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DEPARTMENTOF PERIoDONTics
TOPIC: PERIODONTAL TREATMENT IN
MEDICALLY COMPROMISED AND GEREATRIC
PATIENTS
PRESENTED BY,
GOPIKA SUKUMARAN(INTERN)
content
• Introduction
• Types
• Management
• Conclusion
• Reference
INTRODUCTION
• Many patients seeking dental care might have significant medical
condition which may alter the course of their oral disease and therapy
provided.
• The therapeutic responsibility of clinician includes identification of
medical problems and consultation with or referral of the patient to
appropriate physician may be indicated
TYPES
Hemorrhagic disorder
Renal diseases
Liver diseases
Pulmonary dsisease
Infectious diseases
Pregnancy
Medications and cancer therapies
Hemorrhagic disorders…..!!!!
• Patients with a history of bleeding
problems caused by the disease or
drugs should be managed to minimize
risks of hemorrhage.
• Identification of these patients can be
done by the following methods :
1) Health history
2) Clinical examination
3) Laboratory tests
HEMORRHAGIC DISORDERS
ETIOLOGY
• Nonthrombocytopenic purpuras
• Thrombocytopenic purpuras
• Disorders of coagulation
THROMBOCYTOPENIC PURPURA
• Primary
THROMBOCYTIC PURPURA
NON-THROMBOCYTIC PURPURA
• Vascular wall alteration : infection, chemical, allergy
• Disorder of platelet function
• Genetic defects
• Aspirin, NSAIDs broad-spectrum antibiotic Ampicillin,
Penicillin, Gentamycin, Vancomycin
• Autoimmune disease
NON THROMBOCYTIC PURPURA
DISORDERS OF COAGULATION
• Inherited : Hemophilia A Christmas disease von Willebrand's Disease
• Acquired : Liver disease Vitamin K deficiency
• Anticoagulation drugs (heparin, coumarin)
• Anemia
Evaluation of bleeding disorders
• Take history
• Physical examination
• Screening clinical laboratory tests
• 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
• Oral ulcer
• Hyperplasia of gingiva
Screening laboratory tests
• Platelet count
• BT (Bleeding Time)
• PT (Prothrombin Time)
• aPTT (active Partial Thrombopastin Time)
• TT (Thrombin Time)
ANTICOAGULANTMEDICATION
COUMARIN (VIT K ANATAGONIST)
• Inhibit Vit K action (Factor II,VII,IX,X)
• Duration haft-life 40hrs
• Monitored by PT : INR 1.5-2.5
• Alteration of coumar dosage ( 2-3 days )
HEPARIN
• Complex inhibited ( IXa, Xa, XIa, XIIa )
• 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
• And protamine sulfate can reverse the effect
Aspirin (antiplatelet)
• Inhibit cycloxygenase, TxA2 formation
• Impairs platelet function
• Tests-BT, aPTT
• If tests are abnormal,physcian should be consulted before dental surgery
• Stop aspirin for 5 days, substitute alternative drug in consultation with MD
Thrombocytopenia
• Disease in number of circulation platelets
• Idiopathic thrombocytopenia, secondary thrombocytopenia
• TX : is none indicated unless platelets<20000/mm3, or
excessive bleeding
• TX : Steroid, platelet transfusion
THROMBOCYTOPENIA
VONWILLEBRANDISDISEASE
• Gene mutation on Von Willebrand’s factor; most common Inherited disease
in America ( 1% )
 Type I : 70%-80%, partial loss on quantity
 Type II : poor on quality
 Type III : severe loss on quantity, inactive to DDAVP
HEMOPHILIA
• Sex-linked recessive trait
• Prolong aPTT, normal BT,PT
• Severity of disorder : severe<1%, moderate 1-5%,
mild 6-30%
• TX : Replacement factors, antifibrinilytic agents, steroids
HEMOPHILIA
HEMOPHILIA-DENTAL MANAGEMENT
• Preventive dentistry
1. Tooth brushing, flossing, rubber cup prophylaxis &topical fluoride,
supragingival scaling without prior replacement therapy
• Pain control
1. Block anesthesia: factor level>50%
2. Avoid aspirin, NSAIDs
