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Key Points
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Straightforward research findings can speed changes in
clinical practices.
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Research findings that are extensively disseminated are
most likely to be used.
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Political support for and timeliness of research findings
can be essential for moving them into practice.
- Increasing interactions among researchers, policy-makers,
and practitioners can further hasten research utilization.
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Many factors can facilitate the speed and ease with which research
results are incorporated into practice. The presence of these factors
does not guarantee implementation of research findings, but the more
factors that are in place, the greater the chances of success.
One key factor is the nature and complexity of the research question,
which often determines how easily it can be investigated and how
straightforward the study conclusions will be. Various study designs are
used to evaluate different types of research questions pertaining to
reproductive health. One of two basic categories of studies —
observational — is commonly used to answer questions about disease
prevalence, natural history, cause, and risk groups. Observational
studies may appropriately be used for ethical, financial, or logistical
reasons, or because the research question requires this approach.
However, these studies — while identifying associations among
variables — are less able to identify direct causal relationships than
are randomized controlled trials. Such trials, involving an intervention
to prevent or change the course of a disease, are especially well suited
to test the safety and efficacy of drugs or devices.1
Particularly straightforward findings from a randomized controlled
trial in Uganda are among several unique factors that recently
contributed to rapid and positive changes in clinical practice (see Nevirapine
Results Quickly Put into Practice).
The trial determined the effectiveness of single-dose nevirapine
versus a specific regimen of short-course zidovudine (AZT) to prevent
mother-to-child transmission of HIV.2 Enrollment of some 600
women and their infants occurred quickly, and rates of adherence to the
drug regimens were high. The proportion of women and infants who
remained in the trial through completion, the most important component
of avoiding study bias, was also high. "After eight weeks, 98
percent of mother-infant pairs had been followed-up, and at 16 weeks, 97
percent," says Dr. Willard Cates Jr., president of FHI's Institute
for Family Health . "In any setting, especially in a resource-poor
setting like Uganda, these are phenomenal study vital statistics,"
he says.
The results of the study were also highly significant, demonstrating
that nevirapine was nearly 50 percent more effective than this AZT
regimen at preventing transmission. Moreover, the research had a strong
potential to make a highly desired public health impact of saving the
lives of babies, which it eventually did.
Strategic dissemination
Like the strength of research results, specific ways of disseminating
results can help facilitate their use. Most research findings are
passively disseminated through academic seminars and publication in
peer-reviewed journals, but more active dissemination involving a broad
range of stakeholders — key decision-makers, health professionals, and
the community — can increase their acceptance.
Type and scale of dissemination are among the best predictors of
research utilization, according to a review of eight operations research
projects conducted between 1988 and 1993 by the Population Council's
Africa Operations Research and Technical Assistance Project I.3
(Operations research seeks to assess factors contributing to
programmatic success or failure and to test new and potentially better
approaches to service delivery.) Studies with the most extensive
dissemination efforts were the most utilized, this operations research
in Africa showed.
One study disseminated and utilized most extensively was a pilot
project of community-based distribution of contraceptives, conducted
from 1990 to 1993 by the Ministry of Health in Mali (see Community-Based
Distribution Project Expands Beyond Mali). Dissemination activities
included development and distribution of reports on five different
aspects of the study; dissemination seminars during the study; an
international workshop on the final results; and presentation of study
findings at regional and international meetings. Communicating results
with messages, and through channels, appropriate to specific audiences
was an important dissemination strategy, says Dr. Ian Askew, a
Population Council senior program associate and coauthor of the review
of the eight operations research projects. "This requires many more
resources, but is also much more effective," he says.
Supportive context
Another factor that can facilitate or hinder research utilization is
the economic, political, or programmatic environment in which the
research is conducted and eventually implemented. The timeliness of
research in any of these contexts can be important, as is depicted in a
case study regarding IUD provision in Turkey (see IUD
Insertion by Nurse-Midwives Increases Use).
