Showing posts with label coping. Show all posts
Showing posts with label coping. Show all posts
Thursday, October 16, 2008
Pallimed Case Conferences (cases.pallimed.org) is closed to comments and new posts as of April 25, 2013.
This site will stay online as an archived source, but will no longer be updated.
For active posts on these cases and new cases go to www.pallimed.com.
By David Barnard, Ph.D.
Originally posted at the Institute to Enhance Palliative Care, University of Pittsburgh Medical Center
Case:Mr. L.O. was an elderly Russian immigrant to Canada, admitted to the Palliative Care Unit of a Canadian hospital with advanced rectal cancer. When L.O. was first presented to the multidisciplinary team, his major problems were identified as persistent rectal pain and anxiety. The initial workup of the pain suggested a neuropathic component, and adjustments were made to L.O.’s medications. His complaints of pain and anxiety persisted over the next several days.
L.O. then began to experience terrifying nightmares. Even during the day, when he was awake, he would have what he called “flashes” of frightening imagery, but the nightmares were the worst. L.O. was so fearful of them that he resisted falling asleep as much as he could. The images were horrific, often violent, with L.O. sometimes being the victim of the violence, sometimes the perpetrator. A CT scan was ordered to investigate the possibility of brain metastases as a contributing factor.
At the same time, the attending palliative care physician had a long interview with L.O., in which they explored the content of the nightmares in depth. L.O. was an amateur artist, and the physician suggested that he might sketch the images in his dreams, or, if not the exact images, some rendering of how they made him feel. L.O. did this. Subsequent conversations revealed that L.O. was estranged from his children; the main reason that he needed to be in the Palliative Care Unit was that none of his children cared enough about him to support him while he lived at home. L.O.’s sketches showed a small figure—himself—cowering at the bottom of a deep pit, with another figure standing far above, looking down.
The physician suggested that L.O., who had become physically well enough for a weekend pass, bring some of his previous paintings back with him to the Palliative Care Unit. Within a few days, the sound of hammering could be heard from L.O’s room. He was hanging his pictures, 15 or 20 in all. Most were landscapes, but there were also a portrait of a lovely young woman, and a winter scene, all in black and silvery white, of a snow- and ice-lined brook leading into a dark woods. The next morning L.O. reported that he had dreamed of eating a chicken dinner.
Discussion:
Two features of this case are striking. The first is the necessity of combining medical and psychosocial approaches to L.O.’s nightmares and overwhelming anxiety. Both the CT scan and several psychoactive medications were appropriate and helpful. But it was the in-depth exploration of the content of the imagery, and even more, the suggestion that L.O. use his art to capture his emotional state in drawings, that appeared to unlock the insights and emotions that lay beneath the anxiety and terror. The physician succeeded in helping L.O. find a language to express himself more effectively and concretely than he had been able to do at a purely verbal level. The physician found a form of expression that “fit” the patient, even though that form was somewhat unconventional.
The second feature concerns the possibility of creating a living space in the Palliative Care Unit where L.O. could work his way to a feeling of peace and safety, despite his estrangement. This use of the inpatient palliative care service would almost certainly be impossible in the United States, with our minimal lengths of stay and our restrictive utilization review requirements. L.O. died in this Canadian palliative care unit many days after his physical and emotional symptoms had been brought firmly under control. But the inpatient environment remained critical to his spiritual well-being. Even though the Canadian health care system faces some of the same economic pressures as that in the U.S., the possibility still exists there for more flexibility to respond to the broadest range of patient or family need, compared to the limits imposed by hospice and palliative care financing in the U.S.
References:
1. Pratt A, Wood M (eds). Art Therapy in Palliative Care. London: Routledge, 1998.
2. Lynn J. Serving patients who may die soon and their families: The role of hospice and other services. JAMA, 2001, 285:925-932. (No open access pdf)
3. Raphael C, Ahrens J, Fowler N. Financing end-of-life care in the USA. Journal of the Royal Society of Medicine, 2001, 94:458-461. (Open access PDF avail from Journal and PubMed Central)
(CS: Minor formatting edits for readability)
Thursday, October 16, 2008 by Christian Sinclair ·
Monday, May 26, 2008
Pallimed Case Conferences (cases.pallimed.org) is closed to comments and new posts as of April 25, 2013.
