Pub Date : 2025-02-01DOI: 10.1053/j.jvca.2024.11.018
Nicolò Sella MD , Tommaso Pettenuzzo MD , Sabrina Congedi MD , Maria Bisi MD , Giulio Gianino MD , Agnese De Carolis MD , Carlo Alberto Bertoncello MD , Mario Roccaforte MD , Francesco Zarantonello MD , Paolo Persona MD, PhD , Enrico Petranzan MD , Gabriella Roca MD , Eugenio Biamonte MD , Michele Carron MD , Andrea Dell'Amore MD , Federico Rea MD , Annalisa Boscolo MD, PhD , Paolo Navalesi MD, FERS
Objectives
Primary graft dysfunction (PGD) affects survival after lung transplant (LT). The current hypothesis was that prone positioning (PP), proposed as a rescue maneuver to treat refractory hypoxemia due to PGD, may improve LT outcomes, especially when applied early.
Design
Bilateral LT recipients developing moderate-to-severe PGD within 24 hours from intensive care unit admission were enrolled. From January 2020 to November 2021, patients developing PGD after LT were turned prone between 24 and 48 hours after diagnosis, only in case of radiological or oxygenation worsening (“late PP” group). After November 2021, patients were routinely turned prone within 24 hours from PGD diagnosis (“early PP”). A propensity score–weighted analysis, adjusted for clinically relevant covariates, was applied.
Setting
Intensive care unit.
Participants
Bilateral LT recipients.
Interventions
Early PP, late PP, or supine position.
Measurements and Main Results
130 LT patients were screened and 67 were enrolled. A total of 25 (37%) recipients were treated in the supine position, 24 (36%) in early PP, and 18 (27%) in late PP. After propensity score weighting, both supine treatment (estimated effect for 1 ventilator-free day = 8.23, standard error: 2.97, p = 0.007) and early PP treatment (estimated effect = 9.42, standard error: 2.59, p < 0.001) were associated with greater 28-day ventilator-free days than late PP treatment (reference). Compared with late PP, early PP was also associated with better oxygenation, driving pressure, and static respiratory system compliance. Compared with supine recipients, the early PP group showed better oxygenation at 72 hours after PGD diagnosis.
Conclusions
Early PP in LT recipients with moderate-to-severe PGD seems to be associated with better 28-day ventilator-free days, oxygenation, and driving pressure than late PP.
{"title":"Early Prone Positioning As a Rescue Therapy for Moderate-to-severe Primary Graft Dysfunction After Bilateral Lung Transplant","authors":"Nicolò Sella MD , Tommaso Pettenuzzo MD , Sabrina Congedi MD , Maria Bisi MD , Giulio Gianino MD , Agnese De Carolis MD , Carlo Alberto Bertoncello MD , Mario Roccaforte MD , Francesco Zarantonello MD , Paolo Persona MD, PhD , Enrico Petranzan MD , Gabriella Roca MD , Eugenio Biamonte MD , Michele Carron MD , Andrea Dell'Amore MD , Federico Rea MD , Annalisa Boscolo MD, PhD , Paolo Navalesi MD, FERS","doi":"10.1053/j.jvca.2024.11.018","DOIUrl":"10.1053/j.jvca.2024.11.018","url":null,"abstract":"<div><h3>Objectives</h3><div>Primary graft dysfunction (PGD) affects survival after lung transplant (LT). The current hypothesis was that prone positioning (PP), proposed as a rescue maneuver to treat refractory hypoxemia due to PGD, may improve LT outcomes, especially when applied early.</div></div><div><h3>Design</h3><div>Bilateral LT recipients developing moderate-to-severe PGD within 24 hours from intensive care unit admission were enrolled. From January 2020 to November 2021, patients developing PGD after LT were turned prone between 24 and 48 hours after diagnosis, only in case of radiological or oxygenation worsening (“late PP” group). After November 2021, patients were routinely turned prone within 24 hours from PGD diagnosis (“early PP”). A propensity score–weighted analysis, adjusted for clinically relevant covariates, was applied.</div></div><div><h3>Setting</h3><div>Intensive care unit.</div></div><div><h3>Participants</h3><div>Bilateral LT recipients.