Case Studies: Combined
Sam Clark |
Jonathan Gorstein - Abstract |
Jonathan Gorstein - Outline |
Anne Marie Kimbal |
Ann Kurth
Martina Morris |
Beth Rivin |
Bettina Shell-Duncan |
Clarence Spigner |
Joe Zunt |
Combined
Nevirapine to Prevent Mother to Child Transmission of HIV
Sam Clark
Abstract
The drug
nevirapine can be used in single dose to the mother just before delivery
and following delivery by 72 hours to
the newborn to dramatically reduce the likelihood of transmission of HIV from HIV+ mothers to
their newborn children – see url below
titled “Nevirapine - godsend or a drug from hell?” [I do not agree with all
the conclusions of this piece, but it is
written by a reputable colleague who is knowledgeable.] The object of this treatment is to
dramatically reduce the number of HIV+ babies born to HIV+ mothers.
The
treatment described above is comparatively cheap and easy and very
effective. However, it has many
potential problems that need to be carefully considered before endorsing widespread implementation of
nevirapine monodose therapy to prevent
mother to child transmission.
The first
of these is that this treatment has no particular benefit for the mother. The drug has few side effects, but this still
raises an ethical question regarding whether or not it is acceptable to submit
the mother to a treatment that does have
some individual-level side effects if she gains nothing from it.
Second is
the fact that this regimen has a non-negligible likelihood of quickly selecting
for nevirapine-resistant strains of HIV,
and these strains may linger as a significant fraction of a treated woman’s viral load for a number
of months after treatment. This timescale is
long enough for her to recover from the birth and resume sexual
relationships that may mediate the
transmission of nevirapine-resistant strains to her partners. Further, it
turns out that nevirapine is very
similar to another drug efaverenz and both of these are used routinely to treat adult HIV+ individuals.
Worse, resistance to one usually means
resistance to both. So, the bad news is that nevirapine monodose therapy
to prevent mother to child transmission
may accelerate the spread of nevirapine/efaverenz-resistant strains of HIV in the general population.
Third, what
happens to young children whose mothers are HIV+? The answer is nothing nice, including the imminent loss of the
mother. Orphans of any kind face dramatically
higher risks of dying, and this goes for both the HIV+ and HIV- children
who are born to HIV+ mothers. The
unpleasant reality is that nevirapine monodose therapy will likely save the child from HIV in order to let it
die of “orphanhood”.
How do we decide what to do?
Disciplinary Basis:
Public Health, Medicine, Demography, Sociology, Law (justice,
philosophy?)
Learning Objectives: See: Nevirapine
- godsend or a drug from hell?
http://www.scienceinafrica.co.za/2002/april/nevirapine.htm
The elimination of iodine deficiency through universal salt iodization
Jonathan Gorstein
Abstract
Iodine
deficiency is the world’s most preventable cause of mental retardation, and
places unnecessary constraints on the pace of social and economic development
in a way that no nation can afford. It
is therefore imperative that countries implement programs which assure the
sustainable elimination of iodine deficiency disorders (IDD). Many countries throughout the world, both
industrialized and developing, have
adopted the international strategy of universal salt iodization (USI), i.e. the
iodization of all the salt for human and animal consumption, including the salt
used in food processing, as the main strategy for the prevention of iodine
deficiency. The tools, equipment and procedures for salt iodization have become
widely available and have made it possible for countries to implement
large-scale programs.
The ultimate goal of USI programs is to
ensure that all salt reaching households and consumers is adequately iodized so
as to satisfy the physiological requirements of iodine. However, while the concept of universal salt
iodization seems quite simple, the practical realities of implementing such
programs are challenging as these require a strong collaboration between
Governments and salt producers. This public-private partnership has been
essential in forging successful programs but there are delicate considerations
when there are competing interests and potential implications of the private
sector participating in a social program. In addition, there are issues with
small-scale farmers, many of whom are subsistence producers who are very poor
and cannot comply with mandatory salt iodization requirements. While their participation is vital, so as to
avoid any non-iodized salt leaking to markets, coming up with feasible
mechanisms to ensure that their salt is iodized has required innovative small
business models, such as community co-operatives, to be developed in many
settings . Finally, the selection of table salt as a fortification vehicle is
based on the assumption that all populations consume salt in relatively
consistent quantities regardless of socio-economic status. However, as
hypertension and other chronic diseases emerge, the consumption of salt has
declined, while in other settings, table salt is not as readily consumed as
other salty condiments such as fish sauce or soy sauce, thereby calling into
question the appropriateness of salt as a food vehicle.
