Branimir Anić
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View article: Lung function and skin fibrosis changes as predictors of survival in SSc-associated interstitial lung disease: a EUSTAR study
Lung function and skin fibrosis changes as predictors of survival in SSc-associated interstitial lung disease: a EUSTAR study Open
Objectives This study assessed how changes in lung function, skin fibrosis and digital ulceration (DU) burden predict mortality in patients with SSc-associated interstitial lung disease (SSc-ILD), the leading cause of death in SSc. Methods…
View article: POS0581 INTERSTITIAL LUNG DISEASE IN ANTI-U1RNP SYSTEMIC SCLEROSIS PATIENTS: UPDATED RESULTS FROM THE EUROPEAN SCLERODERMA TRIALS AND RESEARCH (EUSTAR) DATABASE
POS0581 INTERSTITIAL LUNG DISEASE IN ANTI-U1RNP SYSTEMIC SCLEROSIS PATIENTS: UPDATED RESULTS FROM THE EUROPEAN SCLERODERMA TRIALS AND RESEARCH (EUSTAR) DATABASE Open
View article: ABS0882 FREQUENCY OF SPONTANEOUS REPORTS OF MAJOR ADVERSE CARDIOVASCULAR EVENTS AND VENOUS THROMBOEMBOLISM IN PATIENTS ON JAK INHIBITORS COMPARED TO ADALIMUMAB
ABS0882 FREQUENCY OF SPONTANEOUS REPORTS OF MAJOR ADVERSE CARDIOVASCULAR EVENTS AND VENOUS THROMBOEMBOLISM IN PATIENTS ON JAK INHIBITORS COMPARED TO ADALIMUMAB Open
View article: ABS0747 ROLE OF ACE GENE POLYMORPHISMS IN SYSTEMIC SCLEROSIS-ASSOCIATED PERIPHERAL VASCULOPATHY AND SKIN CHANGES
ABS0747 ROLE OF ACE GENE POLYMORPHISMS IN SYSTEMIC SCLEROSIS-ASSOCIATED PERIPHERAL VASCULOPATHY AND SKIN CHANGES Open
View article: Autologous hematopoietic stem-cell transplantation in diffuse cutaneous systemic sclerosis: a single-center experience
Autologous hematopoietic stem-cell transplantation in diffuse cutaneous systemic sclerosis: a single-center experience Open
Systemic sclerosis (SSc) is a chronic autoimmune disorder characterized by multisystem involvement. Patients can be stratified into an indolent or rapidly progressive disease course. A progressive course warrants early and more aggressive …
View article: The effect of hydroxychloroquine on activities of daily living and hand function in systemic sclerosis: results from an analysis of the EUSTAR cohort
The effect of hydroxychloroquine on activities of daily living and hand function in systemic sclerosis: results from an analysis of the EUSTAR cohort Open
View article: Interstitial lung disease in anti-U1RNP systemic sclerosis patients: A European Scleroderma Trials and Research analysis
Interstitial lung disease in anti-U1RNP systemic sclerosis patients: A European Scleroderma Trials and Research analysis Open
Background: Interstitial lung disease is the leading cause of morbidity and mortality in systemic sclerosis, but it is characterized by significant heterogeneity in patient outcomes. So far, little is known about the influence of anti-U1RN…
View article: Does regression of skin thickening predict improvement of internal organ involvement and survival in patients with diffuse cutaneous systemic sclerosis? A EUSTAR analysis
Does regression of skin thickening predict improvement of internal organ involvement and survival in patients with diffuse cutaneous systemic sclerosis? A EUSTAR analysis Open
We found that regression of skin fibrosis is associated with a lower probability of lung progression and better survival at follow up. The link between the disease course of skin and lung fibrosis in SSc can help to better stratify patient…
View article: Critically Ill Patients with Newly Diagnosed Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis: Case Series and Literature Review
Critically Ill Patients with Newly Diagnosed Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis: Case Series and Literature Review Open
ANCA-associated vasculitides (AAVs) are rare diseases with a prevalence of less than 200 cases per million persons and an incidence of less than 25 cases per million person-years. Their presenting features can vary from prodromal and nonsp…
