DefinePK

DefinePK hosts the largest index of Pakistani journals, research articles, news headlines, and videos. It also offers chapter-level book search.

Postpartum Acquired Hemophilia (PAH) – A Rare Entity


Article Information

Title: Postpartum Acquired Hemophilia (PAH) – A Rare Entity

Authors: Safia Mehmood Khan, Saima Siddiqui, Qurat-Ul-Ain Abedin

Journal: National Journal of Health Sciences

HEC Recognition History
Category From To
Y 2024-10-01 2025-12-31
Y 2023-07-01 2024-09-30
Y 2022-07-01 2023-06-30

Publisher: National Institute of Blood Disease Welfare Society

Country: Pakistan

Year: 2022

Volume: 7

Issue: 2

Language: en

Categories

Abstract

Objective: Acquired Hemophilia A (AHA) is a rare autoimmune disease that can result in life threatening bleeding. Formation ofauto-antibodies (inhibitors) against coagulation factor VIII develops the hemorrhagic syndrome that may appear at any age; however,prevalence of AHA is chiefly observed in post-partum and elderly persons. Idiopathic acquired hemophilia is commonest type of acquiredhemophilia whereas it is also associated with autoimmune disease, malignant neoplasm, medication and vaccinations. Post-partum acquiredhemophilia (PAH) may develop due to development of antibodies against fetal FVIII. In this case report, 36-year-old Asian woman presentedwith complain of bruises from 2 months. There was history of cesarean section four months ago. Family history, past medical and drug historywere not significant. As there was no active bleeding, patient was started an oral prednisolone along with azathioprine and was counseledregarding disease and precautions. Patient presented after 2 weeks with severe PV bleed, anemia secondary to self-induced medicine abortion.For this she receives pack cells and cryoprecipitate. Steroids and azathioprine were continued and patient was discharged in stable condition.Her ultrasound pelvis however showed small fibroids. Patient went back to her village where she again develops severe PV bleed and for thatshe underwent hysterectomy. Patient presented in our hospital with severe operative site bleeding, pain and anemia. She was managed withPacked Red Blood (PRBCs), Fresh Frozen Plasma (FFP), Recombinant Activated Clotting Factor VII (rFVIIa), prednisolone IV andazathioprine PO. Her Activated Partial Thromboplastin, Hemoglobin were continuously monitored. After a week bleeding was stopped butActivated Partial Thromboplastin Time (APTT) was still prolonged so we tapered rFVIIa dose and advice two sessions of plasmapheresis.APTT, hemoglobin levels, inhibitor titer, High-Sensitivity C - reactive protein (hs-CRP) levels were improved. Patient was discharged in astable condition and was advised to continue medication at home with supportive care and wound dressing.


Paper summary is not available for this article yet.

Loading PDF...

Loading Statistics...