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Show The Berlin Questionnaire Screens for Obstructive Sleep Apnea in Idiopathic Intracranial Hypertension Matthew J. Thurtell, MBBS, FRACP, Beau B. Bruce, MD, David B. Rye, MD, Nancy J. Newman, MD, Valerie Biousse, MD Background: Obstructive sleep apnea (OSA) may be associated with idiopathic intracranial hypertension (IIH), a disorder most commonly occurring in young obese women. Because polysomnography, the standard test for diagnosing OSA, is expensive and time consuming, questionnaires have been developed to identify persons with OSA. The Berlin questionnaire (BQ) reliably identifies middle-aged and older persons in the community who are at high-risk for OSA. We aimed to validate the BQ as a screening tool for OSA in IIH patients. Methods: Patients with newly diagnosed IIH completed the BQ and then underwent diagnostic polysomnography. The BQ was scored as high or low risk for OSA, and the diagnosis of OSA was based on polysomnography find-ings. OSA was defined as an apnea-hypopnea index of $5 on polysomnography. Results: Thirty patients were evaluated (24 women; 15 white and 15 black; age, 16-54 years [median, 32 years]; body mass index, 27.3-51.7 kg/m2 [median, 39.8 kg/m2]). Twenty patients (66.7%) had a high-risk BQ score and 18 (60%) exhibited OSA. Fifteen of 20 (75%) with a high-risk BQ score had OSA, while 3 of 10 (30%) with a low-risk score had OSA (Fisher test, P = 0.045). The sensitivity and specificity of the BQ for OSA in IIH patients were 83% and 58%, respectively, whereas the positive predictive value was 75%. Conclusion: A low-risk BQ score identifies IIH patients who are unlikely to have OSA. Polysomnography should be considered in those with a high-risk score. Journal of Neuro-Ophthalmology 2011;31:316-319 doi: 10.1097/WNO.0b013e31821a4d54 2011 by North American Neuro-Ophthalmology Society Obstructive sleep apnea (OSA) is a common condition in which there are intermittent partial (viz, hypo-pneas) and complete (viz, apneas) limitations in airflow, with associated hypoxia and sympathetic arousals during sleep (1,2). It is associated with obesity and older age, is more common in men, and, when left untreated, results in increased cardiovascular morbidity and mortality (1-3). Polysomnography is the gold standard test for OSA diagnosis, but requires overnight evaluation (4). The Berlin questionnaire (BQ), which includes questions about snor-ing, daytime somnolence, body mass index (BMI), and hypertension, is a brief and validated screening tool that identifies persons in the community who are at high risk for OSA (5). OSA is thought be associated with idiopathic intracranial hypertension (IIH) (6). Although the BQ has been used as a screening tool for OSA in prior IIH studies (7), validation studies of the BQ have only been performed in middle-aged and older adults living in the community, whereas IIH most often occurs in young obese women (5). Because outcomes may be worse in IIH patients who have OSA (3,8), we obtained diagnostic polysomnography on newly diagnosed IIH patients. We concurrently administered the BQ to evaluate its validity as a screening tool for OSA in IIH patients. Department of Ophthalmology and Visual Sciences (MJT), The University of Iowa, Iowa City, Iowa; Emory Eye Center, Emory University School of Medicine (BBB, NJN, VB), Atlanta, Georgia; and Department of Neuroscience (DBR), Emory University, Atlanta, Georgia. Supported in part by a departmental grant (Department of Ophthalmology) from the Research to Prevent Blindness, Inc, New York, NY, by core grant P30-EY06360. Dr Bruce received research support from the National Institutes of Health/Public Health Service (KL2-RR025009, UL1-RR025008), National Institutes of Health/ National Eye Institute (K23-EY019341), and the Knights Templar Eye Foundation and also the American Academy of Neurology Practice Research Fellowship. Dr Biousse received research support from National Institutes of Health/Public Health Service (UL1-RR025008). Dr Newman is a recipient of the Research to Prevent Blindness Lew R. Wasserman Merit Award. Dr Rye received research support from the NIH/USPHS (NS055015 and MH083746) and is a consultant for the USPHS, Merck Co, Inc, and UCB Inc. The authors report no conflicts of interest. Address correspondence to Valerie