AIDS
INTRODUCTION
Acquired
Immuno Deficiency Syndrome (AIDS) was first identified in
Definition:
Acquired
Immunodeficiency Syndrome is caused by
Human Immunodeficiency virus [ HIV], which is a group of retro virus, HIV-I and
HIV-II. HIV causes an incurable
infection that leads ultimately to a terminal disease called acquired Immuno
Deficiency Syndrome [AIDS].
INCIDENCE:
Incidence
is difficult to work out but the fact remains that the disease is alarmingly
increasing both in the developed and in developing countries.
World
wide 25-30% of infected patients are women and 905 of them are 20 to 49 years
of age.
THE VIRUS
HIV
viruses (HIV-1 and HIV-2) are RND retroviruses having the enzyme reverse
transcriptase, which permits genomic RND to be transcribed into double stranded
DNA. The virus attaches to T lymphocytes
known as CD4+ cells whose action in the immune system is
to combact viruses, bacteria and certain
malignancies. Once the virus is into the
genome of the host, it produces multiple copies of itself, which will eventually
cause host cell damage. There is gradual
depletion of CD4+ cells.
There is also failure of B lymphocytes to produces anti bodies to
HIV. These events leads to progressive
loss of host immune defence and development of AIDS.
INCUBATION
PERIOD:
HIV
positive person can develop AIDS within
10 years usually. Median incubation
period 5-8 years in adults while in infants and children 2-5 years.
MODE OF
TRANSMISSION
1.
Sexual contact
(homosexual or heterosexual)
2.
Transplacental
transmission (perinatal)
3.
Exposure
to infected blood or tissue fluids.
4.
Breast
Feeding
5.
Intraveneous
drug abuses.
6.
Use
of contaminated, needles, needle stick injuries.
7.
Perinatal
transmission
IMMUNO
PATHOGENESIS
Profound
cell mediated immuno deficiency is the basic pathology as the HIV leads to slow
but progressive destruction of T
cells. After a peak viral load, there is
a set point which is a state of balance between the virus’s ability to
replicate and this hosts ability to protect itself by neutralization and
removal of virus.
When the set point
viral load is high
ß
More destruction of
host CD4+ cells
ß
Progressive
immuno-suppression
ß
Opportunistic
infections and cancer
CLINICAL FEATURES
Initial
presentation of an infected patient are
Ø
Fever
Ø
Malaise
Ø
Headache
Ø
Sorethroat
Ø
Lymphadenopathy
Ø
Maculopapular
rash
Ø
Primary
illness may be followed by an asymptomatic period.
Ø
Progression
of the disease may lead to multiple opportunistic infection
Examples:
o
Candida
o
Liberculosis
o
Pneumocystis
Ø
Autoimmune
thrombocytopenia
Ø
Cervical
Carcinoma
Ø
Lymphomas
Ø
Kaposi’s
Sarcoma
Ø
Constitutional
symptoms like
o
Weight
loss
o
Lymph
adenopathy
o
Protected
diarrhea
DIAGNOSSIS
1. History of the mother
a. Any past history of
accident, blood transfusion or surgery.
b. Socio economic status
c. Age
d. Extra marital
relationship
2. Physical Examination
3. CD4+
count L200 cells / mm3
4. Serum test for HIV
a. ELISA test [Enzyme-Linked
Immunosorbent Assay].
b. Western blot or
immunoflurescence assay.
c.
Polymerase
chain reaction technique of amplifying viral DNA.
MANAGEMENT
PRENATAL
CARE
Ø All clients should be
offered voluntary serologic testing for HIV infection.
Ø In Sero-poistive cases,
additional investigations should be done to test for other STDs. Husbands should be offered serologic testing
for HIV.
Ø Counselling about the
risk of HIV transmission to the fetus and neonates should be made and
termination of pregnancy offered.
Ø Tuberculin test is to
be done. If it is positive, a chest
X-ray should be performed. Even if the
chest X-ray is negative chemoprophylaxis with isoniazid (INH) 300mg orally
darty should be administered.
Ø The woman should have
T-lymphycyte count in each trimester. If
the count falls to less than 200 cells / mm3, the woman should be
treated with zidovudine, the woman should receive prohylaxis aganst
pneumocystis carimi infection with trimethoprim 160mg and sulphamethaxazole
800mg orally thrice weekly. Nevirapine
is found to reduce the viral transmission to breast fed infants.
Ø The progression of the disease is assessed by CD-4 lymphycytes
count presence of P24 core antigen and decrease of tiles of P24 antibody.
Ø Anti retroviral
therapy to HIV-1 positive women is highly effective in reducing the viral (HIV,
RNA) load. Triple chemotherapy is
preferred as a first line defence and to be started any time between 14 and 34
weeks and then continued throughout pregnancy, labour and post partum period.
Ø Anti-HIV-1 drugs are
grouped into
Group A - Neucleoside
analogs
- Zidovudine
- Zalcitabline
- Lamivudine
- Stavudine
Group B - Protease
inhibitors
- Indinavir
- Sqauinavir
- Ritonavir
Ø Group C - Nonnucleoside
analogs
- Nevirapine
- Delivirdine
Ø Group D - Integrase
inhibitor
- Elvitegravis
Ø Group E - Entry
inhibitor
- Vicriviroc
Treatment
regimen:
Two
from group A plus one from either group B or groupC.
Example: Zindovudine 100mg given five times
daily it can reduce perinatal transmission.
INTRAPARTUM
CARE
Ø Zidovudine is given Iv
infusion starting at the onset of labour in vaginal delivery or 4 hours before
caesarean section.
Ø Elective caesarean
delivery reduces the risk of vertical transmission by about 50%.
