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Fırat Tıp Dergisi
2022, Cilt 27, Sayı 4, Sayfa(lar) 262-268
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Fungal Pneumonia in Febrile Neutropenia; Clinical and Microbiological Properties
Zehra Gül DUMAN1, Behice KURTARAN2, Filiz KİBAR3, Süheyla KÖMÜR2, Oya BAYDAR TOPRAK4, Ferit KUŞÇU2, Yusuf Kemal ARSLAN5, Ayşe SEZA İNAL2, Ezgi ÖZYILMAZ4, Aslıhan CANDEVİR1, Emel GÜRKAN6, Yeşim TAŞOVA2
1Dışkapı Yıldırım Beyazıt Eğitim ve Araştırma Hastanesi, Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Kliniği, Ankara, Türkiye
2Çukurova Üniversitesi Tıp Fakültesi, Enfeksiyon Hastalıkları ve Klinik Mikrobiyoloji Anabilim Dalı, Adana, Türkiye
3Çukurova Üniversitesi Tıp Fakültesi, Mikrobiyoloji Anabilim Dalı, Adana, Türkiye
4Çukurova Üniversitesi Tıp Fakültesi, Göğüs Hastalıkları Anabilim Dalı, Adana, Türkiye
5Erzincan Binali Yıldırım Üniversitesi Tıp Fakültesi, Biyoistatistik ve Tıbbi Bilişim Anabilim Dalı, Erzincan, Türkiye
6Çukurova Üniversitesi Tıp Fakültesi, Hematoloji Anabilim Dalı, Adana, Türkiye

Objective: Lung infections are an important cause of morbidity and mortality in neutropenic patients. It was aimed to determine the fungal agents, clinical and microbiological characteristics of lung infections in febrile neutropenic patients.

Material and Method: Febrile neutropenic patients whose fever did not regress despite broad-spectrum antibacterial therapy and who were suspected of invasive fungal infection were evaluated. Those with newly developed infiltration on posterior anterior chest radiography or newly developed nodule, ʺhalo signʺ, consolidation, ʺreverse halo signʺ, cavitation, and air-crescent sign on thorax computer tomography were included in the study. Microscopic examination, bacterial and fungal culture cultivation, galactomannan antigen, Aspergillus fumigatus and Pneumocystis jirovecii polymerase chain reaction test were performed on the collected serum and bronchoalveolar lavage samples.

Results: Two patients were classified as definite, 32 patients as probable, 12 patients as suspected invasive fungal infection and 27 patients as non-invasive fungal infection. The sensitivity and specificity of the GM antigen test in serum were found as 74,4% and 100% respectively. In BAL, the sensitivity and specificity were found to be 66,7%, 71,4%, 47,6%, and 100%, respectively, with cut-off values of 0,5 and 1. The sensitivity and specificity of the LightMix A. fumigatus PCR test in serum were calculated as 67,9% and 5,9%, and the sensitivity and specificity in BAL were calculated as 81% and 14,3%, respectively.

Conclusion: In the diagnosis of IFI, LightMix A. fumigatus PCR test may be more helpful in BAL than in serum. Bronchoalveolar lavage GM is more valuable in diagnosis in patients using antifungal treatments/prophylaxis.


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