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Early electrodiagnostic abnormalities in acute inflammatory demyelinating polyneuropathy: a retrospective study of 58 patients.
Clin Neurophysiol. 2014 Sep; 125(9):1900-5.CN

Abstract

OBJECTIVE

Although patients with acute inflammatory demyelinating polyneuropathy (AIDP) are frequently admitted a few days after symptoms onset, electrodiagnostic (EDX) abnormalities in early AIDP are not well characterized. Our aim was to determine the EDX pattern of early AIDP, and, if needed, to propose new EDX diagnostic criteria.

METHODS

In this monocentric study, we retrospectively reviewed the clinical and EDX data of 58 consecutive AIDP patients in whom EDX studies had been performed within 7 days after disease onset, representing 46% of all GBS patients admitted in our hospital in an 11 years interval.

RESULTS

EDX abnormalities were observed in all patients. The most altered parameters were H reflexes (97% of cases), motor nerve conduction velocities (78%) and distal motor latencies (78%). Only 66% of patients fulfilled the most sensitive published AIDP EDX diagnosis criteria. When using a new set of EDX criteria, which require only one marked EDX abnormality, we observed that 81% of patients could be diagnosed with AIDP.

CONCLUSION

This study suggests that exhaustive EDX studies are always abnormal in early AIDP, and that existing EDX diagnosis criteria can be improved.

SIGNIFICANCE

Our findings are useful for the interpretation of EDX studies in early AIDP.

Authors+Show Affiliations

Département de Neurologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France. Electronic address: jean-baptiste.chanson@chru-strasbourg.fr.Département de Neurologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

24529487

Citation

Chanson, Jean-Baptiste, and Andoni Echaniz-Laguna. "Early Electrodiagnostic Abnormalities in Acute Inflammatory Demyelinating Polyneuropathy: a Retrospective Study of 58 Patients." Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology, vol. 125, no. 9, 2014, pp. 1900-5.
Chanson JB, Echaniz-Laguna A. Early electrodiagnostic abnormalities in acute inflammatory demyelinating polyneuropathy: a retrospective study of 58 patients. Clin Neurophysiol. 2014;125(9):1900-5.
Chanson, J. B., & Echaniz-Laguna, A. (2014). Early electrodiagnostic abnormalities in acute inflammatory demyelinating polyneuropathy: a retrospective study of 58 patients. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology, 125(9), 1900-5. https://doi.org/10.1016/j.clinph.2014.01.007
Chanson JB, Echaniz-Laguna A. Early Electrodiagnostic Abnormalities in Acute Inflammatory Demyelinating Polyneuropathy: a Retrospective Study of 58 Patients. Clin Neurophysiol. 2014;125(9):1900-5. PubMed PMID: 24529487.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Early electrodiagnostic abnormalities in acute inflammatory demyelinating polyneuropathy: a retrospective study of 58 patients. AU - Chanson,Jean-Baptiste, AU - Echaniz-Laguna,Andoni, Y1 - 2014/01/27/ PY - 2013/09/13/received PY - 2013/12/15/revised PY - 2014/01/01/accepted PY - 2014/2/18/entrez PY - 2014/2/18/pubmed PY - 2015/5/6/medline KW - Acute inflammatory demyelinating polyneuropathy KW - Demyelination KW - Electrodiagnostic study KW - Guillain–Barré syndrome KW - Sural sparing SP - 1900 EP - 5 JF - Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology JO - Clin Neurophysiol VL - 125 IS - 9 N2 - OBJECTIVE: Although patients with acute inflammatory demyelinating polyneuropathy (AIDP) are frequently admitted a few days after symptoms onset, electrodiagnostic (EDX) abnormalities in early AIDP are not well characterized. Our aim was to determine the EDX pattern of early AIDP, and, if needed, to propose new EDX diagnostic criteria. METHODS: In this monocentric study, we retrospectively reviewed the clinical and EDX data of 58 consecutive AIDP patients in whom EDX studies had been performed within 7 days after disease onset, representing 46% of all GBS patients admitted in our hospital in an 11 years interval. RESULTS: EDX abnormalities were observed in all patients. The most altered parameters were H reflexes (97% of cases), motor nerve conduction velocities (78%) and distal motor latencies (78%). Only 66% of patients fulfilled the most sensitive published AIDP EDX diagnosis criteria. When using a new set of EDX criteria, which require only one marked EDX abnormality, we observed that 81% of patients could be diagnosed with AIDP. CONCLUSION: This study suggests that exhaustive EDX studies are always abnormal in early AIDP, and that existing EDX diagnosis criteria can be improved. SIGNIFICANCE: Our findings are useful for the interpretation of EDX studies in early AIDP. SN - 1872-8952 UR - https://www.unboundmedicine.com/medline/citation/24529487/Early_electrodiagnostic_abnormalities_in_acute_inflammatory_demyelinating_polyneuropathy:_a_retrospective_study_of_58_patients_ DB - PRIME DP - Unbound Medicine ER -