|
Intrauterine devices (IUDs) are contraindicated or considered
undesirable for women at risk of sexually transmitted diseases (STDs),
including HIV, or for women infected with STDs.
Concerns focus on health risks to the woman, as well as to her sexual
partner. Yet, for some of these women and their partners, IUDs may be
effective, safe and desirable as long as the women have access to
appropriate medical tests or services.
Like other nonbarrier contraceptive methods, IUDs do not protect men
or women from any STD. HIV-positive women and men should always be
encouraged to advise their partners of their HIV status and to use
condoms consistently.
The World Health Organization's (WHO) medical eligibility criteria
for safe use of contraceptives state that insertion of a Copper T IUD in
an HIV-infected woman or one who is at high risk of infection is not
usually recommended.1 Safety concerns for HIV-positive women
using IUDs include the fear that a woman's immune system may be weakened
and unable to fight off infections, such as other STDs that could lead
to pelvic inflammatory disease (PID). This inflammation of a woman's
upper genital tract -- quite often caused by the bacteria Neisseria
gonorrhoeae or Chlamydia trachomatis -- can lead to chronic pelvic pain,
infertility, ectopic pregnancy and sometimes even death.
However, recent research conducted in Kenya by investigators at the
University of Nairobi and FHI found that 156 HIV-infected women --
including those whose immune systems were suppressed at the time of IUD
insertion -- had no more overall complications at one, four and 24
months following insertion than did 493 uninfected women.2
Overall complications were defined as PID; removal due to infection,
bleeding or pain; and expulsion or pregnancy.
"There was weak evidence of more infection-related complications
-- defined as PID, pelvic tenderness, and removal due to infection or
pain -- with IUD use longer than five months," says Dr. Charles
Morrison, an FHI epidemiologist who designed the research.
"Nevertheless, PID was rare among both HIV-infected and uninfected
IUD users. These findings suggest that the IUD may be a safe
contraceptive method for appropriately selected HIV-infected women with
continuing access to medical services. It also suggests that IUDs should
continue to be offered in areas with high prevalence of HIV."
WHO guidelines were published in 1996, before the Kenyan study was
conducted. However, until further research clarifies the issue, WHO is
not expected to change its guidelines stating that use of a copper IUD
is not usually recommended for HIV-infected women, says Dr. Patrick
Rowe, medical officer of WHO's Department of Reproductive Health and
Research.
Safety concerns for the sexual partners of HIV-infected IUD users
arise from the fact that IUDs can cause an increase in menstrual
bleeding (heavier or irregular bleeding). Greater exposure to infected
blood theoretically could increase a partner's risk of infection. In
theory, IUDs may also increase cervical shedding of HIV-infected cells,
which may increase a partner's exposure.
However, in the Kenya study of HIV-infected women, no increase in
cervical shedding of HIV occurred four months after IUD insertion,
compared to before IUD insertion.3 And IUD use did not
increase HIV transmission to the male partner in the only study to
consider the effect of IUD use on female-to-male HIV transmission. In a
study among 563 couples, only one of 10 men whose regular partner was an
HIV-infected IUD user became infected. This infection rate was similar
to that of 86 men whose partners were HIV-infected women not using IUDs
or other contraception.4 "The data from these studies
suggest that IUD use by HIV-infected women does not appear to make them
more infectious to their sexual partners," says Dr. Morrison.
Studies of some 1,400 women seen at family planning clinics in
Tanzania and some 800 sex workers seen at an STD clinic in Kenya suggest
that IUD use does not increase a healthy woman's risk of acquiring HIV
from an infected sexual partner,5 although some study results
are conflicting.
|
Percentage of Women Who Developed
Pelvic Inflammatory Disease Following IUD Insertion |
| Country |
Cervical
infection present at insertion |
No
cervical infection present at insertion |
| Kenya1 |
4.3% of 117
women |
1.3% of 670
women |
| Kenya2* |
3.1% of 32
women |
0.4% of 548
women |
| Brazil3 |
5.2% of 19
women |
0.0% of 308
women |
|
* Cervical infection diagnosed at one month
after IUD insertion.
References
- Sinei SK, Schulz KF, Lamptey PR, et al.
Preventing IUCD-related pelvic infection: the efficacy of
prophylactic doxycycline at insertion. B J Obstet Gynaecol 1990;97(5):412-19.
- Morrison CS, Sekadde-Kigondu C, Miller WC,
et al. Use of sexually transmitted disease risk assessment
algorithms for selection of intrauterine device candidates. Contraception
1999;59(2):97-106.
