20 marks university exam PSM

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Topic national leprosy eradication programme national leprosy control programme think as MD community medicine Prof checking answers Sheet then prepare detailed answer

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National Leprosy Eradication Programme NLEP India history objectives strategies MDT 20 marks PSM

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https://dghs.mohfw.gov.in/nlep.php

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National Leprosy Control Programme (NLCP) & National Leprosy Eradication Programme (NLEP)

Model Answer - 20 Marks | PSM / Community Medicine | University Examination


INTRODUCTION (2 marks)

Leprosy (Hansen's disease) is a chronic infectious disease caused by Mycobacterium leprae, primarily affecting the skin, peripheral nerves, upper respiratory tract mucosa, and eyes. It is the leading infectious cause of permanent physical disability. India carries approximately 50-60% of the global leprosy burden. Recognising this, the Government of India launched systematic national programmes beginning in 1955.

NATIONAL LEPROSY CONTROL PROGRAMME (NLCP) - 1955 (3 marks)

Year of launch: 1955 by the Government of India.
Primary aim: To control (not eradicate) leprosy by reducing its prevalence and disease burden.
Key features:
  • Focused on early case detection through surveys and passive surveillance
  • Treatment with Dapsone (DDS - Diaminodiphenylsulfone) monotherapy - given for life (20-30 years) or indefinitely
  • Domiciliary treatment model - patients treated at home rather than isolated
  • Survey, Education, and Treatment (SET) approach
  • Leprosy control units and leprosy clinics established as vertical (standalone) infrastructure
  • Recognition that leprosy could be treated in the community without isolation/stigmatisation
Limitations of NLCP:
  • Dapsone monotherapy led to widespread drug resistance (M. leprae resistance to dapsone)
  • Prolonged treatment (decades) led to poor compliance
  • Disease burden remained high despite years of the programme
  • No curative endpoint - patients treated for life
  • Vertical programme structure was not integrated with general health services

TRANSITION FROM NLCP TO NLEP (2 marks)

YearEvent
1948Hind Kusht Nivaran Sangh established
1955NLCP launched - Dapsone monotherapy
1981WHO Study Group recommends Multi-Drug Therapy (MDT)
1983NLCP restructured into NLEP - MDT introduced
1991World Health Assembly resolution to eliminate leprosy globally by year 2000
1993-2000World Bank Project Phase I - NLEP expanded to all districts
2001-2004World Bank Project Phase II
2004Leprosy integrated into IDSP
2005National-level elimination achieved (PR < 1/10,000)
2005NLEP integrated under National Rural Health Mission (NRHM)
2007Disability Prevention & Medical Rehabilitation (DPMR) guidelines
2025 (April 1)Revised MDT protocol implemented - 3-drug regimen for both PB and MB
The shift occurred because WHO demonstrated MDT was curative (not just controlling), with a fixed duration, addressing the dapsone resistance problem completely.

NATIONAL LEPROSY ERADICATION PROGRAMME (NLEP) - 1983 (8 marks)

Vision

"The Attainment of Leprosy Free Status for the People of India"

Administrative Status

NLEP is a Centrally Sponsored Scheme under the National Health Mission (NHM), implemented by the Ministry of Health & Family Welfare, Government of India. Services are provided free of cost through all public health facilities.

OBJECTIVES of NLEP

Original objectives (1983):
  1. To detect all cases of leprosy irrespective of endemicity of the area
  2. To treat all detected cases and their complications till cure/recovery
  3. To impart training to all categories of health personnel
  4. To recommend grant-in-aid to voluntary agencies engaged in anti-leprosy work
  5. To promote medico-surgical rehabilitation of disease-arrested deformed cases
  6. To encourage research on various aspects of leprosy
Current revised objectives:
  1. To reduce Prevalence Rate (PR) < 1/10,000 population at sub-national and district level
  2. To reduce Grade II disability % < 1% among new cases at national level
  3. To reduce Grade II disability cases < 1 case per million population at national level
  4. Zero disabilities among new child cases
  5. Zero stigma and discrimination against persons affected by leprosy

