Demet Altun
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Demet Altun has a total of 82 co-authors. Here are the top co-authors by number of shared publications:
- Emre Camci
Istanbul Faculty of Medicine, Department of Anesthesiology Istanbul University Istanbul Turkey
10 shared publications - Achmet Ali
Department of Anesthesiology and Reanimation, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey
5 shared publications - Dilek Altun
Department of Anesthesiology and Reanimation, Vocational School of Health Sciences Acıbadem Mehmet Ali Aydınlar University Istanbul Turkey
4 shared publications Emre Çamcı
Istanbul University, Istanbul Faculty of Medicine, Department of Anesthesiology, Istanbul, Turkey
4 shared publications- Mukadder Orhan-Sungur
Department of Anesthesiology and Reanimation, Istanbul Faculty of Medicine, Istanbul University, Istanbul 34093, Turkey
4 shared publications Dilek Altun
Acıbadem Mehmet Ali Aydınlar University, Department of Anesthesiology and Reanimation, Istanbul, Turkey
3 shared publications
Latest Publications
- 6 October 2026
- Published by Wiley in The Laryngoscope
Comparison of the Effects of High‐Flow Nasal Cannula Oxygen and Jet Ventilation Techniques
Objectives: Shared airway management in endolaryngeal surgery conflicts surgical access with adequate ventilation. This study compared the effects of High‐Frequency Jet Ventilation (HFJV) and Transnasal Humidified Rapid‐Insufflation Ventilatory Exchange (THRIVE) via High‐Flow Nasal Cannula (HFNC) on perioperative oxygenation, arterial CO 2 kinetics, and metabolic stability. Methods: In this prospective randomized controlled study, 36 patients (ASA I–II) undergoing elective endolaryngeal procedures were randomized into HFJV ( n = 18) or HFNC ( n = 18) groups. Both cohorts received standardized TIVA and neuromuscular blockade. Primary outcomes were longitudinal PaCO 2 changes at five intervals: baseline (T0), 10 (T1), 20 (T2), 30 (T3) minutes post‐induction, and at surgical conclusion (T4). Secondary outcomes included PaO 2 , pH, and lactate. Results: PaCO 2 levels were comparable at T0 and T1. At 20 min (T2), PaCO 2 was significantly higher in the HFNC group (55.5 vs. 44.5 mmHg; p = 0.002). At surgical conclusion (T4), median PaCO 2 reached 66.5 mmHg in the HFNC group versus 44.5 mmHg in the HFJV group ( p < 0.001). Consequently, the HFNC group exhibited significantly lower pH (7.21 vs. 7.31; p < 0.001) and elevated lactate (3.4 vs. 2.5 mmol/L; p < 0.001) at T4. PaO 2 levels at T3 and T4 were significantly superior in the HFJV group ( p < 0.001). Conclusion: While HFNC offers an ideal tubeless field for short interventions, its use is limited by time‐dependent hypercapnia and progressive respiratory acidosis. We propose a clinical “20‐min threshold” for HFNC; for longer endolaryngeal procedures, HFJV is preferred to maintain ventilatory and metabolic homeostasis. Trial Registration: This clinical trial was registered at ClinicalTrials.gov (registration number NCT05746949). Level of Evidence: 2.
