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Kuldeep Vyas
Asst. Prof. Community HealthHIV/ AIDS 1Kuldeep Vyas M.Sc. CHN
AIDS
 Acquired immuno deficiencysyndrome
 Fatal illness
 Caused by a retrovirusHIV
 It breaks down the body's immunesystem, leaving the
patient vulnerable to a host of life threatening
opportunistic infections, neurological disorders or
unusual malignancies.
2Kuldeep Vyas M.Sc. CHN
Structure of HIV
3Kuldeep Vyas M.Sc. CHN
Epidemiology
 Males>females
 Occurs in all ages and ethnic groups
 All areas of the country are affected
 AIDS is now the second leading cause of death for all men
aged 25-44 years
 (Unintended injuries is #1 and heart disease is #3 for this
age group)
4Kuldeep Vyas M.Sc. CHN
AIDS Worldwide
5Kuldeep Vyas M.Sc. CHN
AIDS
In
India
6
Kuldeep Vyas M.Sc. CHN
7Kuldeep Vyas M.Sc. CHN
8Kuldeep Vyas M.Sc. CHN
HIV- Agent
 It is a RNAvirus
 Which replicates in actively dividing T4lymphocytes.
 Uniqueability todestroyT4 Helpercells
 Reservoir- Once a person gets infected virus remains
in his body lifelong. And the person is a symptomless
carrier foryears before the symptomsactuallyappear.
9Kuldeep Vyas M.Sc. CHN
 Source – Thevirus is found in great concentrations in
blood, CSF and semen.
 Lower concentrations have been found in tears,saliva,
breast milk, urine, cervical and vaginalsecretions.
 Also isolated from brain tissue, lymph nodes,bone
marrow cells andskin.
 Howeveronly blood and semen are known totransmit
thevirus.
10Kuldeep Vyas M.Sc. CHN
HIV in Body Fluids
Semen
11,000 Vaginal
Fluid
7,000
Blood
18,000
Amniotic
Fluid
4,000 Saliva
1
Average number of HIV particles in 1 ml of these body fluids
11Kuldeep Vyas M.Sc. CHN
Host
 Age- Mostcasesareamong sexuallyactivepeopleaged
between age 20- 49years.
 High riskgroups-
Male homosexuals, hetero sexual partners, i.v. drug
abusers, blood transfusion recipients, haemophiliacs
and patients having STDs.
12Kuldeep Vyas M.Sc. CHN
13
HIV Transmission
 HIV enters the bloodstreamthrough:
Open Cuts
Breaks in theskin
Mucous membranes
Direct injection
Kuldeep Vyas M.Sc. CHN
Routes of Transmission of HIV
Sexual Contact: Male-to-male
Male-to-female orvice versa
Female-to-female
Blood Exposure: Injecting drug use/needlesharing
Occupational exposure
Transfusion of blood products
Perinatal: Transmission from mother tobaby
Breastfeeding
14Kuldeep Vyas M.Sc. CHN
15
Routes of Transmission of HIV
Occupational Transmission
Health care worker/ hospitalstaff
Laboratory workers
Otherroutes
Organ transplantation
Artificial insemination
Needle-prick
Kuldeep Vyas M.Sc. CHN
Incubation Period
 The incubation period is from HIV infectiontill
development of AIDS.
 It is from a few months to 10 yearsoreven more.
 However it is estimated that 75% of people infected
with HIV will developAIDS at theend of 10 years.
16Kuldeep Vyas M.Sc. CHN
17
HIV-Infected T-Cell
HIV
Virus
T-Cell
HIV Infected
T-Cell
New HIV
Virus
Kuldeep Vyas M.Sc. CHN
Clinical Manifestations
I] Initial Infection
II] Asymptomatic CarrierState
III] AIDS-related Complex(ARC)
IV] AIDS
18Kuldeep Vyas M.Sc. CHN
I] Initial Infection
 Except fora generally mild illnessof fever, sore throat
and rash, which about 70% of the peopleexperience a
few weeks after the initial infection; Most HIV –
infected people have no symptoms for the first five
years.
 However they can infect others, Once, infectedthe
people a infected forlife.
