CASE REPORT: Multidrug-resistant Pseudomonas keratitis and sequential endophthalmitis treated with chlorhexidine and piperacillin-tazobactam

Louisa Lu, A. Shen, C. DeBoer, V. Mahajan, Charles Lin, Jennifer Rose-Nussbaumer
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Abstract

To report the clinical course and treatment strategies employed in management of a case of multidrug-resistant Pseudomonas aeruginosa keratitis progressing to endophthalmitis. The drug-resistant strain was later traced to use of contaminated EzriCare Artificial Tears in a multi-state cluster outbreak. A 57-year-old male patient with a history of Descemet stripping automated endothelial keratoplasty was referred for a culture-positive Pseudomonas corneal ulcer in the right eye that had been treated with several weeks of topical moxifloxacin, fortified vancomycin and tobramycin, and intravitreal injections for endophthalmitis. His cornea was cultured off of antibiotics and grew only rare Propionibacterium acnes. Topical antibiotics and steroids were reduced, but his condition rapidly deteriorated with leading to corneal melt, perforation, and endophthalmitis. Repeat corneal cultures and sensitivity analyses revealed growth of a strain of Pseudomonas aeruginosa that was resistant to fluoroquinolones, aminoglycosides, cephalosporins, monobactams, and carbapenems, and only intermediate susceptibility to piperacillin-tazobactam. The patient underwent a therapeutic penetrating keratoplasty and was subsequently initiated on an intensive regimen of topical chlorhexidine and polymyxin-B/trimethoprim. He also underwent a pars plana vitrectomy with anterior chamber washout, followed by serial injections of intravitreal piperacillin-tazobactam at a dose of 225 mg/0.1 mL. After 8 weeks of intensive treatment, there was gradual with healing of his ocular surface, regression of his hypopyon and posterior inflammation, and no signs of recurrent infection. A public health investigation ultimately revealed that his infection was one of several cases involved in a multistate cluster outbreak of extensively drug-resistant Pseudomonas ocular infections that were traced to the use of contaminated EzriCare Artificial Tears. Multidrug-resistant keratitis and endophthalmitis caused by multidrug-resistant Pseudomonas keratitis requires consideration of nonconventional antimicrobial agents and experimental therapeutic alternatives. Topical chlorhexidine and intravitreal piperacillin-tazobactam are currently nonconventional therapies in the context of bacterial keratitis and endophthalmitis, but were safe and effective in the management of multidrug-resistant Pseudomonas aeruginosa ocular infection.
病例报告:多药耐药假单胞菌角膜炎和序贯性眼内炎用氯己定和哌拉西林-他唑巴坦治疗
报告1例多药耐药铜绿假单胞菌角膜炎发展为眼内炎的临床过程及治疗策略。耐药菌株后来被追踪到在多州群集爆发中使用了受污染的EzriCare人工泪液。一名57岁男性患者,有Descemet剥离自动内皮角膜移植术史,因右眼培养阳性假单胞菌角膜溃疡而被转诊,该患者曾接受数周的局部莫西沙星、强化万古霉素和妥布霉素治疗,并通过玻璃体内注射治疗眼内炎。他的角膜在没有抗生素的情况下培养,只生长出罕见的痤疮丙酸杆菌。局部抗生素和类固醇减少,但他的病情迅速恶化,导致角膜融化,穿孔和眼内炎。重复角膜培养和敏感性分析显示,一株铜绿假单胞菌对氟喹诺酮类药物、氨基糖苷类药物、头孢菌素、单巴菌素和碳青霉烯类药物耐药,对哌西林-他唑巴坦只有中等敏感性。患者接受了穿透性角膜移植术,随后开始了局部氯己定和多粘菌素- b /甲氧苄啶的强化治疗方案。患者同时行玻璃体切除伴前房冲洗术,随后连续注射剂量为225 mg/0.1 mL的哌拉西林-他唑巴坦玻璃体内注射。强化治疗8周后,患者眼表逐渐愈合,下丘脑和后部炎症消退,无复发感染迹象。一项公共卫生调查最终显示,他的感染是多州广泛耐药假单胞菌眼部感染聚集性爆发的几个病例之一,这些感染可追溯到使用受污染的EzriCare人工泪液。多药耐药角膜炎和眼内炎由多药耐药假单胞菌角膜炎引起,需要考虑非传统抗菌药物和实验性治疗方案。目前,在细菌性角膜炎和眼内炎的治疗中,外用氯己定和玻璃体内注射哌哌西林-他唑巴坦是一种非传统的治疗方法,但在多药耐药铜绿假单胞菌眼部感染的治疗中是安全有效的。
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