Comparison of intraocular pressure as measured by three different non-contact tonometers and goldmann applanation tonometer for non-glaucomatous subjects

Currently, the Goldmann applanation tonometer (GAT) is considered to be the gold standard for IOP measurement in clinical practice [1‐6]. However, since their introduction, non-contact tonometers (NCTs) have become well established in clinical practice. NCT is a rapid, simple and objective method of intraocular pressure (IOP) measurement that can be performed by ancillary staff without the use of corneal anaesthesia [7].

Not all NCTs perform similarly. Although earlier models showed, relative to the GAT, a wider bias and a poor sensitivity for detection of elevated IOP [1, 3, 7, 8], the accuracies of subsequent models are much improved [9‐18]. The Canon TX-20P, Nidek NT-530P, and Topcon CT-1P are the new automatic tonometers currently marketed. Perhaps surprisingly, there are in the literature, to our knowledge, few reports available on the performance of the Canon TX-20P or Nidek NT-530P [10‐15], and none on the Topcon CT-1P. Also, various studies have compared just one or two of the NCTs with the GAT, and there have been few studies comparing the accuracy of various tonometers for non-glaucomatous healthy adult subjects [10, 14, 19‐21].

The purposes of this study were to evaluate the reliability of the three new NCTs and to compare their IOP measurements with those obtained by the GAT for non-glaucomatous subjects. For each tonometer, the relationships between the measured ocular parameters and the IOP measurements also were examined.

Fifty-two eyes of 52 non-glaucomatous healthy subjects aged 21 to 85 years were included in the study. The study was approved by the Institutional Review Board (IRB) of Keimyung University Dongsan Medical Center (IRB no. 2015–12-052) and was performed in accordance with the tenets of the Declaration of Helsinki. None of the subjects had any history of ocular pathology affecting IOP, refractive surgery or trauma, and none had worn contact lenses within the two-week period prior to IOP measurement. Subjects were excluded if they had regular astigmatism greater than 3.50 diopters (D) or any irregular astigmatism. To avoid the double-organ bias, one eye per individual was randomly included in the analysis using a table of random numbers for randomization [22]. In a fixed sequence, all of the subjects were examined with the three NCTs, the GAT and ultrasound pachymeter (850, Humphrey Instruments, Inc., San Leandro, CA, USA) to obtain IOP and central corneal thickness (CCT) measurements, respectively. According to the GAT IOP values, the eyes were categorized into low-teen (<14 mmHg), mid-teen (≥14 and ≤17 mmHg) and high-teen (>17 mmHg) groups.

IOP measurements were made by the same experienced ancillary staff using the three NCTs. The order in which the instruments were used was the Canon TX-20P, followed by the Nidek NT-530P, the Topcon CT-1P and the GAT. Each of the tonometers was calibrated according to the manufacturer’s guidelines prior to its use in this study. In manual measurements using the Nidek NT-530P, on the other hand, the operator aligns the cornea by superimposing a reflection of the target from the subject’s cornea on a stationary ring and depresses the trigger when the cornea is aligned. In the present study, the mean of three measurements was used so as to avoid the effect of fluctuations caused by the cardiac pulse cycle.

IOP measurements were taken with the GAT (AT900; Haag-Streit, Köniz, Switzerland) according to the standard procedures. Before acquisition, one drop of 0.5% proparacaine hydrochloride eye drops (Alcaine®, Alcon Laboratories Inc., Fort Worth, TX, USA) was instilled and a fluorescein strip was applied to the inferior conjunctival fornix. To avoid error introduced by topical anesthesia, the GAT was applied five minutes after eyedrop instillation [23]. The last IOP measurement was obtained using GAT to avoid a corneal-compression-induced aqueous outflow increase that would have affected subsequent IOP readings [24, 25]. Also, the mean of three measurements of GAT was used and each IOP readings were masked to the one clinician (SPB) performing the measurements. Between each instrumentation application, the subjects were allowed a five-minute rest period to recover from the aqueous outflow. All of the measurements were taken between 11:30 am and 1:30 pm in order to minimize the effects of diurnal IOP variation [26].

Pearson correlation analysis, the intraclass correlation coefficient (ICC), the paired t-test were used to assess the correlation, consistency and agreement among the IOP measurements provided by each instrument. We also constructed Bland-Altman plots using Medcalc version 15.2 (Ostend, Belgium) to compare the bias in the IOP measurements of each NCT relative to the GAT. Simple linear regression analysis was used to assess the correlations between CCT and the IOP measurements of each tonometer. The paired t-test was used to analyze the difference between the IOP measurements of each NCT and the GAT in each subgroup divided by the GAT IOP values. Data were analyzed using SPSS version 22 (IBM, Armonk, NY, USA).

Of the 52 participants, 22 were male and 30 were female, with a mean age of 50.56 ± 17.25 years (range: 21–85 years). The mean IOP across all subjects was 17.23 ± 2.94 mmHg (range: 11–21 mmHg) with the Canon TX-20P, 14.87 ± 3.25 mmHg (range: 8–21 mmHg) with the Nidek NT-530P, 16.33 ± 3.01 mmHg (range: 9–21 mmHg) with the Topcon CT-1P, and 15.85 ± 3.05 mmHg (range: 8–21 mmHg) with the GAT. The mean CCT as measured with the ultrasound pachymeter was 541.44 ± 28.49 μm (range: 469–605 μm).

