Early and late invasive pneumococcal infection following stem cell transplantation: a European Bone Marrow Transplantation survey
Identifieur interne : 00B764 ( Main/Exploration ); précédent : 00B763; suivant : 00B765Early and late invasive pneumococcal infection following stem cell transplantation: a European Bone Marrow Transplantation survey
Auteurs : Dan Engelhard [Israël] ; Catherine Cordonnier [France] ; Peter J. Shaw [Australie] ; Terttu Parkalli [Finlande] ; Christine Guenther [Allemagne] ; Rodrigo Martino [Espagne] ; Adriaan W. Dekker [Pays-Bas] ; H. Grant Prentice [Royaume-Uni] ; Anita Gustavsson [Suède] ; Wenzel Nurnberger [Allemagne] ; Per Ljungman [Suède]Source :
- British journal of haematology [ 0007-1048 ] ; 2002.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Cellule souche, Homme.
English descriptors
- KwdEn :
Abstract
Streptococcus pneumoniae (S. pneumoniae) may cause severe and lethal infections months and years following stem cell transplantation (SCT). In a prospective survey over a 3.5-year period, we assessed the incidence, risk factors and outcome for invasive pneumococcal infection (IPI) following SCT. Fifty-one episodes of IPI were reported: 43 episodes after bone marrow transplantation (BMT) and 8 after peripheral blood stem cell transplantation (PBSCT); 35 after allogeneic SCT and 16 after autologous SCT. Seven IPI episodes, all bacteraemias, were defined as early, occurring 1-35 d (median 3 d) post transplantation. Forty-four episodes were defined as late (≥ 100 d post SCT), occurring 4 months to 10 years (median 17 months) post transplantation. The incidences of early and late IPI were 2.03/1000 and 8.63/1000 transplantations respectively (P = 0.001). A higher incidence of late IPI was observed after BMT than after PBSCT (10.99 versus 3.23/1000; P<0.01) and after allogeneic versus autologous SCT (12.20 versus 4.60/1000; P <0.01). There was a higher estimated incidence of IPI in allogeneic patients with than in those without graft-versus-host disease (GVHD) (18.85 versus 8.25/1000; P = 0.015). The mortality rate was 20%, including 2/7 of early and 8/44 of late IPI. S. pneumoniae is a rare but important complication during the aplastic phase after SCT. In conclusion, S. pneumoniae is a significant cause of morbidity late post-transplantation, especially in allogeneic patients, and particularly those with GVHD. The high IPI mortality rate, both early and late post-transplantation, requires preventive approaches, mainly effective immunization.
Affiliations:
- Allemagne, Australie, Espagne, Finlande, France, Israël, Pays-Bas, Royaume-Uni, Suède
- Angleterre, Bavière, Catalogne, District de Düsseldorf, District de Haute-Bavière, Grand Londres, Nouvelle-Galles du Sud, Rhénanie-du-Nord-Westphalie, Utrecht (province), Île-de-France
- Barcelone, Créteil, Düsseldorf, Londres, Munich, Sydney, Utrecht
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Le document en format XML
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<series><title level="j" type="main">British journal of haematology</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Autograft</term>
<term>Bone marrow</term>
<term>Complication</term>
<term>Graft versus host reaction</term>
<term>Hematopoietic cell</term>
<term>Homograft</term>
<term>Human</term>
<term>Late</term>
<term>Pneumococcal infection</term>
<term>Stem cell</term>
<term>Streptococcus pneumoniae</term>
<term>Survey</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Homogreffe</term>
<term>Autogreffe</term>
<term>Maladie greffon hôte</term>
<term>Complication</term>
<term>Tardif</term>
<term>Pneumococcie</term>
<term>Streptococcus pneumoniae</term>
<term>Cellule hématopoïétique</term>
<term>Cellule souche</term>
<term>Moelle osseuse</term>
<term>Enquête</term>
<term>Homme</term>
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<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Cellule souche</term>
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<front><div type="abstract" xml:lang="en">Streptococcus pneumoniae (S. pneumoniae) may cause severe and lethal infections months and years following stem cell transplantation (SCT). In a prospective survey over a 3.5-year period, we assessed the incidence, risk factors and outcome for invasive pneumococcal infection (IPI) following SCT. Fifty-one episodes of IPI were reported: 43 episodes after bone marrow transplantation (BMT) and 8 after peripheral blood stem cell transplantation (PBSCT); 35 after allogeneic SCT and 16 after autologous SCT. Seven IPI episodes, all bacteraemias, were defined as early, occurring 1-35 d (median 3 d) post transplantation. Forty-four episodes were defined as late (≥ 100 d post SCT), occurring 4 months to 10 years (median 17 months) post transplantation. The incidences of early and late IPI were 2.03/1000 and 8.63/1000 transplantations respectively (P = 0.001). A higher incidence of late IPI was observed after BMT than after PBSCT (10.99 versus 3.23/1000; P<0.01) and after allogeneic versus autologous SCT (12.20 versus 4.60/1000; P <0.01). There was a higher estimated incidence of IPI in allogeneic patients with than in those without graft-versus-host disease (GVHD) (18.85 versus 8.25/1000; P = 0.015). The mortality rate was 20%, including 2/7 of early and 8/44 of late IPI. S. pneumoniae is a rare but important complication during the aplastic phase after SCT. In conclusion, S. pneumoniae is a significant cause of morbidity late post-transplantation, especially in allogeneic patients, and particularly those with GVHD. The high IPI mortality rate, both early and late post-transplantation, requires preventive approaches, mainly effective immunization.</div>
</front>
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