Skip to main content
. 2022 Sep 5;23(17):10189. doi: 10.3390/ijms231710189

Table 2.

Morbidities of thalassemia intermedia.

Studies, n (%) ORIENT Study, No Iron Chelation or Fetal Hemoglobin Induction; n = 52 (β-TI) [42] KM Musallamb, 2011, n = 168 (β-TI) [33] OPTIMAL CARE Study, 2010, n = 584 TI [16]
Age (years), mean (SD) 24.1 ± 1.6 (range 2–56) 35.2 (12.6) 25.44 ± 13.86 (2–76)
Male, n (%) 25 (48.1) 73 (42.9) 291:293
Splenectomized, n (%) 30 (57.7) 121 (72.0) 325 (55.7)
Transfusion history, n (%) No regularly blood transfusion
None 44 (26.2) 139 (23.8)
Occasional 80 (47.6) 143 (24.5)
Regular 44 (26.2) 302 (51.7)
Age (years), mean (SD) 24.1 ± 1.6 (range 2–56) 35.2 (12.6) 25.44 ± 13.86 (2–76)
Male, n (%) 25 (48.1) 73 (42.9) 291:293
Splenectomized, n (%) 30 (57.7) 121 (72.0) 325 (55.7)
Morbidity, n (%) 36 (69.2)
Osteoporosis 25 (48.1) 77 (45.8) 134 (22.9)
Extramedullary hematopoiesis 10 (19.2) 43 (25.6) 124 (21.2)
Liver disease 9 (17.3) (No B, C carrier) 54 (32.1) 57 (9.8)
Hypogonadism 4 (7.7) 28 (16.7) 101 (17.3)
DM 4 (7.7) 6 (3.6) 10 (1.7)
Thrombosis 3(5.8) 44 (26.2) 82 (14)
Pulmonary hypertension 1 (1.9) 56 (33.3) 64 (11)
Hypoparathyroidism 1 (1.9)
Leg ulcers 41 (24.4) 46 (7.9)
Hypothyroidism 5 (9.6) 30 (17.9) 33 (5.7)
Heart failure 9 (5.4) 25 (4.3)
cholelithiasis 100 (17.1)