This study compared the IOP-measurement performances of the three new NCTs with the GAT. With the same subjects at the same moment, the IOPs from each NCT were obtained and demonstrated the following tendencies in terms of range: the IOP measurements with the Canon TX-20P and the Topcon CT-1P tended to be higher, whereas those with the Nidek NT-530P tended to be lower than with the GAT. Considering the order of the tonometer measurements, the greatest IOP values of C-IOP could be due to the ‘massage effect’, though the NCTs were less affected than was the GAT [24, 25], and regardless, the five-minute interval between each measurement, enough time to recover from enhanced aqueous outflow due to corneal compression, would minimize such effect.

In terms of study samples, the mean IOPs recorded using the four tonometers were close to those obtained by other authors for healthy subjects (15–16 mmHg on average, SD 2.5–3.0 mmHg) [3, 27]. Similarly, the mean CCT of 541.4 μm determined using the ultrasound pachymeter was close to the population mean of 530.9 μm and within the range found in normal Korean subjects [28].

The relationships observed between the CCT and IOP measurements obtained by the Nidek NT-530P and Topcon CT-1P tonometers are in agreement with the general assumption that CCT affects NCT readings, showing a positive correlation. According to previous reports, CCT affects both GAT and NCT readings [29, 30], the latter being more affected than the former [30‐32]. The moderate correlations observed in this study (R = 0.325 and 0.390) could be attributed to the limited range of CCT in our population (469–605 μm). Other authors argue that for corneas with a CCT less than 575 μm, IOP measurements are unaffected [5, 33]. In our study population, only 6 of the 52 eyes showed a CCT greater than 575 μm.

Through Pearson correlation analysis (Fig. 1), we observed a highly significant relationship between the pressure readings provided by each NCT and those offered by the GAT, confirming the good relationships between NCT- and GAT-determined IOPs reported by others [33]. These results indicate that the three NCTs provide statistically significant predictions of G-IOP measurements.

Many variables affect IOP measurements, including astigmatism, corneal thickness, corneal biomechanics/hysteresis, accommodation, respiration, heart rate and rhythm [34], and diurnal variation [26]. Considering these sources of error, some authors advocate that ±3.0 mmHg should be the maximum clinically acceptable error [19]. In our study, according to the Bland-Altman plots, the 95% LoA between C-IOP and G-IOP were close to this clinically acceptable error (±3.43 mmHg), 92% of the differences falling within this range. This means that the N-IOP showed 8% clinical error in our study subjects, all of whose IOP was within the normal range. In case of N-IOP, the LoA were wider (±3.92 mmHg), and 89% of the differences were within the clinically acceptable limits. The LoA of T-IOP was the widest (±4.16 mmHg), and 87% of the differences were within the clinically acceptable limits. These differences of LoA among the three NCTs might be accounted for in the differences in the alignment methods: the Canon TX-20P and Topcon CT-1P make parallel automatically, whereas the Nidek NT-530P aligns manually. Manual alignments might allow the operator to more accurately adjust subjects’ cornea in the three, axial, vertical and lateral dimensions. The reason for the narrower LoA of the Canon TX-20P than that of the Nidek NT-530P should be clarified by further evaluation with a larger subject cohort.

While there was a statistically significant difference between C-IOP and G-IOP as well as between N-IOP and G-IOP, none such was detected between T-IOP and G-IOP, suggesting that any such differences as might exist are independent of the mean IOP values. Thus, we could argue that the Topcon CT-1P offers relatively closer agreement with the GAT than does the Canon TX-20P or Nidek NT-530P. Furthermore, in the subgroup comparison study by G-IOP, the low- and mid-teen subgroups between C-IOP and G-IOP and the high-teen subgroup between N-IOP and G-IOP showed significant mean differences, demonstrating the tendency of discrepancy between the Canon TX-20P and GAT as well as between the Nidek NT-530P and GAT in these G-IOP ranges.

There are some limitations to this study. The fact that we did not test the instruments across the entire useful range is the main one. We also excluded subjects with irregular astigmatism or astigmatism of more than 3.5 diopters, and thus, our findings may hold true only for subjects with similar refraction characteristics. Furthermore, the sample size of this study was relatively small for the subgroup analysis; future studies will need to include larger populations of ocular hypertensive and glaucoma subjects, with or without irregular/severe astigmatism, for whom any bias between instruments could have clinical implications. Additionally, we were unable to randomize the order in which the NCTs were used due to restraints on access to the equipment. Therefore, we were unable to avoid potential systematic errors and are unable to ensure that the lack of randomization did not influence the outcome. We did implement a five-minute interval between each measurement to minimize the ‘massage effect’. One other limitation was the fact that we did not carry out CCT correction separately with each tonopachymeter; future studies should also investigate the results of CCT correction and comparison of CCT values from the ultrasound pachymeter with those from each tonopachymeter.

In conclusion, this comparative study shows that the only Canon TX-20P provides reliable and repeatable IOP measurements not influenced by CCT within a relatively normal/restricted range of corneal thickness. However, without CCT correction, the Canon TX-20P, Nidek NT-530P and Topcon CT-1P all offer similar accuracy to the GAT. Despite the relatively small sample size of this study and the absence of high IOPs, the instruments demonstrated good performance in measuring IOP in ocular normotensive non-glaucomatous subjects. These results suggest the instruments will prove useful for rapid IOP testing in clinical practice. Indeed, practitioners should keep in mind the differences in the tendencies of the IOP values as measured by the respective NCTs.

Without CCT correction, the Canon TX-20P, Nidek NT-530P and Topcon CT-1P all offer similar accuracy to the GAT.