Extracorporeal Lung Assist with Heparin-Coated Systems

1992 ◽  
Vol 15 (1) ◽  
pp. 29-34 ◽  
Author(s):  
R. Rossaint ◽  
K. Slama ◽  
K. Lewandowski ◽  
R. Streich ◽  
P. Henin ◽  
...  

Extracorporeal lung assist (ELA) has been recommended for the treatment of ARDS if conventional therapy fails. However, the need for nearly complete anticoagulation is a major risk factor for hemorrhagic complications. We describe our experience with 13 ARDS patients treated with ELA using heparin-coated systems (Carmeda). Maintaining partial thromboplastin time and activated clotting time within or close to the normal range, even major surgery (20 thoracotomies and 2 laparotomies) could be performed without undue bleeding complications related to anticoagulation during extracorporeal support. Eight of the 13 patients survived. The use of heparin-coated systems allows prolonged ELA with nearly physiological coagulation function, permitting major surgical intervention. It enhances the safety margin of extracorporeal gas exchange and may ultimately extend its indications.

Perfusion ◽  
1996 ◽  
Vol 11 (4) ◽  
pp. 333-337 ◽  
Author(s):  
Ahmet Hamulu ◽  
Berent Discigil ◽  
Mustafa Özbaran ◽  
Tanzer Çalkavur ◽  
Erkan Kara ◽  
...  

Heparin attachment to synthetic surfaces is one means of improving the biocompatibility of clinically used cardiopulmonary bypass (CPB) circuits. To assess the effect of heparin-coated circuits on complement consumption during CPB, 40 patients undergoing elective myocardial revascularization were prospectively randomized either to a group in which a completely Duraflo II heparin-coated circuit was used for perfusion (heparin-coated Group, n = 20 patients) or to a control group (n = 20 patients) in which an uncoated, but otherwise standard circuit was used. Full systemic heparinization was induced (activated clotting time, 480 seconds) in all the patients included in the study, regardless of which perfusion circuit was used. The two groups did not differ significantly in terms of bodyweight, aortic crossclamp and extracorporeal circulation times. No patient had difficulty in weaning from bypass and the postoperative period was uneventful in all patients. Concentrations of C3 and C4 were found to be within the 'normal' range in the prebypass period in both groups. There were no significant intergroup differences with regard to C3 and C4 consumption during CPB. We conclude that Duraflo II heparin- coated circuits have no effect in reducing complement consumption during CPB in fully heparinized patients.


2002 ◽  
Vol 144 (3) ◽  
pp. 501-507 ◽  
Author(s):  
William B. Hillegass ◽  
Brigitta C. Brott ◽  
Gregory D. Chapman ◽  
Harry R. Phillips ◽  
Richard S. Stack ◽  
...  

Author(s):  
Dong Geum Shin ◽  
Jinhee Ahn ◽  
Sang-Jin Han ◽  
Hong Euy Lim

Introduction: Single-shot ablation has emerged as an effective technique for index atrial fibrillation (AF) ablation, with an advantage of short procedure time. Although recent guidelines recommend peri-procedural uninterrupted oral anticoagulants (OACs), the intra-procedural anticoagulation strategy remains uncertain under non-vitamin K OACs (NOACs). We investigated procedural safety of a single bolus administration of heparin without activated clotting time (ACT) measurement during cryoballoon ablation (CBA). Methods: Two hundred patients (64.2±10.0years, 70% with non-paroxysmal AF) who underwent CBA with uninterrupted NOACs were randomly assigned to No-ACT group and ACT group. A bolus of heparin (100 U/kg) was routinely administered immediately after transseptal puncture. In the ACT group, an additional injection of heparin (30 U/kg) was administered if ACT at 30-min after the initial bolus was <300 s. Results: There were no differences in baseline characteristics including CHA2DS2-VASc score between two groups. The left atrium indwelling and procedure times were 60.4±13.1 min and 78.9±13.9 min, respectively and not significantly different between two groups. The mean ACT was 335.2±59.9 s in the ACT group. Any bleeding rate was 3.2% in all patients and there was no statistically difference in bleeding complications between two groups. In the ACT group, groin hematoma, laryngopharyngeal bleeding, and hemoptysis occurred in 3, 1, and 1 patient, respectively. Cardiac tamponade occurred in 1 patient in the No-ACT group. No thromboembolic events occurred during the 30-day follow-up after CBA. Conclusion: Single bolus administration of heparin without ACT measurement is a feasible anticoagulation strategy for CBA in patients with uninterrupted NOACs intake.


