Evidence map›Paper›PMID 40156227›Full record

ArticleClinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Activated Clotting Time Requires Adaptation Across Altered Measurement Devices: Determination of Appropriate Range During Atrial Fibrillation Ablation.

Haruna Sakanoue, Hirosuke Yamaji, Sayaka Okamoto, Kumi Okano, Yuka Fujita, Shunichi Higashiya, Takashi Murakami, Satoshi Hirohata, Shozo Kusachi

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Article in Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 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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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Haruna SakanoueDepartment of Nursing, Okayama Heart Clinic, Okayama, Japan.
Hirosuke YamajiHeart Rhythm Center, Okayama Heart Clinic, Okayama, Japan.ORCID 0000-0002-7758-154X
Sayaka OkamotoDepartment of Nursing, Okayama Heart Clinic, Okayama, Japan.
Kumi OkanoDepartment of Nursing, Okayama Heart Clinic, Okayama, Japan.
Yuka FujitaDepartment of Nursing, Okayama Heart Clinic, Okayama, Japan.
Shunichi HigashiyaHeart Rhythm Center, Okayama Heart Clinic, Okayama, Japan.
Takashi MurakamiHeart Rhythm Center, Okayama Heart Clinic, Okayama, Japan.
Satoshi HirohataDepartment of Medical Technology, Okayama University Graduate School of Health Sciences, Okayama, Japan.
Shozo KusachiHeart Rhythm Center, Okayama Heart Clinic, Okayama, Japan.ORCID 0000-0002-9531-076X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundMethods for measuring activated clotting time (ACT) are not yet standardized.ObjectivesTo adjust and compare values between two measurement systems and to optimize ACT during atrial fibrillation (AF) ablation.MethodsTwo systems were compared: electromagnetic detection using a rotating tube (EM system; Hemochron Response) and photo-optical detection using a cartridge immersed in blood (PO system; ACT CA-300TM).ResultsACT was measured simultaneously in 124 instances in 53 patients before and during AF ablations using both methods. A linear regression analysis showed ACT (EM system) = 1.19 × ACT (PO system) + 9.03 (p < .001, r = 0.90). Bland-Altman plots indicated an average difference of 50 s between the two systems. In 3364 ACT measurements from 1161 ablations, the EM system recorded a mean ACT of 320 ± 44 s (range 156-487 s). Estimating the target range as mean ± 1 SD range, the EM system's range was 275-365 s, in 5-s increments. The pre-ablation ACT measured on the EM system was 143 ± 28 s (115-170 s). Cardiac tamponade occurred in 4 out of 2085 ablations (0.19%) over 5 years, with ACT values ranging from 330 to 391 s on the EM system. Based on these findings, the estimated optimal ACT range for the PO system was adjusted to 225-300 s to align with the EM system's range of 275-365 s.ConclusionsACT target ranges should be system-specific, and direct extrapolation between devices is not recommended. Adjustment is clinically necessary when switching systems.

Indexed as

Atrial FibrillationCatheter AblationAgedFemaleHumansMaleMiddle AgedWhole Blood Coagulation Timeanticoagulationcatheterheparinpoint-of-care testingsupraventricular arrhythmia

Identifiers

PMID40156227
PMCPMC11954560

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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.