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Covid-19 infection is associated with elevation of inflammatory markers and coagulopathy.
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Anticoagulation practice for severely ill covid-19 patients is variable among physicians.
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Inflammatory markers levels may impact anticoagulation dosages.
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Anticoagulation does not improve 28-day survival.
Abstract
Covid-19 has affected 16Millions people worldwide with 644 K death as of July 26th, 2020. It is associated with inflammation and microvascular thrombosis—anticoagulation in widely used in these patients especially in patients with elevated d-Dimers. The significance of anticoagulation in these patients is not yet established. We aim to define the anticoagulation pattern and its impact on outcomes (28-day survival, LOSICU, DVT, and PE and bleeding complications. We also observe if levels of d-Dimers affect the anticoagulation prescription.
Methods: We analyzed data of all consecutive patients with Covid-19 ARDS admitted to ICU retrospectively. The primary variable of interest was anticoagulation. The daily dose of anticoagulant medication for each patient was recorded. Survival (28-day survival), Length of stay in ICU (LOSICU), the occurrence of DVT, PE, or bleeding were primary outcome variables. We also recorded confounding factors with potential impact on clinical outcomes. We assign Patients to one of the four groups based on anticoagulant dosing during the ICU (increasing dose, decreasing dose, increase followed by a decrease, multiple changes). We analyze the effect of different anticoagulation dosing strategies on 28-day survival, LOSICU, the occurrence of DVT, PE, and bleeding. We also observe if levels of d-Dimers affect the anticoagulation prescription.
Results: The sample includes 149 patients. The most frequently used medication was subcutaneous Enoxaparin (85.2%). The Enoxaparin mean dose per day for the whole sample was 49.5 mg + 15.7 (mean + SD). There was no significant difference in doses of anticoagulants between survivors and nonsurvivors (62.8 mg + 21.7 mg vs. 61.2 mg + 25.7 mg, p 0.3). Multinomial regression showed no difference in 28-day survival among four-dose modification (increasing dose, decreasing dose, increase followed by a decrease, multiple changes). Logistic regression showed that BMI, d-Dimers, platelets, and the use of mechanical ventilation predict 28-day survival. Kaplan-Meier Survival plots for 4 anticoagulant groups showed no survival advantage for any anticoagulant strategy. Secondary outcome analysis showed that d-dimer levels significantly affect anticoagulants doses.
Conclusion: Prescription of anticoagulation is quite variable in patients admitted to ICU for Covid-19 associated ARDS. Anticoagulation dosing strategy has no significant effect on 28-day survival, LOSICU, the occurrence of DVT, PE, or bleeding.
World Health Organization Transmission of SARS-CoV-2 implications for infection prevention precautions: scientific brief, July 09th 2020. No. WHO/2019-nCoV/Sci_Brief/Transmission_modes/2020.
Transmission of SARS-CoV-2. 3. World Health Organization,
2020
Data on anticoagulation in Covid-19 positive patients is evolving. The results of the studies are variable, so is the clinical practice. Skeptical physicians used thromboprophylaxis dose. Other physicians use markers (D-Dimer level) as a guide to change the anticoagulation dose. Firm believers use therapeutic dose anticoagulation recommended to treat deep venous thrombosis (DVT) or pulmonary embolism (PE); Enoxaparin 1 mg/kg subcutaneous every 12 h. The results of different strategies on clinical outcomes are not known. We aim to determine anticoagulation practice patterns. We aim to evaluate the impact of varying anticoagulation patterns on clinical outcomes (28-day survival, LOSICU, DVT, and PE) and bleeding complications.
