<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov:80/entrez/query/static/PubMed.dtd">
<ArticleSet>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>How I changed my practice in the last five years and what is likely to change in the next five years</ArticleTitle>
		<FirstPage>1</FirstPage>
		<LastPage>2</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>W.J.</FirstName>
				<LastName>Fokkens</LastName>
			<Affiliation>Department of Otolaryngology, Academic Medical Center, Amsterdam, The Netherlands</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1306</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin53E1</ArticleId>
		</ArticleIdList>
		<Abstract>
	    The fast development of our field in the last decades has had significant impact on the way we practice our profession. This year my editorials will focus on the impact of these develop- ments on my own daily practice.
When I started in otorhinolaryngology functional endoscopic sinus surgery was the new kid on the Block. We learned to operate as functional as possible. The primary goal of FESS was to restore normal ventilation and remove irreversibly changed mucosa. The concept was that by restoring proper ventilation the sinus would heal itself. In the past decades, we have more and more discovered that CRS and especially CRS with nasal polyps is a mucosal disease that needs intensive medical treat- ment if necessary combined with ESS. The concept of FESS has moved from improving ventilation to opening up sinus for local medical treatment. Local medical treatment has been shown to be more effective when it is able to enter the sinus. Although we do not have all data available yet, rinsing with saline in which local corticosteroids have been dissolved seems to be more effective than using nasal drops and certainly more effective than nasal spray. 
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Efficacy and side effects of antibiotics in the treatment of acute rhinosinusitis: a systematic review</ArticleTitle>
		<FirstPage>3</FirstPage>
		<LastPage>9</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>WJ</FirstName>
				<LastName>Sng</LastName>
			<Affiliation>House Officer, Yong Loo Lin School of Medicine, National University of Singapore, Singapore</Affiliation>
			</Author>
			<Author>
				<FirstName>DY</FirstName>
				<LastName>Wang</LastName>
			<Affiliation>Department of Otolaryngology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1281</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin13.225</ArticleId>
		</ArticleIdList>
		<Abstract>
	    BACKGROUND: Acute rhinosinusitis (ARS) is one of the most common diagnoses for which an antibiotic is prescribed. Although the usage of antibiotics in the treatment of mild, moderate or uncomplicated ARS is not recommended by most international guideli- nes, overuse of antibiotics is still an alarming problem among patients and healthcare practitioners. We thus sought to review the evidence available through a systematic review of the existing literature on antibiotic usage in ARS.
METHODOLOGY: A search of the PubMed database was conducted for studies on antibiotic and placebo usage in the treatment of ARS.
RESULTS: A total of 31 random control trials (RCT) reporting the clinical efficacy of treating ARS and side effects of using cefuroxime axetil, telithromycin, amoxicillin/potassium clavulanate, levofloxacin, moxifloxacin and clarithromycin were included in the review. Among them, 9 studies were performed double-blinded with placebo controls. The results showed that while antibiotics are more efficacious than placebos in the treatment of ARS, the risks of potential side effects need to be weighed against the potential be- nefit that antibiotics give to the patient. This is especially pertinent as usage of the placebo has shown to be almost as efficacious as using the antibiotic therapy, and also much safer.
CONCLUSION: The usage of antibiotics in ARS is widespread and there seems to be only slight added benefit in the usage of antibi- otics over placebo in the treatment of ARS. Hence, larger scale studies should be done in the future to confirm the results of these studies.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Does time to endoscopic sinus surgery impact outcomes in Chronic Rhinosinusitis? Prospective findings from the National Comparative Audit of Surgery for Nasal Polyposis and Chronic Rhinosinusitis</ArticleTitle>
		<FirstPage>10</FirstPage>
		<LastPage>17</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>C.</FirstName>
				<LastName>Hopkins</LastName>
			<Affiliation>ENT Dept , Guy's and St Thomas' Hospitals, London, United Kingdom</Affiliation>
			</Author>
			<Author>
				<FirstName>J.</FirstName>
				<LastName>Rimmer</LastName>
			<Affiliation>Royal National Throat, Nose and Ear Hospital, London, United Kingdom</Affiliation>
			</Author>
			<Author>
				<FirstName>V.J.</FirstName>
				<LastName>Lund</LastName>
			<Affiliation>Royal National Throat, Nose and Ear Hospital, London, United Kingdom</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1251</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin13-217</ArticleId>
		</ArticleIdList>
		<Abstract>
	    OBJECTIVES: Patients with chronic rhinosinusitis refractory to medical management undergo elective surgery. The time from initial diagnosis to surgery varies considerably. The impact of this delay on surgical success has never previously been evaluated.
DESIGN: First-time patients within the National Comparative Audit of Surgery for Nasal Polyposis and Chronic Rhinosinusitis were grouped based on time to surgery: 1) Early cohort: < 12 months; 2) Mid cohort: 12-60 months; and 3) Late cohort: > 60 months. Co-morbidities and preoperative CT scores were analysed for all patients.
