Food fortification in psm

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food fortification PSM Park's preventive social medicine iodine iron vitamin A fluoride

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Food Fortification in PSM (Preventive & Social Medicine)

(Source: Park's Textbook of Preventive and Social Medicine)

Definition

Food fortification is "the process whereby nutrients are added to foods (in relatively small quantities) to maintain or improve the quality of the diet of a group, a community, or a population." - WHO
More broadly, it is a public health measure aimed at reinforcing the usual dietary intake of nutrients with additional supplies to prevent or control nutritional disorders.

Programmes of Demonstrated Effectiveness

The following fortification programmes have proven effectiveness:
ProgrammeVehicleNutrient AddedTarget Condition
Fluoridation of waterWaterFluorideDental caries
Iodization of saltCommon saltIodineEndemic goitre / IDD
Vanaspati/milk fortificationVanaspati, milkVitamins A & DVitamin A deficiency, rickets
Twin fortification of saltCommon saltIodine + IronIDD + anaemia
  • Iodized salt is now widely used in most countries, including India (mandatory under law).
  • Technology has been developed for twin (double) fortification of salt with both iodine and iron to tackle two deficiencies simultaneously.

Criteria for a Suitable Vehicle and Nutrient (WHO, Park's 25th criterion)

For food or the nutrient to qualify for fortification, both must fulfil these conditions:
  1. (a) Consumption pattern - The vehicle must be consumed consistently as part of the regular daily diet by the relevant (or total) population sections targeted.
  2. (b) Safe dose range - The amount of nutrient added must provide an effective supplement for low consumers, without contributing a hazardous excess to high consumers.
  3. (c) Organoleptic acceptability - The addition must not cause any noticeable change in taste, smell, appearance, or consistency of the food.
  4. (d) Affordability - The cost of fortification must not raise the price of the food beyond the reach of the population in greatest need.

Additional Requirement

  • An adequate system of surveillance and control is indispensable for the effectiveness of food fortification programmes.
  • Food fortification is a long-term measure for mitigating specific problems of malnutrition in the community.

Types of Fortification (Global Classification)

TypeDescriptionExample
Mass / Large-scale fortificationNutrients added to foods consumed by the general populationIodized salt, fluoridated water
Targeted fortificationFor specific at-risk groups (children, pregnant women)Iron-fortified infant formula, folic acid in flour for women of reproductive age
Point-of-use fortificationMicronutrient powders added just before consumption (at home/school)Sprinkles for complementary feeding

Common Examples in India (PSM Context)

  1. Iodized salt - Standard salt fortified with potassium iodate (30 ppm at production level; 15 ppm at consumer level) to combat Iodine Deficiency Disorders (IDD). Mandated by Prevention of Food Adulteration Act.
  2. Vanaspati (hydrogenated fat) with Vitamins A & D - Required by the Prevention of Food Adulteration Rules to contain minimum Vitamin A (25 IU/g) and Vitamin D (2.5 IU/g).
  3. Fluoridation of water - Optimal fluoride level: 0.5-0.8 mg/L (ppm) in India (due to warmer climate; 1 ppm in temperate climates) to reduce dental caries without causing fluorosis.
  4. Twin fortification of salt (TFS) - Double fortified with both iodine and iron - addresses the co-existence of IDD and iron-deficiency anaemia; developed by NIN (National Institute of Nutrition), Hyderabad.
  5. Folic acid in cereal flour - Adopted in many countries to prevent neural tube defects (NTDs) in neonates.

Advantages of Food Fortification

  • Reaches a large population without requiring individual behaviour change
  • No change in food habits needed
  • Cost-effective and sustainable over the long term
  • Can be implemented rapidly through existing food supply chains
  • Does not require individual compliance (as opposed to supplementation)

Limitations / Disadvantages

  • Difficult to reach populations who do not consume the vehicle food (e.g., remote tribal populations not using commercial salt)
  • Risk of over-fortification in high consumers of the vehicle
  • Requires robust quality control and surveillance systems
  • May not address multiple concurrent deficiencies with a single vehicle
  • Higher cost may limit access in the most vulnerable populations

Fortification vs. Supplementation vs. Dietary Diversification

StrategyApproachBest For
FortificationAdd nutrients to foodsPopulation-wide, long-term prevention
SupplementationGive high-dose nutrient pills/dropsSevere deficiency, targeted groups (e.g., Vitamin A megadose)
Dietary diversificationImprove variety and quality of dietSustainable community-level change
Food fortification occupies the second of four WHO/FAO strategies to decrease micronutrient deficiencies globally (after dietary diversification, before supplementation and public health measures).

Park's Textbook of Preventive and Social Medicine, Chapter on Nutrition and Health (Food Fortification section, lines 6181-6206)

Botulism in psm

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Botulism in PSM (Preventive & Social Medicine)

(Primary Source: Park's Textbook of Preventive and Social Medicine)

Overview

Botulism is the most serious but rare form of food poisoning. It kills two-thirds of its victims. It is classified under food-borne intoxications (not infections) in PSM.
The name "botulism" derives from the Latin word for sausage - botulus - as early outbreaks were linked to sausage consumption.

Classification of Food Poisoning (PSM Context)

Bacterial food poisoning is classified into 3 types:
TypeMechanismExample
Infection typeIngestion of viable organisms that multiply in gutSalmonella, Shigella
Toxin type (Intoxication)Toxins produced by organisms in foodStaphylococcus enterotoxin
BotulismIngestion of preformed botulinum toxin in preserved foodClostridium botulinum

Aetiology (Agent)

  • Agent: Exotoxin of Clostridium botulinum
  • Types: Generally Type A, B, or E (Types A & B most common; Type E associated with fish)
  • At least 7 antigenic toxin types (A-G) are known; an 8th type (H) has been reported
  • C. botulinum is an anaerobic, spore-forming, gram-positive bacillus

Source / Reservoir

  • The organism is widely distributed in soil, dust, and the intestinal tract of animals
  • Enters food as spores
  • Foods most frequently responsible:
    • Home-canned/home-preserved vegetables
    • Smoked or pickled fish
    • Home-made cheese
    • Similar low-acid foods stored under anaerobic conditions
    • Honey (source of spores in infant botulism)

Incubation Period

TypeIncubation Period
Food-borne botulism18-36 hours (Park's); range 6 hours to 10 days
Infant botulism3-30 days from ingestion of spores
Wound botulism4-14 days from time of injury

Mechanism of Food Poisoning

  • The toxin is preformed in food ("intradietetic") under suitable anaerobic conditions
  • After absorption, botulinum toxin blocks release of acetylcholine (ACh) at the neuromuscular junction (presynaptic blockade)
  • Acts on the parasympathetic nervous system
  • Produces a descending flaccid paralysis - irreversible binding to presynaptic terminals
  • Immunity does NOT develop - patients who recover do not develop antitoxin in the blood

Clinical Features

Botulism differs from other food poisonings - GI symptoms are very slight/absent:

Neurological (Prominent):

  • Dysphagia (difficulty swallowing)
  • Diplopia (double vision)
  • Ptosis (drooping eyelids)
  • Dysarthria (difficulty speaking)
  • Blurring of vision
  • Muscle weakness - descending, symmetric, flaccid
  • Quadriplegia (in severe cases)

Key Distinguishing Features:

  • Fever is generally absent
  • Consciousness is retained (patient fully alert)
  • GI symptoms are very slight (unlike other food poisonings)
  • Condition is frequently fatal - death occurs 4-8 days later due to respiratory or cardiac failure

Types of Botulism

TypeMechanismKey Feature
Food-borneIngestion of preformed toxin in improperly preserved foodMost common PSM type; home-canned foods
Infant botulismSpores ingested → germinate in gut → produce toxin in vivoMost common type globally; honey a source; constipation is early sign
Wound botulismC. botulinum infects traumatized tissue, produces toxin locallyAssociated with crush injuries, "skin popping" of heroin
Iatrogenic/BioterrorismBotulinum toxin is a potential bioterrorism agentAbrupt onset of neurological symptoms

Infant Botulism (Special):

  • Occurs predominantly in infants < 6 months
  • Preceded by or begins with constipation
  • Features: decreased movement, loss of facial expression, poor feeding, weak cry, diminished gag reflex, ocular palsies, loss of head control
  • Due to in vivo toxin production in the gut (unlike food-borne botulism)
  • Honey is an avoidable source - honey should NOT be given to infants < 1 year

