Simon J. Mitchell

Cerebral protection by lidocaine during cardiac operations.

BACKGROUND Lidocaine improves outcome in animal brain injury models. Cardiac operations often cause postoperative neuropsychological (NP) impairment. We investigated cerebral protection by lidocaine in cardiac surgical patients. METHODS Sixty-five patients undergoing left heart valve procedures completed 11 preoperative NP tests, a self-rating inventory for memory, and inventories measuring depression and anxiety. These were repeated 10 days, 10 weeks, and 6 months postoperatively. Patients received a 48-hour double-blinded infusion of either lidocaine in a standard antiarrhythmic dose or placebo, beginning at induction of anesthesia. A postoperative deficit in any test was defined as decline by more than or equal to the group preoperative standard deviation. In addition, sequential postoperative percentage change scores were calculated for each patient in all NP tests and the inventories for memory, depression and anxiety. RESULTS Forty-two patients completed all three reviews, 8 completed two reviews, and 5 patients were reviewed once. Significantly more placebo patients had a deficit in at least one NP test at 10 days (p<0.025) and 10 weeks (p<0.05). The lidocaine group achieved superior sequential percentage change scores in 6 of the 11 NP tests (p<0.05) and in the memory inventory (p<0.025). There were no group differences in the remaining NP tests or the depression and anxiety inventories. CONCLUSIONS These data show that cerebral protection by lidocaine, which is unrelated to any effect on depression or anxiety, and is at a level that is noticed by the patients.

Venous air in the bypass circuit: a source of arterial line emboli exacerbated by vacuum-assisted drainage

BACKGROUND Arterial emboli cause neurocognitive deficits in cardiac surgical patients. Carotid artery emboli, detected ultrasonically, have been observed after venous air entrainment into the cardiopulmonary bypass circuit. We investigated in vitro the extent to which venous air affected emboli detected in the arterial line downstream from a 40-microm filter. METHODS Using salvaged clinical cardiopulmonary bypass circuits, fixed volumes of air were introduced into the venous return line at unrestricted rates and at fixed rates using gravity venous drainage and vacuum-assisted venous drainage. Emboli counts were recorded distal to the arterial line filter using a 2-MHz pulsed-wave Doppler monitor. Emboli counts were similarly recorded after the introduction of carbon dioxide into the venous return line instead of air. RESULTS The number of emboli rose with increasing volumes of entrained venous air (p < 0.001), and there was an almost tenfold increase with vacuum-assisted venous drainage (p < 0.0001) compared with gravity venous drainage. Venous air was entrained at a significantly faster rate under vacuum-assisted venous drainage (p < 0.0001). When the entrainment rate of venous air was fixed, the difference in emboli numbers recorded for gravity and assisted venous drainage was not significant. There was a significant reduction in arterial line emboli when carbon dioxide rather than air was entrained under both vacuum-assisted and gravity drainage (p < 0.001). CONCLUSIONS Entrained venous air during cardiopulmonary bypass is a potential hazard, particularly during vacuum-assisted venous drainage. Every effort should be made to avoid venous air entrainment.

Multimodal system designed to reduce errors in recording and administration of drugs in anaesthesia: prospective randomised clinical evaluation

