EHA Library - The official digital education library of European Hematology Association (EHA)

MANAGEMENT OF ADULT CHRONIC IMMUNE THROMBOCYTOPENIA.SINGLE CENTER EXPERIENCE
Author(s): ,
Claudiu Ionita
Affiliations:
UMF 'Victor Babes' Timisoara,Timisoara,Romania
,
Ioana Ionita
Affiliations:
UMF 'Victor Babes' Timisoara,Timisoara,Romania
,
Despina Calamar-Popovici
Affiliations:
UMF 'Victor Babes' Timisoara,Timisoara,Romania
,
Dacian Nicolae Oros
Affiliations:
UMF 'Victor Babes' Timisoara,Timisoara,Romania
,
Maria Iordache
Affiliations:
UMF 'Victor Babes' Timisoara,Timisoara,Romania
,
Mihai Ionita
Affiliations:
UMF 'Victor Babes' Timisoara,Timisoara,Romania
,
Ioana Pascu
Affiliations:
UMF 'Victor Babes' Timisoara,Timisoara,Romania
,
Marta Ifrose
Affiliations:
UMF 'Victor Babes' Timisoara,Timisoara,Romania
Hortensia Ionita
Affiliations:
UMF 'Victor Babes' Timisoara,Timisoara,Romania
(Abstract release date: 05/18/17) EHA Library. Ionita I. 05/18/17; 182837; PB2124
Ioana Ionita
Ioana Ionita
Contributions
Abstract

Abstract: PB2124

Type: Publication Only

Background
The investigation and management of patients with Chronic immune thrombocytopenic purpura (ITP) varies widely. Although many treatments have been recommended for ITP, there are no evidence-bassed recommendations for when different treatments should be used, or when any treatment should be used rather than managing a patient by observation alone.

Aims

To evaluate the treatment of ITP patients in Departament of Hematology, County Hospital, Timişoara.

Methods
A retrospective study for 350 ITP patients was performed. Patients demographics, medical history, current treatments and side effects, were abstracted from the patient’s medical charts for the 15 months prior to their most recent visit.

Results

The mean age was 45.6 years with 58% women and 42% men. Median time from the diagnosis of ITP to the start of the observational period was 23 months. Regardless of the presence of bleeding symptoms, for majority of patients we started treatment based on plateled count. Treatment was considered when platelet counts are less than 20x109/L in patients without bleeding, and less than 30x109/L in patients with bleeding. Prior to the observational period, 36% of patients had been splenectomized and the most reported treatment was corticosteroids. During the observational period, 72% of all patients were treated. The most frequent reasons given for treatment were platelet count (58%), followed by bleeding symptoms (42%). Corticosteroids represented 52% of treatments, followed by IVIg (20%), azathioprine (12%) rituximab and 8% Nplate. Splenectomies (8% of patients) and platelet transfusions (27% of patients) were performed during the observational period. In the patient survey, 52% of participants were 60 years of age or older and the duration of disease was more than 10 years in 43% of patients. The minimum platelet counts were less than 10x109/L in 49% of patients. The most common symptoms of ITP was fatigue (45%). Approximately 60% of patients reported at least one side effect associated with ITP treatment. The side effects were most frequently associated with corticosteroid use (43%). Overall, 40% of patients required hospitalization. Mean duration of hospitalization was 13,5 days.

Conclusion
The retrospective study of 350 patients provides the results of treatment practices in our country. It showed that bleeding symptoms remained quite frequent among patients with chronic ITP. Corticosteroids were the most widely used treatment.

Session topic: 32. Platelets disorders

Keyword(s): adult, Thrombocytopenia

Abstract: PB2124

Type: Publication Only

Background
The investigation and management of patients with Chronic immune thrombocytopenic purpura (ITP) varies widely. Although many treatments have been recommended for ITP, there are no evidence-bassed recommendations for when different treatments should be used, or when any treatment should be used rather than managing a patient by observation alone.

Aims

To evaluate the treatment of ITP patients in Departament of Hematology, County Hospital, Timişoara.

Methods
A retrospective study for 350 ITP patients was performed. Patients demographics, medical history, current treatments and side effects, were abstracted from the patient’s medical charts for the 15 months prior to their most recent visit.

Results

The mean age was 45.6 years with 58% women and 42% men. Median time from the diagnosis of ITP to the start of the observational period was 23 months. Regardless of the presence of bleeding symptoms, for majority of patients we started treatment based on plateled count. Treatment was considered when platelet counts are less than 20x109/L in patients without bleeding, and less than 30x109/L in patients with bleeding. Prior to the observational period, 36% of patients had been splenectomized and the most reported treatment was corticosteroids. During the observational period, 72% of all patients were treated. The most frequent reasons given for treatment were platelet count (58%), followed by bleeding symptoms (42%). Corticosteroids represented 52% of treatments, followed by IVIg (20%), azathioprine (12%) rituximab and 8% Nplate. Splenectomies (8% of patients) and platelet transfusions (27% of patients) were performed during the observational period. In the patient survey, 52% of participants were 60 years of age or older and the duration of disease was more than 10 years in 43% of patients. The minimum platelet counts were less than 10x109/L in 49% of patients. The most common symptoms of ITP was fatigue (45%). Approximately 60% of patients reported at least one side effect associated with ITP treatment. The side effects were most frequently associated with corticosteroid use (43%). Overall, 40% of patients required hospitalization. Mean duration of hospitalization was 13,5 days.

Conclusion
The retrospective study of 350 patients provides the results of treatment practices in our country. It showed that bleeding symptoms remained quite frequent among patients with chronic ITP. Corticosteroids were the most widely used treatment.

Session topic: 32. Platelets disorders

Keyword(s): adult, Thrombocytopenia

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