Diagnosis

  • Toxin neutralization bioassay in mice (gold standard)
  • In vitro mass spectrometry assay
  • Specimens: serum, stool, enema fluid, gastric aspirate, suspected food
  • EMG: Incremental increase of evoked muscle potentials at high-frequency (20-50 Hz) nerve stimulation (unlike Myasthenia Gravis which shows decrement)
  • Treatment should NOT wait for lab confirmation - start on clinical suspicion

Treatment

  1. Meticulous supportive care - especially respiratory support (mechanical ventilation if needed); recovery may take weeks to months
  2. Antitoxin:
    • Should be given to all individuals who partook of the suspected food (prophylaxis)
    • Dose: 50,000 to 100,000 units IV
    • Antitoxin is of no avail if toxin is already fixed to nervous tissue
    • For infant botulism: BabyBIG (Human Botulism Immune Globulin IV) - licensed FDA
    • For all forms including adults: Heptavalent BAT (equine-derived, available via CDC)
  3. Guanidine hydrochloride (oral): 15-40 mg/kg body weight - shown to reverse the neuromuscular block; useful adjunct when combined with good medical and nursing care
  4. Active immunization with botulinum toxoid is also available (for prevention in high-risk persons)

Prevention and Control

MeasureDetails
Heat food properlyToxin is thermolabile - heating food at 100°C for a few minutes before use makes it safe (destroys preformed toxin)
Proper canning/preservationCommercial canning (autoclaving at 121°C) destroys spores
Avoid low-acid home-preserved foods if improperly processedHome-canned vegetables, pickled fish especially risky
Do not give honey to infants < 1 yearSpores in honey cause infant botulism
Antitoxin prophylaxisGiven to all who consumed the implicated food
Botulinum toxoidFor active immunization in high-risk groups
Key point: The toxin is thermolabile - destroyed at 100°C for a few minutes. However, the spores are heat-resistant and require autoclaving (121°C, 15 min) for destruction.

Comparison with Other Food Poisonings (PSM Exam Favourite)

FeatureStaphylococcalSalmonellaBotulism
TypeIntoxicationInfectionIntoxication
Incubation1-6 hours12-24 hours18-36 hours
FeverAbsentPresentAbsent
GI symptomsProminent (vomiting)Prominent (diarrhoea)Very slight
Nervous systemNoNoProminent
ConsciousnessRetainedRetainedRetained
MortalityLowLowVery high

Sources: Park's Textbook of Preventive and Social Medicine (Botulism, p. 281); Red Book 2021 - Report of the Committee on Infectious Diseases

Reasons of paralysis of muscle

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Reasons (Causes) of Muscle Paralysis

Muscle paralysis results from failure at any point along the motor pathway. Understanding the anatomical level of the lesion is essential for diagnosis.

The Motor Pathway (Overview)

Motor Cortex (UMN)
      ↓
Internal Capsule / Corticospinal Tract
      ↓
Spinal Cord (UMN ends / LMN begins at anterior horn)
      ↓
Anterior Horn Cell (LMN cell body)
      ↓
Peripheral Nerve (LMN axon)
      ↓
Neuromuscular Junction (NMJ)
      ↓
Muscle Fibre
Paralysis can occur due to a lesion at any of these 5 levels.

Level 1 - Upper Motor Neuron (UMN) Lesions

UMN refers to neurons from the cerebral cortex → spinal cord (corticospinal tract). Lesions here cause spastic paralysis.

Signs of UMN Lesions:

FeatureFinding
WeaknessYes
Muscle atrophyMinimal (disuse only)
FasciculationsAbsent
ToneIncreased (spasticity)
ReflexesHyperreflexia
Plantar responseExtensor (Babinski's sign +)
ClonusPresent
Note: In acute UMN lesions (e.g., stroke, spinal shock), initial presentation is flaccid with decreased tone and reflexes - spasticity develops over hours to weeks.

Causes by Location:

A. Cerebral Cortex / Cerebral Hemisphere

  • Stroke (ischaemic or haemorrhagic) - most common cause of hemiplegia
  • Brain tumour (primary or metastatic)
  • Traumatic brain injury
  • Brain abscess
  • Multiple sclerosis (demyelinating plaques)
  • Encephalitis
  • Cerebral palsy (perinatal hypoxic-ischaemic injury)

B. Internal Capsule

  • Lacunar infarct (pure motor hemiplegia - classic)
  • Hypertensive haemorrhage

C. Brainstem

  • Brainstem stroke - produces crossed hemiplegia (ipsilateral cranial nerve + contralateral body weakness)
  • Brainstem tumour (e.g., glioma)
  • Multiple sclerosis

D. Spinal Cord (UMN + LMN features at different levels)

  • Trauma / spinal cord injury → quadriplegia (cervical) or paraplegia (thoracic/lumbar)
  • Transverse myelitis
  • Multiple sclerosis (cord plaques)
  • Spinal cord compression (disc prolapse, tumour, abscess, haematoma)
  • Motor neuron disease (ALS) - both UMN and LMN affected
  • Syringomyelia
  • Subacute combined degeneration (Vitamin B12 deficiency)

Level 2 - Lower Motor Neuron (LMN) Lesions

LMN refers to the anterior horn cell + peripheral nerve. Lesions here cause flaccid paralysis.

Signs of LMN Lesions:

FeatureFinding
WeaknessYes
Muscle atrophyProminent (early)
FasciculationsPresent
ToneDecreased (flaccidity)
ReflexesHyporeflexia / areflexia
Plantar responseFlexor (normal)

Causes:

A. Anterior Horn Cell (Motor Neuron)

  • Poliomyelitis - classic acute flaccid paralysis; destruction of anterior horn cells
  • Amyotrophic Lateral Sclerosis (ALS) - LMN + UMN combined
  • Spinal Muscular Atrophy (SMA) - genetic degeneration of anterior horn cells
  • West Nile virus - acute flaccid paralysis
  • Progressive Muscular Atrophy - pure LMN variant

B. Nerve Root (Radiculopathy)

  • Disc herniation / Prolapsed intervertebral disc (PIVD) - L4-L5, L5-S1 most common
  • Spondylosis
  • Tumour compressing nerve root
  • Guillain-Barre Syndrome (GBS) - acute ascending demyelinating polyneuropathy (affects roots + peripheral nerves)

C. Peripheral Nerve (Neuropathy / Mononeuropathy)

  • Trauma / nerve injury (cutting, compression, stretch)
  • Compression neuropathies:
    • Radial nerve palsy ("Saturday night palsy") - wrist drop
    • Common peroneal nerve palsy - foot drop
    • Ulnar nerve palsy - claw hand
    • Carpal tunnel syndrome (median nerve)
  • Guillain-Barre Syndrome (GBS) - most common acute paralytic polyneuropathy
  • Diabetic neuropathy
  • Vasculitis / mononeuritis multiplex
  • Leprosy - thickened peripheral nerves → mononeuropathy multiplex
  • Diphtheria - demyelinating polyneuropathy (toxin-mediated)
  • Lead poisoning - wrist drop, predominantly motor neuropathy
  • Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease)

Level 3 - Neuromuscular Junction (NMJ) Disorders

The NMJ is where the peripheral nerve terminal meets the muscle membrane. Paralysis results from failure of neurotransmission without structural nerve or muscle damage.
DisorderMechanismKey Feature
Myasthenia GravisAutoantibodies against ACh receptors (or MuSK) → postsynaptic failureFatigable weakness; worse with activity, better with rest; ptosis/diplopia
Lambert-Eaton Myasthenic Syndrome (LEMS)Autoantibodies against presynaptic VGCC → reduced ACh releaseProximal weakness improves transiently with repeated stimulation; associated with lung cancer
BotulismBotulinum toxin blocks presynaptic ACh releaseDescending flaccid paralysis; diplopia, dysphagia, no fever
Organophosphate poisoningInhibits acetylcholinesterase → ACh accumulatesCholinergic crisis; later paralysis
Succinylcholine / neuromuscular blockersCompetitive or depolarizing blockade of ACh receptorIatrogenic (used in anaesthesia)
Congenital myasthenic syndromesGenetic defects in NMJ proteinsPresent in infancy
Tick paralysisTick salivary toxin blocks presynaptic AChAscending flaccid paralysis; resolves after tick removal