This case study will consider the many
dimensions of designing and implementing a salt iodization program to address
iodine deficiency and will consider the real practical issues of such a
program.
Disciplinary Areas:
Nutrition, Public Health, Private-public partnerships
Learning objectives for this capstone
topic could include:
- Understand the importance and epidemiology of iodine deficiency
- Identify the key factors that led to successful implementation of USI
- Identify the obstacles and potential solutions in salt iodization
programs with respect to use of salt as a sole vehicle and dealing with
small-scale salt farmers
- Consider the importance of public-private partnerships in addressing
public health issues
Oil rig worker in the Philippines
Ann-Marie Kimball
Abstract
Mario Nachor (fictitious) is a 40 year old father of five from the Philippines. He
was raised in the countryside 60 km from Manila in a poor district. He pursued his education
through high school, marrying his
highschool girlfriend in a lavish Catholic ceremony. While they had hoped to
defer a family, family planning was not an option in the Catholic family and
community setting where he and his bride resided. Mario soon found himself struggling to
support his family with manual labor jobs. Despite lots of looking, he was
never fully employed, and funds for clothing, food and schooling were very
tight. Mario did not want his wife to work, it was against his belief system.
She had a full time job caring for the children. A cousin from Manila
called him with an opportunity to go and work for an American Oil Company which
was doing exploration in the empty quarter of the Saudi Peninsula.
He leapt at the chance.
To qualify
for a visa to travel he had a health examination certified for a fee by a local
physician known to his family. No physical exam was done, and it was difficult for
Mario to afford the price of a chest x-ray, but he managed. Three months later
he was taken from the airport to the rig by truck with many other workers from
the Philippines, Pakistan, India
and China.
His job was to assure the alignment of the large drill which required daily
inspection and servicing of its complex gears. The drill operated 24 hours a
day.
Mario lived
in dormitory accommodations with forty other men. His bunk was adequate and he
placed pictures of his wife and children prominently around his bed so he could
remember why he had come so far to work. The pay was good, and he worked at the
rig for 6 weeks of long shifts (14 to 18 hours) and then had two weeks off.
Normally workers did not go home, but spend the two weeks in the capital in
dormitory accommodations provided by the company. Most of the pay he sent back
to his wife in Mindanao.
His second
week of work he felt very fatigued. The work was hard and the temperature was
very hot during the day time. He checked into the rig clinic to consult the
nurse about a heavy feeling in his chest and numbness in his arm, but the nurse
reassured him that workers often had to adjust to the conditions.
After
dinner the following week he felt nauseous and had crushing chest pain. He was
sweating and felt dizzy and short of breath. He collapsed on his way to see the
nurse. He passed out. He awoke a day later in a strange hospital with IV tubes
in his arms and a cardiac monitor. Mario was afraid and soon learned he had
suffered a heart attack. Not to worry, he was assured, the company would pay
his hospitalization costs.
Three days
later, he was discharged with a prescription for nitroglycerin and instructions
to follow up with his own physician. He was dismayed to learn that his passage
to Mindinao was paid, but he would not be allowed to return to the rig to work,
and was being discharged for medical reasons. He would receive no compensation
other than what he would have received for his six week stint. Dejected, he
returned to Mindanao to face unemployment once
again.
Outbreak of TB among a Social Network in Seattle, Washington
Ann Kurth
Abstract
In King County,
a TB (TB) outbreak occurred among a group of friends and associates beginning
in late 2003. Most of the people
affected were men in their late teens and early twenties, who were of East
African origin. Most of these young men
came to the United States
as babies or small children with their families seeking to escape political
turmoil and war in their home countries.
Many had a history of incarceration
at juvenile, adult, and INS detention facilities, and were involved both in
dealing and actively using drugs (usually marijuana and crack cocaine). The members of this group also ‘hot boxed’,
which in part accounts for the high rate of transmission within the group. (‘Hot boxing’ is getting high in a car with
the windows rolled up, to maximize marijuana intake). Most of these young men had tenuous shelter,
couch surfing in various apartments with friends for extended periods of
time. One of the friends with whom the
cases stayed was HIV-positive (thus at high risk for TB acquisition or
relapse).
