Determination of plasma volume by indocyanine green - validation of the method and use in patients after cardiopulmonary bypass

Citation
Se. Menth-meier et al., Determination of plasma volume by indocyanine green - validation of the method and use in patients after cardiopulmonary bypass, INTEN CAR M, 27(5), 2001, pp. 925-929
Citations number
10
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
INTENSIVE CARE MEDICINE
ISSN journal
03424642 → ACNP
Volume
27
Issue
5
Year of publication
2001
Pages
925 - 929
Database
ISI
SICI code
0342-4642(200105)27:5<925:DOPVBI>2.0.ZU;2-L
Abstract
Objective: Validation of plasma volume (PV) determination by indocyanine gr een (ICG) in comparison to the gold-standard method with radioiodinated alb umin, and investigation of the effect of commonly used plasma expanders (al bumin, hydroxyethyl starch, and polygelatine) on PV in the early postoperat ive phase in patients undergoing cardiac surgery. Design: Prospective clinical study. Setting: Department of medicine and intensive care unit at a university hos pital. Patients and participants: Ten healthy volunteers and 21 patients after ele ctive open-heart surgery. Measurements and results: PV of subjects was measured by i.v. injecting 5 m u Ci [I-125]albumin (I-ALB). One hour later, PV was determined by a periphe ral i.v. injection of 0.25 mg/kg body weight ICG (ICG1). In five subjects P V was measured repeatedly by ICG (ICG2) 1 h after ICG1. Mean PV of I-ALE an d ICG1 or ICG2 showed consistent results. Further, we investigated central vs peripheral intravenous injection of ICG in six patients after open-heart surgery compared to [I-125]albumin. There was no difference between mean P V measured by [I-125]albumin and peripheral ICG (P = 0.40). PV determined b y central injection of ICG was significantly higher than by the other metho ds. In 15 patients PV was determined by [I-125]albumin. Thereafter, patient s were randomly divided into three groups. Group ALE was infused with 1.75 ml/kg body weight human albumin 20%, group HAES with 5.25 ml/kg body weight hydroxyethyl starch 6%, and group HAEM with 7.0 ml/kg body weight polygela tine 3.5%. PV was measured 1 h and 4 h after infusion by ICG. There were no significant changes in PV between the groups. Conclusions: PV determination by peripheral i.v. injection of ICG produced reliable and consistent results when a reactive hyperaemia was produced by a tourniquet prior to injection. Therefore, central venous injection of ICG may not be prerequisite for precise measurements of PV. The expected acute increase in PV after infusion of commonly used plasma expanders after card iac surgery was not found.