Suh Jeffrey D, Cohen Noam A, Palmer James N
Division of Rhinology, Department of ORL:HNS, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Curr Opin Otolaryngol Head Neck Surg. 2010 Feb;18(1):27-31. doi: 10.1097/MOO.0b013e328334f670.
Rhinosinusitis is one of the most common medical complaints in the United States, affecting up to 16% of the population. It is associated with over 13 million physician visits per year and an estimated aggregated cost of over $6 billion annually. Patients with chronic rhinosinusitis (CRS) demonstrate worse quality-of-life scores than those suffering from chronic obstructive pulmonary disease, congestive heart failure, back pain, or angina. Despite the large societal impact and economic burden, the pathophysiology of CRS remains largely unsolved. One possible mechanism for the chronic nature of this disease is the involvement of bacterial biofilms, which represent a phenotypic change in bacteria that make them resistant to conventional treatment strategies. We will discuss these changes as well as emerging treatment options.
New research involving topical antimicrobials, surfactants, loop diuretics, and macrolide antibiotics can be used as adjuvant therapies to treat biofilm-associated CRS. All have shown some promise in laboratory or small patient studies, but all need further evaluation
Bacterial biofilms are highly organized structures composed of communities of bacteria encased within a protective extracellular matrix. If bacterial biofilms are the cause of certain cases of CRS, then the treatment paradigms will have to be changed. Novel nonantimicrobial therapies may have clinical applications to prevent and destabilize biofilms. We believe that ultimately methods to reduce sinonasal inflammation and protect cilia will be the first step in blocking the attachment and aggregation of bacteria that would otherwise start biofilm formation. Once more is known about the role of biofilms in CRS, new therapies will undoubtedly play a greater role and change our treatment paradigms.
鼻窦炎是美国最常见的医疗问题之一,影响着高达16%的人口。每年因鼻窦炎就诊的人数超过1300万,估计每年总花费超过60亿美元。慢性鼻窦炎(CRS)患者的生活质量评分比慢性阻塞性肺疾病、充血性心力衰竭、背痛或心绞痛患者更差。尽管鼻窦炎对社会有巨大影响且经济负担沉重,但其病理生理学仍 largely未解决。这种疾病慢性化的一种可能机制是细菌生物膜的参与,细菌生物膜代表了细菌的一种表型变化,使其对传统治疗策略产生抗性。我们将讨论这些变化以及新出现的治疗选择。
涉及局部抗菌药物、表面活性剂、襻利尿剂和大环内酯类抗生素的新研究可作为辅助疗法用于治疗与生物膜相关的CRS。所有这些在实验室或小型患者研究中都显示出了一些前景,但都需要进一步评估。
细菌生物膜是由包裹在保护性细胞外基质中的细菌群落组成的高度有组织的结构。如果细菌生物膜是某些CRS病例的病因,那么治疗模式将不得不改变。新型非抗菌疗法可能具有预防和破坏生物膜的临床应用。我们认为最终减少鼻窦炎症和保护纤毛的方法将是阻止细菌附着和聚集的第一步,否则这些细菌会开始形成生物膜。一旦对生物膜在CRS中的作用有了更多了解,新疗法无疑将发挥更大作用并改变我们的治疗模式。