PubMed Health⌕ Search

PubMed · 10149850

Tilt-table testing and syncope.

Abstract

Syncope is a common clinical problem with multiple potential causes. Recent studies have delineated the natural history and most frequent causes of recurrent syncopal episodes. The medical history and detailed physical examination are particularly important. Clinical electrophysiologic testing has also played a critical role in assessing causes of syncope, but recent reports suggest that its value lies primarily in treating patients with evident underlying structural heart disease. Among patients without structural heart disease, the neurally mediated forms of syncope, particularly the emotional or vasovagal faint, are by far the most common basis for symptoms. In these patients, head-up tilt-table testing has proved particularly valuable in defining the origin of the problem and in assessing therapeutic alternatives. Protocols for upright tilt-table testing remain in evolution. Nonetheless, current practice suggests that 25-minute tilt-test duration is reasonable if pharmacologic provocation is to be used for further evaluation of patients with negative initial findings. However, for those laboratories that do not favor pharmacologic intervention, a 45-minute tilt-test duration is probably essential. Overall, tilt-table testing has proved relatively sensitive and appropriately specific for the identification of patients susceptible to neurally mediated syncopal syndromes.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

D G Benditt, A Asso, S Remole, K Lurie. 1992. Tilt-table testing and syncope.. https://pubmed.ncbi.nlm.nih.gov/10149850/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

A new approach to analysing texture-defined motion.

It has been widely accepted that standard low-level computational approaches to motion processing cannot extract texture-defined motion without applying some pre-processing nonlinearity. This has motivated accounts of motion perception in which luminance- and texture-defined motion are processed by separate mechanisms. Here, we introduce a novel method of image description where motion sequences may be described in terms of their local spatial and temporal gradients. This allows us to assess the local velocity information available to standard low-level motion mechanisms. Our analysis of several texture-motion stimuli shows that the information indicating correct texture-motion velocity and/or direction is present in the raw luminance measures. This raises the possibility that luminance-motion and texture-motion may be processed by the same cortical mechanisms. Our analysis offers a way of looking at texture-motion processing that is, to our knowledge, new and original.

Electrophysiology↗

Hydroperoxyl, superoxide and pH gradients in the mitochondrial matrix: a theoretical assessment.

The negative surface charge of many cellular membranes concentrates protons and rarefies superoxide in their vicinity. It was speculated that the low pH near membranes should facilitate superoxide protonation, thereby concentrating hydroperoxyl radical in this region. This process would exacerbate both lipid peroxidation and the transfer of oxidative damage between cellular compartments, as hydroperoxyl is a good initiator of lipid peroxidation and permeates lipid bilayers. Surface-charge-enhancement of hydroperoxyl production in mitochondria--which are main intracellular sources of superoxide--should be particularly relevant. Using a simple model of superoxide metabolism in the mitochondrial matrix, we calculated the gradients of pH, superoxide, and hydroperoxyl, and assessed the previous hypothesis in the light of available experimental data. The following predictions ensued: (i) Near the mitochondrial inner membrane, gradients of superoxide concentration with amplitude up to 36% of the maximal concentration, and pH gradients of up to 0.19 units between membrane and bulk. (ii) These electrostatically induced gradients die out within approximately 4 nm of the membrane. (iii) At high (hundreds of nanometres) inter-cristae separations, owing to enzyme-catalyzed dismutation of superoxide, both superoxide and hydroperoxyl become rarefied towards the midpoint between cristae. (iv) Surface charge should neither enhance superoxide protonation nor concentrate hydroperoxyl near biological membranes.

Electrophysiology↗

Derivation of Poisson and Nernst-Planck equations in a bath and channel from a molecular model.

Permeation of ions from one electrolytic solution to another, through a protein channel, is a biological process of considerable importance. Permeation occurs on a time scale of micro- to milliseconds, far longer than the femtosecond time scales of atomic motion. Direct simulations of atomic dynamics are not yet possible for such long-time scales; thus, averaging is unavoidable. The question is what and how to average. In this paper, we average a Langevin model of ionic motion in a bulk solution and protein channel. The main result is a coupled system of averaged Poisson and Nernst-Planck equations (CPNP) involving conditional and unconditional charge densities and conditional potentials. The resulting NP equations contain the averaged force on a single ion, which is the sum of two components. The first component is the gradient of a conditional electric potential that is the solution of Poisson's equation with conditional and permanent charge densities and boundary conditions of the applied voltage. The second component is the self-induced force on an ion due to surface charges induced only by that ion at dielectric interfaces. The ion induces surface polarization charge that exerts a significant force on the ion itself, not present in earlier PNP equations. The proposed CPNP system is not complete, however, because the electric potential satisfies Poisson's equation with conditional charge densities, conditioned on the location of an ion, while the NP equations contain unconditional densities. The conditional densities are closely related to the well-studied pair-correlation functions of equilibrium statistical mechanics. We examine a specific closure relation, which on the one hand replaces the conditional charge densities by the unconditional ones in the Poisson equation, and on the other hand replaces the self-induced force in the NP equation by an effective self-induced force. This effective self-induced force is nearly zero in the baths but is approximately equal to the self-induced force in and near the channel. The charge densities in the NP equations are interpreted as time averages over long times of the motion of a quasiparticle that diffuses with the same diffusion coefficient as that of a real ion, but is driven by the averaged force. In this way, continuum equations with averaged charge densities and mean-fields can be used to describe permeation through a protein channel.

Electrophysiology↗