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      Quid novi in the eldery patient’s anesthesia

      abstract
      1 , , 1 , 1 ,
      BMC Geriatrics
      BioMed Central
      XXIII Annual Meeting of the Italian Society of Geriatric Surgery
      2-4 December 2010

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          Abstract

          Background Today the availability of new local anesthetics and the use of analgesics, allow the modulation of the analgesia, maintaining a state of consciousness. An answer to the needs of patients >75 years undergoing surgery is the technique Monitored Anesthesia Care (MAC), defined “the middle land” (Figure 1). Figure 1 Monitored anestesia care MAC allows: - the modulation of the level of analgesia at different stages of surgery due to the availability of analgesic action, but with rapid onset-time - the additional analgesia using local anesthetics with prolonged effect without the use of noradrenaline, dangerous for elderly patients the consciousness and cooperation of the patient (Table 1). Table 1 MAC. Conscious Sedation ( MAC ) Unconscious Sedation Altered consciousness Unconsciousness Conscious patient Unconscious patient Protective reflexes intact and active Protective reflexes decreased; airway obstruction may occurVentilation: hypoxia, hypercapniaCardiovascular system: , hypotension, hypertension, bradycardia, tachycardia Stable vital signs Unstable vital signs Analgesia may be present; need for regional analgesia / local or systemic Pain controlled centrally; does not require regional analgesia Limited stay in the units of observation Requiring hospitalization or prolonged hospitalization Low risk of complications High risk of complications Infrequent postoperative complications Frequent postoperative complications Patients with psychiatric problems or mental deficiency may be difficult to manage May be needed to manage patients with mental deficiency Materials and methods With this study we tested the efficacy, safety and limitations of the MAC. The design of the study was a prospective, double-blind, parallel-group, with 42 patients randomly selected from 87 patients recruited between those eligible for inclusion in the circuit one-day surgery (Table 2) Table 2 Patients’ criteria of homogeneity. Patients’ criteria of homogeneity same level of gravity ASA II/III NYHA II class same duration of surgery (40 min ± 10 min Two groups were subjected to two different regimes of sedation with propofol and midazolam, pain controlled with remifentanil. - Primary end-point was verifying the level and quality of sedation achieved - Secondary end-point was identifying and quantifying potential adverse effects (Table 3-4) Table 3 Access Criteria. ACCESS CRITERIA Weight 69 ± 6 Kg Informed consent for MAC procedures ASA II/III with stabilized cardio-circulatory impairments and respiratory parameters: pO2 ≤ 70 e pCO2 < 45 mmHg Patients undergoing operations can be managed only with the cooperation of the patient Age > 75 years Table 4 Exclusion Criteria. EXCLUSION CRITERIA Patient desire ASA III impairment of vital organs in acute and evolutionary phase Patients with unexpected rapid intubation Patients with high risk of bleeding Severe neurological disorders Levels of sedation, pain and mental status were assessed using different clinical approaches : - Observational data (Table 5). Table 5 Observer’ s assessment of alertness/sedation scale (oaa/s scale). Answer Verbal expression Facial expression Eyes Ready to the call, normal tone Normal Normal Normal 5 Torpid to the call, normal tone Initial slowdown Medium relaxation Medium relaxation 4 Only for repeat calls with high tone slowdown Marked relaxation Marked ptosis 3 Only if shaken Not understandable words --- --- 2 No answers, even if shaken --- --- --- 1 We proceeded as follows: 1) O2 inhalation (SpO2 > 98 and normocapnia) 2) during surgical manipulation a continuous infusion of remifentanil: 0.03 to 0.06 mg / kg / h was activated Patients were randomly dichotomized into two arms with two different infusion regimens: -group P (45 patients): starter bolus of 0.5 mg / kg propofol (to fill the central compartment) → P infusion of 1-2 mg / kg / h (to offset the rapid deployment) -group M (41 patients): bolus starter from 0.03 to 0.05 mg / kg midazolam (average dose of 2-4 mg) infusion of 1-2 mg / kg / h Every 10 m’ scores are recorded, BIS and OAA / S scale. - objective parameters based on Ramsay Scale (Table 6). Table 6 Ramsay Scale. 1 Patient anxious and agitated or restless, or both 2 Patient co-operative, orientated and tranquil 3 Patient responds to commands only 4 Brisk response to a light glabellar tap or auditory stimulus 5 Sluggish response to a light glabellar tap or auditory stimulus 6 No response to the stimuli mentioned in items 4 and 5 - Instrumental response with Bispectral Index (Table 7 8 9) Table 7 Average values of clinical and instrumental group P. T10m T20m T30m T40m BIS 72 (42-45) 66 (35-88) 70 (55-82) 74 (52-88) OAA/S 4 (1-5) 3-4 (1-5) 3-4(1-5) 4 (1-5) Table 8 Average values of clinical and instrumental group M. T10m T20m T30m T40m BIS 64 (48-86) 58 (35-73) 62 (36-84) 66 (48-83) OAA/S 4 (1-5) 3-4 (1-5) 3-4 (1-5) 4 (1-5) Table 9 Propofol, Midazolam, Remifentanil during MAC. Propofol Midazolam Remifentanil onset of sedation rapid moderate rapid resolution pharmacological effects rapid lenta rapid injection pain yes no no intraoperative and postoperative pain moderate moderate minimum hemodynamic depression moderate minimum minimum respiratory variations mild desaturation (<30%) minimum moderate PONV minimum minimum minimum Conclusions The combination midazolam-remifentanil presented a lower synergistic effect compared with propofol-remifentanil. The first fact documented a mean BIS of 62.5 +3 vs. 64.7 +4 midazolam-remifentanil association and has finally, although sporadic, incidents of desaturation content and never > 30%. The evaluation of the kinetic values of BIS, the interesting fact that emerges concerns the values> 70, which represented a significant predictor in the study to better recovery of consciousness, which has helped the fast-traking ongoing day-surgery.

