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The late phases in lung and skin tissue are likely to represent the residue of the early response as well as the contribution of active enzymes generic 1mg arimidex mastercard pregnancy fatigue, newly arrived plasma inflammatory cascades arimidex 1 mg online womens health 48858, various cytokines (particularly those inducing endothelial expression of adhesion molecules) ( 57) purchase arimidex line pregnancy diet, and the influx of activated circulating leukocytes. The late inflammatory response is relevant to the progression of asthma in that patients experiencing the late responses have exacerbation of their nonspecific bronchial hyperreactivity, whereas this phenomenon does not occur after isolated early responses. Because mast cells are positioned near small blood vessels and at the host environment interface, and are thus at crucial sites for regulating local nutrient delivery and for the entry of noxious materials, the potential regulatory role of mediators is obvious. They are likely to be especially important in the regulation of flow through small blood vessels, impulse generation in unmyelinated nerves, and smooth muscle and bone structural integrity and function. The ability to recruit and activate plasma proteins and cells may also provide preimmune defense against host invasion by infectious agents. Such a role is most apparent in parasitic infestation but is also likely in the case of other insults. Moreover, the recognition of mast cell heterogeneity implies that differences in mast cells relate to locally important biologic requirements. Although the homeostatic and pathophysiologic role of mast cell mediators is understood imprecisely, the broadening understanding of their chemical nature and function provides a useful framework for addressing their role in health and disease. The diverse potential effector and immunoregulatory roles of mast cells in allergic disease. Ribonuclease-gold ultrastructural localization of heparin in isolated human lung mast cells stimulated to undergo anaphylactic degranulation and recovery in vitro. Dependence of mast cell IgE-mediated cytokine production on nuclear factor-kB activity. Clinical manifestations of the release of histamine and other inflammatory mediators. Histamine and tryptase levels in patients with acute allergic reactions: an emergency department-based study. Platelet activating factor: a potent chemotactic and chemokinetic factor for eosinophils. Effects of platelet activating factor on pulmonary function and bronchial responsiveness in man. The bronchoconstrictor effects of inhaled prostaglandin D2 in normal and asthmatic men. A prostaglandin J2 metabolite binds peroxisome proliferator-activated receptor gamma and promotes adipocyte differentiation. IgE-dependent activation of cytokine primed mouse cultured mast cells induces a delayed phase of prostaglandin D2 generation via prostaglandin endoperoxidase synthase 2. Molecular cloning and characterization of a second human cysteininyl leukotriene receptor: discovery of a subtype selective agonist. A3 adenosine receptor activation triggers phosphorylation of protein kinase B and protects rat basophilic leukemia 2H3 mast cells from apoptosis. Release of neutrophil chemotactic activity during immediate hypersensitivity reactions in humans. Increased biosynthesis of platelet activating factor in activated human eosinophils. Development of a new, more sensitive immunoassay for human tryptase: use in systemic anaphylaxis. Effect of mast cell-derived mediators and mast cell-related neutral proteases on human dermal fibroblast proliferation and type 1 collagen production. Second-generation, nonsedating H 1 receptor antagonists, many of which have been derived from first-generation agents, have added a new dimension to the treatment of allergic disorders. During the past several years, a new field of pharmacoepidemiology has also emerged, largely as a result of postmarketing surveillance of these newer H1 antagonists. In fact, investigations into the adverse drug reactions associated with the second-generation agent terfenadine have served as prototypes for the design of current long-term surveillance studies monitoring the safety of drugs in a variety of clinical situations. The term histamine was adopted because of its prevalence in animal and human tissues (hist, relating to tissue) and its amine structure ( 2,3) (Fig. Subsequently, histamine was found to be synthesized from L-histadine by L-histidine decarboxylase and metabolized by histamine N-methyltransferase to form N-methylhistadine or by diamine oxidase to form imidazole acetic acid ( 5). Histamine is stored in the cytoplasm of mast cells and basophils, attached to anionic carboxylate and sulfate groups on secretory granules ( 5). Histamine is released from mast cell and basophil secretory granules after aggregation of high-affinity immunoglobulin E (IgE) receptors. IgE receptors are coupled to G proteins, which, when activated, lead to a sequence of chemical reactions with the end result being histamine release. This speculation was confirmed by Black and co-workers in 1972, who used the experimental histamine antagonists mepyramine and burimamide to block histamine-induced reactions in animals ( 8). They observed that each of these antagonists inhibited different physiologic responses, suggesting that there were at least two histamine receptors, now referred to as H 1 and H2 (8). Arrang and colleagues discovered a third histamine receptor (H3) with unique physiologic properties, raising the possibility that additional, yet unrecognized, histamine receptors exist ( 9). Effect of histamine on human histamine receptors The first histamine antagonist was serendipitously discovered in 1937 by Bovet and Staub who found that a drug originally being studied for its adrenergic antagonistic properties in guinea pigs also had potent antihistaminic activity ( 3). By 1942, safe and effective antihistamines developed for human use became available. H2 antagonists were first synthesized in 1969 for the purpose of developing a drug capable of inhibiting gastric acid secretion ( 13). These agents have a closer structural resemblance to histamine because most are simple modifications of the histamine molecule itself ( 14,15). Histamine is composed of a single imidazole heterocyclic ring linked to an ethylamine group, whereas H1 antagonists consist of one or two heterocyclic or aromatic rings joined to a linkage atom (nitrogen, oxygen, or carbon) ( 3) (Table 5. Generally, these compounds are rapidly absorbed orally or intravenously, resulting in peak serum concentrations within 2 to 3 hours and symptomatic relief within 30 minutes. They have large volumes of distribution, have slow clearance rates, and are metabolized primarily by hydroxylation in the hepatic cytochrome P-450 system. Most of the parent drug is excreted as inactive metabolites in the urine within 24 hours of dosing. The lipophilic nature of these antihistamines allows them to cross the placenta and the blood brain barrier. Pharmacokinetics of H1 receptor antagonists in healthy young adults Pharmacodynamics The first-generation H1 antagonists compete with histamine for binding to histamine receptors. This competitive inhibition is reversible and, therefore, highly dependent on free drug plasma concentrations. As these agents are metabolized and excreted into the urine as inactive metabolites, the histamine receptors become desaturated, allowing surrounding histamine to bind. This mechanism emphasizes the need to instruct patients in using these agents on a regular basis to achieve a maximal therapeutic benefit (3,22). Interestingly, smaller doses of H 1 antagonists have been found to inhibit mast cell activation in vitro, whereas larger doses cause mast cell activation and histamine release ( 23). Before the availability of pharmacokinetic data, these agents were believed to have short half-lives, which necessitated frequent dosing intervals in order to be effective ( 22). The availability of sustained-release preparations of shorter half-life agents has also allowed less frequent dosing, thereby improving patient compliance and minimizing side effects.
Database/retrieval system on the Internet with joint publication WormBase: the Biology and Genome of C order 1 mg arimidex pregnancy 3 weeks. Database/retrieval system on the Internet with standard date of publication Database of Human Disease Causing Gene Homologues in Dictyostelium Discoideum [Internet] purchase arimidex on line amex zyrtec menstrual cycle. The Alberta Atlas of Human Pathology: a Resource for Teachers and Learners in the Health Sciences [Internet] order discount arimidex on-line pregnancy early symptoms. Database/retrieval system on the Internet with date of copyright instead of date of publication Biozon [Internet]. Database/retrieval system on the Internet with date obtained from earliest material in it PubMed [Internet]. Database/retrieval system on the Internet with unknown date The Internet Acronym Server [Internet]. Database/retrieval system on the Internet with update/revision date Health Library for Disasters [Internet]. Database/retrieval system on the Internet with supplemental note included Is Your Doctor Certified? Pfam is a large collection of multiple sequence alignments and hidden Markov models covering many common protein domains and families. Institutional repository of the University of California Libraries intended to provide comparative and historical information about traditional medical beliefs. Databases/Retrieval Systems on the Internet 1297 Drugs and Lactation Database (LactMed) [Internet]. Sample Citation and Introduction to Citing Parts of Databases on the Internet The general format for a reference to a part of a database on the Internet, including punctuation: Examples of Citations to Parts