STRATEGIES of NLEP

  1. Early case detection and prompt MDT treatment
    • Routine passive case detection through health facilities
    • Active case detection: Leprosy Case Detection Campaigns (LCDC)
    • Household contact surveys
    • Special campaigns in high-endemic districts
  2. Multi-Drug Therapy (MDT) - core intervention (see below)
  3. Integration with General Health Care Services
    • Vertical leprosy services merged into general health infrastructure
    • Services provided at PHCs, CHCs, District Hospitals
    • ASHA involvement in case detection and treatment completion
  4. Disability Prevention and Medical Rehabilitation (DPMR)
    • Prevention of reaction-related disability
    • Reconstructive surgery for established deformities
    • Self-care training for patients with ulcers
    • Physiotherapy and vocational rehabilitation
  5. IEC / BCC (Information, Education, Communication / Behavioural Change Communication)
    • Reduction of social stigma and discrimination
    • Using local and mass media
    • Encouraging self-reporting to PHCs
    • School health education programmes
  6. Involvement of ASHAs
    • Detection of new cases
    • Ensuring treatment completion
    • Providing counselling and community linkage
  7. Surveillance and monitoring
    • Integration with IDSP (since 2004)
    • Simplified Information System (since 2002)
    • District-wise monitoring of PR, new case detection rate, Grade II disability rates

MULTI-DRUG THERAPY (MDT) - KEY COMPONENT

MDT was recommended by WHO in 1981 and introduced in India under NLEP in 1983. MDT is the only effective curative treatment for leprosy.
WHO Classification for MDT (Operational classification):
TypePaucibacillary (PB)Multibacillary (MB)
Skin lesions1-5 patches> 5 patches
Nerve involvementSingle nerve> 1 nerve
Slit-skin smearNegativePositive (or > 5 lesions)
ExamplesTT, BT leprosyBB, BL, LL leprosy
MDT Regimens:
Prior regimen (Pre-April 2025):
DrugPB (6 months)MB (12 months)
Rifampicin 600mgOnce monthly (supervised)Once monthly (supervised)
Dapsone 100mgDaily (self-administered)Daily (self-administered)
Clofazimine 300mg + 50mgNOT included300mg monthly + 50mg daily
Revised regimen (Effective April 1, 2025 - aligned with WHO 2018 guidelines):
  • A uniform 3-drug MDT regimen (Rifampicin + Dapsone + Clofazimine) is now used for BOTH PB and MB cases
  • This enhances uniformity, addresses drug resistance concerns, and improves operational efficiency
  • Duration: PB - 6 months; MB - 12 months (duration maintained)
Advantages of MDT:
  • Bactericidal against M. leprae rapidly (infectious cases rendered non-infectious within days)
  • Prevents drug resistance (multiple drugs with different mechanisms)
  • Fixed, short duration improves compliance
  • Free supply through all public health facilities
  • Relapse rates extremely low (< 0.1% per year)

ORGANISATION / INFRASTRUCTURE

LevelComponent
NationalNLEP HQ under MOHFW; Central Leprosy Division
StateState Leprosy Officer (SLO)
DistrictDistrict Leprosy Officer (DLO)
Block/PHCMedical Officer, Health Visitor, MPW (Multi-Purpose Worker)
CommunityASHA workers for case detection and treatment monitoring
SpecialisedDPMR centres, Referral Centres, Reconstructive Surgery centres
Key training institutes:
  • Central JALMA Institute for Leprosy, Agra (ICMR)
  • National Jalma Institute for Leprosy and Other Mycobacterial Diseases
  • Regional Leprosy Training and Research Institutes (RLTRIs)

MODIFIED LEPROSY ELIMINATION CAMPAIGNS (MLEC)

Conducted periodically in high-endemic areas to detect "hidden" cases through:
  • Door-to-door surveys
  • School surveys
  • Contact surveys
  • Camp approach in remote areas

ACHIEVEMENTS AND CURRENT STATUS (2 marks)

