Yoğun Bakımda Guillain-Barré Sendromu Yönetimi
Özet
48 yaş erkek yaklaşık 2 gündür ellerde ayaklarda uyuşma yaygın güzsüzlük şikayetiyle başvurdu. Derin tendon reflekslerinde azalma, beyin omurilik (BOS) incelemesinde albüminositolojik disosiasyon olan hasta takibinde gelişen hızlı progresyon ve solunum sıkıntısı nedeniyle yoğun bakım ünitesine yatırıldı. Guillain-barré sendromu (GBS) öntanısıyla ıntravenöz immunglobulin (IVIG) başlanan hasta immun tedavi ve destekleyici tedaviden belirgin fayda gördü. Elbette süreçte fizik tedavi desteği ile takip edilen hastanın servis taburculuğunda; kas gücünde düzelme ve klinik iyileşme gözlendi. Hasta GBS için tipik bir vaka örneğiydi. Guillain-Barré sendromu akut başlangıçlı, jeneralize kas güçsüzlüğü ve duysal semptomlarla seyreden bir nörolojik acildir. Klinik progresyon sonrası bilinç ön planda etkilenmezken solunum sıkıntısı mekanik ventilatör ihtiyacı ve disotonomik bulgular hayatı tehtid edebilir. Tedavide destek tedavi yanında IVIG plazmaferez gibi immun tedavilerin yeri vardır. Genellikle monofazik olan bu hastalığın tanı,takip ve tedavi süreçleri tartışılacaktır.
A 48-year-old male presented with complaints of numbness in the hands and feet and generalized weakness that had persisted for approximately two days. Neurological examination revealed decreased deep tendon reflexes. Cerebrospinal fluid (CSF) analysis demonstrated albuminocytologic dissociation. During follow-up, the patient developed rapidly progressive weakness and respiratory distress, necessitating admission to the intensive care unit. With a presumptive diagnosis of Guillain-Barré syndrome (GBS), intravenous immunoglobulin (IVIG) therapy was initiated. The patient benefited significantly from both immunotherapy and supportive management. Physical therapy was also provided during the clinical course. At the time of discharge from the ward, improvement in muscle strength and overall clinical recovery were noted. This case represents a typical presentation of GBS.
Guillain-Barré syndrome is an acute-onset neurological emergency characterized by generalized muscle weakness and sensory symptoms. While consciousness is usually preserved during the clinical progression, respiratory failure requiring mechanical ventilation and autonomic dysfunction may be life-threatening. Treatment involves supportive measures as well as immunomodulatory therapies, such as IVIG and plasma exchange. The disease is generally monophasic in nature. The diagnostic, follow-up, and therapeutic processes will be discussed in detail in this section.
Referanslar
Goodfellow, J.A. and H.J. Willison, Guillain-Barre syndrome; a cen tury of progress. Nat Review Neurology; 2016. 12(12); 723-731
Wijdicks, E.F. and C.J. Klein, Guillain-Barre Syndrome. Mayo Clin Proceedings; 2017. 92(3); 467-479.
Pithadia, Anand B., and Nimisha Kakadia. "Guillain-Barré syndrome (GBS)." Pharmacological reports 62.2 (2010); 220-232.
Hughes, Richard AC. "Guillain-Barré syndrome; looking back… and forward." Journal of Neurology, Neurosurgery & Psychiatry 91.2 (2020); 111-112.
Overell, James R., ve diğerleri. "Fisher sendromu, Bickerstaff beyin sapı ensefaliti ve ilgili bozuklukların tedavisi." Cochrane Sistematik İncelemeler Veritabanı 1 (2007).
Shang, P., Zhu, M., Baker, M., Feng, J., Zhou, C., & Zhang, H. L. (2020). Mechanical ventilation in Guillain–Barré syndrome. Expert Reviewiew of Clinical Immunology, 16(11), 1053–1064.
Shang, P., Feng, J., Wu, W., & Zhang, H. L. (2021). Intensive Care and Treatment of Severe Guillain-Barré Syndrome. Frontiers in pharmacology, 12, 608130.
Greene-Chandos, D. and M. Torbey, Critical Care of Neuromuscular Disorders. Continuum (Minneap Minn), 2018. 24(6); 1753-1775.
Chevret, S., R.A. Hughes, and D. Annane, Plasma exchange for Guil lain-Barre syndrome. Cochrane Database Syst Review, 2017. 2; CD001798.
Hughes, Richard AC, et al. "Corticosteroids for Guillain‐Barré syndrome." Cochrane Database of Systematic Reviewiews 10 (2016).
Hughes RA, Swan AV, van Doorn PA. Intravenous immunoglobulin for Gui lain-Barre syndrome. Cochrane Database Syst Review 2014(9);CD002063.
Patwa HS, Chaudhry V, Katzberg H, Rae-Grant AD, So YT. Evidence-based guideline; intravenous immunoglobulin in the treatment of neuromuscular disorders; report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology 2012;78(13);1009-1015.
Elovaara I, Apostolski S, van Doorn P et al. Efns. EFNS guidelines for the use of intravenous immunoglobulin in treatment of neurological diseases; EFNS task force on the use of intravenous immunoglobulin in treatment of neurological diseases. Eur J Neurol 2008;15(9);893-908.
Korinthenberg R, Schessl J, Kirschner J, Monting JS. Intravenously administered immunoglobulin in the treatment of childhood Gui lain-Barre syndrome; a randomized trial. Pediatrics 2005;116(1);8-14.
Doets AY, Hughes RA, Brassington R, Hadden RD, Pritchard J. Pharmacological treatment other than corticosteroids, intravenous immunoglobulin and plasma exchange for Gui lain-Barre syndrome. Cochrane Database Syst Review 2020;1;CD008630.