View article: Preventive effects of early immunosuppressive treatment on the development of interstitial lung disease in systemic sclerosis
Preventive effects of early immunosuppressive treatment on the development of interstitial lung disease in systemic sclerosis Open
Background Hypothesizing that early treatment yields improved prognosis, we aimed to investigate how the timing of immunosuppressive treatment relates to interstitial lung disease (ILD) development and the course of pulmonary function in s…
View article: #2963 Light chain deposition in the kidney is more frequent in patients with proliferative lupus nephritis
#2963 Light chain deposition in the kidney is more frequent in patients with proliferative lupus nephritis Open
Background and Aims Light chain deposition in the kidney is an important histologic feature having a significant role in the pathogenesis of glomerular and autoimmune diseases, including lupus nephritis (LN). However, there is no study exa…
View article: P78 Thrombotic thrombocytopenic purpura (TTP) in an SLE patient successfully treated with plasma exchange, caplacizumab and rituximab
P78 Thrombotic thrombocytopenic purpura (TTP) in an SLE patient successfully treated with plasma exchange, caplacizumab and rituximab Open
Objective Our aim was to present our first experience with the use of caplacizumab, an anti-von Willebrand factor monoclonal antibody, in an SLE patient who developed TTP. Data on the use of caplacizumab in SLE-associated TTP are scarce. M…
View article: P81 Light chain deposition in the kidneys of patients with lupus nephritis
P81 Light chain deposition in the kidneys of patients with lupus nephritis Open
Objective Light chain deposition has been shown to be an important histologic hallmark with differences in isotype, characteristics and ratio of kappa and lambda light chains having a significant role in pathobiology, pathogenesis and prog…
View article: Mimics of hereditary angioedema
Mimics of hereditary angioedema Open
Nasljedni (hereditarni) angioedem je bolest karakterizirana periodičnim, nepredvidivim oticanjima mekih tkiva različitih lokalizacija i intenziteta s najčešće samoograničavajućim tijekom trajanja, te je u pravilu posredovan bradikininom. B…
View article: Two sisters with one disease: Giant cell arteritis within one family
Two sisters with one disease: Giant cell arteritis within one family Open
Giant cell arteritis (GCA) is the most common of the vasculitides, with the incidence varying from 21.57 in Scandinavia to 7.26 per 100,000 in the rest of Europe. GCA follows a polygenic inheritance pattern and rare familiar clustering.[1-…
View article: Klonalna proliferacija T-limfocita u bolesnika sa sindromom ektodermalne displazije i imunodeficijencijom
Klonalna proliferacija T-limfocita u bolesnika sa sindromom ektodermalne displazije i imunodeficijencijom Open
View article: Cutaneous Manifestations, Clinical Characteristics, and Prognosis of Patients With Systemic Sclerosis Sine Scleroderma
Cutaneous Manifestations, Clinical Characteristics, and Prognosis of Patients With Systemic Sclerosis Sine Scleroderma Open
Importance Systemic sclerosis (SSc) sine scleroderma (ssSSc) is a subset of SSc defined by the absence of skin fibrosis. Little is known about the natural history and skin manifestations among patients with ssSSc. Objective To characterize…
View article: AB0823 A BAYESIAN APPROACH TO DETERMINE THE ROLE OF ORAL ANTICOAGULANTS FOR THE OCCURRENCE OF DIGITAL ULCERS IN SYSTEMIC SCLEROSIS – A EUSTAR OBSERVATIONAL STUDY
AB0823 A BAYESIAN APPROACH TO DETERMINE THE ROLE OF ORAL ANTICOAGULANTS FOR THE OCCURRENCE OF DIGITAL ULCERS IN SYSTEMIC SCLEROSIS – A EUSTAR OBSERVATIONAL STUDY Open
View article: AB0974 TREATMENT OF AXIAL SPONDYLOARTHRITIS WITH SECUKINUMAB: A REAL-LIFE RETROSPECTIVE COHORT STUDY
AB0974 TREATMENT OF AXIAL SPONDYLOARTHRITIS WITH SECUKINUMAB: A REAL-LIFE RETROSPECTIVE COHORT STUDY Open
View article: #6899 MICROVASCULAR LESIONS IN LUPUS NEPHRITIS
#6899 MICROVASCULAR LESIONS IN LUPUS NEPHRITIS Open
