Human Immunodeficiency Viru Sreal

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HUMAN IMMUNODEFICIENCY VIRUS HUMAN IMMUNODEFICIENCY VIRUS SUBMITTED BY- GROUP D1 SUBMITTED BY- GROUP D1 MEDICAL WARD MEDICAL WARD 25.4.2006 25.4.2006

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Transcript of Human Immunodeficiency Viru Sreal

  • 1.HUMAN IMMUNODEFICIENCY VIRUS SUBMITTED BY- GROUP D1 MEDICAL WARD25.4.2006

2.

  • First described in 1981
  • Reported as lymphadenopathy associated virus (LAV) in paris 1983 at Pasteur Institute by Lue Montagrier and associates
  • In U.S. , called human T lymphotropic virus type III (HTLV III) by Robert Gallo and colleagues at National Institute of Health
  • Assigned a uniform name, the Human Immunodeficiency virus (HIV) by the International Committee on the Taxonomy of virus in 1986

3.

  • Family retrovirus
  • RNA virus
  • HIV 1 has widest distribution , world wide
  • HIV 2 found mostly in western Africa
  • HIV 2 less aggressive than HIV 1
  • Second leading cause of disease burden world-wide
  • Leading cause of death in Africa( >20% of deaths

4.

  • In 2000, WHO estimated that over 36 million people living with HIV/AIDS, 5.3 million new infection and 3 million deaths
  • Rising alarmingly in heavily populated parts of the world including some Eastern European countries ( Ukraine , Russia) and South East Asian countries (Thailand , Myanmar)

5. Mode of transmission 6. Major mode of spreads

  • Sexual (vaginal , anal ,oral)
  • parenteral (blood and blood product recipients, injection drugs users and those experiencing occupational injury)
  • Vertical transmission
  • Major route of transmission (>70%) world-wide is hetrosexual

7. Transmission risk after exposure

  • >90 % for blood and blood products
  • 15-40 % for vertical transmission
  • 0.5-1 % for injection drug users
  • 0.2-0.5 % for genital mucous membrane
  • half of patient )
  • (1) Pneumocystic carinii pneumonia most common AIDS defining illness , rarely occur when CD4 counts more than 200cells/ mm3
  • (2)Mycobacterium tuberculosis reactivating latent infection or acquired from open contact develop progressive primary disease , disseminated , miliary or extra pulmonary tuberculosis

23. Cardiac

  • (3)Bacterial infection -S pneumoniae , H influenzae ,Staph aureus , pseudomonas and norcardia infection
  • Myocarditis , cardiomyopathy (25 40 % of the patients ), pericardial effusion , congestive cardiac failure

24. Renal Endocrine

  • HIV associated nephropathy is the most important renal condition usually present with nephrotic syndrome, chronic renal disease or combination of both.
  • Reduced level of testosterone , abnormal adrenal function (hypoadrenalism in 25% of patients )

25. Mucocutaneous

  • Seborrhoeic dermatitis (80%)
  • Herpes infection (20%)
  • Molluscum contagiosum ( 10%)
  • Fungal infection ( candidiasis )
  • Drug allergy Stephen Johnsons syndrome
  • Recurrent apthous ulceration

26. Haematology

  • Disorders of all 3 major cell lines may occur in HIV
  • Most frequent in late-stage disease
  • Anaemia 70 %
  • Leucopenia 50 %
  • Thrombocytopenia 40 %

27. Neoplasms

  • Kaposi sarcoma and Non-Hodgkins lymphoma are most common opportunistic malignancies associated with HIV and are considered AIDS defining diagnosis
  • Primary CNS lymphoma-usually complicate late stage HIV
  • Genital cancer-anogenital (vulval, vaginal, anal, penile) and cervical cancer closely associated with HPV is more frequently observed in HIV

28.

  • HIV associated lymphoma (non-Hodgkins lymphoma it is late manifestation of HIV )

29. Opportunistic infection

  • Protozoa toxoplasmosis , cryptosporidiosis , microsporidiosis,
  • Virus CMV , Herpes , EBV , HPV , Papova virus ,
  • Fungus PCP , Cryptococcus , Candida , Dermatophytes , Aspergillus , Histoplasma
  • Bacteria Mycobacteria ,Staphylococci , Non-typhoidal salmonellosis ,
  • Others Disseminated strongyloidiasis , Giadiasis, Crustes ( Norwegian )scabes

30. Common AIDS defining condition

  • Oesophageal candidiasis
  • Cryptococcal meningitis
  • Chronic cryptosporidial diarrhoea
  • CMV retinitis
  • Chronic mucocutaneous herpes simplex
  • Disseminated Mycobacterium avium intracellulare
  • Miliary or extrapulmonary tuberculosis
  • PCP
  • Progressive multifocal leuco-encephalopathy

31.

