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Featured researches published by Carl J. Getto.


Journal of Pain and Symptom Management | 2003

Fatigue and Sleep Disturbance in Patients with Cancer, Patients with Clinical Depression, and Community-Dwelling Adults

Karen O. Anderson; Carl J. Getto; Tito R. Mendoza; Stephen N Palmer; Xin Shelley Wang; Cielito C. Reyes-Gibby; Charles S. Cleeland

This study compared the severity of fatigue in patients with cancer to the fatigue reported by depressed psychiatric patients and community-dwelling adults. Data were collected for this study during the process of validating a new fatigue assessment tool, the Brief Fatigue Inventory (BFI). The sample included 354 cancer patients, 72 psychiatric patients, and 290 non-patient volunteers. Study subjects reported severity of fatigue and the degree to which fatigue interfered with various aspects of life. Data were also collected on sleep disturbance and demographic variables that might correlate with fatigue. The psychiatric patients reported significantly higher levels of fatigue and fatigue-related interference than the cancer patients, who reported more severe fatigue and interference than the community subjects. The sleep disturbance scores of the cancer patients and the community subjects were significantly correlated with fatigue severity. Although the majority of the psychiatric patients reported sleep disturbance, their sleep disturbance scores were not significantly associated with fatigue severity.


Brain Research Bulletin | 1985

Sugar, opioids and binge eating

Donald T. Fullerton; Carl J. Getto; William J. Swift; Ian H. Carlson

There is evidence that endogenous opiates are involved in the control of feeding in experimental animals. Several types of experimental obesity are associated with increased opiate production and/or increased numbers and sensitivity of opiate receptors. Research with experimental animals suggests that nutrients, particularly sugar, have an effect on feeding behavior that is mediated by opiates. For instance, the obesity-producing effect of a palatable diet in rodents is blocked by opiate antagonists. Stress induced feeding in rodents leads to preferential sucrose ingestion and is blocked by opiate antagonists and beta-endorphin. The effect of nutrients on the endogenous opiate system of humans is less clear. Clinical experience suggest that carbohydrates (sugar in particular) play a role in binge eating and obesity. Many binge eaters preferentially eat sweets during a binge. Many obese individuals consume more than half of their total daily calories as carbohydrates. Sweet snacking is a frequent behavior at times of stress. Recent evidence suggests that sugar can lead to increased beta-endorphin production in obese subjects.


Psychological Medicine | 1986

Plasma immunoreactive beta-endorphin in bulimics.

Donald T. Fullerton; William J. Swift; Carl J. Getto; Ian H. Carlson

The plasma beta-endorphin response to glucose ingestion was compared in 8 bulimics and 8 controls. The bulimics demonstrated a sustained elevation of plasma beta-endorphin unrelated to glucose ingestion throughout the 5-hour study period. It is hypothesized that such an elevation of beta-endorphin is the result of stress and that it may play an important role in the perpetuation of the binge-vomiting cycle.


Appetite | 1984

Plasma immunoreactive beta-endorphin response to glucose ingestion in human obesity

Carl J. Getto; Donald T. Fullerton; Ian H. Carlson

Following the oral administration of 100 g of glucose, morbidly-obese subjects and non-obese controls demonstrated increased levels of plasma immunoreactive beta-endorphin. There was a slow rise in plasma immunoreactive beta-endorphin in the non-obese controls throughout the 3-h observation period. The obese subjects demonstrated a delayed and significantly greater rise of plasma immunoreactive beta-endorphin, when compared to the controls. These findings may have implications for further research in human obesity.


Pain | 1981

A standardized evaluation of psychosocial factors in chronic pain

Robert K. Heaton; Carl J. Getto; Ralph A.W. Lehman; Wilbert E. Fordyce; Ellen Brauer; Stephen E. Groban

Abstract A number of psychosocial factors are generally considered to be important in exacerbating and maintaining chronic pain problems. However, standardized and reliable methods of evaluating these factors are needed. We have developed such an evaluation system, called the Psychosocial Pain Inventory (PSPI), and have obtained normative data from a large sample of chronic pain patients. Scores on the PSPI were approximately normally distributed and had good inter‐rater reliability. Patients with high PSPI scores were more likely to be considered exaggerating their symptoms during their physical examinations, but they did not show less evidence of an organic basis for pain. Significant correlations were obtained between PSPI scores and some measures from the McGill Pain Questionnaire, but scores on the PSPI were essentially unrelated to personality disturbance as measured by the Minnesota Multiphasic Personality Inventory (MMPI). The PSPI and MMPI appear to provide different types of information that can be used in a complementary way in evaluating pain patients. Results of a small pilot study suggest that high scores on the PSPI predict poor response to medical treatment for pain.


Behavior Research Methods | 1981

The computer psychiatrist: How far have we come? Where are we heading? How far dare we go?

Harold P. Edman; John H. Greist; Marjorie H. Klein; James W. Jefferson; Carl J. Getto

The use of computers in psychiatry and psychology is reviewed. It is noted that computers are already being used successfully for consultation, interviewing, and continuing education. Issues related to the usage of computers in mental health are discussed. Guidelines for future work in the area are suggested.


Brain Research Bulletin | 1986

Immunoreactive beta-endorphin increases after IV glucose in obese human subjects

Carl J. Getto; William J. Swift; Ian H. Carlson; Donald T. Fullerton

The plasma beta-endorphin of obese human subjects and non-obese controls was compared following the intravenous infusion of 25 grams of glucose. The plasma beta-endorphin of the obese subjects was significantly higher than controls one hour and four and one half hours after glucose infusion. The increased beta-endorphin of the obese subjects was associated with falling blood sugar.


International Journal of Eating Disorders | 1992

Persistent functional vomiting

Donald T. Fullerton; Susan Neff; Carl J. Getto

Two cases of persistent, spontaneous, effortless, involuntary vomiting are presented as ex- amples of functional vomiting. Their diagnosis is discussed and a suggestion is made for categorizing functional vomiting as either self-induced or psychogenic vomiting. Psychogenic vomiting would be considered rumination when there is reswallowing of vomited material or as a conversion disorder. This classification if adopted would help to define these syndromes and allow for testing of observations regarding associated psychiatric disorders, impairment in other functions, and prognosis.


International Journal of Eating Disorders | 1988

Oral glucose increases plasma beta-endorphin in obese subjects

Donald T. Fullerton; Carl J. Getto; William J. Swift; Ian H. Carlson; Lori D. Gutzmann

Previous studies by the authors have suggested an increased plasma beta-endorphin response to glucose ingestion in obese subjects compared with controls. The present study confirms these earlier findings and demonstrates a parallel increase in plasma ACTH in obese subjects compared with normal-weight controls. It seems likely that this response is the result of increased production of beta-endorphin by the pituitary. Suggestions for further research are made.


International Journal of Eating Disorders | 1988

Differences in the plasma betaendorphin levels of bulimics

Donald T. Fullerton; William J. Swift; Carl J. Getto; Ian H. Carlson; Lori D. Gutzmann

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Donald T. Fullerton

University of Wisconsin-Madison

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Ian H. Carlson

University of Wisconsin-Madison

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William J. Swift

University of Wisconsin-Madison

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Lori D. Gutzmann

University of Wisconsin-Madison

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Charles S. Cleeland

University of Texas MD Anderson Cancer Center

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Cielito C. Reyes-Gibby

University of Texas MD Anderson Cancer Center

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Ellen Brauer

University of Colorado Denver

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Harold P. Edman

University of Wisconsin-Madison

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James W. Jefferson

University of Wisconsin-Madison

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John H. Greist

University of Wisconsin-Madison

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