Copeptin predicts clinical deterioration and persistent instability in community-acquired pneumonia

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

Abstract

RATIONALE: Optimal risk prediction of early clinical deterioration in community-acquired pneumonia (CAP) remains unresolved. We prospectively examined the predictive value of the new biomarkers copeptin and proadrenomedullin (MR-proADM) in comparison to clinical scores and inflammatory markers to predict early high risk prognosis in CAP.

METHODS: 51 consecutive hospitalised adult patients were enrolled. We measured CRB-65- and PSI-scores, the ATS/IDSA 2007 minor criteria to predict ICU-admission and the biomarkers CRP, procalcitonin, copeptin and MR-proADM on admission. Predefined outcome parameters were combined mortality or ICU-admission after 7 days and clinical instability after 72 h.

RESULTS: Copeptin was the only biomarker significantly elevated in patients with either adverse short term outcome (p = 0.003). According to ROC-curve analysis, copeptin predicted ICU admission or death within 7 days (AUC 0.81, cut-off 35 pmol/l: sensitivity 78%, specificity 79%) and persistent clinical instability after 72 h (AUC 0.74). In Kaplan-Meier-analysis patients with high copeptin showed lower ICU-free survival within 7 days (p = 0.001). The diagnostic accuracy of copeptin was superior to the CRB-65 score and comparable to the PSI-score and the ATS/IDSA minor criteria. If copeptin was included as additional minor criterion for combined 7-day mortality or ICU-admission, the diagnostic accuracy of the minor criteria was significantly improved (p = 0.045).

CONCLUSION: Copeptin predicts early deterioration and persistent clinical instability in hospitalised CAP and improves the predictive properties of existing clinical scores. It should be evaluated within a biomarker guided strategy for early identification of high risk CAP patients who most likely benefit from early intensified management strategies.

Details

OriginalspracheEnglisch
Seiten (von - bis)1320-1328
Seitenumfang9
FachzeitschriftRespiratory Medicine
Jahrgang106
Ausgabenummer9
PublikationsstatusVeröffentlicht - Sept. 2012
Peer-Review-StatusJa

Externe IDs

Scopus 84864609839
researchoutputwizard legacy.publication#47883
researchoutputwizard legacy.publication#48303
PubMed 22732597
ORCID /0000-0001-6022-6827/work/142659546

Schlagworte

Schlagwörter

  • Aged, Aged, 80 and over, Biomarkers/metabolism, Community-Acquired Infections/diagnosis, Disease Progression, Female, Glycopeptides/metabolism, Humans, Kaplan-Meier Estimate, Male, Middle Aged, Pneumonia, Bacterial/diagnosis, Prognosis, Prospective Studies, ROC Curve, Risk Assessment