Biomedical subjects

Giovanni Alessio

Publications and source records attributed to Giovanni Alessio.

4 recordsLinked to original sources

PubMed2005

Relationship between eye symptoms and blepharospasm: a multicenter case-control study.

Although patients with primary blepharospasm (BSP) commonly report experiencing ocular symptoms before the onset of orbicular spasms, the precise frequency and pathogenic role of this subjective ocular discomfort are poorly understood. We conducted a multicenter case-control study to investigate symptoms related to disorders of the anterior segment of the eye, administering a questionnaire to 165 patients with BSP and 180 age- and gender-matched control patients with hemifacial spasm. On a validation sample, our questionnaire yielded high accuracy in detecting eye diseases (predominantly, dry eye syndrome) using detailed ophthalmological examination as the criterion. Logistic regression analysis indicated a significant association between ocular symptoms at disease onset and BSP. Ocular symptoms starting in the year preceding disease onset (short-latency symptoms) showed a stronger association with BSP than ocular symptoms occurring earlier in time (long-latency symptoms). The association was stronger when short-latency symptoms developed from 40 to 59 years of age, whereas this was not observed for long-latency symptoms. Our findings support the view that eye symptoms associated with BSP result from eye diseases and may be involved in the pathogenesis of BSP. The differential risk of developing BSP, based on age at onset of ocular symptoms, suggests that age and eye diseases may interact in giving rise to BSP.

Age of Onset↗

PubMed2003

Combined topical anesthesia and sedation for open-globe injuries in selected patients.

PURPOSE: To evaluate the efficacy and safety of topical anesthesia (TA) and IV sedation in surgery for less severe open-globe injury (OGI). DESIGN: Noncomparative consecutive interventional case series. PARTICIPANTS: Of 67 OGI cases reviewed at the Department of Ophthalmology and Otolaryngology, University of Bari, Bari, Italy, in the period from 1999 to 2000, 10 eyes (14.9%) of 10 consecutive patients (age range, 6-58 years) were repaired using TA and IV sedation. All patients belonged to the American Society of Anesthesiologists risk class I or II. Nine eyes had corneoscleral wounds, four had vitreous loss, two had traumatic cataract, and three had an intraocular foreign body (IOFB); one patient had interruption of a continuous penetrating keratoplasty suture. Preoperatively, best-corrected visual acuity (BCVA) ranged from hand movement to 20/20. INTERVENTION: Corneoscleral suture was performed in nine patients, vitreous excision in four, uveal excision or reposition in four, IOFB removal in three, and cataract extraction in two; corneal button resuture was carried out in one patient. All patients received topical oxybuprocaine hydrochloride 0.4%, and IV propofol, midazolam, and fentanyl for anesthesia. MAIN OUTCOME MEASURES: The change in BCVA was evaluated. Within 24 hours after surgery, each patient was asked to grade subjective pain and discomfort on a 4-point scale. The surgeon was asked to report difficulties attributable to the operating conditions. Complications related to anesthesia and to surgery were assessed. RESULTS: Best-corrected visual acuity stabilized or improved in all patients. All patients had grade 1 pain and discomfort during most of the procedure. All patients had grade 2 (mild) pain and discomfort during external bipolar cautery and conjunctival closure. No patient required additional anesthesia. The operating conditions as reported by the surgeons were graded slightly difficult in all cases but one, which was graded moderately difficult. No patient had surgical or anesthesia-related adverse events or life-threatening complications. CONCLUSIONS: Topical anesthesia and IV sedation are safe and effective and could be a reasonable alternative for less severe OGI. The degree of patient discomfort is only marginal during surgery and postoperatively. However, surgical training and patient preparation are the keys to the safe use of this anesthetic modality.

Adolescent↗

PubMed2002

Accuracy of Orbscan optical pachymetry in corneas with haze.

PURPOSE: To compare corneal thickness measurements with the Orbscan instrument (Orbtek, Inc.) and an ultrasonic pachymeter (Alcon Surgical) in corneas with haze. SETTING: Department of Ophthalmology and Otolaryngology, University of Bari, Bari, Italy. METHODS: Six eyes of 6 patients having phototherapeutic keratectomy for treatment of grade 2+ haze were assessed preoperatively and postoperatively by Orbscan optical pachymetry and ultrasonic pachymetry. Contralateral transparent untreated corneas of the same patients were used as controls. Two Orbscan and 5 ultrasound pachymetry measurements were performed at each visit and the mean values recorded. The accuracy and repeatability of the measurements were evaluated. RESULTS: Preoperatively, the median corneal thickness in the 6 eyes with haze was 512.7 microm by ultrasonic pachymetry and 375.0 microm by optical pachymetry. The mean difference of 143.1 microm was statistically significant (Wilcoxon signed rank test, P= .0277). Postoperatively, the median pachymetry was 439.0 microm and 433.0 microm, respectively; the mean difference was 10.7 microm (P= .0277). In the control group, the median ultrasonic pachymetry was 530.9 microm and the median optical pachymetry, 529.0 microm; the mean difference was 4.7 microm (P= .1730). Precision was good in all groups; the standard deviation was less than 6.0 microm. CONCLUSIONS: The Orbscan system showed a decreased accuracy in measuring corneal thickness when clinically significant haze was present. The repeatability of the measures was good, suggesting that the cause of error lies in the optical acquisition process.

Adult↗

PubMed2002

Visual discomfort after acrylic intraocular lens implantation.

A 64-year-old man had phacoemulsification in both eyes. In January 1998, an Allergan SI-30NB silicone intraocular lens (IOL) with a 6.0 mm optic was implanted in the right eye. In April, an Alcon AcrySof MA60BN acrylic IOL with a 6.0 mm optic was implanted in the left eye. The following October, the patient experienced visual discomfort in the left eye. Two superior radial minikeratotomies were performed. The patient continued to have visual discomfort and the next month, a topographic ablation was performed in the same eye. In January 2000, the left IOL was replaced with a 5.5 mm Allergan SI-55NB silicone IOL. Visual impairment resolved 1 day after surgery.

Acrylic Resins↗