In some cases, however, compatibility of research with existing
cultural beliefs may be even more important. Lessons learned from
interventions and operations research to eradicate female genital
cutting (FGC) throughout Africa demonstrate this point. Multiple factors
facilitating research utilization have been present in the settings
where this research is being conducted (including Egypt, Burkina Faso,
Mali, and Kenya). Research clearly shows that FGC has negative health
consequences, including hemorrhage, infections, complications during
childbirth, and psychological scarring. And the political environment is
supportive of eradication: Burkina Faso, Ghana, and Senegal all have
national laws banning FGC. Nevertheless, utilization of the FGC research
has been slow.
In Mali, where FGC prevalence is more than 90 percent, several
nongovernmental organizations (NGOs) have been working to eradicate this
practice. In particular, three local NGOs have educated traditional
practitioners on FGC's negative health effects, trained them to advocate
discontinuation of the practice, and suggested alternative sources of
income. But an evaluation of the work of these three NGOs in 1996 showed
that many practitioners were not convinced that FGC is a harmful
practice and were continuing to perform it, despite the interventions.4
Many of these early efforts by NGOs to eradicate FGC emphasized the
adverse health effects of the practice, says Dr. Askew, who is also an
associate director of the Frontiers in Reproductive Health Program
(carried out by the Population Council, FHI, and Tulane University),
which conducted the evaluation in Mali. But the original emphasis on
health did not sufficiently address the fact that FGC is essentially a
cultural practice. "So several groups are now trying different and
innovative ways of addressing the practice from a sociocultural
perspective," he says.
In Kenya, for example, where FGC is practiced as a traditional rite
of passage for young women, the local NGO Maendeleo Ya Wanawake (MYWO)
has been working for years to encourage communities to abandon FGC. As
an alternative to this tradition, MYWO suggests that families hold
similar ceremonies that do not include genital cutting. An assessment in
2000 of this "alternative rite" program showed that families
who took part in alternative ceremonies were more likely than others to
know about the negative health consequences of FGC and to attribute to
MYWO some of their decisions to abandon FGC.5
Research utilization mediators
Those who have a stake in utilization of research findings can
provide essential support to move research findings into practice. But
different stakeholders do not always have the same views on whether or
how to push findings forward. A mediator — such as an influential
political leader, a researcher, an entire organization, or an advocate
or "champion" for utilization — can also help.
"Anything that can bridge the gap between research and practice
is important," says Matthew Tiedemann, senior program manager and
research utilization expert at FHI. "Use of mediators, which
increases interaction between researchers, policy-makers, and
practitioners, can help ensure that stakeholders are aware of the
others' needs and contributions. That can reduce the time lag between
research and its utilization."
In an ongoing project to implement a new single-visit approach for
cervical cancer prevention in rural Thailand (see A
Single-Visit Approach for Cervical Cancer Prevention), an
influential member of the medical community is acting as a mediator,
says Dr. Paul Blumenthal, director of JHPIEGO's Cervical Cancer
Prevention Program. JHPIEGO is collaborating with the Royal Thai College
of Obstetricians and Gynaecologists (RTCOG) on the project.
This single-visit approach, involving visual inspection of the cervix
with acetic acid and a light source and then immediate treatment of
precancerous lesions with cryotherapy, is safe, acceptable, and feasible
in rural Thailand, a recent study has shown.6 The mediator
— Dr. Khunying Kobchitt Limpaphayom, who is a well-known professor at
Chulalongkorn University in Bangkok, the project director of JHPIEGO's
Cervical Cancer Prevention Program in Thailand, and a member of the
research team — will continue to be especially important as the
project is expanded. "Because she is well respected and well
connected, and because many people recognize that women's health issues
are important to her, Dr. Limpaphayom can draw attention to the
topic," says Dr. Blumenthal. "It is also clear that without
her, we would not have been able to garner as much collaboration and
support as we have."
As president of RTCOG during the project's conception, Dr.
