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Hand <strong>book</strong> <strong>for</strong> <strong>dental</strong> <strong>surgeons</strong> on <strong>dental</strong> management of persons with hemophilia and other haemostatic disorders<br />

DENTAL MANAGEMENT IN PERSONS WITH HEMOPHILIA<br />

AND OTHER HAEMOSTATIC DISORDERS - AN OVER VIEW<br />

Numerous procedures in <strong>dental</strong> practice may cause bleeding. Uncontrolled bleeding after minor surgical<br />

procedures like tooth extraction being one of the main complications encountered in clinical practice in normal<br />

circumstances, <strong>dental</strong> procedures can be per<strong>for</strong>med with little or no risk to the patient. However, a patient,<br />

whose ability to control bleeding is altered by drug or disease is in grave danger unless the dentist identifies the<br />

problem be<strong>for</strong>e per<strong>for</strong>ming any surgery. There<strong>for</strong>e, it is very important that proper medical and family history<br />

of the patient is collected be<strong>for</strong>e commencing any surgical procedure, and routine blood investigations should<br />

be carried to identify the bleeding disorder to reduce the risks associated with <strong>dental</strong> procedures.<br />

The <strong>dental</strong> treatment of patients with inherited bleeding disorders has been widely discussed in the literature<br />

with the aim of developing guidelines <strong>for</strong> common procedures. the majority of guidelines recommend the use of<br />

clotting factor replacement therapy be<strong>for</strong>e invasive oral surgery and the use of the inferior alveolar nerve block<br />

<strong>for</strong> restorative <strong>dental</strong> treatment. the dose of clotting factor used varies and this may be due to problems relating<br />

to both the availability and cost of factor concentrate in different parts of the world.<br />

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Hand <strong>book</strong> <strong>for</strong> <strong>dental</strong> <strong>surgeons</strong> on <strong>dental</strong> management of persons with hemophilia and other haemostatic disorders

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