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Hypercoagulability and Anticoagulation in Patients With COVID-19 Requiring Renal Replacement Therapy

2020; Elsevier BV; Volume: 5; Issue: 9 Linguagem: Inglês

10.1016/j.ekir.2020.07.024

2468-0249

Lara N. Roberts, Kate Bramham, Claire C. Sharpe, Roopen Arya,

COVID-19 and healthcare impacts

Severe acute respiratory coronavirus 2 (SARS-CoV2) and the resulting acute respiratory distress syndrome (coronavirus disease 2019 [COVID-19]) is responsible for a worldwide pandemic, with more than 10 million cases reported as of June 28, 2020.S1 Although severe disease requiring hospitalization is characterized by pneumonia and respiratory failure, a significant proportion also develop acute kidney injury. Within critical care admissions with COVID-19, 16% to 35% are reported as requiring renal replacement therapy (RRT).1Hirsch J.S. Ng J.H. Ross D.W. et al.Acute kidney injury in patients hospitalized with COVID-19.Kidney Int. 2020; 98: 209-218Abstract Full Text Full Text PDF PubMed Scopus (912) Google Scholar–3Argenziano M.G. Bruce S.L. Slater C.L. et al.Characterization and clinical course of 1000 patients with coronavirus disease 2019 in New York: retrospective case series.BMJ. 2020; 369: m1996Crossref PubMed Scopus (477) Google Scholar,S2,S3 There is increasing recognition of an associated coagulopathy in hospitalized patients characterized by a prothrombotic state and increased venous thromboembolism. This brief review presents the current understanding of the coagulopathy associated with COVID-19, the risk of venous thrombosis, and the impact of this on management of RRT in critically ill patients with COVID-19. The complex relationship between coagulation and inflammation is well described and termed "thromboinflammation."S4 COVID-19 pneumonia is associated with pronounced changes in coagulation, with degree of coagulopathy correlating with disease severity.S5,S6 There are multiple reports of markedly elevated D-dimer, fibrinogen, Factor VIII, and von Willebrand factor in patients hospitalized with COVID-19.2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,S6,S7,S8 Progressive increase in D-dimer and fibrinogen over time are associated with intensive care unit (ICU) admission and mortality.S5,S6 Changes in coagulation markers associated with COVID-19 are presented in Table 1.2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,S2,S3,S5–S9 Early reports of disseminated intravascular coagulation have not been confirmed in subsequent case series.S5 Although these findings are presented as novel, one center compared laboratory parameters with a historic cohort with non–COVID-19 acute respiratory distress syndrome and found D-dimer was lower, fibrinogen higher, and antithrombin preserved in those with COVID-19.2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar Viscoelastic testing further confirms hypercoagulability in small cohorts of patients with COVID-19 admitted to ICUs.S8–S10 Additional markers of endothelial activation (soluble P-selectin and soluble thrombomodulin) also have been reported as increased in those with critical illness compared with those receiving ward-based care.S11 The underlying pathophysiological mechanisms remain unknown. Some suggest it is simply a consequence of acute respiratory distress syndrome, coined "pulmonary-induced coagulopathy" and others an "endotheliopathy" as a direct consequence of virus cell entry rather than a more systemic response to cytokine storm.4Connors J.M. Levy J.H. COVID-19 and its implications for thrombosis and anticoagulation.Blood. 