4.0 Article

Assessment of the HScore for reactive haemophagocytic syndrome in patients with rheumatic diseases

Journal

SCANDINAVIAN JOURNAL OF RHEUMATOLOGY
Volume 46, Issue 1, Pages 44-48

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.3109/03009742.2016.1167951

Keywords

-

Categories

Ask authors/readers for more resources

Objectives: Reactive haemophagocytic syndrome (RHS) is a hyperinflammatory disorder often occurring in the background of several disorders such as infections, malignancies, and rheumatic diseases. Recently, a score known as the HScore was developed for the diagnosis of RHS. In the original study, most of the patients had underlying haematological malignancy or infection and the best cut-off value for the HScore was 169 (sensitivity 93%; specificity 86%). In this study we aimed to analyse the performance of the HScore in rheumatic disease-related RHS.Method: The patients with rheumatic disorders evaluated in the Departments of Rheumatology and Paediatric Rheumatology at Hacettepe University, Ankara, Turkey between 2002 and 2014 were reviewed retrospectively. The first group (n=30) consisted of patients with RHS; the control group (n=64) included patients with active rheumatic diseases without RHS.Results: In the RHS group, 14 (46.7%) had adult-onset Still's disease (AOSD), 10 (33.3%) systemic juvenile idiopathic arthritis (SJIA), and six (20%) systemic lupus erythematosus (SLE). The control group (n=64) consisted of 32 (50%) AOSD, 13 (20.3%) SJIA, and 19 (29.7%) SLE patients. Applying the HScore to the RHS patients, the best cut-off value was 190.5 with a sensitivity of 96.7% and specificity of 98.4%. When we excluded the patients from the control group who had not had bone marrow aspiration (n=23), the same cut-off (190.5) performed best (sensitivity 96.7%; specificity 97.6%). Applying the 2004 haemophagocytic lymphohistiocytosis (HLH-2004) criteria gave a sensitivity of 56.6% and a specificity of 100% in the whole study group.Conclusions: In our study, a cut-off value for the HScore different from the original study performed better. Further studies are warranted to determine optimum cut-off values in different studies.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.0
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Rheumatology

The Characteristics of Patients With COVID-19-Associated Pediatric Vasculitis: An International, Multicenter Study

Ezgi D. Batu, Seher Sener, Gulcan Ozomay Baykal, Elif Arslanoglu Aydin, Semanur Ozdel, Alenka Gagro, Esra Esen, Merav Heshin-Bekenstein, Niluefer Akpinar Tekgoz, Fatma G. Demirkan, Kubra Ozturk, Olga Vougiouka, H. Emine Sonmez, Maria Cristina Maggio, Ummusen Kaya Akca, Marija Jelusic, Aysenur Pac Kisaarslan, Banu Acar, Nuray Aktay Ayaz, Betul Sozeri, Seza Ozen

Summary: This study analyzed the characteristics, treatment, and outcomes of COVID-19-associated pediatric vasculitis (excluding KD-like vasculitis in MIS-C). The results showed that COVID-19-associated pediatric IgA vasculitis/Henoch-Schönlein purpura had more severe clinical manifestations and poorer treatment outcomes compared to pre-pandemic cases.

ARTHRITIS & RHEUMATOLOGY (2023)

Article Rheumatology

EULAR recommendations for the management of ANCA-associated vasculitis: 2022 update

Bernhard Hellmich, Beatriz Sanchez-Alamo, Jan H. Schirmer, Alvise Berti, Daniel Blockmans, Maria C. Cid, Julia U. Holle, Nicole Hollinger, Omer Karadag, Andreas Kronbichler, Mark A. Little, Raashid A. Luqmani, Alfred Mahr, Peter A. Merkel, Aladdin J. Mohammad, Sara Monti, Chetan B. Mukhtyar, Jacek Musial, Fiona Price-Kuehne, Marten Segelmark, Y. K. Onno Teng, Benjamin Terrier, Gunnar Tomasson, Augusto Vaglio, Dimitrios Vassilopoulos, Peter Verhoeven, David Jayne

Summary: Since the publication of the EULAR recommendations for the management of AAV in 2016, several clinical trials have been conducted that have the potential to change clinical care. A systematic literature review and expert opinions were used to modify existing recommendations and create new ones. The recommendations provide updated guidance on AAV management.

ANNALS OF THE RHEUMATIC DISEASES (2023)

Article Obstetrics & Gynecology

Fertility, early menopause and pregnancy outcomes of patients with Takayasu?s arteritis

Arzu Taghiyeva, Levent Kilic, Murat Cagan, Ertugrul Cagri Bolek, Gozde Kubra Yardimci, Ozgur Ozyuncu, Sule Apras Bilgen, Omer Karadag

Summary: This study aimed to evaluate fertility, early menopause, and pregnancy outcomes of patients with Takayasu's arteritis (TA) before and after diagnosis. The results showed that TA patients had a higher infertility rate compared to the general population in Turkey (12.5% vs 8.6%) and a lower rate of early menopause (16.7% vs 36.1%). Pregnancy following a TA diagnosis had more maternal complications, and fetal complications were common both before and after diagnosis. Chronic inflammation may contribute to increased infertility and fetal complications.

EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY (2023)

Review Immunology

Tofacitinib experience in patients with enteropathic arthritis

Pinar Akyuez Dagli, Abdulsamet Erden, Serdar Can Gueven, Berkan Armagan, oeykue Tayfur Yuerekli, Yasemin oezderin oezin, Ahmet Omma, Orhan Kuecueksahin

Summary: This study evaluated the effectiveness of tofacitinib in the treatment of enteropathic arthritis. The results showed that after tofacitinib treatment, clinical and laboratory symptoms of both inflammatory bowel disease and arthritis improved in three patients.

IMMUNOTHERAPY (2023)

Article Medicine, General & Internal

Interchangeability and adverse events in originator-rituximab and its biosimilar (CT-P10) among rheumatic patients: a real-life experience

Melda Bahap-Kara, Emine Duran, Aygin Bayraktar-Ekincioglu, Omer Karadag

Summary: CT-P10 is the first biosimilar of rituximab approved in Europe for all indications of originator rituximab. This study provides real-life data on treatment changes and adverse events in patients who received oRTX or CT-P10. The results show that CT-P10 is a safe alternative for rituximab therapy.

INTERNAL AND EMERGENCY MEDICINE (2023)

Article Rheumatology

Tocilizumab in Behcet Disease: A Multicenter Study of 30 Patients

Mohamed-Yacine Khitri, Alessandra Bartoli, Georgina Maalouf, Alban Deroux, Carlo Salvarani, Giacomo Emmi, Omer Karadag, Gerard Espinosa, Mathilde Leclercq, Gabriele Simonini, Mathieu Vautier, Patrice Cacoub, David Saadoun

Summary: This study evaluated the efficacy of tocilizumab in patients with refractory Behcet disease. The results showed that 83% of patients responded to tocilizumab, with 60% achieving complete response and 23% achieving partial response. Tocilizumab also significantly reduced steroid dosage and the need for concomitant disease-modifying antirheumatic drugs. However, a small number of patients experienced mild to moderate side effects and serious adverse events.

JOURNAL OF RHEUMATOLOGY (2023)

Article Rheumatology

Characteristics and outcome of ANCA-associated vasculitides induced by anti-thyroid drugs: a multicentre retrospective case-control study

Julien Culerrier, Yann Nguyen, Omer Karadag, Sule Yasar Bilge, Tuba Demirci Yildrim, Tahir Saygin Ogut, Veli Yazisiz, Cemal Bes, Ayse Celfe, Ayten Yazici, Oznur Sadioglu Cagdas, Andreas Kronbichler, David Jayne, Philipp Gauckler, Alexis Regent, Vitor Teixeira, Sylvain Marchand-Adam, Pierre Duffau, Saskia Ingen- Housz-Oro, Celine Droumaguet, Baptiste Andre, Luminita Luca, Sarah Lechtman, Achille Aouba, Celine Lebas, Amelie Servettaz, Amandine Dernoncourt, Marc Ruivard, Anne-Marie Milesi, Vincent Poindron, Patrick Jego, Roberto Padoan, Paolo Delvino, Frederic Vandergheynst, Christian Pagnoux, Elaine Yacyshyn, Peter Lamprecht, Oliver Flossmann, Xavier Puechal, Benjamin Terrier

Summary: This retrospective multicentre study aimed to investigate the characteristics and outcome of ANCA-associated vasculitis (AAV) induced by anti-thyroid drugs (ATD) compared to primary AAV. The results showed that ATD-induced AAV mainly presented as microscopic polyangiitis (MPA), with the most common manifestations being skin involvement, arthralgia, and glomerulonephritis. However, ATD-induced MPA was less severe and had a lower risk of relapse compared to primary MPA.

RHEUMATOLOGY (2023)

Article Pediatrics

The Effect of Biologics in the Treatment of Multisystem Inflammatory Syndrome in Children (Mis-C): A Single-Center Propensity-Score-Matched Study

Ozge Basaran, Ezgi Deniz Batu, Ummusen Kaya Akca, Erdal Atalay, Muserref Kasap Cuceoglu, Seher Sener, Zeynep Balik, Erdem Karabulut, Selman Kesici, Tevfik Karagoz, Yasemin Ozsurekci, Yelda Bilginer, Ali Bulent Cengiz, Seza Ozen

Summary: This study compared the clinical and laboratory outcomes of MIS-C patients treated with IVIG plus corticosteroids (CS) to those treated with IVIG plus CS and an additional biologic drug. The results showed that the primary outcome was favorable in patients treated with IVIG plus CS, while it was unfavorable in patients treated with IVIG plus CS and a biologic drug.

