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Effectiveness and immunogenicity of pneumococcal vaccination in splenectomized and functionally asplenic patients C. Forstner, S. Plefka, S. Tobudic, H.M.

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Presentation on theme: "Effectiveness and immunogenicity of pneumococcal vaccination in splenectomized and functionally asplenic patients C. Forstner, S. Plefka, S. Tobudic, H.M."— Presentation transcript:

1 Effectiveness and immunogenicity of pneumococcal vaccination in splenectomized and functionally asplenic patients C. Forstner, S. Plefka, S. Tobudic, H.M. Winkler, K. Burgmann, H. Burgmann Department of Internal Medicine I Division of Infectious Diseases and Tropical Medicine Medical University of Vienna Dr. Stephanie Plefka October 2014

2 http://www.news.at/_storage/asset/1650080/storage/newsat:key-visual/file/12967091/spitaeler-akh-proben-311334_e.jpg

3 Background Splenectomized and functionally asplenic patients are at an increased risk of overwhelming post-splenectomy infection (OPSI) and invasive pneumococcal disease (IPD) caused particularly by Streptococcus pneumoniae 1 : Sepsis Meningitis Pneumonia 1 - Di Carlo I, Primo S, Pulvirenti E, Toro A. Should all splenectomised patients be vaccinated to avoid OPSI? Revisiting an old concept: an Italian retrospective monocentric study. Hepatogastroenterology. 2008 Mar-Apr;55(82-83):308-10. - Waghorn DJ. Overwhelming infection in asplenic patients: current best practice preventive measures ar not being followed. J Clin Pathol 2001; 54:214-8 - Ejstrud P, Kristensen ´B, Hansen JB, Madsen KM, Schonheyder HC, Sorensen HT. Risk and patterns of bacteremia after splenectomy: a population-based study. Scand J Infect Dis 2000; 32:521-5 - Kyaw MH, Holmes EM, Toolis F, Wayne B, Chalmers J, Jones IG, et al. Evaluation of severe infection and survival after splenectomy. Am J Med 2006; 110:276e1-7e.

4 Background Current guidelines 2 : Vaccination with the 23-valent pneumococcal polysaccaride vaccine (PPV23) after SPE Revaccination after 3-5 years 2 Davies JM, Lewis MPN, Wimperis J, Rafi I, Ladhani S, Bolton-Maggs HB, Rewiewof guidelines for the prevention andtreatment of infection in patients with an absent or dysfunctional spleen: prepared on behalf of the British committee for standards in haematology by a working part if the haemato-oncology task force. Br J Haematol 2011; 155:308-17.

5 Aims  Investigation of the effectiveness of pneumococcal vaccination, using PPV23 and PCV7, in preventing OPSI and IPD among patients after splenectomy and patients with a congenitally absent or dysfunctional spleen.  Induction of serological response

6 Methods Study Design Single-centre observational trial a.Retrospective analysis b.Prospective determination Ad a.) OPSI or IPD in post-splenectomized patients? Cause of death in deceased patients? Ad b.) Specific anti-pneumococcal antibody concentrations

7 Methods Material Questionnaire (a.) Database (a.) Blood sampling (b.)

8 Methods Retrospective analysis Questionnaire Demographic data Reason and time of SPE/asplenia Time and type of pneumococcal vaccination Number and type of OPSI or IPD Database Number and causes of death obtained from the local central bureau of statistics in Vienna

9 Methods Prospective determination Measurement of serological antibody response Comparison of antibody concentration Vaccinated, splenectomized/asplenic patients Age-matched control group of non-vaccinated, non-splenectomized patients 7 serotypes (4, 6B, 9V, 14, 18C, 19F, 23F) contained in PPV23 and PCV7 - ELISA Excluded: revaccination

10 Methods Patients Criteria of Inclusion: Splenectomy or functionally asplenic Vaccination against Streptococcus pneumoniae btw. 1996 and 2009 at AKH Vaccines: - PPV23 (before March 2002) - PCV7 (replaced PPV23) 19a – 90a

11 Methods Patients

12 Methods Limitations Retrospective analysis of the post-vaccine complications Serological responses Determined only once Limited number of patients Irrespective of the time of vaccination

13 Results

14 Cause of death Progression of the underlying malignant haemato-oncological disease in 68% Septic shock in 13.2% 3 septicaemia as complication of pneumonia 4 fulminant neutropenic sepsis Underlying disease: 3 lymphoma 2 leukaemia 1 immunodeficiency 1 visceral leishmaniasis

15 Results Cause of death

16 Results Post-vaccine complications OPSI 7% of all study patients Mortality 64% (7/11) Diagnosed a median of 1.3a after vaccination 1a in deceased 2.9a in living Cause of death: bacterial sepsis Causative pathogen in survivers: Strep. Pneumoniae No meningitis

17 Results Post-vaccine complications IPD 13% of living patients Pneumonia in 9 Septicaemia in 4 Otitis media in 2 No meningitis Causative pathogen: Strep. Pneumoniae

18 Results Serological antibody response PCV7 within the previous 5 years (n=15) => significantly higher GMCs (of 0.8-6.1µg/mL) against all 7 Strep. Pneumoniae serotypes measured 4, 6B, 9V, 14, 18C, 23F

19 Results

20 Antibodies to Pneumococcal Polysaccarides Serotype 1) PPV23 2) PCV7 3) Control group * p < 0.05 # p < 0.001 GMC: mcg/ml

21 Results 7% OPSI between 1996-2009 (PPV23 and/or PCV7) OPSI of a median of 1.3a after vaccination 64% mortality Causative pathogen: Streptococcus pneumoniae

22 Results PCV7 betw. 2005-2009 – all 46 splenectomized patients still alive in 2009 PPV23 followed by PCV7 All patients died No OPSI

23 Discussion Main indication for splenectomy in all study patients: Malignant haematological neoplasm mostly Thrombocytopenia Langley et al. 2010 Melles et al. 2004 Böhner et al. 1996

24 Discussion Main cause of death: Malignant haemato-oncological disease (68%) But: septic shock in 13.2%

25 Discussion Post-vaccine complications: 7% OPSI in all splenectomized and vaccinated patients All Sepsis, no meningitis Ejstrud et al. 2000

26 Discussion Serological antibody response: Vaccination with PCV7 in the previous 5 years => High GMCs of 0.8-6.1mcg/mL against 4, 6B, 9V, 14, 18C, 19F, 23F Meerwald-Eggink et al. >0.35 mcg/mL against 4 and 9V SPE, non-vaccinated 9/16 <0.35mcg/mLg

27 Discussion Serological antibody response: Vaccination with PCV7 in the previous 5 years -> No deceased => Thesis: High GMCs of 0.8-6.1mcg/mL might be a level to achieve protection

28 Conclusion Underlying diseases in splenectomized patients seem to be the most important predictors of mortality High GMCs after pneumococcal vaccination within the first 5 years after vaccination Post-vaccine pneumococcal sepsis in 3.3% of the splenectomized survivors

29 Special thanks Univ. Prof. Dr. Burgmann Dr. Selma Tobudic Heide-Maria Winkler Secretary of Department

30 Thank you for your attention http://www.alpha-world.info/system/attachments/cms/430d1336395260-wien-special.jpg


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