Vasodepressor reactions after orthotopic cardiac transplantation: Relationship to reinnervation status

Ventricular vagal nerve endings are thought to trigger vasodepressor syncope. Reports of vasodepressor reactions associated with donor bradycardia after cardiac transplantation have led to speculation that vagal reinnervation occurs. We assessed reinnervation status in seven patients 23–36 months (median 24 months) post-transplantation. Heart rate responses to vagal manoeuvres (respiration, Valsalva) and sympathetic stimuli (exercise and injection of tyramine into the coronary artery supplying the sinus node) were measured. All patients underwent 60 min of 60° head-up tilt with foot plate support. During tilt four of the seven had vasodepressor reactions with a fall in mean arterial pressure of 20–90 mmHg. During vasodepression two patients had falls in donor heart rate of 13 and 40% relative to peak heart rate during tilt. These two patients had evidence of functional sympathetic reinnervation. By contrast the two patients without donor bradycardia during vasodepression had only limited or no evidence of sympathetic reinnervation. No patient had consistent evidence of parasympathetic reinnervation as judged by the heart rate response to vagal manoeuvres. Headup tilt can thus produce vasodepressor reactions with donor bradycardia after cardiac transplantation in the absence of consistent evidence of vagal reinnervation. Left ventricular nerve endings may not be the only mediators of tilt-induced vasodepressor reactions in man. Donor bradycardia during vasodepression may reflect sympathetic withdrawal and not vagal reinnervation.     

Essential Cardiac Catheterization

Essential Cardiac Catheterization is a concise new book of 10chapters. It covers various aspects of diagnostic cardiac catheterizationand is primarily aimed at cardiologists in training. Productionof the book has been supported by an educational grant fromthe medical technology company Medtronic. The authors are cardiologists     

Aortic stenosis and non-cardiac surgery

Goldman and colleagues identified severe aortic stenosis asa risk factor for perioperative cardiac complications in non-cardiacsurgery in 1977.¹ Furthermore, they emphasized that this riskwas significantly increased by the presence of coexisting cardiacfailure and dysrhythmias. The National Confidential Enquiryinto Perioperative Deaths has expressed concerns in severalrecent reports about the assessment and management of patientswith aortic stenosis who undergo surgery. In the UK, aorticstenosis is most often a degenerative disease that is increasingin incidence as people live longer; it occurs frequently inpatients with significant comorbidities. The condition is oftenunrecognized before death and post-mortem data suggest an endof life incidence of 1%. Aortic stenosis may also be presentat birth; congenital malformation registry data suggest a livebirth incidence of 0.1%.     

New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation

We performed detailed clinical, histopathological, biochemical, in vitro translation and molecular genetic analysis in patients from two unrelated families harbouring the tRNA(SerUCN) 7472C-insertion mutation. Proband 1 developed a progressive neurodegenerative phenotype characterised by myoclonus, epilepsy, cerebellar ataxia and progressive hearing loss. Proband 2 had a comparatively benign phenotype characterised by isolated myopathy with exercise intolerance. Both patients had the 7472C-insertion mutation in identical proportions and they exhibited a similar muscle biochemical and histopathological phenotype. However, proband 2 also had a previously unreported homoplasmic A to C transition at nucleotide position 7472 in the tRNA(SerUCN) gene. This change lengthens further the homopolymeric C run already expanded by the 7472C-insertion. These data extend the phenotypic range associated with the 7472C-insertion to include isolated skeletal myopathy, as well as a MERRF-like phenotype.     

Multi-detector row computed tomography: imaging in acute aortic syndrome

Acute aortic syndromes (AAS) encompass a spectrum of emergencies. These include those non-traumatic disease entities of the aorta namely, penetrating atherosclerotic ulcer, intramural haematoma, dissection and aneurysm rupture. The various types of AAS cannot be reliably differentiated on clinical grounds alone. Acute thoracic aortic injury is usually included in this group even though clinical presentation is different, i.e., in the context of trauma, the imaging features are very similar. Differentiation of AAS from acute coronary syndrome (ACS) is important, however, it must be remembered that ACS may occur as a result of AAS. Now electrocardiogram (ECG)-gating technology is widely available, ECG-gated multi-detector row computed tomography (MDCT) is a powerful clinical tool in the acute emergency setting, which enables rapid and specific diagnosis of aortic pathology. ECG-gated MDCT significantly reduces motion artefact, avoids potential pitfalls in diagnosis and often provides diagnostic information about the coronary arteries. It should be used as a first-line imaging technique. This article examines the role of MDCT imaging and cardiac gating in the assessment of AAS and discusses the differentiation of this spectrum of aortic diseases with reference to the key imaging findings as obtained by experience in our institution.     

Multi-detector row computed tomography: imaging the coronary arteries

Over the last 2 years, multi-detector row computed tomographic (MDCT) cardiac imaging has continued to rapidly develop and evolve from the experimental research setting to become a useful clinical tool. The increasing availability of MDCT presents today's clinicians with an additional non-invasive diagnostic cardiac imaging method, in particular for the coronary arteries. With the advent and increasing clinical use of 16-detector row machines, and now with the imminent clinical emergence of 64-channel machines, the improvements in spatial and temporal resolution and sophisticated ECG-gating are allowing motion-free, fast, accurate, detailed, contrast-enhanced cardiac imaging that begins to approach the accuracy of traditional invasive diagnostic techniques. Additional diagnostic information may also be provided.