Association between anemic status on admission and clinical outcomes of acute large vessel occlusion
Introduction
Anemia is a common comorbidity in daily clinical practice, especially among the elderly. The same population also has a higher risk of stroke [1]; thus, the prevalence of anemia in patients with acute stroke has been reported to be 21.9% in a meta-analysis of cohort studies [2] or 24.5% in a large registry data [3]. Previous studies have shown that anemia is associated with poor clinical outcomes in patients with any stroke [3], including ischemic stroke [4].
Recent advancements in thrombolytic therapy or endovascular therapy (EVT) have dramatically improved the disability of patients with acute large vessel occlusion (LVO) [5]. However, the risk stratification of patients or optimal candidates for such treatments is controversial in acute stroke management, even in elderly patients [6]. While anemic status should be considered for treatment selection or risk stratification, the availability of data of patients with anemia was limited in patients with LVO who underwent reperfusion therapy. For example, in a multicenter register-based study analyzing 6866 intravenous thrombolysis-treated patients, anemia was associated with poor functional outcomes and mortality [7]. Additionally, a recent analysis of 712 patients who underwent EVT demonstrated that a lower hemoglobin level at baseline and any hemoglobin decline during stroke treatment were associated with poor outcomes, probably due to enlarging and accelerating infarct growth as observed in magnetic resonance imaging (MRI) [8]. However, no large-scale studies have evaluated the associations between anemic status and clinical outcomes in all consecutive LVO patients with and without reperfusion therapy.
Therefore, we investigated the association between anemic status on admission and clinical outcomes in patients with LVO onset using a nationwide registry that enrolled consecutive patients in daily clinical practice.
Section snippets
Study design and participants
The data supporting our results of this study are available from the corresponding author upon reasonable requests. We conducted a post-hoc analysis of the Recovery by Endovascular Salvage for Cerebral Ultra-acute Embolism (RESCUE)-Japan Registry 2, a prospective, multicenter registry that enrolled 2420 consecutive patients with acute ischemic stroke due to LVO from 46 centers in Japan between October 2014 and September 2016 [9]. The study protocol was approved by the respective institutional
Patients
Among the 2420 patients registered in the RESCUE-Japan Registry 2, 12 who did not meet the eligibility criteria and 35 whose hemoglobin data were not available were excluded (Fig. 1). Six patients who were lost to follow-up at day 90 were also excluded from the analyses. Finally, there were 307 (13.0%) patients in the anemia group and 2060 (87.0%) patients in the no-anemia group. (Fig. 1) Of the 307 patients in anemia group, 29 patients have severe anemia (hemoglobin level < 8 g/dL). Among the
Discussion
This study investigated the association between anemic status on admission and clinical outcomes of patients with LVO onset using a nationwide registry that enrolled consecutive patients in daily clinical practice. Herein, 13% of the acute LVO patients were found to have moderate to severe anemia at the onset of acute LVO, and anemia was discovered to be significantly associated with poor outcomes at day 90 after onset. While LVO patients with anemia had more comorbidities and received
Conclusion
Anemic state on admission was associated with poorer clinical outcomes of LVO in real-world clinical practice. The effects of anemic status were larger in LVO patients with lower NIHSS or higher ASPECTS.
Sources of funding
This study was supported in part by the Japan Agency for Medical Research and Development (AMED), the Japanese Society for Neuroendovascular Therapy (JSNET), the Ministry of Health, Labour and Welfare of Japan, Medtronic, Stryker, and Medicos Hirata. The funding sources did not participate in any part of the study, from conception to manuscript preparation.
Declaration of Competing Interest
Dr. Fujiwara: none.
Dr. Sakai reports a research grant from Biomedical Solutions, NeuroVasc, and Terumo; lecturer's fees from Asahi-Intec, Biomedical Solutions, Medtronic, and Terumo; membership on the advisory boards for Johnson&Johnson, Medtronic, and Terumo without related this manuscript.
Dr. Imamura reports lecturer's fees from Medtronic, Stryker, Johnson & Johnson, Terumo, and Asahi-Intec J-sales.
Dr. Tanaka reports lecturer's fee from Johnson & Johnson and Stryker.
Dr. Ohara: none.
Dr.
Acknowledgments
We are indebted to the RESCUE-Japan Registry 2 Investigators (Ryosuke Doijiri, Yukiko Enomoto, Masayuki Ezura, Norihito Fukawa, Eisuke Furui, Akira Handa, Koichi Haraguchi, Taketo Hatano, Makoto Hayase, Nagayasu Hiyama, Koji Iihara, Norio Ikeda, Keisuke Imai, Hideyuki Ishihara, Ryou Itabashi, Yuki Kamiya, Chisaku Kanbayashi, Kazumi Kimura, Kazuo Kitagawa, Yoshihiro Kiura, Junya Kobayashi, Takao Kojima, Ryuji Kondo, Naoya Kuwayama, Yuji Matsumaru, Keigo Matsumoto, Yoshihisa Matsumoto, Kazuo
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