| Literature DB >> 25420615 |
Paul Vaucher1, Daniela Herzig, Isabel Cardoso, Michael H Herzog, Patrice Mangin, Bernard Favrat.
Abstract
BACKGROUND: In many countries, primary care physicians determine whether or not older drivers are fit to drive. Little, however, is known regarding the effects of cognitive decline on driving performance and the means to detect it. This study explores to what extent the trail making test (TMT) can provide indications to clinicians about their older patients' on-road driving performance in the context of cognitive decline.Entities:
Mesh:
Year: 2014 PMID: 25420615 PMCID: PMC4256796 DOI: 10.1186/1471-2318-14-123
Source DB: PubMed Journal: BMC Geriatr ISSN: 1471-2318 Impact factor: 3.921
Figure 1Flow chart for the selection of older drivers. TMT = Trail Making Test, n = sample size.
Characteristics of volunteer, older, home-dwelling drivers and of those considered as healthy drivers
| Determinants | All study participants (n = 404) | Healthy* (n = 197) | “Unhealthy”* (n = 207) | P-value‡ |
|---|---|---|---|---|
| Median (p5–p95) / % (n) | Median (p5–p95) / % (n) | Median (p5–p95) / % (n) | (Chi2or | |
| Age (years) | 75.4 years (70-84) | 74.8 (70–83) | 75.8 (71–85) | P = 0.025 |
| Gender (% male) | 62.6% (n = 253) | 52.8% (n = 104) | 72.0% (n = 149) | P < 0.001 |
| Education (% <12 yrs) | 26.2% (n = 106) | 23.3% (n = 46) | 29.0% (n = 60) | P = 0.198 |
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| Visual acuity (decimal) | 1.0 dec (0.6–1.2) | 1.0 (0.8–1.2) | 1.0 (0.6–1.2) | P = 0.003 |
| Visual field (°) | 180° (150–200) | 180 (160–200) | 180 (150–200) | P = 0.106 |
| Contrast sensitivity (log[CS])† | 1.72 log(CS) (1.6–1.76) | 1.72 (1.6–1.76) | 1.72 (1.6–1.76) | P = 0.429 |
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| Timed up-and-go test – TUG (sec) | 8.0 sec (6.0–13.0) | 8.0 (6.0–12.0) | 8.4 (6.0–14.8) | P < 0.001 |
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| MoCA (points [0-30]) | 27 points (21–30) | 28 (26–30) | 25 (20–29) | P < 0.001 |
| MoCAmod (points [0-29]) | 26 points (20–29) | 27 (24–29) | 24 (19–28) | P < 0.001 |
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| Distance driven per week (km) | 200 km (50–500) | 200 (40–500) | 200 (50–500) | P = 0.832 |
| History of accidents during the previous 2 years | ||||
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| 26.0% (n = 105) | 25.4% (n = 50) | 26.6% (n = 55) | P = 0.785 |
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| 7.4% (n = 30) | 6.6% (n = 13) | 8.2% (n = 17) | P = 0.536 |
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| 1.2% (n = 5) | 0% (n = 0) | 2.4% (n = 5) | P = 0.028 |
| On-road driving performance | P = 0.605 | |||
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| 47.0% (n = 190) | 46.2% (n = 91) | 47.8% (n = 99) | |
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| 27.0% (n = 109) | 27.9% (n = 55) | 26.1% (n = 54) | |
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| 20.5% (n = 83) | 21.8% (n = 43) | 19.3% (n = 40) | |
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| 5.4% (n = 22) | 4.1% (n = 8) | 6.8% (n = 14) |
*The healthy population was defined as drivers with normal optical vision, no cognitive impairment (MoCA ≥ 26), normal functional mobility (TUG < 13.5 sec), no known risk of sudden blackout, and without class III medication affecting driving performance. † MARS contrast sensitivity was not collected from the start of the study and was therefore available for only 158 participants, of whom 76 were healthy. ‡ P-Values are for comparing healthy participants to “unhealthy participants”. CS = contrast sensitivity, MoCA = Montreal cognitive assessment, MoCAmod = Modified MoCA (without TMT or education level).