Limpaphayom was instrumental in developing an initial RTCOG/JHPIEGO
collaboration. She was also pivotal in gaining the support of the
Ministry of Public Health and in creating a project advisory board. That
board helps convey project information to Ministry members who can
consider further project implementation.
"This single-visit approach is important for my country,"
says Dr. Limpaphayom. "It can help save many lives, since, for the
time being, we cannot offer Pap smear screening for all women. My goal
is to decrease mortality from cervical cancer, so I want to get this
research into practice as quickly as possible. There is no time to
waste."
— Kerry L. Wright
References
- Stephenson JM, Babiker A. Overview of study design in clinical
epidemiology. Sex Transm Inf 2000;76(4):244-47.
- Guay LA, Musoke P, Fleming T, et al. Intrapartum and neonatal
single-dose nevirapine compared with zidovudine for prevention of
mother-to-child transmission of HIV-1 in Kampala, Uganda: HIVNET 012
randomised trial. Lancet 1999;354(9181):795-802.
- Solo J, Cerulli A, Miller R, et al. Strengthening the utilization
of family planning operations research: findings from case studies
in Africa. Unpublished paper. New York, NY: Population Council,
1998.
- Frontiers in Reproductive Health. Mali Female Genital Cutting.
FGC Excisors Persist Despite Entreaties, OR Summary 2.
Washington, DC: Population Council, Frontiers in Reproductive
Health, 2000.
- Frontiers in Reproductive Health. Kenya Female Genital Cutting.
Community Sensitization Must Precede Alternative Coming-of-Age Rite,
OR Summary 27. Washington, DC: Population Council, Frontiers in
Reproductive Health, 2002; Chege JN, Askew I, Liku J. An
Assessment of the Alternative Rites Approach for Encouraging
Abandonment of Female Genital Mutilation in Kenya. Nairobi,
Kenya: Population Council, 2001.
- Royal Thai College of Obstetricians and Gynaecologists (RTCOG) and
the JHPIEGO Corporation Cervical Cancer Group. Safety,
acceptability, and feasibility of a single-visit approach to
cervical-cancer prevention in rural Thailand: a demonstration
project. Lancet 2003;361(9360):814-20.
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A randomized controlled trial conducted in the late 1990s in
Kampala, Uganda,1 helped to create — at an
unprecedented pace — a standard for preventing mother-to-child
transmission of HIV in the developing world.
The rate of HIV transmission from mother to child in
developing countries is estimated to be as high as 43 percent,2
with most cases occurring late in pregnancy or during labor and
delivery.3 Recognizing the urgent need to reduce
these transmission rates, the international HIV Network for
Prevention Trials (HIVNET), established by the National
Institute of Allergy and Infectious Diseases (NIAID) in the
United States, supported the Ugandan trial. As trial
coordinator, FHI collaborated with Makerere University in
Kampala, Johns Hopkins University in Baltimore, MD, USA, the
University of Washington and the Fred Hutchinson Cancer Research
Center in Seattle, WA, USA, and several other partners to test
the safety and efficacy of the antiretroviral nevirapine versus
a specific regimen of the antiretroviral zidovudine (AZT) for
preventing transmission from more than 600 pregnant,
HIV-infected women to their infants.
Half of the women in the trial were randomly assigned to
receive a single dose of nevirapine at the onset of labor, and
their infants received a single dose within 72 hours of birth.
The other half of the women were assigned to receive doses of
AZT at the onset of labor and every three hours until delivery,
and their infants received twice-daily doses of AZT for a week
after birth. Results showed that nevirapine was 47 percent more
effective than AZT: Fourteen to 16 weeks after delivery, only 13
percent of infants given nevirapine were infected with HIV,
compared with 25 percent of infants given AZT.