MAIN OUTCOME MEASURES: The 22-item Sino-Nasal Outcome Test scores (SNOT-22) were collected at 0, 3, 12 and 60-months. Absolute and relative SNOT-22 changes from baseline were evaluated.
RESULTS: Asthma and allergies were significantly more prevalent in the Late versus the Early and Mid-cohorts. In addition, patients in the Late cohort had greater symptom burden on the SNOT-22 and more extensive preoperative radiographic disease as determined by Lund-Mackay (LM) scores. SNOT-22 scores demonstrated greater percentage improvements in the Early versus the Mid- and Late cohorts, at all time points after surgery. At 12 and 60 months after surgery, significantly more patients in the Early group achieved a clinically important change in SNOT-22 scores compared with the other groups. These differences were maintained when cohorts were matched for preoperative co-morbidities.
CONCLUSION: Patients with asthma and/or allergies are more likely to experience delayed surgical intervention versus other patients. Overall, patients with delayed surgery reported less improvement in SNOT-22 scores than patients treated at earlier time points, regardless of co-morbid status. Delaying surgical intervention may worsen long term clinical outcomes.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Does time to endoscopic sinus surgery impact outcomes in chronic rhinosinusitis? Retrospective analysis using the UK clinical practice research data</ArticleTitle>
		<FirstPage>18</FirstPage>
		<LastPage>24</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>C.</FirstName>
				<LastName>Hopkins</LastName>
			<Affiliation>Guy s Hospital, ENT Department, London, UK</Affiliation>
			</Author>
			<Author>
				<FirstName>P.</FirstName>
				<LastName>Andrews</LastName>
			<Affiliation>Royal National Throat, Nose and Ear Hospital, London, UK</Affiliation>
			</Author>
			<Author>
				<FirstName>C.E.</FirstName>
				<LastName>Holy</LastName>
			<Affiliation>Acclarent Inc, Menlo Park, CA, USA</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1278</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin14.077</ArticleId>
		</ArticleIdList>
		<Abstract>
	    BACKGROUND: Patients with chronic rhinosinusitis (CRS) refractory to medical management may elect endoscopic sinus surgery (ESS). Recent data showed that clinical outcomes of patients treated earlier outperformed those of patients treated later in the disease continuum. In this study, CRS-related healthcare utilisation of patients treated early versus late was analysed using the UK-based Clinical Practice Research Database.
METHODS: Two cohorts ("Early Cohort": ESS within 12 months of first CRS diagnosis, versus "Late Cohort": &#8805; 5 years from diagnosis to ESS) were matched for age, gender, asthma, polyposis. Healthcare needs related to CRS were analysed post-operatively for 5 years.
RESULTS: Patients in the Late cohort used significantly more CRS-related care than patients in the Early cohort visits and 0.54 prescriptions per patient per year. A sub-analysis of patients with and without asthma indicated that patients in the Late cohort without asthma had healthcare needs equivalent to patients in the Early cohort with asthma.
CONCLUSION: Delayed surgical intervention for CRS is associated with greater post-operative healthcare needs than ESS within 12 months of first CRS diagnosis.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Heredity of nasal polyps</ArticleTitle>
		<FirstPage>25</FirstPage>
		<LastPage>28</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>A.</FirstName>
				<LastName>Bohman</LastName>
			<Affiliation>Department of Otorhinolaryngology, Uppsala University Hospital, Uppsala, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>M.</FirstName>
				<LastName>Oscarsson</LastName>
			<Affiliation>Department of Otorhinolaryngology, Hospital of Skaraborg, Skovde, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>K.</FirstName>
				<LastName>Holmberg</LastName>
			<Affiliation>Department of Otorhinolaryngology, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>L.</FirstName>
				<LastName>Johansson</LastName>
			<Affiliation>Department of Otorhinolaryngology, Hospital of Skaraborg, Skovde, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>E.</FirstName>
				<LastName>Millqvist</LastName>
			<Affiliation>Department of Internal Medicine/Respiratory Medicine and Allergology, The Sahlgrenska Academy at the University of  Gothenburg, Gothenburg, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>S.</FirstName>
				<LastName>Nasic</LastName>
			<Affiliation>Research and Development Centre, Hospital of Skaraborg, Skovde, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>A.</FirstName>
				<LastName>Torinsson-Naluai</LastName>
			<Affiliation>Department of Clinical Genetics, Institute of Biomedicine, The Sahlgrenska Academy at the University of Gothenburg,  Gothenburg, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>M.</FirstName>
				<LastName>Bende</LastName>
			<Affiliation>Department of Otorhinolaryngology, Hospital of Skaraborg, Skovde, Sweden</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1279</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin14.032</ArticleId>
		</ArticleIdList>
		<Abstract>
	    BACKGROUND: Nasal polyps is a common disease but little is known about its' pathogenesis. Our hypothesis was that there are genetic factors involved in the development of this disease. The aim of this study was to examine close relatives of patients with nasal polyps and comparing them with a general population with regard to prevalence of polyps.
