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In practice, Clinical Governance Leads are likely to be appropriate, but they can only do so as named individuals. The information that must be contained in all PGDs is bought premarin online in canada below: Name of the business to which the direction applies; Date the direction comes into force and the date it expires; Description of the medicine(s) to which the direction applies; Class of health professional who may supply or administer the medicine; Signature of a doctor and a pharmacist; Signature on behalf of an appropriate organization; Clinical condition or situation to which the direction applies; Description of those patients excluded from treatment under the direction; Description of the circumstances in which further advice should be sought from a doctor, and arrangements for referral; Details of appropriate dosage and maximum total dosage, quantity, pharmaceutical form and strength, route and frequency of administration, and minimum or maximum period over which the medicine should be administered; Relevant warnings, including potential adverse reactions; Details of any necessary follow-up action; and the circumstances; Statement of the records to be kept for audit purposes. Examples of PGDs relevant to podiatric surgery are shown in Appendix C. Podiatrists are already exempt from certain requirements of the Medicines Act. These exemptions allow them to administer or supply certain specified medicines listed in Chapter affected by provisions for PGDs.

Experience and interpretation of pain is subjective and influenced by previous experience and an individuals physical and mental condition at the time. Sensory nerve endings are found throughout the body in the skin, muscles, joints, blood vessels and internal organs. These nociceptors are sensitive to the effects of potentially damaging mechanical, thermal and chemical stimuli. When cells are damaged they release a variety of chemical mediators, which can activate or sensitize nociceptors to other chemicals.

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Attacks of asthma can be prevented by prophylactic use of cromoglicate, although this drug is of no use in an acute attack or in chronic bronchitis. Leukotriene receptor antagonists can be used to reduce the inflammation of asthma particularly in the late phase. Inhaled corticosteroids are useful for treatment and prophylaxis of asthma and for reducing acute exacerbations of bronchitis.

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An infants liver is unable to metabolize certain drugs; for example, inability to metabolize chloramphenicol resulted in grey baby syndrome. Up until at least the age of the kidneys are not as efficient as an adults, so drug elimination may be reduced. Due to the existence of these factors, it is unsatisfactory simply to adjust doses for children because of weight alone.

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This can be prevented by concurrent use of a bronchodilator. Leukotriene receptor antagonists are a relatively new class of drugs that directly bind to leukotriene receptors in the lung preventing the inflammatory actions of leukotrienes particularly in the late phase of asthma. They are used in cases of asthma where there is a poor response to bronchodilators alone. Current examples are montelukast and zafirlukast, both of which are given orally, either alone or in combination with corticosteroids. They are not recommended for use in chronic bronchitis.

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British Hypertension Society guidelines for the management of hypertension have recently been changed to be in line with European guidelines. Drugs that are used to treat hypertension include diuretics, ACE inhibitors, angiotensin II receptor antagonists, β-blockers, calcium channel blockers, α acting antihypertensives. Groups of drugs are described together with their relevant therapeutic indications because often the same drugs are used for different conditions. Cardiac glycosides are used to treat cardiac failure and atrial flutter and atrial fibrillation. Digoxin and digitoxin are cardiac glycosides that improve cardiac contractility, which in turn increases cardiac output.

They have a lower incidence of side effects than aspirin, but are more expensive and probably no more effective. Mefenamic acid, and piroxicam and tenoxicam have a spectrum of side effects between that of aspirin and the ibuprofen type. The oxicams have a markedly longer duration of action than the majority of other NSAIDs and are therefore useful in chronic pain. Indometacin is a much more potent anti-inflammatory drug but poorer analgesic than aspirin. It is more likely to produce serious side effects and is only recommended for chronic pain when other analgesics do not work.

I especially want to thank Leah Greene for her technical expertise and unfailing assistance with computer applications. I am grateful to Alison Barlow and Peter Bowden for their helpful ideas with matters relating to podiatry and Louise Stuart, MBE for an insight into supplementary prescribing; to Jan Dodgeon for help with topics relevant to radiography and Chris Frames and Chris ONeal for their help with devising physiotherapy case studies. Special thanks are due to those who contributed to Chapter Peter Hogg and his co-authors, and Anthony Waddington (Podiatric Surgeon).

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