The index case was a twenty-one year
old male from Somalia
who was diagnosed with TB while in a detention facility. In late February of 2004, he complained of
two weeks of fever and weight loss. A
chest x-ray showed left hilar adenopathy (one of the hallmark of TB). The source case was a twenty-year old male
who came to the US from Ethiopia as an
infant. He was hospitalized in early
April of 2004. He had symptoms of cough,
weight loss, and fever for several months.
A chest x-ray revealed countless bilateral cavities and sputum smears
were 4+ for acid-fast bacilli (AFB).
This young man had sought treatment for the same symptoms in late
December 2003 at an emergency room setting, where a chest x-ray revealed
cavitary TB (a characteristic feature
of ‘secondary’ or ‘adult type’) – but the diagnosis of TB was not
recognized at the time, and the public health TB program was not notified.
Between April and September
of 2004, ten more cases linked to this outbreak were found. Six of the twelve cases had cavitary TB and
were 3+ to 4+ smear positive for AFB.
Three of the twelve cavitary cases had normal chest x-rays two months
prior to diagnosis. All eleven of these
cases completed treatment. The twelfth case was identified as a contact early
in the outbreak. He had a positive PPD
and normal chest x-ray. He declined
treatment for latent TB infection in King county. He moved to another state, became symptomatic
for TB and was diagnosed there with clinical TB—negative sputum cultures, but
improved symptoms and chest x-ray while on treatment for TB. He returned to King county and continued with
TB treatment here. Eventually, he
refused further treatment and was lost to follow-up.
In all, about 130 contacts were
identified. Challenges in identification
included the fact that some cases and contacts were reluctant to give contact
information due to fears of police, INS, and the government. The team of nurses and other Health
Department staff were able to overcome this by building trusting relationships,
facilitating access to housing, food, public assistance, primary care, and
assistance with legal issues (letters, visits in jail). Funding from the
Centers for Disease Control allowed the Health Department to hire as a staffer
someone who was a member of the patient community. Lack of Health Department resources meant
that field-based directly observed preventive therapy was limited, and where it
was done, involved a great deal of staff time ‘chasing after’ highly mobile
clients from place to place via cellphone.
Self-administered therapy (every day for 9 months) did not work well, as
adherence was poor due to a variety of competing life concerns and the fact
that therapy is required even though one doesn’t feel sick. Therefore most patients had to come in to the
clinics for 6-month therapy, which meant that follow-up was not optimal. Very few of the 130 have received treatment
for latent TB infection, because they have declined treatment. To date, no new cases have been identified in
King County since September 2004, and
monitoring by Health Department staff of a high-risk subset of individuals
continues.
Disciplinary basis: UW Epidemiology and Nursing (A. Kurth, CNM, PhD)
and Public Health Seattle-King, (Darla Mosse, RN)
Learning objectives:
- the interconnectedness of immigration and incarceration policies
- lack of primary care/limits of emergency care settings
- social support mechanisms for infectious disease screening, treatment, and control.
The 3 by 5 Initiative
Martina Morris
On World AIDS Day 2003, WHO
and UNAIDS released a detailed and concrete plan to reach the 3 by 5 target of
providing antiretroviral treatment to three million people living with AIDS in
developing countries and those in transition by the end of 2005. This is a
vital step towards the ultimate goal of providing universal access to AIDS
treatment to all those who need it.
The Problem is URGENT
- 30 million people have died in two decades. 40
million more people are infected.
- In poor countries, 6 million people with
HIV/AIDS need immediate ART. Less than 8% get it.
- Worst hit is sub-Saharan Africa.
With 28.5 million people infected, HIV/AIDS has destroyed communities,
health care systems and put a shadow upon the future of entire countries.
Why antiretroviral therapy (ART)?
- ART prolongs lives, making HIV/AIDS a chronic
disease, not a death sentence. Affluent countries have seen a 70% decline
in HIV/AIDS deaths.
- ART will help calm fears and change attitudes towards HIV.
