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Dive into the research topics where Federica Machetta is active.

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Featured researches published by Federica Machetta.


Cornea | 2006

Corneal endothelium evaluation with 2 noncontact specular microscopes and their semiautomated methods of analysis.

Ugo de Sanctis; Federica Machetta; Luca Razzano; Paola Dalmasso; Federico Grignolo

Purpose: Noncontact specular microscopes and semiautomated methods of endothelial analysis are widely used in the clinical practice and for research purposes. In this study, the interexaminer reproducibility between two noncontact specular microscopes using different semiautomated methods was assessed in normal corneas. Methods: Average cell size (ACS), endothelial cell density (ECD), coefficient of variation (CV), and hexagonality values were independently calculated by two examiners with the Topcon SP 2000P Image-NET retraced method and the Konan CC7000 center method in 49 normal subjects. Interexaminer reproducibility and correlation between instruments/methods were assessed through 95% limits of agreement, intra-class correlation coefficient (ICC), Pearson correlation coefficient, and Spearman rank test. Results: Interexaminer reproducibility was good for ACS and ECD measurements (ICC> 0.85) but weak for CV and hexagonality (ICC < 0.65). Significantly higher ACS and lwer ECD values (P <0.05) were obtained with the Topcon in comparison with the Konan method by both examiners. ACS and ECD mean differences were respectively, +26&mgr;m2 and −184 cell/mm2 for examiner 1 and +36&mgr;m2 and −228 cell/mm2 for examiner 2. No significant difference (P > 0.05) between instruments/methods was found in CV or hexagonality values; however, the correlation for these parameters was low (r < 0.20). Conclusions: Either instrument or method allows reproducible and accurate ACS and ECD measurements on normal corneas, but the difference between the two instruments is systematic and significant. The difference found were not clinically meaningful however for research/longitudinal study purposes, the data collected with the two systems cannot be used interchangeably.


The Open Ophthalmology Journal | 2014

In Vivo Confocal Microscopic Evaluation of Corneal Langerhans Cells in Dry Eye Patients

Federica Machetta; Antonio Maria Fea; Alessandro Guido Actis; Ugo de Sanctis; Paola Dalmasso; Federico Grignolo

Purpose. To assess inflammatory involvement of cornea in dry eye by means of confocal microscopy, evaluating the presence and distribution of Langherans cells (LCs). Methods: 98 eyes of 49 subjects were enrolled: 18 subjects affected by Sjögren Syndrome Dry Eye (SSDE), 17 with Non-Sjögren Syndrome Dry Eye (NSSDE), 14 healthy volunteeers. Dry eye symptoms, tear film, ocular surface damage and corneal confocal microscopy were analized. Results: A significant increase of LCs density was observed at sub-basal nerve plexus (SSDE = 79 cells/mm2 andNDE = 22 cells/mm2; p = 0,0031) and sub-epithelial nerve plexus (SSDE = 38 cells/mm2 and NDE = 3 cells/mm2; p = 0,0169) in central cornea of SSDE group. An increased number of LCs from the center to the periphery of the cornea was observed, significant only in healthy volunteers group. In dry eye patients there was an increase in LCs density in both peripheral and central cornea with a significant difference between NDE (14,66 cells/mm2) and SSDE (56,66 cells/mm2) only in central cornea (p = 0,0028). In SSDE group, mean density of LCs in central cornea results also superior to NSSDE group (29,33 cells/mm2). There was no correlation between LCs density and dry eye symptoms, tear film deficiency and ocular surface damage. Conclusion: This study demonstrates the activation of an inflammatory and immunological reaction in cornea of NSSDE and SSDE patients. Confocal microscopy can be an important diagnostic tool in evaluation and follow-up of dry eye disease.


