Davies H D, McGeer A, Schwartz B, Green K, Cann D, Simor A E, Low D E
Division of Infectious Diseases, Hospital for Sick Children, Toronto, Canada.
N Engl J Med. 1996 Aug 22;335(8):547-54. doi: 10.1056/NEJM199608223350803.
Several reports suggest that the incidence of invasive group A streptococcal infections, including streptococcal toxic shock syndrome and necrotizing fasciitis, is increasing.
During 1992 and 1993 we conducted prospective, population-based surveillance of invasive group A streptococcal disease in Ontario, Canada. We reviewed clinical and laboratory records, searched for secondary cases of invasive disease, and cultured specimens from household contacts.
We identified 323 patients with invasive group A streptococcal infections, for an annual incidence of 1.5 cases per 100,000 population. The rates were highest in young children and the elderly. Fifty-six percent of the patients had underlying chronic illness. Risk factors for disease included infection with the human immunodeficiency virus, cancer, diabetes, alcohol abuse, and chickenpox. The most common clinical presentations were soft-tissue infection (48 percent), bacteremia with no septic focus (14 percent), and pneumonia (11 percent). Necrotizing fasciitis occurred in 6 percent of patients, and toxic shock in 13 percent. The mortality rate was 15 percent overall, but it was 29 percent among those over 64 years of age (P<0.001) and 81 percent among those with toxic shock (P<0.001). Fourteen percent of the cases were nosocomial, and 4 percent occurred in nursing home residents, often in association with disease outbreaks. Invasive disease occurred in 2 household contacts of patients with infection, for an estimated risk of 3.2 per 1000 household contacts (95 percent confidence interval, 0.39 to 12 per 1000).
The elderly and those with underlying medical conditions are at greatest risk for invasive group A streptococcal disease, toxic shock, and necrotizing fasciitis. Invasive steptococcal infection is associated with a substantial risk of transmission in households and health care institutions.
多项报告表明,包括链球菌中毒性休克综合征和坏死性筋膜炎在内的侵袭性A组链球菌感染的发病率正在上升。
1992年至1993年期间,我们在加拿大安大略省对侵袭性A组链球菌病进行了基于人群的前瞻性监测。我们查阅了临床和实验室记录,寻找侵袭性疾病的二代病例,并对家庭接触者的标本进行培养。
我们确定了323例侵袭性A组链球菌感染患者,年发病率为每10万人1.5例。发病率在幼儿和老年人中最高。56%的患者有潜在的慢性病。疾病的危险因素包括感染人类免疫缺陷病毒、癌症、糖尿病、酗酒和水痘。最常见的临床表现为软组织感染(48%)、无脓毒症病灶的菌血症(14%)和肺炎(11%)。6%的患者发生坏死性筋膜炎,13%的患者发生中毒性休克。总体死亡率为15%,但64岁以上患者的死亡率为29%(P<0.001),中毒性休克患者的死亡率为81%(P<0.001)。14%的病例为医院感染,4%发生在养老院居民中,且常与疾病暴发有关。2例感染患者的家庭接触者发生了侵袭性疾病,估计每1000名家庭接触者中的风险为3.2(95%置信区间,每1000名接触者0.39至12)。
老年人和有基础疾病的人患侵袭性A组链球菌病、中毒性休克和坏死性筋膜炎的风险最大。侵袭性链球菌感染在家庭和医疗机构中具有较高的传播风险。