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| ¿µ¹® | injection | ÇÑ±Û | ÁÖÀÔ |
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| ECG | Electro-Cardio-Graphy(-Gram); ½ÉÀüµµ = EKG 1. Conducting System Structu... |
|---|---|
| misc | miscarriage; miscellaneous |
| SI | International System of Units [Fr. le Systeme International d'Unites]; sacroiliac; saline infusion; ... |
| IT | immunological test; immunotherapy; implantation test; individual therapy; information technology; in... |
| EPO | eosinophil peroxidase; erythropoiesis; erythropoietin; evening primrose-oil; exclusive provider orga... |
| PORT | Patient Outcome Research Team |
|---|---|
| PMGH | Port Moresby General Hospital |
| PWS | Port Wine Stain |
| AIP | Acute Intermittent Porphyria |
| CIC | Clean intermittent catheterisation |
| port | This is an implated access device which allows professional carers to draw blood and make intravenous (or intra-arterial) injections into a patient in an easier way without having to locate and insert a canulla into a new vessel. Some ports are connected for intrathecal, intraperitoneal or intracavitary injections. These devices are expensive and are not free of problems, they should not be implated without good indications. Normally implantation is performed by a surgeon with experience in this technique, in a operational theatre under local anaesthetic. (16 Dec 1997) |
|---|---|
| port-wine mark | Flame nevus, a large congenital vascular nevus having a purplish colour; it is usually found on the head and neck and persists throughout life. See: Sturge-Weber syndrome. Synonym: port-wine mark, port-wine stain. (05 Mar 2000) |
| port-wine stain | <technique> A mark on the skin that resembles port wine (porto) in its rich ruby red colour. Due to an abnormal aggregation of capillaries, a port-wine stain is a type of haemangioma. It occurs on the face as a sign of sturge-weber syndrome. (12 Dec 1998) |
| acute intermittent porphyria | <gastroenterology, haematology> A group of rare inherited metabolic disorders that result from a disturbance in porphyrin metabolism, causing increased formation and excretion of porphyrin or its precursors. It is caused by hepatic overproduction of d-aminolevulinic acid, which has greatly increased urinary excretion and of porphobilinogen, and some increase of uroporphyrin, due to a deficiency of porphobilinogen deaminase. Clinical features: intermittent acute attacks of hypertension, abdominal colic, psychosis, and polyneuropathy, but with no photosensitivity. It is exacerbated by the ingestion of certain drugs such as; barbiturates). Inheritance: autosomal dominant. (20 Sep 2002) |
| Charcot's intermittent fever | Fever, chills, right upper quadrant pain, and jaundice associated with intermittently obstructing common duct stones. (05 Mar 2000) |
| porphyria, acute intermittent | A form of hepatic porphyria (porphyria, hepatic) characterised by periodic attacks of gastrointestinal disturbances, abdominal colic, paralyses, and psychiatric disorders. The onset of this condition is usually in the third or fourth decade of life. (12 Dec 1998) |
| hepatic intermittent fever | Ague-like paroxysms of fever occurring in cases of one or more stones in the common bile duct. (05 Mar 2000) |
| spontaneous intermittent mandatory ventilation | Intermittent mandatory ventilation spontaneously initiated by the patient, to increase tidal volume, and subsequently synchronised with patient's respiratory cycle. Synonym: synchronised intermittent mandatory ventilation. (05 Mar 2000) |
| synchronised intermittent mandatory ventilation | Intermittent mandatory ventilation spontaneously initiated by the patient, to increase tidal volume, and subsequently synchronised with patient's respiratory cycle. Synonym: synchronised intermittent mandatory ventilation. (05 Mar 2000) |
| intermittent | Occurring at separated intervals, having periods of cessation of activity. (18 Nov 1997) |
| intermittent acute porphyria | <gastroenterology, haematology> A group of rare inherited metabolic disorders that result from a disturbance in porphyrin metabolism, causing increased formation and excretion of porphyrin or its precursors. It is caused by hepatic overproduction of d-aminolevulinic acid, which has greatly increased urinary excretion and of porphobilinogen, and some increase of uroporphyrin, due to a deficiency of porphobilinogen deaminase. Clinical features: intermittent acute attacks of hypertension, abdominal colic, psychosis, and polyneuropathy, but with no photosensitivity. It is exacerbated by the ingestion of certain drugs such as; barbiturates). Inheritance: autosomal dominant. (20 Sep 2002) |
| intermittent albuminuria | <nephrology> Functional albuminuria occurring at intervals, such as cyclic albuminuria or albuminuria of athletes. (05 Mar 2000) |
| intermittent arthralgia | A condition in which pain and swelling of one or more joints, most commonly the knee, occurs at regular intervals; there is sometimes abdominal pain, purpura, or oedema. Synonym: intermittent arthralgia. (05 Mar 2000) |
| intermittent claudication | <symptom> A symptom complex characterised by leg pain and weakness brought on by walking, with the disappearance of the symptoms following a brief rest. (12 Dec 1998) |
| intermittent cramp | 1. Hyperexcitability of nerves and muscles due to decrease in concentration of extracellular ionised calcium, which may be associated with such conditions as parathyroid hypofunction, vitamin D deficiency and alkalosis or result from ingestion of alkaline salts, it is characterised by carpopedal spasm, muscular twitching and cramps, laryngospasm with inspiratory stridor, hyperreflexia and choreiform movements. 2. Tetanus. (18 Nov 1997) |
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