The Grand Rapids Dip Revisited
The Grand Rapids Dip Revisited
1994
Copyright 6 1994 Efsevier Science Ltd
Pergamon P&&d in the USA. All rights reserved
~~-4S75/94 $6.00 + .oO zyxwvutsrq
iConsultant, Alcohol and Traffic Safety, Pukerua Bay, New Zealand; *Victoria University of Wellington,
New Zealand; 3Land Transport Safety Authority, Wellington, New Zealand zyxwvutsrqponmlkjihgfedc
Abstract-This analysis addresses an issue that has concerned road safety authorities for some 28 years:
the celebrated “Grand Rapids Dip.” This, most readers will recognise, is the below-baseline excursion,
which occurs in the blood alcohol concentration (BAC) interval of .Ol%-.04%, of the relative risk curve for
accident risk versus blood alcohol, derived from the 1964 Grand Rapids Study data. The present analysis
has its starting place in the explanation advanced by Allsop, who noted that the case/control comparisons
were biased due to the disproportionate representation of demographic subgroups in different blood alcohol
concentration class intervals. Indeed, when relative-risk curves are derived separately for subgroups of
differing drinking habits, the resulting separate risk curves all show monotonic increases at al1 blood alcohol
concentration ranges. Such separate relative risk curves are unpopular, and most of the road safety community
pays them little heed. Thus, the original concept of the “dip” remains with us. For this reason, we have
derived, using a simple but realistic statisticat model, a single relative-hazard curve from the Grand Rapids
data, one that is free from the distortion introduced by unequal representation of different demographic
subgroups in different blood alcohol concentration class intervals. This curve indicates that accident risk
increases with increased blood alcohol concentration regardless of self-reported drinking frequency. However
more frequent drinkers have less risk at all blood alcohol concentration levels, including zero, than less
frequent drinkers at the times and places sampled.
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who believe that the Grand Rapids Dip is actually only self-reported drinking frequency but also age,
evidence, of at least tentative quality, that a little sex, education, economic status, and driving expe-
alcohol improves driving. Perhaps this is because rience. However, this would have required the
people prefer to think in terms of “a” curve, or original raw data, which are no longer available.
relative hazard function, rather than a number of Accordingly, we chose the strongest single attri-
separate ones. For this reason, we thought it desir- bute, self-reported drinking frequency. The data
able to derive, using a simple but realistic statistical available to us from the Grand Rapids study con-
model, a single relative-hazard curve from the Grand sisted of a table of case and control counts for
Rapids data, without the distortion previously five self-reported drinking frequency classes (daily,
caused by the inadequate representation of different thrice-weekly, weekly, monthly, and yearly or less)
subpopulations in different blood alcohol concentra- and five blood alcohol concentration classes (.OO%.
tion class intervals. .Ol-.04%, .05-.07%, .08-.lO%, .ll+%). Unfortu-
nately , in the cases of “yearly or less” and
“monthly” drinkers, accident counts for the three
OUR METHOD
higher blood alcohol concentration classes had in
It would have been most elegant to adjust the each case been accumulated into just one cell
relative hazard function for simultaneous variations (Table 1). In our analysis we treated the two cells
in a number of moderating influences, including not that result as a blood alcohol concentration of
The Grand Rapids Dip revisited 649
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Fig. 2. Relative risk by blood alcohol concentration and self-reported drinking frequency.
Note: The counts marked * are presented as an aggregate for all cases over .05% in Borkenstein et al. (19641,
such that (I + zyxwvutsrqponmlkjihgfedcbaZYXWVUTSRQPONMLKJIHGFEDCBA
b + c = 34 and d + r + f‘ = 49.
650 P. M. HURST et al.
.08-.lO%, being the “average” cell over which and observed values will be denoted by lower-case
the accumulation had taken place. characters.
A brief description of the way the data were Further, let ‘pijbe the probability that a journey
sampled in the original study follows. Accident data in the ijth class results in an accident and define Zijk
over a one-year period were classified according to as such:
each involved driver’s self-reported drinking habits
and measured blood or breath alcohol at the time of
0 if the kth journey in class ij
the accident. results in no accident
Using an historical set of accident data, previ- z,, =
ous accident sites, dates, and times of day were 1 if the kth journey in class ij
1 results in an accident,
extracted and tabulated. This information was used
to furnish guidelines for the selection of a “control”
then
group of drivers. About four drivers were stopped
at each historical accident site at an anniversary date
and time. They were asked about drinking fre- wy = ‘pjj (1)
quency, among other matters, and given breath
tests. and
We can therefore think of the situation as af-
fording two contingency tables involving accident Var (Z,,) = E[Z$.,] - E[Z,J2
and control drivers. Both tables have the same for-
mat, with rows representing reported drinking fre- = cpjj(l - cpij). (2)
quency and columns the estimated blood alcohol
Using these definitions
equivalent resulting from breath tests.
