Optimal time-window duration for computing time/frequency representations of normal phonocardiograms in dogs.

The optimal duration of the time-window used to compute the time-frequency representation (spectrogram) of the phonocardiogram was studied in four dogs by using intracardiac and thoracic measurements of the PCG. The power and cross-spectrograms of the intracardiac and thoracic PCGs were computed using a fast Fourier transform algorithm and a sine-cosine window with 10 per cent decaying functions. A coherence spectrogram was also computed for each dog to study the linear relationship between the two signals and determine the optimal time-window duration. Results show that the optimal range of the time-window duration is between 16 and 32 ms. A time-window shorter than 16 ms spreads out low-frequency components into the higher frequencies and generates a spectrographic representation with poor frequency resolution (> or = 62.5 Hz). A window larger than 32 ms increases the frequency resolution but smears the spectrographic representation of the signal in the time domain and thus cannot correctly reflect the time-varying properties of the signal. In both cases, the amplitude of the coherence function computed between the left ventricular and the thoracic phonocardiograms is overestimated.

Interaction between the aortic valve leaflets and a Millar dual-micromanometer catheter during recording of the aortic component of the second heart sound in dogs.

The influence of the closure of the aortic valve leaflets on a dual-micromanometer Millar catheter is investigated with respect to the power spectrum of the aortic component (A2) of the second heart sound in dogs. The catheter inserted through the aortic valve is used to simultaneously record A2 in the left ventricle and in the aorta and to study the transmission of A2 up to the body surface. Results indicate that the interaction of the valve leaflets with the Millar dual-micromanometer catheter during the closure and vibration of the aortic valve does not produce a clapping artefact. The main effect is a change in the natural modes of vibration (resonant frequencies) of the aortic valve resulting from a modification of the vibrating structure (combined structure composed of the catheter, the aortic valve and the surrounding blood and tissues) because of the tight mechanical coupling between the aortic valve leaflets and the catheter. In addition, this modification of the natural modes of resonance does not invalidate the estimation of the frequency response of the transfer function between the aortic root and the thoracic recording site, even if the mean gain of the transfer function is affected and the phase slightly increased with frequency. On the contrary, the interaction of the aortic valve leaflets with the catheter seems to slightly increase the spectral contribution (coherence) of the intra-aortic A2 to the thoracic A2.

Acoustic transmission of the aortic component of the second heart sound within the ascending aorta of dogs.

The spectral characteristics of the acoustic transmission of the aortic component of the second heart sound within the ascending aorta was studied using a Millar dual-micromanometer catheter. The tip micromanometer was located close to the aortic valve leaflets while the second micromanometer was located 3 cm above the aortic valve. The frequency response of the transmission properties (amplitude and phase) of the blood and the aortic wall was modelled by an equivalent acoustic transmission system. The signal recorded by the tip micromanometer located near the aortic valve was considered to be the input signal of the equivalent system and the signal recorded by the second micromanometer was used as the output signal. Results of the spectral analysis of the input and output signals show that the acoustic transmissibility of blood in the ascending aorta is high at 20 Hz (the attenuation is negligible). Between 20 and 60 Hz, the transmissibility decreases at a rate of -3 dB per octave while between 60 and 120 Hz it decreases at a rate of -14 dB per octave. Above 120 Hz the transmissibility is low and the resulting attenuation is greater than 20 dB. The phase of the transfer function is shifted by -60 degrees at 20 Hz and decreases at a mean rate of -2.0 degrees Hz-1 between 20 and 100 Hz and -0.75 degrees Hz-1 up to 400 Hz. The phase velocity of the sound transmission is relatively constant (5.5 ms-1) between 40 and 100 Hz and increases up to 9 ms-1 at 300 Hz.

Spectral analysis and acoustic transmission of mitral and aortic valve closure sounds in dogs. Part 3. Effects of altering heart rate and P-R interval.

A surgical protocol was designed to implant, in seven dogs, a programmable sequential atrioventricular pacemaker after destruction of the bundle of His to produce a chronic heart block. The heart rate and P-R interval were then varied independently and their influence on the spectra and acoustic transmission of the mitral M1 and aortic A2 valve closure sounds was studied. Results indicate that the major effects of varying the P-R interval are a strong change in the intensity of M1 and modifications of its acoustic transmission across the heart/thorax acoustic system. No similar influence is observed on the intensity and acoustic transmission of A2. Varying the heart rate has a small effect of the intensity of M1 but none on the intensity of A2. In addition, changes in either the P-R interval or the heart rate do not seem to modify the spectral profile of the intracardiac and thoracic M1 and A2 components.

