Abstract
Purpose
To report an outbreak of endophthalmitis in three eyes of two patients following intravitreal methotrexate, caused by Ralstonia pickettii.
Design
Retrospective, noncomparative, consecutive case series.
Methods
Medical records and microbiology results of two patients who presented with acute endophthalmitis following intravitreal methotrexate injection in November 2013 were reviewed.
Results
Following intravitreal injections, the patients experienced pain and decrease in vision in the affected eye within 24 hours of receiving intravitreal methotrexate injection. The presenting visual acuity in case 1 was 20/50 in the left eye. The presenting visual acuity in case 2 was hand motions in the right eye and counting fingers at 1 m in the left eye. Both the patients received methotrexate prepared in the same manufacturing facility. Both the patients underwent vitreous biopsy and intravitreal injection of vancomycin 1 mg/0.1 mL, amikacin 400 µg/0.1 mL, and dexamethasone 400 µg/0.1 mL. Microbiology cultures from vitreous, and used and unused vials of methotrexate from the same batch grew R. pickettii. After 8 months of follow-up, both the patients had visual acuity 20/60 or better.
Conclusion
R. pickettii can be rarely associated with outbreak of endophthalmitis. Timely intervention can be associated with good visual outcome in such patients.
Keywords: Ralstonia pickettii, intravitreal injection, intravitreal methotrexate
Introduction
Intravitreal methotrexate was first used in the treatment of primary intraocular lymphoma.1 Over the years, it has been used to treat posterior and intermediate uveitis.2–4 Methotrexate injected directly into the vitreous cavity is generally well tolerated and has very few complications. The incidence of endophthalmitis, following intravitreal injections ranges from 0.02% to 0.05%.5,6 Most reports have described endophthalmitis following intravitreal injections of anti-VEGFs or long-acting corticosteroids.7,8 We report two cases of endophthalmitis following intravitreal injection with methotrexate contaminated by Ralstonia pickettii. Although Ralstonia species are considered to be a rare infectious organism, recent reports suggest that the organism may be more virulent and widespread than previously thought and may cause infections ranging from asymptomatic colonization to septicemia and death.9
Methods
The current study is a retrospective, noncomparative, consecutive case series. Informed consent was obtained prior to intraocular injections. Intraocular injections were done in the operating room under topical anesthesia and prophylactic povidone-iodine eye drops were used pre- and postinjections. Separate sterile drape, speculum, topical anesthetic drops, povidone-iodine preparation, syringe, and needle were used for each eye. All eyes received intravitreal injections from different vials. Vitreous biopsy was done to obtain the vitreous sample. The age, sex, the affected eye, lens status, the date of the most recent injection, the underlying diagnosis, clinical indication for intravitreal injection, the preinjection visual acuity, the presenting symptoms and signs, management, as well as the microbiology result and postinjection visual acuity were documented.
Results
Case report 1
A 28-year-old male presented with pain, redness, and diminution of vision in the left eye 24 hours after intravitreal methotrexate injection for idiopathic retinal vasculitis. On examination, his best-corrected visual acuity (BCVA) in the left eye was 20/50. His preinjection BCVA had been recorded as 20/30. The conjunctiva was congested with 4+ cells in the anterior chamber and a 2% hypopyon.10 The view to the posterior segment was hazy, with a media clarity of grade 2.11 He was diagnosed with acute-onset endophthalmitis and underwent vitreous biopsy and injection of intravitreal vancomycin 1 mg/0.1 mL, amikacin 400 µg/0.1 mL, and dexamethasone 400 µg/0.1 mL. The patient was started on oral ciprofloxacin along with oral and topical corticosteroids. The visual acuity started improving within 1 week, and the patient had a BCVA of 20/50 after 8 months of follow-up.
Case report 2
A 46-year-old male patient presented with diminution of vision, pain, and watering in both the eyes 6 hours after intravitreal methotrexate injection for pars planitis with cystoid macular edema. On examination, his BCVA was hand motions in the right eye and counting fingers at 1 m in the left eye. Preinjection visual acuity had been recorded as 20/20 in both eyes. Both the eyes had conjunctival congestion with 3–4+ cells in the anterior chamber and a 5% hypopyon.10 On fundus evaluation, the disc could be hazily seen with a media clarity of grade 3.11 He was diagnosed with acute-onset endophthalmitis. The patient underwent vitreous biopsy and injection of intravitreal vancomycin 1 mg/0.1 mL, amikacin 400 µg/0.1 mL, and dexamethasone 400 µg/0.1 mL in both eyes and received oral ciprofloxacin and oral corticosteroids along with frequent topical corticosteroids (Figure 1A). The visual acuity started improving within 1 week (Figure 1B), and at last follow-up visit 8 months later, the patient had a BCVA of 20/60 in right eye and 20/50 in the left eye.
