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  1. Article ; Online: Postoperative Pain Management and the Incidence of Ipsilateral Shoulder Pain After Thoracic Surgery at an Australian Tertiary-Care Hospital: A Prospective Audit.

    Hodge, Anthony / Rapchuk, Ivan L / Gurunathan, Usha

    Journal of cardiothoracic and vascular anesthesia

    2020  Volume 35, Issue 2, Page(s) 555–562

    Abstract: Objectives: Ipsilateral shoulder pain (ISP) is a common but variably occurring (42%-85%) complication after thoracic surgery. Multiple potential treatments, including upper limb blocks, intrapleural local anaesthetic infiltration, and systemic opioids, ... ...

    Abstract Objectives: Ipsilateral shoulder pain (ISP) is a common but variably occurring (42%-85%) complication after thoracic surgery. Multiple potential treatments, including upper limb blocks, intrapleural local anaesthetic infiltration, and systemic opioids, have undergone trials, with limited efficacy. Phrenic nerve infiltration is a potential intervention that may prevent ISP. The aim of this study was to assess the incidence and severity of ISP after thoracic surgery at the authors' institution, where phrenic nerve infiltration is commonly used.
    Design: Observational cohort study.
    Setting: A single- center study in a tertiary referral center in Brisbane, Australia.
    Participants: This study comprised all adult patients undergoing thoracic surgery at a tertiary- care referral center from May to July 2018.
    Measurements and main results: Surgical procedures were divided into open thoracotomy, video-assisted thoracic surgery (VATS) and VATS-guided mini-thoracotomy. The primary outcome was a comparison of incidence of ISP among the 3 types of surgical procedures. Data were analyzed using Stata (StataCorp), with significance testing by Kruskal-Wallis equality of populations rank test. A p value of < 0.05 was deemed significant. Sixty thoracic surgeries were performed during the audit period. Nineteen patients had thoracotomies performed for lobectomy or pneumonectomy, all of whom received phrenic nerve infiltration. The incidence of moderate-to-severe ipsilateral shoulder pain among the thoracoctomy cohort was 15.8% (3/19). Of the 36 VATS procedures audited, 7 patients (19.4%) received infiltration of their phrenic nerve, none of whom reported postoperative ISP. Of the remaining twenty-nine patients who did not receive phrenic nerve infiltration, there were 4 cases of moderate-to-severe ipsilateral shoulder pain (11.1%). Four of the 5 patients (80%) who underwent VATS-guided mini-thoracotomies received phrenic nerve infiltration intraoperatively. Three patients reported moderate-to-severe ISP and of these 3 patients, 2 patients had phrenic nerve infiltration, and 1 patient did not receive infiltration. Overall, there were no statistically significant differences in rest or dynamic pain scores across the surgical groups at any time point. Mann-Whitney test revealed that the participants with ISP were significantly older than those without ISP (p = 0.006). However, there were no significant differences in sex or body mass index between those with and without ISP.
    Conclusion: The authors observed a lower (15.8%) incidence of moderate-to-severe ISP among their thoracotomy patients than reported in prior literature. Injection of local anesthetic into the phrenic nerve fat pad at the level of the diaphragm appeared to be an effective and safe surgical intervention that may eliminate a significant cause of ISP. None of the VATS patients who received phrenic nerve infiltration experienced ISP. Postoperative pain in VATS is expected to be reduced by avoiding the use of a rib spreader, severing of the intercostal nerves, and division of muscle tissue, which may account for the lower observed rates of ISP in the VATS cohort who did not receive phrenic nerve infiltration. Further randomized controlled trials are warranted to establish if patients undergoing various VATS procedures benefit from this intervention.
    MeSH term(s) Adult ; Australia/epidemiology ; Humans ; Incidence ; Pain Measurement ; Pain, Postoperative/diagnosis ; Pain, Postoperative/epidemiology ; Pain, Postoperative/etiology ; Pneumonectomy ; Shoulder Pain/diagnosis ; Shoulder Pain/epidemiology ; Shoulder Pain/etiology ; Tertiary Care Centers ; Thoracic Surgery ; Thoracic Surgery, Video-Assisted/adverse effects ; Thoracotomy/adverse effects
    Language English
    Publishing date 2020-08-01
    Publishing country United States
    Document type Journal Article ; Observational Study
    ZDB-ID 1067317-9
    ISSN 1532-8422 ; 1053-0770
    ISSN (online) 1532-8422
    ISSN 1053-0770
    DOI 10.1053/j.jvca.2020.07.078
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  2. Article ; Online: Ultrasound probe modification to optimise ultrasound-guided peripheral vascular access.