• Periodontal therapy
1. No contraindication of probing and supragingival scaling
DENTALMANAGEMENTOF BLEEDINGDISORDERS
Replacement therapy :
1. Platelet concentrate : thrombocytopenia ( 1 unit= 30,000/ uL enough for 1 day )
2. Fresh frozen plasma : liver disease, Hemophilia B, vWD type III
3. Factor VIII,IX concentrate : Hemophilia A
( 1 unit /kg can add 2%, so 50 unit /kg add 100% )
4. Factor IX concentrate : Hemophilia B
5. DDAVP : Hemophilia A, vWD type I,II
Antifibrinolytic therapy:
1. E-aminocaproic acid (EACA)
2. Tranexamic acid (AMCA, Transamin)
RENAL
DISEASES
CAUSESOF RENAL FAILURE
• Glomerulonephritis
• Kidney cystic disease
• Renovascular disease
• Drug nephropathy
• Obstructive uropathy
• Hypertension
Renal failure result in:
• Severe electrolyte imbalances
• Cardiac arrhythmias
• Pulmonary congestion
• Congestive heart failure
• Prolonged bleeding
ORAL MANIFESTATIONSOF RENALDISEASE
• Halitosis
• Altered taste sensation
• Xerostomia
• Gingivitis
• Enamel hypoplasia
• Infections
TREATMENT
• Consult the patient’s physician
• Monitor Blood Pressure
(patients in end stage renal failure are usually hypertensive)
• Check laboratory values: PTT, PT, bleeding time, platelet count, blood
urea nitrogen and serum creatinine
• Frequent recall and appointments should be scheduled
• Drugs that are nephrotoxic or metabolized by the kidney should not
be given (eg: tetracycline, aminoglycoside antibiotics)
• Acetaminophen used for analgesia, diazepam for sedation.
• The patients who are receiving dialysis requires modification in treatment
planning
MODES OF DIALYSIS:
Intermittent Periodontal Dialysis (IPD)
Chronic ambulatory peritoneal dialysis (CAPD)
Hemodialysis
RECOMMENDATIONFOR HEMODIALYSIS
• Screen for Hepatitis B and C antigens antibody before any treatment
• Provide antibiotic prophylaxis
• Periodontal treatment should be provided on the day after dialysis
due to the effects of heparinization
• BP reading should be taken from the other arm.
LIVER DISEASES
INTRODUCTION
• Liver is the site of production for most of the clotting factors
• Excessive bleeding during or after periodontal treatment may occur
in patients with severe liver disease
• Many drugs are metabolized in the liver. So the liver disease alters
the normal drug metabolism.
CAUSESOF LIVER DISEASES
• Drug toxicity
• Cirrhosis
• Viral infections (hepatitis B and C)
• Neoplasms
• Biliary tract disorders
ORAL MANIFESTATIONSOF LIVER DISEASE
• Candidiasis
• Angular cheilitis
• Atropic glossitis
• Petechiae
• Lichen planus
TREATMENT
• Consultation with the physician concerning current stage of disease,
risk for bleeding, potential drugs to be prescribed during treatment
And required alterations to periodontal therapy.
• Screening for hepatitis B and C
• Check laboratory values for PT and PTT
PULMONARY DISEASES
INTRODUCTION
• Pulmonary diseases range from obstructive lung diseases
(eg: asthma, emphysema, bronchitis) to restrictive ventilatory
disorders that could
• interfere with effective ventilation
• Acute respiratory distress may be caused by slight airway obstruction
or depression of respiratory function.
• Patients with acute respiratory distress might alter their position in
attempts to improve their ventilatory efficiency
• sed by muscle weakness,scarring,obesity
ORAL MANIFESTATIONS:
• Xerostomia
• Gingivitis
• Halitosis
• Candidiasis
TREATMENT
• Increased respiratory rate, cyanosis, clubbing of the fingers, chronic
cough, chest pain, hemoptysis, dyspnea and wheezing- need
consultation from the physician and medication details.
Avoid elicitation of respiratory depression or distress.