</div></div><div><h3>Interventions</h3><div>Early PP, late PP, or supine position.</div></div><div><h3>Measurements and Main Results</h3><div>130 LT patients were screened and 67 were enrolled. A total of 25 (37%) recipients were treated in the supine position, 24 (36%) in early PP, and 18 (27%) in late PP. After propensity score weighting, both supine treatment (estimated effect for 1 ventilator-free day = 8.23, standard error: 2.97, p = 0.007) and early PP treatment (estimated effect = 9.42, standard error: 2.59, p < 0.001) were associated with greater 28-day ventilator-free days than late PP treatment (reference). Compared with late PP, early PP was also associated with better oxygenation, driving pressure, and static respiratory system compliance. Compared with supine recipients, the early PP group showed better oxygenation at 72 hours after PGD diagnosis.</div></div><div><h3>Conclusions</h3><div>Early PP in LT recipients with moderate-to-severe PGD seems to be associated with better 28-day ventilator-free days, oxygenation, and driving pressure than late PP.</div></div>","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":"39 2","pages":"Pages 479-488"},"PeriodicalIF":2.3,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142828599","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-01DOI: 10.1053/j.jvca.2024.10.012
Jordi Miralles Bagán MD, PhD , Laura Parrilla Quiles MD , Pilar Paniagua Iglesias MD, PhD , Antoni J. Betbesé Roig MD, PhD , Sergi Sabaté Tenas MD, PhD , Sergio Pérez García MD , Mercedes García Álvarez MD, PhD
Objectives
Cardiac surgery–associated acute kidney injury (CSA-AKI) is a common complication with high morbidity and mortality. This study was designed to determine whether adding human albumin to the cardiopulmonary bypass (CPB) priming solution reduces the incidence of CSA-AKI.
Design
A double-blind, randomized controlled trial (RCT) involving 248 patients scheduled for cardiac surgery with CPB.
Setting
A single-center tertiary university hospital.
Participants
Adults with a baseline estimated glomerular filtration rate (eGFR) of ≥60 mL/min/1.73 m2 and left ventricular ejection fraction ≥40%.
Interventions
Patients were randomized to receive either a crystalloid priming solution (Plasma-Lyte) plus 4% albumin (intervention group, n = 126) or a crystalloid solution alone (control group, n = 122) for CPB.
Measurements and Main Results
Data analyses were performed using the Chi-square test and Student's t-test, or their nonparametric equivalent. The primary outcome was the incidence of CSA-AKI, as defined by the Kidney Disease Improving Global Outcomes criteria, within 5 days postoperatively. Both cohorts were comparable in baseline and perioperative characteristics, including preoperative albumin levels. The incidence of CSA-AKI was 29.3% (n = 37) in the intervention group compared with 31.2% (n = 38) in the control group (odds ratio: 0.91, 95% confidence interval: 0.53-1.58). The observed difference in CSA-AKI incidence between the groups was not statistically significant. A post-hoc subgroup analysis of patients with a baseline eGFR of 60 to 70 mL/min/1.73 m² indicated a trend toward a reduced incidence of CSA-AKI in the intervention group compared with the control group (35.7% v 57.6%; odds ratio: 0.41, 95% confidence interval: 0.16-1.03). This trend was not observed in patients with an eGFR greater than 70 mL/min/1.73 m². No significant differences were observed between groups for the need for inotropes or vasoconstrictors, incidence of cardiogenic or distributive shock, bleeding, need for transfusion, or use of nephrotoxic drugs.
Conclusions
Adding albumin to the CPB priming solution did not decrease the incidence of CSA-AKI in patients with normal preoperative renal function. These findings suggest that albumin might benefit patients with impaired renal function, warranting further investigation.
