Surgical interventions in childhood rare factor deficiencies: a single-center experience from Turkey

Blood Coagul Fibrinolysis. 2013 Dec;24(8):854-61. doi: 10.1097/MBC.0b013e3283655667.

Abstract

Congenital rare factor deficiencies may present in infancy by life-threatening bleedings or may not show any symptoms until adulthood. It is reported more commonly in countries having consanguineous marriages. Data regarding surgical interventions of rare congenital factor deficiencies are based on case reports and records of guidelines. There are no well documented and separately prepared directories related to pre-surgical and prophylactic approaches of surgical interventions of these deficiencies. Our retrospective study consisted of 171 rare factor deficiencies that were followed up in our clinic, and of whom 61 had 88 surgical interventions between 1990 and 2012. Of these patients, 45 were having factor VII deficiency, and factor V, X, XI, XIII and fibrinogen deficiencies were present in five, four, three, two and two patients, respectively. In 23 patients, factor coagulant activities were under 5% (37.7%), in 15 it was between 5 and 30% (24.6%), and in 23 between 30 and 50% (37.7%). Twenty-eight were symptomatic and 33 were asymptomatic. Information of 51 (83.6%) male and 10 (16.4%) female patients with an age range of 5-25 years (13 ± 5.27), whose age at presentation ranged between 3 weeks and 18 years (7 ± 4.66), were retrieved from patient records and from the records contained in the data-processing environment introduced in 2005. The rate of familial consanguinity was 49.2%. Of the surgical interventions, 24 (27.3%) were major, 24 (27.3%) were minor and 40 (45.4%) were circumcision. We used fresh frozen plasma in 32, recombinant factor (rF)VIIa in 20, prothrombin complex concentrate in five and fibrinogen in three patients during surgical interventions. In 18 patients, antifibrinolytic agents were also used. In 27 patients, surgical interventions were applied without any replacement therapy. No additional doses were required after surgical prophylaxis doses. Thrombotic events were not observed. Antibody occurrence was not detected in these patients. In our study, we evaluated preparation for surgical procedures, factor replacement therapy before surgical intervention and postoperative follow-up in patients with rare coagulation factor deficiency.

MeSH terms

  • Adolescent
  • Adult
  • Antifibrinolytic Agents / therapeutic use
  • Asymptomatic Diseases
  • Blood Coagulation Factors / therapeutic use
  • Child
  • Child, Preschool
  • Coagulation Protein Disorders / blood*
  • Coagulation Protein Disorders / drug therapy
  • Coagulation Protein Disorders / surgery*
  • Consanguinity
  • Female
  • Humans
  • Male
  • Preoperative Care
  • Retrospective Studies
  • Turkey

Substances

  • Antifibrinolytic Agents
  • Blood Coagulation Factors
  • prothrombin complex concentrates