of Databases on the Internet Rather than citing a whole database, portions of a database may be cited. They are contributions when the database has individual records or other components written by various authors, usually called contributors. A reference should start with the individual or organization with responsibility for the intellectual content of the publication: Begin a reference to a part of a database with a citation to the database itself, followed by information about the part. For parts that contain hyperlinks, however, such as those shown in example 11, it will not be possible to provide the length. Citation Rules with Examples for Parts of Databases on the Internet Components/elements are listed in the order they should appear in a reference. Name and Number/Letter of the Part of a Database on the Internet (required) General Rules for Name and Number/Letter Enter the name of the part as it appears in the database Capitalize the name, such as Record, Table, Chart You may abbreviate Number to No. Otdel 6 Romanize or translate titles in character-based languages (Chinese, Japanese). 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Part of a database on the Internet with a date of publication separate from the date of the database as a whole Current Controlled Trials [Internet]. Part of a database on the Internet with a date of update/revision Cornell University Poisonous Plants Informational Database [Internet]. Alzheimer disease; [updated 2008 Oct 20; reviewed 2006 Oct; cited 2008 Oct 22]; [about 6 screens]. Part of a Database on the Internet with location (pagination) expressed as number of pages Antimicrobial Resistance Information Bank [Internet].
The first is the rate of 25 -0 - Control growth organism killing and whether increasing drug concen- - - Cefazolin 12 purchase discount arimidex online women's health issues heart disease. Simultaneous drug activity and in fact have been demonstrated to be serum cefazolin concentrations are also shown 1mg arimidex menopause signs and symptoms. Baltimore generic arimidex 1mg on-line menstruation after mirena removal, Williams & Wilkins,1996, pp it is important to maximize the duration of time for which 296-329. The pharmacologic goal of dosing regimens with these Antifungal compounds have also been shown to have agents would be to maximize concentrations by adminis- prolonged persistent effects. Nearly all antibacterials appear to be capable of producing per- On the basis of these two time-course characteristics sistent effects with staphylococci. This pattern of killing and per- did not appreciably increase the rate of killing. Thus high The dosing frequency is usually not a major factor in concentrations will not kill the organisms faster or more determining the efficacy of these drugs. Effect of increasing the dose or U 1 changing the dosing interval of a hypothetical E drug on the C.. These however, vary dosing frequency comparing the efficacy relationships have been examined primarily in in vitro and of continuous vs. Investigation in human clinical tri- otics, including cefamandole, in febrile neutropenic als to support or refute the observations from in vitro and patients. Two other studies have impact of higher doses of drug on efficacy with usually all compared continuous and intermittent infusions of cef- tazidime in the treatment of gram-negative infections. However, much of the Although it can be difficult to vary dosing regimens interdependence among pharmacodynamic parameters can in clinical trials enough to reduce the inherent parameter be eliminated with dosing regimens that use different dosing interrelationships, studies in animal infection models do intervals. I nterrelationship among dosing interval number and the pharmacokinetic and pharmacodynamic parameters. The 02 value represents the percentage of variation in bacterial numbers that could be attributed to differences in each of 0 20 40 60 80 3 30 300 3000 3 30 300 3000 the individual pharmacodynamic parameters. Pairs of neutropenic mice were treated with drugs 12,13 For example, Blaser et al demonstrated superior multiple dosage regimens of meropenem that varied both efficacy with single compared with multiple aminoglyco- in the total dose and dosing interval. The dotted line reflects the 5 00 00 number of bacteria at the initiation of therapy. Various studies, however, concentrations are used, and for different sites of infec- have demonstrated the impact of dose and dosing interval tion. Most recently this type of 100 analysis has been used in the development of antimicro- 50 bial treatment guidelines for otitis media, sinusitis, and community-acquired pneumonia. Antimicrob Agents about 50% of the dosing interval, similar to the rela- Chemother 1998;42:2375-2379. This pharmacodynamic target ences in kinetics, one would expect that the patterns of is based upon results from animal model studies. As one would expect, the primary therapeutic