2000
DOI: 10.1016/s0140-6736(00)02485-5
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Pumpless extracorporeal lung assist and adult respiratory distress syndrome

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Cited by 104 publications
(54 citation statements)
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“…Most studies in humans have described a significant rise in Pa,O 2 after implementation of iLA treatment [6][7][8][16][17][18]. The patients evaluated in the current study had a Pa,O 2 /FI,O 2 ratio of 69 mmHg before iLA treatment, which increased to 94 mmHg within 2 h (p,0.001).…”
Section: Effects On Oxygen Transportmentioning
confidence: 50%
See 1 more Smart Citation
“…Most studies in humans have described a significant rise in Pa,O 2 after implementation of iLA treatment [6][7][8][16][17][18]. The patients evaluated in the current study had a Pa,O 2 /FI,O 2 ratio of 69 mmHg before iLA treatment, which increased to 94 mmHg within 2 h (p,0.001).…”
Section: Effects On Oxygen Transportmentioning
confidence: 50%
“…Optimised technical design, especially the development of low-resistance oxygenators, made the use of pumpless devices in humans possible. Early clinical results in small series of patients were encouraging [5][6][7][8] and meanwhile interventional lung assist (iLA) has become commercially available. Prospective controlled trials, which are still lacking, have been demanded [9] and have commenced recently.…”
mentioning
confidence: 99%
“…DECAPSMART is a classic example of pulmonary/renal support and has been used successfully in isolated instances [10,74]. This adaptation can also be extended to other ECCO2R devices and can also be used with AVCO2R [75]. …”
Section: Pulmonary/renal Support – Mostmentioning
confidence: 99%
“…Der Einsatz der oben dargestellten Polymethylpentenmembran statt einer herkömmlichen mikroporösen Polypropylenmembran macht den Oxygenator Plasma-leakage-resistent, und das reduzierte Risiko einer Luftembolie erlaubt einen deutlich höheren Gasfluss mit einer verbesserten Kohlendioxidelimination.In einer ersten unkontrollierten Studie wurden 20 ARDS-Patienten (p a O 2 45,9± 7 mmHg bei F I O 2 1,0) mit dieser arteriovenösen pumpenlosen ECLA für 1-32 Tage behandelt.Der durchschnittliche Blutfluss der ECLA lag deutlich höher als in der anderen Studie bei 2,6±0,6 l/min entsprechend etwa 25% des HZV [19,28] …”
Section: Arteriovenöse Pumpenlose "Extracorporeal Lung Assist"unclassified