Kawamura Kodai, Ichikado Kazuya, Suga Moritaka, Yoshioka Masakazu
Division of Respiratory Medicine, Saiseikai Kumamoto Hospital, Kumamoto, Japan.
Respiration. 2014;87(6):478-84. doi: 10.1159/000358443. Epub 2014 Apr 30.
Acute exacerbation of chronic fibrosing interstitial pneumonia (AE-CFIP) is an often fatal condition with no established treatment. Recently, macrolides were found to be beneficial in cases of acute lung injury.
To examine the clinical effectiveness and safety of intravenous azithromycin in patients hospitalized for AE-CFIP.
A prospective, open-label study with historical controls was conducted. Twenty consecutive patients with AE-CFIP received azithromycin. They were compared with a historical cohort treated with fluoroquinolone (n = 56). All patients received high-dose steroid pulse therapy. The primary end point was mortality at 60 days. The secondary end point was safety of intravenous azithromycin in patients with AE-CFIP. Inverse probability of treatment weighting (IPTW) using the propensity score was performed to investigate the relationship between azithromycin use and survival time.
Mortality was significantly lower in the patients treated with azithromycin than in those treated with fluoroquinolone (mortality rate at 60 days: 20 vs. 69.6%, p < 0.001; median survival time: not reached vs. 29.5 days, p < 0.001). The IPTW adjusted hazard of mortality at 60 days in patients receiving azithromycin was 0.17 (95% CI 0.05-0.61). No serious adverse events were observed.
Azithromycin was associated with improved outcomes in patients with AE-CFIP. Further studies are needed to verify this finding (Clinical trial JMA-IIA00095).
慢性纤维化间质性肺炎急性加重(AE-CFIP)是一种常致命且尚无既定治疗方法的疾病。最近发现大环内酯类药物对急性肺损伤病例有益。
研究静脉注射阿奇霉素对因AE-CFIP住院患者的临床有效性和安全性。
进行了一项有历史对照的前瞻性开放标签研究。连续20例AE-CFIP患者接受阿奇霉素治疗。将他们与接受氟喹诺酮治疗的历史队列(n = 56)进行比较。所有患者均接受大剂量类固醇脉冲治疗。主要终点是60天的死亡率。次要终点是静脉注射阿奇霉素对AE-CFIP患者的安全性。使用倾向评分进行治疗权重逆概率(IPTW)分析,以研究阿奇霉素使用与生存时间之间的关系。
接受阿奇霉素治疗的患者死亡率显著低于接受氟喹诺酮治疗的患者(60天死亡率:20% 对69.6%,p < 0.001;中位生存时间:未达到对29.5天,p < 0.001)。接受阿奇霉素治疗的患者60天IPTW调整后的死亡风险为0.17(95%CI 0.05 - 0.61)。未观察到严重不良事件。
阿奇霉素与AE-CFIP患者预后改善相关。需要进一步研究以验证这一发现(临床试验JMA-IIA00095)。