agents used in these respiratory tract treatment trials have (t/O included a variety of R-lactams and macrolide antibiotics. Ambrose et al observed a similar association in ceftazidime dose administered via continuous infusion the treatment of community-acquired pneumonia. Continuous infu- study of cefuroxime therapy compared continuous infu- sion is best suited for R-lactam drugs with short elimina- sion of 1. This regimen design can be convenient in the macrolides have also been examined in double-tap otitis outpatient setting because of the reduction in the number. As with P-lactams, when serum levels necessary to achieve the pharmacodynamic goal. For example, treatment against susceptible choose this as a target steady state concentration for con- S. One could estimate the dose and patients treated with erythromycin and clarithromycin, rate of infusion with a simple calculation. In these trials, both erythromycin and clarithromycin resulted in bacteriologic success rates similar to those 60 that would be observed with placebo (50% or less). One clini- Although in vitro susceptibility testing with antifungals has cal nosocomial pneumonia trial also reported a clinical only recently been standardized, data from a number of ani- response rate (reduction in fever and leukocytosis) in mal model studies and clinical trials suggest that triazole more than 90% of patients when the C. With dose escalation to 400 or 800 mg/day, a simi- 40 lar ratio would be seen at the susceptible-dose-dependent 20 0 breakpoints (16-32 pg/mL), again similar to the parameter 0 magnitude observed in animal infection models. If, however, this param- produce pharmacodynamic parameter magnitudes equal eter magnitude is relevant for other organisms, it would to those shown to be successful in the treatment of sus- suggest that we are currently overdosing this compound ceptible pathogens. Current administra- namic studies with amoxicillin and amoxicillin- tion of 100 to 150 mg/kg/day in four divided doses would clavulanate against a large number of strains of S. Analysis of cefprozil ther- drug toxicity by occasionally allowing the administration of apy in this model has demonstrated similar results. Various of techniques to examine the effects of different antimi- types of data have been factored into breakpoint determi crobial classes in combination. R 2, percentage of variation in bacterial numbers that could be attrib- uted to differences in each of the pharmacodynamic parameters. The susceptibility breakpoints for the Pallares et al were the first to address this issue. There are numerous case independent of the susceptibility of the pathogen (Table reports of meningitis treatment failures to support these 1-5). This would Pneumococci on Mortality in Community- include macrolide- and ketolide-resistant pathogens with Acquired Pneumonia methylase mutations and fluoroquinolone mutations in Mortality/Patients in group (%) one of the gyrases. There has, however, been a general resistance mechanism for which the degree of in vitro Penicillin resistance does not appear to predict the in vivo behavior. However, Animal model studies with numerous fluoroquinolones, there is also a clear association between antimicrobial macrolides, and ketolides have likewise demonstrated that exposure and the selection or development of resistance. Antimicrobial Pharmacokinetics and Pharmacodynamics 1 17 Resistance Mutations significantly reduce the emergence of resistant subpopula- tions with fluoroquinolones and aminoglycosides. Thomas et al similarly examined data from a that long half-life drugs that provide sustained but sub- larger cohort of 107 patients with pneumonia. Both amoxicillin-clavulanate and azithromycin were suc- It is not clear if the same magnitudes for the C. Further studies are necessary to examine the clinical relevance of these observations. Pharmacokinetic and pharmacodynamic parameters are the major determinants of the efficacy of antimicrobial Selection of Resistant Mutants therapy. The ability of a drug to reach the magnitude of Although it has been difficult for animal infection models the parameter required for efficacy against common to examine the relationship between the time course of pathogens and emerging resistant organisms should be antimicrobial exposure and the development of resistance considered in drug and dosage regimen selection for mutations, these models have been useful for describing empiric therapy (Table 1-8). Antimicrobial pharmacody- the relationship between antimicrobial pharmacodynam- namic analyses have been useful for the development of ics and the selection of resistant subpopulations. For (1) in vitro susceptibility breakpoints, (2) antimicrobial example, several animal and in vitro studies have sug- treatment guidelines, (3) new drug formulations (e. In Lorian V enhancement: Increased susceptibility of bacteria pretreated (ed): Antibiotics in Laboratory Medicine, 4th ed.
