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a Clinic for Psychiatry and Psychotherapy of Children and Adolescents, University of Cologne, Cologne, Germany; b EORTC Data Center, Quality of Life Unit, Brussels, Belgium
Correspondence: Henning Flechtner, M.D., Ph.D., Clinic for Psychiatry and Psychotherapy of Children and Adolescents, University of Cologne, Robert-Koch-Str. 10, D, 50931 Cologne, Germany. Telephone: 49-221-478-6121; Fax: 49-221-478-6104; e-mail: henning.flechtner{at}medizin.uni-koeln.de
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LEARNING OBJECTIVES
Top
Learning Objectives
Abstract
Introduction
What Is Fatigue?
Why Should We Assess...
How Do We Assess...
What Have We Learned?
What Are Our Goals?
References
After completing this course, the reader will be able to:
| ABSTRACT |
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Key Words. Fatigue • Quality of life • Anemia • Neoplasms
| INTRODUCTION |
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| WHAT IS FATIGUE? |
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Healthy people will typically feel exhausted and fatigued after sleep deprivation. But this is normal fatigue; if healthy people sleep, their fatigue dissipates, and they feel recovered. People with diseases, even very common diseases (e.g., a simple flu), can feel extremely fatigued. Once the flu is over, however, the fatigue is gone.
Fatigue in oncology patients is a very different concept. These patients experience fatigue, in relation to their therapy and their tumor, that has very specific phenomena and that differs not only from fatigue in healthy people, but also from fatigue in people suffering from other diseases. A simple definition of fatigue is that it is a feeling and a state of tiredness that exceeds the norm and is experienced as clearly unpleasant.
The medical context of fatigue is very broad. It can be a symptom (e.g., a symptom of depression) or a syndrome (e.g., fatigue syndrome in relation to cancer). It can even be regarded asalthough this is still controversiala disease on its own (e.g., chronic fatigue syndrome). It can be a result of side effects of chemotherapy or late effects after radiation.
Any discussion of fatigue should address at least two dimensions of the problem. There is the subjective dimension, or what patients say they experience when they talk about fatigue. In general, this dimension has at least three aspects: physical, emotional, and cognitive. There is also an objective dimension. This is related to the functional parameters of organ systems; for example, fatigue can originate in the hematopoietic system and may appear as anemia (for which drugs are available). But other organ systems, such as the respiratory system and the immune system, may also be responsible for fatigue. These two dimensions correlate with two descriptions of fatigue: A) as a general phenomenon relating to a patients overall well-being and B) as a specific phenomenon in the sense of cancer-related fatigue.
| WHY SHOULD WE ASSESS FATIGUE? |
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The impact of fatigue on the quality of life of oncology patients is under-recognized. Fatigue is associated with a range of negative effects, starting with a decrease in activity requiring physical exertion and including the profound loss of the feeling of being in control. Many patients report that they cannot partake in activities as they did before, so they lose control of parts of their life; ultimately, this can lead to feelings of loneliness and isolation and a further decrease in activity. This vicious cycle puts the patient in a distressing position.
The prevalence of cancer-related fatigue is another major reason that fatigue assessment is important. As noted earlier, it is present in the majority of patients. An estimated 60%96% of cancer patients in treatment experience fatigue, including 60%93% of those on radiotherapy and 80%96% of those on chemotherapy. Fatigue is very common after surgery or treatment with a biologic response modifier. In addition to treatment, fatigue is associated with neoplasms and other comorbid conditions. It increases with advanced disease and is related to anemia, depression, cachexia, pain, and insomnia [2].
In Germany, and within the European Organization for Research and Treatment of Cancer (EORTC), we recently conducted an investigation of fatigue levels in a patient population of 389 female cancer patients and 1,139 healthy female controls (Fig. 1
) [3]. As expected, normal fatigue increased with age, as shown on a scale from 0 to 100 where 0 represented no fatigue and 100 represented the highest level of fatigue. Cancer patients reported much higher levels of fatigue. Scores for the healthy German female population ranged from around 10 to 15, although they increased to more than 30 in older women. The cancer patients scored much higher, with younger patients scoring in the range of 30 to 40 and older patients scoring higher. In general, levels over 40 suggest an inpatient population reporting on fatigue.
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| HOW DO WE ASSESS FATIGUE? |
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Fatigue is objectively assessed using a variety of instruments. Some, like the EORTC questionnaire [4], the Functional Assessment of Cancer Therapy (FACT) questionnaire by Cella et al. [5], and the Profile of Mood States [6], address fatigue in certain parts of the instrument (e.g., the fatigue scale of the EORTC QLQ-C30). In addition, there have been new, fatigue-specific instruments developed that deal with fatigue as a multidimensional phenomenon. Some instruments measure the intensity of fatigue; others also deal with its interference in the activities of daily living or with the duration of fatigue.
