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本文引用的文献

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Prevention of antibiotic-nonsusceptible Streptococcus pneumoniae with conjugate vaccines.用结合疫苗预防抗生素耐药性肺炎链球菌。
J Infect Dis. 2012 Feb 1;205(3):401-11. doi: 10.1093/infdis/jir755. Epub 2011 Dec 7.
2
Effectiveness of the new serotypes in the 13-valent pneumococcal conjugate vaccine.13 价肺炎球菌结合疫苗中新血清型的有效性。
Vaccine. 2011 Nov 15;29(49):9127-31. doi: 10.1016/j.vaccine.2011.09.112. Epub 2011 Oct 5.
3
Pervasive sign epistasis between conjugative plasmids and drug-resistance chromosomal mutations.普遍存在的接合质粒与耐药染色体突变的符号上位性。
PLoS Genet. 2011 Jul;7(7):e1002181. doi: 10.1371/journal.pgen.1002181. Epub 2011 Jul 28.
4
The impact of antiretroviral treatment on the burden of invasive pneumococcal disease in South African children: a time series analysis.抗逆转录病毒治疗对南非儿童侵袭性肺炎球菌病负担的影响:时间序列分析。
AIDS. 2011 Feb 20;25(4):453-62. doi: 10.1097/QAD.0b013e328341b7f1.
5
A trial of a 7-valent pneumococcal conjugate vaccine in HIV-infected adults.HIV 感染者 7 价肺炎球菌结合疫苗的临床试验。
N Engl J Med. 2010 Mar 4;362(9):812-22. doi: 10.1056/NEJMoa0903029.
6
Burden of disease caused by Streptococcus pneumoniae in children younger than 5 years: global estimates.5岁以下儿童肺炎链球菌所致疾病负担:全球估计数
Lancet. 2009 Sep 12;374(9693):893-902. doi: 10.1016/S0140-6736(09)61204-6.
7
Risk factors for nasopharyngeal carriage of drug-resistant Streptococcus pneumoniae: data from a nation-wide surveillance study in Greece.耐多药肺炎链球菌鼻咽部携带的危险因素:来自希腊一项全国性监测研究的数据。
BMC Infect Dis. 2009 Jul 29;9:120. doi: 10.1186/1471-2334-9-120.
8
Molecular characterization of emerging non-levofloxacin-susceptible pneumococci isolated from children in South Africa.从南非儿童中分离出的新出现的非左氧氟沙星敏感肺炎球菌的分子特征
J Clin Microbiol. 2009 May;47(5):1319-24. doi: 10.1128/JCM.02280-08. Epub 2009 Mar 4.
9
Effect of pneumococcal conjugate vaccine on pneumococcal meningitis.肺炎球菌结合疫苗对肺炎球菌性脑膜炎的影响。
N Engl J Med. 2009 Jan 15;360(3):244-56. doi: 10.1056/NEJMoa0800836.
10
Serotype replacement and multiple resistance in Streptococcus pneumoniae after the introduction of the conjugate pneumococcal vaccine.引入肺炎球菌结合疫苗后肺炎链球菌的血清型替换和多重耐药性。
Microb Drug Resist. 2008 Jun;14(2):101-7. doi: 10.1089/mdr.2008.0782.

南非高艾滋病毒流行地区,疫苗时代前(2003 年至 2008 年),耐多药侵袭性肺炎球菌病的危险因素。

Risk factors for multidrug-resistant invasive pneumococcal disease in South Africa, a setting with high HIV prevalence, in the prevaccine era from 2003 to 2008.

机构信息

Division of Public Health Surveillance and Response, National Institute for Communicable Diseases, National Health Laboratory Service, Johannesburg, South Africa.

出版信息

Antimicrob Agents Chemother. 2012 Oct;56(10):5088-95. doi: 10.1128/AAC.06463-11. Epub 2012 Jul 16.

