You are on page 1of 5

MAJOR ARTICLE

Recurrent Guillain-Barre Syndrome Following Vaccination


Roger Baxter,1 Ned Lewis,1 Nandini Bakshi,2 Claudia Vellozzi,3 Nicola P. Klein,1 and the CISA Network
1Kaiser Permanente Vaccine Study Center; 2The Permanente Medical Group, Oakland, California; and 3Immunization Safety Office, Centers for Disease Control and Prevention, Atlanta, Georgia

Background. Guillain-Barre syndrome (GBS) is an acute polyradiculopathy, thought to be autoimmune, which has been reported following vaccinations. The Advisory Committee on Immunization Practices recommends not administering inuenza vaccine to individuals who have had a history of GBS within 6 weeks of a prior inuenza vaccination if they are not at high risk of severe complications from inuenza illness. Methods. We identied GBS cases from the Kaiser Permanente Northern California databases from 1995 into 2006 using hospital discharge codes; each medical record was neurologist-reviewed and only GBSconrmed cases were included for follow-up. We followed conrmed cases through 2008 for vaccinations and recurrent GBS. Results. We identied 550 cases of GBS over 33 million person-years. Following their GBS diagnoses, 989 vaccines were given to 279 of these individuals, including 405 trivalent inactivated inuenza vaccines (TIV) administered to 107 individuals with a prior diagnosis of GBS. Among the 550 total cases of GBS, 18 initially had onset within 6 weeks of TIV; of these, 2 were revaccinated with TIV without a recurrence of GBS. Only 6 individuals of 550 (1.1%) had a second (recurrent) diagnosis of GBS. Among these 6 individuals, none had any vaccine exposure at all in the 2 months prior to the second onset of GBS. Conclusions. In our population of over 3 million members, during an 11-year period, risk of GBS recurrence was low. There were no cases of recurrent GBS after inuenza vaccination and none within 6 weeks after any vaccine.

Downloaded from http://cid.oxfordjournals.org/ by guest on August 9, 2012

Guillain-Barre syndrome (GBS) is an acute, rapidly evolving polyradiculoneuropathy, typically presenting with bilateral muscle weakness and paresthesias, in association with absent or diminished deep tendon reexes. The severity of weakness in cases of GBS ranges from mild weakness to total paralysis, which can lead to death. The annual average incidence rate of GBS, depending on the population being assessed and the method of surveillance, is between 0.4 and 4 cases per 100 000 population [13]. Persons of any age are at risk; however, the incidence is much higher among the elderly [4, 5].

Received 21 September 2011; accepted 15 November 2011; electronically published 19 January 2012. Correspondence: Roger Baxter, MD, Kaiser Permanente Vaccine Study Center, 1 Kaiser Plaza, 16th Floor, Oakland, CA 94612 (roger.baxter@kp.org). Clinical Infectious Diseases 2012;54(6):8004 The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com. DOI: 10.1093/cid/cir960

GBS is thought to be an autoimmune disorder; the most widely accepted current hypothesis is that of molecular mimicry in which the immune response to specic antigens (including infectious organisms) is characterized by an attack on cross-reactive epitopes in the host peripheral nervous system, causing inammation and demyelination [5]. Numerous antecedent events have been temporally associated with subsequent development of GBS, including viral and bacterial infections, and surgery [611]. An antecedent illness has been reported in up to two-thirds of patients with GBS [2, 7, 12]. Receipt of vaccines has also been temporally associated with GBS, including rabies [10], combined diphtheria, pertussis and tetanus, rubella, tetanus toxoid [8], hepatitis B, hepatitis A [13], polio [14], inuenza [1517], and meningococcal conjugate vaccines [2, 18, 19]. In most cases, the association of vaccination with subsequent GBS is temporal only, and causality is rarely established [20, 21]. The most accurately characterized relationship between GBS and vaccines is that which was seen following the 1976 swine inuenza vaccine [15].

