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社区获得性肺炎概述。预后与临床特征。

Overview of community-acquired pneumonia. Prognosis and clinical features.

作者信息

Campbell G D

机构信息

Department of Medicine, Louisiana State University Medical Center, Shreveport.

出版信息

Med Clin North Am. 1994 Sep;78(5):1035-48. doi: 10.1016/s0025-7125(16)30118-3.

Abstract

Despite the introduction of newer antibiotics, vaccinations, and better supportive care, CAP remains a common, frequently fatal disease. Age and coexisting illness influence which infectious agents are most likely to cause infection. Severity of illness and clinical features are influenced by various host factors and by the virulence of the infectious agent. Mortality and morbidity are reduced by the rapid institution of appropriate antimicrobial therapy. Because of the limitations of presently available diagnostic tests, many patients are begun on empiric regimens, and in up to half of these individuals, a cause is not identified. Although there are a number of potential pathogens, it is possible to identify likely pathogens based on easily identifiable clinical factors (age, presence of coexisting disease, severity of illness at presentation, and the need for hospitalization). Using this approach, CAP in immunocompetent adults may be divided into four categories. Once empiric therapy has been initiated, therapy should be continued for at least 72 hours unless clinical deterioration is noted. Within 4 days, fever and leukocytosis should return to baseline, but abnormal physical findings (i.e., crackles) require longer to resolve, especially with coexisting illness, and chest radiographic findings are the last to return to baseline and are especially delayed if the patient is bacteremic or has structural lung disease. Not all patients respond to initial empiric therapy. Reasons for this include antimicrobial resistance, the presence of nonbacterial pathogens (respiratory viruses), unusual bacterial pathogens, noninfectious causes that may mimic CAP, infectious complications (i.e., empyema), and pneumonia occurring in patients with unrecognized severe immunosuppression. Failure to improve after 72 hours and development of deterioration are indications for repeat diagnostic workup and consideration of alternative diagnoses. More invasive diagnostic tests are appropriate in severely ill patients and in those whose condition is deteriorating rapidly.

摘要

尽管引入了更新的抗生素、疫苗接种以及更好的支持治疗,但社区获得性肺炎(CAP)仍然是一种常见且往往致命的疾病。年龄和并存疾病会影响哪些感染因子最有可能导致感染。疾病的严重程度和临床特征受多种宿主因素以及感染因子毒力的影响。通过迅速开始适当的抗菌治疗可降低死亡率和发病率。由于目前可用诊断测试存在局限性,许多患者开始接受经验性治疗方案,其中多达一半的患者病因无法确定。虽然有多种潜在病原体,但根据易于识别的临床因素(年龄、并存疾病的存在、就诊时疾病的严重程度以及住院需求),有可能识别出可能的病原体。采用这种方法,免疫功能正常的成年人的CAP可分为四类。一旦开始经验性治疗,除非出现临床恶化情况,治疗应持续至少72小时。在4天内,发热和白细胞增多应恢复至基线水平,但异常的体格检查结果(即啰音)需要更长时间才能消退,尤其是伴有并存疾病时,而胸部X线检查结果是最后恢复至基线水平的,并且如果患者有菌血症或存在结构性肺病,恢复会特别延迟。并非所有患者对初始经验性治疗都有反应。其原因包括抗菌药物耐药性、非细菌性病原体(呼吸道病毒)的存在、不常见的细菌病原体、可能模拟CAP的非感染性病因、感染性并发症(即脓胸)以及在未被识别的严重免疫抑制患者中发生的肺炎。72小时后病情未改善以及病情恶化是重复进行诊断检查和考虑其他诊断的指征。对于重症患者以及病情迅速恶化的患者,更具侵入性的诊断测试是合适的。

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