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Pethidine-augmented white cell scintigraphy in inflammatory bowel disease.

Authors :
Davidson J
Poon FW
Bessent RG
Neilly JB
Gray HW
Source :
European journal of nuclear medicine [Eur J Nucl Med] 2000 Jun; Vol. 27 (6), pp. 656-9.
Publication Year :
2000

Abstract

Technetium-99m hexamethylpropylene amine oxime (99mTc-HMPAO) white cell scintigraphy is invaluable for assessing the presence and extent of disease activity in patients with inflammatory bowel disease. Interpretation of images can be compromised by physiological excretion of tracer into the bowel via the biliary tree. This study assesses the effect of intravenous pethidine administered with the labelled white cells in an attempt to reduce the enterohepatic circulation of the tracer. Ninety-one subjects with proven or suspected inflammatory bowel disease were included in this study, all of whom underwent 99mTc-HMPAO white cell scintigraphy. The control group of 50 subjects underwent the standard protocol for this study performed in our department. The other 41 subjects received an intravenous injection of 0.3 mg/kg of pethidine at the same time as re-injection of the labelled white cells. Images were graded using a five-point scale at both 1 and 2.5 h and categorised as positive, negative or non-diagnostic. Each scan was also assessed for the presence of a visible gall-bladder. The pethidine group had significantly fewer non-diagnostic scans than the control group (P=0.003), and significantly (P=0.001) more studies in which the gall-bladder was visualised. It is concluded that the use of pethidine appears to reduce biliary excretion of tracer during 99mTc-HMPAO white cell scintigraphy. This may allow the delayed images, and early images with low-grade tracer uptake in the bowel, to be interpreted with greater confidence and thereby reduce the number of scans classified as non-diagnostic.

Details

Language :
English
ISSN :
0340-6997
Volume :
27
Issue :
6
Database :
MEDLINE
Journal :
European journal of nuclear medicine
Publication Type :
Academic Journal
Accession number :
10901451
Full Text :
https://doi.org/10.1007/s002590050559