The purpose of this longitudinal pilot study is to characterize the symptoms experienced and the feeding volumes infused over time for adults with cancer who are receiving prescribed enteral feedings at home. Since varied symptoms have been reported with enteral feedings, it is important to know when these sensations and symptoms are experienced by adults with cancer, in order to prepare them for this nutrient therapy. In addition, there are no published reports addressing the relationship between symptoms and the amount of the prescribed feeding that is actually delivered.
Specific aims for this longitudinal pilot study of adults with cancer receiving enteral feedings are to: 1) describe patterns of symptoms and changes in characteristics of symptoms over a 12 week period; 2) explore the relationships among enteral feeding volumes, level of adherence to prescribed feedings, and symptoms experienced over a 12 week period; and 3) examine four feasibility elements of long-term weekly data collection for nutritionally compromised cancer patients. A longitudinal design will be used for this pilot study of 20 adults, 19 years or older, diagnosed with head or neck cancer, beginning enteral feedings for the first time, and discharged home from a health care agency within 48 hours of contact. Each patient will be interviewed by telephone weekly for 12 weeks. During the interviews, patients will be asked to describe current enteral feeding status, including volumes infusing per feeding and per day. Patients also will be asked to describe any sensations experienced since the last interview, and provide a comparison with the previous week. Analysis will focus on data from each time point by sensation and sensation group (GI, tube-related, and other sensations), as well as comparisons among sensations and infused volumes, using Generalizing Estimating Equations. Distress scores for each symptom and symptom group will be calculated. The results till serve as a basis for developing an informational intervention to be used with adult oncology patients who are going to be starting, or are receiving enteral feedings.

Agency
National Institute of Health (NIH)
Institute
National Institute of Nursing Research (NINR)
Type
Exploratory Grants (P20)
Project #
5P20NR007807-02
Application #
6660147
Study Section
Special Emphasis Panel (ZNR1)
Project Start
2002-09-01
Project End
2003-08-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Oregon Health and Science University
Department
Type
DUNS #
009584210
City
Portland
State
OR
Country
United States
Zip Code
97239
Elsea, Collin R; Roberts, Daniel A; Druker, Brian J et al. (2008) Inhibition of p38 MAPK suppresses inflammatory cytokine induction by etoposide, 5-fluorouracil, and doxorubicin without affecting tumoricidal activity. PLoS One 3:e2355
Winters-Stone, Kerri M; Bennett, Jill A; Nail, Lillian et al. (2008) Strength, physical activity, and age predict fatigue in older breast cancer survivors. Oncol Nurs Forum 35:815-21
Nail, Lillian M (2006) Cognitive changes in cancer survivors. Cancer and cancer treatment often cause cognitive deficits, but no guidelines exist for screening or treatment. Am J Nurs 106:48-54
Wood, Lisa J; Nail, Lillian M; Perrin, Nancy A et al. (2006) The cancer chemotherapy drug etoposide (VP-16) induces proinflammatory cytokine production and sickness behavior-like symptoms in a mouse model of cancer chemotherapy-related symptoms. Biol Res Nurs 8:157-69
Wood, Lisa J; Nail, Lillian M; Gilster, April et al. (2006) Cancer chemotherapy-related symptoms: evidence to suggest a role for proinflammatory cytokines. Oncol Nurs Forum 33:535-42
Nail, Lillian M (2006) Cognitive changes in cancer survivors. Cancer Nurs 29:48-54
Fromme, Erik K; Tilden, Virginia P; Drach, Linda L et al. (2004) Increased family reports of pain or distress in dying Oregonians: 1996 to 2002. J Palliat Med 7:431-42
Nail, Lillian M (2004) My get up and go got up and went: fatigue in people with cancer. J Natl Cancer Inst Monogr :72-5
Hickman, Susan E; Tilden, Virginia P; Tolle, Susan W (2004) Family perceptions of worry, symptoms, and suffering in the dying. J Palliat Care 20:20-7