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*AIDS

   By-Dr.Mimosa Chatterjee
   http://www.pediatricdentists.blogspot.com/
Acquired Immuno Deficiency Syndrome

   INTRODUCTION:

 AIDS, the acquired immuno deficiency syndrome (some times called “ slim

 disease”) is a fatal illness caused by a retro virus known as human immuno

 deficiency virus (HIV) which breaks down the body’s immune system, leaving

 the victim vulnerable       to a host of life threatening opportunistic

 infections, neurological disorders or unusual malignancies. Among the special

 feature of HIV infection are that once infected, probable that a person will be

 infected for life. Strictly speaking the term AIDS refers only to the last stage of

 the HIV infection. AIDS can be called our modern pandemic affecting both

 industrialized & developing countries.
Epidemiology
*The first case of AIDS was detected in 1981 in USA & in India
 1st case was detected in1986 in chennai. In 2004’ who
 estimated that there were 39.4 million people living with AIDS,
 4.9 new infections & 3.1 million deaths. In India high
 prevalence states are MAHARASTRA, TAMIL NADU,
 KARNATAKA, ARUNACHAL PRADESH, MANIPUR &
 NAGALAND.
                     Epidemiological
                         feature

                   Agent
                                       Host
                   factor
EPIDEMIOLOGICAL FEATURES
* 1) Agent Factor: when the virus was first identified, a FRENCH SCIENTEST
 called it lymphadenopathy-associated virus. Researchers in USA called it
 human T-cell lymphotropic virus III. In 1986, International committee of
 taxonomy gave it name HIV. HIV virus is spherical in shape with 100-140
 nm in size. it has a core having core protein P24 &P18. It contains 2 stands
 of genomic RNA & a double layer of lipid membrane. The membrane is
 studded with 2 viral glycoprotein: gp120&gp41.the virus is able to spread
 through out the body. Two types of HIV- HIV1 & HIV2. Heat easily kills the
 virus. Readily get inactivated by ether, acetone, and ethanol but resistant
 to ionizing radiation & u-v radiation.
a)   Reservoir of infection: These are the case &carriers. Once person is a
     infected virus remains in body life long. HIV infection can take years to
     manifest it self.
b)   Source of infection: The virus has been found in greatest concentration
     in blood, semen &CSF &in lower concentration in tears, saliva, breast
     milk, urine &vaginal secretions. To date only blood & semen have been
     conclusively shown to transmit virus.
HIV Virus




            AIDS Virus
2) Host factors

(a) Age: 20-49yrs., children below 15 makes less than 3%

(b) Sex: In North America, Europe &Australia about 70%arehomosexual or bisexual men.

   In Africa the sex ratio is equal.

(c) High-risk groups: Male homosexual& bisexual, heterosexual partners, I.V drug

   abusers, transfusion recipients of blood & blood products, hemophiliacs.

(d) Immunology: Immune system disorder occur primarily due to gradual depletion in CD4

   cells. HIV selectively infects T-helper cells. Virus reproduce & infected T- helper cells

   are destroyed. There is overall low white blood cell count. There is profound

   lymphopenia with lymphocyte count below 500cmm. The alteration in T- cell function is

