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The Death of Nasogastric Tube Feeding Reprinted from Eating
Disorders Review At our hospital, we have developed a different approach to treating inpatients with eating disorders. With it we have been able to do away with some coercive methods once thought to be essential for care and recovery of severely ill patients. After an initial assessment in the BC Children’s Hospital Eating Disorders Program, a youth with a severe eating disorder may be referred to our Intensive Treatment Service (ITS). She and her family will then undergo pre-care interviews. During these interviews, the content of the treatment program and the expectations from her and her family will be carefully detailed and discussed. She will be told that we do not use nasogastric tube feeding or nutritional supplements and that, with our support, she will be expected to complete all her meals. She will also be told that, unless medically indicated (and this is rare), we do not use bed rest or wheelchairs, and she will participate in supervised physical activities. Finally, she and her parents will be reminded that her participation is voluntary and she will be able to leave if she feels it is not helpful. This program has been very successful, according to the feedback we receive from patients and families, and the ITS has a waiting list. Patients gain weight (when necessary) at a rate of approximately 1 kg (2.2 lb) a week, just as before, when nasogastric tube feeding and bed rest were utilized. Almost all patients eventually decide to participate. However, others are sometimes followed in our outpatient clinic for weeks before they arrive at that decision. Having worked in other programs, I do not believe that the patients in British Columbia are any different from those elsewhere in North America. Then, how can one explain why this approach—which is very different from one I myself may have taken 15 years ago— is as effective as more standard treatment and is clearly appreciated by patients and their families?
The Culture and Practice of Medicine The following exploration is not meant to be critical or judgmental of past and current approaches to treating patients with eating disorders. It is also too brief to do justice to a fuller discussion of this issue. It is meant, rather, to encourage clinicians to review and consider their approach to treatment.
Coercive Approaches Also, we now have a better appreciation of the “benefits” a patient may believe an eating disorder brings to her life. These benefits can be valued, particularly early on in the illness, prior to the accumulation of the negative side effects. These perceived benefits are real and not delusional, although they may seem overvalued to us. Acknowledging and exploring them are often the first steps to establishing the therapeutic alliance that will be needed when the benefits wear out—as they will eventually—for the majority of patients
Costs to Patients The option of training and providing staff for meal support therapy may not be welcomed by healthcare administrators, but this can be achieved on an outpatient or day hospitalization basis, which may make it more economical. To facilitate this, we have produced two manuals and videos (one aimed primarily at professionals, and one for families and friends) on how to provide meal support for patients. (See further information at the end of the article.) But the construction of eating disorders by Western medicine is not limited to this issue.
DSM Systems
Then, what may be the ‘benefits’ to high recognition of comorbidity?
Should the Hospital Be the Primary Site for Treatment? Through mostly qualitative research on patients and families’ views of illness and recovery, we are starting to consider different ways of understanding eating disorders and their treatment. The importance of the “wish to change,” the reconnection with meaningful others, including therapists, acceptance of the self, and maturation for youth are emerging as consistent messages. The main theme seems to point toward patience and collaboration in our interventions. Hence, we owe it to our patients and our families to pay heed to the words Adelaide Nutting, a nurse, wrote in 1925: We need to realize and affirm anew that ‘medicine’ is one of the most difficult of arts. Compassion may provide the motive, but knowledge is our only working power. Perhaps, too, we need to remember that growth in our work must be preceded by ideas — and that conditions which suppress thought must retard growth. Surely we shall not be satisfied in perpetuating methods and traditions. Surely we shall wish to be more involved in creating them. The videos mentioned in the article are available by writing to: Program Secretary, Eating Disorders Program, DC Children’s Hospital, 4480 Oak Street D411, Vancouver, BC Canada V6H 3V4, or by e-mail at: mcatamo@cw.bc.ca. click
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