• Minimize the stress of periodontal appointment
• Patient with emphysema should be treated in the aftenoon
• Avoid medications that cause respiratory depression
(eg: narcotics, sedatives or general anesthetics)
• Avoid bilateral mandibular block anesthesia which could cause
increased airway obstruction.
• Position the patient to allow maximal ventilator efficiency
• Keep the patients throat clear and avoid excess periodontal packing
• Do not use equipments that produce aerosol.
eg: ultrasonic scalers
• For asthmatic patient – inhaler should be available
• Infectious patients should not be treated unless the periodontal
procedure is emergency
PREGNANCY
ORAL MANIFESTATIONS
• Gingivitis
• Pregnancy tumour
• Tooth mobility
• Tooth surface loss
AIMOF PERIODONTAL THERAPY
• To minimize the potential inflammatory response related to
pregnancy associated hormonal alterations.
• Plaque control, scaling, root planning, and polishing can be done.
• The second trimester is the safest time to perform treatment.
• The supine position of patient cause obstruction of venacava and
aorta leads to supinehypotensive syndrome.
• Patient should be placed on her left side by elevating the right hip
during treatment.
• Appointments should be short and the patient should be allowed to
change the position frequently.
• No medications should be prescribed ideally
• Safer drugs:
Lidocaine, prilocaine, analgesics: paracetamol, antibiotics: amoxicillin
INFECTIOUS DISEASES
TYPES
• Hepatitis
• HIV
• Tuberculosis
HEPATITIS
• Hepatitis A and E are both self-limiting infections with no associated
chronic liver disease.
• Hepatitis B infection may result in chronic liver disease in about 5
10% of infected individuals
• Hepatitis D requires the presence of HBV for its survival
• Hepatitis C is the most serious of all viral hepatitis infection because
of its high chronic infection rate. Only 15% of patients recover
completely; 85% develop chronic HCV infection, which dramatically
increases the risk for cirrhosis, liver Ca. and failure.
• Hepatitis G appears as a co-infection with hepatitis A,B or C
• TTV is often present in patients with hepatitis and chronic liver
disease and it is also associated with HCV.
GUIDELINESFOR TREATINGHEPATITIS PATIENT
• If the disease is active – do not provide periodontal treatment unless
emergency.
• Patients with history of hepatitis consultation from physician
required
• For recovered HAV or HEV patients perform routine periodontal care.
• Patients with anti HBs positive and HBsAg negative may be treated
routinely.
PRECAUTIONS TO BE USED
• If bleeding occurs during or after treatment- measure PT nd Bleeding
time.
• Usage of masks,gloves,eye shields,disposable gowns,disposable
covers,headrest covers,covering light handles,drawer handles and
bracket trays is also essential.
• After treatment all disposable items should be disposed.
• Minimize aerosol production by not using ultrasonic
instrumentation,air syringe or high speed handpieces.
• Prerinsing with chlorhexidine gluconate is highly recommended.
• All equipment should be scrubbed and sterilised
• If a percutaneous or permucosal injury occurs during treatment
of a HBV carrier , CDC guidelines recommend administration of
Hepatitis B immune globulin (HBIG)
hiv
PERIODONTAL TREATMENT FOR HIV PATIENTS
• HEALTH STATUS
• INFECTION CONTROL MEASURES
• SUPPORTIVE PERIODONTAL THERAPY
1.Healthstatus
• Should be determined from the health history, physical evaluation
and consultation with the patient’s physician.
• Treatment decisions will vary depending on the patient’s state of
health.
• Information should be obtained regarding-
CD4+ T4 lymphocyte level
current viral load
difference from previous counts and load
2. INFECTIONCONTROL MEASURES
GOALS OF THERAPY
• Restoration and maintenance of oral health.
• Treatment should be directed toward control of HIV- associated
mucosal diseases such as chronic candidiasis and recurrent oral
ulcerations.
• Effective oral hygiene maintenance
• Conservative, nonsurgical periodontal therapy should be a treatment
option for virtually all HIV patients.
• NUP & NUS can be severely destructive to periodontal structures and
should be treated appropriately.
