A representative sample of the adult population in Germany was screened for dizziness / vertigo. Lifetime prevalence of MV was 0.98% (95% CI 0. To 1.37), the 12-month prevalence 0.89% (95% CI 0. To 1.27) age-adjusted health-related quality of life scores (SF-8 health survey) were consistently lower in participants with MV compared to dizziness-free controls.
A representative sample of the adult population in Germany was screened for dizziness / vertigo. Lifetime prevalence of MV was 0.98% (95% CI 0. To 1.37), the 12-month prevalence 0.89% (95% CI 0. To 1.27) age-adjusted health-related quality of life scores (SF-8 health survey) were consistently lower in participants with MV compared to dizziness-free controls.
A representative sample of the adult population in Germany was screened for dizziness / vertigo. Lifetime prevalence of MV was 0.98% (95% CI 0. To 1.37), the 12-month prevalence 0.89% (95% CI 0. To 1.27) age-adjusted health-related quality of life scores (SF-8 health survey) were consistently lower in participants with MV compared to dizziness-free controls.
H.K. Neuhauser, MD, MPH; A. Radtke, MD; M. von Brevern, MD; M. Feldmann; F. Lezius; T. Ziese, MD; and T. Lempert, MD AbstractObjective: To investigate the epidemiology of migrainous vertigo (MV) in the general population by assessing prevalence, clinical features, comorbid conditions, quality of life, and health care utilization. Methods: We screened a representative sample of the adult population in Germany (n 4,869) for moderate or severe dizziness/vertigo and followed up with validated neurotologic telephone interviews (n 1,003). Diagnostic criteria for MV were as follows: 1) recurrent vestibular vertigo; 2) migraine according to the International Headache Society; 3) migrainous symptoms during at least two vertiginous attacks (migrainous headache, photophobia, phonophobia, or aura symptoms); and 4) vertigo not attributed to another disorder. In a concurrent validation study (n 61) the interviews had a sensitivity of 84% and a specificity of 94% for vestibular vertigo and 81% and 100% for migraine. Results: The lifetime prevalence of MV was 0.98% (95% CI 0.70 to 1.37), the 12-month prevalence 0.89% (95% CI 0.62 to 1.27). Spontaneous rotational vertigo was reported by 67% of participants with MV while 24% had positional vertigo. Twenty-four percent always experienced headaches with their vertigo. Logistic regression analysis comparing participants with MV with dizziness-free migraineurs showed an independent association with coronary heart disease but not with sex, age, migrainous aura, education, stroke, hyperten- sion, hyperlipidemia, body mass index, or depression. Age-adjusted health-related quality of life scores (SF-8 Health Survey) were consistently lower in participants with MV compared to dizziness-free controls. Two thirds of participants with MV had consulted a doctor but only 20% of these were diagnosed with MV. Conclusions: Migrainous vertigo is relatively common but underdiagnosed in the general population and has considerable personal and healthcare impact. NEUROLOGY 2006;67:10281033 Migrainous vertigo (MV) is a frequent cause of recur- rent vertigo in patients presenting to specialized diz- ziness clinics 1,2 and is also frequent in headache clinic patients. 2 In the general population, lifetime prevalences are estimated at 7% for vertigo 3 and 16% for migraine. 4 The frequency of MV, i.e., of vertigo causally related to migraine, however, is not known at the population level. This recently recognized syn- drome has thus far been investigated in specialized care settings. 2,5-7 In this study, we sought to estimate the popula- tion prevalence of MV in a nationally representative sample of the general population in Germany through validated neurotologic interviews applying explicit diagnostic criteria. We further aimed to de- scribe the clinical characteristics of MV, associated sociodemographic characteristics, comorbid condi- tions, health-related quality of life, and health care utilization in an unselected general population sample. Methods. The neurotologic survey is a cross-sectional study which investigated the epidemiology of dizziness and vertigo in the general population with neurotologic interviews. 