2020; 135: 2033-2040Crossref PubMed Scopus (154) Google Scholar,S5,S12 Virus entry follows adhesion to the angiotensin-converting enzyme 2 receptor on endothelial cells, and subsequent viral replication leads to inflammatory cell infiltrate, apoptosis, and microvascular hypercoagulability, with recent autopsy reports confirming viral inclusions within endothelial cells.S13Table 1Coagulation markers in coronavirus disease 2019 (COVID-19)Coagulation markerValues in COVID-19Platelet countS2,S3,S6,S8Normal–mildly ↓Prothrombin timeS6,S8Normal–mildly ↑Fibrinogen2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,S5–S9Normal–markedly ↑D-dimer2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,S2,S3,S5–S9Normal–markedly ↑Factor V2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google ScholarMildly ↑Factor VIII2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,S5,S7,S8Normal–markedly ↑Von Willebrand antigen2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,S7,S8Normal–markedly ↑Von Willebrand activity2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,S7,S8Normal–markedly ↑ADAMTS-13S7Normal–mildly ↓Soluble P-selectinS11Normal–↑Soluble thrombomodulinS11Normal–↑AntithrombinS8,S9Normal–mildly ↓Protein CS8Normal–mildly ↑Protein S antigenS8Normal–↓↑, increased; ↓, decreased. Open table in a new tab ↑, increased; ↓, decreased. There are an increasing number of case series reporting increased rates of venous thromboembolic events (VTE), particularly in those with critical illness and in centers using screening for VTE. The first report from China was of 81 patients admitted to ICU with 4% mortality rate and 85% discharged at the time of reporting.S14 Deep vein thrombosis was reported in 25%. No thromboprophylaxis was used, and the criteria for imaging were not reported. Subsequent case series in Europe and the United States, where thromboprophylaxis is routinely used, have reported an increased incidence in patients admitted to ICU of 5% to 69%.2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,5Al-Samkari H. Karp Leaf R.S. Dzik W.H. et al.COVID and coagulation: bleeding and thrombotic manifestations of SARS-CoV2 infection.Blood. 2020; 136: 489-500Crossref PubMed Scopus (15) Google Scholar,S15–S21 Of note, the series with the lowest incidence (5% of 79 patients) excluded segmental/subsegmental pulmonary embolism (designated "immunothrombosis") and line-associated deep vein thrombosis from their primary endpoint.S15 In contrast, the series with the highest incidence involved a small number of patients (n = 25) and performed deep vein thrombosis imaging in all patients on admission and at 1 week post admission to ICU.S21 Of studies reporting all VTE following imaging based on clinical suspicion, VTE (predominantly pulmonary embolism) was confirmed in 16.7% to 35.0%, with cumulative incidence of up to 49.0% at 14 days.2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,S17,S22 The data for symptomatic VTE are summarized in Table 2.2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,5Al-Samkari H. Karp Leaf R.S. Dzik W.H. et al.COVID and coagulation: bleeding and thrombotic manifestations of SARS-CoV2 infection.Blood. 2020; 136: 489-500Crossref PubMed Scopus (15) Google Scholar,S14,S15,S17–S20,S22 Of note, 3 series also reported bleeding rates, with major bleeding complicating 2.7% to 11.0% of ICU admissions.2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,5Al-Samkari H. Karp Leaf R.S. Dzik W.H. et al.COVID and coagulation: bleeding and thrombotic manifestations of SARS-CoV2 infection.Blood. 2020; 136: 489-500Crossref PubMed Scopus (15) Google Scholar,S15Table 2Rates of venous thromboembolism in critically ill patients with coronavirus disease 2019Author, countryNCriteria for imagingProportion imagedProportion of total n with VTECumulative incidence (95% CI)Al-Samkari et al., United States5Al-Samkari H. Karp Leaf R.S. Dzik W.H. et al.COVID and coagulation: bleeding and thrombotic manifestations of SARS-CoV2 infection.Blood. 