Professional Documents
Culture Documents
DENTISTRY 2 LEC
ORIENTATION 2ND SEMESTER 2020-
2021
WELCOME TO THE SCHOOL OF
DENTISTRY
VIRTUAL CLASS HOUSE
RULES
GOAL?
Lesson 1- Definition, Importance, Major and
Accessory Parts of a Medical Record
• patient has been given an appointment for surgical procedure or specialized investigations that must • admissions from casualty
take place in the hospital
• usually from the ER
• short stays where patients undergo a surgical procedure (hospital dental service)
g. Dental and oral surgical patients with coagulopathies and other medical conditions that may require f. any infections or injuries that have the potential to cause airway compromise
transfusions or intravenous medications
LESSON 1- HOSPITAL
ADMISSION
3 admitting categories: 3 admitting types:
1.elective 1.private
2.emergency 2.service
3.urgent 3.continuity of care
LESSON 1- HOSPITAL
ADMISSION
Three Primary elements of admission 3. History and Physical Examination
1. Admitting orders HISTORY
•a full set of orders (diagnostic, therapeutic, routine maintenance •chief complaint
intervention) written by a practitioner on the patient’s chart •HPI
•if expired, must be rewritten •Past medical history
•automatically cancelled if patient undergoes surgery or transferred •Medications
to another service
•Allergies
•ADC VAAN DIMEL (Admit, Diagnosis, Condition, Vital
Sign, Activity, Allergies, Nursing, DIET, IV meds and •Family History
fluids, Medication, Extras, Laboratory studies) •Social History
2. Admitting note •Review of Symptoms
•includes history, results of PE (head, neck, oral), lab test results, PHYSICAL EXAMINATION
radiographic findings, differential diagnosis, plans for treatment
•performed after history taking
•if ELECTIVE:
• consent form signed and attached to chart •comprehensive, emphasis on areas related to CC
• pre-op instructions (NPO), meds to be taken •vital signs
LESSON 2 - THE OUT-PATIENT
AND IN-PATIENT ADMISSIONS
OUT-PATIENT Admission Criteria for a PROCEDURE:
Ambulatory Admissions
1. physiologic derangements produced by the
•one-day surgery, ambulatory surgery, day surgery, short-stay operation must not require hospital care
surgery
•patients have greater control in scheduling the procedure 2. blood loss must not be great enough to
•insurance feels it reduces costs
require transfusion
•discharge depends more on recovery from anesthesia than the 3. post-operative pain is controllable with safe
procedure doses of oral analgesics
Patient selection guidelines:
4. no risk of airway obstruction
1.ASA physical status
2.Reliability and compliance 5. potential complications must not immobilize
the patient
3.Discharge situation
4.Age
LESSON 2 - THE OUT-PATIENT
AND IN-PATIENT ADMISSIONS
Patient examination requirements: Required forms for admission
•Similar to any operation 1.Hospital forms
1. Medical history
2. Physical examination 2.Patient information forms
3. Laboratory studies
3.Medical history and PE forms
Protocols
4.Informed consent
•patient’s agreement, predetermination of
insurance benefits and preauthorization must
all be in writing
•accepted date of procedure is cleared with the
hospital admission office to permit firm
scheduling
LESSON 2 - THE OUT-PATIENT
AND IN-PATIENT ADMISSIONS
IN-PATIENT Admission Automatic admissions
Cardiac Arrest
• Cessation of cardiac mechanical activity
• Unresponsiveness, absence of detectable pulse and
apnea (agonal respirations)
EXTRINSIC
• Foreign bodies
2. Do abdominal thrust
Heimlich maneuver
Chest Thrust
Back blows and chest thrust
LESSON 2 – FOREIGN BODY
AIRWAY OBSTRUCTION
LESSON 2 – FOREIGN BODY
AIRWAY OBSTRUCTION
LESSON 2 – FOREIGN BODY
AIRWAY OBSTRUCTION
For INFANTS
• Awake, unable to cough, cry, breathe
• 5 back blows and 5 chest thrusts
LESSON 2 – FOREIGN BODY
AIRWAY OBSTRUCTION
LESSON 2 – FOREIGN BODY
AIRWAY OBSTRUCTION
If becomes UNCONSCIOUS If becomes UNRESPONSIVE
•Gently guide patient to the floor •Carefully lower patient to a firm, flat
surface
•Get astride the victim’s thigh and place
the heel of one hand at approximately the •Send someone to get an AED
belly button
•Begin CPR with chest compression
•Put your other hand on top and give 5
•Open airway and check person’s mouth
abdominal thrusts toward the victim’s
nose for any visible object
• Use finger sweep motion to remove the
object
• DO NOT perform a blind finger sweep
Lesson 1- Types, Diagnostics, and
3.Fat metabolism
4.Protein metabolism
5.Removal, excretion, detoxification and
inactivation of drugs, hormones and toxins take
place in the liver
LESSON 2 – WHAT IS
HEPATITIS?
