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GUİLLAİN-BARRE SENDROMLU HASTALARDA KLİNİK SEYİR VE PROGNOZ İLE İLİŞKİLİ FAKTÖRLERİN DEĞERLENDİRİLMESİ

Yıl 2023, Cilt: 5 Sayı: 1, 47 - 52, 15.01.2023
https://doi.org/10.37990/medr.1150691

Öz

Amaç: Guillain-Barré sendromunda (GBS) kötü prognozla ilişkili öngörücü faktörleri belirlemek, hastalığın seyrinde etkin tedaviyi erken dönemde sağlamak önemlidir. Bu çalışmada amaç; GBS tanılı hastaların klinik, labaratuvar, elektrofizyolojik ve demografik özelliklerini saptamak ve taburculuk esnasındaki prognoz üzerine katkısı olan faktörleri belirlemektir.
Gereç ve Yöntem: Çalışmaya 2013 Ocak ve 2017 Aralık tarihleri arasında kliniğimizde yatırılarak tedavisi yürütülen 138 hasta dahil edildi. Hasta kayıtları retrospektif olarak incelendi. Hastaların yatış ve taburculuk esnasındaki Hughes skorları, demografik özellikleri, klinik ve labaratuvar verileri kaydedildi.
Bulgular: Hastaların 61’i kadın (%44,2), 77’si erkek (%55,8)’ti. Yaş ortalamaları 58,119,7 yıl idi. Hastaların yatış muayenelerinde Hughes skorları ve taburculuk muayenelerinde Hughes skorları değerlendirildi. Buna göre taburculuk esnasında 112 hasta iyi prognozlu, 20 hasta kötü prognozlu olarak kabul edildi. Prognoz üzerine etkili olan faktörler ileri yaş, yüksek WBC sayısı, sepsis, hastane yatış süresinin fazla olması, yatış esnasında yüksek Hughes skoru olması ve mekanik ventilatör ihtiyacı olarak belirlendi
Sonuçlar: En sık görülen GBS alt tipi akut enflamatuvar demiyelinizan polinöropatiydi. Taburculuk prognozları açısından kötü prognostik faktörler; MV ihtiyacı, yatış gün sayısının fazla olması, yatış esnasında kötü motor fonksiyon, yüksek WBC sayısı, sepsis ve ileri yaştır.

