Management strategies for newly diagnosed immune thrombocytopenia in Italian AIEOP Centres: do we overtreat? Data from a multicentre, prospective cohort study

The aim of the present study was to assess management strategies for immune thrombocytopenia (ITP) among Italian paediatric haematologists, and to compare these with those of recent international guidelines. Predictors of early remission or disease chronicity were also evaluated. During a period of...

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Veröffentlicht in:Blood transfusion = Trasfusione del sangue 2020-09, Vol.18 (5), p.396-405
Hauptverfasser: Parodi, Emilia, Russo, Giovanna, Farruggia, Piero, Notarangelo, Lucia D, Giraudo, Maria T, Nardi, Margherita, Giona, Fiorina, Giordano, Paola, Ramenghi, Ugo, Barone, Angelica, Boscarol, Gianluca, Cesaro, Simone, Fioredda, Francesca, Ladogana, Saverio, Licciardello, Maria, Rossi, Francesca, Rubert, Laura, Spinelli, Marco, Tucci, Fabio
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container_issue 5
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container_title Blood transfusion = Trasfusione del sangue
container_volume 18
creator Parodi, Emilia
Russo, Giovanna
Farruggia, Piero
Notarangelo, Lucia D
Giraudo, Maria T
Nardi, Margherita
Giona, Fiorina
Giordano, Paola
Ramenghi, Ugo
Barone, Angelica
Boscarol, Gianluca
Cesaro, Simone
Fioredda, Francesca
Ladogana, Saverio
Licciardello, Maria
Rossi, Francesca
Rubert, Laura
Spinelli, Marco
Tucci, Fabio
description The aim of the present study was to assess management strategies for immune thrombocytopenia (ITP) among Italian paediatric haematologists, and to compare these with those of recent international guidelines. Predictors of early remission or disease chronicity were also evaluated. During a period of 1 year, 205 children (age: 1 month-18 years) with newly diagnosed ITP were prospectively enrolled by 16 centres belonging to the Italian Association of Paediatric Haematology and Oncology (AIEOP). We collected the subjects demographic data, history, clinical symptoms, platelet count and treatment at presentation and at subsequent visits. Of the 205 patients, 47 (23%) were initially managed with a wait-and-see approach. Compared to these patients, children administered platelet-enhancing therapies were significantly younger (median age: 4.75 vs 7.96 years; p
doi_str_mv 10.2450/2020.0041-20
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Data from a multicentre, prospective cohort study</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Parodi, Emilia ; Russo, Giovanna ; Farruggia, Piero ; Notarangelo, Lucia D ; Giraudo, Maria T ; Nardi, Margherita ; Giona, Fiorina ; Giordano, Paola ; Ramenghi, Ugo ; Barone, Angelica ; Boscarol, Gianluca ; Cesaro, Simone ; Fioredda, Francesca ; Ladogana, Saverio ; Licciardello, Maria ; Rossi, Francesca ; Rubert, Laura ; Spinelli, Marco ; Tucci, Fabio</creator><creatorcontrib>Parodi, Emilia ; Russo, Giovanna ; Farruggia, Piero ; Notarangelo, Lucia D ; Giraudo, Maria T ; Nardi, Margherita ; Giona, Fiorina ; Giordano, Paola ; Ramenghi, Ugo ; Barone, Angelica ; Boscarol, Gianluca ; Cesaro, Simone ; Fioredda, Francesca ; Ladogana, Saverio ; Licciardello, Maria ; Rossi, Francesca ; Rubert, Laura ; Spinelli, Marco ; Tucci, Fabio ; “AIEOP-ITP Study Group” (Appendix 1)</creatorcontrib><description>The aim of the present study was to assess management strategies for immune thrombocytopenia (ITP) among Italian paediatric haematologists, and to compare these with those of recent international guidelines. Predictors of early remission or disease chronicity were also evaluated. During a period of 1 year, 205 children (age: 1 month-18 years) with newly diagnosed ITP were prospectively enrolled by 16 centres belonging to the Italian Association of Paediatric Haematology and Oncology (AIEOP). We collected the subjects demographic data, history, clinical symptoms, platelet count and treatment at presentation and at subsequent visits. Of the 205 patients, 47 (23%) were initially managed with a wait-and-see approach. Compared to these patients, children administered platelet-enhancing therapies were significantly younger (median