Level 4 - Muscle Disorders (Myopathies)

Paralysis/weakness from intrinsic muscle disease. No fasciculations, reflexes mildly reduced only late.
CategoryExamples
Muscular dystrophiesDuchenne MD (dystrophin gene deletion), Becker MD, Fascioscapulohumeral dystrophy, Limb-girdle dystrophy
Inflammatory myopathiesPolymyositis, Dermatomyositis, Inclusion body myositis
Metabolic myopathiesMcArdle's disease (glycogen storage), Mitochondrial myopathies
Channelopathies (periodic paralysis)Hypokalemic periodic paralysis, Hyperkalemic periodic paralysis - ion channel mutations causing episodic weakness
Endocrine myopathiesHypothyroid myopathy, Cushing's syndrome (steroid myopathy), Thyrotoxic myopathy
Toxic myopathiesStatins (rhabdomyolysis), Alcohol, Corticosteroids
Congenital myopathiesNemaline myopathy, Central core disease, Centronuclear myopathy
Infectious myositisViral myositis (influenza), pyomyositis, trichinosis

Special Patterns of Paralysis and Their Localisation

PatternLesion Location
Monoplegia (one limb)Contralateral cortex (parasagittal) or ipsilateral cord/root
Hemiplegia (arm + leg, same side)Contralateral cortex, internal capsule, brainstem
Paraplegia (both legs)Thoracic/lumbar spinal cord, bilateral cortex (parasagittal)
Quadriplegia/TetraplegiaCervical spinal cord or bilateral hemispheres
Crossed hemiplegia (ipsilateral CN palsy + contralateral body)Brainstem
Ascending paralysisGBS, transverse myelitis
Descending paralysisBotulism
Proximal > distal weaknessMyopathy, LEMS
Distal > proximal weaknessNeuropathy, Charcot-Marie-Tooth
Fatigable weaknessMyasthenia Gravis (NMJ)
Episodic weaknessPeriodic paralysis (channelopathy)

UMN vs LMN vs NMJ vs Myopathy - Quick Comparison

FeatureUMNLMNNMJMyopathy
ToneIncreased (spastic)Decreased (flaccid)NormalNormal/decreased
ReflexesIncreasedDecreased/absentNormalNormal/slightly reduced
FasciculationsAbsentPresentAbsentAbsent
AtrophyMinimalProminentAbsentVariable
BabinskiPresentAbsentAbsentAbsent
Weakness distributionContralateral, pyramidalSegmental/nerve territoryProximal/ocularProximal
EMGUMN patternDenervationDecrement (MG) / Increment (LEMS)Myopathic

Sources: Neuroanatomy through Clinical Cases 3rd Ed; Bradley and Daroff's Neurology in Clinical Practice; General Anatomy - Thieme Atlas; Localization in Clinical Neurology 8e

Icds in psm

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ICDS (Integrated Child Development Services) in PSM

(Source: Park's Textbook of Preventive and Social Medicine)

Introduction

  • ICDS = Integrated Child Development Services
  • Started: 1975, in pursuance of the National Policy for Children
  • India's largest and most unique programme for early childhood care and development
  • It is designed both as a preventive and developmental effort
  • The programme has a strong nutrition component - supplementary nutrition, Vitamin A prophylaxis, and iron and folic acid distribution

Administrative Unit

AreaAdministrative UnitPopulation Covered
Rural areasCommunity Development Block~1,00,000
Tribal areasTribal Development Block~35,000
Urban areasGroup of slums-
  • Preference given to areas inhabited by backward tribes, drought-prone areas, and areas with rampant nutritional deficiencies
  • By end of 2019: ~7,075 ICDS projects and 13.77 lakh Anganwadi Centres / Mini-AWCs functional in the country

Beneficiaries

Beneficiary GroupAge
Children0-6 years
Pregnant women-
Nursing (lactating) mothers-
Other women15-45 years
Adolescent girls11-18 years
Note: Below Poverty Line (BPL) is NOT a criterion - the scheme is universal.

Objectives (5 Objectives)

  1. (a) To improve the nutritional and health status of children in the age group 0-6 years
  2. (b) To lay the foundations for proper psychological, physical and social development of the child
  3. (c) To reduce mortality, morbidity, malnutrition and school drop-out
  4. (d) To achieve effective coordination of policy and implementation among various departments working for child development
  5. (e) To enhance the capability of the mother to meet the nutritional and health needs of the child through proper nutrition and health education

Package of Services (6 Services)

The ICDS provides the following integrated package of early childhood services:
S.No.Service
1Supplementary Nutrition
2Immunization
3Health Check-up
4Medical Referral Services
5Nutrition and Health Education
6Non-formal Pre-school Education (children up to 6 years)
Services 2, 3, and 4 (immunization, health check-up, referral) are provided through public health infrastructure - sub-centres, PHC, and CHC.

Services Provided to Each Beneficiary

BeneficiaryServices
Pregnant womenHealth check-up, Tetanus immunization, Supplementary nutrition, Nutrition & health education
Nursing mothersHealth check-up, Supplementary nutrition, Nutrition & health education
Other women (15-45 yrs)Nutrition and health education only
Children < 3 yearsSupplementary nutrition, Immunization, Health check-up, Referral services
Children 3-6 yearsSupplementary nutrition, Immunization, Health check-up, Referral services, Non-formal pre-school education
Adolescent girls (11-18 yrs)Supplementary nutrition, Nutrition and health education

Delivery of Services (Details)

1. Supplementary Nutrition

Given 300 days in a year from locally available foods:
BeneficiaryCaloriesProtein
Child 6-72 months (normal)500 kcal12-15 g
Severely malnourished child 6-72 months800 kcal20-25 g
Pregnant / nursing woman600 kcal18-20 g
Revised feeding norms:
  • Children coming to AWC: morning snack (milk/banana/egg/seasonal fruit/micronutrient-fortified food) + hot cooked meal
  • Children < 3 years and pregnant/lactating mothers: "Take Home Ration" (THR)
Action based on malnutrition grade:
  • 1st degree: Nutrition education + health education to mother
  • 2nd and 3rd degree: Supplementary/therapeutic food
  • 4th degree: Recommended hospitalization
Children are weighed every month.

2. Nutrition and Health Education

  • Given to all women aged 15-45 years (priority to nursing and expectant mothers)
  • Imparted through organized courses in village during home visits by Anganwadi workers

3. Immunization

  • Children: Against 9 vaccine-preventable diseases
  • Expectant mothers: Tetanus immunization

4. Health Check-up

  • Antenatal care for expectant mothers (minimum 3 physical examinations)
  • Postnatal care for nursing mothers and newborns
  • Care of children under 6 years including:
    1. Weight and height recorded at periodical intervals
    2. Watch over developmental milestones
    3. Immunization
    4. General check-up every 3-6 months
    5. Treatment for common illnesses (diarrhoea, dysentery, RTI)
    6. Deworming
    7. Prophylaxis against Vitamin A deficiency and anaemia
    8. Referral of serious cases
  • Iron, folic acid tablets, and protein supplements given to expectant mothers

5. Non-formal Pre-school Education

  • For children 3-6 years at the anganwadi in each village (~1000 population)
  • Objective: Develop desirable attitude, values and behaviour
  • Uses locally produced, inexpensive toys and materials

6. Medical Referral Services

  • Serious cases referred to hospitals/appropriate institutions for special care

Infrastructure and Functionaries

Anganwadi Centre (AWC) Norms:

  • 1 AWC for 300-800 population (previously stated as 400-800)
  • 1 Mini-AWC for 150-300 population (previously 150-400)

Key Personnel:

FunctionaryRole
Anganwadi Worker (AWW)Focal point for service delivery; selected from community; trained for 4 months; paid honorarium Rs. 1500/month; covers population of 400-800
Child Development Project Officer (CDPO)In-charge of each ICDS project; supervises 4 Supervisors and 100 AWWs
Supervisor (Mukhya Sevika)Each responsible for 20-25 anganwadis; mentors AWWs; assists in record-keeping; provides on-the-job training
Mahila MandalsNetwork of women's groups built up in ICDS areas to help AWWs
AWW functions:
  • Provides direct link to children and mothers
  • Assists CDPO in survey of community and beneficiaries
  • Organizes non-formal education sessions
  • Provides health and nutrition education to mothers
  • Assists PHC staff in providing health services
  • Maintains records of immunization, feeding and pre-school attendance