- ART, as part of a prevention plan, can
significantly reduce HIV transmission.
- ART, once very costly,
is now much more affordable.
- ART can reduce overall health care costs and restore quality of life.
- WHO and UNAIDS are working to make ART accessible to all.
What will 3 by 5 DO?
To reach the 3 by 5 target, WHO and UNAIDS will focus on five critical areas:
- Simplified, standardized tools to deliver antiretroviral therapy.
- A new service to ensure an effective, reliable supply of medicines and diagnostics.
- Rapid identification, dissemination and
application of new knowledge and successful strategies.
- Urgent, sustained support for countries.
- Global leadership, strong partnership and
advocacy.
- WHO, countries and other
partners need to train 100 000 health workers, develop health systems and
build infrastructure and standards.
The funding gap: US$ 5.5 billion
over current commitments.
Potential Problems:
- Is HIV the
most important priority for global funding and activities?
- Will mass treatment
lead to rapid development of antiviral resistance?
- Will treatment lead to behavioral disinhibition?
Disciplinary basis:
Epidemiology, Health Services, Methods/Statistics/Modeling, Biology, Social Sciences
Learning objectives:
- How should priorities be defined?
- What is the right metric? Death? DALY? Morbidity? QALY? Orphans?
- Does donor interest matter?
- Does capacity building matter?
- Should we focus on eradication or reducing prevalence?
- How seriously should we take
the arguments that AIDS is not caused by HIV?
- Measuring the burden of disease
- Where do the data come from?
- Which agencies have comprehensive data?
- Sentinel surveillance vs. pop based surveys (representative samples)
- Response rate bias
- What does capacity buildinginvolve?
- Health service organizations
- Public infrastructure (roads, water, safety)
- Human resources (training models and brain drain)
- The difference between individual and population level outcomes
- Metrics for patient improvement
- Metrics for population health
- Mechanisms that link individual and population outcomes
- Conflicting goals
- Individual health and freedom vs. evolution of drug resistance
- Individual health and freedom vs. compensating behavioral change
- Reducing death rates vs. reducing incidence
‘The highest attainable standard
of health is one of the fundamental rights of every human being, without
distinction of race, religion, political belief, economic or social
conditions’
~ Constitution of WHO
What does it mean to say that “the highest attainable standard of health” is a right
regardless of economic and social conditions?
HIV positive woman seeking care for a compound fracture
Beth Rivin
Bvitri Susalo is 26 years old and on
the orthopedic ward of a big hospital in Jakarta, Indonesia
getting prepared for her operation. She
needs a surgical repair of a complex fracture which she sustained when her
husband threw her down the stairs one night after a fight they had. This happens often.
He comes home late at night and hurts her.
Bvitri doesn’t know if she should
tell the doctor of her HIV positive status.
She has been told by her activist friends that disclosing her status
could hurt her and her family. After
many hours of confusion about this, she finally decides to tell her surgeon
that she is HIV positive.
Within an hour of the disclosure,
the nurses rush in and tell her that she should go home. The surgeon has cancelled the operation and
has left the hospital for his private practice.
She calls her friend who works for an NGO called Yayasan Spiritia. They are a resource for people like Bvitri. Yayasan and many other organizations working
for the rights of PLWA start to look for an orthopedic surgeon who will operate
on Bvitri.
Female “Circumcision”: The Uneasy Alliance Between Health and Human Rights
Bettina Shell-Duncan
Abstract
Female
“circumcision” is a practice involving the partial or complete removal of the
external female genitalia. A recent
study estimated that 132 million women worldwide experienced some form of
genital cutting. Although this custom
has been practiced for thousands of years in some parts of Africa,
it only recently obtained enormous international attention, becoming the
centerpiece of a global campaign aimed at eliminating “harmful traditional
practices.”
Although efforts to eliminate female
circumcision have been underway since the early part of the 20th century, the
current wave of opposition can be traced back to the U.N. Decade for Women
(1975-1985), during which a series of conferences were held that drew
international attention to the practice as one that should be ended with urging
and aid from the international community.