- 6 October 2026
- Published by Wiley in The Laryngoscope
Comparison of the Effects of High‐Flow Nasal Cannula Oxygen and Jet Ventilation Techniques
Objectives: Shared airway management in endolaryngeal surgery conflicts surgical access with adequate ventilation. This study compared the effects of High‐Frequency Jet Ventilation (HFJV) and Transnasal Humidified Rapid‐Insufflation Ventilatory Exchange (THRIVE) via High‐Flow Nasal Cannula (HFNC) on perioperative oxygenation, arterial CO 2 kinetics, and metabolic stability. Methods: In this prospective randomized controlled study, 36 patients (ASA I–II) undergoing elective endolaryngeal procedures were randomized into HFJV ( n = 18) or HFNC ( n = 18) groups. Both cohorts received standardized TIVA and neuromuscular blockade. Primary outcomes were longitudinal PaCO 2 changes at five intervals: baseline (T0), 10 (T1), 20 (T2), 30 (T3) minutes post‐induction, and at surgical conclusion (T4). Secondary outcomes included PaO 2 , pH, and lactate. Results: PaCO 2 levels were comparable at T0 and T1. At 20 min (T2), PaCO 2 was significantly higher in the HFNC group (55.5 vs. 44.5 mmHg; p = 0.002). At surgical conclusion (T4), median PaCO 2 reached 66.5 mmHg in the HFNC group versus 44.5 mmHg in the HFJV group ( p < 0.001). Consequently, the HFNC group exhibited significantly lower pH (7.21 vs. 7.31; p < 0.001) and elevated lactate (3.4 vs. 2.5 mmol/L; p < 0.001) at T4. PaO 2 levels at T3 and T4 were significantly superior in the HFJV group ( p < 0.001). Conclusion: While HFNC offers an ideal tubeless field for short interventions, its use is limited by time‐dependent hypercapnia and progressive respiratory acidosis. We propose a clinical “20‐min threshold” for HFNC; for longer endolaryngeal procedures, HFJV is preferred to maintain ventilatory and metabolic homeostasis. Trial Registration: This clinical trial was registered at ClinicalTrials.gov (registration number NCT05746949). Level of Evidence: 2.
- 16 July 2026
- Published by Elsevier in International Journal of Pediatric Otorhinolaryngology
- Vol. 208, 112932
Evaluation of anatomical and ultrasonographic parameters to predict difficult airway in pediatric patients
- 16 July 2026
- Published by Elsevier in International Journal of Pediatric Otorhinolaryngology
- Vol. 208, 112932
Evaluation of anatomical and ultrasonographic parameters to predict difficult airway in pediatric patients
- Open Access
- 2 September 2023
- Published by Wiley in Laryngoscope Investigative Otolaryngology
- Vol. 8 (5) , 1169-1177
Airway management during unusual tracheal stenosis: A clinical feasibility trial
Objectives: Prolonged intubation is a known risk factor of LTS. LTS related to COVID‐19 may result in a different phenotype: pronation affects the location of stenosis and COVID‐19 pneumonia can decline lung mechanics. Therefore, airway management in these patients may carry unique challenges for both anesthesiologists and surgeons.This prospective observational feasibility trial aims to evaluate the use of a novel thin, cuffed, endotracheal tube (Tritube) in combination with flow‐controlled ventilation (FCV) in the management of patients with COVID‐19‐related LTS undergoing laryngeal surgery.Methods: 20 patients suffering from COVID‐19‐related LTS, as diagnosed by CT, requiring endolaryngeal surgery, with or without CO2 laser, were included. Ultrathin endotracheal tube Tritube, together with FCV was used for airway management and ventilation. Feasibility, ventilation efficiency, and surgical exposure were evaluated.Results: Median duration of mechanical ventilation during their ICU stay was 17 days, (range, 7–27), and all patients had been pronated. In 18/20 patients, endoscopic diagnosis confirmed the initial CT diagnosis: posterior subglottic stenosis. Surgeons’ satisfaction on the view was rated 9 out of 10 (range 7–10), where 0 was the worst view and 10 was the best view. Hemodynamic and respiratory variables were within the normal clinical range during the surgical procedure. One patient that had a SpO2 of 90% before induction of anesthesia, a temporal drop to 89%, caused meeting the predefined requirement of “respiratory complication.”Conclusion: This study demonstrates the feasibility of using Tritube with FCV in patients with relatively unusual subglottic posterior location tracheal stenosis, undergoing laryngotracheal surgery. Tritube provides a good surgical field and FCV provides highly adequate ventilation especially in patients with compromised lung mechanics.Level of Evidence: IV, non‐comparitive prospective clinical trial with 20 patients.
