The burden of invasive pneumococcal disease in children with underlying risk factors in North America and Europe.

M A Rose, D Christopoulou, T T H Myint, I de Schutter
Author Information
  1. M A Rose: Children's Hospital, Goethe University, Frankfurt, Germany.

Abstract

BACKGROUND: Characterisation of risk groups who may benefit from pneumococcal vaccination is essential for the generation of recommendations and policy.
METHODS: We reviewed the literature to provide information on the incidence and risk of invasive pneumococcal disease (IPD) in at-risk children in Europe and North America. The PubMed database was searched using predefined search terms and inclusion/exclusion criteria for papers reporting European or North American data on the incidence or risk of IPD in children with underlying medical conditions.
RESULTS: Eighteen references were identified, 11 from North America and 7 from Europe, with heterogeneous study methods, periods and populations. The highest incidence was seen in US children positive for human immunodeficiency virus infection, peaking at 4167 per 100,000 patient-years in 2000. Studies investigating changes in incidence over time reported decreases in the incidence of IPD between the late 1990s and early 2000s. The highest risk of IPD was observed in children with haematological cancers or immunosuppression. Overall, data on IPD in at-risk children were limited, lacking incidence data for a wide range of predisposing conditions. There was, however, a clear decrease in the incidence of IPD in at-risk children after the introduction of 7-valent pneumococcal conjugate vaccine into immunisation programmes, as previously demonstrated in the general population.
CONCLUSION: Despite the heterogeneity of the studies identified, the available data show a substantial incidence of IPD in at-risk children, particularly those who are immunocompromised. Further research is needed to determine the true risk of IPD in at-risk children, particularly in the post-PCV period, and to understand the benefits of vaccination and optimal vaccination schedules.