METHODOLOGY: Patients with nasal polyps who attended the clinic were recruited to the study and were asked whether they had any close adult relatives (siblings, parents or children). We intended to recruit two relatives per patient, one of each gender, for nasal endoscopy. The prevalence of nasal polyps in these relatives was compared with the prevalence of nasal polyps in a general population.
RESULTS: During a 4-year period, 368 patients and 410 relatives were recruited to the study. Although we were unable to recruit two close relatives for every patient, we were able to calculate nasal polyp prevalence within families as being 19.2%. Compared with the prevalence of nasal polyps among individuals in a general Swedish population from the same geographical area, the relative risk for polyps among relatives was almost five times higher.
CONCLUSION: This study strongly indicates that heredity is a factor of importance for development of nasal polyps.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Olfactory cleft opacity and CT score are predictive factors of smell recovery after surgery in nasal polyposis</ArticleTitle>
		<FirstPage>29</FirstPage>
		<LastPage>34</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>C.</FirstName>
				<LastName>Vandenhende-Szymanski</LastName>
			<Affiliation>1 Department of Otorhinolaryngology and Head and Neck surgery, Huriez Hospital, University of Lille, France</Affiliation>
			</Author>
			<Author>
				<FirstName>B.</FirstName>
				<LastName>Hochet</LastName>
			<Affiliation>Department of Otorhinolaryngology and Head and Neck surgery, Huriez Hospital, University of Lille, France</Affiliation>
			</Author>
			<Author>
				<FirstName>D.</FirstName>
				<LastName>Chevalier</LastName>
			<Affiliation>Department of Otorhinolaryngology and Head and Neck surgery, Huriez Hospital, University of Lille, France</Affiliation>
			</Author>
			<Author>
				<FirstName>G.</FirstName>
				<LastName>Mortuaire</LastName>
			<Affiliation>Department of Otorhinolaryngology and Head and Neck surgery, Huriez Hospital, University of Lille, France</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1285</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin14.160</ArticleId>
		</ArticleIdList>
		<Abstract>
	    OBJECTIVES: To assess subjective improvement of olfactory function following endoscopic sinus surgery (ESS) in chronic rhinosinusitis associated with nasal polyps (CRSwNP) and to analyse factors of recovery with the European Test of Olfactory Capabilities (ETOC).
METHODS: We carried out a prospective study of 30 patients with CRSwNP from November 2011 to April 2013. The ETOC was filled the day before surgery and in the short term follow-up. Sixteen suprathreshold odorants with a detection task and a forced choice verbal identification task were tested.
RESULTS: The mean composite score (MCS) improved at 3 and 6 months. The preoperative MCS was correlated to the Lund-Mackay score and to the olfactory cleft opacification on preoperative computed tomography (CT) scan. Multivariate linear regression modelling of patients with preoperative anosmia showed that the olfactory recovery at 3 months was predicted by the preoperative Lund-Mackay score and the age, and at 6 months by the preoperative Lund-Mackay score.
CONCLUSION: With a convenient psychophysical test, we showed that olfactory cleft opacification and CT scan score could be predictive factors of olfaction disorder severity and improvement after ESS in CRSwNP. These results need to be strengthened in the long term with a larger panel of patients.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Treatment outcomes of midfacial segment pain: experience from the Liverpool multi-disciplinary team facial pain clinic</ArticleTitle>
		<FirstPage>35</FirstPage>
		<LastPage>40</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>S.C.</FirstName>
				<LastName>Leong</LastName>
			<Affiliation>Department of Otolaryngology - Head and Neck Surgery Royal Liverpool University Hospital, Liverpool, United Kingdom</Affiliation>
			</Author>
			<Author>
				<FirstName>L.</FirstName>
				<LastName>Lazarova</LastName>
			<Affiliation>Department of Otolaryngology - Head and Neck Surgery Royal Liverpool University Hospital, Liverpool, United Kingdom</Affiliation>
			</Author>
			<Author>
				<FirstName>H.K.</FirstName>
				<LastName>Tsang</LastName>
			<Affiliation>Department of Anesthesiology and Pain Management, Royal Liverpool University Hospital, Liverpool, United Kingdom</Affiliation>
			</Author>
			<Author>
				<FirstName>G.</FirstName>
				<LastName>Banhegyi</LastName>
			<Affiliation>Department of Otolaryngology - Head and Neck Surgery Royal Liverpool University Hospital, Liverpool, United Kingdom</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1291</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin14.156</ArticleId>
		</ArticleIdList>
		<Abstract>
	    OBJECTIVES: Midfacial segment pain (MSP) has the characteristics of tension-type headache which is confined to the midface cor- responding to the second division of the trigeminal nerve. This review presents treatment outcomes of MSP patients managed at the Multi-disciplinary Team (MDT) Facial Pain Clinic in Liverpool.
