Hansen R M, Hanson G, Anderson T
Arch Intern Med. 1985 Jan;145(1):93-4.
A three-year review of the medical records of 76 patients with apparent thalassemic syndromes (mean corpuscular volume, greater than 75 cu micron; RBC count, greater than 5 X 10(6)/cu mm) was performed to assess overall physician response to this information at a midwestern teaching institution. Abnormal indices were recognized in only 50% of the cases; in only 32% of cases was a thalassemic syndrome considered in the differential diagnosis. Residents in internal medicine failed to recognize microcytic indices and to consider thalassemic syndromes 42% and 59% of the time, respectively. Even though hemoglobin electrophoresis was performed in 25 patients, in only 15 (56%) of the 25 cases was beta-thalassemia proved or alpha-thalassemia presumptively diagnosed. In 17% of all cases, the patients were treated with iron without diagnostic findings on iron studies and/or in spite of data suggesting a thalassemic syndrome. The RBC indices are an underused portion of the complete blood cell count, and readily apparent thalassemic syndromes are often not considered.
对76例疑似地中海贫血综合征患者(平均红细胞体积大于75立方微米;红细胞计数大于5×10⁶/立方毫米)的病历进行了为期三年的回顾,以评估中西部一所教学机构的医生对这些信息的整体反应。仅50%的病例识别出异常指标;鉴别诊断中仅32%的病例考虑了地中海贫血综合征。内科住院医师分别有42%和59%的时间未能识别小细胞指标和考虑地中海贫血综合征。尽管对25例患者进行了血红蛋白电泳,但25例中仅15例(56%)确诊为β地中海贫血或疑似诊断为α地中海贫血。在所有病例中,17%的患者在铁研究无诊断结果且/或尽管有数据提示地中海贫血综合征的情况下接受了铁剂治疗。红细胞指标在全血细胞计数中未得到充分利用,明显的地中海贫血综合征常常未被考虑。