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P-2300. Invasive Pulmonary Aspergillosis-Mimicking Pseudomonas aeruginosa Pneumonia in Immunocompromised Patients

医学 铜绿假单胞菌 肺炎 微生物学 曲菌病 曲霉 肺曲菌病 病原生物 内科学 免疫学 细菌 生物 遗传学
作者
Choseok Yoon,Euijin Chang,Seongman Bae,Jiwon Jung,Min Jae Kim,Yong Pil Chong,Sang-Oh Lee,Sang‐Ho Choi,Yang Soo Kim,Sung‐Han Kim
出处
期刊:Open Forum Infectious Diseases [Oxford University Press]
卷期号:12 (Supplement_1)
标识
DOI:10.1093/ofid/ofae631.2453
摘要

Abstract Background Pseudomonas aeruginosa (PA) pneumonia is occasionally misdiagnosed as invasive pulmonary aspergillosis (IPA) in immunocompromised patients, especially transplant recipients or those with hematologic malignancy who have risk factors for IPA. However, there are limited data on this area. We thus investigated the clinical features and CT findings of PA pneumonia in immunocompromised patients. Methods All immunocompromised patients who were diagnosed as PA pneumonia was retrospectively reviewed in a tertiary hospital between 2017 and 2023. PA pneumonia was classified as follows; “confirmed”: positive culture from sterile tissues (blood, tissue, etc.) with radiologic compatible findings with pneumonia, “probable”: i) abnormalities on chest X-ray, ii) culture growth from non-sterile sources such as sputum or bronchoalveolar lavage fluid, iii) improvement with the use of anti-pseudomonal antibiotics without the use of antifungal agents, and “possible”: cases that do not meet the above criteria but cannot rule out PA pneumonia. Results Of 16 immunocompromised with PA pneumonia, 13 (81%) were male, and 9 (56%) were transplant recipients. Of these 16 patients, 9 (56%) were classified as “confirmed”, 5 (31%) “probable”, and the remaining 2 (13%) “possible”. 7 (44%) patients with PA pneumonia had concurrent IPA, with 1 proven IPA and 6 probable IPA. The remaining 9 patients with PA pneumonia alone revealed macronodules (n=5), mass-like consolidation (n=6), cavitary lesions (n=6), and halo sign (n=4) in initial CT findings. Of the 16 patients with PA pneumonia, 4 (25%) received inappropriate antifungal therapy. Conclusion About half of immunocompromised patients with PA pneumonia had concurrent IPA, but about one quarter of immunocompromised patients with PA pneumonia received inappropriate antifungal therapy. Disclosures All Authors: No reported disclosures
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