Biousse, MD, Neuro-Ophthal-mology Unit, Emory Eye Center, 1365-B Clifton Road NE, Atlanta, GA 30322; E-mail: vbiouss@emory.edu 316 Thurtell et al: J Neuro-Ophthalmol 2011; 31: 316-319 Original Contribution Copyright © North American Neuro-Ophthalmology Society. Unauthorized reproduction of this article is prohibited. METHODS Standard Protocol Approvals and Patient Consents The study was approved by our institutional review board. As data were collected retrospectively, patients were not required to give written informed consent. Patients Since March 2008, all newly diagnosed IIH patients seen in the Neuro-Ophthalmology Unit at our institution have completed the BQ and been referred for overnight poly-somnography as part of their evaluation; polysomnography could not be obtained in some patients (e.g., if they declined or did not have medical insurance). We retrospectively included all newly diagnosed patients satisfying the updated modified Dandy criteria for IIH (9) who had completed the BQ and had undergone polysomnography. We excluded patients who were pregnant, were younger than 16 years, had a prior diagnosis of IIH, or had another cause for their increased intracranial pressure. Berlin Questionnaire The BQ (Fig. 1) incorporates questions about snoring (category 1), daytime somnolence (category 2), and hy-pertension and BMI (category 3) (5). The BQ was ad-ministered at the time of the patient's initial visit. When available, the patient's family or bed partner was asked to confirm the accuracy of responses to the questions about snoring. The overall BQ score was determined, as in pre-vious studies, from the responses to the 3 categories: scores from the first and second categories were positive if the responses indicated frequent symptoms (.3-4 times/week), whereas the score from the third category was positive if there was a history of hypertension or a BMI .30 kg/m2 (5). Patients were scored as being at high risk for OSA if they had a positive score on 2 or more categories, while those who did not were scored as being at low risk (5). FIG. 1. The BQ for OSA (5). The questionnaire incorporates questions about snoring (category 1), daytime somnolence (category 2), and hypertension and BMI (category 3). BQ, Berlin questionnaire; OSA, obstructive sleep apnea; BMI, body mass index. Thurtell et al: J Neuro-Ophthalmol 2011; 31: 316-319 317 Original Contribution Copyright © North American Neuro-Ophthalmology Society. Unauthorized reproduction of this article is prohibited. Polysomnography All patients had overnight laboratory-based video polysomnography, including electroencephalogram, electro-oculography, surface mentalis and anterior tibialis electro-myogram, electrocardiogram, respiratory airflow (measured by thermistor) and effort (measured by piezoelectric sensors), and oxyhemoglobin saturation. The presence of apneas and hypopneas was determined using conventional criteria (4). The polysomnographic technologists scoring the study and the board-certified sleep specialists who interpreted the studies were blinded to the results of the BQ. The apnea-hypopnea index (AHI) was then calculated as the average number of apneas and hypopneas per hour. OSA was diagnosed when the AHI was $5 (4). Data Analysis Univariate analyses were used to summarize the results. The sensitivity and specificity of the BQ for OSA were deter-mined by comparing the number of IIH patients with high-risk and low-risk BQ scores to the number with and without OSA, while the significance of the association between BQ score and OSA was determined using the Fisher exact test. RESULTS Patient Demographics Thirty newly diagnosed IIH patients were included. Twenty-four were women. The median age was 32 years (range, 16-54 years). Fifteen were whites, and 15 were blacks. The median BMI was 39.8 kg/m2 (range, 27.3-51.7 kg/m2). There was no difference in age, race, or BMI be-tween patients who underwent polysomnography and those who did not (P . 