Oshima S, Kikuiri T, Murakami T, Ujiie A, Itoh C, Yajima O, Nitta Y, Tango M, Ichishima Y, Ogi M
Jpn J Antibiot. 1983 Oct;36(10):2769-812.
Cefamandole sodium (CMD), a new cephalosporin-derivative, was synthesized in the Laboratory of Eli-Lilly Co. Ltd. U.S.A. in 1972. CMD, which is several times more active than cefmetazole (CMZ, a cephamycin antibiotic) against Gram-positive cocci, is only as active as the latter antibiotic against Gram-negative bacilli. Against Haemophilus influenzae, CMD exhibits an antimicrobial activity which is as strong as that of ampicillin sodium. Our previous comparative tests on efficacy and safety of CMD versus cefazolin (CEZ) demonstrated that CMD was as effective and safe as CEZ in the treatment of respiratory tract infections. In the present clinical trial, the efficacy and safety of CMD are evaluated by a comparative double blind method using CMZ, a more recently synthesized cephamycin antibiotic, as a reference drug. For this purpose, a comparative double blind study was carried out in 50 institutions and clinics in Tohoku and Hokkaido districts in Japan. A total of 272 inpatients, who was aged over 16 years and was diagnosed as having pneumonia, lung abscess or acute infectious exacerbation of chronic obstructive pulmonary diseases, was included in this trial. They received 2 g of CMD or CMZ twice a day by intravenous drip infusions, as a rule, for 14 days. Of these patients, 264 (133 received CMD and 131 CMZ) were available for the evaluation of safety and usefulness. Two hundred and thirty-eight patients (122 received CMD and 116 CMZ) were adopted for the evaluation of efficacy. Prior to the treatment, there was no significant difference with respect to age, sex, severity of infection and underlying diseases between subjects in 2 treatment groups. An excellent or good clinical response was obtained in 82% of the patients treated with CMD, and in 81% of those treated with CMZ. Thus, there was no significant difference in cure rate between 2 treatment groups. However, an excellent clinical response was found in 12.3% of the patients treated with CMD, whereas only in 4.3% of those treated with CMZ. This difference in percentage of excellent clinical response between 2 treatment groups was statistically significant (P less than 0.05). Of the 87 patients with moderate to severe infection who were treated with CMD, 13 showed an excellent response. Only 4 of 90 patients treated with CMZ showed an excellent response. Statistically the difference in the rate of excellent response between these 2 groups was significant (P less than 0.05).(ABSTRACT TRUNCATED AT 400 WORDS)
头孢孟多酯钠(CMD)是一种新型头孢菌素衍生物,于1972年由美国礼来公司实验室合成。CMD对革兰氏阳性球菌的活性比头孢美唑(CMZ,一种头霉素类抗生素)高几倍,而对革兰氏阴性杆菌的活性与后一种抗生素相当。针对流感嗜血杆菌,CMD表现出与氨苄西林钠一样强的抗菌活性。我们之前对CMD与头孢唑林(CEZ)的疗效和安全性进行的对比试验表明,CMD在治疗呼吸道感染方面与CEZ一样有效且安全。在本次临床试验中,以一种较新合成的头霉素类抗生素CMZ作为对照药物,采用双盲对比法评估CMD的疗效和安全性。为此,在日本东北和北海道地区的50家机构和诊所进行了一项双盲对比研究。共有272名16岁以上、被诊断患有肺炎、肺脓肿或慢性阻塞性肺疾病急性感染加重的住院患者纳入该试验。通常,他们每天通过静脉滴注接受2克CMD或CMZ,持续14天。在这些患者中,264名(133名接受CMD,131名接受CMZ)可用于安全性和有效性评估。238名患者(122名接受CMD,116名接受CMZ)被纳入疗效评估。治疗前,两个治疗组的受试者在年龄、性别、感染严重程度和基础疾病方面无显著差异。接受CMD治疗的患者中有82%获得了良好或优秀的临床反应,接受CMZ治疗的患者中有81%获得了良好或优秀的临床反应。因此,两个治疗组的治愈率无显著差异。然而,接受CMD治疗的患者中有12.3%获得了优秀的临床反应,而接受CMZ治疗的患者中只有4.3%获得了优秀的临床反应。两个治疗组在优秀临床反应百分比上的差异具有统计学意义(P小于0.05)。在接受CMD治疗的87名中重度感染患者中,13名表现出优秀反应。在接受CMZ治疗的90名患者中,只有4名表现出优秀反应。这两组在优秀反应率上的差异具有统计学意义(P小于0.05)。(摘要截取自400字)