Discriminative performance of pancreatic stone protein in predicting ICU mortality and infection severity in adult patients with infection: a systematic review and individual patient level meta-analysis.

Zuercher, Patrick; Moser, André; Garcia de Guadiana-Romualdo, Luis; Llewelyn, Martin J; Graf, Rolf; Reding, Theresia; Eggimann, Philippe; Que, Yok-Ai; Prazak, Josef (2023). Discriminative performance of pancreatic stone protein in predicting ICU mortality and infection severity in adult patients with infection: a systematic review and individual patient level meta-analysis. Infection, 51(6), pp. 1797-1807. Springer 10.1007/s15010-023-02093-w

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BACKGROUND

Several studies suggested pancreatic stone protein (PSP) as a promising biomarker to predict mortality among patients with severe infection. The objective of the study was to evaluate the performance of PSP in predicting intensive care unit (ICU) mortality and infection severity among critically ill adults admitted to the hospital for infection.

METHODS

A systematic search across Cochrane Central Register of Controlled Trials and MEDLINE databases (1966 to February 2022) for studies on PSP published in English using 'pancreatic stone protein', 'PSP', 'regenerative protein', 'lithostatin' combined with 'infection' and 'sepsis' found 46 records. The search was restricted to the five trials that measured PSP using the enzyme-linked immunosorbent assay technique (ELISA). We used Bayesian hierarchical regression models for pooled estimates and to predict mortality or disease severity using PSP, C-Reactive Protein (CRP) and procalcitonin (PCT) as main predictor. We used statistical discriminative measures, such as the area under the receiver operating characteristic curve (AUC) and classification plots.

RESULTS

Among the 678 patients included, the pooled ICU mortality was 17.8% (95% prediction interval 4.1% to 54.6%) with a between-study heterogeneity (I-squared 87%). PSP was strongly associated with ICU mortality (OR = 2.7, 95% credible interval (CrI) [1.3-6.0] per one standard deviation increase; age, gender and sepsis severity adjusted OR = 1.5, 95% CrI [0.98-2.8]). The AUC was 0.69 for PSP 95% confidence interval (CI) [0.64-0.74], 0.61 [0.56-0.66] for PCT and 0.52 [0.47-0.57] for CRP. The sensitivity was 0.96, 0.52, 0.30 for risk thresholds 0.1, 0.2 and 0.3; respective false positive rate values were 0.84, 0.25, 0.10.

CONCLUSIONS

We found that PSP showed a very good discriminative ability for both investigated study endpoints ICU mortality and infection severity; better in comparison to CRP, similar to PCT. Combinations of biomarkers did not improve their predictive ability.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Intensive Care, Emergency Medicine and Anaesthesiology (DINA) > Clinic of Intensive Care
04 Faculty of Medicine > Pre-clinic Human Medicine > Department of Clinical Research (DCR)

UniBE Contributor:

Zürcher, Patrick, Moser, André, Que, Yok-Ai, Prazak, Josef

Subjects:

600 Technology > 610 Medicine & health

ISSN:

0300-8126

Publisher:

Springer

Language:

English

Submitter:

Pubmed Import

Date Deposited:

15 Sep 2023 07:53

Last Modified:

20 Feb 2024 14:15

Publisher DOI:

10.1007/s15010-023-02093-w

PubMed ID:

37707744

Additional Information:

Zuercher and Moser contributed equally to this work.
Open Access Funding provided by University of Bern.

Uncontrolled Keywords:

Biomarker Infection Mortality PSP Pancreatic stone protein

BORIS DOI:

10.48350/186330

URI:

https://boris.unibe.ch/id/eprint/186330

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