| BEAM | brain electrical activity monitoring |
|---|---|
| BGM | bedside glucose monitoring |
| BM | Bachelor of Medicine; barium meal; basal medium; basal metabolism; basement membrane; basilar membra... |
| BMS | Bachelor of Medical Science; betamethasone; biomedical monitoring system; biomedical science; bleomy... |
| CAMS | computer-assisted monitoring system |
| uterine monitoring | Measurement or recording of contraction activity of the uterine muscle. It is used to determine progress of labour and assess status of pregnancy. It is also used in conjunction with foetal monitoring to determine foetal response to stress of maternal uterine contractions. (12 Dec 1998) |
|---|---|
| baby, foetal alcohol syndrome | <syndrome> Alcohol is capable of causing birth defects. FAS (foetal alcohol syndrome) always involves brain damage. And impaired growth. FAS also always involves head and face abnormalities. No amount of alcohol has been proven safe during pregnancy. Women who are or may become pregnant are advised to avoid alcohol. (12 Dec 1998) |
| baseline foetal heart rate | <paediatrics> The average heart rate for a particular foetus during the diastolic phase of uterine contractions. (05 Mar 2000) |
| baseline variability of foetal heart rate | The beat-to-beat changes in foetal heart rate as recorded on a graph. (05 Mar 2000) |
| rate, foetal mortality | The ratio of foetal deaths divided by the sum of the births (the live births + the foetal deaths) in that year. In the united states, the foetal mortality rate plummeted from 19.2 per 1,000 births in 1950 to 9.2 per 1,000 births in 1980. (12 Dec 1998) |
| marked foetal bradycardia | A foetal heart rate less than 100 beats per minute. (05 Mar 2000) |
| version, foetal | The manual conversion of or changing of the polarity of the foetus with reference to the mother. (12 Dec 1998) |
| maternal-foetal exchange | Exchange of substances between the maternal blood and the foetal blood through the placental barrier. It excludes microbial or viral transmission. (12 Dec 1998) |
| persistent foetal circulation syndrome | <syndrome> A syndrome of persistent pulmonary hypertension in the newborn infant, without demonstrable cardiac disease. It is characterised by cyanosis and acidosis, severe pulmonary vasoconstriction, hypertrophy of pulmonary arterial muscle, and elevated pulmonary vascular resistance, with resultant right-to-left shunting of blood through a patent ductus arteriosus and at times a patent foramen ovale. (12 Dec 1998) |
| circulation, foetal | The blood circulation in the foetus (the unborn baby). Before birth, the blood from the heart that is destined (in the pulmonary artery) for the lungs is shunted away from the lungs and returned to the greatest of arteries (the aorta). The shunt is through a short vessel called the ductus arteriosus. When this shunt is open, it is said to be a patent (pronounced pá tent) ductus arteriosus (PDA). The PDA usually closes at or shortly after birth and blood is permitted to course freely to the lungs. (12 Dec 1998) |
| mild foetal bradycardia | A foetal heart rate less than 120 beats per minute. (05 Mar 2000) |
| mortality rate, foetal | The ratio of foetal deaths to the sum of the births (the live births + the foetal deaths) in that year. In the united states, the foetal mortality rate plummeted from 19.2 per 1,000 births in 1950 to 9.2 per 1,000 births in 1980. (12 Dec 1998) |
| heart rate, foetal | The heart rate of the foetus. The normal range at term is between 120 and 160 beats per minute. (12 Dec 1998) |
| hereditary persistence of foetal haemoglobin | <haematology> Hereditary persistence of foetal haemoglobin is a genetic condition where adult types of haemoglobin fail to develop and the types of haemoglobin the individual had as a foetus remains present well past the point when they would normally have stopped being produced. (09 Oct 1997) |
| hypoplastic foetal chondrodystrophy | A developmental error of the epiphyses characterised by severe deformities, epiphyses ossified from several discrete centres and with a stippled appearance, and thickened shafts of the long bones; congenital cataract and mental retardation are often present. There is an autosomal dominant form and an autosomal recessive form. Synonym: chondrodysplasia punctata, chondrodystrophia calcificans congenita, hypoplastic foetal chondrodystrophy, stippled epiphysis. (05 Mar 2000) |