Evidence map›Paper›PMID 41803386›Full record

ArticlePediatric nephrology (Berlin, Germany)2026

Safety and efficacy of low-dose initial citrate infusion for continuous kidney replacement therapy in critically ill children.

Muhterem Duyu, Ayşe Aşık

Abstract read
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Article in Pediatric nephrology (Berlin, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Muhterem DuyuDepartment of Pediatric Intensive Care, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Istanbul, Turkey, 34722. drmuhteremduyu@gmail.com.ORCID http://orcid.org/0000-0001-7892-2927
Ayşe AşıkDepartment of Pediatric Intensive Care, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Istanbul, Turkey, 34722.ORCID http://orcid.org/0000-0003-0973-8098

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCircuit survival (CS) is critical for the maintenance of continuous kidney replacement therapy (CKRT). Regional citrate anticoagulation (RCA) is widely used, effective, and relatively safe; however, it is associated with complications such as citrate accumulation (CA). We aimed to analyze how a lower citrate infusion dose (CID) protocol could impact CS and risks for CA.

methodsThis retrospective single-center cohort study compared the efficacy and safety of standard CID (3.0 mmol/L) and low CID (2.2-2.5 mmol/L) at initial administration in patients receiving RCA for CKRT in a pediatric intensive care unit.

resultsA total of 127 patients received 239 circuits (115 circuits in 55 recipients of standard CID, and 124 filters in 72 recipients of low CID). When filter life was limited to 72 h, median CS for all filters was similar between the standard and low CID groups (51.0 h [IQR: 25.0-72.0] vs. 49.5 h [IQR: 24.0-72.0]; p = 0.857). CS was also similar in circuits terminated due to clotting (standard CID: 38.0 h [IQR: 20.0-58.0], low CID: 37.5 h [IQR: 18.0-55.0]). Recipients of the low CID protocol had significantly lower frequencies of metabolic alkalosis, CA, and hypocalcemia. Multivariate regression identified two independent CA risk factors: longer circuit runtime (OR 1.013, 95% CI 1.002-1.025) and higher weight-adjusted blood flow rates (OR 1.208, 95% CI 1.022-1.427).

conclusionsAdministering a low CID when initializing RCA significantly reduces the likelihood of citrate-related complications while maintaining anticoagulant efficacy.

Indexed as

Acute Kidney InjuryAnticoagulantsCitric AcidContinuous Renal Replacement TherapyChildChild, PreschoolCritical IllnessFemaleHumansInfantInfusions, IntravenousIntensive Care Units, PediatricMaleRetrospective StudiesTreatment OutcomeAnticoagulantsCitric AcidCircuit survivalCitrate-related complicationsContinuous kidney replacement therapyPediatric intensive careRegional citrate anticoagulation

Identifiers

PMID41803386
PMCPMC13337807

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.