{"title":"The Potential Role of Albumin in Reducing Cardiac Surgery–Associated Acute Kidney Injury: A Randomized Controlled Trial","authors":"Jordi Miralles Bagán MD, PhD , Laura Parrilla Quiles MD , Pilar Paniagua Iglesias MD, PhD , Antoni J. Betbesé Roig MD, PhD , Sergi Sabaté Tenas MD, PhD , Sergio Pérez García MD , Mercedes García Álvarez MD, PhD","doi":"10.1053/j.jvca.2024.10.012","DOIUrl":"10.1053/j.jvca.2024.10.012","url":null,"abstract":"<div><h3>Objectives</h3><div>Cardiac surgery–associated acute kidney injury (CSA-AKI) is a common complication with high morbidity and mortality. This study was designed to determine whether adding human albumin to the cardiopulmonary bypass (CPB) priming solution reduces the incidence of CSA-AKI.</div></div><div><h3>Design</h3><div>A double-blind, randomized controlled trial (RCT) involving 248 patients scheduled for cardiac surgery with CPB.</div></div><div><h3>Setting</h3><div>A single-center tertiary university hospital.</div></div><div><h3>Participants</h3><div>Adults with a baseline estimated glomerular filtration rate (eGFR) of ≥60 mL/min/1.73 m<sup>2</sup> and left ventricular ejection fraction ≥40%.</div></div><div><h3>Interventions</h3><div>Patients were randomized to receive either a crystalloid priming solution (Plasma-Lyte) plus 4% albumin (intervention group, n = 126) or a crystalloid solution alone (control group, n = 122) for CPB.</div></div><div><h3>Measurements and Main Results</h3><div>Data analyses were performed using the Chi-square test and Student's <em>t</em>-test, or their nonparametric equivalent. The primary outcome was the incidence of CSA-AKI, as defined by the Kidney Disease Improving Global Outcomes criteria, within 5 days postoperatively. Both cohorts were comparable in baseline and perioperative characteristics, including preoperative albumin levels. The incidence of CSA-AKI was 29.3% (n = 37) in the intervention group compared with 31.2% (n = 38) in the control group (odds ratio: 0.91, 95% confidence interval: 0.53-1.58). The observed difference in CSA-AKI incidence between the groups was not statistically significant. A post-hoc subgroup analysis of patients with a baseline eGFR of 60 to 70 mL/min/1.73 m² indicated a trend toward a reduced incidence of CSA-AKI in the intervention group compared with the control group (35.7% <em>v</em> 57.6%; odds ratio: 0.41, 95% confidence interval: 0.16-1.03). This trend was not observed in patients with an eGFR greater than 70 mL/min/1.73 m². No significant differences were observed between groups for the need for inotropes or vasoconstrictors, incidence of cardiogenic or distributive shock, bleeding, need for transfusion, or use of nephrotoxic drugs.</div></div><div><h3>Conclusions</h3><div>Adding albumin to the CPB priming solution did not decrease the incidence of CSA-AKI in patients with normal preoperative renal function. These findings suggest that albumin might benefit patients with impaired renal function, warranting further investigation.</div></div>","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":"39 2","pages":"Pages 453-460"},"PeriodicalIF":2.3,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143286194","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-01DOI: 10.1053/S1053-0770(25)00023-0
{"title":"Articles to Appear in Future Issues","authors":"","doi":"10.1053/S1053-0770(25)00023-0","DOIUrl":"10.1053/S1053-0770(25)00023-0","url":null,"abstract":"","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":"39 2","pages":"Page xiii"},"PeriodicalIF":2.3,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143286440","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-01DOI: 10.1053/j.jvca.2024.11.037
Miklos D. Kertai MD, MMHC, PhD , Rachel Rayl BA , Daniel B. Larach MD , Ashish S. Shah MD , Stephen Bruehl PhD
Objectives
This study was designed to test whether a negative affect phenotype reflecting depression, anxiety, anger, and pain catastrophizing predicts inpatient and outpatient opioid use outcomes following cardiac surgery.
Design
In a single-center prospective observational pilot study, the authors obtained validated measures of negative affect and opioid-related phenotype preoperatively and collected opioid use and opioid misuse-related outcomes at 30-day postoperative follow-up.
Setting
Quaternary medical center.
Participants
The final dataset included 30 adult patients undergoing elective cardiac surgery procedures between August 19, 2022, and August 29, 2023.
Interventions
None.
Measurements and Main Results
Opioid outcomes included: (1) total inpatient postoperative opioid use (in milligram morphine equivalents), (2) self-reported number of days that prescribed outpatient opioids were used during the 30-day follow-up period (Timeline Followback method), and (3) number of opioid misuse-related behaviors (Current Opioid Misuse Measure–9) at 30-day follow-up. Generalized linear model analyses using a Poisson distribution indicated that greater preoperative depression, anxiety, anger, pain catastrophizing, and opioid misuse risk (indexed by the Screener and Opioid Assessment for Patients with Pain- Revised) were all significantly (p < 0.002) associated with greater inpatient and outpatient postoperative opioid use, as well as more opioid misuse-related behaviors at 30-day follow-up (p < 0.001).
