|
The purpose of this
course is to update healthcare professionals on current trends and
treatments of human immunodeficiency virus (HIV) and acquired immune
deficiency syndrome (AIDS).
This course is designed so that the
healthcare professional will be able
to:
|
1. |
describe HIV/AIDS, |
| |
|
|
2. |
discuss how HIV affects the
immune system, |
| |
|
|
3. |
identify ways HIV is
transmitted, |
| |
|
|
4. |
identify methods to prevent
transmission of HIV, and |
| |
|
|
5. |
discuss the most up to date
treatment of HIV/AIDS. |
HIV kills and damages cells of the
body's immune system by destroying
the body's ability to fight
infections and certain cancers. You
cannot get AIDS without first having
HIV. AIDS is the end stage of HIV
infection.
Prevalence is the number of people
living with HIV/AIDS in a given
year.
AIDS is the most catastrophic
disease in modern history. It has
become the world's deadliest
infectious disease and is
threatening to eliminate up to a
sixth of the world's population. An
estimated 33.2 million people
worldwide are infected with HIV and
2.1 million died of AIDS in 2007, of
which 1.7 Million were Adults, and
330,000 were children less than 15
years old (UNAIDS, 2007). UNAIDS and
the World Health Organization (WHO)
estimate there are 30.8 million
adults living with HIV, 15.4 million
Women, and 2.5 million children less
than 15 years of age.
Since the 1990s two significant
changes have occurred in the course
of HIV/AIDs: antiretroviral
medications were developed and
deaths from the disease decreased (Trynka,
& Erlen, 2004). The annual number of
deaths from AIDS peaked between 1991
and 1996. Deaths declined 14%
between 1998 and 2002 (Trynka, &
Erlen, 2004). This trend is directly
attributed to the widespread use of
antiretroviral medication (Trynka, &
Erlen, 2004).
HIV
Incidence Estimate
Incidence is the number of new HIV
infections that occur during a given
year.
The Center for Disease Control (CDC)
estimated that approximately 56,300
people were newly infected with HIV
in 2006. 53% of these new infections
occurred in gay and bisexual men.
African American men and women were
also strongly affected and were
estimated to have an incidence rate
than was 7 times greater than among
whites, (Hall HI, Ruiguang S, Rhodes
P, et al., 2008).
|
Data for 34 states: |
Year of diagnosis of HIV: |
|
Age
at diagnosis(yr) |
2004 |
2005 |
2006 |
2007 |
|
<13 |
212 |
189 |
169 |
159 |
|
13-14 |
41 |
40 |
45 |
40 |
|
15-19 |
1,081 |
1,216 |
1,409 |
1,703 |
|
20-24 |
3,714 |
3,875 |
41,84 |
4,907 |
|
25-29 |
4,524 |
4,547 |
4,884 |
5,771 |
|
30-34 |
5,353 |
5,024 |
4,686 |
5,089 |
|
35-39 |
6,359 |
5,907 |
5,678 |
6,088 |
|
40-44 |
6,011 |
5,889 |
6,003 |
6,554 |
|
45-49 |
4,286 |
4,338 |
4,377 |
5,172 |
|
50-54 |
2,645 |
2,698 |
2,862 |
3,489 |
|
55-59 |
1,473 |
1,531 |
1,512 |
1,938 |
|
60-64 |
771 |
729 |
741 |
942 |
|
>65 |
696 |
657 |
643 |
803 |
|
|
37166 |
36640 |
33009 |
42655 |
|
Race/Ethnicity |
|
|
|
|
|
American Indian/Alaska Native |
177 |
180 |
163 |
228 |
|
Asian |
308 |
329 |
332 |
455 |
|
Black/African American |
19,309 |
18,479 |
18,975 |
21,549 |
|
Hispanic/Latino |
6,183 |
6,383 |
6,590 |
7,484 |
|
Native Hawaiian/Other Pacific Islander |
39 |
43 |
49 |
46 |
|
White |
10,838 |
10,818 |
10,815 |
12,556 |
|
Transmission
category |
|
|
|
|
|
Male-to-male sexual contact |
17,898 |
18,333 |
18,894 |
22,472 |
|
Injection drug use |
3,198 |
2,990 |
2,931 |
3,133 |
|
Male-to-male sexual contact and Injection drug
use |
1,413 |
1,308 |
1,195 |
