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Life After Gynecologic Cancer—A Review of Patients Quality of Life, Needs, and Preferences in Regard to Follow-up
Abstract
Objective: This article reviews the literature on
quality of life (QoL) of gynecologic cancer survivors, their needs and
preferences regarding follow-up, and possible predictors of long-term
QoL.
Methods: A systematic literature search was made in
the following databases: MEDLINE (PubMed), Bibliotek.dk, CINAHL,
Cochrane, EMBASE, PsycINFO, and SveMed+. We searched the period
1995–2012 for English-language literature. The search was made during
July 2011 to February 2012. When possible, the search was made using
MeSH terms. Additional reports were collected by systematically viewing
the reference lists of the retrieved articles.
Results: Overall studies indicate that survivors after
gynecologic cancer do not have impaired QoL in the long term. In
general, the patients are highly satisfied with the follow-up program.
The patients’ greatest concern is fear of recurrence. The most frequent
reported unmet need is help in dealing and living with the fear of
recurrence. It seems that psychosocial status at time of diagnosis is
determining for QoL and well-being in the long term. Association has
been found between coping style and QoL, risk of depression, and anxiety
in the long term after cancer.
Conclusions: Even though long-term QoL does not seem
to be impaired, the patients are struggling with fear of recurrence, and
the way of coping with this fear is a possible predictor for long-term
QoL after cancer. However, there is a lack of evidence on QoL, needs,
and preferences regarding follow-up of the survivors after gynecologic
cancer. The quality of the follow-up regimen is questionable, and it is
not evidence based. Thus, it is extremely important to optimize the
follow-up program and move focus to life quality. There is a need for an
evidence-based strategy regarding follow-up for low-risk gynecologic
cancer patients.
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