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1.
Eur J Ophthalmol ; 34(2): 529-533, 2024 Mar.
Article in English | MEDLINE | ID: mdl-37654069

ABSTRACT

PURPOSE: comparison between two anesthetic techniques on the ability to reduce pain during panretinal photocoagulation (PRP) treatment. METHODS: Observational retrospective single center study. Medical charts of patients who underwent PRP for proliferative diabetic retinopathy were revised. Patients were included if they had the first eye treated with oxybuprocaine hydrochloride drops, and in case of severe pain, the fellow eye received topical anesthesia in combination with 2% subconjunctival lidocaine. The groups were compared for pain perception using an analog visual scale (VAS), number of laser spots, number of interruptions, and laser session duration. RESULTS: Forty-two eyes of 21 patients (mean age: 58.3 ± 7.6 years) were analyzed. The mean number of laser spots was significantly higher under combined anesthesia (+84.2 ± 155.9 spots, p = 0.01), with a reduced time for laser execution (-2.5 ± 3.12, p = 0.0008). The use of combined anesthesia significantly decreased the number of interruptions (-40.8%, p < 0.0001) into a single session. On the pain grading scale, the pain perception was significantly lower in the combined anesthesia group (p < 0.0001). In eyes receiving topical anesthesia the treatment was stopped for pain in 5 eyes (23.8%), while 5 eyes under combined anesthesia presented subconjunctival hemorrhage (23.8%). CONCLUSION: Using combined anesthesia in patients subjected to PRP appeared to reduce pain perception limiting the treatment duration and the interruptions for pain without significant complications. Further studies on a larger scale would be desirable to replicate such findings and standardize the analgesic procedures in ophthalmology.


Subject(s)
Diabetes Mellitus , Diabetic Retinopathy , Humans , Middle Aged , Aged , Diabetic Retinopathy/surgery , Retrospective Studies , Laser Coagulation/methods , Anesthesia, Local , Pain/etiology
2.
Eur Rev Med Pharmacol Sci ; 21(4): 662-668, 2017 02.
Article in English | MEDLINE | ID: mdl-28272719

ABSTRACT

OBJECTIVE: To assess vitreous and plasma changes of vascular endothelial growth factor A (VEGF-A), adrenomedullin (ADM) and endothelin-1 (ET-1) in proliferative diabetic retinopathy (PDR). PATIENTS AND METHODS: 9 patients with PDR in type 2 diabetes (T2DM) and 11 age-matched non-diabetic patients were enrolled. The levels of VEGF-A, ADM and ET-1 were measured using an enzyme (ELISA) and a radioimmunoassay (RIA) both in vitreous and plasma samples. RESULTS: Vitreous ADM and VEGF-A levels were significantly higher in PDR patients (p=0.04 and p=0.02), whereas no differences were found in ET-1 levels (p=0.29). Plasma ADM levels were significantly higher in the PDR group (p<0.01), whereas no significant differences were found in the plasma ET-1 and VEGF-A levels (p=0.30 and p=0.37). The ADM vitreous/plasma ratio was significantly reduced in PDR group. CONCLUSIONS: The role of ET-1 in advanced PDR is still controversial; it has been supposed a role limited to induce hypoxic state and promote angiogenesis in the early phases. Once the neo-angiogenic process starts, other mediators are mainly involved as VEGF and ADM. Our findings suggest that ADM is an important marker of advanced PDR as well as VEGF. Conversely, ET-1 is not significantly involved in the advanced stage of PDR.


Subject(s)
Adrenomedullin/metabolism , Diabetic Retinopathy/metabolism , Endothelin-1/metabolism , Vascular Endothelial Growth Factor A/metabolism , Adrenomedullin/blood , Adult , Aged , Aged, 80 and over , Case-Control Studies , Diabetes Mellitus, Type 2/metabolism , Endothelin-1/blood , Endothelium, Vascular/metabolism , Enzyme-Linked Immunosorbent Assay , Female , Humans , Male , Middle Aged , Vascular Endothelial Growth Factor A/blood , Vitreous Body/metabolism
3.
Clin Ter ; 165(5): 261-8, 2014.
Article in Italian | MEDLINE | ID: mdl-25366947

ABSTRACT

We report a rare case of acute posterior multifocal placoid pigment epitheliopathy (APMPPE) in an elderly patient and a review of the recent scientific literature. A 65-year-old Caucasian man, forty-five days after return from tropical travel he developed right-sided facial palsy with right hemiplegia, dysarthria and a positive Babinski sign. He started prednisone 90 mg/day. Clinical, laboratory and imaging examinations were reported. Five months later there was a complete neurological and ophthalmological recovery. Although APMPPE was described primarily in young adults, we report the first case of APMPPE associated with neurological involvement in an older patient with a complete restitutio ad integrum.


Subject(s)
Choroiditis/diagnosis , Choroiditis/drug therapy , Pigment Epithelium of Eye/pathology , Retinal Diseases/drug therapy , Retinal Diseases/pathology , Retinal Pigment Epithelium/pathology , Acute Disease , Aged , Fluorescein Angiography , Humans , Male , Multifocal Choroiditis , Prednisolone/therapeutic use , Prednisone/therapeutic use
4.
Clin Ophthalmol ; 7: 947-9, 2013.
Article in English | MEDLINE | ID: mdl-23723687

ABSTRACT

Hyoscine-N-butyl bromide is a widely used antispasmodic belonging to the belladonna alkaloid class of semisynthetic quaternary ammonium compounds. These compounds exert a spasmolytic action on the smooth muscles of the bile-gastrointestinal tract, genitourinary tract, salivary glands (xerostomia), and also on the visual apparatus - in particular, the irido-ciliary complex. As a consequence, they provoke collateral effects such as mydriasis and accommodation disturbances. We report the case of a 23-year-old woman who complained of not only "dry mouth" but also "cloudy vision" and a "diplopia", both of temporary type, 2 hours after oral administration of hyoscine-N-butyl bromide.

5.
Clin Ter ; 163(2): e85-94, 2012.
Article in Italian | MEDLINE | ID: mdl-22555841

ABSTRACT

Waadernburg syndrome (WS) is an autosomal dominant disease clinically and genetically heterogeneous. It is characterized by non-progressive sensorineuronal hearing loss of variable degree and anomalous pigmentation (of the eyes, skin and stria vascularis of cochlear duct) caused by melanocytes absence. The syndrome is caused by mutations in genes that regulate the melanocytes differentiation from the neural crest during embriogenetic development. This study will review the literature on WS and explain more in detail the ocular findings in WS, while reporting new findings on two newly diagnosed cases.


Subject(s)
Waardenburg Syndrome , Adult , Child , Female , Humans , Male , Waardenburg Syndrome/classification , Waardenburg Syndrome/diagnosis
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