22 research outputs found

    A solution for global hygienic challenges regarding the application of heater-cooler systems in cardiac surgery

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    71.759 surgical procedures were performed in 2019 with the aid of cardiopulmonary bypass in Germany. To adjust the patient’s body temperature on extracorporeal circulation, the application of a heater-cooler unit (HCU) is mandatory. However, in case of insufficient sanitisation of HCU, life-threatening infections can be transmitted by the device to the patients, including Legionella bacteria, Mycobacterium chimaera, Pseudomonas aeruginosa. To avoid disease transmission, as a requirement for safe medical practice established by regulatory authorities, HCUs must be regularly disinfected by hazardous chemicals posing a danger for both handling humans and the environment. Therefore, to comply with regulations, HCU manufacturers have introduced both timely and financially extensive sanitisation procedures. Our paper describes a novel, effective and easy to handle disinfection method for the above problematics without utilising hazardous chemicals. The method’s technical principle is electrolysis, resulting in drinking water quality regarding the analysed germs in the worldwide most commonly utilised heater-cooler device. The main aim of the study was to prove the efficacy and reliability of the device cleansing process. Furthermore, the economic impact of the novel method was evaluated. Therefore, we have undertaken 60 microbiological sampling series between December 2019 and November 2020 from a conventional HCU (3T LivaNova, Germany). During the total investigational period, no contamination with Pseudomonas aeruginosa or Legionellae could have been demonstrated in the HCU. The extreme slow-growing nontuberculous M. chimaera was detected only in one sample obtained from diamond electrode cleansed HCU water, and source of contamination was promptly eliminated by a simple technical modification of the device test-site. Additionally, the diamond electrode application is beneficial for eliminating potentially hazardous cleansing material from the process, which may affect otherwise both patients operated on cardiopulmonary bypass and the perfusionists

    Quantitative assessment of peripheral limb perfusion using a modified distal arterial cannula in venoarterial ECMO settings

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    In cases of severe cardiopulmonary deterioration, quick establishment of venoarterial extracorporeal membrane oxygenation (ECMO) represents a support modality. After successful arterial peripheral cannulation, a certain grade of peripheral limb malperfusion is a fairly common phenomenon. Detection of peripheral malperfusion is vital, since it can result in compartment syndrome or even loss of the affected limb. To prevent or resolve emerging lower limb ischaemia, a newly designed perfusion catheter is placed into the superficial femoral artery, distal to the arterial cannula via ECMO. The aim of our study was to evaluate flow and haemodynamic characteristics of this novel distal limb perfusion cannula for ECMO therapy and present these important findings for the first time. The distal perfusion cannula blood flow increases in linear correlation with ECMO blood flow The variability of distal perfusion cannula blood flow with a 15 Fr cannula ranges between 160 +/- 0.40 mL min(-1) at 1.5 L min(-1) ECMO flow rate and 480 +/- 80 mL min(-1) at 5.0 L min(-1) ECMO blood flow, respectively. Comparatively, the 17-Fr-sized cannula performs on a scale of 140 +/- 20 to 390 +/- 60 mL distal perfusion cannula blood flow at 1.5-5.0 L min(-1) ECMO blood flow, respectively. The quantitative assessment of the distal perfusion cannula blood flow has revealed that distal perfusion cannula blood flow can measure up to 10% of the ECMO blood flow. Furthermore, it has been also well demonstrated that the novel distal perfusion cannula is sufficient to compensate peripheral limb ischaemia

    Central Cannulation by Seldinger Technique: A Reliable Method in Type A Aortic Dissection Repairs