Conclusions
Patients with higher preoperative levels of negative affect (depression, anxiety, anger, and pain catastrophizing) use more inpatient and outpatient opioid analgesics following cardiac surgery, a pattern similar to noncardiac surgery populations. Results support further study of patient-specific approaches to opioid prescribing to reduce the risk for opioid use disorder post–cardiac surgery.
{"title":"Predicting Extent of Opioid Use Following Cardiac Surgery: A Pilot Study","authors":"Miklos D. Kertai MD, MMHC, PhD , Rachel Rayl BA , Daniel B. Larach MD , Ashish S. Shah MD , Stephen Bruehl PhD","doi":"10.1053/j.jvca.2024.11.037","DOIUrl":"10.1053/j.jvca.2024.11.037","url":null,"abstract":"<div><h3>Objectives</h3><div>This study was designed to test whether a negative affect phenotype reflecting depression, anxiety, anger, and pain catastrophizing predicts inpatient and outpatient opioid use outcomes following cardiac surgery.</div></div><div><h3>Design</h3><div>In a single-center prospective observational pilot study, the authors obtained validated measures of negative affect and opioid-related phenotype preoperatively and collected opioid use and opioid misuse-related outcomes at 30-day postoperative follow-up.</div></div><div><h3>Setting</h3><div>Quaternary medical center.</div></div><div><h3>Participants</h3><div>The final dataset included 30 adult patients undergoing elective cardiac surgery procedures between August 19, 2022, and August 29, 2023.</div></div><div><h3>Interventions</h3><div>None.</div></div><div><h3>Measurements and Main Results</h3><div>Opioid outcomes included: (1) total inpatient postoperative opioid use (in milligram morphine equivalents), (2) self-reported number of days that prescribed outpatient opioids were used during the 30-day follow-up period (Timeline Followback method), and (3) number of opioid misuse-related behaviors (Current Opioid Misuse Measure–9) at 30-day follow-up. Generalized linear model analyses using a Poisson distribution indicated that greater preoperative depression, anxiety, anger, pain catastrophizing, and opioid misuse risk (indexed by the Screener and Opioid Assessment for Patients with Pain- Revised) were all significantly (p < 0.002) associated with greater inpatient and outpatient postoperative opioid use, as well as more opioid misuse-related behaviors at 30-day follow-up (p < 0.001).</div></div><div><h3>Conclusions</h3><div>Patients with higher preoperative levels of negative affect (depression, anxiety, anger, and pain catastrophizing) use more inpatient and outpatient opioid analgesics following cardiac surgery, a pattern similar to noncardiac surgery populations. Results support further study of patient-specific approaches to opioid prescribing to reduce the risk for opioid use disorder post–cardiac surgery.</div></div>","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":"39 2","pages":"Pages 461-469"},"PeriodicalIF":2.3,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142853976","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-01DOI: 10.1053/j.jvca.2024.11.006
Natalie J. Bodmer MD, Matthew W. Vanneman MD
{"title":"Updating “Optimal” Perioperative Care for Stable Angina","authors":"Natalie J. Bodmer MD, Matthew W. Vanneman MD","doi":"10.1053/j.jvca.2024.11.006","DOIUrl":"10.1053/j.jvca.2024.11.006","url":null,"abstract":"","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":"39 2","pages":"Pages 343-346"},"PeriodicalIF":2.3,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142755171","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-01DOI: 10.1053/j.jvca.2024.11.016
Lisa Q. Rong MD, MS , Edan Leshem BA , Joel A. Kaplan MD
{"title":"Further Retractions of Dr. Joachim Boldt in the Journal of Cardiothoracic and Vascular Anesthesia","authors":"Lisa Q. Rong MD, MS , Edan Leshem BA , Joel A. Kaplan MD","doi":"10.1053/j.jvca.2024.11.016","DOIUrl":"10.1053/j.jvca.2024.11.016","url":null,"abstract":"","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":"39 2","pages":"Pages 360-363"},"PeriodicalIF":2.3,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142794719","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-01DOI: 10.1053/j.jvca.2024.12.001
Janne Moilanen MD , Marika Pada MD , Pasi Ohtonen MSc , Timo Kaakinen MD, PhD , Matti Pokela MD, PhD , Eeva-Riitta Savolainen MD, PhD , Tiina Erkinaro MD, PhD
Objectives
According to the manufacturer, the Hemochron ACT-LR cuvette is designated for heparin concentrations of 0 to 2.5 IU/mL, while the optimal concentration range for the ACT+ cartridge is 1 to 6 IU/mL. We hypothesized that at low to moderate heparin concentrations, the ACT-LR is more reliable than the ACT+.
