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DOI 10.1016/j.pediatrneurol.2023.04.018

Медицинская библиотека · Pediatric neurology · 2023

Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study.

Sarıkaya Uzan Gamze, Vural Atay, Yüksel Deniz, Aksoy Erhan, Öztoprak Ülkühan, Canpolat Mehmet, Öztürk Selcan, Yıldırım Çelebi, Güleç Ayten, Per Hüseyin, Gümüş Hakan, Okuyaz Çetin, Çobanoğulları Direk Meltem, Kömür Mustafa, Ünalp Aycan, Yılmaz Ünsal, Bektaş Ömer, Teber Serap, Aliyeva Nargiz, Olgaç Dündar Nihal, Gençpınar Pınar, Gürkaş Esra, Keskin Yılmaz Sanem, Kanmaz Seda, Tekgül Hasan, Aksoy Ayşe, Öz Tuncer Gökçen, Acar Arslan Elif, Tosun Ayşe, Ayanoğlu Müge, Kızılırmak Ali Burak, Yousefi Mohammadreza, Bodur Muhittin, Ünay Bülent, Hız Kurul Semra, Yiş Uluç

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Аннотация

BACKGROUND

To evaluate the clinical features, demographic features, and treatment modalities of pediatric-onset chronic inflammatory demyelinating polyneuropathy (CIDP) in Turkey.

METHODS

The clinical data of patients between January 2010 and December 2021 were reviewed retrospectively. The patients were evaluated according to the Joint Task Force of the European Federation of Neurological Societies and the Peripheral Nerve Society Guideline on the management of CIDP (2021). In addition, patients with typical CIDP were divided into two groups according to the first-line treatment modalities (group 1: IVIg only, group 2: IVIg + steroid). The patients were further divided into two separate groups based on their magnetic resonance imaging (MRI) characteristics.

RESULTS

A total of 43 patients, 22 (51.2%) males and 21 (48.8%) females, were included in the study. There was a significant difference between pretreatment and post-treatment modified Rankin scale (mRS) scores (P < 0.05) of all patients. First-line treatments include intravenous immunoglobulin (IVIg) (n = 19, 44.2%), IVIg + steroids (n = 20, 46.5%), steroids (n = 1, 2.3%), IVIg + steroids + plasmapheresis (n = 1, 2.3%), and IVIg + plasmapheresis (n = 1, 2.3%). Alternative agent therapy consisted of azathioprine (n = 5), rituximab (n = 1), and azathioprine + mycophenolate mofetil + methotrexate (n = 1). There was no difference between the pretreatment and post-treatment mRS scores of groups 1 and 2 (P > 0.05); however, a significant decrease was found in the mRS scores of both groups with treatment (P < 0.05). The patients with abnormal MRI had significantly higher pretreatment mRS scores compared with the group with normal MRI (P < 0.05).

CONCLUSIONS

This multicenter study demonstrated that first-line immunotherapy modalities (IVIg vs IVIg + steroids) had equal efficacy for the treatment of patients with CIDP. We also determined that MRI features might be associated with profound clinical features, but did not affect treatment response.

Для цитирования: Sarıkaya Uzan Gamze, Vural Atay, Yüksel Deniz, Aksoy Erhan, Öztoprak Ülkühan, Canpolat Mehmet, Öztürk Selcan, Yıldırım Çelebi, Güleç Ayten, Per Hüseyin, Gümüş Hakan, Okuyaz Çetin, Çobanoğulları Direk Meltem, Kömür Mustafa, Ünalp Aycan, Yılmaz Ünsal, Bektaş Ömer, Teber Serap, Aliyeva Nargiz, Olgaç Dündar Nihal, Gençpınar Pınar, Gürkaş Esra, Keskin Yılmaz Sanem, Kanmaz Seda, Tekgül Hasan, Aksoy Ayşe, Öz Tuncer Gökçen, Acar Arslan Elif, Tosun Ayşe, Ayanoğlu Müge, Kızılırmak Ali Burak, Yousefi Mohammadreza, Bodur Muhittin, Ünay Bülent, Hız Kurul Semra, Yiş Uluç. Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study.. Pediatric neurology. 2023. DOI: 10.1016/j.pediatrneurol.2023.04.018.

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