Division of Public Health Surveillance and Response, National Institute for Communicable Diseases, National Health Laboratory Service, Johannesburg, South Africa.
Antimicrob Agents Chemother. 2012 Oct;56(10):5088-95. doi: 10.1128/AAC.06463-11. Epub 2012 Jul 16.
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.
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。