Literature DB >> 16123995

Prolongation of the prothrombin time and activated partial thromboplastin time in children with sickle cell disease.

Leslie J Raffini1, Alison E Niebanck, Joanne Hrusovsky, Amanda Stevens, Anne Blackwood-Chirchir, Kwaku Ohene-Frempong, Janet L Kwiatkowski.   

Abstract

BACKGROUND: Patients with sickle cell disease (SCD) have high rates of perioperative complications, including bleeding 1,2. PROCEDURES: We conducted a retrospective review of pre-operative coagulation studies in pediatric patients with SCD followed by a prospective study of 100 well children with SCD to determine the prevalence of abnormal coagulation screening tests, and to evaluate potential etiologies.
RESULTS: In the retrospective study, 32/84 (38.1%) had a prolonged prothrombin time (PT), compared to 8/100 in the prospective study. Prolongations of the activated partial thromboplastin time (aPTT) were less common. Children in the prospective study with prolonged PTs had significantly lower levels of Factor V and VII compared to those with normal PTs. Factor VII levels were <50% in 4/8 with long PTs, compared to 3/92 with normal PTs, P=0.001. Though retrospectively, several patients had normalization of their PT with vitamin K, there was no laboratory evidence of vitamin K deficiency in the prospective study. In the retrospective analysis, six of seven children who had pre-operative coagulation studies and significant intraoperative blood loss had prolonged PTs (P=0.04).
CONCLUSIONS: Children with SCD admitted for surgical procedures were more likely to have prolonged PTs than those tested at a well visit. There was intra-patient variability in coagulation studies that may be related to clinical status, hepatocellular dysfunction, and/or increased clotting factor consumption. Future well-designed prospective studies to determine whether abnormal coagulation studies are associated with an increased risk of perioperative bleeding in children with SCD are necessary. Copyright (c) 2005 Wiley-Liss, Inc.

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Year:  2006        PMID: 16123995     DOI: 10.1002/pbc.20579

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  2 in total

1.  Severity of Anaemia Has Corresponding Effects on Coagulation Parameters of Sickle Cell Disease Patients.

Authors:  Samuel Antwi-Baffour; Ransford Kyeremeh; Lawrence Annison
Journal:  Diseases       Date:  2019-12-17

2.  Coagulation profile of Sudanese children with homozygous sickle cell disease and the effect of treatment with omega-3 fatty acid on the coagulation parameters.

Authors:  Shiekh Awoda; Ahmed A Daak; Nazik Elmalaika Husain; Kebreab Ghebremeskel; Mustafa I Elbashir
Journal:  BMC Hematol       Date:  2017-11-09
  2 in total

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