Ashley Polski

Ashley Polski

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

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Previous Organizations / Institutes

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Ashley Polski has a total of 110 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    The Role of Stress Reduction and Mindfulness Meditation in Glaucoma Management: A Review

    by Ashley Polski, Anthony P. Mai, Brian C. Stagg, Barbara M. Wirostko

    Glaucoma is a progressive optic neuropathy that is increasing in prevalence worldwide and can lead to devastating vision loss and even blindness if left untreated. Current medical and surgical approaches to glaucoma treatment all aim to lower intraocular pressure (IOP), which is a well-known risk factor for glaucoma development and progression. Although the exact pathogenesis of glaucoma is not yet fully elucidated, multiple studies suggest that mental stress and elevated cortisol levels may contribute to IOP elevation and glaucomatous progression. In recent decades, various randomized-controlled trials have also demonstrated a significant reduction of IOP in patients practicing stress-reduction techniques, including mindfulness meditation and yoga. In this review, we discuss the relationship between mental stress and glaucoma and review the supporting literature to highlight the potential role of mindfulness meditation as an adjunctive strategy to reduce stress and thereby lower IOP in glaucoma patients.


  • Open Access

    Uveitis-Glaucoma-Hyphema Syndrome From Subtle Malposition of a Hydrus Microstent

    by Ashley Polski, Theresa Long, Brian C. Stagg, Barbara Wirostko

    Uveitis-glaucoma-hyphema (UGH) syndrome is a rare condition characterized by intraocular inflammation, elevated intraocular pressure, and recurrent hyphema. Although UGH syndrome is typically caused by chafing between an intraocular lens and the iris or ciliary body, microinvasive glaucoma devices are becoming increasingly recognized as potential causes of recurrent intraocular inflammation. Herein, we discuss a case of UGH syndrome due to the subtle malposition of a Hydrus microstent that ultimately required surgical removal to manage. This represents the first case of Hydrus-related UGH syndrome to include high-quality anterior segment imaging, which led us to suspect Hydrus-iris contact and supported the decision to proceed with microstent explantation.


  • Open Access

    Incident glaucoma and ocular hypertension after periocular and intravitreal steroid injections: a claims-based analysis

    by Ashley Polski, Katy C Liu, Divakar Gupta, Dilraj S Grewal, Joshua Horns, Barbara M Wirostko, Brian C Stagg

    Background/aims This study aims to determine the incidence and risk of open-angle glaucoma or ocular hypertension (OHT) following ocular steroid injections using healthcare claims data. Methods We retrospectively reviewed deidentified insurance claims data from the IBM MarketScan Database to identify 19 156 adult patients with no prior history of glaucoma who received ocular steroid injections between 2011 and 2020. Patient demographics and steroid treatment characteristics were collected. Postinjection glaucoma/OHT development was defined as a new diagnosis of glaucoma/OHT, initiation of glaucoma drops, and/or surgical or laser glaucoma treatment. Cox proportional hazards models were used to determine the risk of glaucoma/OHT development within 5 years after first steroid injection. Results Overall, 3932 (20.5%) patients were diagnosed with new glaucoma/OHT, 3345 (17.5%) started glaucoma drops and 435 (2.27%) required a laser or surgical glaucoma procedure within 5 years of first steroid injection. Triamcinolone subconjunctival injections were associated with a lower risk of glaucoma/OHT development than retrobulbar or intravitreal steroid injections (pConclusion Patients receiving ocular steroid injections are at risk of developing glaucoma/OHT, even with no prior glaucoma/OHT diagnosis or treatment. Patients should be closely monitored for the development of glaucoma following ocular steroid injections, particularly in the setting of intravitreal and/or repeated steroid administration.


  • Open Access

    Data from Chromosome 6p Amplification in Aqueous Humor Cell-Free DNA Is a Prognostic Biomarker for Retinoblastoma Ocular Survival

    by Liya Xu, Ashley Polski, Rishvanth K. Prabakar, Mark W. Reid, Patricia Chevez-Barrios, Rima Jubran, Jonathan W. Kim, Peter Kuhn, David Cobrinik, James Hicks, et al.

    Aqueous humor contains tumor-derived cell-free DNA (cfDNA) and can serve as a liquid biopsy for retinoblastoma. We previously associated somatic copy-number alteration (SCNA) 6p gain with a 10-fold increased risk of enucleation. Here we provide a 2-year update to further explore 6p gain as a prognostic biomarker for ocular survival. Patients diagnosed with retinoblastoma from December 2014 to July 2019 from whom aqueous humor was sampled were included. cfDNA was extracted and shallow whole-genome sequencing performed to identify highly recurrent retinoblastoma SCNAs (gain of 1q, 2p, 6p, loss of 13q, 16q). 116 aqueous humor samples from 50 eyes of 46 patients were included: 27 eyes were salvaged, 23 were enucleated. Highly recurrent retinoblastoma SCNAs were found in 66% eyes. 6p gain was the most prevalent SCNA (50% eyes). It was particularly more prevalent in enucleated eyes (73.9%) than in salvaged eyes (29.6%; P = 0.004). 6p gain in aqueous humor cfDNA portended nearly 10-fold increased odds of enucleation (OR = 9.87; 95% confidence interval = 1.75–55.65; P = 0.009). In the enucleated eyes, 6p gain was associated with aggressive histopathologic features, including necrosis, higher degrees of anaplasia, and focal invasion of ocular structures. With extended follow-up and nearly double the aqueous humor samples, we continue to demonstrate 6p gain as a potential prognostic biomarker for retinoblastoma.Implications:Aqueous humor is a high-yield source of tumor-derived DNA in retinoblastoma eyes. Detection of 6p gain in the aqueous humor allows for targeted, patient-centered therapies based on this molecular prognostic marker. Prospective, multicenter studies with aqueous humor sampled from all eyes at diagnosis are warranted to validate these findings.

