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Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi

Yıl 2022, , 32 - 39, 22.04.2022
https://doi.org/10.46332/aemj.874209

Öz

Amaç: Hemolitik üremik sendrom (HÜS) mikroanjiopatik hemolitik anemi, trombositopeni ve akut böbrek hasarı ile karakterize bir tablodur. Şiga toksini üreten Escherchia coli ilişkili HÜS (STEC-HÜS) çocuklarda en sık nedendir. Farklı dönemlerde salgınlar şeklinde karşımıza çıkan HÜS vakalarında son yıllarda merkezimizde de artış görülmüştür ve bu yazımızda on yıllık HÜS ile takipli hastaların klinik özellikleri değerlendirilmiştir.
Araçlar ve Yöntem: 2008-2018 yılları arasında HÜS tanısı alan hastalar çalışmaya alındı. Hastaların demografik özellikleri, başvuru klinik bulguları, başvuru anında ve hastalığın akut fazında hematolojik ve biyokimyasal bulguları, kompleman değerleri, HÜS’e bağlı organ tutulumları, uygulanan tedaviler ve böbrek yerine koyma tedavileri değerlendirildi.
Bulgular: Kırk üç hasta çalışmaya alındı. Hastaların %86’sında ishal öyküsü vardı ve bu hastaların yarısında ishal kanlı idi. Nörolojik tutulum hastaların %30’unda vardı. On sekiz hastaya ekulizumab tedavisi verildi. Ekulizumab tedavisi alan hastaların proteinüri, hipertansiyon gibi böbrek hastalığının progresyonunu gösteren parametreleri daha belirgin idi. İki hastada takipte son dönem böbrek yetmezliği gelişti.
Sonuç: Akut böbrek hasarının önemli bir nedeni olan HÜS çocuk hastalarda en sık ishal ilişkili olarak karşımıza çıkmaktadır. Nörolojik tutulum en sık böbrek dışı tutulum şeklidir. Hastaların çoğunda (%70) böbrek yerine koyma tedavisine gereksinim duyulmakta ve ekulizumab tedavisini progresyonu kötü olan olgularda daha sık kullanılmaktadır. 

