Clinical characteristics of Chlamydia psittaci pneumonia: a single-center, retrospective study over 5 years
- PMID: 40819069
- PMCID: PMC12358061
- DOI: 10.1186/s12879-025-11450-z
Clinical characteristics of Chlamydia psittaci pneumonia: a single-center, retrospective study over 5 years
Abstract
Background: Psittacosis pneumonia is not uncommon, and it can progress to severe illness or even death. Identifying the clinical characteristics of Chlamydia psittaci (C. psittaci ) pneumonia and its risk factors were the aim of improving decision-making regarding diagnosis and treatment.
Methods: According to the guidelines for CAP, 59 patients with C. psittaci pneumonia were divided into a non-severe pneumonia group and a severe pneumonia group, and their clinical characteristics and the differences were analyzed and compared.
Results: The incidence of consciousness disorders is higher(P = 0.020), and the time from onset to diagnosis is longer (8 days vs. 14 days, P = 0.002), it is more prone to myocardial injury, kidney injury, hypoalbuminemia, coagulation abnormalities, and venous thrombosis (P < 0.05) in the severe group, while fatigue is more common in the non-severe group (P = 0.022). On laboratory indicators, the severe pneumonia group had a significantly longer prothrombin time (P = 0.007), higher WBC and neutrophil percentages and lower lymphocyte count and percentages, higher lactate dehydrogenase and D-dimer values (all P < 0.001). After adjustment for sex and age, logistic regression analysis identified myocardial injury as an independent risk factor for severe C. psittaci pneumonia (OR, 124.3, [95%CI, 4.25 ~ 3633.24]; P = 0.005).
Conclusions: Impaired consciousness indicates severe illness and myocardial injury is an independent risk factor for severe C. psittaci pneumonia.
Keywords: Chlamydia psittaci; Community-acquired; Outcome; Pneumonia; Risk.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: This study was conducted in accordance with the ethical principles of the Declaration of Helsinki. Its was approved by the Ethics Committee of the First Affiliated Hospital of University of Science and Technology of China (No.2025-RE-097) and all methods were carried out in accordance with relevant guidelines and regulations. Confidentiality of the information related to study participates was assured during and after the data collection, and informed consent was waived by Ethics committee of the First Affiliated Hospital of University of Science and Technology of China because of its retrospective characterization. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests. Clinical trial number: Not applicable.
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