3 In brief, the sampling design had two stages. First, a representative sample of the adult general population in Germany consisting of 4,869 par- ticipants of the German National Telephone Health Interview Survey (GNT-HIS) 2003 aged 18 years were invited to partici- pate in a further interview and were screened for moderate or severe dizziness or vertigo in their past life. Out of 1,157 eligible participants with dizziness and vertigo, 1,003 completed a de- tailed neurotologic interview by telephone. The response rates were 52% for the GNT-HIS 2003 and 87% for the neurotologic survey. We developed the neurotologic interview in a specialized dizzi- ness clinic with the aim to differentiate vestibular vertigo from non-vestibular dizziness and to identify four specific syndromes according to explicit diagnostic criteria: MV, benign paroxysmal positional vertigo (BPPV), Menie`res disease, and orthostatic diz- ziness. Vestibular vertigo was defined according to diagnostic cri- teria that had been developed for this survey through piloting and validation in a specialized dizziness clinic (table 1). MV was de- fined according to previously published diagnostic criteria for def- inite MV 2 (table 1). Some patients with MV do not fulfill all of these criteria, e.g., have an International Headache Society (IHS) migraine but do not show typical migraine symptoms during the vertigo attacks or do not have a history of IHS migraine but report typical migraine precipitants for their vertigo or response to anti- migraine medication. These patients can be diagnosed with prob- able MV. 2 However, we did not aim to investigate the prevalence of probable migraine in this study since this would have length- ened the interview considerably as shown in the pilot study. Sim- ilarly, the prevalence of non-vestibular dizziness related to migraine such as orthostatic dizziness during migraine attacks was not investigated. Migraine was diagnosed according to the criteria of the IHS. 8 The interviews had a specificity of 94% and a sensitivity of 84% for vestibular vertigo and 100% and 81% for migraine as shown in a concurrent validation study (n 61). The interviews were conducted by two medical student interviewers (F.L., M.F.) who had been extensively trained in a neurotologic dizziness clinic over a period of 1 year. Each interview was dis- From the Department of Epidemiology (H.K.N., T.Z.), Robert Koch Institute; Vestibular Research Group (H.K.N., A.R., M.v.B., M.F., F.L., T.L.), Department of Neurology, Charite; and Department of Neurology (T.L.), Schlosspark-Klinik, Berlin, Germany. Disclosure: The authors report no conflicts of interest. Received December 23, 2005. Accepted in final form May 12, 2006. Address correspondence and reprint requests to Dr. H. Neuhauser, Robert Koch-Institut, Seestr. 10, D-13353 Berlin, Germany; e-mail: neuhauserh@rki.de 1028 Copyright 2006 by AAN Enterprises, Inc. cussed with an experienced neurotologist (H.N., M.v.B., A.R., or T.L.). The prevalence of MV was calculated taking into account the two-stage sampling design by multiplying the proportion of MV in neurotologic survey participants with the proportion of dizziness/ vertigo in GNT-HIS participants. 3 Thereby, non-responders and those lost to follow-up between the two sampling stages were assumed to have the same probability of MV as participants of the neurotologic survey. The CI for the prevalences were calculated using the conservative Wilson method 9 and taking into account the loss of power through non-response and loss to follow-up be- tween the GNT-HIS and the neurotologic survey. The analysis includes comparisons of participants with MV and two different control groups of dizziness-free individuals from the general population participating in the GNT-HIS. For the analysis of the association of MV with demographic factors and comorbid conditions we have chosen a control group of dizziness- free migraineurs in order to avoid confounding by migraine (since MV patients also all have migraine). Migraine was assessed in the neurotologic survey and in the GNT-HIS 2004 but not in the GNT-HIS 2003. Therefore, the first control group came from the GNT-HIS 2004. Thirty participants with MV in the past 12 months were compared to consecutive migraineurs participating in the GNT-HIS 2004 without vertigo/dizziness in the past 12 months (n 589). The GNT-HIS 2004 belongs to the same pro- gram of nationally representative health interview surveys as the GNT-HIS 2003, has the same sampling design, an almost identi- cal response rate, and a migraine questionnaire based on the IHS criteria. Both in cases and controls only visual auras were in- quired about. The questions on sociodemographic factors and co- morbid conditions were identical for the cases and controls. Comorbid conditions were self-reported physician diagnoses ex- cept for depression, which was self-reported by the participants. Chi-square test and Fisher exact test were used to test for univariate associations of categorical variables and the t test for differences in means of numerical variables. Results were consid- ered significant at p 0.05. To test for independent associations with MV, we performed a stepwise backward logistic regression analysis. The second comparison focused on health-related quality of life as measured with the eight-item short form questionnaire (SF-8). The SF-8 is a generic instrument for measuring health-related quality of life in the past 4 weeks constructed for use in population-based studies. 