TY - JOUR
T1 - Cardiac wall motion abnormality after bleeding from vertebral artery aneurysms
AU - Inamasu, Joji
AU - Hayashi, Takuro
AU - Oheda, Motoki
AU - Yamashiro, Kei
AU - Tateyama, Shinichiro
AU - Kogame, Hirotaka
AU - Yamada, Yasuhiro
AU - Sugimoto, Keiko
AU - Watanabe, Eiichi
AU - Kato, Yoko
AU - Hirose, Yuichi
N1 - Publisher Copyright:
© 2014, Springer-Verlag Berlin Heidelberg.
PY - 2014/12/5
Y1 - 2014/12/5
N2 - Objective: Lesions in the medulla oblongata may be causally associated with cardiac wall motion abnormality (WMA). Although subarachnoid hemorrhage (SAH) patients occasionally develop WMA, the relationship between aneurysmal locations and the frequency of WMA has rarely been investigated. The objective of this study was to evaluate whether the frequency of WMA was higher after the rupture of vertebral artery (VA) aneurysms than that of non-VA aneurysms.Methods: We performed a retrospective chart analysis of 244 SAH patients who underwent transthoracic echocardiography and plasma catecholamine measurements. The frequencies of WMA and electrocardiographic (ECG) abnormalities were compared among patients classified by the location of aneurysms. Multivariate regression analysis was conducted to identify variables correlated with WMA. Furthermore, the relationship between plasma catecholamine levels and aneurysmal locations was evaluated.Results: The frequency of WMA was significantly higher in patients with VA aneurysms than in those with non-VA aneurysms (45 vs. 22 %, p = 0.01). However, there was no significant difference in the frequency of ECG abnormalities. Multivariate regression analysis showed that VA aneurysms (OR, 3.317; 95 % CI, 1.129–9.745), poor-grade SAH (OR, 2.733; 95 % CI, 1.320–5.658) and concomitant hydrocephalus (OR, 3.658; 95 % CI, 1.690–7.917) correlated with WMA. There were no significant intergroup differences in plasma catecholamine levels.Conclusion: VA aneurysms are close to several medullary nuclei that integrate autonomic inputs. A transient deformation and ischemia of the medulla oblongata caused by the mechanical stress related to the rupture of a VA aneurysm and/or a concomitant hydrocephalus may be responsible for the disproportionately high frequency of WMA.
AB - Objective: Lesions in the medulla oblongata may be causally associated with cardiac wall motion abnormality (WMA). Although subarachnoid hemorrhage (SAH) patients occasionally develop WMA, the relationship between aneurysmal locations and the frequency of WMA has rarely been investigated. The objective of this study was to evaluate whether the frequency of WMA was higher after the rupture of vertebral artery (VA) aneurysms than that of non-VA aneurysms.Methods: We performed a retrospective chart analysis of 244 SAH patients who underwent transthoracic echocardiography and plasma catecholamine measurements. The frequencies of WMA and electrocardiographic (ECG) abnormalities were compared among patients classified by the location of aneurysms. Multivariate regression analysis was conducted to identify variables correlated with WMA. Furthermore, the relationship between plasma catecholamine levels and aneurysmal locations was evaluated.Results: The frequency of WMA was significantly higher in patients with VA aneurysms than in those with non-VA aneurysms (45 vs. 22 %, p = 0.01). However, there was no significant difference in the frequency of ECG abnormalities. Multivariate regression analysis showed that VA aneurysms (OR, 3.317; 95 % CI, 1.129–9.745), poor-grade SAH (OR, 2.733; 95 % CI, 1.320–5.658) and concomitant hydrocephalus (OR, 3.658; 95 % CI, 1.690–7.917) correlated with WMA. There were no significant intergroup differences in plasma catecholamine levels.Conclusion: VA aneurysms are close to several medullary nuclei that integrate autonomic inputs. A transient deformation and ischemia of the medulla oblongata caused by the mechanical stress related to the rupture of a VA aneurysm and/or a concomitant hydrocephalus may be responsible for the disproportionately high frequency of WMA.
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U2 - 10.1007/s10286-014-0256-8
DO - 10.1007/s10286-014-0256-8
M3 - Article
C2 - 25273609
AN - SCOPUS:84919839735
SN - 0959-9851
VL - 24
SP - 259
EP - 264
JO - Clinical Autonomic Research
JF - Clinical Autonomic Research
IS - 6
ER -