Association Between the Rate of Treatment Response and Short-Term Outcomes in Childhood Guillain-Barré Syndrome

Abstract

Introduction: Few studies have examined the association between the rate of treatment response and the outcome of pediatric Guillain-Barré syndrome (GBS). Therefore, our study aimed to identify treatment response in relation to the short-term outcomes of GBS. Further, we investigated its potential predictive value for prognosis.Methods: Our retrospective study included children diagnosed with GBS in the Pediatric Neurology Department of the Children's Hospital of Hebei Province from 2016 to 2020. According to the rate of response from the standard intravenous immunoglobulin (IVIg) treatment, patients were divided into two groups: rapid-response GBS (initial response within 7 days) and slow-response (initial response within 8–30 days). The GBS disability score (Hughes Functional Grading Scale) was used to assess the children's functional disability at nadir, 1 month, and 6 months after onset.Results: Among the 36 children included in the study, 18 (50%) and 18 (50%) were rapid and slow responders, respectively. Time from IVIg treatment to the initial response was significantly shorter in the rapid-response group (5 [3–6.25] days vs. 10.5[8.75–15] days in slow-response GBS, p < 0.001). Hughes score at 1 month was worse than the rapid responders (Fisher's exact test, p = 0.006). Survival analysis (Kaplan–Meier) with respect to regaining the ability to walk independently (Hughes Functional Grading Scale of 2) within 1 month after onset was significantly different among the two groups (log-rank test for trend, p = 0.024). The abnormal levels of cerebral spinal fluid proteins and autonomic dysfunction were more frequent in the slow-response group than those in the rapid group (p < 0.05).Conclusion: The rate of response to IVIg treatment was correlated with short-term outcomes in children with GBS and had predictive value for prognosis. The role of patient's initial responses to treatment could be significantly valuable in developing more effective and efficient treatment options.

Association Between A-Waves and Outcome in Pediatric Guillain-Barré Syndrome

“…The prognosis of patients with GBS is considered good; however, approximately 20% of patients are unable to walk unaided (9), and about 7% of patients died (10). As a special group, most children with GBS have a good prognosis (11,12). In this study, 29.2% (19/65) of patients at 1 month and 7.7% (5/65) of patients at 6 months had poor prognoses, respectively.…”

Case Report: Chlamydia psittaci pneumonia complicated by Guillain-Barré syndrome detected using metagenomic next-generation sequencing

“…The recommended dosage in adults is 0.4 g•kg -1 •d -1 for 5 consecutive days (Van den Berg et al, 2014;Liu et al, 2018;Svacǐna et al, 2019). The response rate after immunoglobulin treatment was found to correlate with clinical outcomes, and the short-term outcomes of patients that started with intravenous immunoglobulin within 1 week were significantly better than those of patients that started treatment after 1 week (Jin et al, 2021). Grattan et al (1982) reported a case of psittacosis complicated by GBS.…”

Cerebrospinal fluid neurofilament light chain predicts short-term prognosis in pediatric Guillain-Barré syndrome

“…The prognosis of GBS tends to be good after effective treatments, however, about one-fifth of the patients are unable to walk independently at 6 months after symptom onset, and about 7% of patients die ( 16 ). Many studies have shown that pediatric GBS has a good prognosis ( 17 , 18 ). In the present study, seven (7/26, 26.9%) and 19 patients (19/26, 73.1%) showed poor and good prognoses, respectively, at 1 month after symptom onset, whereas none of the patients was unable to walk independently at 6 months after symptom onset.…”