10 The control group consisted of all dizziness-free participants of the GNT-HIS 2003 subsample on which the neurotologic survey was based (the GNT-HIS 2004 did not include questions on health-related quality of life). Age- adjusted SF-8 scores and 95% CI in all eight subscales and in the two summary measures were compared for the 14 participants with MV in the past 4 weeks and 2,816 dizziness-free controls using a general linear model univariate procedure. We additionally investigated the consequences of MV at the general population level by asking about sick leave, overall impact on daily activities, and health care utilization. Results. We identified 243 participants with vestibular vertigo, corresponding to a general population lifetime prevalence of 7.4%. A total of 109 participants had a his- tory of both vestibular vertigo and migraine, corresponding to a general population lifetime prevalence of 3.2%. Thirty- three participants had migrainous vertigo according to the study criteria (27 women and 6 men). These were 14% of all participants with vestibular vertigo and 3% of all par- ticipants with moderate to severe dizziness or vertigo. The lifetime prevalence of MV in the general population was calculated at 0.98% (95% CI 0.70 to 1.37), and the 12- month prevalence at 0.89% (95% CI 0.62 to 1.27). The clinical characteristics of MV are summarized in table 2. Vestibular symptoms were spontaneous rotational vertigo (67%) or positional vertigo (24%) in the vast major- ity of patients. Three participants (9%) reported recurrent dizziness with nausea and either oscillopsia or episodic imbalance. The most frequent migrainous symptom during MV attacks was headache (91%). However, headache al- ways accompanied vertigo in only 24% of participants. Only 4 out of 33 participants with MV (12%) had vertigo with the typical duration of an aura (5 to 60 minutes) and in close temporal relationship to headache, and only in two did the vertigo regularly precede the headache. Cochlear symptoms during vertigo were reported by 12 patients with MV (36%) but none had progressive hearing loss as would be expected in Menie`res disease. Sixty-one percent noted at least one typical migraine trigger (men- struation, stress, or sleep irregularities) for both their headache and MV attacks. Age at onset of MV ranged from 8 to 53 years (median 23 years) and MV attacks had occurred over a period rang- ing from 1 to 48 years (median 13 years). Migraine head- ache manifested before MV in 74% of participants and in more than half of these (52%) migraine headache preceded MV by more than 5 years, in 26% even by more than 10 years. The vast majority of patients (85%) had experienced both active MV and active migraine headaches during the last 12 months. We analyzed the association of MV with sociodemo- graphic factors and comorbid conditions comparing partic- ipants with MV in the past 12 months with dizziness-free migraineurs selected from the general population (GNT- HIS 2004 participants) (table 3). In univariate analysis, only coronary heart disease (CHD) was associated with MV, while age, sex, education, migraine aura, stroke, dia- betes, body mass index, hypertension, elevated blood lip- ids, and self-reported depression were not. In a logistic regression model analysis including age, sex, level of edu- cation, elevated blood lipids, diabetes, and CHD, only CHD was independently associated with MV and the association of diabetes with MV was marginally significant. Age-adjusted health-related quality of life scores were consistently lower both in men and women with MV com- pared to dizziness-free general population controls from the GNT-HIS 2003 in all eight scales of the SF-8 and in the summary measure scales. However, this comparison had low power due to the few MV patients with vertiginous attacks in the last 4 weeks (n 14) and the confidence intervals are wide (figure). Forty percent of working MV patients reported sick leave from work. The overall impact of MV on daily activi- ties was rated as mild by 21% of participants with MV, as Table 1 Diagnostic criteria for vestibular vertigo and migrainous vertigo used in the neurotologic survey Vestibular vertigo (one has to be fulfilled): 1. Rotational vertigo 2. Positional vertigo 3. Recurrent dizziness with nausea and either oscillopsia or imbalance Migrainous vertigo (AD have to be fulfilled): A. Recurrent vestibular symptoms of at least moderate severity B. Current or previous history of migraine according to the criteria of the International Headache Society C. At least one migrainous symptom during at least two vertiginous attacks: migrainous headache, photophobia, phonophobia, or visual auras D. Not attributed to another disorder September (2 of 2) 2006 NEUROLOGY 67 1029 moderate by 46%, and as severe by 33%. Impact was de- fined as mild when activities during the days with MV could be