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

Table 3.

Characteristics and clinical outcomes of individuals with severe primaquine-associated hemolysis

Clinical manifestations of severe hemolysis Probable PQ associated (n = 48) Possible PQ associated (n = 53) Uncertain PQ associated (n = 62)
N n (%) N n (%) N n (%)
Symptoms and signs
 Dark urine 36 29 (80.6) 38 34 (89.5) 39 38 (97.4)
 Pallor 40 38 (95.0) 35 31 (88.6) 40 36 (90.0)
 Dyspnea 33 9 (27.3) 26 7 (26.9) 30 2 (6.7)
 Dizziness 17 9 (52.9) 9 4 (44.4) 8 3 (37.5)
 Fever 38 24 (63.2) 31 16 (51.6) 32 7 (21.9)
 Severe fatigue 20 13 (65.0) 6 5 (83.3) 3 2 (66.7)
 Heart failure 31 3 (9.7) 31 6 (19.4) 33 0 (0.0)
 Chest pain 7 1 (14.3) 3 0 (0.0) 0 0 (0.0)
 Jaundice 44 39 (88.6) 48 44 (91.7) 54 47 (87)
 Low urine output 14 2 (14.3) 4 0 (0.0) 5 2 (40)
Laboratory findings
 Glucose 6-phosphate dehydrogenase
  Normal 47 0 (0.0) 51 1 (2.0) 61 5 (8.2)
  Intermediate 47 2 (4.4) 51 0 (0.0) 61 0 (0.0)
  Deficient 47 45 (95.7) 51 50 (98.0) 61 56 (91.8)
 Total bilirubin, > 1 mg/dL 37 31 (83.8) 38 35 (92.1) 52 46 (88.5)
 Indirect bilirubin, > 0.8 mg/dL 36 30 (83.3) 36 33 (91.7) 43 37 (86.1)
 Urine dipstick blood, positive 21 10 (47.6) 27 19 (60.4) 31 21 (67.7)
 Urine dipstick urobilinogen, positive 20 3 (15) 25 14 (66) 30 12 (40)
 White blood cell count, > 12,000/μL 32 20 (62.5) 38 20 (52.6) 36 10 (27.8)
Target daily dose of PQ
 0.25 mg/kg/day 47 5 (10.6) 52 12 (23.1) 57 14 (24.6)
 0.5 mg/kg/day 47 36 (76.6) 52 39 (75.0) 57 43 (75.4)
 0.75 mg/kg/day 47 2 (4.3) 52 0 (0.0) 57 0 (0.0)
 1.0 mg/kg/day 47 4 (8.5) 52 1 (1.9) 57 0 (0.0)
Management
 Blood transfusion 48 45 (93.8) 42 31 (73.8) 43 0 (0.0)
 Renal replacement therapy 39 4 (10.3) 41 4 (9.8) 42 0 (0.0)
 Hospitalized (no blood transfusion or renal replacement therapy) 48 3 (6.3) 41 8 (19.5) 42 42 (100)
Outcome
 Died 48 0 (0.0) 53 7 (13.2) 62 0 (0.0)

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