LESSON 2 – WHAT IS
HEPATITIS?
Hepatitis - Is a general term that means Types of Hepatitis:
inflammation of the liver. The Ancient Greek 1.Infectious – Viral infection of the liver
word hepa refers to the liver, and itis means due to acute or chronic viral hepatitis
inflammation. (HAV, HBV, HCV, HDV, HEV).
Inflammation of the liver has several 2.Non-infectious – Due to excessive or
possible causes, including: prolonged use of toxic substances that
•Toxins and chemicals such as excessive are metabolized in the liver (e.g.
amounts of alcohol acetaminophen, alcohol, halothane,
ketoconazole, methyldopa and
•Autoimmune diseases that cause the immune methotrexate) and sometimes due to auto
system to attack healthy tissues in the body immune system response in the body.
•Fat which may cause fatty liver disease
•Microorganisms, including viruses
LESSON 3 – TYPES OF
VIRAL HEPATITIS
LESSON 3 – TYPES OF VIRAL
HEPATITIS
1.Hepatitis A (RNA-Piconavirus)
Transmission: enteric (fecal-oral route)
Often occurs as an epidemic because the reservoir for
infection is frequently a common food or water source
Incubation period: ̴25 days
Persons of any age may be infected but occurs
primarily in children and young adults
Mild severity
No carrier state
Recovery conveys immunity against infection
Vaccine developed in 1995
LESSON 3 – TYPES OF VIRAL
HEPATITIS
2. Hepatitis B (DNA-Hepadnavirus)
•Transmission:
• Direct percutaneous inoculation or transfusion of infected blood or products
• Indirect percutaneous introduction of infected blood and blood products
through minute skin cuts or abrasion
• Absorption of infected blood or blood specimen into the mucosal surface of
the mouth or eye
• Absorption of infected secretions like saliva and semen into mucosal
surfaces
• Transfer of infected serum or plasma through inanimate environmental
surfaces
2.2nd phase – Icteric phase
2. Clinical jaundice (yellowish brown hue of the eyes, skin, oral
mucosa and urine)
3. Some prodromal symptoms may subside but gastrointestinal
symptoms increases
4. 2-8 weeks
5. (+) hepato- and splenomegaly
3.3rd phase – Convalescent/Recovery phase [post-icteric]
3. Symptoms disappear but abnormal liver function and hepatomegaly
may persist
4. Recovery period usually completed ̴4 months after onset of
jaundice. Hepa B and C have longer recovery periods
Lesson 1- Diagnosis of
Dental Considerations:
•Preoperative glyceryl trinitrate & oral sedation advised sometimes.
•Dental care carried with minimal anxiety & oxygen saturation
•Monitor pulse & blood pressure
•Post angioplasty elective dental care deferred for 6 months,
emergency dental care in a hospital setting.
•Patients with bypass grafts – anti biotic cover against infective
endocarditis. – local anesthesia containing adrenaline is
contraindicated
•Patients with vascular stents – no antibiotic cover except during 1st 6
week postop for emergency dental care.
•DRUGS used in t/t of angina may cause oral adverse effects.
LESSON 2 – MANAGEMENT OF
CARDIOVASCULAR DISEASE
MYOCARDIAL INFARCTION • If coronary artery stent is in place and if it
is more than 24 weeks after placement,
Dental Management: antibiotic prophylaxis is not necessary.
