• Dental procedures
  resulting in bleeding can
  have serious
  consequences in a pt.
  having bleeding
  disorder……… severe
  hemorrhage or even
  death.
• 2 theories:::

                           ( MARKOWITZ----
  1903)
                                  (1964)-the
  coagulation mechanism results in a final
  explosive change of a liquid to a gel.
fibrinolysis
                          (tPA)

PLASMINOGEN    PLASMIN.

                 [FDPs]
Factor XII                  Factor XIIa                             tPA
                                          + high Mol.wt
                                            kininogen


      parakallikren                       kallikren

                                                             FV           F VIII
                      plasminogen                         plasmin




                                             fibrin
                                                                          FDPs
tPA:
   Used in thromboembolic
disoders asso with Myocardial
infarction.(effective within 1st
     6 hrs postinfarction.
Fibrinolytic system activation
          turned off
         α
 by…… 2antiplasmin/ by
   plasminogen activator
          inhibitors
       ( PAI-1,PAI-2)
CLINICAL LABORATARY TESTS
• Help to




                  Platelet count
                  Bleeding time
                   PFA-100 CT
                      PT/INR
                       aPTT
                        TT
                       FDPs
                  Factor assays
            Tests of capillary fragility
PLATELET COUNT:
• Normal-150,000 to 450,000/mm3
• If < 50,000/mm3
                            Hemorrhagic
                                stroke
                          Surgical/traumatic
                             hemorrhage
                           etc. may occur.
• In such cases platelet transfusion may be
  necessary.
TESTS OF PLATELET FUNCTION:



      ADV



                      Dis ADV
INR Intro.by WHO(1983):itz
the ratio of PT that adjusts for
     the sensitivity of the
thromboplastin reagants,such
   that normal coagulation
 profile is reported as an INR
              of 1.0
USES of PT/INR:
• Measured using a specific latex
  agglutination system.


                     Evaluates the presence
                         of a D-dimer of
                    fibrinogen / fibrin above
                          normal levels.
CUSHING’S syndrome:
Resulting from excessive corticosteroid
Intake / production.
Patient shows skin bleeding & easy bruising.
syndrome:
• Autosomal dominant disorder:
• Fragile skin vessels & easy bruising.
•   HHT
•   Abnormal telangiectatic capillaries.
•   Frequent episodes of nasal & GI bleeding.
•   Telangiectases common on lips, tongue &
    palate.
:
•   Cryotherapy.
•   Laser ablation.
•   Electrocoagulation.
•   Blood replacement & iron therapy.
Thrombocytopaenia    Quantity of platelets when
  reduced by    *

                 *

                 *
TREATMENT
Thrombocytopathies Qualitative
Corticosteroids
      Splenectomy
       Rituximab
         Anti-D
Thrombopoietin like agents.
TTP:
• CAUSES:metastaticmalignancy,pregnancy,m
  itomycin & high dose chemotherapy.
• SYMPTOMS:
                  Thrombocytopaenia
               Microangiopathic hemolytic
                        anemia
                   Renal dysfunction
                    Occasional fever
                 Fluctuating neurologic
                     abnormalities.
• Platelet count may also decreased by
  medications.
• ASPIRIN
• ASPIRIN :
• USES----
              ANTIPLATELET THERAPY
              FOR THROMBOEMBOLIC
                   PROTECTION.



• INEXPENSIVE & EFFECTIVE
• No racial
• AGE                        6

• SIGNS H
  H           H   GI
  B               h
        s              bleeding.
  H
DISADV
Viral transmission
  Large volume
     needed.
F VIII CONCENTRATES:
• 1U= Amount present in 1ml fresh normal
  plasma.
• High purity F VIII products mfg. by
  recombinant & monoclonal antibody
  purification tech.          VIRAL SAFETY
Highly purified recombinant &
monoclonal FIX conc.(mononine)
F IX complex conc.(prothrombin
      complex conc.---PCC)
                     proplex-T,
                     Autoplex-T
Complications of factor
 replacement therapy



          Allergic reactions
             Viral disease
       transmission(hepatitis
          B & C, CMV,HIV)
          thromboembolic
               disorder,
                 DIC,
         Devpt.of antibodies
        against factor concs.
•
• Fibrin stabilizing factor def &
  Fibrinogen def.
• Very rare.
• Autosomal recessive traits.
• Rx -Factor replacement
  therapy & FFP.
• TREATMENT:
                  heparin LMWH


           activated protein C ,
 Antithrombin III.
• Surveying the patient for current medication
  use.
• History of heavy alcohol intake.
• Medical conditions – hepatitis/cirrhosis,renal
  disease,hematologic
  malignancy&thrombocytopenia predispose
  patients to bleeding problems.
Bleeding & clotting disorders
Bleeding & clotting disorders

