NADESH 1
NADESH 1
NADESH 1
TABLE OF CONTENT
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TITLE............................................................................................................................................. i
TABLE OF CONTENT....................................................................................................................... ii
LISTS OF ABREVIATION..................................................................................................................iv
LISTS OF FIGURES..................................................................................................................... v
List of table................................................................................................................................... vi
DEFINITION OF TERM................................................................................................................... vii
CHAPTER ONE............................................................................................................................1
INTRODUCTION..........................................................................................................................1
1.1. Background of study............................................................................................................1
1.2. Statement of problem.........................................................................................................2
1.3. Objectives of study..............................................................................................................3
1.3.1 Main objective............................................................................................................... 3
1.3.2 Specific objective.......................................................................................................... 3
1.4 Research questions............................................................................................................... 3
1.5 Significance of the study...................................................................................................... 3
CHAPTER TWO............................................................................................................................... 4
LITERATURE REVIEW...........................................................................................................4
2.1 DEFINITION...........................................................................................................................4
2.2 pathogenesis........................................................................................................................ 4
2.3 mode of transmission........................................................................................................... 5
2.4 Persons at risk of HIV infection...........................................................................................6
2.6 Diagnosis.............................................................................................................................. 7
2.7 Complications.......................................................................................................................8
2.8 Classification........................................................................................................................ 9
2.9 Treatment............................................................................................................................ 9
2.10 Nursing intervention........................................................................................................ 10
2.11 Prevention of HIV/AIDS....................................................................................................11
CHAPTER THREE...........................................................................................................................13
MATERIALS AND METHOD....................................................................................................... 13
3.1 Study design and period.....................................................................................................13
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3.2 Research setting................................................................................................................. 13
3.2.1 Historical Back ground of the MIFI...............................................................................13
3.2.2 Geographical location of the MDH..............................................................................13
3.2.3 Infrastructure, Organization and functioning of the MDH..................................................15
3.3 Study participants.............................................................................................................. 16
3.4 Selection criteria................................................................................................................ 16
3.4.1 Inclusive criteria.......................................................................................................... 16
3.4.2 Exclusive criteria..........................................................................................................16
3.5 Sample size and sampling.................................................................................................. 16
3.6 Study procedure.................................................................................................................16
3.7 Data processing and analysis..............................................................................................16
3.8. Data storage and data quality and control........................................................................16
3.9. Ethical consideration.........................................................................................................17
TIME TABLE OF ACTIVITIES.......................................................................................................... 18
BUDJET......................................................................................................................................... 19
REFRENCES...................................................................................................................................20
QUESTIONNAIRE.......................................................................................................................... 23
LISTS OF ABREVIATION
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AIDS: Acquire Immunodeficiency Syndrome.
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LISTS OF FIGURES
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List of table
Table 1: Table of activities......................................................................................18
Table 2: budget......................................................................................................19
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DEFINITION OF TERM
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CHAPTER ONE
INTRODUCTION
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1.2. Statement of problem
Mother –to-child transmission (MTCT) of HIV remains a significant public health challenge in
Cameroon, despite advancements in the prevention of mother to child transmission (PMTCT)
programs [11]. Cameroon is among the countries with high HIV prevalence, where pregnant
women and children remain particularly vulnerable [12]. The national prevalence of HIV among
women of reproductive age is approximately3.4%, contributing significantly to the burden of
pediatric HIV infections if timely interventions are not implemented to mother to child
transmission can be drastically reduced to less than 5% through the use of antiretroviral therapy
(ART), appropriate obstetric interventions, and safe infant feeding practices [13]. However, gaps
in knowledge, attitude and practices related to MTCT persist among HIV-positive pregnant
women in Cameroon, exacerbated by socio-cultural factors, stigma, and limited access to
healthcare services [14]. Study and awareness regarding PMTCT strategies, misconceptions
about HIV transmission, and inadequate adherence to ART significantly increase the risk of
vertical transmission [15]. Additionally, structural challenge healthcare infrastructure,
insufficient trained personnel, and economic barriers further hinder the success of PMTCT
programs [16]. Understanding the level of knowledge and practice pregnant women is essential
for addressing these challenges [17]. Without targeted interventions to enhance awareness,
promote positive attitudes and improve adherence to prevention protocols, the goal of
eliminating pediatric HIV in Cameroon by 2030 will remain unattainable [18].Therefore the aim
of this study will be to assess the knowledge, attitude and practices of mother to child
transmission of HIV/AIDS among HIV infected pregnant women attending ANC at the Mifi
District Hospital Bafoussam.