800

CID 2012:54 (15 March)

Baxter et al

Concerns about the association of GBS with inuenza vaccine have resulted in caution regarding revaccination in individuals with a history of GBS [15]. The Advisory Committee on Immunization Practices (ACIP) currently recommends avoiding inuenza vaccination in persons who are not at high risk for severe inuenza illness complications and who have a history of GBS within 6 weeks after a previous inuenza vaccination [22]. While persons with a history of GBS have a greater likelihood of subsequently experiencing GBS (regardless of any potential etiologies, including vaccination) than persons without such a history [23, 24], there is little evidence to support these recommendations. Further, this recommendation may be interpreted to mean avoidance of inuenza vaccination for anyone with a history of GBS, not just those who had GBS temporally associated with a previous inuenza vaccination; this may also cause avoidance of other vaccines as well. Studies [25, 26] and case reports [2729] of the recurrence of GBS following immunization suggest that the rate of recurrence is low, but evidence and population-based recommendations regarding vaccinating persons with a history of GBS are needed. The purpose of this study is to describe the vaccination and GBS recurrence rate in individuals with a history of GBS, and to determine whether they have an increased risk of disease recurrence following vaccination. METHODS
Study Population

Kaiser Permanente of Northern California (KPNC) is a large, integrated healthcare delivery system with a membership of over 3.2 million. The KPNC population is diverse with regard to age, sex, race, and socioeconomic status, and is similar to the regions demographic distribution, except for the extremes of wealth and poverty [30, 31]. Members of the health plan receive almost all medical care at KPNC facilities, and information on all visits is recorded in the electronic medical record. Laboratory tests, medications, and most other services are covered by the plan, and are provided at KP facilities. Hospitalizations and emergency department visits that are not covered by the health plan are captured via claims. Vaccinations are provided at no additional cost to members, and are mostly received and recorded [32] in a unique immunization tracking system. Inuenza vaccines in particular are delivered to multiple areas during the season to make vaccination as convenient as possible for members.
Study Design

this younger age group. All identied cases underwent chart review by trained medical records analysts (MRAs). If the record review indicated that the case was diagnosed prior to the visit identied, we searched for earlier diagnoses, and extensively examined the medical record to determine the GBS onset date. We included all cases, including those in which subsequent review determined that the GBS onset date was prior to the study period. An abstraction form was used that was designed to validate the diagnosis of GBS and determine etiologic factors, including vaccination. Cases were rejected by an MRA if there was no reference to GBS in the chart, or if GBS was ruled out. All cases that were not rejected were subsequently reviewed by a neurologist and classied as level 1, 2, or 3 according to the Brighton Collaboration criteria [33]. Level 1 denotes a laboratoryconrmed case, while levels 2 and 3 denote probable cases without all laboratory variables and possible cases with clinical criteria only, respectively. Chronic inammatory demyelinating polyradiculoneuropathy (CIDP) is an illness that presents with signs and symptoms similar to GBS but has a chronic or relapsing course, rather than a monophasic course typical of GBS. CIDP may be difcult to distinguish from GBS in the early stages [34], and may be misclassied as a recurrence of GBS [35]. Cases primarily identied as CIDP by ICD-9 codes were excluded from the initial data extraction. Among cases with the ICD-9 code 357.0 (GBS), subsequent chart review sometimes revealed that the disease was later conrmed as CIDP, and these cases were also excluded. Recurrent GBS was dened as 2 or more episodes of acute monophasic neuropathy followed by near complete recovery between episodes [36]. After identifying the rst episode of GBS, we searched inpatient and outpatient databases as well as our immunization databases for vaccination and GBS recurrence through 2008, until the patient died or left the health plan, or until 25 years had elapsed since the rst episode of GBS. The neurologist reviewed all cases and determined whether or not a recurrence of GBS had, in fact, occurred. Follow-up time for the study was determined by the total number of person-years in the KPNC cohort $5 years of age during the study years. Follow-up time after the onset of GBS was determined by total person-time from the date of GBS diagnosis of all cases to the end of 2008, death, or disenrollment from the health plan. This study was approved by the KPNC Institutional Review Board. RESULTS Out of a total of 896 individual cases of GBS that were identied on the basis of the ICD-9 codes, medical records were available for 892. Of these, 114 (12.8%) were rejected by the MRAs as being inconsistent with GBS. Of the remaining 778 potential
d