Intervention was at first justified on health grounds, arguing that that
female genital cutting exposes women to unnecessary, and often severe, health
risks, and consequently a medical argument formed the foundation of most
anticircumcision campaigns. Under the
impetus of an international women’s health movement, female circumcision has
been targeted to be “eradicated” as though it were a disease. One outspoken advocate has written: “Genital
mutilation should be treated as a public health problem and recognized as an impediment
to development that can be prevented and eradicated much like any
disease.” (Hosken, 1978: 155)
This approach has spawned
intervention efforts that feature education on health complications, assuming
that as practitioners are made aware of the adverse health consequences, they
will become motivated to abandon the practice.
Two key problems have emerged from this approach: 1) the
repeat recitation of the “medical sequelae” has drawn attention to the quality
of epidemiological evidence on the adverse health consequences, and 2) many individuals convinced of the unnecessary
health risks have, instead of abandoning the practice, sought medical
assistance.
In response to these problems, the practice is now being
recast as a “human rights violation” rather than a health issue. However, the search for international human
rights conventions that are applicable to the issue of female circumcision has
been frought with problems, and most experts agree that the most tenable
solution is to frame the issue as a “right to health.” Therefore, efforts to divorce the health
approach from the human rights approach are unsuccessful.
Disciplinary Areas: Anthropology, Public Health, Human Rights Law
Learning objectives for this capstone topic could include:
- Assessing the range of practices classified as female “circumcision”
- Overviewing common reasons that the practice is perpetuated
- Critically reviewing intervention efforts aimed at eliminating female circumcision
- Critically reviewing the evidence on long-term and short-term health risks
- Examining ways that the practice has become medicalized, and arguments for opposing this
phenomenon
- Summarize international human rights conventions that may apply to the practice
- Debating how to weigh cultural rights against human rights
- Assessing the priority of eliminating female circumcision in comparison to other pressing health
concerns in practicing communities
- Assessing the socio-political factors motivating the global campaign to eliminate female circumcision
Angry Man
Clarence Spigner
Abstract
The fact that Arnold Blackthorn was
never legally married makes little difference to him. He has been divorced and is now without
“wife” and child. Arnold
is presently caught up in a bureaucratic maze of welfare rules and legalese
that seems totally hostile to just him.
He’s is worried to the point of hysteria about his 6 year-old
daughter. He feels little Rayna’s
situation grows worst by the minute due to her mothers’ negligence of which
only he has witnessed, and possibly from the new man now in the house.
Child Protective Services has no
record of Rayna being abuse. Arnold is the one the
case-workers do not like. His brooding
mood and intense demeanor is off-putting, and his unscheduled drop-ins with complaints
expressed in a rage does not his promote his alleged case of child abuse. Arnold knows the deck is
stacked against him, but he can not understand why child’s mother is
automatically given the benefit of the doubt?
Arnold has a high school education. He works for a construction company by day
and drives a cab at night. His dream is
to start his own home repair business.
Having been singled all of his adult life (he’s now 43 years old), Arnold use to live only
for himself. Then he met Rayna’s mother,
and her child came into his life. A
system of child welfare seems built just to keep him away.
Rayna is not Arnold’s biological child. When asked his
relationship to the little girl, without hesitation he responded that he is her
father. To him, this was a true statement. But he now realizes that the
“truth” in his eyes will only diminish his credibility as a concerned
“father.” He realizes when it’s found
out that he lied to officials, his declaration of parent-hood will sink his
case of the child being at-risk.
All he can think about is the physical and psychological abuse that surely will be visited upon his
daughter.
Disciplinary Bases: Public Health; Social Work; Public Policy; Law; Psychology; Sociology
Learning Objectives:
- To allow students to address issues of the organization based in the theories of Max Weber.
- To critically analyze gender dynamics in terms of issues surround vulnerability.
- To address the dynamics of defining “family” in terms of the health and well-being of children.
Child of God
Clarence Spigner
Abstract
Elana Billings always knew she was
adopted. She came from Philippines as
a baby, and that is just about all information about her background she has
been able to get from her parents. They
lived on what was left of a farm in a back-water town of 15,000 people located somewhere in the northeast corner of
the State of Oregon. Elena’s father, Jack Billings, was a red-neck
with a heart-of-gold. You’d have to know
Jack to understand that description. Her
mother, Abigail, worked as a nurses’ aid in the State’s mental institution
before it was converted to a minimum security prison. Jack now works as prison guard there. His job has done little to improve his view
of humanity.
