Leibovitz Eugene, Piglansky Lolita, Raiz Simon, Greenberg David, Hamed Kamal A, Ledeine Jean-Marie, Press Joseph, Leiberman Alberto, Echols Roger M, Pierce Phillip F, Jacobs Michael R, Dagan Ron
Pediatric Infectious Disease Unit, Soroka University Medical Center, Ben-Gurion University, PO Box 151, Beer-Sheva 84101, Israel.
Pediatr Infect Dis J. 2003 Nov;22(11):943-9. doi: 10.1097/01.inf.0000095468.89866.14.
Gatifloxacin is an 8-methoxyfluoroquinolone with good activity against respiratory pathogens.
To document the bacteriologic and clinical efficacy of gatifloxacin in recurrent/nonresponsive acute otitis media (AOM).
One hundred sixty patients 6 to 48 months of age with recurrent/nonresponsive AOM received gatifloxacin suspension (10 mg/kg once daily for 10 days). Recurrent AOM was defined as > or =3 AOM episodes during the previous 6 months or > or =4 AOM episodes during the previous 12 months. Nonresponsive AOM was defined as AOM occurring < or =14 days after completing antibiotic treatment or not improving after > or =48 h of therapy. Middle ear fluid (MEF) obtained by tympanocentesis pretreatment (Day 1) and 3 to 5 days after initiation of treatment (Days 4 to 6) was cultured. Additional MEF cultures were obtained if clinical failure or recurrence of AOM occurred. Bacteriologic failure was defined by culture-positive MEF during treatment. Patients were followed until Days 22 to 28. Susceptibility was determined by broth microdilution.
One hundred twenty-eight (80%) patients completed treatment, and 32 discontinued the study prematurely (adverse events, 17; lost to follow-up, 10; consent withdrawal, 3; and laboratory abnormalities, 2). From 89 patients (median age, 1 year; median number of prior AOM episodes, 4; range, 0 to 12), 121 pathogens were recovered: Haemophilus influenzae, 74 (61%); Streptococcus pneumoniae, 36 (30%); Moraxella catarrhalis, 9 (7%); and Streptococcus pyogenes, 2 (2%). The 36 S. pneumoniae isolates were susceptible to gatifloxacin (MIC50 0.25 microg/ml); 26 of 36 (72%) were penicillin-nonsusceptible (15 fully resistant). All 74 H. influenzae isolates were susceptible to gatifloxacin (MIC < or = 0.03 mg/ml). Fourteen of 74 (19%) and 9 of 9 (100%) H. influenzae and M. catarrhalis isolates, respectively, produced beta-lactamase. Bacteriologic eradication was achieved for 118 of 121 (98%) pathogens: 74 of 74 H. influenzae; 34 of 36 (94%) S. pneumoniae; 9 of 9 M. catarrhalis; and 1 of 2 S. pyogenes. Clinical improvement/cure at end of treatment was seen in 103 of 114 (90%) clinically evaluable patients. Clinical recurrence of AOM after completion of therapy occurred in 31 patients. Of the 27 recurrent AOM cases in which tympanocentesis was performed, there were 16 (59%) new infections, 4 (15%) culture-negative results and only 7 (26%) true bacteriologic relapses. Adverse events were recorded in 21 of 160 (13%) patients: vomiting, 16; diarrhea, 3; maculopapular rash, 2. No articular adverse events were recorded.
Gatifloxacin is efficacious and safe for the treatment of recurrent/nonresponsive AOM.
加替沙星是一种8 - 甲氧基氟喹诺酮类药物,对呼吸道病原体具有良好的活性。
记录加替沙星治疗复发性/难治性急性中耳炎(AOM)的细菌学和临床疗效。
160例6至48个月大的复发性/难治性AOM患者接受加替沙星混悬液治疗(10mg/kg,每日1次,共10天)。复发性AOM定义为在前6个月内发生≥3次AOM发作或在前12个月内发生≥4次AOM发作。难治性AOM定义为在完成抗生素治疗后≤14天内发生AOM或在治疗≥48小时后无改善。在治疗前(第1天)及开始治疗后3至5天(第4至6天)通过鼓膜穿刺获取中耳积液(MEF)进行培养。如果发生临床治疗失败或AOM复发,则获取额外的MEF培养物。细菌学失败定义为治疗期间MEF培养阳性。对患者进行随访直至第22至28天。通过肉汤微量稀释法测定药敏性。
128例(80%)患者完成治疗,32例患者提前终止研究(不良事件,17例;失访,10例;撤回同意书,3例;实验室异常,2例)。从89例患者(中位年龄1岁;既往AOM发作的中位次数4次;范围0至12次)中分离出121种病原体:流感嗜血杆菌74株(61%);肺炎链球菌36株(30%);卡他莫拉菌9株(7%);化脓性链球菌2株(2%)。36株肺炎链球菌分离株对加替沙星敏感(MIC50为0.25μg/ml);36株中有26株(72%)对青霉素不敏感(15株完全耐药)。所有74株流感嗜血杆菌分离株对加替沙星敏感(MIC≤0.03mg/ml)。74株流感嗜血杆菌分离株中有14株(19%)和9株卡他莫拉菌分离株中的9株(100%)产生β - 内酰胺酶。121种病原体中的118种(98%)实现了细菌学清除:74株流感嗜血杆菌中的74株;36株肺炎链球菌中的34株(94%);9株卡他莫拉菌中的9株;2株化脓性链球菌中的1株。在114例可进行临床评估的患者中,103例(90%)在治疗结束时临床症状改善/治愈。治疗完成后31例患者发生AOM临床复发。在27例进行鼓膜穿刺的复发性AOM病例中,有16例(59%)为新感染,4例(15%)培养结果阴性,仅7例(26%)为真正的细菌学复发。160例患者中有21例(13%)记录到不良事件:呕吐16例;腹泻3例;斑丘疹2例。未记录到关节不良事件。
加替沙星治疗复发性/难治性AOM有效且安全。