Point prevalence
Note: The "point" in point prevalence may, for all practical purposes, consist of a day, several days, or even a few weeks - depending on the time it takes to examine the population sample.
| Type | Definition |
|---|---|
| Point prevalence | Cases existing at a single point in time |
| Period prevalence | Cases existing during a defined time interval (e.g., annual) |

Prevalence = 10 × 5 = 50 per 1,000 population
Period prevance and incidence rate
Period prevalence is considered a less commonly used measure compared to point prevalence.
Important: Incidence rate must always include the unit of time in the expression (e.g., "per 1,000 per year"). Writing "16.7 per 1,000" alone is inadequate.
| Feature | Detail |
|---|---|
| Counts | New cases only |
| Time frame | During a given period (usually one year) |
| Denominator | Population at risk |
| Duration | Not influenced by disease duration |
| Common use | Acute conditions |
| Spells | Can also count new episodes (e.g., a person with 2 colds contributes 2 spells) |

| Measure | Cases |
|---|---|
| Incidence (Jan-Dec) | 3, 4, 5, 8 (new cases that started during the year) |
| Point prevalence (Jan 1) | 1, 2, 7 (active on Jan 1) |
| Point prevalence (Dec 31) | 1, 3, 5, 8 (active on Dec 31) |
| Period prevalence (Jan-Dec) | 1, 2, 3, 4, 5, 7, 8 (present at any time during the year) |
| Feature | Incidence Rate | Point Prevalence | Period Prevalence |
|---|---|---|---|
| Cases counted | New only | Old + new at one moment | Old + new over a time span |
| Time dimension | Rate over time | Snapshot | Duration |
| Denominator | Population at risk | Population at same point | Mid-interval population |
| Best used for | Acute disease, causation studies | Burden at a moment | Burden over time |
| Relationship | P = I × D | - | - |
Case control and cohort study
The unit is the individual (not the group). The focus is on a disease that has already developed.
| Suspected Risk Factor | Cases (Disease present) | Controls (Disease absent) |
|---|---|---|
| Present | a | b |
| Absent | c | d |
| Total | a+c | b+d |
Note: The Relative Risk (RR) cannot be directly calculated from a case-control study. The OR approximates RR when the disease is rare.
| Bias | Description |
|---|---|
| Recall (memory) bias | Cases recall past exposures more readily than healthy controls |
| Selection bias | Cases/controls may not represent the general population |
| Berkesonian bias | Different hospital admission rates for different diseases distort results |
| Interviewer bias | Interviewer probes cases more thoroughly if aware of the hypothesis |
| Confounding bias | Controlled by matching |
| Advantages | Disadvantages |
|---|---|
| Relatively easy and quick to conduct | Relies on memory or past records (uncertain accuracy) |
| Inexpensive compared to cohort studies | Prone to recall bias |
| Requires few subjects | Difficult to validate information |
| Ideal for rare diseases | Not suitable for rare exposures |
| Can study multiple aetiological factors simultaneously | Cannot directly calculate incidence or RR |
| No attrition problems (no follow-up required) | Temporal relationship (cause before effect) may be hard to establish |
| Ethical problems minimal | Selection of appropriate controls is difficult |
| Cohort | Disease: YES | Disease: NO | Total |
|---|---|---|---|
| Exposed | a | b | a+b |
| Not exposed | c | d | c+d |
Relative risk can be exactly determined only from a cohort study.
| Advantages | Disadvantages |
|---|---|
| Can determine incidence of disease directly | Time-consuming and expensive |
| Can calculate Relative Risk directly | Requires large numbers of subjects |
| Temporal sequence of cause → effect is clear | Attrition (loss to follow-up) is a major problem |
| Reduces recall bias | Not suitable for rare diseases |
| Can study multiple outcomes from a single exposure | Changes in diagnostic criteria over time can distort results |
| Most reliable design for showing association between risk factor and disease | Ethical concerns if harmful exposure is suspected |
| Eliminates many problems of case-control study |
"A well-designed cohort study is considered the most reliable means of showing an association between a suspected risk factor and subsequent disease."
