Infections in non‐splenectomized persistent or chronic primary immune thrombocytopenia adults: risk factors and vaccination effect

Essentials The risk factors for infection in immune thrombocytopenia are not well known. We conducted a national pharmacoepidemiological study. Pulmonary disease, corticosteroids and rituximab were the main risk factors for infections. Pneumococcal and influenza vaccines were protective against infe...

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Veröffentlicht in:Journal of thrombosis and haemostasis 2017-04, Vol.15 (4), p.785-791
Hauptverfasser: Moulis, G., Lapeyre‐Mestre, M., Palmaro, A., Sailler, L.
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container_issue 4
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creator Moulis, G.
Lapeyre‐Mestre, M.
Palmaro, A.
Sailler, L.
description Essentials The risk factors for infection in immune thrombocytopenia are not well known. We conducted a national pharmacoepidemiological study. Pulmonary disease, corticosteroids and rituximab were the main risk factors for infections. Pneumococcal and influenza vaccines were protective against infections. Summary Introduction Risk factors for infection and protective effect of vaccines in immune thrombocytopenia (ITP) patients in the era of rituximab therapy are unknown. Objectives To assess the risk factors for serious and non‐serious infections (respectively, SIs and NSIs) in non‐splenectomized adults treated for persistent or chronic primary ITP, including the effect of pneumococcal and influenza vaccines. Patients/Methods The population was the 2009–2012 FAITH cohort (n = 1805), which is the cohort of all incident (newly diagnosed) primary ITP adults treated > 3 months in France built into the national health insurance database (SNIIRAM). SIs were hospitalizations with any infection as the primary diagnosis code. NSIs were identified using out‐of‐hospital antibiotic dispensing. Cox models were performed. Results Incidence rates were 6.3/100 patient‐years (95% confidence interval [CI], 5.4–7.4) for SIs (lower respiratory tract in 42.8% of the cases) and 100.5/100 patient‐years (95% CI, 95.0–106.3) for NSIs. In multivariate analyses, increasing age and chronic pulmonary disease were associated with both SI and NSI occurrence. The hazard ratios (HRs) for corticosteroids and rituximab were, respectively, 3.83 (95% CI, 2.76–5.31) and 2.60 (95% CI, 1.67–4.03) for SIs and 2.46 (95% CI, 2.19–2.76) and 1.49 (95% CI, 1.28–1.74) for NSIs. Pneumococcal vaccine showed a protective effect for both SIs and NSIs (0.38 [95% CI, 0.20–0.73] and 0.52 [95% CI, 0.43–0.65], respectively), as did influenza vaccine (0.42 [95% CI, 0.27–0.64] and 0.49 [95% CI, 0.41–0.59], respectively). Conclusions Chronic pulmonary disease, corticosteroids and rituximab are the main risk factors for infections, whereas pneumococcal and influenza vaccines are protective against SIs and NSIs.
doi_str_mv 10.1111/jth.13622
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We conducted a national pharmacoepidemiological study. Pulmonary disease, corticosteroids and rituximab were the main risk factors for infections. Pneumococcal and influenza vaccines were protective against infections. Summary Introduction Risk factors for infection and protective effect of vaccines in immune thrombocytopenia (ITP) patients in the era of rituximab therapy are unknown. Objectives To assess the risk factors for serious and non‐serious infections (respectively, SIs and NSIs) in non‐splenectomized adults treated for persistent or chronic primary ITP, including the effect of pneumococcal and influenza vaccines. Patients/Methods The population was the 2009–2012 FAITH cohort (n = 1805), which is the cohort of all incident (newly diagnosed) primary ITP adults treated &gt; 3 months in France built into the national health insurance database (SNIIRAM). SIs were hospitalizations with any infection as the primary diagnosis code. NSIs were identified using out‐of‐hospital antibiotic dispensing. Cox models were performed. Results Incidence