AIDS(ACQUIRED
IMMUNO DEFICIENCY SYNDROME)
INTRODUCTION
India’s first known
HIV infection was diagnosed in a female sex worker in Chennai in February 1986.
It is highly probable that HIV had been circulating for some years before that,
since screening during 1986-87 found as many as 3%-4% of sex workers infected
in Vellore and Madurai, and 1% of STD patients infected in Mumbai. As there
were already over 20,000 cases in the world before any case was identified in
India, screening for HIV infections began in India in 1985, almost as soon as
tests for the HIV antibody were available. In India, too, for the first time in
2006, HIV testing was a part of the National Family Health Survey (NFHS).
DEFINITION
Acquired immune deficiency syndrome or acquired immunodeficiency syndrome (AIDS) is a disease
of the human immune system caused by the human
immunodeficiency virus (HIV)
HIV POSITIVE MOTHER AND HER BABY
Women who are
infected with HIV are at risk of passing the infection on to their babies.
Approximately 25% of all babies born to HIV-positive pregnant women are
infected with the virus. HIV can be transmitted from an HIV-positive woman to
her child either during pregnancy, or during labour and delivery, or by
breast-feeding. In Europe and the USA, about 15 to 20%of babies born to
HIV-positive women who are not taking anti-HIV drugs are infected. In most cases, HIV is thought to be
transmitted during the last weeks of pregnancy or during delivery.
However, the risks of
mother-to-child transmission of HIV can be reduced to below 1% by
the appropriate use of anti-HIV drugs during pregnancy and labour; by having a
caesarean delivery if you have a detectable viral load; and (when safe alternatives
are available) by not breastfeeding. In 2010, a
study showed that there were no cases of mother-to-child transmission when
guidelines to prevent this were properly followed.
EPIDEMIOLOGY OF AIDS IN INDIA
*
In India there is an estimated 2-5 million people infected
with HIV in India today. The most rapid and well-documented spread of
infection has occurred in Bombay and the State of Tamil Nadu.
*
In Bombay, HIV
prevalence has reached 50% in sex workers, 36% in STD patients, and 2.5% in
women seen in antenatal clinics.
*
The infection affects both urban and rural areas.
*
In Bombay, seroprevalence rose from 2-3% in patients
seen in STD clinics in 1990 to 36% in 1994 and in rural areas 3-4% of some
populations have an STD.
*
In India, there are an estimated 1-2 million cases of
tuberculosis every year. TB is the most prevalent form of POI (opportunistic
infection) in over 60% of AIDS cases. In Bombay alone, 10% of the
patients with TB are HIV-positive.
*
The epidemiology of HIV
infections and AIDS is quite different
in children (diagnosed when younger than
13 year of age). About 1% of all AIDS cases occur in population and the vast
majority (about 90% results from vertical transmission of virus from infected
motler to the fetus or newborn.
*
Mother To Infant
Transmission Mother to infant vertical
transmission is the major cause of
pediatric AIDS. Three routes are
involved in utero, by transplacental spread
intrapartum, during delivery
and via ingestion of HIV
contaminated breast milk. Of these the transplacental
and intrapartum routes account for most cases. Vertical transmission rates
world side vary from 25% . Vertical transmission rates world side vary from
25% to 35% with a
15% to 25% rate reported in the United States, higher rates of infection occur with
high maternal viral load and or the presence of
presumably by increasing placental accumulation of inflammatory cells.
NATIONAL FAMILY HEALTH SURVEY-III
According to NFHS-II figures, India
had an estimated 2.5 million people (range 2 and 3.1 million) between the ages
of 15 and 49 years living with HIV in 2006 – less than half the previous year’s
estimate of more than 5 million. The country’s adult HIV prevalence is halved
as well, and is now estimated to be approximately 0.36%. HIV prevalence among
adult women is 0.29%; for men it is 0.43%. This puts India behind South Africa
and Nigeria in numbers living with HIV.
*
HIV prevalence was highest among women whose
spouses were employed in the transport industry. In Manipur and Nagaland, HIV
prevalence was the highest among women whose spouses were industry/factory
workers.
*
In 2006, HIV prevalence among mothers attending
antenatal clinics is more than 1% in 118
districts. Eighty-one districts have an HIV prevalence of more than 5% in one
or more of the high risk groups.
*
The HIV epidemic in the north-eastern states of
Manipur, Mizoram and Nagaland continues unabated. In 2006, HIV seropositivity
among pregnant women was 1.39%, 1.36% and 0.94% in Manipur, Nagaland and
Mizoram respectively. In addition, HIV prevalence among sex workers appears to
be increasing in Nagaland and Mizoram.
*
Further, there has been a rise in HIV prevalence
in the northern and eastern regions: 26 districts -- mostly in Madhya Pradesh,
Uttar Pradesh, West Bengal, Orissa, Rajasthan and Bihar – are high prevalence
districts. In West Bengal, prevalence has gone up from 0.21% in 2005, to 0.30%
in 2006. In some districts of West Bengal high HIV transmission is seen among
sex workers and IDUs. Among migrants at one site in Orissa, HIV prevalence was
5%. In Rajasthan, HIV prevalence has gone from 0.12% in 2005 to 0.17% in 2006.
*
Karnataka: HIV prevalence at
antenatal clinics in Karnataka has been over 1% for some years. A 2005-2006
survey found that 0.69% of the general population was infected. The average HIV
prevalence among female sex workers in Karnataka was 18% in 2005.
HIV SCREENING IN PREGNANCY
In many countries across the world, women are tested for HIV during pregnancy. There are a number of important reasons
for this:
- HIV infection can be passed on
to a baby during pregnancy, labour and delivery, and breastfeeding.
- In areas where antiretroviral therapy
is available, a pregnant woman can receive these drugs if she tests HIV
positive during pregnancy.
