The management approach recommended in this manual is based on the
principle that testing and treatment can take place during the same visit
and that both can take place at the lowest level of the healthcare system
where the majority of at-risk women will go at least once in their lives.
Given that healthcare providers most often posted to such levels are
nurses or nurse-midwives, this approach assumes that both testing and
treatment can be performed competently by these or similar cadres of
healthcare personnel. A major advantage of the test and immediately treat
approach is that it offers a potential solution to the problem of
loss-to-followup (generally at least 20%) that occurs as a consequence of
delays in receiving laboratory-based screening results (e.g., between Pap
smear processing and return of lab results to local clinic) or referrals
to a different facility for treatment.
Currently, a test and treat approach to managing precancerous lesions
is increasingly being used when women undergo colposcopic examination for
a previous positive Pap smear. That is, if colposcopy confirms the results
of the Pap smear, many practitioners will proceed to treatment without
waiting for histological confirmation. To date, there is no large-scale
experience using a test and treat approach in conjunction with VIA. Data
from a recent South Africa study using VIA (Megevand et al 1996), however,
suggest that a VIA-based test and treat approach could work. In this
study, 76 (3.1%) out of 2,426 women screened were positive on VIA. Of
these, 61 (80.3%) had SIL on Pap smear, 65 (85.5%) on colposcopy and 55
(72.4%) on biopsy. In other words, 72% of women who tested positive with
VIA had a confirmed precancerous lesion on histology.
Treating Women with Unconfirmed Disease
For many developing countries, determining how best to test and treat
women on a large scale remains a problem. While the specificity of VIA is
relatively high, the positive predictive value (PPV) even in a high
prevalence setting was only about 20%. This means that four of every five
women in that population who tested positive on VIA did not have a
high-grade (CIN III) lesion and could potentially have been treated
(University of Zimbabwe/JHPIEGO Cervical Cancer Project 1999). Because of
the low morbidity associated with cryotherapy, however, as well as its
other advantages, treatment of all women with an abnormal VIA test
(test-positive) could be considered acceptable because of the potential to
significantly reduce future cervical cancer risk (see below). Also, if the
patient is unlikely to return for followup, some degree of over treatment
may be justified.
While this "over treatment" may translate into unnecessary
costs to the healthcare system as well as unnecessary discomfort and
potential side effects experienced by the women, in a low-resource
environment most women are unlikely to ever have the opportunity to have a
diagnosis confirming their true disease state. In such an environment,
offering treatment for suspicious precancerous lesions, which potentially
represent either no disease or only low-grade (CIN I) lesions, could be
considered a preventive measure against the later development of cervical
cancer. This is because cryotherapy has the potential to significantly
reduce the probability of developing cancer or precancerous lesions for at
least 5 to 10 years in women determined to be at high risk (Lonky et al
1997). Also, in many settings (especially third world settings) it is
standard practice to use cryotherapy or electrocautery for treatment of
chronic cervicitis. In such instances, either procedure results in
resolution of the cervicitis and reduction of cervical ectopy, which could
have a long-term protective effect against acquiring both HPV and HIV.
Lastly, recurrences after cryotherapy are more likely to involve one or
more types of HPV other than the one present before treatment. By
contrast, those seen following excisional treatment (e.g., LEEP) tend to
be of the same type (Nuovo, Banbury and Calayag 1991). Thus, if a woman
who is VIA test-positive is carrying one of the high-risk HPV types and is
treated by cryotherapy, this treatment could eliminate her existing HPV
type and possibly prevent her from ever developing a precancerous lesion.
Association Between HIV and Precancer of the Cervix
(CIN)
Data on the association between HIV and CIN are increasingly convincing.
Two studies, both from high HIV prevalence areas, demonstrate an
association between HIV and CIN (Table 8).
Table 8. Risk of CIN Among Women with HIV Compared to HIV Negative
Women
| Author |
Country |
Date |
Odds
Ratio
(of having) |
| Miotti et al |
Malawi |
1996 |
2.2
(1.10-4.8) |
| Maggwa et al |
Kenya |
1993 |
2.69
(1.29-5.49) |
The implications of these studies on the outpatient treatment for CIN
are significant. For example:
- Should women who are known to be HIV positive and who have cervical
dysplasia be offered treatment for CIN? If treatment is not offered or
accepted, will disease progress more quickly and the chance to prevent
development of cancer be lost?
- Will treatment of CIN in HIV-positive women be as effective? Will
recurrence rates be greater? Will complication rates be higher?
