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1.
Curr Opin Ophthalmol ; 35(4): 322-328, 2024 Jul 01.
Article in English | MEDLINE | ID: mdl-38813738

ABSTRACT

PURPOSE OF REVIEW: Meibomian gland dysfunction (MGD) is one of the most common disorders encountered by ophthalmologists, and its management can prove challenging for both clinicians and patients. Intense pulsed light (IPL), which has been historically used in the field of dermatology, has emerged as a tool to help improve meibomian gland function. The goal of this review is to assess the clinical efficacy, utility, and safety of IPL for the treatment of MGD. RECENT FINDINGS: In recent randomized controlled trials, IPL has been shown to improve meibomian gland function, and subsequently tear film quality and dry eye symptoms. The mechanism of action still remains unclear. Recent literature suggests that IPL may also be used in conjunction with other therapies, such as meibomian gland expression, low-level light therapy, and thermal pulsation. Careful attention should be placed on each patient's Fitzpatrick skin type, as well as protecting the ocular structures to reduce the risk of adverse effects. Cost, accessibility, as well as a limited duration of efficacy may be drawbacks. SUMMARY: There is significant evidence supporting that IPL may be used as a potential well tolerated and effective treatment for MGD, though there are certain caveats regarding its long-term efficacy, accessibility, and cost.


Subject(s)
Intense Pulsed Light Therapy , Meibomian Gland Dysfunction , Humans , Meibomian Gland Dysfunction/therapy , Intense Pulsed Light Therapy/methods , Meibomian Glands , Treatment Outcome , Dry Eye Syndromes/therapy , Dry Eye Syndromes/physiopathology
2.
J Cell Physiol ; 234(6): 9247-9254, 2019 06.
Article in English | MEDLINE | ID: mdl-30444003

ABSTRACT

The aim of the study was to evaluate the effects of the Quiet eye (QE) phenomenon on performances during the shooting section of "Laser Run" of Modern Pentathlon, in two samples of athletes (novices and experts). The "Laser Run" consists of running and shooting activities. The study involved 18 experienced athletes of the Italian National Team of Modern Pentathlon (i.e., "elite" group) and 18 young and nonexpert athletes of a local Pentathlon club (i.e., "novice" group). Participants performed, in ecological conditions, five trials of four series of shootings (as it occurs in the real competitions), for a total of 20 series. During the shooting trials, athletes wore a mobile Eye Tracking System to record eye movements (saccades, blinks, and fixations). Key measures of the study were QE parameters (QE Duration [QED], Relative QED [RQED], and QE Onset), as well as the performance (accuracy and time to perform the event). The results revealed that both groups of athletes had a longer QED, RQED, and an earlier onset during their best shots than during the worse ones. Furthermore, differences between the groups showed that elite athletes had an earlier onset and a shorter QED than the novice group of athletes. These results provide insightful information about different cognitive and perceptual processes involved in Modern Pentathlon's athletes' performances at both the elite and non-elite level.


Subject(s)
Athletes , Eye Movements/physiology , Running/physiology , Adolescent , Adult , Athletic Performance , Humans , Male , Young Adult
3.
J Neuroophthalmol ; 31(1): 29-33, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21164358

ABSTRACT

A 56-year-old man developed a pupil-involving left third nerve palsy. Imaging studies of the brain and intracranial vessels were normal. Neurological examination demonstrated a sensory polyneuropathy and mild distal weakness. Nerve conduction studies showed prolonged distal motor latencies. An enzyme-linked immunosorbent assay test detected high titers of anti-myelin-associated glycoprotein (MAG) antibodies. The patient improved with prednisone and rituximab treatment. Anti-MAG neuropathy should be considered when evaluating a patient with an undiagnosed cranial neuropathy, especially in the setting of a sensory neuropathy.


Subject(s)
Autoantibodies/blood , Myelin-Associated Glycoprotein/immunology , Oculomotor Nerve Diseases/diagnosis , Oculomotor Nerve Diseases/pathology , Peripheral Nervous System Diseases/diagnosis , Peripheral Nervous System Diseases/pathology , Pupil , Autoantibodies/biosynthesis , Humans , Male , Middle Aged , Oculomotor Nerve Diseases/immunology , Peripheral Nervous System Diseases/immunology , Pupil/physiology
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