Downloaded from http://cid.oxfordjournals.org/ by guest on August 9, 2012

We identied all persons $5 years of age in KPNC databases discharged from the hospital with a rst occurrence of the ICD-9 code corresponding to GBS (357.0) during the study period 19952006. The study cohort excluded persons ,5 years of age to minimize the effect of the multiple vaccination schedule in

Vaccination and Recurrence of Guillain-Barre Syndrome

CID 2012:54 (15 March)

801

cases, 220 (28.3%) were rejected by the reviewing neurologist due to information in the chart that was incompatible with GBS, and 8 (1.0%) were rejected for insufcient information in the medical record to determine a diagnosis. The remaining 550 (61.4% of the original set identied) were veried as GBS cases, of which 139 were classied as Brighton level 1 (laboratory-conrmed), 360 cases as level 2 (met some but not all laboratory criteria), and 51 cases as level 3 (clinical diagnosis only). The earliest conrmed case was in September 1958 and the latest conrmed case was in February 2008. We included all 550 rst-episode cases in our analysis. Of the 550 cases, 91 were determined to have occurred prior to the study period. The 459 remaining cases occurred over 31 305 844 person-years, resulting in an overall incidence of GBS of 1.47 per 100 000 person-years for ages $5 years (95% Poisson condence interval [CI], 1.341.61). We assessed vaccines administered to individuals subsequent to their GBS diagnosis and observed that a total of 989 vaccines were given to 279 individuals with a history of GBS (Table 1). There was a wide range of vaccines administered, with the most common being trivalent inactivated (killed) inuenza vaccine (TIV; 405 doses were given to 107 individuals), pneumococcal polysaccharide vaccine (151 doses), and tetanus-diphtheria vaccines (143 doses). We estimated the overall incidence of recurrent GBS by identifying and conrming individuals with recurrent GBS. Out

Table 1. Vaccines Given to People After the Diagnosis of Guillain Barre Syndrome (GBS), Northern California Kaiser, 19952006 (Total Number of GBS Cases N 5 550)
Vaccine Type Trivalent injectable inuenza Pneumovax Tetanus diphtheria Hepatitis A Hepatitis B Combined MMR Injectable polio Tetanus, reduced diphtheria, reduced acellular pertussis Diphtheria, tetanus, acellular pertussis Zoster Injectable typhoid Meningococcal conjugate Meningococcal polysaccharide Othera Any vaccine
a

N 405 151 136 78 42 19 17 43

Percent 41.0 15.3 13.8 7.9 4.3 1.9 1.7 4.4

Individuals 107 132 126 53 30 18 16 43

of the 896 cases initially suspected as having GBS, 37 individuals initially appeared in the electronic database as having multiple episodes of GBS. Chart review and further neurologist adjudication determined that 11 (29.7%) of these were eventually diagnosed as CIDP, and 20 (54.1%) were either not recurrent (ie, the diagnosis was documented later, but turned out to be referring to the history of the earlier episode) or not conrmed to be GBS. The remaining 6 individuals (1.1% of the group of 550 conrmed cases) were conrmed as having recurrent GBS; these 6 individuals each had only 1 episode of recurrent GBS. There were 3974 person-years of follow-up in the 550 GBS patients after the conrmed diagnosis of GBS. The calculated rate of recurrence of GBS was 1.5 per 1000 person-years (95% Poisson CI, .63.3). Table 2 shows time to recurrence for the recurrent cases. Among the 6 individuals with conrmed GBS recurrence, only 1 had any vaccine exposure within the year prior to the recurrent GBS episode. The vaccine exposure was a single dose of measles-mumps-rubella administered 4 months prior to the onset of the recurrent GBS episode. Of the 550 cases of GBS, 18 (3.3%) had the initial onset within 6 weeks of TIV. This is the group for which the ACIP recommends caution for inuenza revaccination. These 18 people were less likely to have received further inuenza vaccines than those who developed GBS with no temporal association with TIV (2 [11%] of the 18 received subsequent inuenza vaccines vs 105 of 532 [20%] of those who developed GBS not in relation to TIV), but the difference was not signicant (P 5 .6 by Fisher exact test). None of the GBS cases followed receipt of live intranasal inuenza vaccine. Among the 107 individuals with a previous diagnosis of GBS who received a total of 405 doses of TIV, there were no cases of recurrent GBS within the year following TIV (95% binomial CI, 0.91 per 100 doses). None of the 18 GBS cases which originally followed TIV, including the 2 with subsequent TIV administration, had a recurrence of GBS.