3. SUPPORTIVE PERIODONTAL THERAPY
• Patient should be encouraged to maintain meticulous personal oral
hygiene.
• Recall visits should be conducted at short intervals (2 to 3 months)
• Systemic antibiotic therapy should be administered with caution
• Blood and other medical laboratory tests may be required to
monitor
• The patients overall health status and consultation and coordination
with the patient’s physician are necessary
TUBERCULOSIS
• Patients with the tuberculosis should receive only emergency care
following the guidelines.
• The sputum culture for mycobacterium tuberculosis should be done.
• If the results are negative patients may be treated normally.
Anticancer drug
• Bisphosphate is used to treat cancer(iv)
• Potential risk factors contribute to the development are steroid
therapy, alcohol, smoking, poor oral hygiene, chemotherapy,
extractions, root canal treatment, periodontal infections, periodontal
surgery and implant surgery.
• Invasive treatment should be avoided.
• Caution and careful consideration of risks must be evaluated for
individuals with a history of talking oral bisphosphonates for periods
longer than 3 years
Anticoagulant/antiplatelet therapy
• Discontinue therapy about 3 to 5 (antiplatelet) or 7 to 10
(anticoagulant) days before planned surgical procedures.
• Simple extractions or periodontal surgery can be done without
discontinuation of therapy.
• In case of intraoperative bleeding local measures are sufficient to
control bleeding.
corticosteroids
• Administration of corticosteroid is not required in case of
uncomplicated minor surgical procedures.
• Supplementation is indicated in lengthy and major surgical
procedures.
chemotherapy
• Should be conservative and palliative.
• The treatment should be done before the day of chemotherapy when
the white cell counts are above 2000/mm3
• Teeth with a poor prognosis should be extracted.
• The clinician should teach the importance of good oral hygiene.
• Antimicrobial rinses such as chlorhexidine is
recommened to prevent secondary infections
Radiationtherapy
• Used to treat head and neck tumors.
• Complication includes:
 Mucositis
 Xerostomia
 Trismus
 Radiation caries
 Dysphagia
 Osteoradionecrosis
Before radiation therapy:
• Teeth that are restorable or severely periodontally diseased should be
extracted atleast 2 weeks before radiation.
• Extractions should be performed in a manner that allows primary
closure.
• Mucoperiosteal flaps should be elevated and teeth should be
extracted in segments.
• Alveolopasty should be performed allowing no bony spicules to
remain.
During radiation therapy:
• Patients should receive weekly prophylaxis
• Oral hygiene instructions.
• Professionally applied fluoride treatments.
• Patient should be instructed to brush daily with a 0.4% stannous fluoride or
1% sodium fluoride gel.
After radiation therapy:
• Viscous lidocaine prescribed for painful mucositis
• Salivary substitutes given for xerostomia.
• Radiation caries may be prevented by topical fluoride application daily
and maintenance of good oral hygiene.
• After 3 month recall interview is ideal.
NOTE: Tooth extraction after radiation treatment involves a high risk for
developing OSTEORADIONECROSIS.
Conclusion
• In managing medically compromised patients, the clinician should
always obtain a physcian consult before any periodontal treatment.
• Changes in recommendations for medically compromised patients
are continually occurring.
• Dentists should follow the recommendations from the patient’
physician and utilize the appropriate protocol.
• Thus all clinicians need to be cognizant of the systemic implications
of periodontal diseases and their treatment, and should stay up to
date to give the best possible treatment.
