Readings with the Goldmann applanation tonometer were made at various intraocular hydrostatic pressures and compared with central corneal thickness and radius in rabbit and in man. Linear correlations were established between hydrostatic pressure and applanation readings, with correlation coefficients close to 1.0. In rabbits the tonometer readings were generally too low. In human eyes with a normal corneal thickness tonometer readings and hydrostatic pressure coincided, with thick corneas the readings were too high, with thin corneas too low. The correlation between corneal thickness and the error of applanation tonometry (LIP) was statistically highly significant (P < 0.001). No statistical correlation could be established between corneal radius and AP. Multiple regression, taking thickness as well as corneal radius into consideration, revealed only slightly higher correlation coefficients. It is concluded that the central corneal thickness is a parameter which should be taken into consideration when evaluating applanation tonometer readings. A Table is presented showing the correction to be added to the applanation reading at differing corneal thickness. A clinical study of the normal human central corneal thickness. Kruse Hansen, F. PC Ehlers, N. (1971) Elevated tonometer readings caused by a thick Mishima, S. & Hedbys, B. 0. (1968). Measurement of corneal thickness with the Haag-Acta ophthal. (Kbh.) 49, 82-89. cornea. Acta ophthal. (Kbh.) 49, 775-778. Streit pachometer. Arch. Ophthal. (Chicago) 80, 710-7 13.

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The endothelium of 30 pairs of human cadaver corneas was stained by trypan blue and the intercellular spaces were visualized by induced dilation prior to corneal culture. Trypan blue staining and induced dilation of intercellular spaces by 0.9% and 0.45% NaCl were found to be atraumatic. Only a fraction of damaged cells were stained by trypan blue. Endothelial cell losses in culture did not correlate with the number of trypan-blue stained cells, the post-mortem time, or donor age.

Thirty-nine corneas were removed within 6 h post mortem and stored in a moist chamber at 4 degrees C before grafting. The mean donor age was 33 years and the average time between death and grafting was 11 h. Thirty cadaver corneas were selected after trypane blue staining and cultured at 31 degrees C for 24 h before grafting. The mean donor age was 61 years and the mean time between death and culture was 18 h. During the first 10 postoperative days fresh grafts were thinner than cultured grafts. One year after the transplantation the two groups did not differ significantly in regard to the clinical result, corneal thickness, or endothelial cell loss. This indicates that corneas from old donors with extended post mortem time can be used for transplantation after individual evaluation and corneal culture.