Khyber Medical University Journal (Mar 2017)

HEMOPHILIA B DIAGNOSTIC DISCREPANCY: A SURVEY TO CONFIRM THE DIAGNOSIS OF HEMOPHILIA B

  • Muhammad Tariq Masood Khan,
  • Arshi Naz,
  • Abid Sohail Taj,
  • Tahir Sultan Shamsi,
  • Muahmmad Tariq Hamayun Khan,
  • Nazish Farooq,
  • Jawad Ahmed

Journal volume & issue
Vol. 9, no. 1
pp. 19 – 23

Abstract

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OBJECTIVES: To determine the frequency of misdiagnosis among doc­umented factor IX (FI) deficient (hemophilia B) patients of Khyber Pakhtunkhwa (KP) province of Pakistan and to discern role of different diagnostic tests employed in this regard. METHODS: Patients were identified through registries at transfusion centers. Out of 83 FIX deficient patients registered at transfusion cen­ters and hemophilia care centers of KP province, 32 patients could be contacted and only 30 patients consented to be enrolled into the study. A comprehensive questionnaire depicting demographic details, clinical history and physical examination was filled out for each enrolled patient. Their blood samples were posed to first and second line coagulation tests both manually and on two different automated coagulation analyzers. RESULTS: The registered FIX deficient patients’ pool was found to have a mean age of 17.39±9.8 years. Out of 30 enrolled patients, di­agnosis was correct in 18 (60.0%) patients and wrong in 12 (40.0%) patients. The misdiagnosed cases were hemophilia-A (n=9; 30%) and hypo-fibrinogenemia (n=3; 10.0%). All cases diagnosed previously on the basis of factor assays (n=8, 100%) were found to be correct while those diagnosed previously with mixing studies, only 08/18 (44.44%) had FIX deficiency. Out of 4 cases diagnosed on circumstantial evidence of isolated prolonged APTT along with established FIX deficiency in another sibling or maternal cousin, 2 had FIX deficiency. CONCLUSION: A large fraction of patients documented as FIX deficient on the basis of mixing studies are misdiagnosed. In clinical practice factor assays are more valid in comparison to mixing studies. Key Words Hemophilia B (MeSH), Factor IX Deficiency (Non-MeSH), Diagnostic Discrepancy (Non-MeSH), Mixing Studies (Non-MeSH)