Destekleyen Kurum

yok

Kaynakça

  • 1. Bitzan M. Glomeruler Diseases. Phadke K, Goodyer P, Bitzan M, Ed. Manuel of Pediatr Nephrol. 1. ed. Newyork: Springer; 2014:215–225.
  • 2. Nester CM, Andreoli S. Renal involvement in Children with HUS. Avner ED, Harmon WE, Niaudet P, Yoshikava N, Emm a F, Goldstein SL, editörler. Pediatr Nephrol. 7. ed. New York: Springer Reference; 2016:1490–1513.
  • 3. Vivarelli M, Thurman JM. Complement-mediated glomerulonephritis and thrombotic microangiopathy. Bomback AS, Perazella MA, Tonelli M, editörler. Primer on Kidney Diseases. 7. ed. Philadelphia: Elsevier; 2018:208–219.
  • 4. Gasser C, Gautier E, Steck A, Siebenmann R, Oechslin R. Hemolytic-uremic syndrome: bilateral necrosis of the renal cortex in acute acquired hemolytic anemia. Schweiz Med Wochenschr. 1955;85(38-39):905-909.
  • 5. Corrigan JJ, Boineau FG. Hemolytic-uremic syn-drome. Pediatr Rev. 2001;22(11):365-369.
  • 6. Noris M, Remuzzi G. Atypical hemolytic-uremic syndrome. N Eng J Med. 2009;361(17):1676-1687.
  • 7. Cody EM, Dixon BP. Hemolytic uremic syndrome. Pediatr Clin North Am. 2019;66(1):235-246.
  • 8. Fakhouri F, Zuber J, Frémeaux-Bacchi V, Loirat C. Haemolytic uraemic syndrome. Lancet. 2017;390 (10095):681-696.
  • 9. Frank C, Werber D, Cramer JP, et al. Epidemic profile of shiga-toxin–producing. N Eng J Med. 2011;365 (19):1771-1780.
  • 10. Yıldırım ZY, Yılmaz A, Yavaş Aksu B ve ark. Diyare öyküsü olan hemolitik üremik sendrom tanılı hastaların klinik özellikleri. İst Tıp Fak Derg. 2015;78(2):46-50.
  • 11. Goodyer P, K P. Evaluation of renal disease. Phadke K, Goodyer P, Bitzan M, editörler. Manuel of Pediatric Nephrology. 1st ed. New York: Springer; 2014:1-64.
  • 12. KDIGO 2012 Clinical Practice Guideline for the evaluation and management of chronic kidney disease. Kidney Int. 2013;3(1):1-163.
  • 13. IBM Corp. IBM SPSS Statistics for Windows, Version 22.0. Armonk, New York: IBM Corp. Released 2013.
  • 14. Watanabe Y, Ozasa K, Mermin JH et al. Factory outbreak of Escherichia coli O157:H7 infection in Japan. Emerg Infect Dis. 1999;5(3):424-428.
  • 15. Ekinci Z, Candan C, Alpay H et al. Hemolytic uremic syndrome outbreak in Turkey in 2011. Turk J Pediatr. 2013;55(3):246-252.
  • 16. Yun YS, Kim NO, Chun JH, Hwang KJ, Hong S. The prevalence and characteristics of Shiga toxin producing Escherichia coli isolated by enteric pathogens active surveillance network (Enter-Net) in the republic of Korea, 200-9-2018. Microb Pathog. 2021;158: 105005.
  • 17. Canpolat N. Hemolytic uremic syndrome. Turk Arch Pediatr. 2015;50(2):73-82.
  • 18. Keenswijk W, Raes A, De Clerck M, Vande Walle J. Is plasma exchange efficacious in shiga toxin-associated hemolytic uremic syndrome? A narrative review of current evidence. Ther Apher Dial. 2019;23(2):118-125.
  • 19. Kielstein JT, Beutel G, Fleig S et al. Best supportive care and therapeutic plasma exchange with or without eculizumab in Shiga-toxin-producing E. coli O104:H4 induced haemolytic-uraemic syndrome: An analysis of the German STEC-HUS registry. Nephrol Dial Transpl. 2012;27(10):3807-3815.
  • 20. Walsh PR, Johnson S. Eculizumab in the treatment of Shiga toxin haemolytic uraemic syndrome. Pediatr Nephrol. 2019;34(9):1485-1492.
  • 21. Buchholz U, Bernard H, Werber D et al. German outbreak of Escherichia coli O104:H4 associated with sprouts. N Eng J Med. 2011;365(19):1763-1770.
  • 22. German Society of Nephrology. "Advice of the German Society of Nephrology on the use of Eculizumab during the 2011 EHEC HUS outbreak" http://www.dgfn.eu/aktuell/ehec-informationen/fuer-das-fachpublikum/advice-on-the-useof-ecilizumab.ht ml. Erişim tarihi: 10 Haziran, 2011.
  • 23. Siegler RL, Pavia AT, Christofferson RD, Milligan MK. A 20-year population-based study of post-diarrheal hemolytic uremic syndrome in Utah. Pediatrics. 1994;94(1):35-40.
  • 24. Mody RK, Gu W, Griffin PM, et al. Postdiarrheal hemolytic uremic syndrome in United States children: Clinical spectrum and predictors of in-hospital death. J Pediatr. 2015;166(4):1022-1029.

Hemolytic Uremic Syndrome; 10 Year Single Center Experience

Yıl 2022, , 32 - 39, 22.04.2022
https://doi.org/10.46332/aemj.874209

Öz

Purpose: Hemolytic uremic syndrome (HUS) is a clinical syndrome characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. Shiga toxin producing Escherchia coli-associated HUS (STEC-HUS) is the most common cause in children. In recent years, an increase has been observed in our center in the cases of HUS, which appeared as outbreaks in different periods, and in this study, the clinical characteristics of patients with HUS were evaluated.
Materials and Methods: Patients diagnosed with HUS between 2008-2018 were included in the study. The demographic characteristics of the patients, clinical findings at admission, hematological and biochemical findings at the time of admission and in the most active period of the disease, complement values, organ involvement due to HUS, applied treatments and kidney replacement treatments were evaluated.
Results: Forty-three patients were included in the study. 86% of the patients had a history of diarrhea and half of these patients had diarrhea with blood. Neurological involvement was present in 30% of the patients. Eighteen patients were given eculizumab treatment. Parameters showing the progression of kidney disease such as proteinuria and hypertension were more prominent in patients who received eculizumab treatment. End-stage kidney disease developed in two patients during follow-up.
Conclusion: HUS, which is an important cause of acute kidney damage, is most frequently associated with diarrhea in pediatric patients. Neurological involvement is the most common extra-renal manifestation. Kidney replacement therapy is required in most patients (70%) and eculizumab therapy is used more frequently in severe cases.

