Perio Exam 1 Flashcards

(45 cards)

1
Q

1) What legal ethical requirements are we obligated to provide. (4)

A
  1. Must diagnose disease 2. Must inform patient of existing disease
  2. Must offer appropriate treatment or refer
    for treatment
  3. Must treat to the standard of care
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2
Q

2) Know the variables associated with probing. (5)

A

Variables

  1. Inflammation
  2. Probe Diameter
  3. Tapered vs. Parallel
  4. Force (0.15 N to 0.75 N)
  5. Band Width (0.7 mm to 1.0 mm)
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3
Q

3) Localized vs. Generalized Chronic Periodontitis

A
Localized Chronic Periodontitis:
≤ 30% of teeth involved
Slight
Moderate
Severe
Generalized Chronic Periodontitis:
 > 30% of teeth involved
Slight
Moderate
Severe
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4
Q

4) Know the initial, early, established, advanced lesions of gingivitis and periodontitis. When do things occur

A
A.    Normal=Healthy
B1.  Initial Lesion=Gingivitis
B2.  Early Lesion=Gingivitis
B3.  Established Lesion=Gingivitis
C.  Advanced Lesion=Periodontitis
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5
Q

5) You will be asked to calculate clinical attachment loss, based on the data provided.

A
GM= Gingival Margin
PD= Probing Depth
CAL= Clinical Attachment Loss
GM + PD = CAL
ex.
GM=CEJ, 3 mm coronal, 3 mm apical
PD= 6mm, 9mm, 3mm
CAL= 6mm, 6mm, 6mm
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6
Q

6) Know about probing, how to do it and factors involved, when is it worse, when is it less, when do we exaggerate it, etc.

A

Always check interproximal/interdental crater clinically. X-ray may not show bone loss well enough.

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7
Q

7) Know about biological width.

A

Junctional Epithelium + Connective Tissue Attachment = Biological Width.

CEJ to Crest of Alveolar Bone = 1.5-2mm (biological width)

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8
Q

8) Know about mobility. How do we detect it, what is class 1, what is class 2.

A

Detect Mobility using two instruments, never fingers.

Average width of PDL in adults is: 0.17mm
Class I
	> 0.2 mm but < 1 mm
Class II
	> 1 mm
Class III
	> 1 mm + Axial Displacement
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9
Q

9) Important concept, commonly confused.

A

When we record data every time and over time it shows disease progression or disease stability. This is an important concept. Probing depth, one day tells you what it is today, but over the year it gives an indication of the patient’s disease. Bleeding on probing indicates disease activity for that day

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10
Q

10) Know the normal distance between CEJ and alveolar bone.

A

CEJ to Crest of Alveolar Bone = 1.5-2mm (biological width)

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11
Q

11) The average width of the PDL

A

0.17

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12
Q

13) When we measure furcations we use a particular type of probe and that probe measures??.

A

Cowhorn or Nabors Furca Probes for Horizontal Bone Loss.

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13
Q

14) Know the difference between gingivitis and periodontitis.

GINGIVITIS

A

Gingivitis:

  1. Plaque-Induced
  2. Gingival Diseases Modified by Systemic Factors
    ex. puberty, pregnancy, diabetes, leukemia.
  3. Gingival Diseases Modified by Med’s
    ex. dilantin, ca channel blockers, cyclosporine ask zak
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14
Q

15) Know the clinical presentation of gingivitis versus periodontitis.

A
Everybody develops gingivitis but only  
susceptible patients will develop periodontitis.
Therefore, patient’s immunology is 
extremely important in the pathogenesis 
of periodontal disease
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15
Q

16) What are the characteristics of clinically healthy gingiva? (5)

A
  1. Some neutrophils and macrophages present
  2. A few neutrophils migrating through the JE
  3. No collagen destruction
  4. Intact epithelial barrier
  5. Gingival crevicular fluid present
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16
Q

18) Know the data that we collect to diagnose.

A
  1. Probing Depth
  2. Bleeding on Probing
  3. Clinical Attachment Levels
  4. Width of Attached Gingiva
  5. Gingival Recession
  6. Furcation Involvements
  7. Tooth Mobility
  8. Radiographic Evidence of Bone Loss
  9. Plaque and Calculus
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17
Q

*****19) Know about chronic periodontitis. What does it look like clinically, what are the manifestations, is it associated with pain, etc.

A

Chronic Perio
Slight: 1-2mm CAL
Moderate: 3-4mm
Advanced: >5mm

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18
Q

20) Highlighted a few slides by Dr.Loe and Dr.Cobb that have some research data on them, those are important to know.

A

Loe: The average rate of clinical attachment loss
in patients with untreated chronic periodontitis
ranges from 0.1 to 0.3 mm per year for facial
and lingual surfaces and 0.3 mm per year for
interproximal areas.
Cobb: During the same time period, untreated periodontal patients will lose 3.5 times more teeth than will those patients who receive treatment.
OR
In a ten year period, untreated periodontal patients will lose 3.5 – 4.0 teeth while those patients who receive treatment will lose 1 tooth.

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19
Q

21) You will be asked about periodontal progression (4), the asynchronous burst model. (4)

A
  1. Plaque-induced
  2. susceptible host is required (immune system).
  3. Only a small % of the population experiences advanced destruction.
  4. The progression of the disease is probably
    an asynchronous multiple burst model
  5. Several sites have one or more bursts of activity
  6. Prolonged period of inactivity
  7. Cumulative extent of destruction varies among
    sites
  8. Some sites don’t develop attachment loss
20
Q

22) Know how we diagnose.

