Steenhoff Andrew P, Wood Sarah M, Rutstein Richard M, Wahl Allison, McGowan Karin L, Shah Samir S
Division of Special Immunology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Pediatr Infect Dis J. 2008 Oct;27(10):886-91. doi: 10.1097/INF.0b013e3181734f8f.
The heptavalent pneumococcal conjugate vaccine (PCV7) has decreased the incidence of pediatric invasive pneumococcal disease (IPD) in the United States. Few data exist on the changing IPD incidence in HIV-infected children.
Diagnostic codes and clinical microbiology laboratory records identified cases of IPD from 1989 to 2006 in perinatally-infected children <18 years of age followed at an urban HIV clinic. IPD incidence was calculated and serotype distribution and antibiotic resistance were recorded.
Two-hundred fifty-six patients were followed for 1756 person-years (PY). The sample was 59% female, 76% black, 14% white, and 8% Hispanic. Of 21 episodes of IPD (1200/100,000 PY), 17 (81%) were female. IPD cases had a median age of 6.3 years (interquartile range [IQR]: 2.3-9.9 years), median CD4% of 17% (IQR: 11-28%), and median CD4 count of 415 cells/mm (range, 2-1699 cells/mm). Bacteremia was the commonest form of IPD (19 episodes; 1080/100,000 PY). After HAART introduction in 1996, the incidence of IPD decreased 84% from 1862/100,000 PY in 1989-1995 to 292/100,000 PY in 1997-1999 (incidence rate ratio [IRR]: 0.16, P = 0.03). After PCV7 introduction in 2000, IPD incidence showed a nonsignificant increase from 292 of 100,000 PY in 1997-1999 to 860 of 100,000 PY in 2001-2006 (IRR: 2.94; P = 0.16). The percentages of IPD isolates nonsusceptible to penicillin and trimethoprim-sulfamethoxazole were 19% and 33%, respectively. Vaccine serotypes accounted for 38% of isolates, vaccine-related 14%, nonvaccine 33%, and the serotype was unknown in 14%.
The incidence of IPD among perinatally HIV-infected children decreased after the introduction of HAART. Ongoing monitoring is required to determine the effect of PCV7 on IPD in this vulnerable population.
七价肺炎球菌结合疫苗(PCV7)已降低了美国儿童侵袭性肺炎球菌疾病(IPD)的发病率。关于HIV感染儿童中IPD发病率变化的数据很少。
通过诊断编码和临床微生物学实验室记录,确定了1989年至2006年在一家城市HIV诊所随访的18岁以下围产期感染儿童中的IPD病例。计算IPD发病率,并记录血清型分布和抗生素耐药性。
256例患者随访了1756人年(PY)。样本中59%为女性,76%为黑人,14%为白人,8%为西班牙裔。在21例IPD发作(1200/100,000 PY)中,17例(81%)为女性。IPD病例的中位年龄为6.3岁(四分位间距[IQR]:2.3 - 9.9岁),CD4%中位数为17%(IQR:11 - 28%),CD4细胞计数中位数为415个细胞/mm³(范围:2 - 1699个细胞/mm³)。菌血症是IPD最常见的形式(19例发作;1080/100,000 PY)。1996年引入高效抗逆转录病毒治疗(HAART)后,IPD发病率从1989 - 1995年的1862/100,000 PY下降了84%,至1997 - 1999年的292/100,000 PY(发病率比[IRR]:0.16,P = 0.03)。2000年引入PCV7后,IPD发病率从1997 - 1999年的292/100,000 PY至2001 - 2006年的860/100,000 PY呈非显著性增加(IRR:2.94;P = 0.16)。对青霉素和甲氧苄啶 - 磺胺甲恶唑不敏感的IPD分离株百分比分别为19%和33%。疫苗血清型占分离株的38%,与疫苗相关的占14%,非疫苗血清型占33%,14%的血清型未知。
围产期HIV感染儿童中IPD的发病率在引入HAART后有所下降。需要持续监测以确定PCV7对这一脆弱人群中IPD的影响。