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

Autor: 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
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Male
p<
56 patients had chronic ITP
which was significantly associated with younger age. Chronicity at 12 months was not affected by different therapeutic approaches at diagnosis or response to therapy
thrombocytopenia
0.001) . At 1 year
95% confidence interval: 1.09-2.98). In total
Background - 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. Materials and methods - 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. Results - 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<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<0.001)
and recent viral infection (p<0.001) . At 1 year
56 patients had chronic ITP
which was associated with older median age (7.54 vs 5.35 years

p<0.001)
and a family history of autoimmunity (p<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. Discussion - 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

Prospective Studies
Child
Children
clinical symptoms
which was associated with older median age (7.54 vs 5.35 years
treatment
Background - The aim of the present study was to assess management strategies for immune thrombocytopenia (ITP) among Italian paediatric haematologists
Immunoglobulins
Intravenous

Italy
80 steroids). Response to intravenous immunoglobulins did not have an effect on remission rate at 12 months. Discussion - Pediatric hematologists in Italian Centre treat over three-quarters of patients with newly diagnosed ITP
Child
Preschool

Practice Guidelines as Topic
Female
Steroids
Guideline Adherence
history
thrombocytopenia
pediatric
treatment

and to compare these with those of recent international guidelines. Predictors of early remission or disease chronicity were also evaluated. Materials and methods - During a period of 1 year
0.001)
Adolescent
platelet count and treatment at presentation and at subsequent visits. Results - Of the 205 patients
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
despite recent international guidelines. Almost 80% of patients with mild clinical symptoms received pharmacological treatment at diagnosis
Humans
IVIG
Purpura
Thrombocytopenic
Idiopathic

Platelet Count
0.05
357 pharmacological treatments were recorded (216 intravenous immunoglobulins
Immune thrombocytopenia
ITP
Infant
47 (23%) were initially managed with a wait-and-see approach. Compared to these patients
92/202 patients (46%) had persistent ITP. Recovery within 3 months was predicted by younger median age (5.3 vs 7.8 years
and recent viral infection (p<
pediatric
Others
and a family history of autoimmunity (p<
0.001) and had lower platelet counts. At the 3-month follow-up
Follow-Up Studies
children administered platelet-enhancing therapies were significantly younger (median age: 4.75 vs 7.96 years
Zdroj: Blood Transfus
Popis: BACKGROUND: 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. MATERIALS AND METHODS: 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. RESULTS: 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
Databáze: OpenAIRE