1,260 |
|
High-risk heterosexual contact |
4,167 |
3,923 |
4,029 |
4,551 |
|
Other |
140 |
120 |
132 |
102 |
|
Female adult or adolescent |
|
|
|
|
|
Injection drug use |
2,065 |
1,834 |
1,729 |
1,805 |
|
High-risk heterosexual contact |
7,967 |
7,852 |
8,033 |
9,076 |
|
Other |
103 |
90 |
80 |
96 |
|
Child (<13 yrs at diagnosis) |
|
|
|
|
|
Perinatal |
177 |
162 |
134 |
139 |
|
Other |
37 |
30 |
36 |
20 |
Table above is the estimated numbers
of cases of HIV/AIDS, by year of
diagnosis and selected
characteristics, 2004-2007-34 states
And 5 U.S., dependent areas with
confidential name-based HIV
infection reporting
Note. These numbers of HIV
infections (CDC, 2008) do not
represent reported case counts.
Rather, these numbers are point
estimates, which result from
adjustments of reported case counts.
The reported case counts have been
adjusted for reporting delays and
missing risk-factor. Specifics on
the above numbers: information, but
not for incomplete reporting.
|
a. |
Includes Asian/Pacific
Islander legacy cases (see
Technical Notes). |
| |
|
|
b. |
Hispanics/Latinos can be of
any race. |
| |
|
|
c. |
Heterosexual contact with a
person known to have, or to
be at high risk for, HIV
infection. |
| |
|
|
d. |
Includes hemophilia, blood
transfusion, perinatal
exposure, and risk factor
not reported or not
identified. |
| |
|
|
e. |
Includes hemophilia, blood
transfusion, and risk factor
not reported or not
identified. |
| |
|
|
f. |
Includes persons of unknown
race or multiple races and
persons of unknown sex.
|
In the most recent CDC data over
6,800 persons become infected with
HIV every day and over 5,700 persons
die daily from AIDS. This is mostly
due to inadequate access to HIV
prevention and treatment services.
The HIV pandemic remains the most
serious of infectious diseases and
is a major challenge world wide.
Currently the 2007 epidemiologic
assessment suggests the following:
|
the global prevalence of HIV
infection or percentage of
persons infected with HIV
remains at the same level
and the global number to
persons living with HIV is
increasing because of
ongoing accumulation of new
infections with longer
survival times, measured
over a continuously growing
general population; |
| |
|
|
specific countries
demonstrate a localized
reduction in prevalence;
|
| |
|
|
with a scaling up of
treatment access there has
been a reduction of
HIV-associated deaths;
|
| |
|
|
globally, there has been a
reduction of new HIV
infections. |
Globally, the survival of those with
HIV without treatment has increased
from 9 to 11 years.
Regional and global trends in 2007
suggest the pandemic has formed two
broad patterns:
|
1. |
epidemics sustained in the
general populations of many
sub-Saharan African
countries, primarily in the
southern area of the
continent, and |
| |
|
|
2. |
epidemics in the rest of the
world primarily are
concentrated among those
populations at risk, such as
men who have sex with men,
sex workers, injecting drug
users, and sexual partners
of these groups. |
In 2007 33.2 million people were
estimated to be living with HIV, 2.5
million people became newly infected
and 2.1 million dies of AIDS.
Sub- Saharan Africa still remains
the most seriously affected area,
with AIDS the leading cause of
death. There were an estimated 1.7
million new HIV infections in
sub-Saharan Africa in 2007, a
significant reduction since 2001.
There is an estimated 22.5 million
living with HIV. 68% of the global
total of those living with HIV are
in sub-Saharan Africa.
