scholarly journals Coagulation parameters and major bleeding in critically ill patients with cirrhosis

Hepatology ◽  
2016 ◽  
Vol 64 (2) ◽  
pp. 556-568 ◽  
Author(s):  
Andreas Drolz ◽  
Thomas Horvatits ◽  
Kevin Roedl ◽  
Karoline Rutter ◽  
Katharina Staufer ◽  
...  
Author(s):  
Alexandra Jayne Nelson ◽  
Brian W Johnston ◽  
Alicia Achiaa Charlotte Waite ◽  
Gedeon Lemma ◽  
Ingeborg Dorothea Welters

Background. Atrial fibrillation (AF) is the most common cardiac arrhythmia in critically ill patients. There is a paucity of data assessing the impact of anticoagulation strategies on clinical outcomes for general critical care patients with AF. Our aim was to assess the existing literature to evaluate the effectiveness of anticoagulation strategies used in critical care for AF. Methodology. A systematic literature search was conducted using MEDLINE, EMBASE, CENTRAL and PubMed databases. Studies reporting anticoagulation strategies for AF in adults admitted to a general critical care setting were assessed for inclusion. Results. Four studies were selected for data extraction. A total of 44087 patients were identified with AF, of which 17.8-49.4% received anticoagulation. The reported incidence of thromboembolic events was 0-1.4% for anticoagulated patients, and 0-1.3% in non-anticoagulated patients. Major bleeding events were reported in three studies and occurred in 7.2-8.6% of the anticoagulated patients and up to 7.1% of the non-anticoagulated patients. Conclusions. There was an increased incidence of major bleeding events in anticoagulated patients with AF in critical care compared to non-anticoagulated patients. There was no significant difference in the incidence of reported thromboembolic events within studies, between patients who did and did not receive anticoagulation. However, the outcomes reported within studies were not standardised, therefore, the generalisability of our results to the general critical care population remains unclear. Further data is required to facilitate an evidence-based assessment of the risks and benefits of anticoagulation for critically ill patients with AF.


2020 ◽  
Vol 58 ◽  
pp. 34-40
Author(s):  
Yosuf W. Subat ◽  
Hamza Rayes ◽  
Andrew C. Hanson ◽  
Madeline Q. Johnson ◽  
Phillip J. Schulte ◽  
...  

2021 ◽  
Vol 50 (1) ◽  
pp. 494-494
Author(s):  
Phil Grgurich ◽  
Lily Vitali ◽  
Tara Lech ◽  
Leah Mangini

2015 ◽  
Vol 45 (1) ◽  
pp. 90-93 ◽  
Author(s):  
Christina Routsi ◽  
Stelios Kokkoris ◽  
Evangelia Douka ◽  
Foteini Ekonomidou ◽  
Ilias Karaiskos ◽  
...  

Author(s):  
Anne Godier ◽  
Darless Clausse ◽  
Simon Meslin ◽  
Myriame Bazine ◽  
Elodie Lang ◽  
...  

2016 ◽  
Vol 12 (1) ◽  
pp. 63-67
Author(s):  
Masuma Ahmed Salsabil ◽  
Md Manirul Islam ◽  
Jannatul Ferdous ◽  
Shameem Montasir Hossain

Introduction: Haematological status is an important parameter for the management of critically ill patients. Objective: To see the status of the haematological changes of critically ill patients admitted in CMH, Dhaka. Materials and Methods: This cross sectional study was conducted in the Department of Haematology of Armed Forces Institute of Pathology and Intensive Care Unit of Combined Military Hospital, Dhaka from March 2014 to September 2014 for a period of 6 months. All the patients who were admitted in the Intensive Care Unit of Combined Military Hospital, Dhaka at any age with either sex were included in this study. The complete blood count and coagulation parameters were considered and data sheet was prepared. Results: A total number of 862 samples were analyzed. Male female ratio was 1.8:1. Anaemia was found in 43.2% patients and 22.3% patients had Erythrocytosis. Normocytic Normochromic Anaemia was the most common morphological subtype of Anaemia. 13.8% patients had Leukopenia and 55.1% patients had Leukocytosis; 7.3% patients had Neutropenia and 49.0% patients had Neutrophilia. 10.0% patients had Eosinophilia. 26.3% patients had Lymphopenia and 14.7% patients had Lymphocytosis. 39.1% patients had Thombocytopenia and 20.3% patients had Thrombocytosis. MCV (Mean Corpuscular Volume) was below normal in 36.5% patients and was above normal in 16.8% patients. MCH (Mean Corpuscular Hemoglobin) was below normal among 49.7% patients and 11.1% patients above normal. MCHC (Mean Corpuscular Haemoglobin Content) was below normal level in 61.8% patients and 3.7% patients had above normal. Abnormal coagulation parameters that is prolonged PT, APTT and raised FDP was found in 36.3%, 18.6% and 35.8% patients. Conclusion: Critically ill patients were suffering from anaemia and thrombocytopenia with significant changes in other blood cells counts and coagulation parameters. Journal of Armed Forces Medical College Bangladesh Vol.12(1) 2016: 63-67


