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Biomedical subjects

A J Bron

Publications and source records attributed to A J Bron.

At least 145 records · Page 8Linked to original sources

Unsuspected hypoglycaemia, haemoglobin A1 and diabetic control.

Control of diabetes in a group of 82 insulin-treated diabetics was assessed by in-patient 24-hour plasma glucose profiles and haemoglobin A1 (HbA1) estimation. Thirty-two of these patients (39 per cent) had hypoglycaemia (plasma glucose less than or equal to 2 mmol/l) which was rarely associated with symptoms. Twenty-seven (61 per cent) of 44 patients who took a series of out-patient pre-prandial capillary blood samples over a three-day period had hypoglycaemia. Conventional measurements of diabetic control including fasting plasma glucose and HbA1, were lower in patients with hypoglycaemia than in those without. Rebound hyperglycaemia following hypoglycaemia was not seen and its absence was not due to diabetic autonomic neuropathy. Cortisol/creatinine ratios in early morning urine samples were similar in patients with and without nocturnal hypoglycaemia, consistent with the absence or rebound hyperglycaemia. Diabetic retinopathy was less prevalent in patients with hypoglycaemia, possibly reflecting better long-term diabetic control in this group. HbA1 concentration reflects overall blood glucose control in diabetes but near-normal levels must be interpreted with caution since they may be associated with recurrent hypoglycaemia.

Adult↗

Clinical and biochemical heterogeneity in gyrate atrophy.

Two patients had milder variants of the usual form of gyrate atrophy. Although the appearance of the chorioretinal degeneration was identical, the progression of the clinical signs and symptoms were slower with night blindness, cataracts, and decreased vision occurring at an older age. Additionally, the level of hyperornithinemia, although still increased above normal, was lower than that usually found in such patients (between 448 and 676 microM). Additionally, one of our patients responded to high dosage vitamin B6 with a 27% reduction in plasma ornithine. The difference in the quantitation of the increase in plasma ornithine, the difference in responsiveness to vitamin B6, and the difference in the clinical consequences of this underlying biochemical abnormality, indicated a variant form of gyrate atrophy, suggesting the presence of genetic heterogeneity.

Adolescent↗

West Indian punctate keratopathy in a Caucasian.

We present a patient with the picture of corneal white spots, very similar in morphology to those described in native West Indians, occurring here in a Caucasian. Their aetiology remains obscure.

Adult↗

Epithelial deposition of gold in the cornea in patients receiving systemic therapy.

Epithelial gold deposits were demonstrated biomicroscopically in 13 of 15 patients receiving gold therapy for rheumatoid arthritis. Only one of six further patients who had received gold therapy in the past showed such deposits. Deposits appeared with a cumulative dose of sodium thiomalate exceeding 100 mg. The earliest appearance was after seven months of therapy and deposits were visible in one subject as long as nine months after therapy had stopped. The density of deposit does not appear to increase over the whole of the dose range, possibly as a result of the effect of epithelial turnover. No symptoms attributable to the deposit were encountered in any patient.

Adolescent↗

The intraocular penetration of cefuroxime after parenteral administration.

Cefuroxime (Zinacef) is a new second generation cephalosporin which is resistant to beta-lactamases produced by both Gram-negative and Gram-positive organisms, with an antibacterial spectrum that includes practically all likely ocular pathogens except pseudomonas. It is shown to penetrate into the eye after intravenous (1.5g) or intramuscular (1 g) injection and achieve therapeutic concentrations, with absence of side effects. Cefuroxime is therefore a useful antibiotic for ophthalimic infections and should have a role in combination with gentamicin in intraocular infections, particularly those of unknown aetiology.

Adult↗

Streptococcus suis type II (group R) as a cause of endophthalmitis.

A case is reported of a patient with bilateral endophthalmitis, meningitis, sensorineural deafness, labyrinthitis, and septicaemia due to Streptococcus suis type II (group R). The organism is known to produce epidemic meningitis, septicaemia, and purulent arthritis in piglets, but human infection is rare, and no other case reports of ocular infection are known. The organism was sensitive to penicillin at a minimum inhibitory concentration of 0.03 mg/1.

Deafness↗

Television slit-lamp biomicroscopy.

The basic requirements for performing television slit-lamp biomicroscopy are outlined, and the methods of demonstrating particular features of ocular anatomy and ocular disease are discussed. The technique has a particular role in teaching in the clinical setting.

Eye↗

Role of tears in maintaining corneal integrity.

In addition to providing a smooth optical surface, the tear film moistens and protects the cornea by providing a wide variety of antimicrobial substances. Accessory secretions of the conjunctiva and tarsal glands play an important protective role in lubricating, promiting wetting of the corneal epithelium by tears, stabilizing the extremely thin precorneal film, and reducing evaporation.

Conjunctiva↗

Superficial lines and associated disorders of the cornea.

In a clinical classification of fine superficial corneal lines, we recognized five major types of line: mare's tail lines, fibrillary lines, fingerprint lines, lacunar dystrophy or map-like changes, and tram lines. The fingerprint lines were further classified into several subgroups. There was a relationship between certain lines, in particular, fingerprint lines and lacunar dystrophy or map-like change with the occurrence of Cogan's microcystic dystrophy and recurrent erosion.

Adult↗

Morgagnian cataract.

It appears that morgagnian cataract is a special form of cortico-nuclear cataract. It is assumed that the process of fibre dissolution which is encountered in cortical cataract in general is speeded up and occurs en masse in morgagnian cataract. Enzymatic degradation of membrane and crystallin fibre components could then occur to produce liquefaction of the fibres and resorption of the cortical fluid. Factors responsible for the resistance of the nucleus to this process have been discussed. The high levels of calcium in the capsule and nucleus in this form of cataract could be due to the precipitation of calcium orthophosphate in the capsule and of calcium oxalate in the nucleus.

Calcium↗