METHODOLOGY: Prospective clinical outcome performed in a tertiary referral centre for complex facial pain syndromes.
MAIN OUTCOME MEASURES: Sino-Nasal Outcome Test (SNOT). Clinical "success" was defined as an improvement in total SNOT score
of >9 points and a reduction of the ear-facial symptoms sub-domain score by &#8805;50% from baseline.
RESULTS: The average age of the cohort was 49 years, with an average follow-up of 12 months. The overall pre-treatment total SNOT-22 score was 59.5 which improved significantly to 42 at latest follow-up. Although the average scores of all sub-domains improved, only the ear-facial symptoms and psychological issues sub-domains achieved statistical significance. When the criterion for success was applied, nine patients fulfilled this definition at an average of 12 months follow-up. The baseline total SNOT score in this cohort improved from 60.6 to 19.7. Half of these patients achieved success within 18 months of commencing treatment and the probability of attaining success at long-term follow-up was high.
CONCLUSIONS: Treatment of midfacial segment facial pain is complex and requires follow-up to achieve any meaningful clinical outcome.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		<Replaces IdType="pubmed">25756077</Replaces>
		<ArticleTitle>A computational study of functional endoscopic sinus surgery and maxillary sinus drug delivery</ArticleTitle>
		<FirstPage>41</FirstPage>
		<LastPage>49</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>M.R.</FirstName>
				<LastName>Wofford</LastName>
			<Affiliation>Department of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, NC, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>J.S.</FirstName>
				<LastName>Kimbell</LastName>
			<Affiliation>Department of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, NC, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>D.O.</FirstName>
				<LastName>Frank-Ito</LastName>
			<Affiliation>Department of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, NC, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>V.</FirstName>
				<LastName>Dhandha</LastName>
			<Affiliation>Department of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, NC, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>K.A.</FirstName>
				<LastName>McKinney</LastName>
			<Affiliation>Department of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, NC, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>G.M.</FirstName>
				<LastName>Fleischman</LastName>
			<Affiliation>Department of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, NC, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>C.S.</FirstName>
				<LastName>Ebert, Jr.</LastName>
			<Affiliation>Department of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, NC, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>A.M.</FirstName>
				<LastName>Zanation</LastName>
			<Affiliation>Department of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, NC, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>B.A.</FirstName>
				<LastName>Senior</LastName>
			<Affiliation>Department of Otolaryngology/Head and Neck Surgery, University of North Carolina, Chapel Hill, NC, USA</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1302</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin13.065</ArticleId>
		</ArticleIdList>
		<Abstract>
	    BACKGROUND: Topical medication is increasingly used following functional endoscopic sinus surgery (FESS). Information on particle sizes that maximise maxillary sinus (MS) delivery is conflicting, and the effect of antrostomy size on delivery is unclear. The purpose of this study was to estimate antrostomy and particle size effects on topical MS drug delivery.
METHODOLOGY: Sinonasal reconstructions were created from a pre- and a post-FESS CT scan in each of four chronic rhinosinusitis patients. Additional models were created from each post-FESS reconstruction representing four alternative antrostomy sizes. Airflow and particle deposition were simulated in each reconstruction using computational fluid dynamics for nebulised and sprayed delivery.
RESULTS: MS ventilation and drug delivery increased following FESS, the largest virtual antrostomy led to greatest delivery, and MS delivery was sensitive to particle size. Particles within a 5-18 &#956;m and 5-20 &#956;m size range led to peak MS deposition for nebulised and sprayed particles, respectively. Post-FESS increases in drug delivery varied across individuals and within individuals by the type of antrostomy created.