- For many women, especially in
resource-poor areas, pregnancy will be the only time in their young adult
lives when they access healthcare services on a regular basis. It
therefore presents an excellent opportunity not only to screen for HIV,
but also to educate and advise about the dangers of the virus.
RECOMMENDATIONS
1. All
pregnant women should be offered HIV screening with appropriate counselling.
This testing must be voluntary. Screening should be considered a standard of
care, although women must be informed of the policy, its risks and benefits,
and the right of refusal. Women must not be tested without their knowledge.
2. Pre-test
counselling and the patient’s decision about testing should be documented in
the patient’s chart.
3. Women
who decline screening should still have concerns discussed and should continue
to receive optimum antenatal care.
4. Women
should be offered HIV screening at their first prenatal visit.
5. Women
who test negative for HIV and continue to engage in high-risk behaviour should
be retested in each trimester.
6. Women
with no prenatal care and unknown HIV status should be offered testing when
admitted to hospital for labour and delivery. Women at high risk for HIV and
with unknown status should be offered HIV prophylaxis in labour, and HIV
prophylaxis should be given to the infant post partum.
7. Women
who test positive for HIV should be followed by practitioners who are
knowledgeable in the care of HIV-positive women.
HIGH-RISK
BEHAVIOURS
¨ Sharing
needles or any other components during intravenous drug use
¨ Unprotected
sex with multiple partners
¨ Unprotected
sex with a known HIV-positive individual
¨ Unprotected
sex with a partner who is from an HIV-endemic area.
¨ Unprotected sex with a partner participating
in known high-risk behaviour
HIV TEST-
HIV
tests are usually performed on venous blood. Many laboratories use fourth
generation screening tests which detect anti-HIV antibody (IgG and IgM) and
the HIV p24 antigen. The detection of HIV antibody or antigen in a patient
previously known to be negative is evidence of HIV infection. Individuals whose
first specimen indicates evidence of HIV infection will have a repeat test on a
second blood sample to confirm the results.
The
window period (the time between initial infection and the development of detectable
antibodies against the infection) can vary since it can take 3–6 months to
seroconvert and to test positive. Detection of the virus using polymerase chain
reaction (PCR) during the window period is possible, and evidence suggests that
an infection may often be detected earlier than when using a fourth generation
EIA screening test.
Positive results obtained by PCR are confirmed by
antibody tests.[ Routinely used HIV tests for infection in
neonates and infants (ie, patients younger than 2 years), born to HIV-positive
mothers, have no value because of the presence of maternal antibody to HIV in
the child's blood. HIV infection can only be diagnosed by PCR, testing for HIV
pro-viral DNA in the children's lymphocytes
LABORATORY TEST FOR DIAGNOSING AND TRACKING HIV AND
ASSESSING IMMUNE STATUS
TESTS
|
FINDINGS IN
HIV INFECTION
|
ELISA(enzyme linked immunosorbant assay)
|
Antibodies are detected, resulting in
positive results and making the end of the window period.
|
WESTERN BLOT
|
Detects antibodies to HIV; used to confirm
ELISA
|
VIRAL LOAD
|
Measures HIV RNA in the plasma
|
CD4-CD8
RATIO
|
These are lymphocytes; HIV kills CD4 cells,
which results in a significant impaired immune system.
|
Blood samples are tested
with two different blood test to determine the presence of antibodies to HIV.ELISA
identifies antibodies against HIV. The western blot test is used to confirm
seropositivity when the ELISA is positive. People whose blood contain antibodies for HIV are seropositive. Saliva
can also be tested using the ELISA antibody test.
VIRAL LOAD TESTS
It measures plasma HIV
RNA level. Currently these test are used to track viral load and response to treatment to HIV
infection.HIV culture or quantitative plasma culture and plasma viremia are additional test that measure viral burden but they are used infrequently. The
lower the viral load, the longer the time to AIDS diagnosis and the longer the
survival time.
PARENT TO CHILD TRANSMISSION
• Without interventions the risk of MTCT is
25-40% . The change of PMCTC to PPTCT is to involve the father in the prevention of transmission of
HIV infection to the child
• Combination interventions can reduce MTCT
rate by up to 40% in breastfeeding populations
• Because ARV prophylaxis alone does not treat
the mother’s infection, ongoing care and support is needed
• MCH services can act as an entry point to
the range of services that can provide care and support to the HIV-positive
women and affected family members
• Linkages to community services can provide
enhanced care and support
• An important component of the Indian
government’s AIDS control programme
• Parent-to-child transmission (PTCT) of HIV,
or perinatal transmission, accounts for 2.72 percent of the total HIV infection
load in the country.(India)
• Parent-To Child Transmission (PTCT) of HIV
can occur during pregnancy, at the time of delivery or through breastfeeding.
• If
an HIV positive woman becomes pregnant, there is a 25-30% chance that the baby
will also be infected.
Rationale for PPTCT in India
o
27 million pregnancies per year
o
1,62,000 infected pregnancies
o
Cohort of 48,600 infected newborns per year
o
0.6% prevalence
o
30% transmission
o
Most of these children die within 2-5 years
The Terminology of HIV/AIDS
• MTCT
– mother-to-child transmission
• PMTCT
– prevention of MTCT
• PTCT
– parent-to-child transmission
• PPTCT
– prevention of PTCT
• PLWHA
– people living with HIV/AIDS
Estimated MTCT Rates
• Without
intervention
• During
pregnancy 5 - 10%
• During
labour and delivery 15- 20 %
• During
breastfeeding 5 - 15%
• Total
25 - 45%
Elements of the PPTCT programme:
• Primary prevention of HIV infection in young
people & women of child bearing age through promotion and provision of
free, subsidized or commercially marketed condoms, provide diagnosis for
treatment of sexually transmitted diseases, and behaviour change communication
efforts to reduce behaviour that place individuals at risk, and information
about risks of PTCT during pregnancy, delivery, breastfeeding &
encouragement to see VCT counselor or health provider for information on how to
prevent HIV/AIDS among infants & young children.
