Immune Thrombocytopenia Purpura

Key Points Two Types: Acute and ChronicDiagnosis: Established by excluding known causes of thrombocytopeniaTreatment: Depends on the platelet count and the presence and severity of bleeding.When therapy is indicated, the primary treatment options for the newly diagnosed patient are: CorticosteroidsIntravenous immunoglobulinIntravenous anti-D Ig

2017 ◽  
Vol 1 (24) ◽  
pp. 2295-2301 ◽  
Author(s):  
Cindy E. Neunert

Abstract Immune thrombocytopenia resulting from antibody-mediated platelet destruction combined with impaired platelet production is a common cause of thrombocytopenia. The decision to treat newly diagnosed patients is based on several factors including ceasing hemorrhagic manifestations, increasing the platelet count, prevention of bleeding, and inducing remission. Current standard first-line therapy is a course of corticosteroids. Although this treatment paradigm increases the platelet count in the majority of patients, a high percentage relapse after discontinuation of corticosteroid therapy. For this reason, intensification of first-line therapy that results in superior long-term remission rates would be desirable. This manuscript focuses primarily on adults with idiopathic thrombocytopenic purpura (ITP), highlighting pediatric data and practice when applicable. The primary aim is to outline upfront strategies for treatment-naive patients with ITP to enhance remission rates, taking into account assessment of the risks and benefits of these approaches.


Blood ◽  
2013 ◽  
Vol 121 (11) ◽  
pp. 1976-1981 ◽  
Author(s):  
Sif Gudbrandsdottir ◽  
Henrik Sverre Birgens ◽  
Henrik Frederiksen ◽  
Bjarne Anker Jensen ◽  
Morten Krogh Jensen ◽  
...  

Key Points In newly diagnosed ITP, addition of rituximab to dexamethasone yields higher sustained response rates than dexamethasone alone.


Blood ◽  
2014 ◽  
Vol 124 (22) ◽  
pp. 3295-3307 ◽  
Author(s):  
Katja M. J. Heitink-Pollé ◽  
Joyce Nijsten ◽  
Chantal W. B. Boonacker ◽  
Masja de Haas ◽  
Marrie C. A. Bruin

Key Points Older age, insidious onset, no preceding infection, mild bleeding, and higher platelet count are the strongest risk factors for chronic ITP. Intravenous immunoglobulin treatment seems to protect against development of chronic ITP.


Blood ◽  
2016 ◽  
Vol 127 (3) ◽  
pp. 296-302 ◽  
Author(s):  
Yu Wei ◽  
Xue-bin Ji ◽  
Ya-wen Wang ◽  
Jing-xia Wang ◽  
En-qin Yang ◽  
...  

Key Points HD-DXM is a preferred strategy to conventional prednisone as first-line management of newly diagnosed adult primary ITP.


2020 ◽  
Vol 46 (03) ◽  
pp. 256-263
Author(s):  
Annemarie E. Fogerty

AbstractThe impact of thrombocytopenia varies widely depending on the underlying pathophysiology driving it. The biggest challenge in managing thrombocytopenia in pregnancy is accurately identifying the responsible pathophysiology—a task made difficult given the tremendous overlap in clinical and laboratory abnormalities associated with different thrombocytopenia processes. The most common etiologies of thrombocytopenia in pregnancy range from physiology deemed benign to those that are life-threatening to the mother and fetus. Even in cases in which the responsible etiology is deemed benign, such as gestational thrombocytopenia, there are still implications for the management of labor and delivery, a time where hemostatic challenges may prove life-threatening. In most institutions, a minimum platelet count will be mandated for epidural anesthesia to be deemed a safe option. The causes of thrombocytopenia can also include diagnoses that are pregnancy-specific (such as preeclampsia or gestational thrombocytopenia), potentially triggered by pregnancy (such as thrombotic thrombocytopenic purpura), or unrelated to or predating the pregnancy (such as liver disease, infections, or immune thrombocytopenia purpura). It is imperative that the source of thrombocytopenia is identified accurately and expeditiously, as intervention can range from observation alone to urgent fetal delivery. In this review, the approach to diagnosis and the pathophysiological mechanisms of the most common etiologies of thrombocytopenia in pregnancy and associated management issues are presented.


Blood ◽  
2014 ◽  
Vol 123 (25) ◽  
pp. 3906-3908 ◽  
Author(s):  
David Gómez-Almaguer ◽  
Miguel A. Herrera-Rojas ◽  
José C. Jaime-Pérez ◽  
Andrés Gómez-De León ◽  
Olga G. Cantú-Rodríguez ◽  
...  

Key Points Eltrombopag/dexamethasone is a safe and effective combination for treating newly diagnosed ITP patients. This treatment may prove useful in achieving lasting responses without additional immunosuppression in some patients.


Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 1056-1056
Author(s):  
Salim Mezaache ◽  
Thibault Comont ◽  
Johanne Germain ◽  
François Montastruc ◽  
Natacha Brun ◽  
...  