pursued, moderate when there was interference with daily activities, and severe when daily activities had to be abandoned. Two thirds of participants with MV had consulted a physician for their vertigo and almost all of them had undergone at least one diagnostic procedure (table 4). Most patients could report a diagnosis as the result of the con- sultation. This diagnosis, however, was MV only in four patients (21% of diagnoses). The others had been labeled with non-vestibular diagnoses including anemia, diabetes, cervical dizziness, psychosomatic dizziness, and hypovole- mia. Forty percent of participants with MV had taken medication for their vertigo but only one third reported a good response. Discussion. The main finding of our study is that MV has a lifetime prevalence of approximately 1% and thus is a frequent condition at the general popu- lation level. This is in line with the high prevalence of MV in specialized dizziness and migraine clin- ics, 1,7,11,12 which however cannot be extrapolated to the general population since the selection effects in specialized care settings produce a considerable bias. Another important finding is that migraine head- aches and vestibular vertigo concur in the general population about three times more often than ex- pected by chance: at a lifetime migraine prevalence of 16% 4 and vestibular vertigo of 7%, 3 chance concur- rence is expected in 1.1% of the population but was actually found in 3.2% of the population in our study. Strengths of our study are the nationally repre- sentative general-population setting, the use of vali- dated neurotologic interviews for vestibular vertigo with high specificity and sensitivity, and the use of explicit diagnostic criteria for MV. In addition, we sought to minimize misclassification by a detailed assessment of the most common differential diag- Table 2 Clinical characteristics in 33 participants with migrainous vertigo (%) Main vestibular Spontaneous rotational vertigo 67 sympton* Position triggered rotational vertigo 12 Position triggered nonrotational vertigo 12 Vestibular dizziness 9 Additional vestibular Oscillopsia 36 symptoms Imbalance 61 Vestibular head motion intolerance 49 IHS migraine With visual aura 36 Without visual aura 64 Migrainous symptoms Headache with vertigo Sometimes 67 Always 24 Photophobia Sometimes 47 Always 16 Phonophobia Sometimes 47 Always 9 Visual aura Sometimes 36 Always 0 2 Migrainous symptoms with vertigo Sometimes 67 Always 12 Cochlear symptoms Tinnitus 15 with vertigo Aural fullness 15 Hearing loss 9 Typical duration 1 min 25 of attacks 15 min 22 560 min 22 124 h 28 24 h 3 Total no. of attacks 220 12 (lifetime) 21-50 50 50 38 Shared precipitants Menstruation 33 of migraine and MV Stress 41 Sleep irregularities 38 * Leading to the classification as vestibular vertigo. Vestibular dizziness: recurrent dizziness with nausea and either oscillop- sia or episodic imbalance during at least two attacks. Percent of women with migrainous vertigo (MV). IHS International Headache Society. Table 3 Sociodemographic factors and comorbidity in 30 participants with migrainous vertigo in the past 12 months compared to 589 dizziness-free migraineurs Prevalence (%) Migrainous vertigo Control group Univariate p Multivariate* OR (95% CI) Women 83 76 NS 1.7 (0.65.0) Age, y, mean (SD) 43 (15) 38 (12) NS 1.1 (0.81.6) Secondary school education, y NS 10 35 22 10 39 39 10 27 30 Migraine with visual aura 33 26 NS Self-reported depression in the past year 19 18 NS Hypertension 27 21 NS Elevated blood lipids 31 21 NS Diabetes 11 2 NS 4.8 (0.924.9) Coronary heart disease 15 2 0.01 4.4 (1.117.9) Stroke 0 1 NS Body mass index, kg/m 2 , mean (SD) 25 (4) 24 (4) NS * Backward stepwise logistic regression including age, sex, and all factors with p 0.25 in univariate analysis, leading to a model including age, sex, coronary heart disease, and diabetes. The OR for age is reported for an increase in age of 10 years. Self-reported physician diagnosis. NS not significant at p 0.05. 1030 NEUROLOGY 67 September (2 of 2) 2006 noses of MV (BPPV, Menie`res disease, and ortho- static dizziness). As with any epidemiologic study, we cannot ex- clude selection bias. However, the willingness of GNT-HIS participants to undergo a further inter- view was not associated with having dizziness/ver- tigo. More importantly, non-responder analysis of the neurotologic survey, which included a compari- son of the GNT-HIS sample on which the neuroto- logic survey was based with national population statistics, showed very similar distributions of demo- graphic features and selected health indicators (age, sex, BMI, and smoking). 