Furthermore buy 1 mg arimidex mastercard women's health center templeton, it will For almost 50 years the focus was on the prevention of develop other activities generic arimidex 1mg with amex menstrual 1 day period, including advocacy cheap arimidex 1mg fast delivery menopause gas bloating. Research reveals that such therapies are effective in the reduction of chronic pain and absenteeism from work (22). Relaxation techniques, hydrotherapy and exercise are helpful in the management of painful conditions that have a musculoskeletal com- ponent. There is good evidence that multimodal treatment and rehabilitation programmes are effective in the treatment of chronic pain (23, 24). All health-care workers who treat pain, especially chronic pain, whatever its cause, can expect about 20% of patients to develop symptoms of a depressive disorder. Among patients attending pain clinics, 18% have moderate to severe depression when pain is chronic and persistent. It is known that the presence of depression is associated with an increased experience of pain whatever its origin and also reduced tolerance for pain. Therefore the quality of life of the patient is signicantly reduced, and active treatment for depression is an important aspect of the manage- ment of the chronic pain disorder. Service delivery The management of neurological diseases is primarily a matter for specialist medical and nursing staff, both in developed and developing countries. The relief of pain should be one of the fundamental objectives of any health service. Good practice should ensure provision of evidence-based, high quality, adequately resourced services dedicated to the care of patients and to the continuing education and development of staff. Multidisciplinary pain centre The centre comprises a team of professionals from several disciplines (e. Multidisciplinary pain clinic The clinic is a health-care delivery facility with a team of trained professionals who are devoted to the analysis and treatment of pain. Pain clinic Pain clinics vary in size and stafng complements but should not be run single-handed by a clinician. Modality-orientated clinic The clinic offers a specic type of treatment and does not conduct comprehensive as- sessment or management. They are met to a much lesser extent in developing countries, where other health priorities, costs of treatment and availability of trained personnel are all contributing factors to the relative lack of resources. Nevertheless, strenuous efforts to improve services for people in pain are being made in many developing countries. Even though services for neurological disorders are better provided, many patients with pain of neurologi- cal origin may never reach such centres. There is therefore a great need for health-care providers to devote more resources to pain relief in general, which in turn will bring about an improvement in the treatment facilities available for neurological patients with pain. Its Special Interest Group on Neuropathic Pain provides a forum for scientic exchange on neuropathic pain and other types of pain that are related to neurological disorders (26). In Germany, a medical subspecialty, specialized pain therapy, is supervised by a licensed training centre and carried out after nishing a residency in one of the traditional medical specialties. More general training in pain management does exist but it is very variable within and between specialist medical areas and between countries. Training programmes for nurses who will specialize in pain management are growing steadily. Such programmes exist mainly in relation to palliative care, post-operative pain management and the work of pain clinics in developed countries but, increasingly, also in countries in the developing world. Physiotherapy is a discipline in which pain management is an integral part of the working day and therefore should be a major aspect of the training of all physiotherapists. Clinical psychologists have a major role in the treatment of chronic pain patients. Usually they specialize in pain management after a period of postgraduate training in general clinical psychol- ogy and practise either independently or in specialist pain centres. Very few clinical psychologists are available for work with patients in pain, whether attributable to neurological conditions or not, in developing countries. However, specialist training in pain management for medical practitioners who work in hospitals or the community in developing countries is spreading gradually. Neurologists and non-neurologists who have responsibility for patients with neurological disorders should ensure that pain is assessed carefully and recorded in terms of its origins, nature and severity as part of an overall clinical assessment prior to diagnosis and management. Postgraduate training is also neglected in many countries, though specialization in pain management is increasing steadily, particularly in