- Faúndes A, Telles E, Cristofoletti ML, et
al. The risk of inadvertent intrauterine device insertion in
women carriers of endocervical Chlamydia trachomatis.
Contraception 1998;58(2):105-9.
|
Other STDs
Any woman with a cervical infection -- particularly gonorrhea or
chlamydia -- is at greater risk of PID than an uninfected woman, whether
or not she is using an IUD. Women at high risk for cervical infections
include those living in areas with a high prevalence of the diseases,
and those who engage in high-risk sexual behaviors, such as having
multiple sexual partners or having sex with a man who has multiple
partners.
"Among women who have an IUD inserted, women with cervical
infections appear more likely to develop PID than are women who do not
have a cervical infection," Dr. Morrison says. What accounts for
this small increase in PID risk? It is thought that the process of IUD
insertion can introduce STD-causing bacteria from the cervix into the
uterus and fallopian tubes, which can later cause PID. WHO studies
involving nearly 23,000 IUD insertions demonstrated that IUD users
rarely develop PID after the first 20 days following insertion. The rate
of PID immediately after insertion was 9.7 per 1,000 woman-years.
Thereafter, for up to eight years later, PID risk among IUD users was
1.4 per 1,000 woman-years.6 PID risk among non-IUD users
varies, largely depending upon the STD prevalence in an area.
Recent studies have shown that about 95 percent of women with
cervical infections did not develop PID in the months following IUD
insertion. Yet, identifying women with cervical infections or those who
are at increased risk is desirable, since the PID risk is higher for
these women.
Women who are identified with cervical infections usually are denied
IUD use. WHO's medical eligibility criteria for safe use of
contraceptives state that current infection with an STD contraindicates
IUD use, as does any previous STD infection that has not been cured for
at least three months. An IUD usually is considered undesirable for a
woman at increased risk of STDs.7
Current research, however, indicates IUD use may be unnecessarily
restricted for some women, says Dr. David Grimes, FHI vice president of
biomedical affairs. For example, after the insertion period, most pelvic
inflammatory disease in IUD users is thought to be acquired from men
with STDs. "While international guidelines recommend that women who
choose any other contraceptive method -- pills, injectables, implants,
sterilization -- use male latex condoms for STD protection, guidelines
do not suggest such dual method use for IUD users," he says.
"Guidelines simply prohibit use of IUDs and recommend women choose
another contraceptive." Dr. Grimes suggests that recommending dual
method use may be appropriate for some IUD users.
While some providers are becoming aware that new research raises
questions about the guidelines, they continue to follow them to be
prudent. "What we teach students about IUDs and currently practice
in Kenya is based upon WHO recommendations," says Dr. Boaz
Otieno-Nyunya of Moi University, Eldoret, Kenya, and a former FHI
fellow. "We are being conservative."
|
Antibiotics
Before Insertion |
|
In general, giving women antibiotics before IUD insertion has
little impact on the rate of pelvic inflammatory disease (PID),
although such antibiotic use may be justified in some populations
with high STD prevalence. Further research is needed to resolve
the question of whether to offer antibiotics prophylactically to
certain IUD recipients.
Dr. David Grimes and Dr. Ken Schulz of FHI recently analyzed
four randomized, controlled trials of antibiotic use before IUD
insertion that were conducted in Kenya, Nigeria, the United States
and Turkey.1 "A uniform finding of these trials," they
wrote, "was the low risk of IUD-associated infection, with or
without the use of antibiotic prophylaxis. However, in populations
with a high prevalence of STDs, antibiotic prophylaxis may offer
modest protection against PID."
In the FHI-sponsored study in Kenya, where the prevalences of
gonorrhea and chlamydial infections were high (3 percent and 11
percent, respectively, among all women in the trial), the rate of
PID was about a third lower among women receiving 200 mg of
doxycycline orally at the time of IUD insertion, compared with
women receiving a placebo. This difference, however, was not
statistically significant.
In a similar FHI-sponsored trial in Nigeria, where the
prevalences of gonorrhea and chlaymdial infections were lower than
in Kenya (1 percent and 7 percent, respectively, among all women
in the trial), the rate of PID was no different among women
receiving doxycycline than among those receiving a placebo. The
United States and Turkish studies found no significant overall
benefit of using the antibiotics doxycycline or azithromycin
before IUD insertion to reduce risk of PID.
-- Kim Best
Reference
- Sinei SK, Schulz KF, Lamptey PR, et al.
Preventing IUCD-related pelvic infection: the efficacy of
prophylactic doxycycline at insertion. Br J Obstet Gynaecol
1990;97(5):412-19; Ladipo OA, Farr G, Otolorin E, et al.