Schemes for Adolescent Girls under ICDS

  1. Kishori Shakti Yojana (KSY): Targets girls 11-18 years; addresses self-development, nutrition, literacy, numerical and vocational skills; implemented using ICDS infrastructure
  2. Nutrition Programme for Adolescent Girls (NPAG): Pilot in 51 identified districts; targets undernourished girls (< 30 kg in 11-15 yrs; < 35 kg in 15-19 yrs); provides 6 kg free food grain/month
  3. SABLA (Rajiv Gandhi Scheme for Empowerment of Adolescent Girls): For age group 11-18 years to improve nutritional and health status
  4. IGMSY (Indira Gandhi Matritva Sahyog Yojana): Conditional cash transfer to pregnant and lactating mothers to improve their nutritional and health status

Poshan Abhiyan (National Nutrition Mission)

  • Launched: 18th December 2017 by Government of India
  • Coverage: All 36 states/UTs for 3 years starting 2017-18
  • Ensures convergence of various programmes (Anganwadi services, PMMVY, Janani Suraksha Yojana, NHM, Swachh Bharat Mission etc.)
Targets:
TargetReduction
Stunting in children (0-6 yrs)Reduce by 6% (2%/year)
Undernutrition/underweight in children (0-6 yrs)Reduce by 6% (2%/year)
Anaemia in children (6-59 months)Reduce by set targets
Low birth weightReduce by set targets

Impact of ICDS Programme

The programme has shown measurable impact:
  • Increased birth weight
  • Reduced incidence of malnutrition
  • Increased immunization coverage
  • Reduced infant and child mortality rate in covered areas

Summary - Key Numbers to Remember

ItemNumber
Year started1975
Beneficiary age (children)0-6 years
Adolescent girls11-18 years
Other women15-45 years
AWC population coverage300-800
Mini-AWC population150-300
AWWs per ICDS project~100
Supervisors per CDPO4
AWCs per Supervisor20-25
AWW training duration4 months
Supplementary nutrition days/year300 days
Calories for child (6-72 months)500 kcal + 12-15 g protein
Calories for severely malnourished child800 kcal + 20-25 g protein
Calories for pregnant/lactating mother600 kcal + 18-20 g protein
Weighing of childrenEvery month
Immunization for children9 vaccine-preventable diseases
Total ICDS projects (2019)~7,075
Total AWCs functional (2019)~13.77 lakh

Source: Park's Textbook of Preventive and Social Medicine, Chapter on Nutrition and Health / Health Programmes (ICDS section, pp. 686-688, 757)

Poshan abhiyan in psm

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Poshan Abhiyan 2.0 PSM features objectives life cycle approach India nutrition mission

I now have complete data from Park's PSM and updated information on Poshan 2.0 from official sources. Here is the full answer:

Poshan Abhiyan in PSM

(Primary Source: Park's Textbook of Preventive and Social Medicine)

Introduction

  • Full name: POSHAN Abhiyan = PM's Overarching Scheme for Holistic Nourishment
  • Also known as the National Nutrition Mission (NNM)
  • Launched: 18th December 2017 (officially rolled out 8th March 2018, International Women's Day, from Jhunjhunu, Rajasthan)
  • Coverage: All 36 States/UTs
  • Duration: Initially for 3 years commencing 2017-18 (later extended/upgraded to Poshan 2.0)
  • Nodal Ministry: Ministry of Women and Child Development (MoWCD)
  • Budget: Rs. 9046.17 crore (2017-20)

Objective / Goal

The Abhiyan aims to reduce malnutrition in the country through a life cycle approach.
Goal: Achieve improvement in the nutritional status of:
  • Children 0-6 years
  • Adolescent girls
  • Pregnant women
  • Lactating mothers

Targets (5 Fixed Targets)

S.No.TargetReductionRate
1Prevent and reduce stunting in children (0-6 years)By 6%2% per year
2Prevent and reduce undernutrition/underweight in children (0-6 years)By 6%2% per year
3Reduce prevalence of anaemia among children (6-59 months)By 9%3% per year
4Reduce prevalence of anaemia among girls and women (15-49 years)By 9%3% per year
5Reduce Low Birth Weight (LBW)By 6%2% per year
Memory aid: Targets 1, 2, 5 = 6% total (2%/year); Targets 3, 4 = 9% total (3%/year)

Approach: Life Cycle Approach

Poshan Abhiyan follows a life cycle approach - addressing nutrition at every critical stage of life:
Pre-pregnancy / Adolescent girl
        ↓
Pregnant woman (especially first 1,000 days - conception to 2 years)
        ↓
Lactating mother / Newborn
        ↓
Child under 6 years (pre-school)
        ↓
School-age child / Adolescent
Special emphasis on the first 1,000 days (conception to 2 years of age) as this period is critical for physical growth, brain development, and long-term health outcomes.

Convergence of Programmes

Poshan Abhiyan ensures convergence of multiple programmes across ministries:
ProgrammeMinistry
Anganwadi Services (ICDS)MoWCD
Pradhan Mantri Matru Vandana Yojana (PMMVY)MoWCD
Schemes for Adolescent Girls (SABLA)MoWCD
Janani Suraksha Yojana (JSY)Ministry of Health & Family Welfare
National Health Mission (NHM)Ministry of Health & Family Welfare
Swachh Bharat MissionMinistry of Jal Shakti

Key Features / Pillars

1. Technology-driven monitoring

  • Poshan Tracker Application - real-time monitoring of >14 lakh Anganwadi Centres and ~9 crore beneficiaries
  • Use of IT-based tools for tracking beneficiaries, monitoring growth, and accountability

2. Jan Andolan (People's Movement)

  • Community mobilization and mass awareness on nutrition
  • Poshan Maah (Nutrition Month) - celebrated every September with community-level activities
  • Poshan Pakhwada (Nutrition Fortnight) - twice yearly nutritional awareness campaigns
  • The Jan Andolan approach has generated over 150 crore activities nationwide

3. Convergence

  • Convergence of services across multiple schemes and ministries (detailed above)
  • Targets convergent actions at the AWC level

4. Incentive structure

  • States/districts given incentives for achieving targets
  • Incremental improvements rewarded

5. Behavioral Change Communication (BCC)

  • Focused nutrition and health education
  • Community-based activities involving families and frontline workers

Additional Schemes Under ICDS / Poshan Abhiyan

(a) SABLA - Rajiv Gandhi Scheme for Empowerment of Adolescent Girls

  • Target: Girls 11-18 years
  • Aim: Improve nutritional and health status, self-development, literacy, vocational skills

(b) IGMSY - Indira Gandhi Matritva Sahyog Yojana

  • Conditional cash transfer to pregnant and lactating mothers
  • Aim: Improve nutritional and health status of mothers

ICDS Status (2019 data from Park's)

IndicatorFigure
ICDS projects functional~7,075
Anganwadi Centres / Mini-AWCs functional13.77 lakh
Pre-school education beneficiaries (children)305.09 lakh
Supplementary nutrition beneficiaries (children + PLMs)836.25 lakh

Poshan 2.0 (Mission POSHAN 2.0) - Updated

After the initial 3-year phase, the government upgraded to Mission POSHAN 2.0 by amalgamating:
  • Supplementary Nutrition Programme (SNP)
  • POSHAN Abhiyan
Under one umbrella - Saksham Anganwadi and POSHAN - to create synergies and adopt an integrated approach to nutrition services.
Central Theme of Poshan 2.0: "Maximizing Brain Development in the First Six Years of Life"
Key focus areas:
  • Mother and Child Nutrition
  • Early stimulation for brain development
  • Play-based education in early years
  • Role of parents and community in minimizing screen time
  • Strengthening the Anganwadi as a community hub
  • Community-based management of acute malnutrition (CMAM) protocols

Significance in PSM

FeatureDetails
Type of programmePreventive + Promotive + Developmental
Level of carePrimary (village/AWC level)
ApproachLife cycle + convergence + technology + community participation
Key beneficiaries0-6 yr children, adolescent girls, pregnant & lactating mothers
Frontline workerAnganwadi Worker (AWW)
Monitoring toolPoshan Tracker App
Awareness monthPoshan Maah = September