2020; 136: 489-500Crossref PubMed Scopus (15) Google Scholar144Clinical suspicionaPatients treated for VTE without diagnostic imaging not presented here.Not reported7.6%4.8%/100 patient-weeksCui et al., ChinaS1481Not reportedNot reported25% DVTNot reportedDesborough et al., EnglandS1566Clinical suspicion29% CTPA10% DVT scan15% VTE5% "true" VTEb"True" VTE excludes segmental/subsegmental PE and line-associated DVT.Not reportedHelms et al., France2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar150Clinical suspicion or increase in D-dimer66%16.6% PENot reportedKlok et al., NetherlandsS16,S22184Clinical suspicionNot reported7 dS16: 15.2% VTE14 dS22: 35.3% PE7 d: 27% (17–37)14 d: 49% (41–57)Lodigiani et al., ItalyS1761Clinical suspicion∼20%8.3% VTE27.6%Middeldorp et al., NetherlandsS1875Clinical suspicioncThirty-eight patients had DVT screening, patients with asymptomatic VTE are excluded from the table.Not reported28% VTE7 d: 15% (8–24)14 d: 28% (18–39)21 d: 24% (21–46)Poissy et al., FranceS20107Clinical suspicion31.8%22.4% VTEPE 15 d: 20.4% (13.1–28.7)Thomas et al., EnglandS1962Clinical suspicion17.7%9.6% VTE27% (10–47)CI, confidence interval; CTPA, computed tomography pulmonary angiogram; DVT, deep vein thrombosis; PE, pulmonary embolism; VTE, venous thromboembolism.a Patients treated for VTE without diagnostic imaging not presented here.b "True" VTE excludes segmental/subsegmental PE and line-associated DVT.c Thirty-eight patients had DVT screening, patients with asymptomatic VTE are excluded from the table. Open table in a new tab CI, confidence interval; CTPA, computed tomography pulmonary angiogram; DVT, deep vein thrombosis; PE, pulmonary embolism; VTE, venous thromboembolism. RRT was not been consistently reported in the preceding series, with 4 studies reporting use in 8.3% to 37.0% of the whole cohort, and one study reporting RRT use in 5 of 10 patients with VTE (VTE in 28% of patients on RRT).2Helms J. Tacquard C. Severac F. et al.High risk of thrombosis in patients with severe SARS-CoV-2 infection: a multicenter prospective cohort study.Intensive Care Med. 2020; 46: 1089-1098Crossref PubMed Scopus (1871) Google Scholar,5Al-Samkari H. Karp Leaf R.S. Dzik W.H. et al.COVID and coagulation: bleeding and thrombotic manifestations of SARS-CoV2 infection.Blood. 2020; 136: 489-500Crossref PubMed Scopus (15) Google Scholar,S15,S16,S19 Although RRT can be associated with an increased bleeding rate, the high prevalence of VTE supports the use of routine thromboprophylaxis in this patient cohort in the absence of active bleeding or severe thrombocytopenia. Acute kidney injury is common in critical illness, developing in up to half of patients, with 10% to 20% requiring RRT.S23 Continuous RRT is generally preferred in this setting due to the lesser impact on haemodynamic stability and opportunity for strict volume control. Blood exposure to the artificial circuit results in activation of coagulation and can lead to thrombosis with subsequent increased blood loss, nursing work load, and cost, in addition to adverse impacts on control of uremia, acidemia, and fluid balance.S24 Options to minimize circuit thrombosis include regional anticoagulation with citrate or heparin (unfractionated heparin [UFH] or low molecular weight heparin) or systemic anticoagulation (UFH, low molecular weight heparin, or prostacyclin). Citrate chelates calcium, a key cofactor for coagulation, thereby inhibiting its activation. Heparin anticoagulation is associated with an increased risk of major bleeding, reported as 10% to 50% in small case series.S25 Recent randomized controlled trials have demonstrated regional citrate is as effective in maintaining filter patency with reduced bleeding risk compared with systemic heparinization.S26,S27 Acute kidney injury is common in patients hospitalized with COVID, with rates of 5.1% to 78.0% reported.1Hirsch J.S. Ng J.H. Ross D.W. et al.Acute kidney injury in patients hospitalized with COVID-19.Kidney Int. 2020; 98: 209-218Abstract Full Text Full Text PDF PubMed Scopus (912) Google Scholar3Argenziano M.G. Bruce S.L. Slater C.L. et al.Characterization and clinical course of 1000 patients with coronavirus disease 2019 in New York: retrospective case series.BMJ. 2020; 369: m1996Crossref PubMed Scopus (477) Google Scholar Acute kidney injury is associated with disease severity and is more common in those critically ill. The etiology is likely multifactorial and may include dehydration, direct kidney tubular injury by viral infection, thrombotic processes, collapsing glomerulopathy, and rhabdomyolysis.S28,S29 The proportion of critically ill patients with COVID-19 requiring RRT ranges from 15% to 