  • Recurrent non-typhi salmonella septicaemia
  • Cerebral toxoplasmosis
  • Karposis sarcoma
  • Non-Hodgkins lymphoma
  • Primary cerebral lymphoma
  • HIV associated wasting
  • HIV associated dementia

32. CLINICAL COURSE 33. Primary infection

  • Mild in most patients and only identify by retrospective enquiry
  • Symptoms appear 2 to 4 wks after exposure ( seroconversion illness)
  • Manifest as fever , erythematous or maculopapular rash over the body , fatigue , pharyngitis , cervical lymphadenopathy , myalgia , arthralgia , retro-orbital headache, mucosal ulceration

34.

  • Rarely present with aseptic meningitis, encephalitis, myelitis , polyneuritis
  • Coincides with surge in plasma HIV RNA level and fall in CED4 count .
  • Recover after 1- 2 wks associated with fall in viral load and rise in CD4 count but not to its previous value .
  • HIV antibody appear at 3 12 wks

35. Asymptomatic infection (CD4> 500/cumm)

  • Variable period in which infected individual remains well with no evidence of disease
  • May present with persistent generalized lymphadenopathy ( PGL)( enlarged lymph nodes at two or more extra inguinal sites persists for 3 months without any other causes of generalized lymphadenopathy )
  • Sustained viraemia with decline in CD 4 counts

36. Mildly symptomatic disease ( ARC)( CD4 200-500/cumm)

  • Impaired cellular immunity median interval from infection is 7-10 yrs
  • Chronic weight loss, fever , diarrhoea , oral or vaginal candidiasis , oral hairy leucoplakia, recurrent herpes zoster infection , severe pelvic inflammatory disease , bacillary angiomatosis , ITP and cervical dysplasia

37. Acquired immune deficiency syndrome

  • Development of
  • - 1) specified opportunistic infection ,
  • - 2) tumors ,
  • - 3) wasting and
  • - 4) dementia
  • Disease correlate with level of CD 4 count

38.

  • CD 4 < 200 PCP pneumonia , mucocutaneous herpes simplex , cryptosporidiosis , microsporidiasis, oesophageal candidiasis, miliary or extra pulmonary TB , wasting and peripheral neuropathy
  • CD 4 < 100 Cerebral toxoplasmosis , cryptococcal meningitis , primary CNS lymphoma , non Hodgkins lymphoma , dementia and progressive multifocal leucoencephalopathy
  • CD 4 < 50 Cytomegalovirus retinitis , gastrointestinal disease , disseminated mycobacterium avian intracellulare

39. Major signs

  • weight loss >10 %
  • Diarrhoea > 1 month
  • Fever > 1 month

CRITERIA USED IN MYANMAR 40. Minor signs

  • Persistent cough > 1 month ( not due to tuberculosis )
  • Candidiasis ( oropharyngeal )
  • Herpes zoster ( recurrent )
  • Herpes simplex ( chronic progressive and disseminated)
  • Generalized pruritic dermatitis
  • Generalized lymphadenopathy

41. INVESTIGATION 42. laboratory confirmation

  • Serology test using ELISA antibody testing { false positive are rare but it is important that any (+)ve results are confirmed by using other immunoassays ,e.g. immunoblot }
  • Seroconversion ( HIV antibody negative ) and vertical transmission ( HIV antibody positive ) , ELISA test is unhelpful and HIV RNA must be measured by using PCR ( reverse transcriptase ) , b DNA , NASBA technique
  • Ag detection for P24 Ag

43. Pre and post test counselling

  • Prior to HIV antibody testing , the patient must see a counsellor
  • Pretest counselling involve assessment of the risk of exposure and explore a persons knowledge about HIV infection
  • Post-test counselling ( return +ve)- to provide emotional support , organised continuous contact and medical follow up , safer sex and needle exchange

44. Baseline investigations

  • all patients
  • -CD4 count-viral load
  • -HBV surface antigen-HCV antibody
  • -HBV core antibody-HAV IgG antibody
  • -Toxoplasma antibody
  • -CMV IgG antibody
  • -Treponema serology
  • -Chest radiograph

45.

  • CD 4350 200-350