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2.
Front Med (Lausanne) ; 10: 1103842, 2023.
Article in English | MEDLINE | ID: covidwho-2278714

ABSTRACT

Introduction: Variable D-dimer trends during hospitalization reportedly result in distinct in-hospital mortality. In this multinational case series from the first and second waves, we show the universality of such D-dimer trends. Methods: We reviewed 405 patients with COVID-19 during the first wave admitted to three institutions in the United States, Italy, and Colombia, and 111 patients admitted to the U.S. site during the second wave and 55 patients during the third wave. D-dimer was serially followed during hospitalization. Results: During the first wave, 66 (15%) patients had a persistently-low pattern, 33 (8%) had early-peaking, 70 (16%) had mid-peaking, 94 (22%) had fluctuating, 30 (7%) had late-peaking, and 112 (26%) had a persistently-high pattern. During the second and third waves, similar patterns were observed. D-dimer patterns were significantly different in terms of in-hospital mortality similarly in all waves. Patterns were then classified into low-risk patterns (persistently-low and early-peaking), where no deaths were observed in both waves, high-risk patterns (mid-peaking and fluctuating), and malignant patterns (late-peaking and persistently-high). Overall, D-dimer trends were associated with an increased risk for in-hospital mortality in the first wave (overall: HR: 1.73) and stayed the same during the second (HR: 1.67, p < 0.001) and the third (HR: 4.4, p = 0.001) waves. Conclusion: D-dimer behavior during COVID-19 hospitalization yielded universal categories with distinct mortality risks that persisted throughout all studied waves of infection. Monitoring D-dimer behavior may be useful in the management of these patients.

5.
Rheumatology (Oxford) ; 61(SI2): SI136-SI142, 2022 06 28.
Article in English | MEDLINE | ID: covidwho-1784398

ABSTRACT

OBJECTIVES: Patients with APS and triple-positive for aPL are at high risk of recurrent events. As COVID-19 and COVID-19 vaccination may induce thrombotic complications, the objective of the study was to assess the course of COVID-19 and adverse events after vaccination in these patients. METHODS: This is a nationwide multicentre survey conducted in nine APS referral centres by means of a questionnaire. Included patients are thrombotic APS with triple-positive aPL confirmed 12 weeks apart. Reference specialist physicians used a four-graded scale of severity for COVID-19 [from 0 (asymptomatic) to 3 (hospitalization in intensive care unit)] and a six-graded scale for adverse reactions to vaccination [from 0 (transient local injection site sign/symptoms) to 5 (potentially life-threatening reactions)]. Outcomes were considered within a 30-day period. RESULTS: Out of 161 patients interviewed, 18 (11%) had COVID-19. All of them fully recovered without any progression to severe disease nor thromboembolic event. A total of 146 patients received the first (92%) and 129 (80%) the second dose of vaccine; side effects were minimal and, in most cases (83% after the first and 68% after the second vaccination) limited to a sore arm. Fifteen patients (9%) were unvaccinated. Most of them raised doubts on the need for vaccination, complained of poor safety and in general were reluctant about COVID-19 vaccination. CONCLUSION: Patients with triple-positive thrombotic APS did not suffer from severe COVID-19 outcomes. Importantly, COVID-19 vaccination was well tolerated. These data may reassure patients and physicians and contribute to reducing hesitancy in unvaccinated patients.


Subject(s)
Antiphospholipid Syndrome , COVID-19 , Thrombosis , Antibodies, Antiphospholipid , Antiphospholipid Syndrome/complications , COVID-19/complications , COVID-19/epidemiology , COVID-19/prevention & control , COVID-19 Vaccines/adverse effects , Humans , Surveys and Questionnaires , Thrombosis/epidemiology , Thrombosis/etiology , Vaccination/adverse effects
6.
Front Immunol ; 12: 741589, 2021.
Article in English | MEDLINE | ID: covidwho-1441110

ABSTRACT

Autoantibodies targeting prothrombin (aPT) can be found in antiphospholipid syndrome (APS) patients. However, their detection has proven difficult to standardize. Here, we developed a new ELISA assay to improve the identification of aPT and compared its performance with currently available anti-phosphatidylserine/prothrombin antibodies (aPS/PT) and autoantibodies targeting prothrombin bound to the plastic plate (aPT-A) assays using a cohort of 27 APS patients at high risk of thrombosis. We generated a novel prothrombin variant, ProTS525A-Biot, carrying an artificial tag at the C-terminus suitable for site-specific biotinylation and added the mutation S525A to improve stability. ProTS525A-Biot was immobilized to neutravidin-coated plates at the desired density and with a defined orientation, i.e., pointing the N-terminal fragment-1 toward the solvent. Antibodies against ProTS525A-Biot (aPT-Bio) were found in 24 out of 27 triple-positive APS patients (88%). When compared to aPS/PT and aPT-A, aPT-Bio showed an excellent linear correlation with aPS/PT (R2 = 0.85) but not with aPT-A (R2 = 0.40). Since aPS/PT but not aPT-A are an emerging biomarker of thrombosis in APS, this method may find utility for detecting pathogenic aPT in APS but also other prothrombotic conditions such as COVID-19.


