Direct antiglobulin test (DAT)-negative (DAT-)
autoimmune hemolytic anemia (AIHA) is empirically thought to show the same clinical conditions as DAT-positive (DAT+)AIHA, with the exception of an adequate amount of red blood cell (RBC)-bound
immunoglobulin (Ig)G. We investigated the clinical characteristics of DAT-AIHA in comparison with DAT+AIHA. Of the 582 patients referred to our laboratory with undiagnosed
hemolytic anemia, AIHA was clinically diagnosed in 216 patients (DAT-AIHA, n = 154; DAT+AIHA, n = 62). The percentage of reticulocytes, mean corpuscular volume, RBC-
IgG levels, white blood cell count, and total
protein (TP) levels were significantly higher in patients with DAT+AIHA than patients with DAT-AIHA. The
hemoglobin level was significantly lower in patients with DAT+AIHA. No significant differences between patients with DAT-AIHA and DAT+AIHA existed with respect to age, gender, idiopathic/secondary nature, complications such as
Evans syndrome, effectiveness of
steroid treatment, or survival rate at 1 year following diagnosis. Patients with DAT-AIHA required significantly lower doses of
steroids for maintenance
therapy. Based on multivariate analysis of idiopathic DAT-AIHA (n = 110), TP and
Evans syndrome were associated with the effectiveness of
steroids (adjusted odds ratio [aOR], 1.36/[0.1 g/dl]; 95% confidence interval [CI], 1.01-1.84) and survival at the 1-year follow-up (aOR, 0.1; 95% CI, 0.01-0.88). Our results indicate that patients with DAT-AIHA generally suffer milder
anemia and
hemolysis than patients with DAT+AIHA, respond equally well to
steroids, and have comparable survival at 1-year.