35%.1Hirsch J.S. Ng J.H. Ross D.W. et al.Acute kidney injury in patients hospitalized with COVID-19.Kidney Int. 2020; 98: 209-218Abstract Full Text Full Text PDF PubMed Scopus (912) Google Scholar, 3Argenziano M.G. Bruce S.L. Slater C.L. et al.Characterization and clinical course of 1000 patients with coronavirus disease 2019 in New York: retrospective case series.BMJ. 2020; 369: m1996Crossref PubMed Scopus (477) Google Scholar,S2,S3 There are anecdotal reports of RRT circuit clotting in patients with COVID-19, but few published data supporting this.6National Institute for Health and Clinical ExcellenceCOVID-19 rapid guideline: acute kidney injury in hospital.www.nice.org.uk/guidance/ng175/resources/covid19-rapid-guideline-acute-kidney-injury-in-hospital-pdf-66141962895301Date: 2020Date accessed: June 19, 2020Google Scholar In a multicenter French cohort of 150 patients, 29 were receiving RRT. Of those, 28 (97%) experienced circuit thrombosis, with reduced circuit lifespan compared with a matched historical cohort.3Argenziano M.G. Bruce S.L. Slater C.L. et al.Characterization and clinical course of 1000 patients with coronavirus disease 2019 in New York: retrospective case series.BMJ. 2020; 369: m1996Crossref PubMed Scopus (477) Google Scholar Circuit anticoagulation was not specifically reported; however, all patients received at least thromboprophylaxis with 30% receiving therapeutic heparin. In a further single-center study of 69 critically ill patients with COVID-19, 9 of 11 patients were escalated to therapeutic UFH infusions due to recurrent circuit thrombosis.S30 A third single-center study reported filter circuit clotting in 8 of 12 critically ill patients with COVID-19 on hemofiltration, despite prophylactic dose anticoagulation.5Al-Samkari H. Karp Leaf R.S. Dzik W.H. et al.COVID and coagulation: bleeding and thrombotic manifestations of SARS-CoV2 infection.Blood. 2020; 136: 489-500Crossref PubMed Scopus (15) Google Scholar This led to escalation to therapeutic anticoagulation with UFH infusion, with 2 of 8 having recurrent filter thrombosis. Of the 4 patients with no filter thrombotic event, 3 were on therapeutic UFH infusion for a preexisting thrombosis at time of initiation of hemofiltration. National guidance published in England acknowledges the hypercoagulable state associated with COVID-19 and suggests the following actions in the event of frequent circuit clotting: optimizing vascular access, consideration of alternate/combined anticoagulation strategies including combined citrate and heparin (systemic or via circuit), heparin and epoprostenol or argatroban, along with excluding other prothrombotic disorders.6National Institute for Health and Clinical ExcellenceCOVID-19 rapid guideline: acute kidney injury in hospital.www.nice.org.uk/guidance/ng175/resources/covid19-rapid-guideline-acute-kidney-injury-in-hospital-pdf-66141962895301Date: 2020Date accessed: June 19, 2020Google Scholar An Italian group recommend regional citrate as the preferred anticoagulant, and based on their experience suggest a post filter ionized calcium of 0.25 to 0.35 mmol/l (over usual target of 0.3–0.45 mmol/l) to prolong filter patency. For low molecular weight heparin, they suggest a starting dose of 3.5 mg/h with a target systemic anti-factor Xa of 0.25 to 0.35 IU/ml and for UFH 10 to 14 unit/kg per hour targeting an activated partial thromboplastin time (APTT) of 60 to 90 seconds. They acknowledge these targets as indicators based on their experience with the need to individually tailor. Approaches to anticoagulation to prolong haemofilter patency are summarized in Figure 1.7Ronco C. Reis T. Husain-Syed F. Management of acute kidney injury in patients with COVID-19.Lancet Respir Med. 2020; 8: 738-742Abstract Full Text Full Text PDF PubMed Scopus (381) Google Scholar Monitoring UFH with APTT in any inflammatory state may not reflect underlying anticoagulant activity. APTT measures the time to initial clot formation following addition of calcium and an activator of the intrinsic pathway. High Factor VIII and fibrinogen can therefore shorten the