    Kunju, Shakeel Meeran / Rapchuk, Ivan L

    The journal of vascular access

    2014  Volume 15, Issue 2, Page(s) 141–142

    MeSH term(s) Catheterization, Peripheral/instrumentation ; Catheterization, Peripheral/methods ; Equipment Design ; Humans ; Punctures ; Ultrasonography, Interventional/instrumentation ; Ultrasonography, Interventional/methods
    Language English
    Publishing date 2014-03
    Publishing country Italy
    Document type Letter
    ZDB-ID 2252820-9
    ISSN 1724-6032 ; 1129-7298
    ISSN (online) 1724-6032
    ISSN 1129-7298
    DOI 10.5301/jva.5000188
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  3. Article ; Online: Determining sex-specific preoperative haemoglobin levels associated with intraoperative red blood cell transfusion in cardiac surgery: a retrospective cohort study.

    Cavalli, Leonardo B / Pearse, Bronwyn L / Craswell, Alison / Anstey, Christopher M / Naidoo, Rishendran / Rapchuk, Ivan L / Perel, Joanne / Hobson, Kylie / Wang, Mingzhong / Fung, Yoke-Lin

    British journal of anaesthesia

    2023  Volume 131, Issue 4, Page(s) 653–663

    Abstract: Background: Anaemic cardiac surgery patients are at greater risk of intraoperative red blood cell transfusion. This study questions the application of the World Health Organization population-based anaemia thresholds (haemoglobin <120 g L: Methods: A ...

    Abstract Background: Anaemic cardiac surgery patients are at greater risk of intraoperative red blood cell transfusion. This study questions the application of the World Health Organization population-based anaemia thresholds (haemoglobin <120 g L
    Methods: A retrospective cohort study was conducted on adults ≥18 yr old undergoing cardiopulmonary bypass surgery. Logistic regression was applied to define sex-specific preoperative haemoglobin concentrations with reduced probability of intraoperative red blood cell transfusion for cardiac surgery patients.
    Results: Data on 4384 male and 1676 female patients were analysed. Binarily stratified multivariable logistic regression odds of receiving intraoperative red blood cell transfusion increased in cardiac surgery patients >45 yr old (odds ratio [OR] 1.84; 95% confidence interval [CI] 1.33-2.55), surgery urgency <30 days (OR 2.03; 95% CI 1.66-2.48), combined coronary artery bypass grafting and valve surgery, or other surgery types (OR 2.24; 95% CI 1.87-2.67), and female sex (OR 1.92; 95% CI 1.62-2.28). The odds decreased by 8.4% with each 1 g L
    Conclusions: The World Health Organization female anaemia threshold of haemoglobin <120 g L
    MeSH term(s) Adult ; Humans ; Female ; Male ; Erythrocyte Transfusion ; Retrospective Studies ; Cardiac Surgical Procedures ; Coronary Artery Bypass ; Probability
    Language English
    Publishing date 2023-08-29
    Publishing country England
    Document type Journal Article
    ZDB-ID 80074-0
    ISSN 1471-6771 ; 0007-0912
    ISSN (online) 1471-6771
    ISSN 0007-0912
    DOI 10.1016/j.bja.2023.06.062
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  4. Article ; Online: Role of high flow nasal oxygen in the management of a case of anaesthesia related aspiration pneumonia.