DOI:10.1128/AAC.06463-11
PMID:22802256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3457358/
Abstract

The emergence of multidrug-resistant (MDR) Streptococcus pneumoniae complicates disease management. We aimed to determine risk factors associated with MDR invasive pneumococcal disease (IPD) in South Africa and evaluate the potential for vaccination to reduce disease burden. IPD data collected by laboratory-based surveillance from 2003 through 2008 were analyzed. Multidrug resistance was defined as nonsusceptibility to any three or more different antibiotic classes. Risk factors for multidrug resistance were evaluated using multivariable logistic regression. Of 20,100 cases of IPD identified, 3,708 (18%) had MDR isolates, with the proportion increasing from 16% (461/2,891) to 20% (648/3,326) (P < 0.001) over the study period. Serotypes included in the 13-valent pneumococcal conjugate vaccine (PCV13) accounted for 94% of MDR strains. Significant risk factors for MDR IPD included PCV13 (1,486/6,407; odds ratio [OR] of 6.3; 95% confidence interval [CI] of 5.0 to 7.9) and pediatric (3,382/9,980; OR of 12.8; 95% CI of 10.6 to 15.4) serotypes, age of <5 (802/3,110; OR of 2.0; 95% CI of 1.8 to 2.3) or ≥65 (39/239; OR of 1.5; 95% CI of 1.0 to 2.2) years versus age of 15 to 64 years, HIV infection (975/4,636; OR of 1.5; 95% CI of 1.2 to 1.8), previous antibiotic use (242/803; OR of 1.7; 95% CI of 1.4 to 2.1), previous hospital admissions (579/2,450; OR of 1.2; 95% CI of 1.03 to 1.4), urban location (883/4,375; OR of 2.0; 95% CI of 1.1 to 3.5), and tuberculosis treatment (246/1,021; OR of 1.2; 95% CI of 1.03 to 1.5). MDR IPD prevalence increased over the study period. The effect of many of the MDR risk factors could be reduced by more judicious use of antibiotics. Because PCV13 serotypes account for most MDR infections, pneumococcal vaccination may reduce the prevalence of multidrug resistance.

摘要

耐多药(MDR)肺炎链球菌的出现使疾病管理复杂化。我们旨在确定与南非耐多药侵袭性肺炎球菌病(IPD)相关的危险因素,并评估疫苗接种降低疾病负担的潜力。对 2003 年至 2008 年通过实验室监测收集的 IPD 数据进行了分析。将对任何三种或更多种不同抗生素类别的药物不敏感定义为耐多药。使用多变量逻辑回归评估了耐多药的危险因素。在确定的 20100 例 IPD 病例中,3708 例(18%)为 MDR 分离株,这一比例从研究期间的 16%(461/2891)增加到 20%(648/3326)(P<0.001)。13 价肺炎球菌结合疫苗(PCV13)中包含的血清型占 MDR 菌株的 94%。MDR IPD 的显著危险因素包括 PCV13(1486/6407;比值比[OR]为 6.3;95%置信区间[CI]为 5.0 至 7.9)和儿科(3382/9980;OR 为 12.8;95%CI 为 10.6 至 15.4)血清型,年龄<5 岁(802/3110;OR 为 2.0;95%CI 为 1.8 至 2.3)或≥65 岁(39/239;OR 为 1.5;95%CI 为 1.0 至 2.2)与 15 至 64 岁年龄相比,HIV 感染(975/4636;OR 为 1.5;95%CI 为 1.2 至 1.8)、先前使用抗生素(242/803;OR 为 1.7;95%CI 为 1.4 至 2.1)、先前住院治疗(579/2450;OR 为 1.2;95%CI 为 1.03 至 1.4)、城市位置(883/4375;OR 为 2.0;95%CI 为 1.1 至 3.5)和结核病治疗(246/1021;OR 为 1.2;95%CI 为 1.03 至 1.5)。MDR IPD 的患病率在研究期间有所增加。许多 MDR 危险因素的影响可以通过更明智地使用抗生素来降低。由于 PCV13 血清型占大多数 MDR 感染,肺炎球菌疫苗接种可能会降低耐多药的流行率。