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. 2010 Apr;51(4):1918–1926. doi: 10.1167/iovs.09-4186

Table 2.

Cell Densities Measured by the ConfoScan 4 and Tandem Scanning Confocal Microscopes in 16 Corneas

Stromal Layer ConfoScan 4
TSCM
Automatic Manual Difference Auto − Manual Automatic Difference TSCM − ConfoScan 4
Anterior 10% 31,677 ± 4,886 31,358 ± 5,506 319 ± 4,009 44,126 ± 6,680 12,449 ± 8,326*
10%–33% 25,890 ± 3,517 26,062 ± 4,046 −172 ± 2,695 27,582 ± 4,553 1,692 ± 4,843
33%–66% 24,419 ± 3,498 25,939 ± 2,828 −1,520 ± 2,172 23,317 ± 5,043 −1,103 ± 6,107
66%–90% 24,493 ± 3,092 24,983 ± 2,171 −490 ± 2,765 24,498 ± 3,475 5 ± 5,433
90%–100% 22,728 ± 4,930 23,610 ± 3,096 −883 ± 3,418 23,230 ± 4,798 502 ± 7,506
Unweighted mean, n = 80 layers 25,841 ± 5,027 26,391 ± 4,486 −549 ± 3,065 24,647 ± 4,661 2,709 ± 8,114*
274 ± 5,994

Cell densities are expressed as the mean cells per cubic millimeter ± SD. These corneas were independent of corneas used to determine selection criteria for the automatic method. The differences were not significant (P > 0.1), except where indicated. TSCM, Tandem Scanning confocal microscope.

*

ConfoScan 4 significantly different from TSCM, P < 0.001, paired t-test.

Automatic significantly different from manual, P = 0.014, paired t-test.

Mean difference between 10% and 100% stromal thickness.