不断变化的儿童溶血性尿毒症流行病学和预后:波兰儿科 HUS 登记处和波兰儿童肾脏替代疗法登记处的前瞻性全国队列研究》(Polish Pediatric HUS Registry and the Polish Registry of Renal Replacement Therapy in Children)。
Ilona Zagożdżon, Maria Szczepańska, Beata Leszczyńska, Wioleta Jarmużek, Monika Miklaszewska, Marcin Tkaczyk, Anna Medyńska, Anna Wieczorkiewicz-Płaza, Jacek Zachwieja, Piotr Protas, Paulina Rosińska, Urszula Jacher, Elżbieta Trembecka-Dubel, Danuta Zwolińska, Aleksandra Żurowska
{"title":"不断变化的儿童溶血性尿毒症流行病学和预后:波兰儿科 HUS 登记处和波兰儿童肾脏替代疗法登记处的前瞻性全国队列研究》(Polish Pediatric HUS Registry and the Polish Registry of Renal Replacement Therapy in Children)。","authors":"Ilona Zagożdżon, Maria Szczepańska, Beata Leszczyńska, Wioleta Jarmużek, Monika Miklaszewska, Marcin Tkaczyk, Anna Medyńska, Anna Wieczorkiewicz-Płaza, Jacek Zachwieja, Piotr Protas, Paulina Rosińska, Urszula Jacher, Elżbieta Trembecka-Dubel, Danuta Zwolińska, Aleksandra Żurowska","doi":"10.3390/jcm13216499","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background/Objectives</b>: Hemolytic uremic syndrome (HUS) is a known cause of acute kidney injury in children, but there are few recent reports on its epidemiology and outcome. We aimed to investigate trends in the incidence and the long-term outcomes of both Shiga toxin-producing <i>Escherichia coli</i> -HUS (STEC-HUS) and atypical HUS (aHUS) in Poland over the last 12 years (2012-2023), based on the Polish Pediatric HUS and Pediatric Renal Replacement Therapy (RRT) Registries. <b>Methods</b>: A total of 436 patients (301 with STEC-HUS and 135 with aHUS) were included. <b>Results</b>: The incidence of STEC-HUS increased during the observation period, with a mean of 3.9 cases per million age-related population (marp). The incidence of aHUS was relatively constant with a mean of 1.8/marp. The majority of patients fully recovered, although kidney sequelae were observed at 5-year follow-ups in 31% of children with STEC-HUS, 57% of aHUS subjects in the pre-eculizumab era, and 37% of aHUS subjects who had received eculizumab. The overall mortality rate was 2% for STEC-HUS and 3.7% for aHUS, with no deaths reported in children on eculizumab and mortality mainly attributed to neurological damage. A decreasing incidence of chronic kidney disease stage 5 (CKD5) due to HUS was observed. <b>Conclusions</b>: Despite an unchanging incidence of aHUS and an increasing incidence of STEC-HUS, the kidney outcomes of both diseases have improved significantly over the last 12 years. Mortality from HUS has dropped due to improved symptomatic treatment and the introduction of anti-C5 therapy. The development of CKD5 in childhood as a consequence of HUS has become exceptional.</p>","PeriodicalId":15533,"journal":{"name":"Journal of Clinical Medicine","volume":"13 21","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11546500/pdf/","citationCount":"0","resultStr":"{\"title\":\"Changing Epidemiology and Outcomes of Hemolytic Uremic Syndrome in Children: A Prospective National Cohort Study from the Polish Pediatric HUS Registry and the Polish Registry of Renal Replacement Therapy in Children.\",\"authors\":\"Ilona Zagożdżon, Maria Szczepańska, Beata Leszczyńska, Wioleta Jarmużek, Monika Miklaszewska, Marcin Tkaczyk, Anna Medyńska, Anna Wieczorkiewicz-Płaza, Jacek Zachwieja, Piotr Protas, Paulina Rosińska, Urszula Jacher, Elżbieta Trembecka-Dubel, Danuta Zwolińska, Aleksandra Żurowska\",\"doi\":\"10.3390/jcm13216499\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Background/Objectives</b>: Hemolytic uremic syndrome (HUS) is a known cause of acute kidney injury in children, but there are few recent reports on its epidemiology and outcome. We aimed to investigate trends in the incidence and the long-term outcomes of both Shiga toxin-producing <i>Escherichia coli</i> -HUS (STEC-HUS) and atypical HUS (aHUS) in Poland over the last 12 years (2012-2023), based on the Polish Pediatric HUS and Pediatric Renal Replacement Therapy (RRT) Registries. <b>Methods</b>: A total of 436 patients (301 with STEC-HUS and 135 with aHUS) were included. <b>Results</b>: The incidence of STEC-HUS increased during the observation period, with a mean of 3.9 cases per million age-related population (marp). The incidence of aHUS was relatively constant with a mean of 1.8/marp. The majority of patients fully recovered, although kidney sequelae were observed at 5-year follow-ups in 31% of children with STEC-HUS, 57% of aHUS subjects in the pre-eculizumab era, and 37% of aHUS subjects who had received eculizumab. The overall mortality rate was 2% for STEC-HUS and 3.7% for aHUS, with no deaths reported in children on eculizumab and mortality mainly attributed to neurological damage. A decreasing incidence of chronic kidney disease stage 5 (CKD5) due to HUS was observed. <b>Conclusions</b>: Despite an unchanging incidence of aHUS and an increasing incidence of STEC-HUS, the kidney outcomes of both diseases have improved significantly over the last 12 years. Mortality from HUS has dropped due to improved symptomatic treatment and the introduction of anti-C5 therapy. 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Changing Epidemiology and Outcomes of Hemolytic Uremic Syndrome in Children: A Prospective National Cohort Study from the Polish Pediatric HUS Registry and the Polish Registry of Renal Replacement Therapy in Children.
Background/Objectives: Hemolytic uremic syndrome (HUS) is a known cause of acute kidney injury in children, but there are few recent reports on its epidemiology and outcome. We aimed to investigate trends in the incidence and the long-term outcomes of both Shiga toxin-producing Escherichia coli -HUS (STEC-HUS) and atypical HUS (aHUS) in Poland over the last 12 years (2012-2023), based on the Polish Pediatric HUS and Pediatric Renal Replacement Therapy (RRT) Registries. Methods: A total of 436 patients (301 with STEC-HUS and 135 with aHUS) were included. Results: The incidence of STEC-HUS increased during the observation period, with a mean of 3.9 cases per million age-related population (marp). The incidence of aHUS was relatively constant with a mean of 1.8/marp. The majority of patients fully recovered, although kidney sequelae were observed at 5-year follow-ups in 31% of children with STEC-HUS, 57% of aHUS subjects in the pre-eculizumab era, and 37% of aHUS subjects who had received eculizumab. The overall mortality rate was 2% for STEC-HUS and 3.7% for aHUS, with no deaths reported in children on eculizumab and mortality mainly attributed to neurological damage. A decreasing incidence of chronic kidney disease stage 5 (CKD5) due to HUS was observed. Conclusions: Despite an unchanging incidence of aHUS and an increasing incidence of STEC-HUS, the kidney outcomes of both diseases have improved significantly over the last 12 years. Mortality from HUS has dropped due to improved symptomatic treatment and the introduction of anti-C5 therapy. The development of CKD5 in childhood as a consequence of HUS has become exceptional.
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