 Antibody Response usually takes 2-12 weeks to appear
in the blood stream. This period is called ‘the window
period’. (Tests- Negative)
19Kuldeep Vyas M.Sc. CHN
20
HIV Infection And Antibody Response
6 month ~ Years ~ Years ~ Years ~ Ye
Virus
Antibody
Infection
Occurs
AIDS Symptoms
Initial Stage---------------- --------Intermediate or Latent Stage-----------------Illness Stage
Flu-like Symptoms
Or
No Symptoms Symptom-free
<
----
Kuldeep Vyas M.Sc. CHN
21
The Acute HIV Syndrome
Follows 3-6 wks following primary infection
Kuldeep Vyas M.Sc. CHN
Asymptomatic Carrier State
 Infected peoplewith antibodies butwithoutanyovert
signs of the disease, except persistent generalized
lymphadenopathy.
 It is howevernot firmlyclearabout how long does the
asymptomatic stagelasts.
22Kuldeep Vyas M.Sc. CHN
AIDS-Related Complex
 Has illnesses caused by damage to immune system,
butwithout theopportunistic infectionsand cancers
associated withAIDS.
 They mayexhibit-
Unexplained diarrhea(lasting more than a month),
fatigue, malaise, loss of body weight(>10%), fever,
night sweats.
Signs of Mild infections like oral thrush, generalized
lymphadenopathy, enlarged spleen.
23Kuldeep Vyas M.Sc. CHN
24
Common manifestation of AIDS
Lung infection:
P.Cariniipneumonia
Gastrointestinal infection:
candidiasis of mouth
or oesophagus
Skin infection: Kaposi’s
sarcoma - red or violet
macules or papules
Central nervous
System Infection:
Toxoplasmosis
Dementia
Meningitis
Primary CNS Lymphomas.
Progressive Multifocal
Leucoencephalopathy.
Kuldeep Vyas M.Sc. CHN
25
Source: NACO
Opportunistic Infections Among Reported AIDS Cases in India
25Kuldeep Vyas M.Sc. CHN
26
Kuldeep Vyas M.Sc. CHN
27
Kaposi sarcoma
Candidiasis Of Mouth
Kuldeep Vyas M.Sc. CHN
Swollen parts of the body
28Kuldeep Vyas M.Sc. CHN
Deterioration of the body tissues
29Kuldeep Vyas M.Sc. CHN
30
Extreme Wt loss
Lymphadenopathy
Kuldeep Vyas M.Sc. CHN
31
P.Carinii pneumonia
Primary CNS Lymphoma
Kuldeep Vyas M.Sc. CHN
Causes/Contributors of HIV Risk
Structural Level
Resource Availability
Physical Environment
Organizational Systems
Laws/Policies
Individual Susceptibility
Macro Level
Racism, Stigma, Poverty, Gender Inequality, Migration
Community Level
Community Norms
Social Networks
Social Capital/Collective
Efficacy
Relationships
Individual Level
Behavior
Attitudes
Knowledge
Perceptions
Biology
32Kuldeep Vyas M.Sc. CHN
33Kuldeep Vyas M.Sc. CHN
Primary
• Primary HIV prevention refers to activity focused on
preventing uninfected people becoming infected.
Secondary
• Secondary HIV prevention aimed at enabling people
with HIV to stay well (e.g. testing to allow people to
know their status; welfare rights advice; lifestyle
behaviour ; anti–discriminatory lobbying).
Tertiary
• Tertiary HIV prevention aims to minimise the effects
of ill–health experienced by someone who is
symptomatic with HIV disease (e.g. the prophylactic
use of drugs and complementary therapies )
34
Kuldeep Vyas M.Sc. CHN
Diagnosis of HIV
• HIV antibody test – using different antigen &/ orwith
different principle of thetest
• Viral antigen test - used forscreening blood donors in
USA
• Detection of viral nucleic acid inblood.
• Determining the CD4 counts toassess thedisease
progression.
35Kuldeep Vyas M.Sc. CHN
Testing-
(Integrated Counseling & Testing ICTC centre
Centre)
 District Hospitals
 Medical colleges
 Free HIV testing
 Confidential counseling
 Referral to nearest ART (Anti Retroviral Therapy)
centre .
36Kuldeep Vyas M.Sc. CHN
ANTIRETROVIRAL DRUGS
NRTI NNRTI PI
Zidovudine (AZT)* Nevirapine(NVP)* Indinavir(IDV)*
Lamivudine (3TC)* Efavirenz(EFV)* Nelfinavir(NFV)*
Stavudine (d4T)* Delavirdine(DLV) Saquinavir(SQV)*
Didanosine (ddl)*
INTEGRASE
INHIBITORS Ritonavir(RTV)*
Zalcitabine(ddC)* Raltegravir Amprenavir(APV)
Abacavir(ABC)* CCR5 antagonists Lopinavir(LPV)*
Tenofovir(TFV)* Maraviroc Atazanavir(ATV)*
Emtricitabine(FTC) Foseamprenavir
MAMC- Feb2009
FusionInhibitor:Enfuvirtide(T-20)
* Available in India , available under national programme
Cost of Therapy reduced from Rs.30,000 in 1998 to Rs1000 per month in 2006, no. of pills from 32 to 1 or 2 per day,37Kuldeep Vyas M.Sc. CHN
PREVENTION
 Avoid multiple partners – useCondoms.