  • India achieved national-level elimination (PR < 1/10,000) in December 2005, well ahead of some targets
  • New Case Detection Rate (NCDR): significantly reduced from >5 lakh cases/year in early 1980s to approximately 1.2-1.5 lakh new cases/year currently
  • Grade II disability among new cases has been progressively declining
  • Child proportion among new cases serves as a sensitive indicator of active transmission in the community
  • India remains the country with the highest absolute number of new leprosy cases globally, highlighting the need for sustained programme efforts
Current challenges:
  • Hidden/undetected cases in remote/tribal areas
  • Social stigma preventing self-reporting
  • Drug resistance (rare, but emerging concern - addressed by 2025 revised protocol)
  • Post-elimination complacency in health system
  • High proportions in certain states (Bihar, Chhattisgarh, Jharkhand, Odisha, West Bengal, Maharashtra)

CONCLUSION (1 mark)

The NLCP laid the foundation and NLEP built upon it by introducing curative MDT, transforming India's approach from lifelong control to time-bound eradication. The programme's integration with NHM, involvement of grassroots workers (ASHAs), free MDT services, and sustained IEC activities have driven dramatic reductions in disease burden. Achieving a truly leprosy-free India requires maintaining high-quality services, sustained active case detection in endemic pockets, reducing stigma, and preventing disability in those already affected.

EXAMINER'S SCORING GUIDE (20 marks)

ComponentMarks
Introduction - leprosy, its significance, India's burden1
NLCP - year, aim, Dapsone monotherapy, limitations3
Transition timeline (1955 → 1983 → 2005)2
NLEP - vision, status (centrally sponsored, NHM)1
NLEP Objectives (original + current)2
NLEP Strategies (all 7 listed with explanation)3
MDT - WHO classification, drug regimens PB/MB, advantages4
Organisation and infrastructure1
Achievements + current challenges2
Conclusion1
Total20

Sources: Park's Textbook of Preventive and Social Medicine (PSM); Harrison's Principles of Internal Medicine 22e (2025); DGHS/MOHFW - NLEP Official Programme Page; National Health Mission Guidelines. The 3-drug uniform MDT protocol (April 2025) is the most recent update - mention this to impress the examiner.

Next national tuberculosis elimination programme

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National Tuberculosis Elimination Programme NTEP India 2025 objectives strategies DOTS NSP 2017-2025 PSM community medicine

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NTEP India Nikshay Poshan Yojana drug regimen DR-TB treatment 2025 organisation structure TU STS STLS

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National Tuberculosis Elimination Programme (NTEP)

Model Answer - 20 Marks | PSM / Community Medicine | University Examination


INTRODUCTION (2 marks)

Tuberculosis (TB) is a chronic infectious disease caused by Mycobacterium tuberculosis. It is a major public health problem and was declared a Global Emergency by WHO in 1993. India carries approximately 26% of the global TB burden - the highest of any country in the world. TB is predominantly a disease of poverty and is closely linked to malnutrition, overcrowding, HIV co-infection, and poor living conditions. Recognising this burden, India has had a national TB control programme since 1962, which has evolved significantly over decades.

EVOLUTION / HISTORICAL BACKGROUND (3 marks)

1. National Tuberculosis Programme (NTP) - 1962

  • Launched in 1962 as the first organised national TB programme
  • Based on the District Tuberculosis Centre (DTC) model
  • Strategy: Domiciliary treatment, sputum microscopy, BCG vaccination
  • Treatment: Non-standardised, irregular drug supply, self-administered
  • Problems / Failures of NTP:
    • Treatment success rates unacceptably low
    • High death and default (lost to follow-up) rates
    • Spread of multidrug-resistant TB (MDR-TB)
    • Inadequate drug supply, poor supervision
    • Programme never achieved its targets despite 30 years of operation

2. Revised National TB Control Programme (RNTCP) - 1993/1997

  • In 1993, GOI decided to revitalise NTP with international assistance
  • RNTCP formulated in 1993; pilot phase launched in 1993; nationwide expansion from 1997
  • Adopted the internationally recommended DOTS (Directly Observed Treatment Short-course) strategy
  • Fully covered the whole country by March 2006
  • Based on WHO Stop TB Strategy (2006)

3. National TB Elimination Programme (NTEP) - 2020

  • RNTCP was renamed NTEP in 2020
  • GOI committed to eliminate TB by 2025 - 5 years ahead of the global SDG target of 2030
  • Aligned with the National Strategic Plan (NSP) 2017-2025 and WHO's End TB Strategy (2014)
  • Governed under National Health Mission (NHM) as a Centrally Sponsored Scheme