CONCLUSION: Our findings suggest that FESS, particularly with larger antrostomies, improves topical drug delivery, and that certain particle sizes improve this delivery. Further research is needed to contextualise these findings with other post-surgical effects.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		<Replaces IdType="pubmed">25756078</Replaces>
		<ArticleTitle>Accuracy of a questionnaire for identifying respiratory allergies in epidemiological studies</ArticleTitle>
		<FirstPage>49</FirstPage>
		<LastPage>53</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>R.</FirstName>
				<LastName>Pedotti</LastName>
			<Affiliation>Neuroimmunology and Neuromuscular Disorders Unit, Foundation IRCCS Neurological Institute C. Besta, Milan, Italy</Affiliation>
			</Author>
			<Author>
				<FirstName>L.</FirstName>
				<LastName>Losappio</LastName>
			<Affiliation>Department of Allergology and Immunology, Niguarda Ca Granda Hospital, Milan, Italy</Affiliation>
			</Author>
			<Author>
				<FirstName>M.</FirstName>
				<LastName>Farinotti</LastName>
			<Affiliation>Neuroepidemiology Unit, Foundation IRCCS Neurological Institute C. Besta, Milan, Italy</Affiliation>
			</Author>
			<Author>
				<FirstName>D.</FirstName>
				<LastName>Preziosi</LastName>
			<Affiliation>Department of Allergology and Immunology, Niguarda Ca Granda Hospital, Milan, Italy</Affiliation>
			</Author>
			<Author>
				<FirstName>I.</FirstName>
				<LastName>Tramacere</LastName>
			<Affiliation>Neuroepidemiology Unit, Foundation IRCCS Neurological Institute C. Besta, Milan, Italy</Affiliation>
			</Author>
			<Author>
				<FirstName>C.</FirstName>
				<LastName>Stafylaraki</LastName>
			<Affiliation>Department of Allergology and Immunology, Niguarda Ca Granda Hospital, Milan, Italy</Affiliation>
			</Author>
			<Author>
				<FirstName>A.</FirstName>
				<LastName>Mascheri</LastName>
			<Affiliation>Department of Allergology and Immunology, Niguarda Ca Granda Hospital, Milan, Italy</Affiliation>
			</Author>
			<Author>
				<FirstName>G.</FirstName>
				<LastName>Filippini</LastName>
			<Affiliation>Neuroepidemiology Unit, Foundation IRCCS Neurological Institute C. Besta, Milan, Italy</Affiliation>
			</Author>
			<Author>
				<FirstName>E.A.</FirstName>
				<LastName>Pastorello</LastName>
			<Affiliation>Department of Allergology and Immunology, Niguarda Ca Granda Hospital, Milan, Italy</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1276</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin14.047</ArticleId>
		</ArticleIdList>
		<Abstract>
	    BACKGROUND: The assessment of allergic asthma (AA) and allergic rhinitis (AR) in epidemiological studies is often challenging. We performed a cross-sectional study to test the accuracy of a Questionnaire aimed at Identifying subjects with Respiratory Allergy (QIRA) in a simple and fast way.
METHODS: One hundred-thirty subjects, 18-76 years of age, admitted consecutively at the Allergy Center of the Niguarda Ca' Granda Hospital of Milan were included. The questionnaire (index test) investigated the presence of AA and AR with seven questions enquiring history of symptoms, diagnosis made by a doctor, allergy tests performed, and treatments. After completing the questionnaire, all subjects were subsequently diagnosed by an allergist (reference standard).
RESULTS: The accuracy of the questionnaire for the diagnosis of AA and AR was high (sensitivity 94.7% [95% confidence interval CI: 74.0-99.9] and specificity 99.1% [95% CI 95.1-100.0] for AA; sensitivity 82.8% [95% CI 71.3-91.1] and specificity 98.5% [95% CI 91.8-100.0] for AR).
CONCLUSION: The questionnaire significantly distinguished subjects with respiratory allergy from those without. The QIRA represents a valid and accurate tool for classifying subjects as having or not AA and/or AR in epidemiological studies.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Quality of life after septorhinoplasty measured with the Functional Rhinoplasty Outcome Inventory 17 (FROI-17)</ArticleTitle>
		<FirstPage>54</FirstPage>
		<LastPage>58</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>O.C.</FirstName>
				<LastName>Bulut</LastName>
			<Affiliation>Department of Otolaryngology, University of Heidelberg, Germany</Affiliation>
			</Author>
			<Author>
				<FirstName>F.</FirstName>
				<LastName>Wallner</LastName>
			<Affiliation>Department of Otolaryngology, University of Heidelberg, Germany</Affiliation>
			</Author>
			<Author>
				<FirstName>P.K.</FirstName>
				<LastName>Plinkert</LastName>
			<Affiliation>Department of Otolaryngology, University of Heidelberg, Germany</Affiliation>
			</Author>
			<Author>
				<FirstName>S.</FirstName>
				<LastName>Prochnow</LastName>
			<Affiliation>Department of Otolaryngology, University of Heidelberg, Germany</Affiliation>
			</Author>
			<Author>
				<FirstName>C.</FirstName>
				<LastName>Kuhnt</LastName>
			<Affiliation>Department of Otolaryngology, University of Heidelberg, Germany</Affiliation>
			</Author>
			<Author>
				<FirstName>I.</FirstName>
				<LastName>Baumann</LastName>
			<Affiliation>Department of Otolaryngology, University of Heidelberg, Germany</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1290</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin14.008</ArticleId>
		</ArticleIdList>
		<Abstract>
	    BACKGROUND: Quality of life measurements in septorhinoplasty patients so far have taken place only to a small extent. The aim of the present study was a prospective measurement of disease-specific quality of life with a newly developed and validated instrument, the Functional Rhinoplasty Outcome Inventory 17 (FROI-17).
METHODS: The patients completed the FROI-17 and the Rhinoplasty Outcome Evaluation (ROE) as disease-specific instruments preoperatively as well as 12 months postoperatively. As a general instrument, the Short Form 36 Health Survey (SF-36) was used. Furthermore, additional general questions were answered at both time points. 