When she reached age18, Elena won a
scholarship and went away to college.
With her long black hair, dark
features and almond eyes, she was often mistaken for an American Indian,
especially in her home-town. Now away
at college, she “blended-in” with many of the other ethnic groups there. Many thought her to be a Latina,
or from South Asia, or sometimes Italian, and
once for a Sephardic Jew.
Stories about the “nature” of Black
inferiority still tore at her. Her mother cautioned that father’s opinions came
from ignorance and his own sense of inferiority. Still, Elana wrestled with personal feelings
of inferiority which exacerbated when she begin to suspect that her biological
father might have been an African American soldier.
Still, she gravitated towards her
new found “blackness” both politically and socially at college. Blacks seem to reach out to her under a
collective assumption that she obviously was “one of them.” She saw little reason to debate it since she
enjoyed the social cohesion. She joined
Black political and cultural organizations; dated Black, and studied African
and African American history. She
developed interests in biology and the social sciences, and combining them,
built an academic background for a career in public health or cultural
medicine.
Her studies started focusing on the
determinants of health: i.e., genetics, the role of the social and cultural
environment, lifestyle factors, and the health delivery infrastructure. These approaches re-sparked her concern about
just how “black” she might be. For instance, how biologically predisposed to
certain diseases was she? Was she more
or less vulnerable to certain socio-environmental assaults? Did culturally-based assumptions about health
behaviors foster blame or credit; and how would she fit-into the status-quo of
the health and medical establishment?
Disciplinary Bases: Public Health; Sociology; Biology; Psychology; Semantics; Public Policy
Learning Objectives:
- To allow students to critically examine the social construction of “race” and well-being.
- To address the “positive” and “negative” health, i.e., social, physical and emotional, consequences
of labeling.
- To promote a discussion on the social determinants of health.
The Un-Chosen
Clarence Spigner
Abstract
Jefro Snider was a very sick
man. The night was cold and the pain in
his side was excruciating. He urinated
behind a dumpster in the alley, and could not tell if red color in his pee came
as a result of the neon sign that reflected from a bar over-head or not. He shuffled to a doorway to sleep, and wait
for the morning sun.
Jefro grew up during the Jim Crow
Era in South Carolina. His father, an impoverished share-cropper,
died young, leaving him and his two younger brothers, Henry and John, to be
were raised by their mother. The boys
were all in their teens when their mother died, and so they moved north to New York City to make
their way in the world.
For a time, the brothers stuck
together. Henry had only a high school
diploma but found good employment working at a bank. John, the youngest, attended City College
for a teaching certificate. But Jefro
drifted… from a series of odd jobs such as dish-washer, janitor, day laborer,
and for a while, as telephone installer/repairmen for New York Bell, but
nothing lasted.
When he met Cathy, a middle-class
young woman from a troubled family, it was as if the two would form an
everlasting bond and shelter each-other from a heartless world. But in less than a year, Cathy left. That was
seven years ago and Jefro has been roaming the back allies of major American
cities since.
Disciplinary Bases: Public Health; Anthropology; Sociology; Public Policy; Geography; History
Learning Objectives: To allow for a critical examination of health and homelessness.
Are you really an Indian?
Jonathan Warren
In the municipal of Aracuai, located in the sertão (dry
hinterlands) of northeastern Brazil
which is also the poorest region in the country, two communities have emerged
in the past ten years: an indigenous community called the Arana and a maroon
community named the Bau. Until recently individuals in these communities
identified as poor, mixed-race Brazilians. However, now they are asserting
identities in which race is centered and that have very different meanings and
consequences in the regional and national context where they reside.
This raises a whole new set of opportunities and limitations
to the difficult lives that most Brazilians confront in this region. To take a
few examples: First their new identities are both stigmatized and not accepted.
Indianness is both romanticized and denigrated, and the Arana, for example, are
considered racial charlatans. What are constructive ways of dealing with such a
symbolically violent context? Second, they are emphasizing memories that are
both therapeutic and painful and that the broader society considers
inappropriate to discuss. The Bau, for instance, have begun remembering and
telling stories about its painful experiences with slavery – memories which
most Brazilians choose to forget. How can a community be assisted in dealing
with atrocities that they and their immediate relatives suffered? Third, they
are identifying with communities, namely indigenous and black, that impose their
own expectations for behavior and criteria for membership – the policing of
which has even resulted in physical violence. Are their any strategies or
skills that might help communities and its members navigate these tensions
around community membership?