The strength of the study findings and their potential for a
substantial public health impact — uniquely coupled with other
facilitating factors such as political interest and support,
strong advocacy, and nevirapine's low cost, readily available
supplies, and relatively easy storage and administration —
helped propel the findings into practice. In July 1999, interim
data were reviewed by the data and safety monitoring board
overseeing the study, and the findings were immediately released
to the public. In August 1999, nevirapine was included on the
agenda of an international working group meeting on
mother-to-child transmission of HIV, held by the Joint United
Nations Programme on HIV/AIDS (UNAIDS) to develop
recommendations for using new antiretroviral regimens. In
September 1999, the findings were formally published. By the
next year, the Elizabeth Glaser Pediatric AIDS Foundation had
raised more than U.S. $15 million to establish a "Call to
Action" project to support implementation of the findings.
Approximately 50 nevirapine programs have now been
established in at least 17 countries, and this simple regimen is
now the standard for preventing mother-to-child transmission of
HIV in many parts of the developing world. Recent research has
confirmed the safety and effectiveness of nevirapine,4
which may help governments in other countries adopt the
practice.
"We estimate that more than 250,000 women have been
offered voluntary HIV counseling and testing through Call to
Action programs established by the Elizabeth Glaser Pediatric
AIDS Foundation, more than 27,000 HIV-infected women have been
identified, and at least half of these women have received
nevirapine," says Dr. Willard Cates Jr., president of FHI's
Institute for Family Health. "Thousands of infants have
been spared HIV infection as a result of this finding and its
utilization."
— Kerry L. Wright
References
- Guay LA, Musoke P, Fleming T, et al. Intrapartum and
neonatal single-dose nevirapine compared with zidovudine for
prevention of mother-to-child transmission of HIV-1 in
Kampala, Uganda: HIVNET 012 randomised trial. Lancet
1999;354(9181):795-802.
- The Working Group on Mother-to-Child Transmission of HIV.
Rates of mother-to-child transmission of HIV-1 in Africa,
America, and Europe: results from 13 perinatal studies. J
Acquir Immune Defic Syndr Hum Retrovirol
1995;8(5):506-10.
- Rouzioux C, Costagliola D, Burgard M, et al. Estimated
timing of mother-to-child human immunodeficiency virus type
I (HIV-1) transmission by use of a Markov model. The HIV
Infection in Newborns French Collaborative Study Group. Am
J Epidemiol 1995;142(12):1330-37; Bertolli J, St. Louis
ME, Simonds RJ, et al. Estimating the timing of
mother-to-child transmission of human immunodeficiency virus
in a breast-feeding population in Kinshasa, Zaire. J
Infect Dis 1996;174(4):722-26.
- Moodley D, Moodley J, Coovadia H, et al. A multicenter
randomized controlled trial of nevirapine versus a
combination of zidovudine and lamivudine to reduce
intrapartum and early postpartum mother-to-child
transmission of human immunodeficiency virus type 1. J
Infect Dis 2003;187(5):725-35.
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Community-Based
Distribution Project Expands beyond Mali
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An operations research project to introduce community-based
distribution (CBD) of contraceptives into two rural areas of
Mali has expanded to thousands of Malian villages and has been
replicated in at least six countries. This is also an excellent
example of how research and program implementation can inform,
build upon, and strengthen each other through repeated
interplay.
According to the 1987 Mali Demographic and Health Survey,
nearly half of Malian women wished to use a contraceptive
method. But, largely due to lack of information or family
planning services in rural areas, contraceptive prevalence was
only 1 percent.1
Spurred by this dramatic evidence of unmet need, the Family
Health Division of the Ministry of Health (MOH), with funding
from the U.S. Agency for International Development (USAID)
mission in Mali, began in 1990 a three-year CBD pilot project to
bring contraceptive services to rural Malians.
"Community involvement was a very important part of the
project," says Dr. Seydou Doumbia, a program associate in
the Mali office of the New York-based Population Council, which
provided technical assistance through its Africa Operations
Research and Technical Assistance Project I. At the start of the
CBD project, the study team held meetings with community leaders
and members from 54 Malian villages in the Sikasso and Koulikoro
regions to gain commitment to the project. Because men are
traditionally the heads of households and the decision-makers in
Mali, it was especially important to reach them. This took some
time, says Dr. Doumbia, but after nine months of meetings, the
study team gained their support.