 Use sterile needles each time for injection
 Never share needles
 Avoid unnecessary blood transfusions
 All pregnant women should be testedfor
HIV
38Kuldeep Vyas M.Sc. CHN
Prevention
 Use standard work precautions – handhygiene,
personal protectivegear.
 Proper disposal of biomedicalwaste.
 Immunization againstHBV
 Education
39Kuldeep Vyas M.Sc. CHN
Occupational Exposure
HCW comes in contactwith potentially infectious body
fluids due to–
 A percutaneous injury ( needlestick, cutwith sharp
object)
 Contact with mucousmembrane
 Contactwith non intactskin (abraded, chapped,
dermatitis )
40Kuldeep Vyas M.Sc. CHN
Management of Exposure site
 Do notpanic
 Skin
 Wash wound & surrounding withsoap/water
 Rinsewell
 Do notscrub
 Do not use Antisepticor Skin washes
41Kuldeep Vyas M.Sc. CHN
Management of Exposure site
 Splash of Blood/OPIM
 Eye
 Eye irrigation with wateror Saline
 If using contact lens leave them in place while irrigating
.Removeonceeye is cleaned remove them & clean
 Mouth
 Spit fluid immediately
 Rinse mouth thoroughlywith water / saline repeatedly
 Do not use soap ordisinfectant
42Kuldeep Vyas M.Sc. CHN
PEP Prescription
 Contact ARTspecialist
 Decision of starting PEP based on Exposure type&
HIV status of source
 Decide PEP regimens
 Basic regimen
 Expanded regimen
2 drugcombination
3 drug combination
 If source person is on ART drugs expert should be
consulted after starting 2drugs
43Kuldeep Vyas M.Sc. CHN
Post Exposure Prophylaxis
 In India recommended for occupationalexposure
 It should be started as early as possible (within 72
hours)
 ARV is given for 4weeks
 HIV testing should be done at baseline, 6wks, 3mths &
6mths
44Kuldeep Vyas M.Sc. CHN
HIV from beinga
VIRTUAL DEATH SENTENCE
has been brought down to being a
CHRONIC MANAGABLE DISEASE
45Kuldeep Vyas M.Sc. CHN
Thank you!
46Kuldeep Vyas M.Sc. CHN

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HIV AIDS

  • 1. Kuldeep Vyas Asst. Prof. Community HealthHIV/ AIDS 1Kuldeep Vyas M.Sc. CHN
  • 2. AIDS  Acquired immuno deficiencysyndrome  Fatal illness  Caused by a retrovirusHIV  It breaks down the body's immunesystem, leaving the patient vulnerable to a host of life threatening opportunistic infections, neurological disorders or unusual malignancies. 2Kuldeep Vyas M.Sc. CHN
  • 3. Structure of HIV 3Kuldeep Vyas M.Sc. CHN
  • 4. Epidemiology  Males>females  Occurs in all ages and ethnic groups  All areas of the country are affected  AIDS is now the second leading cause of death for all men aged 25-44 years  (Unintended injuries is #1 and heart disease is #3 for this age group) 4Kuldeep Vyas M.Sc. CHN
  • 9. HIV- Agent  It is a RNAvirus  Which replicates in actively dividing T4lymphocytes.  Uniqueability todestroyT4 Helpercells  Reservoir- Once a person gets infected virus remains in his body lifelong. And the person is a symptomless carrier foryears before the symptomsactuallyappear. 9Kuldeep Vyas M.Sc. CHN
  • 10.  Source – Thevirus is found in great concentrations in blood, CSF and semen.  Lower concentrations have been found in tears,saliva, breast milk, urine, cervical and vaginalsecretions.  Also isolated from brain tissue, lymph nodes,bone marrow cells andskin.  Howeveronly blood and semen are known totransmit thevirus. 10Kuldeep Vyas M.Sc. CHN
  • 11. HIV in Body Fluids Semen 11,000 Vaginal Fluid 7,000 Blood 18,000 Amniotic Fluid 4,000 Saliva 1 Average number of HIV particles in 1 ml of these body fluids 11Kuldeep Vyas M.Sc. CHN
  • 12. Host  Age- Mostcasesareamong sexuallyactivepeopleaged between age 20- 49years.  High riskgroups- Male homosexuals, hetero sexual partners, i.v. drug abusers, blood transfusion recipients, haemophiliacs and patients having STDs. 12Kuldeep Vyas M.Sc. CHN
