A5V4d
A5V4d
A5V4d
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Feverish illness in children<br />
Few studies were found looking at the usefulness of markers of bacterial infection in the management<br />
of children with fever without apparent source presenting to the paediatric specialist who were<br />
considered sufficiently unwell that intravenous anti-bacterial treatment should be initiated empirically.<br />
GDG translation<br />
‘Green’ group<br />
Because tests such as CRP, PCT and WBC do not improve the detection of SBI in this group, the<br />
GDG concluded that routine blood tests on well-appearing children with fever are not justified. This<br />
would not change current practice since well-appearing children over 3 months old with fever rarely<br />
have blood tests in the UK at present. In contrast, there is a significant risk of UTI in this group and<br />
only by testing the urine will this be identified.<br />
‘Amber’ and ‘Red’ groups<br />
Although PCT is more sensitive than CRP in identifying sepsis and meningitis in young children with<br />
fever, the GDG did not feel that this difference was sufficient to recommend PCT over CRP,<br />
potentially changing current UK practice. The GDG noted that there was only limited evidence on the<br />
use of PCT in children with fever without apparent source, and they decided to call for more research<br />
in this area. In children with no symptoms or signs of pneumonia, a combination of temperature<br />
> 39°C and a WBC > 20 × 10 9 /litre has a high specificity for bacterial pneumonia and therefore the<br />
GDG concluded that a chest X-ray is indicated in this small group of children. In children considered<br />
sufficiently unwell to require empiric antibiotics, the GDG acknowledged that the result of a CRP or<br />
WBC would not influence immediate management. However, they should be measured as an aid to<br />
ongoing management of this group.<br />
Procalcitonin and C-reactive protein<br />
Introduction<br />
A review question comparing procalitonin (PCT) and C-reactive protein (CRP) was outlined as new<br />
evidence had become available since the 2007 guideline was published.<br />
PCTCRP are found in the bloodstream and the levels of both increase in response to the presence of<br />
bacterial infection, but not (or less so) to viral illness. This response starts approximately 6 hours after<br />
the start of infection with PCT and 12 hours afterwards for CRP. The tests are used to differentiate<br />
between viral and bacterial infections, and to determine the seriousness of bacterial infection.<br />
Review question<br />
The clinical question set out on the scope asks for: ’The predictive value of pro-calcitonin and/or Creactive<br />
protein markers.’ This translates into the following review question “What is the predictive<br />
value of procalcitonin compared to C-reactive protein for detecting serious illness in fever without<br />
apparent source in children under 5?”<br />
Overview of review<br />
In the 2007 guideline the use of CRP was recommended, but not the use of PCT. A research<br />
recommendation was outlined stating the need for studies comparing PCT and CRP. The focus of this<br />
question was to review the literature comparing PCT and CRP.<br />
A literature search was undertaken from 2005 onwards. A total of 594 studies were identified. In<br />
addition, studies included in the 2007 guideline were reviewed for inclusion in the updated guideline.<br />
Description of included studies<br />
A total of 16 observational studies were included in this review (Galetto-Lacour et al., 2003; Guen et<br />
al., 2007; Lacour et al., 2001; Thayyil et al., 2005; Manzano et al., 2011; Olaciregui et al., 2009;<br />
Andreola et al., 2007; Maniaci et al., 2008; Hsaio et al, 2006; Berger et al, 1996; Isaacman et a, 2002;<br />
Pratt et al, 2007 ; Pulliam et al, 2001; Gomez et al, 2010; Luaces-Cubells et al, 2012; Woelker et al,<br />
2012). Fifteen of these assessed CRP and ten assessed PCT. Eight of these studies directly<br />
compared CRP with PCT (Galetto-Lacour et al., 2003; Guen et al., 2007; Lacour et al., 2001; Thayyil<br />
et al., 2005; Manzano et al., 2011; Olaciregui et al., 2009; Andreola et al., 2007; Luaces-Cubells et al,<br />
2012). Six studies included CRP but not PCT (Hsaio et al, 2006; Berger et al, 1996; Gomez et al,<br />
2010; Isaacman et a, 2002; Pratt et al, 2007; Pulliam et al, 2001). Two studies examined PCT only<br />
(Maniaci et al., 2008; Woelker et al, 2012). Fourteen studies were prospective studies and two were<br />
158<br />
2013 Update