Table 1.
Baseline characteristics of patients with eosinophilia during anti-tuberculosis treatment
Variable | All (n = 262) |
---|---|
Age, yr | 60 (45–73) |
Male sex | 175 (66.8) |
Type of TB | |
Pulmonary TB | 162 (61.8) |
Extrapulmonary TB | 100 (38.2) |
Adverse reactions | |
GI disorder | 118 (45.0) |
Abnormal liver function | 32 (12.2) |
Abnormal renal function | 10 (3.8) |
CADRs | 161 (61.5) |
Pruritus only | 76 (47.2) |
Skin rash | 77 (47.8) |
DRESS | 7 (4.4) |
SJS/TEN | 1 (0.6) |
Fever | 15 (5.7) |
History of previous anti-TB treatment | |
New treatment | 238 (90.8) |
Retreatment | 24 (9.2) |
Peripheral blood eosinophilia | |
Eosinophil count before start of anti-TB treatment, /mL | 110 (70–200) |
Eosinophil percentage before start of anti-TB treatment, % of total white blood cell count | 1.9 (0.9–3.1) |
Initial eosinophil count/mL | 400 (300–500) |
Initial eosinophil percentage, % of total white blood cell count | 6.2 (5.4–7.7) |
Peak eosinophil count/mL | 465 (300–650) |
Peak eosinophil percentage, % of total white blood cell count | 7.7 (6.0–10.7) |
Values are presented as median (interquartile range) or number (%).
TB, tuberculosis; GI, gastrointestinal; CADR, cutaneous adverse drug reaction; DRESS, drug reaction with eosinophilia and systemic symptom; SJS/TEN, Stevens-Johnson syndrome/toxic epidermal necrolysis.