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. 2023 Aug 21;109(4):761–769. doi: 10.4269/ajtmh.23-0280

Table 4.

Clinical and laboratory manifestations of patients with probable or possible severe primaquine-associated hemolysis by clinical outcome

Clinical or laboratory manifestation Blood transfusion (N = 76) Renal replacement therapy (N = 8) Death (N = 7) All patients (N = 101)
N n (%) N n (%) N n (%) N n (%)
Clinical manifestations
 Dark urine 57 48 (84.2) 5 5 (100) 4 4 (100) 74 63 (85.1)
 Pallor 60 56 (93.3) 8 7 (87.5) 2 2 (100) 75 69 (92.0)
 Dyspnea 47 8 (17.0) 7 2 (28.6) 3 3 (100) 59 16 (27.1)
 Dizziness 22 11 (50.0) 4 1 (25.0) 0 0 (0.0) 26 13 (50.0)
 Fever 58 37 (63.8) 7 4 (57.1) 1 1 (100) 69 40 (57.8)
 Severe fatigue 21 15 (71.4) 0 0 (0.0) 0 0 (0.0) 26 18 (69.2)
 Heart failure 51 7 (13.7) 6 6 (100) 0 0 (0.0) 62 9 (14.5)
 Chest pain 8 1 (12.5) 8 0 (0.0) 0 0 (0.0) 10 1 (10.0)
 Jaundice 67 59 (88.1) 7 7 (100) 6 6 (100) 92 83 (90.2)
 Low urine output 14 2 (14.3) 3 2 (66.7) 0 0 (0.0) 18 2 (11.1)
Laboratory findings
 Hemoglobin > 3 g/dL decrease 11 9 (81.8) 0 0 (0.0) 0 0 (0.0) 14 12 (85.7)
 Hemoglobin > 25% decrease 11 11 (100) 0 0 (0.0) 0 0 (0.0) 14 14 (100)
 Total bilirubin > 1 mg/dL 59 51 (86.4) 7 5 (71.4) 1 1 (100) 75 66 (88.0)
 Indirect bilirubin > 0.8 mg/dL 59 51 (86.4) 7 5 (71.4) 1 1 (100) 72 63 (87.5)
 Urine dipstick blood, positive 31 17 (54.8) 6 3 (50.0) 5 5 (100) 48 29 (60.4)
 Urobilinogen dipstick, positive 30 5 (16.7) 5 1 (20.0) 3 3 (100) 45 17 (37.8)
 White blood cell count > 12,000/μL 56 33 (58.9) 7 4 (57.1) 3 3 (100) 70 40 (57.1)

N = number of patients for whom data were available, n = number of patients with manifestation present.

Patients could present with more than one outcome. Thus, the total number of patients does not equal the summation of those who received a blood transfusion and/or renal replacement therapy, or who died.