Kaynakça

  • 1. Sejvar JJ, Baughman AL, Wise M, Morgan OW. Population incidence of Guillain-Barré syndrome: a systematic review and meta-analysis. Neuroepidemiology. 2011;36:123-33.
  • 2. Head VA, Wakerley BR. Guillain–Barré syndrome in general practice: clinical features suggestive of early diagnosis. Br J Gen Pract. 2016;66:218-19.
  • 3. Dalakas MC. Pathogenesis of immune-mediated neuropathies. Biochim Biophys Acta. 2015;1852:658-66.
  • 4. Willison HJ, Jacobs BC, van Doorn PA. Guillain-barre syndrome. Lancet. 2016;388:717-27.
  • 5. Piccione EA, Salame K, Katirji B. Guillain-Barré syndrome and related disorders. In: Katirji B, Kaminski H, Ruff R, eds, Neuromuscular Disorders in Clinical Practice. New York: Springer. 2014:573-603.
  • 6. Leonhard SE, Mandarakas MR, Gondim FA et al. Diagnosis and management of Guillain–Barré syndrome in ten steps. Nat Rev Neurol. 2019;15:671- 83.
  • 7. Zhang Y, Zhao Y, Wang Y. Prognostic factors of Guillain-Barré syndrome: a 111-case retrospective review. Chin Neurosurg. 2018;4:1-9.
  • 8. Walgaard C, Lingsma H, Ruts L, et al: Early recognition of poor prognosis in Guillain-Barre syndrome. Neurology. 2011;76:968-75.
  • 9. Asbury AK, Cornblath DR. Assessment of current diagnostic criteria for Guillain‐Barré syndrome. Ann Neurol. 1990;27:21-4.
  • 10. Hughes R, Newsom-Davis J, Perkin GD, Pierce JM: Controlled trial of prednisolone in acute polyneuropathy. Lancet. 1978;312:750-53.
  • 11. Sipilä JO, Soilu‐Hänninen M, Ruuskanen JO, et al. Epidemiology of Guillain‐Barré syndrome in Finland 2004–2014. J Peripher Ner Syst. 2017;22:440-45.
  • 12. McGrogan A, Madle GC, Seaman HE, De Vries CS. The epidemiology of Guillain-Barré syndrome worldwide. Neuroepidemiology. 2009;32:150-63.
  • 13. Khan F, Pallant J, Ng L, Bhasker A. Factors associated with long-term functional outcomes and psychological sequelae in Guillain–Barre syndrome. J Neurol. 2010;257:2024-31.
  • 14. Sudulagunta SR, Sodalagunta MB, Sepehrar M, et al. Guillain-Barré syndrome: clinical profile and management. Ger Med Sci. 2015;13:Doc16.
  • 15. Webb AJ, Brain SA, Wood R, et al. Seasonal variation in Guillain-Barré syndrome: a systematic review, meta-analysis and Oxfordshire cohort study. J Neurol, Neurosurg, Psychiatry.2015; 86:1196-201.
  • 16. Rocha MSG, Brucki SMD, Carvalho AAdS, et al. Epidemiologic features of guillain- barré syndrome in São Paulo, Brazil. Arq Neuropsiquiatr. 2004;62:33-7.
  • 17. Ozbey G, Tasdemir BJVi: Seasonality and antibiotic resistance of Campylobacter in Turkish chicken meat. Vet Ital. 2014;50:277-83.
  • 18. Mathew T, Srinivas M, Nadig R, Arumugam R, Sarma GRK. Seasonal and monthly trends in the occurrence of Guillain-Barre syndrome over a 5-year period: A tertiary care hospital-based study from South India. Ann Indian Acad Neurol. 2014;17:239-41.
  • 19. Meşe S, Uyanik A, Özakay A, et al. Influenza surveillance in Western Turkey in the era of quadrivalent vaccines: A 2003–2016 retrospective analysis. Hum Vaccin Innunother. 2018;14:1899-908.
  • 20. Çetiner M, Seyit M, Akdağ G, et al. Guillain-Barré Sendromlu Hastalarda Prognozla İlişkili Faktörler. Turk J Neurol. 2019;25:140-45.
  • 21. Gazioglu S, Tomak T, Boz C. Guillain Barre Sendromunda Klinik Özellikler ve Prognoz. J Neurol Sci. 2013;30:124-34.
  • 22. Tam CC, O’Brien SJ, Petersen I, Islam A, Hayward A, Rodrigues LC. Guillain-Barré syndrome and preceding infection with campylobacter, influenza and Epstein-Barr virus in the general practice research database. PLoS One. 2007;2:e344.
  • 23. Arami MA, Yazdchi M, Khandaghi R. Epidemiology and characteristics of Guillain-Barre syndrome in the northwest of Iran. Annals of Saudi Medicine. 2006;26:22-7.
  • 24. Eşref A, Varol S, Taşkın A, Arıkanoğlu A, Tamam Y, Öztürk Ü. Guillain-Barre sendromunda klinik ve demografik özellikler. Dicle Medical Journal. 2014;41:707- 11.
  • 25. Tian J, Cao C, Li T, Zhang K, Li P, Liu Y, Liu X. Electrophysiological subtypes and prognostic factors of Guillain-Barre syndrome in northern china. Frontiers in Neurology. 2019;10:714.
  • 26. Rajabally YA, Uncini A. Outcome and its predictors in Guillain–Barré syndrome. Journal of Neurology, Neurosurgery, Psychiatry. 2012;83:711-8.
  • 27. Wang Y, Lang W, Zhang Y, Ma X, Zhou C, Zhang H-L. Long-term prognosis of Guillain- Barré syndrome not determined by treatment options? Oncotarget.2017;8:79991.
  • 28. Fletcher DD, Lawn ND, Wolter TD, Wijdicks EF. Long-term outcome in patients with Guillain–Barré syndrome requiring mechanical ventilation. Neurology. 2000;54:2311-5.
  • 29. Hashim NA, Mohamed WS, Emad EM. Neutrophil–lymphocyte ratio and response to plasmapheresis in Guillain–Barré syndrome: a prospective observational study. The Egyptian Journal of Neurology, Psychiatry and Neurosurgery. 2020;56:17.

