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1.
ESC Heart Fail ; 7(4): 1982-1986, 2020 08.
Article in English | MEDLINE | ID: mdl-32351016

ABSTRACT

Post-operative right coronary artery occlusion is a serious complication that demands acute coronary revascularization to prevent myocardial infarction. We present two cases with acute right coronary artery obstruction caused by (1) transfemoral aortic valve implantation and (2) acute type A aortic dissection. Although coronary artery bypass grafting was performed intraoperatively, right heart failure was observed in both cases. The Impella RP® device offers temporary right ventricular mechanical support; wherefore, we decided to deploy it in both patients. The devices were uneventfully and successfully implanted to bridge for recovery of the right heart. We report the perioperative course of the patients as well as their condition at 1 year follow-up.


Subject(s)
Heart Failure , Heart-Assist Devices , Myocardial Infarction , Heart Failure/etiology , Heart Ventricles , Humans , Treatment Outcome
2.
Anesthesiology ; 107(1): 33-44, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17585213

ABSTRACT

BACKGROUND: Neuraxial blockade is used as primary anesthetic technique in one third of surgical procedures. The authors tested whether bisoprolol would protect patients at risk for cardiovascular complications undergoing surgery with spinal block. METHODS: The authors performed a double-blinded, placebo-controlled, multicenter trial to compare the effect of bisoprolol with that of placebo on 1-yr composite outcome including cardiovascular mortality, nonfatal myocardial infarction, unstable angina, congestive heart failure, and cerebrovascular insult. Bisoprolol was given orally before and after surgery for a maximum of 10 days. Adrenergic receptor polymorphisms and safety outcome measures of bisoprolol therapy were also determined. RESULTS: A total of 224 patients were enrolled. Spinal block could not be established in 5 patients. One hundred ten patients were assigned to the bisoprolol group, and 109 patients were assigned to the placebo group. The mean duration of treatment was 4.9 days in the bisoprolol group and 5.1 days in the placebo group. Bisoprolol therapy reduced mean heart rate by 10 beats/min. The primary outcome was identical between treatment groups and occurred in 25 patients (22.7%) in the bisoprolol group and 24 patients (22.0%) in the placebo group during the 1-yr follow-up (hazard ratio, 0.97; 95% confidence interval, 0.55-1.69; P = 0.90). However, carriers of at least one Gly allele of the beta1-adrenergic receptor polymorphism Arg389Gly showed a higher number of adverse events than Arg homozygous (32.4% vs. 18.7%; hazard ratio, 1.87; 95% confidence interval, 1.04-3.35; P = 0.04). CONCLUSIONS: Perioperative bisoprolol therapy did not affect cardiovascular outcome in these elderly at-risk patients undergoing surgery with spinal block.


Subject(s)
Adrenergic beta-Antagonists/therapeutic use , Anesthesia, Spinal , Bisoprolol/therapeutic use , Cardiovascular Diseases/prevention & control , Intraoperative Complications/prevention & control , Postoperative Complications/prevention & control , Receptors, Adrenergic/genetics , Cardiomyopathy, Dilated/mortality , Cardiomyopathy, Dilated/prevention & control , Cardiovascular Diseases/mortality , Coronary Disease/mortality , Coronary Disease/prevention & control , Double-Blind Method , Electrocardiography, Ambulatory , Follow-Up Studies , Genotype , Humans , Intraoperative Complications/mortality , Myocardial Infarction/mortality , Myocardial Infarction/prevention & control , Postoperative Complications/mortality , Proportional Hazards Models , Respiratory Function Tests , Risk , Switzerland , Treatment Outcome
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