Clearly, more studies on the role of HIV infection as it relates to
increased susceptibility to CIN and the effectiveness of treatment for CIN
are needed. In addition, there is preliminary evidence that women who are
seropositive for HIV have increased shedding of HIV following treatment
(e.g., cryotherapy or LEEP) and during the healing process (Wright 1999).
Therefore, because of the increasing prevalence of HIV/AIDS in many
countries coupled with the limited availability of HIV testing to reduce
risks of HIV transmission before providing treatment, women need to be
counseled to either:
- abstain from sexual intercourse for up to 4 weeks (or until the
vaginal discharge is gone) following treatment, or
- use condoms if they have intercourse.
Linking cervical cancer screening and treatment services with other
reproductive health services is essential and logical, yet these services
remain distinctly separate in much of the world. This separation leaves
women without access to reproductive healthcare and contributes
significantly to women’s poor overall health status. The integration of
cervical cancer prevention with existing reproductive health services
clearly answers the broad-based call for making it "accessible
through the primary healthcare system, to all individuals of appropriate
ages as soon as possible" (ICPD 1994). Testing, treatment and the
necessary followup care for gynecological cancers is considered an
integral part of reproductive health by a range of international
organizations and was included in the Cairo Programme of Action (Jones
1999).
Overall, it is quite clear that the way to reduce the incidence of
cervical cancer is to:
- screen a large proportion of women at high risk at least once using
appropriate techniques, and
- treat women who test positive for possible high-grade dysplasia (VIA
positive) by simple outpatient techniques.
Table 9 provides information on the cervical
cancer screening and treatment services appropriate to different
healthcare facility levels and the need for community involvement to
promote awareness of cervical cancer prevention. There is now general
agreement that the interventions needed to save the lives and preserve the
health of women must form part of a broad strategy to improve reproductive
health. This strategy implies that interventions should be applied
holistically within a general health context that promotes equity in
access to and quality of care. Finally, in order to make the best use of
existing resources, these essential services should be integrated into and
operate through the existing primary healthcare systems.
As shown in Table 9, the district-level
health system is the basic unit for planning and implementing the
interventions outlined in this manual in developing countries. The
district provides a mechanism for linking families and communities with
health centers and hospitals in a functional, cost-effective manner.
Through district-based implementation of interventions, it is possible to
ensure that health services are available as close as possible to people’s
homes. Treatment procedures for precancerous disease of the cervix should
be carried out by the healthcare worker closest to the community who is
competent to perform them safely and effectively. The person best equipped
to provide community-based, appropriate technology, and safe and
cost-effective care to women during their reproductive lives is usually
the nurse or midwife who works in the community near the women she serves.
She can ensure that the healthcare system serves women fairly and
effectively and that the health services available respond to the needs of
the people.
Table 9. Provision of Cervical Cancer Prevention Services (by Level of
Healthcare Facility and Staff)
| Level |
Staff May Include |
Services |
Requirements |
|
Community |
Community
leadersb
Women’s groups
Community health
workers (CHWs) |
Recognition of
importance of
cervical cancer
Referral to
facilities where
screening is
available |
Community
mobilization
IEC (awareness):
radio messages,
pamphlets and other
public information
|
|
Primary
Level
a
(Primary
Health,
Family
Planning or
Polyclinics)
|
Nurses, midwives
or physician
assistants (PAs) |
Above activities,
plus:
Counseling
(sexual and
cancer risk)
Visual
inspection with
acetic acid
(VIA)
Treatment with
cryotherapy or
referral |
Pelvic exam
Infection prevention
Basic equipment, CO2 and
supplies |
|
First
Referral
Level
(District
Hospital)
|
Above plus:
Medical officers
Nurse midwives
(Ob/Gyn
specialists) |
Above activities
(VIA, cryotherapy)
plus:
VIAM or HPV
testing
LEEP or cone
biopsy
Simple
hysterectomy |
Limited specialty
hospital
General anesthesia
LEEP machine and
thin wire loops |
|
Secondary
and
Tertiary
Level
(Regional
or
Referral
Hospital)
|
Above plus:
Ob/Gyn
specialists
(Ob/Gyn
oncologists)
(Radiotherapist) |
Above activities,
plus:
Full diagnostics
(colposcopy,
biopsy, HPV)
Radical surgery
Radiotherapy |
Full specialty
hospital
Radiation therapy
services
Chemotherapy |
aLevel where VIA and cryotherapy appropriate
bKnowledgeable people, local nongovernmental organizations and private
groups