1988 ◽  
Vol 11 (4) ◽  
pp. 255-258 ◽  
Author(s):  
L. Preuschof ◽  
F. Keller ◽  
J. Seemann ◽  
G. Offermann

Heparinization during hemodialysis may cause severe bleeding complications in patients with high bleeding risk. Heparin-free hemodialyses (n=208) were performed in 46 unselected patients with high bleeding risk after kidney transplantation (n=25), after major surgery (n=10), and with bleeding disorders (n=11). Dialyser and blood lines were primed without heparin. In addition to the established measures (high blood flow, intermittent rinsing), system clotting was prevented by prophylactically changing the dialyser and blood lines in 107 of 208 dialyses (52 percent). Total system clotting with blood loss ranging from 100 to 250 ml occurred in six cases (3 percent). Mean hemodialysis time (± SD) was 4.1 hours (± 0.4), rising volume of the extracorporeal system 1.4 liters/hour (± 0.6), blood flow 244 ml/min (± 38), clotting time 12 min (+ 4), and weight loss 2.5 kg (± 1.5). Mean hemodialysis creatinine clearance was 110 ml/min (± 34) and BUN clearance 138 ml/min (± 48). Heparin-free hemodialysis with prophylactic change of system is thus a safe and practical method of treatment for patients at high bleeding risk, but it is less effective, more expensive and the patient requires closer care.


2003 ◽  
Vol 31 (1) ◽  
pp. 95-98 ◽  
Author(s):  
M. J. Lennon ◽  
N. M. Thackray ◽  
N. M. Gibbs

The activated clotting time (ACT) may be an unreliable monitor of coagulation for patients with the antiphospholipid syndrome. We describe a patient with antiphospholipid syndrome in whom adequate anticoagulation during cardiopulmonary bypass was confirmed by monitoring both the ACT and anti-factor Xa levels. The cardiopulmonary bypass was uneventful, and there were no thrombotic or bleeding complications. The use of anti-factor Xa levels provided confirmation of adequate anticoagulation (and reversal of anticoagulation) that was not possible using the ACT alone.


EP Europace ◽  
2021 ◽  
Vol 23 (Supplement_3) ◽  
Author(s):  
T Mine ◽  
R Kitagaki ◽  
E Fukuhara ◽  
M Ishihara

Abstract Funding Acknowledgements Type of funding sources: None. Background Direct thrombin inhibitors (DTIs) unlike factor Xa-inhibitors (Xa-inhibitors) is associated with fewer bleeding complications than warfarin in patients who had catheter ablation (CA) for atrial fibrillation (AF). However, the mechanisms remains unclear, and activated clotting time (ACT) is used to control heparin-dose for thromboembolic prevention during CA. Methods: We retrospectively studied 543 patients taking direct oral anticoagulant (DOAC) who underwent CA for AF (375 males, age 67 ± 10, 251 non-paroxysmal AF, 142 DTIs). Patients with off-label usage of DOAC were excluded. ACT was measured before (Pre-ACT) and after (post-ACT) initial heparin administration (3000U + 100U/kg), and total heparin-dose was evaluated. Results: Pre-ACT and post-ACT were extended in patients with DTIs (150 ± 21 vs 123 ± 15; P &lt; 0.0001 and 322 ± 39 vs 309 ± 42 sec; P = 0.0013). Patients with Xa-inhibitors required higher total heparin-dose (199 ± 43 vs 175 ± 34 U/kg; P &lt; 0.0001). During and after CA, none had thromboembolic events and 14 patients (3 DTIs, 11 Xa-inhibitor) showed bleeding events (Figure). Conclusions: ACT is extended in patients taking DTIs. Xa-inhibitors might have anticoagulant effects which are not reflected in ACT. Abstract Figure.


Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 2137-2137
Author(s):  
Kanak Parmar ◽  
Wasawat Vutthikraivit ◽  
Amritpal Singh ◽  
Christina Morataya ◽  
Gaspar Del Rio Pertuz ◽  
...  

Abstract Background Veno-Venous Extracorporeal Membrane Oxygenation (ECMO) technology provides as a alternative approach in the intensive care of patients with respiratory failure due to varied causes who are not responsive to conventional treatment. As per the 2014 Extracorporeal Life Support Organization (ELSO) guidelines, in order to to maintain circuit patency and minimize thromboembolic complications, anticoagulation is used, but the optimal strategy remains to be defined. Activated clotting time (ACT) is the most utilized bedside test to adjust anticoagulation. Therefore, we performed an extended analysis of all published studies on the incidence of thromboembolic and bleeding events in patients with acute respiratory distress syndrome who were put on ECMO. Methods A comprehensive search of several databases from inception to November 25, 2020, limited to English language and excluding animal studies, was conducted. The databases included Ovid MEDLINE(R) and Epub Ahead of Print, In-Process & Other Non-Indexed Citations and Daily, Ovid Embase, Ovid Cochrane Central Register of Controlled Trials, Ovid Cochrane Database of Systematic Reviews, and Scopus. The studies were classified into low anticoagulation target (ACT&lt;180) or high anticoagulation target (ACT&gt;180). A meta-analysis was performed of all eligible studies with the data on the incidences of thromboembolic and bleeding complications in patients with ARDS on VV-ECMO during different intensities of anticoagulation. Results A total of 6 eligible studies (4 retrospective and 2 case series) were identified, including in total 190 patients for 100 patient years. Our study showed that there is two times higher chances of bleeding when ACT goal is &gt;180 versus a lower ACT range of &lt;180 (Risk ratio 2.07, 95% CI 1.23-3.46, P 0.0056). The incidence of thrombosis did not change in the two group (Risk ratio 1.17, 95% CI 0.45-3, P 0.7516). Conclusions Currently there is a lack of data for anticoagulation strategies during VV-ECMO for patients in respiratory failure. Our study aimed to find an appropriate anticoagulation target for this patient group. The results show that although anticoagulation is required for circuit patency, there is an increased risk of bleeding when higher anticoagulation targets are set. Disclosures No relevant conflicts of interest to declare.


2019 ◽  
Vol 28 ◽  
pp. S380-S381
Author(s):  
A. Bailey ◽  
M. Fryer ◽  
K. Hall ◽  
E. Hogg ◽  
E. Levy ◽  
...  

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 1178-1178
Author(s):  
Dearbhla Doherty ◽  
Anjali Patel ◽  
Margaret Nolan ◽  
Mary Byrne ◽  
Sonia Aguila ◽  
...  