Spectral analysis and acoustic transmission of mitral and aortic valve closure sounds in dogs. Part 4: Effect of modulating cardiac inotropy.

A surgical protocol was designed to implant in dogs a programmable atrioventricular pacemaker and to destroy the bundle of His with one to four 0.1 ml formaldehyde injections. The heart rate and P-R interval were paced at 100 beats min-1 and 75 ms, respectively. Cardiac inotropy was then varied in five animals by using injections or infusions of cardiotonic drugs (Dobutamine, Betalol and Quinidine). Their effect on the spectra and acoustic transmission of the mitral M1 and aortic A2 closure sound components produced within the left heart and transmitted up to the body surface was studied. Results indicate that changes in cardiac inotropy strongly modify the intensity of M1 and A2 but do not markedly affect their spectral distribution. They also affect the transfer function of the heart/thorax acoustic system, but this influence is small compared with that of a 12 min reference interval. In addition, it was shown that the intensity of M1 is more sensitive to the cardiotonic agents than the intensity of A2.

Spectral analysis and acoustic transmission of mitral and aortic valve closure sounds in dogs. Part 1. Modelling the heart/thorax acoustic system.

A system model based on the simultaneous recording and analysis of the intracardiac and thoracic phonocardiograms to estimate the time-varying properties of the heart/thorax acoustic system of the dog is described. The presence of instrumental noise in the recording of intracardiac phonocardiograms is characterised, and it is demonstrated that its effect on the estimate of the transfer and coherence functions of the system can be quantified and corrected. Application of the model to study the spectral characteristics and the acoustic transmission properties of the mitral component M1 of the first heart sound and of the aortic component A2 of the second heart sound in the dog shows that the heart/thorax acoustic system acts like a bandpass filter having a higher attenuation for A2 than for M1. Between 20 and 100 Hz, the mean attenuation of M1 is 30 dB while that of A2 is 46 dB. Above 100 Hz, the attenuation slope is -12 dB per octave for M1 and -6 dB per octave for A2.

Spectral analysis and acoustic transmission of mitral and aortic valve closure sounds in dogs. Part 2. Effects of neuromuscular blockade, sternotomy and pacemaker control, and a two-week recovery period.

The paper describes the effects of neuromuscular blockade, sternotomy and atrio-ventricular pacing, and a two-week recovery period on the spectra and acoustic transmission of mitral M1 and aortic A2 sound components in dogs. Results indicate that neuromuscular blockade does not affect the attenuation properties of the heart/thorax acoustic system even if it modifies the intensity of M1 and the phase of the transfer function. The immediate effect of sternotomy and cardiac pacing is an important increase in the attenuation of the heart/thorax acoustic system. This increased attenuation is different for both sounds (20 dB for M1 and 11 dB for A2) and disappears after a two-week recovery period. However, the resulting controlled dog model shows slightly different acoustic characteristics than those of the normal animal model.

An assessment of the risk of neoplasia in long-term ileal reservoirs using the DMH rodent model.

This study was undertaken to determine if the construction of an ileal reservoir induces mucosal changes that can potentiate the effect of a chemical carcinogen (1,2-dimethylhydrazine) on ileal mucosa. Animals were divided into three groups: 1) sham operation (n = 19), 2) total colectomy with ileorectal anastomosis (n = 20), 3) total colectomy with an ileal reservoir made of terminal ileum sutured to the rectum (n = 20). An adaptation period of 12 weeks was allowed to promote fecal stasis and the histologic changes before exposure to weekly subcutaneous injections of DMH (25 mg/kg) for 16 weeks. Sodium butyrate was added to the diet as a tumor promotor. All animals were sacrificed one month later. Fecal stasis, along with enlargement, occurred in all the reservoirs (mean dimensions, 74 X 58 X 43 mm). Their mean volume was 88 +/- 14 ml. The histologic changes in the ileal reservoirs were: chronic inflammation (14/20), villous atrophy (14/20), and atrophy of the glands (8/20). In group 3, five carcinomas were seen. There were three in the duodenum and two in the reservoirs. In contrast, 21 carcinomas were detected in the control groups. There were 17 in the colon, 3 in the jejunum, and 1 in the ileum. No significant difference in the number of carcinomas was seen in the ileum with and without reservoir. Although it is possible to induce carcinomas in ileal reservoirs, the incidence remained significantly less than in the colon. In conclusion, the histologic changes induced by the construction of an ileal reservoir do not increase the risk of malignant transformation in the DMH model for intestinal carcinogenesis.