• Prevention of unintended pregnancies in HIV
positive women through reproductive health services, which include family
planning.
• Prevention of transmission from an HIV
positive women to her infant through anti-retroviral (ARV) prophylaxis and
safer delivery practices
• Care and support services to HIV-infected
women who are enrolled with the programme and to their children and families,
including counselling on infant feeding.
Comprehensive PPTCT services include 4 prongs:
• Prong
1 Primary prevention of HIV infection
• Prong
2 Prevention of unintended pregnancies among HIV-infected women
• Prong
3 Prevention of HIV transmission from HIV-infected women to their infants.
•
Prong 4 Provision of care and support to HIV-infected women, their infants, and
their families
PPTCT: Interventions to Decrease Risk of HIV Transmission to Infant
During pregnancy
o
Decrease viral load (ARV prophylaxis and
treatment)
o
Monitor and treat infections
o
Support optimal nutrition
PPTCT: Interventions to Decrease Risk During labour and delivery
Avoid
• Premature
rupture of membranes
• Invasive
delivery techniques
• Unresolved
infections such as STIs
Provide
• Elective
caesarean section when safe and feasible
PPTCT: Interventions to Decrease Risk
• Promote
safer infant feeding
• Replacement
feeding
• Exclusive
breastfeeding for limited time
• Avoidance
of mixed feeding
• Reporting
breast problems
• Support
for optimal nutrition
For parents-to-be . . . the ABCs
• A
= Abstinence
• B
= Be faithful to one HIV-uninfected partner
• C = Condoms — use consistently and
correctly
PROPHYLAXIS
MEDICAL
TREATMENT
Effective treatment would require both the destruction
or inactivation of the virus in the body
and the restimulation of the
immunesystem.
Ø
ANTIVIRAL AGENTS
HIV contains enzyme
,’reverse transcriptase, which is necessary for
viral replication.
COMMON MEDICATIONS
Drug
|
Actions
|
Interventions
|
NUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITORS (NRTis)
|
||
Zidovudine (AZT, ZOV) Retrovir
|
Nucleoside analog, Prevents the initial step in
which HIV turns its RNA into DNA and integrates itself into human genes. Drugs acts as decoy
preventing the replication of HIV
|
Monitor for bone marrow suppression anemia or
neutropenia
Monitor for GI intolerance, headache, insomia,
asthemia.
Monitor for
drug effectiveness
Teach patients/significant other regarding drug
dose schedule,a nd possible adverse effects.
|
Didanosine (ddl) Videx
|
Nucleoside analog. Prevents the replications of
HIV
|
Monitor for
drug associated pancreatitis,
peripheral neuropathy nausea, diarrhea.
Monitor CD4 cell counts for drug effectiveness Teach patient significant other regarding drug dose schedule and possible adverse effects.
|
Zalcitabine (ddc) Hivid
|
Nucleoside analog. Prevents replication of HIV
|
Monitor for
peripheral neuropathy, stomatitis.
Monitor for
drug effectiveness.
Teach patient/significant other regarding drug
dose schedule, and possible adverse effects.
|
Stavudine (d4T) Zerit
|
Nucleoside analog. Prevents replication of HIV.
|
Monitor for
peripheral neuropathy
Monitor for
drug effectives.
Teach patient/significant other regarding drug dose schedule and
possible adverse effects.
|
Lamivudine (3TC) Epivir
|
Nucleoside
analog. Prevents replication of HIV
|
Minimal toxicity noted.
Monitor for
drug effectiveness.
Teach patient
significant other regarding drug dose schedule and possible adverse effects.
|
NONNUCLEOSIDE REVERSE
TRANSCRIPTASE INHIBITORS (NNRTIs)
|
||
Nevirapine
Viramune
|
Blocks HIV replication by protecting non HIV infected cells
|
Monitor for rash.
Monitor
drug effectiveness.
Drug interactions rifampin, rifabutin, oral
contraceptives protease inhibitors .
|
Delavirudine Rescriptor
|
Blocks HIV
replications
|
Monitor for rash
Do not administer within 1 hour of antacids.
Drug interactions : terfenadine, astemizole alprazolam midazolam, cisapride, rifabutin,
rifampin.
Drugs that decrease drug effectiveness phenytoin,
carbamazepine Phenobarbital.
Increases drug levels of calrithromycin, dapsone.
Rifabutin ergot alkaloids,
dihydropyrides quinidine, warfarin, indinaviro,
saquinavir.
|
Drug
|
Actions
|
Interventions
|
|
PROTEASE INHIBITORS
|
|||
Indinavir
Crixivan
|
Protease inhibitors interfere with the step of HIV replication in which the
virus makes the long protein chains necessary to reproduce itself from DNA. The long protein chains
must be cut by a protease enzyme in order to turn the proteins into the
correct length to create HIV. Protease inhibitors interfere with this step of the
process, rendering the virus non infections. The defective viruses are not
able to infect or destroy immune cells.
|
Monitor CD4
cells and viral load for drugs
effectiveness.
Teach patient/significant other about drug dose,
schedule, and potential side effects.
Monitor for
nephrolithiasis, GI intolerance headache, asthenia, blurred vision,
dizziness, rash, metallic taste,
thrombocytopenia.
Drug
interactions rifampin
terfenadine, astemizole cisapride triazolam, ergot
alkaloids ketoconazole
rifabutin, midazolam.
|
|
Ritonavir Norvir
|
Protease inhibitor
|
Monitor CD4
cells and viral load for drug
effectiveness
Teach patient/significant other about drug dose, schedule, and potential side effects.
Monitor for GI intolerance nausea, vomiting diarrhea.