Blood ◽  
2011 ◽  
Vol 118 (21) ◽  
pp. 3293-3293
Author(s):  
Jerrold H Levy ◽  
Nigel S. Key ◽  
Andrew F Shorr ◽  
Michael A Kurz ◽  
Victor J. Marder

Abstract Abstract 3293 Background: Prophylaxis for venous thromboembolism (VTEP) is recommended for critically ill patients with limited mobility or those undergoing major surgery. Commonly used agents are heparin-based therapies (unfractionated or low-molecular-weight heparin (H); fondaparinux) which are of limited utility in patients with thrombocytopenia (TCP) due to concerns about bleeding risk and the possibility of heparin-induced thrombocytopenia (HIT). The DESIRABLE trial was designed to examine the safety profile of desirudin (Iprivask®, recombinant hirudin), the only parenteral heparin alternative approved for VTEP in the US, in a broad range of perioperative and critically ill patients requiring VTEP. DESIRABLE was a multicenter, open-label, single-arm study which enrolled 516 subjects at 19 centers. Desirudin was administered for as long as clinically required at 15 mg Q12H SC. Patients with uncontrolled bleeding were excluded. The primary endpoint was Major Bleeding; secondary endpoints included incidence of new symptomatic VTE. The present analysis was performed to evaluate the safety profile of desirudin in DESIRABLE patients who were thrombocytopenic at enrollment. Methods: Case report forms were reviewed to identify subjects with TCP, defined as having a platelet count of <150 × 106/mL. Demographic characteristics, incidence of Major Bleeding, VTE, and serious adverse events were determined for comparison to the overall cohort. Results: Analysis of case report forms identified 93 subjects with TCP (<150 × 106/mL), 50 (54%) of whom had a platelet count <100 × 106/mL. Compared to subjects with normal platelet counts, TCP subjects were older (median age 66 vs. 59), more likely to be male (65% vs 34%) and underweight (BMI <25: 37% vs 23%), and less likely to be morbidly obese (BMI >35, 14% vs 31%). TCP subjects were also more likely to have a recent (<3 months or concurrent) history of cardiac surgery (CABG or valve, 24% vs 3%), coronary artery disease (47% vs 20%), congestive heart failure (18% vs 7%) and/or atrial fibrillation (16% vs 4%). HIT was suspected in 27 (29%) of TCP subjects, although the presence of HIT was not confirmed by SRA testing. No subjects had clinical evidence of thrombosis at enrollment. Treatment duration was similar between TCP subjects and the overall cohort (5.1±3.3 days vs 4.9±3.2 days, p=NS). The incidence of new VTE was similar between TCP and non-TCP subjects: 2 (2.2%) TCP subjects developed a VTE vs 6 of 423 non-TCP subjects (1.4%, p=NS). There were no bleeding events meeting criteria for the Primary Endpoint in either group. Serious adverse events occurred in 16 (17%) TCP subjects, all considered unrelated to study drug. Serious adverse events were reported in 64 (15%) non-TCP subjects, 5 of which were considered “possibly related” to study drug. Conclusions: DESIRABLE demonstrated the clinical utility and safety of desirudin in a broad population of critically ill perioperative and medical patients. The present subanalysis indicates that this finding holds true for hospitalized TCP patients, suggesting that desirudin may be a useful alternative for VTE prophylaxis patients for whom HIT is suspected or heparin-based therapies are considered inappropriate. Additional randomized trials in TCP patients are needed to confirm these findings. Disclosures: Levy: Canyon Pharmaceuticals: Consultancy. Off Label Use: Desirudin is approved for VTE prophylaxis following elective hip arthroplasty. Data presented may describe use of desirudin for VTE prophylaxis in patients who did not undergo total hip arthroscopy. Kurz:Canyon Pharmaceuticals: Employment. Marder:Canyon Pharmaceuticals: Clinical Trial Steering Committee.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lorenzo Falsetti ◽  
Matteo Rucco ◽  
Marco Proietti ◽  
Giovanna Viticchi ◽  
Vincenzo Zaccone ◽  
...  