This site will stay online as an archived source, but will no longer be updated.
For active posts on these cases and new cases go to www.pallimed.com.
By Winifred G. Teuteberg, MD
Originally posted at the Institute to Enhance Palliative Care, University of Pittsburgh Medical Center
Case:MM is a 77-year-old woman who presented to the emergency department with flu-like symptoms. On exam she had a large palpable mass in her left breast.
I came into the patient’s room and introduced myself, saying, “I see many of the breast cancer patients on this floor.” The patient stopped me, saying, “I don’t have cancer.” I apologized and asked if I might sit down and talk with her. I asked her to explain what she understood of her illness. She said she had fallen several months before and bruised her left breast. It had been sore ever since but she was otherwise fine until she developed “flu” and came to the emergency department. She understood that a scan showed “something in my liver,” but believed that without the biopsy she did not have cancer.
I explained that her doctors were concerned she had cancer. I then asked her what she was most worried about. She told me that her husband died from lung cancer the year before after a two-year battle with the disease. She said, “I’m afraid I’ll suffer the way he did with chemotherapy and radiation and die anyway.” I counseled her that some patients with metastatic breast cancer choose to focus on comfort, rather than pursue aggressive therapies that may not help them achieve more quality time. She was relieved to hear that this was possible. She was discharged with a plan to discuss treatment options with her oncologist but was also considering referral to hospice.
Discussion:
A large part of my clinical practice involves providing inpatient palliative care consults to breast cancer patients. During my three years of practice in this setting, I frequently encounter women presenting with palpable, often fungating, breast masses. In nearly all of these cases patients sought medical attention for a symptom not obviously related to the mass or at the request of a concerned friend or family member. Even after being told their diagnosis, patients often did not accept it and continued to believe their symptoms were related to something else. They can continue in this belief for months and sometimes years. When other health care providers encounter these patients, they are struck by the magnitude of their denial.
Upon review of the literature, denial of obvious breast cancer and delay in presentation for medical care is quite common. Approximately one third of patients present for evaluation more than 12 weeks after developing symptoms and about 5% present more than a year after noticeable symptoms. Most of these patients present with locally advanced or metastatic disease. Studies identify several reasons for this delay, most of them related to the patients’ initial psychological response to their symptoms. Patients who delayed presentation were more likely to have significant fear of cancer itself and/or therapies for cancer including disfiguring surgery. Many patients noticed a lump but believed that the lump would go away or attributed it to another cause. Others did not know that breast cancer is a potentially curable illness and fatalistically did not seek treatment because they believed they were going to die no matter what they did. In several studies patients reported that they knew the symptom was serious, but were too busy caring for others such as young children or sick family members to take time to seek medical advice.
Interestingly, although some studies found a small increased incidence of psychiatric illness in patients who delayed presentation, studies found no significant differences in psychological well-being between patients with early versus late presentation.
When caring for such patients, it is important to realize that their reasons for delaying presentation or even acknowledging their illness are significant for them. Rather than initially attempting to change their beliefs and force them to accept their diagnosis, it is best to first explore their fears and identify ways to help allay these fears. In the case of MM, her fear was that she would suffer the way her husband did and die anyway. Although I was not able to cure her cancer, I was able to provide comfort by offering her a way to avoid the suffering that her husband endured.
1. Phelan M, Dobbs J, David AS. ‘I thought it would go away’: patient denial in breast cancer. J R Soc Med 1992;85;206-207. Full PDF
2. Mohamed IE, Williams KS, Tamburrino MB , et al. Understanding locally advanced breast cancer: What influences a woman’s decision to delay treatment? Preventive Medicine 2005;41:399-405. 10.1016/j.ypmed.2004.12.012 [doi]
3. Burgess CC, Potts HWW, Hamed H, et al. Why do older women delay presentation with breast cancer symptoms? Psycho-Oncology 2006;15:962-968. 10.1002/pon.1030 [doi]
Monday, May 26, 2008 by Christian Sinclair ·
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