Tramper-Stranders Gerdien A, Wolfs Tom F W, Fleer André, Kimpen Jan L L, van der Ent Cornelis K
Department of Pediatric Pulmonology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
Pediatr Infect Dis J. 2007 Jan;26(1):8-12. doi: 10.1097/01.inf.0000247109.44249.ac.
Maintenance azithromycin therapy may improve pulmonary function in patients with cystic fibrosis (CF) with Pseudomonas aeruginosa infection because of its antiinflammatory properties. However, azithromycin therapy might increase macrolide resistance in Staphylococcus aureus cultured from respiratory secretions. We studied the emergence of macrolide resistance in S. aureus and correlated this to pulmonary function decline in pediatric patients with CF on daily azithromycin therapy.
Respiratory cultures of 100 patients with CF were analyzed for S. aureus colonization and its resistance pattern before and during 3 years after initiation of azithromycin maintenance therapy. Mean annual change in forced expiratory volume as percent of predicted (FEV1 %) was calculated to compare pulmonary function before and after azithromycin therapy.
Staphylococcal colonization did not significantly decrease after initiation of azithromycin (50% versus 48%). Before start of therapy, 10% of patients with staphylococcal colonization had macrolide-resistant strains. Staphylococcal resistance increased to 83% in the first year; 97% in the second and 100% in the third year after initiation of azithromycin therapy (P < 0.001). Half of macrolide-resistant S. aureus comprised the macrolide-lincosamide-streptogramin phenotype. Percent forced expiratory volume in 1 second improved in the first year after initiation of azithromycin (mean annual change: -4.75% before versus +3.09% after initiation; P < 0.01) but decreased during the second and third years after initiation (-5.15% and -3.65%, respectively). Emergence of macrolide-resistant S. aureus was not related to pulmonary function decline.
Maintenance azithromycin therapy in patients with CF leads to macrolide resistance in nearly all S. aureus carriers. Pulmonary function improvement after initiation of azithromycin therapy seems to be temporary and appears not to be related to macrolide resistance of S. aureus.
维持性阿奇霉素治疗可能因其抗炎特性而改善患有铜绿假单胞菌感染的囊性纤维化(CF)患者的肺功能。然而,阿奇霉素治疗可能会增加从呼吸道分泌物培养出的金黄色葡萄球菌对大环内酯类药物的耐药性。我们研究了接受每日阿奇霉素治疗的CF患儿中金黄色葡萄球菌大环内酯类耐药性的出现情况,并将其与肺功能下降相关联。
对100例CF患者的呼吸道培养物进行分析,以检测阿奇霉素维持治疗开始前及开始后3年内金黄色葡萄球菌的定植情况及其耐药模式。计算用力呼气量占预计值百分比(FEV1%)的年均变化,以比较阿奇霉素治疗前后的肺功能。
阿奇霉素治疗开始后,葡萄球菌定植情况未显著降低(50%对48%)。治疗开始前,10%的葡萄球菌定植患者有大环内酯类耐药菌株。阿奇霉素治疗开始后,第一年葡萄球菌耐药率增至83%;第二年为97%,第三年为100%(P<0.001)。一半的大环内酯类耐药金黄色葡萄球菌具有大环内酯-林可酰胺-链阳菌素表型。阿奇霉素治疗开始后的第一年,一秒用力呼气量百分比有所改善(年均变化:治疗前为-4.75%,治疗后为+3.09%;P<0.01),但在治疗开始后的第二和第三年下降(分别为-5.15%和-3.65%)。大环内酯类耐药金黄色葡萄球菌的出现与肺功能下降无关。
CF患者接受维持性阿奇霉素治疗会导致几乎所有金黄色葡萄球菌携带者出现大环内酯类耐药。阿奇霉素治疗开始后肺功能的改善似乎是暂时的,且似乎与金黄色葡萄球菌的大环内酯类耐药性无关。