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1.
N Z Med J ; 132(1500): 25-28, 2019 08 16.
Article in English | MEDLINE | ID: mdl-31415496

ABSTRACT

AIM: To assess the impact of anticoagulation on patients having cataract surgery. METHODS: Patients who underwent cataract surgery with phacoemulsification and intraocular lens insertion between 1 January 2015 and 31 December 2015 at Christchurch Hospital were identified and retrospectively audited. The outcome measures were the occurrence of intraoperative and postoperative haemorrhage, and thromboembolic events within two weeks after surgery. A control group was included to assess the outcome measures in a sample of patients who were not on anticoagulants or antiplatelets. RESULTS: Forty-four anticoagulated patients (46 eyes) and 41 controls (46 eyes) were identified. Seventy-four percent of those anticoagulated were on warfarin and 26% were on dabigatran. The incidence of haemorrhagic complications was 18%, 25% and 11% in the warfarin, dabigatran and control groups, respectively, although these differences were not statistically significant. Apart from one vitreous haemorrhage, which may have been present preoperatively, the haemorrhages that occurred were minor and not visually significant. No thromboembolic events were noted in any of the groups. CONCLUSION: There is no statistically significant increase in haemorrhagic complications in cataract surgery patients who were on warfarin or dabigatran. Therefore, continuing the anticoagulation in this setting may be appropriate.


Subject(s)
Anticoagulants/adverse effects , Phacoemulsification , Postoperative Complications/epidemiology , Adult , Aged , Aged, 80 and over , Dabigatran/adverse effects , Female , Humans , Male , Middle Aged , Phacoemulsification/adverse effects , Phacoemulsification/statistics & numerical data , Postoperative Hemorrhage/epidemiology , Retrospective Studies , Thromboembolism/epidemiology , Warfarin/adverse effects
2.
Aust N Z J Public Health ; 36(3): 257-62, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22672032

ABSTRACT

OBJECTIVE: To determine whether diabetic retinal screening services and retinopathy referral centres in New Zealand meet the national guidelines for referral and assessment of screen detected moderate retinal and mild macular diabetic eye disease. METHODS: Diabetic retinal screening pathways and the data collected at four main centre retinal screening services were described and compared with recommendations in the national diabetes retinal screening guidelines. A retrospective audit of photoscreen detected moderate retinopathy (grade R3), and mild maculopathy (grades M2B and M3) during May to August 2008 was undertaken. Data collected by retinopathy referral centres were used to examine the follow-up of screen detected cases and to make comparisons with the national recommendations. RESULTS: All four screening services used the guidelines for grading, but the recommended dataset was incomplete. Not all recorded data were readily accessible. The retinal photos of 157 (2.4%) patients were graded as R3, M2B, M3 or a combination. The proportion of those screened with these grades varied across the four centres from 1.2% to 3.4%. Follow-up of the 157 screen positive patients did not always comply with guideline recommendations. Seventy five (48%) were referred for review by an ophthalmologist as recommended, 45 (60% of referred) were seen within the recommended six months. Nine patients (15% of the 60 with a documented assessment) were referred for or received laser treatment at 12-months follow-up. CONCLUSION: Quality diabetic retinal screening data systems and quality assurance programs are required to improve the monitoring and quality of retinal screening in New Zealand.


Subject(s)
Data Collection/standards , Diabetic Retinopathy/diagnosis , Guideline Adherence , Mass Screening , Quality Assurance, Health Care , Female , Follow-Up Studies , Humans , Male , Mass Screening/standards , New Zealand , Practice Guidelines as Topic , Referral and Consultation
3.
J Cataract Refract Surg ; 33(7): 1278-83, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17586387

ABSTRACT

PURPOSE: To report the outcomes of cataract extraction with intraoperative intravitreal triamcinolone (IVTA) in eyes with a history of posterior uveitis. SETTING: Moorfields Eye Hospital Uveitis Service, London, United Kingdom. METHODS: Nineteen eyes of 17 patients with posterior uveitis thought to require systemic corticosteroid prophylaxis for cataract surgery were included. The use of systemic corticosteroids at the time of surgery would have been problematic in 7 of the patients, who had a history of systemic hypertension. Three of the 7 patients were also diabetic. All patients were not happy about using oral corticosteroids. RESULTS: Median visual acuity 1 day after surgery was 20/40 (range 20/20 to counting fingers). At final follow-up (mean 25.2 months; range 7 to 41 months), 17 eyes (89.5%) eyes achieved visual acuity of 20/40 or better; 2 eyes failed to achieve a final visual acuity of 20/40 or better, 1 as a result of optic atrophy and the other as a result of macular edema. No patient lost acuity and no eye developed macular edema within 4 months of surgery. Intraocular pressure elevation occurred after surgery in 3 eyes; all were controlled by topical medication that was discontinued after 3 months. One patient developed severe intraocular inflammation after surgery that resolved with intensive topical corticosteroid therapy within 1 week. CONCLUSIONS: Cataract extraction by phacoemulsification with concurrent IVTA appears a useful treatment option. Targeted delivery of corticosteroid is achieved without the risks of systemic corticosteroid prophylaxis. The incidence of postoperative macular edema was markedly reduced. Levels of visual acuity after cataract surgery, similar to those in eyes without uveitis, were achieved in eyes with posterior uveitis.


Subject(s)
Glucocorticoids/therapeutic use , Lens Implantation, Intraocular , Phacoemulsification , Triamcinolone Acetonide/therapeutic use , Uveitis, Posterior/drug therapy , Adult , Aged , Female , Humans , Injections , Intraocular Pressure , Intraoperative Care , Macular Edema/prevention & control , Male , Middle Aged , Pilot Projects , Prospective Studies , Treatment Outcome , Visual Acuity , Vitreous Body
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