Simultaneous bedside assessment of global cerebral blood flow and effective cerebral perfusion pressure in patients with intracranial hypertension.

BACKGROUND: We examined a bedside technique transcerebral double-indicator dilution (TCID) for global cerebral blood flow (CBF) as well as the concept of effective cerebral perfusion pressure (CPP(eff)) during different treatment options for intracranial hypertension, and compared global CBF and CPP(eff) with simultaneously obtained conventional parameters. METHODS: Twenty-six patients developing intracranial hypertension in the course of traumatic brain injury or subarachnoid hemorrhage were prospectively analyzed using a combined assessment during elevated ventilation (n = 15) or osmotherapy (hypertonic saline or mannitol). For calculation of global CBF, injections of ice-cold indocyanine green boluses were performed and temperature and dye concentration changes were monitored in the thoracic aorta and the jugular bulb. CBF was then calculated according to the mean transit time principle. Estimation of CCP, the arterial pressure at which cerebral blood flow becomes zero, was performed by synchronized registration of corresponding values of blood flow velocity in the middle cerebral artery and arterial pressure and extrapolation to zero-flow velocity. CPP(eff) was calculated as mean arterial pressure minus critical closing pressure (CPP(eff) = MAP(c) - CCP). RESULTS: Elevated ventilation causes a decrease in both ICP (P < 0.001) and CBF (P < 0.001). While CPP(conv) increased (P < 0.001), CPP(eff) decreased during this observation (P = 0.002). Administration of osmotherapeutic agents resulted in a decrease of ICP (P < 0.001) and a temporary increase of CBF (P = 0.052). CPP(conv) and CPP(eff) showed no striking difference under osmotherapy. CONCLUSION: TCID allows repeated measurements of global CBF at the bedside. Elevated ventilation lowered and osmotherapy temporarily raised global CBF. In situations of increased vasotonus, CPP(eff) is a better indicator of blood flow changes than conventional CPP.

Influence of fentanyl, alfentanil, and sufentanil on motor evoked potentials.

The effects of the opioids fentanyl, alfentanil, and sufentanil on motor pathways were studied in a total of 30 rabbits. Compound muscle action potentials (CMAP) were recorded from the extensor muscles of the upper extremity as well as evoked spinal cord potentials (ESCP) from the thoracic epidural space in response to electrical stimulation of the motor cortex. After establishing stable baseline values, an equipotent intravenous bolus of one of the three opioids was applied that abolished reflex motor response to noxious stimulation. Motor evoked potentials (MEP) were recorded from the time of bolus administration until recovery of MEP amplitudes and latencies. Afterwards, the opioids were administered continuously with cumulative dosage up to total absence of motor evoked response. Our results show a dose-dependent suppression of the CMAP: When reflex movement to noxious stimulation was extinguished, we found a significant (P < .001) reduction of the amplitudes to 34+/-18% (mean +/- SD) in the fentanyl group, to 43+/-24% in the alfentanil group, and to 53+/-20% of baseline values in the sufentanil group. Increasing opioid plasma levels were associated with complete extinction of the CMAP. We hypothesize that the descending volleys within motor pathways are mainly inhibited at a spinal level, because ESCP, particularly the number of spinal I-waves, are not severely affected even when CMAP are completely suppressed. In conclusion, intraoperative monitoring of descending pathways by means of MEP during anesthesia with opioids is feasible at anesthetic plasma concentrations maintaining a surgical level of analgesia. Even with high opioid plasma levels, a valid MEP monitoring could be performed evaluating neural activity of spinal MEP.

Influence of nitrous oxide on motor-evoked potentials.

STUDY DESIGN: Rabbits were used as an experimental model in the study of motor-evoked potentials. OBJECTIVES: To evaluate the effect of nitrous oxide on motor-evoked potentials while monitoring direct muscle and spinal cord responses. SUMMARY OF BACKGROUND DATA: Motor-evoked potential monitoring provides a promising tool for intraoperative assessment of descending pathways function. However, to date, this technique is still at an experimental stage, since its routine use is mainly limited because of intraoperative recording difficulties caused by the influence of anesthesia. METHODS: Eight male rabbits weighing between 3000 g and 3500 g were studied. Motor-evoked potentials were recorded from the extremity muscles and from the epidural space of the thoracic cord in response to electrical stimulation of the motor cortex at baseline conditions and at increasing nitrous oxide concentrations (10-70 vol%). RESULTS: The authors found a major suppressive effect of high nitrous oxide concentrations on the electromyographic responses. With 50 vol% nitrous oxide, electromyographic amplitudes were suppressed to 46% (fore leg) and 14% (hind leg) of the baseline values, whereas latencies did not change significantly. In contrast to muscular activity, spinal evoked responses representing neural activity were not affected by any concentration of nitrous oxide. CONCLUSIONS: Intraoperative monitoring of descending pathways by means of motor-evoked potentials during anesthesia of the rabbits based on nitrous oxide is feasible when neural activity is evaluated. Higher doses of nitrous oxide, however, are not compatible with recording of muscular activity.

[Effect of premedication and barbiturate hypnotics on motor evoked potentials induced by magnetic cortex stimulation]. / Einfluss von Prämedikation und Barbiturathypnotika auf motorisch evozierte Potentiale mittels magnetischer Kortexstimulation.

OBJECTIVE: The aim of this study was to investigate the influence of the premedication and the influence of the two barbiturates methohexital and thiopental on magnetically evoked compound muscle action potentials (magnet MEP) in humans. METHODS: 40 Patients (ASA-PS I-II) undergoing lumbar nucleotomy were included in this study after obtaining written informed consent. The study was approved by the local ethical committee. All patients were premedicated with 0.5 mg atropine, 25 mg promethazine and 50 mg pethidine. For induction of anaesthesia patients randomly received methohexital or thiopental by continuous infusion with increasing infusion rates every 15 seconds up to a minimal anaesthesia level in 15 minutes. Transcranial magnetic stimulation was delivered by the magstim 200 magnetic stimulator. Magnetic MEPs were recorded from the surface of the short abductor pollices muscle. MEP-examination was performed preoperatively, after premedication and every two minutes during the induction of anaesthesia. Every other two minutes the patients level of consciousness were assessed and documented. Statistical calculations were performed with the U-test. RESULTS: No statistical differences were found for the mean induction time in the two groups. No statistical difference in amplitude and latency could be observed between the preoperative values and the values measured after premedication. During anaesthesia induction the amplitude decreased in both groups. In 25 of the 40 cases, the MEP disappeared completely before the patients fell asleep. The thiopental group showed a significantly lower incidence of MEP preservation (20%) compared to methohexital (50%). CONCLUSIONS: Premedication with atropine, promethazine and pethidine has no influence on magnetic MEP. Methohexital allows the highest incidence of successful MEP recordings with sufficient anaesthesia. A success rate of only 50% even in cases without motorpathway affection makes the application of magnetic MEP an unreliable tool for intraoperative monitoring.