Copyright 2016 American Medical Association. All rights reserved.
D
izziness is among themost common chief complaints
among patients presenting to frontline clinicians.
1,2
Whereas dizziness is a symptom with many causes,
evaluation by an otolaryngologist is commonly recom-
mended. Treatment of patients with vestibular disorders is
complex, requires additional clinic time, and uses greater re-
sources (eg, videonystagmography [VNG], rotary chair). Many
patients are found not to have otologic disease, leading to pa-
tient and clinician frustration and delays in diagnosis.
Patient history plays a critical role in the evaluation of ves-
tibular complaints.
3,4
The nature of the dizziness (ie, vertigo,
lightheadedness, imbalance), the temporal pattern of the
dizziness (ie, single episode, recurrent), the duration of at-
tacks (ie, seconds, hours), and associated symptoms (ie, hear-
ing loss, headache) can identify otologic vs nonotologic dis-
ease, and even a specific diagnosis.
5
Physical examinationmay
help establish a vestibular diagnosis but often has normal re-
sults. Similarly, vestibular testing may be useful in establish-
ing a diagnosis but requires a narrowdifferential diagnosis for
correct test selection and interpretation of test results.
3
A questionnaire focusing on key elements of the history
may provide adequate information for development of a nar-
row differential diagnosis prior to the office visit.
4,6
Our pro-
gram began using a vestibular disorders intake questionnaire
in September 2012. This 10-page questionnaire was designed
as a quality improvement measure to provide more efficient
and timely care to patients. The results of the questionnaire
have been used to direct appointments (eg, to physician,
vestibular therapist, nurse practitioner, neurologist) and to
inform choice of testing (eg, VNG, rotary chair, posturogra-
phy, vestibular evoked myogenic potentials [VEMPs]). Sub-
jectively this appears to have improved clinical efficiency but
places time burden on administrative and clinical staff toman-
age this system.
We performed data analyses of the triage questionnaire.
This study used414 consecutive patient questionnaires for de-
scriptive analyses andpredictivemodel building. Results of this
studymay be generalized to practicemanagement for allocat-
ing resources and improving efficiency of patient evaluation.
Methods
Approval was obtained from the Medical College of Wiscon-
sin institutional review board. Informed consent was waived
due to the retrospective nature of this study. This project ana-
lyzes a clinically used intake questionnaire specifically de-
signed to triage new patients with vestibular disorders.
Questionnaire
Thequestionnairewas developedatMayoClinic andwasmodi-
fiedslightlybeforebeing implemented inour institution. Atotal
of 162 data variables were captured from each questionnaire.
The questionnaire captures demographic information includ-
ing medical, family, and social history, and current medica-
tion use. There are sections that focus on:
1. The nature of the dizziness perception. This includes a
series of check boxes to describe the dizziness, and ques-
tions as to the onset, duration, and frequency of spells (epi-
sodes), triggers for spells, and the relationship of spells to
motion.
2. Headache, migraine, and migraine-associated symptoms.
3. Otologic problems including hearing loss, tinnitus, aural
pressure, otalgia, and otorrhea.
4. Prior tests and results including audiograms, imaging,
VEMPs, VNG, rotary chair, cardiacHoltermonitors, tilt table
testing, and so forth.
Predictive Model Development
The development of predictivemodels for the diagnosis of be-
nign paroxysmal positional vertigo (BPPV), Ménière’s disease,
andvestibularmigraine incorporatedan initial data set for iden-
tifying key variables for further data collection and a large data
set for predictive model building. The initial group consisted
of 212 consecutive newpatient intake questionnaires. All vari-
ables and fields were collected from these questionnaires for
analysis.Weinitially tried todevelopmodels using all available
variables, but this resulted in complex algorithms with unsat-
isfactory sensitivity and specificity. By repetitively narrowing
the data set, and checking for improvements in sensitivity and
specificity, we identified a set of factorswith strong correlation
with specific diseases. Asubsequent 202 consecutivequestion-
naires were then interrogated for this narrow set of variables.
These variables from the combined 414 questionnaires were
then analyzed to build the statistical models for diagnosis
predictions.
Statistical Analysis
The initial data set was screened to identify variables using 3
criteria: (1) significant (
P
< .05) associationwith the 3 diagno-
ses, (2) sufficient number of observations (≥5 per cell after
cross-tabulation with the outcome), and (3) clinical impor-
tance and relevance. All variableswere converted intodichoto-
mous form (ie, 0 = absent; 1 = present).
The final data set had information on 414 individuals, of
which 381 were ultimately fully evaluable (see Results). Lo-
gistic regression analyses were performed to build parsimo-
nious predictive models with model variables significant at
P
< .05. All 2-way interactions between significantmodel vari-
ables were investigated for statistical significance. A forward
stepwise variable selectionprocedurewas used. The 3 final par-
simonious models included only variables significant at the
P
< .02 level, more stringent than the initially planned signifi-
cance cutoff of .05. The receiver operating characteristic (ROC)
curve, area under ROC curve, sensitivity, and specificity at se-
lected cutoffs (ie, linear predictor [LP] values) were assessed
using 10-fold cross-validation.
Thestatisticalanalysiswasperformedusingtheopen-source
software R, version 3.1.1
( http://www.r-project.org).Two-
tailed Wald tests were used for statistical significance testing.
Results
Of the 414 questionnaires analyzed, 381 had clinical informa-
tionnecessary to define a final diagnosis (
Figure
). Of these, 183
Research
Original Investigation
Statistical Model for the Prediction of Common Vestibular Diagnoses
JAMA Otolaryngology–Head & Neck Surgery
April 2016 Volume 142, Number 4
(Reprinted)
jamaotolaryngology.com18




