Prevalence of mycoplasma pneumoniae from symptomatic pediatric patients referred to a child outpatient clinic of a university hospital Bir üniversite hastanesinde çocuk sağlığı ve hastalıkları kliniklerine başvuran hastalarda mycoplasma pneumoniae sıklığının araştırılması


KÖKSAL M. O., KABA Ö., BEKA H., ÖNEL M., KARA E. M., HANÇERLİ TÖRÜN S., ...Daha Fazla

Cocuk Enfeksiyon Dergisi, cilt.15, sa.1, 2021 (ESCI) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 15 Sayı: 1
  • Basım Tarihi: 2021
  • Doi Numarası: 10.5578/ced.20219918
  • Dergi Adı: Cocuk Enfeksiyon Dergisi
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, CINAHL, EMBASE, TR DİZİN (ULAKBİM)
  • Anahtar Kelimeler: Respiratory tract infection, Mycoplasma pneumoniae, ELISA, RT-PCR, COMMUNITY-ACQUIRED PNEUMONIA, INFECTIONS, PCR, EPIDEMIOLOGY, DIAGNOSIS
  • İstanbul Üniversitesi Adresli: Evet

Özet

Objective: Lower respiratory tract infections are one of the major causes of morbidity and mortality in children worldwide. Besides, epidemiolog-ical data on this subject is very limited. Mycoplasma pneumoniae is an important bacterial agent in community-acquired pneumonia (CAP) and may cause mild, moderate and severe lower respiratory tract infections. Clinical diagnosis is very difficult. Material and Methods: In this study, it was aimed to determine the se-roprevalence of M. pneumoniae in children aged 0-17 years admitted to a medical faculty in Istanbul with lower respiratory tract complaints or non-respiratory findings such as cytopenia and arthritis/arthralgia and to determine the prevalence of infection among children in various age groups. One hundred and thirty-four patients were included in the pres-ent study. Venous blood and nasopharyngeal swab samples were taken from study patients. M. pneumoniae IgG and IgM antibodies were deter-mined by ELISA (Enzyme Liquid Immunoassay) test in blood samples and M. pneumoniae Real-time polymerase chain reaction (RT-PCR) test was performed in nasopharengeal swab samples. Results: Seropositivity was seen in 50 (37.3%) patients, only specific IgM antibody positivity in 5 (3.7%) patients, both specific IgM antibody and specific IgG antibody positivity in 8 (6%) patients and 37 (27.6%) patients specific IgG antibody was also observed. The number of M. pneumoni-ae DNA RT-PCR positive samples was shown to be only 2 (1.5%), both of which were not serologically positive. Conclusion: Our results show a significant prevalence of M. pneumoniae in children diagnosed with acute respiratory infection. It also highlight the importance of laboratory detection for appropriate and rapid antibiotic treatment.