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Table 3 Clinical Characteristics. SCD-related clinical characteristics for patients: Children of parent participants (Group 1) and adolescent patient participants (Group 2) patients are both included here. Patients who were a part of a dyad are only represented once

From: Patient and family experience with chronic transfusion therapy for sickle cell disease: A qualitative study

Patient Characteristics (n = 18)

Genotype, n (%)

 HbSS or HbS-β0 thalassemia

18 (100)

Transfusion Type, n (%)

 Simple

11 (61.1)

 Erythracytapheresis

5 (27.8)

 Partial manual exchange

2 (11.1)

Duration of CTT, median years (IQR)

6.8 (4.3–9.8)

Indication for CTT, n (%)

 Abnormal TCD

5 (27.8)

 Overt or silent stroke

12 (66.6)

 Splenic sequestration

1 (5.6)

Chelation type, n (%)

 None

3 (16.7)

 Deferasirox

15 (83.3)

Taking hydroxyurea, n (%)

3 (16.7)

Current or prior CTT-related complications, n (%)

 Iron overload

17 (94.4)

 Red cell antibodies

9 (50.0)

 Port complications

3 (16.7)

 Renal complications

2 (11.1)