In Sub-Saharan Africa, continued
treatment scale-up and HIV
prevention efforts are bringing
results in some countries, but
mortality from AIDS remains high in
Africa due to the extensive unmet
treatment needs. Cote d'Ivoire,
Kenya and Zimbabwe have all seen
downward trends in their national
prevalence. Beyond Sub-Saharan
Africa, declines in new HIV
infections have occurred in South
and South-East Asia, notably in
Cambodia, Myanmar and Thailand.
There is a need to adapt and revive
HIV prevention efforts as some
countries are seeing a reversal of
declining trends. Burundi’s
declining trend from the late 1990’s
did not continue beyond 2005. HIV
prevalence started to increase again
at most surveillance sites. Despite
achievements in reversing the
epidemic in Thailand, HIV prevalence
is rising among men who have sex
with men and has remained high among
injecting drug users over the past
15 years, ranging from 30% to 50%.
UNAIDS and WHO officials point out
that the new estimates do not change
the need for immediate action and
increased funding to scale up
towards universal access to HIV
prevention, treatment, care and
support services is vitally needed.
|
Adult Prevalence (15-49) [%] in 2008
[Source: AIDS
Epidemic Update, UNAIDS, December 2008] |
 |
|
Sub-Saharan Africa |
5.0% |
|
Middle East and North Africa |
0.3% |
|
South and South-East Asia |
0.3% |
|
East Asia |
0.1% |
|
Oceania |
0.4% |
|
Latin America |
0.5% |
|
Caribbean |
1.1% |
|
Eastern Europe and Central Asia |
0.8% |
|
Western and Central Europe |
0.3% |
|
North America |
0.6% |
|
Adults and Children Estimated to be Living with
HIV during 2008
[Source: AIDS
Epidemic Update, UNAIDS, December 2008] |
 |
|
Sub-Saharan Africa |
22.0 million |
|
Middle East and North Africa |
380,000 |
|
South and South-East Asia |
4.2
million |
|
East Asia |
740,000 |
|
Oceania |
74,000 |
|
Latin America |
1.7
million |
|
Caribbean |
230,000 |
|
Eastern Europe and Central Asia |
1.5
million |
|
Western and Central Europe |
730
000 |
|
North America |
1.2
million |
|
Total |
33 million |
|
Estimated Adult and Child Deaths due to AIDS
during 2008
[Source: AIDS
Epidemic Update, UNAIDS, December 2008] |
 |
|
Sub-Saharan Africa |
1.5
million |
|
Middle East and North Africa |
27,000 |
|
South and South-East Asia |
340,000 |
|
East Asia |
40,000 |
|
Oceania |
1,000 |
|
Latin America |
63,000 |
|
Caribbean |
14,000 |
|
Eastern Europe and Central Asia |
58,000 |
|
Western and Central Europe |
8,000 |
|
North America |
23,000 |
|
Total |
2.0 million |
|
Adults and Children Estimated to be Newly
Infected with HIV during 2008
[Source: AIDS
Epidemic Update, UNAIDS, December 2008] |
 |
|
Sub-Saharan Africa |
1.9
million |
|
Middle East and North Africa |
40,000 |
|
South and South-East Asia |
330,000 |
|
East Asia |
52,000 |
|
Oceania |
13,000 |
|
Latin America |
140,000 |
|
Caribbean |
20,000 |
|
Eastern Europe and Central Asia |
110,000 |
|
Western and Central Europe |
27,000 |
|
North America |
54,000 |
|
Total |
2.7 million |
Healthcare Workers
The main cause of infection in
healthcare work settings is exposure
to HIV-infected blood via a
percutaneous injury (i.e. from
needles, instruments, bites which
break the skin, etc. The average
risk for HIV transmission after such
exposure to infected blood is low;
about 3 per 1,000 injuries (CDC,
2007). Certain specific factors may
mean a percutaneous injury carries a
higher risk, for example:
|
A deep injury |
| |
|
|
Late-stage HIV disease in
the source patient |
| |
|
|
Visible blood on the device
that caused the injury |
| |
|
|
Injury with a needle that
had been placed in a source
patient's artery or vein |
If
Percutaneous exposure occurs then
the site of exposure should be
washed liberally with soap and water
but, without scrubbing. Bleeding
should be encouraged by pressing
gently around the site of the
injury. It is important not to press
immediately on the injury site and
to cleanse wound under running
water. Although infection through
needle-stick injury does not often
occur, it can be devastating for the
person.