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1.3. Objectives of study
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CHAPTER TWO
LITERATURE REVIEW
2.1 DEFINITION
HIV (Human immunodeficiency virus) is a virus that attack the immune system, specifically
targeting CD4 cells which are crucial for the body’s ability to fight off infection.
AIDS is the final stage of HIV infection, characterized by severe immune system damage
and increase susceptibility to opportunistic infection .The scale of the HIV/AIDS pandemic has
exceeded all expectation since its identification 20 years ago. Globally, an estimated 36 million
people are currently living with HIV and some 20 million people have already died, with the
worst of the pandemic centered on the sub –Saharan Africa [19]. The HIV/AIDS pandemic has
become a public health crises. Which researchers has deepened out understanding of how the
virus replicates, manipulation and hides in an infected person. Antiretroviral treatment has
transformed AIDS from an inevitably fatal condition to a chronic manageable disease in some
setting [20].
2.2 pathogenesis
When HIV enter a new host, the virus targets CCR5+ CD4+ effector memory T cells,
resulting in acute, massive damage of these cells from mucosal effector sites. This depletion does
not initially compromise the regenerative capacity of the immune system because the most
central memory T cells are spread. Here, we will talk on evidence suggesting that frequent
activation of these spread cells during chronic phase of HIV infection supplies mucosal tissues
with short lived CCRT+ CD4+ effector cells that prevent life threatening infections. This
immune activation may lead to infection and killing of target T cells by HIV. There are
selective and the impact on effector cells life span is limited. We propose however that,
persistent activation progressively destroys the functional organization of immune system
reducing its regenerative capacity and facilitating viral evolution that leads to loss of the
exquisite target cell. Sparing selectivity of viral replication, ultimately resulting in AIDS [21].
Infection with HIV begins without any symptoms and is accompanied by slight changes in the
immune system. This stage might take up to three months after infection until seroconversion,
where HIV specific antibodies can be detected in individuals following recent exposure. The
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outcome of infection and duration for a disease progression with clinical symptoms may vary
greatly between individuals, but often it progresses fairly slowly [22]. It take several years from
primary infection to the development of symptoms of advance HIV disease and
immunosuppression.
During primary infection, individuals may look healthy, but the virus is actively replicating
in the lymph nodes and blood stream of those who are infected. AS a result, the immune system
may get slowly damaged because of the burst in the viral load in the bodies [23].
Symptomatic stage of disease shows the late phase of HIV disease (AIDS) where
individuals may be open to other opportunistic infections such as mycobacterium avium,
mycobacterium tuberculosis, pneumocystis carina, toxoplasmosis and candidiasis. It has been
discovered that infected individuals develop an AIDS status when their plasma HIV load is high
and the CD4+T count is less than 200mm. The availability of the highly active antiretroviral
therapy may question the dilemma as to whether everyone who seroconverts HIV will develop
AIDS [24].
This led to the discovery of the chemokine receptor as essential coreceptors for HIV -1.
There are different types of these coreceptors for different cell types that HIV variants can use
for infection of cells. Two main chemokine receptors have been identified to play a major role in
HIV entry, CCR5 and CXCR4 (or fusing) [25]. HIV -1 is one of the most polymorphic viruses
known and exists as a swarm of genetically related variants. The polymorphic viruses nature of
HIV-1 can be directly attributed to its error prone reverse transcriptase and complexity of its
cDNA formation. Together with other factors, the evolution of the viral genome underlies all of
the changes in the biological characteristics of HIV-1 including cytopathic ability, immune
evasion, coreceptors usage and tropism.
