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2024, Cilt 54, Sayı 1, Sayfa(lar) 040-048
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The Association of Prolonged Cough in Adults with Bordetella pertussis Infection: A Cross-Sectional Assessment Using Culture, PCR, and Serological Methods
Pınar Yürük Atasoy1, Cumhur Artuk2, Cemile Sönmez3, Selin Nar Ötgün4, Meral Turan5, Selçuk Kılıç6
1Ankara Bilkent Şehir Hastanesi, Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji, Ankara, Türkiye
2Sağlık Bilimleri Üniversitesi, Gülhane Eğitim ve Araştırma Hastanesi, Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji, Ankara, Türkiye
3Sağlık Bakanlığı, Halk Sağlığı Genel Müdürlüğü Mikrobiyoloji Referans Laboratuvarları ve Biyolojik Ürünler Daire Başkanlığı, Aşı ile Önlenebilir Bakteriyel Hastalıklar Seroloji Laboratuvarı, Ankara, Türkiye
4Sağlık Bakanlığı, Halk Sağlığı Genel Müdürlüğü Mikrobiyoloji Referans Laboratuvarları ve Biyolojik Ürünler Daire Başkanlığı, Ulusal Solunum Yolu Patojenleri Referans Laboratuvarı, Ankara, Türkiye 5Sağlık Bakanlığı, Halk Sağlığı Genel Müdürlüğü Mikrobiyoloji Referans Laboratuvarları ve Biyolojik Ürünler Daire Başkanlığı, Ulusal Yüksek Riskli Patojenler Referans Laboratuvarı, Ankara, Türkiye
6Sağlık Bilimleri Üniversitesi, Savunma Sağlık Bilimleri Enstitüsü, Tıbbi, Kimyasal, Biyolojik, Radyolojik ve Nükleer Savunma Anabilim Dalı, Ankara, Türkiye
Keywords: Bordetella pertussis, Polymerase Chain Reaction (PCR), Serology

Objective: Pertussis is a contagious respiratory tract infection caused by Bordetella pertussis that can affect all age groups despite widespread vaccination. The aim of this study was to evaluate the complaints of prolonged cough due to B. pertussis infection in individuals aged 18 years and older using culture, polymerase chain reaction (PCR) and serologic tests.

Methods: This study was conducted at a tertiary hospital in Ankara, focusing on individuals aged ≥ 18 years who reported coughing symptoms lasting for two weeks or longer. The study included 68 adults with coughing symptoms persisting for more than two weeks and 65 control individuals without coughing symptoms. Nasopharyngeal swab samples collected from the participants were used for culture and PCR. Additionally, sera derived from the blood samples of patients were evaluated using serological tests to ascertain the presence of antibodies against B. pertussis.

Results: Detection of B. pertussis in culture was not possible. However, 22% of the patients tested positive for PCR, and 13% were found to have positive Anti- Pertussis Toxin IgG levels. The average age of the patients with positive diagnostic test results was 38.5, while the average age was determined as 36.8.

Conclusion: Although the culture method is considered the gold standard for the diagnosis of pertussis, PCR was found to be more sensitive than culture in the present study. Pertussis should be considered in the differential diagnosis of prolonged cough symptoms in adults. Furthermore, there is a need to raise awareness regarding pertussis and conduct broader studies.


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