   responsible for development of neoplasm’s & opportunistic infections.
Pathogenesis
* HIV infect CD4 immune cells chiefly T helper lymphocytes
* Other cells like B-lymphocytes, monocytes, dendritic cells are also
  infected.
* Glycoprotein GP120 present on surface has affinity for CD4
  molecules present on surface of immune cells.
* Co- receptor such as CXCR4 present on lymphocyte & CCR5 present
  on monocytes are also needed for binding.
* HIV enters the cell.
* Its genomic RNA is released in to cytoplasm & converted in to viral
  DNA by reverse transcriptase.
* The viral DNA is integrated into host cells DNA & captures the
  genetic machinery of host cells.
* This leads to rapid production of viral genome, which attains the
  shape of full virus with the help of protease enzyme
Pathogenesis of AIDS
Pathogenesis of AIDS
Mode Of Transmission
* a)   SEXUAL TRANSMISSION: It is first and fore most
 sexually transmitted disease.
* b)   PARENTRAL ROUTE:
* i.   BLOOD AND BLOOD PRODUCTS: Transmitted by
 contaminated blood transfusion of WBC, platelets &
 factor viii & ix.
* ii. INJECTION &DRUG USERS
* iii. OCCUPATIONAL INJURY
* iv. EARPIERCING, TATTOING, ACUPUNCTURE.
* C) MATERNAL-FOETAL TRANSMISSION: HIV can pass
 through an infected mother to her fetus, through
 placenta, during delivery or by breast-feeding.
CLINICAL MANIFESTATIONS
* IT CAN BE CLASSIFIED IN TO FOUR BROAD CATEGORIES: -
* 1.     INITIAL INFECTION WITH THE VIRUS & THE DEVELOPMENT OF ANTIBODIES: -
  Except for a generally mild illness like fever, sore throat & rash about 70% of people have
  no symptoms for the first five years. They look healthy & well although they can transmit
  virus to others. Antibodies usually take between 2-12 weeks to appear in the blood
  stream.
* 2.       ASYMTOMATIC CARRIER STATE:
          Infected people have antibodies.
           Persistent generalized lymphadenopathy.
          It is not clear that how long this stage last.
* 3.       AIDS RELATED COMPLEX: - A person in this phase has illness caused due to
  immune system, but without the opportunistic infections but they exhibit one or more of
  the following clinical signs: - unexplained diarrhoea lasting longer then
  months, fatigue, malaise, loss of more than 10% body weight, fever, night sweats or other
  mild opportunistic infections such as oral thrush, generalized lymphadenopathy or
  enlarged spleen.
* 4.       AIDS: - AIDS is the end stage of HIV infection. A number of opportunistic infection
  commonly occurs at this stage. death is due to uncontrolled or untreated infections. There
  is significant decrease in CD4 count. Important opportunistic infections are
  tuberculosis, oroesophageal candidiasis, pneumonia etc.
Oral Manifestations
1)   Fungal                                  3)   Viral
·    Candidiasis                             ·    Varicella zoster
·    Aspergillosis                           ·    Epstein-Barr including hairy leukoplakia
·    Histoplasmosis                          ·    HPV virus
·    Cryptococcus neoformans                 ·    CMV virus
·    Geotrichosis                            4)   Neoplasm
2)   Bacterial                               ·    Kaposi’s sarcoma
·    HIV gingivitis                          ·    Non-Hodgkin lymphoma
·    HIV periodontitis                       ·    Squamous cell carcinoma
·    Necrotizing gingivitis                  5)   Lymphadenopathy
·    Mycobacterium avium intracellulare      6)   Neurologic disorders
·    Klebsiella pneumonia                    ·    Paraesthesia
·    Enterobacterium cloacae                 ·    Facial palsy
·    E.coli                                  ·    Hyperesthesia
·    Salmonella enteritidis                  ·    Dysphagia
·    Sinusitis
·    Exacerbation of apical periodontistis
·    Submandibular cellulitis
Oral Manifestations
7)   Miscellaneous
·     Recurrent apthous ulceration
·     Progressive necrotizing ulceration
·     Toxic epidermolysis
·     Delayed wound healing
·     Thrombocytopenia
 Xerostomia & sicca type syndrome
 Herpes Simplex
·     HIV embryopathy
·     Hyperpigmentation
·     Granuloma annulare
·     Exfoliative cheilitis
·     Lichenoid & other drug Reaction
Diagnosis

             LABORATORY
CLINICAL
               FINDINGS
Diagnosis
Clinical
1) WHO CASE DEFINATION OF AIDS SURVEILLANCE: -
An adult or adolescent is considered to have aids it at least 2 major &
attest one minor signs are present & if these signs are not known to be due
to a condition unrelated to HIV infection.
             MAJOR                           MINOR                      Presence of either Kaposi sarcoma or
                                                                 cryptococcal meningitis –diagnosis of AIDS
     Wt loss > 10% of body           Persistent cough for more   for surveillance.

