Kaye Alan D, Shah Shivam S, LaHaye Leon, Hennagin John A, Ardoin Anna K, Dubuisson Alexandra, Ahmadzadeh Shahab, Shekoohi Sahar
Departments of Anesthesiology and Pharmacology, Toxicology and Neurosciences, Louisiana State University Health Sciences Center Shreveport, Shreveport, LA 71103, USA.
School of Medicine, Louisiana State University Health Sciences Center at Shreveport, Shreveport, LA 71103, USA.
Toxics. 2025 May 9;13(5):382. doi: 10.3390/toxics13050382.
Nitrofurantoin, a commonly prescribed antibiotic for urinary tract infections, has been associated with rare but potentially serious pulmonary toxicity, which can present in acute, subacute, or chronic forms. Acute toxicity typically manifests in the form of hypersensitivity pneumonitis, which is characterized by fever, dyspnea, and eosinophilia, often resolving rapidly after drug discontinuation. However, chronic toxicity can lead to interstitial lung disease with progressive fibrosis, causing significant and sometimes irreversible pulmonary impairment. The pathophysiology of nitrofurantoin-induced lung injury is thought to involve oxidative stress, immune-mediated mechanisms, and direct cytotoxic effects; however, the exact pathways remain incompletely understood. Clinical diagnosis is challenging due to nonspecific symptoms that often resemble other respiratory conditions, leading to delays in recognition and treatment. Radiographic findings vary, with acute cases showing diffuse ground-glass opacities, while chronic cases may demonstrate reticular interstitial changes and fibrosis. The discontinuation of nitrofurantoin is the primary intervention, but corticosteroids may be beneficial, particularly in chronic cases with persistent inflammation or fibrosis, though their efficacy remains uncertain. Given the risk of long-term respiratory complications, heightened awareness among healthcare providers is essential for early diagnosis and intervention. Future research is needed to better define risk factors, improve diagnostic criteria, and explore alternative treatment strategies that mitigate the potential for pulmonary toxicity while maintaining effective antimicrobial therapy. This review explores the pathophysiology, clinical presentation, diagnostic challenges, and management strategies for nitrofurantoin-induced pulmonary toxicity.
呋喃妥因是一种常用于治疗尿路感染的抗生素,它与罕见但可能严重的肺部毒性有关,这种毒性可表现为急性、亚急性或慢性形式。急性毒性通常表现为过敏性肺炎,其特征为发热、呼吸困难和嗜酸性粒细胞增多,停药后通常迅速缓解。然而,慢性毒性可导致伴有进行性纤维化的间质性肺病,造成严重且有时不可逆的肺损伤。呋喃妥因所致肺损伤的病理生理学被认为涉及氧化应激、免疫介导机制和直接细胞毒性作用;然而,确切途径仍未完全明确。由于非特异性症状常与其他呼吸道疾病相似,临床诊断具有挑战性,导致识别和治疗延迟。影像学表现各异,急性病例表现为弥漫性磨玻璃影,而慢性病例可能显示网状间质改变和纤维化。停用呋喃妥因是主要干预措施,但皮质类固醇可能有益,特别是在伴有持续炎症或纤维化的慢性病例中,尽管其疗效仍不确定。鉴于长期呼吸并发症的风险,医护人员提高认识对于早期诊断和干预至关重要。需要进一步研究以更好地确定危险因素、改进诊断标准,并探索替代治疗策略,在维持有效抗菌治疗的同时减轻肺部毒性的可能性。本综述探讨了呋喃妥因所致肺部毒性的病理生理学、临床表现、诊断挑战和管理策略。