莫西沙星治疗护理及卫生保健相关性肺炎的疗效和安全性

The Japanese journal of antibiotics Pub Date : 2013-10-01
Kei Yamasaki, Kazuhiro Yatera, Toshinori Kawanaml, Yu Suzuki, Yasuo Choujin, Kentarou Akata, Takaaki Ogoshi, Susumu Tokuyama, Shuya Nagata, Naomasa Inoue, Shingo Noguchi, Chinatsu Nishida, Takeshi Orihashi, Yugo Yoshida, Yukiko Kawanami, Yuusuke Taura, Hiroshi Ishimoto, Tatsunori Kawajiri, Hideto Obata, Yukikazu Awaya, Chiharu Yoshii, Hiroshi Mukae
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摘要

莫西沙星(MFLX)是一种呼吸用喹诺酮类药物,不仅对革兰氏阳性和阴性细菌有效,而且对厌氧菌也有效。目前还没有前瞻性研究评估MFLX对护理和医疗保健相关性肺炎(NHCAP)患者的疗效和安全性。因此,我们评估了MFLX在NHCAP患者中的有效性和安全性。2011年4月至2012年3月,日本呼吸学会社区获得性肺炎指南A-DROP系统评定的轻、中度NHCAP患者来我院就诊。评估临床症状、胸部x线片和/或计算机断层扫描、外周血白细胞、红细胞和血小板计数、血清CRP、AST、ALT、BUN、肌酐。最终评估40例患者,平均年龄74.1岁,男女比例21/19,92.5%(37/40)患者有一种或多种合并症。MFLX给药的中位持续时间为7.1天(4-15天)。MFLX在所有患者中的有效率为87.5%(35/40)。各年龄组有效率分别为87.9%(65岁以上)、85.7%(64岁以下),A-DROP系统肺炎严重程度组有效率分别为91.7%(轻度)、85.7%(中度)。开始服用MFLX后,1例患者(2.5%)出现腹泻和乳房肿胀。轻度转氨酶升高3例(7.5%),轻度肾功能不全2例(5.0%)。所有异常升高的转氨酶和血清肌酐水平在停用MFLX后恢复。MFLX对NHCAP患者有效且安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Efficacy and safety of moxifloxacin in patients with nursing and healthcare-associated pneumonia].

Moxifloxacin (MFLX) is a respiratory quinolone, and is effective against not only Gram-positive and negative bacteria but also anaerobes. There has been no prospective studies evaluating the efficacy and safety of MFLX in patients with nursing and healthcare-associated pneumonia (NHCAP). Therefore, we assessed the efficacy and safety of MFLX in patients with NHCAP. NHCAP patients with mild and moderate severity assessed by the A-DROP system in community-acquired pneumonia guideline proposed by Japan Respiratory Society visited our hospitals from April 2011 to March 2012. Clinical symptoms, chest X-ray films and/or computed tomography, peripheral white and red blood cell and platelet counts, serum CRP, AST, ALT, BUN, creatinine were evaluated. Forty patients were eventually evaluated, and average age was 74.1 years old, male/female were 21/19, 92.5% (37/40) of them had one or more comorbidities. Median duration of MFLX administration was 7.1 days (4-15 days). The efficacy of MFLX in all patients was 87.5% (35/40). The efficacies in each age group were 87.9% (aged over 65 years old), 85.7% (aged under 64 years old), and in each pneumonia severity group by the A-DROP system were 91.7% (mild), 85.7% (moderate). Diarrhea and swelling of the breast were observed in one patient (2.5%) after starting MFLX administration. Mild elevated transaminases were observed in three patients (7.5%), and mild renal dysfunction was observed in two patients (5.0%). All abnormally increased levels of transaminases and serum creatinine were recovered after a cessation of MFLX. MFLX is effective and safe in patients with NHCAP.

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