3 As an exception to this, participants with a lower secondary school education were underrepresented in the GNT-HIS, whereas those with a middle and higher educational level were overrepresented. Since vertigo has been shown to occur less frequently in individuals with a higher educational level, 3 the effect is likely to be an under- estimation of the true MV prevalence. The difference between the lifetime and the 1-year prevalence of MV is surprisingly small and may be due to recall bias, i.e., that more remote attacks of MV may be more easily forgotten, in particular ac- companying migrainous symptoms. This, however, would result in an underestimation rather than an overestimation of the true lifetime prevalence of MV. With regard to recall bias, we refrained from includ- ing benign paroxysmal vertigo of childhood, which is an early childhood manifestation of migrainous ver- tigo. Benign paroxysmal vertigo of childhood is characterized by brief attacks of vertigo or disequi- librium, anxiety, and often nystagmus or vomiting that occur recurrently for months or years in other- wise healthy young children. 13 Many of these chil- dren later develop migraine, often years after vertigo attacks have ceased. 14 In a population-based study, the prevalence of recurrent vertigo probably related to migraine was estimated at 2.8% in children be- tween 6 and 12 years. 15 Our estimates of the prevalence of MV are also likely to be conservative since both the validated in- terview diagnostic criteria for vestibular vertigoas a prerequisite for diagnosis of MVand the diagnos- tic criteria for MV had an emphasis on specificity rather than sensitivity. These prevalence estimates do not include probable MV since identifying pa- tients with probable MV would have involved inquir- ing in detail about migraine precipitants of vertigo and response to migraine medication, which was not possible in the time frame of the interviews. How- ever, probable MV is likely to be frequent as well. In an earlier dizziness clinic case series, probable MV accounted for a further 4% of diagnoses in addition to the 7% of patients with definite MV. 2 In the neurotologic survey, 109 participants had a history of both vestibular vertigo and migraine, cor- responding to a general population prevalence of 3.2%. Based on a lifetime prevalence of vestibular vertigo of 7% 3 and migraine 16%, 4 around 1% of the population can be expected to have a chance concur- rence of vertigo and migraine. We have found that an additional 1% of the population has migrainous vertigo, i.e., a vertigo syndrome causally linked to migraine. It is likely that among the remaining 1%, Table 4 Health care utilization in 33 participants with migrainous vertigo (%) Medical consultation 67 General practitioner/internal medicine 58 ENT 27 Neurologist 24 Radiologist 15 Orthopedist 9 Other 3 More than one specialist 37 Diagnostic procedures 36 Audiometric test 27 EEG 27 Brainstem auditory evoked potentials 21 Cranial CT or MRI 21 Caloric test 18 Ultrasound of carotid and vertebral arteries 12 Cranial or cervical X-ray 9 Cervical CT or MRI 6 More than one diagnostic procedure 30 Figure. Age-adjusted health-related quality of life in 14 participants with MV during the last 4 weeks compared to a representative general population sample of 2,816 dizziness-free controls (short form eight item health status survey [SF-8] scores with 95% CI). September (2 of 2) 2006 NEUROLOGY 67 1031 there are quite a few cases of probable migrainous vertigo. However, since other vestibular disorders in- cluding BPPV and Me nie` res disease have been shown to be associated with migraine, 16,17 the propor- tion of patients with suspected probable MV cannot be estimated from these figures. We also aimed at investigating the association of MV with sociodemographic factors and comorbid con- ditions which have been previously linked to dizzi- ness or vertigo. The choice of a control group of unselected migraineurs from a general population sample has the advantage of avoiding confounding by migraine. However, the analysis had low power due to the small number of cases and was limited by the cross-sectional design and the assessment of risk factors by self-report rather than measurement. An interesting finding is that the proportion of women did not differ significantly between partici- pants with MV and dizziness-free migraineurs (83% vs 76%). After adjustment for age and other factors in multivariate analysis, the OR for female sex still was not significantly different from one. This is the first analysis of the association of sex and MV ad- justed for migraine and suggests thatunless it is a power problemthe female preponderance among patients with MV merely reflects the female prepon- derance among migraineurs in general. The proportion of 33% MV patients with visual auras seems rather high. However, it is not signifi- cantly higher than in the control group of dizziness- free migraineurs (26%). In addition, since well over 90% of migraineurs with aura have been reported to have visual auras, 18,19 the overall proportion of mi- graine with visual aura in the MV group probably still lies within the range of reported proportions of 18% to 36% of migraine with aura from population- based studies. 