 22 条
[1]  
[Anonymous], 2010, Stata statistical software: Release 11
[2]  
[Anonymous], 2003, The Statistical Evaluation of Medical Tests for Classification and Prediction
[3]   Quantitation of bleeding symptoms in children with von Willebrand disease: use of a standardized pediatric bleeding questionnaire [J].
Biss, T. T. ;
Blanchette, V. S. ;
Clark, D. S. ;
Bowman, M. ;
Wakefield, C. D. ;
Silva, M. ;
Lillicrap, D. ;
James, P. D. ;
Rand, M. L. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2010, 8 (05) :950-956
[4]   Generation and validation of the Condensed MCMDM-1VWD Bleeding Questionnaire for von Willebrand disease [J].
Bowman, M. ;
Mundell, G. ;
Grabell, J. ;
Hopman, W. M. ;
Rapson, D. ;
Lillicrap, D. ;
James, P. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2008, 6 (12) :2062-2066
[5]   Health-related quality of life among adult patients with moderate and severe von Willebrand disease [J].
de Wee, E. M. ;
Mauser-Bunschoten, E. P. ;
van der Bom, J. G. ;
Degenaar-Dujardin, M. E. L. ;
Eikenboom, H. C. J. ;
Fijnvandraat, K. ;
de Goede-Bolder, A. ;
Laros-Van Gorkom, B. A. P. ;
Meijer, K. ;
Raat, H. ;
Leebeek, F. W. G. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2010, 8 (07) :1492-1499
[6]   Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD) [J].
Goodeve, Anne ;
Eikenboom, Jeroen ;
Castaman, Giancarlo ;
Rodeghiero, Francesco ;
Federici, Augusto B. ;
Batlle, Javier ;
Meyer, Dominique ;
Mazurier, Claudine ;
Goudemand, Jenny ;
Schneppenheim, Reinhard ;
Budde, Ulrich ;
Ingerslev, Jorgen ;
Habart, David ;
Vorlova, Zdena ;
Holmberg, Lars ;
Lethagen, Stefan ;
Pasi, John ;
Hill, Frank ;
Soteh, Mohammad Hashemi ;
Baronciani, Luciano ;
Hallden, Christer ;
Guilliatt, Andrea ;
Lester, Will ;
Peake, Ian .
BLOOD, 2007, 109 (01) :112-121
[7]   The power of a standardized bleeding score in diagnosing paediatric type 1 von Willebrand's disease and platelet function defects [J].
Marcus, P. D. ;
Nire, K. G. ;
Grooms, L. ;
Klima, J. ;
O'Brien, S. H. .
HAEMOPHILIA, 2011, 17 (02) :223-227
[8]  
NIEUWENHUIS HK, 1987, BLOOD, V70, P620
[9]   High prevalence of bleeders of unknown cause among patients with inherited mucocutaneous bleeding. A prospective study of 280 patients and 299 controls [J].
Quiroga, Teresa ;
Goycoolea, Manuela ;
Panes, Olga ;
Aranda, Eduardo ;
Martinez, Carlos ;
Belmont, Sabine ;
Munoz, Blanca ;
Zuniga, Pamela ;
Pereira, Jaime ;
Mezzano, Diego .
HAEMATOLOGICA, 2007, 92 (03) :357-365
[10]   How to estimate bleeding risk in mild bleeding disorders [J].
Rodeghiero, F. ;
Tosetto, A. ;
Castaman, G. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2007, 5 :157-166