developed countries. There is a need to continue and expand postgraduate training in pain management and to develop specialized pain management centres. Recognized international guidelines for the use of powerful analgesics should be observed and unduly restrictive regulations should be suitably modied to ensure availability on a reasonable basis. Guidelines should be made available on the use of co-analgesic drugs and other treatments used to relieve or control very severe pain. Classication of chronic pain: descriptions of chronic pain syndromes and denitions of pain terms, 2nd ed. Persistent pain and well-being: a World Health Organization study in primary care. Screening of neuropathic pain components in patients with chronic back pain associated with nerve root compression: a prospective observational pilot study. Therapeutic outcome in neuropathic pain: relationship to evidence of nervous system lesion. A 5-year follow-up evaluation of the health and economic consequences of an early cognitive behavioural intervention for back pain: a randomized controlled trial. Treatment outcome of chronic non-malignant pain patients managed in a Danish multi- disciplinary pain centre compared with general practice: a randomized controlled trial. Urinary disturbances, orthostatic hypotension and neuropsychiatric disturbances (dementia, hallucinations and delirium) usually become evident and troublesome after several years in the course of the disease (3). Overt dementia is a late complication that most frequently affects older patients with prolonged disease duration (4). Late-onset motor symptoms include postural instability and falls, freezing of gait, speech and swallowing difculties. The consequence of this denervation process is an imbalance in the striato-pallidal and pallido-thalamic output pathways, which is responsible for the major motor decits (5). Genetic predisposing factors in combination with environmental factors are thought to be responsible for the cellular changes leading to progressive neuronal degeneration in which mitochondrial dysfunction, oxidative mechanisms and failure of the protein degradation machinery at the cellular level are probably involved (6). These criteria are used worldwide and provide for a denite neurological disorders: a public health approach 141 diagnosis with a high degree of accuracy. Clinicopathological studies based on brain bank material from Canada and the United Kingdom have shown that clinicians diagnose the disease incorrectly in about 25% of patients. In these studies, the most common reasons for misdiagnosis were presence of essential tremor, vascular parkinsonism and atypical parkinsonian syndromes (8). The quest for environmental exogenous triggering factors has remained elusive and supported only through indirect evidence gathered from numerous and extensive epidemiological studies. The wide variation in incidence estimates probably reects differences in methodology and case ascertainment as well as age distribution of the sample population. As this is a chronic disorder with a prolonged course, prevalence is much higher than incidence. Crude prevalence estimates vary from 18 per 100 000 persons in a population survey in Shanghai, China, to 328 per 100 000 in a door-to-door survey of the Parsi community in Bombay, India.
For an analysis see Max Gluckman buy generic arimidex 1mg line menstruation 2 weeks early, Order and Rebellion in Tribal Africa (New York: Free Press generic arimidex 1mg mastercard menstruation education for kids, 1963) order arimidex with a visa breast cancer epidemiology. Ackerknecht, "Natural Diseases and Rational Treatment in Primitive Medicine," Bulletin of the History of Medicine 19 (May 1946): 467-97. Titmuss, The Gift Relationship (New York: Pantheon, 1971), compares the market for human blood under U. But see also the judgment of Ibn Khaldun, The Muqaddimak: An Introduction to History, trans. Roth, "Ritual and Magic in the Control of Contagion," American Sociological Review 22 (June 1957): 310-14. Belief in the danger of contagion from tuberculosis patients leads to ritualized procedures and irrational practices. For instance, the rules compelling patients to wear protective masks are strictly enforced when they go to X-ray services but not when they go to movies or socials. Shapiro, "Factors Contributing to the Placebo Effect: Their Implications for Psychotherapy," American Journal of Psychotherapy 18, suppl. Beecher, "Surgery as Placebo: A Quantitative Study of Bias," Journal of the American Medical Association 176 (1961): 1102-7. I argue here that similar effects can be sociopolitically transmitted by highly visible interventions. Beecher, "Nonspecific Forces Surrounding Disease and the Treatment of Disease," Journal of the American Medical Association 179 (1962): 437-40. Victims of Haitian magic have ominous and persistent fears, which cause intense action of the sympatico-adrenal system and a sudden fall