rates were 6.3/100 patient‐years (95% confidence interval [CI], 5.4–7.4) for SIs (lower respiratory tract in 42.8% of the cases) and 100.5/100 patient‐years (95% CI, 95.0–106.3) for NSIs. In multivariate analyses, increasing age and chronic pulmonary disease were associated with both SI and NSI occurrence. The hazard ratios (HRs) for corticosteroids and rituximab were, respectively, 3.83 (95% CI, 2.76–5.31) and 2.60 (95% CI, 1.67–4.03) for SIs and 2.46 (95% CI, 2.19–2.76) and 1.49 (95% CI, 1.28–1.74) for NSIs. Pneumococcal vaccine showed a protective effect for both SIs and NSIs (0.38 [95% CI, 0.20–0.73] and 0.52 [95% CI, 0.43–0.65], respectively), as did influenza vaccine (0.42 [95% CI, 0.27–0.64] and 0.49 [95% CI, 0.41–0.59], respectively). Conclusions Chronic pulmonary disease, corticosteroids and rituximab are the main risk factors for infections, whereas pneumococcal and influenza vaccines are protective against SIs and NSIs.</description><identifier>ISSN: 1538-7933</identifier><identifier>ISSN: 1538-7836</identifier><identifier>EISSN: 1538-7836</identifier><identifier>DOI: 10.1111/jth.13622</identifier><identifier>PMID: 28078756</identifier><language>eng</language><publisher>England: Elsevier Limited</publisher><subject>Adrenal Cortex Hormones - adverse effects ; Adrenal Cortex Hormones - therapeutic use ; Adult ; Aged ; Cohort Studies ; Female ; France ; glucocorticoids ; Humans ; immune thrombocytopenia ; infection ; Infections ; Influenza ; Influenza Vaccines - therapeutic use ; Lung Diseases - complications ; Male ; Middle Aged ; Multivariate Analysis ; Pneumococcal Vaccines - therapeutic use ; Proportional Hazards Models ; Purpura, Thrombocytopenic, Idiopathic - complications ; Risk Factors ; rituximab ; Rituximab - adverse effects ; Rituximab - therapeutic use ; Spleen ; Splenectomy ; Treatment Outcome ; vaccine ; Vaccines</subject><ispartof>Journal of thrombosis and haemostasis, 2017-04, Vol.15 (4), p.785-791</ispartof><rights>2017 International Society on Thrombosis and Haemostasis</rights><rights>2017 International Society on Thrombosis and Haemostasis.</rights><rights>Copyright © 2017 International Society on Thrombosis and Haemostasis</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3882-56fd0fd3dac2eca879b07365020212f160dd739587c5d8574841cbb25556a9183</citedby><cites>FETCH-LOGICAL-c3882-56fd0fd3dac2eca879b07365020212f160dd739587c5d8574841cbb25556a9183</cites><orcidid>0000-0001-9953-4640</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28078756$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moulis, G.</creatorcontrib><creatorcontrib>Lapeyre‐Mestre, M.</creatorcontrib><creatorcontrib>Palmaro, A.</creatorcontrib><creatorcontrib>Sailler, L.</creatorcontrib><title>Infections in non‐splenectomized persistent or chronic primary immune thrombocytopenia adults: risk factors and vaccination effect</title><title>Journal of thrombosis and haemostasis</title><addtitle>J Thromb Haemost</addtitle><description>Essentials The risk factors for infection in immune thrombocytopenia are not well known. We conducted a national pharmacoepidemiological study. Pulmonary disease, corticosteroids and rituximab were the main risk factors for infections. Pneumococcal and influenza vaccines were protective against infections. Summary Introduction Risk factors for infection and protective effect of vaccines in immune thrombocytopenia (ITP) patients in the era of rituximab therapy are unknown. Objectives To assess the risk factors for serious and non‐serious infections (respectively, SIs and NSIs) in non‐splenectomized adults treated for persistent or chronic primary ITP, including the effect of pneumococcal and influenza vaccines. Patients/Methods The population was the 2009–2012 FAITH cohort (n = 1805), which is the cohort of all incident (newly diagnosed) primary ITP adults treated &gt; 3 months in France built into the national health insurance database (SNIIRAM). SIs were hospitalizations with any infection as the primary diagnosis code. NSIs were identified using out‐of‐hospital antibiotic dispensing. Cox