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https://dora.health.qld.gov.au/qldresearchjspui/handle/1/12232| Title: | Retrospective case-series of Paecilomyces lilacinus ocular mycoses in Queensland, Australia, 2000-2023 | Authors: | Van Der Nagel, A. C.;Nguyen, T. ;Conrad, D. | Issue Date: | 2025 | Source: | Clinical and Experimental Ophthalmology, 2025 (53) p.101 | Pages: | 101 | Journal Title: | Clinical and Experimental Ophthalmology | Abstract: | Purpose: (i) To update a previous case-series of Paecilomyces lilacinus infections with a further 15 cases since 2015; (ii) to present the varied clinical manifestations of Paecilomyces lilacinus ocular mycoses; (iii) to identify risk factors and exposure events associated with disease onset; (iv) to discuss treatment regimens/surgery utilised; (v) to determine if outcomes have improved with time given the advent of newer technologies and treatments. Methods: A retrospective case series of 36 cultureproven individuals participated, who were identified via a review of the pathology reporting system utilised in the Queensland public health system. All culture proven individuals were subjected to a systematic chart review. Results: Thirty-six culture-proven cases of Paecilomyces lilacinus ocular mycoses were identified in Queensland from 1998-2023. To date, this is the largest such caseseries pertaining to this pathogen. Immunosuppression via either systemic or topical route was the primary riskfactor identified, as in 75% of cases. 78.78% of cases had an intact epithelial surface prior to onset. 58.3% of cases had no previous ocular history. 33.33% of cases occurred following initiation of topical steroids for other ophthalmic conditions. A striking range of treatments were used, with wide variability seen across eye drop regimens. Visual outcomes remained generally poor, with 44.44% of cases resulting in a final best corrected visual acuity of HM or worse. Conclusion: Paecilomyces lilacinus is a rare but devastating cause of ophthalmic disease, mostly affecting the immunocompromised. Prognosis remains poor, owing to delayed recognition and lack of consistent and effective treatment guidelines. | DOI: | 10.1111/ceo.14486 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L650018536&from=export http://dx.doi.org/10.1111/ceo.14486 |
Type: | Conference Abstract |
| Appears in Sites: | Children's Health Queensland Publications Queensland Health Publications |
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