HIV has been acquired through
contact with non-intact skin or
mucous membranes (i.e. splashes of
infected blood in the eye) in a
small number of situations. Research
suggests that the risk of HIV
infection after mucous membrane
exposure is less than 1 in 1000. If
mucocutaneous exposure occurs then
the affected area should be washed
thoroughly with soap and water. If
the eye is affected, it should be
irrigated thoroughly.
|
If intact skin is exposed to
HIV infected blood then
there is no risk of HIV
transmission. |
The immune system is a network of
cells and organs that work together
to defend the body against infection
by germs such as HIV.
Antibodies attach themselves to the
enemy to slow them down so that the
phagocytes can engulf them. When all
the enemy cells are engulfed and the
battle is won, T suppressor cells
send out the recall signal.
Phagocytes come in to clean up and
eat the dead cells. After the
battle, most of the cells die off.
Some T cells survive and become T
memory cells. These memory cells
remember the battle and are able to
fight again should the same invader
strike. Thus, the body is said to be
immune to that infection. HIV
disguises itself by mutating the
outer cell coating. This mutation
helps the virus evade antibody
detection because the T memory cells
only recognize previously
encountered invaders (Staff, 2004c).
HIV is classified as a retrovirus
that has a long latency period. HIV
invades the body through the
bloodstream and uses the immune
system against itself. As the
macrophages recognize the invader,
they attack just as they would for
any other foreign substance. Some of
the HIV are destroyed when the
helper T cells join the battle;
however, the HIV attach themselves
to the T cells and the T cells
accept the foreign HIV cells as
their own. The outer coverings of
the two cells fuse.
Once inside the T-4 cell, HIV uses a
reverse transcriptase enzyme to
translate its own genetic program
ribonucleic acid (RNA) into the T-4
cells' genetic material
deoxyribonucleic acid (DNA). Instead
of fighting against the infection
the T cell is reprogrammed to either
produce more HIV cells or to remain
dormant.
People infected with HIV eventually
develop symptoms that usually last a
long time and are often severe.
These symptoms include enlarged
lymph glands, fever, tiredness, loss
of appetite and weight loss,
diarrhea, yeast infections of the
mouth and vagina, and night sweats.
As the immune system becomes weaker,
the infected person becomes more
susceptible to illnesses that
normally do not occur in healthy
people. These illnesses are called
Opportunistic infections. The most
common opportunistic infections are
Pneumocystis Carinii Pneumonia
(PCP), yeast infections of the mouth
and esophagus, and Kaposi's sarcoma,
a cancer of certain blood vessels.
HIV Infection Cycle:
|
1. |
Window Period: The time
period after contracting the
infection and until the body
has developed enough
antibodies for an accurate
positive test results. This
can range from two weeks to
six months. The HIV infected
person is infectious during
this time. HIV is confirmed
upon receiving a positive
HIV antibody test and having
another test reconfirm the
results. |
| |
|
|
2. |
Incubation Period: An HIV
infected person may not feel
sick or exhibit symptoms of
the disease for five to ten
years or longer. The disease
can still be spread during
this period. |
| |
|
|
3. |
AIDS: Symptoms appear and
the immune system begins to
break down. When an HIV
infected person's CD4 count
drops to below 200, he is
said to have AIDS. A healthy
person's CD4 count is from
800 to 1200. AIDS also means
that the HIV infected person
has one or more of the many
opportunistic infections. |
| |
|
AIDS Lifecycle (NLM, nd)
Stage 1
HIV virus is passed from one person
to another. The virus travels
through the bloodstream to many
different places in the body.