age: 4.75 vs 7.96 years; p&lt;0.001) and had lower platelet counts. At the 3-month follow-up, 92/202 patients (46%) had persistent ITP. Recovery within 3 months was predicted by younger median age (5.3 vs 7.8 years; p&lt;0.001), and recent viral infection (p&lt;0.001) . At 1 year, 56 patients had chronic ITP, which was associated with older median age (7.54 vs 5.35 years; p&lt;0.001), and a family history of autoimmunity (p&lt;0.05; relative risk: 1.81; 95% confidence interval: 1.09-2.98). In total, 357 pharmacological treatments were recorded (216 intravenous immunoglobulins, 80 steroids). Response to intravenous immunoglobulins did not have an effect on remission rate at 12 months. Pediatric hematologists in Italian Centre treat over three-quarters of patients with newly diagnosed ITP, despite recent international guidelines. Almost 80% of patients with mild clinical symptoms received pharmacological treatment at diagnosis, which was significantly associated with younger age. Chronicity at 12 months was not affected by different therapeutic approaches at diagnosis or response to therapy.</description><identifier>ISSN: 1723-2007</identifier><identifier>EISSN: 2385-2070</identifier><identifier>DOI: 10.2450/2020.0041-20</identifier><identifier>PMID: 32931416</identifier><language>eng</language><publisher>Italy: Edizioni SIMTI - SIMTI Servizi Srl</publisher><subject>Adolescent ; Child ; Child, Preschool ; Female ; Follow-Up Studies ; Guideline Adherence ; Humans ; Immunoglobulins, Intravenous - administration &amp; dosage ; Immunoglobulins, Intravenous - adverse effects ; Infant ; Italy ; Male ; Others ; Platelet Count ; Practice Guidelines as Topic ; Prospective Studies ; Purpura, Thrombocytopenic, Idiopathic - blood ; Purpura, Thrombocytopenic, Idiopathic - drug therapy</subject><ispartof>Blood transfusion = Trasfusione del sangue, 2020-09, Vol.18 (5), p.396-405</ispartof><rights>SIMTI Servizi Srl 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7592159/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7592159/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32931416$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Parodi, Emilia</creatorcontrib><creatorcontrib>Russo, Giovanna</creatorcontrib><creatorcontrib>Farruggia, Piero</creatorcontrib><creatorcontrib>Notarangelo, Lucia D</creatorcontrib><creatorcontrib>Giraudo, Maria T</creatorcontrib><creatorcontrib>Nardi, Margherita</creatorcontrib><creatorcontrib>Giona, Fiorina</creatorcontrib><creatorcontrib>Giordano, Paola</creatorcontrib><creatorcontrib>Ramenghi, Ugo</creatorcontrib><creatorcontrib>Barone, Angelica</creatorcontrib><creatorcontrib>Boscarol, Gianluca</creatorcontrib><creatorcontrib>Cesaro, Simone</creatorcontrib><creatorcontrib>Fioredda, Francesca</creatorcontrib><creatorcontrib>Ladogana, Saverio</creatorcontrib><creatorcontrib>Licciardello, Maria</creatorcontrib><creatorcontrib>Rossi, Francesca</creatorcontrib><creatorcontrib>Rubert, Laura</creatorcontrib><creatorcontrib>Spinelli, Marco</creatorcontrib><creatorcontrib>Tucci, Fabio</creatorcontrib><creatorcontrib>“AIEOP-ITP Study Group” (Appendix 1)</creatorcontrib><title>Management strategies for newly diagnosed immune thrombocytopenia in Italian AIEOP Centres: do we overtreat? Data from a multicentre, prospective cohort study</title><title>Blood transfusion = Trasfusione del sangue</title><addtitle>Blood Transfus</addtitle><description>The aim of the present study was to assess management strategies for immune thrombocytopenia (ITP) among Italian paediatric haematologists, and to compare these with those of recent international guidelines. Predictors of early remission or disease chronicity were also evaluated. During a period of 1 year, 205 children (age: 1 month-18 years) with newly diagnosed ITP were prospectively enrolled by 16 centres belonging to the Italian Association of Paediatric Haematology and Oncology (AIEOP). We collected the subjects demographic data, history, clinical symptoms, platelet count and treatment at presentation and at subsequent visits. Of the 205 patients, 47 (23%) were initially managed with a wait-and-see approach. Compared to these patients, children administered