| PCCM | pediatric critical care medicine; primary care case management; primary care case manager |
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| PCP | parachlorophenate; patient care plan; pentachlorophenol; 1-(1-phenylcyclohexyl)piperidine; periphera... |
| PH | parathyroid hormone; partial hepatectomy; partial hysterectomy; passive hemagglutination; past histo... |
| PHC | personal health costs; posthospital care; premolar hypodontia, hyperhidrosis, [premature] canities [... |
| PI | first meiotic prophase; isoelectric point; pacing impulse; package insert; pancreatic insufficiency;... |
| failure | The state of insufficiency or nonperformance. (05 Mar 2000) |
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| failure to thrive | <paediatrics> A clinical finding in infants often associated with poor weight gain, malnutrition, poor feeding and a weight for age that is less than the 5th percentile. (27 Sep 1997) |
| kidney failure | <nephrology> The inability of the kidneys to adequately remove wastes from the bloodstream, resulting in severe metabolic derangement's. See: acute renal failure. (27 Sep 1997) |
| kidney failure, acute | A clinical syndrome characterised by a sudden decrease in glomerular filtration rate, often to values of less than 1 to 2 ml per minute. It is usually associated with oliguria (urine volumes of less than 400 ml per day) and is always associated with biochemical consequences of the reduction in glomerular filtration rate such as a rise in blood urea nitrogen (bun) and serum creatinine concentrations. (12 Dec 1998) |
| kidney failure, chronic | An irreversible and usually progressive reduction in renal function in which both kidneys have been damaged by a variety of diseases to the extent that they are unable to adequately remove the metabolic products from the blood and regulate the body's electrolyte composition and acid-base balance. Chronic kidney failure requires haemodialysis or surgery, usually kidney transplantation. (12 Dec 1998) |
| forward heart failure | A concept (formerly considered mutually exclusive of backward heart failure) that maintains that the phenomena of congestive heart failure result from the inadequate cardiac output, and especially from the consequent inadequacy of renal blood flow with resulting retention of sodium and water. Compare: backward heart failure. (05 Mar 2000) |
| left-sided heart failure | Inability of the left heart to maintain its circulatory load with corresponding rise in pressure in the pulmonary circulation usually with pulmonary congestion and ultimately pulmonary oedema. (05 Mar 2000) |
| left ventricular failure | <cardiology> A disorder where the left side of the heart fails to pump blood effectively. This results in a back flow (and pressure) and congestion of blood into the lungs. The causes of this condition include, valvular heart disease, cardiomyopathy, anaemia, hyperthyroidism, atrial myxoma, drug toxicity and congenital heart disease. Risk factors include diabetes, alcoholism, obesity and smoking. Symptoms include increasing shortness of breath with activity and while lying flat. Other symptoms include cough, palpitations, fatigue, decreased urine production and waking in the middle of the nigh with difficulty breathing. Complications include pulmonary oedema, arrhythmias and pleural effusion. (27 Sep 1997) |
| liver failure | A condition of severe end-stage liver dysfunction that is accompanied by a decline in mental status that may range from confusion (hepatic encephalopathy) to unresponsiveness (hepatic coma). Other features include a mousy odour to the breath, difficulty with balance and walking, tremor and impaired speech. (27 Sep 1997) |
| liver failure, acute | A form of liver failure with rapid onset. It is often induced by the toxic effect of drugs and various toxic substances in experimental studies in animals and in clinical states in humans. If coma ensues, the constellation of neurological symptoms is referred to as hepatic encephalopathy. (12 Dec 1998) |
| low output failure | Heart failure in which the cardiac output is subnormal, as is usually seen in failure due to coronary, hypertensive, or valvular heart disease. (05 Mar 2000) |
| acute primary haemorrhagic meningoencephalitis | A disease characterised by acute onset of fever, followed by convulsions, delirium, and coma, and associated with perivascular demyelination and haemorrhagic foci in the central nervous system. Synonym: acute primary haemorrhagic meningoencephalitis, Strumpell's disease. (05 Mar 2000) |
| acyclic monoterpene primary alcohol - NADP oxidoreductase | <enzyme> From catmint nepeta racemosa; involved in the biosynthesis of iridoid monoterpenes; oxidises geraniol, nerol, and their 10-hydroxy derivatives in the presence of nadp(+). Registry number: EC 1.1.1.- Synonym: monoterpene primary alcohol - nadp oxidoreductase, ampano (26 Jun 1999) |
| anterior primary division | <anatomy, nerve> The larger, anterolaterally-directed major terminal branch (with the dorsal primary ramus) of all 31 pairs of mixed spinal nerves, formed at the intervertebral foramen. Most ventral primary rami, especially those involved in the innervation of the limbs, participate in the formation of the major nerve plexuses (cervical, brachial, and lumbosacral) and lose their identities. Most in the thoracic region, however, remain separate from adjacent rami to become the intercostal and subcostal nerves. Ventral primary rami provide innervation to the anterolateral body wall and trunk. Nomina Anatomica lists ventral primary rami as "rami ventrales" for each group of spinal nerves: 1) cervical (nervorum cervicalium ), 2) thoracic (nervorum thoracicorum ), 3) lumbar (nervorum lumbalium ), 4) sacral (nervorum sacralium )m, and 5) coccygeal (nervi coccygei ). Synonym: ramus ventralis nervi spinalis, anterior primary division. (05 Mar 2000) |
| aphasia, primary progressive | A type of aphasia appearing gradually and gradually worsening without any major change in other cognitive functions. It is regarded by some authors as a syndrome which may be due to various degenerative diseases of the cerebral cortex (notably alzheimer disease, owing to its frequency), while others see in it an autonomous disease related to a neuropathological process that is distinct from the main degenerative dementias. The principal clinical peculiarity of primary progressive aphasia is that it spares the patient's autonomy for a long time, but ultimately turns into global dementia. (12 Dec 1998) |