Normal blood pressure Systolic <120 mmHg and diastolic <80 mmHg
•HIV infects the T helper cell because it has the protein CD4 on its
surface, which HIV uses to attach itself to the cell before gaining entry
•This is why the T helper cell is sometimes referred to as a CD4+
lymphocyte. Once it has found its way into a cell, HIV produces new
copies of itself, which can then go on to infect other cells
•Over time, HIV infection leads to a severe reduction in the number of T
helper cells available to help fight disease. The number of T helper cells
is measured by having a CD4 test and is referred to as the CD4 count
•It can take several years before the CD4 count declines to the point that
an individual is said to have progressed to AIDS
•HIV infection can generally be broken down into four distinct stages:
primary infection, clinically asymptomatic stage, symptomatic HIV
infection, and progression from HIV to AIDS
LESSON 1- HIV
•STAGE 1 : Primary HIV infection
• This stage of infection lasts for a few weeks
and is often accompanied by a short flu-like
illness
• In up to about 20% of people the HIV
symptoms are serious enough to consult a
doctor, but the diagnosis of HIV infection is
frequently missed
• During this stage there is a large amount of
HIV in the peripheral blood and the immune
system begins to respond to the virus by
producing HIV antibodies and cytotoxic
lymphocytes
• This process is known as seroconversion
• If an HIV antibody test is done before
seroconversion is complete then it may not be
positive
LESSON 1- HIV
•STAGE 2 : Clinically asymptomatic stage
• This stage lasts for an average of ten years
and, as its name suggests, is free from major
symptoms, although there may be swollen
glands
• The level of HIV in the peripheral blood
drops to very low levels but people remain
infectious and HIV antibodies are detectable
in the blood, so antibody tests will show a
positive result
• Research has shown that HIV is not dormant
during this stage, but is very active in the
lymph nodes
• A test is available to measure the small
amount of HIV that escapes the lymph nodes
• This test which measures HIV RNA (HIV genetic
material) is referred to as the viral load test, and it
has an important role in the treatment of HIV
infection
LESSON 1- HIV
•STAGE 3 : Symptomatic HIV infection
• Over time the immune system becomes severely damaged by
HIV
• This is thought to happen for three main reasons:
• The lymph nodes and tissues become damaged or 'burnt out' because of the
years of activity;
• HIV mutates and becomes more pathogenic, in other words stronger and more
varied, leading to more T helper cell destruction;
• The body fails to keep up with replacing the T helper cells that are lost
• As the immune system fails, symptoms develop. Initially many
of the symptoms are mild, but as the immune system deteriorates
the symptoms worsen
• Symptomatic HIV infection is mainly caused by the emergence
of certain opportunistic infections that the immune system
would normally prevent
• This stage of HIV infection is often characterized by multi-
system disease and infections can occur in almost all body
systems
• Treatment for the specific infection is often carried out, but the
underlying cause is the action of HIV as it erodes the immune
system
• Unless HIV itself can be slowed down the symptoms of immune
suppression will continue to worsen
LESSON 1- HIV
•STAGE 4 : Progression from HIV to AIDS as the
immune system becomes more and more damaged the
individual may develop increasingly severe
opportunistic infections and cancers, leading eventually
to an AIDS diagnosis
•A clinical criteria is used by WHO to diagnose the
progression to AIDS, this differs slightly between adults
and children under five
•In adults and children (5+) the progression to AIDS is
diagnosed when any condition listed in clinical stage 3
or stage 4 is diagnosed and/or the CD4 count is less that
350 cells/mm3
•In children younger than five, an AIDS diagnosis is
based on having any stage 3 or stage 4 condition and/or
a CD4 count of less than between 20 cells/mm3and 30
cells/mm3 depending on the child's age in months
LESSON 2 – CLINICAL
STAGES OF HIV
LESSON 2 – CLINICAL
STAGES OF HIV
•Clinical Stage I: •Clinical Stage III:
• Asymptomatic • Unexplained* severe weight loss (over 10% of
presumed or measured body weight)**
• Persistent generalized lymphadenopathy
• Unexplained* chronic diarrhea for longer than one
month
•Clinical Stage II:
• Unexplained* persistent fever (intermittent or
• Moderate unexplained* weight loss (under constant for longer than one month)
10% of presumed or measured body weight)**
• Persistent oral candidiasis
• Recurrent respiratory tract infections (sinusitis, • Oral hairy leukoplakia
tonsillitis, otitis media, pharyngitis)
• Pulmonary tuberculosis
• Herpes zoster • Severe bacterial infections (e.g. pneumonia,
• Angular chelitis empyema, pyomyositis, bone or joint infection,
• Recurrent oral ulceration meningitis, bacteremia)
• Acute necrotizing ulcerative stomatitis, gingivitis or
• Papular pruritic eruptions periodontitis
• Seborrhoeic dermatitis • Unexplained* anemia (below 8 g/dl), neutropenia
• Fungal nail infections (below 0.5 billion/l) and/or chronic thrombocytopenia
(below 50 billion/l)
LESSON 2 – CLINICAL
STAGES OF HIV
•Clinical Stage IV: • HIV encephalopathy
• HIV wasting syndrome • Extrapulmonary cryptococcosis including
meningitis
• Pneumocystis pneumonia
• Disseminated non-tuberculous mycobacteria
• Recurrent severe bacterial pneumonia infection
• Chronic herpes simplex infection (orolabial, • Progressive multifocal leukoencephalopathy
genital or anorectal of more than one month’s • Chronic cryptosporidiosis
duration or visceral at any site)
• Chronic isosporiasis
• Esophageal candidiasis (or candidiasis of
trachea, bronchi or lungs) • Disseminated mycosis (extrapulmonary
histoplasmosis, coccidiomycosis)
• Extrapulmonary tuberculosis
• Recurrent septicemia (including non-typhoidal
• Kaposi sarcoma Salmonella)
• Cytomegalovirus infection (retinitis or infection • Lymphoma (cerebral or B cell non-Hodgkin
of other organs) • Invasive cervical carcinoma
• Central nervous system toxoplasmosis • Atypical disseminated leishmaniasis
• Symptomatic HIV-associated nephropathy or
HIV-associated cardiomyopathy
LESSON 2 – CLINICAL
STAGES OF HIV
Enzyme-linked immunosorbent assay (ELISA) is a
labeled immunoassay that is considered the gold standard
of immunoassays. This immunological test is very
sensitive and is used to detect and quantify substances,
including antibodies, antigens, proteins, glycoproteins,
and hormones.
