CHANGES IN INFLAMMATORY MEDIATORS AND TOTAL-BODY WATER DURING EXTRACORPOREAL MEMBRANE-OXYGENATION (ECMO) - A PRELIMINARY-STUDY

Citation
Mj. Underwood et al., CHANGES IN INFLAMMATORY MEDIATORS AND TOTAL-BODY WATER DURING EXTRACORPOREAL MEMBRANE-OXYGENATION (ECMO) - A PRELIMINARY-STUDY, International journal of artificial organs, 18(10), 1995, pp. 627-632
Citations number
15
Categorie Soggetti
Engineering, Biomedical
ISSN journal
03913988
Volume
18
Issue
10
Year of publication
1995
Pages
627 - 632
Database
ISI
SICI code
0391-3988(1995)18:10<627:CIIMAT>2.0.ZU;2-4
Abstract
We studied six patients (5 paediatric, 1 neonate) treated with ECMO to quantify changes in inflammatory mediators (neutrophil elastase (NE), free radical activity (FR), interleukin 8 (IL8)) and total body wafer (TBW). Blood samples were taken before instigation of ECMO, 4, 12, 24 hours post-ECMO and daily for six days. FR activity was quantified us ing the oxidised IgG FI/UV ration. NE and IL8 levels were measured by ELISA. TBW was assessed by electrical bioimpedance. Statistical analys is was made using repeated measures analysis of variance and modified t-test where appropriate. Results are presented as mean +/- standard e rror of the mean. FR activity increased 4 hours after instigation of E CMO (IgG FI/UV 32.1 +/- 3.2 from 24.1 +/- 3.0 p=0.005) and remained el evated. NE also increased by 4 hours (94.8 mu g/L +/- 8.9 to 678 mu g/ L +/- 153.4, p=0.005) but returned to pre-ECMO values by day 6. IL8 le vels rose after ECMO (from 98 pg/ml +/- 39, to 24 pg/ml +/- 117.4) alt hough no statistical difference was noted over time due to the large v ariation between subjects (p=0.009). TBW (% pre-ECMO body weight) fell by 24 hours (from 118.6 +/- 12.6 to 96.5 +/- 8.2 p=0.0004). This stud y demonstrated that ECMO stimulates an 'inflammatory' response to extr acorporeal perfusion (increased FR, NE) but despite this, results in a reduction in total body wafer. The complex relationship between the i nflammatory response to prolonged extracorporeal perfusion and its eff ect on tissue oedema merits further investigation.