models were performed. Results Incidence rates were 6.3/100 patient‐years (95% confidence interval [CI], 5.4–7.4) for SIs (lower respiratory tract in 42.8% of the cases) and 100.5/100 patient‐years (95% CI, 95.0–106.3) for NSIs. In multivariate analyses, increasing age and chronic pulmonary disease were associated with both SI and NSI occurrence. The hazard ratios (HRs) for corticosteroids and rituximab were, respectively, 3.83 (95% CI, 2.76–5.31) and 2.60 (95% CI, 1.67–4.03) for SIs and 2.46 (95% CI, 2.19–2.76) and 1.49 (95% CI, 1.28–1.74) for NSIs. Pneumococcal vaccine showed a protective effect for both SIs and NSIs (0.38 [95% CI, 0.20–0.73] and 0.52 [95% CI, 0.43–0.65], respectively), as did influenza vaccine (0.42 [95% CI, 0.27–0.64] and 0.49 [95% CI, 0.41–0.59], respectively). Conclusions Chronic pulmonary disease, corticosteroids and rituximab are the main risk factors for infections, whereas pneumococcal and influenza vaccines are protective against SIs and NSIs.</description><subject>Adrenal Cortex Hormones - adverse effects</subject><subject>Adrenal Cortex Hormones - therapeutic use</subject><subject>Adult</subject><subject>Aged</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>France</subject><subject>glucocorticoids</subject><subject>Humans</subject><subject>immune thrombocytopenia</subject><subject>infection</subject><subject>Infections</subject><subject>Influenza</subject><subject>Influenza Vaccines - therapeutic use</subject><subject>Lung Diseases - complications</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Pneumococcal Vaccines - therapeutic use</subject><subject>Proportional Hazards Models</subject><subject>Purpura, Thrombocytopenic, Idiopathic - complications</subject><subject>Risk Factors</subject><subject>rituximab</subject><subject>Rituximab - adverse effects</subject><subject>Rituximab - therapeutic use</subject><subject>Spleen</subject><subject>Splenectomy</subject><subject>Treatment Outcome</subject><subject>vaccine</subject><subject>Vaccines</subject><issn>1538-7933</issn><issn>1538-7836</issn><issn>1538-7836</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kLtOwzAUhi0EglIYeAFkiYmhrS917LAhxKWoEkuZI8d2VJfGDnYCKhMDD8Az8iS4tLBxFh8dffp--QfgBKMhTjNatPMhphkhO6CHGRUDLmi2-7vnlB6AwxgXCOGcEbQPDohAXHCW9cDHxFVGtda7CK2Dzruv98_YLI1LV1_bN6NhY0K0sTWuhT5ANQ_eWQWbYGsZVtDWdecMbNO5Lr1atb4xzkoodbds4wUMNj7BSiZbiFA6DV-kUtbJdSY01Tr9COxVchnN8fbtg8eb69nV3WD6cDu5upwOFBWCDFhWaVRpqqUiRknB8xJxmjFEEMGkwhnSmtOcCa6YFoyPxRirsiSMsUzmWNA-ONt4m-CfOxPbYuG74FJkgYWgGI8Rx4k631Aq-BiDqYrtVwuMinXfReq7-Ok7sadbY1fWRv-RvwUnYLQBXu3SrP43Ffezu43yGzh-jVI</recordid><startdate>201704</startdate><enddate>201704</enddate><creator>Moulis, G.</creator><creator>Lapeyre‐Mestre, M.</creator><creator>Palmaro, A.</creator><creator>Sailler, L.</creator><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0001-9953-4640</orcidid></search><sort><creationdate>201704</creationdate><title>Infections in non‐splenectomized persistent or chronic primary immune thrombocytopenia adults: risk factors and vaccination effect</title><author>Moulis, G. ; Lapeyre‐Mestre, M. ; Palmaro, A. ; Sailler, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3882-56fd0fd3dac2eca879b07365020212f160dd739587c5d8574841cbb25556a9183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adrenal Cortex Hormones - adverse effects</topic><topic>Adrenal Cortex Hormones - therapeutic use</topic><topic>Adult</topic><topic>Aged</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>France</topic><topic>glucocorticoids</topic><topic>Humans</topic><topic>immune thrombocytopenia</topic><topic>infection</topic><topic>Infections</topic><topic>Influenza</topic><topic>Influenza Vaccines - therapeutic use</topic><topic>Lung Diseases - complications</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Pneumococcal Vaccines - therapeutic use</topic><topic>Proportional Hazards Models</topic><topic>Purpura, Thrombocytopenic, Idiopathic - complications</topic><topic>Risk Factors</topic><topic>rituximab</topic><topic>Rituximab - adverse effects</topic><topic>Rituximab - therapeutic use</topic><topic>Spleen</topic><topic>Splenectomy</topic><topic>Treatment Outcome</topic><topic>vaccine</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moulis, G.