- 2 September 2023
- Published by Wiley in Laryngoscope Investigative Otolaryngology
- Vol. 8 (5) , 1169-1177
Open AccessAirway management during unusual tracheal stenosis: A clinical feasibility trial
Objectives: Prolonged intubation is a known risk factor of LTS. LTS related to COVID‐19 may result in a different phenotype: pronation affects the location of stenosis and COVID‐19 pneumonia can decline lung mechanics. Therefore, airway management in these patients may carry unique challenges for both anesthesiologists and surgeons.This prospective observational feasibility trial aims to evaluate the use of a novel thin, cuffed, endotracheal tube (Tritube) in combination with flow‐controlled ventilation (FCV) in the management of patients with COVID‐19‐related LTS undergoing laryngeal surgery.Methods: 20 patients suffering from COVID‐19‐related LTS, as diagnosed by CT, requiring endolaryngeal surgery, with or without CO2 laser, were included. Ultrathin endotracheal tube Tritube, together with FCV was used for airway management and ventilation. Feasibility, ventilation efficiency, and surgical exposure were evaluated.Results: Median duration of mechanical ventilation during their ICU stay was 17 days, (range, 7–27), and all patients had been pronated. In 18/20 patients, endoscopic diagnosis confirmed the initial CT diagnosis: posterior subglottic stenosis. Surgeons’ satisfaction on the view was rated 9 out of 10 (range 7–10), where 0 was the worst view and 10 was the best view. Hemodynamic and respiratory variables were within the normal clinical range during the surgical procedure. One patient that had a SpO2 of 90% before induction of anesthesia, a temporal drop to 89%, caused meeting the predefined requirement of “respiratory complication.”Conclusion: This study demonstrates the feasibility of using Tritube with FCV in patients with relatively unusual subglottic posterior location tracheal stenosis, undergoing laryngotracheal surgery. Tritube provides a good surgical field and FCV provides highly adequate ventilation especially in patients with compromised lung mechanics.Level of Evidence: IV, non‐comparitive prospective clinical trial with 20 patients.
- Open Access
- 8 June 2023
- Published by Cambridge University Press (CUP) in The Journal of Laryngology & Otology
- Vol. 138 (1) , 67-74
The effect of pharyngeal packing on gastric volume in patients undergoing nasal surgery: a randomised, controlled trial
Objective: To explore the effects of pharyngeal packing on antral cross-sectional area, gastric volume and post-operative complications.Methods: In this prospective, randomised, controlled study, 180 patients were randomly assigned to a control group or a pharyngeal packing group. Gastric antral dimensions were measured with pre- and post-operative ultrasound scanning. Presence and severity of post-operative nausea and vomiting and sore throat were recorded.Results: Post-operative antral cross-sectional area and gastric volume were significantly larger in the pharyngeal packing group compared to the control group. The incidence and severity of post-operative nausea and vomiting were significantly less in the pharyngeal packing group. More frequent and severe sore throat was observed in the control group within the ward. An increased Apfel simplified risk score and post-operative antral cross-sectional area were associated with post-operative nausea and vomiting during the first 2 hours, whereas septorhinoplasty and functional endoscopic sinus surgery, absent pharyngeal packing, and lower American Society of Anesthesiologists’ physical status were associated with post-operative nausea and vomiting within the ward.Conclusion: Regardless of operation type, pharyngeal packing use resulted in smaller gastric volume, which was associated with reduced post-operative nausea and vomiting frequency and severity, and lower sore throat incidence.
