Haemostatic Profile in Patients of Myeloproliferative Neoplasms-A Tertiary Care Centre Experience

Introduction: Patients of MPN commonly present with abnormalities in laboratory coagulation tests that are consistent with hypercoagulable state. Some individuals with MPN exhibit a pattern of exclusive bleeding or thrombotic events; many others have both bleeding and thrombosis during the cours...

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Main Authors: Yatendra Parashar, Rashmi Kushwaha, Ashutosh Kumar, Kamal Agarwal, U.S Singh, Mili Jain, S.P Verma, A.K Tripathi
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2016-11-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/8840/19985_CE(Ra1)_F(AK)_PF1(ROAK)_PFA(AK)_PF2(OPR_P).pdf
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author Yatendra Parashar
Rashmi Kushwaha
Ashutosh Kumar
Kamal Agarwal
U.S Singh
Mili Jain
S.P Verma
A.K Tripathi
author_facet Yatendra Parashar
Rashmi Kushwaha
Ashutosh Kumar
Kamal Agarwal
U.S Singh
Mili Jain
S.P Verma
A.K Tripathi
author_sort Yatendra Parashar
collection DOAJ
description Introduction: Patients of MPN commonly present with abnormalities in laboratory coagulation tests that are consistent with hypercoagulable state. Some individuals with MPN exhibit a pattern of exclusive bleeding or thrombotic events; many others have both bleeding and thrombosis during the course of the disease. Aim: This study was undertaken to assess the haemostatic defects and platelet functions in patients of MPN. Materials and Methods: One year prospective study was conducted at a tertiary care centre in North India in Department of Pathology in collaboration with Department of Clinical Haematology. All recently diagnosed cases of MPN along with 30 age and sex matched controls were included. Patients on antiplatelet drugs, antimyeloproliferative treatment, vitamin K agonists or antagonists, OCPs, Platelet count <1,00,000/µl, high grade fever, liver disease, pregnancy were excluded from this study. All the patients underwent screening investigations like CBC, peripheral smear evaluation, BT, PT, aPTT, Protein C and S measurement (clot based assay) and aggregation studies with ADP (5µM) (Optical Aggregometry with AGGRO/LINK 8 software and CHRONOLOG 700 aggregometer). Results: In present study, 50 cases were included. There was an occult prothrombotic state, suggested by significantly (p<0.001) reduced levels of Protein C and Protein S, but no patient presented with frank thrombosis while 8 out of 50 patients had haemorrhagic manifestations ranging from subdural haematoma to pin point petechial haemorrhages. Patients of CML-CP, ET, PV, PMF, MPN-NOS showed significantly reduced maximal aggregation with ADP (5µM) when compared to control (p<0.001). MPV also showed a statistically significant increase in these patients. Conclusion: Thrombohaemorrhagic complications significantly affect the morbidity and mortality of MPN patients. This can be assessed by the use of platelet aggregation studies, Protein C and S activities and other coagulation studies. Timely diagnosis of these prothrombotic/haemorrhagic states can decrease the morbidity in these patients.
