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. 2017 Jun 21;7(6):e015734. doi: 10.1136/bmjopen-2016-015734

Table 2.

Clinical and biological data collection planning

D0* D1 (D2) D2‡ D3/4 D5/7 D13/18 D26/36 D52/68 D90
Inclusion/exclusion criteria x§
Consent form x§
Demography x§
Weight x§
Size x§
Description of hospital stay x§
IGS II score x§
McCabe score x§
CHARLSON score x§
Documentation of the x§
septic shock, surgery,
burn or trauma
SOFA score x x x x X
Treatments against infections Steadily x x x x
Therapeutic management Steadily
Exposition to medical devices Steadily
Surveillance of healthcare Steadily x x x x
associated infections
Concomitant events Steadily x x x x
Vital status** x x x x
Life quality (EQ5D) x
Biology
PAXgene tube sampling x x x x X x x x
EDTA tubes sampling x x x x X x x x
Heparin tubes sampling x x x x X x x x
Haematology x x x x X x x x
Lactate x†† x†† x†† x†† x††
pH x†† x†† x†† x†† x††
Liver results (ASAT, ALAT, PAL) x†† x†† x†† x†† x††
Procalcitonin x†† x†† x†† x†† x†† x†† x†† x†† x††
Serology (CMV, HSV1) X§

*Only for patients of the surgery group

†For the septic shock and burn patients: The enrollment at D2 will be accepted if D1 is not available

‡Only for patients of the trauma group

§Evaluation on day 0 for patients of the surgery group (not repeated on day 1)

¶Only if related to a new hospitalisation

**Also at ICU release and Hospital release

††If available