The diagnostic accuracy of mid-regional pro-adrenomedullin for sepsis: a systematic review and meta-analysis
- PMID: 34134460
- DOI: 10.23736/S0375-9393.21.15585-3
The diagnostic accuracy of mid-regional pro-adrenomedullin for sepsis: a systematic review and meta-analysis
Abstract
Introduction: The incidence and mortality of sepsis are high, and common biomarkers are not perfect. To identify a biomarker with high specificity and sensitivity for sepsis, we evaluated the current literature on the performance of mid-regional pro-adrenomedullin (MR-proADM) in the diagnosis of sepsis.
Evidence acquisition: According to appropriate eligibility and exclusion criteria, PubMed, EMBASE, Cochrane Library, China Journal full-text Database, Wanfang Database and Chinese Journal Full Text Database were searched for "mid-regional pro-adrenomedullin," "MR-proADM," "sepsis," "pyemia," "pyohemia," "septicemia," and "blood poisoning." The publication dates considered for the search were from inception until August 31st, 2020. The risk of bias was assessed according to QUADAS-2 criteria.
Evidence synthesis: Eleven studies involving 2038 cases were included. MR-proADM had high sensitivity and specificity in the diagnosis of sepsis, with values of 0.83 (95% CI: 0.79-0.87) and 0.90 (95% CI: 0.83-0.94), respectively. The odds ratio of a combined diagnosis was 41.35, and the area under the curve (AUC) was 0.91. The best cut-off value for MR-proADM diagnosis of sepsis is 1-1.5 nmol/L. MR-proADM may also have value in distinguishing pathogens and identifying sepsis severity and organ failure.
Conclusions: MR-proADM is an excellent biomarker for the diagnosis of sepsis with high sensitivity and specificity. The best cut-off value for MR-proADM diagnosis of sepsis is 1-1.5 nmol/L.
Comment in
-
Phenotyping the host immune response to infection: the critical role of biomarkers in sepsis.Minerva Anestesiol. 2021 Oct;87(10):1067-1069. doi: 10.23736/S0375-9393.21.15992-9. Epub 2021 Aug 2. Minerva Anestesiol. 2021. PMID: 34337927 No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
