非甲、非乙型肝炎的管理:问题及其治疗。

H C Thomas, M R Jacyna, J Main
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引用次数: 0

摘要

非甲、非乙(NANB)肝炎由至少三种尚未查明的病毒引起,可因输血、使用血液制品、隐蔽或公开的经皮接触以及流行的水传播感染暴发而发生。这三种病毒的特点是潜伏期;短时间为2-4周,长时间为6-12周,水传播的NANB肝炎病毒为中间期。急性乙型肝炎比乙型肝炎轻,转氨酶峰值水平较低。但也有部分发展为暴发性肝炎,存活率较低,为0.13%。10 - 100%的急性患者会发展为慢性乙型肝炎。研究发现,每周3次注射3-5兆单位(MU)的α -淋巴母细胞样干扰素可在6-8周内使转氨酶水平恢复正常。约80%的患者在治疗第8周时达到正常水平,并维持在2.5-3 MU,每周3次;耐受良好的剂量。需要长期、低剂量的治疗来维持缓解。
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Management of non A, non B hepatitis: the problem and its treatment.

Non A, non B (NANB) hepatitis is caused by at least three, as yet unidentified, viruses and can occur as a result of blood transfusions, the use of blood products, covert or overt percutaneous exposure and epidemic waterborne outbreaks of infection. The three types of viruses are characterised by their incubation times; a short time of 2-4 weeks, a longer time of 6-12 weeks and a intermediate period for the waterborne NANB hepatitis virus. Acute NANB hepatitis is milder than HBV hepatitis with lower peak transaminase levels. However, some develop into fulminant hepatitis with a lower survival rate of 0.13%. Ten to 100% of acute patients progress to chronic NANB hepatitis. It was found that alpha-lymphoblastoid interferon at levels of 3-5 megaunits (MU) thrice weekly returned transaminase levels to normal within 6-8 weeks. Approximately 80% had normal levels by the eighth week of treatment and this was maintained on 2.5-3 MU thrice weekly; a well tolerated dose. Long term, low-dose therapy is needed to maintain remission.

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