Pentraxin-3 as a marker of disease severity and risk of death in patients with necrotizing soft tissue infections: a nationwide, prospective, observational study

TY - JOUR

T1 - Pentraxin-3 as a marker of disease severity and risk of death in patients with necrotizing soft tissue infections

T2 - a nationwide, prospective, observational study

AU - Hansen, Marco Bo

AU - Rasmussen, Lars Simon

AU - Garred, Peter

AU - Bidstrup, Daniel

AU - Madsen, Martin Bruun

AU - Hyldegaard, Ole

PY - 2016/2/15

Y1 - 2016/2/15

N2 - Background: New biomarkers are needed to assess the severity of necrotizing soft tissue infection (NSTI) at an early stage and to individualize treatment strategies. We assessed pentraxin-3 (PTX3) as a marker of disease severity and risk of death in patients with NSTI. Methods: We conducted a prospective, observational study in the intensive care unit at Copenhagen University Hospital, where treatment of NSTI is centralized at a national level. We compared PTX3, procalcitonin and C-reactive protein in septic shock versus nonshock patients and in amputated versus nonamputated patients using the Mann-Whitney U test. The prognostic value of the markers for 180-day mortality was assessed using Cox regression analyses. Results: Patients with NSTI (n = 135) were included over 25months with up to 2.5-year follow-up; 71% had septic shock, amputation was undertaken in 20% and the 180-day mortality was 27%. Baseline plasma PTX3 level was significantly higher in patients with septic shock (67.3 versus 24.6ng/mL, p < 0.0001) and in patients who underwent amputation (118.6 versus 43.6ng/mL, p = 0.019). No significant differences in baseline procalcitonin or C-reactive protein levels were found according to amputation (25.2 versus 7.0μg/L, p = 0.060 and 202 versus 225mg/L, p = 0.123), respectively. Baseline PTX3 level above the median was associated with death (p = 0.009, log-rank test) and the univariate Cox regression analysis revealed a significant association between PTX3 level upon admission and 180-day mortality (hazard ratio 2.60 (95% confidence interval 1.28-5.29), p = 0.008). When adjusted for age, sex, chronic disease and Simplified Acute Physiology Score II, no significant association was found. Conclusions: High PTX3 level is associated with septic shock, amputation and risk of death in patients with NSTI, but it is not an independent predictor of 180-day mortality in this patient group. Trial registration: ClinicalTrials.gov Identifier: NCT02180906. Date of registration: June 29, 2014.

AB - Background: New biomarkers are needed to assess the severity of necrotizing soft tissue infection (NSTI) at an early stage and to individualize treatment strategies. We assessed pentraxin-3 (PTX3) as a marker of disease severity and risk of death in patients with NSTI. Methods: We conducted a prospective, observational study in the intensive care unit at Copenhagen University Hospital, where treatment of NSTI is centralized at a national level. We compared PTX3, procalcitonin and C-reactive protein in septic shock versus nonshock patients and in amputated versus nonamputated patients using the Mann-Whitney U test. The prognostic value of the markers for 180-day mortality was assessed using Cox regression analyses. Results: Patients with NSTI (n = 135) were included over 25months with up to 2.5-year follow-up; 71% had septic shock, amputation was undertaken in 20% and the 180-day mortality was 27%. Baseline plasma PTX3 level was significantly higher in patients with septic shock (67.3 versus 24.6ng/mL, p < 0.0001) and in patients who underwent amputation (118.6 versus 43.6ng/mL, p = 0.019). No significant differences in baseline procalcitonin or C-reactive protein levels were found according to amputation (25.2 versus 7.0μg/L, p = 0.060 and 202 versus 225mg/L, p = 0.123), respectively. Baseline PTX3 level above the median was associated with death (p = 0.009, log-rank test) and the univariate Cox regression analysis revealed a significant association between PTX3 level upon admission and 180-day mortality (hazard ratio 2.60 (95% confidence interval 1.28-5.29), p = 0.008). When adjusted for age, sex, chronic disease and Simplified Acute Physiology Score II, no significant association was found. Conclusions: High PTX3 level is associated with septic shock, amputation and risk of death in patients with NSTI, but it is not an independent predictor of 180-day mortality in this patient group. Trial registration: ClinicalTrials.gov Identifier: NCT02180906. Date of registration: June 29, 2014.

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

U2 - 10.1186/s13054-016-1210-z

DO - 10.1186/s13054-016-1210-z

M3 - Journal article

C2 - 26880104

SN - 1364-8535

VL - 20

JO - Critical Care

JF - Critical Care

M1 - 40

ER -