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2.
Stud Health Technol Inform ; 124: 801-6, 2006.
Article in English | MEDLINE | ID: mdl-17108612

ABSTRACT

This paper proposes a number of revisions to CEN/TS 14463 (ClaML), which is a pre-standard mark-up language for the electronic publication of classification coding schemes. A CEN Taskforce in close collaboration with the WHO network carefully analysed 70 classifications from the healthcare domain. All were transformed in ClaML using a dedicated classification management tool. The proposal removes all formatting elements and adds a number of layout structuring elements. Several elements have been replaced by attributes to enforce internal consistency. A modest number of extensions are proposed to help users and authors in maintenance and version control. A pilot implementation has shown that ICD10 as one of the most complex traditional classifications can be adequately represented to produce quality printed output.


Subject(s)
Forms and Records Control/standards , Medical Informatics , Programming Languages , International Classification of Diseases
3.
Schmerz ; 14(2): 97-103, 2000 Apr.
Article in German | MEDLINE | ID: mdl-12800046

ABSTRACT

ICD-10 was implemented for morbidity coding in Germany in January 2000. The electronic versions of ICD-10 are introduced. For everyday work with the classification and for epidemiological research further tools are provided by DIMDI: ICD-10 meta files, ICD conversion tables, ICD-10 thesaurus of diagnostic terms. All files are available free of charge via the INTERNET.

4.
Anaesthesist ; 48(12): 924-30, 1999 Dec.
Article in German | MEDLINE | ID: mdl-10672359

ABSTRACT

ICD-10 is to be implemented for morbidity coding in Germany soon. The electronic versions of ICD-10 are introduced. For everyday work with the classification and for epidemiological research further tools are provided by DIMDI:ICD-10 meta files, ICD conversion tables, ICD-10 thesaurus of diagnostic terms. All files are available free of charge via the INTERNET.


Subject(s)
Disease/classification , Internet , Germany
5.
Eur J Appl Physiol Occup Physiol ; 62(3): 228-34, 1991.
Article in English | MEDLINE | ID: mdl-2044531

ABSTRACT

As a result of our recently published studies we have thought that altitude diuresis resulting from hypoxic stimulation of the arterial chemoreceptors reduces the cardiac volume overload. To test this hypothesis, cardiovascular, endocrine and renal responses to stepwise acute exposure to simulated altitude (6,000 m) were compared in ten acclimatized recumbent mountaineers a mean of 24 days, SD 11, after descending from Himalayan altitudes of at least 4,000 m, with those found in ten non-acclimatized recumbent volunteers. The results showed that natriuresis and diuresis typified the renal responses to altitude exposure of both the acclimatized as well as non-acclimatized subjects, as long as altitude was well tolerated. It was concluded that the renal effects were mediated by atrial natriuretic peptide release and slight suppression of arginine-vasopressin (AVP) secretion, that the increased urine flow at altitude offset the cardiac (volume) overload resulting from hypoxic stimulation of the arterial chemoreceptors, and that enhanced AVP secretion, as found in the non-acclimatized subjects at and above 4,000 m, coincided with subjective and objective distress, i.e. with inadequate altitude adjustment owing to insufficient chemoreflex effects and central hypoxia.


Subject(s)
Acclimatization , Altitude , Diuresis , Endocrine Glands/physiopathology , Hypoxia/physiopathology , Kidney/physiopathology , Acute Disease , Adult , Cardiovascular System/physiopathology , Humans , Male , Middle Aged
6.
Article in English | MEDLINE | ID: mdl-2022205

