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1.
Br J Haematol ; 205(2): 404-405, 2024 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-38922871

RESUMO

Historically understudied and regarded as a mild type of sickle cell disease, HbSC can be associated with significant, progressive complications. Prospective studies are urgently needed to address treatment gaps for HbSC disease. Commentary on: Nelson et al. The clinical spectrum of HbSC sickle cell disease-not a benign condition. Br J Haematol 2024;205:653-663.


Assuntos
Doença da Hemoglobina SC , Humanos , Doença da Hemoglobina SC/complicações , Anemia Falciforme/sangue
2.
Pediatr Crit Care Med ; 25(7): e328-e337, 2024 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-38713010

RESUMO

OBJECTIVES: The activated partial thromboplastin time (aPTT) is the most frequently used monitoring assay for bivalirudin in children and young adults on mechanical circulatory support including ventricular assist devices (VADs) and extracorporeal membrane oxygenation (ECMO). However, intrinsic variability of the aPTT complicates management and risks bleeding or thrombotic complications. We evaluated the utility and reliability of a bivalirudin-calibrated dilute thrombin time (Bival dTT) assay for bivalirudin monitoring in this population. DESIGN: Retrospective analysis of clinical data (including aPTT, dilute thrombin time [dTT]) and results of residual plasma samples from VAD patients were assessed in two drug-calibrated experimental assays. One assay (Bival dTT) was validated for clinical use in VAD patients, and subsequently used by clinicians in ECMO patients. Pearson correlation and simple linear regression were used to determine R2 correlation coefficients between the different laboratory parameters using Statistical Package for Social Sciences (Armonk, NY). SETTING: ICUs at Cincinnati Children's Hospital Medical Center. SUBJECTS: Children on VAD or ECMO support anticoagulated with bivalirudin. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: One hundred fifteen plasma samples from 11 VAD patients were analyzed. Both drug-calibrated experimental assays (anti-IIa and Bival dTT) showed excellent correlation with each other ( R2 = 0.94) and with the dTT ( R2 = 0.87), but poor correlation with aPTT ( R2 = 0.1). Bival dTT was selected for validation in VAD patients. Subsequently, clinically ordered results (105) from 11 ECMO patients demonstrated excellent correlation between the Bival dTT and the standard dTT ( R2 = 0.86) but very poor correlation with aPTT ( R2 = 0.004). CONCLUSIONS: APTT is unreliable and correlates poorly with bivalirudin's anticoagulant effect in ECMO and VAD patients. A drug-calibrated Bival dTT offers superior reliability and opportunity to standardize results across institutions. Additional studies are needed to determine an appropriate therapeutic range and correlation with clinical outcomes.


Assuntos
Antitrombinas , Oxigenação por Membrana Extracorpórea , Coração Auxiliar , Hirudinas , Fragmentos de Peptídeos , Proteínas Recombinantes , Humanos , Hirudinas/administração & dosagem , Oxigenação por Membrana Extracorpórea/métodos , Estudos Retrospectivos , Fragmentos de Peptídeos/sangue , Fragmentos de Peptídeos/uso terapêutico , Criança , Masculino , Feminino , Pré-Escolar , Proteínas Recombinantes/uso terapêutico , Proteínas Recombinantes/administração & dosagem , Antitrombinas/uso terapêutico , Tempo de Tromboplastina Parcial , Adolescente , Lactente , Reprodutibilidade dos Testes , Monitoramento de Medicamentos/métodos
3.
J Artif Organs ; 2024 Apr 06.
Artigo em Inglês | MEDLINE | ID: mdl-38581568

RESUMO

Critically ill pediatric patients supported on ventricular assist devices (VADs) are increasingly being anticoagulated on bivalirudin, but with difficulty monitoring anticoagulation. Activated partial thromboplastin time (aPTT) has recently been shown to poorly correlate with bivalirudin plasma concentrations, while dTT had excellent correlation. However, aPTT is the more common monitoring test and dTT testing is rarely used. In addition, effects of frequent clinical VAD scenarios (such as inflammation) on the accuracy of aPTT and dTT testing remains uncertain. We reviewed the effects of clinical scenarios (infection/inflammation, chylothorax, and steroids administration) on anticoagulation monitoring in 10 pediatric VAD patients less than 3 years at Cincinnati Children's Hospital Medical Center from 10/27/2020 to 5/6/2022 using bivalirudin for anticoagulation. There were 16 inflammation/infection, 3 chylothorax, and 6 steroids events. Correlation between dTT and aPTT was significantly lower after infection/inflammation, with dTT increasing prior to inflammation/infection while aPTT remained unchanged. In addition, steroids are administered to VAD patients to reduce inflammation and thus additionally stabilize anticoagulation. However, this anticoagulation stabilization effect was reflected more accurately by dTT compared to aPTT. In children requiring VAD support utilizing bivalirudin anticoagulation, inflammation/infection is a common occurrence resulting in anticoagulation changes that may be more accurately reflected by dTT as opposed to aPTT.

4.
J Thromb Haemost ; 22(7): 2081-2092, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38642706

RESUMO

In response to growing recognition that nonadherence prevents children, adolescents, and young adults from achieving the therapeutic benefits of anticoagulant medication, the International Society on Thrombosis and Haemostasis Scientific and Standardization Committee Subcommittee on Pediatric and Neonatal Thrombosis and Hemostasis convened a working party on medication adherence. The primary aim of this article was to synthesize recommendations from the larger adherence science literature to provide guidance regarding the classification, collection, and interpretation of anticoagulation adherence data. The secondary aim of this article was to evaluate the degree to which trials published from 2013 to 2023 adhered to these guidance recommendations. As less than half of all trials reported on adherence and none included all recommended elements, the proposed International Society on Thrombosis and Haemostasis Scientific and Standardization Committee guidance has the potential to enhance the rigor and reproducibility of pediatric anticoagulant research.


Assuntos
Anticoagulantes , Ensaios Clínicos como Assunto , Hemostasia , Adesão à Medicação , Trombose , Humanos , Anticoagulantes/uso terapêutico , Anticoagulantes/efeitos adversos , Criança , Trombose/prevenção & controle , Trombose/tratamento farmacológico , Trombose/etiologia , Adolescente , Recém-Nascido , Pré-Escolar , Hemostasia/efeitos dos fármacos , Lactente , Projetos de Pesquisa/normas , Fatores Etários , Fidelidade a Diretrizes
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