Must be
kept refrigerated
Drug interactions, meperidine piroxicam, flecainde quinidine
rifampin, bepridil, terfenadine
cisapride bupropion, clozapine,
diazepam, alprazolam, dihydroergotamine,
ergotamine.
|
|
Saquinavir
Invirase
|
Protease inhibitor
|
Monitor CD4 cells and viral load for drug
effectiveness
Teach patient significant other about drug dose, schedule and potential side effects.
Monitor for
GI intolerance nausea, diarrhea, headache,
elevated transaminase enzymes.
Drug
interactions rifampin , rifabutin
astemizole, terfenadine, cisapride.
|
|
Nelfinavir
Viracept
|
Protease inhibitor
|
Monitor for
diarrhea.
Monitor CD4 celsl and viral load for drug
effectiveness.
Teach patient significant other about drug dose,
schedule and potential side effects.
Drug interactions rifampin, astemiozole
terfenadine, cisapride, midazolam, triazolam.
|
|
Risks and Benefits of Early
Antiretroviral Therapy for the Asymptomatic
HIV infected Person
POTENTIAL
BENEFITS
• Potential
reduction of viral load
• Control
of viral replication and mutation
• Prevention
of progressive immunodeficiency
• Delayed progression
from HIV infection to AIDS
• Decreased risk of resistance
• Decreased
risk of drug toxicity
POTENTIAL RISKS
• Reduction
in quality of life from side effects of
drug therapy
• Earlier
development of drug resistance
• Limited
choice of antiretroviral agents for future use
• Risk
of dissemination of drug resistant virus
• Unknown
long term toxicity
• Unknown
duration of drug effectiveness.
IMMUNOSUPPRESANT
THERAPY
HIV infects some but
certainly not all T4-nhelper cells.When these cells are stimulated,infected T4 helper cells may provoke an autoimmune
disease.Each time T4helper cells are stimulated,there is a further autoimmune
destruction of both infected and non- infected T4 cells.Immunosuppressive drugs
,such as cyclosporine A are being investigated
as one means of controlling this possible autoimmune mechanism.
IMMUNE
STIMULATION OR RECONSTRUCTION
As the primary defect in
patients with HIV related illness is a depressed immne system,investigators
have explored the role of immunostimulants such as interleukin2 and
interferone.As they stimulate T4 helper cells ,viral replication and disease
progression is accelerated.
A
VACCINE AGAINST HIV INFECTION
Researchers in the USA
have recently been successful in
inserting one of the genes from HIV into
the Vaccinia virus .When the altered vaccinia virus is injected into mice and
rhesus monkeys , they produce antibodies
against the outer envelope of HIV
without developing AIDS.Approaches using recombinant DNA anti-
idiotype antibodies and immunostimulating complexes are also being explored.The chief difficulty
in producing a vaccine against HIV is
that this retrovirus shows
marked”antigenic drift.
Postexposure
Prophylaxis
For
Health Care Providers
If you sustain a needle stick injury take the following actions immediately
- Wash the
area with soap and water.
- Alert your
supervisor and initiate the injury
reporting system used in the
setting.
- Identify
the source patient, who may need to be rested for HIV, hepatitis, B an Hepatitis C. (state laws will determine if written informed consent must be obtained from
the source patient prior to his or her testing.
- Report to
the employee health services the emergency department or other designated treatment facility
- Give
consent for baseline testing for
HIV, hepatitis B and Hepatitis C.
- Get post
exposure prophylaxis for HIV in accordance with CDC
guidelines. Start the prophylaxis medications within 2 hours after
exposure . Make sure that you are being monitored for symptoms of toxicity. Practice safer sex until
follow up testing is complete.
- Follow
up with post exposure testing at 6 weeks, 3 months and 6 months and perhaps 1 year.
- Document the exposure in detail for your own records as well as for the employer.
STANDARD
SAFETY PRECAUTIONS
The following
guidelines were developed to prevent the transmission of infection during patient care for all
patients, regardless of known or unknown infectious status.
Hand
Washing/Hand Hygiene
- Wash
hands/perform hand hygiene after touching blood body fluids, secretions, excretions, and contaminated items whether or not gloves are worn
- Wash hands perform hand hygiene immediately gloves are removed, between patient
contacts and when other wise indicated to avoid transfer of microorganisms to other
patient or environments.
- Wash
hand/perform hand hygiene between
tasks and procedures on the same patient to prevent cross contamination of
different body sites.
- Use a plain
(non antimicrobial) soap or
alcohol base hand rub for
routine hand washing.
- Use an antimicrobial agent or waterless antiseptic agent for
specific circumstances (control of outbreaks or hyperendemic infections)
Gloves
- Wear
clean, nonsterile gloves when touching blood, body fluids secretions, excretions, and contaminated items.
- Put on
clean gloves just before touching
mucous membranes and nonintact skin
- Change
gloves between tasks and procedures
on the same patient after contact
with materials that may
contain a high concentration of microorganisms.
- Remove gloves promptly after use, before touching noncontraminated items and environmental
surfaces, and before going to
another patient.
- Wash hands/perform hand hygiene immediately after removing gloves.
Mask, Eye
Protection, Face Shield
- Wear a mask
and eye protection or a face
shield to protect mucous
membranes of the eyes, and mouth during procedures and patient care activities
that are likely to generate splashers
or sprays of blood, body fluids secretions, or excretions.
Gown
- Wear a clear nonsterile, gown to protect skin and prevent soiling
of clothing during procedures and patient care activities that are likely
to generate splashers or sprays of
blood body fluids secretions or
secretions .
- Select a
gown that is appropriate for the activity and amount of fluid likely to be encountered
- Remove a soiled
as promptly as possible and
wash hands/perform hand hygiene to
prevent he transfer of microorganisms to other patients or environments.
Patient
Care Equipment
- Handle used
patient care equipment soiled with blood, body fluids, secretions and excretions in a manner that prevents
skin and mucous membrane exposures, contamination of clothing and transfer of microorganisms to other patients and environments.
- Ensure that
reusable equipment is not used for the care of another
patient until has been cleaned and
reprocessed appropriately.