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From mother to child during childbirth: This is the most common way for HIV to
be transmitted from mother to child during pregnancy, labor and delivery or
breastfeeding. Without any interventions, the risk of vertical transmission is 15% -45%.
However, this risk can be reduce to below 5% with the used of antiretroviral therapy,
safe infant feeding methods [26].
Blood transfusion and organ transplants: Although rare in countries with strict
screening procedures, HIV can be transmitted through contaminated blood transfusions
or organ transplants [27].
Unprotected sexual contact: HIV is spread commonly through unprotected vaginal,
anal, or oral sex with an infected partner. The risk of transmission is higher if there are
open sores or cuts in the genital area and especially those with limited access to HIV
testing and preventions services.
Sharing of needles or syringes: HIV can be spread through sharing needles or
syringes contaminated with infected blood, such as in the case of intravenous drug use.
Unsterilized medical equipment: Reuse of unsterilized medical equipment in
healthcare settings can lead to the transmission of HIV between patients.
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prevention services, such as poverty, lack of education, geographic
isolation, maybe at a higher risk of infection [29].
The symptoms of HIV and AIDS vary, depending on the phase of infection some people
infected by HIV develop a flu-like illness within 2 to 4 weeks after the virus enters the body
[30]. This illness is known as primary HIV infection may last for few week’s possible sign and
symptoms include:
Fever
Headache
Muscle aches and joint pain
Rash sore throat and painful mouth sore swollen lymph nodes, mainly on the neck.
Diarrhea
Weight loss, cough
Night sweats.
The next stage is the clinical latent infection (chronic HIV). In this stage of infection
many people may not have any symptoms. This stage can last for many years. When it
reaches AIDS, the various symptoms can be seen [31].
Sweats
Chills
Recurring fever
Chronic diarrhea
Persistent white sports or unusual lesions on your tongue or mouth. Persistent,
unexplained fatigue, skin rashes.
2.6 Diagnosis
Diagnosis tests for HIV infection have undergone considerable evolution since the first enzyme
immunoassay (EIA) and western blot were introduced 2 decades ago. Newer methods detect
infection sooner and yield the results much faster. Rapid test represent a major advance for HIV
screening. 6 rapid tests have been approved by the food and drug administration (FDA) since
November 2002. Four of these tests can be done in point of care and non- clinical settings
because they use whole blood or oral fluid and are simple to perform. An assay for detection of
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HIV-1 RNA has been approved by the FDA to detect HIV infection before seroconversion has
occurred [32].
2.7 Complications
Patients with HIV infection often develop multiple complications and comorbidities.
Opportunistic infections should always be considered in the evaluation of symptomatic patients
with advanced HIV and AIDS, although, the overall incidence of these infections has decreased.
Complications of HIV infection can vary widely and can affect different parts of the body. Some
common complications include;
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Metabolic complications: HIV and certain antiretroviral medications can lead to
metabolic complications such as insulin resistance, dyslipidemia, and lip dystrophy,
which can increase the risk of diabetes and cardiovascular disease.
Bone disorders: HIV and certain antiretroviral medications can affect bone health,
leading to conditions such as osteoporosis and osteopenia, which can increase the risk of
fracture [33].
2.8 Classification
At present, three classification systems are in use. The first defines primary isolates as
macrophage (M)- tropic or T- cell- line(T)- tropic. However, this system disguises the fact that
all primary isolates replicate in activated, primary CD4+ T- lymphocytes. The second system
categorizes isolate as being either syncytium- inducing non-syncytium- inducing (NSI) on the
basis of whether they form syncytia in MT-2 cells, which express CXCR4 but not CCR5 [34].
However, NSI viruses can readily form syncytia with CCR5- positive cells. The third system
defines viruses as either slow/low (SL) or rapid/ high (RH) depending on their growth kinetics in
culture2. These classifications are often used interchangeably, but they are not synonymous.
