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EFFICACY











                                TABLE 1. Visual Function, Intraocular Pressure, and Blood Pressure (N   15)
                                                           Prestudy Baseline                Poststudy Baseline
               Visual field mean deviation (db)              3.85   1.76                       3.37   1.67
               CPSD                                         3.78   1.02                       3.86   1.12

                                                   Timolol (Control)               Timolol   Dorzolamide
                                            Baseline          Drug            Baseline          Drug
               Visual acuity                .11   .04        .14   .04        .11   .03        .09   .03
               Contrast sensitivity (log units)
                3 cycles per degree       1.641   .075     1.548   .062     1.524   .083      1.593   0.47
                6 cycles per degree       1.697   .078     1.707   .086     1.684   .050      1.722   .058
                12 cycles per degree      1.248   .107     1.092   .086     1.255   .103      1.201   .094
                18 cycles per degree      0.783   .098     .0759   .068     0.847   .092      0.757   .107
               Intraocular pressure (mm Hg)  14.7   0.9     14.0   1.1       14.7   1.0       13.4   0.7*
               Systolic pressure (mm Hg)   118   4           122   4          123   4          126   3
               Diastolic pressure (mm Hg)   74   2           76   3           78   2           76   2
               Heart rate (beats/minute)    67   3           66   2           67   2           64   3
                CPSD   corrected pattern standard deviation.
                *Indicates P   .05 versus matched baseline.


             as the maximum minus the minimum. Similarly, 10%  size of 15 was chosen, on the basis of past studies of the
             arrival time (the amount of time required to reach bright-  reproducibility of measures of ocular blood flow and visual
             ness 10% above baseline) was analyzed for each area, as a  function. With an average variability of 15%, this study
             six-region mean, and as a maximum minus minimum.  had statistical power of 90% to detect significant differ-
             Finally, dye duration (analyzed as time between 70% dye  ences as small as 12.5%. To correct for multiple compari-
             arrival and return to 70% maximal dye intensity) was  sons, Bonferonni’s t procedure was used.
             determined for each area, as a six-region mean, and as a
             maximum minus minimum.
              Color Doppler imaging is an ultrasound technique that          RESULTS
             combines b-scan gray scale imaging of tissue structure with
             colored representation of blood movement toward or away  THE MEAN DEVIATION OF THE VISUAL FIELD TESTING WAS
             from the sensor based on Doppler-shifted frequencies, and  unchanged by participation in the study (Table 1); the
             pulsed-Doppler measurement of blood velocities. Blood  corrected pattern standard deviation was unaltered as well
             velocities were measured in the ophthalmic, central reti-  (Table 1). Neither timolol (control) nor timolol plus
             nal, and nasal and temporal posterior ciliary arteries.  dorzolamide treatment affected visual acuity (Table 1), or
              A Siemens Quantum 2000 color Doppler imaging system  altered contrast sensitivity at 3, 6, 12, or 18 cycles per
             (Siemens Quantum, Issaquah, Washington) with a 7.5-MHz  degree (Table 1).
             linear probe was used. Samples of pulsed-Doppler signal from  Intraocular pressure was significantly reduced by dorzo-
             within a 0.2-mm by 0.2-mm sample area were analyzed to  lamide-timolol combination as compared with timolol
             calculate blood velocities. In each vessel, peak systolic and  alone (P   .05, Table 1). Intraocular pressure was un-
             end-diastolic velocities were determined, and Pourcelot’s  changed during the control series on timolol (Table 1).
             resistance index was calculated as follows: (peak systolic  Baseline measurements were taken after a timolol run-in.
             velocity   end-diastolic velocity)/peak systolic velocity.  The addition of dorzolamide to timolol did not alter
              During testing, subjects reclined in a chair as acoustic  systemic arterial blood pressure and heart rate (Table 1).
             coupling gel was placed over a closed eye and the probe  The dorzolamide-timolol combination accelerated supe-
             was gently positioned. After identification of the appropri-  rior temporal arterial arteriovenous passage of fluorescein
             ate vessel, the sample area was placed in the center of the  dye as compared with timolol treatment alone, from 2.13
             vessel, the angle of incidence was selected, and several  to 1.76 seconds (P   .01, Figure 1). Retinal arteriovenous
             seconds of Doppler waveform were recorded.     passage time from the superior temporal artery to the
              Data from each experimental series were compared with  corresponding vein was unaltered by treatment with timo-
             their respective (timolol) baseline, using t tests, with P less  lol. In the inferotemporal artery and vein, no significant
             than .05 regarded as statistically significant. The sample  effect of either drug was present (Figure 1 shows results from

             492                           AMERICAN JOURNAL OF OPHTHALMOLOGY                  OCTOBER 2001


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