- Ensure that
single use items are discarded properly.
Environmental
Control
- Ensure that the hospital has adequate procedures for the routine care, cleaning and disinfection of environmental
surfaces, beds, bed rails,
bedside equipment and other
frequently touched surfaces.
- Ensure
that procedures are being
followed.
Linen
- Handle transport, and process used linen
soiled with blood body fluids, secretions, and excretions in a manner that prevents skin and mucous membrane
exposure and
contamination of clothing and that
avoids transfer of
microorganisms to other patients
and environments.
Occupational Health and Bloodborne Pathogens
- Take care
to prevent injuries when using
needles scalpels and other sharp instruments or devices.
- When
handling sharp instruments after procedures
- When
cleaning used instruments
- When
disposing of used needles.
- Never recap
used needles or otherwise manipulate them by using both hands or use any technique that involves directing the point of the needle toward any part of the body.
- Use either
a one handed scoop technique or a mechanical device designed for holding the needle sheath.
- Do not remove used needles from disposable syringes by hand and do not bend break otherwise manipulate used needles by hand.
- Place used
disposable syringes and needles, scalpel blades, and other sharp items in a
appropriate puncture resistant
containers as close as practical to the
area in which the items were used.
- Place reusable
syringes and needles in a puncture resistant container for
transport to the reprocessing area.
- Use mouthpieces
resuscitation bags, or other
ventilation devices as an
alternative to mouth to mouth to resuscitation methods in areas where needs for
resuscitation is predictable.
Patient Placement
- Place a
patient who contaminates the environment or who does not or cannot be expected
to assist in
maintaining appropriate hygiene or environmental control in a private room.
- If a
private room is not available consult with infection control
professionals regarding patient placement or other alternatives.
HIV COUNSELING
Counselling in HIV and AIDS has
become a core element in a holistic model of health care, in which
psychological issues are recognised as integral to patient management.
HIV and AIDS counselling has two general aims:
(1) the prevention of HIV transmission and
(2) the
support of those affected directly and indirectly by HIV.
It is vital that HIV counselling
should have these dual aims because the spread of HIV can be prevented by
changes in behaviour. One to one prevention counselling has a particular
contribution in that it enables frank discussion of sensitive aspects of a
patient's life—such discussion may be hampered in other settings by the
patient's concern for confidentiality or anxiety about a judgmental response. Also,
when patients know that they have HIV infection or disease, they may suffer
great psychosocial and psychological stresses through a fear of rejection,
social stigma, disease progression, and the uncertainties associated with
future management of HIV. Good clinical management requires that such issues be
managed with consistency and professionalism, and counselling can both minimise
morbidity and reduce its occurrence. All counsellors in this field should have
formal counselling training and receive regular clinical supervision as part of
adherence to good standards of clinical practice.
Factors
that affect Voluntary Counselling and HIV Testing among antenatal pregnant
women
Factors that affect voluntary
counselling and HIV testing among antenatal pregnant women revolve primarily
around stigma and discrimination. Stigma and discrimination fuel the HIV &
AIDS epidemic, with the adverse effects extending beyond the infected
individuals into the broad society. Stigma is predominantly fuelled by domestic
and societal pressures, as well as some cultural and religious ethos. Another
factor is the emotionally-laden disclosure of status, especially as it affects
children. Relevant factors that determine whether or not an individual will
disclose his or her status include:
- Adverse reaction from relatives and the fear of hurting
the parents: relatives of the subject including the parents might not take
the news easily, especially as the condition is regarded as a terminal
situation. For adults, it will be taken that the affected is/was
promiscuous.
- Apprehension of an employer’s reaction: the subject
might be worried about the way the employer will take the news, including
the possibility of severance. This is predominant in organisations that
subject their employees to HIV & AIDS tests.
- Loss of acquaintances: friends and associates of the
affected might reduce interaction with the infect individual.
- Feeling of guilt, especially for members of same
cultural community: this situation arises when such cultural affiliations
attach much value to subjects revolving around sexual ethics, etc.
- The likelihood of having the integrity of one’s sexual
relationship questioned or of losing a relationship: when one sexual
partner tests positive, this might lead to questioning the sexual fidelity
of the infected.
- The probability of being subjected to prejudice and
stigma: this is very common especially in developing countries /
societies. This is fuelled by ignorance about HIV & AIDS issues.
- The prospect of being labelled an unfit parent: this is
also predominantly propelled by ignorance. There is the tendency to label
the affected as being ‘sick’ with HIV.
- Vulnerability to violence, and in this context a woman
intending to disclose to her partner. The difficulty here is that the
woman needs to be supported and shielded from physical and emotional
abuses as well as to prevent being re-infected or infecting her partner if
sero-discordant. These are ultimately the responsibility of the partner to
provide for, including economic support.
All of these factors highlight the
necessity of social support in advocating for and implementing voluntary
testing and counselling of antenatal pregnant women and preventing
mother-to-child transmission of HIV.
BREAST
FEEDING
HIV transmission from mothers to infants occurs during
pregnancy, at the time of labor and delivery, and postnatal through
breastfeeding. In the absence of any interventions to prevent or reduce
transmission, about 5-10 percent of HIV infected mothers pass the virus to
their infants during pregnancy; between 10-20 percent during labor and
delivery; and another 10-20 percent
postnatally through breastfeeding to 24 months.
Labor and delivery is the single time point of
greatest risk with as much infection occurring within 24 hours as occurs
postnatally within 24 months of breastfeeding. Most ARV prophylaxis regimens aim to reduce
HIV transmission during this time.
BREAST FEEDING ISSUES
§ Warmth for newborn
§ Nutrition for newborn
§ Protection against other infections
§ Safety – unclean water, diarrheal diseases
§ Risk of HIV transmission
§ Contraception for mother
§ Cost
Risk factors for postnatal transmission
§ Prolonged breastfeeding
§ Mixed breastfeeding
§ High plasma viral load, low CD4
§ Seroconversion during lactation
§ Mastitis
§ Cracked bleeding nipples,
abscesses
§ Sub-clinical mastitis (raised Na/K ratio)
§ High viral load in breast milk
§ Oral thrush in infant
How does HIV transmission during breastfeeding
occur?
