NEET MDS Lessons
Public Health Dentistry
When testing a null hypothesis, two types of errors can occur:
-
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.
-
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.
Case-Control Study and Cohort Study are two types of epidemiological studies
commonly used in dental research to identify potential risk factors and
understand the causality of diseases or conditions.
1. Case-Control Study:
A case-control study is a retrospective analytical study design in which
researchers start with a group of patients who already have the condition of
interest (the cases) and a group of patients without the condition (the
controls) and then work backward to determine if the cases and controls have
different exposures to potential risk factors. It is often used when the
condition is relatively rare, when it takes a long time to develop, or when it
is difficult to follow individuals over time.
In a case-control study, the cases are selected from a population that already
has the disease or condition being studied. The controls are selected from the
same population but do not have the disease. The researchers then compare the
two groups to see if there is a statistically significant difference in the
frequency of exposure to a particular risk factor.
Example in Dentistry:
Suppose we want to investigate whether there is a link between periodontal
disease and cardiovascular disease. A case-control study might be set up as
follows:
- Cases: Patients with a diagnosis of periodontal disease.
- Controls: Patients without a diagnosis of periodontal disease but otherwise
similar to the cases (same age, gender, socioeconomic status, etc.).
- Exposure of Interest: Cardiovascular disease.
The researchers would collect data on the medical and dental histories of both
groups, looking for a history of cardiovascular disease. They would compare the
proportion of cases with a history of cardiovascular disease to the proportion
of controls with the same history. If a significantly higher proportion of cases
have a history of cardiovascular disease, this suggests that there may be an
association between periodontal disease and cardiovascular disease. However,
because the study is retrospective, it does not prove that periodontal disease
causes cardiovascular disease. It merely suggests that the two are associated.
Advanatages:
- Efficient for studying rare diseases.
- Relatively quick and inexpensive.
- Can be used to identify multiple risk factors for a condition.
- Useful for generating hypotheses for further research.
Disadvantages:
- Can be prone to selection and recall bias.
- Cannot determine the temporal sequence of exposure and outcome.
- Cannot calculate the incidence rate or the absolute risk of developing the
disease.
- Odds ratios may not accurately reflect the relative risk in the population if
the disease is not rare.
2. Cohort Study:
A cohort study is a prospective longitudinal study that follows a group of
individuals (the cohort) over time to determine if exposure to specific risk
factors is associated with the development of a particular disease or condition.
Cohort studies are particularly useful in assessing the risk factors for
diseases that take a long time to develop or when the exposure is rare.
In a cohort study, participants are recruited and categorized based on their
exposure to a particular risk factor (exposed and non-exposed groups). The
researchers then follow these groups over time to see who develops the disease
or condition of interest.
Example in Dentistry:
Let's consider the same hypothesis as before, but this time using a cohort study
design:
- Cohort: A group of individuals who are initially free of
cardiovascular disease, but some have periodontal disease (exposed) and others
do not (non-exposed).
- Follow-up: Researchers would follow this cohort over a
certain period (e.g., 10 years).
- Outcome Measure: Incidence of new cases of cardiovascular
disease.
The researchers would track the incidence of cardiovascular disease in both
groups and compare the rates. If the exposed group (those with periodontal
disease) has a higher rate of developing cardiovascular disease than the
non-exposed group (those without periodontal disease), this would suggest that
periodontal disease may be a risk factor for cardiovascular disease.
Advanatges:
- Allows for the calculation of incidence rates.
- Can determine the temporal relationship between exposure and outcome.
- Can be used to study the natural history of a disease.
- Can assess multiple outcomes related to a single exposure.
- Less prone to recall bias since exposure is assessed before the outcome
occurs.
Disdvanatges:
- Can be expensive and time-consuming.
- Can be difficult to maintain participant follow-up, leading to loss to
follow-up bias.
- Rare outcomes may require large cohorts and long follow-up periods.
- Can be affected by confounding variables if not properly controlled for.
Both case-control and cohort studies are valuable tools in dental research.
Case-control studies are retrospective, quicker, and less costly, but
may be limited by biases. Cohort studies are prospective, more robust for
establishing causal relationships, but are more resource-intensive and require
longer follow-up periods. The choice of study design depends on the
research question, the availability of resources, and the nature of the disease
or condition being studied.
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
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.
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:
- 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).
- 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.
- 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:
- First Stage: The population is divided into clusters (e.g., geographic areas, schools, or communities). A random sample of these clusters is selected.
- 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.
- 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.
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.
1. Disease is multifactorial in nature; difficult to identify one particular cause
a. Host factors
(1) Immunity to disease/natural resistance
(2) Heredity
(3) Age, gender, race
(4) Physical or morphologic factors
b. Agent factors
(1) Biologic—microbiologic
(2) Chemical—poisons, dosage levels
(3) Physical—environmental exposure
c. Environment factors
(1) Physical—geography and climate
(2) Biologic—animal hosts and vectors
(3) Social —socioeconomic, education, nutrition
2. All factors must be present to be sufficient cause for disease
3. Interplay of these factors is ongoing: to affect the disease, attack at the weakest link
Some Terms
1. Epidemic—a disease of significantly greater prevalence than normal; more than the expected number of cases; a disease that spreads rapidly through a demographic segment of a population
2. Endemic—continuing problem involving normal disease prevalence; the expected number of cases; indigenous to a population or geographic area
3. Pandemic—occurring throughout the population of a country, people, or the world
4. Mortality—death
5. Morbidity—disease
6. Rate—a numerical ratio in which the number of actual occurrences appears as the numerator and number of possible occurrences appears as the denominator, often used in compilation of data concerning the prevalence and incidence of events; measure of time is an intrinsic part of the denominator.