of blood pressure resulting in death. Wolf, "Effects of Suggestion and Conditioning on the Action of Chemical Agents in Human Subjects: The Pharmacology of Pa. Ackerknecht offers an important corrective to the Parsonian prejudice that all societies incorporate a specific kind of power in the healer. He shows that medicine man and modern physician are antagonists rather than colleagues: both take care of disease, but in all other ways they are different. Deals with the healing powers traditionally attributed to outcastes and marginals such as executioners, gravediggers, prostitutes, and millers. Troels-Lund, Gesundheit and Krankheit in der Ansctumung alter Zeiten (Leipzig, 1901), is an early study of the shifting frontiers of sickness in different cultures. For orientation on the evolution of recent discussion see David Mechanic, Medical Sociology: A Selective View (New York: Free Press, 1968), especially pp. Frake, "The Diagnosis of Disease Among the Subanun of Mindanao," American Anthropologist 63 (1961): 113-32. Henderson, "Physician and Patient as a Social System," New England Journal of Medicine 212 (1935): 819-23, was perhaps the first to suggest that the physician exonerates the sick from moral accountability for their illness. For the classical formulation of the modern, almost morality-free sick-role, see Talcott Parsons, "Illness and the Role of the Physician" (orig. He rejects the notion that illness starts with the presentation of symptoms to a professional. The latter, a service to the patient, can be provided in two profoundly distinct ways. It can be the output of an institution and its functionaries executing policies, or it can be the result of personal, spontaneous interaction within a cultural setting. The distinction has been elaborated by Jacques Ellul, The Technological Society (New York: Random House, 1964). The phenomenology of personal care has been developed by Milton Mayeroff, On Caring (New York: Harper & Row, 1971). Notwithstanding the prevailing logical and rational explanations for their sickness, they too grapple with it in religious, cosmic, and especially moral terms. In the first six months of 1970, 5 million working days were lost in Britain owing to industrial disputes. In comparison, over 300 million working days were lost through absence due to certified sickness. According to Karier, tests given outside the schools are a more powerful device for discrimination than tests given within a pedagogical situation. In the same way, it can be argued that medical testing becomes an increasingly powerful means for classification and discrimination, as the number of test results accumulate for which no significant treatment is feasible. Once the patient role becomes universal, medical labeling turns into a tool for total social control. Since the sixties a citizen without a medically recognized status has come to constitute an exception. A case study by a criminologist of the conflict between two monopolistic professional empires. The medicalization of all diagnosis denies the deviant the right to his own values: he who accepts the patient role implies by this submission that, once restored to health (which is just a different kind of patient role in our society), he will conform. The medicalization of his complaint results in the political castration of his suffering. Pitts, "Social Control: The Concept," International Encyclopedia of the Social Sciences (1968), 14:391. On the rise of the pan-therapeutic society in which morality-charged roles are extinguished. Buytendijk, Allgemeine Theone der menschlichen Haltung tmd Bewegung (Berlin: Springer, 1956). Through a comparison with other species, he comes to describe man as a physiologically and psychologically self-structuring organism. Pappe, "On Philosophical Anthropology," Australasian Journal of Philosophy 39 (1961): 47-64. Man has no built-in evolutionary mechanisms that would lead him to an equilibrium; his creative availability gives to his environment (Umwelt) characteristics different from those it has for other species: it turns habitat into home. Ackerknecht, "Primitive Medicine and Culture Patterns," Bulletin of the History of Medicine 12 (November 1942): 545-74. Sigerist states: "Culture, whether or not primitive, always has a certain configuration. It is one expression of it, and cannot be fully understood if it is studied separately. Evans-Pritchard, Witchcraft, Oracles and Magic Among the Azande (New York: Oxford Univ. I argue here that health and my ability to remain responsible for my behavior in suffering are correlated. Dunn, "Traditional Asian Medicine and Cosmopolitan Medicine as Adaptative Systems," mimeographed, Univ. He claims that 95% of the ethnographic (and also anthropological) literature on health-enhancing behavior and on the beliefs underlying it deals with curing and not with the maintenance and expansion of health.
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