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Sue A. Aicher

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Open access Jul 2026

Ocular Symptoms After Refractive Surgery.

Importance Characterizing individual ocular symptom trajectories following laser-assisted in situ keratomileusis (LASIK) and photorefractive keratectomy (PRK) may provide a longitudinal, patient-centered perspective on postoperative recovery and help identify patients at risk of prolonged symptom courses. Objective To characterize longitudinal ocular symptom trajectories after refractive surgery, describe associated symptom descriptors over time, and identify baseline factors associated with pain trajectories. Design, Setting, and Participants This prospective, multicenter cohort study was conducted at 2 academic ophthalmology centers in the US from April 2021 to July 2025. Adults undergoing bilateral LASIK or PRK were enrolled and evaluated preoperatively and at postoperative day 1 (POD 1) and months 3 (POM 3) and 6 (POM 6). Participants eligible for refractive surgery were included. Exclusion criteria included pregnancy, corneal abnormality (scar, ectasia, corneal surgery), eye diseases that could confound ocular pain (glaucoma, herpetic eye disease), and age younger than 18 years. Main Outcomes and Measures Ocular pain intensity measured using numerical rating scale (NRS; 0-10) at baseline, POD 1, POM 3, and POM 6. Clinically relevant pain was defined as an NRS score of 3 or greater. Trajectories were classified based on clinically relevant pain presence across time points; baseline demographic, clinical, surgical, and ocular surface factors were evaluated as associated factors. Results Among 326 participants with complete pain data (mean [SD] age, 34.3 [7.9] years; 196 [60.1%] female), pain trajectories were heterogeneous. No clinically relevant pain was observed in 94 participants (28.8%), pain at POD 1 only in 143 participants (43.9%), and prolonged pain (at POM 3 or POM 6) in 59 participants (18.1%); 30 participants had uncommon pain trajectories. Prolonged pain was independently associated with PRK (vs LASIK: odds ratio [OR], 2.73; 95% CI, 1.29-5.77) and several preoperative factors, including lubricating drop use (OR, 2.41; 95% CI, 1.17-4.96), chronic low back pain (OR, 2.45; 95% CI, 1.14-5.25), and greater ocular symptom burden (5-Item Dry Eye Questionnaire score: OR, 1.11; 95% CI, 1.01-1.22). The presence of corneal staining at 6 months after surgery was associated with lower odds of prolonged pain (OR, 0.79; 95% CI, 0.64-0.97). Conclusions and Relevance In this cohort study, postoperative ocular symptom trajectories after refractive surgery followed distinct longitudinal patterns, suggesting these trajectories may have been associated with specific baseline factors. This trajectory-based, symptom-specific approach may provide clinically relevant insight into patient recovery and may improve risk stratification, counseling, and targeted perioperative management, but further corroboration is warranted.

Sujin Kang, Jason Betz, E. Locatelli et al. · 0 citations
Aug 2026

Perineuronal nets preferentially surround parvalbumin interneurons in the prelimbic cortex: A rat and mouse comparison.

Recent work has shown the importance of perineuronal nets (PNNs) in modulating neuronal function and plasticity. Functional studies increasingly manipulate PNNs to probe their role in learning and memory, yet interpreting these manipulations requires knowing which cell types PNNs surround, information that remains incomplete for several brain regions. This study focuses on the prelimbic cortex to determine the percentage of specific interneurons and pyramidal cells that are surrounded by PNNs in male rats and mice. We used immunohistochemistry to assess prelimbic cortex cells containing parvalbumin (PV), glutamate decarboxylase (GAD65/67), and/or calcium kinase II (CamKII), and Wisteria floribunda agglutinin to identify PNNs. Cells with PV, GAD65/67 and/or CamKII were counted and the percentage with PNNs was calculated. Among the cell types examined, PV-expressing interneurons showed the highest frequency of PNN association in the prelimbic cortex of both rats and mice, followed by GAD65/67-expressing interneurons. No CamKII-positive cells had PNNs in rats or mice. PV-only and GAD-only cells were much more likely to have PNNs in mice than in rats. In both species, a small percentage of PNNs surround cells that had no detectable immunolabeling. These findings indicate that PV interneurons are most likely to have PNNs in layers 5/6 of the prelimbic cortex, but species differences suggest caution in designing and interpreting experiments that manipulate PNNs, particularly when generalizing between rat and mouse models.

A. Jenike, Travis E. Brown, S. Impey et al. · 0 citations

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