Objective To clinically evaluate a new patented multimodal system (SAFERSleep) designed to reduce errors in the recording and administration of drugs in anaesthesia. Design Prospective randomised open label clinical trial. Setting Five designated operating theatres in a major tertiary referral hospital. Participants Eighty nine consenting anaesthetists managing 1075 cases in which there were 10 764 drug administrations. Intervention Use of the new system (which includes customised drug trays and purpose designed drug trolley drawers to promote a well organised anaesthetic workspace and aseptic technique; pre-filled syringes for commonly used anaesthetic drugs; large legible colour coded drug labels; a barcode reader linked to a computer, speakers, and touch screen to provide automatic auditory and visual verification of selected drugs immediately before each administration; automatic compilation of an anaesthetic record; an on-screen and audible warning if an antibiotic has not been administered within 15 minutes of the start of anaesthesia; and certain procedural rules—notably, scanning the label before each drug administration) versus conventional practice in drug administration with a manually compiled anaesthetic record. Main outcome measures Primary: composite of errors in the recording and administration of intravenous drugs detected by direct observation and by detailed reconciliation of the contents of used drug vials against recorded administrations; and lapses in responding to an intermittent visual stimulus (vigilance latency task). Secondary: outcomes in patients; analyses of anaesthetists’ tasks and assessments of workload; evaluation of the legibility of anaesthetic records; evaluation of compliance with the procedural rules of the new system; and questionnaire based ratings of the respective systems by participants. Results The overall mean rate of drug errors per 100 administrations was 9.1 (95% confidence interval 6.9 to 11.4) with the new system (one in 11 administrations) and 11.6 (9.3 to 13.9) with conventional methods (one in nine administrations) (P=0.045 for difference). Most were recording errors, and, though fewer drug administration errors occurred with the new system, the comparison with conventional methods did not reach significance. Rates of errors in drug administration were lower when anaesthetists consistently applied two key principles of the new system (scanning the drug barcode before administering each drug and keeping the voice prompt active) than when they did not: mean 6.0 (3.1 to 8.8) errors per 100 administrations v 9.7 (8.4 to 11.1) respectively (P=0.004). Lapses in the vigilance latency task occurred in 12% (58/471) of cases with the new system and 9% (40/473) with conventional methods (P=0.052). The records generated by the new system were more legible, and anaesthetists preferred the new system, particularly in relation to long, complex, and emergency cases. There were no differences between new and conventional systems in respect of outcomes in patients or anaesthetists’ workload. Conclusions The new system was associated with a reduction in errors in the recording and administration of drugs in anaesthesia, attributable mainly to a reduction in recording errors. Automatic compilation of the anaesthetic record increased legibility but also increased lapses in a vigilance latency task and decreased time spent watching monitors. Trial registration Australian New Zealand Clinical Trials Registry No 12608000068369.

Anaphylaxis Is More Common with Rocuronium and Succinylcholine than with Atracurium

Background:Intraoperative anaphylaxis is a rare but serious occurrence, often triggered by neuromuscular-blocking drugs (NMBDs). Previous reports suggest that the rates of anaphylaxis may be greater for rocuronium than for other NMBDs, but imprecise surrogate metrics for new patient exposures to NMBDs complicate interpretation. Methods:This was a retrospective, observational cohort study of intraoperative anaphylaxis to NMBDs at two hospitals between 2006 and 2012. Expert anesthetic and immunologist collaborators investigated all referred cases of intraoperative anaphylaxis where NMBDs were administered and identified those where a NMBD was considered responsible. New patient exposures for each NMBD were extracted from electronic anesthetic records compiled during the same period. Anaphylaxis rates were calculated for each NMBD using diagnosed anaphylaxis cases as the numerator and the number of new patient exposures as the denominator. Results:Twenty-one patients were diagnosed with anaphylaxis to an NMBD. The incidence of anaphylaxis was 1 in 22,451 new patient exposures for atracurium, 1 in 2,080 for succinylcholine, and 1 in 2,499 for rocuronium (P < 0.001). Conclusions:In Auckland, the rate of anaphylaxis to succinylcholine and rocuronium is approximately 10-fold higher than to atracurium. Previous estimates of NMBD anaphylaxis rates are potentially confounded by inaccurate proxies of new patient exposures. This is the first study to report anaphylaxis rates using a hard denominator of new patient exposures obtained directly from anesthetic records.

Bubble generation and venous air filtration by hard-shell venous reservoirs: a comparative study