RESULTS: Out of the 103 patients, 69 patients (32 men, 37 women) responded after 12 months (response rate 67%). Thirteen patients (18%) were not satisfied with the result of surgery. However, all scales of FROI-17 and also ROE showed a significant postoperative improvement of subjective assessments by the patients. In the SF-36, this was true in 2 out of 8 scales (mental health and role-functioning physical). Furthermore, we found significant correlations between the FROI-17 and the SF-36 scales but not between the ROE and the SF-36 scales.
CONCLUSION: The disease-specific quality of life was significantly improved by septorhinoplasty. FROI-17 scales detect more functional aspects compared with the ROE thus establishing significant correlations with general quality of life measured by SF-36. The application of both FROI-17 and ROE in future clinical trials in septorhinoplasty patients is recommended. 
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Septoplasty with concomitant inferior turbinate reduction reduces the need for revision procedure</ArticleTitle>
		<FirstPage>59</FirstPage>
		<LastPage>65</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>T.R.</FirstName>
				<LastName>Karlsson</LastName>
			<Affiliation>Sahlgrenska University Hospital, Gothenburg, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>M.</FirstName>
				<LastName>Shakeel</LastName>
			<Affiliation>Department of Otolaryngology - Head and Neck Surgery, University of Aberdeen, Aberdeen Royal Infirmary Aberdeen, Scotland, United Kingdom</Affiliation>
			</Author>
			<Author>
				<FirstName>M.</FirstName>
				<LastName>Supriya</LastName>
			<Affiliation>Department of Otolaryngology - Head and Neck Surgery, University of Aberdeen, Aberdeen Royal Infirmary Aberdeen, Scotland, United Kingdom</Affiliation>
			</Author>
			<Author>
				<FirstName>B.</FirstName>
				<LastName>Ram</LastName>
			<Affiliation>Department of Otolaryngology - Head and Neck Surgery, University of Aberdeen, Aberdeen Royal Infirmary Aberdeen, Scotland, United Kingdom</Affiliation>
			</Author>
			<Author>
				<FirstName>K.W.</FirstName>
				<LastName>Ah-See</LastName>
			<Affiliation>Department of Otolaryngology - Head and Neck Surgery, University of Aberdeen, Aberdeen Royal Infirmary Aberdeen, Scotland, United Kingdom</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1272</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin12.059</ArticleId>
		</ArticleIdList>
		<Abstract>
	    OBJECTIVE: Septoplasty is an accepted and common surgical intervention to improve the nasal airway. However, the role of concomitant surgery on the inferior turbinate remains debated. This study aims to investigate if the inferior turbinate surgery at the time of septoplasty would impact on the likelihood of revision nasal surgery - septoplasty or septorhinoplasty.
STUDY DESIGN: Retrospective review of consecutive patients undergoing septoplasty with or without inferior turbinate reduction over 12 years (1998 - 2010) at Aberdeen Royal Infirmary.
METHODS: Patients were identified from the theatre log books and were excluded if they underwent any other nasal procedure. Data collected include demographics, type of primary surgery, and grade of surgeon along with revision nasal surgery in this cohort.
RESULTS: 2168 eligible patients with a mean age of 39 years were investigated. Two groups were identified: Group A, with 788 patients who underwent septoplasty only, and Group B, in which 1380 patients underwent septoplasty with concomitant inferior turbinate reduction. The majority of operations were performed by the surgeons in training. The incidence of revision surgery was 5.1 % (21 revision septoplasties and 19 corrective septorhinoplasties) in Group A compared to 2.2 % (20 revision septoplasties and 10 corrective septorhinoplasties) in Group B. 
CONCLUSION: Based on this study, it would appear that concomitant inferior turbinate reduction may decrease the likelihood of revision nasal surgery. 
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Comparison of acoustic rhinometry and nasal inspiratory peak flow as objective tools for nasal obstruction assessment in patients with chronic rhinosinusitis</ArticleTitle>
		<FirstPage>66</FirstPage>
		<LastPage>74</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>E.K.</FirstName>
				<LastName>Proimos</LastName>
			<Affiliation>ENT Department, Chania General Hospital, Chania, Crete, Greece</Affiliation>
			</Author>
			<Author>
				<FirstName>D.E.</FirstName>
				<LastName>Kiagiadaki</LastName>
			<Affiliation>ENT Department, Chania General Hospital, Chania, Crete, Greece</Affiliation>
			</Author>
			<Author>
				<FirstName>T.S.</FirstName>
				<LastName>Chimona</LastName>
			<Affiliation>ENT Department, Chania General Hospital, Chania, Crete, Greece</Affiliation>
			</Author>
			<Author>
				<FirstName>F.G.</FirstName>
				<LastName>Seferlis</LastName>
			<Affiliation>ENT Department, Chania General Hospital, Chania, Crete, Greece</Affiliation>
			</Author>
			<Author>
				<FirstName>N.J.</FirstName>
				<LastName>Maroudias</LastName>
			<Affiliation>ENT Department, New Ionian General Hospital, Athens, Greece</Affiliation>
			</Author>
			<Author>
				<FirstName>C.E.</FirstName>
				<LastName>Papadakis</LastName>
			<Affiliation>ENT Department, Chania General Hospital, Chania, Crete, Greece</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1271</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin13.203</ArticleId>
		</ArticleIdList>
		<Abstract>
	    BACKGROUND: Chronic rhinosinusitis (CRS) is a disease with increasing incidence, characterized by persistent symptoms and negative impact on patient's quality of life. Nasal inspiratory peak flow (NIPF) and acoustic rhinometry (AR) were studied and compared as assessment tools for CRS with or without nasal polyps (NP), as well as, in follow up monitoring of conservative medical treatment.