Key Numbers Summary for Exam

ItemValue
Launch date18 Dec 2017 / 8 Mar 2018
Duration3 years (2017-18 to 2020-21)
States/UTs covered36
Stunting reduction target6% total (2%/year)
Underweight reduction target6% total (2%/year)
Anaemia reduction target (children 6-59 m)9% total (3%/year)
Anaemia reduction target (women 15-49 yrs)9% total (3%/year)
LBW reduction target6% total (2%/year)
ApproachLife cycle approach
Monitoring appPoshan Tracker
Awareness campaignPoshan Maah (September)

Source: Park's Textbook of Preventive and Social Medicine, Poshan Abhiyan section (lines 405-477, p. 687-688); PIB - Mission Poshan 2.0

Mid day meal scheme

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PM POSHAN scheme mid day meal renamed 2021 features calorie norms India PSM

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Mid-Day Meal Scheme in PSM

(Primary Source: Park's Textbook of Preventive and Social Medicine)

Introduction and Names

VersionNameYear
OriginalMid-Day Meal Programme (MDMP) / School Lunch ProgrammeSince 1961
Centrally Sponsored SchemeNational Programme of Nutritional Support to Primary Education (NP-NSPE)Launched 15th August 1995
RenamedNational Programme of Mid-Day Meal in SchoolsOctober 2007
Current NamePM POSHAN (Pradhan Mantri Poshan Shakti Nirman)September 2021
  • It is one of the largest school feeding programmes in the world
  • Reaches over 11 crore children in more than 11 lakh schools

Objectives

Primary Objective (Park's):

To attract more children for admission to schools and retain them so that literacy improvement could be brought about.

Expanded Objectives (NP-NSPE/PM POSHAN):

  1. Universalization of primary education by increasing:
    • Enrolment
    • Retention
    • Attendance
  2. Simultaneously impacting on nutritional status of school children
  3. Reorientation of eating habits
  4. Incorporating nutrition education into the school curriculum
  5. Encouraging use of local commodities
  6. Improving educational performance of pupils

Historical Milestones

YearEvent
1961Mid-day meal programme started throughout India
5th Five Year PlanProgramme became part of Minimum Needs Programme
15th August 1995Relaunched as centrally sponsored scheme (NP-NSPE)
1997-98Covered whole country in phased manner (started in 2,408 blocks in 1st year)
October 2002Extended to Education Guarantee Scheme and Alternative & Innovative Education Centres
2004Revised
October 2007Renamed National Programme of Mid-Day Meal in Schools
September 2021Renamed PM POSHAN (Pradhan Mantri Poshan Shakti Nirman)

Coverage / Beneficiaries

  • Originally: Classes I to V (primary stage) in government, local body and government-aided schools
  • Extended to: Classes I to VIII (upper primary added later)
  • PM POSHAN further extended to: Pre-primary (Bal Vatika) classes in government and government-aided schools

Nutritional Norms

Original Scheme (Park's - for primary classes I-V):

ComponentAmount
Food grain (central assistance)100 g per student per day (from nearest FCI godown)
CaloriesMinimum 300 kcal
Protein8-12 g

MDM Rules 2015 (Updated norms):

ClassCaloriesProtein
Primary (Classes I-V)450 kcal12 g
Upper Primary (Classes VI-VIII)700 kcal20 g
Park's key principle: The meal should supply at least one-third of total energy requirement and half of protein need of the child.

Model Menu (Park's - Table 39)

A model mid-day school meal composition:
FoodstuffAmount (g/day/child)
Cereals and millets75 g
Pulses30 g
Oils and fats8 g
Leafy vegetables30 g
Non-leafy vegetables30 g
  • The National Institute of Nutrition (NIN), Hyderabad has prepared model recipes suitable for both North and South Indians
  • Minimum feeding days required: 250 days per year (to have desired impact)

Principles of Formulating Mid-Day Meals (6 Principles - Park's)

  1. (a) The meal should be a supplement and NOT a substitute to the home diet
  2. (b) The meal should supply at least one-third of total energy requirement and half of protein need
  3. (c) The cost of the meal should be reasonably low
  4. (d) The meal should be easily prepared in schools; no complicated cooking process
  5. (e) As far as possible, locally available foods should be used (reduces cost)
  6. (f) The menu should be frequently changed to avoid monotony

Suggestions for Nutritious and Economical Meals (Park's)

  • Use whole wheat or broken wheat (dalia) for preparation
  • Rice should preferably be parboiled or unpolished
  • Single dish meals using broken wheat/rice + pulse + seasonal vegetable + edible oil - saves time and fuel (e.g., broken wheat pulao, leafy khicheri, upma, dal-vegetable bhaat)
  • Cereal-pulse combination is necessary for good quality protein; cereal:pulse ratio = 3:1 to 5:1
  • Use sprouted pulses - they have more nutrients
  • Fermentation improves nutritive value - idli, dosa, dhokla should be encouraged
  • Leafy vegetables should be washed before cutting, not after
  • Soaking of rice/dal reduces cooking time; wash grains thoroughly
  • Rice water should never be thrown away - mix with dal
  • Cook with lid on to avoid nutrient loss
  • Avoid overcooking
  • Avoid reheating of oil used for frying
  • Leafy tops of carrots, radish, turnips should be utilized, not discarded
  • Only iodized salt should be used for cooking

Funding Structure

  • Central Government: Provides free food grain from nearest Food Corporation of India (FCI) godown + transport subsidy
  • Cost sharing: Centre 60% : States 40%
  • Central assistance for cooking cost, honorarium for cook-cum-helpers, infrastructure, etc.

Important Goals of School Feeding Programme

School feeding should not be considered an end in itself. The important goals are:
  1. Reorientation of eating habits of children
  2. Incorporating nutrition education into the curriculum
  3. Encouraging use of local commodities
  4. Improving school attendance and educational performance
  5. Since numbers to be fed are in millions - maintaining balance between resources and number to be fed

PM POSHAN (2021 Update) - New Features

  • New name: Pradhan Mantri Poshan Shakti Nirman (PM POSHAN)
  • Approved for 5 years (2021-22 to 2025-26)
  • Extended coverage to pre-primary (Bal Vatika) children in government schools
  • Emphasis on nutritional quality and dietary diversity
  • Convergence with Poshan Abhiyan / Mission Poshan 2.0
  • Encourages inclusion of locally grown nutritious items like millets, eggs, fruits, and vegetables

Benefits / Impact

BenefitDetails
Increased school enrolmentParticularly for girls and disadvantaged groups
Improved attendance and retentionChildren come to school for the meal
Reduced classroom hungerImproves concentration and learning
Nutritional improvementAddresses protein-energy malnutrition
Social equityChildren of all castes eat together (promotes social cohesion)
EmploymentCreates livelihood for cook-cum-helpers (mainly women)

Key Numbers Summary for Exam

ItemValue
Original start year1961
Centrally sponsored launch15th August 1995
Current namePM POSHAN (Sep 2021)
Beneficiaries>11 crore children
Schools covered>11 lakh
Feeding days per year (NIN recommendation)250 days
Food grain per child per day100 g
Calories - Primary (I-V)450 kcal (Park's original: 300 kcal)
Calories - Upper Primary (VI-VIII)700 kcal
Protein - Primary12 g
Protein - Upper Primary20 g
Cereal:pulse ratio3:1 to 5:1
One-third energy + half protein rulePrinciple (b) of formulation
Model recipes byNIN Hyderabad
Cost sharingCentre 60% : State 40%

Source: Park's Textbook of Preventive and Social Medicine, Chapter on Nutrition and Health, Sections 7 & 8 - Mid-Day Meal Programme (lines 6452-6545, pp. 757-758)

Ors with example of appropriate technology in psm

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ORS as an Example of Appropriate Technology in PSM

(Source: Park's Textbook of Preventive and Social Medicine)

Part 1: Appropriate Technology - Definition and Concept

Definition (Park's):

"Technology that is scientifically sound, adaptable to local needs, and acceptable to those who apply it and those for whom it is used, and that can be maintained by the people themselves in keeping with the principle of self-reliance with the resources the community and country can afford."

