Page 28
allied
academies
August 23-24, 2018 | London, UK
Hematology and Oncology
2
nd
International Conference on
Journal of Hematology and Blood Disorder | Volume 2
Manifestation of Antiphospholipid Syndrome among Saudi patients; Examining the applicability of
Sapporo
Farjah H AlGahtani
King Saud Universty ,Saudi Arabia
A
ntiphospholipidsyndrome(APS)isasystematicautoimmune
disease featured with vascular thrombosis and pregnancy
morbidity, which is likely to be under-diagnosed in the clinical
practice. The Sapporo classification criteria of APS was revised
in 2006 and are used as the main diagnosis guideline, which
validity as standardmeasurements is still in debate. Few studies
had been tackled the clinical and laboratory manifestations of
APS among Saudi Arabic population. A total of 72 (90%) females
and 8 (10%) males were included, female-to-male ratio was 9:1.
The mean (±SD) age at diagnosis was 28.1 (± 8.7) years (range
11-63 years). 22 patients (27.5%) fulfilled the revised Sapporo
criteria (definitive APS). There was no significant difference
in the clinical manifestations or treatment between the two
group (p>0.2). However, we found definitive APS cases had
significantly higher percentage of serological manifestation
presence than possible APS cases. Although not reaching
statistical significance, definitive APS cases had higher odds of
experiencing vascular thrombosis (OR=1.61, 95%CI 0.55, 4.71;
P=0.39) and DVT/PE (OR=1.53, 95%CI 0.55, 4.31; P=0.42), and
lower odds of experiencing recurrent DVT/PE (OR=0.67, 95%CI
0.12, 3.81; P=0.65) and pregnancy morbidity (OR=0.63, 95%CI
0.21, 1.92; P=0.42) than the possible APS cases.
e:
falgahtani@gmail.com