19 research outputs found

    The crucial role of bilateral infraclavicular nerve blocks in the anesthetic management of a trauma patient

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    Bilateral brachial plexus blocks and regional anesthesia in trauma patients are rarely performed due to potential complications when using these techniques. We illustrate a case in which bilateral infraclavicular nerve blocks were placed as part of a multimodal approach to pain management in a trauma patient. We discuss potential hazards, important considerations, and rationale for attempting this procedure. Ultimately, performing bilateral brachial plexus nerve blocks in trauma patients is a viable option when choosing pain management techniques

    Quantification of respiratory depression during pre-operative administration of midazolam using a non-invasive respiratory volume monitor.

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    BACKGROUND:Pre-operative administration of benzodiazepines can cause hypoventilation-a decrease in minute ventilation (MV)-commonly referred to as "respiratory compromise or respiratory depression." Respiratory depression can lead to hypercarbia and / or hypoxemia, and may heighten the risk of other respiratory complications. Current anesthesia practice often places patients at risk for respiratory complications even before surgery, as respiratory monitoring is generally postponed until the patient is in the operating room. In the present study we examined and quantified the onset of respiratory depression following the administration of a single dose of midazolam in pre-operative patients, using a non-invasive respiratory volume monitor that reports MV, tidal volume (TV), and respiratory rate (RR). METHODS:Impedance-based Respiratory Volume Monitor (RVM) data were collected and analyzed from 30 patients prior to undergoing orthopedic or general surgical procedures. All patients received 2.0 mg of midazolam intravenously at least 20 minutes prior to the induction of anesthesia and the effects of midazolam on the patient's respiratory function were analyzed. RESULTS:Within 15 minutes of midazolam administration, we noted a significant decrease in both MV (average decrease of 14.3% ± 5.9%, p<0.05) and TV (22.3% ± 4.5%, p<0.001). Interestingly, the corresponding RR increased significantly by an average of 10.3% ± 4.7% (p<0.05). Further analysis revealed an age-dependent response, in which elderly patients (age≥65 years, n = 6) demonstrated greater reductions in MV and TV and a lack of compensatory RR increase. In fact, elderly patients experienced an average decrease in MV of 34% ± 6% (p<0.05) compared to an average decrease of 9% ± 6% (p<0.05) in younger patients. CONCLUSIONS:We were able to quantify the effects of pre-operative midazolam administration on clinically significant respiratory parameters (MV, TV and RR) using a non-invasive RVM, uncovering that the respiratory depressive effect of benzodiazepines affect primarily TV rather than RR. Such respiratory monitoring data provide the opportunity for individualizing dosing and adjustment of clinical interventions, especially important in elderly patients. With additional respiratory data, clinicians may be able to better identify and quantify respiratory depression, reduce adverse effects, and improve overall patient safety

    A time-lapse capturing one representative patient’s onset of respiratory depression during the 20 minutes following the administration of midazolam.

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    <p>Note that this is the same patient as in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0172750#pone.0172750.g003" target="_blank">Fig 3A and 3B</a> (31 y/o male). MV and TV decrease about 3–4 minutes after the dose and remain low as compared to pre-dose values, whereas RR increases and remains above baseline.</p

    Thirty-second snapshots of RVM traces from a 66 y/o male patient (165 cm, 78 kg, BMI: 29 kg/m<sup>2</sup>) undergoing a left hip replacement surgery.