Evaluation of Factors Associated with the Clinical Course and Prognosis of Patients with Guillain-Barre Syndrome

Yıl 2023, Cilt: 5 Sayı: 1, 47 - 52, 15.01.2023
https://doi.org/10.37990/medr.1150691

Öz

Aim: This study aims to investigate the clinical, laboratory, electrophysiological, and demographic characteristics of patients with Guillain-Barre Syndrome (GBS) who were admitted to our clinic and underwent treatment and the factors contributing to the prognosis at discharge.
Materials and Methods: The study included 138 patients admitted to our clinic for treatment between January 2013 and December 2017, whose patient records were reviewed retrospectively. The Hughes scores, demographic characteristics, and clinical and laboratory data of the patients at admission and discharge were recorded.
Results: The study sample comprised 61 female (44.2%) and 77 male (55.8%) patients with a mean age of 58.1 years. In evaluations of the Hughes scores at admission and discharge, 117 patients were considered to have a good prognosis and 21 patients to have a poor prognosis at discharge. In the poor prognosis group, advanced age (p=0.028), being in the acute motor axonal neuropathy (AMAN) subtype (p=0.001), development of sepsis (p=0.007), need for mechanical ventilation (p<0.001), high Hughes scores on admission (p<0.001), extended hospitalization (p=0.030), increased WBC count (p=0.033), presence of hyponatremia (p<0.001), abnormal liver function test (p=0.08) were higher than the good prognosis group.
Conclusion: Early identification of GBS patients who may have a poor prognosis and rapid application of appropriate treatment methods are essential in creating positive effects on the clinical course and prognosis in this patient group.