           weight                       than months

   Chronic diarrhoea for more          Generalised pruritic

       than month                        dermatitis

    Prolonged fever for more            H/o herpes zostor

     then one month

                                    Oropharyngeal candidiasis

                                Generalized lymphadenopathy
Diagnosis
2) Expanded WHO case definition for AIDS surveillance: -
. HIV antibody test positive
. One or more of the following condition present.
1.      WT LOSS > 10% OF BODY WEIGHT or cachexia with diarrhea or
fever or both, intermittent or constant for at least 1 month.
2.     Cryptococcal meningitis
3.     Tuberculosis
4.     Kaposi sarcoma
5.     Neurological impairment
6.     Candidiasis of Oesophagus
7.     Recurrent episodes of Pneumonia
8.     Invasive cervical cancer
Diagnosis
LABORATORY DIAGNOSIS
a)     Screening test: ELISA
b)     Specific test: Western blot
c)     Non-specific test: anemia, leucopoenia, thrombocytopenia, and
absolute CD4 count.
Control Of AIDS
1.     Prevention:
a.     Education: Health education
•      Avoiding indiscriminate sex
•      Use of condoms
•      Avoid sharing razors and tooth brushes
•      Comprehensive sex education programmers in school.
•      Public awareness campaigns for HIV.
•     Educational material and guideline for prevention should
be made wide available.
•      All mass media channels should be involved in educating
the people on AIDS, its nature of transmission & prevention.
Control Of AIDS
b.     Prevention of blood borne HIV transmission:
      People with high risk should be urged to refrain from donating blood,
body organs, sperm or other tissues.
      All blood should be screened before transfusion
      Transmission of infection to haemophiliacs can be reduced by
introducing heat treatment of factor viii & ix.
c.     Strict sterilization practice in hospitals and clinics
d.     Disposable needles and syringes should be used
e.     Universal precautions by health care workers.
Control Of AIDS
2.   ANTIRETROVIRAL TREATMENT: - It will not cure the disease but can
     prolong the life of severely ill patients.

                     HIV infected with viral load > 5000-1000 or
                     CD4 < 500/ul




            zidovudi        Didanosin            Zidovudine        Zidovudine
           1st lin
            ne Lami         e                    Didanosine
            vudine                                                 Zalcitabine


            1dt line treatment
Control Of AIDS
Intolerance to regime                  Progression of diseases or
                                       viral load does not
                                       decrease by >.5 log with
                                       initiation of treatment or
                                       increase of viral load by
                                       >. 5log while on
Change to alternative                  treatment
first line treatment
    2nd line treatment




Saquinqv        Ritonavi   Indinavir      Stavudin      Stavudine
ir Zidov        r          Zidovudin      e Lamiv         Didnosin
udine           Zidovudi   e              udine         e
                ne
Control Of AIDS

     Progression of diseases or viral load does not
     decrease by >.5 log with initiation of treatment
     or increase of viral load by >. 5log while on
     treatment




3rd line treatment




 Saquinqvir                  Indinavir                    Nelfinavir
 Indinavir                   Zidovudine                   Zidovudine
 Zidovudine                   Didnosine