REFERENCES
1CARRANZA 11TH EDITION
2.DENTAL MANAGEMENT CONSIDERATION FOR DIABETIC
PATIENT.RAJESH ET AL JADA VOL 132,2003
3. TR E A T M E N T O F H E M O P H I L I A MAY 2006 • NOV 40
4.DENTAL CONSIDERATIONS IN CARDIOVASCULAR PATIENTS: A
PRACTICAL PERSPECTIVE SWANTIKA CHAUDHRY A,*, RITIKA
JAISWAL A, SURENDER SACHDEVA ,JANUARY 2016
Periodontal management of medically compromised patients

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Periodontal management of medically compromised patients

  • 1. DEPARTMENTOF PERIoDONTics TOPIC: PERIODONTAL TREATMENT IN MEDICALLY COMPROMISED AND GEREATRIC PATIENTS PRESENTED BY, GOPIKA SUKUMARAN(INTERN)
  • 2. content • Introduction • Types • Management • Conclusion • Reference
  • 3. INTRODUCTION • Many patients seeking dental care might have significant medical condition which may alter the course of their oral disease and therapy provided. • The therapeutic responsibility of clinician includes identification of medical problems and consultation with or referral of the patient to appropriate physician may be indicated
  • 4. TYPES Hemorrhagic disorder Renal diseases Liver diseases Pulmonary dsisease Infectious diseases Pregnancy Medications and cancer therapies
  • 6. • Patients with a history of bleeding problems caused by the disease or drugs should be managed to minimize risks of hemorrhage. • Identification of these patients can be done by the following methods : 1) Health history 2) Clinical examination 3) Laboratory tests
  • 7. HEMORRHAGIC DISORDERS ETIOLOGY • Nonthrombocytopenic purpuras • Thrombocytopenic purpuras • Disorders of coagulation THROMBOCYTOPENIC PURPURA • Primary
  • 9. NON-THROMBOCYTIC PURPURA • Vascular wall alteration : infection, chemical, allergy • Disorder of platelet function • Genetic defects • Aspirin, NSAIDs broad-spectrum antibiotic Ampicillin, Penicillin, Gentamycin, Vancomycin • Autoimmune disease
  • 11. DISORDERS OF COAGULATION • Inherited : Hemophilia A Christmas disease von Willebrand's Disease • Acquired : Liver disease Vitamin K deficiency • Anticoagulation drugs (heparin, coumarin) • Anemia
  • 12.
  • 13. Evaluation of bleeding disorders • Take history • Physical examination • Screening clinical laboratory tests • Observation of excessive bleeding following a surgical procedure
  • 14. 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..
  • 15. PHYSICAL EXAMINATION • Jaundice • Petechiae :< 0.2 cm • Purpura :0.2 cm-1 cm • Eccymoses :> 1 cm • Oral ulcer • Hyperplasia of gingiva
  • 16. Screening laboratory tests • Platelet count • BT (Bleeding Time) • PT (Prothrombin Time) • aPTT (active Partial Thrombopastin Time) • TT (Thrombin Time)
  • 17.
  • 18. ANTICOAGULANTMEDICATION COUMARIN (VIT K ANATAGONIST) • Inhibit Vit K action (Factor II,VII,IX,X) • Duration haft-life 40hrs • Monitored by PT : INR 1.5-2.5 • Alteration of coumar dosage ( 2-3 days )
  • 19. HEPARIN • Complex inhibited ( IXa, Xa, XIa, XIIa ) • 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 • And protamine sulfate can reverse the effect
  • 20. Aspirin (antiplatelet) • Inhibit cycloxygenase, TxA2 formation • Impairs platelet function • Tests-BT, aPTT • If tests are abnormal,physcian should be consulted before dental surgery • Stop aspirin for 5 days, substitute alternative drug in consultation with MD
  • 21. Thrombocytopenia • Disease in number of circulation platelets • Idiopathic thrombocytopenia, secondary thrombocytopenia • TX : is none indicated unless platelets<20000/mm3, or excessive bleeding • TX : Steroid, platelet transfusion
  • 23. VONWILLEBRANDISDISEASE • Gene mutation on Von Willebrand’s factor; most common Inherited disease in America ( 1% )  Type I : 70%-80%, partial loss on quantity  Type II : poor on quality  Type III : severe loss on quantity, inactive to DDAVP
  • 24.