| Feature | Case-Control | Cohort |
|---|---|---|
| Direction | Backward (effect → cause) | Forward (cause → effect) |
| Starting point | Disease outcome | Exposure status |
| Cases at start | Disease already present | Disease-free at start |
| Time | Fast | Slow (years to decades) |
| Cost | Low | High |
| Sample size | Small | Large |
| Rare disease | Ideal | Impractical |
| Rare exposure | Impractical | Ideal |
| Measure of association | Odds Ratio (OR) | Relative Risk (RR) |
| Incidence calculable | No | Yes |
| Bias | Recall bias, selection bias | Attrition bias |
| Classic example | DES and vaginal adenocarcinoma | Framingham Heart Study |
Scanning in pregnant woman with trimester
| Parameter | Purpose |
|---|---|
| Presence, size, location of gestational sac | Confirm intrauterine pregnancy |
| Crown-Rump Length (CRL) | Gestational age dating (most accurate in 1st trimester) |
| Cardiac activity | Confirm viability |
| Number of fetuses + chorionicity | Detect multiple pregnancy |
| Amniotic fluid volume | Qualitative assessment |
| Maternal uterus and adnexa | Rule out fibroids, ovarian cysts, ectopic |
| Structure | Specific Assessment |
|---|---|
| Fetal number + cardiac activity | Confirm viability and presentation |
| Biometry | BPD, HC, AC, FL - gestational age + growth |
| Brain/Head | Intracranial anatomy, ventricles, cerebellum, cisterna magna |
| Spine | Integrity, spina bifida |
| Thorax | Four-chamber heart, lungs, diaphragm |
| Abdomen | Stomach, kidneys, bladder, abdominal wall |
| Limbs | Long bones, hands, feet |
| Placenta | Location (rule out placenta praevia), appearance |
| Amniotic fluid | Amniotic fluid index (AFI) |
| Umbilical cord | Insertion site, number of vessels |
| Ultrasound Finding | Associated Abnormality |
|---|---|
| Cardiac defect (AVSD) | Trisomy 13, 18, 21 |
| Clenched overlapping fingers | Trisomy 18 |
| Cystic hygroma / hydrops | Trisomy 13, 18, 21; Turner syndrome |
| Duodenal atresia ("double bubble") | Trisomy 21, Turner syndrome |
| Exomphalos | Trisomy 13, 18 (50% of cases) |
| Rocker-bottom foot | Trisomy 18 |
| Parameter | Purpose |
|---|---|
| Fetal biometry (BPD, HC, AC, FL) | Growth velocity; detect IUGR or macrosomia |
| Amniotic fluid index (AFI) | Oligohydramnios / polyhydramnios |
| Placenta | Final confirmation of location; rule out placenta praevia |
| Fetal presentation | Cephalic / breech / transverse |
| Umbilical artery Doppler | Assess fetoplacental circulation |
| Biophysical Profile (BPP) | Fetal wellbeing (tone, movement, breathing, AFI, NST) |
In diabetic pregnancies: "The goals of third-trimester management are to prevent stillbirth and asphyxia while optimizing safe vaginal delivery - involving monitoring fetal growth and biophysical profile or non-stress testing at least weekly."
| Trimester | Week | Scan Name | Key Purpose |
|---|---|---|---|
| 1st | 6-10 wks | Viability scan | Confirm live intrauterine pregnancy |
| 1st | 11-14 wks | Dating + NT scan | CRL dating, nuchal translucency, early anomaly detection |
| 2nd | 18-20 wks | Anomaly / Morphology scan | Structural survey, fetal anatomy, biometry |
| 2nd/3rd | 20-24 wks | Cervical length (if indicated) | Risk of preterm labour |
| 3rd | 28-36 wks | Growth scan | IUGR surveillance, Doppler, presentation |
| 3rd | 36+ wks | Presentation scan | Confirm cephalic, placental position |
Diet history chart S PERNPARK
S PERNPARK mnemonic diet history chart Park's Preventive Social Medicine
"S PERNPARK" OR "SPERNPARK" diet history nutritional assessment mnemonic
diet history methods "S" "P" "E" "R" "N" "P" "A" "R" "K" nutritional assessment Park PSM
| Letter | Method | Description |
|---|---|---|
| S | Dietary Score method | Assigns scores based on consumption of key foods; quick screening tool for dietary adequacy |
| P | Prospective method (Weighment/Record method) | Food is weighed/recorded before consumption; most accurate but burdensome |
| E | Expenditure pattern method | Estimates food intake based on household expenditure on food items |
| R | Recall method (24-hour Recall) | Subject recalls all food consumed in the previous 24 hours; retrospective, quick, widely used |
| N | Nutrition (Food) Balance Sheet | National-level data on food availability per capita; macro-level assessment |
| P | Precise (Chemical analysis / Duplicate Sample) method | Laboratory chemical analysis of duplicate food portions; most accurate, used in research |
| A | Appraisal by Food Frequency Questionnaire (FFQ) | Assesses how often specific foods are consumed over a reference period |
| R | Recording method (Food diary) | Subject records all food consumed over several days (3-7 days); prospective |
| K | Key (Inventory) method | Records food stocks at beginning and end of a defined period; used at household level |
| Prospective (recorded before/during eating) | Retrospective (recalled after eating) |
|---|---|
| Weighment method | 24-hour Recall |
| Food diary / Recording method | Diet History |
| Duplicate sample method | Food Frequency Questionnaire |
| Food Balance Sheet |
Important note: The exact mnemonic "S PERNPARK" is a teaching aid used in Indian PSM coaching/notes and is not formally printed in Park's textbook. The textbook lists these methods under "Assessment of Nutritional Status - Dietary Surveys" without using this specific acronym. If your notes or coaching material assigns slightly different full forms to any letter, those should be given priority in your exam preparation.
diet history as per park
"The value of nutritional assessment is greatly enhanced when it is supplemented by an assessment of food consumption. Direct assessment of food consumption involves dietary surveys which may be household inquiries or individual food consumption surveys."
Reference used: ICMR publication - "Nutritive Value of Indian Foods"
| Method | Type | Level | Duration |
|---|---|---|---|
| Weighment of raw foods | Direct, prospective | Household | 7 days (1 dietary cycle) |
| Weighment of cooked foods | Direct, prospective | Household | Variable |
| Oral questionnaire (24-hr recall) | Direct, retrospective | Individual | Previous 24-48 hrs |
| Food balance sheet | Indirect | National | Periodic |
Note on "S PERNPARK": Park's textbook does NOT use this mnemonic. It simply lists the above methods under "Assessment of Dietary Intake" (Method 5 of the 7 assessment methods). The mnemonic is a coaching/notes-based teaching aid not present in the original textbook.