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          Electroencephalographic bispectral index correlates with intraoperative recall and depth of propofol-induced sedation.

          The bispectral (BIS) index and 95% spectral edge frequency (SEF) of the electroencephalograph (EEG) have been used to study the anesthetic and sedative effects of intravenously (i.v.) administered drugs. This prospective study was designed to evaluate the effectiveness of the BIS index and 95% SEF for assessing the level of propofol-induced sedation and amnesia during regional anesthesia. Ten consenting adult patients undergoing surgery with regional anesthesia were administered propofol in increments of 10-20 mg i.v., every 5-10 min until they became unresponsive to tactile stimulation (i.e., mild prodding or shaking). The BIS index and 95% SEF were continuously recorded from a bifrontal montage (Fp1-Cz and Fp2-Cz) using the Aspect B500 monitor. The depth of sedation was assessed clinically at 5- to 10-min intervals using the observer's assessment of alertness/sedation (OAA/S) scale, with 1 = no response to tactile stimulation to 5 = wide awake. Each patient was shown a picture of an animal (cat) prior to administration of an initial dose of propofol, 40 mg i.v.. Subsequently, patients were administered intermittent bolus doses of propofol, 10-20 mg i.v., and shown different pictures upon achieving OAA/S scores of 4, 3, and 2 during the onset of and recovery from propofol-induced sedation. Picture recall was tested upon arrival of the patient in the postanesthesia care unit (PACU). Of the two EEG variables studied, the BIS index exhibited a better correlation with the OAA/S scores during both the onset (Spearman's rho = 0.744) and recovery (Spearman's rho = 0.705) phases of propofol-induced sedation. With the increasing depth of sedation, there was a progressive decrease in the BIS index (OAA/S score of 5, BIS = 94.5 +/- 2.9; 4, 93.3 +/- 3.3; 3, 89 +/- 6.1; 2, 80.1 +/- 8.7; 1, 75.6 +/- 7.5; mean +/- SD). Conversely, there was a progressive increase in the BIS value during recovery from propofol sedation (OAA/S score of 1, BIS = 75.6 +/- 7.5; 2, 82.4 +/- 10.5; 3, 84.9 +/- 5.9; 4, 93.8 +/- 0.8). Although the changes in the 95% SEF values were less consistent during the onset phase, this EEG variable increased from 16.4 +/- 5.0 to 19.3 +/- 5.6 as the OAA/S score increased from 1 to 4 during the recovery phase. Patient recall of the intraoperative pictures decreased with increasing depth of sedation and decreasing BIS values (OAA/S:% BIS:% recall = 5:94.5 +/- 2.9:100%; 4:93.4 +/- 3:63%; 3:87.3 +/- 6.1:40%; 2:80.8 +/- 8.3:0%; 1:75.6 +/- 7.5:0%). The BIS index appears to be a useful variable for assessing the depth of propofol-induced sedation. Increasing depth of sedation was associated with a significant decrease in intraoperative picture recall.
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            Development of a measure of patient satisfaction with monitored anesthesia care: the Iowa Satisfaction with Anesthesia Scale.