Primary infection of HIV also known as the acute stage may last for few weeks with
possible symptoms of fever, headache, and muscle ache. These symptoms can be so mild that
you might not even notice the manifestations [35]. However, the amount of virus in your blood
stream (viral load) is quite high at this time. As a result, the infection spreads more easily during
primary infection than during the next stage [36]. Clinical latent infection (chronic HIV). In this
stage of infection, HIV is still present in the body and in white blood cells however, many people
may not have any symptoms or infection during this time [37]. This stage can last for many years
if you are not receiving antiretroviral therapy (ART). Some people develop more severe disease
much sooner. Symptomatic HIV infection as the virus continues to multiply and destroy your
immune cells. The cells in your body that help fight off germs you may develop mild infections
[38].
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2.9 Treatment
The treatment of HIV/AIDS typically involves a combination of antiretroviral drugs (ARVs) that
target the virus at different stages of its life cycle. The treatment regimen may vary based on the
stage of the disease, the individual’s overall health, and any co- existing conditions. Here is a
general overview of the different stages of HIV/AIDS and the corresponding treatment drugs:
Acute HIV infection: During the acute phase of HIV infection, the virus rapidly
replicates and spreads throughout the body. Treatment during this stage aims to reduce
viral replication and establish viral suppression. Commonly used ARVs during this stage
may include:
Tenofovir disoproxil fumarate( TDF)
Emtricitabine (FTC)
Dolutegravir (DTG)
Raltegravir (RAL)
Chronic HIV infection (asymptomatic stage): In this stage, the virus remains
active but may not cause any symptoms for many years. Treatment aims to maintain viral
suppression, prevent disease progression, and preserve immune function. Commonly
used ARVs during this stage may include:
Tenofovir alafenamide (TAF)
Emtricitabine/ tenofovir alafenamide (FTC/TAF)
Efavirenz (EFV)
Atazanavir (ATV)
Symptomatic HIV infection (AIDS): As the disease progresses to AIDS, the immune
system becomes severely compromised, leading to opportunistic infections and other
complications [39].Treatment during this stage focuses on managing complications,
preventing opportunistic infections, and maintaining quality of life. Commonly used
ARVs during this stage may include:
Lopinavir/ ritonavir (LPV/r)
Darunavir (DRV)
Abacavir (ABC)
Lamivudine (3TC).
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2.10 Nursing intervention
Nursing interventions for patients with HIV/AIDS focus on promoting health, preventing
complications, managing symptoms, and supporting emotional well-being. Some possible
nursing interventions are;
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Education and awareness: Providing comprehensive education about HIV
transmission, prevention methods, and the importance of regular testing can help
individuals make informed decisions about their sexual health and reduce the risk of
transmission.
Condom use: Consistent and correct use of condoms during sexual activity can greatly
reduce the risk of HIV transmission. Condoms are readily available and are an effective
barrier method for preventing the spread of the virus.
Testing and counseling: Regular HIV testing is important for early detection and
treatment. Individuals who are aware of their HIV status can take steps to protect
themselves and their partners, seek appropriate medical care, and access support services
[42].
Pre-exposure prophylaxis (PrEP): PrEP is a medication taken by HIV negative
individuals to reduce their risk of acquiring the virus through sexual activity or injection
drug use. When taken as prescribed, PrEP can be highly effective in preventing HIV
transmission.
Needle exchange programs: Providing access to clean needle and syringes for
individuals who inject drugs can reduce the risk of HIV transmission through sharing of
contaminated equipment.
Harm reduction programs: Implementing harm reduction strategies, such as opioid
substitution therapy and supervised injection facilities, can help reduce the risk of HIV
transmission among individuals who use drugs.
