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Gewählte Publikation:

Haidmayer, R; Kurz, R; Kenner, T; Wurm, H; Pfeiffer, KP.
Physiological and clinical aspects of respiration control in infants with relation to the sudden infant death syndrome.
Klin Wochenschr. 1982; 60(1):9-18 Doi: 10.1007/BF01721582
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Führende Autor*innen der Med Uni Graz
Haidmayer Reinhard
Co-Autor*innen der Med Uni Graz
Kenner Thomas
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Abstract:
We have examined the behavior of several variables which are related to respiratory control in 114 infants (up to 6 months of age) in order to assess the risk for the sudden infant death syndrome (SIDS), 23 of the infants had already had demonstratable serious or life threatening apneas or respiratory problems during surgical anesthesia. These infants were assigned as a risk group, and the rest of the investigated babies was taken as a control group. We found that practically all infants of the risk group had apneas during sleep, which lasted longer than 8 s each. Only 22% of the infants of the control group had apneas of such a duration. As a statistical parameter, calculated from at least 1 hour recording of respiration, we defined the mean apnea duration (MA-value) as average value of apnea duration time in seconds per minute of recording. The MA-value proved to be significantly elevated in the infants of the risk group. The trend to hypoxia in the infants of the risk group was also indicated by the observation of lower transcutaneous PO2-values (tc-PO2) during sleep, when compared with control infants. In agreement with this observation is the increase of the 2,3-DPG concentration and the decrease of the density of erythrocytes of the infants of the risk group. Breathing hypoxic gas mixtures tended to depress respiration in all infants tested, and, especially in the risk group, to elicit irregular respiratory patterns. On the other hand, we observed that inhalation of pure oxygen markedly stimulated respiration in all infants investigated. We conclude from these observations that a risk for SIDS may be related to a particular response pattern of the respiratory center during the early postnatal life. We are able to distinguish infants with a higher risk for SIDS from other children by determination of the MA-value during sleep.
Find related publications in this database (using NLM MeSH Indexing)
Aminophylline - pharmacology
Apnea - physiopathology
Carbon Dioxide - physiopathology
Female - physiopathology
Humans - physiopathology
Infant - physiopathology
Infant, Newborn - physiopathology
Infant, Newborn, Diseases - physiopathology
Male - physiopathology
Oxygen - physiopathology
Partial Pressure - physiopathology
Respiration - physiopathology
Risk - physiopathology
Sudden Infant Death - etiology

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