- 8 June 2023
- Published by Cambridge University Press (CUP) in The Journal of Laryngology & Otology
- Vol. 138 (1) , 67-74
Open AccessThe effect of pharyngeal packing on gastric volume in patients undergoing nasal surgery: a randomised, controlled trial
Objective: To explore the effects of pharyngeal packing on antral cross-sectional area, gastric volume and post-operative complications.Methods: In this prospective, randomised, controlled study, 180 patients were randomly assigned to a control group or a pharyngeal packing group. Gastric antral dimensions were measured with pre- and post-operative ultrasound scanning. Presence and severity of post-operative nausea and vomiting and sore throat were recorded.Results: Post-operative antral cross-sectional area and gastric volume were significantly larger in the pharyngeal packing group compared to the control group. The incidence and severity of post-operative nausea and vomiting were significantly less in the pharyngeal packing group. More frequent and severe sore throat was observed in the control group within the ward. An increased Apfel simplified risk score and post-operative antral cross-sectional area were associated with post-operative nausea and vomiting during the first 2 hours, whereas septorhinoplasty and functional endoscopic sinus surgery, absent pharyngeal packing, and lower American Society of Anesthesiologists’ physical status were associated with post-operative nausea and vomiting within the ward.Conclusion: Regardless of operation type, pharyngeal packing use resulted in smaller gastric volume, which was associated with reduced post-operative nausea and vomiting frequency and severity, and lower sore throat incidence.
- Open Access
- 24 May 2023
- Published by Springer Nature in Research Square
Airway management during unusual tracheal stenosis: A Clinical Feasibility Trial
BackgroundWhile actual figures are still lacking, this incidence of laryngotracheal stenosis (LTS) is expected to increase because of the high COVID-19 patient numbers requiring (prolonged) invasive mechanical ventilation. While prolonged intubation is a known risk factor of LTS, LTS related to COVID-19 may be result in a different phenotype: pronation affects the location of stenosis and COVID-19 pneumonia can decline lung mechanics. Therefore, airway management in patients with COVID-19 related LTS has unique challenges for both anesthesiologists and surgeons for its location and severity. This prospective observational feasibility trial aims to evaluate the use of a novel thin, cuffed, endotracheal tube (Tritube) in combination with flow_controlled ventilation (FCV) in the management of patients with LTS secondary to COVID-19 related LTS undergoing laryngeal surgery.Methods20 patients suffering from COVID-19 related LTS, as diagnosed by CT, requiring endolaryngeal surgery were included. Ultrathin endotracheal tube Tritube, together with FCV was used for airway management and ventilation. Feasibility, ventilation efficiency and surgical exposure were evaluated.ResultsMedian duration of mechanical ventilation during their ICU stay was 17 days, [range (7-27] and the prone position was used in all patients. In 18/20 patients endoscopic diagnosis, confirmed the initial CT diagnosis: posterior subglottic stenosis. Visual Analogue Scale (VAS) score was 9 out of 10 (range 7-10). FCV ventilation was performed with or without CO2laser. All hemodynamic and respiratory variables were within the normal clinical range. In 1 patient a respiratory complication occurred, meaning that the SpO2temporarily dropped to 89 %. Note that this patient had SpO2of 90 % before induction of anesthesia.ConclusionThis study shows that it is feasible to use Tritube with FCV in patients with unusual location of tracheal stenosis, namely a subglottic posterior location, undergoing laryngotracheal surgery. Tritube provides a good surgical field and FCV provided highly adequate ventilation especially in patients with compromised lung mechanics.Trial registrationClinical trial registration was done prospectively (NCT05317923) on 08/04/2022.