Kaynakça

  • 1. Bitzan M. Glomeruler Diseases. Phadke K, Goodyer P, Bitzan M, Ed. Manuel of Pediatr Nephrol. 1. ed. Newyork: Springer; 2014:215–225.
  • 2. Nester CM, Andreoli S. Renal involvement in Children with HUS. Avner ED, Harmon WE, Niaudet P, Yoshikava N, Emm a F, Goldstein SL, editörler. Pediatr Nephrol. 7. ed. New York: Springer Reference; 2016:1490–1513.
  • 3. Vivarelli M, Thurman JM. Complement-mediated glomerulonephritis and thrombotic microangiopathy. Bomback AS, Perazella MA, Tonelli M, editörler. Primer on Kidney Diseases. 7. ed. Philadelphia: Elsevier; 2018:208–219.
  • 4. Gasser C, Gautier E, Steck A, Siebenmann R, Oechslin R. Hemolytic-uremic syndrome: bilateral necrosis of the renal cortex in acute acquired hemolytic anemia. Schweiz Med Wochenschr. 1955;85(38-39):905-909.
  • 5. Corrigan JJ, Boineau FG. Hemolytic-uremic syn-drome. Pediatr Rev. 2001;22(11):365-369.
  • 6. Noris M, Remuzzi G. Atypical hemolytic-uremic syndrome. N Eng J Med. 2009;361(17):1676-1687.
  • 7. Cody EM, Dixon BP. Hemolytic uremic syndrome. Pediatr Clin North Am. 2019;66(1):235-246.
  • 8. Fakhouri F, Zuber J, Frémeaux-Bacchi V, Loirat C. Haemolytic uraemic syndrome. Lancet. 2017;390 (10095):681-696.
  • 9. Frank C, Werber D, Cramer JP, et al. Epidemic profile of shiga-toxin–producing. N Eng J Med. 2011;365 (19):1771-1780.
  • 10. Yıldırım ZY, Yılmaz A, Yavaş Aksu B ve ark. Diyare öyküsü olan hemolitik üremik sendrom tanılı hastaların klinik özellikleri. İst Tıp Fak Derg. 2015;78(2):46-50.
  • 11. Goodyer P, K P. Evaluation of renal disease. Phadke K, Goodyer P, Bitzan M, editörler. Manuel of Pediatric Nephrology. 1st ed. New York: Springer; 2014:1-64.
  • 12. KDIGO 2012 Clinical Practice Guideline for the evaluation and management of chronic kidney disease. Kidney Int. 2013;3(1):1-163.
  • 13. IBM Corp. IBM SPSS Statistics for Windows, Version 22.0. Armonk, New York: IBM Corp. Released 2013.
  • 14. Watanabe Y, Ozasa K, Mermin JH et al. Factory outbreak of Escherichia coli O157:H7 infection in Japan. Emerg Infect Dis. 1999;5(3):424-428.
  • 15. Ekinci Z, Candan C, Alpay H et al. Hemolytic uremic syndrome outbreak in Turkey in 2011. Turk J Pediatr. 2013;55(3):246-252.
  • 16. Yun YS, Kim NO, Chun JH, Hwang KJ, Hong S. The prevalence and characteristics of Shiga toxin producing Escherichia coli isolated by enteric pathogens active surveillance network (Enter-Net) in the republic of Korea, 200-9-2018. Microb Pathog. 2021;158: 105005.
  • 17. Canpolat N. Hemolytic uremic syndrome. Turk Arch Pediatr. 2015;50(2):73-82.
  • 18. Keenswijk W, Raes A, De Clerck M, Vande Walle J. Is plasma exchange efficacious in shiga toxin-associated hemolytic uremic syndrome? A narrative review of current evidence. Ther Apher Dial. 2019;23(2):118-125.
  • 19. Kielstein JT, Beutel G, Fleig S et al. Best supportive care and therapeutic plasma exchange with or without eculizumab in Shiga-toxin-producing E. coli O104:H4 induced haemolytic-uraemic syndrome: An analysis of the German STEC-HUS registry. Nephrol Dial Transpl. 2012;27(10):3807-3815.
  • 20. Walsh PR, Johnson S. Eculizumab in the treatment of Shiga toxin haemolytic uraemic syndrome. Pediatr Nephrol. 2019;34(9):1485-1492.
  • 21. Buchholz U, Bernard H, Werber D et al. German outbreak of Escherichia coli O104:H4 associated with sprouts. N Eng J Med. 2011;365(19):1763-1770.
  • 22. German Society of Nephrology. "Advice of the German Society of Nephrology on the use of Eculizumab during the 2011 EHEC HUS outbreak" http://www.dgfn.eu/aktuell/ehec-informationen/fuer-das-fachpublikum/advice-on-the-useof-ecilizumab.ht ml. Erişim tarihi: 10 Haziran, 2011.
  • 23. Siegler RL, Pavia AT, Christofferson RD, Milligan MK. A 20-year population-based study of post-diarrheal hemolytic uremic syndrome in Utah. Pediatrics. 1994;94(1):35-40.
  • 24. Mody RK, Gu W, Griffin PM, et al. Postdiarrheal hemolytic uremic syndrome in United States children: Clinical spectrum and predictors of in-hospital death. J Pediatr. 2015;166(4):1022-1029.
Toplam 24 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Klinik Tıp Bilimleri
Bölüm Bilimsel Araştırma Makaleleri
Yazarlar