The next step was to select CBD workers. One male and one
female CBD worker were selected from each of the 54 villages.
They were then trained to provide family planning information
and to sell condoms, spermicides, and oral contraceptive pills.
The main component of the project was a large information,
education, and communication strategy designed specifically for
Mali, where oral communication and theater groups are the
traditional communication channels. CBD workers held weekly
meetings with village members to deliver family planning
messages; they also made home visits to counsel clients and
provide contraceptives. A local theater group then emphasized
the CBD workers' messages during performances at the village
meetings.2
An evaluation of the project in 1993 showed that knowledge of
family planning increased from 40 percent to 85 percent in
project areas, and contraceptive prevalence increased from less
than 1 percent to more than 30 percent, says Dr. Doumbia. After
an aggressive campaign to disseminate project findings, the MOH
decided to create a national CBD program, and the USAID mission
in Mali provided about U.S. $8 million for the expansion.
"From 1993 to 1999, we expanded the project to five
regions in Mali, and now we are working in about 3,000 villages
with 6,000 CBD workers," says Dr. Doumbia. "Through
this project, we were able to bring family planning services to
more than 20 percent of rural villages in Mali."
The CBD program in Mali is now being sustained through the
MOH (without USAID funding) and has been adapted in many West
African countries, including Burkina Faso, Cameroon, Côte
d'Ivoire, Guinea, Niger, and Senegal.
"Senegal represents the most recent example of the CBD
expansion," says Dr. Diouratié Sanogo, program associate
for the Frontiers in Reproductive Health Program, which is
leading the effort, and a Population Council representative in
Dakar.
There, researchers are comparing two models for providing
reproductive health services to rural communities. One involves
strengthening the capacity of traditional community health huts
by updating equipment and retraining workers to provide
reproductive health services. (Health hut workers, including
traditional birth attendants, hygienists, and health
communicators, are traditionally trained to provide only basic
health care and prevention services to rural community members
who visit the huts). To provide more mobile services, the second
model uses voluntary community workers who are trained to
provide reproductive health services and act as CBD workers.
Evaluation of the two models is under way.
— Kerry L. Wright
References
- Centre d'Études et de Recherches sur la Population pour
le Développement, Institut du Sahel and Demographic and
Health Surveys Institute for Resource
Development/Westinghouse. Enquête Démographique et de
Santé au Mali 1987. Bamako, Mali, and Columbia, MD:
Centre d'Études et de Recherches sur la Population pour le
Développement, Institut du Sahel and Demographic and Health
Surveys Institute for Resource Development/Westinghouse,
1989.
- Doumbia S. Male and community involvement in family
planning: community-based distribution project in Mali
(1990-1999). The 122nd annual meeting of the American Public
Health Association, Washington, DC, 1994.
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IUD Insertion
by Nurse-Midwives Increases Use
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| Over a 15-year period, intrauterine device
(IUD) prevalence more than doubled in Turkey after
recommendations from a collaborative operations research effort
influenced ratification in 1983 of the national family planning
law that, among other changes, allowed trained nonphysicians to
provide IUD services.
Before that, in the 1970s, only physicians
could provide IUDs, and most physicians were male. But many
women were uncomfortable being examined or having an IUD
inserted by a male physician, thus limiting acceptance and use
of the IUD.
Together, the Ministry of Health (MOH) and
researchers in the Public Health Department of Hacettepe
University in Ankara, Turkey, recognized this problem. Supported
by the World Health Organization (WHO) Programme in Human
Reproduction, the researchers began studying whether trained
nonphysicians — particularly nurse-midwives — could
adequately provide IUD services.
"The lead investigator from Hacettepe
University had the foresight to involve the Ministry of Health
in the project from the outset," says Dr. Iqbal Shah of the
Department of Reproductive Health and Research at WHO.