  • 25. HEMOPHILIA • Sex-linked recessive trait • Prolong aPTT, normal BT,PT • Severity of disorder : severe<1%, moderate 1-5%, mild 6-30% • TX : Replacement factors, antifibrinilytic agents, steroids
  • 27. HEMOPHILIA-DENTAL MANAGEMENT • Preventive dentistry 1. Tooth brushing, flossing, rubber cup prophylaxis &topical fluoride, supragingival scaling without prior replacement therapy • Pain control 1. Block anesthesia: factor level>50% 2. Avoid aspirin, NSAIDs • Periodontal therapy 1. No contraindication of probing and supragingival scaling
  • 28. DENTALMANAGEMENTOF BLEEDINGDISORDERS Replacement therapy : 1. Platelet concentrate : thrombocytopenia ( 1 unit= 30,000/ uL enough for 1 day ) 2. Fresh frozen plasma : liver disease, Hemophilia B, vWD type III 3. Factor VIII,IX concentrate : Hemophilia A ( 1 unit /kg can add 2%, so 50 unit /kg add 100% ) 4. Factor IX concentrate : Hemophilia B 5. DDAVP : Hemophilia A, vWD type I,II
  • 29. Antifibrinolytic therapy: 1. E-aminocaproic acid (EACA) 2. Tranexamic acid (AMCA, Transamin)
  • 30.
  • 31.
  • 33. CAUSESOF RENAL FAILURE • Glomerulonephritis • Kidney cystic disease • Renovascular disease • Drug nephropathy • Obstructive uropathy • Hypertension
  • 34. Renal failure result in: • Severe electrolyte imbalances • Cardiac arrhythmias • Pulmonary congestion • Congestive heart failure • Prolonged bleeding
  • 35.
  • 36. ORAL MANIFESTATIONSOF RENALDISEASE • Halitosis • Altered taste sensation • Xerostomia • Gingivitis • Enamel hypoplasia • Infections
  • 37.
  • 38. TREATMENT • Consult the patient’s physician • Monitor Blood Pressure (patients in end stage renal failure are usually hypertensive) • Check laboratory values: PTT, PT, bleeding time, platelet count, blood urea nitrogen and serum creatinine • Frequent recall and appointments should be scheduled • Drugs that are nephrotoxic or metabolized by the kidney should not be given (eg: tetracycline, aminoglycoside antibiotics) • Acetaminophen used for analgesia, diazepam for sedation.
  • 39. • The patients who are receiving dialysis requires modification in treatment planning MODES OF DIALYSIS: Intermittent Periodontal Dialysis (IPD) Chronic ambulatory peritoneal dialysis (CAPD) Hemodialysis
  • 40.
  • 41.
  • 42.
  • 43. RECOMMENDATIONFOR HEMODIALYSIS • Screen for Hepatitis B and C antigens antibody before any treatment • Provide antibiotic prophylaxis • Periodontal treatment should be provided on the day after dialysis due to the effects of heparinization • BP reading should be taken from the other arm.
  • 45. INTRODUCTION • Liver is the site of production for most of the clotting factors • Excessive bleeding during or after periodontal treatment may occur in patients with severe liver disease • Many drugs are metabolized in the liver. So the liver disease alters the normal drug metabolism.
  • 46. CAUSESOF LIVER DISEASES • Drug toxicity • Cirrhosis • Viral infections (hepatitis B and C) • Neoplasms • Biliary tract disorders
  • 47.
