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

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Pentraxin-3 as a marker of disease severity and risk of death in patients with necrotizing soft tissue infections : a nationwide, prospective, observational study. / Hansen, Marco Bo; Rasmussen, Lars Simon; Garred, Peter; Bidstrup, Daniel; Madsen, Martin Bruun; Hyldegaard, Ole.

In: Critical Care, Vol. 20, 40, 2016.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hansen, MB, Rasmussen, LS, Garred, P, Bidstrup, D, Madsen, MB & Hyldegaard, O 2016, 'Pentraxin-3 as a marker of disease severity and risk of death in patients with necrotizing soft tissue infections: a nationwide, prospective, observational study', Critical Care, vol. 20, 40. https://doi.org/10.1186/s13054-016-1210-z

APA

Hansen, M. B., Rasmussen, L. S., Garred, P., Bidstrup, D., Madsen, M. B., & Hyldegaard, O. (2016). Pentraxin-3 as a marker of disease severity and risk of death in patients with necrotizing soft tissue infections: a nationwide, prospective, observational study. Critical Care, 20, [40]. https://doi.org/10.1186/s13054-016-1210-z

Vancouver

Hansen MB, Rasmussen LS, Garred P, Bidstrup D, Madsen MB, Hyldegaard O. Pentraxin-3 as a marker of disease severity and risk of death in patients with necrotizing soft tissue infections: a nationwide, prospective, observational study. Critical Care. 2016;20. 40. https://doi.org/10.1186/s13054-016-1210-z

Author

Hansen, Marco Bo ; Rasmussen, Lars Simon ; Garred, Peter ; Bidstrup, Daniel ; Madsen, Martin Bruun ; Hyldegaard, Ole. / Pentraxin-3 as a marker of disease severity and risk of death in patients with necrotizing soft tissue infections : a nationwide, prospective, observational study. In: Critical Care. 2016 ; Vol. 20.

Bibtex

@article{b1c7d9fed58e4f5a9f2c6d7a75d052b1,
title = "Pentraxin-3 as a marker of disease severity and risk of death in patients with necrotizing soft tissue infections: a nationwide, prospective, observational study",
abstract = "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 25 months 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 24.6 ng/mL, p < 0.0001) and in patients who underwent amputation (118.6 versus 43.6 ng/mL, p = 0.019). No significant differences in baseline procalcitonin or C-reactive protein levels were found according to amputation (25.2 versus 7.0 μg/L, p = 0.060 and 202 versus 225 mg/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.",
keywords = "Journal Article, Research Support, Non-U.S. Gov't",
author = "Hansen, {Marco Bo} and Rasmussen, {Lars Simon} and Peter Garred and Daniel Bidstrup and Madsen, {Martin Bruun} and Ole Hyldegaard",
year = "2016",
doi = "10.1186/s13054-016-1210-z",
language = "English",
volume = "20",
journal = "Critical Care",
issn = "1364-8535",
publisher = "BioMed Central Ltd.",

}

RIS

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

Y1 - 2016

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 25 months 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 24.6 ng/mL, p < 0.0001) and in patients who underwent amputation (118.6 versus 43.6 ng/mL, p = 0.019). No significant differences in baseline procalcitonin or C-reactive protein levels were found according to amputation (25.2 versus 7.0 μg/L, p = 0.060 and 202 versus 225 mg/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 25 months 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 24.6 ng/mL, p < 0.0001) and in patients who underwent amputation (118.6 versus 43.6 ng/mL, p = 0.019). No significant differences in baseline procalcitonin or C-reactive protein levels were found according to amputation (25.2 versus 7.0 μg/L, p = 0.060 and 202 versus 225 mg/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

VL - 20

JO - Critical Care

JF - Critical Care

SN - 1364-8535

M1 - 40

ER -

ID: 165009214