Normative data for healthy, home-dwelling, older drivers (n = 197)
| TMT-A (seconds) | TMT-B (seconds) | |||||
|---|---|---|---|---|---|---|
| Mean | SD | Median [p5-p95] | Mean | SD | Median [p5-p95] | |
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| Female (n = 93) | 43.8 | 14.6 | 40 [26-68] | 94.5 | 31.2 | 91 [54-157] |
| Male (n = 104) | 45.6 | 17.9 | 40 [27-80] | 117.6 | 59.0 | 98 [56-204] |
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| <75 years (n = 101) | 43.2 | 14.6 | 40 [26-67] | 103.3 | 47.8 | 91 [53-187] |
| 75 to 79 years (n = 61) | 43.3 | 14.9 | 40 [24-72] | 97.6 | 34.2 | 90 [58-172] |
| ≥ 80 years (n = 35) | 51.7 | 22.0 | 44 [29-113] | 132.8 | 65.3 | 129 [66-214] |
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| > 12 years of schooling (n = 151) | 44.7 | 16.4 | 40 [26-72] | 101.6 | 45.8 | 90 [54-182] |
| ≤ 12 years of schooling (n = 46) | 44.8 | 16.9 | 42 [28-76] | 123.8 | 56.3 | 102 [70-214] |
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| 44.8 | 16.5 | 41 [26-74] | 106.7 | 49.2 | 93 [54-187] |
For this analysis designed to provide normative values for healthy older adults, we excluded measures from patients with health conditions that might have affected their performance. Therefore, normative data is provided for older drivers with normal optical vision, no cognitive impairment (MoCA ≥ 26), normal functional mobility (TUG < 13.5 sec), no known risk of sudden blackout, and without class III medication affecting driving performance. TMT = trail making task, SD = standard deviation.
Modeling the psychophysical components of the TMT-B (n = 45)
| TMT-B | ||
|---|---|---|
| IRR†[CI95%] | R2 | |
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| Age (years) | 1.05 [0.91 to 1.20] | 0.006 |
| Gender (male) | 1.14 [0.89 to 1.45] | 0.016 |
| Education (years of schooling) | 0.91 [0.79 to 1.04] | 0.150 |
| Literacy (KHE [sec]) | 1.23 [1.09 to 1.39]* | 0.146 |
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| Visual acuity (FrACT arc minutes) | 0.97 [0.88 to 1.06] | 0.004 |
| Contrast sensitivity (75% threshold Gabor patch) | 1.12 [1.02 to 1.22]* | 0.075 |
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| Visio-spatial search (TMT-A [sec]) | 1.25 [1.10 to 1.41]* | 0.157 |
| Mental flexibility (Perseverative errors WCST [%]) | 1.11 [0.96 to 1.29] | 0.035 |
| Working memory (Digit backwards [n°]) | 0.75 [0.62 to 0.91]* | 0.109 |
| Verbal fluency ([animals + fruit–veg.] /2 [n°/min]) | 0.85 [0.73 to 0.98]* | 0.074 |
| Functional mobility (timed up-and-go test - TUG [sec]) | 1.11 [0.99 to 1.11] | 0.047 |
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| Visual processing (Vernier’s Task) | ||
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| 1.12 [0.93 to 1.34] | 0.023 |
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| 1.12 [0.90 to 1.40] | 0.015 |
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| 1.11 [0.97 to 1.27] | 0.035 |
| Simple response time (ms) | 1.11 [0.93 to 1.32] | 0.029 |
| Visual search (RT [ms]) | 1.12 [0.96 to 1.32] | 0.040 |
| Motion direction sensitivity (% dots) | 1.17 [1.06 to 1.29]* | 0.125 |
| Orientation discrimination sensitivity | 1.17 [1.09 to 1.25]* | 0.091 |
| Biological motion | 0.95 [0.80 to 1.13] | 0.005 |
| Simon’s effect (Δt [ms]) | 1.03 [0.86 to 1.25] | 0.002 |
*Significant at p < 0.05. † Incidence risk ratio was measured using Poisson regression. Continuous values were transformed to be normally distributed and have a range of 0 to 1 from the twenty-fifth to the seventy-fifth percentile of the population. FrACT = Freiburg Visual Acuity and Contrast Test, IRR = Incidence-rate ratio, R2 = Coefficient of determination, SOA = Stimulus-onset-asynchrony.
