Guillain-Barré syndrome natural history, complications, and prognosis: Difference between revisions

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==Overview==
==Overview==
Approximately 80% of patients have a complete recovery within a few months to a year, although minor findings may persist. A patient's outcome is most likely to be very good when the symptoms go away within 3 weeks after they first started. Complications like [[paralysis]], [[respiratory failure]] and [[hypotension]] can be seen in these patients.
 
==Natural History, Complications, and Prognosis==
==Natural History, Complications, and Prognosis==


=== Natural history ===
=== Natural history ===
* The symptoms of Guillain Barre syndrome typically develop 1 to 3 weeks after the Antecedent Infection.
* The symptoms of Guillain Barre syndrome typically develop 1 to 3 weeks after the Antecedent Infection.
* If left untreated, 65% of patients with Guillain Barre syndrome will recover with may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
* If left untreated, 65% of patients with Guillain Barre syndrome will recover with no permanent disability.
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated. GBS has a different natural history in every patient based on age and the speed of symptoms occurrence, so it can lead to death or patients may fully recover no matter what the etiology is.<ref name="pmid9818934">{{cite journal |vauthors=Hadden RD, Cornblath DR, Hughes RA, Zielasek J, Hartung HP, Toyka KV, Swan AV |title=Electrophysiological classification of Guillain-Barré syndrome: clinical associations and outcome. Plasma Exchange/Sandoglobulin Guillain-Barré Syndrome Trial Group |journal=Ann. Neurol. |volume=44 |issue=5 |pages=780–8 |date=November 1998 |pmid=9818934 |doi=10.1002/ana.410440512 |url=}}</ref><ref name="pmid1565119">{{cite journal |vauthors=Bradshaw DY, Jones HR |title=Guillain-Barré syndrome in children: clinical course, electrodiagnosis, and prognosis |journal=Muscle Nerve |volume=15 |issue=4 |pages=500–6 |date=April 1992 |pmid=1565119 |doi=10.1002/mus.880150415 |url=}}</ref>
* 35% of them will not fully recover. 8% of these 35% will die from complication and others will have permanent disabilities.
 
* Treatment will just reduce the recovery period and has no effect on natural history of the disease.
 
* The first symptoms are lower extremities weakness and paresthesia.<ref name="pmid9818934">{{cite journal |vauthors=Hadden RD, Cornblath DR, Hughes RA, Zielasek J, Hartung HP, Toyka KV, Swan AV |title=Electrophysiological classification of Guillain-Barré syndrome: clinical associations and outcome. Plasma Exchange/Sandoglobulin Guillain-Barré Syndrome Trial Group |journal=Ann. Neurol. |volume=44 |issue=5 |pages=780–8 |date=November 1998 |pmid=9818934 |doi=10.1002/ana.410440512 |url=}}</ref><ref name="pmid1565119">{{cite journal |vauthors=Bradshaw DY, Jones HR |title=Guillain-Barré syndrome in children: clinical course, electrodiagnosis, and prognosis |journal=Muscle Nerve |volume=15 |issue=4 |pages=500–6 |date=April 1992 |pmid=1565119 |doi=10.1002/mus.880150415 |url=}}</ref><ref name=":0">{{cite book | last = Mattle | first = Heinrich | title = Fundamentals of neurology : an illustrated guide | publisher = Thieme | location = Stuttgart New York | year = 2017 | isbn = 9783131364524 }}</ref>
===Complications===
===Complications===
* Common complications of GBS include:<ref name="pmid15668421">{{cite journal |vauthors=Dornonville de la Cour C, Jakobsen J |title=Residual neuropathy in long-term population-based follow-up of Guillain-Barré syndrome |journal=Neurology |volume=64 |issue=2 |pages=246–53 |date=January 2005 |pmid=15668421 |doi=10.1212/01.WNL.0000149521.65474.83 |url=}}</ref><ref name="pmid9344309">{{cite journal |vauthors=Meythaler JM |title=Rehabilitation of Guillain-Barré syndrome |journal=Arch Phys Med Rehabil |volume=78 |issue=8 |pages=872–9 |date=August 1997 |pmid=9344309 |doi= |url=}}</ref>
* Common complications of GBS include:<ref name="pmid15668421">{{cite journal |vauthors=Dornonville de la Cour C, Jakobsen J |title=Residual neuropathy in long-term population-based follow-up of Guillain-Barré syndrome |journal=Neurology |volume=64 |issue=2 |pages=246–53 |date=January 2005 |pmid=15668421 |doi=10.1212/01.WNL.0000149521.65474.83 |url=}}</ref><ref name="pmid9344309">{{cite journal |vauthors=Meythaler JM |title=Rehabilitation of Guillain-Barré syndrome |journal=Arch Phys Med Rehabil |volume=78 |issue=8 |pages=872–9 |date=August 1997 |pmid=9344309 |doi= |url=}}</ref>

Revision as of 19:47, 17 December 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editors-In-Chief: Fahimeh Shojaei, M.D.

Overview

Natural History, Complications, and Prognosis

Natural history

  • The symptoms of Guillain Barre syndrome typically develop 1 to 3 weeks after the Antecedent Infection.
  • If left untreated, 65% of patients with Guillain Barre syndrome will recover with no permanent disability.
  • 35% of them will not fully recover. 8% of these 35% will die from complication and others will have permanent disabilities.
  • Treatment will just reduce the recovery period and has no effect on natural history of the disease.
  • The first symptoms are lower extremities weakness and paresthesia.[1][2][3]

Complications

Prognosis

  • About 65% of patients with GBS will fully recover with no permanent disability.
  • 35% of them do not fully recover. 8% of this group will die from GBS complication and others will have permanent disabilities.
  • Treatment of GBS just reduce the recovery time and doesn’t affect prognosis.[6]
  • Overally, older patients will have worst prognosis in comparison to children who discover very fast.[1][2]

References

  1. 1.0 1.1 Hadden RD, Cornblath DR, Hughes RA, Zielasek J, Hartung HP, Toyka KV, Swan AV (November 1998). "Electrophysiological classification of Guillain-Barré syndrome: clinical associations and outcome. Plasma Exchange/Sandoglobulin Guillain-Barré Syndrome Trial Group". Ann. Neurol. 44 (5): 780–8. doi:10.1002/ana.410440512. PMID 9818934.
  2. 2.0 2.1 Bradshaw DY, Jones HR (April 1992). "Guillain-Barré syndrome in children: clinical course, electrodiagnosis, and prognosis". Muscle Nerve. 15 (4): 500–6. doi:10.1002/mus.880150415. PMID 1565119.
  3. Mattle, Heinrich (2017). Fundamentals of neurology : an illustrated guide. Stuttgart New York: Thieme. ISBN 9783131364524.
  4. Dornonville de la Cour C, Jakobsen J (January 2005). "Residual neuropathy in long-term population-based follow-up of Guillain-Barré syndrome". Neurology. 64 (2): 246–53. doi:10.1212/01.WNL.0000149521.65474.83. PMID 15668421.
  5. Meythaler JM (August 1997). "Rehabilitation of Guillain-Barré syndrome". Arch Phys Med Rehabil. 78 (8): 872–9. PMID 9344309.
  6. Rees JH, Thompson RD, Smeeton NC, Hughes RA (January 1998). "Epidemiological study of Guillain-Barré syndrome in south east England". J. Neurol. Neurosurg. Psychiatry. 64 (1): 74–7. PMC 2169900. PMID 9436731.

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