Biomarker | Study (ref) | Study design | Nb patients, n (setting) | Level of evidence | End-point | Main results, absolute risk reduction (ARR) or odds ratio (OR; 95% CI) |
---|---|---|---|---|---|---|
 | 1 st author, [Ref] |  |  |  |  |  |
PCT | Stolz D, [20] | Single-centre, randomised, controlled open study | 208 | High | Antibiotic exposure and rate of initiation of antibiotic therapy, based on PCT level > 0.25 μg/L | ARR = 32% (40% vs. 72%) of antibiotic prescriptions in the PCT-guided group. |
 |  |  | (AECB) |  |  |  |
 |  |  |  |  |  | Ab exposure OR = 0.56 [0.43-0.73] |
PCT | Schuetz P, [25] | Multicentre, open RCT | 1359 | High | Antibiotic exposure | ARR = 12% (75.4% vs. 87.7%) in PCT group, Overall antibiotic exposure = - 35% (5.7 vs. 8.7 days). |
 |  | Noninferiority study | (ED) |  | Based on a PCT level > 0.25 μg/L for initiating prescription. |  |
PCT | Christ-Crain M, [18] | Single-centre open RCT | 302 | High | Antibiotic initiation rate | ARR = 14% (85% vs. 99%) in initial antibiotic prescription in PCT group |
 |  |  | (ED, ward) |  | Antibiotic exposure |  |
 |  |  |  |  | Based on a PCT level > 0.25 μg/L to initiate therapy | Overall ab exposure: OR = 0.52 [0.48–0.55] |
PCT | Kristoffersen KB, [19] | Single-centre, open, RCT | 210 | High | Antibiotic prescription rate, based on a PCT level > 0.25 μg/L to initiate therapy in PCT group | 3% increase in antibiotic prescription (88% vs. 85%) in the PCT group |
 |  |  | (ED, ward) |  |  |  |
PCT | Long W, [23] | Single-centre, open RCT | 127 | High | Antibiotic prescription rate, based on a PCT level > 0.25 μg/L in the PCT group | ARR = 11% of antibiotic prescriptions in the PCT group |
 |  |  | (ED) |  |  |  |
PCT | Long W, [22] | Single-centre, open RCT | 156 | High | Antibiotic prescription rate, based on a PCT level > 0.25 μg/L in the PCT group | ARR = 13% of antibiotic prescriptions in the PCT group |
 |  |  | (ED) |  |  |  |
PCT | Burkhardt O, [16] | Single-centre, open RCT, noninferiority | 550 | High | Antibiotic prescription rate, based on a PCT level > 0.25 μg/L in the PCT group | ARR = 15% (21.5% vs. 36.7%) for antibiotic prescription rate in the PCT group |
 |  |  | (PC) |  |  |  |
PCT | Briel M, [15] | Multicentre, open RCT, noninferiority | 458 | High | Antibiotic prescription rate, based on a PCT level > 0.25 μg/L in the PCT group | ARR = 72% [95% CI 66-78] for antibiotic prescription rate in the PCT group |
 |  |  | (PC) |  |  |  |
PCT | Schuetz P, [30] | Meta-analysis of 14 RCTs | 3 119 | High | Â | Risk reduction of initial antibiotic therapy: OR = 0.24 (95% CI, 0.2-0.29) |
 |  |  |  |  |  | Overall antibiotic exposure: |
 |  |  |  |  |  | OR = 0.1 (95% CI = 0.07-0.14), without difference in mortality rates |
PCT | Van der Meer V, [28] | Literature review on the use of CRP (13 studies) | 13 | High | Prediction of LRTI | Bacterial LRTI predicted with a sensitivity varying from 8% to 99% and a specificity varying from 27% to 95% |
PCT | Schuetz P, [29] | Review of 8 RCTs using an PCT-based algorithm for the initiation of antibiotic therapy | 3 457 | High | Antibiotic prescription rate | ARR varying from 6% to 72% |
CRP | Cals JW, [24] | Multicentre, open cluster-RCT, testing a CRP-based algorithm | 431 | High | Antibiotic prescription rate and antibiotic exposure, based on a CRP value < 20 : no antibiotic; CRP >100 : atb recommended, and 20<CRP<99 : reassess for possible therapy | ARR = 22% (31% vs. 53%) of initial antibiotic prescriptions in the CRP group |
 |  |  |  |  |  | Overall antibiotic exposure: - 13% (45% vs. 58%) |
PCT | Christ-Crain M, [17] | Multicentre, open, cluster-RCT | 243 | High | Antibiotic prescription rate, based on a PCT level > 0.25 μg/L in the PCT group | ARR = 39% for antibiotic prescription rate in the PCT group |
 |  |  | (ED) |  |  |  |
Summary of evidence table: Lower respiratory tract infection | ||||||
Number of studies, n | Total number of patients, n | Highest level of evidence | Directness* | Consistency** | Overall strength of evidence | |
12 | 4 412 | High | Yes | Yes | Strong |