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tooth extraction in patients with blood and hematopoietic disorders is complex due to risks such as?
delete healing
excessive bleeding
increased susceptibility to infection
when doing tooth extraction in patients with blood and hematopoietic disorders, dental clinicians must
take a thorough history
perform relevant clinical and lab investigations
consult the patient's physician before any invasive procedures
role of white blood cells in dental health - disorders of white blood cells
primary defence against infections
crucial for immune response
abnormal WBC's → delayed healing, mucous alteration, infection and even fatal complications
types of WBC disorders
leukaemia: cut out of WBC's in bone marrow and blood
acute leukaemia = the rapid accumulation of immature and functionless WBC's in bone marrow and blood
chronic leukaemia = slower, more functional WBC production
lymphoma: cancel lymphoid tissues, present as tissue masses
types = Hodgkin's disease, non Hodgkins lymphoma, burkitts lymphoma, multiple myeloma
List The types of dental management of leukemic patients
detection
referral
Pre dental treatment consultation
routine dental care
emergency dental care
surgical planning
prescribe dental management During detection in leukemic patients
history and clinical exam
lab = WBC count, differential count, blood smear, haemoglobin/ hematocrit, platelet count
describe dental management during referral of leukemic patients
refer to physician for diagnose and treatment
describe dental management during pre dental treatment consultation of leukaemia patients
assess current medical status
Determine dental treatment plan based on patient's condition
describe dental management during routine dental care in leukemic patients
avoid in patients with acute symptoms
allow after disease is controlled
invasive care considerations e.g scaling and surgical procedures:
— platelet count > 50,000 = proceed
— platelet count <40,000 = Require platelet replacement
— neutropenic patient → antibiotic prophylaxis needed
describe dental management during emergency dental care of leukemic patients
ulcers = antibiotics, bland rinses, and antihistamines, orabase
oral candidiasis: antifungals
pain/infection: conservative management, antibiotic sensitivity test, strong analgesics
describe dental management during surgical planning for leukemic patients
get platelet count and bleeding time on procedure day
platelet replacement if thrombocytopenic and delay procedure until physician is consulted
in Hodgkin's disease with splenectomy: prophylactic antibiotics recommended
regimen: penicillin VK 2g, 1 hr before, and 500 mg x4/day for 1 week
what are bleeding disorders
conditions that alter ability of blood vessels, platelets and coagulation factors to maintain homeostasis
what are the types of bleeding disorders
Inherited
acquired
list and describe the inherited and acquired bleeding disorders
inherited
haemophilia A = factor VIII deficiency
hemophilia B (christmas disease) = factor IX deficiency
rare = deficiencies and other clotting factors
acquired
result of diseases that affect vascular water integrity, platelets, coagulation factors, drugs, radiotherapy or chemotherapy
the liver disease, DIC
vitamin K deficiency
drug induced (e.g anticoagulants, aspirin, NSAID's, alcohol)
dental management during assessment of patients with bleeding disorders
no surgery without bleeding history assessment and lab tests
refer to haematologists for diagnosis and tests are abnormal
simple management during medication considerations of patients with bleeding disorders
aspirin = even low doses impair platelets (thromboxane inhibition)
if PFA-100 is moderately prolonged, minor surgery may proceed unless another bleeding disorder is present
in emergencies with PFA-100, desmopressin (DDAVP) can be used to shorten bleeding time
Elective = stop aspirin three days before, if approved
NSAID's = reversible COX inhibition
bleeding risk enhanced with alcohol, anticoagulants, liver disease
wait for three half lives of the drug to pass before preceding the surgery to allow normal platelet function to return
describe precautions needed when treating patients with haemophilia A (factor VIII) deficiency)
requires haematologist consultation
determine = severity, inhibitors, responder status, Need for hospitalisation
avoid = the block, lingual infiltration, floor of mouth, intramuscular injections without factor replacement
replacement therapy is required = periodontal surgery, extractions, flap surgeries, 3rd molar removal (prefer buccal approach)
mild/moderate forms = may use desmopressin, EACA, tranexamic acid
pain control = paracetamol ± codeine
always monitor for allergic reactions to factor products