Publikasi Scopus 2024 per tanggal 31 Mei 2024 (409 artikel)

Rasyid A.; Harris S.; Kurniawan M.; Mesiano T.; Hidayat R.; Wiyarta E.
Rasyid, Al (56703146700); Harris, Salim (55325116600); Kurniawan, Mohammad (57196001182); Mesiano, Taufik (57204830976); Hidayat, Rakhmad (57225289998); Wiyarta, Elvan (57221521342)
56703146700; 55325116600; 57196001182; 57204830976; 57225289998; 57221521342
Predictive value of admission D-dimer levels in patient with acute ischaemic stroke and COVID-19: a second-wave prospective cohort study
2024
BMJ Open
14
4
e077500
0
Department of Neurology, Faculty of Medicine, Universitas Indonesia-Dr Cipto Mangunkusumo National Hospital, Jakarta, Indonesia
Rasyid A., Department of Neurology, Faculty of Medicine, Universitas Indonesia-Dr Cipto Mangunkusumo National Hospital, Jakarta, Indonesia; Harris S., Department of Neurology, Faculty of Medicine, Universitas Indonesia-Dr Cipto Mangunkusumo National Hospital, Jakarta, Indonesia; Kurniawan M., Department of Neurology, Faculty of Medicine, Universitas Indonesia-Dr Cipto Mangunkusumo National Hospital, Jakarta, Indonesia; Mesiano T., Department of Neurology, Faculty of Medicine, Universitas Indonesia-Dr Cipto Mangunkusumo National Hospital, Jakarta, Indonesia; Hidayat R., Department of Neurology, Faculty of Medicine, Universitas Indonesia-Dr Cipto Mangunkusumo National Hospital, Jakarta, Indonesia; Wiyarta E., Department of Neurology, Faculty of Medicine, Universitas Indonesia-Dr Cipto Mangunkusumo National Hospital, Jakarta, Indonesia
Objectives This study aimed to evaluate the predictive value of admission D-dimer levels for in-hospital mortality in patients with COVID-19 and acute ischaemic stroke. Design Cohort (prospective). Setting Tertiary referral hospital in the capital city of Indonesia conducted from June to December 2021. Participants 60 patients with acute ischaemic stroke and COVID-19 were included. Patients were classified into D-dimer groups (low and high) according to a 2 110 ng/ mL cut-off value, determined via receiver operating characteristic analysis. Primary and secondary outcome measures The primary outcome was in-hospital mortality, with admission D-dimer levels as the major predictor. Secondary outcomes included associations between other demographic and clinical variables and the admission D-dimer value. Kaplan-Meier method was used to carry out survival analysis, with univariable and multivariable Cox regression performed to assess the association of D-dimer levels and other confounding variables (including demographic, clinical and laboratory parameters) with in-hospital mortality. Results The findings demonstrated an association between elevated admission D-dimer levels (≥2 110 ng/ mL) and an increased likelihood of death during hospitalisation. The adjusted HR was 14.054 (95% CI 1.710 to 115.519; p=0.014), demonstrating an increase in mortality risk after accounting for confounders such as age and diabetes history. Other significant predictors of mortality included a history of diabetes and increased white blood cell count. Conclusions Admission D-dimer levels may be a useful predictive indicator for the likelihood of death during hospitalisation in individuals with COVID-19 and acute ischaemic stroke. © Author(s) (or their employer(s)) 2024.
Biomarkers; Brain Ischemia; COVID-19; Diabetes Mellitus; Fibrin Fibrinogen Degradation Products; Hospitalization; Humans; Ischemic Stroke; Prognosis; Prospective Studies; Retrospective Studies; Stroke; D dimer; fibrinogen; hemoglobin; biological marker; fibrin degradation product; fibrin fragment D; activated partial thromboplastin time; acute ischemic stroke; adult; Article; cohort analysis; confounding variable; controlled study; coronavirus disease 2019; female; follow up; glucose blood level; human; in-hospital mortality; international normalized ratio; length of stay; leukocyte count; major clinical study; male; middle aged; platelet count; predictive value; prothrombin time; radiodiagnosis; survival analysis; tertiary care center; treatment outcome; brain ischemia; cerebrovascular ac
BMJ Publishing Group
20446055
38580372
Article
Q1
1059
3829