Literature DB >> 27586406

[Hereditary heterozygous factor VII deficiency in patients undergoing surgery : Clinical relevance].

D Woehrle1, M Martinez2, D Bolliger3.   

Abstract

BACKGROUND: A hereditary deficiency in coagulation factor VII (FVII) may affect the international normalized ratio (INR) value. However, FVII deficiency is occasionally associated with a tendency to bleed spontaneously. We hypothesized that perioperative substitution with coagulation factor concentrates might not be indicated in most patients.
METHODS: In this retrospective data analysis, we included all patients with hereditary heterozygous FVII deficiency who underwent surgical procedures at the University Hospital Basel between December 2010 and November 2015. In addition, by searching the literature, we identified publications reporting patients with FVII deficiency undergoing surgical procedures without perioperative substitution.
RESULTS: We identified 22 patients undergoing 46 surgical procedures, resulting in a prevalence of 1:1500-2000. Coagulation factor concentrates were administered during the perioperative period in 15 procedures (33 %), whereas in the other 31 procedures (66 %), FVII deficiency was not substituted. No postoperative bleeding or thromboembolic events were reported. In addition, we found no differences in pre- and postoperative hemoglobin and coagulation parameters, with the exception of an improved postoperative INR value in the substituted group. In the literature review, we identified five publications, including 125 patients with FVII deficiency, undergoing 213 surgical procedures with no perioperative substitution. DISCUSSION: Preoperative substitution using coagulation factor concentrates does not seem to be mandatory in patients with an FVII level ≥15 %. For decision-making on preoperative substitution, patient history of an increased tendency to bleed may be more important than the FVII level or increased INR value.

Entities:  

Keywords:  Bleeding risk; FVII deficiency; Perioperative coagulopathy; Rare bleeding disorders; Thromboembolic events

Mesh:

Substances:

Year:  2016        PMID: 27586406     DOI: 10.1007/s00101-016-0217-9

Source DB:  PubMed          Journal:  Anaesthesist        ISSN: 0003-2417            Impact factor:   1.041


  25 in total

1.  The anticoagulant effect of protamine sulfate is attenuated in the presence of platelets or elevated factor VIII concentrations.

Authors:  Daniel Bolliger; Fania Szlam; Marc Azran; Kaoru Koyama; Jerrold H Levy; Ross J Molinaro; Kenichi A Tanaka
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Review 3.  Potential predictors of bleeding risk in inherited factorVII deficiency. Clinical, biological and molecular criteria.

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4.  Pregnancy in women with congenital factor VII deficiency.

Authors:  A A Kulkarni; C A Lee; R A Kadir
Journal:  Haemophilia       Date:  2006-07       Impact factor: 4.287

Review 5.  Rare coagulation deficiencies.

Authors:  F Peyvandi; S Duga; S Akhavan; P M Mannucci
Journal:  Haemophilia       Date:  2002-05       Impact factor: 4.287

Review 6.  Factor VII deficiency: defining the clinical picture and optimizing therapeutic options.

Authors:  M Lapecorella; G Mariani
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8.  Epidemiological investigation of the prevalence of von Willebrand's disease.

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Review 9.  Usefulness of standard plasma coagulation tests in the management of perioperative coagulopathic bleeding: is there any evidence?

Authors:  T Haas; D Fries; K A Tanaka; L Asmis; N S Curry; H Schöchl
Journal:  Br J Anaesth       Date:  2014-09-08       Impact factor: 9.166

10.  Bleeding symptoms at disease presentation and prediction of ensuing bleeding in inherited FVII deficiency.

Authors:  Matteo Nicola Dario Di Minno; Alberto Dolce; Guglielmo Mariani
Journal:  Thromb Haemost       Date:  2013-03-21       Impact factor: 5.249

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  1 in total

1.  A new perspective on perioperative coagulation management in a patient with congenital factor VII deficiency: A case report.

Authors:  Yongliang Sun; Lingling Jia; Zhiying Yang; Wenqian Chen
Journal:  Medicine (Baltimore)       Date:  2018-11       Impact factor: 1.817

  1 in total

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