TIMELINE AT A GLANCE

YearMilestone
1962National Tuberculosis Programme (NTP) launched
1978District TB Programme established
1992NTP reviewed - found ineffective
1993RNTCP formulated; DOTS pilot introduced
1997RNTCP expanded nationally
2006RNTCP covers entire country; Stop TB Strategy adopted
2012TB Notification made mandatory
2012Serological tests for TB banned
2014WHO End TB Strategy approved
2017NSP 2017-2025 launched; daily FDC regimen introduced
2018Nikshay Poshan Yojana (NPY) launched
2020RNTCP renamed NTEP
2022PM TB Mukt Bharat Abhiyaan (PMTBMBA) launched
2025 (target)TB Elimination in India

OBJECTIVES OF NTEP / NSP 2017-2025 (2 marks)

  1. Detect all drug-sensitive (DS-TB) and drug-resistant TB (DR-TB) cases, especially from private providers and high-risk undiagnosed populations
  2. Treat all diagnosed patients with appropriate anti-TB treatment with patient-friendly systems and social support
  3. Prevent emergence of TB in susceptible populations
  4. Build and strengthen enabling policies, empowered institutions, human resources, and financial support
Expected NSP Targets (by 2025):
  • 80% reduction in TB incidence (from 2015 baseline)
  • 90% reduction in TB mortality (from 2015 baseline)
  • Zero patients facing catastrophic expenditure due to TB

STRATEGIES OF NTEP - THE FOUR PILLARS (D-T-P-B) (6 marks)

Pillar 1: DETECT

  • Active Case Finding (ACF):
    • TB Mukt Bharat campaign - high visibility awareness for early case finding
    • Community screening
    • Institutional screening
    • Targeted screening of high-risk groups: prisoners, migrants, PLHIV/AIDS, contacts of confirmed cases, tribal populations, slum dwellers
  • Diagnostics:
    • Sputum smear microscopy - at Tuberculosis Diagnostic Centres (TDCs), formerly Designated Microscopy Centres (DMCs)
    • Nucleic Acid Amplification Tests (NAAT) / CB-NAAT (CBNAAT/Xpert MTB/RIF) - first-line test for diagnosis and rifampicin resistance detection; 68.3 lakh NAAT tests done in 2023
    • TRUNAT, LPA (Line Probe Assay) for rapid DR-TB detection
    • Culture & DST (C&DST) for drug resistance pattern
    • Sputum smear serology BANNED since 2012 (poor specificity, not acceptable)
  • TB Notification (Mandatory since 2012):
    • All healthcare providers (public AND private) must notify every TB case to District Health Officer monthly
    • NIKSHAY portal used for real-time notification and surveillance
  • Private Sector Engagement:
    • Private providers notified and linked for free drug supply
    • Incentives to private practitioners for notification

Pillar 2: TREAT

DOTS Strategy - Core Mechanism:
DOTS (Directly Observed Treatment Short-course) remains the cornerstone. It consists of 5 components:
  1. Political will and administrative commitment
  2. Diagnosis by quality-assured sputum smear microscopy
  3. Adequate supply of quality-assured short-course chemotherapy drugs
  4. Directly Observed Treatment (DOT) - all drugs under direct supervision, especially in intensive phase
  5. Systematic monitoring and accountability
DOT Agents: MPWs, ASHA workers, Anganwadi workers, teachers, ex-patients, social workers. Paid Rs.150 honorarium per patient completing treatment.
Current Treatment Regimen (NTEP Daily FDC Regimen):
All treatment under NTEP uses daily Fixed Dose Combinations (FDCs) based on weight bands:
CategoryPatientsRegimen
Category I (New cases)New smear +ve PTB, new smear -ve PTB, new EP-TB2HRZE / 4HR (2 months Intensive + 4 months Continuation)
Category II (Previously treated)Retreatment (relapse, failure, defaulter)2HRZES / 1HRZE / 5HRE
Paediatric TBChildrenDaily weight-band FDC
MDR-TB / DR-TBRifampicin-resistant casesBedaquiline-based regimens (BPaL, BPaLM)
H = Isoniazid, R = Rifampicin, Z = Pyrazinamide, E = Ethambutol, S = Streptomycin
New drugs for DR-TB:
  • Bedaquiline - introduced in India; highly effective against MDR-TB
  • Delamanid - for XDR-TB
  • Shorter Treatment Regimen (STR) for DR-TB - 9-12 months (vs. old 24 months)
  • BPaL / BPaLM regimen (Bedaquiline + Pretomanid + Linezolid ± Moxifloxacin)
Patient Support - Nikshay Poshan Yojana (NPY):
  • Financial incentive of Rs. 500/month given directly to TB patients throughout treatment for nutritional support
  • Transferred via Direct Benefit Transfer (DBT) linked to Aadhaar
  • Helps address malnutrition and improves treatment adherence
Digital Adherence:
  • 99DOTS - mobile technology-based adherence monitoring
  • NIKSHAY portal - real-time patient tracking, outcome monitoring

