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Procalcitonin is a valuable prognostic marker in cardiac surgery but not specific for infection
H Dörge1, F A Schöndube, P Dörge
1Thoracic Cardiovascular Surgery, Heart Center Göttingen, Georg-August-University Göttingen, Germany. doerge@med.uni-goettingen.de
Insights
Elevated procalcitonin (PCT) levels post-cardiac surgery indicate higher mortality, infection, and complication risks. While PCT is a valuable prognostic marker, it cannot distinguish between infectious and non-infectious complications.
Area of Science:
- Biomarkers in Critical Care
- Cardiac Surgery Outcomes
- Infectious Disease Markers
Background:
- The prognostic significance of procalcitonin (PCT) in early post-cardiac surgery patients on cardiopulmonary bypass (CPB) is not well-established.
- Investigating PCT's utility as a prognostic marker for mortality, complications, and infections after cardiac surgery is crucial.
Purpose of the Study:
- To evaluate the prognostic value of serum procalcitonin (PCT) levels in patients undergoing cardiac surgery with cardiopulmonary bypass (CPB).
- To determine if PCT can predict mortality, severe complications, and infections, and if it specifically indicates infections.
Main Methods:
- A prospective study of 80 high-risk patients (APACHE II-score: 25.1 ± 4.7) undergoing cardiac surgery.
- Serum PCT levels were measured preoperatively and on postoperative day 1.
- Demographic, operative data, and clinical outcomes (mortality, infection, severe complications) were documented.
Main Results:
- Postoperative PCT levels were significantly higher in non-survivors, patients with severe complications, and those with infections compared to their counterparts.
- PCT demonstrated predictive value for mortality (AUC: 0.772), infections (AUC: 0.720), and complications (AUC: 0.861).
- Preoperative PCT levels were normal; however, PCT did not differentiate between infectious and non-infectious complications.
Conclusions:
- Elevated postoperative procalcitonin (PCT) levels are associated with increased mortality, infections, and severe complications following cardiac surgery with CPB.
- PCT serves as a valuable prognostic marker in this patient population.
- PCT levels do not distinguish between infectious and non-infectious causes of complications.
Background:
The prognostic value of elevated serum levels of procalcitonin (PCT) in patients early after cardiac surgery on cardiopulmonary bypass (CPB) remains unclear. In a prospective study, we investigated whether PCT is useful as a prognostic marker in cardiac surgery with respect to mortality, complications and infections, and whether PCT is a specific marker for occurrence of infections.
Methods:
Within 8 months, a subset of 80 high-risk patients (APACHE II-score: 25.1 +/- 4.7 (mean +/- SD)) out of a consecutive cohort of 776 patients was investigated. Demographic data, operative data and clinical endpoints (mortality, infection, severe complication) were documented. Serum levels of PCT were analyzed preoperatively and at postoperative day 1.
Results:
Hospital mortality in this high-risk group was 21.3 %, infections occurred in 33.8 % and complications in 58.8 % of the patients. Preoperative PCT was normal in all patients. Postoperative PCT was increased in non-survivors compared to survivors (34.3 +/- 7.0 ng/ml vs. 15.9 +/- 4.9 ng/ml; p < 0.05), in patients with severe complications (30.3 +/- 6.7 ng/ml vs. 5.5 +/- 1.4 ng/ml; p < 0.05) and in patients with infections (38.4 +/- 11.3 ng/ml vs. 10.8 +/- 1.6 ng/ml; p < 0.05). Area under receiver operating characteristic curve for PCT as predictor of mortality, infections and complications was 0.772 (95 %-confidence-interval (CI): 0.651 - 0.894), 0.720 (95 %-CI: 0.603 - 0.837) and 0.861 (95 %-CI: 0.779 - 0.943), respectively. PCT was not different with infectious compared to non-infectious complications.
Conclusions:
High levels of PCT are associated with mortality, infections, and severe complications early after cardiac surgery using cardiopulmonary bypass and therefore provide a valuable prognostic marker. However, PCT does not discriminate between infectious and non-infectious complications.
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