There are other issues at play as well. In their endeavors
to legitimate and develop their communities, both the Bau and Arana are
attempting to be federally recognized as quilombo and indigenous communities
respectfully. If they are recognized, tensions with the surrounding community
could be heightened considerably. They are also seeking aide from international
NGOs to help with the construction of an arts and crafts/community house,
school and irrigation system. This means not only acquiring the knowledge of
grant writing but also successfully navigating NGOs’ conceptions of authentic
Indianness and Blackness; something that can be very different from how the
federal government and surrounding communities define these racial locations.
To get a better education, many young adults leave their communities for 2 or 3
years – leaving their children with their parents and sometimes creating a
feeling of detachment between these individuals and their communities. Basic
health care is of poor quality; the infant mortality rate, for example, is very
high. How might these new identities affect, both positively and negatively,
the quality of health care? Finally they are struggling with how to build the
economic base of their communities; unemployment is rampant and will likely
intensify as they assert their new identities. What sort of constraints and
possibilities do their new identities present for micro-development
projects?
Learning Objectives:
- Identity formation – genetic, cultural and political dimensions
- Defining mental health
- Status-based access to health care resources
Sex (workers) and the city
Joe Zunt
Abstract
Under Peru's criminal legislation,
prostitution is not classified as an offense for persons who engage in it and are
eighteen years of age or older. However,
any person promoting or favoring the prostitution of another will be sentenced
to a prison term of not less than two nor more than five years. The Barton Clinic
in Lima’s port city of Callao,
is one of four reference centers for sexually transmitted infections (STI) in
the Lima
metropolitan area. Under a national
program organized by the Peruvian Ministry of Health’s Program for the Control
of STI and AIDS (PROCETSS), the Clinic provides free periodic medical attention
to female sex workers, including clinical evaluation, diagnostic testing and
counseling services every 28 days. Each woman receives an official stamp on her
carnet after each screening that she is
required to show the brothel owner prior to renting a room for the day. The ability of the
Clinic to offer diagnostic and treatment services depends upon availability of
laboratory reagents, antibiotics and equipment from the Ministry of
Health. Periodic shortages can limit the
Clinic’s ability to provide some diagnostic services. The laboratory staff at the Clinic has
adapted to deficiencies of equipment: lack of an ELISA reader for HIV testing
means that ELISA results are interpreted manually; a broken incubator means
that diagnosis of gonorrheal infection is based on Gram stain rather than
culture. The centrifuge in use no longer
functions correctly.
After an afternoon of screening
female sex workers for STI in the public health clinic, the social worker,
physician and laboratory technologist have just enough time to grab an Inca
cola and snack from a street vendor before loading up the mobile medical van
with educational brochures and supplies before heading out to set up a
temporary examination room in a nearby hostel.
The social worker approaches a young woman standing on the corner
outside a bar. Once the social worker
identifies herself as part of a public health team providing healthcare to
female sex workers, the young woman accepts an invitation to discuss STI and
receive a gynecologic examination. The
young woman is 16 years old and has heard of HIV and syphilis, but is unable to
name any other STI or note what symptoms such infections may produce. She states she tries to use condoms with
clients when condoms are available and the client is willing. Sometimes she’ll have sex without a condom if
the client agrees to pay a higher price.
She is the third of five children and completed grade school; her
siblings earn money by selling newspapers and toys on the street corners. Her father is away most of the year working
in the copper mines but occasionally sends money home to buy food. The examination does not reveal an STI, but
her pregnancy test is positive.
Disciplinary Perspectives:
Public health, Public policy, International law, Medicine, Social work
Learning Objectives:
- Discuss effective approaches to surveillance and treatment of sexually transmitted
infections in high risk populations and their clients.
- Evaluate the impact of Peruvian law on access to care for commercial sex workers.
- Examine how Peru has adopted aspects International law regarding sex workers.
- Identify impediments to health care access for adolescent sex workers.
- Explore how social service agencies and NGOs could provide useful services to CSW
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