Prevention of IUD-related pelvic infection: the efficacy of
prophylactic doxycycline at IUD insertion. Adv Contracept 1991;7(1):43-54;
Walsh T, Grimes DA, Frezieres R, et al. Randomised controlled
trial of prophylactic antibiotics before insertion of
intrauterine devices. Lancet 1998;351(9108):1005-8;
Zorlu CG, Aral K, Cobanoglu O, et al. Pelvic inflammatory
disease and intrauterine devices: prophylactic antibiotics to
reduce febrile complications. Adv Contracept 1993;9(4):299-302.
|
Screening
Identifying women with cervical infections can be difficult. When
available, laboratory tests to identify STDs associated with the
development of PID can rule out infection, making IUD insertion safe as
long as a woman abstains from sexual relations or uses a condom
correctly and consistently between the time of the test and IUD
insertion. But current lab tests require an additional clinic visit --
prior to the IUD insertion visit -- which entails time, money and
inconvenience for clients. Requiring such tests can discourage some
women from obtaining an IUD. Also, many clinics in developing countries
cannot afford laboratory tests for women requesting IUDs.
The WHO guidelines discouraging IUD use in women at STD risk were
designed with this in mind, says Dr. Rowe of WHO. "They are aimed
primarily at IUD providers in developing countries where there are no
laboratory facilities for ruling out current lower genital tract
infection," he says.
Providers lacking laboratory facilities can predict the likelihood of
STD infection by screening women requesting IUDs, such as asking about a
client's personal history. But this is a less precise way of ruling out
STD infection.
In a Brazilian study in which 327 women were deemed eligible for an
IUD after rigorous STD screening based on their sexual history and a
clinical exam, 19 (6 percent) were found after IUD insertion to have a
positive chlamydia laboratory test result, and one woman was diagnosed
with PID within two weeks of insertion.8 Screening included
questions about the socioeconomic characteristics and sexual behavior of
women and their partners, and evaluation of patients' gynecological
symptoms and signs.
The study's authors noted that the PID rate was low. Still, screening
procedures "were not as effective as previously assumed in
preventing insertion of the IUD among women with endocervical
infection," they concluded.
Yet, rigorous STD screening for IUD candidates, based on personal
history and clinical exams, should be maintained, says Dr. Soledad Díaz,
director of the Instituto Chileno de Medicina Reproductiva in Santiago,
Chile. Dr. Díaz, a member of the International Medical Advisory Panel
of the International Planned Parenthood Federation (IPPF), was one of
the experts who developed the WHO medical eligibility criteria. Such
screening is used successfully in Chile, where some 70 percent of women
receiving public-sector family planning services use the IUD. "As a
result of rigorous screening and treatment before IUD insertion of all
women with signs of infection, only one of some 5,000 patients receiving
an IUD in our clinic developed severe PID, and that occurred more than
one year after the insertion," says Dr. Díaz.
"Rigorous screening of women to identify those likely to have an
STD at the time of IUD insertion is especially important in developing
countries," she says. "If PID due to an undetected STD occurs
after an IUD is inserted, the PID can nearly always be treated with
antibiotics; however, many women in developing countries lack access to
medical services and treatment."
U.S. Agency for International Development guidelines recommend using
personal history and sociodemographic factors (such as marital status)
to predict the likelihood that an IUD candidate has an STD. A physical
exam of the reproductive organs may also detect some STDs. In some
settings, the guidelines state, it may be appropriate to supplement such
screening with laboratory tests.9
In the Republic of Karakalpakstan (Uzbekistan), where the majority of
contracepting women use IUDs, laboratory testing for syphilis, gonorrhea
and trichomoniasis is readily available through the public health
system, despite limited resources. "In addition, we have found it
helpful to provide screening and a clinical exam for women requesting
IUDs," says Dr. Oral Ataniyazova of the Karakalpak Center for
Reproductive Health and Environment.
However, criteria for identifying a woman's risk for STD are not
clearly stated in most family planning programs worldwide. Researchers
from AVSC International, in collaboration with the Instituto Mexicano
del Seguro Social (IMSS), recently found that the IMSS had no
established STD risk assessment protocol. The finding was part of a
larger assessment of the capacity of Mexican service delivery systems to
provide IUDs safely.10
Researchers also found that providers' clinical assessments of women
requesting IUDs were often incomplete. Providers conscientiously
reviewed medical histories and performed speculum exams, but did not
consistently perform manual exams. Speculum exams help providers observe
the cervix and any discharge associated with infection. Manual exams can
enable providers to identify abdominal tenderness caused by infection or
more serious conditions.