Why "Appropriate" Is Emphasized:

  • In some countries, large, luxurious hospitals totally inappropriate to local needs are built, absorbing a major part of the national health budget, effectively blocking any improvement in general health services
  • Similarly, costly equipment and procedures are used when cheaper, scientifically valid and acceptable alternatives are available
  • The word "appropriate" distinguishes technology that truly serves the community's needs from technology that is expensive, complex, or inaccessible

Examples of Appropriate Technology (Park's):

  1. Oral Rehydration Fluid (ORS) - for diarrhoea management (the classic example)
  2. Standpipes for water supply - socially acceptable and financially more feasible than house-to-house connections

Context in Primary Health Care:

  • Appropriate technology is one of the 8 essential components of Primary Health Care (Alma-Ata Declaration, 1978)
  • It embodies the PHC philosophy of "Health by the People" - placing people's health in people's hands

Part 2: ORS (Oral Rehydration Salts/Solution)

Why ORS is the Best Example of Appropriate Technology:

ORS fulfils ALL criteria of appropriate technology -
  • Scientifically sound - based on proven glucose-sodium co-transport mechanism
  • Adaptable to local needs - usable in any setting, from hospitals to homes
  • Acceptable - easy to administer by mothers and community health workers
  • Maintainable by the people themselves - can be prepared at home with simple ingredients
  • Affordable - inexpensive ingredients, low cost
  • Called a "major breakthrough" in the fight against cholera and diarrhoeal diseases

Part 3: ORS - Full PSM Details

Background and Principle:

  • Introduced by WHO; firmly established that ORT can be used for acute diarrhoeas of all aetiologies, in all age groups, and in all countries
  • Aim: To prevent dehydration and reduce mortality
  • Scientific basis: Glucose given orally enhances intestinal absorption of salt and water (glucose-sodium co-transport mechanism), and is capable of correcting the electrolyte and water deficit
  • Experience from Kolkata: 90-95% of all cases of cholera and acute diarrhoea can be treated by oral fluids alone

Evolution of ORS Composition:

GenerationCompositionNotes
1st (original)Sodium bicarbonate-basedLess stable
2ndTrisodium citrate replaced sodium bicarbonateMore stable; less stool output in cholera
3rd (current - Reduced Osmolarity ORS)Reduced glucose + NaCl concentrationLower osmolarity (245 mOsm/L); better efficacy

Benefits of Reduced Osmolarity ORS over standard ORS:

  • Unscheduled IV therapy need fell by 33%
  • Stool output decreased by 20%
  • Vomiting reduced by 30%
  • As safe and effective as standard ORS for cholera too
  • India was the FIRST country in the world to launch this formulation (since June 2004)
  • Since January 2004 - the only formulation procured by UNICEF

Composition of Reduced Osmolarity ORS (WHO/UNICEF - Current Standard):

In grams per litre:

Ingredientg/litre
Sodium chloride2.6 g
Glucose, anhydrous13.5 g
Potassium chloride1.5 g
Trisodium citrate, dihydrate2.9 g
Total weight20.5 g

In mmol per litre (electrolyte concentrations):

Componentmmol/litre
Sodium (Na⁺)75
Chloride (Cl⁻)65
Glucose, anhydrous75
Potassium (K⁺)20
Citrate10
Total osmolarity245 mOsm/L
Compare: Standard/old ORS had osmolarity of 311 mOsm/L (Na 90 mmol/L); the reduced osmolarity version has 245 mOsm/L (Na 75 mmol/L)

Home-Made ORS (Sugar-Salt Solution):

When WHO-ORS packet is not available:
  • 1 level teaspoon of table salt + 6 level teaspoons of sugar dissolved in 1 litre of drinking water
  • Safe to use until proper ORS mixture is obtained
  • Earlier the treatment is instituted, the better

Assessment of Dehydration (Park's Table 3):

SignMild DehydrationSevere Dehydration
AppearanceThirsty, alert, restlessDrowsy, limp, cold, sweaty; may be comatose
Radial pulseNormal rate and volumeRapid, feeble, sometimes impalpable
Blood pressureNormal< 80 mmHg; may be unrecordable
Skin elasticity (pinch)Retracts immediatelyRetracts very slowly (>2 seconds)
TongueMoistVery dry
Anterior fontanelleNormalVery sunken
Urine flowNormalLittle or none
% body weight lost4-5%10% or more
Estimated fluid deficit40-50 ml/kg100-110 ml/kg

Guidelines for ORT Administration (Park's Table 4 - First 4 hours):

AgeWeightORS volume in 4 hours
Under 4 months< 5 kg200-400 ml
4-11 months5-7.9 kg400-600 ml
12-23 months8-10.9 kg600-800 ml
2-4 years11-15.9 kg800-1200 ml
5-14 years16-29.9 kg1200-2200 ml
15 years and above30 kg or more2200-4000 ml
General rule: If weight not known, set deficit at approximately 75 ml/kg

Practical Administration Rules (Park's):

  • Children < 2 years: Give 1 teaspoon every 1-2 minutes; offer frequent sips from cup for older children
  • Adults: May drink as much as they like
  • After each loose stool:
    • Children < 2 years: 50-100 ml (¼ to ½ large cup)
    • Children 2-10 years: 100-200 ml (½ to 1 large cup)
    • Older children/adults: as much as they want
  • If child vomits: Wait 10 minutes, then give slowly - 1 spoonful every 2-3 minutes
  • Breastfeeding should be continued during ORS treatment
  • Give as much as the child wants - if no vomiting and dehydration signs gone, rehydration complete
  • ORS packet dissolved in 1 litre of drinking water
  • Prepare fresh daily - use within 24 hours
  • Do NOT boil or sterilize the solution

Recommended Household Fluids (when ORS not available):

Acceptable fluids (with/without salt):
  • Rice water (kanji)
  • Unsalted soup
  • Yoghurt drinks
  • Green coconut water
  • Weak tea
  • Add 3 g salt/litre to unsalted drinks
Fluids to AVOID during diarrhoea:
  • Commercial carbonated beverages (cause osmotic diarrhoea and hypernatraemia)
  • Commercial fruit juices
  • Sweetened tea
  • Coffee
  • Medicinal teas or infusions with stimulant/purgative/diuretic effects

Feeding During Diarrhoea:

  • Infant's usual diet of cereals, vegetables and other foods should be CONTINUED during diarrhoea
  • Food should NEVER be withheld
  • Child's usual food should NEVER be diluted
  • Aim: Give as much nutrient-rich food as the child will accept
  • Resume normal feeding as soon as possible

Intravenous Rehydration (when ORS fails):

Reserved for severely dehydrated patients in shock or unable to drink. Recommended IV solutions:
  1. Ringer's Lactate (Hartmann's solution) - Best commercially available; supplies Na, K; lactate corrects acidosis
  2. Diarrhoea Treatment Solution (DTS) - WHO recommended polyelectrolyte solution
  • Normal saline: can be given if nothing else available (poorest option - does not correct acidosis or replace K)
  • Plain glucose/dextrose: should NOT be used (provide only water and glucose)
  • Recommended IV dose: 100 ml/kg

Part 4: ORS as Appropriate Technology - Why It Qualifies

Criterion of Appropriate TechnologyHow ORS Fulfils It
Scientifically soundBased on glucose-Na co-transport; proven to treat 90-95% diarrhoea/cholera cases
Adaptable to local needsUsed in hospitals, PHCs, sub-centres, and homes
Acceptable to usersAdministered by mothers and community workers; no special training needed
Maintainable by people themselvesHome preparation with salt + sugar + water
AffordableLow-cost ingredients; free at PHCs, sub-centres
Self-relianceReduces dependence on IV fluids and hospitals
Reduced mortalityMajor breakthrough in reducing deaths from diarrhoeal diseases
Empowers communityMothers can treat children at home
"The introduction of oral rehydration fluid has not only reduced the cost of treatment, but also made possible treatment of patients in their own homes by primary health workers or relatives of patient." - Park's PSM

Key Numbers Summary for Exam

ItemValue
% cholera/diarrhoea treatable by ORS alone90-95%
ORS total osmolarity (current - reduced)245 mOsm/L
ORS total osmolarity (old standard)311 mOsm/L
Sodium in reduced ORS75 mmol/L
Total weight of ORS per litre20.5 g
NaCl in ORS2.6 g/L
Glucose in ORS13.5 g/L
KCl in ORS1.5 g/L
Trisodium citrate in ORS2.9 g/L
Reduction in need for IV therapy with new ORS33%
Reduction in stool output20%
Reduction in vomiting30%
Home ORS (sugar-salt): salt1 level teaspoon
Home ORS (sugar-salt): sugar6 level teaspoons
Water for ORS preparation1 litre
ORS shelf life after preparation24 hours
IV fluid dose for severe dehydration100 ml/kg
India launched new ORS formulationJune 2004 (first country in world)
UNICEF procures only new ORS sinceJanuary 2004

Source: Park's Textbook of Preventive and Social Medicine - Section on Appropriate Technology (p. 998) and Diarrhoeal Diseases Control Programme / ORS (pp. 265-267)

Bmi in psm

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BMI (Body Mass Index) in PSM

(Source: Park's Textbook of Preventive and Social Medicine)

Definition

Body Mass Index (BMI) is a simple index of weight-for-height that is commonly used to classify underweight, overweight, and obesity in adults.
Also known as Quetelet's Index (after the Belgian statistician Adolphe Quetelet who developed it).