We have previously shown significant bubble formation in Medtronic Maxima hard-shell venous reservoirs (HSVRs). In the present study, we not only investigated the mechanism of this bubble formation, but also the extent of bubble clearance by membrane oxygenators and arterial line filters. In addition, we also compared the performance of five HSVRs with respect to bubble formation and venous air filtration. Salvaged clinical CPB circuits containing different HSVRs were studied by downstream Doppler monitoring under fixed flow - decreasing volume, fixed volume - increasing flow, and entrained venous air conditions. Bubbles formed in the Medtronic Maxima top entry HSVR at volumes below 800 ml and flows above 3.5 l min-1, and were incompletely removed by a membrane oxygenator and arterial line filter. Decreased bubbling was seen when the reservoir atmosphere was flushed with CO2, suggesting that these bubbles formed in a fountain at the venous inflow. The Medtronic Maxima Forte HSVR formed significantly fewer bubbles at low volumes, and filtered venous air effectively. Negligible bubble formation occurred in the Sorin, Terumo, or Baxter reservoirs. The minimum recommended operating volume for the Medtronic Maxima top entry reservoir should be reset at 600 ml and this device should always be used with an arterial filter. Bubble formation is substantially reduced in the new Medtronic Maxima Forte HSVR and this device is a good filter for venous air.

Cerebral Protection by Lidocaine During Cardiac Operations: A Follow-Up Study

BACKGROUND A previous study showed less postoperative neurocognitive impairment in open-chamber cardiac surgery patients given lidocaine for 48 hours after induction of anesthesia. In the present study, we aimed to test the benefit of a 12-hour infusion in a broader group of cardiac surgery patients, including those undergoing coronary artery bypass graft surgery. METHODS This was a randomized, double-blind, intention-to-treat trial. Before cardiac surgery, 158 patients completed 7 neurocognitive tests and a self-rating scale for memory. They received a 12-hour infusion of either lidocaine in a standard antiarrhythmic dose or placebo, beginning at induction of anesthesia. The cognitive tests and memory scale were repeated at postoperative weeks 10 and 25. A deficit in any cognitive test was defined as a decline in score by more than or equal to the preoperative group standard deviation. RESULTS All tests were completed by 118 and 107 patients at 10 and 25 weeks, respectively. The proportions of patients in the lidocaine and placebo groups exhibiting a deficit in one or more tests were as follows: 45.8% versus 40.7% at 10 weeks, and 35.2% versus 37.7% at 25 weeks (not significant). There were no significant differences between groups in self-ratings of memory function or length of intensive care unit or hospital stay. CONCLUSIONS Lidocaine was not neuroprotective. The result of the previous trial may represent a type 1 error. Alternatively, benefit may be more likely for open-chamber surgery patients exposed to larger numbers of emboli or with a longer lidocaine infusion.

A prospective, observational study of the effects of implementation strategy on compliance with a surgical safety checklist

Background The reported benefits of using the WHO Surgical Safety Checklist (SSC) are likely to depend on compliance with its correct use. Compliance with SSC administration in centres that have introduced the checklist under a research protocol may differ from centres where the SSC is introduced independently. Objective To compare compliance with SSC administration at an original WHO pilot study centre (Hospital 1) with that at a similar neighbouring hospital (Hospital 2) that independently integrated the SSC with pre-existing practice. Methods This was a prospective, observational study. One hundred operations were observed at each hospital. We recorded: compliance with administration of SSC domains (Sign In, Time Out and Sign Out) and individual domain items; timing of domain administration; and operating room team engagement during administration. Results Domain compliance at Hospital 1 and Hospital 2, respectively, was: 96% and 31% (p<0.0005) for Sign In; 99% and 48% (p<0.0005) for Time Out and 22% and 9% (p=0.008) for Sign Out. Engagement of two or more teams during Sign In and Time Out occurred more frequently at Hospital 2 than at Hospital 1. Discussion Compliance with administration of SSC domains was lower at Hospital 2 which introduced the SSC outside the context of a strict study protocol. This finding mandates caution in extrapolation of benefits identified in SSC studies to non-study hospitals. Staff engagement was better at Hospital 2 where checklist administration leadership is strategically shared among anaesthetic, surgical and nursing team members as compared with exclusive nursing leadership at Hospital 1. Study registry number Australian and New Zealand Clinical Trials Registry: Ref: ACTRN12612000135819, http://www.anzctr.org.au/trial_view.aspx?ID=362007

The physiological kinetics of nitrogen and the prevention of decompression sickness