Design
An in vitro study.
Setting
A tertiary care university hospital.
Participants
Twenty healthy adult volunteers.
Interventions
Donor blood samples were spiked with unfractionated heparin to concentrations of 0, 0.5, 1.0, 1.5, 2.0, and 2.5 IU/mL. From each concentration, 3 measurements were made with each test cassette using 3 different Hemochron Signature Elite devices, for a total of 720 ACT tests. The Bland-Altman method and intraclass correlation coefficients were used to analyze the data.
Measurements and Main Results
All 360 ACT+ tests yielded a result. Of 360, 38 (11%) ACT-LR tests ran above the upper measurement range; of these, 36 were from the 120 measurements at heparin concentrations ≥2.0 IU/mL. The bias between all ACT-LR and ACT+ measurements was 52 (95% CI, 48-56) celite seconds, and the limits of agreement were wide. Based on the intraclass correlation coefficients, the reliability of ACT+ was better than or equal to that of ACT-LR.
Conclusions
The performance of ACT+ is equal to that of ACT-LR up to a concentration of 0.5 IU/mL, above which ACT+ is superior to ACT-LR, questioning the rationale for a specific low-range test. However, there is a significant bias between ACT-LR and ACT+ measurements that needs to be considered if switching from one test to the other.
{"title":"Performance of Hemochron ACT-LR and ACT+ Test Cuvettes in Monitoring Low to Moderate Heparin Concentrations: An In Vitro Study","authors":"Janne Moilanen MD , Marika Pada MD , Pasi Ohtonen MSc , Timo Kaakinen MD, PhD , Matti Pokela MD, PhD , Eeva-Riitta Savolainen MD, PhD , Tiina Erkinaro MD, PhD","doi":"10.1053/j.jvca.2024.12.001","DOIUrl":"10.1053/j.jvca.2024.12.001","url":null,"abstract":"<div><h3>Objectives</h3><div>According to the manufacturer, the Hemochron ACT-LR cuvette is designated for heparin concentrations of 0 to 2.5 IU/mL, while the optimal concentration range for the ACT+ cartridge is 1 to 6 IU/mL. We hypothesized that at low to moderate heparin concentrations, the ACT-LR is more reliable than the ACT+.</div></div><div><h3>Design</h3><div>An in vitro study.</div></div><div><h3>Setting</h3><div>A tertiary care university hospital.</div></div><div><h3>Participants</h3><div>Twenty healthy adult volunteers.</div></div><div><h3>Interventions</h3><div>Donor blood samples were spiked with unfractionated heparin to concentrations of 0, 0.5, 1.0, 1.5, 2.0, and 2.5 IU/mL. From each concentration, 3 measurements were made with each test cassette using 3 different Hemochron Signature Elite devices, for a total of 720 ACT tests. The Bland-Altman method and intraclass correlation coefficients were used to analyze the data.</div></div><div><h3>Measurements and Main Results</h3><div>All 360 ACT+ tests yielded a result. Of 360, 38 (11%) ACT-LR tests ran above the upper measurement range; of these, 36 were from the 120 measurements at heparin concentrations ≥2.0 IU/mL. The bias between all ACT-LR and ACT+ measurements was 52 (95% CI, 48-56) celite seconds, and the limits of agreement were wide. Based on the intraclass correlation coefficients, the reliability of ACT+ was better than or equal to that of ACT-LR.</div></div><div><h3>Conclusions</h3><div>The performance of ACT+ is equal to that of ACT-LR up to a concentration of 0.5 IU/mL, above which ACT+ is superior to ACT-LR, questioning the rationale for a specific low-range test. However, there is a significant bias between ACT-LR and ACT+ measurements that needs to be considered if switching from one test to the other.</div></div>","PeriodicalId":15176,"journal":{"name":"Journal of cardiothoracic and vascular anesthesia","volume":"39 2","pages":"Pages 447-452"},"PeriodicalIF":2.3,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142872065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}