Search PubMed⌕ Search

Biomedical subjects

B W Fleck

Publications and source records attributed to B W Fleck.

At least 37 records · Page 2Linked to original sources
PubMed1995

Diode laser treatment for retinopathy of prematurity: structural and functional outcome.

AIMS: The anatomical and functional outcome of 13 babies with retinopathy of prematurity (ROP) treated with binocular indirect ophthalmoscope diode laser photocoagulation was assessed. METHODS: Thirteen babies (25 eyes) at median postmenstrual age (PMA) 25.5 weeks and median birth weight 725 g were treated with binocular indirect ophthalmoscope (BIO) diode laser photocoagulation when threshold retinopathy of prematurity (ROP) was detected at median PMA 35 weeks. Retinopathy was more severe in the nasal retina in 15 eyes. The median severity of retinopathy was 6 clock hours grade 3 disease. All babies were treated under general anaesthetic with no significant ocular or systemic complications during treatment. The median number of burns was 1200. RESULTS: Resolution of active retinopathy occurred 1-2 weeks following treatment in all but one baby. All eyes had favourable anatomical and functional outcome as defined by the Cryo-ROP study group at a median age of 19.5 months of follow up. CONCLUSION: BIO diode laser treatment is as effective as cryotherapy with less morbidity.

Female↗
PubMed1995

An audit of the 1995 Royal College of Ophthalmologists guidelines for screening for retinopathy of prematurity applied retrospectively in one regional neonatal intensive care unit.

To test the effectiveness of the 1995 Royal College of Ophthalmologists (RCO) guidelines for screening for retinopathy of prematurity (ROP) in one regional neonatal intensive care unit, an analysis was carried out of screening examination results over a 4 year period, retrospectively applying the rules of the 1995 RCO guidelines. Four hundred and forty-eight examinations would have been performed in 258 infants, significantly fewer than the 764 examinations which had been performed using our existing screening protocol. Threshold ROP developed in 36 infants, and would have been detected promptly in every case. No case of threshold ROP developed in infants of birth weight greater than 1250 g. The 1995 RCO guidelines for ROP screening provide an effective and efficient means of detecting treatable ROP. The need to include infants of birth weight > 1250 g should be reviewed at a future date, following a period of further national data collection.

Birth Weight↗
PubMed1992

A photometric study of the effect of pupil dilatation on Nd:YAG laser iridotomy area.

A photometric study of the effect of pupil dilatation on Nd:YAG laser iridotomy area was performed in 21 eyes of 21 patients. The iridotomy area was 0.075 (0.055) mm-2 (mean (SD)) before pupil dilatation and 0.073 (0.070) mm-2 after pupil dilatation (t test NS). Iridotomy area after pupil dilatation correlated with iridotomy area before pupil dilatation (r = 0.815, p < 0.01) but did not significantly correlate with measures of iridotomy shape or position, or with changed iris area following pupil dilatation. Two iridotomies became reduced to less than 20% of their initial area following pupil dilatation. Our findings suggest that the only effective method of avoiding development of unacceptably small iridotomy area after pupil dilatation is to create a sufficiently large iridotomy at the time of initial laser surgery.

Acute Disease↗
PubMed1992

Blood viscosity and retinopathy of prematurity: a preliminary report.

Whole blood viscosity (WBV) and haematocrit (Hct) were measured in 8 very low birth weight premature neonates developing acute severe retinopathy of prematurity (ROP) and 7 control neonates without retinopathy or mild ROP. Single samples were collected at 32-34 weeks conceptual age. There was no statistically significant difference in WBV or Hct between the two groups. The results of this preliminary report suggest that WBV does not appear to play a major role in the development of advanced ROP, though larger studies are required to investigate this further.

Blood Viscosity↗
PubMed1991

A randomised, prospective comparison of Nd:YAG laser iridotomy and operative peripheral iridectomy in fellow eyes.

A prospective, randomised comparison of Nd:YAG laser iridotomy and operative peripheral iridectomy in the fellow eye of 52 patients presenting with acute angle closure glaucoma has been undertaken. Nd:YAG laser iridotomy resulted in a significantly higher incidence of iris bleeding at the time of treatment (p less than 0.05), higher intraocular pressure one hour (p less than 0.02) and three hours (p less than 0.02) following treatment, and a higher incidence of focal corneal oedema 24 hours following treatment (p less than 0.001). One laser treated patient developed acute angle closure glaucoma two weeks following treatment despite the presence of a small patent iridotomy. After a mean follow-up period of 11.8 months there was no significant difference between the two groups in visual acuity, or intraocular pressure. It is concluded that Nd:YAG laser iridotomy is a satisfactory alternative to operative peripheral iridectomy in the prophylactic treatment of fellow eyes.

Adult↗
PubMed1991

Case of penetrating orbitocranial injury caused by wood.

A case of retained intraorbital and intracerebral wooden foreign body following an orbitocranial penetrating injury through the lower lid of an adult is described. Initial failure to recognise the true nature of the injury led to intracerebral abscess formation and monocular blindness. Diagnosis and management of such cases are discussed.

Adult↗
PubMed1991

Argon laser pretreatment 4 to 6 weeks before Nd:YAG laser iridotomy.