Furthermore, the Director General of Maternal and Child Health
and Family Planning at the time was a coinvestigator of the
project, facilitating wide dissemination of results and
mobilizing support for research utilization, he says.
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Research has shown that the Copper T IUD
can be safely provided by trained nonphysicians.
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In 1979, 13 female nurse-midwives from a
district near Ankara learned to provide IUD services using a
training program designed specifically for this research. The
program involved use of a specially developed WHO manual for
providing IUD services, followed by practice. Nurse-midwives in
training used pelvic models, gave real pelvic examinations, and
performed supervised IUD insertions.1 Researchers
then determined how well the trained nurse-midwives provided IUD
services, compared with six male and two female physicians.2
After 238 IUD insertions by physicians and 257 by
nurse-midwives, no significant differences were found in terms
of IUD expulsions, IUD removals, pregnancies, losses to
follow-up, and referrals to obstetrician/gynecologists.
Study findings were published in February
1983 and disseminated to the MOH, policy-makers, and the medical
community in Turkey. Findings from a similar, unpublished
WHO-supported study of some 200 nurse-midwives were also
disseminated, with a recommendation that legislation be changed
to allow nonphysicians with appropriate training to provide IUD
services. Policy-makers and the medical community showed some
resistance, but the MOH and Hacettepe University countered with
several advocacy meetings to convince the two groups of the
proposal's merits.3
The resistance eventually weakened. On May
24, 1983, the second anti-natalist population planning law,
which included a provision allowing nonphysicians to provide IUD
services, went into effect.
"In my opinion, if we had not performed
this operations research on these sensitive issues, it would
have been either impossible or too hard to change the existing
population planning law" to include that provision, says
Dr. Ayse Akin, the lead investigator from Hacettepe University.
Training of nurse-midwives to provide IUD
services was added to regular national training programs, and in
the 15 years after the law was ratified, IUD prevalence among
contracepting women steadily increased from 9 percent to 20
percent, says Dr. Akin.
The studies that influenced ratification of
the population planning law in Turkey, which also included
research from the Philippines,4 focused on the Lippes
loop IUD. FHI and others have conducted similar studies on
Copper T IUD provision in Turkey, Mexico, Nigeria, Brazil, and
Thailand, showing that nonphysicians with proper training can
also safely provide services involving this type of IUD.5
—Kerry L. Wright
References
- Akin A, Gray RH, Ramos R. Training auxiliary
nurse-midwives to provide IUD services in Turkey and the
Philippines. Stud Fam Plann 1980;11(5):178-87.
- Eren N, Ramos R, Gray RH. Physicians vs. auxiliary
nurse-midwives as providers of IUD services: a study in
Turkey and the Philippines. Stud Fam Plann
1983;14(2):43-47.
- Akin A, Ozvariüs SB, Fisek N. Integrating an Expanded
Range of Reproductive Health Services in Primary Health
Care: Turkey's Experience. International Council on
Management of Population Programmes. Available online.
- Akin, Gray, Ramos; Eren.
- Farr G, Rivera R, Amatya R. Non-physician insertion of
IUDs: clinical outcomes among TCu380A insertions in three
developing-country clinics. Adv Contracept
1998;14(1):45-57; Lassner KJ, Chen CHC, Kropsch LAJ, et al.
Comparative study of safety and efficacy of IUD insertions
by physicians and nursing personnel in Brazil. Bull Pan
Am Health Organ 1995;29(3):206-15; Wright NH, Sujpluem
C, Rosenfield AG, et al. Nurse-midwife insertion of copper T
in Thailand: performance, acceptance, and programmatic
effects. Stud Fam Plann 1977;8(9):237-43.
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A Single-Visit
Approach for Cervical Cancer Prevention
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The recent demonstration of the safety and acceptability of a
single-visit approach for cervical cancer prevention in rural
Thailand emphasizes the importance of having appropriate
resources and infrastructure to implement research findings.