Stage 2
The immune system, which helps the
body fight off illness, fights back
in three ways:
Stage 3
This defense is coordinated by the
helper T cells. But HIV has an
ingenious battle strategy; it
attacks the T cells themselves,
crippling the body's defenses.
Stage 4
HIV has a special shape on its
surface which, like a piece of a
jigsaw puzzle, fits perfectly into a
shape on the T cell. This shape is a
protein called CD4. HIV uses CD4 to
enter the cells it infects. This is
why the T helper cell is referred to
as a CD4 lymphocyte.
Stage 5
Once inside a T helper cell, HIV
takes over the cell and the virus
then replicates. The virus's genetic
information (RNA) is transcribed
into a form that is identical to the
cell's genetic information (DNA).
The virus, now in the form of DNA,
hides out inside the nucleus of the
cell, escaping from the body's
defenses.
Stage 6
After a while, HIV comes out of
hiding and begins to reproduce.
Stage 7
The proteins are cut into usable
pieces and packaged with the RNA.
Stage 8
The new viruses then bud from the
cell. Each new virus may then go on
to infect and destroy other T cells,
weakening the immune system's
defense.
Stage 9
After a lot of T cells are
destroyed, the person is said to
have AIDS. A person with AIDS will
probably develop one or many
opportunistic infections. A person
with AIDS will usually die of an
opportunistic infection.
Enzyme immunoassay (EIA) is a
screening test for HIV. A blood
sample is drawn, sent to a lab, and
the results are available within
several days to several weeks. A
negative screening test means a
person is not infected with HIV, and
does not require further testing. If
a person has risky behaviors they
could be in the window period and a
repeat test is suggested in six
months. A positive screening test
means the person needs further
testing. A Western Blot, or
immunofluorescence assay (IFA), is
performed to confirm the diagnosis
of HIV.
A rapid test licensed by the Food
and Drug Administration (FDA), known
as the Single Use Diagnostic System
for HIV-1 (SUDS) can give HIV-1 test
results in 5 to 30 minutes. Another
rapid test is Ora Quick Rapid HIV
Test.
In March 2004, the Ora Quick Rapid
HIV Test was approved, by the FDA,
for use on Oral Fluid. A reactive
HIV test result from either of these
tests needs to be confirmed by an
additional, more specific test (CDC,
n.d.a).
The patient having a rapid test can
be advised immediately of their
screening test results, and
counseled on HIV prevention and
transmission. A negative rapid test
result is always negative, unless
the patient has been tested before
the antibodies have formed (window
period).
The blood, semen, vaginal fluid, and
breast milk of people infected with
HIV has enough of the virus in it to
infect other people. It has not been
documented as fact that HIV can be
transmitted through tears and
saliva, but CDC has kept saliva on
the list of body fluids that require
the healthcare professional to
exercise standard precautions. CDC
and the American Dental
Association's Council on Dental
Therapeutics suggest assuming that
saliva containing a lot of blood
could potentially carry HIV and
other harmful pathogens).
An HIV infected person who has no
signs of an infection or illness can
still infect others.
There are four known common ways HIV
is transmitted:
|
1. |
sexual intercourse, |
| |
|
|
2. |
sharing of needles and
syringes, |
| |
|
|
3. |
body fluids (blood, semen,
vaginal fluid, and breast
milk, and |
| |
|
|
4. |
babies born of infected
mothers and drinking breast
mile of infected mothers. |
HIV can enter the body through
certain types of tissues that line
the anus, vagina, or penis. It also
can enter through cuts or tears in
the vagina, rectum, penis, or mouth.
HIV can be spread through
unprotected sexual intercourse from
male-to-male, male-to-female, or
female-to-female. Unprotected sexual
intercourse means sexual intercourse
without correct and consistent use
of a latex condom or any other
physical barrier to HIV. It is
possible to catch HIV through oral
sex if there are open sores in a
person's mouth or bleeding gums.
