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Том 22 №4 2020 год - Нефрология и диализ
Клинические практические рекомендации IPNA по диагностике и лечению детей со стероид-резистентным нефротическим синдромом
Агнес Траутманн
Марина Виварелли
Сьюзан Самуэль
Дебби Джипсон
Адити Синха
Франц Шафер
Нг Кар Хуи
Оливия Бойер
Мойн А Салим
Луциана Фельтран
Янина Мюллер-Дайле
Ян Ульрих Беккер
Франциско Кано
Хонг Сю
Ям Нго Лим
Уильям Смойер
Ифеома Аночи
Коичи Наканиси
Элизабет Ходсон
Дитер Хаффнер
DOI: 10.28996/2618-9801-2020-4-435-473
Аннотация: Идиопатический нефротический синдром ежегодно выявляется у 1-3 детей на 100 000 детской популяции. Примерно в 85% случаев наблюдается полная ремиссия протеинурии после лечения глюкокортикостероидами. У пациентов, не достигших полной ремиссии в течение 4-6 недель стероидной терапии, имеет место стероид-резистентный нефротический синдром (СРНС). У 10-30% пациентов со СРНС могут быть обнаружены мутации в генах, ассоциированных с подоцитами, в то время как у остальных детей в генезе заболевания предполагаются циркулирующие факторы иммунного происхождения. Диагностика и лечение СРНС представляет собой сложную задачу в связи с гетерогенной этиологией заболевания, частым отсутствием эффекта при дальнейшей иммуносупрессивной терапии, а также с тяжелыми осложнениями и развитием хронической болезни почек (ХБП) 5 стадии и возвратом заболевания после трансплантации почек. Группа экспертов, включающая детских нефрологов и генетиков из Международной ассоциации педиатрической нефрологии (IPNA), ренального патоморфолога и взрослого нефролога, разработала клинические практические рекомендации по диагностике и лечению СРНС у детей. Экспертная группа провела систематический обзор литературы по 9 клинически значимым вопросам PICO (Patient or Population covered, Intervention, Comparator, Outcome/Пациент или Популяция, Вмешательство, Сравнение, Исход), сформулировала рекомендации и присвоила им степень на консенсусном совещании с участием представителей пациентов и диетолога, выступавшего в качестве внешнего консультанта, а также группы детских нефрологов, участвующих в голосовании.
Для цитирования: Агнес Траутманн, Марина Виварелли, Сьюзан Самуэль, Дебби Джипсон, Адити Синха, Франц Шафер, Нг Кар Хуи, Оливия Бойер, Мойн А Салим, Луциана Фельтран, Янина Мюллер-Дайле, Ян Ульрих Беккер, Франциско Кано, Хонг Сю, Ям Нго Лим, Уильям Смойер, Ифеома Аночи, Коичи Наканиси, Элизабет Ходсон, Дитер Хаффнер Клинические практические рекомендации IPNA по диагностике и лечению детей со стероид-резистентным нефротическим синдромом. Нефрология и диализ. 2020. 22(4):435-473. doi: 10.28996/2618-9801-2020-4-435-473
Весь текст
Ключевые слова: стероид-резистентный нефротический синдром,
дети,
хронические заболевания почек,
генетика,
исход,
педиатрия,
иммуносупрессивное лечение,
steroid-resistant nephrotic syndrome,
children,
chronic kidney disease,
genetics,
outcome,
pediatrics,
immunosuppressive treatmentСписок литературы:- Noone DG, Iijima K, Parekh R (2018) Idiopathic nephrotic syndrome in children. Lancet (London, England) 392 (10141):61-74. doi:10.1016/s0140-6736(18)30536-1
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