The control table consists of the total number
of drivers stopped, interviewed, and tested. The
margins of the control table will be random, but
the total number of drivers is predetermined. The Then
control table provides us with relative exposure by
types of drivers (based on reported drinking fre- -wijl = zyxwvutsrqponmlkjihgfedcbaZYXWVU
a&jJmqjl
quency) at times and sites at which accidents have
previously occurred. It must be carefully noted that = PijE[wijl, (3)
this control group is not typical of the general driver
population, but is rather typical of the population of i.e. the expected number of accidents equals the
drivers using the roads at the times and places of probability of an accident times the expected num-
the accidents recorded a year earlier. Therefore, the ber of journeys. Also
absolute number of drivers in each cell is not so
much of interest as the ratio of numbers in different E[ Y;] = E[WJE[Z;.J + E[Wij (WV - l)]zz[Z,,]?
cells (relative exposure). By performing a chi-square
= E[W,,](E[Z&] - E[Z~J’> + E[W$E[Z,J2
test on the control table, one can test the hypothesis
that self-reported drinking frequency is independent = E[ WJ Var (Z,,)
of blood alcohol concentration. The test statistic is
+ _f?[W$E[Z,,]* (from eq 2). (4)
very large and this hypothesis is clearly rejected.
In fact it can be easily seen that blood alcohol is
positively correlated with self-reported drinking Now, consider a sample of drivers taken at
frequency. some other time and let Xi be the number of these
sampled drivers (journeys) in the ijth class. Then
an estimator of the number of journeys in the “acci-
dent” interval observed is given by rXij, where Y >
MODEL DESCRIPTION 0 is some scaling constant, and so
Let Y, be the number of accidents, during some
period of time, of drivers in the ith self-reported E[W,,] = rE[X& (5)
drinking frequency class and the jth BAC interval.
Let Wi, be the total number of journeys in the ijth and from eq 3,
class in the same period of time. Note that random
variables will be denoted by upper-case characters E[Y,] = cpijrE[XJ. (6)
The Grand Rapids Dip revisited 651
Therefore an estimator for the number of accidents lf!lu = exp (a; + pj + 8,)
-WY, - v&J*1
k[(y.. - r(p..X_)2]
rJ rJ rJ
=
( !Q11 +
_Q
6..
rJ’
= rEIXJcpij(l - CpJ + Y@[XJ + r*$O;EIXjj] This is based on eq 7. PROC NLIN in the SAS
(SAS Institute Inc., Cary, NC) package was used
= rt&S[XJ( 1 + r(pij) to achieve this. A number of iterations are required
before convergence is achieved. The parameter esti-
=(I+%) E[ Y,,] (from eq 6). (7) mates could also be calculated with other packages
such as Genstat and GLIM. For a general descrip-
tion of this class of models see McCullagh and
Therefore, the actual value of r, which is not known, Nelder (1990).
is not needed. There is then sufficient information to The risk ratios were calculated as exponentials
calculate the relative risks and the relevant standard of the corresponding parameter estimates.
errors.
The expected number of accidents during the re-
cording period is modelled by eq. 6. We used the RESULTS
control survey results, xij, as estimates for E[XJ. The accident risk was assumed to be of the form
Thus the estimated number of accidents, fig, is
$6 = exp (a; + pj),
pij = x&
This model assumes that the interaction term, 6,, is
where I& is an estimate of rpij. Note that I$~/&~~is zero.
an estimate of (pijl(pili.or the relative accident risk. An assessment of the validity of our model can
We assume that the risk is multiplicative, thus be achieved by considering the Pearson residuals.
652 P. M. zyxwvutsrqponmlkjihgfedcbaZYXWVUTSRQPONMLKJIHG
HURSTet al.
Table 2. Estimated relative risks goodness-of-fit of the model. Our model gives
Self-reported Blood alcohol concentration (70) 11.171/(21 - 9) = 0.931, indicating that the ob-
drinking served variability is comparable to that predicted by
frequency .oo .Ol-.04 .os-.07 .08-.I0 .l I+ our model (i.e. close to one). The largest residual
Yearly or less 1.00 1.17 1.71 3.93 10.68 value (1.84) originates from the cell: self-reported
Monthly 1.03 1.20 1.I7 4.05 11.01 drinking frequency of yearly or less with a blood
Weekly 0.78 0.91 1.33 3.05 8.29 alcohol concentration of O.OS%-0.10%. This is not
3 times per week 0.59 0.70 1.02 2.34 6.35
Daily 0.37 0.43 0.63 1.45 3.93 unexpected, as our knowledge of blood alcohol con-
centration for this cell is more uncertain than for
other cells. However, such a value is still within
The mean sum of squares of the Pearson residuals, acceptable limits.
i.e. The risk in the (i, j)th cell relative to the (1, 1)th
cell is given by
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