A

Meaning slight, moderate, severe, how much clinical attachment loss for each. Is it localized or is it generalized. How do you know based on how many percentages of sites, know the numbers and the know how to come up with a diagnosis.

21
Q

23) Different types of walls of a defect, definition of them, prognosis of them.

A

Intrabony Pockets (Vertical Bone Loss)
1 wall (worst prognosis)
2 wall
3 wall-best prognosis (most remaining walls)
circumferential
interdental: 35% max intrabony defects & 63% of mand. intrabony defects

22
Q

24) There will be a drawing of the wall defect.

A

slide 13 chronic perio slide

23
Q

25) You will be asked about diabetes in terms of periodontal disease, multiple abscesses, treatment of, and their response to treatment. A well-controlled diabetic responds just as well as a non-diabetic treatment.

A
Diabetes Causes:
xerostomia
obesity (increases susceptibility to bacterial infection- aka perio disease)
Periodontal abscesses
Rapid alveolar bone loss
increased bone resorption
increased plaque activity
impaired wound healing
altered pmn chemotaxis
24
Q

26) The pyogenic granuloma associated with pregnancy comes from what bacteria?

A

what is p. intermedia because it’s tissue invasive and associated with gingival inflammation and pyogenic granuloma.

25
27) The medication induced gingival types of gingival inflammation or gingival excess.
Dilantin Cyclosporine Ca Channel Blockers
26
28) antibiotics for pregnant women
ok to use: penecillin, erythromycin, clindamycin (with caution), cephalosporins, gentamicin (caution), vanocomycin (caution) avoid: tetracycline, ciprofloxacin, metronidazole, clarithromycin. review slides 17-19
27
29) How many months do you need to wait if a patient reports an MI before you treat the patient?
6 months.
28
30) Red Complex
porphy ging tannerella forsythia treponema denticola AA (aggresive) & prev intermedia (chronic)
29
31) There are pictures on the exam associated with the pictures you have seen in the power points; the wall defects for example, patterns of bone loss pictures (pseudopocket, intrabony..etc).
psuedopocket: gingivitis pocket intrabondy: vertical loss suprabony: horizontal loss
30
33) Diabetes, multiple abscess, how do you treat them.
chx, antibiotics??
31
1) Know the rational for treatment,
1. Control etiology 2. Control inflammation 3. Control pain and discomfort 4. Restore periodontal health 5. Maintain long-term function of the dentition 6. Regeneration of lost bone and soft tissues. 7. Maintain or restore to esthetic level as desired by patient 8. Control of the local inflammatory response contributes to control of the systemic inflammatory response and thereby promotes good general systemic health.
32
1) why do we treat the patient,
``` 1. The disease in an INFECTION Initiated by bacteria Provokes both a local and systemic inflammatory response in the host. 2. The disease is CHRONIC Cannot be cured Can be controlled 3. CANNOT REMOVE all plaque and calculus Re-infection may occur ```
33
3) Probing Depth
Rang of Probing Depth for Normal Periodontium is: | 0-3mm
34
4) When do we see bleeding on probing, things of that nature.
``` BOP Negative: No Active Disease Healthy Microbial Flora Sulcus/Pocket Epithelial Integrity Intact BOP Positive: Active Disease Presence of Microbial Biofilm/Plaque Ulcerative Sulcus/Pocket Epithelium ```
35
14) Know the difference between gingivitis and periodontitis. PERIODONTITIS
Chronic: localized and generalized Aggressive: localized and generalized Perio as manifestation of systemic disease: leukemia, neutropenia, and genetic disorders.
36
14) Know the difference between gingivitis and periodontitis.
slide 19-27 evolution inflam
37
Initial Lesion
``` 2-4 days nuetrophils vasculitis loss of CT no bone loss or CAL ```
38
Early Lesion
``` 4-7 days acute inflamm persists (nuetrophils) macrophages start to appear 70 % collagen loss pseudopocket formation begins increased GCF flow loss of stipling bleeding on probing ```
39
Established Lesion
2-3 weeks nuetrophils persist but macrophages dominate proliferation of JE elongation of rete pegs no bone loss collagen and fibroblasts continue to degrade final stage of gingivitis, can remain stable for months until=if it develops into periodontitis
40
Advanced Lesion
``` Alveolar Bone Resorption activation of osteoclasts, mmps, cytokines, prostaglandins, leukotrienes. pmns, plasma cells, macrophages loss of collagen continues CAL periodontal pocket formation radiographic bone loss 30-50 % volume ```
41
Important Cytokines
slide 39 evo
42
Stages of Gingivitis
slide 61 evo
43
Oral Signs and Symptoms of Diabetes (5)
1. Xerostomia 2. burning mouth 3. perio abscesses 4. dental caries 5. candidiasis
44
Puberty
Increase estro/proges = increase gingivitis = increase levels of prevotella intermedia management: OHI, scaling, CHX,
45
Pregnancy
Primary Objectives: healthy oral enviro & maintain optimal oral hygiene Elective: 1st tri = no tx, no radio 2nd tri = safest time frame for tx, but postpone perio surgery 3rd tri = selective tx