</creatorcontrib><creatorcontrib>Lapeyre‐Mestre, M.</creatorcontrib><creatorcontrib>Palmaro, A.</creatorcontrib><creatorcontrib>Sailler, L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><jtitle>Journal of thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moulis, G.</au><au>Lapeyre‐Mestre, M.</au><au>Palmaro, A.</au><au>Sailler, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Infections in non‐splenectomized persistent or chronic primary immune thrombocytopenia adults: risk factors and vaccination effect</atitle><jtitle>Journal of thrombosis and haemostasis</jtitle><addtitle>J Thromb Haemost</addtitle><date>2017-04</date><risdate>2017</risdate><volume>15</volume><issue>4</issue><spage>785</spage><epage>791</epage><pages>785-791</pages><issn>1538-7933</issn><issn>1538-7836</issn><eissn>1538-7836</eissn><abstract>Essentials The risk factors for infection in immune thrombocytopenia are not well known. We conducted a national pharmacoepidemiological study. Pulmonary disease, corticosteroids and rituximab were the main risk factors for infections. Pneumococcal and influenza vaccines were protective against infections. Summary Introduction Risk factors for infection and protective effect of vaccines in immune thrombocytopenia (ITP) patients in the era of rituximab therapy are unknown. Objectives To assess the risk factors for serious and non‐serious infections (respectively, SIs and NSIs) in non‐splenectomized adults treated for persistent or chronic primary ITP, including the effect of pneumococcal and influenza vaccines. Patients/Methods The population was the 2009–2012 FAITH cohort (n = 1805), which is the cohort of all incident (newly diagnosed) primary ITP adults treated &gt; 3 months in France built into the national health insurance database (SNIIRAM). SIs were hospitalizations with any infection as the primary diagnosis code. NSIs were identified using out‐of‐hospital antibiotic dispensing. Cox models were performed. Results Incidence rates were 6.3/100 patient‐years (95% confidence interval [CI], 5.4–7.4) for SIs (lower respiratory tract in 42.8% of the cases) and 100.5/100 patient‐years (95% CI, 95.0–106.3) for NSIs. In multivariate analyses, increasing age and chronic pulmonary disease were associated with both SI and NSI occurrence. The hazard ratios (HRs) for corticosteroids and rituximab were, respectively, 3.83 (95% CI, 2.76–5.31) and 2.60 (95% CI, 1.67–4.03) for SIs and 2.46 (95% CI, 2.19–2.76) and 1.49 (95% CI, 1.28–1.74) for NSIs. Pneumococcal vaccine showed a protective effect for both SIs and NSIs (0.38 [95% CI, 0.20–0.73] and 0.52 [95% CI, 0.43–0.65], respectively), as did influenza vaccine (0.42 [95% CI, 0.27–0.64] and 0.49 [95% CI, 0.41–0.59], respectively). Conclusions Chronic pulmonary disease, corticosteroids and rituximab are the main risk factors for infections, whereas pneumococcal and influenza vaccines are protective against SIs and NSIs.</abstract><cop>England</cop><pub>Elsevier Limited</pub><pmid>28078756</pmid><doi>10.1111/jth.13622</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-9953-4640</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adrenal Cortex Hormones - adverse effects
Adrenal Cortex Hormones - therapeutic use
Adult
Aged
Cohort Studies
Female
France
glucocorticoids
Humans
immune thrombocytopenia
infection
Infections
Influenza
Influenza Vaccines - therapeutic use
Lung Diseases - complications
Male
Middle Aged
Multivariate Analysis
Pneumococcal Vaccines - therapeutic use
Proportional Hazards Models
Purpura, Thrombocytopenic, Idiopathic - complications
Risk Factors
rituximab
Rituximab - adverse effects
Rituximab - therapeutic use
Spleen
Splenectomy
Treatment Outcome
vaccine
Vaccines
title Infections in non‐splenectomized persistent or chronic primary immune thrombocytopenia adults: risk factors and vaccination effect
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