    Meeran Kunju, Shakeel Arsad / Rapchuk, Ivan L

    Journal of clinical anesthesia

    2017  Volume 38, Page(s) 72–73

    MeSH term(s) Aged, 80 and over ; Anesthesia, General/adverse effects ; Anesthesia, General/instrumentation ; Anesthesia, General/methods ; Cannula ; Endoscopy, Gastrointestinal/adverse effects ; Humans ; Intubation, Intratracheal/adverse effects ; Intubation, Intratracheal/instrumentation ; Intubation, Intratracheal/methods ; Laryngopharyngeal Reflux/etiology ; Lung/diagnostic imaging ; Male ; Oxygen/administration & dosage ; Pneumonia, Aspiration/diagnostic imaging ; Pneumonia, Aspiration/etiology ; Pneumonia, Aspiration/therapy ; Positive-Pressure Respiration/adverse effects ; Radiography ; Vomiting/diagnostic imaging
    Chemical Substances Oxygen (S88TT14065)
    Language English
    Publishing date 2017
    Publishing country United States
    Document type Case Reports ; Letter
    ZDB-ID 1011618-7
    ISSN 1873-4529 ; 0952-8180
    ISSN (online) 1873-4529
    ISSN 0952-8180
    DOI 10.1016/j.jclinane.2017.01.033
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  5. Article ; Online: Radiological outcomes of whole lung lavage for artificial stone-associated silicosis.

    Chambers, Daniel C / Apte, Simon H / Deller, David / Masel, Philip J / Jones, Catherine M / Newbigin, Katrina / Matula, Michael / Rapchuk, Ivan L

    Respirology (Carlton, Vic.)

    2021  Volume 26, Issue 5, Page(s) 501–503

    Language English
    Publishing date 2021-02-24
    Publishing country Australia
    Document type Journal Article
    ZDB-ID 1435849-9
    ISSN 1440-1843 ; 1323-7799
    ISSN (online) 1440-1843
    ISSN 1323-7799
    DOI 10.1111/resp.14018
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  6. Article ; Online: Combined use of fascia iliaca block, subarachnoid block and dexmedetomidine sedation for patients having fractured femur surgery.

    Rapchuk, Ivan L / Glover, Patrick

    Journal of anesthesia

    2012  Volume 27, Issue 1, Page(s) 149–150

    MeSH term(s) Aged ; Aged, 80 and over ; Anesthesia, General ; Deep Sedation ; Dexmedetomidine ; Female ; Femoral Fractures/surgery ; Humans ; Hypnotics and Sedatives ; Male ; Nerve Block/methods ; Orthopedic Procedures/methods ; Peripheral Nerves
    Chemical Substances Hypnotics and Sedatives ; Dexmedetomidine (67VB76HONO)
    Language English
    Publishing date 2012-09-26
    Publishing country Japan
    Document type Letter
    ZDB-ID 1107821-2
    ISSN 1438-8359 ; 0913-8668
    ISSN (online) 1438-8359
    ISSN 0913-8668
    DOI 10.1007/s00540-012-1481-8
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  7. Article ; Online: Association of Obesity With Septic Complications After Major Abdominal Surgery: A Secondary Analysis of the RELIEF Randomized Clinical Trial.

    Gurunathan, Usha / Rapchuk, Ivan L / Dickfos, Marilla / Larsen, Peter / Forbes, Andrew / Martin, Catherine / Leslie, Kate / Myles, Paul S

    JAMA network open

    2019  Volume 2, Issue 11, Page(s) e1916345

    Abstract: Importance: Body mass index (BMI) has been the most common obesity measure to assess perioperative risk; however, cardiometabolic risk is associated with the burden of visceral fat. Definitive evidence on the association of visceral fat measures, such ... ...