Decompression sickness (DCS) is a potentially crippling disease caused by intracorporeal bubble formation during or after decompression from a compressed gas underwater dive. Bubbles most commonly evolve from dissolved inert gas accumulated during the exposure to increased ambient pressure. Most diving is performed breathing air, and the inert gas of interest is nitrogen. Divers use algorithms based on nitrogen kinetic models to plan the duration and degree of exposure to increased ambient pressure and to control their ascent rate. However, even correct execution of dives planned using such algorithms often results in bubble formation and may result in DCS. This reflects the importance of idiosyncratic host factors that are difficult to model, and deficiencies in current nitrogen kinetic models.Models describing the exchange of nitrogen between tissues and blood may be based on distributed capillary units or lumped compartments, either of which may be perfusion- or diffusion-limited. However, such simplistic models are usually poor predictors of experimental nitrogen kinetics at the organ or tissue level, probably because they fail to account for factors such as heterogeneity in both tissue composition and blood perfusion and non-capillary exchange mechanisms.The modelling of safe decompression procedures is further complicated by incomplete understanding of the processes that determine bubble formation. Moreover, any formation of bubbles during decompression alters subsequent nitrogen kinetics. Although these factors mandate complex resolutions to account for the interaction between dissolved nitrogen kinetics and bubble formation and growth, most decompression schedules are based on relatively simple perfusion-limited lumped compartment models of blood : tissue nitrogen exchange. Not surprisingly, all models inevitably require empirical adjustment based on outcomes in the field.Improvements in the predictive power of decompression calculations are being achieved using probabilistic bubble models, but divers will always be subject to the possibility of developing DCS despite adherence to prescribed limits.

Emboli generation by the Medtronic Maxima hard shell adult venous reservoir in cardiopulmonary bypass circuits: a preliminary report

Increases in right common carotid artery Doppler ultrasound signals typical of emboli were found in cardiopulmonary bypass patients when the Medtronic Maxima hard-shell adult combined venous and cardiotomy reservoir was operated at reservoir blood volumes near the manufacturer;s recommended minimum of 300 ml. The signals were reduced by increasing the reservoir blood volume. Possible microembolus generation in the top- and bottom-entry versions of this reservoir was investigated using an in vitro circuit and a colour flow Doppler monitor that was interfaced with a microprocessor to count the signals. The reservoir blood volume was progressively lowered in 100 ml increments below 1000 ml, and signals were counted over five minutes at each new level. Signal counts downstream of the reservoir increased exponentially after the volume was decreased below 1000 ml in the bottom-entry version, and 700 ml in the top-entry version. Ultrasonic monitor ing, both upstream and downstream of the reservoir, showed that the source of these signals was the reservoir itself, and that recirculation of emboli around the circuit accounted for only a small proportion of the measured increase. Changes in circuit blood prime haematocrit within the range 0.11-0.31 did not alter the signal counts. However, counts were profoundly affected by exposure of the circuit to nitrous oxide via a membrane oxygena tor ; this showed that the emboli were bubbles. Bubble formation may occur where venous blood enters the reservoir as this results in a fountaining effect when the reservoir volume is low. This effect appears to have been serendipi tously reduced, but not eliminated, in the design of the top-entry version. It is

Selective vulnerability of the inner ear to decompression sickness in divers with right-to-left shunt: the role of tissue gas supersaturation

Inner ear decompression sickness has been strongly associated with the presence of right-to-left shunts. The implied involvement of intravascular bubbles shunted from venous to arterial circulations is inconsistent with the frequent absence of cerebral symptoms in these cases. If arterial bubbles reach the labyrinthine artery, they must also be distributing widely in the brain. This discrepancy could be explained by slower inert gas washout from the inner ear after diving and the consequent tendency for arterial bubbles entering this supersaturated territory to grow because of inward diffusion of gas. Published models for inner ear and brain inert gas kinetics were used to predict tissue gas tensions after an air dive to 4 atm absolute for 25 min. The models predict half-times for nitrogen washout of 8.8 min and 1.2 min for the inner ear and brain, respectively. The inner ear remains supersaturated with nitrogen for longer after diving than the brain, and in the simulated dive, for a period that corresponds with the latency of typical cases. It is therefore plausible that prolonged inner ear inert gas supersaturation contributes to the selective vulnerability of the inner ear to short latency decompression sickness in divers with right-to-left shunt.