  • 13. 13 HIV Transmission  HIV enters the bloodstreamthrough: Open Cuts Breaks in theskin Mucous membranes Direct injection Kuldeep Vyas M.Sc. CHN
  • 14. Routes of Transmission of HIV Sexual Contact: Male-to-male Male-to-female orvice versa Female-to-female Blood Exposure: Injecting drug use/needlesharing Occupational exposure Transfusion of blood products Perinatal: Transmission from mother tobaby Breastfeeding 14Kuldeep Vyas M.Sc. CHN
  • 15. 15 Routes of Transmission of HIV Occupational Transmission Health care worker/ hospitalstaff Laboratory workers Otherroutes Organ transplantation Artificial insemination Needle-prick Kuldeep Vyas M.Sc. CHN
  • 16. Incubation Period  The incubation period is from HIV infectiontill development of AIDS.  It is from a few months to 10 yearsoreven more.  However it is estimated that 75% of people infected with HIV will developAIDS at theend of 10 years. 16Kuldeep Vyas M.Sc. CHN
  • 18. Clinical Manifestations I] Initial Infection II] Asymptomatic CarrierState III] AIDS-related Complex(ARC) IV] AIDS 18Kuldeep Vyas M.Sc. CHN
  • 19. I] Initial Infection  Except fora generally mild illnessof fever, sore throat and rash, which about 70% of the peopleexperience a few weeks after the initial infection; Most HIV – infected people have no symptoms for the first five years.  However they can infect others, Once, infectedthe people a infected forlife.  Antibody Response usually takes 2-12 weeks to appear in the blood stream. This period is called ‘the window period’. (Tests- Negative) 19Kuldeep Vyas M.Sc. CHN
  • 20. 20 HIV Infection And Antibody Response 6 month ~ Years ~ Years ~ Years ~ Ye Virus Antibody Infection Occurs AIDS Symptoms Initial Stage---------------- --------Intermediate or Latent Stage-----------------Illness Stage Flu-like Symptoms Or No Symptoms Symptom-free < ---- Kuldeep Vyas M.Sc. CHN
  • 21. 21 The Acute HIV Syndrome Follows 3-6 wks following primary infection Kuldeep Vyas M.Sc. CHN
  • 22. Asymptomatic Carrier State  Infected peoplewith antibodies butwithoutanyovert signs of the disease, except persistent generalized lymphadenopathy.  It is howevernot firmlyclearabout how long does the asymptomatic stagelasts. 22Kuldeep Vyas M.Sc. CHN
  • 23. AIDS-Related Complex  Has illnesses caused by damage to immune system, butwithout theopportunistic infectionsand cancers associated withAIDS.  They mayexhibit- Unexplained diarrhea(lasting more than a month), fatigue, malaise, loss of body weight(>10%), fever, night sweats. Signs of Mild infections like oral thrush, generalized lymphadenopathy, enlarged spleen. 23Kuldeep Vyas M.Sc. CHN
  • 24. 24 Common manifestation of AIDS Lung infection: P.Cariniipneumonia Gastrointestinal infection: candidiasis of mouth or oesophagus Skin infection: Kaposi’s sarcoma - red or violet macules or papules Central nervous System Infection: Toxoplasmosis Dementia Meningitis Primary CNS Lymphomas. Progressive Multifocal Leucoencephalopathy. Kuldeep Vyas M.Sc. CHN
  • 25. 25 Source: NACO Opportunistic Infections Among Reported AIDS Cases in India 25Kuldeep Vyas M.Sc. CHN
  • 27. 27 Kaposi sarcoma Candidiasis Of Mouth Kuldeep Vyas M.Sc. CHN
  • 28. Swollen parts of the body 28Kuldeep Vyas M.Sc. CHN
  • 29. Deterioration of the body tissues 29Kuldeep Vyas M.Sc. CHN
  • 31. 31 P.Carinii pneumonia Primary CNS Lymphoma Kuldeep Vyas M.Sc. CHN
  • 32. Causes/Contributors of HIV Risk Structural Level Resource Availability Physical Environment Organizational Systems Laws/Policies Individual Susceptibility Macro Level Racism, Stigma, Poverty, Gender Inequality, Migration Community Level Community Norms Social Networks Social Capital/Collective Efficacy Relationships Individual Level Behavior Attitudes Knowledge Perceptions Biology 32Kuldeep Vyas M.Sc. CHN
