{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:48:52Z","timestamp":1787017732513,"version":"build-2736575974"},"reference-count":40,"publisher":"Wiley","license":[{"start":{"date-parts":[[2015,1,1]],"date-time":"2015-01-01T00:00:00Z","timestamp":1420070400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/3.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Case Reports in Infectious Diseases"],"published-print":{"date-parts":[[2015]]},"abstract":"<jats:p>\n                    <jats:italic>Introduction. P. aeruginosa<\/jats:italic>\n                    is the primary cause for pulmonary destruction and premature death in cystic fibrosis (CF). Therefore, prevention of airway colonization with the pathogen, ubiquitously present in water, is essential. Infection of CF patients with\n                    <jats:italic>P. aeruginosa<\/jats:italic>\n                    after dentist treatment was proven and dental unit waterlines were identified as source, suggesting prophylactic measures. For their almost regular sinonasal involvement, CF patients often require otorhinolaryngological (ORL) attendance. Despite some fields around ORL-procedures with comparable risk for acquisition of\n                    <jats:italic>P. aeruginosa<\/jats:italic>\n                    , such CF cases have not yet been reported. We present four CF patients, who primarily acquired\n                    <jats:italic>P. aeruginosa<\/jats:italic>\n                    around ORL surgery, and one around dentist treatment. Additionally, we discuss risks and preventive strategies for CF patients undergoing ORL-treatment. Perils include contact to pathogen-carriers in waiting rooms, instrumentation, suction, drilling, and flushing fluid, when droplets containing pathogens can be nebulized. Postsurgery mucosal damage and debridement impair sinonasal mucociliary clearance, facilitating pathogen proliferation and infestation. Therefore, sinonasal surgery and dentist treatment of CF patients without chronic\n                    <jats:italic>P. aeruginosa<\/jats:italic>\n                    colonization must be linked to repeated microbiological assessment. Further studies must elaborate whether all CF patients undergoing ORL-surgery require antipseudomonal prophylaxis, including nasal lavages containing antibiotics. Altogether, this underestimated risk requires structured prevention protocols.\n                  <\/jats:p>","DOI":"10.1155\/2015\/438517","type":"journal-article","created":{"date-parts":[[2015,3,18]],"date-time":"2015-03-18T18:07:08Z","timestamp":1426702028000},"page":"1-9","source":"Crossref","is-referenced-by-count":7,"title":["<i>Pseudomonas aeruginosa<\/i>\n                    Acquisition in Cystic Fibrosis Patients in Context of Otorhinolaryngological Surgery or Dentist Attendance: Case Series and Discussion of Preventive Concepts"],"prefix":"10.1155","volume":"2015","author":[{"given":"Jochen G.","family":"Mainz","sequence":"first","affiliation":[{"name":"Cystic Fibrosis Center, Pediatric Pneumology, Jena University Hospital, 07740 Jena, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrea","family":"Gerber","sequence":"additional","affiliation":[{"name":"Cystic Fibrosis Center, Pediatric Pneumology, Jena University Hospital, 07740 Jena, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael","family":"Lorenz","sequence":"additional","affiliation":[{"name":"Cystic Fibrosis Center, Pediatric Pneumology, Jena University Hospital, 07740 Jena, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ruth","family":"Michl","sequence":"additional","affiliation":[{"name":"Cystic Fibrosis Center, Pediatric Pneumology, Jena University Hospital, 07740 Jena, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Julia","family":"Hentschel","sequence":"additional","affiliation":[{"name":"Cystic Fibrosis Center, Pediatric Pneumology, Jena University Hospital, 07740 Jena, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anika","family":"Nader","sequence":"additional","affiliation":[{"name":"Cystic Fibrosis Center, Pediatric Pneumology, Jena University Hospital, 07740 Jena, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James 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