An antibody is a type of protein produced by an
individual’s immune system. This protein type has specific
regions that bind to antigens. An antigen is a protein that
can come from some foreign source and, when bound to
an antibody, induces a cascade of events through the
body’s immune system.
This interaction is utilized in ELISA testing and allows
for identifying specific protein antibodies and antigens,
with only small amounts of a test sample. ELISA testing is
used to diagnose HIV infection, pregnancy tests, and
blood typing, among others.
LESSON 2 – CLINICAL
STAGES OF HIV
The Western blot assay is a method in which individual proteins
of an HIV-1 lysate are separated according to size by
polyacrylamide gel electrophoresis. The viral proteins are then
transferred onto nitrocellulose paper and reacted with the patient's
serum. Any HIV antibody from the patient's serum is detected by
an antihuman immunoglobulin G (IgG) antibody conjugated with
an enzyme that in the presence of substrate will produce a colored
band. Positive and negative control serum specimens are run
simultaneously to allow identification of viral proteins.
The HIV-1 Western blot (WB), the historic gold standard for
laboratory diagnosis of HIV-1 infection, is no longer part of the
recommended algorithm. The two main reasons for this are the
inability of the WB to detect acute infection and the potential to
misclassify HIV-2 infection as an HIV-1 infection
Lesson 1- Oral Cancers, clinical features and etiology
M5H – CANCER
Lesson 2 – Diagnosis and Treatment Modalities for
Oral Cancers
• Frequently involves mandible than maxilla Classification of SCCA (based on degree of differentiation of the neoplastic
proliferating cells)
• Mainly observed in female than male older than 50yrs
old. Grade 1- Well differentiated- cells are generally large and show distinct cell
membrane, individual cell keratinization, keratin pearls of varying size
• Gingival SCCA does not show a strong association
with classical risk factors (tobacco use, alcohol) Grade 2- moderately differentiated- tumor cells less differentiated, have less
resemblance to squamous cell epithelium
Normal Histologic appearance of the oral Grade 3- poorly differentiated- proliferation of anaplastic cells, highly
mucosa: invasive with poor prognosis, high mitotic figures
Spindle Cell- arises from surface epithelium, usually of the lips, appears as a
proliferation of spindle cells that may be mistaken as sarcoma
Complications/Side Effects
alopecia
bone marrow suppression (risk to infection and bleeding tendencies)
mucositis
nausea and vomiting
reproductive function suppression
Treatment Modifications
1.Prior to RT
• Teeth with poor prognosis should be removed PRIOR to RT.
• An interval of at least 10 days to 2 weeks between extracting the teeth and starting RT is ideal
• No bone should be left exposed in the mouth when RT begins since, once the blood supply is damaged by RT, wound healing is jeopardized.
• Meticulous oral hygiene should be implemented and preventive oral health care instituted
•2. On-Going RT
• During RT, mucosal and salivary gland protection is critical
• amifostine can minimize mucositis and xerostomia
• chlorhexidine mouthwash, 0.2%, helps maintain oral hygiene
• antifungal drugs such as nystatin suspension q4
• 3. Post RT
• If extractions become unavoidable:
• trauma should be kept to a minimum, sharp bone edges removed, and suture carefully
• prophylactic antibiotics from 24–48 hours preop are indicated and continued for at least 4 weeks; clindamycin 300mg q6h is an appropriate antibiotic since it
penetrates bone well
• HBO may be indicated.
• oral hygiene and preventive dental care should be continued
• radiation caries and dental hypersensitivity can be controlled with a non-cariogenic diet, and daily topical fluoride applications (sodium fluoride mouthwash,
stannous fluoride gel or acidulated fluoride phosphate gel)
• salivary substitutes and sialagogues are usually required.