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Featured researches published by Gianmarco Paris.


Antimicrobial Agents and Chemotherapy | 2006

Topical Voriconazole as a Novel Treatment for Fungal Keratitis

William E. Sponsel; Nancy Chen; Demi Dang; Gianmarco Paris; John R. Graybill; Laura K. Najvar; Lei Zhou; Kwok Wai Lam; Randolph D. Glickman; Frank W. Scribbick

ABSTRACT Paecilomyces lilacinus is a fungal pathogen which is generally resistant to amphotericin B and certain other antifungals and is an uncommon cause of devastating fungal keratitis. In the present studies, we evaluated topical voriconazole as therapy for P. lilacinus keratitis in rabbits. Thirty eyes of 15 rabbits were studied. In five animals, the uninfected left eye was treated twice daily with voriconazole (drug control, uninfected eye). In these same animals, the right eye was infected with P. lilacinus but not treated with voriconazole (infection control eye). By day 5, the infection controls had lesions of >2.4 mm in diameter, with conjunctivitis and severe hypopyon, and were sacrificed. In the other 10 rabbits (voriconazole treatment), the right eyes were infected with P. lilacinus and treated with voriconazole beginning on day 3 after infection. Voriconazole therapy caused lesions to decrease during 8 days of therapy, after which rabbits were sacrificed (11 days postinfection). Hyphal masses were present in the control infected eyes and absent in treated infected eyes. Voriconazole was detected in all tissues of treated eyes. Topical voriconazole is effective treatment for P. lilacinus experimental keratitis, and it penetrates more deeply than the corneal tissue.


American Journal of Ophthalmology | 2002

Latanoprost and brimonidine: therapeutic and physiologic assessment before and after oral nonsteroidal anti-inflammatory therapy.

William E. Sponsel; Gianmarco Paris; Yolanda Trigo; Melanie Pena; Anke Weber; Keith Sanford; S.J. McKinnon

PURPOSE To assess, before and during oral nonsteroidal anti-inflammatory drug coadministration, latanoprosts and brimonidines hypotensive action in eyes at risk of glaucomatous progression, assessing the effect of each drug on ocular perfusion and visual function. METHODS Twenty consenting adults with open-angle glaucoma or ocular hypertension underwent a double-masked, bilateral, randomized prospective study. Treatment started with either latanoprost 0.005% in the morning and placebo in the evening, or brimonidine 0.2% twice daily in one eye; after 1 week starting the other in the fellow eye. After another week, oral indomethacin 25 mg four times a day, commenced for 2 more weeks. Intraocular pressure, ocular circulation, and visual function were monitored pretreatment, after unilateral monotherapy (day 7), bilateral ocular therapy (day 14), and coadministered oral indomethacin (day 28). Intrasubject differences (interocular and intraocular relative to baseline) were determined by two-tailed paired t test. RESULTS A loss of the significance of intraocular pressure reduction with brimonidine was noted after oral indomethacin coadministration (-14%; P =.004 for brimonidine alone versus -11%; P =.3 with indomethacin). Significant intraocular pressure reduction with latanoprost persisted despite indomethacin (-25%; P <.0001 for latanoprost alone versus -30%; P <.0001 with indomethacin). Pulsatile ocular blood flow increased 40% with latanoprost, but was unchanged with brimonidine (interdrug difference, P =.004). Midperipheral retinal microcirculation increased 23% (P =.03) with latanoprost. Humphrey perimetry and contrast sensitivity remained consistently at or above baseline with both latanoprost and brimonidine. Indomethacin had no significant effect on ocular perfusion or visual function measures. CONCLUSIONS Circulatory and hydrodynamic findings differed substantially for the two drugs. The loss of significance of intraocular pressure reduction with brimonidine during indomethacin treatment may be clinically important.


American Journal of Ophthalmology | 2002

Comparative Effects of Latanoprost (Xalatan) and Unoprostone (Rescula) in Patients With Open-angle Glaucoma and Suspected Glaucoma