OBJECTIVES: Seventy-eight patients were prospectively studied. Objective assessment included NIPF and AR at baseline and at 4 and 8 weeks after onset medical treatment. Measurements were studied in correlation with Sinonasal Outcome Test-22 (SNOT-22) questionnaire, Visual Analogue Scale (VAS) and endoscopic appearance score (EAS).
RESULTS: Both NIPF and AR improved significantly, after medical treatment. NIPF score reflected CRS symptoms' improvement according to SNOT-22 total score at the end of treatment protocol, showing moderate to strong correlation with nasal obstruction VAS grading during the treatment period. AR measures were associated with EAS in all sets of examinations and correlated moderately with VAS scoring at 8 weeks. 
CONCLUSION: NIPF and AR were proven to be promising methods for objective evaluation and monitoring of nasal obstruction based on different aspects of nasal physiology in patients with CRS.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Sinonasal malignancies in Sweden 1960-2010; a nationwide study of the Swedish population</ArticleTitle>
		<FirstPage>75</FirstPage>
		<LastPage>80</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>A.</FirstName>
				<LastName>Elliot</LastName>
			<Affiliation>Department of Oto-Rhino-Laryngology, Head and Neck Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>M.</FirstName>
				<LastName>Jangard</LastName>
			<Affiliation>Department of Oto-Rhino-Laryngology, Head and Neck Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>L.</FirstName>
				<LastName>Marklund</LastName>
			<Affiliation>Department of Oto-Rhino-Laryngology, Head and Neck Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>N.</FirstName>
				<LastName>Hakansson</LastName>
			<Affiliation>Institute of Environmental Medicine Karolinska Institutet, Stockholm, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>P.</FirstName>
				<LastName>Dickman</LastName>
			<Affiliation>Institute of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>L.</FirstName>
				<LastName>Hammarstedt-Nordenvall</LastName>
			<Affiliation>Department of Oto-Rhino-Laryngology, Head and Neck Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>P.</FirstName>
				<LastName>Stjarne</LastName>
			<Affiliation>Department of Oto-Rhino-Laryngology, Head and Neck Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1282</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin14.070</ArticleId>
		</ArticleIdList>
		<Abstract>
	    INTRODUCTION: Sinonasal malignancies (SNM) are rare and the prognosis is generally poor. Recently, a change in incidence for SNM has been reported. In this study, we investigated population-based trends for SNM in Sweden.
METHODS: We identified 3,221 patients from the Swedish National Cancer Registry diagnosed with primary malignancies arising from the nasal cavity, paranasal sinuses, or both, during the period 1960 through 2010. Incidence, gender and age, anatomical sites and relative survival were investigated.
RESULTS: The incidence for SNM decreased except for sinonasal malignant melanoma (SNMM) and adenoid cystic cancer (even though a very small group) during the study period. More than 50 % of the malignancies involved the nasal cavity. The five-year relative survival was highest for adenoid cystic cancer followed by adenocarcinoma. SNMM and undifferentiated carcinoma had the poorest prognosis.
CONCLUSION: We found that the incidence for SNM has decreased during the study period 1960 through 2010, except for SNMM that has increased.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>The natural history of community-acquired common colds symptoms assessed over 4-years</ArticleTitle>
		<FirstPage>81</FirstPage>
		<LastPage>88</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>T.J.</FirstName>
				<LastName>Witek</LastName>
			<Affiliation>Healthcare Innovation and Technology Laboratory at Columbia University in The City of New York, NY 10032 USA </Affiliation>
			</Author>
			<Author>
				<FirstName>D.L.</FirstName>
				<LastName>Ramsey</LastName>
			<Affiliation>Procter and Gamble, Personal Health Care Division, Mason, OH 45040, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>A.N.</FirstName>
				<LastName>Carr</LastName>
			<Affiliation>Procter and Gamble, Personal Health Care Division, Mason, OH 45040, USA</Affiliation>
			</Author>
			<Author>
				<FirstName>D.K.</FirstName>
				<LastName>Riker</LastName>
			<Affiliation>On Point Advisors, LLC, PO Box 5450, Chattanooga, TN  37406, USA</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1280</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin14.149</ArticleId>
		</ArticleIdList>
		<Abstract>
	    BACKGROUND: The common cold is the most frequently experienced infection among humans, but limited data exist to characterize the onset, duration, severity and intersection of symptoms in community-acquired colds.  A more complete understanding of the symptom frequency and burden in naturally occurring colds is needed.