Downloaded from http://cid.oxfordjournals.org/ by guest on August 9, 2012

Table 2. Characteristics of Recurrent Guillain-Barre Syndrome, Northern California Kaiser, 19952006


1st Episode 2nd Episode Age 36 45 79 66 31 54 Prior Illness Respiratory Strep pharyngitis Respiratory None GI Respiratory

11 10 10 7 8 52 989

1.1 1.0 1.0 0.7 0.8 5.3 100

11 10 9 7 6 36 279 Case 1 2 3 4 5 6 Sex F F M F F M

Years to Recurrence 11.0 1.8 13.2 40.0 2.9 2.9

Age 25 43 66 26 28 52

Prior Illness Respiratory Respiratory Respiratory None GI Respiratory

Abbreviation: MMR, measles-mumps-rubella. Each with fewer than 10 (1%) total.

Abbreviation: GI, gastrointestinal.

802

CID 2012:54 (15 March)

Baxter et al

DISCUSSION The ACIP strives to makes vaccine recommendations based on available evidence. In the absence of evidence, the ACIP has chosen to be cautious in their recommendations to not vaccinate persons with a history of GBS following previous inuenza vaccination who are also at low risk of inuenza illness complications. Contributing to the knowledge of the risk of GBS recurrence after revaccination will support the work of advisory committees such as ACIP. In our series, the overall incidence rate of GBS of 1.47 per 100 000 person-years was consistent with rates of 0.44 per 100 000 person-years found worldwide, and conrms tighter estimates in European studies of 1.21.9 per 100 000 person-years [4, 5]. We found that patients diagnosed with GBS subsequently received multiple vaccines of various types, including inuenza vaccines. With over 30 million person-years of follow-up over the study period and nearly 1000 vaccines administered after a diagnosis of GBS (including over 400 inuenza vaccinations), we did not observe a single recurrent case of GBS that could be considered associated with vaccination. Based on this observation, it appears that vaccination does not increase the risk of recurrent GBS, although our insufcient sample size detracts from the complete condence we have for this conclusion. Because recurrent GBS is so rare and our study was small in size, we were only able to rule out a recurrence risk of GBS greater than about 1 per 100 doses of TIV (our upper CI limit was .91 per 100). We identied only 18 cases (3.3% of the total) that would potentially be considered at higher risk of recurrence because they originally experienced onset of GBS within 6 weeks of TIV. The paucity of data does not allow us to evaluate the ACIP recommendation that GBS patients who developed the condition within 6 weeks of an inuenza vaccine should not be revaccinated unless they have a compelling need. Limitations of our study included reliance on inpatient diagnoses to identify GBS cases. It is possible that we could have detected more cases if we had used the outpatient databases as well. However, we think it would be unusual in our practice setting for GBS to be treated solely as an outpatient, particularly since patients often receive plasmapheresis, which is generally done as an inpatient procedure. Another limitation is the possibility that members received vaccines outside of KPNC. However, for the reasons cited above, we think that the vast majority of vaccines of all types are captured by our immunization tracking system. In conclusion, we found no evidence that vaccination is associated with recurrent GBS. We also did not observe any recurrent GBS in the 18 GBS cases that initially occurred within 6 weeks following receipt of inuenza vaccine; however, we did not have enough power to evaluate an association of repeat inuenza vaccination and recurrent GBS. It may not be possible to obtain