Insects such as mosquitoes, bugs or
animals do not spread HIV. HIV is
also not spread through casual
contact of any kind such as:
|
1. |
Sharing a telephone |
| |
|
|
2. |
Toilet seats/ doorknobs |
| |
|
|
3. |
Sharing dishes |
| |
|
|
4. |
Holding hands, hugging, etc |
Reducing high risk behaviors through
educational efforts can prevent HIV
infections. To prevent HIV
infections, the Center of Disease
Control (CDC) (n.d.b) offers the
Following suggestions:
|
do not have sex with an HIV
infected person, |
| |
|
|
do not share needles with an
HIV infected person, and |
| |
|
|
avoid any risky behaviors
that might result in contact
with blood, semen, vaginal
secretions, or other body
fluids |
The best way for a healthcare worker
to avoid contracting HIV and
developing AIDS is to follow CDC's
recommendations to treat every
patient as though they are HIV
positive. The Occupational Health
and Safety Administration (OSHA) and
CDC recommend the use of standard
precautions whenever there is a risk
of a person being exposed to
contaminated blood or body fluids.
It is recommended that all
individuals be treated as if they
could be infected. Hand washing is
the single most important factor in
preventing HIV and other diseases.
Keeping hands away from ones face
and not eating or drinking in any
environment that may be contaminated
is recommended.
Barrier precautions should always be
used to prevent exposure to blood
and other body fluids. Vinyl or
latex gloves must be worn before
touching any blood, body fluids,
non-intact skin, mucous membranes,
or excretions. Wearing a clean
waterproof, non-sterile gown will
protect the healthcare worker from
exposure to contaminated body
fluids. Both OSHA and CDC recommend
the use of blood and body fluid
precautions for all invasive
procedures. An invasive procedure is
a procedure requiring surgical entry
into tissues, organs, cavities, or
repair of traumatic injury. These
precautions prevent the transmission
of pathogens from all body
substances. When doing CPR, masks,
ventilation bags, and other
intubation equipment should be used
to prevent exposure to saliva.
The most direct way of spreading HIV
is through a puncture wound from a
contaminated needle or other object
that causes a break in the skin.
Needles should NEVER be recapped,
bent, broken, or removed from
contaminated syringes. Sharps should
be disposed into a puncture-proof
container and then transported to a
reprocessing area. One out of every
four needle stick injuries involves
IV therapy equipment.
Specimens should be placed in
leak-proof bags or containers with
an identifiable Biohazard Warning
label. Used equipment and
instruments need to be
systematically cleansed and
sterilized. The HIV virus can easily
be destroyed on surfaces by exposure
to common cleansing agents and by
all routine methods of
sterilization.
Prompt initiation of antiretroviral
therapy soon after occupational
exposure to HIV was found to
substantially reduce the risk of HIV
seroconversion (Pinkerton, et al.,
2004). Therefore, the US Public
Health Service recommends
Post-exposure prophylaxis (PEP) with
antiretroviral agents for persons
with occupational HIV exposures if
there is a recognized transmission
risk. These medications are only
available with a prescription. PEP
should begin as soon as possible
within 72 hours. Treatment is with 2
or 3 antiretroviral medications for
4 weeks if tolerated. PEP is not
100% effective and does not
guarantee that exposure to HIV will
not become a case of HIV infection
(AIDS InfoNet, 2007).
The US Public Health Service does
not recommend for or against
antiretroviral agents for
non-occupational situations because
of the lack of efficacy data
(Pinkerton, et al., 2004, AIDS
InfoNet, 2007).
Presently there is no cure for HIV.
Vaccines are under development but
are not yet available. Human testing
has begun at the University of
Massachusetts (Staff, 2004c).
Current treatment consists of
medications to slow down the process
of HIV duplication and weakening of
the body's immune system. Highly
Active Anti-Retroviral Therapy (HAART)
is the combination of three or four
antiretroviral agents (CDC, n.d.b).
The following are a list of
medications that may be used in
HAART.