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spelling doaj.art-a2fb4ffebe194dbcab5bc80bc6b914212022-12-21T19:20:07ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2016-11-011011EC01EC0410.7860/JCDR/2016/19985.8840Haemostatic Profile in Patients of Myeloproliferative Neoplasms-A Tertiary Care Centre ExperienceYatendra Parashar0Rashmi Kushwaha1Ashutosh Kumar2Kamal Agarwal3U.S Singh4Mili Jain5S.P Verma6A.K Tripathi7Junior Resident, Department of Pathology, King George’s Medical University, Lucknow, Uttar Pradesh, India. Associate Professor, Department of Pathology, King George’s Medical University, Lucknow, Uttar Pradesh, India.Professor and Head, Department of Pathology, King George’s Medical University, Lucknow, Uttar Pradesh, India.Professor, Department of Pathology, King George’s Medical University, Lucknow, Uttar Pradesh, India.Professor, Department of Pathology, King George’s Medical University, Lucknow, Uttar Pradesh, India.Assistant Professor, Department of Pathology, King George’s Medical University, Lucknow, Uttar Pradesh, India.Assistant Professor, Department of Clinical Hematology, King George’s Medical University, Lucknow, Uttar Pradesh, India.Head of Department of Clinical Hematology, King George’s Medical University, Lucknow, Uttar Pradesh, India.Introduction: Patients of MPN commonly present with abnormalities in laboratory coagulation tests that are consistent with hypercoagulable state. Some individuals with MPN exhibit a pattern of exclusive bleeding or thrombotic events; many others have both bleeding and thrombosis during the course of the disease. Aim: This study was undertaken to assess the haemostatic defects and platelet functions in patients of MPN. Materials and Methods: One year prospective study was conducted at a tertiary care centre in North India in Department of Pathology in collaboration with Department of Clinical Haematology. All recently diagnosed cases of MPN along with 30 age and sex matched controls were included. Patients on antiplatelet drugs, antimyeloproliferative treatment, vitamin K agonists or antagonists, OCPs, Platelet count <1,00,000/µl, high grade fever, liver disease, pregnancy were excluded from this study. All the patients underwent screening investigations like CBC, peripheral smear evaluation, BT, PT, aPTT, Protein C and S measurement (clot based assay) and aggregation studies with ADP (5µM) (Optical Aggregometry with AGGRO/LINK 8 software and CHRONOLOG 700 aggregometer). Results: In present study, 50 cases were included. There was an occult prothrombotic state, suggested by significantly (p<0.001) reduced levels of Protein C and Protein S, but no patient presented with frank thrombosis while 8 out of 50 patients had haemorrhagic manifestations ranging from subdural haematoma to pin point petechial haemorrhages. Patients of CML-CP, ET, PV, PMF, MPN-NOS showed significantly reduced maximal aggregation with ADP (5µM) when compared to control (p<0.001). MPV also showed a statistically significant increase in these patients. Conclusion: Thrombohaemorrhagic complications significantly affect the morbidity and mortality of MPN patients. This can be assessed by the use of platelet aggregation studies, Protein C and S activities and other coagulation studies. Timely diagnosis of these prothrombotic/haemorrhagic states can decrease the morbidity in these patients.https://jcdr.net/articles/PDF/8840/19985_CE(Ra1)_F(AK)_PF1(ROAK)_PFA(AK)_PF2(OPR_P).pdfhaemorrhageplatelet dysfunctionthrombosis
spellingShingle Yatendra Parashar
Rashmi Kushwaha
Ashutosh Kumar
Kamal Agarwal
U.S Singh
Mili Jain
S.P Verma
A.K Tripathi
Haemostatic Profile in Patients of Myeloproliferative Neoplasms-A Tertiary Care Centre Experience
Journal of Clinical and Diagnostic Research
haemorrhage
platelet dysfunction
thrombosis
title Haemostatic Profile in Patients of Myeloproliferative Neoplasms-A Tertiary Care Centre Experience
title_full Haemostatic Profile in Patients of Myeloproliferative Neoplasms-A Tertiary Care Centre Experience
title_fullStr Haemostatic Profile in Patients of Myeloproliferative Neoplasms-A Tertiary Care Centre Experience
title_full_unstemmed Haemostatic Profile in Patients of Myeloproliferative Neoplasms-A Tertiary Care Centre Experience
title_short Haemostatic Profile in Patients of Myeloproliferative Neoplasms-A Tertiary Care Centre Experience
title_sort haemostatic profile in patients of myeloproliferative neoplasms a tertiary care centre experience
topic haemorrhage
platelet dysfunction
thrombosis
url https://jcdr.net/articles/PDF/8840/19985_CE(Ra1)_F(AK)_PF1(ROAK)_PFA(AK)_PF2(OPR_P).pdf
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