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Coagulation Disorders
1. Inherited: Hemophilia A
Christmas disease
von Willebrandis Disease
2. Acquired: Liver disease
Vitamin K deficiency
Anticoagulation drugs
(heparin, coumarin)
Anemia
Evaluation of bleeding disorders
1. Take history
2. Physical examination
3. Screening clinical laboratory tests
4. Observation of excessive bleeding following a surgical
procedure
History
• Bleeding problems in relatives
• Bleeding problems following operations and tooth
extractions, trauma
• Use of drugs for prevention of coagulation or pain
• Spontaneous bleeding from nose mouth etc..
Physical Examination
• Jaundice
• Petechiae: <0.2 cm
• Purpura: 0.2 cm-1 cm
• Eccymoses : >1 cm
• Spider angioma
• Oral ulcer
• Hyperplasia of gingiva
• Hemarthrosis
Screening laboratory tests
• 1. Platelet count
• 2. BT (Bleeding Time)
• 3. PT (Prothrombin Time)
• 4. aPTT (active Partial Thrombopastin Time)
• 5. TT (Thrombin Time)
Anticoagulant (Heparin)
• Complex inhibited ( IXa, Xa, Xla, XIla)
• Used in deep vein thrombosis, renal dialysis > Rapid
onset, Duration 4-6hrs (given IV)
• Monitoring by aPTT: 50-65 sec
• Discontinue 6 hrs before surgery then reinstituting
therapy 6-12hrs post-op
Antiplatelet (Asprin)
• Inhibit cycloxygenase, TXA2 formation!
• Analgesic drug impairs platelet function
• Arterial thrombosis, MI
• Tests-BT, aPTT
• If tests are abnormal, MD should be consulted
before dental surgery is done
• Stop aspirin for 5 days, substitute alternative drug
in consultation with MD
Thrombocytopenic purpura
• Thrombocytopenic purpura is a blood disorder
characterized by an abnormal decrease in the number of
platelets in the blood
• This disease is caused by an immune reaction against one's
own platelets. It has also been called autoimmune
thrombocytopenic purpura.
• A decrease in platelets can result in easy bruising, bleeding
gums, and internal bleeding
Treatment
Platelet count of <20,000 is an indication of
treatment. 20,000-50,000 patients are
monitored. >50,000 treatment is not necessary.
• • Steroids i.e prednisone.
• Immunoglobulins (IgG).
• Anti-D administration.
• • Thrombopoietin Rececptor agonists are available.
Romiplostim & Eltrombopag.
• Surgery (splenctomy).
• Antibiotics used for the treatment of Helicobacter.pylori.
• Platelet transfusion.
Non Thrombocytopenic purpura
• Nonthrombocytopenic purpuras result from either vascular wall
fragility or thrombasthenia .
• Vascular wall fragility may result from hypersensitiv- ity
reactions, scurvy, infections, chemicals (phenacetin and
aspirin), dysproteinemia, and other causes.
• Thrombasthenia occurs in uremia, Glanzmann disease, aspirin
ingestion, and von-Willebrand disease
• Both types of nonthrombocytopenic purpura may result in
Treatment
1) Treatment consists primarily of direct pressure
applied for at least 15 min.
2) This initial pressure should control the bleed- ing
unless coagulation times are abnormal or reinjury
occurs.
3) Surgical therapy should be avoided until the
qualitative and quantitative platelet problems are
resolved.

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Coagulation and Bleeding Disorders Guide

  • 1. Coagulation Disorders 1. Inherited: Hemophilia A Christmas disease von Willebrandis Disease 2. Acquired: Liver disease Vitamin K deficiency Anticoagulation drugs (heparin, coumarin) Anemia
  • 2. Evaluation of bleeding disorders 1. Take history 2. Physical examination 3. Screening clinical laboratory tests 4. Observation of excessive bleeding following a surgical procedure
  • 3. History • Bleeding problems in relatives • Bleeding problems following operations and tooth extractions, trauma • Use of drugs for prevention of coagulation or pain • Spontaneous bleeding from nose mouth etc..
  • 4. Physical Examination • Jaundice • Petechiae: <0.2 cm • Purpura: 0.2 cm-1 cm • Eccymoses : >1 cm • Spider angioma • Oral ulcer • Hyperplasia of gingiva • Hemarthrosis
  • 5. Screening laboratory tests • 1. Platelet count • 2. BT (Bleeding Time) • 3. PT (Prothrombin Time) • 4. aPTT (active Partial Thrombopastin Time) • 5. TT (Thrombin Time)
  • 6. Anticoagulant (Heparin) • Complex inhibited ( IXa, Xa, Xla, XIla) • Used in deep vein thrombosis, renal dialysis > Rapid onset, Duration 4-6hrs (given IV) • Monitoring by aPTT: 50-65 sec • Discontinue 6 hrs before surgery then reinstituting therapy 6-12hrs post-op
  • 7. Antiplatelet (Asprin) • Inhibit cycloxygenase, TXA2 formation! • Analgesic drug impairs platelet function • Arterial thrombosis, MI • Tests-BT, aPTT • If tests are abnormal, MD should be consulted before dental surgery is done • Stop aspirin for 5 days, substitute alternative drug in consultation with MD
  • 8. Thrombocytopenic purpura • Thrombocytopenic purpura is a blood disorder characterized by an abnormal decrease in the number of platelets in the blood • This disease is caused by an immune reaction against one's own platelets. It has also been called autoimmune thrombocytopenic purpura. • A decrease in platelets can result in easy bruising, bleeding gums, and internal bleeding
  • 9. Treatment Platelet count of <20,000 is an indication of treatment. 20,000-50,000 patients are monitored. >50,000 treatment is not necessary. • • Steroids i.e prednisone. • Immunoglobulins (IgG). • Anti-D administration. • • Thrombopoietin Rececptor agonists are available. Romiplostim & Eltrombopag. • Surgery (splenctomy). • Antibiotics used for the treatment of Helicobacter.pylori. • Platelet transfusion.
  • 10. Non Thrombocytopenic purpura • Nonthrombocytopenic purpuras result from either vascular wall fragility or thrombasthenia . • Vascular wall fragility may result from hypersensitiv- ity reactions, scurvy, infections, chemicals (phenacetin and aspirin), dysproteinemia, and other causes. • Thrombasthenia occurs in uremia, Glanzmann disease, aspirin ingestion, and von-Willebrand disease • Both types of nonthrombocytopenic purpura may result in
  • 11. Treatment 1) Treatment consists primarily of direct pressure applied for at least 15 min. 2) This initial pressure should control the bleed- ing unless coagulation times are abnormal or reinjury occurs. 3) Surgical therapy should be avoided until the qualitative and quantitative platelet problems are resolved.