Rolfe Robert, Steed Lisa L, Salgado Cassandra, Kilby J Michael
Internal Medicine Residency Training Program, The University of Alabama of Birmingham, Birmingham, Alabama.
Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina.
Am J Med Sci. 2016 Jul;352(1):53-62. doi: 10.1016/j.amjms.2016.03.003. Epub 2016 Mar 18.
Actinomyces, particularly Actinomyces israelii, may cause indolent, persistent infections or represent normal mucosal flora, leading to management dilemmas.
Prompted by a refractory Actinomyces meyeri infection complicating AIDS, clinical data for all Actinomyces isolates at our hospital laboratory since 1998 were analyzed.
A total of 140 cases had a positive result for Actinomyces cultures. Of 130 cases with adequate follow-up, 36 (28%) cases had end-organ or disseminated disease treated with prolonged antibiotics or surgery or both (Group 1). A. meyeri was more common than A. israelii (33% versus 8%; P < 0.05) in Group 1, particularly thoracic infections. Another 56 (43%) cases were considered local pathogens, treated with drainage only or short-course antibiotics (Group 2). Another 38 (29%) cases were deemed commensals (Group 3). Immunosuppression was less frequent in Group 1 versus Group 2 or 3 (P = 0.05) and human immunodeficiency virus or AIDS was uncommon. Foreign bodies or devices (Group 1 versus Group 2 or 3, P = 0.003) and alcoholism (Group 1 versus Group 2 or 3; P = 0.03) were associated with actinomycosis. Isolates from the central nervous system and musculoskeletal sites were more often treated as definitive disease; skin, abdominal or pelvic or single blood culture isolates were more likely commensals (all P < 0.05). Disease progression or recurrence did not occur in Groups 2 and 3, whereas Group 1 had complex and variable courses, including 2 deaths.
In the absence of disseminated or end-organ disease, avoiding prolonged therapy for Actinomyces isolates was not associated with adverse outcomes. Alcoholism or foreign bodies were associated with actinomycosis. A. meyeri may be a more common cause of actinomycosis than previously recognized.
放线菌,尤其是衣氏放线菌,可引起隐匿性、持续性感染,或作为正常黏膜菌群存在,从而导致治疗难题。
受1例并发艾滋病的耐甲氧西林放线菌难治性感染病例的启发,我们分析了自1998年以来本院实验室所有放线菌分离株的临床资料。
共有140例放线菌培养结果呈阳性。在130例有充分随访资料的病例中,36例(28%)出现终末器官或播散性疾病,接受了长期抗生素治疗或手术治疗或两者兼用(第1组)。在第1组中,迈氏放线菌比衣氏放线菌更常见(33%对8%;P<0.05),尤其是在肺部感染中。另外56例(43%)被视为局部病原体,仅接受引流或短期抗生素治疗(第2组)。另有38例(29%)被认为属于共生菌(第3组)。与第2组或第3组相比,第1组免疫抑制情况较少见(P=0.05),人类免疫缺陷病毒或艾滋病并不常见。异物或器械(第1组与第2组或第3组相比,P=0.003)和酗酒(第1组与第2组或第3组相比;P=0.03)与放线菌病有关。来自中枢神经系统和肌肉骨骼部位的分离株更常被视为确诊疾病;皮肤、腹部或盆腔分离株或单次血培养分离株更可能是共生菌(所有P<0.05)。第2组和第3组未出现疾病进展或复发,而第1组病程复杂且多变,包括2例死亡。
在无播散性或终末器官疾病的情况下,避免对放线菌分离株进行长期治疗不会导致不良后果。酗酒或异物与放线菌病有关。迈氏放线菌可能是比以往认识到的更常见的放线菌病病因。