BioMed Research International | 2016

The Effect of Autologous Platelet Lysate Eye Drops: An In Vivo Confocal Microscopy Study

Antonio Maria Fea; Vittoria Aragno; Valeria Testa; Federica Machetta; Simone Parisi; Sergio D'Antico; Roberta Spinetta; Enrico Fusaro; Federico Grignolo

Purpose. To determine the effectiveness of autologous platelet lysate (APL) eye drops in patients with primary Sjögren syndrome (SS) dry eye, refractory to standard therapy, in comparison with patients treated with artificial tears. We focused on the effect of APL on cornea morphology with the in vivo confocal microscopy (IVCM). Methods. Patients were assigned to two groups: group A used autologous platelet lysate QID, and group B used preservative-free artificial tears QID, for 90 days. Ophthalmological assessments included ocular surface disease index (OSDI), best corrected visual acuity (BCVA), Schirmer test, fluorescein score, and breakup time (BUT). A subgroup of patients in group A underwent IVCM: corneal basal epithelium, subbasal nerves, Langerhans cells, anterior stroma activated keratocytes, and reflectivity were evaluated. Results. 60 eyes of 30 patients were enrolled; in group A (n = 20 patients) mean OSDI, fluorescein score, and BUT showed significant improvement compared with group B (n = 10 patients). The IVCM showed a significant increase in basal epithelium cells density and subbasal nerve plexus density and number and a decrease in Langerhans cells density (p < 0.05). Conclusion. APL was found effective in the treatment of SS dry eye. IVCM seems to be a useful tool to visualize cornea morphologic modifications.


Clinical Ophthalmology | 2008

The trabecular bypass stent in a pseudophakic glaucoma patient: A 1-year follow-up

Antonio Maria Fea; Monica Dogliani; Federica Machetta; Gabriella Lale-Lacroix; B. Brogliatti; Federico Grignolo

Purpose To describe the 1-year success of a trabecular stent implant in a pseudophakic glaucoma patient. The stent is implanted through a small corneal incision under gonioscopic control. Intraocular pressure control was reported in cultured human anterior segment. Design Observational case report. Methods We report the case of a patient who was implanted and followed-up for 1 year at the Dipartimento di Fisiopatologia Clinica. The main outcome measures were intraocular pressure and visual field. Results The patient’s intraocular pressure was controlled with topical beta-blockers for 6 months and without therapy for 6 months. Two diurnal curves demonstrated achievement of target pressure during the day. The 1-year visual field was unchanged. Conclusions We are not aware of previous reports of trabecular stent implantation in pseudophakic patients. The trabecular stent had minimal peri-operative morbidity. Identification of the implantation site is challenging and reduction of efficacy over time may occur.


Clinical Ophthalmology | 2014

Terson syndrome and leukemia: a case report

Umberto Lorenzi; Elisa Buschini; Antonio Maria Fea; Federica Machetta; Federico Grignolo

Background Terson syndrome is defined as intraocular hemorrhage associated with intracranial bleeding. This syndrome can occur in the event of intracranial hemorrhage or elevated intracranial pressure. To our knowledge, it has never been associated with chronic myeloid leukemia. A 45-year-old woman suffering from chronic myeloid leukemia was referred to our clinic with Terson syndrome after intracranial bleeding. We followed this patient for a year, performing visual acuity assessment, fundus examination, color retinography, and A-scan and B-scan ultrasonography. At presentation, her best-corrected visual acuity on the right was 20/63 and on the left was 20/320. In the right eye, retinoscopy showed blurring of the optic margins surrounded by retinal and preretinal hemorrhages, preretinal fibrosis of the optic disc along the vascular arcades, and perivascular retinal infiltrates. In the left eye, the optic disc was surrounded by retinal and preretinal hemorrhages, and massive fibrosis with hard exudates and severe preretinal hemorrhage were observed at the posterior pole. Roth spots and many circular hemorrhages were noted at the periphery of the retina. A-scan and B-scan ultrasonography did not show intraocular leukemic infiltration. The clinical picture remained stable over the following 12 months. In this patient, we observed the ophthalmoscopic features of chronic myeloid leukemia, but also coexistence of features typical of Terson syndrome. To our knowledge, no similar cases have been reported previously.