    Abstract Importance: Body mass index (BMI) has been the most common obesity measure to assess perioperative risk; however, cardiometabolic risk is associated with the burden of visceral fat. Definitive evidence on the association of visceral fat measures, such as waist circumference and waist-to-hip ratio (WHR), with postoperative complications is lacking.
    Objective: To compare the value of waist circumference with the value WHR and BMI in predicting adverse outcomes, including major septic complications and persistent disability, following major abdominal surgery.
    Design, setting, and participants: This planned secondary analysis of the Restrictive vs Liberal Fluid Therapy for Major Abdominal Surgery (RELIEF) randomized clinical trial took place at 47 centers in 7 countries between October 2013 and September 2016, with 90-day follow-up. A total of 2954 adult RELIEF participants were coenrolled in this secondary analysis. Data analysis took place from December 2018 to September 2019.
    Exposures: Waist circumference, WHR, and BMI measurements.
    Main outcomes and measures: The primary outcomes were 30-day major septic complications and 90-day persistent disability or death.
    Results: Of 2954 eligible participants, 2755 were included (mean [SD] age, 65.9 [12.9] years; 1426 [51.8%] men) in the final analysis. A total of 564 participants (20.6%) experienced at least 1 major septic complication within 30 days after surgery (sepsis, 265 [9.7%]; surgical site infection, 409 [14.9%]; anastomotic leak, 78 [2.8%]; pneumonia, 104 [3.8%]). Waist circumference had a statistically significantly larger odds ratio (OR) and discrimination indices as well as a smaller prediction error than WHR or BMI for 30-day major septic complications or death (waist circumference: OR, 1.44; 95% CI, 1.28-1.62; P < .001; area under the receiver operating characteristic curve, 0.641; net reclassification index, 0.266; integrated discrimination improvement [score × 104], 152.98; Brier score, 0.162; WHR: OR, 1.15; 95% CI, 1.03-1.28; P = .01; area under the receiver operating characteristic curve, 0.621; net classification index, 0.199; integrated discrimination improvement [score × 104], 28.47; Brier score, 0.164; BMI: OR, 1.33; 95% CI, 1.17-1.50; P < .001; area under the receiver operating characteristic curve, 0.629; net reclassification index, 0.205; integrated discrimination improvement [score × 104], 85.61; Brier score, 0.163) but not for any other outcomes.
    Conclusions and relevance: In this secondary analysis of the RELIEF randomized clinical trial, waist circumference was observed to be superior to other adiposity indices in predicting 30-day major septic complications alone or in conjunction with death following elective major abdominal surgery. Findings suggest that waist circumference is a useful adiposity measure that should be incorporated in preoperative risk assessment for such complications.
    Trial registration: ClinicalTrials.gov identifier: NCT01424150.
    MeSH term(s) Abdomen/surgery ; Aged ; Body Mass Index ; Female ; Humans ; Male ; Obesity/complications ; Postoperative Complications/etiology ; Risk Factors ; Sepsis/etiology ; Waist Circumference
    Language English
    Publishing date 2019-11-01
    Publishing country United States
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ISSN 2574-3805
    ISSN (online) 2574-3805
    DOI 10.1001/jamanetworkopen.2019.16345
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  8. Article ; Online: Prophylactic Postoperative High Flow Nasal Oxygen Versus Conventional Oxygen Therapy in Obese Patients Undergoing Bariatric Surgery (OXYBAR Study): a Pilot Randomised Controlled Trial.

    Fulton, Rachel / Millar, Jonathan E / Merza, Megan / Johnston, Helen / Corley, Amanda / Faulke, Daniel / Rapchuk, Ivan L / Tarpey, Joe / Fanning, Jonathon P / Lockie, Philip / Lockie, Shirley / Fraser, John F

    Obesity surgery

    2021  Volume 31, Issue 11, Page(s) 4799–4807

    Abstract: Background: Patients with obesity are predisposed to a reduction in end-expiratory lung volume (EELV) and atelectasis after anaesthesia. High flow nasal oxygen (HFNO) may increase EELV, reducing the likelihood of postoperative pulmonary complications ( ... ...

