Concise Encyclopedia of Chronic Fatigue Syndrome
eBook - ePub

Concise Encyclopedia of Chronic Fatigue Syndrome

  1. English
  2. ePUB (mobile friendly)
  3. Available on iOS & Android
eBook - ePub

Concise Encyclopedia of Chronic Fatigue Syndrome

About this book

Are you in touch with the latest CFS information?The Concise Encyclopedia of Chronic Fatigue Syndrome summarizes current knowledge about Chronic Fatigue Syndrome (CFS) to help doctors and those working with CFS patients become familiar with recent developments and lessons learned about this and related fatiguing disorders. The information has been thoughtfully organized so that you will be able to easily access and become familiar with highlights of the most relevant topics.The Concise Encyclopedia of Chronic Fatigue Syndrome will bring you up-to-date on advances in cardiovascular medicine, endocrinology, epidemiology, immunology, infectious diseases, neurology, psychiatry, and psychology which have served as the basis for the formulation of new lines of research and novel therapeutic interventions for CFS. You'll find valuable information on the A-to-Z of CFS in the Concise Encyclopedia of Chronic Fatigue Syndrome, including the relationships between:

  • AIDS and fatigue
  • brain injury and fatigue
  • cancer and fatigue as well as:
  • demographics of CFS
  • interstitial cystitis
  • MAO inhibitors
  • neuropsychology of CFS
  • psychosocial measures
  • stress factors
  • tumor necrosis factors ...and much moreComprehensive and thorough, the Concise Encyclopedia of Chronic Fatigue Syndrome highlights areas that need more research and gives you greater awareness of this widespread and growing problem. This compendium will educate and create greater CFS awareness among healthcare professionals and the general public.

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Yes, you can access Concise Encyclopedia of Chronic Fatigue Syndrome by Roberto Patarca Montero in PDF and/or ePUB format, as well as other popular books in Medicina & Neurología. We have over one million books available in our catalogue for you to explore.

Information

Publisher
CRC Press
Year
2021
eBook ISBN
9781000156669
Subtopic
Neurología

I

Iceland disease:

Iceland disease or Akureyri disease is characterized by prolonged chronic fatigue that results in anxiety disorders following infection. The more serious psychiatric disorders (agoraphobia with panic attacks, agoraphobia without panic attacks, social phobia, simple phobia, schizophrenia, and alcohol dependence) do not seem to play a major role in the long run.1

Illness beliefs:

The literature on the role of illness beliefs/attributions on the part of both patients and health care professionals is widely divided and some have gone as far as suggesting that chronic fatigue is merely a question of attribution.13 The findings in a study4 of 60 CFS patients suggested that physical illness attributions were less important in determining outcome (at least in treatment studies), and that good outcome was associated with change in avoidance behavior and related beliefs, rather than causal attributions. Another study5 of 137 CFS patients concluded that the belief that one’s actions can influence outcomes modified the relationship between illness accommodation and both fatigue and impairment; adverse outcomes were associated with accommodating to illness only in the context of lower levels of perceived control. It was suggested, therefore, that interventions that either discourage avoidance of activity or enhance perceived control could benefit the course of the illness. A series of regression analyses in one study6 showed illness representations to be stronger predictors of adaptive outcome than coping scores.
Some studies emphasize the patient’s attributions of disease as the cause for symptomatology. For instance, a study7 of 153 women from the Toronto area who were attending a women’s health symposium yielded an overwhelming endorsement of social determinants as the cause of their persistent fatigue. Although depression and anxiety formed the most robust associations with persistent fatigue in primary care and community studies, women in this sample ranked these factors in seventh place in their attributions. Similarly, although physicians often assume physical causes for fatigue, women rank physical health low in their own attributions. A study8 comparing medical records of 133 CFS and 75 multiple sclerosis permanent health insurance claimants and 162 nonclaimant controls cases showed that CFS patients recorded significantly more illnesses at time of proposal for insurance than the two control groups, and had significantly more claims between proposal and diagnosis of their disorder. These observations led the authors to conclude that there is no support for a specific viral or immunological explanation for CFS and that abnormal illness behavior is of great importance.
Other studies have emphasized the role of the physician in disease perpetuation. For instance, a study9 of 2,097 individuals in the Netherlands found that more psychosocially attributed fatigue was found to correlate with consultations characterized by less physical examination, more diagnostic procedures to reassure, fewer diagnostic procedures to discover underlying pathology, more counseling, less medical treatment, less prescription, and a longer duration than consultations with more somatically attributed fatigue. The study concluded that general practitioners do not discriminate between social groups when attributing fatigue to either somatic or psychosocial causes. The presence and character of other complaints and underlying diseases/problems, rather, relate to the general practitioners’ somatic psychosocial attributions, which are then associated with particular aspects of the consultation. Research in one study10 of 609 CFS patients suggested several patterns of relationships between doctors and patients, and attitudes to health and illness, which may alert doctors to patients’ perceptions, beliefs, encoded constructs, and patterns of relating that affect responses to treatment. The study suggested that more attention from doctors to patients who are experiencing the stress of chronic illness is indicated. The latter view is reinforced by another study11 that found that CFS patients complained about insufficient informational as well as emotional support from their doctors and, as a consequence, most opted for alternative or complementary forms of treatment. In addition, disagreements over illness etiology and treatment precluded effective cooperation.
Some studies have addressed the influence of illness attributions by family members on the disease process. A study12 of adolescents with CFS in the Netherlands concluded that factors contributing to the persistence of fatigue are somatic attributions, illness-enhancing cognitions, and behavior of parents as well as physical inactivity. The role of the physician and the role of parents can enhance the problems. The treatment should focus on decreasing the somatic attributions, on reinforcement by the parents of healthy adolescent behavior, on the gradual increase of physical activity, and on decreasing attention (including medical attention) for the somatic complaints. A women’s study13 showed that some women respondents were able to identify specific ways in which family and important others could help them to decrease or prevent their fatigue. However, many expressed the belief that significant others were unconcerned and unwilling to assist them in any substantive way. Analysis of responses in one study14 of 66 CFS participants indicated that, whereas the most commonly described explanation for the illness was a physical one, more than half the patients also believed “stress” had played a role. Patients believed that they could partially control the symptoms by reducing activity, but felt helpless to influence the physical disease process and hence the course of the illness. Patients reported that they had arrived at these beliefs about the illness after prolonged reflection on their own experiences combined with the reading of media reports, self-help books, and patient group literature. The views of health professionals played a relatively small role.
In conclusion, attribution contributes to the course of CFS, but it is not its sole determinant.15 The presence of strong somatic attributions appears to be one of the perpetuating factors in CFS, but not the only one. Many CFS patients present a self-diagnosis. Communication problems...

