2013, Number 3
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Rev Hematol Mex 2013; 14 (3)
Immune thrombocytopenia in northern México. A single institution experience
Jaime-Pérez JC, López-Razo ON, Marfil- Rivera LJ, Herrera-Garza JL, González-Llano O, Gómez-Almaguer D
Language: Spanish
References: 20
Page: 131-137
PDF size: 380.65 Kb.
ABSTRACT
Background and Objective: Immune Thrombocytopenic Purpura
(ITP) is a disorder characterized by the production of anti-platelet
antibodies leading to platelet destruction. There is a lack of information
regarding the characteristics of ITP patients in northeast México.
Material and Methods: All patients diagnosed with ITP at the “Dr.
José Eleuterio González” University Hospital during a 5-year period
were included. The clinical presentation, treatment and outcome
for children and adults, as well as Relapse Free Survival (RFS)
were determined. Hazard Ratio (HR) for relapse was estimated by
univariate Cox analysis.
Results: 72 patients were included, 35 were <16 years, 53.4%
belonged to the male gender and 45.7% were females. Thirty-seven
patients were ≥16 years, 29.7% males and 70.3% females. 43% of
the children had a recent history of infectious disease. The one-year
Relapse Free Survival (RFS) for children and adults was 74.6% and
51.2%, respectively P= 0.656. 45.5 of adults did not comply with
follow-up visits. 22.9% of those <16 years (n=8) and 37.8% of adults
(n=14) relapsed; the platelet count at relapse was 15.10x109/L (SD
8.10) on patients <16 years of age and 15.46x109/L (SD 14.13) in
adults. No deaths occurred.
Conclusion: Although the clinical presentation, diagnosis, treatment
and outcome of the ITP in children and adults during the period of
the study was similar to published data some interesting differences
in the clinical course were documented
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