Table 2.
Author | CURB‐65 (2–5) | End point | Cutoff of NLR | Sensitivity | Specificity | Prognostic effect estimates (HR, OR) | AUC | Variables | Conclusion |
---|---|---|---|---|---|---|---|---|---|
de Jager et al. 13 | 123 | Adverse event (mortality/adverse events) | 10 | 74 (95% CI: 59.66–85.37) | 53.33 (95% CI: 47.91–58.69) | N/A | N/A | Age, gender, comorbidities, medications, pathogens, CRP level | NLR better‐predicted mortality compared to CRP levels, WBC count, neutrophil count, and lymphocyte count |
In‐hospital mortality | 10 | 78.26 (95% CI: 56.3–92.54) | 51.61 (95% CI: 46.4–56.8) | N/A | 0.701 | ||||
Avci and Perincek 14 | N/A | 30‐day mortality | N/A | N/A | N/A | N/A | 0.577 (95%CI 0.501‐0.650) | Age, smoking, comorbidities, complication, clinical parameters | NLR showed low 30‐day mortality estimation accuracy than PSI class, PSI scores and procalcitonin |
Cataudella et al. 15 | 175 | 30‐day mortality | 11.2 | 100 (95% CI: 92.45–100) | 77.7 (95% CI: 70.14–84.13) | N/A | 0.94 | Age, sex, CURB‐65, PSI, comorbidities | NLR predicted mortality better than PSI, CURB‐65, CRP, and WBC count |
13.4 | 91.49 (95% CI: 76.84–89.33) | 83.78 (95% CI: 76.84–89.33) | N/A | ||||||
Curbelo et al. 16 | 128 | 30‐day mortality | 10 | 63.6 (95% CI: 35.4–84.3) | 65 (95% CI: 56.8–72.4) | OR = 1.04 (1.0–1.1) | 0.88 (95% CI: 0.79–0.98) | Age, sex, vaccination, comorbidities, PSI, CURB‐65, CRP, procalcitonin, proadrenomedullin | NLR was not inferior to proadrenomedullin and significantly better than other biomarkers |
Masbang et al. 17 | N/A | Predicting HR from LR and MR | 10.24 | 56.4 | 66.8 | N/A | 0.726 | Age, gender, comorbidity, smoking, symptoms, vital signs, radiologic finding | NLR predicts CAP severity more than WBC count. NLR can better predict HR from LR and MR |
Ozmen et al. 18 | N/A | 30‐day mortality | N/A | N/A | N/A | HR = 1.04 (0.99–1.01) | 0.64 (0.49–0.79) | Age, gender, comorbidity, smoking, biochemistry, ventilation, ABG finding | Higher NT‐pro BNP values (above 2000 pg/ml) and NLR can be used to predict pneumonia severity and higher NLR on admission to ICU has a higher risk of 180‐day mortality |
Mortality 180 days after ICU admission | N/A | N/A | N/A | HR = 1.04 (1.01–1.07) | 0.63 (0.52–0.74) | ||||
ICU mortality | N/A | N/A | N/A | N/A | 0.60(0.46–0.75) | ||||
Postma et al. 12 | N/A | 30‐day mortality | Median = 10.4 | N/A | N/A | OR = 1.19 (95% CI: 1.02–1.38) | N/A | Age, sex, comorbidities, clinical parameters, mortality scores | NLR had a moderate bivariate association with mortality, but was not statistically significant when added to the model with either PSI or CURB‐65 |
90‐day mortality | N/A | N/A | N/A | OR = 1.18 (95% CI: 1.05–1.32) | N/A | ||||
Yang et al. 19 | 67 | In‐hospital mortality (in patient) | Median in patient who died (11.96; IQR: 7.26–30.68) | 82.61 | 72.2 | N/A | 0.799 | Age, sex, PCT, CRP, comorbidities, PSI, CURB‐65 | NLR is a simple promising marker for predicting in‐hospital mortality |
In‐hospital mortality (ICU) | Median in patient who did not die (4.19; IQR : 2.39–7.52) | N/A | N/A | N/A | N/A | ||||
Cutoff = 7.12 | |||||||||
Kaya 20 | N/A | In‐patient mortality | N/A | N/A | N/A | N/A | N/A | Age, sex, comorbidities, PSI, CURB, laboratory values | NLR can be used in estimating mortality, but is not superior to the commonly used scoring system (PSI, CURB‐65) |
ICU Mortality | Dead NLR = 13.5 ± 9 | N/A | N/A | N/A | 0.743 (95% CI: 0.627–0.860) | ||||
Survived NLR = 7.9 ± 6.8 | N/A | N/A | N/A |
Abbreviations: AUC, area under the ROC curve; CI, confidence interval; CRP, C‐reactive protein; CURB‐65, Confusion, Respiratory rate, Blood pressure, 65 years of age and older; HR, high risk; HR, hazard ratio; ICU, intensive care unit; IQR, interquartile range; LR, low risk; MR, medium risk; N/A, not available; NLR, neutrophil–lymphocyte ratio; NT‐proBNP, N‐terminal (NT)‐prohormone B‐type natriuretic peptide; OR, odds ratio; PCT, procalcitonin; PSI, Pneumonia Severity Index; WBC, white blood cell.