                     Antiretroviral combination therapy
Control Of AIDS
3.   POST EXPOSURE PROPHYLACTIC TREATMENT:
•   It refers to anti retroviral drug therapy with in hrs. Following accidental
exposure to virus.
•    Following needle stick injury, the part should be thoroughly washed with soap
& water. The injured finger should not be reflex to put in the mouth. Open wounds
should be irrigated with saline. Antiseptic agent can be applied but caustic agents
should be avoided.
•    Following treatment is recommended by the US center for disease control
and prevention for health care workers accidentally exposed to HIV: -
•   zidovudine( 200mg three times daily) +Lamivudine (150 mg twice daily) for
4 weeks
•    if “ source individual have advance aids : Nelfinavir(750 mg 3 times daily)
+zidovudine +lamivudine
•    if “ source” individual failed on zidovudine +lamivudine therapy then
stavudine +didanosine
Control Of AIDS
4.     PREVENTION OF INFECTION TO BABY BY HIV POSITIVE MOTHER: -
a)     zidovudine( 300mg three times daily) –to pregnant mothers from 10-
12th week of pregnancy or immediately after diagnosis.
b)     During labour- zidovudine I.V
c)     New born -Syrup zidovudine( three times daily for 6 weeks)
d)     Single dose of Neverpin (200 mg) at the time of labour.
Control Of AIDS

6.        PRIMERY HEALTH CARE: -
*        Because of its wide range of implication, AIDS touches all aspects of
    primary health care including mother & child health, Family planning &
    education.
*          It is important that AIDS control programmes should not be developed
    in isolation.
*         Integration in to country’s primary health care system is essential.
Conclusion
         Aids is caused by HIV virus which breaks down the body’s immune
    system leading to cause of opportunistic infections like tuberculosis, herpes
    simplex & zoster, hairy leukoplakia, pneumonia etc.
         Death in aids is actually because of opportunistic infections.
         Aids don’t pass on by: -
•         Sharing crockery and cutlery.
•         Touching, hugging or shaking hands.
•         Using same toilets.
•         Insect and animal bites
•      In can only pass on by having sex with infected person, from infected
blood and injections and infected mother to her child
        As it is said that mouth is the mirror of once health. Patient of aids
    have many oral manifestations.
Conclusion
A wide increase in the awareness about this disease is required.
Much advancement has now been made in field of science & medicine.
 Many types of therapy & drugs have been introduced but still then………….



                      We have not been able to cure AIDS
                       Prevention is only cure for AIDS
In the present day awareness campaign through multimedia has made easy
 the efforts to reach large segment of people. The print medias, electronic
 media, press campaign holds the key to success
A massive media campaign was launched by NACO in 1996, through well
 defined generic materials, posters, pamphlets, booklets, newspapers,
 advertisement, film clippings, TV spots, wall paintings and cinema slides
 were prepared in Hindi and all regional languages.
Conclusion
Ethics/moral duty of a doctor towards HIV ve patient
•      He should educate the patient
•      He should never refuse treatment to HIV positive patient. A dentist
who refuses treatment is in violation of law and subject to penalties.
           Every year on 1st December world AIDs day is celebrated
Thank you
    http://www.pediatricdentists.blogspot.com/

