
Dr Kieu Thi Phuong Nhan
Dean of the Medicine Faculty, Buon Ma Thuot Medical University;
Head of the Internal Medicine Department, Buon Ma Thuot Medical University Hospital, Vietnam.
The American Thoracic Society (ATS) has recently updated its guidelines for community-acquired pneumonia (CAP). These updates were prompted by recent advances in evidence, clinical experiences and emerging technologies that have reshaped the approach to the diagnosis and management of CAP.1
In this interview, Dr Kieu Thi Phuong Nhan from Buon Ma Thuot Medical University Hospital discussed how the new 2025 ATS guidelines for CAP have influenced the diagnosis and management of CAP in Vietnam.
Q1: The recently published 2025 ATS guidelines for CAP now recommend lung ultrasound (LUS) as an alternative to chest radiography for the diagnosis of CAP.1 What are the opportunities and challenges of implementing the use of LUS in Vietnam?
There is a strong potential for implementing the use of LUS in Vietnam2:
While implementing LUS in Vietnam offers significant opportunities, it also presents notable challenges3:
Q2: As CAP can be caused by a variety of aetiologies (e.g., bacterial, viral and fungal pathogens), how do you decide on a recommended course of action in your clinical practice? When do you consider antibiotics (e.g., quinolones), and what guides that decision?
In clinical practice, identifying the causative agent of pneumonia can sometimes be challenging, especially at the initial stage when microbiological test results cannot be performed or results are not yet available. We need to rely on a clinical examination and some paraclinical tests that can suggest the pathogen, such as blood count, C-reactive protein, procalcitonin, and imaging from a chest X-ray, pleural ultrasound, or occasionally computed tomography scan.4,5
The empiric diagnosis of bacterial agents causing pneumonia is based on6,7: (1) the severity of the pneumonia; and (2) the patient’s background, including their age, lifestyle habits and comorbidities (pulmonary and systemic). The selection of an antibiotic should be based on the causative pathogen and the antimicrobial spectrum of various antibiotics, which then guides the empiric antibiotic regimen. Since bacterial pathogens of CAP often coexist with viruses, and there are currently no rapid and accurate tests to determine if the cause is solely viral. It is crucial to start an empiric antibiotic regimen early whenever a bacterial or co-bacterial/viral cause is suspected.8
Common bacterial pathogens causing CAP include Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and intracellular bacteria, with Streptococcus pneumoniae being the most common cause.9 Accordingly, the three most common antibiotic classes used to treat CAP are β-lactams, macrolides, and fluoroquinolones.7
Respiratory fluoroquinolones (e.g., levofloxacin and moxifloxacin) have a broad antimicrobial spectrum that covers both S. pneumoniae and atypical bacteria.10 However, this class of antibiotics should be reserved for the later line and not be a first-line choice for outpatients without comorbidities, those who do not have risk factors for drug-resistant S. pneumoniae infection, or those who have not recently used antibiotics, in order to reduce the risk of antibiotic resistance.1
Q3: Given the new guideline recommendation to limit antibiotic treatment for clinically stable outpatients with CAP to 5 days or shorter, have you observed any differences in patient recovery or relapse risk between shorter versus longer antibiotic courses?
The recommendation to limit antibiotic treatment for clinically stable outpatients with CAP to 5 days or shorter is based on numerous randomised controlled trials and meta-analyses.1 The overwhelming conclusion from this evidence is that shorter courses of antibiotics are non-inferior to longer courses for the majority of patients with uncomplicated CAP.1 For stable outpatients with CAP, using antibiotics for 5 days or less has shown comparable effectiveness to longer courses.1
In reality, many outpatients with CAP in Vietnam are prescribed a 7- to 10-day course of antibiotics. However, most patients stop taking the medication after 3 to 5 days when they feel better or have fully recovered. Shorter treatment durations do not appear to increase the likelihood of infection recurrence. While shorter treatment durations offer greater convenience for outpatients, improve adherence, and may provide effective treatment outcomes, it is important to note that prematurely discontinuing antibiotics before completing the prescribed course may contribute to antimicrobial resistance.11,12
Q4: The updated guidelines recommend against prescribing corticosteroids for hospitalised patients with non-severe CAP.1 Based on your clinical experience, are quinolones alone sufficient for this patient population? When do you consider prescribing corticosteroids, and what guides your decision?
In most cases, quinolones (or other appropriate antibiotic regimens) are sufficient for hospitalised patients with non-severe CAP. The core principle of treating non-severe CAP is to use effective antimicrobial therapy to eliminate the bacterial pathogen. Due to their broad-spectrum coverage, quinolones can be used as a monotherapy.8
Based on the evidence that guides the new recommendations, corticosteroids are not for routine use in non-severe CAP.1 Instead, their use is limited to a specific subset of patients where the potential benefits outweigh significant risks.1 The decision to prescribe corticosteroids is guided by the severity of the illness and the presence of a dysregulated, hyper-inflammatory response.1
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