Ø Cord should be clamped
as early as possible.
Ø Baby should be bathed
immediately.
Ø A maternal sample for
plasma viral load should be taken at delivery.
Ø To avoid procedures
that might result in break in the skin or mucous membrane of the infants.
Ø Amniotomy, Attachment
of scalp electrode and determination of scalp blood pH should best be avoid.
Ø Caps, masks, gowns and
double gloves should be worn. Protective eye wear should be used by
physician and midwives.
Ø Mechanical suctioning
devices should be used to remove secretions from the neonates airways.
Ø Blunt tipped needles
should be used to avoid needle stick injury and washing of any blood
contaimination off the skin immediately.
Ø Health care workers
should be protected from contact with potentially infected body fluids.
Ø Post exposure
prohylaxis with triple therapy for 4 weeks, reduces the risk of seroconversion
by more than 80% [Zudovudine 200mg tid + lamivudin 150mg bd + indinavir 800 mg
tid].
Ø Disposable syringes
and needles are used and they are deposited in the puncture proof containers.
POSTPARTUM
CARE
Ø Mothers must be
counseled about the risk and benefits of breast feeding and hlped to make an
informed choice.
Ø Zidovudine syrip 2 mg
/ kg is given to the neonates 4 times daily for first 6 weeks.
Ø Mother should be
encouraged to manage the baby’s care herself with the support of the midwife.
Ø Gloves must be worn
for examining the perineum lochia or cesarian wound.
Ø Disposal of sanitary
napkins and disinfection and cleaning of any 8 pilled blood must be done
correctly.
CARE OF
BABY SOON AFTER BIRTH
1.
Suction
any secretion from the oral cavity first and then from the nose to prevent the
baby from swalloing any secretion.
2.
Do
not milk the umbilical cord.
3.
Cut
the cord as soon as pulsation are not felt.
4.
Wipe
the baby’s body with a warm clean towel to remove any blood stained secretion.
5.
Administer
single dose of syp neviapine to the child within 72 hours after birth.
REDUCING
THE RISK OF INFECTION THROUGH BREAST FEEDING
Ø Ensure good nutrition
during pregnancy and post natal period.
Ø Preparation of Breast
in the antenatal period
i.
Examine
her breast for any bifid nipples and
flat nipples.
ii.
Prepare
the nipple for suckling by massaging them with oil every day.
Ø Adopting proper
position for breast feeding for herself and the baby. Baby in facing mother and is close to her,
babys tummy flat against moter tummy.
CORRECT
ATTACHMENT
Ø Baby’s chin is
touching the breast.
Ø Baby’s mouth covers
all the areola.
Ø Baby’s lower lip is
curled outward.
TREATMENT
Therapy
of HIV is complicated by the fact that the HIV Genome is incorporated into the
host cell genoma and can remain there in a dormant state for prolonged periods
until it is reactivated. Effective
therapy must be directed against both free virus and virus – infected
cells. Although a number of substances
with in vitro anti – HIV activity has been described, only a few drugs exhibit anti HIV activity in vivo at tolerable
toxicities. The main group of substances
described are:-
1.
Nucleoside
analogues reverse transcriptase inhibitors.
AZT, DDC, DDI and lamu vidine.
2.
Non-Nucleoside
analogue reverse transcriptase inhibitors eg., Nevirapine
3. HIV protease inhibitors eg., Ritonair, Indivavir. They are the most potent inhibitors of HIV replication to date.
PREVENTION
Ø Use
of condoms or diaphragms can prevent sexual transmission of the disease. Hormonal contraceptives and IUCD do not
protect from the risk of infection.
Ø Screening
of blood donors should be mandatory.
Ø Frozen
semen in artificial donor insemination should be prechecked.
Ø Screening
of all high risk cases in the population.
Ø Cessation
of smoking.
Ø Additionally,
patients with CD45 count less than 200 or those with symptoms should receive
trimethoprim and sulphamethoxazole or aerosol pentamidine.
DURING PREGNANCY
Zidovudine reduces viral load, and
100mg three times a day may be given after 14th week of pregnancy.
Ø The
neonate with positive HIV antigen should receive zidovudine.
Ø ABC
approach to AIDS prevention is widely accepted as a model to approach
adolescent and young adults where HIV infection has been spreading most
rapidly.
A – Abstain
B – Be faithful to one
partner
C
– Use condoms
Ø Another
new approach for prevention of AIDS is
SCAAB
– P way
S - Safe
Sex
C - Condom
Promotion
A - Avoid
substances abuse
A
- Adopt
traditional customs safely
B - Blood management and haling of body
fluids safely
P - Prevention of mother to child
transmission
COUNSELING
Pre-pregnancy
and early pregnancy counseling for HIV infected patient is essential. The women suffering from AIDS should be
advised against pregnancy and if pregnant, termination of pregnancy should be
offered. The counselor must provide
uptodate knowledge which enables the patient to make an informed consent.
The highest HIV prevalence rates are
found in
Estimated number of people living with
HIV / AIDS 2009
People living with HIv / AIDS – 2.7
million adult (15 years or above) HIV prevalence 0.4%.
The percentage of adults living with
HIV globally has remained stable since 2000.
use of antiretroviral therapy has increased.
In the end of 2007 only 335 of HIV
infected women had received anti retroviral drugs to reduce the risk of mother
to child transmission.
HIV STATISTICS 2008-2009
The National Family Health Survey
conducted between 2008 and 2009 measured HIV prevalence among the general adult
population of
CONCLUSION
AIDS is the emergency of the “Third
Generation” of sexually transmitted diseases.
Prevalence rate in
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