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AIDS

  • 1. *AIDS By-Dr.Mimosa Chatterjee http://www.pediatricdentists.blogspot.com/
  • 2. Acquired Immuno Deficiency Syndrome INTRODUCTION: AIDS, the acquired immuno deficiency syndrome (some times called “ slim disease”) is a fatal illness caused by a retro virus known as human immuno deficiency virus (HIV) which breaks down the body’s immune system, leaving the victim vulnerable to a host of life threatening opportunistic infections, neurological disorders or unusual malignancies. Among the special feature of HIV infection are that once infected, probable that a person will be infected for life. Strictly speaking the term AIDS refers only to the last stage of the HIV infection. AIDS can be called our modern pandemic affecting both industrialized & developing countries.
  • 3.
  • 4. Epidemiology *The first case of AIDS was detected in 1981 in USA & in India 1st case was detected in1986 in chennai. In 2004’ who estimated that there were 39.4 million people living with AIDS, 4.9 new infections & 3.1 million deaths. In India high prevalence states are MAHARASTRA, TAMIL NADU, KARNATAKA, ARUNACHAL PRADESH, MANIPUR & NAGALAND. Epidemiological feature Agent Host factor
  • 5. EPIDEMIOLOGICAL FEATURES * 1) Agent Factor: when the virus was first identified, a FRENCH SCIENTEST called it lymphadenopathy-associated virus. Researchers in USA called it human T-cell lymphotropic virus III. In 1986, International committee of taxonomy gave it name HIV. HIV virus is spherical in shape with 100-140 nm in size. it has a core having core protein P24 &P18. It contains 2 stands of genomic RNA & a double layer of lipid membrane. The membrane is studded with 2 viral glycoprotein: gp120&gp41.the virus is able to spread through out the body. Two types of HIV- HIV1 & HIV2. Heat easily kills the virus. Readily get inactivated by ether, acetone, and ethanol but resistant to ionizing radiation & u-v radiation. a) Reservoir of infection: These are the case &carriers. Once person is a infected virus remains in body life long. HIV infection can take years to manifest it self. b) Source of infection: The virus has been found in greatest concentration in blood, semen &CSF &in lower concentration in tears, saliva, breast milk, urine &vaginal secretions. To date only blood & semen have been conclusively shown to transmit virus.
  • 6. HIV Virus AIDS Virus
  • 7. 2) Host factors (a) Age: 20-49yrs., children below 15 makes less than 3% (b) Sex: In North America, Europe &Australia about 70%arehomosexual or bisexual men. In Africa the sex ratio is equal. (c) High-risk groups: Male homosexual& bisexual, heterosexual partners, I.V drug abusers, transfusion recipients of blood & blood products, hemophiliacs. (d) Immunology: Immune system disorder occur primarily due to gradual depletion in CD4 cells. HIV selectively infects T-helper cells. Virus reproduce & infected T- helper cells are destroyed. There is overall low white blood cell count. There is profound lymphopenia with lymphocyte count below 500cmm. The alteration in T- cell function is responsible for development of neoplasm’s & opportunistic infections.
  • 8. Pathogenesis * HIV infect CD4 immune cells chiefly T helper lymphocytes * Other cells like B-lymphocytes, monocytes, dendritic cells are also infected. * Glycoprotein GP120 present on surface has affinity for CD4 molecules present on surface of immune cells. * Co- receptor such as CXCR4 present on lymphocyte & CCR5 present on monocytes are also needed for binding. * HIV enters the cell. * Its genomic RNA is released in to cytoplasm & converted in to viral DNA by reverse transcriptase. * The viral DNA is integrated into host cells DNA & captures the genetic machinery of host cells. * This leads to rapid production of viral genome, which attains the shape of full virus with the help of protease enzyme
  • 11.
  • 12. Mode Of Transmission * a) SEXUAL TRANSMISSION: It is first and fore most sexually transmitted disease. * b) PARENTRAL ROUTE: * i. BLOOD AND BLOOD PRODUCTS: Transmitted by contaminated blood transfusion of WBC, platelets & factor viii & ix. * ii. INJECTION &DRUG USERS * iii. OCCUPATIONAL INJURY * iv. EARPIERCING, TATTOING, ACUPUNCTURE. * C) MATERNAL-FOETAL TRANSMISSION: HIV can pass through an infected mother to her fetus, through placenta, during delivery or by breast-feeding.