0.18). Berlin Questionnaire Scores Twenty of 30 patients (66.7%) had a high-risk score for OSA on the BQ, while 10 (33.3%) had a low-risk score (Table 1). Sixteen of 24 women (66.7%) and 4 of 6 men (66.7%) had a high-risk score. Eleven of 15 white patients (73.3%) and 9 of 15 black patients (60%) had a high-risk score. Of 30 patients, 17 (56.7%) had a positive score in category 1 of the BQ, 17 (56.7%) had a positive score in category 2, and 28 (93.3%) had a positive score in category 3, in most cases because their BMI was .30 kg/m2. Snoring could not be determined in 3 patients (10%), as they did not have a bed partner who could corroborate their per-ceived absence of snoring. Polysomnography Results Eighteen of 30 patients (60%) had OSA (Table 1), with 7 (23.3%) having mild, 4 (13.3%) having moderate, and 7 (23.3%) having severe OSA. Fourteen of 24 women (58.3%) and 4 of 6 men (66.7%) had OSA. Ten of 15 white patients (66.7%) and 8 of 15 black patients (53.3%) had OSA. Berlin Questionnaire Sensitivity and Specificity Fifteen of 20 patients (75%) with a high-risk BQ score had polysomnographically verified OSA, whereas 7 of 10 (70%) with a low-risk BQ score did not have OSA (Table 1). The sensitivity of the BQ for OSA in IIH patients was 83.3%, the specificity was 58.3%, the positive predictive value was 75%, and the negative predictive value was 70% (Fisher test, P = 0.045). DISCUSSION Overnight laboratory-based polysomnography is the gold standard test for diagnosing OSA (4), but given the expense, time requirement, and inconvenience of polysomnography for many patients, it would be preferable to first use a simple and sensitive screening test to determine an IIH patient's risk for OSA. The BQ can be completed in a few minutes and has been validated as a useful screening tool for iden-tifying persons in the community who are at high-risk for OSA (5). In a large study, 744 community-dwelling adults completed the BQ; similar numbers of men and women were studied, but most were middle-aged or older (48.9 6 17.5 years, mean 6 SD) (5). After completing the BQ, 100 of the participants underwent polysomnography. Fifty-nine of 69 participants (86%) with a high-risk score had OSA, and 7 of 31 (23%) with a low-risk score had OSA. Thus, the sensitivity and specificity of the BQ for identifying OSA were 86% and 77%, respectively (5). The BQ is not as predictive of OSA in specialized sleep clinics. Indeed, a lower threshold for performing diagnostic polysomnograms on a mixed patient population likely ac-counts for a lower sensitivity and specificity (68% and 49%, respectively) for identifying OSA in such clinics (10). In contrast to study and sleep clinic populations, IIH patients are typically young. Therefore, it was uncertain whether the BQ would reliably identify IIH patients with OSA (5,10). Because OSA may be associated with IIH (6,8,11,12), and OSA has been shown to increase cardiovascular morbidity and mortality (3), we felt compelled to evaluate all IIH patients for OSA with polysomnography until the BQ was validated in the IIH population. TABLE 1. Contingency table of OSA determined by polysomnography (AHI $ 5) vs BQ score BQ OSA Present Absent High risk 15 5 Low risk 3 7 Fisher test: P = 0.045. OSA, obstructive sleep apnea; AHI, apnea-hypoxia index. 318 Thurtell et al: J Neuro-Ophthalmol 2011; 31: 316-319 Original Contribution Copyright © North American Neuro-Ophthalmology Society. Unauthorized reproduction of this article is prohibited. We routinely administered the BQ and obtained di-agnostic polysomnography on newly diagnosed IIH patients and found 83% sensitivity, 58% specificity, and 75% positive predictive value of the BQ for identifying OSA in IIH patients. The frequency of snoring might have been underestimated by the BQ, as several patients lacked a family member or bed partner to confirm the question-naire responses. Nonetheless, our findings demonstrate that the sensitivity of the BQ in IIH patients is comparable to that observed in older individuals in the general community. It is important to note that this study was not designed to evaluate for an association between OSA and IIH. Although the majority of our patients had OSA by polysomnography, comparison with age-, sex-, race-, and BMI-matched con-trols is required to determine if there is any evidence of an association between IIH and OSA. Our study has several limitations. First, it was retro-spective rather than prospective. Yet, all patients were evaluated in a standardized fashion, which should have substantially reduced the biases usually associated with retrospective studies. Second, not all of our IIH patients underwent polysomnography. 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