Table of contents

  1. Cover Page
  2. Half Title Page
  3. Series Page
  4. Title Page
  5. Copyright Page
  6. Contents Page
  7. About the Author Page
  8. Preface Page
  9. List of Abbreviations Page
  10. Acquired immunodeficiency syndrome (AIDS) and fatigue
  11. Age
  12. Adrenocorticotropin hormone (ACTH)
  13. Akureyri disease
  14. Allergies
  15. Amantadine
  16. Ankylosing spondylitis
  17. Antidiuretic hormone (ADH)/Arginine vasopressin
  18. Anxiety disorders
  19. Apoptosis
  20. Atopy
  21. Attention
  22. Attributions
  23. Autoantibodies
  24. Autoimmunity
  25. Autonomic function
  26. Beta-2 microglobulin
  27. Blood volume
  28. Borna disease virus (BDV)
  29. Brain injury and fatigue
  30. Brain positron emission tomography (PET)
  31. Branched-chain amino acids (BCAA)
  32. Cancer and fatigue
  33. Cardiovascular deconditioning
  34. Celiac disease
  35. Chlorinated hydrocarbons
  36. Chronic fatigue syndrome (CFS), definition
  37. Ciguatera
  38. Circadian rhythms
  39. Circulating immune complexes
  40. Cognitive behavioral therapy
  41. Cognitive function
  42. Concentration
  43. Connective tissue and rheumatologic disorders
  44. Coping
  45. Core body temperature
  46. Coronary artery disease
  47. Corticotropin-releasing hormone (CRH)
  48. Cortisol
  49. Creatine
  50. Cyanocobalamin
  51. Cysteine
  52. Cytokines
  53. Cytomegalovirus (CMV)
  54. Daytime sleepiness
  55. Demographics
  56. Dental amalgam fillings
  57. Depression
  58. Dermatomyositis
  59. Dexamethasone
  60. Dieting disorders
  61. Disability
  62. Energy expenditure
  63. Enteroviruses
  64. Environmental chemicals
  65. Eosinophils
  66. Epidemiology
  67. Epstein-Barr virus (EBV)
  68. Exercise
  69. Familial chronic fatigue syndrome
  70. Fatigue
  71. Fibromyalgia
  72. Folic acid
  73. Fluoxetine
  74. Food intolerance
  75. Gait
  76. Gastric emptying
  77. Gastrointestinal pathology
  78. Gender
  79. Glandular fever
  80. Glucocorticoids
  81. Glutamine/L-Glutamine
  82. Glutathione
  83. Glycogen
  84. Glyconutrients
  85. Growth hormone (GH)
  86. Gulf War syndrome
  87. Gynecology
  88. Heart rate variability
  89. Herpesviruses
  90. HLA-DR
  91. Hirsutism
  92. Homocysteine
  93. Human herpesvirus-6 (HHV-6)
  94. Human herpesvirus-7 (HHV-7)
  95. Hydrocortisone
  96. Hyperventilation
  97. Hypothalamus-pituitary-adrenal (HPA) axis
  98. Hypothyroidism
  99. Iceland disease
  100. Illness beliefs
  101. Immune cell phenotypic distributions
  102. Immunoglobulins
  103. Inflammatory bowel disease
  104. Information processing
  105. Inner ear disorders
  106. Inomapil
  107. Insulin-like growth factors (IGFs)
  108. Interferons (IFNs)
  109. Interleukin-1 (IL-1) and soluble IL-1 receptors
  110. Interleukin-2 (IL-2) and soluble IL-2 receptor
  111. Interleukin-4 (IL-4)
  112. Interleukin-6 (IL-6) and soluble IL-6 receptor
  113. Interleukin-10 (IL-10)
  114. Interstitial cystitis
  115. Ion channels
  116. Irritable bowel syndrome
  117. Juvenile onset chronic fatigue syndrome
  118. Lactate
  119. Lead poisoning
  120. Learning