Abstract Recent international consensus guidelines recommend that patients with significant bleeding phenotypes and plasma VWF levels in the 30-50 IU/dL range should be classified as Low von Willebrand factor (Low VWF). Critically however, evidence-based guidelines regarding optimal clinical management strategies for this cohort have not been defined. In particular, data regarding the need for hemostatic cover for procedures in Low VWF are limited. To address this deficit, as part of the Low Von Willebrand in Ireland Cohort (LoVIC) study we conducted a systematic retrospective review of all procedures in a large cohort of well characterised patients with Low VWF. Methods: Following written informed consent, we collated data on all procedures performed in LoVIC patients over a 17 year period (1/1/00-12/31/17). Case notes were reviewed and data collected in a standard proforma - age at intervention, choice of hemostatic cover, perioperative VWF, haemoglobin (Hgb) levels and reported bleeding. Procedures were categorised as dental extractions (DE), minor (e.g. endoscopies, joint injections) or major surgery. Tranexamic acid (TA) was prescribed 1g TDS. All desmopressin (DDAVP) was administered intravenously (IV, 0.3mg/kg). Results: 165 procedures in 65 LoVIC participants were identified. The procedural group was significantly older (median 45 vs 38.8 years, p<0.0001) and with a longer duration of Low VWF (9.0 vs 6.5 years, p=0.02) compared to the rest of the cohort. The majority of procedures were either minor (69.1%) or DEs (24.2%), with only 11 major procedures. Overall, 41 (24.8%) were covered with TA alone; 103 (62.4%) with DDAVP+/- TA; clotting factor concentrate (CFC) was used in only 4 procedures. Dental extractions: DDAVP+/-TA was used in 72.5% of DEs with no excess bleeding. Of the 10 DE with only TA, 4 developed bleeding requiring treatment (DDAVP/suturing/TA). On comparison of the DDAVP/TA and TA groups, no significant difference in ISTH BAT (median 9 vs 7, p=0.3) or plasma VWF levels (Table 1) at time of procedure was seen. However, the TA only cohort were significantly older (median 55.1 vs 29.3 years, y, p=0.0002), influencing treatment choice. Of interest, in the 4/10 with TA only who bled, pre-DE plasma VWF levels were close to or within the normal range (VWF:RCo 47- 79 IU/dL). Minor procedures: Of the 114 minor procedures, 45.6% (52) were endoscopies, 31 with biopsy. The other 62 procedures were dermatological (19), orthopaedic (19), gynecological (8) or other (e.g. minor biopsies, 14). 17 procedures with low bleeding risk were performed with no hemostatic cover independent of the coagulation service. Excessive bruising was reported in 2/17 procedures, both patients were older (54 and 70 years) with pre-op plasma VWF levels within the normal range. For the remaining 97 procedures, 3 patients had CFC cover (unsuitable for DDAVP); 68 DDAVP/TA and 26 received only TA. Age contributed to prophylaxis choice, with TA cohort significantly older than the DDAVP/TA group (median 65.6 vs 42.5y, p=0.0004). However, phenotype also influenced with ISTH BAT scores significantly lower in the TA only cohort (median 3 vs 10.5, p<0.0001). No bleeding or significant change in perioperative Hgb levels were reported in any procedure covered with prophylaxis. Major : Data on major procedures were limited to 11 procedures covered with TA or DDAVP/TA. Plasma VWF levels were maintained following a single dose of DDAVP in all cases. A significant reduction in post-op Hgb levels was observed in TA only patients but no significant bleeding occurred (Table 1). The TA group were significantly older than DDAVP/TA patients (54.8 vs 33.6,p=0.03) but no significant difference in ISTH BAT score, pre-operative plasma VWF or Hgb levels or inpatient stay was seen, although numbers are limited. Conclusion: This study represents the largest analysis of procedural outcomes in patients with Low VWF to date. Our data suggest that age and ISTH BAT score significantly influence choice of hemostatic prophylaxis. Bleeding complications were observed only in LoVIC patients undergoing DE covered by TA, or with minor procedures with no hemostatic cover. Interestingly, patients who developed bleeding were typically older (median 59.7y) and, critically in this subgroup, bleeding occurred despite that plasma VWF levels had corrected to within the normal range, clearly raising the possibility that age-corrected normal ranges may need to be considered. Table Table. Disclosures Lavin: Shire: Honoraria, Research Funding, Speakers Bureau. O'Donnell:Bayer: Research Funding, Speakers Bureau; Baxter: Research Funding, Speakers Bureau; Shire: Research Funding, Speakers Bureau; Novo Nordisk: Research Funding, Speakers Bureau; Leo Pharma: Speakers Bureau; Octapharma: Speakers Bureau; CSL Behring: Consultancy; Daiichi Sankyo: Consultancy; Pfizer: Consultancy, Research Funding.


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