医学
无色杆菌
囊性纤维化
铜绿假单胞菌
抗药性
抗生素
痰
木糖氧化酶无色杆菌
美罗培南
抗生素耐药性
重症监护医学
内科学
微生物学
生物
假单胞菌
病理
细菌
遗传学
肺结核
作者
Andrew B. Gainey,Anna‐Kathryn Burch,Michael Brownstein,David E. Brown,Joseph Fackler,Bri’Anna Horne,Biswajit Biswas,Brittany N. Bivens,Francisco Malagón,Robert Daniels
摘要
Cystic fibrosis is associated with significant morbidity and early mortality due to recurrent acute and chronic lung infections. The chronic use of multiple antibiotics without pathogen eradication increases the possibility of extensive drug resistance or even pan-drug resistance (PDR). It is imperative that new or alternative treatment options be explored. We present a clinical case of a 10-year-old female cystic fibrosis patient, infected with a PDR Achromobacter spp. She was treated with cefiderocol, meropenem/vaborbactam, and bacteriophage therapy (Ax2CJ45ϕ2) during two separate admissions in an attempt to clear her infection and restore baseline pulmonary function. The Centers for Disease Control and Prevention confirmed antibiotic susceptibilities, which showed resistance to both cefiderocol and meropenem/vaborbactam. However, after using all three agents concomitantly during the second treatment course, our patient's pulmonary function improved dramatically, and the Achromobacter spp. could not be isolated from sputum samples obtained 8 and 16 weeks after completion of therapy. Overall, the treatment regimen consisting of cefiderocol, meropenem/vaborbactam, and bacteriophage was safe and well-tolerated in our patient.
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