  • 48. ORAL MANIFESTATIONSOF LIVER DISEASE • Candidiasis • Angular cheilitis • Atropic glossitis • Petechiae • Lichen planus
  • 49. TREATMENT • Consultation with the physician concerning current stage of disease, risk for bleeding, potential drugs to be prescribed during treatment And required alterations to periodontal therapy. • Screening for hepatitis B and C • Check laboratory values for PT and PTT
  • 51. INTRODUCTION • Pulmonary diseases range from obstructive lung diseases (eg: asthma, emphysema, bronchitis) to restrictive ventilatory disorders that could • interfere with effective ventilation • Acute respiratory distress may be caused by slight airway obstruction or depression of respiratory function. • Patients with acute respiratory distress might alter their position in attempts to improve their ventilatory efficiency • sed by muscle weakness,scarring,obesity
  • 52. ORAL MANIFESTATIONS: • Xerostomia • Gingivitis • Halitosis • Candidiasis
  • 53. TREATMENT • Increased respiratory rate, cyanosis, clubbing of the fingers, chronic cough, chest pain, hemoptysis, dyspnea and wheezing- need consultation from the physician and medication details. Avoid elicitation of respiratory depression or distress. • Minimize the stress of periodontal appointment • Patient with emphysema should be treated in the aftenoon • Avoid medications that cause respiratory depression (eg: narcotics, sedatives or general anesthetics)
  • 54. • Avoid bilateral mandibular block anesthesia which could cause increased airway obstruction. • Position the patient to allow maximal ventilator efficiency • Keep the patients throat clear and avoid excess periodontal packing • Do not use equipments that produce aerosol. eg: ultrasonic scalers • For asthmatic patient – inhaler should be available • Infectious patients should not be treated unless the periodontal procedure is emergency
  • 56. ORAL MANIFESTATIONS • Gingivitis • Pregnancy tumour • Tooth mobility • Tooth surface loss
  • 57. AIMOF PERIODONTAL THERAPY • To minimize the potential inflammatory response related to pregnancy associated hormonal alterations. • Plaque control, scaling, root planning, and polishing can be done. • The second trimester is the safest time to perform treatment. • The supine position of patient cause obstruction of venacava and aorta leads to supinehypotensive syndrome. • Patient should be placed on her left side by elevating the right hip during treatment.
  • 58.
  • 59. • Appointments should be short and the patient should be allowed to change the position frequently. • No medications should be prescribed ideally • Safer drugs: Lidocaine, prilocaine, analgesics: paracetamol, antibiotics: amoxicillin
  • 62. HEPATITIS • Hepatitis A and E are both self-limiting infections with no associated chronic liver disease. • Hepatitis B infection may result in chronic liver disease in about 5 10% of infected individuals • Hepatitis D requires the presence of HBV for its survival • Hepatitis C is the most serious of all viral hepatitis infection because of its high chronic infection rate. Only 15% of patients recover completely; 85% develop chronic HCV infection, which dramatically increases the risk for cirrhosis, liver Ca. and failure.
  • 63. • Hepatitis G appears as a co-infection with hepatitis A,B or C • TTV is often present in patients with hepatitis and chronic liver disease and it is also associated with HCV.
  • 64. GUIDELINESFOR TREATINGHEPATITIS PATIENT • If the disease is active – do not provide periodontal treatment unless emergency. • Patients with history of hepatitis consultation from physician required • For recovered HAV or HEV patients perform routine periodontal care. • Patients with anti HBs positive and HBsAg negative may be treated routinely.
  • 65.
  • 66. PRECAUTIONS TO BE USED • If bleeding occurs during or after treatment- measure PT nd Bleeding time. • Usage of masks,gloves,eye shields,disposable gowns,disposable covers,headrest covers,covering light handles,drawer handles and bracket trays is also essential. • After treatment all disposable items should be disposed. • Minimize aerosol production by not using ultrasonic instrumentation,air syringe or high speed handpieces.
  • 67. • Prerinsing with chlorhexidine gluconate is highly recommended. • All equipment should be scrubbed and sterilised • If a percutaneous or permucosal injury occurs during treatment of a HBV carrier , CDC guidelines recommend administration of Hepatitis B immune globulin (HBIG)
  • 68. hiv PERIODONTAL TREATMENT FOR HIV PATIENTS • HEALTH STATUS • INFECTION CONTROL MEASURES • SUPPORTIVE PERIODONTAL THERAPY
  • 69. 1.Healthstatus • Should be determined from the health history, physical evaluation and consultation with the patient’s physician. • Treatment decisions will vary depending on the patient’s state of health. • Information should be obtained regarding- CD4+ T4 lymphocyte level current viral load difference from previous counts and load
  • 70.
  • 72. GOALS OF THERAPY • Restoration and maintenance of oral health. • Treatment should be directed toward control of HIV- associated mucosal diseases such as chronic candidiasis and recurrent oral ulcerations. • Effective oral hygiene maintenance • Conservative, nonsurgical periodontal therapy should be a treatment option for virtually all HIV patients. • NUP & NUS can be severely destructive to periodontal structures and should be treated appropriately.
