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骨髓纤维化所致难治性贫血对盐酸吡哆醇的反应

Response to pyridoxine hydrochloride in refractory anemia due to myelofibrosis.

作者信息

Rojer R A, Mulder N H, Nieweg H O

出版信息

Am J Med. 1978 Oct;65(4):655-60. doi: 10.1016/0002-9343(78)90854-9.

Abstract

Eleven of 14 patients with primary myelofibrosis were given a therapeutic trial with 250 mg of pyridoxine hydrochloride daily because of refractory anemia. The effect on the hemoglobin level and the hematocrit value was studied and compared to that in a group of untreated patients with the same degree of anemia. Six of 11 treated patients responded within three months with a rise in the hemoglobin level (at least 3 g/100 ml) and/or an increase in the hematocrit value (at least 10 per cent), and transfusions were no longer required. Deliberate discontinuation of pyridoxine treatment in one responding patient was followed by a relapse of the anemia; resumption of therapy once again induced an erythropoietic response. Spontaneous remissions of anemia were not observed in the untreated group. It is concluded that a trial with pyridoxine is warranted in patients with myelofibrosis and refractory anemia.

摘要

14例原发性骨髓纤维化患者中有11例因难治性贫血接受了每日250毫克盐酸吡哆醇的治疗试验。研究了其对血红蛋白水平和血细胞比容值的影响,并与一组贫血程度相同的未治疗患者进行了比较。11例接受治疗的患者中有6例在三个月内有反应,血红蛋白水平升高(至少3克/100毫升)和/或血细胞比容值增加(至少10%),不再需要输血。一名有反应的患者故意停用吡哆醇治疗后,贫血复发;再次恢复治疗再次诱导了红细胞生成反应。未治疗组未观察到贫血的自发缓解。结论是,对骨髓纤维化和难治性贫血患者进行吡哆醇试验是有必要的。

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