Methods
We included all patients with confirmed Covid-19 infection admitted to the ICU of Dubai hospital, retrospectively. We excluded patients with age <18 years and patients treated with extracorporeal membrane oxygenation therapy (ECMO). ECMO requires closely monitored larger dose anticoagulation for ECMO circuit patency. The primary variable of interest was anticoagulation. Daily doses of anticoagulant medication for each patient were recorded for all days of ICU stay. We assigned patients to one of the four groups (fixed-dose, increasing amount, decreasing dose, multiple changes in quantities). Primary clinical outcomes were 28-day survival, LOSICU, and DVT, PE, and bleeding. The secondary aim was to observe if d-Dimer levels have any impact on anticoagulant dosing. We also recorded confounding factors that may affect clinical outcomes. Demographics: age, gender, body mass index (BMI), nationality, clinical parameters, swab positivity for viral DNA, number of swabs, days to turn swab test negative, days of symptoms, presence of symptoms, cough, fever, dyspnea, gastric complaints. We also recorded diabetes, hypertension, coronary disease, renal failure, and outpatient dialysis. We recorded inpatient clinical data, including vital signs; fever, tachycardia, Blood Pressure, hypoxia, use of oxygen l/m, mechanical ventilation, vasopressors, or inpatient dialysis. Laboratory parameters: markers of inflammation (CRP, Ferritin, procalcitonin), hematologic indices (WBC, platelets count), chemistries (electrolytes), and organism culture studies, including blood cultures bacteremia, were also recorded since secondary bacterial infection with bacteria impact the clinical outcome. Anticovid-19 medication therapies; chloroquine, antivirals, and Steroids were also recorded as they may be significant confounding factors. We calculated APACHE 2 scores within 24 h of admission to the ICU to assess illness severity.
Statistical analysis
We assess four anticoagulation practice patterns (Fixed-dose, increasing dose, decreasing dose, variable quantity) with Multinomial regression analysis to determine the impact on outcome variables, 28-day survival, and LOSICU adjusting for confounding factors. We constructed Kaplan-Meier plots to detect survival differences among these four groups.
Results
The sample includes 149 patients. The sample characteristics are described in Tables 1 and 2. The practice pattern of anticoagulation is summarized in Table 3. The most frequently used medication was subcutaneous Enoxaparin (85.2%). Therefore, all anticoagulation pattern analyses include Enoxaparin only. Mean dose of enoxaparin per 24 h for sample was 49.5 mg + 15.7 (mean + SD). There was no significant difference in dose of anticoagulants between survivors and nonsurvivors (62.8 mg + 21.7 vs. 61.2 mg + 25.7, p 0.3).
Only 20% of patients have a fixed dose of anticoagulant, while 80% have changes in doses throughout the ICU stay. Logistic regression analysis for anticoagulant dose (set versus changing dosage) showed no impact on 28-day survival (p-value 0.7). Multinomial regression showed no difference in 28-day survival among four strategies of dose modification. Kaplan-Meier Survival plot showed no survival advantage for any group (Fig. 1). Only BMI, d-Dimers, platelets, and the use of mechanical ventilation predict 28-day survival (Table 4).
For LOSICU, multiple regression analyses showed that anticoagulation doses or patterns do not predict LOSICU. Factors predicting LOSICU include mechanical ventilation (P=.01) and Lactate (p=.01).
DVT, PE, and bleeding occurrences: no patients had any documentation of DVT or PE. One patient developed retroperitoneal bleeding, who also had severe thrombocytopenia and renal failure. Another patient developed significant gastrointestinal bleeding requiring gastroscopy and colonoscopies; both patients had treatment with variable anticoagulation doses. Despite the highly variable practice of anticoagulation DVT, PE and bleeding complications were exceptionally low in our sample, not enough to make any comparisons among the four groups.
Linear regression analysis between d-Dimer levels and Enoxaparin's average daily dose showed positive interaction (p=.04) (Fig. 2).
Fig. 2Relationship between d-Dimer levels and Anticoagulant daily dose.
The possible mechanism includes activation of the complement cascade and endothelial dysfunction induced by the virus, with or without the antiphospholipid syndrome, leading to Disseminated intravascular coagulation.
Nadkarni et al. compared prophylactic and therapeutic anticoagulation in 4389 COVID-19 patients and found therapeutic anticoagulation was associated with lower mortality, though not statistically significant.
Paranjpe et al. documented in their sample of mechanically ventilated Covid-19 patients (n = 395) an in-hospital reduction mortality (29.1% with therapeutic dose anticoagulation versus 62.7% in the control group).