- 24 May 2023
- Published by Springer Nature in Research Square
Open AccessAirway management during unusual tracheal stenosis: A Clinical Feasibility Trial
BackgroundWhile actual figures are still lacking, this incidence of laryngotracheal stenosis (LTS) is expected to increase because of the high COVID-19 patient numbers requiring (prolonged) invasive mechanical ventilation. While prolonged intubation is a known risk factor of LTS, LTS related to COVID-19 may be result in a different phenotype: pronation affects the location of stenosis and COVID-19 pneumonia can decline lung mechanics. Therefore, airway management in patients with COVID-19 related LTS has unique challenges for both anesthesiologists and surgeons for its location and severity. This prospective observational feasibility trial aims to evaluate the use of a novel thin, cuffed, endotracheal tube (Tritube) in combination with flow_controlled ventilation (FCV) in the management of patients with LTS secondary to COVID-19 related LTS undergoing laryngeal surgery.Methods20 patients suffering from COVID-19 related LTS, as diagnosed by CT, requiring endolaryngeal surgery were included. Ultrathin endotracheal tube Tritube, together with FCV was used for airway management and ventilation. Feasibility, ventilation efficiency and surgical exposure were evaluated.ResultsMedian duration of mechanical ventilation during their ICU stay was 17 days, [range (7-27] and the prone position was used in all patients. In 18/20 patients endoscopic diagnosis, confirmed the initial CT diagnosis: posterior subglottic stenosis. Visual Analogue Scale (VAS) score was 9 out of 10 (range 7-10). FCV ventilation was performed with or without CO2laser. All hemodynamic and respiratory variables were within the normal clinical range. In 1 patient a respiratory complication occurred, meaning that the SpO2temporarily dropped to 89 %. Note that this patient had SpO2of 90 % before induction of anesthesia.ConclusionThis study shows that it is feasible to use Tritube with FCV in patients with unusual location of tracheal stenosis, namely a subglottic posterior location, undergoing laryngotracheal surgery. Tritube provides a good surgical field and FCV provided highly adequate ventilation especially in patients with compromised lung mechanics.Trial registrationClinical trial registration was done prospectively (NCT05317923) on 08/04/2022.
- 20 September 2022
- Published by Turkish Society of Intensive Care in Turkish Journal of Intensive Care
- Vol. 20, 7-13
The Relationship Between Preoperative Prognostic Nutritional Index and Postoperative Mortality in Patients with Hip Fracture
Amaç: Kalça kırıkları geriatrik hasta grubunda önemli bir sağlık sorunudur. Malnütrisyonun saptanması, perioperatif tedavi planının oluşturulması, prognozun belirlenmesi ve böylece morbidite ve mortalitenin azaltılması açısından önemlidir. Prognostik beslenme indeksi (Prognostic nutritional index, PNI), hastaların beslenme durumunun bir göstergesi olan basit, uygun maliyetli ve kolay uygulanabilir bir parametredir. Bu çalışmanın amacı, postoperatif kalça kırığı hastalarında preoperatif PNI ile mortalite arasındaki ilişkiyi incelemektir. Gereç ve Yöntem: Bu prospektif gözlemsel çalışmaya, kalça kırığı sonrası ilk 48 saat içinde ameliyat edilen, Amerikan Anesteziyoloji Derneği skoru I-IV arası olan, 65-95 yaş arası 183 hasta dahil edildi. Hastalar PNI’nın 37,25 eşik değerine göre 2 gruba ayrıldı. Toplamda 172 hasta çalışmayı tamamladı: 53’ü grup düşük PNI’da ve 119’u grup yüksek PNI’da sınıflandı. Bulgular: Hastanede kalış süresi grup düşük PNI’da anlamlı olarak daha yüksekti (p=0,035). Postoperatif deliryum grup düşük PNI’da anlamlı olarak daha yüksek bulundu (p=0,001). Üç aylık mortalite grup düşük PNI’da anlamlı olarak daha yüksekti (p=0,0001). Sonuç: Rutin taramalarda kullanılabilecek kolay hesaplanabilen, objektif ve ucuz bir biyobelirteç olan PNI ile kalça kırıklarında malnütrisyon tanısı konarak optimize bir tedavi planı oluşturmak ve mortaliteyi azaltmak mümkün olabilir.