Addressing stigma and discrimination: Stigma and discrimination related to HIV
can create barriers to prevention efforts and discourage individuals from seeking testing
and treatment. Promoting understanding, empathy, and acceptance can help create a
supportive environment for HIV prevention and care [43]
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CHAPTER THREE
Also, the MDH is found in the west region of Cameroon, mifi Division and precisely in
Bafoussam town.
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Figure 1: geographical location of mifi District Hospital Bafoussam
http:www.localization of the Mifi District hospital Bafoussam
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3.2.3 Infrastructure, Organization and functioning of the MDH
The MDH is structure surrounded by a barrier up of blocs, painted in yellow. It has 3 modest
buildings with many departments such as;
The emergency ward; where new patients are booked and emergency cases are equally
handled here. It is an emergency ward that is in charge of sending patients to the précised
ward or unit of the hospital.
The men ward; here, male patients of 15 years and above are handled here.
The women ward; here, female patients of 5 years and above are been taken care of.
The surgical ward; here surgical acts are being done by a surgeon with many assistants.
The maternity; women in labor and sick pregnant women are being handle here.
The ANC unit; pregnant women coming for ANC and family planning are received here.
Physiotherapy; it takes care of patients with nerves problems and those with broken arm
or leg that need massage.
The dentistry; it takes care of patients with tooth problems.
The ultrasound room; here, ultrasound and x-ray examination are being carried out.
The pharmacy; drugs are stored and sold here.
The laboratory; various test are being carried out here.
The antenatal clinic in MDH is an active clinic that runs from Monday to Friday of every
week between 8am – 3:30pm. The ANC unit is located in the building that host the
podiatry and the women ward, the activities of the clinic includes; booking visits, for
new pregnant women and routine antenatal visit for booked clients.
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3.3 Study participants
The participants of the study will be all infected HIV pregnant women attending ANC at the
MDH Bafoussam.
A semi structured questionnaire containing closed ended questions will be used, which contain 4
sections that is Socio- demographic characteristics, Knowledge on HIV/AIDS prevention,
Assessing the attitude score toward the prevention of HIV/AIDS, explore the practices toward
HIV/AIDS, will be administered to study participants for them to fill and return them back.
Those who will be unable to fully understand the questions will be help by the researcher.
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The data collected will be stored in computer, USB key, Hard, soft copy as back up before it will
be analyzed.
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TIME TABLE OF ACTIVITIES
Defense
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BUDJET
Table 2: budget
N/S Activities Amount Justification
Correction.
Total 93,000
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REFRENCES
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16. Nkenfou ,C.N;et al (2018).knowledge PMTCT amongst HIV –Positive pregnant women
in cameroon .BMC public ,Health ,18,845.
17. Cherish ,M.F, et al (2017).Adherence to ART and MTCT Prevention ;Insights from sub-
saharan Africa.The lancet HIV,4(2).e63-e71.
18. Zash ,R;et al.(2022).Advances from high –burden setting .Journal of Acquired Immune
Deficiency Syndromes (JAIDS),90(2),123-130.
19. Viviana Simon et Al. HIV and AIDS epidemiology, the lancet, 368 (9534), 489-504,
2006.
20. MD. Et Al. Condoms and HIV prevention centers for disease control and prevention,
centers for disease. Control, vol 4 (1), 2014.
21. Cunningham Al, L IS, Tuarez j. The level of HIV infection of macrophages is determined
by interaction of viral and host cell genotype, leukoc Biol, 68:311-7, 2000.
22. Anna Maria, Rukundo et Al. Health sciences, health 8(10), 2016.
23. M Atrouni W, Berbari E, Temesgen Z. HIV associated with opportunistic infections,
bacterial infections, pub med 54:80-3, 2006.
24. Chun TW, Fauci AS. HIV reservoirs, AIDS, 26:1261-8, 2012.
25. Mofenson, L.M (2010) Advance in the prevention if vertical transmission of human
Immunodifiency virus 001.Seminars in pediatric infectious Disease, 21 (4). 293-300
https://doi.org/10.1053/j spid. 2010. 08. 001.