Nearly half a million women develop cervical cancer each year
worldwide, and it is the leading cause of death due to cancer
among women in developing countries. Several countries,
including Thailand, have traditional cervical cancer prevention
programs based on the Pap smear, a cytology-based screening
tool. But Pap smears require special training, laboratory
equipment, and repeat visits for clients. (Screening can be
performed in one visit, but results can take quite a while to
obtain, diagnoses can only be confirmed later, and women must
return to the clinic if treatment is necessary.) The
infrastructure in many resource-poor settings cannot sustain
such programs, and screening rates remain low. In Thailand, only
about 5 percent of women have been screened.1
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Nurses in Thailand learn to use a new single-visit
approach to cervical cancer prevention that research
has shown to be safe, effective, and inexpensive.
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An alternative to Pap smears is visual inspection of the
cervix with acetic acid and a light source, followed by
provision of cryotherapy (freezing) of suspected precancerous
cervical lesions — all in a single visit.
Researchers from U.S.-based JHPIEGO's Cervical Cancer
Prevention Program and the Royal Thai College of Obstetricians
and Gynaecologists (RTCOG), with support from the Ministry of
Public Health in Thailand, conducted a demonstration study of
this single-visit approach in Roi-et Province in 2000.2
Twelve nurses were trained to use the approach and then used it
to screen nearly 6,000 women in village centers and district
hospitals. Both low-cost3 and effective at detecting
most precancerous lesions,4 the single-visit approach
also proved safe and very acceptable to women.
"Now it is time for the local Ministry of Health to
decide whether it wants to adopt this approach on a larger, if
not a national, scale," says Dr. Paul Blumenthal, director
of JHPIEGO's Cervical Cancer Prevention Program.
For now, the Ministry of Public Health has decided not to
officially change any national service delivery policies to
include the new approach. But it is supporting implementation in
more provinces, as long as the provinces have sufficient
resources.
The most difficult step for the provinces is going to be
program start-up, says Dr. Blumenthal. This will require
extensive training, purchases of equipment, and development of
infrastructures to deliver the new services. Once these factors
are in place and the programs are running well, they should be
sustainable, he says.
The chief provincial health officer of Roi-et Province at the
time of the initial study has since moved to Nong Kai Province,
where he and the Ministry of Public Health are spearheading an
effort to expand the single-visit approach. The team from
JHPIEGO and RTCOG has provided training and supervision of nurse
providers for the program, which screened its first patient
earlier in 2003.
"We are also helping in training and preparation for
another four provinces in northeast Thailand to implement this
single-visit approach," says Dr. Khunying Kobchitt
Limpaphayom, project director of JHPIEGO's Cervical Cancer
Prevention Program in Thailand. "Northeast Thailand is
considered the area with the fewest resources, so implementation
will require a lot of leadership and commitment from the chief
provincial health officers there. The results remain to be
seen."
— Kerry L. Wright
References
- Royal Thai College of Obstetricians and Gynaecologists (RTCOG)
and the JHPIEGO Corporation Cervical Cancer Group. Safety,
acceptability, and feasibility of a single-visit approach to
cervical-cancer prevention in rural Thailand: a
demonstration project. Lancet 2003;361(9360):814-20.
- Royal Thai College of Obstetricians and Gynaecologists (RTCOG).
- Mandelblatt JS, Lawrence WF, Gaffikin L, et al. Costs and
benefits of different strategies to screen for cervical
cancer in less-developed countries. J Natl Cancer Inst
2002;94(19):1469-83; Goldie SJ, Kuhn L, Denny L, et al.
Policy analysis of cervical cancer screening strategies in
low-resource settings: clinical benefits and
cost-effectiveness. JAMA 2001;285(24):3107-15.
- University of Zimbabwe and JHPIEGO Cervical Cancer
Project. Visual inspection with acetic acid for
cervical-cancer screening: test qualities in a primary-care
setting. Lancet 1999;353(9360):869-73.
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For more information, visit Family Health International's Website at www.fhi.org
Go to FHI's Network
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