18,20 Of note, in the vast majority of cases, MV misses not only the duration criterion for an aura as defined by the IHS, but also the temporal relationship to migraine headaches. 11 There was also no evidence of an association of MV with depression, although previous studies have shown an association of vestibular vertigo with de- pression. However these studies did not exclude con- founding by migraine. 3,21,22 Both the significant association of MV with CHD and the marginally sig- nificant association with diabetes are rather surpris- ing and do not necessarily reflect a causal relationship. Diabetes has been previously discussed as a risk factor for peripheral vestibular dysfunction, 23-25 but the overall evidence has re- mained inconclusive. CHD was associated with non- vestibular dizziness in previous studies 26,27 but not with vestibular disorders. Of note, while migraine was not associated with early onset CHD in several studies, 28,29 this association has not been thoroughly investigated yet among migraineurs with aura. In addition, adult migraineurs, particularly those with aura, had a higher cardiovascular risk profile. 30 Mi- graine with aura however is unlikely to explain the association of MV with CHD in our study since the two groups do not differ significantly with respect to visual auras and the overall proportions of migraine with aura are likely to be similar as well. In our analysis, the proportion of migraineurs with aura in the MV group (33%) compared to the control group (26%) may have contributed to the as- sociation of MV with vascular factors, but cannot explain it entirely. We compared this unselected general population sample of patients with MV with patients with MV from our specialized dizziness clinic, who were diag- nosed according to the same criteria. 2 The two groups showed a similar age and sex distribution, as well as a similar proportion of patients with sponta- neous rotational vertigo and patients with migrain- ous headaches in close temporal association to their vertiginous attacks. However, neurotologic survey participants with MV had shorter attacks than dizzi- ness clinic patients with MV: 47% vs 18% had at- tacks shorter than 5 minutes and only 3% vs 27% had attacks longer than 24 hours. This may explain why one third of survey participants with MV never consulted a doctor for their vertigo. Our results suggest that MV is not only a frequent disorder but also has a considerable impact both at the personal and at the societal level. The differences in the age-adjusted quality of life subscales and sum- mary measures consistently point toward lower qual- ity of life in MV patients compared to dizziness-free controls. As our results are based on a small sample, they could be adjusted only for age. It would be inter- esting to investigate health-related quality of life in a larger group of patients with MV compared to a control group of dizziness-free migraineurs and to control for other comorbid conditions. A 1-year population prevalence of 0.9% and a medical consultation rate of almost 70% prompting various diagnostic procedures in the majority of pa- tients suggest considerable health care costs due to MV. The low recognition rate of MV is worrisome and confirms that MV is not a well-known condition in primary care. 31 References 1. Brandt T. 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Dizziness among older adults: a possible geriatric syndrome. Ann Intern Med 2000;132:337344. 28. Cook NR, Bensenor IM, Lotufo PA, et al. Migraine and coronary heart disease in women and men. Headache 2002;42:715727. 29. Rose KM, Carson AP, Sanford CP, et al. Migraine and other headaches: associations with Rose angina and coronary heart disease. Neurology 2004;63:22332239. 30. Scher AI, Terwindt GM, Picavet HSJ, Verschuren WMM, Ferrari MD, Launer LJ. Cardiovascular risk factors and migraine. Neurology 2005; 64:614620. 31. Hanley K, OD T. Symptoms of vertigo in general practice: a prospective study of diagnosis. Br J Gen Pract 2002;52:809812. MARK YOUR CALENDARS! Plan to attend the 59th Annual Meeting in Boston, April 28-May 5, 2007 The 59th Annual Meeting Scientific Program highlights leading research on the most critical issues facing neurolo- gists. More than 1,000 poster and platform presentations cover the spectrum of neurologyfrom updates on the latest diagnostic and treatment techniques to prevention and practice management strategies. For more information contact AAN Member Services at memberservices@aan.com; (800) 879-1960, or (651) 695- 2717 (international). AAN 60th Annual Meeting in Chicago, Illinois April 12-19, 2008 AAN 61st Annual Meeting in Seattle, Washington April 25May 2, 2009 September (2 of 2) 2006 NEUROLOGY 67 1033