Abstract Background: The incidence ofadverse drug reactions (ADRs) related to immune thrombocytopenia (ITP) drugs is not well known in the real-life practice. Aim: The principal aim of this study was to assess the incidence of ADRs related to ITP drugs. The secondary aims were to compare the incidence of ADRs depending on the drugs, and to assess the factors associated to corticosteroids-related ADR occurrence. Methods: Study population was the patients included between June 2013 and December 2014 in the CARMEN (Cytopénies Auto-immunes: Registre Midi-PyréneEN) registry. This multicenter registry is carried out on behalf of the French national center for autoimmune cytopenia and the French national center for rare diseases in immunohematology. It is aimed at the prospective follow-up of all newly diagnosed ITP adults in the French Midi-Pyrénées region (3 million inhabitants). Each investigator prospectively follows every patient newly diagnosed for ITP in routine visit or hospital stay, providing informed consent was received. ITP is defined in accordance with French guidelines: platelet count <150 x 109/L and exclusion of other causes of thrombocytopenia. CARMEN is dedicated to pharmacoepidemiological studies, with detailed recording of treatment exposure and prospective reporting of every ADR that the investigator judge significant. All ADRs are analyzed by two independent investigators at the Midi-Pyrénées Center for Pharmacovigilance. Only ADRs with a World Health Organization causality score at least "possible" were included in this study. For incidence calculations, the denominator was the period of exposure to ITP drugs. To assess the factors associated with corticosteroids-related ADRs, we performed univariate and multivariate (backward procedure) Cox models. The variables included were: age, gender, secondary vs.primary ITP, bleeding score and platelet count at diagnosis, diabetes mellitus, Charlson's comorbidity score, and number of concomitant drugs. Results: Out of 116 patients, 81 were exposed to at least one ITP drug and had at least one follow-up visit. At diagnosis, median age was 64 years (range: 18-95), 48.1% were female, 74.1% had primary ITP, 69.1% had bleeding symptoms and median platelet count was 7 x109/L. Eighty patients (98.8%) of the patients were exposed to corticosteroids, 46 (56.8%) to intravenous immunoglobulin (IVIg), 11 (13.6%) to thrombopoietin receptor agonists (TPO-RA), 7 (8.6%) to danazol and 7 to dapsone, 6 (7.4%) to rituximab. Thirty-nine patients (48.1%) experienced at least one significant ADR (58 ADRs in total). The most frequent ADRs were infections (25.0%) and endocrinal diseases (18.5%). Twenty-two (37.9%) ADRs were serious (leading to hospitalization, necessitating a new drug) and 2 were lethal. The overall incidence of ADRs related to ITP drugs was 4.2/100 persons-weeks (95% confidence interval - 95% CI: 3.2-5.2). Corticosteroids showed the highest incidence of ADR (5.2/100 persons-weeks; 95% CI: 3.6-6.8). In multivariate analysis, the 2 remaining variables associated with corticosteroids-related ADR occurrence were an age >60 years (hazard ratio - HR: 1.79, 95% CI: 0.77-4.15) and diabetes mellitus (HR: 2.73, 95% CI: 1.08-6.87). Conclusion: This first study assessing the incidence of ADRs related to ITP drugs in a real-life setting showed that they are frequent. Corticosteroids were the first drug responsible for ADRs, stressing the need of second-line treatments, particularly in older and diabetic patients. Disclosures Godeau: Roche: Research Funding; Amgen: Speakers Bureau; Novartis: Membership on an entity's Board of Directors or advisory committees, Speakers Bureau. Adoue:AMGEN: Other: Symposium presentations; Novartis: Consultancy, Membership on an entity's Board of Directors or advisory committees; GSK: Other: Symposium presentations; OCTAPHARMA: Other: Symposium presentations; PFIZER: Other: Symposium presentations; LFB: Other: Symposium presentations; ACTELION: Other: Symposium presentations.


Blood ◽  
2016 ◽  
Vol 128 (10) ◽  
pp. 1329-1335 ◽  
Author(s):  
Dongmei Sun ◽  
Nadine Shehata ◽  
Xiang Y. Ye ◽  
Sandra Gregorovich ◽  
Bryon De France ◽  
...  

Key Points Maternal platelet count response was not different for IVIg and corticosteroids in this retrospective study of pregnant women with ITP. Neonatal outcomes were overall favorable and similar after treatment of maternal ITP with IVIg or corticosteroids.


Hematology ◽  
2017 ◽  
Vol 2017 (1) ◽  
pp. 400-405 ◽  
Author(s):  
Cindy E. Neunert

Abstract Immune thrombocytopenia resulting from antibody-mediated platelet destruction combined with impaired platelet production is a common cause of thrombocytopenia. The decision to treat newly diagnosed patients is based on several factors including ceasing hemorrhagic manifestations, increasing the platelet count, prevention of bleeding, and inducing remission. Current standard first-line therapy is a course of corticosteroids. Although this treatment paradigm increases the platelet count in the majority of patients, a high percentage relapse after discontinuation of corticosteroid therapy. For this reason, intensification of first-line therapy that results in superior long-term remission rates would be desirable. This manuscript focuses primarily on adults with idiopathic thrombocytopenic purpura (ITP), highlighting pediatric data and practice when applicable. The primary aim is to outline upfront strategies for treatment-naive patients with ITP to enhance remission rates, taking into account assessment of the risks and benefits of these approaches.


2018 ◽  
Vol 9 (10) ◽  
pp. 309-317 ◽  
Author(s):  
David Gómez-Almaguer

Immune thrombocytopenia (ITP) is a bleeding disorder caused by a decrease in platelet count resulting from increased destruction and insufficient production of platelets. Although impaired regulatory T-lymphocyte activity plays a critical role in platelet destruction, many other immunologic abnormalities are also likely to be involved. Importantly, patients with ITP appear to have defects in a thrombopoietin-mediated physiological mechanism that compensates for a decrease in platelet count by increasing platelet production. Thus, simultaneous treatment of multiple pathogenic pathways involved in ITP could potentially result in synergistic efficacy. While conventional treatments for ITP suppress or modulate the immune system to reduce platelet destruction, a unique class of ITP therapy, namely thrombopoietin receptor agonists (TPO-RAs), improves platelet production by activating the thrombopoietin pathway. As hypothesized, preliminary studies show that combinations of eltrombopag, an oral TPO-RA, with conventional treatments improve outcomes in both newly diagnosed and refractory patients. In this review, the clinical experience with eltrombopag-based combinations in patients with ITP is summarized and the implications of the available data are discussed.


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