- 20 September 2022
- Published by Turkish Society of Intensive Care in Turkish Journal of Intensive Care
- Vol. 20, 7-13
The Relationship Between Preoperative Prognostic Nutritional Index and Postoperative Mortality in Patients with Hip Fracture
Amaç: Kalça kırıkları geriatrik hasta grubunda önemli bir sağlık sorunudur. Malnütrisyonun saptanması, perioperatif tedavi planının oluşturulması, prognozun belirlenmesi ve böylece morbidite ve mortalitenin azaltılması açısından önemlidir. Prognostik beslenme indeksi (Prognostic nutritional index, PNI), hastaların beslenme durumunun bir göstergesi olan basit, uygun maliyetli ve kolay uygulanabilir bir parametredir. Bu çalışmanın amacı, postoperatif kalça kırığı hastalarında preoperatif PNI ile mortalite arasındaki ilişkiyi incelemektir. Gereç ve Yöntem: Bu prospektif gözlemsel çalışmaya, kalça kırığı sonrası ilk 48 saat içinde ameliyat edilen, Amerikan Anesteziyoloji Derneği skoru I-IV arası olan, 65-95 yaş arası 183 hasta dahil edildi. Hastalar PNI’nın 37,25 eşik değerine göre 2 gruba ayrıldı. Toplamda 172 hasta çalışmayı tamamladı: 53’ü grup düşük PNI’da ve 119’u grup yüksek PNI’da sınıflandı. Bulgular: Hastanede kalış süresi grup düşük PNI’da anlamlı olarak daha yüksekti (p=0,035). Postoperatif deliryum grup düşük PNI’da anlamlı olarak daha yüksek bulundu (p=0,001). Üç aylık mortalite grup düşük PNI’da anlamlı olarak daha yüksekti (p=0,0001). Sonuç: Rutin taramalarda kullanılabilecek kolay hesaplanabilen, objektif ve ucuz bir biyobelirteç olan PNI ile kalça kırıklarında malnütrisyon tanısı konarak optimize bir tedavi planı oluşturmak ve mortaliteyi azaltmak mümkün olabilir.
- Open Access
- 9 September 2022
- Published by Galenos Yayinevi in Balkan Medical Journal
- Vol. 39 (5) , 351-357
Comparison of Stroke Volume Variation-based goal-directed Therapy Versus Standard Fluid Therapy in Patients Undergoing Head and Neck Surgery: A Randomized Controlled Study
Perioperative fluid therapy is used to avoid dehydration and hypovolemia. Optimum perioperative fluid administration may improve postoperative outcomes after major surgery, and the optimal strategy remains controversial and uncertain. The primary outcome was the total amount of intraoperative fluids given between perioperative goal-directed fluid therapy (GDFT) guided by a hemodynamic monitoring system and standard fluid therapy based on “mean arterial pressure-diuresis” data in patients undergoing head and neck surgery. The secondary outcomes were the hemodynamics and laboratory variables, postoperative complications, length of mechanical ventilation, intensive care unit and hospital stay. A randomized controlled study. Sixty patients were scheduled and randomized into two groups of 30 patients each: in the study group, an arterial pressure catheter was inserted and connected to the FloTrac system, whereas in the control group, an arterial pressure catheter was inserted and integrated into the hemodynamic monitoring system with a special transducer. The control group had fluids administered at the discretion of the anesthesiologist according to the mean arterial pressure >65 mmHg and diuresis >0.5 ml/kg/h. In the study group, fluid management was administered to achieve a target value of ≤13% through the stroke volume variation. The total amounts of fluid in the intraoperative period were different between the groups, with the study group receiving significantly more fluids (P = 0.0455). The length of hospital stay was significantly longer in the study group than in the control group (P = 0.012), but prolonged oxygen demand was significantly more frequent in the control group than in the study group (P = 0.017). No difference was found in hemodynamics, lactate kinetics, and vasoactive agent requirements. The standard fluid therapy guided by conventional circulatory parameters appears sufficient for patients with low-to-moderate risk during head and neck surgery.