    Abstract Background: Patients with obesity are predisposed to a reduction in end-expiratory lung volume (EELV) and atelectasis after anaesthesia. High flow nasal oxygen (HFNO) may increase EELV, reducing the likelihood of postoperative pulmonary complications (PPC). We conducted a pilot randomised controlled trial (RCT) of conventional oxygen therapy versus HFNO after bariatric surgery. The aim was to investigate the feasibility of using electrical impedance tomography (EIT) as a means of assessing respiratory mechanics and to inform the design of a definitive RCT.
    Methods: We performed a single-centre, parallel-group, pilot RCT. Adult patients with obesity undergoing elective bariatric surgery were eligible for inclusion. We excluded patients with a known contraindication to HFNO or with chronic lung disease.
    Results: Fifty patients were randomised in equal proportions. One patient crossed over from conventional O
    Conclusions: These data suggest that a large-scale RCT of HFNO after bariatric surgery in an 'all-comers' population is likely infeasible. While EIT was an effective means of assessing respiratory mechanics, it was impractical over time. Similarly, the infrequency of PPC precludes its use as a primary outcome. Future studies should focus on identifying patients at the greatest risk of PPC.
    MeSH term(s) Adult ; Bariatric Surgery ; Humans ; Obesity/complications ; Obesity/surgery ; Obesity, Morbid/surgery ; Oxygen ; Pilot Projects
    Chemical Substances Oxygen (S88TT14065)
    Language English
    Publishing date 2021-08-13
    Publishing country United States
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 1070827-3
    ISSN 1708-0428 ; 0960-8923
    ISSN (online) 1708-0428
    ISSN 0960-8923
    DOI 10.1007/s11695-021-05644-y
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  9. Article: Polyhexamethylene biguanide discs versus unmedicated dressings for prevention of central venous catheter-associated infection in the intensive care unit: A pilot randomised controlled trial to assess protocol safety and feasibility.

    Pearse, India / Marsh, Nicole / Rickard, Claire M / Ullman, Amanda J / Larsen, Emily / Pelecanos, Anita / McGuinness, Nicola / Irvine, Lacey / Rapchuk, Ivan L / Ziegenfuss, Marc / Corley, Amanda

    Australian critical care : official journal of the Confederation of Australian Critical Care Nurses

    2021  Volume 35, Issue 5, Page(s) 512–519

    Abstract: Background: Central venous catheters are prone to infectious complications, affecting morbidity, mortality and healthcare costs. Polyhexamethylene biguanide-impregnated discs at the catheter insertion site may prevent local and bloodstream infection; ... ...

    Abstract Background: Central venous catheters are prone to infectious complications, affecting morbidity, mortality and healthcare costs. Polyhexamethylene biguanide-impregnated discs at the catheter insertion site may prevent local and bloodstream infection; however, efficacy has not been established in a critical care setting.
    Objective: The objective of this study was to pilot test polyhexamethylene biguanide-impregnated discs compared to standard unmedicated dressings for central venous catheter infection prevention in critically ill patients.
    Methods: This was a single-centre pilot randomised controlled trial. Adults admitted to intensive care requiring a central venous catheter for >72 h were eligible. Patients with a current bloodstream infection, concurrent central venous catheter, chlorhexidine or polyhexamethylene biguanide allergy, or sensitive skin were excluded. Patients were randomised to receive standard central venous catheter dressings with/without polyhexamethylene biguanide discs.
    Outcome measures: The primary outcome was feasibility, defined by patient eligibility, recruitment, retention, protocol adherence, missing data, and staff satisfaction. Secondary outcomes included: central line-associated infection; primary bloodstream infection; local infection; skin complications; device/dressing dwell time; serious adverse events, and cost-effectiveness.
    Results: Of 309 patients screened, 80 participants were recruited with 98% (n = 78) receiving an internal jugular catheter which dwelled for a median of 5 days (interquartile range = 4.0, 6.0). Feasibility criteria were predominantly met (recruitment 88%; retention 100%; protocol fidelity 91%); however, eligibility criteria were not met (32%; most commonly owing to short predicted catheter dwell). Staff acceptability criteria were met, with 83% of staff scoring dressing application and removal ≥7 on a numerical rating scale. There were no central line-associated bloodstream infections and no local infections. Insertion site itch occurred in 4% (control [n = 0], intervention [n = 3]) of participants, while 32% (24/76) reported pain, and 46% (35/76) tenderness.
    Conclusions: Polyhexamethylene biguanide discs appear safe for central venous catheter infection prevention. Feasibility of a large efficacy trial was established with some modifications to screening processes. Large, adequately powered randomised controlled trials are needed to test the infection prevention hypotheses.
    MeSH term(s) Adult ; Bandages/adverse effects ; Biguanides ; Catheter-Related Infections/prevention & control ; Catheterization, Central Venous/adverse effects ; Chlorhexidine ; Feasibility Studies ; Humans ; Intensive Care Units ; Pilot Projects ; Randomized Controlled Trials as Topic ; Sepsis/drug therapy
    Chemical Substances Biguanides ; polihexanide (322U039GMF) ; Chlorhexidine (R4KO0DY52L)
    Language English
    Publishing date 2021-07-25
    Publishing country Australia
    Document type Journal Article ; Randomized Controlled Trial
    ZDB-ID 1159493-7
    ISSN 1878-1721 ; 1036-7314
    ISSN (online) 1878-1721
    ISSN 1036-7314
    DOI 10.1016/j.aucc.2021.05.015
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  10. Article ; Online: The effect of pregabalin and celecoxib on the analgesic requirements after laparoscopic cholecystectomy: a randomized controlled trial.