  • 13. CLINICAL MANIFESTATIONS * IT CAN BE CLASSIFIED IN TO FOUR BROAD CATEGORIES: - * 1. INITIAL INFECTION WITH THE VIRUS & THE DEVELOPMENT OF ANTIBODIES: - Except for a generally mild illness like fever, sore throat & rash about 70% of people have no symptoms for the first five years. They look healthy & well although they can transmit virus to others. Antibodies usually take between 2-12 weeks to appear in the blood stream. * 2. ASYMTOMATIC CARRIER STATE:  Infected people have antibodies.  Persistent generalized lymphadenopathy.  It is not clear that how long this stage last. * 3. AIDS RELATED COMPLEX: - A person in this phase has illness caused due to immune system, but without the opportunistic infections but they exhibit one or more of the following clinical signs: - unexplained diarrhoea lasting longer then months, fatigue, malaise, loss of more than 10% body weight, fever, night sweats or other mild opportunistic infections such as oral thrush, generalized lymphadenopathy or enlarged spleen. * 4. AIDS: - AIDS is the end stage of HIV infection. A number of opportunistic infection commonly occurs at this stage. death is due to uncontrolled or untreated infections. There is significant decrease in CD4 count. Important opportunistic infections are tuberculosis, oroesophageal candidiasis, pneumonia etc.
  • 14. Oral Manifestations 1) Fungal 3) Viral · Candidiasis · Varicella zoster · Aspergillosis · Epstein-Barr including hairy leukoplakia · Histoplasmosis · HPV virus · Cryptococcus neoformans · CMV virus · Geotrichosis 4) Neoplasm 2) Bacterial · Kaposi’s sarcoma · HIV gingivitis · Non-Hodgkin lymphoma · HIV periodontitis · Squamous cell carcinoma · Necrotizing gingivitis 5) Lymphadenopathy · Mycobacterium avium intracellulare 6) Neurologic disorders · Klebsiella pneumonia · Paraesthesia · Enterobacterium cloacae · Facial palsy · E.coli · Hyperesthesia · Salmonella enteritidis · Dysphagia · Sinusitis · Exacerbation of apical periodontistis · Submandibular cellulitis
  • 15. Oral Manifestations 7) Miscellaneous · Recurrent apthous ulceration · Progressive necrotizing ulceration · Toxic epidermolysis · Delayed wound healing · Thrombocytopenia  Xerostomia & sicca type syndrome  Herpes Simplex · HIV embryopathy · Hyperpigmentation · Granuloma annulare · Exfoliative cheilitis · Lichenoid & other drug Reaction
  • 16. Diagnosis LABORATORY CLINICAL FINDINGS
  • 17. Diagnosis Clinical 1) WHO CASE DEFINATION OF AIDS SURVEILLANCE: - An adult or adolescent is considered to have aids it at least 2 major & attest one minor signs are present & if these signs are not known to be due to a condition unrelated to HIV infection. MAJOR MINOR Presence of either Kaposi sarcoma or cryptococcal meningitis –diagnosis of AIDS Wt loss > 10% of body Persistent cough for more for surveillance. weight than months Chronic diarrhoea for more Generalised pruritic than month dermatitis Prolonged fever for more H/o herpes zostor then one month Oropharyngeal candidiasis Generalized lymphadenopathy
  • 18. Diagnosis 2) Expanded WHO case definition for AIDS surveillance: - . HIV antibody test positive . One or more of the following condition present. 1. WT LOSS > 10% OF BODY WEIGHT or cachexia with diarrhea or fever or both, intermittent or constant for at least 1 month. 2. Cryptococcal meningitis 3. Tuberculosis 4. Kaposi sarcoma 5. Neurological impairment 6. Candidiasis of Oesophagus 7. Recurrent episodes of Pneumonia 8. Invasive cervical cancer
  • 19. Diagnosis LABORATORY DIAGNOSIS a) Screening test: ELISA b) Specific test: Western blot c) Non-specific test: anemia, leucopoenia, thrombocytopenia, and absolute CD4 count.
  • 20. Control Of AIDS 1. Prevention: a. Education: Health education • Avoiding indiscriminate sex • Use of condoms • Avoid sharing razors and tooth brushes • Comprehensive sex education programmers in school. • Public awareness campaigns for HIV. • Educational material and guideline for prevention should be made wide available. • All mass media channels should be involved in educating the people on AIDS, its nature of transmission & prevention.
  • 21. Control Of AIDS b. Prevention of blood borne HIV transmission:  People with high risk should be urged to refrain from donating blood, body organs, sperm or other tissues.  All blood should be screened before transfusion  Transmission of infection to haemophiliacs can be reduced by introducing heat treatment of factor viii & ix. c. Strict sterilization practice in hospitals and clinics d. Disposable needles and syringes should be used e. Universal precautions by health care workers.