William E. Sponsel; Gianmarco Paris; Yolanda Trigo; Melanie Pena

PURPOSE To compare, in paired eyes of open-angle glaucoma patients and glaucoma suspects, hydrodynamic and visual changes after 1 month of topical latanoprost in one eye and unoprostone in the other. DESIGN Single-center, institutional randomized clinical trial. METHODS After completing a washout period off all topical medication, 25 adults (mean age 54 +/- SEM 2 years) with bilateral open-angle glaucoma or glaucoma suspect status underwent morning (8 to 10 AM) and afternoon (1 to 3 PM) measurements of intraocular pressure (IOP), pulsatile ocular blood flow (POBF), contrast, sensitivity, frequency doubling technology, and Humphrey 10-2 perimetry (HVFA II) in both eyes. Each then started unoprostone 0.15% (Rescula) in one randomly assigned eye and latanoprost 0.005% (Xalatan) in the other. Unoprostone was administered at 8 AM and 8 PM and latanoprost at 8 PM with placebo at 8 AM, both from masked bottles. After 28 days, differences were determined for each measured variable by two-tailed paired t test. RESULTS Starting from similar baseline IOP levels, after 1 month of treatment, the mean morning IOP values differed according to the topical agent received (16.2 +/- SEM 0.6 mm Hg for latanoprost vs 17.9 +/- 0.7 mm Hg for unoprostone; P =.001). These morning pressures were 2.6 mm Hg lower than baseline in the eyes receiving latanoprost (P <.0001), and 1.6 mm Hg lower in unoprostone-treated eyes (P =.02). Afternoon values were 3.1 +/- SEM 0.6 lower than corresponding baseline in eyes receiving latanoprost, and 2.4 +/- SEM 0.6 mm Hg in unoprostone-treated eyes (P <.0001 from baseline for both medications; interdrug mean IOP difference; P =.04). Eyes receiving unoprostone showed a 1.7-db improvement in frequency doubling mean deviation (P =.03), the only significant visual function change observed. Pulsatile ocular blood flow increased 30% relative to baseline in eyes receiving latanoprost, (P <.0001) and 16% in eyes receiving unoprostone (P =.05) by the morning of day 28. That afternoon, mean POBF had increased 30% (P <.0001) relative to afternoon baseline values among eyes receiving latanoprost and 18% (P =.03) among those receiving unoprostone (interdrug change difference, P =.05). Humphrey perimetry and contrast sensitivity remained stable with both prostanoids. CONCLUSIONS Both latanoprost and unoprostone produced significant reductions in IOP and increases in POBF, with stable central and perimacular visual function. Latanoprost once daily produced IOP reduction and POBF increases nearly twofold greater than those obtained with unoprostone twice daily. These differences in IOP and POBF change between unoprostone and latanoprost were statistically significant.


American Journal of Ophthalmology | 2003

Spontaneous regression of choroidal metastasis from renal cell carcinoma

Amjad M. Hammad; Gianmarco Paris; Wichard A.J. van Heuven; Ian M. Thompson; Thomas D. Fitzsimmons

PURPOSE To describe a patient with choroidal metastasis from renal cell carcinoma that spontaneously regressed after nephrectomy. DESIGN Interventional case report. METHOD A 48-year-old Hispanic woman presented with reduced vision in the left eye attributable to an elevated choroidal lesion and associated exudative retinal detachment. Oncology workup revealed a left kidney renal cell carcinoma with pulmonary metastases. The patient underwent primary nephrectomy, without specific treatment of choroidal or pulmonary metastases. RESULTS The metastatic choroidal lesion regressed and the retinal detachment completely resolved, as evidenced by fundus photographs and ultrasonography. CONCLUSIONS Choroidal metastasis from renal cell carcinoma may spontaneously regress after removal of the primary tumor.


Clinical and Experimental Ophthalmology | 2004

Operative revision of non-functioning filtering blebs with 5-fluorouracil to regain intraocular pressure control

Gianmarco Paris; Ming Zhao; William E. Sponsel

Purpose: To determine the efficacy of extensive microsurgical needling revision of failed filtering blebs followed by serial 5‐fluorouracil subconjunctival injections.


International Ophthalmology | 2001

Sildenafil increases ocular perfusion

Gianmarco Paris; William E. Sponsel; Sal S. Sandoval; W. Rowe Elliott; Yolanda Trigo; Donald K. Sanford; Joseph M. Harrison


The New England Journal of Medicine | 2000

Sildenafil and ocular perfusion.

William E. Sponsel; Gianmarco Paris; Sal S. Sandoval; Donald K. Sanford; Joseph M. Harrison; W. Rowe Elliott; Yolanda Trigo


Archive | 2002

Prostanoids augment ocular drug penetration

William E. Sponsel; Randolph D. Glickman; Gianmarco Paris; Vanessa Bernal; John R. Graybill


Documenta Ophthalmologica | 2005

Retinal Function Assessed by ERG Before and After Induction of Ocular Aspergillosis and Treatment by the Anti-fungal, Micafungin, in Rabbits

Joseph M. Harrison; Randolph D. Glickman; Charles S. Ballentine; Yolanda Trigo; Melanie Pena; Pearl Kurian; Laura K. Najvar; Neeru Kumar; Ankit H. Patel; William E. Sponsel; John R. Graybill; William C. Lloyd; Margaret M. Miller; Gianmarco Paris; Fernando Trujillo; Aaron Miller; Robert F. Melendez


Investigative Ophthalmology & Visual Science | 2004

Comparison of Two Antifungal Agents, Natamycin and Micafungin, for Fungal Keratitis

F. Trujillo; Gianmarco Paris; L. Woodward; J. Graybill; Melanie Pena; L. Najvar; Yolanda Trigo; William E. Sponsel

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William E. Sponsel

University of the Incarnate Word

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Yolanda Trigo

University of Texas Health Science Center at San Antonio

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Melanie Pena

University of Texas Health Science Center at San Antonio

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John R. Graybill

University of Texas Health Science Center at San Antonio

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Joseph M. Harrison

University of Texas Health Science Center at San Antonio

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Randolph D. Glickman

University of Texas Health Science Center at San Antonio

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Charles S. Ballentine

University of Texas Health Science Center at San Antonio

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Donald K. Sanford

University of Texas Health Science Center at San Antonio

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F. Trujillo

University of Texas Health Science Center at San Antonio

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Laura K. Najvar

University of Texas Health Science Center at San Antonio

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