A good fatigue scale requires minimal patient input. It is valid and reliable, with easily understood items. Scoring and interpretation are straightforward. It should be easily translated and cross-culturally valid. One example is the Multidimensional Fatigue Inventory (MFI), first published by Smets et al. in 1995 [7], which has many of these characteristics. It is a 20-item instrument that includes five different fatigue subdimensions: general fatigue, physical fatigue, mental fatigue, reduced activity, and reduced motivation. It has demonstrated good psychometric properties in some trials, but it is not yet fully internationally validated.
| WHAT HAVE WE LEARNED? |
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Perhaps the most prominent study on this subject published over the past few years is by Littlewood et al. [9]. Using a randomized, controlled design and measuring the effect of the erythropoietin treatment using the FACT scales of anemia and fatigue, these investigators demonstrated that treatment with epoetin alfa to increase hemoglobin level had positive effects on patients quality of life.
But what do these data mean? Recent follow-on studies by Cella et al. [10] and Patrick et al. [11] using two different methodologies address the clinical significance of changes in quality of life scores. These studies independently conclude that the changes seen in the Littlewood trial [9] are clinically meaningful to patients.
Effect of Fatigue Intensity
In some trials from the EORTC Lymphoma Group and the German Hodgkin Study Group, we assessed fatigue using the subscale of a general assessment questionnaire, the EORTC QLQ-C30, and the five subscales of the MFI [12]. Longitudinal data obtained from healthy control groups and a cross-sectional trial indicate that patients scored quite high on the physical functioning scale of the EORTC quality-of-life instrument. Almost 7 years after the end of treatment, these people had recovered and stayed in the midrange of functioning; they did not recover fully, but they stabilized in general. This is a finding expected in many populations of cancer survivors; patients show limitations after the end of treatment, but ultimately reach a reasonably good level of functioning.
Looking into subpopulations of these total populations produces a totally different picture. The control group usually scored around 10 on the fatigue assessment scale. Cancer patients who expressed very low levels of fatigue, scoring less than 20 on the scale, showed almost no limitations in physical functioning, even at early time points after the end of treatment; they returned to normal after treatment. They resembled a healthy control group. Those who scored over 40 at the time of treatment, however, reported quite extreme limitations in physical functioning. They recovered after treatment, but they did not recover fully. At least some subpopulations experienced much higher levels of fatigue and limitations of functioning.
This phenomenon is evident in other quality-of-life domains as well. In the area of emotional functioning, again there are differences between patients who scored low on the fatigue scale and those who scored high. There were extreme limitations in emotional functioning among those with high fatigue scores; a low level of emotional functioning, a low spirit, was apparent. Even those who felt relatively well physically did not return to high levels of emotional functioning.
An examination of the overall quality of life produced a similar picture. The quality of life for those patients with low levels of fatigue returned essentially to normal, while that for those patients with high levels of fatigue remained substandard even 67 years after the end of treatment.
Patterns of Recovery
Analyses of these data suggest that there are at least four recovery patterns among people who have undergone cancer treatment for diseases like Hodgkins disease.
In various quality-of-life domains, we were able to separate patients into groups according to their limitations in functioning and patterns of recovery over time. We have assessments on these patients from 6 months until 68 years after the end of therapy. More than 40% of the patients scored lower than 60 on physical functioning (0100 scale with 100 being the maximum of functioning) shortly after therapy, which we expected, and from which they did recover. This percentage went down as time passed after treatment, and at the end, only about 20% reported very low physical functioning and limitations. But still, 20% were physically not well. The percentage of the population reporting a high functioning level (i.e., scores of 80 and above) and the least limitation in physical functioning increased over time to almost 70% of all patients.
In the area of emotional functioning, findings are different. Not much change over time was evident here. Seven years after treatment, 50% of the patients still reported limitations in emotional functioning. The picture gets even worse in the area of global quality of life. After 67 years, only 40% reported a good quality of life, while almost 60% reported limitationsand this was in a cancer-free population.
Results from these trials point to the potential for a new and disturbing finding. Fatigue scores of 40 to 100 as the high parameter cover 45% of the patients. These patients reported higher levels of fatigue 6 months after the end of treatment. This percentage declined until year 2 to 3 (to 18%) and then rose again. At the end of the observation period, almost 30% reported high levels of fatigue again. The midrange population did not change very much, and the population reporting low levels of fatigue reached 40%; however, this means that 60% of patients had medium to high levels of fatigue after 5 cancer-free years.
Almost one third of patients reported severe limitations due to fatigue, and the profession must deal with this. We need to determine what is happening and to resolve this condition not only with psychological treatment, but also with other interventions. Investigations are essential to determine the current status of long-term survivors in more detail and to link it to the conditions observed during the treatment of acutely ill patients.
| WHAT ARE OUR GOALS? |
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| ACKNOWLEDGMENT |
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| REFERENCES |
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This article has been cited by other articles:
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E. J. Corwin, L. E. Murray-Kolb, and J. L. Beard Low Hemoglobin Level Is a Risk Factor for Postpartum Depression J. Nutr., December 1, 2003; 133(12): 4139 - 4142. [Abstract] [Full Text] [PDF] |
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E. K. Rowinsky Crossing the Cancer Cell Membrane to Improve Clinical Outcomes Oncologist, December 1, 2003; 8(90003): 1 - 4. [Full Text] [PDF] |
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P. A. Daly Introduction: All Ireland Fatigue Coalition Oncologist, February 1, 2003; 8(90001): 1 - 2. [Abstract] [Full Text] [PDF] |
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