26. Suy, A., Martinez, E., Coll O., Lonca, M., palacio, M., de Lazzari, E., … and Gatell, J.M.
(2006). Increased risk of preterm delivery in HIV infected women treated with highly
active antiretroviral therapy.
27. WHO. (2010). Toward 100% voluntary Blood Donation: A Global framework for action
Retrieved from https://www.who.int/bloodsafety/voluntary-donation/en/.
28. United Nations office on Drug .(2021). World Drug Report. 2021. Retrrieved from
https://www.unodc.org/unodclen/data.analysis/wdr2021.html.
29. Strathdee, S.A., and stock man, j.k (2010). Epidemiology of HIV among injecting drug
users: current trends and implications for interventions .Current HIV/AIDS Report, 7
(2),99-106.
30. Fauci As. 25 years of of HIV, nature, p453:289-90, 2008.
xxviii
31. Hassan M Naif, L IS, Alali M, J virol. CCR5 expression correlates with susceptibility of
maturing monocytes to human immunodeficiency virus type, PMC Free articals 72:830-
6.
32. WHO. (2021) Consolidated guidelines on HIV testing services for a changing epidemic.
33. Fouchier R, Groenink M, Koostra N. Phenotype association sequence variation in the
third variable domain of the human immunodeficiency virus type, 66:33183-7.
34. E.A. Berger, RW Doms, RA Weiss, EM Fenya, BTM Korner, DR Littman, JP Moore, QJ
Sattentau. A new classification for HIV, nature,391,240, 1998.
35. Fenyo, EJ virol. A new classification for HIV, nature, 1998.
36. Moore, JP,TrKola, A and Dragic, T. Curr.A new classification for HIV, nature1997.
37. Rachel A. Royce,PHD, MPH, Arlene Sena, MD,Willard cartes, Jr,MD, and Myron’s S.
Cohen. Sexual transmission of HIV, the new England Journal of medicine, 1997.
38. World Health Organization (WHO) consolidate guideline on the use of antiretroviral
drugs for treating and preventing HIV infection 2016.
39. American nurses association HIV/AIDS nursing: scope and standards of practice 2018.
40. The body pro, psychosocial issues in HIV/AIDS care 2018.
41. Marco Florida, Marina Giuliano,Lucia Palmisane, Stefano vella.Gender differences in
the treatment of HIV infection, pharmacology research 58 (3-4), 173-182, 2008.
42. Carl W Dieffenbach, Anthony S faice. Thirty years of HIV and AIDS, Annals of internal
medicine,154 (11), 766-771, 2011.
43. Namaitijiang Maimaiti, Jalan Yaacob Latiff, Bandar Tun Razak, Cheras Knowledge,
Attitude and Practice Regarding HIV/AIDS October 2010 published by Canadian center
of science and Education.
44. National institute of health . US department of health and human services. Workshop
summary: scientific evidence on condom effectiveness for sexually transmitted diseases
prevention. 12-13 june 2000.
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QUESTIONNAIRE
Dear respondent,
5- Religion:
A) Catholic B) Presbyterian C) Baptist D) Others
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7- How is HIV transmitted from mother to child?
A) Yes B) No C) Not
10-Are you aware of the importance of early testing for HIV during pregnancy?
12- Do you feel comfortable discussing HIV prevention with your friends?
13-The use of condoms during sexual activity is an effective way to prevent the spread of
HIV.
14- Are you aware of the different ways in which HIV can be transmitted?
15- Do you support the initiatives that promote HIV testing and encourage people to know
their status?
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A) Agree B) Strongly agree C) Neutral D) Disagree E) Strongly disagree.
16- Do you believe that stigma and discrimination against people living with HIV should be
addressed to prevent further spread of the virus?
A) Yes B) No.
19- Do you avoid sharing needle or syringes with others to prevent the risk of HIV
transmission?
20- Do you think that regular HIV testing is important for preventing the spread of
HIV/AIDS?
21-Do you think that education and awareness programs about HIV prevention are
effective in reducing the risk of HIV transmission?
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