TY - JOUR
T1 - Association of kidney function with effectiveness of procalcitonin-guided antibiotic treatment: a patient-level meta-analysis from randomized controlled trials
AU - Heilmann, Eva
AU - Gregoriano, Claudia
AU - Wirz, Yannick
AU - Luyt, Charles-Edouard
AU - Wolff, Michel
AU - Chastre, Jean
AU - Tubach, Florence
AU - Christ-Crain, Mirjam
AU - Bouadma, Lila
AU - Annane, Djillali
AU - Damas, Pierre
AU - Kristoffersen, Kristina B.
AU - Oliveira, Carolina F.
AU - Stolz, Daiana
AU - Tamm, Michael
AU - de Jong, Evelien
AU - Reinhart, Konrad
AU - Shehabi, Yahya
AU - Verduri, Alessia
AU - Nobre, Vandack
AU - Nijsten, Maarten
AU - Delange, Dylan W.
AU - van Oers, Jos A. H.
AU - Beishuizen, Albertus
AU - Girbes, Armand R. J.
AU - Mueller, Beat
AU - Schuetz, Philipp
N1 - Funding Information:
Competing interests: PS and BM report receiving grants from Thermofisher, Roche Diagnostics and BioMerieux. CEL received lecture fees from Thermofisher Brahms, BioMérieux. YS has received unrestricted research grants from Thermo-fisher, BioMérieux, Orion Pharma, and Pfizer. MCC, DS and MT have received research support from Thermo-Fisher. All other authors declare that they have no conflicts of interest. The National Institute for Health Research provided a grant for the initial Cochrane analysis. Roche Diagnostics provided an unrestricted research grant for this analysis. The funders of the study had no bearing on study design, data collection, data analysis, data interpretation, or writing of the report. The corresponding author had full access to all the data in the study and had final responsibility for the decision to submit for publication.
Publisher Copyright:
© 2020 Eva Heilmann et al., published by De Gruyter, Berlin/Boston.
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2021/2/1
Y1 - 2021/2/1
N2 - Patients with impaired kidney function have a significantly slower decrease of procalcitonin (PCT) levels during infection. Our aim was to study PCT-guided antibiotic stewardship and clinical outcomes in patients with impairments of kidney function as assessed by creatinine levels measured upon hospital admission. We pooled and analyzed individual data from 15 randomized controlled trials who were randomly assigned to receive antibiotic therapy based on a PCT-algorithms or based on standard of care. We stratified patients on the initial glomerular filtration rate (GFR, ml/min/1.73 m2) in three groups (GFR >90 [chronic kidney disease; CKD 1], GFR 15-89 [CKD 2-4] and GFR<15 [CKD 5]). The main efficacy and safety endpoints were duration of antibiotic treatment and 30-day mortality. Mean duration of antibiotic treatment was significantly shorter in PCT-guided (n=2,492) compared to control patients (n=2,510) (9.5-7.6 days; adjusted difference in days -2.01 [95% CI, -2.45 to -1.58]). CKD 5 patients had overall longer treatment durations, but a 2.5-day reduction in treatment duration was still found in patients receiving in PCT-guided care (11.3 vs. 8.6 days [95% CI -3.59 to -1.40]). There were 397 deaths in 2,492 PCT-group patients (15.9%) compared to 460 deaths in 2,510 control patients (18.3%) (adjusted odds ratio, 0.88 [95% CI 0.78 to 0.98)]. Effects of PCT-guidance on antibiotic treatment duration and mortality were similar in subgroups stratified by infection type and clinical setting (p interaction >0.05). This individual patient data meta-analysis confirms that the use of PCT in patients with impaired kidney function, as assessed by admission creatinine levels, is associated with shorter antibiotic courses and lower mortality rates.
AB - Patients with impaired kidney function have a significantly slower decrease of procalcitonin (PCT) levels during infection. Our aim was to study PCT-guided antibiotic stewardship and clinical outcomes in patients with impairments of kidney function as assessed by creatinine levels measured upon hospital admission. We pooled and analyzed individual data from 15 randomized controlled trials who were randomly assigned to receive antibiotic therapy based on a PCT-algorithms or based on standard of care. We stratified patients on the initial glomerular filtration rate (GFR, ml/min/1.73 m2) in three groups (GFR >90 [chronic kidney disease; CKD 1], GFR 15-89 [CKD 2-4] and GFR<15 [CKD 5]). The main efficacy and safety endpoints were duration of antibiotic treatment and 30-day mortality. Mean duration of antibiotic treatment was significantly shorter in PCT-guided (n=2,492) compared to control patients (n=2,510) (9.5-7.6 days; adjusted difference in days -2.01 [95% CI, -2.45 to -1.58]). CKD 5 patients had overall longer treatment durations, but a 2.5-day reduction in treatment duration was still found in patients receiving in PCT-guided care (11.3 vs. 8.6 days [95% CI -3.59 to -1.40]). There were 397 deaths in 2,492 PCT-group patients (15.9%) compared to 460 deaths in 2,510 control patients (18.3%) (adjusted odds ratio, 0.88 [95% CI 0.78 to 0.98)]. Effects of PCT-guidance on antibiotic treatment duration and mortality were similar in subgroups stratified by infection type and clinical setting (p interaction >0.05). This individual patient data meta-analysis confirms that the use of PCT in patients with impaired kidney function, as assessed by admission creatinine levels, is associated with shorter antibiotic courses and lower mortality rates.
KW - Antibiotic stewardship
KW - chronic kidney disease
KW - procalcitonin
UR - http://www.scopus.com/inward/record.url?scp=85092790423&partnerID=8YFLogxK
U2 - 10.1515/cclm-2020-0931
DO - 10.1515/cclm-2020-0931
M3 - Article
C2 - 32986609
VL - 59
SP - 441
EP - 453
JO - Clinical Chemistry and Laboratory Medicine
JF - Clinical Chemistry and Laboratory Medicine
SN - 1434-6621
IS - 2
ER -