Better communication between cancer
survivors and primary care physicians needed to ensure appropriate screening and
surveillance
A team led by investigators from The Cancer Institute
of New Jersey (CINJ) has published new research in the current edition of the
Journal of General Internal Medicine (Vol. 24, Issue 2). The study suggests that
more intervention is needed to ensure that cancer survivors are having their preventative
screening and cancer surveillance needs met as they transition from cancer treatment
back to primary care. CINJ is a Center of Excellence of UMDNJ-Robert Wood Johnson
Medical School.
According to the National Cancer Policy Board and the
Institute of Medicine, there are nearly 40-million physician office visits made
for cancer care each year, with nearly one-third of those in the primary care
setting. To date, data have been limited in the area of whether cancer survivors
are learning about preventative cancer screenings and surveillance testing through
their regular family doctors.
The new study, Breast, Colorectal and Prostate Cancer
Screening for Cancer Survivors and Non-Cancer Patients in Community Practices,
utilized data for 750 patients from the National Cancer Institute (NCI)-funded
Supporting Colorectal Cancer Outcomes through Participatory Enhancements (SCOPE)
study. Of the patients studied, 109 were cancer survivors.
Women in community-based primary care practices were
surveyed on whether they remember receiving preventative screening for colorectal,
breast and cervical cancers or if they recall their primary care doctor recommending
such screenings. Men were asked the same questions regarding colorectal and prostate
cancers. All participants were asked questions about their health and medical
histories and their satisfaction with the care provided by their primary care
practice.
The investigative team found that cancer survivors had
higher rates of screening than those without cancer. Results show self-reported
screening rates for breast, colorectal and prostate cancers ranged from 72 to
81 percent for cancer survivors compared to 53 to 69 percent for non-cancer patients.
For colorectal and prostate cancers specifically, marriage was a significant predictor
of self-reporting as was older age. The study also found no significant differences
in breast cancer screening rates among cancer survivors and non-cancer patients.
"Because a great potential exists for recurrence in cancer
survivors, it is encouraging to see such high numbers in self-reported screenings
among this group," said the paper's lead author, Shawna V. Hudson, Ph.D., director
of community research at CINJ and assistant professor of family medicine at UMDNJ-Robert
Wood Johnson Medical School. However, those responses may not tell the full story.
Researchers also examined the medical records of the patients studied, and a number
of their survey answers did not match information contained in their patient records.
It is unclear whether patient recall errors are responsible
for the discrepancies, or whether they reflect instances where screening may have
been sought elsewhere. In cases where the data reflect a lack of awareness by
patients about the details of screening and other aspects of follow-up care, Dr.
Hudson sees some cause for concern. "It is widely believed that the more knowledge
patients and their physicians have, the better equipped they will be to build
upon the efforts of the whole health care team," she said. "When cancer survivors
who are making a transition back to primary care lack some of this basic knowledge,
they may be less able to take full advantage of the care that is available."
The study's senior investigator, Benjamin Crabtree, Ph.D.,
program leader of the Quality and Outcomes of Cancer Research Program (formerly
the Population Science Program) at CINJ and professor of family medicine at UMDNJ-Robert
Wood Johnson Medical School, notes the research shows a need for intervention
strategies for cancer survivors. "With the estimated number of cancer survivors
expected to surpass new cancer cases just a few decades from now, greater demands
are going to be placed on our healthcare system by this population. The creation
and implementation of a 'survivor care plan' could help improve communication
between survivors and their primary care doctors so that optimal care can be administered,"
he said.
Along with Drs. Hudson and Crabtree, the author team
consists of Karissa A. Hahn, MPH, UMDNJ-Robert Wood Johnson Medical School; Pamela
Ohman-Strickland, Ph.D., UMDNJ-Robert Wood Johnson Medical School and UMDNJ-School
of Public Health; Regina S. Cunningham, Ph.D., The Tisch Cancer Institute, New York;
and Suzanne M. Miller, Ph.D., Fox Chase Cancer Center, Philadelphia.
The research was supported through grants from the NCI
(K01 CA131500, R01 CA112387) and was conducted in conjunction with the New Jersey
Family Medicine Research Network, which is a shared resource of CINJ. CINJ's Survey
Research and Qualitative Methods Shared Resource also supported the study.
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