platelet-enhancing therapies were significantly younger (median age: 4.75 vs 7.96 years; p&lt;0.001) and had lower platelet counts. At the 3-month follow-up, 92/202 patients (46%) had persistent ITP. Recovery within 3 months was predicted by younger median age (5.3 vs 7.8 years; p&lt;0.001), and recent viral infection (p&lt;0.001) . At 1 year, 56 patients had chronic ITP, which was associated with older median age (7.54 vs 5.35 years; p&lt;0.001), and a family history of autoimmunity (p&lt;0.05; relative risk: 1.81; 95% confidence interval: 1.09-2.98). In total, 357 pharmacological treatments were recorded (216 intravenous immunoglobulins, 80 steroids). Response to intravenous immunoglobulins did not have an effect on remission rate at 12 months. Pediatric hematologists in Italian Centre treat over three-quarters of patients with newly diagnosed ITP, despite recent international guidelines. Almost 80% of patients with mild clinical symptoms received pharmacological treatment at diagnosis, which was significantly associated with younger age. 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Data from a multicentre, prospective cohort study</atitle><jtitle>Blood transfusion = Trasfusione del sangue</jtitle><addtitle>Blood Transfus</addtitle><date>2020-09</date><risdate>2020</risdate><volume>18</volume><issue>5</issue><spage>396</spage><epage>405</epage><pages>396-405</pages><issn>1723-2007</issn><eissn>2385-2070</eissn><abstract>The aim of the present study was to assess management strategies for immune thrombocytopenia (ITP) among Italian paediatric haematologists, and to compare these with those of recent international guidelines. Predictors of early remission or disease chronicity were also evaluated. During a period of 1 year, 205 children (age: 1 month-18 years) with newly diagnosed ITP were prospectively enrolled by 16 centres belonging to the Italian Association of Paediatric Haematology and Oncology (AIEOP). We collected the subjects demographic data, history, clinical symptoms, platelet count and treatment at presentation and at subsequent visits. Of the 205 patients, 47 (23%) were initially managed with a wait-and-see approach. Compared to these patients, children administered platelet-enhancing therapies were significantly younger (median age: 4.75 vs 7.96 years; p&lt;0.001) and had lower platelet counts. At the 3-month follow-up, 92/202 patients (46%) had persistent ITP. Recovery within 3 months was predicted by younger median age (5.3 vs 7.8 years; p&lt;0.001), and recent viral infection (p&lt;0.001) . At 1 year, 56 patients had chronic ITP, which was associated with older median age (7.54 vs 5.35 years; p&lt;0.001), and a family history of autoimmunity (p&lt;0.05; relative risk: 1.81; 95% confidence interval: 1.09-2.98). In total, 357 pharmacological treatments were recorded (216 intravenous immunoglobulins, 80 steroids). Response to intravenous immunoglobulins did not have an effect on remission rate at 12 months. Pediatric hematologists in Italian Centre treat over three-quarters of patients with newly diagnosed ITP, despite recent international guidelines. Almost 80% of patients with mild clinical symptoms received pharmacological treatment at diagnosis, which was significantly associated with younger age. Chronicity at 12 months was not affected by different therapeutic approaches at diagnosis or response to therapy.</abstract><cop>Italy</cop><pub>Edizioni SIMTI - SIMTI Servizi Srl</pub><pmid>32931416</pmid><doi>10.2450/2020.0041-20</doi><tpages>10</tpages></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Adolescent
Child
Child, Preschool
Female
Follow-Up Studies
Guideline Adherence
Humans
Immunoglobulins, Intravenous - administration & dosage
Immunoglobulins, Intravenous - adverse effects
Infant
Italy
Male
Others
Platelet Count
Practice Guidelines as Topic
Prospective Studies
Purpura, Thrombocytopenic, Idiopathic - blood
Purpura, Thrombocytopenic, Idiopathic - drug therapy
title Management strategies for newly diagnosed immune thrombocytopenia in Italian AIEOP Centres: do we overtreat? Data from a multicentre, prospective cohort study
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