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    none11Background: Extensive type A aortic dissections that involve peripheral great vessels can complicate the choice of a cannulation site for cardiopulmonary bypass. We started to employ direct cannulation of the true lumen on the concavity of the aortic arch by Seldinger technique and evaluated the efficacy of this access technique as an alternative arterial inflow target in aortic surgery.Material/Methods: Twenty-four consecutive patients (mean age: 59 +/- 14 years) underwent type A aortic dissection repair using selective antegrade cerebral perfusion. Direct aortic cannulation was used in 14 cases, subclavian access in 6 patients, and femoral entry in 4 patients. Perioperative factors were evaluated to identify the reliability and eventual benefits of direct cannulation method at the aortic arch.Results: There were no operative deaths and cumulative 30-day mortality rate was 25% (6). Permanent neurological deficits were not observed; in 1 patient transient changes occurred (4%). Time to reach circulatory arrest was the shortest in the direct access group, with mean 27 +/- 11 (CI: 20.6-33.3) min vs. 43 +/- 22 (28.0-78.0) min (p=0.058) and 32 +/- 8 (23.6-40.4) min (p=0.34) by femoral cannulation and subclavian entry, respectively. Direct arch cannulation resulted in the best renal function in the first 72 h after surgery and similar characteristics were observed in lactic acid levels.Conclusions: Ultrasound-guided direct cannulation on the concavity of the aortic arch using a Seldinger technique is a reliable method in dissection repairs. Prompt antegrade perfusion provides not only cerebral but also peripheral organ and tissue protection, which is an advantage in this high-risk group of patients.noneGobolos, L; Ugocsai, P; Foltan, M; Philipp, A; Thrum, A; Miskolczi, S; Malvindi, PG; di Gregorio, V; Pousios, D; Navaratnarajah, M; Ohri, SKGobolos, L; Ugocsai, P; Foltan, M; Philipp, A; Thrum, A; Miskolczi, S; Malvindi, Pg; di Gregorio, V; Pousios, D; Navaratnarajah, M; Ohri, S

    Patient data and characteristics before ECMO initiation.

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    <p>Data are median (interquartile range).</p><p>SOFA, Sequential Organ Failure Assessment; LIS, Murray lung injury score; apH, arterial pH value; PaCO<sub>2</sub>, partial pressure of arterial carbon dioxide; PaO<sub>2</sub>/FiO<sub>2</sub>, ratio of partial pressure of arterial oxygen and fraction of inspired oxygen; PIP, peak inspiratory pressure; PEEP, positive end-expiratory pressure; TV, tidal volume; BMI, body mass index; ARF, acute renal failure.</p><p><sup>a</sup> bacterial, viral, fungal, aspiration pneumonia and H1N1 infection.</p><p><sup>b</sup> other pathologies (eg. pulmonary fibrosis, near drowning, extensive bronchiectasis, pulmonary hemorrhage, tracheal laceration).</p><p>Patient data and characteristics before ECMO initiation.</p

    Association of technical and clinical parameters with fHb and LDH as a marker for hemolysis in vvECMO therapy.

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    <p><sup>a</sup> p-values refer to the linear mixed model based on ranks with the respective continuous parameter as independent and fHb or LDH as dependent variable. Respective p-values were mentioned in the text.</p><p><sup>b</sup> p-values refer to the linear mixed model based on ranks with the respective categorical parameter as independent and fHb or LDH as dependent variable (respective p-values were mentioned in the text). Pairwise comparisons (all vs. control) were only performed in case of a significant main effect (p≤0.05).</p><p><sup>c</sup> Single-lumen backflow (diameter, 15, 17, 19, 21 Fr), dual-lumen cannulae (Avalon 23, 27 Fr) (all Maquet), Twinport 24 Fr (Novalung).</p><p><sup>d</sup> bacterial, viral, fungal, aspiration pneumonia, H1N1 infection.</p><p><sup>e</sup> other pathologies (pulmonary fibrosis, pulmonary hypertension, extensive bronchiectasis, pulmonary bleeding, tracheal laceration).</p><p>RBC, red blood cells (one RBC contained 300 ml volume); CVVHF, continuous venovenous hemofiltration. fHb, free hemoglobin; LDH, lactate dehydrogenase; Fr, French.</p><p>Association of technical and clinical parameters with fHb and LDH as a marker for hemolysis in vvECMO therapy.</p
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