Dergiler / Ege Tıp Dergisi / 2006 / Cilt: 45 - Sayı: 1

Mikoplazma pnömonisi tanısı alan 21 olgunun klinik, radyolojik ve fizik muayene bulguları yönünden değerlendirilmesi

Laboratory findings, physical and clinical features of Mycoplasma pneumoniae infections. Analysis of 21 cases

Sayfa
63–67
Yayın Tarihi
2022-10-17
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Early identification of the pathogen and treatment improves the outcome of the pneumonia and reduces the associated mortality and morbidity.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Background: Mycoplasma pneumoniae (M. pneumoniae) is a well known causative agent of infection in childhood but clinical presentation may be variable.
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Temel Bulgular & Veri:In this study we aimed to evaluate laboratory findings, physical and clinical features of pneumonia due to M. pneumonia in 21 children retrospectively.
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Sonuç & Katkı:Early identification of the pathogen and treatment improves the outcome of the pneumonia and reduces the associated mortality and morbidity.
🔬Tür:Araştırma Makalesi
📍Kapsam:2004 Verileri
⚙️Değişkenler:Alan Parametreleri

Özet

Background: Mycoplasma pneumoniae (M. pneumoniae) is a well known causative agent of infection in childhood but clinical presentation may be variable. In this study we aimed to evaluate laboratory findings, physical and clinical features of pneumonia due to M. pneumonia in 21 children retrospectively. Methods: Clinical data of 21 children with pneumonia due to M. pneumoniae who were hospitalized in our institution from 1998 through 2004, were collected from the medical records and entered into a database. M. pneumoniae was diagnosed with antibody immünofluorescent assay (IFA) test system in 21 patients. In all patients, the diagnosis of active infection relied on the presence of Ig M antibodies. Results: Patients with M. pneumoniae infection included 17 female and 4 male. Mean age of patients was 7.90 ± 3.30 years (range, 2-16 years). Most of our cases had bilateral lung involvement. Most frequent X-ray finding was perihilar linear opacities. No significant complication was observed during the therapy. Conclusions: Children with pneumonia needed admission to the hospital emphasizes the need for early identification. Routine laboratory studies are not likely to distinguish between low respiratory tract infections due to M. pneumoniae and to viruses. Early identification of the pathogen and treatment improves the outcome of the pneumonia and reduces the associated mortality and morbidity.

Abstract

Background: Mycoplasma pneumoniae (M. pneumoniae) is a well known causative agent of infection in childhood but clinical presentation may be variable. In this study we aimed to evaluate laboratory findings, physical and clinical features of pneumonia due to M. pneumonia in 21 children retrospectively. Methods: Clinical data of 21 children with pneumonia due to M. pneumoniae who were hospitalized in our institution from 1998 through 2004, were collected from the medical records and entered into a database. M. pneumoniae was diagnosed with antibody immünofluorescent assay (IFA) test system in 21 patients. In all patients, the diagnosis of active infection relied on the presence of Ig M antibodies. Results: Patients with M. pneumoniae infection included 17 female and 4 male. Mean age of patients was 7.90 ± 3.30 years (range, 2-16 years). Most of our cases had bilateral lung involvement. Most frequent X-ray finding was perihilar linear opacities. No significant complication was observed during the therapy. Conclusions: Children with pneumonia needed admission to the hospital emphasizes the need for early identification. Routine laboratory studies are not likely to distinguish between low respiratory tract infections due to M. pneumoniae and to viruses. Early identification of the pathogen and treatment improves the outcome of the pneumonia and reduces the associated mortality and morbidity.

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Bu Makaleye Atıf Yap

ÖZÇETİN, M., DEMİR, E., TANAÇ, R., ALTINÖZ, S., ZEYREK, D., ÇAĞLI, R., ALTUĞLU, İ., GÜLEN, F. (2022). Mikoplazma pnömonisi tanısı alan 21 olgunun klinik, radyolojik ve fizik muayene bulguları yönünden değerlendirilmesi. Ege Tıp Dergisi, Cilt: 45 - Sayı: 1, 63–67. https://ajindex.com/articles/496189

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Kaynakça (18)

  1. Waites KB, Talkington DF. Mycoplasma Pneumoniae And Its Role As A Human Pathogen. Clinical Microbiology Reviews 2004;17: 697-728
  2. Weiner LB, McMillan AJ. Mycoplasma pneumoniae: Long SS, Pickering LK, Prober CG, eds. Principles and practice of pediatric infectious disease. Second ed. Philadelphia: Churcil Livingstone; 2003: 1005-08
  3. Mansel JK, Rosenow III EC, Smith TF, Martin JW Jr. Mycoplasma pneumoniae pneumonia. Chest 1989; 95: 639-46
  4. Silva LC, Mutti A, Moreira JS, Porto NS. Pneumonia por Mycoplasma pneumoniae. Rev AMRIGS 1996; 30:191-8
  5. Lichenstein R. Pediatric pneumonia. Emerg Med Clin North Am 2003; 21: 437-51
  6. Dominguez A, Minguell S, Torres J, Serrano A, Vidal J, Salleras L. Community outbreak of acute respiratory infection by Mycoplasma pneomoniae. Eur J Epidemiol 1996; 12: 131-34
  7. Feikin DR, Moroney JF, Talkington DF, et al. An outbreak of acute respiratory disease caused by Mycoplasma pneumoniae and adenovirus at federal service training academy: new implications from an old scenario. Clin Infect Dis 1999; 29: 1545-50
  8. Centers for Disease Control and Prevention. Outbreak of community-acquired pneumonia caused by Mycoplasma pneumoniae-Colorado, 2000. JAMA 2001; 285: 2073-74
  9. Broughton RA. Infections due to Mycoplasma pneumoniae. Pediatr Infect Dis 1986; 5: 71-85
  10. Weiser OL, Higaki HH, Nolte LB. Mycoplasma pneumoniae. Complement-fixing antibody titers at birth. Am J Clin Pathol 1967;47: 641-42
  11. Luby JP. Pneumonia caused by Mycoplasma pneumoniae infection. Clin Chest Med 1991; 12: 237-44
  12. Barker CE, Sillis M, Wreghitt TG. Evaluation of Serodia Myco II particle agglutinationtest for detecting Mycoplasma pneumoniae antibody comparison with mu-capture ELISA and indirect immunofluorescence. J Clin Pathol 1990; 43: 163-65
  13. Stevens D, Swift PGF, Johnston PGB, et al. Mycoplasma pneumoniae infections in children. Arch Dis Child 1978; 53: 38
  14. Narita M, Matsuzono Y, Itakura O, et al. Analysis of mycoplasmal pleural effusion by the polymerase chain reaction. Arch Dis Child 1998; 78: 67
  15. Clyde WA Jr, Denny FW. Mycoplasma infections in childhood. Pediatrics 1967; 40: 669
  16. Niitu Y. M neumoniae respiratory disease: Clinical features-children. Yale J Biol Med 1983; 56: 493
  17. Guckel C, Benz-Bohm G, Widemann B. Mycoplasmal pneumonias in childhood: Roentgen features, differential diagnosis and review of literature. Pediatr Radiol 1989; 19: 499
  18. Esposito S, Blasi F, Bellini F, Allegra L, Principi N. the Mow