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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

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