•
Exact mechanisms unknown
•
HIV virus in blood passes to breast milk
– cell-associated,
cell-free virus observed
– Virus
shed intermittently (undetectable ~ 25-35%)
– levels
vary between breasts in samples taken at same time
– Virus
may also come directly from infected cells in mammary gland
– produced
locally in mammary macrophages, lymphocytes, epithelial cells
Making
breastfeeding safer in terms of HIV transmission with the current knowledge we
have
§ Exclusive breastfeeding up to 6 mths
§ Shorter duration – 6 months??
§ Encourage condom use during
lactation period
§ Good lactation management (attachment, positioning)
to avoid mastitiS
§ No feeding from breast with
cracked bleeding nipples or abscesses
(express milk from affected side and continue feeding from unaffected
side)
§ Prompt treatment of oral thrush
§ Heat treatment of expressed breast milk
§ Anti-retrovirals to infant
during breastfeeding period
2010
WHO Infant Feeding Guidelines
Mother takes ARVs from
14th week of pregnancy until 1 week after labor or for an indefinite amount of
time if the mother is taking ARVs for their own health.
Ø Long
ARV regimen during breastfeeding period for either mother and/or infant
Ø Exclusive
breastfeeding for 6 months
Ø Gradually
wean from breast milk
Ø Mixed
(complementary) feed after 6 months
Ø Recommended
to breastfeed and mix feed in conjunction with ARVs
LEGAL AND ETHICAL ISSUES
1. Planned
Pregnancy
A woman
who knows that she or her partner is HIV positive before she becomes pregnant
should consider effective contraception. This may help to protect her, her
partner and her baby. Being pregnant may cause her CD4 count to drop slightly,
but it should return to its pre-pregnancy level soon after her baby is born.
2. Protection
at conception
An HIV
positive woman with an HIV negative partner can become pregnant without
endangering her partner; by using artificial insemination (the process by which
sperm is placed into a female's genital tract using artificial means rather
than by natural sexual intercourse). This simple technique provides total
protection for the man, but does nothing to reduce the risk of HIV transmission
to the baby.
If the man
has HIV then the only effective way to prevent transmission is sperm washing.
This involves separating sperm cells from seminal fluid, and then testing these
for HIV before artificial insemination or in vitro fertilisation.
When both
partners are HIV positive, it might still be sensible for them not to engage in
frequent unprotected sex, because there might be a small risk of one
re-infecting the other with a different strain of HIV
3. Benefit of being tested during pregnancy
By knowing the HIV status, one can
decide on the best treatment for her and the baby and can take steps to prevent
mother-to-child transmission of
HIV.
4. Benefit of baby being tested for HIV
Health care
providers recommend that all babies born to HIV positive mothers be tested for
HIV. Some states require that babies receive a mandatory HIV test if the status
of the mother is unknown. Some states are only required to offer an HIV test to
pregnant women (not their babies), which they can either accept or refuse.
5. HIV positive mother taking anti-HIV
medications
If the woman is
HIV positive and pregnant, it is recommended that she take anti-HIV medications
to prevent her baby from becoming infected with HIV and for own health. These medications
are recommended for all infected pregnant women regardless of CD4 count and viral load.
6. The best HIV treatment regimen
It depends on
many factors include: risk that the HIV infection may become worse, risks and
benefits of delaying treatment, potential drug toxicities and interactions with
other drugs she is taking.
7. Treatment Regimen During Pregnancy For
The First Time Diagnosed Mother
The best
treatment options depend on when mother is diagnosed with HIV, when she found
out were pregnant, and whether she need treatment for own health. Women who are
in the first trimester of pregnancy and who do not have symptoms of HIV disease
may consider delaying treatment until after 10 to 12 weeks into their
pregnancies. After the first trimester, pregnant women with HIV should receive
at least AZT (Retrovir or zidovudine); The doctor may recommend additional
medications depending on your CD4 count, viral load, and drug resistance
testing.
8.
Drug effect on the baby
The long-term
effects of babies’ exposure to anti- HIV medications in utero are
unknown. In general, protease inhibitors (PIs) are associated with
increased levels of blood sugar (hyperglycemia), development of diabetes
mellitus or worsening of diabetes mellitus symptoms and diabetic
ketoacidosis. Two non-nucleoside reverse transcriptase inhibitors
(NNRTIs), Rescriptor (delavirdine) and Sustiva (efavirenz), are not
recommended for the treatment of HIV-infected pregnant women. Use of these
medications during pregnancy may lead to birth defects. Another NNRTI, Viramune
(nevirapine), may be part of your HIV treatment regimen.
Will the mother need treatment during
labour and delivery?
Most
mother-to-child transmission of HIV occurs around the time of labour and
delivery. Therefore, HIV treatment during this time is very important for protecting
baby from HIV infection. Several treatments can be used together to reduce the
risk of transmission to the baby.
1. Highly active antiretroviral
therapy (HAART) is recommended even for HIV-infected pregnant women who do
not need treatment for their own health. HAART should include Intravenous AZT
(Retrovir or zidovudine).
3. The baby should take AZT (in liquid
form) every 6 hours for 6 weeks after birth.
9. Delivery options for a HIV positive
mother
Depending on the
health and treatment status, plan either a caesarean or a vaginal delivery.