Bleeding & clotting disorders

  • 2.
    • Dental procedures resulting in bleeding can have serious consequences in a pt. having bleeding disorder……… severe hemorrhage or even death.
  • 8.
    • 2 theories::: ( MARKOWITZ---- 1903) (1964)-the coagulation mechanism results in a final explosive change of a liquid to a gel.
  • 12.
    fibrinolysis (tPA) PLASMINOGEN PLASMIN. [FDPs]
  • 13.
    Factor XII Factor XIIa tPA + high Mol.wt kininogen parakallikren kallikren FV F VIII plasminogen plasmin fibrin FDPs
  • 14.
    tPA: Used in thromboembolic disoders asso with Myocardial infarction.(effective within 1st 6 hrs postinfarction. Fibrinolytic system activation turned off α by…… 2antiplasmin/ by plasminogen activator inhibitors ( PAI-1,PAI-2)
  • 17.
    CLINICAL LABORATARY TESTS •Help to Platelet count Bleeding time PFA-100 CT PT/INR aPTT TT FDPs Factor assays Tests of capillary fragility
  • 18.
    PLATELET COUNT: • Normal-150,000to 450,000/mm3 • If < 50,000/mm3 Hemorrhagic stroke Surgical/traumatic hemorrhage etc. may occur. • In such cases platelet transfusion may be necessary.
  • 19.
    TESTS OF PLATELETFUNCTION: ADV Dis ADV
  • 20.
    INR Intro.by WHO(1983):itz theratio of PT that adjusts for the sensitivity of the thromboplastin reagants,such that normal coagulation profile is reported as an INR of 1.0
  • 22.
  • 26.
    • Measured usinga specific latex agglutination system. Evaluates the presence of a D-dimer of fibrinogen / fibrin above normal levels.
  • 32.
    CUSHING’S syndrome: Resulting fromexcessive corticosteroid Intake / production. Patient shows skin bleeding & easy bruising.
  • 33.
    syndrome: • Autosomal dominantdisorder: • Fragile skin vessels & easy bruising.
  • 34.
    HHT • Abnormal telangiectatic capillaries. • Frequent episodes of nasal & GI bleeding. • Telangiectases common on lips, tongue & palate.
  • 35.
    : • Cryotherapy. • Laser ablation. • Electrocoagulation. • Blood replacement & iron therapy.
  • 36.
    Thrombocytopaenia Quantity of platelets when reduced by * * * TREATMENT Thrombocytopathies Qualitative
  • 39.
    Corticosteroids Splenectomy Rituximab Anti-D Thrombopoietin like agents.
  • 40.
    TTP: • CAUSES:metastaticmalignancy,pregnancy,m itomycin & high dose chemotherapy. • SYMPTOMS: Thrombocytopaenia Microangiopathic hemolytic anemia Renal dysfunction Occasional fever Fluctuating neurologic abnormalities.
  • 41.
    • Platelet countmay also decreased by medications. • ASPIRIN
  • 42.
    • ASPIRIN : •USES---- ANTIPLATELET THERAPY FOR THROMBOEMBOLIC PROTECTION. • INEXPENSIVE & EFFECTIVE
  • 47.
    • No racial •AGE 6 • SIGNS H H H GI B h s bleeding. H
  • 50.
    DISADV Viral transmission Large volume needed.
  • 51.
    F VIII CONCENTRATES: •1U= Amount present in 1ml fresh normal plasma. • High purity F VIII products mfg. by recombinant & monoclonal antibody purification tech. VIRAL SAFETY
  • 54.
    Highly purified recombinant& monoclonal FIX conc.(mononine) F IX complex conc.(prothrombin complex conc.---PCC) proplex-T, Autoplex-T
  • 55.
    Complications of factor replacement therapy Allergic reactions Viral disease transmission(hepatitis B & C, CMV,HIV) thromboembolic disorder, DIC, Devpt.of antibodies against factor concs.
  • 60.
  • 62.
    • Fibrin stabilizingfactor def & Fibrinogen def. • Very rare. • Autosomal recessive traits. • Rx -Factor replacement therapy & FFP.
  • 74.
    • TREATMENT: heparin LMWH activated protein C , Antithrombin III.
  • 78.
    • Surveying thepatient for current medication use. • History of heavy alcohol intake. • Medical conditions – hepatitis/cirrhosis,renal disease,hematologic malignancy&thrombocytopenia predispose patients to bleeding problems.