Gcf. Chan et al., END-TIDAL CARBON-MONOXIDE CONCENTRATION IN CHILDHOOD HEMOLYTIC DISORDERS, Journal of paediatrics and child health, 34(5), 1998, pp. 447-450
Objectives: Endogenous carbon monoxide (CO) is produced mainly by heme
catabolism. As CO is excreted solely by the lung, a simple technique
for measuring the end tidal carbon monoxide (ETCO) level was assessed
as a method for screening for haemolytic disease in children. Methods:
Two end expiratory breath samples were collected from normal children
and from children with haemolytic disease using a one way valve conne
ctor between a mouth piece and an anaesthetic bag. The samples were an
alysed by gas chromatography for CO and carbon for dioxide (CO2). The
CO2 value was used to normalise the CO value to an alveolar concentrat
ion. Carboxyhaemoglobin (HbCO) also was measured in the patient group
for correlation analysis with ETCO. Results: A total of 21 children wi
th beta thalassaemia major, 15 children with other haemolytic diseases
(hereditary spherocytosis n=8, haemoglobin H disease n=3 and thalassa
emia intermedia n=4) and 23 normal children were studied. The mean ETC
O concentrations in the three groups were 3.21 p.p.m., 7.41 p.p.m. and
0.69 p.p.m., respectively, which were significantly different from ea
ch other (P<0.0001). There was a significant correlation between ETCO
and HbCO in the patient groups (r=0.85; P<0.0001). Conclusions: The en
d expiratory breath collection device is a simple and feasible sample
collection method. The results confirm that ETCO can be used clinicall
y to distinguish children with a variety of haemolytic disorders from
normal subjects.