  121. Lentiviruses
  122. Light therapy
  123. Low cysteine-glutathione syndrome
  124. Lung function
  125. Lymphocytes
  126. Magnesium
  127. Magnetic resonance imaging (MRI)
  128. Marital relationship
  129. Melatonin
  130. Memory
  131. Menstrual Cycle
  132. Midodrine
  133. Mitochondria
  134. Moclobemide
  135. Monoamine oxidase (MAO) inhibitors
  136. Monocytes
  137. Motor function
  138. Multiple chemical sensitivity (MCS) syndrome
  139. Multiple sclerosis (MS)
  140. Muscle fibers
  141. Muscle physiology
  142. Myalgic encephalomyelitis
  143. Mycoplasma
  144. Myofascial pain
  145. Natural killer (NK) cells
  146. Neopterin
  147. Neurally mediated hypotension
  148. Neurasthenia
  149. Neuroendocrinology
  150. Neurofeedback treatment
  151. Neuroimaging
  152. Neurophysiology
  153. Neuropsychology
  154. Neutrophils
  155. Nighttime hypotension
  156. Nitric oxide
  157. Nutrition
  158. Occupational medicine
  159. Orthostatic hypotension
  160. Ovarian cysts
  161. Overtraining
  162. Pain
  163. Parvovirus B19
  164. Pediatric chronic fatigue syndrome
  165. Personality traits
  166. Phosphate
  167. Phosphorus magnetic resonance spectroscopy
  168. Physical activity
  169. Platelet volume
  170. Polio vaccination
  171. Polycystic ovarian syndrome
  172. Polysomnography
  173. Post-dialysis fatigue
  174. Post-Lyme disease syndrome (PLS)
  175. Post-polio syndrome
  176. Post-Q-fever fatigue syndrome
  177. Postural tachycardia syndrome
  178. Premenstrual syndrome
  179. Prevalence
  180. Progesterone
  181. Prognosis
  182. Prolactin
  183. Protein kinase RNA (PKR)
  184. Prozac
  185. Psychiatric morbidity
  186. Psychoneuroimmunology
  187. Psychopathology
  188. Psychosocial measures
  189. Psychosomatic disorders
  190. Q fever
  191. Quality of life (QOL)
  192. Red blood cell distribution width
  193. Red blood cell mass
  194. Regulation of respiration
  195. Rehabilitation
  196. REM sleep
  197. Reticular activating system
  198. Rh blood group
  199. Rheumatoid arthritis
  200. Rhinitis
  201. RNase L
  202. Ross River virus
  203. Seasonal affective disorder
  204. Selective serotonin reuptake inhibitors (SSRIs)
  205. Selegeline
  206. Self-efficacy
  207. Serotonin
  208. Sick building syndrome (SBS)
  209. Silicone breast implants
  210. Sjögren’s syndrome
  211. Sleep
  212. Socioeconomic status
  213. Sociosomatics
  214. Soluble CDS (sCD8)
  215. Soluble ICAM-1 (sICAM-1)
  216. Somatization
  217. Somatoform disorder
  218. Somatomedin C
  219. Spasmophilia
  220. SPECT SCAN
  221. Spleen
  222. Stealth viruses
  223. Stress
  224. Sub-anaerobic threshold exercise test
  225. Sympathetic hypersensitivity
  226. Systemic lupus erythematosus (SLE)
  227. Tapanui flu
  228. Temporomandibular disorders
  229. Testosterone
  230. Thyroxine
  231. Transfer factors (TFs)
  232. Tryptophan
  233. Tumor growth factor-beta (TGF-beta)
  234. Tumor necrosis factors (TNFs) and soluble TNF receptors
  235. Tyrosine
  236. Urinary metabolites
  237. Vitamins
  238. Yersinia
  239. Notes
  240. Index