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Public Health Dentistry - NEETMDS- courses
Public Health Dentistry

Plaque index (PlI)    

    0 = No plaque in the gingival area.
    1 = A thin film of plaque adhering to the free gingival margin and adjacent to the area of the tooth. The plaque is not readily visible, but is recognized by running a periodontal probe across the tooth surface.
    2 = Moderate accumulation of plaque on the gingival margin, within the gingival pocket, and/or adjacent to the tooth surface, which can be observed visually.
    3 = Abundance of soft matter within the gingival pocket and/or adjacent to the tooth surface.


Gingival index (GI)    

    0 = Healthy gingiva.
    1= Mild inflammation: characterized by a slight change in color, edema. No bleeding observed on gentle probing.
    2 = Moderate inflammation: characterized by redness, edema, and glazing. Bleeding on probing observed.
    3 = Severe inflammation: characterized by marked redness and edema. Ulceration with a tendency toward spontaneous bleeding.


Modified gingival index (MGI)    

    0 = Absence of inflammation.
    1 = Mild inflammation: characterized by a slight change in texture of any portion of, but not the entire marginal or papillary gingival unit.
    2 = Mild inflammation: criteria as above, but involving the entire marginal or papillary gingival unit.
    3 = Moderate inflammation: characterized by glazing, redness, edema, and/or hypertrophy of the marginal or papillary gingival unit.
    4 = Severe inflammation: marked redness, edema, and/or hypertrophy of the marginal or papillary gingival unit, spontaneous bleeding, or ulceration.
    
Community periodontal index (CPI)    

    0 = Healthy gingiva.
    1 = Bleeding observed after gentle probing or by visualization.
    2 = Calculus felt during probing, but all of the black area of the probe remains visible (3.5-5.5 mm from ball tip).
    3 = Pocket 4 or 5 mm (gingival margin situated on black area of probe, approximately 3.5-5.5 mm from the probe tip).
    4 = Pocket > 6 mm (black area of probe is not visible).
    
Periodontal screening and recording (PSR)    

    0 = Healthy gingiva. Colored area of the probe remains visible, and no evidence of calculus or defective margins is detected.
    1 = Colored area of the probe remains visible and no evidence of calculus or defective margins is detected, but bleeding on probing is noted.
    2 = Colored area of the probe remains visible and calculus or defective margins is detected.
    3 = Colored area of the probe remains partly visible (probe depth between 3.5-5.5 mm).
    4 = Colored area of the probe completely disappears (probe depth > 5.5 mm).
 

Factors Considered for Prescribing Fluoride Tablets

Child's Age:

  • Different age groups require different dosages.
  • Children older than 4 years may receive lozenges or chewable tablets, while those younger than 4 are typically prescribed liquid fluoride drops.

Fluoride Concentration in Drinking Water:

  • The fluoride level in the child's drinking water is crucial.
  • If the fluoride concentration is less than 1 part per million (ppm), systemic fluoride supplementation is recommended.

Risk of Dental Caries:

  • Children at higher risk for dental decay may need additional fluoride supplementation.
  • Regular dental assessments help determine the need for fluoride.

Overall Health and Dietary Needs:

  • Consideration of the child's overall health and any dietary restrictions that may affect fluoride intake.

Recommended Doses of Fluoride Tablets

For Children Aged 6 Months to 4 Years:

  • Liquid drops are typically prescribed in doses of 0.125, 0.25, and 0.5 mg of fluoride ion.

For Children Aged 4 Years and Older:

  • Chewable tablets or lozenges are recommended, usually at doses of 0.5 mg to 1 mg of fluoride ion.

Adjustments Based on Water Fluoride Levels:

  • Doses may be adjusted based on the fluoride content in the child's drinking water to ensure adequate protection against dental caries.

Duration of Supplementation:

  • Fluoride supplementation is generally continued until the child reaches 16 years of age, depending on their fluoride exposure and dental health status.

Terms

Health—state of complete physical, mental, and social well-being where basic human needs are met. not merely the absence of disease or infirmity; free from disease or pain

Public health — science and art of preventing disease. prolonging life, and promoting physical and mental health and efficiency through organized community efforts

1. Public health is concerned with the aggregate health of a group, a community, a state, a nation. or a group of nations

2. Public health is people’s health

3. Concerned with four broad areas

a. Lifestyle and behavior

b. The environment

c. Human biology

d. The organization of health programs and systems

Dental public health—science and art of preventing and controlling dental diseases and promoting dental health through organized community efforts; that form of dental practice that serves the community as a patient rather than the individual; concerned with the dental education of the public, with applied dental research, and with the administration of group dental care programs. as well as the prevention and control of dental diseases on a community basis

Community health—same as public health full range of health services, environmental and personal, including major activities such as health education of the public and the social context of life as it affects the community; efforts that are organized to promote and restore the health and quality of life of the people

Community dental health services are directed to ward developing, reinforcing, and enhancing the oral health status of people either as individuals or collectively as groups and communities

When testing a null hypothesis, two types of errors can occur:

  1. Type I Error (False Positive):

    • Definition: This error occurs when the null hypothesis is rejected when it is actually true. In other words, the researcher concludes that there is an effect or difference when none exists.
    • Consequences in Dentistry: For example, a study might conclude that a new dental treatment is effective when it is not, leading to the adoption of an ineffective treatment.
  2. Type II Error (False Negative):

    • Definition: This error occurs when the null hypothesis is not rejected when it is actually false. In this case, the researcher fails to detect an effect or difference that is present.
    • Consequences in Dentistry: For instance, a study might conclude that a new dental material is not superior to an existing one when, in reality, it is more effective, potentially preventing the adoption of a beneficial treatment.