Cesarean delivery is recommended for an HIV positive mother when, her viral
load is unknown or is greater than 1,000 copies/mL at 36 weeks of pregnancy,
she has not taken any anti-HIV medications or has only taken AZT (Retrovir or
zidovudine) during her pregnancy. For preventing transmission, the caesarean
should be scheduled at 38 weeks or should be done before the rupture of membranes. Vaginal
delivery is recommended for an HIV positive mother when, she has been receiving
prenatal care throughout her pregnancy, she has a viral load less than 1,000
copies/mL at 36 weeks, and Vaginal delivery may also be recommended if a mother
has ruptured membranes and labor is progressing rapidly.
10. Preliminaries of labour and delivery
Intravenous
AZT
should be started 3 hours before a scheduled caesarean/vaginal delivery and
should be continued until delivery. It is also important to minimize the baby's
exposure to the mother's blood. This can be done by avoiding any invasive
monitoring and forceps- or vacuum-assisted delivery.
11. Testing baby for HIV infection
Babies born to HIV positive mothers are
tested for HIV differently than adults. Adults are tested by looking for
antibodies to HIV in their blood. A baby keeps antibodies from its mother,
including antibodies to HIV, for many months after birth. Therefore, an
antibody test given before the baby is 18 months old may be positive even if
the baby does not have HIV infection. For the first 18 months, babies are
tested for HIV directly, and not by looking for antibodies to HIV. When babies
are more than 18 months old, they no longer have their mother's antibodies and
can be tested for HIV using the antibody test. Preliminary HIV tests for babies
are usually performed at three time points, they are; birth to 14 days, at 1 to
2 months of age, and at 3 to 6 months of age. If babies test negative on two of these
preliminary tests and negative for HIV antibodies at 12 – 18 months are not HIV
infected. Babies are considered HIV positive if they test positive on
two of these preliminary HIV tests and are need to be retested at 15 to 18
months. A positive HIV antibody test given after 18 months of age confirms HIV
infection in children.
Babies born to
HIV positive mothers should have a complete
blood count (CBC) for signs of anemia,
which is the main negative side effect caused by the 6-week AZT (Retrovir, or
zidovudine) regimen. They may also undergo other routine blood tests and
vaccinations for babies.
12. HIV Policies of Different State
The U.S.
Department of Health and Human Services (HHS) can provide with HIV testing
information for each state.
PSYCHOSOCIAL
ISSUES
1.
Mental Health
There are high
rates of mental health problems, ranging from distress to suicidal ideation, among
women living with HIV/AIDS.
2. Violence
& Abuse
66% of HIV-positive women found
that had experienced some form of domestic violence in their lifetime and 31%
had been sexually abused as children. Interventions to help women with HIV is
reduce the abuse and violence in their lives to improving their mental health,
increasing their access to antiretrovirals and building their ability to
negotiate safer sex practices, including condom use.
3. Substance
Use
There is a need for substance
abuse treatment programs that specifically target HIVpositive women
4. Family
& Children
Family can be a strong source of
psychosocial support for women living with HIV.
5. Sexuality/Prevention
for Positives
Relationships with sexual
partners are another key psychosocial issue for HIV-positive women. As with
family, disclosure is a major issue in sexual relationships. The need to create
culturally appropriate, on-going
risk reduction counselling programs for HIV-positive women and their partners
that take into account the impact of HAART, sterilization, housing instability,
drug use and poverty on condom use.
REHABILITATION
OF HIV INFECTED WOMEN
The
aims are;
Strengthening
women’s economic security and rights and empowering women to enjoy secure
livelihoods.
Engendering
governance and peace building to increase women’s leadership in the decision-making
processes that shape their lives.
Promoting
women’s human rights and eliminating all forms of violence against women to
transform development into a more equitable and sustainable process.
1.
HIV/AIDS
Prevention: Making sure
young people know how to avoid infection and have access to services like ensure
that condoms are readily available and are used consistently and correctly
2. helping pregnant women protect against
infection
3. Young People: To
ensure that adolescents and young people have accurate information as well as
non-judgmental counselling, and comprehensive and affordable services to
prevent unwanted pregnancy and STIs including HIV/AIDS.
4.
Safe
Motherhood: To help reduce
the 500,000 preventable maternal deaths in developing countries. To promote
wider access to skilled delivery assistance and emergency obstetric care.
5.
Reproductive
Health Supplies: To provide logistic
support and commodities to help countries improve access to high quality and
affordable means of contraception and STI
prevention, including condoms.
6.
Response
to Emergencies: Have lifesaving
services such as assisted delivery, and prenatal and post-partum care; and it
works to reduce their vulnerability to HIV infection, sexual exploitation and
violence.
7.
Women’s
Empowerment: Take action to
promote women’s rights and prevent
gender-based
violence including
female genital cutting.
8.
Population
and Development: To support for
data collection and analysis, and for policy formulation, to help countries
meet the needs of growing populations.
9.
Advocacy: Regarding reproductive
health and rights; lower infant and maternal mortality; closing the gender gap
in education; gender equality and equity; women’s empowerment; and increasing
resources for population and development initiatives.
ROLE OF NURSE
Caring for a women who is positive during
pregnancy and childbirth calls for a
great sensitivity to respect the women as a patient with a baffling yet fatal
disease but to encourage her to continue with prenatal care.Nurses need to
remain current on recommendations for therapy as well as prevention.The role of
nurse is explained under various headings.