Ocular Immunology and Inflammation | 2011

In vitro susceptibility to different topical ophthalmic antibiotics of bacterial isolates from patients with conjunctivitis.

Franco Giardini; Giuseppe Grandi; Ugo de Sanctis; Chiara M. Eandi; Federica Machetta; Cristina Pollino; Federico Grignolo

Purpose: To test in vitro the susceptibility to different commercially-available topical antibiotics of isolates from patients with conjunctivitis, evaluated at the Microbiology Service of Turin Ophthalmic Hospital between January 2005-February 2007. Methods: Bacterial isolates were cultured using both liquid and solid media. The four most frequent isolates were analyzed and their in vitro susceptibility to levofloxacin, ofloxacin, norfloxacin, lomefloxacin, tobramycin, netilmycin, ampicillin, and chloramphenicol was tested, using the Kirby-Bauer diffusion method and National Committee for Clinical Laboratory Standards (NCCLS) serum standards. Results: The four most common bacteria isolates were: Staphylococcus aureus (27%), viridians Streptococci (22%), Staphylococcus epidermidis (16%) and streptococcus pneumoniae (13%). The in vitro susceptibility to levofloxacin was highest (p<0.01) for all bacterial isolates. Conclusions: In vitro susceptibility tests showed that levofloxacin had the highest cumulative efficacy against bacterial isolates. Netilmycin showed the highest efficacy against staphylococcus aureus, the most common bacterial isolate in this study.


Ocular Immunology and Inflammation | 2017

Severe Ocular Bacterial Infections: A Retrospective Study Over 13 Years

Carmela Attisano; Monica Cibinel; Guido Strani; Giovanna Panepinto; Cristina Pollino; Gabriella Furfaro; Franco Giardini; Federica Machetta; Federico Grignolo; Giuseppe Grandi

ABSTRACT Purpose: To report data of samples collected from January 2000 to August 2013, in the Department of Diagnosis and Laboratory Analysis, Ophthalmic Hospital, Turin, Italy, from different types of ocular infections and their antibiotic susceptibility. Methods: Collected samples were cultured using both liquid and solid media. Then bacterial isolates were tested for antibiotic susceptibility using the Kirby–Bauer diffusion method and the National Committee for Clinical Laboratory Standards (NCCLS) serum standards. Results: Staphylococcus aureus is the most common bacteria isolated in ocular samples. Conclusions: In vitro susceptibility tests showed that levofloxacin and moxifloxacin (introduced only in 2010) had the highest efficacy against bacterial isolates.


Clinical Ophthalmology | 2017

Treatment of refractory uveitic macular edema: results of a first and second implant of long-acting intravitreal dexamethasone

Marta Zola; Cristina Briamonte; Umberto Lorenzi; Federica Machetta; Federico Grignolo; Antonio Maria Fea

Purpose The purpose of this study was to report the functional and anatomical outcomes of a prospective study resulting from repeated dexamethasone intravitreal implants in patients with uveitic refractory macular edema. Methods Twelve eyes of 9 patients with intermediate and posterior noninfectious inflammatory uveitis complicated with refractory macular edema were regularly reviewed after a dexamethasone intravitreal implant. Patients were examined at baseline, 30, 90, 135, and 180 days with best-corrected visual acuity (BCVA), complete slit-lamp examination, intraocular pressure (IOP), optical coherence tomography, and fluorescein angiography. After 6 months of follow-up, eyes were reassessed to receive a second implant. Results BCVA significantly improved when comparing the baseline values after the first and second implant (16.2 and 25.8 letters, respectively, 9.6 letters improvements, p<0.05). BCVA was better after the second implant compared to the first one throughout the follow-up, but without statistical significance. Mean central macular thickness (CMT) was 446.3±129.9 μm at baseline and was significantly reduced until day 135 (p<0.05). CMT reductions after the second injection showed a similar pattern, though differences were not statistically significant. Cataract progression was observed in 4 of 8 phakic eyes (50%) after the first implant, and in 2 of 3 phakic eyes following the second implant, with 1 eye requiring cataract surgery. One eye developed an IOP >30 mmHg 30 days after the second implant, treated topically. Conclusion Repeated dexamethasone intravitreal implants in uveitic patients with refractory macular edema can be used effectively in a clinical setting with an acceptable safety profile.