    Gurunathan, Usha / Rapchuk, Ivan L / King, Gillian / Barnett, Adrian G / Fraser, John F

    Journal of anesthesia

    2016  Volume 30, Issue 1, Page(s) 64–71

    Abstract: Purpose: Early postoperative pain is a common complaint after elective laparoscopic cholecystectomy. The use of non-opioid medications as a part of multimodal analgesia has been increasingly advocated in the management of acute post-surgical pain. This ... ...

    Abstract Purpose: Early postoperative pain is a common complaint after elective laparoscopic cholecystectomy. The use of non-opioid medications as a part of multimodal analgesia has been increasingly advocated in the management of acute post-surgical pain. This randomized, double-blinded, placebo-controlled study evaluated the efficacy of pregabalin, celecoxib, and their combination in the management of acute postoperative pain in patients undergoing elective laparoscopic cholecystectomy.
    Methods: One hundred ASA I/II patients scheduled to undergo elective laparoscopic cholecystectomy were assigned to receive two perioperative doses, 12 h apart, of either pregabalin alone, celecoxib alone, their combination, or a placebo. Standard anesthetic protocol was followed. The primary outcomes were postoperative pain at rest and with movement. Secondary outcomes were fentanyl requirements and side effects, which were assessed at 1, 2, 4, 8, 12, and 24 h following surgery. Patient satisfaction with pain relief was recorded at discharge. Differences in main outcomes were analyzed using an intention-to-treat approach.
    Results: There was no statistically significant difference (p > 0.05) between the four groups in terms of outcomes such as rest pain, movement pain, postoperative fentanyl requirements, or changes in anxiety scores. Patients who had only celecoxib had significantly higher satisfaction with pain management (p = 0.013). Patients who had only pregabalin were at three-times-higher odds of having drowsiness (p = 0.040) and four-times-higher odds of having lightheadedness (p = 0.019) when compared with the placebo group.
    Conclusions: Pregabalin, celecoxib alone, or in combination offers no analgesic superiority over standard opioid care in the treatment of postoperative pain following laparoscopic cholecystectomy.
    MeSH term(s) Adult ; Aged ; Analgesics/administration & dosage ; Analgesics, Opioid/administration & dosage ; Celecoxib/administration & dosage ; Cholecystectomy, Laparoscopic/adverse effects ; Cholecystectomy, Laparoscopic/methods ; Double-Blind Method ; Elective Surgical Procedures/methods ; Female ; Fentanyl/administration & dosage ; Humans ; Male ; Middle Aged ; Pain, Postoperative/drug therapy ; Patient Satisfaction ; Pregabalin/administration & dosage ; Prospective Studies
    Chemical Substances Analgesics ; Analgesics, Opioid ; Pregabalin (55JG375S6M) ; Celecoxib (JCX84Q7J1L) ; Fentanyl (UF599785JZ)
    Language English
    Publishing date 2016-02
    Publishing country Japan
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 1107821-2
    ISSN 1438-8359 ; 0913-8668
    ISSN (online) 1438-8359
    ISSN 0913-8668
    DOI 10.1007/s00540-015-2078-9
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