
Inadequate utilization of routine electronic RBC counts to identify beta thalassemia carriers.
Author(s) -
Oded Shalev,
E Yehezkel,
Eliezer A. Rachmilewitz
Publication year - 1988
Publication title -
american journal of public health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.284
H-Index - 264
eISSN - 1541-0048
pISSN - 0090-0036
DOI - 10.2105/ajph.78.11.1476
Subject(s) - thalassemia , beta thalassemia , medicine , minor (academic) , pediatrics , law , political science
We investigated physician awareness of the diagnosis of beta thalassemia minor as suggested by RBC indices obtained from routine electronic counts; and, the knowledge of the carriers of their genetic trait. Out of 17,000 counts, 324 were compatible with the diagnosis of beta thalassemia minor, but, only 175 (54 per cent) were identified by physicians as possibly thalassemic and in 47 of these (27 per cent) was the diagnosis verified. Twenty-four of 39 interviewed patients in whom the diagnosis of beta thalassemia minor was established knew about their carrier state.