Ayşe Seda Pınarbaşı 0000-0002-2443-4378

Sibel Yel 0000-0001-8946-0481

Neslihan Günay 0000-0002-0995-8501

Hakan Poyrazoğlu 0000-0003-4783-4339

Aynur Gencer Balaban 0000-0002-1984-1091

İsmail Dursun 0000-0002-0191-4344

Zübeyde Gündüz Bu kişi benim 0000-0003-1358-7632

Ruhan Düşünsel Bu kişi benim 0000-0003-0599-7199

Yayımlanma Tarihi 22 Nisan 2022
Yayımlandığı Sayı Yıl 2022

Kaynak Göster

APA Pınarbaşı, A. S., Yel, S., Günay, N., Poyrazoğlu, H., vd. (2022). Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi. Ahi Evran Medical Journal, 6(1), 32-39. https://doi.org/10.46332/aemj.874209
AMA Pınarbaşı AS, Yel S, Günay N, Poyrazoğlu H, Gencer Balaban A, Dursun İ, Gündüz Z, Düşünsel R. Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi. Ahi Evran Med J. Nisan 2022;6(1):32-39. doi:10.46332/aemj.874209
Chicago Pınarbaşı, Ayşe Seda, Sibel Yel, Neslihan Günay, Hakan Poyrazoğlu, Aynur Gencer Balaban, İsmail Dursun, Zübeyde Gündüz, ve Ruhan Düşünsel. “Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi”. Ahi Evran Medical Journal 6, sy. 1 (Nisan 2022): 32-39. https://doi.org/10.46332/aemj.874209.
EndNote Pınarbaşı AS, Yel S, Günay N, Poyrazoğlu H, Gencer Balaban A, Dursun İ, Gündüz Z, Düşünsel R (01 Nisan 2022) Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi. Ahi Evran Medical Journal 6 1 32–39.
IEEE A. S. Pınarbaşı, S. Yel, N. Günay, H. Poyrazoğlu, A. Gencer Balaban, İ. Dursun, Z. Gündüz, ve R. Düşünsel, “Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi”, Ahi Evran Med J, c. 6, sy. 1, ss. 32–39, 2022, doi: 10.46332/aemj.874209.
ISNAD Pınarbaşı, Ayşe Seda vd. “Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi”. Ahi Evran Medical Journal 6/1 (Nisan 2022), 32-39. https://doi.org/10.46332/aemj.874209.
JAMA Pınarbaşı AS, Yel S, Günay N, Poyrazoğlu H, Gencer Balaban A, Dursun İ, Gündüz Z, Düşünsel R. Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi. Ahi Evran Med J. 2022;6:32–39.
MLA Pınarbaşı, Ayşe Seda vd. “Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi”. Ahi Evran Medical Journal, c. 6, sy. 1, 2022, ss. 32-39, doi:10.46332/aemj.874209.
Vancouver Pınarbaşı AS, Yel S, Günay N, Poyrazoğlu H, Gencer Balaban A, Dursun İ, Gündüz Z, Düşünsel R. Hemolitik Üremik Sendrom; 10 Yıllık Tek Merkez Deneyimi. Ahi Evran Med J. 2022;6(1):32-9.

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