Similar studies were conducted by AVSC International in Kenya, Ghana
and Russia. Researchers found that manual exams of the reproductive
organs were not consistently performed, except in Ghana and one site in
Kenya, says Dr. Mark Barone, AVSC International medical associate and a
principal researcher for the studies. In all four countries, providers
were inconsistent in the questions they asked clients to assess their
risks of STDs.
Population Council researchers have measured the effect on
contraceptive method choice of giving Mexican women information about
contraceptives (including IUDs), their benefits and risks, and
information about STDs and PID. Half of the 2,107 women in the study,
which was conducted in a family planning clinic, were assigned to a
group that received this information and half were assigned to a
standard care group. Laboratory tests identified 2 percent of women as
having chlamydia or gonorrhea, although this information was not shared
with the women or their doctors until after they had indicated a
preferred method for themselves or their patients.
No infected woman actually received an IUD. But, despite being
trained to recognize the signs and symptoms of STDs, the doctors
recommended the use of IUDs to 95 percent of 21 infected women in the
standard care group. In contrast, only half of 23 infected women in the
informed group chose the IUD as an appropriate contraceptive for
themselves.
"This indicates that doctors can be trained about STDs and still
not be able to identify cervical infection" without the help of
laboratory tests, says Dr. Beverly Winikoff, program director of
reproductive health at the Population Council. "In addition, it may
be difficult for physicians to discuss STD risk with their patients.
Sexual behavior is a sensitive subject. A woman may know something that
puts her at risk, but not be able to recognize fully or admit the danger
to a health professional."
Some developing countries use algorithms -- a list of simple
questions about a client's behavior and social circumstances -- to
assess risk of infections. Even providers with little training can use
the algorithms to help decide whether women are eligible for IUDs when
laboratory tests are not available. However, the algorithms tend to be
imprecise. Researchers from the University of Nairobi and FHI have
developed an STD risk assessment algorithm to predict cervical infection
among IUD candidates seen at family planning clinics. Preliminary
findings are promising, but the new algorithm must be evaluated further.11
-- Kim Best
References
- World Health Organization. Improving Access to
Quality Care in Family Planning: Medical Eligibility Criteria for
Contraceptive Use. (Geneva: World Health Organization, 1996)132.
- Sinei SK, Morrison CS, Sekadde-Kigondu C, et al.
Complications of use of intrauterine devices among HIV-1 infected
women. Lancet 1998;351(9111):1238-41; Morrison C,
Sekadde-Kigondu C, Sinei S, et al. Is the IUD appropriate
contraception for HIV-infected women? Presentation at Thirteenth
Meeting of the International Society for Sexually Transmitted
Diseases Research, Denver, CO, USA, July 11-14, 1999.
- Richardson BA, Morrison CS, Sekadde-Kigondu C, et
al. Effect of intrauterine device use on cervical shedding of HIV-1
DNA. AIDS 1999;13(15):2091-97.
- European Study Group on Heterosexual Transmission
of HIV. Comparison of female to male and male to female transmission
of HIV in 563 stable couples. BMJ 1992;304(6830):809-13.
- Kapiga SH, Lyamuya EF, Lwihula GK, et al. The
incidence of HIV-1 infection among women using family planning
methods in Dar es Salaam, Tanzania. AIDS 1998;12(1):75-84;
Martin HL Jr., Nyange PM, Richardson BA, et al. Hormonal
contraception, sexually transmitted diseases, and risk of
heterosexual transmission of Human Immunodeficiency Virus Type 1. J
Infect Dis 1998;178(4):1053-59.
- Farley TM, Rosenberg MJ, Rowe PJ, et al.
Intrauterine devices and pelvic inflammatory disease: an
international perspective. Lancet 1992;339(8796):785-88.
- World Health Organization, 132.
- Faúndes A, Telles E, Cristofoletti ML, et al. The
risk of inadvertent intrauterine device insertion in women carriers
of endocervical Chlamydia trachomatis. Contraception 1998;58(2):105-9.
- U.S. Agency for International Development. Recommendations
for Updating Selected Practices in Contraceptive Use: Volume I.
(Washington: U.S. Agency for International Development, 1994)90.
- Factors Affecting the Safe Provision of IUDs: A
Service Delivery Perspective from Mexico. New
York: AVSC International and Instituto Mexicano del Seguro Social
(IMSS), 1999.
- Morrison CS, Sekadde-Kigondu C, Miller WC, et al.
Use of sexually transmitted disease risk assessment algorithms for
selection of intrauterine device candidates. Contraception 1999;59(2):97-106.
For more information, visit Family Health International's Website at www.fhi.org
Go to FHI's Network |