  • 34. Primary • Primary HIV prevention refers to activity focused on preventing uninfected people becoming infected. Secondary • Secondary HIV prevention aimed at enabling people with HIV to stay well (e.g. testing to allow people to know their status; welfare rights advice; lifestyle behaviour ; anti–discriminatory lobbying). Tertiary • Tertiary HIV prevention aims to minimise the effects of ill–health experienced by someone who is symptomatic with HIV disease (e.g. the prophylactic use of drugs and complementary therapies ) 34 Kuldeep Vyas M.Sc. CHN
  • 35. Diagnosis of HIV • HIV antibody test – using different antigen &/ orwith different principle of thetest • Viral antigen test - used forscreening blood donors in USA • Detection of viral nucleic acid inblood. • Determining the CD4 counts toassess thedisease progression. 35Kuldeep Vyas M.Sc. CHN
  • 36. Testing- (Integrated Counseling & Testing ICTC centre Centre)  District Hospitals  Medical colleges  Free HIV testing  Confidential counseling  Referral to nearest ART (Anti Retroviral Therapy) centre . 36Kuldeep Vyas M.Sc. CHN
  • 37. ANTIRETROVIRAL DRUGS NRTI NNRTI PI Zidovudine (AZT)* Nevirapine(NVP)* Indinavir(IDV)* Lamivudine (3TC)* Efavirenz(EFV)* Nelfinavir(NFV)* Stavudine (d4T)* Delavirdine(DLV) Saquinavir(SQV)* Didanosine (ddl)* INTEGRASE INHIBITORS Ritonavir(RTV)* Zalcitabine(ddC)* Raltegravir Amprenavir(APV) Abacavir(ABC)* CCR5 antagonists Lopinavir(LPV)* Tenofovir(TFV)* Maraviroc Atazanavir(ATV)* Emtricitabine(FTC) Foseamprenavir MAMC- Feb2009 FusionInhibitor:Enfuvirtide(T-20) * Available in India , available under national programme Cost of Therapy reduced from Rs.30,000 in 1998 to Rs1000 per month in 2006, no. of pills from 32 to 1 or 2 per day,37Kuldeep Vyas M.Sc. CHN
  • 38. PREVENTION  Avoid multiple partners – useCondoms.  Use sterile needles each time for injection  Never share needles  Avoid unnecessary blood transfusions  All pregnant women should be testedfor HIV 38Kuldeep Vyas M.Sc. CHN
  • 39. Prevention  Use standard work precautions – handhygiene, personal protectivegear.  Proper disposal of biomedicalwaste.  Immunization againstHBV  Education 39Kuldeep Vyas M.Sc. CHN
  • 40. Occupational Exposure HCW comes in contactwith potentially infectious body fluids due to–  A percutaneous injury ( needlestick, cutwith sharp object)  Contact with mucousmembrane  Contactwith non intactskin (abraded, chapped, dermatitis ) 40Kuldeep Vyas M.Sc. CHN
  • 41. Management of Exposure site  Do notpanic  Skin  Wash wound & surrounding withsoap/water  Rinsewell  Do notscrub  Do not use Antisepticor Skin washes 41Kuldeep Vyas M.Sc. CHN
  • 42. Management of Exposure site  Splash of Blood/OPIM  Eye  Eye irrigation with wateror Saline  If using contact lens leave them in place while irrigating .Removeonceeye is cleaned remove them & clean  Mouth  Spit fluid immediately  Rinse mouth thoroughlywith water / saline repeatedly  Do not use soap ordisinfectant 42Kuldeep Vyas M.Sc. CHN
  • 43. PEP Prescription  Contact ARTspecialist  Decision of starting PEP based on Exposure type& HIV status of source  Decide PEP regimens  Basic regimen  Expanded regimen 2 drugcombination 3 drug combination  If source person is on ART drugs expert should be consulted after starting 2drugs 43Kuldeep Vyas M.Sc. CHN
  • 44. Post Exposure Prophylaxis  In India recommended for occupationalexposure  It should be started as early as possible (within 72 hours)  ARV is given for 4weeks  HIV testing should be done at baseline, 6wks, 3mths & 6mths 44Kuldeep Vyas M.Sc. CHN
  • 45. HIV from beinga VIRTUAL DEATH SENTENCE has been brought down to being a CHRONIC MANAGABLE DISEASE 45Kuldeep Vyas M.Sc. CHN