A test of significance in dentistry, as in other fields of research, is a statistical method used to determine whether observed results are likely due to chance or if they are statistically significant, meaning that they are reliable and not random. It helps dentists and researchers make inferences about the validity of their hypotheses.

The procedure for conducting a test of significance typically involves the following steps:

1. Formulate a Null Hypothesis (H0) and an Alternative Hypothesis (H1): The null hypothesis is a statement that assumes there is no significant difference between groups or variables being studied, while the alternative hypothesis suggests that there is a significant difference. For example, in a dental study comparing two different toothpaste brands for their effectiveness in reducing plaque, the null hypothesis might be that there is no difference in plaque reduction between the two brands, while the alternative hypothesis would be that one brand is more effective than the other.

2. Choose a significance level (α): This is the probability of incorrectly rejecting the null hypothesis when it is true. Common significance levels are 0.05 (5%) or 0.01 (1%).

3. Determine the sample size: Depending on the research question, power analysis or literature review may help determine the appropriate sample size needed to detect a clinically significant difference.

4. Collect data: Gather data from a sample of patients or subjects under controlled conditions or from existing databases.

5. Calculate test statistics: This involves calculating a value that represents the magnitude of the difference between the observed data and what would be expected if the null hypothesis were true. Common test statistics include the t-test, chi-square test, and ANOVA (Analysis of Variance).

6. Determine the p-value: The p-value is the probability of obtaining the observed results or results more extreme than those observed if the null hypothesis were true. It is calculated based on the test statistic and the chosen significance level.

7. Compare the p-value to the significance level (α): If the p-value is less than the significance level, the result is considered statistically significant. If the p-value is greater than the significance level, the result is not statistically significant, and the null hypothesis is not rejected.

8. Interpret the results: Based on the p-value, make a decision about the null hypothesis. If the p-value is less than the significance level, reject the null hypothesis and accept the alternative hypothesis. If the p-value is greater than the significance level, fail to reject the null hypothesis.

Here is a simplified example of a test of significance applied to dentistry:

Suppose you are comparing two different toothpaste brands to determine if there is a significant difference in their effectiveness in reducing dental plaque. You conduct a study with 50 participants who are randomly assigned to use either brand A or brand B for a month. After a month, you measure the plaque levels of all participants.

1. Null Hypothesis (H0): There is no significant difference in plaque reduction between the two toothpaste brands.
2. Alternative Hypothesis (H1): There is a significant difference in plaque reduction between the two toothpaste brands.
3. Significance Level (α): 0.05

Now, let's say you collected the data and found that the mean plaque reduction for brand A was 25%, with a standard deviation of 5%, and for brand B, the mean was 30%, with a standard deviation of 4%. You could use an independent samples t-test to compare the two groups' means.

4. Calculate the t-statistic: t = (Mean of Brand B - Mean of Brand A) / (Standard Error of the Difference)
5. Find the p-value associated with the calculated t-statistic. If the p-value is less than 0.05, you reject the null hypothesis.

If the p-value is less than 0.05, you can conclude that there is a statistically significant difference in plaque reduction between the two toothpaste brands, supporting the alternative hypothesis that one brand is more effective than the other. This could lead to further research or a change in dental hygiene recommendations.

In dental applications, tests of significance are commonly used in studies examining the effectiveness of different treatments, materials, and procedures. For instance, they can be applied to compare the success rates of different types of dental implants, the efficacy of various tooth whitening methods, or the impact of oral hygiene interventions on periodontal health. Understanding the statistical significance of these findings allows dentists to make evidence-based decisions and recommendations for patient care.

Multiphase and multistage random sampling are advanced sampling techniques used in research, particularly in public health and social sciences, to efficiently gather data from large and complex populations. Both methods are designed to reduce costs and improve the feasibility of sampling while maintaining the representativeness of the sample. Here’s a detailed explanation of each method:

Multiphase Sampling

Description: Multiphase sampling involves conducting a series of sampling phases, where each phase is used to refine the sample further. This method is particularly useful when the population is large and heterogeneous, and researchers want to focus on specific subgroups or characteristics.

Process:

  1. Initial Sampling: In the first phase, a large sample is drawn from the entire population using a probability sampling method (e.g., simple random sampling or stratified sampling).
  2. Subsequent Sampling: In the second phase, researchers may apply additional criteria to select a smaller, more specific sample from the initial sample. This could involve stratifying the sample based on certain characteristics (e.g., age, health status) or conducting follow-up surveys.
  3. Data Collection: Data is collected from the final sample, which is more targeted and relevant to the research question.