The patients presented with diminution of vision along with pain within 24 hours of injection. The vitreous samples of the patients along with the used vials of methotrexate and two unused vials from the same batch were sent for culture and sensitivity. Microbiology cultures from both vitreous samples, and used and unused vials of methotrexate from the same batch grew R. pickettii. The sensitivities were detected using the Kirby–Bauer disc diffusion method. Microbiological identification was done using the Vitek 2 system (bioMérieux Inc, Marcy l’Etoile, France). Each of the isolates was susceptible to ciprofloxacin, amikacin, imipenem, moxifloxacin and was resistant to ceftazidime, chloramphenicol, and gentamicin. Both these patients were not able to tolerate systemic methotrexate and hence were injected with intravitreal methotrexate. Following the resolution of infection, clearance of hypopyon and intraocular inflammation occurred.
The profile of the patients, clinical features, and the result of treatment are summarized in Table 1.
Table 1.
Case | Age/sex | Eye | Preinjection visual acuity | Visual acuity at presentation | Anterior chamber reaction10 | Media haze11 | Intervention | Final visual acuity |
---|---|---|---|---|---|---|---|---|
1 | 28 years/M | OS | 20/30 | 20/50 | 4+, Hypopyon | Grade 2 | Vitreous biopsy + intraocular antibiotic | 20/50 |
2 | 46 years/M | OD | 20/20 | Hand motions | 4+, Hypopyon | Grade 3 | Vitreous biopsy + intraocular antibiotic | 20/60 |
OS | 20/20 | Counting fingers at 1 meter | 4+, Hypopyon | Grade 3 | Vitreous biopsy + intraocular antibiotic | 20/50 |
Abbreviations: OS, left eye; OD, right eye; M, male.
Discussion
Endophthalmitis outbreaks following intravitreal injections, although rare, have been reported all over the world.12 Most of these outbreaks were caused by drug contamination at the compounding pharmacies or even spurious drugs, and majority of the culture-positive cases involved Staphylococcus and Streptococcus species.13,14
R. pickettii previously known as Burkholderia pickettii or Pseudomonas pickettii is a nonfermenting Gram-negative bacillus and an opportunistic pathogen in both the hospital setting and from environmental sources.15 It has been isolated from multiple clinical specimens including blood, urine, and cerebrospinal fluid.16 A wide variety of infections ranging from minor skin infections to septicemia may be caused by this organism. Most of the cases of infection with R. pickettii have been attributed to contaminated solutions, including water for injection, saline solutions made with purified water, and sterile drug solutions.17–20 Contamination of the product usually happens at the manufacturing stage and may be due to the ability of R. pickettii to pass through both 0.45-mm and 0.2-mm filters that are used for the terminal sterilization of several medicinal products.21 The organism can also form a biofilm and can survive hospital disinfectants like chlorhexidine and ethacridine lactate.22,23
In the current study, the infection could be traced to the contaminated vials of methotrexate. The vials were of the same batch and had been manufactured at the same facility where the breach in sterility may have occurred. The cultured isolates from each of the vials and vitreous had similar antibiotic susceptibility patterns. The isolates were resistant to ceftazidime, a third-generation cephalosporin which is commonly used for empirical therapy in endophthalmitis. Resistance to β-lactam antibiotics is most commonly due to production of β-lactatamase, which leads to the enzymatic deactivation of the drug. It has been reported previously that Ralstonia may produce a variety of β-lactamases, including ceftazidime and imipenem, hydrolyzing OXA-60.24 This can have implications in the treatment of Ralstonia-associated endophthalmitis. Polymerase chain reaction (PCR) may also be helpful in identifying organisms like Ralstonia, which are not commonly implicated in postoperative endophthalmitis.25 Good clinical outcome has been reported before in patients with PCR-proven R. pickettii endohthalmitis, with intravitreal ceftazidime.25 This indicates that all isolates may not be ceftazidime resistant.
Conclusion
R. pickettii is an important pathogen that may cause an outbreak of endophthalmitis. Prompt and early intervention in such outbreaks can be associated with favorable visual outcomes.
Footnotes
Disclosure
The authors report no conflicts of interest in this work.
References
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