Kaynakça

  • 1. Sejvar JJ, Baughman AL, Wise M, Morgan OW. Population incidence of Guillain-Barré syndrome: a systematic review and meta-analysis. Neuroepidemiology. 2011;36:123-33.
  • 2. Head VA, Wakerley BR. Guillain–Barré syndrome in general practice: clinical features suggestive of early diagnosis. Br J Gen Pract. 2016;66:218-19.
  • 3. Dalakas MC. Pathogenesis of immune-mediated neuropathies. Biochim Biophys Acta. 2015;1852:658-66.
  • 4. Willison HJ, Jacobs BC, van Doorn PA. Guillain-barre syndrome. Lancet. 2016;388:717-27.
  • 5. Piccione EA, Salame K, Katirji B. Guillain-Barré syndrome and related disorders. In: Katirji B, Kaminski H, Ruff R, eds, Neuromuscular Disorders in Clinical Practice. New York: Springer. 2014:573-603.
  • 6. Leonhard SE, Mandarakas MR, Gondim FA et al. Diagnosis and management of Guillain–Barré syndrome in ten steps. Nat Rev Neurol. 2019;15:671- 83.
  • 7. Zhang Y, Zhao Y, Wang Y. Prognostic factors of Guillain-Barré syndrome: a 111-case retrospective review. Chin Neurosurg. 2018;4:1-9.
  • 8. Walgaard C, Lingsma H, Ruts L, et al: Early recognition of poor prognosis in Guillain-Barre syndrome. Neurology. 2011;76:968-75.
  • 9. Asbury AK, Cornblath DR. Assessment of current diagnostic criteria for Guillain‐Barré syndrome. Ann Neurol. 1990;27:21-4.
  • 10. Hughes R, Newsom-Davis J, Perkin GD, Pierce JM: Controlled trial of prednisolone in acute polyneuropathy. Lancet. 1978;312:750-53.
  • 11. Sipilä JO, Soilu‐Hänninen M, Ruuskanen JO, et al. Epidemiology of Guillain‐Barré syndrome in Finland 2004–2014. J Peripher Ner Syst. 2017;22:440-45.
  • 12. McGrogan A, Madle GC, Seaman HE, De Vries CS. The epidemiology of Guillain-Barré syndrome worldwide. Neuroepidemiology. 2009;32:150-63.
  • 13. Khan F, Pallant J, Ng L, Bhasker A. Factors associated with long-term functional outcomes and psychological sequelae in Guillain–Barre syndrome. J Neurol. 2010;257:2024-31.
  • 14. Sudulagunta SR, Sodalagunta MB, Sepehrar M, et al. Guillain-Barré syndrome: clinical profile and management. Ger Med Sci. 2015;13:Doc16.
  • 15. Webb AJ, Brain SA, Wood R, et al. Seasonal variation in Guillain-Barré syndrome: a systematic review, meta-analysis and Oxfordshire cohort study. J Neurol, Neurosurg, Psychiatry.2015; 86:1196-201.
  • 16. Rocha MSG, Brucki SMD, Carvalho AAdS, et al. Epidemiologic features of guillain- barré syndrome in São Paulo, Brazil. Arq Neuropsiquiatr. 2004;62:33-7.
  • 17. Ozbey G, Tasdemir BJVi: Seasonality and antibiotic resistance of Campylobacter in Turkish chicken meat. Vet Ital. 2014;50:277-83.
  • 18. Mathew T, Srinivas M, Nadig R, Arumugam R, Sarma GRK. Seasonal and monthly trends in the occurrence of Guillain-Barre syndrome over a 5-year period: A tertiary care hospital-based study from South India. Ann Indian Acad Neurol. 2014;17:239-41.
  • 19. Meşe S, Uyanik A, Özakay A, et al. Influenza surveillance in Western Turkey in the era of quadrivalent vaccines: A 2003–2016 retrospective analysis. Hum Vaccin Innunother. 2018;14:1899-908.
  • 20. Çetiner M, Seyit M, Akdağ G, et al. Guillain-Barré Sendromlu Hastalarda Prognozla İlişkili Faktörler. Turk J Neurol. 2019;25:140-45.
  • 21. Gazioglu S, Tomak T, Boz C. Guillain Barre Sendromunda Klinik Özellikler ve Prognoz. J Neurol Sci. 2013;30:124-34.
  • 22. Tam CC, O’Brien SJ, Petersen I, Islam A, Hayward A, Rodrigues LC. Guillain-Barré syndrome and preceding infection with campylobacter, influenza and Epstein-Barr virus in the general practice research database. PLoS One. 2007;2:e344.
  • 23. Arami MA, Yazdchi M, Khandaghi R. Epidemiology and characteristics of Guillain-Barre syndrome in the northwest of Iran. Annals of Saudi Medicine. 2006;26:22-7.
  • 24. Eşref A, Varol S, Taşkın A, Arıkanoğlu A, Tamam Y, Öztürk Ü. Guillain-Barre sendromunda klinik ve demografik özellikler. Dicle Medical Journal. 2014;41:707- 11.
  • 25. Tian J, Cao C, Li T, Zhang K, Li P, Liu Y, Liu X. Electrophysiological subtypes and prognostic factors of Guillain-Barre syndrome in northern china. Frontiers in Neurology. 2019;10:714.
  • 26. Rajabally YA, Uncini A. Outcome and its predictors in Guillain–Barré syndrome. Journal of Neurology, Neurosurgery, Psychiatry. 2012;83:711-8.
  • 27. Wang Y, Lang W, Zhang Y, Ma X, Zhou C, Zhang H-L. Long-term prognosis of Guillain- Barré syndrome not determined by treatment options? Oncotarget.2017;8:79991.
  • 28. Fletcher DD, Lawn ND, Wolter TD, Wijdicks EF. Long-term outcome in patients with Guillain–Barré syndrome requiring mechanical ventilation. Neurology. 2000;54:2311-5.
  • 29. Hashim NA, Mohamed WS, Emad EM. Neutrophil–lymphocyte ratio and response to plasmapheresis in Guillain–Barré syndrome: a prospective observational study. The Egyptian Journal of Neurology, Psychiatry and Neurosurgery. 2020;56:17.
Toplam 29 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular İç Hastalıkları
Bölüm Özgün Makaleler
Yazarlar

Recep Baydemir 0000-0001-9753-8461

Duygu Kurt Gök 0000-0003-0994-0325

Erken Görünüm Tarihi 15 Ocak 2023
Yayımlanma Tarihi 15 Ocak 2023
Kabul Tarihi 15 Aralık 2022
Yayımlandığı Sayı Yıl 2023 Cilt: 5 Sayı: 1

Kaynak Göster

AMA Baydemir R, Kurt Gök D. Evaluation of Factors Associated with the Clinical Course and Prognosis of Patients with Guillain-Barre Syndrome. Med Records. Ocak 2023;5(1):47-52. doi:10.37990/medr.1150691

 Chief Editors

Assoc. Prof. Zülal Öner
Address: İzmir Bakırçay University, Department of Anatomy, İzmir, Turkey

Assoc. Prof. Deniz Şenol
Address: Düzce University, Department of Anatomy, Düzce, Turkey

E-mail: medrecsjournal@gmail.com

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