Annals of the Rheumatic Diseases | 2016

SAT0326 Efficacy and Safety of Autologous Platelet Lysate Eye Drops in Sjögren's Syndrome: A New Approach

Simone Parisi; Vittoria Aragno; V. Testa; M. Scarati; M. Priora; Federica Machetta; C.L. Peroni; S. D'Antico; Enrico Fusaro; R. Caporali; C. Montecucco

Background Sjögrens Sydrome (SS) is a chronic multisystem autoimmune disease characterized by hypofunction of salivary and lacrimal glands. The result of the immune-mediate infiltration of the lacrimal gland is a severe dry eye disease. None of the commercially available artificial tear preparations and anti-inflammatory topical treatment has the properties of the human tears as Growth factors (GFs), that are necessary for maintenance of normal corneal epithelium. Platelet alfa granules are a major source of GFs and are rich in platelet derived growth factor (PDGF), which plays an important role in the maintenance of ocular surface and tear film stability (1). Objectives To determine the efficacy and safety of autologous platelet lysate (APL) eye drops in patients with primary SS dry eye, refractory to standard therapy, in comparison to patients treated with artificial tears. We focused on the effect of APL on cornea morphology with the in vivo confocal microscopy (IVCM). Methods We included patients with a diagnosis of SS according to the classification criteria of the American-European Consensus (2), a dry eye severity level ≥2 (Dry Eye Severity Grading Scheme, Workshop 2007). Patients were assigned in two groups, according to the randomization criteria 1:1 – Group A used autologous platelet lysate (BiomedDevice) QID for 90 days.– Group B used preservative-free artificial tears QID (Ialuronic Acid 0,2%) for 90 days. Ophthalmological assessments included: ocular surface disease index (OSDI), Schirmer test, fluoresceine score and break up time (BUT). Both Group A and Group B underwent IVCM; corneal basal epithelium, sub basal nerves, Langherans cells, anterior stroma activated keratocytes were evaluated. The study was conducted in accordance with the Declaration of Helsinki (1964) and approved by our Ethics Committee. Results 43 patients (female:male =42:43) with mean age of 59,75 years (SD±13,10) affected by primary SS from 7,48 years (SD±5,56) were enrolled. The two groups (A=22 pts; B=21 pts) did not have significant differences at baseline in terms of disease (duration, autoantibodies) and treatment (steroids, DMARDs) characteristics. In group A, the mean of improvement of OSDI, fluorescein score and BUT values (Δ38.82; Δ1.0; Δ1.5 respectively) were higher than group B (Δ7.07; Δ0.0; Δ0.0 respectively) with statistical significance (p<0.05). The IVCM showed a significant increase in basal epithelium cells density, sub basal nerve plexus density and number and a decrease in Langerhans cells density (p<0.05) only in group A. No adverse events were observed in all patients treated. Conclusions APL has proved to be effective and safety in the treatment of SS dry eye and IVCM seems to be a useful tool to visualize cornea morphologic modifications. Further studies are required to evaluate the long-term effects and the timing of retreatment. References Pezzotta S, Del Fante C, Scudeller L et al. Autologous platelet lysate for treatment of refractory ocular GVHD. Bone Marrow Transplantation 2012; 47, 1558–1563. Vitali C, Bombardieri S, Jonsson R, et al. Classification criteria for Sjogrens syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann Rheum Dis. 2002; 61:554–8. Disclosure of Interest None declared


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Simone Parisi

Casa Sollievo della Sofferenza

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