Mv. Merrick et al., LONG-TERM FOLLOW-UP TO DETERMINE THE PROGNOSTIC VALUE OF IMAGING AFTER URINARY-TRACT INFECTIONS .2. SCARRING, Archives of Disease in Childhood, 72(5), 1995, pp. 393-396
Long term follow up of children with urinary tract infections, in whom
imaging investigations were performed at presentation, has been used
to identify features that distinguish those at greatest risk of progre
ssive renal damage. No single investigation at presentation was able t
o predict subsequent deterioration but, by employing a combination of
imaging investigations, it was possible to separate groups with high o
r low probability of progressive damage. In the low risk group the inc
idence of progressive damage was 0.2% (95% confidence interval (CI) 0
to 1.3%). The combination of both scarring and reflux at presentation,
or one only of these but accompanied by subsequent documented urinary
tract infection, was associated with a 17-fold (95% CI 2.5 to 118) in
crease in the relative risk of progressive renal damage compared with
children without these features. The recommended combination of invest
igations at presentation for girls of any age and boys over 1 year is
ultrasound and dimercaptosuccinic acid (DMSA) scintigraphy in all, to
detect both scarring and significant structural abnormalities, renogra
phy in children with dilatation of any part of the urinary tract on ul
trasound, to distinguish dilatation from obstruction, and an isotope v
oiding study in all who have acquired bladder control. This gives the
best separation between those at high and those at low risk of progres
sive damage with least radiation dose and lowest rate of instrumentati
on. Micturating cystourethrography (MCU) should be restricted to girls
who have not acquired bladder control, unless there is reason to susp
ect a significant structural abnormality such as urethral valves. A si
ngle non-febrile urinary tract infection that responds promptly to tre
atment is not a justification for performing MCU in boys under 1 year
or in children of any age with bladder control. No case can be made fo
r any abbreviated schedule of investigation. These risk factors should
be taken into account when designing follow up protocols.