Sjövall J
J Int Med Res. 1977;5(5):313-21. doi: 10.1177/030006057700500505.
In an open multicentre study of bacampicillin (Penglobe), a new orally well absorb ed prodrug of ampicillin, 516 patients with acute exacerbations of chronic bronchitis or pneumonia were treated by a group of Belgian pneumologists or internists. Bacampicillin was given in a dosage regimen of 400 mg or 800 mg three times daily. In patients with acute exacerbations of chronic bronchitis the clinical success rate was high, over 95% in both groups. An improvement in the sputum purulence score was seen in 93% of the patients with an initially purulent sputum and 69% had a normal mucoid sputum at follow-up. The clinical success rate in patients with pneumonia was also similar in both dosage groups with success rates over 96%. The total number of patients with adverse reactions was not more than 5-4%, of which the majority were considered mild or moderate. Each type of side-effect occurred in a frequency of 1-2% or less. There were no differences between the two dosage regiments as regards the frequency of side-effects indicates a remarkably good tolerance of bacampicillin also with the higher dosage.
在一项关于巴卡西林(Penglobe)的开放性多中心研究中,巴卡西林是一种口服吸收良好的新型氨苄西林前体药物,516例慢性支气管炎急性加重或肺炎患者由一组比利时肺病学家或内科医生进行治疗。巴卡西林的给药方案为每日三次,每次400毫克或800毫克。在慢性支气管炎急性加重患者中,临床成功率很高,两组均超过95%。在初始痰液为脓性的患者中,93%的患者痰液脓性评分有所改善,随访时69%的患者黏液样痰液恢复正常。两个剂量组肺炎患者的临床成功率也相似,均超过96%。出现不良反应的患者总数不超过5 - 4%,其中大多数被认为是轻度或中度。每种副作用的发生率为1 - 2%或更低。两个给药方案在副作用发生频率方面没有差异,这表明巴卡西林即使使用较高剂量也具有非常好的耐受性。