Pillar 3: PREVENT

  1. Airborne Infection Control (AIC):
    • Administrative measures (triaging, fast-tracking)
    • Environmental controls (ventilation, UV germicidal irradiation)
    • Personal respiratory protection
  2. TB Preventive Therapy (TPT) / Isoniazid Preventive Therapy (IPT):
    • For contacts of bacteriologically-confirmed TB cases
    • PLHIV on ART (high-priority group)
    • Children < 5 years exposed to TB
  3. BCG Vaccination:
    • Protects against severe childhood TB (miliary TB, TB meningitis)
    • Part of UIP; given at birth
  4. Addressing Social Determinants:
    • Intersectoral approach addressing poverty, malnutrition, overcrowding
    • Linking TB with PM Poshan, PMJAY, etc.
  5. TB/HIV Co-management:
    • All TB patients screened for HIV
    • All HIV patients screened for TB
    • Co-treatment with ART + Anti-TB therapy

Pillar 4: BUILD

  1. Strengthening health system infrastructure
  2. Creation of sub-district TB Unit (TU) level - major organisational change
  3. Human resource capacity building - training STS, STLS, MO-TC
  4. Adequate financial resources for programme implementation
  5. Research and innovation - new diagnostics, drugs, regimens, vaccine
  6. Policy and legal framework - mandatory notification, ban on serology

ORGANISATION / INFRASTRUCTURE OF NTEP (3 marks)

NTEP is a Centrally Sponsored Scheme under NHM, with resource sharing between Central and State governments.
LevelUnitKey Personnel
NationalCentral TB Division (CTD), MoHFWDeputy Director General (TB)
StateState TB CellState TB Officer (STO)
DistrictDistrict TB Centre (DTC)District TB Officer (DTO)
Sub-districtTuberculosis Unit (TU)MO-TC + STS + STLS
PeripheralPHI (PHC, CHC, Hospital)Medical Officer
LaboratoryTDC (Tuberculosis Diagnostic Centre)Lab Technician + STLS
CommunityASHADOT provision + referral
Key TU-level staff:
  • MO-TC (Medical Officer - TB Control): overall management of TB programme at TU level
  • STS (Senior TB Treatment Supervisor): 1 per TU / block (~1.5-2.5 lakh population); supervises treatment
  • STLS (Senior TB Laboratory Supervisor): 1 per 5 DMCs (~5 lakh population); quality control of smear microscopy
NIKSHAY Portal: National IT-based web application for real-time TB patient registration, notification, tracking, and outcome reporting. Linked to Aadhaar for DBT of Nikshay Poshan Yojana.