  • 22. Control Of AIDS 2. ANTIRETROVIRAL TREATMENT: - It will not cure the disease but can prolong the life of severely ill patients. HIV infected with viral load > 5000-1000 or CD4 < 500/ul zidovudi Didanosin Zidovudine Zidovudine 1st lin ne Lami e Didanosine vudine Zalcitabine 1dt line treatment
  • 23. Control Of AIDS Intolerance to regime Progression of diseases or viral load does not decrease by >.5 log with initiation of treatment or increase of viral load by >. 5log while on Change to alternative treatment first line treatment 2nd line treatment Saquinqv Ritonavi Indinavir Stavudin Stavudine ir Zidov r Zidovudin e Lamiv Didnosin udine Zidovudi e udine e ne
  • 24. Control Of AIDS Progression of diseases or viral load does not decrease by >.5 log with initiation of treatment or increase of viral load by >. 5log while on treatment 3rd line treatment Saquinqvir Indinavir Nelfinavir Indinavir Zidovudine Zidovudine Zidovudine Didnosine Antiretroviral combination therapy
  • 25. Control Of AIDS 3. POST EXPOSURE PROPHYLACTIC TREATMENT: • It refers to anti retroviral drug therapy with in hrs. Following accidental exposure to virus. • Following needle stick injury, the part should be thoroughly washed with soap & water. The injured finger should not be reflex to put in the mouth. Open wounds should be irrigated with saline. Antiseptic agent can be applied but caustic agents should be avoided. • Following treatment is recommended by the US center for disease control and prevention for health care workers accidentally exposed to HIV: - • zidovudine( 200mg three times daily) +Lamivudine (150 mg twice daily) for 4 weeks • if “ source individual have advance aids : Nelfinavir(750 mg 3 times daily) +zidovudine +lamivudine • if “ source” individual failed on zidovudine +lamivudine therapy then stavudine +didanosine
  • 26. Control Of AIDS 4. PREVENTION OF INFECTION TO BABY BY HIV POSITIVE MOTHER: - a) zidovudine( 300mg three times daily) –to pregnant mothers from 10- 12th week of pregnancy or immediately after diagnosis. b) During labour- zidovudine I.V c) New born -Syrup zidovudine( three times daily for 6 weeks) d) Single dose of Neverpin (200 mg) at the time of labour.
  • 27. Control Of AIDS 6. PRIMERY HEALTH CARE: - * Because of its wide range of implication, AIDS touches all aspects of primary health care including mother & child health, Family planning & education. * It is important that AIDS control programmes should not be developed in isolation. * Integration in to country’s primary health care system is essential.
  • 28. Conclusion  Aids is caused by HIV virus which breaks down the body’s immune system leading to cause of opportunistic infections like tuberculosis, herpes simplex & zoster, hairy leukoplakia, pneumonia etc.  Death in aids is actually because of opportunistic infections.  Aids don’t pass on by: - • Sharing crockery and cutlery. • Touching, hugging or shaking hands. • Using same toilets. • Insect and animal bites • In can only pass on by having sex with infected person, from infected blood and injections and infected mother to her child  As it is said that mouth is the mirror of once health. Patient of aids have many oral manifestations.
  • 29. Conclusion A wide increase in the awareness about this disease is required. Much advancement has now been made in field of science & medicine. Many types of therapy & drugs have been introduced but still then…………. We have not been able to cure AIDS Prevention is only cure for AIDS In the present day awareness campaign through multimedia has made easy the efforts to reach large segment of people. The print medias, electronic media, press campaign holds the key to success A massive media campaign was launched by NACO in 1996, through well defined generic materials, posters, pamphlets, booklets, newspapers, advertisement, film clippings, TV spots, wall paintings and cinema slides were prepared in Hindi and all regional languages.
  • 30. Conclusion Ethics/moral duty of a doctor towards HIV ve patient • He should educate the patient • He should never refuse treatment to HIV positive patient. A dentist who refuses treatment is in violation of law and subject to penalties. Every year on 1st December world AIDs day is celebrated
  • 31. Thank you http://www.pediatricdentists.blogspot.com/