| Report Finds High Rates of Cervical
Cancer Indicate Broader Problems in Access to Care
A new report released today by the National Cancer
Institute, part of the National Institutes of Health,
finds that high rates of cervical cancer are indicators
of larger problems in access to health care. The report
also finds that cervical cancer mortality, which is
higher in certain geographic areas and populations,
is a marker for other health disparities. The authors
of the new report, compiled by NCI’s Center to Reduce
Cancer Health Disparities (CRCHD) and titled Excess
Cervical Cancer Mortality: A Marker for Low Access to
Health Care in Poor Communities*,
conclude that the nation’s public health system must
improve its delivery of cervical cancer education, screening,
and treatment and related health care to women at risk.
Despite a consistent decline in cervical cancer deaths
in the United States overall, patterns of high cervical
cancer mortality have existed for decades in specific
geographic areas and populations. Those groups with
the highest mortality rates include African American
women in the South, Hispanic women along the Texas-Mexico
border, white women in Appalachia, American Indians
of the Northern Plains, Vietnamese American women, and
Alaska Natives.
The authors of this report hypothesize that cervical
cancer is an indicator of larger health system concerns,
including medical care access, cultural issues, and
health communication and education issues. To examine
the underlying causes of this ongoing disparity, CRCHD
embarked on a two-phase project, the Cervical Cancer
Mortality Project. In the first phase, researchers reviewed
the literature and analyzed both historical and current
data on cervical cancer incidence, screening, treatment
and mortality in the United States. An analysis of the
literature showed that women suffering from high cervical
cancer mortality share several life conditions: they
tend not to have a usual source of health care; have
lower rates of preventative health services, including
cancer screening; have low incomes and educational levels;
and live in regions with high rates of screenable and
treatable diseases, such as breast cancer, colorectal
cancer, cerebrovascular disease, and infant mortality.
CRCHD Director Harold P. Freeman, M.D., emphasized
the importance of efforts to find a solution to this
problem. “Effectively addressing cervical cancer mortality
can provide a model for action and an opportunity to
address not only the health problems facing women who
are dying from cervical cancer, but also the full set
of human circumstances that lead to health disparities.”
The authors of the report outline specific actions
and targeted interventions to eliminate cervical cancer
mortality disparities. These actions fall into four
key strategy areas: access (services, outreach,
and navigation); information and communication; collaborations,
partnerships, and advocacy; and research.
The authors recommend that health care workers intensify
outreach to women who have rarely or never been screened
for cervical, breast, or colon cancer and other screenable
diseases. To achieve this outreach, the report suggests
that it is very important for women at risk for cervical
cancer and other cancers to have a “medical home” — a
usual source of medical care where they can receive
screening and counseling, experience continuity of care,
and build relationships with the medical caregivers.
The authors also recommend pairing all women with patient
navigators at local hospitals or primary health centers,
who can help at-risk women through the health system
once an abnormality has been detected. Increased patient
navigator programs would help improve communication
between primary care, screening services, and follow-up/treatment
at hospitals.
The report also suggests strategies to remove cultural
and economic barriers to care. When only male physicians
are available to conduct examinations, distrust and
cultural taboos may cause at-risk women to avoid screening.
Increasing the number of female providers, particularly
those of the patient’s race/ethnicity, is an important
step in breaking down resistance to screening. The report
also calls for improved coverage and reimbursement for
cancer-related services. Specifically, the report recommends
that any uninsured woman with cervical or other cancer
should be considered eligible for Medicaid or Medicare
for the duration of her treatment and follow-up care.
Native-born populations in high cervical cancer mortality
areas tend to reach lower educational status and require
materials written at a level that matches their reading
levels. The authors of the report recommend working
with community members to develop linguistically and
culturally appropriate information about this disease.
Effective translation is an integral part of reaching
women in high-risk populations, and the report recommends
improving provider-patient communication through provider
tools and availability of language translation.
Additional research is needed to study the effects
of numerous factors on cervical cancer mortality, including
insurance status, transportation, lack of a medical
home, human papillomavirus (HPV) prevalence, smoking,
sexual practices, and condom use. The authors emphasize
the need to optimize HPV testing and vaccine development
to eliminate the cause of 90 percent to 95 percent of
all cervical cancers. They also noted a need for additional
research to develop better and more affordable screening
tests for all women.
The authors recommend that all government, state, and
local programs with an interest in women’s health pursue
collaborations which promote a “whole woman” approach
to health care. “The problem of cervical cancer mortality
underscores the urgent need to analyze our entire health
care system,” said Freeman. “Change can occur if the
will exists to make it happen. We need to courageously
craft the changes that will eliminate disparities and
save lives.”
To order a copy of the report, visit NCI’s Publications
Locator Web site at https://cissecure.nci.nih.gov/ncipubs.
To view a HPV Q&A from the NCI Web site, please
visit http://www.nci.nih.gov/cancertopics/factsheet/HPVCervicalQandA.
For more information about NCI’s Center to Reduce
Cancer Health Disparities, visit http://crchd.nci.nih.gov/.
For more information about cancer, visit the NCI
Web site at http://www.cancer.gov or
call NCI’s Cancer Information Service at 1-800-4CANCER
(1-800-422-6237).
The National Institutes of Health (NIH) — The
Nation's Medical Research Agency — is comprised
of 27 Institutes and Centers and is a component of the
U. S. Department of Health and Human Services. It is the
primary Federal agency for conducting and supporting basic,
clinical, and translational medical research, and investigates
the causes, treatments, and cures for both common and
rare diseases. For more information about NIH and its
programs, visit www.nih.gov. |