- 9 September 2022
- Published by Galenos Yayinevi in Balkan Medical Journal
- Vol. 39 (5) , 351-357
Open AccessComparison of Stroke Volume Variation-based goal-directed Therapy Versus Standard Fluid Therapy in Patients Undergoing Head and Neck Surgery: A Randomized Controlled Study
Perioperative fluid therapy is used to avoid dehydration and hypovolemia. Optimum perioperative fluid administration may improve postoperative outcomes after major surgery, and the optimal strategy remains controversial and uncertain. The primary outcome was the total amount of intraoperative fluids given between perioperative goal-directed fluid therapy (GDFT) guided by a hemodynamic monitoring system and standard fluid therapy based on “mean arterial pressure-diuresis” data in patients undergoing head and neck surgery. The secondary outcomes were the hemodynamics and laboratory variables, postoperative complications, length of mechanical ventilation, intensive care unit and hospital stay. A randomized controlled study. Sixty patients were scheduled and randomized into two groups of 30 patients each: in the study group, an arterial pressure catheter was inserted and connected to the FloTrac system, whereas in the control group, an arterial pressure catheter was inserted and integrated into the hemodynamic monitoring system with a special transducer. The control group had fluids administered at the discretion of the anesthesiologist according to the mean arterial pressure >65 mmHg and diuresis >0.5 ml/kg/h. In the study group, fluid management was administered to achieve a target value of ≤13% through the stroke volume variation. The total amounts of fluid in the intraoperative period were different between the groups, with the study group receiving significantly more fluids (P = 0.0455). The length of hospital stay was significantly longer in the study group than in the control group (P = 0.012), but prolonged oxygen demand was significantly more frequent in the control group than in the study group (P = 0.017). No difference was found in hemodynamics, lactate kinetics, and vasoactive agent requirements. The standard fluid therapy guided by conventional circulatory parameters appears sufficient for patients with low-to-moderate risk during head and neck surgery.
- 26 July 2022
- Published by Wiley in Journal of Cardiac Surgery
- Vol. 37 (12) , 4234-4242
A retrospective analysis of dexmedetomidine and morphine in the fast‐track and ultra‐fast‐track extubation protocol after congenital cardiac surgery
After congenital cardiac surgery, the duration of mechanical ventilation (MV) is related to the clinical status, type of operation, and the sedative-analgesic agents used postoperatively. This study aims to examine the effects of dexmedetomidine and morphine on the fast-track extubation (FTE) and ultra-fast-track extubation (UFTE) protocol after congenital cardiac surgery. A total of 251 pediatric patients were divided into two groups: 118 patients in the morphine group (Group M) and 133 patients in the dexmedetomidine group (Group D). We retrospectively reviewed medical data including hemodynamic parameters, duration of MV and cardiovascular intensive care unit (CICU), additional sedative/analgesic requirement, adverse events, the need for reintubation, and noninvasive MV, sedation, and pain scores. The mean mechanical ventilation duration of Group D was significantly shorter than Group M (3.74 ± 0.83 h in Group D, 5.72 ± 1.54 h in Group M, respectively) (p = .001; p < .05). In Group D, the success rate of FTE was 92.5% (n = 123) and UFTE was 7.5% (n = 10) (p = .001). In Group M, the success rate of FTE was 72.9% (n = 86) and UFTE was 0% (n = 0) (p > .05). Dexmedetomidine and morphine have clinical benefits which encourage their use for FTE protocol. Dexmedetomidine has more benefits compared to morphine. It can be used in UFTE protocol, besides its use in FTE protocol with fewer side effects.
- 26 July 2022
- Published by Wiley in Journal of Cardiac Surgery
- Vol. 37 (12) , 4234-4242
A retrospective analysis of dexmedetomidine and morphine in the fast‐track and ultra‐fast‐track extubation protocol after congenital cardiac surgery
After congenital cardiac surgery, the duration of mechanical ventilation (MV) is related to the clinical status, type of operation, and the sedative-analgesic agents used postoperatively. This study aims to examine the effects of dexmedetomidine and morphine on the fast-track extubation (FTE) and ultra-fast-track extubation (UFTE) protocol after congenital cardiac surgery. A total of 251 pediatric patients were divided into two groups: 118 patients in the morphine group (Group M) and 133 patients in the dexmedetomidine group (Group D). We retrospectively reviewed medical data including hemodynamic parameters, duration of MV and cardiovascular intensive care unit (CICU), additional sedative/analgesic requirement, adverse events, the need for reintubation, and noninvasive MV, sedation, and pain scores. The mean mechanical ventilation duration of Group D was significantly shorter than Group M (3.74 ± 0.83 h in Group D, 5.72 ± 1.54 h in Group M, respectively) (p = .001; p < .05). In Group D, the success rate of FTE was 92.5% (n = 123) and UFTE was 7.5% (n = 10) (p = .001). In Group M, the success rate of FTE was 72.9% (n = 86) and UFTE was 0% (n = 0) (p > .05). Dexmedetomidine and morphine have clinical benefits which encourage their use for FTE protocol. Dexmedetomidine has more benefits compared to morphine. It can be used in UFTE protocol, besides its use in FTE protocol with fewer side effects.