Background and Aims Microvascular lesions (MVL) can be found in the kidneys of lupus nephritis (LN) patients and might be associated with worse outcomes. There are very few studies which evaluated MVLs in these patients and we aimed to pro…
View article: Diagnosis and classification criteria of Sjögren’s syndrome
Diagnosis and classification criteria of Sjögren’s syndrome Open
sjögren's syndrome (ss) is a chronic, systemic autoimmune disease of unknown aetiology that manifests with various clinical manifestations.it is characterized by dense lymphocytic infiltration of exocrine glands which leads to functional i…
View article: Rescue treatment of severe lupus myocarditis and proliferative lupus nephritis with immunoadsorption
Rescue treatment of severe lupus myocarditis and proliferative lupus nephritis with immunoadsorption Open
View article: Long-term prophylaxis of hereditary angioedema
Long-term prophylaxis of hereditary angioedema Open
Hereditary angioedema (HAE) is a rare inherited disease characterized by recurrent attacks of painful swelling of the subcutaneous and submucosal tissues. Recurrent attacks of angioedema lead to functional impairment, reduced quality of li…
View article: Delphi-Based Consensus on Interstitial Lung Disease Screening in Patients with Connective Tissue Diseases (Croatian National-Based Study)
Delphi-Based Consensus on Interstitial Lung Disease Screening in Patients with Connective Tissue Diseases (Croatian National-Based Study) Open
The aim of this study was to develop a Croatian Delphi-based expert consensus for screening interstitial lung disease (ILD) associated with connective tissue disease (CTD). A systematic literature review was conducted on risk factors for t…
View article: Stratification in systemic sclerosis according to autoantibody status versus skin involvement: a study of the prospective EUSTAR cohort
Stratification in systemic sclerosis according to autoantibody status versus skin involvement: a study of the prospective EUSTAR cohort Open
View article: POSTERS
POSTERS Open
Upalna bolest crijeva s vrlo ranim početkom (VEO-IBD) predstavlja skupinu upalnih bolesti crijeva (IBD) koje se javljaju prije 6. godine života.Iako genetika ima ulogu u IBD-u bilo koje dobi, monogenska etiologija
View article: Cohort Enrichment Strategies for Progressive Interstitial Lung Disease in Systemic Sclerosis From European Scleroderma Trials and Research
Cohort Enrichment Strategies for Progressive Interstitial Lung Disease in Systemic Sclerosis From European Scleroderma Trials and Research Open
View article: Systemic sclerosis-associated interstitial lung disease in the EUSTAR database: analysis by region
Systemic sclerosis-associated interstitial lung disease in the EUSTAR database: analysis by region Open
Objectives The prevalence and characteristics of SSc-associated interstitial lung disease (SSc-ILD) vary between geographical regions worldwide. The objectives of this study were to explore the differences in terms of prevalence, phenotype…
View article: Glucocorticoids prescribing practices in systemic sclerosis: an analysis of the EUSTAR database
Glucocorticoids prescribing practices in systemic sclerosis: an analysis of the EUSTAR database Open
Objectives To estimate the prevalence of long-term exposure to glucocorticoids (GCs) and to identify factors associated with, and variations in prescribing practices over time and across recruiting countries. Methods We included patients w…
View article: Use of platelet inhibitors for digital ulcers related to systemic sclerosis: EUSTAR study on derivation and validation of the DU-VASC model
Use of platelet inhibitors for digital ulcers related to systemic sclerosis: EUSTAR study on derivation and validation of the DU-VASC model Open
Objective To develop and validate the prognostic prediction model DU-VASC to assist the clinicians in decision-making regarding the use of platelet inhibitors (PIs) for the management of digital ulcers in patients with systemic sclerosis. …