  • Open Access

    Data from Chromosome 6p Amplification in Aqueous Humor Cell-Free DNA Is a Prognostic Biomarker for Retinoblastoma Ocular Survival

    by Liya Xu, Ashley Polski, Rishvanth K. Prabakar, Mark W. Reid, Patricia Chevez-Barrios, Rima Jubran, Jonathan W. Kim, Peter Kuhn, David Cobrinik, James Hicks, et al.

    Aqueous humor contains tumor-derived cell-free DNA (cfDNA) and can serve as a liquid biopsy for retinoblastoma. We previously associated somatic copy-number alteration (SCNA) 6p gain with a 10-fold increased risk of enucleation. Here we provide a 2-year update to further explore 6p gain as a prognostic biomarker for ocular survival. Patients diagnosed with retinoblastoma from December 2014 to July 2019 from whom aqueous humor was sampled were included. cfDNA was extracted and shallow whole-genome sequencing performed to identify highly recurrent retinoblastoma SCNAs (gain of 1q, 2p, 6p, loss of 13q, 16q). 116 aqueous humor samples from 50 eyes of 46 patients were included: 27 eyes were salvaged, 23 were enucleated. Highly recurrent retinoblastoma SCNAs were found in 66% eyes. 6p gain was the most prevalent SCNA (50% eyes). It was particularly more prevalent in enucleated eyes (73.9%) than in salvaged eyes (29.6%; P = 0.004). 6p gain in aqueous humor cfDNA portended nearly 10-fold increased odds of enucleation (OR = 9.87; 95% confidence interval = 1.75–55.65; P = 0.009). In the enucleated eyes, 6p gain was associated with aggressive histopathologic features, including necrosis, higher degrees of anaplasia, and focal invasion of ocular structures. With extended follow-up and nearly double the aqueous humor samples, we continue to demonstrate 6p gain as a potential prognostic biomarker for retinoblastoma.Implications:Aqueous humor is a high-yield source of tumor-derived DNA in retinoblastoma eyes. Detection of 6p gain in the aqueous humor allows for targeted, patient-centered therapies based on this molecular prognostic marker. Prospective, multicenter studies with aqueous humor sampled from all eyes at diagnosis are warranted to validate these findings.

  • Open Access

    Supplementary Table 1 from Chromosome 6p Amplification in Aqueous Humor Cell-Free DNA Is a Prognostic Biomarker for Retinoblastoma Ocular Survival

    by Liya Xu, Ashley Polski, Rishvanth K. Prabakar, Mark W. Reid, Patricia Chevez-Barrios, Rima Jubran, Jonathan W. Kim, Peter Kuhn, David Cobrinik, James Hicks, et al.

    Supplementary Table 1. Retinoblastoma (RB) patient demographics, clinical outcomes, and RB somatic copy number alterations (SCNAs) at a large RB treatment center.

  • Open Access

    Supplementary Table 1 from Chromosome 6p Amplification in Aqueous Humor Cell-Free DNA Is a Prognostic Biomarker for Retinoblastoma Ocular Survival

    by Liya Xu, Ashley Polski, Rishvanth K. Prabakar, Mark W. Reid, Patricia Chevez-Barrios, Rima Jubran, Jonathan W. Kim, Peter Kuhn, David Cobrinik, James Hicks, et al.

    Supplementary Table 1. Retinoblastoma (RB) patient demographics, clinical outcomes, and RB somatic copy number alterations (SCNAs) at a large RB treatment center.

  • Open Access

    The Effects of Breastfeeding on Retinoblastoma Development: Results from an International Multicenter Retinoblastoma Survey

    by Jasmeen K. Randhawa, Mary E. Kim, Ashley Polski, Mark W. Reid, Kristen Mascarenhas, Brianne Brown, Ido Didi Fabian, Swathi Kaliki, Andrew W. Stacey, Elizabeth Burner, et al.

    The protective effects of breastfeeding on various childhood malignancies have been established but an association has not yet been determined for retinoblastoma (RB). We aimed to further investigate the role of breastfeeding in the severity of nonhereditary RB development, assessing relationship to (1) age at diagnosis, (2) ocular prognosis, measured by International Intraocular RB Classification (IIRC) or Intraocular Classification of RB (ICRB) group and success of eye salvage, and (3) extraocular involvement. Analyses were performed on a global dataset subgroup of 344 RB patients whose legal guardian(s) consented to answer a neonatal questionnaire. Patients with undetermined or mixed feeding history, family history of RB, or sporadic bilateral RB were excluded. There was no statistically significant difference between breastfed and formula-fed groups in (1) age at diagnosis (p = 0.20), (2) ocular prognosis measures of IIRC/ICRB group (p = 0.62) and success of eye salvage (p = 0.16), or (3) extraocular involvement shown by International Retinoblastoma Staging System (IRSS) at presentation (p = 0.74), lymph node involvement (p = 0.20), and distant metastases (p = 0.37). This study suggests that breastfeeding neither impacts the sporadic development nor is associated with a decrease in the severity of nonhereditary RB as measured by age at diagnosis, stage of disease, ocular prognosis, and extraocular spread. A further exploration into the impact of diet on children who develop RB is warranted.