Formula

$$\text{BMI} = \frac{\text{Weight (kg)}}{\text{Height}^2 \text{(m}^2\text{)}}$$
Unit: kg/m²

Example (Park's):

An adult who weighs 70 kg and whose height is 1.75 m:
BMI = 70 ÷ (1.75)² = 70 ÷ 3.0625 = 22.9 kg/m² → Normal range

WHO Classification of Adults by BMI (Park's Table 2)

ClassificationBMI (kg/m²)Risk of Comorbidities
Underweight< 18.50Low (but risk of other clinical problems increased)
Normal range18.50 - 24.99Average
Overweight≥ 25.00-
- Pre-obese25.00 - 29.99Increased
- Obese Class I30.00 - 34.99Moderate
- Obese Class II35.00 - 39.99Severe
- Obese Class III (Morbid obesity)≥ 40.00Very severe
  • BMI values are age-independent and the same for both sexes
  • The WHO classification is based primarily on the association between BMI and mortality
  • The risks associated with increasing BMI are continuous and graded and begin at a BMI above 25

Further subdivision of Underweight:

GradeBMI
Grade I CED (Mild)17.0 - 18.49
Grade II CED (Moderate)16.0 - 16.99
Grade III CED (Severe)< 16.0
(CED = Chronic Energy Deficiency)

Asian / Indian Cut-offs (Modified WHO)

WHO recognized that the relationship between BMI and body fat differs across ethnic groups. For South Asians / Indians, the risk of comorbidities occurs at lower BMI levels:
ClassificationWHO (Global)Asian / Indian Cut-off
Normal18.5 - 24.9918.5 - 22.9
Overweight (risk)≥ 25.0≥ 23.0
Obesity≥ 30.0≥ 27.5
  • Indians tend to have higher body fat percentage at the same BMI compared to Caucasians
  • This is related to the "thin-fat Indian" phenotype - relatively lean body but excess visceral/central fat

BMI - Other Indices Used in Assessment of Obesity (Park's)

The BMI is the most widely used, but Park's lists other indicators:
IndexFormula
(1) BMI (Quetelet's Index)Weight (kg) / Height² (m)
(2) Ponderal IndexHeight (cm) / ∛Body weight (kg)
(3) Brocca IndexHeight (cm) - 100 = ideal weight in kg
(4) Lorentz FormulaHt(cm) - 100 - [Ht(cm) - 150] / 2 (women) or 4 (men)
(5) Corpulence IndexActual weight / Desirable weight (should not exceed 1.2)
The BMI and Brocca index are most widely used. A FAO/WHO/UNU report gives reference tables for BMI usable internationally.
Brocca Index example: A person of height 160 cm → Ideal weight = 160 - 100 = 60 kg

Limitations of BMI (Park's)

  1. Does NOT distinguish between weight associated with muscle and weight associated with fat
    • A muscular athlete may have a BMI ≥ 30 without excess fat
  2. The relationship between BMI and body fat content varies by:
    • Body build and proportion
    • Ethnic group - Polynesians have lower fat % than Caucasians at identical BMI
    • Age - % body fat increases with age up to 60-65 years in both sexes
    • Sex - % body fat is higher in women than men of equivalent BMI
  3. BMI values should be interpreted with caution in cross-sectional comparisons when estimating body fat
  4. Not applicable directly to children (need age and sex-specific percentile charts)

Other Methods of Assessing Obesity / Body Fat (Park's)

1. Body Weight

  • Widely used but not accurate for excess fat
  • Epidemiologically: +2 SD from median weight-for-height = cut-off for overweight; +3 SD = obesity

2. Skinfold Thickness

  • Large proportion of total body fat is subcutaneous
  • Measured with Harpenden Skin Callipers (non-invasive, rapid)
  • Sites: Mid-triceps, biceps, subscapular, suprailiac (4 sites)
  • Sum of measurements should be:
    • < 40 mm in boys
    • < 50 mm in girls
  • Drawbacks: No universal standards for subcutaneous fat; impossible in extreme obesity; poor repeatability

3. Waist Circumference and Waist:Hip Ratio (WHR)

  • Waist measured at midpoint between lower rib border and iliac crest
  • Correlates closely with BMI and WHR
  • Index of intra-abdominal (central) fat and total body fat
  • Changes in waist circumference reflect changes in cardiovascular risk

Cut-offs for increased metabolic risk:

MenWomen
Waist circumference≥ 102 cm≥ 88 cm
Waist:Hip Ratio (WHR)> 1.0> 0.85
(For Asians: Waist ≥ 90 cm in men; ≥ 80 cm in women)

4. Advanced Methods (not for routine use):

  • Total body water measurement
  • Total body potassium measurement
  • Body density measurement
  • Fat cell measurement - opened new field in obesity research

Intra-abdominal (Central) Fat and Health Risk (Park's)

Compared with subcutaneous fat, intra-abdominal (visceral) adipose tissue has:
  • More cells per unit mass
  • Higher blood flow
  • More glucocorticoid (cortisol) receptors
  • More androgen (testosterone) receptors
  • Greater catecholamine-induced lipolysis
  • Located upstream from the liver in the portal circulation → increased flux of non-esterified fatty acids to liver
Result: Strong evidence that abdominal obesity causes insulin resistance and metabolic syndrome (hyperinsulinaemia, dyslipidaemia, glucose intolerance, hypertension) linking obesity to CHD.

Hazards of Obesity (Park's)

(a) Increased Morbidity:

Risk LevelConditions
Greatly increasedType 2 diabetes, Gall bladder disease, Dyslipidaemia, Insulin resistance, Breathlessness, Sleep apnoea
Moderately increasedCHD, Hypertension, Osteoarthritis (knees), Hyperuricaemia/gout
Slightly increasedBreast/endometrial/colon cancer, PCOS, Impaired fertility, Low back pain
Additional morbidities: varicose veins, abdominal hernia, osteoarthritis of hips and lumbar spine, flat feet, psychological stress in adolescence, increased surgical risk, lowered fertility.

(b) Increased Mortality:

  • Framingham Heart Study (USA): Dramatic increase in sudden death among men >20% overweight vs normal weight
  • Increased mortality mainly due to: hypertension and CHD
  • Excess deaths also from renal diseases
  • Obesity lowers life expectancy

BMI in PSM - Specific Applications

ApplicationDetails
Epidemiological surveysAssess prevalence of overweight/obesity in community
Nutritional assessmentClassify CED (underweight) and obesity
Non-communicable disease riskScreening for diabetes, HTN, CVD risk
Population-level monitoringTrack nutrition transition in India
Clinical screeningIdentify individuals needing intervention
Cut-off for obese class III≥ 40 = "morbid obesity" - surgical/bariatric intervention

BMI in Children and Adolescents

  • Not applicable using adult cut-offs in children
  • Uses age- and sex-specific percentile charts (CDC/WHO growth charts)
  • At-risk for overweight: ≥ 85th percentile
  • Overweight: ≥ 95th percentile
  • Underweight: < 5th percentile

