Table 4.

Characteristics of ITP

CharacteristicsN = 28
At the time of TPO-RA introductionAt the end of study
ITP duration (y) (0-24)   
Chronic or persistent ITP 22 (78.6%) 28 (100%) 
Indication of antiplatelet drugs or anticoagulant (7.1%) (14.3%) 
Immunoglobulin replacement therapy 11 (39.3%) 22 (78.6%) 
Second-line therapies for ITP 10 (35.7%) (25.0%) 
Immunosuppressants (17.9%) (17.9%) 
Splenectomy (7.1%) (14.3%) 
Rituximab received at least once (17.9%) 14 (50.0%) 
CharacteristicsN = 28
At the time of TPO-RA introductionAt the end of study
ITP duration (y) (0-24)   
Chronic or persistent ITP 22 (78.6%) 28 (100%) 
Indication of antiplatelet drugs or anticoagulant (7.1%) (14.3%) 
Immunoglobulin replacement therapy 11 (39.3%) 22 (78.6%) 
Second-line therapies for ITP 10 (35.7%) (25.0%) 
Immunosuppressants (17.9%) (17.9%) 
Splenectomy (7.1%) (14.3%) 
Rituximab received at least once (17.9%) 14 (50.0%) 
CharacteristicsIn the month before TPO-RA introductionDuring the treatment with TPO-RA
Patients reporting bleeding events 16 (57.1%) 10 (35.7%) 
Patients reporting bleeding events with Khellaf score >8 (21.4%) (7.1%) 
CharacteristicsIn the month before TPO-RA introductionDuring the treatment with TPO-RA
Patients reporting bleeding events 16 (57.1%) 10 (35.7%) 
Patients reporting bleeding events with Khellaf score >8 (21.4%) (7.1%) 

Quantitative variables are presented as median (range, minimum to maximum); and qualitative variables as frequency (percentage).

Median age at PID diagnosis was similar across these 4 populations.

NS, not specified.

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