PubMed HealthSearch

PubMed · 7259599

Pneumatic intraocular microscissors.

Abstract

Intraocular microscissors were developed based on a vitreous cutter-like actuation and control by the console and foot pedal. They are right angled for resection of periretinal membranes and 20 gauge for compatibility with the vitrectomy system.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

S Charles, C Wang. 1981. Pneumatic intraocular microscissors.. https://doi.org/10.1001/archopht.1981.03930020125014

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Low-frequency submicron fluctuations of red blood cells in diabetic retinopathy.

OBJECTIVE: To characterize cell membrane mechanical fluctuations of red blood cells (RBCs) in patients with diabetic retinopathy. METHODS: Point dark-field microscopy-based recordings of these local displacements of the cell membrane in human erythrocytes were compared between patients with severe proliferative diabetic retinopathy and healthy controls. The study was performed on discoid RBCs. RESULTS: The average of the maximal displacement amplitude in the diabetic patients was 13.9% +/- 1.7% (236 +/- 29 nm) compared with 18.7% +/- 1.75% (318 +/- 30 nm) for the controls (P<.001). The decrease of the RBCs' average displacement amplitude was not correlated with the variation in negative curvature of the central area of discoid cells. CONCLUSIONS: Microdisplacements of the cell membrane, which reflect the bending deformability of the RBCs, are directly connected with its efficiency in passing through capillaries narrower than its own diameter. These microdisplacements were significantly reduced in patients with severe diabetic retinopathy because of an increase in viscoelasticity of the cell membrane. Such reduced cell membrane microdisplacements, which reflect lower bending deformability of the RBC, reduce the ability of the cell to enter and pass through small capillaries, increasing tissue ischemia and consequently contributing to the development of diabetic retinopathy.

Diabetic Retinopathy

Transforming growth factor beta2 in the vitreous in proliferative diabetic retinopathy.

OBJECTIVE: To evaluate the hypothesis that transforming growth factor beta2 (TGF-beta2) is involved in the cause of proliferative diabetic retinopathy (PDR). METHODS: We assayed TGF-beta2 levels in the vitreous of patients with PDR and other vitreoretinal disorders. Forty-nine vitreous specimens were obtained from eyes of patients with PDR undergoing vitrectomy, and 19 vitreous specimens from nondiabetic subjects served as controls. We assessed TGF-beta2 levels using an enzyme-linked immunosorbent assay. Both mature and total TGF-beta2 levels were quantified. RESULTS: The mean (+/- SD) total levels of TGF-beta2 were 2634 (+/- 1652) pg/mL in the patients with PDR and 1305 (+/- 972) pg/mL in controls. The mean (+/- SD) levels of mature TGF-beta2 were 244 (+/- 316) pg/mL in patients with PDR and 79 (+/- 81) pg/mL in controls. Total and mature TGF-beta2 levels were significantly greater in patients with PDR (total TGF-beta2, P <.001; mature TGF-beta2, P <.01). Mature TGF-beta2 levels were higher in the vitreous of patients who had severe fibrous proliferation. CONCLUSION: The results indicate increased levels of both total and mature TGF-beta2 in the vitreous of patients with PDR, suggesting that TGF-beta2 plays an important role in the pathogenesis of PDR.

Diabetic Retinopathy