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    <p>These traces show a clear and immediate decrease in both MV and TV following midazolam administration, coupled with marginal and delayed decrease in RR. (<b>A</b>) Pre-midazolam values (2 min pre-dose) were taken as baseline. (<b>B</b>) Within 5 min of the dose, breathing was notably depressed with MV and TV effectively decreased by half, while RR marginally increased. (<b>C</b>) Ten minutes post-midazolam, MV and TV had decreased from pre-dose values by 69.3% and 62.9% respectively (MV: 9.9 to 3.0 L/min; TV 600 to 220 ml) while RR only decreased by 17.9% (16.4 to 13.6 b/min). (<b>D</b>) At 15 minutes post-midazolam, MV and TV had further decreased from pre-dose values by 81.9% and 70.4%, respectively (MV: 9.9 to 1.8L/min; TV: 600 to 180ml). RR finally shows a substantial decrease of 39.0% (RR: 16.4 to 10.0 breaths per minute).</p

    Examples of two different patterns of respiratory depression in two representative subjects. Panels A and B: 31 y/o male, 185 cm, 82 kg, BMI: 24 kg/m<sup>2</sup>. Panels C and D: 61 y/o female, 173 cm, 82 kg, BMI: 27 kg/m<sup>2</sup>.

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    <p>Comparison of traces before (<b>A</b> and <b>C</b>) and after (<b>B</b> and <b>D</b>) benzodiazepine administration shows that respiratory depression may manifest as both tachypnea with low TV (<b>B</b>) as well as intermittent apnea (<b>D</b>).</p

    Average RVM measurements across the entire thirty patient cohort pre (left) and post (right) administration of 2mg of midazolam.

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    <p>(<b>A</b>) MV decreased significantly from 7.41 ± 0.62 L/min (mean ± SEM) to 5.95 ± 0.46 L/min, with an average decrease of 14.3% ± 5.9% (p<0.05). (<b>B</b>) Similarly, TV decreases significantly from 460 ± 30 mL to 340 ± 30 mL, an average decrease of 22.3% ± 4.5% (p<0.001). (<b>C</b>) In contrast, RR increased slightly from 16.6 ± 0.7 breaths per minute to 17.8 ± 0.7 breaths per minute, an average increase of 10.3% ± 4.7% (p<0.05).</p

    Distributions of EtCO<sub>2</sub> instrument sensitivity to changes in MV.

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    <p>For each patient group (General Anesthesia (top, blue), Procedural Sedation (middle, red), and Awake Volunteers (bottom, green)), the distribution of EtCO<sub>2</sub> instrument sensitivity is presented as both a box-plot and histogram. Each box-plot shows the median EtCO<sub>2</sub> instrument sensitivity (middle vertical line), the box extends from the 25th to 75th percentile, the whiskers extend to the most extreme non-outlier data points, and statistical outliers are plotted individually (plus signs). The median EtCO<sub>2</sub> instrument sensitivities were -85.1°, -38.1°, and -20.2° for the General Anesthesia, Procedural Sedation, and Awake Vounteer cohorts, respectively. The General Anesthesia and Awake Volunteer cohorts had unimodal distributions of EtCO<sub>2</sub> instrument sensitivity and single normal distributions were fit to these data (black lines). EtCO<sub>2</sub> instrument sensitivities were significantly higher in the intubated patients under General Anesthesia (θ = -83.6 ± 9.9°, vertical dashed blue line) compared to non-intubated Awake Volunteers over a range of prescribed breathing patterns (θ = -24.7 ± 19.7°, vertical dashed green line, p < 0.0001). The distribution of EtCO<sub>2</sub> instrument sensitivity for the Procedural Sedation cohort was bimodal. Therefore, a mixture of two normal distributions was therefore fit to these data. Approximately half of the patients experienced high EtCO<sub>2</sub> instrument sensitivity (θ = -96.6 ± 15.0°), consistent with the General Anesthesia patients, while the remaining patients had low instrument sensitivity (θ = -1.2 ± 22.4°), consistent with the awake volunteers. Clinically-relevant EtCO<sub>2</sub> is indicated by the shaded gray area. The majority of General Anesthesia patients (43/54, 80%) had clinically-relevant EtCO<sub>2</sub> instrument sensitivity. In contrast, less than half of Procedural Sedation patients (24/58, 41%) and no patients in the Awake Volunteer cohort demonstrated clinically-relevant EtCO<sub>2</sub> instrument sensitivity of -76°.</p
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