Literature DB >> 24709665

Current management of von Willebrand disease and von Willebrand syndrome.

Marc E Stone1, Michael Mazzeffi, Jeffrey Derham, Andre Korshin.   

Abstract

PURPOSE OF REVIEW: Anesthesiologists frequently care for patients with altered hemostasis and coagulation. Where a clear history of familial and personal bleeding exists, a thoughtful plan can be developed in advance to manage the issue perioperatively. However, in some cases, it may not be known that the patient has a disorder until excessive bleeding is noted during or after surgery. Recognition of the issue and appropriate targeted therapy are the keys to successful management. RECENT
FINDINGS: With an estimated prevalence approaching 1% of the population, von Willebrand disease (vWD) is the most common hereditary bleeding diathesis, but the estimated prevalence of acquired vWD (often termed von Willebrand syndrome or vWS) is now believed to be significantly higher, especially in patients with malignancies, autoimmune diseases, cardiac valvular lesions, and in patients on mechanical circulatory support devices. Acquired vWD may also occur with certain medications.
SUMMARY: The mainstay of the diagnosis of vWD is laboratory testing. Preoperative clinical assessment and a high level of suspicion are often effective to alert the anesthesiologist to the possibility of vWS, thus allowing for appropriate testing and potential prophylaxis in elective situations, as well as appropriately targeted therapy of unexpected bleeding when a hemostatic derangement was not anticipated preoperatively.

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Year:  2014        PMID: 24709665     DOI: 10.1097/ACO.0000000000000083

Source DB:  PubMed          Journal:  Curr Opin Anaesthesiol        ISSN: 0952-7907            Impact factor:   2.706


  5 in total

1.  Peri-operative DDAVP Use Leading to Severe Hyponatremia after Total Shoulder Replacement in a Patient with von Willebrand's Disease.

Authors:  James S MacKenzie; Stuart C Kozinn
Journal:  HSS J       Date:  2015-07-17

2.  Hemostatic abnormalities in adult patients with Marfan syndrome.

Authors:  Katharina T I Kornhuber; Heide Seidel; Claudia Pujol; Christian Meierhofer; Franz Röschenthaler; Axel Pressler; Alexander Stöckl; Nicole Nagdyman; Rhoia C Neidenbach; Philipp von Hundelshausen; Martin Halle; Stefan Holdenrieder; Peter Ewert; Harald Kaemmerer; Michael Hauser
Journal:  Cardiovasc Diagn Ther       Date:  2019-10

Review 3.  Acquired von Willebrand syndrome: focused for hematologists.

Authors:  Massimo Franchini; Pier Mannuccio Mannucci
Journal:  Haematologica       Date:  2020-06-18       Impact factor: 9.941

4.  Perioperative management of a pediatric patient with suspected type 1 von Willebrand disease undergoing tonsillectomy: a case report.

Authors:  Hiroyuki Oshika; Yukihide Koyama; Koichi Tsuzaki; Kohmei Ida; Tomio Andoh
Journal:  JA Clin Rep       Date:  2019-08-27

5.  Dental invasive procedures in von Willebrand disease outpatients treated with high purity FVIII/VWF complex concentrate (Fanhdi®): experience of a single center.

Authors:  Valeria De Padua; Umberto Romeo; Cristina Santoro; Riccardo Bosco; Erminia Baldacci; Antonietta Ferretti; Francesco Malaspina; Maria Gabriella Mazzucconi; Domenico Gaglioti
Journal:  Heliyon       Date:  2020-02-25
  5 in total

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