- 24 November 2021
- Published by Wiley in Journal of Cardiac Surgery
- Vol. 37 (3) , 535-541
Measuring potassium level in packed red blood cells before using: Word of caution for congenital cardiac surgery
Background and Aim of the Study Transfusion-associated hyperpotassemia is a serious complication of packed red blood cell (PRBC) transfusion after congenital cardiac surgery. Our study aimed to identify risk factors and potential preventive measures of transfusion-associated hyperpotassemia in neonates and infants after congenital cardiac surgery. Methods Pediatric patients who underwent congenital cardiac surgery and need transfusion were enrolled in this prospective study. The potassium concentration of PRBC was checked from the sample taken from the segment. The volume of transfusion, age of PRBC, potassium concentration of unit were recorded. The estimated increment of potassium level in patients after PRBC transfusion was calculated. Results Seventy-four individual patients, 95 distinct transfusions, 112 blood products were evaluated. The mean age of the blood unit was 3.8 ± 1.4 days. The mean potassium concentration in the PRBCs was 9.9 ± 2.4 mmol/L. A weak correlation was observed between the potassium value of the PRBC and the age of PRBC (p = 0.049, r = 0.2, y = 0.24 × x + −0.68). There was a weak correlation between the potassium value of PRBCs and the age of the unit (p < 0.001, r = 0.37, y = 2.8 × x + −3.6). Conclusions Before transfusion, even PRBC is fresh, measuring the potassium level of PRBC and the potassium that will be given to the pediatric patient with transfusion can prevent transfusion-related hyperpotassemia and related complications. Otherwise, high potassium levels, which may be overlooked despite being fresh, may cause serious complications, even cardiac arrest, especially in neonates and infants.
- 24 November 2021
- Published by Wiley in Journal of Cardiac Surgery
- Vol. 37 (3) , 535-541
Measuring potassium level in packed red blood cells before using: Word of caution for congenital cardiac surgery
Background and Aim of the Study Transfusion-associated hyperpotassemia is a serious complication of packed red blood cell (PRBC) transfusion after congenital cardiac surgery. Our study aimed to identify risk factors and potential preventive measures of transfusion-associated hyperpotassemia in neonates and infants after congenital cardiac surgery. Methods Pediatric patients who underwent congenital cardiac surgery and need transfusion were enrolled in this prospective study. The potassium concentration of PRBC was checked from the sample taken from the segment. The volume of transfusion, age of PRBC, potassium concentration of unit were recorded. The estimated increment of potassium level in patients after PRBC transfusion was calculated. Results Seventy-four individual patients, 95 distinct transfusions, 112 blood products were evaluated. The mean age of the blood unit was 3.8 ± 1.4 days. The mean potassium concentration in the PRBCs was 9.9 ± 2.4 mmol/L. A weak correlation was observed between the potassium value of the PRBC and the age of PRBC (p = 0.049, r = 0.2, y = 0.24 × x + −0.68). There was a weak correlation between the potassium value of PRBCs and the age of the unit (p < 0.001, r = 0.37, y = 2.8 × x + −3.6). Conclusions Before transfusion, even PRBC is fresh, measuring the potassium level of PRBC and the potassium that will be given to the pediatric patient with transfusion can prevent transfusion-related hyperpotassemia and related complications. Otherwise, high potassium levels, which may be overlooked despite being fresh, may cause serious complications, even cardiac arrest, especially in neonates and infants.