Hon Kam-Lun E, Fu Antony, Leung Ting Fan, Poon Terence C W, Cheung Wai Hung, Fong Chor Yiu, Ho Yee Ting Christina, Lee Tsui Yin Jamie, Ng Tam Man, Yu Wai Ling, Cheung Kam Lau, Lee Vivian, Ip Margaret
Department of Paediatrics, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong.
Clin Respir J. 2015 Jan;9(1):45-52. doi: 10.1111/crj.12103. Epub 2014 Feb 19.
The streptococci are important bacteria that cause serious childhood infections. We investigated cardiopulmonary morbidity associated with streptococcal infection and pediatric intensive care unit (PICU) admission.
A retrospective study between 2002 and 2013 of all children with a laboratory isolation of streptococcus.
There were 40 (2.3%) PICU patients with streptococcal isolations including Streptococcus pyogenes (Group A streptococcus, GAS, n = 7), Streptococcus agalactiae (Group B streptococcus, GBS, n = 5), Streptococcus pneumoniae (SP, n = 20), alpha-hemolytic (n = 4), beta-hemolytic (n = 2) and gama-hemolytic (n = 2) streptococci. Comparing among GAS, GBS and SP, respiratory isolates were more likely positive for GAS or SP (P = 0.033), whereas cerebrospinal fluid was more likely positive for GBS (P = 0.002). All GAS and GBS, and the majority of SP (90%) were sensitive to penicillin. All SP specimens were sensitive to cefotaxime and vancomycin. These infections were associated with high PICU mortality of 43%, 20% and 25%, respectively. Isolation of streptococci was associated with a 30% mortality and high rates of need for mechanical ventilatory and inotropic supports. Patients with GAS, SP or any streptococcal isolation had relative risks [95% confidence interval (CI), P value] of PICU deaths of 7.5 (CI 3.1-18.1, P < 0.0001), 4.5 (CI 2.0-9.8, P < 0.0002) and 5.7 (CI 3.4-9.5, P < 0.0001), respectively. In SP, older children had significantly higher prevalence of premorbid conditions such as malignancy, mental retardation/cerebral palsy ± seizure disorders, chromosomal or genetic disorders (P = 0.003) than children <5 years of age. Serotypes were available for some of these specimens that included 19A, 6B, 3 and 6C. There were four SP deaths with multiorgan system failure and hemolytic uremic syndrome (two 19A and two serotype 3).
Severe streptococcal infections are associated with significant morbidity and mortality despite treatment with systemic antibiotics and intensive care unit support. GAS and SP affect the lungs of children, whereas GBS more likely causes meningitis in infants. The expanded coverage of newer polyvalent pneumococcal vaccines can probably prevent infections by serotypes 19A, 19F, 6B and 3.
链球菌是导致儿童严重感染的重要细菌。我们调查了与链球菌感染及儿科重症监护病房(PICU)收治相关的心肺疾病发病率。
对2002年至2013年间所有实验室分离出链球菌的儿童进行回顾性研究。
40例(2.3%)PICU患者分离出链球菌,包括化脓性链球菌(A组链球菌,GAS,n = 7)、无乳链球菌(B组链球菌,GBS,n = 5)、肺炎链球菌(SP,n = 20)、α溶血链球菌(n = 4)、β溶血链球菌(n = 2)和γ溶血链球菌(n = 2)。在GAS、GBS和SP之间比较,呼吸道分离株GAS或SP呈阳性的可能性更大(P = 0.033),而脑脊液GBS呈阳性的可能性更大(P = 0.002)。所有GAS和GBS以及大多数SP(90%)对青霉素敏感。所有SP标本对头孢噻肟和万古霉素敏感。这些感染分别伴有43%、20%和25%的高PICU死亡率。链球菌分离与30%的死亡率以及高机械通气和血管活性药物支持需求率相关。GAS、SP或任何链球菌分离的患者PICU死亡的相对风险[95%置信区间(CI),P值]分别为7.5(CI 3.1 - 18.1,P < 0.0001)、4.5(CI 2.0 - 9.8,P < 0.0002)和5.7(CI 3.4 - 9.5,P < 0.0001)。在SP感染中,年龄较大儿童的恶性肿瘤、智力发育迟缓/脑瘫±癫痫、染色体或遗传疾病等病前状况的患病率显著高于5岁以下儿童(P = 0.003)。部分标本可检测到血清型,包括19A、6B、3和6C。有4例SP感染死亡病例伴有多器官系统衰竭和溶血尿毒综合征(2例19A和2例血清型3)。
尽管采用全身抗生素治疗和重症监护病房支持,严重链球菌感染仍伴有显著的发病率和死亡率。GAS和SP影响儿童肺部,而GBS更易导致婴儿脑膜炎。新型多价肺炎球菌疫苗扩大覆盖范围可能预防19A、19F、6B和3血清型感染。