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Query: UMLS:C0020505 (hyperphagia)
 6,116 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In a Mapleson D circuit the carbon dioxide content of gases, sampled at the breathing bag or near the bellows of the ventilator, is virtually constant throughout the phases of respiration. Assuming that after induction of anaesthesia the fresh gas inflow, if kept constant, is essentially equal in volume to the gas vented at the expiratory valve, CO2 output can be calculated by multiplying the fresh gas inflow by the CO2 content of the vented gas measured with a suitable CO2 analyzer. Anaesthesia with nitrous oxide-oxygen, supplemented with low doses of alphaprodine or halothane was compared in two groups of young patients who underwent dental surgery and who were breathing spontaneously. While the CO2 output in the group supplemented with alphaprodine increased from about 100 to 130 ml/m2/min, the halothane group showed a constant CO2 output of about 90 ml/m2/min followed by a significant rise within 5 minutes after halothane was discontinued. In 42 patients on controlled ventilation, no significant difference was found in the CO2 output estimated one hour after induction of anaesthesia in nitrous oxide-oxygen anaesthesia supplemented by halothane, ethrane or alphaprodine. The values obtained were 87 +/- 11 ml/m2/min for halothane (11 patients), 98 +/- 19 ml/m2/min for ethrane (14) and 93 +/- 13 ml/m2/min for the narcotic supplemented anaesthesia (17). The mean CO2 output for all 42 patients was 93 +/- 14 ml/m2/min. Six markedly obese patients under the same anaesthetic technique had a CO2 output of 114 +/- 17 ml/m2/min; however, their CO2 output was similar to normal patients when calculated on the basis of body weight. A marked increase in CO2 output to a mean of 160 +/- 25 ml/m2/min was found in eight patients undergoing operation while on hyperalimentation. The technique described appears suitable to monitor CO2 output under anaesthesia. In order to avoid hypercarbia when using a partial rebreathing system, the fresh gas inflow must be increased above recommended values in cases with increased metabolic activity (e.g. patients receiving hyperalimentation). In obese patients the fresh gas inflow should be calculated on the basis of body weight.
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PMID:Carbon dioxide output in anaesthesia. 125 73

Exercise training has been considered suitable only in cystic fibrosis (CF) patients with mild to moderate pulmonary dysfunction without progressive hypoxaemia during exercise. We trained 16 CF patients, all with advanced lung disease (mean standardized forced expiratory volume in 1 s (FEV1), 30% pred.), with a ventilatory limitation to exercise and a progressive hypoxaemia and hypercapnia at low maximal exercise capacity, Wmax (mean Wmax, 50% pred). Exercise training was performed on a cycle ergometer twice a day for 20 min at approximately 75% of the maximal predicted heart rate for at least 3 weeks. Supplemental oxygen was administered to reach a haemoglobin oxygen saturation of 90% during training. Patients considered malnourished because of a Quetelet Index of less than 20 kg m-2 received hyperalimentation orally or by duodenal tube (total 3500-4000 kcal day-1). Evaluation directly after the training period showed a statistically significant improvement in Wmax, maximal oxygen consumption, maximal minute ventilation, pulse, PaCO2 at rest, FEV1 and body weight. None of the pretraining variables was able to predict the outcome of the training programme in the individual patient. We detected no adverse effects of the programme. This study shows that oxygen-assisted exercise training in combination with correction of the nutritional status is safe and beneficial in CF patients with severe lung disease.
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PMID:Oxygen-assisted exercise training in adult cystic fibrosis patients with pulmonary limitation to exercise. 193 21

Congenital central hypoventilation syndrome (CCHS) is a rare disorder with uncertain nosology that usually presents early in life. The syndrome is characterized by ventilatory response impairment to carbon dioxide and may result in respiratory failure at birth. Recent reports have identified a similar clinical presentation beyond infancy called late-onset central hypoventilation syndrome (LO-CHS) as a disease continuum of CCHS with similar and overlapping pathophysiology. However, some have proposed that the syndrome accompanied by hypothalamic dysfunction (HD) be classified as a distinct clinical entity, LO-CHS/HD. To the best of our knowledge, the case reported herein is the oldest case of LO-CHS/HD in childhood, at 13 years old. He suffered from recurrent pulmonary edema, acute convulsive seizures, hypersomnia, hyperphagia, obesity, impaired glucose tolerance test, and hypercapnia, diagnosed as LO-CHS/HD, and was successfully treated with nasal bi-level positive airway pressure.
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PMID:A case of late-onset central hypoventilation syndrome with hypothalamic dysfunction: through a new phenotype. 2056 Feb 60