Figure 2Driving performance and results from tests including TMT. Open dots correspond to each individual observation, grey blocks’ upper borders correspond to mean observed TMT duration on a log scale. Interval bars represent 95% CI. P-values correspond to F statistics comparing poor drivers to excellent drivers. For figures A &B, doted lines represent the threshold (TMT-A ≥54 sec; TMT-B ≥150 sec) from which TMT duration can evoke unfitness to drive. For figure C, doted lines represent threshold of the MoCA to differentiate drivers without cognitive impairment (NoCI), those with mild cognitive impairment (MCI), and those with severe cognitive impairment (SCI).
Crude and adjusted odds of having poor driving competencies (N = 404)
| Determinants | Crude | Model 1-TMT-A | Model 2-TMT-B | |||
|---|---|---|---|---|---|---|
| R2 = 0.081 | R2 = 0.107 | |||||
| OR [CI95%, p-value] | R2 | ORadj | P-value | ORadj | P-value | |
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| TMT-A* | 5.1 [1.5 to 17.4, p = 0.010] | 0.036 | 3.8 | 0.041 | - | - |
| TMT-B* | 7.6 [2.2 to 25.8, p = 0.001] | 0.058 | - | - | 6.3 | 0.005 |
| MoCA | 0.043 | |||||
| NoCI (MoCA ≥ 26) | Reference | |||||
| MCI (MoCA < 26 & ≥19) | 0.60 [0.20 to 1.8, p = 0.368] | |||||
| SCI (MoCA < 19) | 16.7 [2.2 to 127, p = 0.006] | |||||
| MoCAmod*† | 4.4 [1.4 to 13.7, p = 0.010] | 0.034 | - | - | ||
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| Age* | 1.6 [0.43 to 6.0, p = 0.468] | 0.003 | 0.85 | 0.821 | 0.83 | 0.797 |
| Gender (female) | 2.1 [0.88 to 5.0 p = 0.093] | 0.016 | - | - | - | - |
| Education (<12 yrs) | 0.81 [0.3 to 2.3, p = 0.701] | <0.001 | - | - | 0.59 | 0.349 |
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| Timed up-and-go test (TUG) | 3.2 [0.9 to 11.1, p = 0.066] | 0.020 | 2.4 | 0.178 | 2.2 | 0.210 |
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| Distance driven per week*† | 5.4 [1.6 to 17.4, p = 0.004] | 0.043 | 4.1 | 0.022 | 3.9 | 0.031 |
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| Visual acuity*† | 1.5 [0.44 to 5.3, p = 0.514] | 0.002 | - | - | ||
*Odds ratio was measured using logistic regression. Continuous values were transformed to be normally distributed and have a range of 0 to 1 from the fifth to the ninety-fifth percentile of the population. † Scale was inverted for high scores to represent worsening conditions. We used multiple imputations (50) to replace missing data (TUG, n = 10; distance per week, n = 2; visual acuity, n = 3). MCI = mild cognitive impairment; MoCA = Montreal Cognitive Assessment, MoCAmod = Modified Montreal Cognitive Assessment (First subtask similar to TMT-B omitted), NoCI = No cognitive impairement; R2 = McFadden's pseudo R-squared coefficient of determination; SCI = severe cognitive impairment.