Nucleoside/Nucleotide Reverse
Transcriptase Inhibitors (NRTIs)
|
Zidovudine (AZT, ZDV) (Retrovir®) |
| |
|
|
Didanosine (ddI) (Videx®) |
| |
|
|
Lamivudine (3TC) (Epivir®) |
| |
|
|
Stavudine (d4T) (Zerit®) |
| |
|
|
Tenofovir (Viread™) |
| |
|
|
Zalcitabine (ddC) (HIVID®) |
| |
|
|
Abacavir (Ziagen™) |
| |
|
|
Zidovudine + Lamivudine (Combivir™) |
| |
|
|
Zidovudine + Lamivudine +
Abacavir (Trizivir®) |
Protease Inhibitors (PIs)
|
Saquinavir (Invirase™ &
Fortovase™) |
| |
|
|
Ritonavir (Norvir™) |
| |
|
|
Indinavir (Crixivan®) |
| |
|
|
Nelfinavir (Viracept®) |
| |
|
|
Amprenavir (Agenerase®) |
| |
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Ritonavir/Lopinavir (Kaletra™) |
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Non-Nucleoside Reverse
Transcriptase Inhibitors (NNRTIs) |
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Nevirapine (Viramune®) |
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Delavirdine (Rescriptor®) |
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Efavirenz (Sustiva™) |
The success of this therapy is
dependent not only on the HAART
treatment plan, but also on the
patient's ability to strictly adhere
to the new medication regimen and
tolerate the side effects of these
powerful drugs. Side effects that
may seem minor, such as fever,
nausea, and fatigue, can mean there
are serious problems. More serious
side effects of HAART are (CDC,
n.d.b):
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liver problems, |
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diabetes, |
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fat maldistribution (lipodystrophy
syndrome), |
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high cholesterol, |
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increased bleeding in
patients with hemophilia, |
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decreased bone density, and |
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skin rash. |
It is important for the healthcare
team to be aware of side effects
(CDC, n.d.b).
AIDS is a stigmatized disease in
most societies causing the AIDS
patient to not seek treatment and
not follow the treatment plan. The
patient requires emotional,
physical, and psychological support.
It is not important to know the
details. Censure and condemnation
are not acceptable in providing care
for the individual with this fatal
disease. The caregiver must provide
hope, compassion, and respect to the
AIDS patient as his disease
progresses. In the terminal stages
of this disease, more and more
physical and emotional support is
required.
In the hospital setting, CDC does
not recommend special isolation for
HIV/AIDS patients. It is not
acceptable to identify or flag a
patient with HIV/AIDS in any way
that is different from any other
patient. Patients with HIV/AIDS may
have other conditions that require
isolation, such as tuberculosis,
infectious diarrhea, or other
communicable diseases. Isolation
procedures in these cases should be
applied as they would be done for
any other patient.
Many states, as well as the Federal
Government have enacted statutes and
regulations related to the care of
patients with HIV/AIDS. Addressed
are topics dealing with the
documentation of HIV/AIDS and
related diagnosis, issues of
informed consent, and the
maintenance of patient
confidentiality. The State of
Florida developed legislation
directed towards confidentiality and
testing for HIV and AIDS.
The following is the Florida Senate
Bill Number 1436: Section 381:609,
(3), Human Immunodeficiency Virus
Testing; Informed Consent; Results;
Counseling; Confidentiality.
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(A) No person in this state shall
perform a test designed to identify
the Human Immunodeficiency Virus, or
its antigen or antibody, without
first obtaining the informed consent
of the person upon whom the test is
being performed, except as specified
in paragraph (i). Informed consent
shall be preceded by an explanation
of the right of confidential
treatment of information identifying
the subject of the test and the
results of the test to the extent
provided by law. Consent need not be
in writing providing there is
documentation in the medical record
that the test has been explained and
the consent has been obtained.