Key Numbers Summary for Exam

ItemValue
FormulaWeight(kg) / Height²(m²)
Also known asQuetelet's Index
Normal BMI18.5 - 24.99
Underweight< 18.5
Overweight (pre-obese)25 - 29.99
Obese Class I30 - 34.99
Obese Class II35 - 39.99
Obese Class III (Morbid)≥ 40
Asian/Indian overweight cut-off≥ 23
Asian/Indian obesity cut-off≥ 27.5
Waist circumference risk - Men≥ 102 cm (Asian: ≥ 90 cm)
Waist circumference risk - Women≥ 88 cm (Asian: ≥ 80 cm)
WHR risk - Men> 1.0
WHR risk - Women> 0.85
Skinfold sum (boys)< 40 mm
Skinfold sum (girls)< 50 mm
Corpulence index upper limit1.2
BMI classification basis (WHO)BMI vs mortality association

Source: Park's Textbook of Preventive and Social Medicine, Chapter on Non-communicable Diseases (BMI section, pp. 449-451)

BMR

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BMR (Basal Metabolic Rate) in PSM

(Sources: Park's Textbook of PSM; Guyton & Hall Textbook of Medical Physiology)

Definition

Basal Metabolic Rate (BMR) is the minimum level of energy required by the body to exist - i.e., to perform all vital chemical reactions while at complete rest, awake, and in a post-absorptive (fasting) state.
"Even when a person is at complete rest, considerable energy is required to perform all the chemical reactions of the body. This minimum level of energy required to exist is called the BMR." - Guyton & Hall
  • Also called Resting Metabolic Rate (RMR) or Resting Energy Expenditure (REE) (RMR differs very little from BMR)
  • Accounts for 50-70% of total daily energy expenditure in most sedentary persons

Conditions for Measuring BMR (Standard Conditions)

BMR is measured under strictly basal conditions:
  1. The person must NOT have eaten food for at least 12 hours (post-absorptive state)
  2. Determined after a night of restful sleep
  3. No strenuous activity for at least 1 hour before the test
  4. All psychic and physical factors causing excitement must be eliminated
  5. Temperature of air must be comfortable - between 68°F and 80°F (20-26.7°C)
  6. No physical activity permitted during the test
  7. Person should be lying still and awake

Normal Value of BMR

  • Average BMR in a 70-kg adult man = 65-70 Calories (kcal) per hour
  • Expressed as: kcal/hour/m² body surface area (to correct for body size differences)
  • BMR is calculated from height and weight (surface area)

Method of Measurement

The standard method is measuring the rate of oxygen (O₂) utilization over a given period under basal conditions (indirect calorimetry).

Harris-Benedict Equation (Predictive formula):

Men: BMR = 66.5 + (13.75 × weight in kg) + (5.003 × height in cm) - (6.775 × age in years)
Women: BMR = 655 + (9.563 × weight in kg) + (1.850 × height in cm) - (4.676 × age in years)
(Also: Mifflin-St Jeor equation is now considered more accurate)

Factors Affecting BMR

Factors That INCREASE BMR:

FactorEffectMagnitude
Thyroid hormone (Thyroxine)Increases chemical reaction rates of cellsMax secretion → BMR rises 50-100% above normal
Male sex hormone (Testosterone)Anabolic effect → increases skeletal muscle massIncreases BMR 10-15%
Growth hormoneStimulates cellular metabolism + skeletal muscleIncreases BMR by ~20%
FeverIncreases chemical reactions of body10-12% for every 1°C rise in temperature
Cold climateThyroid adapts → increased secretionArctic BMR 10-20% higher than tropical
Sympathetic stimulation / AdrenalineStimulates cellular oxidationIncreases BMR
Physical activity (not truly BMR but TEE)Skeletal muscle activityUp to 50x normal briefly
PregnancyExtra tissue deposition, fetal metabolism+350 kcal/day
LactationMilk secretion+600 kcal/day (0-6 months)
Growth (children/adolescents)Puberty spurtChildren >13 yrs need as much as adults

Factors That DECREASE BMR:

FactorEffectMagnitude
AgeingLoss of muscle mass, replaced by adipose tissue2% decline per decade in resting metabolism
Female sexLower muscle%, higher fat% vs menLower BMR than men at same BMI
SleepDecreased CNS activity + decreased muscle tone10-15% below normal
Malnutrition / StarvationPaucity of food substances in cells20-30% decrease
HypothyroidismLoss of thyroid secretionBMR falls to 40-60% of normal
Hot climateThyroid adapts → decreased secretionLower BMR
Advancing age after 40FAO/WHO: reduce by 5%/decade up to 60, then 10%/decadeProgressive fall

BMR and Age (Park's - ICMR 2020)

  • Energy requirements decrease with age because of:
    1. Fall in BMR
    2. Decrease in physical activity
FAO/WHO recommendation:
  • After age 40: Reduce energy requirement by 5% per decade (up to age 60)
  • After age 60: Reduce by 10% per decade
  • Overall: 2% decline in resting metabolism per decade for adults
Children (>13 years): Need as much energy as adults - due to:
  • High physical activity (almost equal to hard work in adults)
  • Puberty: spurt in growth + increase in metabolic rate

Components of Total Energy Expenditure (TEE)

Total daily energy expenditure has three components:
ComponentContributionDetails
BMR / RMR50-70% of TEEMinimum energy for vital functions
Physical Activity20-30% of TEEMost variable component
Thermic Effect of Food (TEF / SDA)~10% of TEEEnergy for digestion/absorption/metabolism of food

Key Related Terms (Park's)

Physical Activity Ratio (PAR):

$$\text{PAR} = \frac{\text{Energy cost of an activity per minute}}{\text{Energy cost of basal metabolism per minute}}$$
  • PAR is unitless
  • Advantage: Can be used for both sexes, all ages, all body sizes (covariates appear in numerator and denominator and cancel out)

Physical Activity Level (PAL):

  • Ratio of TEE to BMR over 24 hours
  • Used to classify activity levels:
    • Sedentary: PAL 1.40-1.69
    • Moderate: PAL 1.70-1.99
    • Heavy: PAL ≥ 2.00

Total Energy Expenditure (TEE):

  • TEE = BMR × PAL

Caloric Values of Macronutrients (Park's)

NutrientEnergy yield
Protein4 kcal/g
Carbohydrate4 kcal/g
Fat9 kcal/g
Dietary Fibre2 kcal/g (fermentable only)
Alcohol7 kcal/g

ICMR 2020 Daily Energy Requirements (Park's Table 23)

Adults:

CategoryActivityICMR 2020 (kcal/day)ICMR 2010 (kcal/day)
Adult MenSedentary21102320
Moderate work27102730
Heavy work34703490
Adult WomenSedentary16601900
Moderate work21302230
Heavy work27202850
Pregnant women-+350+350
Lactating (0-6 months)-+600+600
Lactating (7-12 months)-+520+520

Infants and Children:

Age GroupICMR 2020 (kcal/day)
Infants 0-6 months550
Infants 6-12 months670
Children 1-3 years1010
Children 4-6 years1360
Children 7-9 years1700
Boys 10-12 years2220
Girls 10-12 years2060
Boys 13-15 years2860
Girls 13-15 years2400
Boys 16-18 years3320
Girls 16-18 years2500

Key Numbers Summary for Exam

ItemValue
BMR definitionMinimum energy to maintain vital functions at rest
BMR normal (70-kg adult man)65-70 kcal/hour
BMR as % of TEE50-70%
BMR unitkcal/hour/m² body surface area
Fasting before BMR test12 hours
Temperature for BMR test68-80°F (20-26.7°C)
Thyroid (max) effect on BMR+50-100%
Hypothyroid effect on BMR40-60% of normal
Fever effect on BMR+10-12% per °C
Sleep effect on BMR-10-15%
Male sex hormone effect+10-15%
Malnutrition effect on BMR-20-30%
Arctic vs tropical BMR difference10-20% higher in Arctic
Age-related BMR decline2% per decade
FAO/WHO: after age 40Reduce energy by 5% per decade
FAO/WHO: after age 60Reduce energy by 10% per decade
Sedentary adult man (ICMR 2020)2110 kcal/day
Sedentary adult woman (ICMR 2020)1660 kcal/day
Extra energy in pregnancy+350 kcal/day
Extra energy in lactation (0-6 m)+600 kcal/day
PAR formulaEnergy cost of activity / Energy cost of BMR (per minute)

Sources: Park's Textbook of Preventive and Social Medicine, Nutrition chapter (pp. 729-731); Guyton & Hall Textbook of Medical Physiology, Chapter 73 (pp. 887-889)
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