Considerations for Acquired and Inherited Blood Disorders
Course Number: 685
Course Contents
Proper Use of Clotting Factor Concentrates
Due to the complexity of managing bleeding disorders, communication between the dental provider, patient, and the patient’s hematologist is essential. Once the dentist has established a treatment plan, they must communicate with the hematologist to determine if the patient will require factor replacement prior to, post treatment or both. In addition, the hematology treatment plan must be communicated to the patient or caregiver, as well as the dentist.
Replacement factor is very expensive and there is a risk to the patient of developing antibodies or inhibitors to the factor if unnecessarily prescribed.26 A single dose of factor may cost $5,000-$10,000, and a simple plan may use 1-4 doses of factor. Factor replacement involves either human plasma-derived or human recombinant factor concentrates, some of which may be chemically modified for extended duration. In addition, other therapies include non-factor therapies (i.e. emicizumab, a bispecific antibody that links Factor IX and X and mimics Factor VIIIa’s tenase function), desmopressin (an IV medication), antifibrinolytic drugs, platelets, or fresh frozen plasma depending on the specific bleeding disorder.27 Treatments that do not pose a severe hemostatic challenge, such as restorations, should be completed in as few appointments as possible to minimize unnecessary infusions.
Many patients with bleeding disorders are capable to self-infusing IV medications at home either from a port or a butterfly needle before a procedure. Indeed, some people with severe hemophilia self-infuse factor at home two or three times a week to prevent bleeding. However, some patients may not be able to self-infuse, or they may require medications to be given at an infusion center before going to the dental provider for the dental procedure. Physical impairment from prior bleeding events resulting in arthropathy, IV access difficulty, insurance or cost concerns, and other medical illness can be barriers to self-infusion.
Because of the high costs, logistical barriers, and insurance limitations to obtain bleeding disorder treatments, it can take many weeks (or even months) to obtain the medication necessary to complete an otherwise straightforward treatment plan. However, forgoing such therapy can lead to a traumatic experience from bleeding with a dental procedure that makes the patient hesitant for future dental care. Some patients may already have medications at home, and a procedure(s) could be scheduled once a treatment plan is made.
Figure 6 demonstrates medications community used for patients with bleeding disorders that may be prescribed by the patient’s hematologist/HTC
| Types and Indications of Medications Community Used for Patients with Bleeding Disorders | |
|---|---|
| Factor Concentrate Replacement Therapy | Specifically used for factor VIII, IX, or severe von Willebrand deficiency28, 29. These factors are all given intravenously (IV) or through an injection port. |
| Human recombinant replacement factor | These are recombinant versions of human factors to replace human plasma-derived factors and their concomitant risk of blood borne infections (i.e. HIV). Several formulations from different manufacturers exist. There are also extended duration formulations where the factors have been modified chemically to stay longer in circulation and reduce the frequency of IV injections. |
| Nonfactor therapy (i.e. emicizumab) | Emicizumab is used specifically for treatment of Hemophilia A, especially if an inhibitor is present. Other agents are in clinical trials (i.e. Mim8). |
| Rebalancing agents | Several agents are in clinical trials that improve coagulation by reducing amounts of coagulation-controlling proteins such as antithrombin (i.e. Fitusiran), Tissue-Factor Pathway Inhibitor (i.e. concizumab, marstacimab) and activated protein C (i.e. serpin PC) |
| Activated prothrombin complex concentrate (aPCC) | Emergency medication given to treat bleeds not controlled by replacement factor. Nonfactor therapy may trigger thrombosis and ischemic infarcts if aPCCs are given. |
| Desmopressin (DDAVP) |
Synthetic hormone used to elevate natural factor VIII and vWD concentrations in the blood.
DDAVP is:
|
| Tranexamic Acid |
Antifibrinolytic agent used to help prevent clot degradation for minor bleeds. Maybe useful as a oral rinse or when applied on cotton sponge to improve coagulation from oral wounds.
Tranexamic acid is:
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| Aminocaproic Acid |
Aminocaproic acid, which inhibits fibrinolysis of a clot. Maybe useful as a oral rinse or when applied on cotton sponge to improve coagulation from oral wounds.
Aminocaproic acid is:
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