Subject(s)
Antiphospholipid Syndrome/blood , Enzyme-Linked Immunosorbent Assay/methods , Immunoglobulin G/blood , Prothrombin/immunology , Antiphospholipid Syndrome/immunology , Biotinylation , Humans , Immunoglobulin G/immunology , Mutation , Phosphatidylserines/immunology , Prothrombin/genetics , Risk , Thrombosis
7.
Int J Cardiol ; 329: 266-269, 2021 04 15.
Article in English | MEDLINE | ID: covidwho-971117

ABSTRACT

BACKGROUND: Coronavirus disease 2019 (COVID-19) global pandemic has strikingly high mortality rate with hypercoagulability state being part of the imputed mechanisms. We aimed to compare the rates of in hospital mortality in propensity score matched cohorts of COVID-19 patients in chronic anticoagulation versus those that were not. METHODS: In this population-based study in the Veneto Region, we retrospectively reviewed all patients aged 65 years or older, with a laboratory-confirmed COVID-19 diagnosis. We compared, after propensity score matching, those who received chronic anticoagulation for atrial fibrillation with those who did not. RESULTS: Overall, 4697 COVID-19 patients fulfilled inclusion criteria, and the propensity score matching yielded 559 patients per arm. All-cause mortality rate ratio was significantly higher among non-anticoagulated patients (32.2% vs 26.5%, p = 0.036). On time to event analysis, all-cause mortality was found lower among anticoagulated patients, although the estimate was not statistically significant. (HR 0.81, 95%CI 0.65-1.01, p = 0.054). CONCLUSION: Among elderly patients with COVID-19, those on chronic oral anticoagulant treatment for atrial fibrillation seem to be at lower risk of all-cause mortality compared to their propensity score matched non-anticoagulated counterpart. This finding needs to be confirmed in further studies.


Subject(s)
Anticoagulants/administration & dosage , COVID-19/complications , Population Surveillance , Propensity Score , Thromboembolism/prevention & control , Administration, Oral , Aged , Aged, 80 and over , COVID-19/epidemiology , Cause of Death/trends , Female , Humans , Italy/epidemiology , Male , Retrospective Studies , Risk Factors , SARS-CoV-2 , Survival Rate/trends , Thromboembolism/epidemiology , Thromboembolism/etiology
8.
Am J Cardiovasc Drugs ; 20(6): 559-570, 2020 Dec.
Article in English | MEDLINE | ID: covidwho-910261

ABSTRACT

In patients with coronavirus disease 2019 (COVID-19), the prevalence of pre-existing cardiovascular diseases is elevated. Moreover, various features, also including pro-thrombotic status, further predispose these patients to increased risk of ischemic cardiovascular events. Thus, the identification of optimal antithrombotic strategies in terms of the risk-benefit ratio and outcome improvement in this setting is crucial. However, debated issues on antithrombotic therapies in patients with COVID-19 are multiple and relevant. In this article, we provide ten questions and answers on risk stratification and antiplatelet/anticoagulant treatments in patients at risk of/with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection based on the scientific evidence gathered during the pandemic.


Subject(s)
Anticoagulants/pharmacology , Anticoagulants/therapeutic use , COVID-19/complications , Thrombosis/etiology , Thrombosis/prevention & control , Age Factors , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Anticoagulants/administration & dosage , Anticoagulants/classification , Antiviral Agents/pharmacology , Atrial Fibrillation/drug therapy , Chemoprevention/adverse effects , Chemoprevention/methods , Disseminated Intravascular Coagulation/drug therapy , Drug Interactions , Humans , Italy , Pandemics , Risk Factors , Risk Management , SARS-CoV-2 , Severity of Illness Index , Sex Factors , Thrombosis/drug therapy , Thrombosis/physiopathology
9.
G Ital Cardiol (Rome) ; 21(7): 489-501, 2020 Jul.
Article in Italian | MEDLINE | ID: covidwho-611791

ABSTRACT

Given the high prevalence of preexisting cardiovascular diseases and the increased incidence of adverse cardiovascular events in patients hospitalized for SARS-CoV-2 infection, the identification of optimal antithrombotic approaches in terms of risk/benefit ratio and outcome improvement appears crucial in this setting. In the present position paper we collected current evidence from the literature to provide practical recommendations on the management of antithrombotic therapies (antiplatelet and anticoagulant) in various clinical contexts prevalent during the SARS-CoV-2 outbreak: in-home management of oral anticoagulant therapy; interactions between drugs used in the SARS-CoV-2 infection and antithrombotic agents; in-hospital management of antithrombotic therapies; diagnosis, risk stratification and treatment of in-hospital thrombotic complications.


Subject(s)
Atherosclerosis/drug therapy , Atherosclerosis/epidemiology , Coronavirus Infections/epidemiology , Disease Outbreaks/statistics & numerical data , Fibrinolytic Agents/therapeutic use , Pneumonia, Viral/epidemiology , Thrombosis/drug therapy , Atherosclerosis/diagnosis , Betacoronavirus , COVID-19 , Comorbidity , Coronavirus Infections/diagnosis , Evidence-Based Medicine , Female , Humans , Incidence , Italy , Male , Pandemics , Pneumonia, Viral/diagnosis , Practice Guidelines as Topic , Risk Assessment , SARS-CoV-2 , Thrombosis/diagnosis , Thrombosis/epidemiology , Treatment Outcome
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