FLAGSHIP INITIATIVES (2 marks)

1. PM TB Mukt Bharat Abhiyaan (PMTBMBA) - 2022

  • Launched by PM Modi on September 9, 2022
  • Ni-kshay Mitra programme - volunteers/organisations adopt TB patients to provide nutritional, diagnostic, and vocational support
  • Aims at community participation in TB elimination

2. Nikshay Poshan Yojana (NPY) - 2018

  • Rs. 500/month direct cash transfer to all notified TB patients for nutritional support
  • Addresses the TB-malnutrition-poverty cycle

3. Jan Aushadhi / Free Drug Supply

  • All first and second-line TB drugs supplied free through NTEP
  • Daily FDC (Fixed Dose Combinations) in weight bands introduced to replace thrice-weekly regimen

4. CBNAAT / TrueNat Expansion

  • Universal DST (Drug Susceptibility Testing) for all TB cases
  • Rapid molecular diagnostics replacing conventional smear microscopy as first-line test

STOP TB STRATEGY (WHO, 2006) - adopted by RNTCP

  1. Pursuing quality DOTS - expansion and enhancement
  2. Addressing TB/HIV and MDR-TB
  3. Contributing to health system strengthening
  4. Engaging all care providers (public, private, NGO)
  5. Empowering patients and communities
  6. Enabling and promoting research (diagnostics, treatment, vaccine)

END TB STRATEGY (WHO, 2014) - guiding NTEP

  • Vision: Zero deaths, disease and suffering due to TB
  • Goal: End global TB epidemic
  • 3 Pillars:
    1. Integrated, patient-centred TB care and prevention
    2. Bold policies and supportive systems
    3. Intensified research and innovation
  • Milestones by 2025: 75% reduction in TB deaths, 50% reduction in TB incidence
  • Target by 2030 (SDG): 90% reduction in deaths, 80% reduction in incidence

CURRENT STATUS & CHALLENGES (1 mark)

Achievements:
  • India TB Report 2024: ~1.89 crore sputum smear tests and 68.3 lakh NAAT tests performed in 2023
  • Significant increase in case notifications (improved detection)
  • Treatment success rate improved to ~87% for new cases
  • Bedaquiline rollout for MDR-TB nationwide
Challenges:
  • 32% increase in drug-resistant cases (MDR/XDR-TB)
  • TB/HIV co-infection burden
  • Undetected cases in private sector, tribal areas, urban slums
  • COVID-19 pandemic setback (2020-21) - missed cases, treatment interruptions
  • Malnutrition and poverty as underlying drivers
  • India did not achieve 2025 elimination target - goal extended with renewed commitment

CONCLUSION (1 mark)

The evolution from NTP (1962) to RNTCP (1993) to NTEP (2020) reflects India's commitment to a progressively more scientific, evidence-based, and patient-centred approach to TB control. NTEP's NSP 2017-2025 with the D-T-P-B framework, universal DST, daily FDC regimens, new DR-TB drugs, NIKSHAY digital platform, Nikshay Poshan Yojana, and PM TB Mukt Bharat Abhiyaan represent a multi-pronged strategy. While national-level elimination by 2025 was not fully achieved, the programme has produced significant declines in incidence and mortality, and India remains committed to a TB-free future.

EXAMINER'S SCORING GUIDE (20 marks)

ComponentMarks
Introduction - TB burden, India's significance1
NTP 1962 - features + failures2
RNTCP 1993 - DOTS, 5 components2
NTEP 2020 - renaming, NSP, targets (80%/90%/0%)2
D-T-P-B - Detect (ACF, CBNAAT, notification)2
D-T-P-B - Treat (DOTS, FDC regimens, DR-TB drugs, NPY)3
D-T-P-B - Prevent (IPT, BCG, AIC, TB/HIV)2
D-T-P-B - Build (organisation, NIKSHAY)1
Organisation structure (National to community level)2
Flagship initiatives (PMTBMBA, NPY, CBNAAT)1
Achievements + Challenges1
Conclusion1
Total20

High-yield exam points to include:
  • "Eliminate TB by 2025 - 5 years ahead of SDG 2030 target"
  • NSP targets: 80% incidence reduction, 90% mortality reduction, 0% catastrophic expenditure
  • 5 components of DOTS
  • NIKSHAY portal - mandatory notification since 2012
  • Nikshay Poshan Yojana - Rs. 500/month DBT
  • Bedaquiline + Delamanid for DR-TB
  • TB serology banned since 2012
  • PM TB Mukt Bharat Abhiyaan - Ni-kshay Mitra volunteers
Sources: Park's Textbook of Preventive and Social Medicine; DGHS/MoHFW NTEP guidelines; India TB Report 2024; NSP 2017-2025; iHatePSM (community medicine resource)
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