Classifications of epidemiologic research

1. Descriptive research —involves description, documentation, analysis, and interpretation of data to evaluate a current event or situation

a. incidence—number of new cases of a specific disease within a defined population over a period of time

b. Prevalence—number of persons in a population affected by a condition at any one time

c. Count—simplest sum of disease: number of cases of disease occurrence

d. Proportion—use of a count with the addition of a denominator to determine prevalence:

does not include a time dimension: useful to evaluate prevalence of caries in schoolchildren or tooth loss in adult populations

e. Rate— uses a standardized denominator and includes a time dimension. for example. the number of deaths of newborn infants within first year of life per 1000 births

2. Analytical research—determines the cause of disease or if a causal relationship exists between a factor and a disease

a. Prospective study—planning of the entire study is completed before data are collected and analyzed; population is followed through time to determine which members develop the disease; several hypotheses may be tested at on time

b. Cohort study—individuals are classified into groups according to whether or not they pos- sess a particular characteristic thought to be related to the condition of interest; observations occur over time to see who develops dis ease or condition

c. Retrospective study— decision to carry out an investigation using observations or data that have been collected in the past; data may be incomplete or in a manner not appropriate for study

d. Cross-sectional study— study of subgroups of individuals in a specific and limited time frame to identify either initially to describe current status or developmental changes in the overall group from the perspective of what is typical in each subgroup

e. Longitudinal study—investigation of the same group of individuals over an extended period of time to identify a change or devel opment in that group

3. Experimental research—used when the etiology of the disease is established and the researcher wishes to determine the effectiveness of altering some factor or factors; deliberate applying or withholding of the supposed cause of a condition and observing the result

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.

Here are some common types of bias encountered in public health dentistry, along with their implications:

1. Selection Bias

Description: This occurs when the individuals included in a study are not representative of the larger population. This can happen due to non-random sampling methods or when certain groups are more likely to be included than others.

Implications:

• If a study on dental care access only includes patients from a specific clinic, the results may not be generalizable to the broader community.
• Selection bias can lead to over- or underestimation of the prevalence of dental diseases or the effectiveness of interventions.

2. Information Bias

Description: This type of bias arises from inaccuracies in the data collected, whether through measurement errors, misclassification, or recall bias.

Implications:

• Recall Bias: Patients may not accurately remember their dental history or behaviors, leading to incorrect data. For example, individuals may underestimate their sugar intake when reporting dietary habits.
• Misclassification: If dental conditions are misdiagnosed or misreported, it can skew the results of a study assessing the effectiveness of a treatment.

3. Observer Bias

Description: This occurs when the researcher’s expectations or knowledge influence the data collection or interpretation process.

Implications:

• If a dentist conducting a study on a new treatment is aware of which patients received the treatment versus a placebo, their assessment of outcomes may be biased.
• Observer bias can lead to inflated estimates of treatment effectiveness or misinterpretation of results.

4. Confounding Bias

Description: Confounding occurs when an outside variable is associated with both the exposure and the outcome, leading to a false association between them.

Implications:

• For example, if a study finds that individuals with poor oral hygiene have higher rates of cardiovascular disease, it may be confounded by lifestyle factors such as smoking or diet, which are related to both oral health and cardiovascular health.
• Failing to control for confounding variables can lead to misleading conclusions about the relationship between dental practices and health outcomes.

5. Publication Bias

Description: This bias occurs when studies with positive or significant results are more likely to be published than those with negative or inconclusive results.

Implications:

• If only studies showing the effectiveness of a new dental intervention are published, the overall understanding of its efficacy may be skewed.
• Publication bias can lead to an overestimation of the benefits of certain treatments or interventions in the literature.

6. Survivorship Bias

Description: This bias occurs when only those who have "survived" a particular process are considered, ignoring those who did not.

Implications:

• In dental research, if a study only includes patients who completed a treatment program, it may overlook those who dropped out due to adverse effects or lack of effectiveness, leading to an overly positive assessment of the treatment.

7. Attrition Bias

Description: This occurs when participants drop out of a study over time, and the reasons for their dropout are related to the treatment or outcome.

Implications:

• If patients with poor outcomes are more likely to drop out of a study evaluating a dental intervention, the final results may show a more favorable outcome than is truly the case.

Addressing Bias in Public Health Dentistry

To minimize bias in public health dentistry research, several strategies can be employed:

• Random Sampling: Use random sampling methods to ensure that the sample is representative of the population.
• Blinding: Implement blinding techniques to reduce observer bias, where researchers and participants are unaware of group assignments.
• Standardized Data Collection: Use standardized protocols for data collection to minimize information bias.
• Statistical Control: Employ statistical methods to control for confounding variables in the analysis.
• Transparency in Reporting: Encourage the publication of all research findings, regardless of the results, to combat publication bias.

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.

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).
 

EPIDEMIOLOGY

Epidemiology is the study of the Distribution and determinants of disease frequency in Humans.

Epidemiology— study of health and disease in human populations and how these states are influenced by the environment and ways of living; concerned with factors and conditions that determine the occurrence and distribution of health. disease, defects. disability and deaths among individuals

Epidemiology, in conjunction with the statistical and research methods used, focuses on comparison between groups or defined populations

Characteristics of epidemiology:

1. Groups rather than individuals are studied

2. Disease is multifactorial; host-agent-environment relationship becomes critical

3. A disease state depends on exposure to a specific agent, strength of the agent.  susceptibility of the host, and environmental conditions

4. Factors

• Host: age, race, ethnic background, physiologic state, gender, culture
• Agent: chemical, microbial, physical or mechanical irritants, parasitic, viral or bacterial
• Environment: climate or physical environment, food sources, socioeconomic conditions

5. Interaction among factors affects disease or health status

Uses of epidemiology

I. Study of patterns among groups

2. Collecting data to describe normal biologic processes

3. Understanding the natural history of disease

4. Testing hypotheses for prevention and control of disease through special studies in populations

5. Planning and evaluating health care services

6. Studying of non disease entities such as suicide or accidents

7. Measuring the distribution of diseases in populations

8. Identifying risk factors and determinants of disease