METHODOLOGY: We characterized common cold symptoms from 226 cold episodes experienced by 104 male or female subjects.  Subjects were enrolled in the work environment in an attempt to start symptom evaluation (frequency and severity) at the earliest sign of their cold.  We also assessed the symptom that had the greatest impact on the subject by asking them to identify their single most bothersome symptom.
RESULTS: Symptom reporting started within 24 hours of cold onset for most subjects.  Sore throat was a harbinger of the illness but was accompanied by multiple symptoms, including nasal congestion, runny nose and headache.  Cough was not usually the most frequent symptom, but was present throughout the cold, becoming most bothersome later in the cold. Nasal congestion, pain (eg, sore throat, headache, muscle pains) or feverishness and secretory symptoms (eg, runny nose, sneezing), and even cough, were simultaneously experienced with high incidence over the first 4 days of illness.  The single most bothersome symptom was sore throat on day 1, followed by nasal congestion on days 2-5 and cough on days 6 and 7.
CONCLUSION: There is substantial overlap in the appearance of common cold symptoms over the first several days of the common cold.  Nasal congestion, secretory and pain symptoms frequently occur together, with cough being somewhat less prominent, but quite bothersome when present.  These data establish the typical symptomatology of a common cold and provide a foundation for the rational treatment of cold symptoms typically experienced by cold sufferers.
		</Abstract>
	</Article>
	<Article>
		<Journal>
			<PublisherName>International Rhinologic Society</PublisherName>
			<JournalTitle>Rhinology</JournalTitle>
			<Issn>0300-0729</Issn>
			<Volume>53</Volume>
			<Issue>1</Issue>
			<PubDate PubStatus="ppublish">
				<Year>2015</Year>
				<Month>3</Month>
				<Day>1</Day>
			</PubDate>
		</Journal>
		
		<ArticleTitle>Even cognitively well-functioning adults are unaware of their olfactory dysfunction: Implications for ENT clinicians and researchers</ArticleTitle>
		<FirstPage>89</FirstPage>
		<LastPage>94</LastPage>
		<Language>EN</Language>
		<AuthorList>
			<Author>
				<FirstName>E.</FirstName>
				<LastName>Wehling</LastName>
			<Affiliation>Department of Biological and Medical Psychology, University of Bergen, Norway</Affiliation>
			</Author>
			<Author>
				<FirstName>A.J.</FirstName>
				<LastName>Lundervold</LastName>
			<Affiliation>Department of Biological and Medical Psychology, University of Bergen, Norway</Affiliation>
			</Author>
			<Author>
				<FirstName>T.</FirstName>
				<LastName>Espeset</LastName>
			<Affiliation>Department of Psychology, University of Oslo, Norway</Affiliation>
			</Author>
			<Author>
				<FirstName>I.</FirstName>
				<LastName>Reinvang</LastName>
			<Affiliation>Department of Psychology, University of Oslo, Norway</Affiliation>
			</Author>
			<Author>
				<FirstName>A.</FirstName>
				<LastName>Bramerson</LastName>
			<Affiliation>Department of Otorhinolaryngology, Central Hospital, Skovde, Sweden</Affiliation>
			</Author>
			<Author>
				<FirstName>S.</FirstName>
				<LastName>Nordin</LastName>
			<Affiliation>Department of Psychology, Umea University, Sweden</Affiliation>
			</Author>
		</AuthorList>
		<ArticleIdList>
			<ArticleId IdType="pii">1300</ArticleId>
			<ArticleId IdType="doi">10.4193/Rhin14.081</ArticleId>
		</ArticleIdList>
		<Abstract>
	    BACKGROUND: Past findings of an impact of cognitive impairment on awareness of olfactory dysfunction, and high prevalence of age-associated cognitive impairment motivated the present study of whether middle-aged and elderly adults are unaware of an olfactory dysfunction despite being carefully screened for cognitive impairment.
METHODOLOGY: The sample included 203 Norwegian participants, aged 46-79 years, 134 women and 69 men, who underwent comprehensive neuropsychological assessment for screening of cognitive impairment. Subjective assessment of olfactory function ("How would you estimate your sense of smell?") was compared with outcome on objective assessment of olfactory function with the Scandinavian Odor Identification Test, which in the present study was shown to be valid for use on Norwegian populations.
RESULTS: We found that 79% of this cognitively healthy sample with objectively assessed olfactory dysfunction reported normal olfactory function (57% of functionally anosmics reported normal function). In contrast, only 9% with objectively assessed normal olfactory function reported olfactory dysfunction.
CONCLUSION: A large proportion of cognitively well-functioning middle-aged and elderly adults with an olfactory dysfunction are unaware of their dysfunction. The ENT physician who suspects that the sense of smell may be compromised should, in addition to an anamnesis, assess the patient's olfactory function objectively.
		</Abstract>
	</Article>
</ArticleSet>