Use of the SNOT-22 and UPSIT to Appropriately Select Pediatric Patients With Cystic Fibrosis Who Should Be Referred to an Otolaryngologist Cross-sectional Study

被引:29
作者
Thamboo, Andrew [1 ]
Santos, Rachelle C. Dar [1 ]
Naidoo, Lalenthra [1 ]
Rahmanian, Ronak [1 ]
Chilvers, Mark A. [2 ]
Chadha, Neil K. [1 ]
机构
[1] BC Childrens Hosp, Div Pediat Otolaryngol Head & Neck Surg, Vancouver, BC V6H 3V4, Canada
[2] BC Childrens Hosp, Div Respirol, Vancouver, BC V6H 3V4, Canada
关键词
SMELL IDENTIFICATION TEST; QUALITY-OF-LIFE; CLINICAL CHARACTERISTICS; CHRONIC SINUSITIS; NASAL POLYPOSIS; GENOTYPE ANALYSIS; CHILDREN; DISEASE;
D O I
10.1001/jamaoto.2014.1650
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
IMPORTANCE Sinonasal disease and, specifically, nasal polyps, occur frequently in children with cystic fibrosis (CF). As survival rates have improved, it has become imperative that otolaryngologists become involved in the care of patients with CF to provide appropriate medical and surgical interventions for sinonasal disease. Despite significant variability in the subjective reporting of clinical symptoms, previous work has suggested there may be a relationship between clinical indicators and sinonasal disease in this population. OBJECTIVE To determine whether the 22-item Sino-Nasal Outcome Test (SNOT-22), the University of Pennsylvania Smell Identification Test (UPSIT), and other measures of sinonasal disease could be used to predict the presence of subclinical nasal polyps in children with CF. DESIGN, SETTING, AND PARTICIPANTS This was a cross-sectional study performed from May 2012 through April 2013 at a cystic fibrosis clinic at BC Children's Hospital in Vancouver, British Columbia, Canada. There were 72 eligible children with CF for this study (with a confirmed diagnosis of CF based on genetic testing; their ages ranged from 6 to 18 years, and they were not actively being treated by an otolaryngologist). Thirty-seven of these patients (23 males, 14 females) consented to participate in this study. Twenty-three declined participation, and 12 could not be contacted. MAIN OUTCOMES AND MEASURES Potential clinical predictors for the presence of subclinical nasal polyps were determined a priori. All 37 recruited participants completed a full study assessment. Nasal endoscopy (the gold standard) was performed to determine the presence of nasal polyps. Potential predictors that were assessed included age, sex, genotype, pancreatic function, SNOT-22 and UPSIT scores, oral culture swab result, and severity of forced expiratory volume in 1 second (FEV1). RESULTS A SNOT-22 score of greater than 11 was the only statistically significant predictor of nasal polyps (P = .04). The positive predictive value was 68.1%, the negative predictive value was 66.7%, and the positive likelihood ratio was 1.82. CONCLUSIONS AND RELEVANCE Given that the SNOT-22 is easy to administer and inexpensive, this sinus disease-specific questionnaire seems to be an appropriate tool for routine use by respirologists when assessing patients with CF to help predict subclinical nasal polyps.
引用
收藏
页码:934 / 939
页数:6
相关论文
共 23 条
[1]   CYSTIC-FIBROSIS - AN OTOLARYNGOLOGIC PERSPECTIVE [J].
CEPERO, R ;
SMITH, RJH ;
CATLIN, FI ;
BRESSLER, KL ;
FURUTA, GT ;
SHANDERA, KC .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 1987, 97 (04) :356-360
[2]   Clinical characteristics and genotype analysis of patients with cystic fibrosis and nasal polyposis [J].
Cimmino, M ;
Cavaliere, M ;
Nardone, M ;
Plantulli, A ;
Orefice, A ;
Esposito, V ;
Raia, V .
CLINICAL OTOLARYNGOLOGY, 2003, 28 (02) :125-132
[3]  
Daele J. J., 1997, Acta Oto-Rhino-Laryngologica Belgica, V51, P285
[4]   DEVELOPMENT OF THE UNIVERSITY-OF-PENNSYLVANIA SMELL IDENTIFICATION TEST - A STANDARDIZED MICROENCAPSULATED TEST OF OLFACTORY FUNCTION [J].
DOTY, RL ;
SHAMAN, P ;
DANN, M .
PHYSIOLOGY & BEHAVIOR, 1984, 32 (03) :489-502
[5]   Adults with cystic fibrosis - responding to a new ageing population [J].
Edwards, Jill ;
Clarke, Amanda ;
Greenop, Daz .
CHRONIC ILLNESS, 2013, 9 (04) :312-319
[6]   The united allergic airway: Connections between allergic rhinitis, asthma, and chronic sinusitis [J].
Feng, Charles H. ;
Miller, Michaela D. ;
Simon, Ronald A. .
AMERICAN JOURNAL OF RHINOLOGY & ALLERGY, 2012, 26 (03) :187-190
[7]   Nasal polyposis and cystic fibrosis (CF): review of the literature [J].
Feuillet-Fieux, Marie-Noelle ;
Lenoir, Gerard ;
Sermet, Isabelle ;
Elie, Caroline ;
Djadi-Prat, Juliette ;
Ferrec, Magali ;
Magen, Maryse ;
Simon, Marie ;
Couloigner, Vincent ;
Manach, Yves ;
Lacour, Bernard ;
Bonnefont, Jean-Paul .
RHINOLOGY, 2011, 49 (03) :347-355
[8]   An assessment of sinus quality of life and pulmonary function in children with cystic fibrosis [J].
Friedman, Ellen M. ;
Stewart, Michael .
AMERICAN JOURNAL OF RHINOLOGY, 2006, 20 (06) :568-572
[9]   Patterns of sinusitis in cystic fibrosis [J].
Gentile, VG ;
Isaacson, G .
LARYNGOSCOPE, 1996, 106 (08) :1005-1009
[10]   Bacterial Pattern in Chronic Sinusitis and Cystic Fibrosis [J].
Godoy, Jose M. ;
Godoy, Andres N. ;
Ribalta, Gloria ;
Largo, Isabel .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2011, 145 (04) :673-676