  • 73. 3. SUPPORTIVE PERIODONTAL THERAPY • Patient should be encouraged to maintain meticulous personal oral hygiene. • Recall visits should be conducted at short intervals (2 to 3 months) • Systemic antibiotic therapy should be administered with caution • Blood and other medical laboratory tests may be required to monitor • The patients overall health status and consultation and coordination with the patient’s physician are necessary
  • 74.
  • 75. TUBERCULOSIS • Patients with the tuberculosis should receive only emergency care following the guidelines. • The sputum culture for mycobacterium tuberculosis should be done. • If the results are negative patients may be treated normally.
  • 76.
  • 77.
  • 78. Anticancer drug • Bisphosphate is used to treat cancer(iv) • Potential risk factors contribute to the development are steroid therapy, alcohol, smoking, poor oral hygiene, chemotherapy, extractions, root canal treatment, periodontal infections, periodontal surgery and implant surgery. • Invasive treatment should be avoided. • Caution and careful consideration of risks must be evaluated for individuals with a history of talking oral bisphosphonates for periods longer than 3 years
  • 79.
  • 80. Anticoagulant/antiplatelet therapy • Discontinue therapy about 3 to 5 (antiplatelet) or 7 to 10 (anticoagulant) days before planned surgical procedures. • Simple extractions or periodontal surgery can be done without discontinuation of therapy. • In case of intraoperative bleeding local measures are sufficient to control bleeding.
  • 81.
  • 82. corticosteroids • Administration of corticosteroid is not required in case of uncomplicated minor surgical procedures. • Supplementation is indicated in lengthy and major surgical procedures.
  • 83. chemotherapy • Should be conservative and palliative. • The treatment should be done before the day of chemotherapy when the white cell counts are above 2000/mm3 • Teeth with a poor prognosis should be extracted. • The clinician should teach the importance of good oral hygiene. • Antimicrobial rinses such as chlorhexidine is recommened to prevent secondary infections
  • 84.
  • 85. Radiationtherapy • Used to treat head and neck tumors. • Complication includes:  Mucositis  Xerostomia  Trismus  Radiation caries  Dysphagia  Osteoradionecrosis
  • 86.
  • 87. Before radiation therapy: • Teeth that are restorable or severely periodontally diseased should be extracted atleast 2 weeks before radiation. • Extractions should be performed in a manner that allows primary closure. • Mucoperiosteal flaps should be elevated and teeth should be extracted in segments. • Alveolopasty should be performed allowing no bony spicules to remain.
  • 88. During radiation therapy: • Patients should receive weekly prophylaxis • Oral hygiene instructions. • Professionally applied fluoride treatments. • Patient should be instructed to brush daily with a 0.4% stannous fluoride or 1% sodium fluoride gel.
  • 89. After radiation therapy: • Viscous lidocaine prescribed for painful mucositis • Salivary substitutes given for xerostomia. • Radiation caries may be prevented by topical fluoride application daily and maintenance of good oral hygiene. • After 3 month recall interview is ideal. NOTE: Tooth extraction after radiation treatment involves a high risk for developing OSTEORADIONECROSIS.
  • 90. Conclusion • In managing medically compromised patients, the clinician should always obtain a physcian consult before any periodontal treatment. • Changes in recommendations for medically compromised patients are continually occurring. • Dentists should follow the recommendations from the patient’ physician and utilize the appropriate protocol. • Thus all clinicians need to be cognizant of the systemic implications of periodontal diseases and their treatment, and should stay up to date to give the best possible treatment.
  • 91. REFERENCES 1CARRANZA 11TH EDITION 2.DENTAL MANAGEMENT CONSIDERATION FOR DIABETIC PATIENT.RAJESH ET AL JADA VOL 132,2003 3. TR E A T M E N T O F H E M O P H I L I A MAY 2006 • NOV 40 4.DENTAL CONSIDERATIONS IN CARDIOVASCULAR PATIENTS: A PRACTICAL PERSPECTIVE SWANTIKA CHAUDHRY A,*, RITIKA JAISWAL A, SURENDER SACHDEVA ,JANUARY 2016