            The authors describe development of the Iowa Satisfaction with Anesthesia Scale (ISAS) for monitored anesthesia care (MAC). Patients complete the self-administered written questionnaire before discharge from the hospital. The authors designed the ISAS to measure satisfaction with MAC itself, not the perioperative experience. Patients respond to eleven statements (e.g., "I felt pain") by placing a mark along a six-choice vertical response column (e.g., "Disagree moderately") below each statement. The mean of their responses to each of the 11 statements gives a single number, which is a quantitative measure of a patient's satisfaction with their MAC. Adult, English-speaking patients completed the questionnaires following admission to a phase II postanesthesia care unit after MAC. Response rate for MAC was 92% (86 of 94 patients). Patients completed the questionnaire in 4.6 +/- 2.3 min. Internal consistency, Cronbach's alpha, equaled 0.80. Patients' scores were positively correlated with those predicted by their anesthesia provider (r2 = 0.23) and with responses to the question "I was satisfied with my anesthetic care" (Kendall's tau = +0.41). Scores on initial and repeat questionnaires were positively correlated (r2 = 0.74). Scores on initial questionnaires and those completed within 4.4 +/- 1.7 days postoperatively were positively correlated (r2 = 0.76). The authors have developed and tested an internally consistent, reliable, and valid measure of patient satisfaction with MAC.
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              Target-controlled remifentanil in combination with propofol for spontaneously breathing day-case patients.

              Remifentanil is a new potent opioid with a very short duration of action irrespective of duration of infusion. It may have a role in day-case anaesthesia as part of a balanced total intravenous anaesthetic technique with propofol. We examined the respiratory depressant effects of remifentanil in 20 patients undergoing day-case anaesthesia. The target plasma concentration of remifentanil was varied while maintaining a constant target-controlled infusion of 4.5 microg x ml-1 propofol. In only 12 patients was satisfactory spontaneous respiration maintained. In these patients the median remifentanil target concentration was 1.6 ng x ml-1 and was achieved with a median infusion rate of 0.05 microg x kg-1 x min-1. The range of target concentrations associated with satisfactory spontaneous respiration was wide and varied over a 4.7-fold range from 0.6 to 2.8 ng x ml-1.
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                Author and article information

                Conference
                BMC Geriatr
                BMC Geriatrics
                BioMed Central
                1471-2318
                2011
                24 August 2011
                : 11
                : Suppl 1
                : A26
                Affiliations
                [1 ]Department of Anaesthesia, Surgical and Emergency Science, Second University of Naples, Italy
                Article
                1471-2318-11-S1-A26
                10.1186/1471-2318-11-S1-A26
                3194352
                7a64cc3e-cca1-4942-89a4-a88561896330
                Copyright ©2011 Lettieri et al; licensee BioMed Central Ltd.

                This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                XXIII Annual Meeting of the Italian Society of Geriatric Surgery
                Lecce, Italy
                2-4 December 2010
                History
                Categories
                Meeting Abstract

                Geriatric medicine
                Geriatric medicine

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