ABSTRACT

Respiratory, circulatory and neuropsychological responses to stepwise, acute exposure at rest to simulated altitude (6,000 m) were compared in ten acclimatized recumbent mountaineers 24 days, SD 11 after descending from Himalayan altitudes of at least 4,000 m with those found in ten non-acclimatized recumbent volunteers. The results showed that hypoxic hyperpnoea and O2 consumption at high altitudes were significantly lower in the mountaineers, their alveolar gases being, however, similar to those of the control group. In the acclimatized subjects the activation of the cardiovascular system was less marked, systolic blood pressure, pulse pressure, heart rate and thus (calculated) cardiac output being always lower than in the controls; diastolic blood pressure and peripheral vascular resistance, however, were maintained throughout in contrast to the vasomotor depression induced by central hypoxia which occurred in the non-acclimatized subjects at and above 4,000 m [alveolar partial pressure of O2 less than 55-50 mmHg (7.3-6.6 kPa)]. It was concluded that in the acclimatized subjects at high altitude arterial vasodilatation and neurobehavioural impairment, which in the non-acclimatized subjects reflect hypoxia of the central nervous system, were prevented; that acclimatization to high altitude resulted in a significant improvement of respiratory efficiency and cardiac economy, and that maintaining diastolic blood pressure (arterial resistance) at and above 4,000 m may represent a useful criterion for assessing hypoxia acclimatization.


Subject(s)
Acclimatization/physiology , Altitude , Cardiovascular System/physiopathology , Hypoxia/physiopathology , Mental Processes/physiology , Respiration/physiology , Adult , Humans , Male , Middle Aged , Mountaineering , Oxygen Consumption
7.
J Appl Physiol (1985) ; 66(4): 1785-8, 1989 Apr.
Article in English | MEDLINE | ID: mdl-2732171

ABSTRACT

This study was carried out to investigate the early changes in erythropoietin (EPO) formation in humans in response to hypoxia. Six volunteers were exposed to simulated altitudes of 3,000 and 4,000 m in a decompression chamber for 5.5 h. EPO was measured by radioimmunoassay in serum samples withdrawn every 30 min during altitude exposure and also in two subjects after termination of hypoxia (4,000 m). EPO levels during hypoxia were significantly elevated after 114 and 84 min (3,000 and 4,000 m), rising thereafter continuously for the period investigated. Mean values increased from 16.0 to 22.5 mU/ml (3,000 m) and from 16.7 to 28.0 mU/ml (4,000 m). This rise in EPO levels corresponds to 1.8-fold (3,000 m) and 3.0-fold (4,000 m) increases in the calculated production rate of the hormone. After termination of hypoxia, EPO levels continued to rise for approximately 1.5 h and after 3 h declined exponentially with an average half-life time of 5.2 h.


Subject(s)
Atmospheric Pressure , Erythropoietin/biosynthesis , Hypoxia/metabolism , Adult , Erythropoietin/analysis , Humans , Male , Radioimmunoassay
8.
Eur J Appl Physiol Occup Physiol ; 58(4): 419-25, 1989.
Article in English | MEDLINE | ID: mdl-2522042

ABSTRACT

Diuresis at altitude was thought to be the result of chemoreceptor stimulation leading to a reduction of cardiac volume overload. This hypothesis was tested in ten young, healthy subjects by infusion of almitrine (0.5 mg.kg-1 body mass within 30 min) assuming analogous sites of action, i.e. arterial chemoreceptors and pulmonary vessels, for almitrine as for hypoxic hypoxia. The results show that almitrine increases ventilation, heart rate, systolic blood pressure, central venous pressure and natriuresis, but fails to increase significantly atrial natriuretic peptide plasma concentration and diuresis. It is concluded: (1) that almitrine has similar sites of action as hypoxic hypoxia at about 5000 m, (2) that natriuresis during arterial chemoreceptor stimulation might reduce cardiac volume overload, (3) that the volume excretion hypothesis, in particular the pathways from the cardiac volume overload to the water diuresis, need, for an understanding of the hypoxia-induced diuresis, further direct investigations at altitude.


Subject(s)
Arginine Vasopressin/blood , Atrial Natriuretic Factor/blood , Diuresis/drug effects , Piperazines/pharmacology , Respiration/drug effects , Adult , Almitrine , Altitude , Blood Pressure/drug effects , Chemoreceptor Cells/physiology , Heart Rate/drug effects , Humans , Hypoxia , Infusions, Intravenous , Natriuresis/drug effects
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