Low von Willebrand Factor in Children and Adolescents A Review

被引:1
|
作者
Srivaths, Lakshmi [1 ]
Kouides, Peter A. [2 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, McGovern Sch Med, Dept Pediat, Gulf States Hemophilia & Thrombophilia Ctr, 6655 Travis St,Ste 400, Houston, TX 77030 USA
[2] Univ Rochester, Sch Med, Mary M Gooley Hemophilia Ctr, Rochester, NY USA
关键词
ABO BLOOD-GROUP; BLEEDING SYMPTOMS; DISEASE; DIAGNOSIS; TYPE-1; MANAGEMENT; COHORT; GUIDELINES; CLEARANCE; INSIGHTS;
D O I
10.1001/jamapediatrics.2021.2186
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This narrative review of low von Willebrand factor in children and adolescents summarizes the observations of several studies on low von Willebrand factor and bleeding and available diagnostic modalities and treatment options. Importance Recent studies have documented increased bleeding symptoms and related complications in patients with low von Willebrand factor (VWF), highlighting the clinical significance of this entity. Because children and adolescents with VWF deficiencies often present to primary care physicians with bleeding symptoms, physicians need to be aware of this condition for early detection. Observations Studies have found that children and adolescents with low VWF (VWF levels of 30-50 IU/dL) can present with clinically significant bleeding, including mucosal, menstrual, postsurgical, and posttraumatic bleeding, leading to complications such as anemia, iron deficiency, transfusion, hospitalization, and poor quality of life. Detecting and promptly managing low VWF in children and adolescents with bleeding are essential because failure to do so can lead to significant morbidity in adulthood, especially among female patients, including continued heavy menstrual bleeding; postpartum hemorrhage; related gynecologic complications, such as hemorrhagic ovarian cysts; and surgical interventions for heavy menstrual bleeding, including hysterectomy. This narrative review summarizes the observations of several studies that have shed light on the pathophysiologic mechanisms of low VWF and bleeding in these patients and the available diagnostic modalities and treatment options. Conclusions and Relevance Studies in children and adolescents have provided important insights into the clinical phenotype, complications, pathophysiologic mechanisms, evaluation, and management of low VWF, now recognized as an important clinicopathologic entity, as presented in this review. As gatekeepers, primary care physicians play an important role in guiding patients with this recently recognized clinicopathologic entity toward appropriate specialty care and providing continued comanagement to prevent future complications as the patients enter adulthood.
引用
收藏
页码:1060 / 1067
页数:8
相关论文
共 50 条
  • [21] von Willebrand factor
    Ruggeri, ZM
    JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (11): : S41 - S46
  • [22] Unexpected finding of low von willebrand factor levels or von Willebrand disease in pediatric patients with scoliosis
    Castillo, B.
    Kate Hartman, S.
    Gorena, M.
    Wingate, J.
    Hui, S-K R.
    Teruya, J.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2015, 13 : 736 - 736
  • [23] Von Willebrand factor
    Ruggeri, ZM
    CURRENT OPINION IN HEMATOLOGY, 2003, 10 (02) : 142 - 149
  • [24] Evaluation of von Willebrand factor activity in factor VIII/von Willebrand factor concentrates with the automated von Willebrand factor: activity IL test
    Mori, Filippo
    Rossi, Paola
    Nardini, Ilaria
    Gambelli, Davide
    Farina, Claudio
    BLOOD COAGULATION & FIBRINOLYSIS, 2010, 21 (03) : 221 - 228
  • [25] Evaluation of a microfluidic flow assay to screen for von Willebrand disease and low von Willebrand factor levels
    Lehmann, M.
    Ashworth, K.
    Manco-Johnson, M.
    Di Paola, J.
    Neeves, K. B.
    Ng, C. J.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2018, 16 (01) : 104 - 115
  • [26] The spectrum and severity of bleeding in adolescents with low von Willebrand factor-associated heavy menstrual bleeding
    Srivaths, Lakshmi
    Minard, Charles G.
    O'Brien, Sarah H.
    Wheeler, Allison P.
    Mullins, Eric
    Sharma, Mukta
    Sidonio, Robert
    Jain, Shilpa
    Zia, Ayesha
    Ragni, Margaret, V
    Kulkarni, Roshni
    Dietrich, Jennifer E.
    Kouides, Peter A.
    BLOOD ADVANCES, 2020, 4 (13) : 3209 - 3216
  • [27] von Willebrand factor levels in the diagnosis of von Willebrand disease: a systematic review and meta-analysis
    Kalot, Mohamad A.
    Husainat, Nedaa
    El Alayli, Abdallah
    Abughanimeh, Omar
    Diab, Osama
    Tayiem, Sammy
    Madoukh, Bader
    Dimassi, Ahmad B.
    Qureini, Aref
    Ameer, Barbara
    Eikenboom, Jeroen C. J.
    Giraud, Nicolas
    McLintock, Claire
    McRae, Simon
    Montgomery, Robert R.
    O'Donnell, James S.
    Scappe, Nikole
    Sidonio, Robert F.
    Brignardello-Petersen, Romina
    Flood, Veronica H.
    Connell, Nathan T.
    James, Paula D.
    Mustafa, Reem A.
    BLOOD ADVANCES, 2022, 6 (01) : 62 - 71
  • [28] Von Willebrand factor/factor VIII concentrates in the treatment of von Willebrand disease
    Batlle, Javier
    Fernanda Lopez-Fernandez, Maria
    Loures Fraga, Esther
    Rodriguez Trillo, Angela
    Almudena Perez-Rodriguez, Maria
    BLOOD COAGULATION & FIBRINOLYSIS, 2009, 20 (02) : 89 - 100
  • [29] Introduction to a review series on von Willebrand factor, factor VIII, and factor IX
    Ortel, Thomas L.
    BLOOD, 2024, 144 (21) : 2157 - 2158
  • [30] Von Willebrand factor binding to heparin in von Willebrand disease
    Rastegar-Lari, G
    Legendre, P
    Ajzenberg, N
    Meyer, D
    Baruch, D
    THROMBOSIS AND HAEMOSTASIS, 1999, : 510 - 511