Applications:

  • Public Health Surveys: In a study assessing health behaviors, researchers might first sample a broad population and then focus on specific subgroups (e.g., smokers, individuals with chronic diseases) for more detailed analysis.
  • Qualitative Research: Multiphase sampling can be used to identify participants for in-depth interviews after an initial survey has highlighted specific areas of interest.

Multistage Sampling

Description: Multistage sampling is a complex form of sampling that involves selecting samples in multiple stages, often using a combination of probability sampling methods. This technique is particularly useful for large populations spread over wide geographic areas.

Process:

  1. First Stage: The population is divided into clusters (e.g., geographic areas, schools, or communities). A random sample of these clusters is selected.
  2. Second Stage: Within each selected cluster, a further sampling method is applied to select individuals or smaller units. This could involve simple random sampling, stratified sampling, or systematic sampling.
  3. Additional Stages: More stages can be added if necessary, depending on the complexity of the population and the research objectives.

Applications:

  • National Health Surveys: In a national health survey, researchers might first randomly select states (clusters) and then randomly select households within those states to gather health data.
  • Community Health Assessments: Multistage sampling can be used to assess oral health in a large city by first selecting neighborhoods and then sampling residents within those neighborhoods.

Key Differences

  • Structure:

    • Multiphase Sampling involves multiple phases of sampling that refine the sample based on specific criteria, often leading to a more focused subgroup.
    • Multistage Sampling involves multiple stages of sampling, often starting with clusters and then selecting individuals within those clusters.
  • Purpose:

    • Multiphase Sampling is typically used to narrow down a broad sample to a more specific group for detailed study.
    • Multistage Sampling is used to manage large populations and geographic diversity, making it easier to collect data from a representative sample.

Decayed-Missing-Filled Index ( DMF ) which was introduced by Klein, Palmer and Knutson in 1938 and modified by WHO:

1. DMF teeth index (DMFT) which measures the prevalence of dental caries/Teeth.
2. DMF surfaces index (DMFS) which measures the severity of dental caries.
The components are:

D component:
Used to describe (Decayed teeth) which include:
1. Carious tooth.
2. Filled tooth with recurrent decay.
3. Only the root are left.
4. Defect filling with caries.
5. Temporary filling.
6. Filled tooth surface with other surface decayed

M component:
Used to describe (Missing teeth due to caries) other cases should be excluded these are:
1. Tooth that extracted for reasons other than caries should be excluded, which include:
 a- Orthodontic treatment.
 b- Impaction.
 c- Periodontal disease.
2. Unerupted teeth.
3. Congenitally missing.
4. Avulsion teeth due to trauma or accident.

F component:
Used to describe (Filled teeth due to caries).

Teeth were considered filled without decay when one or more permanent restorations were present and there was no secondary (recurrent) caries or other area of the tooth with primary caries.
A tooth with a crown placed because of previous decay was recorded in this category.

Teeth restored for reason other than dental caries should be excluded, which include:
1. Trauma (fracture).
2. Hypoplasia (cosmatic purposes).
3. Bridge abutment (retention).
4. Seal a root canal due to trauma.
5. Fissure sealant.
6. Preventive filling.

 

1. A tooth is considered to be erupted when just the cusp tip of the occlusal surface or incisor edge is exposed.
The excluded teeth in the DMF index are:
a. Supernumerary teeth.
b. The third molar according to Klein, Palmer and Knutson only.

2. Limitations - DMF index can be invalid in older adults or in children because index can overestimate caries record by cases other than dental caries.

1. DMFT: a. A tooth may have several restorations but it counted as one tooth, F. b. A tooth may have restoration on one surface and caries on the other, it should be counted as D . c. No tooth must be counted more than once, D M F or sound.

2. DMFS: Each tooth was recorded scored as 4 surfaces for anterior teeth and 5 surfaces for posterior teeth. a. Retained root was recorded as 4 D for anterior teeth, 5 D for posterior teeth. b. Missing tooth was recorded as 4 M for anterior teeth, 5 M for posterior teeth. c. Tooth with crown was recorded as 4 F for anterior teeth, 5 F for posterior teeth.

Calculation of DMFT \ DMFS:

1. For individual

DMF = D + M + F

2. For population 

Minimum score = Zero

Primary teeth index:
1. dmft / dmfs Maximum scores: dmft = 20 , dmfs = 88
2. deft / defs, which was introduced by Gruebbel in 1944: d- decayed tooth. e- decayed tooth indicated for extraction . f- filled tooth.
3. dft / dfs: In which the missing teeth are ignored, because in children it is difficult to make sure whether the missing tooth was exfoliated or extracted due to caries or due to serial extraction.

Mixed dentition:

Each child is given a separate index, one for permanent teeth and another for primary teeth. Information from the dental caries indices can be derived to show the:

1. Number of persons affected by dental caries (%).

2. Number of surfaces and teeth with past and present dental caries (DMFT / dmft - DMFS / dmfs).

3. Number of teeth that need treatment, missing due to caries, and have been treated ( DT/dt, MT/mt, FT/f t).

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