Bleeding Disorders

We offer a range of infusion therapies to support individuals living with bleeding disorders, helping to manage conditions that affect the body’s ability to clot blood effectively. Below, you’ll find an overview of the different conditions we support and the therapies designed to improve outcomes and quality of life.

Acquired coagulation factor deficiency

Acquired coagulation factor deficiency is a condition where the body’s ability to clot blood is impaired due to a decrease in specific clotting proteins, often affecting adults with underlying conditions such as liver disease, autoimmune disorders, or cancer. It typically presents with symptoms such as easy bruising, bleeding gums, and prolonged bleeding from cuts.

Factor X deficiency is a rare genetic bleeding disorder where Factor X, a protein crucial for clotting, is lacking in the blood, affecting individuals of any age or gender. The condition usually presents with symptoms such as nosebleeds, easy bruising, excessive bleeding after injuries, and in severe cases, spontaneous bleeding.

Hemophilia A (factor VIII deficiency) is an inherited bleeding disorder that primarily affects males, where the blood does not clot properly due to low levels of clotting factor VIII. The condition often presents with prolonged bleeding after injuries, frequent nosebleeds, and easy bruising.

Hemophilia B (factor IX deficiency) is a genetic bleeding disorder primarily affecting males, characterized by a deficiency in clotting factor IX leading to impaired blood clotting. Symptoms often include prolonged bleeding following injuries or surgeries, frequent nosebleeds, and easy bruising.

Plasminogen deficiency type 1 (PLGD-1) is a rare genetic disorder affecting individuals of any age, characterized by low levels of plasminogen, a protein essential for breaking down blood clots. This leads to the abnormal growth of fibrin-rich lesions on mucous membranes which can cause symptoms such as respiratory issues, conjunctivitis, and other complications depending on their location in the body.

Rare bleeding disorders are a group of uncommon genetic conditions characterized by deficiencies in specific clotting factors, leading to abnormal bleeding. Although they can affect individuals of any age or gender, these disorders often present early in life. Key symptoms include frequent nosebleeds, prolonged bleeding from cuts, and bruising easily.

Von Willebrand disease is a common genetic bleeding disorder caused by a deficiency or dysfunction of the van Willebrand factor, affecting both males and females. It typically presents with symptoms such as frequent nosebleeds, easy bruising, and prolonged bleeding from cuts.

Why choose AIC?

At AIC, we believe delivering infusion care requires more than medication—it requires a thoughtful, coordinated, patient-centered approach. As part of AIS Healthcare, our Advanced Infusion Care division provides specialized, team-based support to ensure treatment is delivered safely, effectively, and in the setting that best fits each patient’s needs.

With flexible infusion options, we bring care closer to you—whether in the comfort of home or at one of our infusion centers—while partnering closely with healthcare providers to streamline the experience from access and onboarding through ongoing, coordinated care.

We have an experienced therapeutic-focused team of pharmacists and nurses for consistent patient care and service delivery.

We guide you through the onboarding process and take a proactive approach to help you with insurance benefits, coverage, and financial assistance.

You have access to our dedicated team of clinical and support staff whenever you need it.

Our bleeding disorders infusion program supports a broad range of specialty medications used to help manage clotting deficiencies and reduce the risk of bleeding. Available therapies may vary based on individual patient needs. Please consult your healthcare provider with any questions regarding specific treatment options.