CHILDREN-BASEL (2023)

Article Rheumatology

IgG4-related pachymeningitis-Long term follow up and outcome of six patients

Gozde Kubra Yardimci, Doruk Arslan, Berrin Babaoglu, Ertugrul Cagri Bolek, Levent Kilic, Arzu Saglam, Asli Tuncer, Figen Soylemezoglu, Rahsan Gocmen, Kader K. Oguz, Ersin Tan, Omer Karadag

Summary: In this study, the HUVAC database was used to evaluate cases of pachymeningitis in patients with IgG4-related disease. It was found that most of these patients had normal serum IgG4 levels, therefore not useful for diagnosis. Typical radiology and tentorial thickening should raise suspicion of IgG4-related disease and prompt early biopsy. With steroids+ rituximab treatment, there was no long-term relapse related to meningeal involvement.

INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES (2023)

Letter Rheumatology

Serum autoantibodies and the risk of cancer in systemic sclerosis over time Reply

Ezgi D. Batu, Seher Sener, Seza Ozen

ARTHRITIS & RHEUMATOLOGY (2023)

Article Rheumatology

Pediatric mixed connective tissue disease versus other overlap syndromes: a retrospective multicenter cohort study

Ezgi Deniz Batu, Aybuke Gunalp, Sezgin Sahin, Semanur Ozdel, Zehra Kizildag, Aysenur Pac Kisaarslan, Ilknur Bagrul, Muserref Kasap Cuceoglu, Ayse Tanatar, Hafize Emine Sonmez, Erdal Sag, Selcan Demir, Elif Celikel, Sengul Caglayan, Banu Celikel Acar, Betul Sozeri, Nuray Aktay Ayaz, Yelda Bilginer, M. Hakan Poyrazoglu, Erbil Unsal, Oezgur Kasapcopur, Seza Ozen

Summary: This study compared the characteristics and outcomes of pediatric MCTD and other overlap syndromes, finding differences in disease phenotype and prognosis. MCTD may be considered a more severe disease. Analyzing these patients could pave the way for early and effective treatment.

RHEUMATOLOGY INTERNATIONAL (2023)

Article Medicine, General & Internal

Pulmonary hypertension in Behcet?s disease: echocardiographic screening and multidisciplinary approach

Berkan Armagan, Metin Oksul, Yusuf Ziya Sener, Alper Sari, Abdulsamet Erden, Goezde Kuebra Yardimci, Kadir Mutlu Hayran, Levent Kilic, Oemer Karadag, Ergun Baris Kaya, Sadberk Lale Tokgozoglu, Ali Ihsan Ertenli, Ali Akdogan

Summary: This study aimed to investigate the prevalence and causes of pulmonary hypertension (PH) in Behcet's disease (BD). The study found that PH is not rare in BD patients and is mainly due to left heart disease or pulmonary arterial involvement. BD patients with vascular involvement are at a higher risk of developing PH.

TURKISH JOURNAL OF MEDICAL SCIENCES (2023)

Article Medicine, General & Internal

Effects of breast milk on Behcet's disease clinical features

Hatice Ecem Konak, Abdulsamet Erden, Berkan Armagan, Serdar Can Guven, Hakan Apaydin, Pinar Akyuez Dagli, Yagnur Uzun, Merve Kaygisiz, Orhan Kucuksahin, Ahmet Omma

Summary: Breastfeeding may have positive effects on the course of Behcet's disease, as breastfed patients had a lower need for TNF-i and a lower incidence of sacroiliitis. Additionally, patients who were breastfed were diagnosed with the disease at a later age compared to those who were not breastfed.

TURKISH JOURNAL OF MEDICAL SCIENCES (2023)

Article Medicine, General & Internal

The impact of antiphospholipid antibodies in Takayasu arteritis

Esra Firat Senturk, Abdulsamet Erden, Alper Sari, Berkan Armagan, Levent Kilic, Umut Kalyoncu, Oemer Karadag, Sule Apras Bilgen, Sedat Kiraz, Ihsan Ertenli, Ali Akdogan

Summary: This study examines the significance of antiphospholipid antibodies (aPL) in Takayasu arteritis (TA). The results indicate that aPL positivity is not rare in TA patients, but its association with disease-related complications is unclear.

TURKISH JOURNAL OF MEDICAL SCIENCES (2023)

Article Rheumatology

Is it possible to predict a disease course prone to macrophage activation syndrome at systemic juvenile idiopathic arthritis diagnosis?

Ezgi Deniz Batu, Seher Sener, Zeynep Balik, Yagmur Bayindir, Veysel Cam, Muserref Kasap Cuceoglu, Ozan Uysal, Emil Aliyev, Ozge Basaran, Yelda Bilginer, Seza Ozen

Summary: This study compared the characteristics of patients with systemic juvenile idiopathic arthritis (SJIA) who developed macrophage activation syndrome (MAS) during the course of the disease to those who never experienced MAS. It was found that patients with MAS had younger age, longer duration of fever, higher frequency of rash, hepatomegaly, and splenomegaly, and lower frequency of arthralgia/arthritis at the time of SJIA diagnosis compared to patients without MAS.

CLINICAL RHEUMATOLOGY (2023)

No Data Available