Role of nurse in HIV Care &
Treatment
The
specific role of nurses in HIV care and
treatment can vary by country, region or facility
In
general, nurses should:
Ø Understand
when to refer women for ARV therapy and start co-trimoxazole prophylaxis
Ø Recognize:
Ø Common
infections in HIV-infected persons
Ø Common
side effects of ARV therapy & advise patients accordingly
Ø Understand
importance of ARV adherence and provide adherence support
Ø Establish
effective communication and linkages between MCH services and centres for HIV
treatment, care and support
Ø Participate
in ongoing problem-solving as a part of a comprehensive care delivery team
Ø Prevention
of Common Infections in HIV-infected mothers
– Wash daily
– Eat nutritious foods
– Take supplemental multivitamins and
essential minerals
– Keep mouth clean
– Re-hydrate promptly in case of
diarrhoea
– Use safe drinking water
– Obtain adequate rest
– Use condoms to prevent STIs
– Apply a long-acting insecticide to
inside walls, roof of home and domestic animal shelters
– Use insecticide-treated bed nets
– Consider immunization against
hepatitis A, B and flu
– Take medications that prevent common
infections (e.g., co-trimoxazole, INH)
HIV-infected
pregnant women should be evaluated for TB and offered preventive therapy with
INH
All
HIV-infected pregnant women (except those on co-trimoxazole prophylaxis) should
receive at least 3 doses of sulfadoxine-pyrimethamine (SP) as intermittent
preventive treatment (IPT) against malaria during the last 6 months of
pregnancy
§ 1st
dose of SP should be given during 2nd trimester after quickening
§ SP
should be given during routine ANC visits, under HCW observation
§ Educate
all women about malaria prevention
Education of mothers
Review
ARV drug regimen; ensure patient knows ARVs are not a cure
Assist
in planning dosage schedule
Remind
about food/beverage restrictions
Remind
about ARV drugs only work if taken every day at the correct time.
Encourage
patients to disclose HIV status to at least one friend or family member who can
remind her to take the medication
Prevention
of Viral Resistance
Promotion
of all safety precautions to the mother ,family and among health professionals
Social & Psychosocial Support
§ HIV-infected
women may need assistance adjusting to diagnosis, managing illness and/ or
addressing concerns of stigma and discrimination
§ nurses
should be familiar with community-based services available and make referrals
as appropriate to help families access necessary service:
§ Peer
group counselling & clubs
§ Referrals
to other services
§ Provides
mothers who are HIV-infected with spiritual and psychosocial support
§ May
also provide an important sense of belonging to a larger community that offers
them compassionate care
§ nurses
should refer patients in need of ongoing home-based care to local programmes
where available
Palliative Care
o Maximize
comfort
o Help for peaceful death
o Help
the family to cope with grief and bereavement
Post-delivery Care of the Mother
with HIV Infection
o nurses should ensure that all mothers — regardless of place of delivery —
attend postpartum care with their infants or are visited at home
o Mothers
and their HIV-exposed infants should be evaluated at approximately 1 week after
birth and again at 6 weeks
o Subsequent
visits for HIV-exposed infants should be scheduled according to a country’s
immunization schedule
o Screening,
prevention & treatment of common infections, including Opprtunistic
Infections
Infant
feeding: information, counselling and support
o Nutritional
counselling
o Psychosocial
support
o Safer
sex and family planning counselling
o Physical
assessment, clinical staging and referral for ARV therapy according to national
guidelines
o Adherence
counselling for self and infant
o Palliative
care, where indicated
o Co-trimoxazole
prophylaxis
Comprehensive Treatment, Care &
Support: HIV-exposed Infant
§ Prevention
and treatment of common infections, including OIs
§ Diagnosis
of HIV by laboratory measurements and/or clinical symptoms
§ Immunizations
§ Growth,
nutritional status and development monitoring
§ Assessment
and referral for ARV therapy
§ Co-trimoxazole
prophylaxis and adherence support
Comprehensive Treatment, Care &
Support: Family
Links
and relationships with community service organizations and agencies to promote
continuity of care
Follow-up Care for HIV-exposed Infants
·
PMTCT
interventions reduce, but do not eliminate, risk of MTCT
·
HIV
increases risk of illness and failure to thrive
·
Regardless
of whether ARV prophylaxis was administered to mother and/or infant — because
HIV disease can progress extremely rapidly in perinatally-infected infants —
close monitoring and regular follow-up care is critical
·
Follow-up care facilitates early diagnosis and
allows infant to be started on ARV therapy
·
Infant should be seen in the clinic or at home
within two weeks to monitor feeding progress
·
Schedule
subsequent visits according to the immunization schedule. Recommended visit
schedule:
o Ages 6, 10 and
14 weeks
o Once a month
from 14 weeks to 1 year
o
Every 3 months from the ages of 1 to 2 years
PREVENTION OF HIV
– PPTCT-
Education
– Prevent
medical transmission – use of sterile medical equipment and screened blood
products
– Education
to avoid risk behaviours
– Folllow
safety precautions
CONCLUSION
Creating an enabling environment for the better
living of the HIV victims - is a key role of the nurse. Stigmatization can be
broken down through education and discussion.We have to Educate family members,
teachers,peers and other community members on the needs of persons affected by HIV/AIDS.Mass media, health
professionals,NGOs play a major role in creating awareness to people.Though we
are not able to cure the disease we are able to provide quality care to the
persons thus to extend a better living.
BIBLIOGRAPHY
·
Pilliteri A. Maternal and
child health nursing. Philadelphia: Lippincott
Williams and Wilkins; 1999
·
Fraser DM, Cooper MA. Myles
textbook for midwives. 14th edition. London: Churchill Livingstone; 2003
·
Dutta DC. Textbook of
obstetrics. 6th edition. Kolkata: New Central Book Agency; 2004
·
Jacob Annamma . A
Comprehensive Textbook of Midwifery . 2nd edition . New Delhi : Jaypee
·
Brothers Medical Publishers
Pvt Ltd ;2008
·
Lewis, et.al, Medical Surgical Nursing Assessment and
Management of clinical problems. 7th edition. New Delhi: Published by Elsevier ; 2000 page
no: 840-870
·
Daniels Rick. Nosek Laura. contemporary medical surgical
nursing. I edition, Thomson publishers 2007.
·
Joyce M. Black. Jane Hokanson Hewks Medical Surgical
Nursing.volume 2 7th edition
New Delhi: Elsevier publishers ;2005
·
Smeltzer, Brenda G. Bave Brunner and Sudharths text book of
Medical surgical nursing.10th edition. Philadelphia: Lippincott Williams and
Wilkins publishers ;2004.
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