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Infectious complications after out-of-hospital cardiac arrest-A comparison between two target temperatures.
Dankiewicz, Josef; Nielsen, Niklas; Linder, Adam; Kuiper, Michael; Wise, Matthew P; Cronberg, Tobias; Erlinge, David; Gasche, Yvan; Harmon, Matthew B; Hassager, Christian; Horn, Janneke; Kjaergaard, Jesper; Pellis, Tommaso; Stammet, Pascal; Undén, Johan; Wanscher, Michael; Wetterslev, Jørn; Åneman, Anders; Ullén, Susann; Juffermans, Nicole P; Friberg, Hans.
Afiliação
  • Dankiewicz J; Department of Intensive and Perioperative Care, Skåne University Hospital, Lund, Sweden; Department of Clinical Sciences, Lund University, Getingevägen, 22185 Lund, Sweden. Electronic address: Josef.dankiewicz@med.lu.se.
  • Nielsen N; Department of Clinical Sciences, Lund University, Getingevägen, 22185 Lund, Sweden; Department of Anaesthesiology and Intensive Care, Helsingborg Hospital, Helsingborg, Sweden.
  • Linder A; Department of Clinical Sciences, Lund University, Getingevägen, 22185 Lund, Sweden; Division of Infection Medicine, Lund University Hospital, Lund, Sweden.
  • Kuiper M; Department of Intensive Care, Leeuwarden Hospital, Leeuwarden, The Netherlands.
  • Wise MP; Adult Critical Care, University Hospital of Wales, Cardiff, United Kingdom.
  • Cronberg T; Department of Clinical Sciences, Lund University, Getingevägen, 22185 Lund, Sweden; Department of Neurology, Skåne University Hospital, Lund, Sweden.
  • Erlinge D; Department of Clinical Sciences, Lund University, Getingevägen, 22185 Lund, Sweden; Department of Cardiology, Skåne University Hospital, Lund Sweden.
  • Gasche Y; Department of Intensive Care, Geneva University Hospital, Geneva, Switzerland.
  • Harmon MB; Academic Medical Center, Amsterdam, The Netherlands.
  • Hassager C; Department of Cardiology, The Heart Centre, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Horn J; Department of Intensive Care, Academic Medical Centre, Amsterdam, The Netherlands.
  • Kjaergaard J; Department of Cardiology, The Heart Centre, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Pellis T; Department of Intensive Care, Santa Maria degli Ángeli, Pordenone, Italy.
  • Stammet P; Department of Anesthesiology and Intensive Care, Centre Hospitalier de Luxembourg, Luxembourg City, Luxembourg.
  • Undén J; Department of Clinical Sciences, Lund University, Getingevägen, 22185 Lund, Sweden; Department of Intensive and Perioperative Care, Skåne University Hospital, Malmö, Sweden.
  • Wanscher M; Department of Cardiology, The Heart Centre, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Wetterslev J; Copenhagen Trial Unit, Centre of Clinical Intervention Research, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
  • Åneman A; Department of Intensive Care, Liverpool Hospital, Sydney, NSW, Australia.
  • Ullén S; R&D Centre Skåne, Skåne University Hospital, Lund, Sweden.
  • Juffermans NP; Academic Medical Center, Amsterdam, The Netherlands.
  • Friberg H; Department of Intensive and Perioperative Care, Skåne University Hospital, Lund, Sweden; Department of Clinical Sciences, Lund University, Getingevägen, 22185 Lund, Sweden.
Resuscitation ; 113: 70-76, 2017 04.
Article em En | MEDLINE | ID: mdl-27993631
ABSTRACT

BACKGROUND:

It has been suggested that target temperature management (TTM) increases the probability of infectious complications after cardiac arrest. We aimed to compare the incidence of pneumonia, severe sepsis and septic shock after out-of-hospital cardiac arrest (OHCA) in patients with two target temperatures and to describe changes in biomarkers and possible mortality associated with these infectious complications.

METHODS:

Post-hoc analysis of the TTM-trial which randomized patients resuscitated from OHCA to a target temperature of 33°C or 36°C. Prospective data on infectious complications were recorded daily during the ICU-stay. Pneumonia, severe sepsis and septic shock were considered infectious complications. Procalcitonin (PCT) and C-reactive-protein (CRP) levels were measured at 24h, 48h and 72h after cardiac arrest.

RESULTS:

There were 939 patients in the modified intention-to-treat population. Five-hundred patients (53%) developed pneumonia, severe sepsis or septic shock which was associated with mortality in multivariate analysis (Hazard ratio [HR] 1.39; 95%CI 1.13-1.70; p=0.001). There was no statistically significant difference in the incidence of infectious complications between temperature groups (sub-distribution hazard ratio [SHR] 0.88; 95%CI 0.75-1.03; p=0.12). PCT and CRP were significantly higher for patients with infections at all times (p<0.001), but there was considerable overlap.

CONCLUSIONS:

Patients who develop pneumonia, severe sepsis or septic shock after OHCA might have an increased mortality. A target temperature of 33°C after OHCA was not associated with an increased risk of infectious complications compared to a target temperature of 36°C. PCT and CRP are of limited value for diagnosing infectious complications after cardiac arrest.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Choque Séptico / Temperatura Corporal / Proteína C-Reativa / Calcitonina / Reanimação Cardiopulmonar / Sepse / Parada Cardíaca Extra-Hospitalar / Hipotermia Induzida Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Choque Séptico / Temperatura Corporal / Proteína C-Reativa / Calcitonina / Reanimação Cardiopulmonar / Sepse / Parada Cardíaca Extra-Hospitalar / Hipotermia Induzida Idioma: En Ano de publicação: 2017 Tipo de documento: Article