The impedance of skin coated with gel but otherwise unprepared was measured from 1 Hz to 1 MHz at ten sites on the thorax, leg, and forehead of ten subjects. For a 1-cm/sup 2/ area, the 1 Hz impedance varied from 10 k Omega to 1 M Omega , which suggests that the bipotential amplifier input impedance should be very high to avoid common-mode-to-differential-mode voltage conversion. The 1-MHz impedance was tightly clustered about 120 Omega . The 100-kHz impedance was about 220 Omega , which suggests that the variation in skin impedance can cause errors in two-electrode electrical impedance tomographs.<>

Injuries to lower limb muscles are common among football players. Localized bioimpedance analysis (BIA) utilizes electrical measurements to assess soft tissue hydration and cell membrane integrity non-invasively. This study reports the effects of the severity of muscle injury and recovery on BIA variables. We made serial tetra-polar, phase-sensitive 50 kHz localized BIA measurements of quadriceps, hamstring and calf muscles of three male football players before and after injury and during recovery until return-to-play, to determine changes in BIA variables (resistance (R), reactance (Xc) and phase angle (PA)) in different degrees of muscle injury. Compared to non-injury values, R, Xc and PA decreased with increasing muscle injury severity: grade III (23.1%, 45.1% and 27.6%), grade II (20.6%, 31.6% and 13.3%) and grade I (11.9%, 23.5% and 12.1%). These findings indicate that decreases in R reflect localized fluid accumulation, and reductions in Xc and PA highlight disruption of cellular membrane integrity and injury. Localized BIA measurements of muscle groups enable the practical detection of soft tissue injury and its severity.

Magnetic induction tomography (MIT) is a contactless method for mapping the electrical conductivity of tissue. MIT is based on the perturbation of an alternating magnetic field by a conducting object. The perturbation is detected by a voltage change in a receivercoil. At physiologically interesting frequencies (10 kHz-10 MHz) and conductivities (< 2 S m(-1)) the lower limit for the relative voltage change (signal/carrier ratio = SCR) to be resolved is 10(-7)-10(-10). A new MIT hardware has been developed consisting of a coil system with planar gradiometers and a high-resolution phase detector (PD). The gradiometer together with the PD resolves an SCR of 2.5 x 10(-5) (SNR = 20 dB at 150 kHz, acquisition speed: 100 ms). The system operates between 20 and 370 kHz with the possibility of extending the range up to 1 MHz. The feasibility of measuring conductivity spectra in the beta-dispersion range of biological tissues is experimentally demonstrated. An improvement of the resolution towards SCR = 10(-7) with an SNR of > or = 20 dB at frequencies > 100 kHz is possible. On-line spectroscopy of tissue conductivity with low spatial resolution appears feasible, thus enabling applications such as non-invasive monitoring of brain oedema.

Muscle injuries in the lower limb are common among professional football players. Classification is made according to severity and is diagnosed with radiological assessment as: grade I (minor strain or minor injury), grade II (partial rupture, moderate injury) and grade III (complete rupture, severe injury). Tetrapolar localized bioimpedance analysis (BIA) at 50 kHz made with a phase-sensitive analyzer was used to assess damage to the integrity of muscle structures and the fluid accumulation 24 h after injury in 21 injuries in the quadriceps, hamstring and calf, and was diagnosed with magnetic resonance imaging (MRI). The aim of this study was to identify the pattern of change in BIA variables as indicators of fluid [resistance (R)] and cell structure integrity [reactance (Xc) and phase angle (PA)] according to the severity of the MRI-defined injury. The % difference compared to the non-injured contralateral muscle also measured 24-h after injury of R, Xc and PA were respectively: grade I (n = 11; -10.4, -17.5 and -9.0%), grade II (n = 8; -18.4, -32.9 and -16.6%) and grade III (n = 2; -14.1, -52.9 and -43.1%), showing a greater significant decrease in Xc (p < 0.001). The greatest relative changes were in grade III injuries. However, decreases in R, that indicate fluid distribution, were not proportional to the severity of the injury. Disruption of the muscle structure, demonstrated by the localized determination of Xc, increased with the severity of muscle injury. The most significant changes 24 h after injury was the sizeable decrease in Xc that indicates a pattern of disrupted soft tissue structure, proportional to the severity of the injury.

A model describing the rotation of the cardiac vector as a possible mechanism for the presence of respiratory information in the ECG is discussed. The way in which this information is revealed is analyzed, and the predictions subjected to qualitative experimental assessment via spectral analysis. The results show that respiratory frequencies occur in the ECG spectrum as a result of heart movement. Measurements on a patient wearing a pacemaker and ventilated to control respiratory rate show that even in the absence of respiratory sinus arrhythmia there is baseband information in the ECG spectrum, attributable neither to electrode artifacts nor to EMG, and sidebands from the respiratory cycle.<>

The purpose of this study is to compare measurement errors in two commercially available multi-frequency bioimpedance analyzers, a Xitron 4000B and an ImpediMed SFB7, including electrode impedance mismatch. The comparison was made using resistive electrical models and in ten human volunteers. We used three different electrical models simulating three different body segments: the right-side, leg and thorax. In the electrical models, we tested the effect of the capacitive coupling of the patient to ground and the skin-electrode impedance mismatch. Results showed that both sets of equipment are optimized for right-side measurements and for moderate skin-electrode impedance mismatch. In right-side measurements with mismatch electrode, 4000B is more accurate than SFB7. When an electrode impedance mismatch was simulated, errors increased in both bioimpedance analyzers and the effect of the mismatch in the voltage detection leads was greater than that in current injection leads. For segments with lower impedance as the leg and thorax, SFB7 is more accurate than 4000B and also shows less dependence on electrode mismatch. In both devices, impedance measurements were not significantly affected (p > 0.05) by the capacitive coupling to ground.