Prevention of Invasive Pneumococcal Disease Among Black or African American Children With and Without Sickle Cell Disease in the United States After Introduction of 13-Valent Pneumococcal Conjugate Vaccine, 2005 Through 2019

IF 2.4 3区 医学 Q2 HEMATOLOGY
Amanda B. Payne, Ryan Gierke, Wei Xing, Lesley McGee, Mary Hulihan, Thomas V. Adamkiewicz, Miwako Kobayashi, for the Active Bacterial Core Surveillance Team
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Abstract

Background

Administration of pneumococcal vaccines and oral penicillin prophylaxis has been recommended for children with sickle cell disease (SCD) to reduce the risk of invasive pneumococcal disease (IPD). Characterizing changes in IPD cases among children with SCD after 13-valent pneumococcal conjugate vaccine (PCV13) introduction could help inform the need for additional prevention measures.

Methods

Using data from Active Bacterial Core surveillance, we characterized IPD cases among Black or African American (Black) children aged less than 18 years with SCD, non-SCD IPD risk factors, and no IPD risk factors across three time periods (pre-PCV13 [2005–2009], early-PCV13 [2010–2014], and late-PCV13 [2015–2019]), and assessed proportion of IPD cases caused by serotypes in new pneumococcal conjugate vaccines (PCV15, PCV20) recommended after 2019. We analyzed IPD incidence among children with and without SCD.

Results

From 2005 to 2019, 1725 IPD cases were reported among Black children (6.9% with SCD). IPD incidence among children with SCD declined by 50% between pre-PCV13 and late-PCV13 periods (from 332 to 167 per 100,000), although IPD incidence among children with SCD was 42 times that of children without SCD in late-PCV13 period. During late-PCV13 period, greater than 95% of IPD cases among children with SCD were non-PCV13 serotypes; PCV15/non-PCV13 and PCV20/non-PCV15 serotypes caused 19% and 22% of cases, respectively. Increase in penicillin-nonsusceptible IPD cases was not observed.

Conclusions

Despite reductions in IPD incidence after PCV13 introduction, children with SCD are at increased risk of IPD compared to children without SCD. Use of higher valency PCVs may help reduce remaining IPD burden.

2005年至2019年,在美国引入13价肺炎球菌结合疫苗后,患有和不患有镰状细胞病的黑人或非裔美国儿童中侵袭性肺炎球菌疾病的预防
背景:已建议镰状细胞病(SCD)患儿接种肺炎球菌疫苗并口服青霉素进行预防,以降低患侵袭性肺炎球菌疾病(IPD)的风险。在引入 13 价肺炎球菌结合疫苗 (PCV13) 后,描述 SCD 儿童中 IPD 病例的变化有助于了解是否需要采取额外的预防措施:利用主动细菌核心监测的数据,我们描述了三个时间段(PCV13 前 [2005-2009]、PCV13 早期 [2010-2014] 和 PCV13 晚期 [2015-2019])内患有 SCD、非 SCD IPD 危险因素和无 IPD 危险因素的 18 岁以下黑人或非裔美国人(黑人)儿童中 IPD 病例的特征,并评估了 2019 年后推荐的新肺炎球菌结合疫苗(PCV15、PCV20)中由血清型引起的 IPD 病例的比例。我们分析了患有和未患有 SCD 儿童的 IPD 发病率:从 2005 年到 2019 年,黑人儿童中报告了 1725 例 IPD 病例(6.9% 患有 SCD)。在 PCV13 前期和 PCV13 后期,SCD 儿童的 IPD 发病率下降了 50%(从每 10 万人 332 例降至 167 例),但在 PCV13 后期,SCD 儿童的 IPD 发病率是未患 SCD 儿童的 42 倍。在 PCV13 晚期,SCD 儿童中超过 95% 的 IPD 病例为非 PCV13 血清型;PCV15/非 PCV13 和 PCV20/非 PCV15 血清型分别占病例的 19% 和 22%。未观察到对青霉素不敏感的 IPD 病例增加:结论:尽管 PCV13 引入后 IPD 发病率有所下降,但与未患 SCD 的儿童相比,患 SCD 的儿童患 IPD 的风险更高。使用效价更高的 PCV 可能有助于减少剩余的 IPD 负担。
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来源期刊
Pediatric Blood & Cancer
Pediatric Blood & Cancer 医学-小儿科
CiteScore
4.90
自引率
9.40%
发文量
546
审稿时长
1.5 months
期刊介绍: Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.
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