Invited Perspective
Strategies to Overcome Cancer Survivorship Care Barriers Julie K. Silver, MD In 2003, I was in my thirties and newly diagnosed with cancer. I went into treatment, received state-of-the-art care (which included extremely toxic therapies), emerged to find that I had to rehabilitate myself, and eventually transformed into an advocate for implementing cancer rehabilitation into the oncology care continuum. I have found this new focus to be, by turns, incredibly rewarding and exceedingly difficult. I have had the privilege of visiting more hospitals and cancer centers than I can count. I have met with thousands of people at various levels who are involved in survivorship care. The travel, while exhausting, has given me a view of survivorship that few health care professionals have—firsthand knowledge of how this care is being implemented throughout the United States. Throughout my travels, I have been extremely impressed by the dedication of oncology professionals to survivorship care. From small community hospitals to large academic medical centers, exceedingly dedicated individuals are committed to implementing the 10 key recommendations from the report by the Institute of Medicine (IOM) entitled, “From Cancer Patient to Cancer Survivor: Lost in Transition” [1]. In particular, two of these recommendations are being widely adopted: (1) create survivorship as a distinct phase of cancer care, and (2) ensure that every patient is given a survivor care plan. It is truly a privilege to have been invited to take part in the survivorship dialogue with so many health care professionals. In this Invited Perspective, I have an opportunity to offer suggestions that will help advance survivorship care for the more than 12 million cancer survivors in the United States and many others worldwide. I will focus on some barriers to that goal that may not be obvious. Certainly, I could describe the need for more research, clinical guidelines, and resources for the postacute care of cancer survivors. However, in this editorial, I want to share a “from the trenches” viewpoint that many health care professionals likely do not have the opportunity to witness.
RECOGNIZE THAT SURVIVOR CARE PLANS ARE ONLY AS GOOD AS THE SERVICES THEY DOCUMENT In 2006, the pivotal IOM report “From Cancer Patient to Cancer Survivor: Lost in Transition” [1] was released, and this report created a national (and international) movement to—at the very least— offer survivors an electronic document that details their diagnosis, treatment, and follow-up care. The IOM’s recommendations have challenged health care providers to change the way that cancer care is delivered. There has been an enormous response to this report throughout the oncology health care community. An editorial by oncologist Craig Earle, MD, entitled “Failing to Plan is Planning to Fail: Improving Quality of Care with Survivorship Care Plans” [2] further outlined the need to comply with the IOM’s recommendation. Many electronic survivorship plans now exist that are free to both survivors and health care professionals. The American College of Surgeons’ Commission on Cancer (CoC) is trying to ensure that the hospitals (and other facilities) it accredits comply with the IOM recommendations. In fact, beginning in 2011, CoC-accredited hospitals are attempting to offer a survivor care plan for every patient. This recommendation by the CoC is important, because as its Web site notes, “Approximately 71 percent of all newly diagnosed cancer patients in the United States are treated in the more PM&R 1934-1482/11/$36.00 Printed in U.S.A.
J.K.S. Department of Physical Medicine and Rehabilitation, Harvard Medical School, Boston, MA. Address correspondence to: J.K.S.; e-mail: julie_silver@hms.harvard.edu. Disclosure: 1, co-founder Oncology Rehab Partners; 4A, consumer health books Disclosure Key can be found on the Table of Contents and at www.pmrjournal.org Submitted for publication April 21, 2011; accepted April 28, 2011.
© 2011 by the American Academy of Physical Medicine and Rehabilitation Vol. 3, 503-506, June 2011 DOI: 10.1016/j.pmrj.2011.04.014
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