Long-Term Joint Function and Quality of Life Following Emicizumab Prophylaxis in Severe Hemophilia A: A Single-Center

Ramnath P Nevrekar1, Gauri Nilajkar1, Anar Khandeparkar1

  • 1Department of Medicine, Goa Medical College, Goa, IND.

Cureus
|October 3, 2025
PubMed

Background Hemophilia A (HA) is an established inherited bleeding condition caused by the lack of factor VIII, which causes recurrent joint hemorrhages and related adverse outcomes. Emicizumab, a bispecific monoclonal antibody, provides sustained prophylaxis, minimizing bleeding episodes and enhancing treatment adherence. This study assesses its impact on joint health, functional independence, and quality of life (QoL) in Indian patients with severe HA. Methodology This retrospective study, conducted at Goa Medical College, Goa, India, involved 20 patients with severe HA receiving emicizumab prophylactic therapy over a period of one year from January 2023 to January 2024. Outcomes were judged using the Hemophilia Joint Health Score (HJHS), annualized bleed rate (ABR), functional independence score in hemophilia (FISH), and the European Quality of Life 5-Dimension 5-Level (EQ-5D-5L) questionnaire for a period of one year. Ethical approval was secured for the study, and patient confidentiality was upheld. Results This study comprised 20 male participants (median age: 30.15 years), of whom 90% had severe HA and 55% had inhibitors present. Most (90%) participants were on an on-demand treatment protocol. At baseline, 90% of participants had target joints (mean: 4.7±2.51), and the mean ABR was 24.6±9.02. Over 12 months, HJHS decreased from 36.00 to 6.05 (p<0.001), FISH improved from 14.00 to 25.95 (p<0.001), and ABR dropped by 99.8% (median: 0.00, p<0.001). The EQ-5D-5L score significantly improved (p<0.001), indicating better QoL. Treatment adherence was 100%, with no adverse events (AEs). Conclusions Emicizumab demonstrated significant benefits in severe HA, including improved joint health, enhanced functional independence, and a better QoL over the course of 12 months. With 100% adherence and no AEs reported, it proves to be a feasible and well-tolerated prophylactic option. These findings support its long-term role in disease management, warranting further research in diverse patient populations.

Related Concept Videos

Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents01:29

Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents

Crohn's disease is an inflammatory bowel disorder marked by chronic inflammation of the GI tract. Various treatment strategies for Crohn's disease are employed, such as immunomodulatory agents, glucocorticoids, and biologics or anti-TNF therapy. Azathioprine (Imuran), a commonly used immunomodulatory drug for Crohn's disease, is converted in the body to mercaptopurine, which inhibits purine biosynthesis and cell proliferation. Both are utilized in severe cases of Inflammatory Bowel Disease...
Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF01:24

Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF

Tumor Necrosis Factor (TNF), a proinflammatory cytokine, contributes significantly to the inflammation seen in Crohn's disease. It exists as soluble TNF and membrane-bound TNF, with actions mediated through TNF receptors (TNFR). TNFR activation leads to the release of proinflammatory cytokines, T-cell activation, collagen production, and leukocyte migration, all contributing to inflammation in Crohn's disease. Anti-TNF monoclonal antibodies, namely infliximab (Remicade), adalimumab (Humira),...
Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids01:21

Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids

Glucocorticoids, a class of anti-inflammatory drugs, are pivotal in treating moderate to severe Crohn's disease by inducing remission. They exhibit their anti-inflammatory action by inhibiting the production of inflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-1, and chemokines like IL-8. In addition, they reduce the expression of inflammatory cell adhesion molecules and inhibit gene transcription of nitric oxide synthase, phospholipase A2, cyclooxygenase-2 (COX-2),...
Rheumatic Heart Disease I: Introduction01:23

Rheumatic Heart Disease I: Introduction

Rheumatic heart disease or RHD is a chronic condition that results from rheumatic fever, causing permanent damage to the heart valves.Etiology and Risk FactorsIt primarily arises from rheumatic fever, an inflammatory disease that can develop after untreated or inadequately treated group A streptococcal (GAS) pharyngitis. Streptococcus spreads through direct contact with oral or respiratory secretions. While the bacteria are the causative agents, factors like malnutrition, overcrowding, poor...
Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies01:22

Rheumatic Heart Disease II: Clinical Manifestations and Diagnostic Studies

The key clinical manifestations of Rheumatic heart disease (RHD) include several distinct cardiac symptoms.Carditis, a hallmark of acute rheumatic fever, involves inflammation of the heart's endocardium, myocardium, and pericardium. Chronic RHD often results from recurrent episodes of carditis. Its symptoms include the following:Murmurs are caused by valvular damage, especially to the mitral and aortic valves. Mitral stenosis or regurgitation is common, with characteristic heart murmurs...
Rheumatic Heart Disease III: Medical Management01:21

Rheumatic Heart Disease III: Medical Management

Rheumatic heart disease (RHD) management can be divided into two main strategies: prevention and long-term management.Primary PreventionPrimary prevention focuses on timely diagnosis and management of group A streptococcal pharyngitis to prevent acute rheumatic fever. The most widely used antibiotic for treating this condition is intramuscular benzathine penicillin G.Acute Rheumatic Fever TreatmentThe primary treatment goal for a patient diagnosed with acute rheumatic fever is to suppress the...