· human immunodeficiency virus
· 1981- AIDS first identified in USA
· 1982 - AIDS first diagnosed in Australia
· 1983 - HIV virus identified
· 1984 - first confirmed case of AIDS through blood transfusion
· 1985 - laboratory test for HIV introduced
· 1985 - HIV screening of blood supply in USA and Australia
· 1% of US population is HIV-positive
· 0.1% of Australian population is HIV-positive
· 25% of these have AIDS
· M:F = 20:1
· homosexual - 85%
· drug user - 5%
· heterosexual contact - 5%
· haemophilia - 2%
· blood transfusion - 2%
· 20% of AIDS patients require surgery
· up to 10% of ER patients are HIV-positive
Sexual intercourse
· anal
· vaginal
Blood-borne
· sharing of infected needles and syringes by infected drug users
· blood or blood products (none since 1985)
· accidental transmission with infected blood in health care setting
Infected mother to child
· before or during birth
· via breast milk
· belongs to retrovirus family
· can reverse RNA of virus into DNA
· thus incorporate into DNA of infected cell
· uses reverse transcriptase
· primary impairment is CD4 lymphocyte (T-helper cell)
· also affects
· B lymphocyte
· monocyte/macrophage cell line
· production of gamma interferon and lymphokines
· impairs wound healing
· via CD4 and lymphokine deficiency
· causes platelet deficiency
· autoimmune thrombocytic purpura
· causes neuropathy
· via autoimmune neuritis
· affects bacteriocidal functions of leukocytes
· chemotaxis, phagocytosis and secretion of microbicides
· may develop illness at time of acute infection
· within 2-4 wks of exposure
· mononucleosis-type illness
· lympadenopathy, myalgia, fever, rash
· high viraemia and high risk of transmission
· HIV antibodies appear 3 wks to 4 mths after infection
· usually resolves
· some have persistent lymphadenopathy
· proportion will progress to HIV infection
· median time of 8-10 yrs
· associated with
· progressive failure in immune system
· development of opportunistic infections and neoplasms
· progression follows chronological order
· can be divided into stages depending on CD4 count
· early (CD4 > 500)
· intermediate (CD4 200-500)
· late (CD4 < 200)
Early
· CD4 > 500
· average survival 10.9 yrs
· develop autoimmune disorders
· ITP, Guillaine-Barre syndrome, polymyositis
Intermediate
· CD4 200-500
· develop mild infections, esp. of skin and mucosa
· tinea, dermatitis, herpes
Late
· CD4 < 200
· average survival 1.7 yrs
· develop severe infections and malignancy
· see below
Group 1
· acute infection
Group II
· asymptomatic infection
Group III
· persistent generalised lymphadenopathy
Group IV
· other diseases
· A - constitutional disease
· B - neurological disease
· C - infectious disease
· D - malignant disease
· pneumocystis carinii
· Mycobacterium avium complex
· toxoplasmosis
· cryptococcal meningitis
· Kaposi sarcoma
· non Hodgkin’s lymphoma
· primary CNS lymphoma
· increased susceptibility
· most common organisms
· Staph aureus
· Strep pneumoniae
· E coli
· most common infections
· pneumonia
· central line phlebitis
· celllitis
· UTI
· usually benign appearance
· not febrile
· not septic
Polyarthralgia
· similar to that seen in other viral diseases
· self-limiting
Septic arthritis
· prone to joint sepsis
· may be due to
· conventional organisms
· opportunistic infections
Reiter’s syndrome
· classical presentation
Psoriatic arthritis
· similar pattern to HIV-negative patients
Polymyositis
· proximal muscle weakness
· myalgia
· elevated serum CK
· window period
· time from infection to time antibody test becomes positive
· usually 2-6 weeks
· up to 6 months considered for safety
· antibody tests
· ELISA test (sensitive but not specific)
· Western Blot Test (specific)
Complications
· some risks with HIV infection
· increased risk with AIDS
· problems due to
· impaired defences to common surgical pathogens
· delayed wound healing
· risks are
· increased morbidity of sepsis and wound problems
· increased mortality secondary to these and to generalised poor state
Effect on disease progression
· no evidence that surgery accelerates disease progression
Procedure
· need to assess risk/benefit ratio
· increased risks of death, sepsis and wound problems
· decreased benefits with limited longevity and decreased function
Indicators
· factors that correspond with outcome risk are
1. low CD4 level
· < 100
2. anergy
· decreased delayed hypersensitivity response to skin test with mumps and tetanus
3. thrombocytopaenia
· < 60 000
4. leucopaenia
· PMNs < 1 000
5. low serum albumin
· < 25 g/l
6. AIDS-relaed conditions
· opportunistic infection
· neoplasm
Preparation
· granulocyte-stimulating factor
· platelet transfusion
· treatment of opportunistic infection
· vaccination against measles, mumps and rubella
· stop marrow-suppressing AIDS treatment