APTT in vitro, without affecting the in vivo anticoagulant activity measured with an anti-Factor Xa assay.S31 Other studies demonstrate using an anti-Factor Xa assay facilitates reaching target anticoagulant activity sooner with fewer infusion rate changes.S32,S33 Centers have therefore moved toward monitoring UFH with an anti-Factor Xa assay.S34 Heparin resistance, defined as high-dose UFH (>35,000 units per day to achieve target APTT ratio or inability to do so) is a recognized phenomenon and is often due to raised coagulation factors such as Factor VIII and/or fibrinogen, and/or reduced antithrombin. Small case series describe heparin resistance in critically ill patients with COVID-19 and this may contribute to circuit issues. Beun et al.S35 described 4 patients with COVID-19 infection with heparin resistance (from 75 patients admitted to ICU; the number on therapeutic anticoagulation was not reported). Factor VIII, fibrinogen, and D-dimer were markedly high with normal antithrombin activity. A further group studied 69 critically ill patients with COVID-19 and reported evidence of heparin resistance in 8 of 10 patients on therapeutic UFH infusions.S30 Argatroban has been proposed as an alternate strategy given it exerts its anticoagulant effect independent of antithrombin, by direct thrombin inhibition. A small case series of 10 critically ill patients with COVID-19 confirmed thrombosis and heparin resistance were switched to argatroban therapy following confirmation of antithrombin deficiency.S36 No patient had a further thrombotic event but 3 patients experienced bleeding complications (hemorrhagic stroke transformation, rectal artery bleeding requiring embolization, and haemorrhoidal bleeding resolved on temporary interruption of argatroban infusion). Recurrent circuit thrombosis not only affects individual patient clinical course as outlined previously but may also affect provision of effective hemofiltration in the ICU setting. Because of demand at the peak of the pandemic, many centers were forced to adapt hemofiltration protocols to expand RRT capacity. Optimizing circuit anticoagulation to prolong circuit lifespan is an important measure to preserve consumables. Other strategies recommended included increasing procurement supply (but avoiding hoarding), reducing blood flow to minimize citrate consumption, moderating intensity to conserve fluids, or running accelerated filtration at higher clearance to increase number of patients per machine (providing there are no issues with consumable supply).S37 Early transition to intermittent hemodialysis or peritoneal dialysis also should be considered in those patients who are deemed suitable.S38 Multiple international guidelines now recommend all patients hospitalized with COVID-19 receive thromboprophylaxis unless contraindicated.8Spyropoulos A.C. Levy J.H. Ageno W. et al.Scientific and Standardization Committee Communication: clinical guidance on the diagnosis, prevention and treatment of venous thromboembolism in hospitalized patients with COVID-19.J Thromb Haemost. 2020; 8: 1859-1864Crossref Scopus (500) Google Scholar,9Moores LK, Tritschler T, Brosnahan S, et al. Prevention, diagnosis and treatment of venous thromboembolism in patients with COVID-19: CHEST Guideline and Expert Panel Report [e-pub ahead of print]. Chest. https://doi.org/10.1016/j.chest.2020.05.559. Accessed June 6, 2020.Google Scholar Randomized controlled trials to evaluate escalated dosing for thromboprophylaxis are in progress, which will enhance prevention of COVID-19–associated VTE (currently 15 studies listed on ClinicalTrials.gov, accessed June 28, 2020). Meta-analyses of RRT anticoagulation strategies and improved understanding of the complex pathophysiology of this novel coagulopathic state will be needed to determine the optimal approach for managing critically unwell patients with COVID-19. CS has been a consultant for Novartis Pharmaceuticals and speaker for Napp Pharmaceuticals. All the other authors declared no competing interests. Download .pdf (.53 MB) Help with pdf files Supplementary File (PDF)