Argon laser pretreatment followed by Nd:YAG laser iridotomy 4 to 6 weeks later was performed in the right eye of 10 patients. Primary Nd:YAG laser iridotomy was performed in the left eye. Significantly more Nd:YAG laser energy was needed to produce an iridotomy in pretreated eyes (P less than .001). Pretreated eyes developed a significantly larger pigment epithelium defect around the iridotomy site and a greater degree of pigmentation of the inferior part of the trabecular meshwork 6 months following treatment. Argon laser pretreatment followed by Nd:YAG laser iridotomy 4 to 6 weeks later appears to offer no advantages over primary Nd:YAG laser iridotomy.

Aged↗
PubMed1991

Effects of pulsed Nd:YAG laser on the surface of rabbit retina.

Six albino rabbits were subjected to pulsed Nd:YAG laser irradiation to the retinal surface to determine whether such treatment would lead to proliferative vitreoretinopathy. Choroidal, retinal, and preretinal hemorrhages, noted at the time of treatment, resolved after 7 to 10 days. Histological examination showed no signs of anterior segment damage or proliferative vitreoretinopathy. These preliminary findings suggest that more extensive experimentation is warranted to determine if pulsed Nd:YAG laser may in fact safely be used to separate vitreoretinal adhesions in the treatment of retinal detachment.

Animals↗
PubMed1990

How large must an iridotomy be?

Four cases of acute angle closure glaucoma in eyes with a small but patent Nd-YAG laser iridotomy are presented, and similar cases in the literature are reviewed. Theoretically a 15 microns diameter iridotomy should be large enough to prevent angle closure glaucoma due to pupil block. Mechanisms by which larger iridotomies fail to prevent angle closure glaucoma, and the role of provocation tests following iridotomy, are discussed. An iridotomy should be at least 150-200 microns in diameter if acute angle closure glaucoma is to be reliably prevented.

Acute Disease↗
PubMed1988

Nd:YAG laser augmented pneumatic retinopexy.

We present the first ten consecutive cases of rhegmatogenous retinal detachment treated by one surgeon using pneumatic retinopexy with Nd:YAG laser disruption of vitreoretinal adhesions. In nine cases the retina has remained reattached, after a follow-up period of 11 to 18 months. The use of the Nd:YAG laser to disrupt vitreoretinal adhesions at the sites of retinal tears is discussed.

Adult↗
PubMed1985

Screening for antimalarial maculopathy in rheumatology clinics.

Ophthalmoscopy and three tests of visual function were undertaken in 39 patients with rheumatoid arthritis receiving treatment with antimalarial drugs and in a control group of 16 patients with rheumatoid arthritis who were not receiving such treatment. Visual contrast sensitivity, macular threshold to red light, and central visual fields to red targets were not significantly different in treated patients and controls. There were no abnormalities in visual acuity, but 11 of 76 eyes of treated patients showed minor macular abnormalities on ophthalmoscopy that were not seen in control patients, suggesting that ophthalmoscopy may be the most sensitive measure of early drug toxicity. Five rheumatologists were able to identify 52 of 65 minor changes detected by an ophthalmologist. These studies, and a critical review of published reports, suggest that in clinical practice antimalarial drugs can be administered safely to patients with rheumatoid arthritis without the need for repetitive routine examination by an ophthalmologist or the use of complicated physiological tests. Recording of visual acuity in each eye and ophthalmoscopy by the prescribing doctor may be all that are required to detect early antimalarial maculopathy.

Adult↗
PubMedDate not supplied

Screening for retinopathy of prematurity: are a lid speculum and scleral indentation necessary?

We wanted to investigate the value of using a lid speculum and scleral indentation in performing binocular indirect ophthalmoscopy (BIO) in neonates at risk of retinopathy of prematurity (ROP). We performed a prospective masked comparison of BIO examinations using either a lid speculum and scleral indentation (SI) or no scleral indentation (NSI), in our neonatal intensive care unit. We did 57 consecutive BIO examinations of infants weighing less than 1500 g and/or having a gestational age of less than 32 weeks. With NSI, zone I ROP was reliably seen in 53 of 57 examinations; the superior, nasal, and temporal aspects of zone II were seen in 45 of 57 examinations; inferior zone II, in 22 of 57 examinations; and zone III in 1 of 57 examinations. SI facilitated complete peripheral fundus examination in all cases but had to be abandoned in two infants due to acute changes in oxygen saturation levels. Five infants developed threshold disease, and in two of them details of the active ROP ridge were missed with NSI. The gentle use of an eyelid speculum and globe rotation allows rapid and relatively atraumatic assessment of the peripheral fundus, even in babies who are being ventilated. Although threshold ROP may be diagnosed by observation of posterior retinal vessel dilation and tortuosity ("plus" disease), accurate grading of ROP is likely to require SI. In the absence of clearly developed "plus" disease, borderline or prethreshold disease may occasionally be missed using BIO with NSI. SI is necessary to examine the inferior midperipheral retinal vasculature (zone II) and the far peripheral temporal retina (zone III) and is associated with few complications.(ABSTRACT TRUNCATED AT 250 WORDS)

Fundus Oculi↗