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Section 75. Section 455.2224 Florida
statute is created to Read: 455.2224
Hepatitis B or Human
Immunodeficiency Carriers. "The
Department of Professional
Regulation and each appropriate
board within the Division of Medical
Quality Assurance shall have the
authority to establish procedures to
handle, counsel, and provide other
services to healthcare professionals
within their respective boards who
are infected with Hepatitis B or the
Human Immunodeficiency Virus.” |
With the rapid changes taking place
in HIV/AIDS treatment and the
extension of life expectancy among
people with HIV/AIDS, nurses have
the opportunity to enhance quality
of life among those who are
afflicted with this disease (Goldrick,
2000). It is our responsibility as
healthcare providers to be educated
and to keep up to date with research
being done nationally and worldwide.
We must not be afraid to ask
questions while maintaining the
HIPAA rights of all our patients.
Continued education nationally and
worldwide is imperative.
Easy access to prevention and
treatment sites without the fear of
condemnation will enhance our
ability as a society, to keep us all
safe from this deadly disease.
AIDS Info Net fact sheet 2007:
Number 156 Retrieved March 3, 2009
from
www.aids.infonet.org
AIDS/Meds.com. Trizivir. Retrieved
February 27, 2009 from
http://www.aidsmed.com/drugs
AIDS/Meds.com. Combivir. Retrieved
February 27, 2009 from
http://www.aidsmed.com/drugs.
Combivir.htm.
Centers for Disease Control (CDC).
(2003a). Basic Statistics. Retrieved
February 26, 2009 from
http://www.cdc.gov/hiv/stats.htm#cumaids.
CDC. HIV Prevalence Estimates-
United States, 2006. MMWR;
57:1073-1076.
CDC. (2003b). HIV/AIDS Among African
Americans. Retrieved February 26,
2009 from
http://www.cdc.gov/hiv/pubs/facts/afam.htm.
CDC. (2003c). Surveillance of
healthcare personnel with HIV/AIDS,
as of December 2002. Retrieved
February 25, 2009 from
http://www.cdc.gov/ncidod/hip/BLOOD/hivpersonnel.htm.
CDC. (n.d.a). OraQuick rapid HIV
test for oral fluid-frequently asked
questions. Retrieved February 24,
2009 from
http://www.cdc.gov.
CDC. (n.d.b). HIV and its treatment:
What you should know (2nd ed.).
Center for Disease Control, National
Center for HIV, STD and TB
Prevention, Divisions of HIV? AIDS
Prevention. Retrieved February 24,
2009 from
http://aidsinfo.nih.gov/guidelines/adult/brochure/.
Goldrick, B., Baigia, J., Larsen,
J., & Lemert, J. (2000). Nursing
research and HIV infection: State-of
–the-science. Journal of Nursing
Scholarship. 32(3), 233-238.
Retrieved February 24, 2009 from
Proquest.
Hall HI, Ruiguang S, Rhodes P, et
al. Estimation of HIV incidence in
the United States. JAMA. 2008;
300:520-529.
Marks G, Crepaz N, Janssen R.
Estimating sexual transmission of
HIV from persons aware and unaware
that they are infected with the
virus in the USAA. AIDS. 2006;
20:1447-1450. Retrieved March 1,
2009 from
http://aidsonline.com/pt/re/aids/fulltext
Pinkerton, S., Martin, J., Roland,
M., Katz, M. et al. (2004).
Cost-effectiveness of post exposure
prophylaxis after sexual or
injection-drug exposure to human
immunodeficiency virus. Archives of
Internal Medicine. 164(1). P 46-56.
Retrieved February 24, 2009 from
Proquest.
Trynka, S., & Erlen, J. (2004). HIV
disease susceptibility in women and
the barriers to adherence. Medsurg
Nursing, 13(2), p13 (2), p 97-105.
Retrieved February 25, 2009 from
Proquest 13(2), p 13(2), p 97-105.
Retrieved February
UNAIDS Epidemic Update 2008
Retrieved February 26, 2009 from
http://www.unaids.org
UNAIDS/WHO AIDS Epidemic Update:
December 2007. ... AIDS epidemic
update 2007: Report fact sheet: key
facts by region ( en | fr | es | ru
) ...Retrieved February 24, 2009
from
www.unaids.org/en/KnowledgeCentre/HIVData/EpiUpdate/default.asp |