AbstractCritically ill patients affected by atrial fibrillation are at high risk of adverse events: however, the actual risk stratification models for haemorrhagic and thrombotic events are not validated in a critical care setting. With this paper we aimed to identify, adopting topological data analysis, the risk factors for therapeutic failure (in-hospital death or intensive care unit transfer), the in-hospital occurrence of stroke/TIA and major bleeding in a cohort of critically ill patients with pre-existing atrial fibrillation admitted to a stepdown unit; to engineer newer prediction models based on machine learning in the same cohort. We selected all medical patients admitted for critical illness and a history of pre-existing atrial fibrillation in the timeframe 01/01/2002–03/08/2007. All data regarding patients’ medical history, comorbidities, drugs adopted, vital parameters and outcomes (therapeutic failure, stroke/TIA and major bleeding) were acquired from electronic medical records. Risk factors for each outcome were analyzed adopting topological data analysis. Machine learning was used to generate three different predictive models. We were able to identify specific risk factors and to engineer dedicated clinical prediction models for therapeutic failure (AUC: 0.974, 95%CI: 0.934–0.975), stroke/TIA (AUC: 0.931, 95%CI: 0.896–0.940; Brier score: 0.13) and major bleeding (AUC: 0.930:0.911–0.939; Brier score: 0.09) in critically-ill patients, which were able to predict accurately their respective clinical outcomes. Topological data analysis and machine learning techniques represent a concrete viewpoint for the physician to predict the risk at the patients’ level, aiding the selection of the best therapeutic strategy in critically ill patients affected by pre-existing atrial fibrillation.


Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 2436-2436 ◽  
Author(s):  
Cat R Murphree ◽  
Joseph J Shatzel ◽  
Sven R Olson

Background: Extra Corporeal Membrane Oxygenation (ECMO) is being used with increasing frequency in critically ill patients requiring cardiopulmonary life-support. The combined effects of critical illness, ECMO use, and systemic anticoagulation to prevent circuit thrombosis, induces a complex milieu of coagulation, fibrinolytic and platelet derangements. Both bleeding and clotting are expectedly the most frequent and dangerous complications of ECMO; in patients with active or high risk of major bleeding, the prospect of anticoagulation-free ECMO is attractive, although data is limited on the safety and efficacy of this practice. In order to better define the safety of anticoagulation-free ECMO, we performed the following systematic review. Methods: We searched Ovid Medline for publications reporting use of ECMO without therapeutic-dose systemic anticoagulation of any kind for a minimum of 24 hours in adult patients, between the years 1977 to 2019. Studies using general venous thromboembolism prophylaxis were included. We included randomized control trials, cohort studies, case series, and case-control studies that contained sufficient patient-level data. Preclinical studies, meta-analyses, systematic reviews, narrative reviews, and reports involving patients under 18 years of age were excluded. Outcomes of interest collected included all bleeding and thrombotic events involving the patient or circuitry. Results: 443 studies were identified through our search. After removal of duplicates, 441 records were screened. After exclusion, 23 full-text articles were assessed for eligibility. 2 of the full text articles were further excluded due to ambiguity regarding the time patients were off of anticoagulation. 21 studies were ultimately included in the systematic review. These included 8 case series and 13 individual case reports. All were single center studies. Data for a total of 154 patients among all 21 studies analyzed were reviewed. 96 adults were treated with veno-venous (vv) ECMO, and 58 were treated with veno-arterial (va) ECMO. Indications for ECMO included acute respiratory distress syndrome, diffuse alveolar hemorrhage, traumatic brain injury, intra-cranial hemorrhage, and lung transplant. Median total time on anticoagulant-free ECMO was 11.85 days among individual case reports, and 7.03 days for patients included in case series. Of the 154 patients, 9 (5.8%) had new, severe bleeding events, 13 (8.4%) experienced minor bleeding, and 15 (9.7%) were re-explored for bleeding. No new cases of intracranial hemorrhage were seen during ECMO without systemic anticoagulation. 15 patients (9.5%) developed circuitry thrombosis, and 6 (3.9%) developed systemic venous or arterial thrombosis. Full results are listed in Table 1. Conclusions: Our systematic review found that anticoagulant-free ECMO was associated with relatively low rates of major bleeding, circuitry and patient thrombosis; the frequency of these events (5.8%, 9.5%, 3.9%, respectively) is similar, if not lower, than historically-reported rates in ECMO with anticoagulation (at least 16%, 10% and 18%, respectively). Of note, no new instances of intracranial hemorrhage were found, which is crucially important given the high associated mortality. Though based on a small number of patients, our review is valuable as it provides a new perspective on the prevailing theory that systemic anticoagulation is an absolutely necessary component of ECMO to prevent thrombosis. Evolving ECMO technology and improved overall care of critically-ill patients may be contributing to a less thrombotic blood microenvironment, which is typically attributed to inflammation, contact pathway and platelet activation. We acknowledge several limitations of our review, including the identification and inclusion of only non-randomized, retrospective studies, variable definitions and reporting of thrombotic and bleeding events, and likely non-negligible differences in ECMO technology, all of which precludes any definitive conclusions. Our findings are, however, hypothesis-generating; prospective, randomized trials would help better clarify the safety and efficacy of ECMO without anticoagulation, and address a unmet medical need by refining anticoagulation indications for critically ill patients on ECMO. Disclosures Shatzel: Aronora, Inc.: Consultancy.


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