the power to rule out this association, based on the rarity of both the disease and revaccination in GBS cases.
Notes
Acknowledgments. Paula Ray, Ajit DeSilva, and Pat Ross for assistance with data collection; Bruce Fireman, Jerry Tokars, and Ali RowhaniRahbar for manuscript review, and James Sejvar at the CDC for guidance and expertise. Disclaimer. The ndings and conclusions in this report are those of the authors and do not necessarily represent the ofcial position of the Centers for Disease Control and Prevention. Financial support. This study was funded by the Clinical Immunization Safety Assessment Network through a subcontract with Americas Health Insurance Plans under contract 200-2002-00732 from the Centers for Disease Control and Prevention. Potential conicts of interest. R. B. and N. P. K. report research support from Merck & Co., Novartis, GlaxoSmithKline, Pzer, and SanoPasteur. All other authors report no reported conicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conicts of Interest. Conicts that the editors consider relevant to the content of the manuscript have been disclosed.

Downloaded from http://cid.oxfordjournals.org/ by guest on August 9, 2012

References
1. Newswanger DL, Warren CR. Guillain-Barre syndrome. Am Fam Physician 2004; 69:240510. 2. Joseph SA, Tsao CY. Guillain-Barre syndrome. Adolesc Med 2002; 13:48794. 3. Klein NP, Ray P, Carpenter D, et al. Rates of autoimmune diseases in Kaiser Permanente for use in vaccine adverse event safety studies. Vaccine 2010; 28:10628. 4. Hughes RA, Rees JH. Clinical and epidemiologic features of GuillainBarre syndrome. J Infect Dis 1997; 176(suppl 2):S928. 5. Hughes RA, Cornblath DR. Guillain-Barre syndrome. Lancet 2005; 366:165366. 6. Novak M. [Guillain-Barre syndrome as a sequela of inuenza]. Cesk Neurol Neurochir 1975; 38:3146. 7. Jacobs BC, Rothbarth PH, van der Meche FG, et al. The spectrum of antecedent infections in Guillain-Barre syndrome: a case-control study. Neurology 1998; 51:11105. 8. Newton N Jr, Janati A. Guillain-Barre syndrome after vaccination with puried tetanus toxoid. South Med J 1987; 80:10534. 9. Schonberger LB, Hurwitz ES, Katona P, Holman RC, Bregman DJ. Guillain-Barre syndrome: its epidemiology and associations with inuenza vaccination. Ann Neurol 1981; 9(suppl):318. 10. Siddiqui A, Usmani RI, Anwer S, Afsar S. Guillain-Barre syndrome occurring after rabies vaccination. J Pak Med Assoc 2005; 55:878. 11. Tam CC, OBrien SJ, Rodrigues LC. Inuenza, Campylobacter and Mycoplasma infections, and hospital admissions for Guillain-Barre syndrome, England. Emerg Infect Dis 2006; 12:18807. 12. Hughes RA, Charlton J, Latinovic R, Gulliford MC. No association between immunization and Guillain-Barre syndrome in the United Kingdom, 1992 to 2000. Arch Intern Med 2006; 166:13014. 13. Roux X, Gramond C, De Greslan T, et al. [Guillain-Barre syndrome and anti-hepatitis A vaccination]. Med Mal Infect 2010; 40:4902. 14. Kinnunen E, Farkkila M, Hovi T, Juntunen J, Weckstrom P. Incidence of Guillain-Barre syndrome during a nationwide oral poliovirus vaccine campaign. Neurology 1989; 39:10346. 15. Schonberger LB, Bregman DJ, Sullivan-Bolyai JZ, et al. Guillain-Barre syndrome following vaccination in the National Inuenza Immunization Program, United States, 19761977. Am J Epidemiol 1979; 110:10523. 16. Centers for Disease Control and Prevention. Preliminary results: surveillance for Guillain-Barre syndrome after receipt of inuenza A (H1N1) 2009 monovalent vaccineUnited States, 20092010. MMWR Morb Mortal Wkly Rep 2010; 59:65761.

