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大剂量阿昔洛韦与人类白细胞干扰素治疗巨细胞病毒性肺炎

Treatment of cytomegaloviral pneumonia with high-dose acyclovir and human leukocyte interferon.

作者信息

Wade J C, McGuffin R W, Springmeyer S C, Newton B, Singer J W, Meyers J D

出版信息

J Infect Dis. 1983 Sep;148(3):557-62. doi: 10.1093/infdis/148.3.557.

Abstract

Thirteen recipients of bone marrow transplants were given high-dose acyclovir and alpha-interferon (Cantell interferon) for the treatment of biopsy-proven cytomegaloviral pneumonia. Three patients survived. Doses of acyclovir between 500 and 1,000 mg/m2 of body surface area (peak plasma levels, 7-86 micrograms/ml) and doses of interferon between 2 X 10(4) and 40 X 10(4) units/kg per day (peak serum levels, 5-608 units/ml) were given. No consistent antiviral effect was seen despite the large doses employed. Possible marrow toxicity associated with this regimen occurred in five patients, neurologic symptoms in two, and nephrotoxicity in one. Thus, treatment with high-dose acyclovir plus alpha-interferon was moderately toxic but ineffective against cytomegaloviral pneumonia after bone marrow transplantation.

摘要

13名骨髓移植受者接受了大剂量阿昔洛韦和α-干扰素(坎特尔干扰素)治疗经活检证实的巨细胞病毒性肺炎。3名患者存活。给予的阿昔洛韦剂量为每平方米体表面积500至1000毫克(血浆峰值水平,7 - 86微克/毫升),干扰素剂量为每天每千克体重2×10⁴至40×10⁴单位(血清峰值水平,5 - 608单位/毫升)。尽管使用了大剂量药物,但未观察到一致的抗病毒效果。该治疗方案可能导致5名患者出现骨髓毒性,2名患者出现神经症状,1名患者出现肾毒性。因此,大剂量阿昔洛韦加α-干扰素治疗骨髓移植后巨细胞病毒性肺炎毒性中等但无效。

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