Literature DB >> 16172900

[Routine otorhinolaryngological examination in patients with cystic fibrosis].

A Koitschev1, A Wolff, C Koitschev, S Preyer, R Ziebach, M Stern.   

Abstract

OBJECTIVES: Data on the prevalence of otorhinolaryngological (ORL) symptoms in patients with cystic fibrosis (CF) are limited. A standard annual examination would be useful for definition of risk factors and/or management alternatives for these symptoms. STUDY
DESIGN: Prospective observational study of an unselected group of CF patients. PATIENTS AND METHODS: Between 1997 and 2004, 123 CF patients were routinely examined. The examinations included nasal endoscopy and audiological evaluation.
RESULTS: All patients who were approached to take part in the study gave their consent and were extremely cooperative. In 40% of the patients nasal polyps were found endoscopically. In 22% rhinological surgery had already been performed. Of the 123 patients, 13 (12%) showed different grades of sensorineural hearing loss, and all of these patients had received aminoglycoside antibiotics.
CONCLUSIONS: CF patients demonstrate a high prevalence of ORL symptoms. Therefore, an annual standard examination would provide data for identifying potential risk factors and for optimizing the management of these symptoms in CF patients.

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Year:  2006        PMID: 16172900     DOI: 10.1007/s00106-005-1328-9

Source DB:  PubMed          Journal:  HNO        ISSN: 0017-6192            Impact factor:   1.284


  23 in total

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3.  Associations between clinical variables and quality of life in adults with cystic fibrosis.

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5.  Aminoglycoside induced ototoxicity in patients with cystic fibrosis.

Authors:  D Mulherin; J Fahy; W Grant; M Keogan; B Kavanagh; M FitzGerald
Journal:  Ir J Med Sci       Date:  1991-06       Impact factor: 1.568

6.  Treatment and prognosis of nasal polyps in cystic fibrosis.

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7.  Identification of the cystic fibrosis gene: chromosome walking and jumping.

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Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

8.  Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker.

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Journal:  Science       Date:  1985-11-29       Impact factor: 47.728

9.  Localization of cystic fibrosis locus to human chromosome 7cen-q22.

Authors:  B J Wainwright; P J Scambler; J Schmidtke; E A Watson; H Y Law; M Farrall; H J Cooke; H Eiberg; R Williamson
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Review 10.  Measures of health-related quality of life for adults with acute sinusitis. A systematic review.

Authors:  Jeffrey A Linder; Daniel E Singer; Melissa Ancker; Steven J Atlas
Journal:  J Gen Intern Med       Date:  2003-05       Impact factor: 5.128

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  5 in total

Review 1.  Pathogenesis and management of nasal polyposis in cystic fibrosis.

Authors:  Jochen G Mainz; Assen Koitschev
Journal:  Curr Allergy Asthma Rep       Date:  2012-04       Impact factor: 4.806

2.  [Atypical cystic fibrosis. First diagnosed by chronic rhinosinusitis].

Authors:  J G Mainz; S Dornaus; C Dopfer; J F Beck; A Müller
Journal:  HNO       Date:  2009-08       Impact factor: 1.284

Review 3.  [Rhinosinusitis in cystic fibrosis].

Authors:  J G Mainz; A Gerber; C Arnold; J Baumann; I Baumann; A Koitschev
Journal:  HNO       Date:  2015-11       Impact factor: 1.284

4.  Pseudomonas aeruginosa Acquisition in Cystic Fibrosis Patients in Context of Otorhinolaryngological Surgery or Dentist Attendance: Case Series and Discussion of Preventive Concepts.

Authors:  Jochen G Mainz; Andrea Gerber; Michael Lorenz; Ruth Michl; Julia Hentschel; Anika Nader; James F Beck; Mathias W Pletz; Andreas H Mueller
Journal:  Case Rep Infect Dis       Date:  2015-03-18

5.  IL-1β, IL-23, and TGF-β drive plasticity of human ILC2s towards IL-17-producing ILCs in nasal inflammation.

Authors:  Korneliusz Golebski; Xavier R Ros; Maho Nagasawa; Sophie van Tol; Balthasar A Heesters; Hajar Aglmous; Chantal M A Kradolfer; Medya M Shikhagaie; Sven Seys; P W Hellings; Cornelis M van Drunen; Wytske J Fokkens; Hergen Spits; Suzanne M Bal
Journal:  Nat Commun       Date:  2019-05-14       Impact factor: 14.919

  5 in total

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