Vaccination and Recurrence of Guillain-Barre Syndrome

CID 2012:54 (15 March)

803

17. Green SK, Rett M, Weintraub ES, et al. Risk of conrmed GuillainBarre Syndrome following monovalent inactivated inuenza A (H1N1) and seasonal inuenza vaccines in the Vaccine Safety Datalink Project, 20092010. Am J Epidemiol 2011; In press. 18. Centers for Disease Control and Prevention. Update: Guillain-Barre syndrome among recipients of Menactra meningococcal conjugate vaccineUnited States, June 2005September 2006. MMWR Morb Mortal Wkly Rep 2006; 55:11204. 19. Centers for Disease Control and Prevention. Update: Guillain-Barre syndrome among recipients of Menactra meningococcal conjugate vaccineUnited States, October 2005February 2006. MMWR Morb Mortal Wkly Rep 2006; 55:3646. 20. Hughes R, Rees J, Smeeton N, Winer J. Vaccines and Guillain-Barre syndrome. BMJ 1996; 312:14756. 21. Schattner A. Consequence or coincidence? The occurrence, pathogenesis and signicance of autoimmune manifestations after viral vaccines. Vaccine 2005; 23:387686. 22. Fiore AE, Uyeki TM, Broder K, et al. Prevention and control of inuenza with vaccines: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2010. MMWR Recomm Rep 2010; 59:162. 23. Smith NM, Bresee JS, Shay DK, Uyeki TM, Cox NJ, Strikas RA. Prevention and control of inuenza: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Recomm Rep 2006; 55:142. 24. Barohn RJ, Saperstein DS. Guillain-Barre syndrome and chronic inammatory demyelinating polyneuropathy. Semin Neurol 1998; 18: 4961. 25. Pritchard J, Mukherjee R, Hughes RA. Risk of relapse of Guillain-Barre syndrome or chronic inammatory demyelinating polyradiculoneuropathy following immunisation. J Neurol Neurosurg Psychiatry 2002; 73: 3489.

26. Hughes RA, Choudhary PP, Osborn M, Rees JH, Sanders EA. Immunization and risk of relapse of Guillain-Barre syndrome or chronic inammatory demyelinating polyradiculoneuropathy. Muscle Nerve 1996; 19:12301. 27. Seyal M, Ziegler DK, Couch JR. Recurrent Guillain-Barre syndrome following inuenza vaccine. Neurology 1978; 28:7256. 28. Pollard JD, Selby G. Relapsing neuropathy due to tetanus toxoid. Report of a case. J Neurol Sci 1978; 37:11325. 29. Combes A, Goulon M. [Recurrence of Guillain-Barre syndrome]. Ann Med Interne (Paris) 1992; 143:5158. 30. Krieger N. Overcoming the absence of socioeconomic data in medical records: validation and application of a census-based methodology. Am J Public Health 1992; 82:70310. 31. Selby JV, Smith DH, Johnson ES, Raebel MA, Friedman GD, McFarland BH, eds. Kaiser Permanente medical care program. 4th ed. New York, NY: Wiley, 2005. 32. Greene SK, Shi P, Dutta-Linn MM, et al. Accuracy of data on inuenza vaccination status at four Vaccine Safety Datalink sites. Am J Prev Med 2009; 37:5525. 33. Sejvar JJ, Kohl KS, Gidudu J, et al. Guillain-Barre syndrome and Fisher syndrome: case denitions and guidelines for collection, analysis, and presentation of immunization safety data. Vaccine 2011; 29:599612. 34. Ruts L, van Koningsveld R, van Doorn PA. Distinguishing acute-onset CIDP from Guillain-Barre syndrome with treatment related uctuations. Neurology 2005; 65:13840. 35. Research criteria for diagnosis of chronic inammatory demyelinating polyneuropathy (CIDP). Report from an ad hoc subcommittee of the American Academy of Neurology AIDS Task Force. Neurology 1991; 41:6178. 36. Ruts L, Drenthen J, Jacobs BC, van Doorn PA. Distinguishing acuteonset CIDP from uctuating Guillain-Barre syndrome: a prospective study. Neurology 2010; 74:16806.

Downloaded from http://cid.oxfordjournals.org/ by guest on August 9, 2012

804

CID 2012:54 (15 March)

Baxter et al