References

  1. Hum Vaccin. 2009 Mar;5(3):177-80 [PMID: 19202358]
  2. MMWR Suppl. 2006 Apr 28;55(1):20-4 [PMID: 16645578]
  3. Pediatr Infect Dis J. 2009 Feb;28(2):118-22 [PMID: 19116604]
  4. Clin Infect Dis. 2007 Jun 1;44(11):1428-33 [PMID: 17479937]
  5. Emerg Infect Dis. 2008 Jan;14(1):25-33 [PMID: 18258073]
  6. Pediatrics. 2010 Jul;126(1):e9-17 [PMID: 20547641]
  7. Pediatr Infect Dis J. 2011 Mar;30(3):251-3 [PMID: 21164387]
  8. N Engl J Med. 2003 May 1;348(18):1737-46 [PMID: 12724479]
  9. Ann Epidemiol. 2008 Feb;18(2):139-46 [PMID: 18191761]
  10. Pediatrics. 2006 Feb;117(2):284-9 [PMID: 16390918]
  11. Clin Infect Dis. 2008 Aug 15;47(4):476-84 [PMID: 18627249]
  12. JAMA. 2006 Apr 12;295(14):1668-74 [PMID: 16609088]
  13. J Infect. 2012 Jul;65(1):17-24 [PMID: 22394683]
  14. Int J Infect Dis. 2010 Mar;14(3):e197-209 [PMID: 19700359]
  15. Pediatr Infect Dis J. 2008 Oct;27(10):886-91 [PMID: 18776825]
  16. Pediatr Infect Dis J. 2010 Apr;29(4):289-93 [PMID: 19935447]
  17. MMWR Recomm Rep. 2010 Dec 10;59(RR-11):1-18 [PMID: 21150868]
  18. Pediatr Infect Dis J. 2006 Mar;25(3):250-4 [PMID: 16511389]
  19. Can Commun Dis Rep. 2010 Nov 23;36(ACS-12):1-21 [PMID: 31697280]
  20. Gut. 2008 Aug;57(8):1074-80 [PMID: 18270242]
  21. PLoS One. 2012;7(7):e39150 [PMID: 22815698]
  22. N Engl J Med. 2005 May 19;352(20):2082-90 [PMID: 15901861]
  23. Pediatr Infect Dis J. 2005 Jan;24(1):17-23 [PMID: 15665705]
  24. Can J Infect Dis Med Microbiol. 2006 Jan;17(1):19-26 [PMID: 18418479]
  25. Clin Infect Dis. 2010 Dec 1;51(11):1258-65 [PMID: 21034194]
  26. Clin Infect Dis. 2010 May 1;50(9):1238-46 [PMID: 20367225]
  27. Pediatrics. 2008 Jul;122(1):e26-32 [PMID: 18595971]
  28. Pediatr Res. 2009 May;65(5 Pt 2):3R-12R [PMID: 19190530]
  29. Euro Surveill. 2009 Mar 26;14(12): [PMID: 19341605]
  30. Eur J Gastroenterol Hepatol. 2008 Jul;20(7):624-8 [PMID: 18679063]
  31. Lancet. 2009 Sep 12;374(9693):893-902 [PMID: 19748398]
  32. Pediatr Infect Dis J. 2010 Mar;29(3):251-6 [PMID: 19952861]
  33. BMJ. 2012 Oct 26;345:e6879 [PMID: 23103369]
  34. Br J Haematol. 2007 Jun;137(5):457-60 [PMID: 17488489]
  35. Int J Gen Med. 2012;5:967-74 [PMID: 23204861]
  36. J Infect. 2006 Jan;52(1):37-48 [PMID: 16368459]
  37. J Infect Dis. 2010 Jan 1;201(1):32-41 [PMID: 19947881]
  38. Vaccine. 2011 Apr 5;29(16):2856-64 [PMID: 21342667]
  39. Pediatr Transplant. 2005 Apr;9(2):183-6 [PMID: 15787790]
  40. Pediatrics. 2008 Mar;121(3):562-9 [PMID: 18310206]
  41. J Med Microbiol. 2011 Jan;60(Pt 1):1-8 [PMID: 20965923]
  42. J Epidemiol Community Health. 2012 Dec;66(12):1177-81 [PMID: 22493476]
  43. Pediatr Infect Dis J. 2011 Jun;30(6):528-30 [PMID: 21164385]
  44. Wkly Epidemiol Rec. 2012 Apr 6;87(14):129-44 [PMID: 24340399]
  45. Pediatr Infect Dis J. 2006 Jul;25(7):602-7 [PMID: 16804429]
  46. J Infect. 2012 Dec;65(6):521-7 [PMID: 22954752]
  47. Clin Microbiol Rev. 2012 Jul;25(3):409-19 [PMID: 22763632]
  48. Clin Infect Dis. 2007 Apr 15;44(8):1051-6 [PMID: 17366448]
  49. Ital J Pediatr. 2010 Mar 26;36:28 [PMID: 20346141]
  50. Epidemiology. 2010 May;21(3):340-6 [PMID: 20220521]
  51. JAMA. 2007 Apr 25;297(16):1784-92 [PMID: 17456820]
  52. Pediatrics. 2010 Jul;126(1):186-90 [PMID: 20498180]
  53. Vaccine. 2005 Dec 1;23(48-49):5464-73 [PMID: 16188350]

MeSH Term

Adolescent
Bacteremia
Child
Child, Preschool
Chronic Disease
Cost of Illness
Europe
HIV Infections
Humans
Immunocompromised Host
Immunosuppression Therapy
Incidence
Infant
Infant, Newborn
Meningitis, Pneumococcal
North America
Opportunistic Infections
Pneumococcal Infections
Risk Factors

Word Cloud

Created with Highcharts 10.0.0childrenincidenceIPDriskat-riskpneumococcalNorthdatavaccinationEuropeAmericainvasivediseaseunderlyingconditionsidentifiedhighestparticularlyBACKGROUND:CharacterisationgroupsmaybenefitessentialgenerationrecommendationspolicyMETHODS:reviewedliteratureprovideinformationPubMeddatabasesearchedusingpredefinedsearchtermsinclusion/exclusioncriteriapapersreportingEuropeanAmericanmedicalRESULTS:Eighteenreferences117heterogeneousstudymethodsperiodspopulationsseenUSpositivehumanimmunodeficiencyvirusinfectionpeaking4167per100000patient-years2000Studiesinvestigatingchangestimereporteddecreaseslate1990searly2000sobservedhaematologicalcancersimmunosuppressionOveralllimitedlackingwiderangepredisposinghowevercleardecreaseintroduction7-valentconjugatevaccineimmunisationprogrammespreviouslydemonstratedgeneralpopulationCONCLUSION:Despiteheterogeneitystudiesavailableshowsubstantialimmunocompromisedresearchneededdeterminetruepost-PCVperiodunderstandbenefitsoptimalschedulesburdenfactors

Similar Articles

Cited By