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Erschienen in: Indian Journal of Pediatrics 10/2016

25.04.2016 | Original Article

Coagulation Profile at Diagnosis in Patients with Acute Lymphoblastic Leukemia

verfasst von: Shivali Sehgal, Sunita Sharma, Jagdish Chandra, Anita Nangia

Erschienen in: Indian Journal of Pediatrics | Ausgabe 10/2016

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Abstract

Objective

To evaluate the coagulation parameters at the time of diagnosis in pediatric acute lymphoblastic leukemia (ALL) patients.

Methods

A total of 65 newly diagnosed ALL patients upto 18 y of age along with 30 age and sex matched controls were included in the study. Coagulation tests including Prothrombin Time (PT), Activated Partial Thromboplastin Time (APTT), Fibrinogen (FBG) assay, D-dimer (D-DI) assay, Coagulation inhibitor levels and tests for fibrinolysis were performed.

Results

At baseline, APTT of the patients was significantly prolonged (p 0.033), but PT and fibrinogen were comparable in the two groups. Protein C (PC) and Protein S (PS) were both significantly reduced in the cases, while antithrombin was comparable to control values (p < 0.001, p < 0.001 & p = 0.828 respectively). Tissue plasminogen activator levels (tPA) were significantly lower in the cases (p < 0.001) but Plasminogen activator inhibitor type 1 (PAI-1) values were comparable. D-DI levels were significantly high (p < 0.001).

Conclusions

The onset of leukemia is associated with hemostatic derangement favouring hypercoagulability. The coagulopathy is due to thrombin activation (as evidenced by raised d-dimer). The decreased fibrinolysis (due to reduced tPA and raised PAI-1) and low levels of PC and PS contribute to the hypercoagulable state at the time of diagnosis.
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Metadaten
Titel
Coagulation Profile at Diagnosis in Patients with Acute Lymphoblastic Leukemia
verfasst von
Shivali Sehgal
Sunita Sharma
Jagdish Chandra
Anita Nangia
Publikationsdatum
25.04.2016
Verlag
Springer India
Erschienen in
Indian Journal of Pediatrics / Ausgabe 10/2016
Print ISSN: 0019-5456
Elektronische ISSN: 0973-7693
DOI
https://doi.org/10.1007/s12098-016-2114-2

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