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

被引:5
|
作者
Salcioglu, Zafer [1 ]
Tugcu, Deniz [1 ]
Akcay, Arzu [1 ]
Sen, Hulya Sayilan [1 ]
Aydogan, Gonul [1 ]
Akici, Ferhan [1 ]
Demirkaya, Metin [1 ]
Ayaz, Nuray Aktay [1 ]
Sander, Serdar [2 ]
Tireli, Gulay Aydin [2 ]
Baslar, Zafer [3 ]
机构
[1] Kanuni Sultan Suleyman Educ & Res Hosp, Pediat Hematol & Oncol Clin, Istanbul, Turkey
[2] Kanuni Sultan Suleyman Educ & Res Hosp, Pediat Surg Clin, Istanbul, Turkey
[3] Istanbul Univ, Cerrahpasa Med Sch, Dept Internal Med, Istanbul, Turkey
关键词
childhood; rare factor deficiency; surgical intervention; FACTOR-VII DEFICIENCY; BLEEDING DISORDERS; INVASIVE PROCEDURES; HEMOPHILIA; RECOMBINANT; SURGERY; CIRCUMCISION; PHENOTYPES;
D O I
10.1097/MBC.0b013e3283655667
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (C) 2013 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:854 / 861
页数:8
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