Studies like this during pandemic peak had a significant impact on anticoagulation practice.
Our clinical observation suggests that anticoagulation prescription is highly variable in patients treated for ARDS secondary to Covid-19 infection. It ranges from fixed preventive dose, fixed therapeutic dose, to changing dosages often daily as a physician taking care of patients also considers a dynamic picture of risk profile as suggested by daily test results. We found none of these differences impact survival or LOSICU in our sample. BMI, d-Dimers, platelets, and the use of mechanical ventilation were the only factors found to affect survival. Only mechanical ventilation and lactate level predicted LOSICU. We observe significant differences between lactate and sodium bicarbonate levels, most likely from the liberal use of sodium bicarbonate infusion in emergency department while awaiting a bed in ICU or CRRT machines for hemodialysis. Therefore, lactate results may not apply to other populations.
may be from a different population, sample size, methodology, and analysis. Studies showing survival improvement did not include several predictors of survival as we did. Therefore, it may also be possible that they may have overestimated the survival benefits. Most such studies recorded anticoagulation on admission day, only assuming it is kept constant throughout the hospital stay, which may not be accurate. We question the survival benefit attributed to anticoagulation when medication may or may not be used subsequently as our data showed a highly variable dosing pattern. Conversely, a variable dose of anticoagulation in our study may be why not translating into a survival benefit. A well-designed prospective study should be considered to address the impact of therapeutic anticoagulation on survival while considering all significant factors that are urgently required.
We found Body mass index, d-Dimers, platelets, and use of mechanical ventilation to be a significant predictor of survival in our study. Others have documented similar results.
Despite the variable practice of anticoagulation, occurrences of DVT and PE were low in our sample. Most likely because of the clinician's high threshold for studies requiring visits to the radiology department when study results were thought less likely to change the management. Therefore it is expected that we might have missed DVT and PE. Many patients in our sample eventually died of secondary bacterial infection, multiorgan failure, including respiratory and cardiac failure. Since none of the patients had post mortem studies, We can not exclude coexistent DVT and PE. Llitjos et al. reported a remarkably high incidence of DVT (56%) even with therapeutic dose anticoagulation in severe COVID‐19 patients. They studied only 26 patients with severe disease. Their patients had additional risk factors of higher BMI >30 and had coexisting medical conditions (hypertension). They also actively screened patients for asymptomatic DVT by ultrasonography.
Bleeding rates were meager in our sample, even in the therapeutic dose anticoagulation group. Others have also reported that bleeding complications, even in patients with disseminated intravascular coagulopathy, are rare in Covid-19 patients.
We found that d-dimers level effects anticoagulant doses; This suggests that d-dimer may be a significant factor for the physician in the decision for daily dosing of Enoxaparin. Additional factors could play a significant role; planning invasive procedures, platelet counts, renal impairment, prothrombin, or activated partial thromboplastin time. Tang et al. reported that prolong APTT has been reported in patients with Covid-19,
as a possible reason to avoid the use of anticoagulation at both therapeutic and prophylactic doses. D‐dimer has been suggested to guide anticoagulant treatment in COVID‐19 patients by experts
although data to support this practice in Covid-19 is lacking.
Variability in the anticoagulation pattern has not been documented before in patients with COVID-19, to our knowledge. Existed data included anticoagulation practice on admission day only, without any follow up. Our observation suggests that dose is frequently changed later depending upon clinical conditions (coagulopathy, renal impairment, thrombocytopenia). Our study highlights the importance of anticoagulation, its dose variability, and its impact (or lack of) on clinical outcomes.
We identify the following weakness of our study. A single-center study with a small sample size in a relatively young patient population comprises Asian patients, so the result may not apply to other communities. A small number of patients in each anticoagulation strategy group may lack the power to detect survival benefits, producing false-negative results.
Conclusion
Prescription of anticoagulation is quite variable in patients treated for ARDS from Covid-19 admitted to ICU. Different patterns of anticoagulant medication seem not to impact survival. Well-designed prospective studies are urgently required to define this particularly important therapeutic issue affecting millions of patients.
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