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1.
Eye (Lond) ; 37(3): 506-510, 2023 02.
Article in English | MEDLINE | ID: mdl-35190668

ABSTRACT

BACKGROUND: Temporal artery biopsy (TAB) is often performed by ophthalmology trainees without direct supervision. The traditional model of 'see one, do one, teach one' still prevails in most units. Whilst it is generally a safe procedure, damage to the temporal branch of the facial nerve has been reported when harvesting the frontal branch of the superficial temporal artery. METHODS: A survey of trainees from Wessex, Wales, London and Severn deaneries was performed to look at current training techniques, anatomical knowledge and practice. RESULTS: 38 trainees responded to the survey, with complete responses from 28 participants. Formal teaching of the anatomical considerations in TAB was not reported by any trainee, with informal teaching being standard practice. Whilst 61% of respondents reported having learnt about the anatomical 'danger zone' for facial nerve damage, 97% of trainees chose an incision that fell within this zone when given a choice between potential incision sites. CONCLUSION: TAB remains a largely trainee-taught, trainee-performed procedure. Most trainees are not aware of how to avoid the risk of damage to the temporal branch of the facial nerve. We suggest harvesting the parietal branch of the temporal artery via an incision outside the anatomical 'danger zone'. In our experience, this is an easily taught technique that minimises the potential risk of damage to the frontal branch of the facial nerve.


Subject(s)
Surgical Wound , Temporal Arteries , Humans , Temporal Arteries/pathology , Facial Nerve , Biopsy/methods , Surgical Wound/pathology , London
2.
Eye (Lond) ; 36(7): 1468-1475, 2022 07.
Article in English | MEDLINE | ID: mdl-34234292

ABSTRACT

OBJECTIVE OR PURPOSE: To develop and test a patient-reported outcome measure for assessing health-related quality of life (HRQOL) in surgically amenable epiphora. DESIGN: Questionnaire development and validation study. PARTICIPANTS: 201 patients with a cause of epiphora amenable to surgical intervention, recruited across three independent centres. METHODS, INTERVENTION OR TESTING: The watery eye quality of life (WEQOL) questionnaire was developed and refined according to defined psychometric standards. Both surgical and non-surgical participants completed WEQOL at baseline and follow-up (>3 months), along with the Lacrimal Symptom Questionnaire (Lac-Q), RAND Short Form Health Survey (SF-36) and Glasgow Benefit Inventory (GBI). Convergent validity of WEQOL was evaluated according to correlation (R > 0.40) with each of these additional tests. Responsiveness of WEQOL to intervention was evaluated according to patient-reported success. Test-retest reliability was assessed by the Bland-Altman method and intraclass correlation (ICC) in a subset of 64 participants at baseline. MAIN OUTCOME MEASURES: WEQOL construct validity, responsiveness and test-retest reliability. RESULTS: WEQOL was moderately correlated (R > 0.4) with the Lac-Q and several subscales of the SF-36 (physical role limitation, social, emotional role limitation and emotional well-being). A stronger correlation was found between the change in WEQOL at follow-up and GBI (R = 0.61). An appropriate graded response was found with a significant change in WEQOL score being observed in patients reporting successful (-28%, p < 0.0001) and partially successful surgery (-6%, p = 0.04), but not in those reporting unsuccessful surgery (+2%, p = 0.9). High test-retest reliability was observed (ICC = 0.93). CONCLUSIONS: The WEQOL questionnaire has been developed systematically according to modern psychometric standards and has been designed to evaluate the quality of life in patients with epiphora that is of a surgically amenable cause. In this study, it has demonstrated appropriate test-retest reliability, responsiveness and construct validity.


Subject(s)
Lacrimal Apparatus Diseases , Quality of Life , Humans , Lacrimal Apparatus Diseases/diagnosis , Lacrimal Apparatus Diseases/surgery , Patient Reported Outcome Measures , Reproducibility of Results , Surveys and Questionnaires
3.
Pediatr Infect Dis J ; 36(5): 502-503, 2017 May.
Article in English | MEDLINE | ID: mdl-28060049

ABSTRACT

Cushing's syndrome after topical ocular corticosteroid use is extremely rare. We describe a case of symptomatic Cushing's syndrome in an adolescent male with sight-threatening vernal keratoconjunctivitis on antiretroviral therapy for HIV-1 infection that included ritonavir, a potent cytochrome p450 CYP3A4 inhibitor. CYP3A4 inhibition reduces the metabolism of exogenous corticosteroids leading to suppression of endogenous steroid production and Cushing's syndrome.


Subject(s)
Adrenal Cortex Hormones/adverse effects , Anti-Inflammatory Agents/adverse effects , Conjunctivitis, Allergic/drug therapy , Cushing Syndrome/chemically induced , HIV Infections/drug therapy , HIV Protease Inhibitors/adverse effects , Ritonavir/adverse effects , Adolescent , Adrenal Cortex Hormones/administration & dosage , Anti-Inflammatory Agents/administration & dosage , Conjunctivitis, Allergic/complications , Cushing Syndrome/pathology , Cytochrome P-450 CYP3A Inhibitors/administration & dosage , Cytochrome P-450 CYP3A Inhibitors/adverse effects , Drug Interactions , HIV Infections/complications , HIV Protease Inhibitors/administration & dosage , Humans , Male , Ritonavir/administration & dosage
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