Journals / Erciyes Medical Journal / 2022 / Cilt: 44 - Sayı: 2

Management of Patients with Factor VII Deficiency in Surgery: A Single-center Experience

Pages
222–224
Publication Date
2022-10-11
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

No bleeding or thromboembolism was observed in any of the 5 patients.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Factor VII deficiency is a rare condition characterized by a broad spectrum of clinical phenotypes, from asymptomatic status to severe, life-threatening bleeding, such as central nervous system or gastrointestinal bleeding.
📊
Key Findings & Data:Importantly, bleeding may also occur in patients with a factor level of 20% to 50%.
💡
Conclusion & Impact:No bleeding or thromboembolism was observed in any of the 5 patients.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Factor VII deficiency is a rare condition characterized by a broad spectrum of clinical phenotypes, from asymptomatic status to severe, life-threatening bleeding, such as central nervous system or gastrointestinal bleeding. Factor VII deficiency is usually diagnosed after a bleeding attack or as a result of screening tests performed in cases with a family history. Importantly, bleeding may also occur in patients with a factor level of 20% to 50%. This report describes the approach to management before, during, and after surgery used in 5 patients with varying factor levels. The use of recombinant factor VIIa (15–30 μg kg) was required in 3 of the patients. No bleeding or thromboembolism was observed in any of the 5 patients.

🔖

Cite This Article

ÜMİT, E. G., KIRKIZLAR, H. O., DEMİR, A. M., GÜLSARAN, S. K., DEMİRCİ, U., BAŞ, V. (2022). Management of Patients with Factor VII Deficiency in Surgery: A Single-center Experience. Erciyes Medical Journal, Cilt: 44 - Sayı: 2, 222–224. https://ajindex.com/articles/502156

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (6)

  1. Gorkom BL, Holme PA, Joch C, Rogosch T, Feussner A, McKeand W, et al. Pharmacokinetics and pharmacodynamics of a recombinant fusion protein linking activated coagulation factor VII with human albumin (rVIIa-FP) in patients with congenital FVII deficiency. Hematology 2020; 25(1): 17–25
  2. Bernardi F, Mariani G. Biochemical, molecular and clinical aspects of coagulation factor VII and its role in hemostasis and thrombosis. Haematologica 2021; 106(2): 351–62
  3. Peyvandi F, Palla R, Menegatti M, Siboni SM, Halimeh S, Faeser B, et al; European Network of Rare Bleeding Disorders Group. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders. J Thromb Haemost 2012; 10(4): 615–21
  4. Napolitano M, Siragusa S, Mariani G. Factor VII deficiency: Clinical phenotype, genotype and therapy. J Clin Med 2017; 6(4): 38
  5. Lee EJ, Burey L, Abramovitz S, Desancho MT. Management of pregnancy in women with factor VII deficiency: A case series. Haemophilia 2020; 26(4): 652–6
  6. Szczepanik A, Wiszniewski A, Oses-Szczepanik A, Dąbrowski W, Pielaciński K, Misiak A. Surgery in patients with congenital factor VII deficiency - a single center study. Pol Przegl Chir 2018; 90(5): 1–5.