Bleeding risk assessment in immune thrombocytopenia.

Bleeding Disorder Bleeding Risk ITP Immune Thrombocytopenia Platelet Dysfunction Sonoclot Thrombocytopenia

Journal

Annals of hematology
ISSN: 1432-0584
Titre abrégé: Ann Hematol
Pays: Germany
ID NLM: 9107334

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 07 08 2023
accepted: 18 09 2023
pubmed: 23 9 2023
medline: 23 9 2023
entrez: 22 9 2023
Statut: ppublish

Résumé

The bleeding risk in immune thrombocytopenia (ITP) is related not only to low platelet count but also to the presence of platelet dysfunction. However, diagnosing a concomitant platelet dysfunction is challenging as most of the available platelet function assays (PFAs) require a platelet count of greater than 100,000/μL. Sonoclot coagulation and platelet function analyzer works on the principle of viscoelastometry, and results remain unaffected by the platelet counts. To assess the platelet function in adult acute ITP patients with the help of sonoclot coagulation and platelet function analyzer and correlate it with the risk of bleeding. Newly diagnosed acute ITP patients with a platelet count less than 20,000/μL were divided into two groups based on WHO bleeding grade: ITP non-bleeder (ITP-NB) group (WHO bleeding grade ≤1) and ITP bleeder (ITP-B) group (WHO bleeding grade ≥2). Platelet function was assessed by sonoclot in both groups. The patients without significant bleeding (ITP-NB) were followed up monthly for six months with the assessment of platelet function during each contact. Eighty patients (30 ITP-B and 50 ITP-NB) were prospectively included in this study. The median age of patients in the two groups was 37 years and 30 years, respectively. The female-to-male ratio was 4:1 and 1:1 in ITP-B and ITP-NB groups. The median platelet count in ITP-B and ITP-NB was 12000/μL (range 1000-19000/μL) and 8000/μL (range 1000-19000/μL), respectively. Mean platelet functions by sonoclot in both groups were lower than the normal cut-off (>1.6). However, the mean platelet function in the ITP-B group (0.2 + 0.17) was significantly lower than the ITP-NB group (1.2 ± 0.52) (p = 0.01). During the follow-up period of 6 months, patients in ITP-NB with a normal platelet function (>1.6) on sonoclot had lesser episodes (one episode) of clinically significant bleeding than patients with a low platelet function (4 episodes). Patients with acute severe thrombocytopenia and bleeding phenotype have a greater abnormality on platelet function by sonoclot than patients with non-bleeding phenotype. This information may help in taking therapeutic decisions in patients with acute ITP.

Identifiants

pubmed: 37740064
doi: 10.1007/s00277-023-05466-1
pii: 10.1007/s00277-023-05466-1
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3007-3014

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Kundan Mishra (K)

Department of Clinical Hematology and Medical Oncology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India. mishrak20@gmail.com.
Department of Clinical Hematology, Army Hospital (Research and Referral), New Delhi, 110010, India. mishrak20@gmail.com.

Aditya Jandial (A)

Department of Clinical Hematology and Medical Oncology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Rajeev Sandal (R)

Department of Clinical Hematology and Medical Oncology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Regional Cancer Centre, Indira Gandhi Medical College, Shimla, 171001, India.

Ashok Meshram (A)

Department of Clinical Hematology and Medical Oncology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Deepesh Lad (D)

Department of Clinical Hematology and Medical Oncology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Gaurav Prakash (G)

Department of Clinical Hematology and Medical Oncology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Alka Khadwal (A)

Department of Clinical Hematology and Medical Oncology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Rajan Kapoor (R)

Department of Clinical Hematology, Army Hospital (Research and Referral), New Delhi, 110010, India.

Jasmina Ahluwalia (J)

Department of Hematology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Neelam Varma (N)

Department of Hematology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Subhash Varma (S)

Department of Clinical Hematology and Medical Oncology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

R K Dhiman (RK)

Department of Hepatology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Pankaj Malhotra (P)

Department of Clinical Hematology and Medical Oncology, Post-Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.

Classifications MeSH