TY  - JOUR
PY  - 2022//
TI  - Acute nitrous oxide-induced neuropathy mimicking Guillain-Barré Syndrome
JO  - Journal of the Peripheral Nervous System
A1  - Qin, Xing
A1  - Kang, Li
A1  - Liu, Xiao
A1  - Jin, Jiaoting
A1  - Hu, Fangfang
A1  - Lu, Wenhui
A1  - Deng, Yongning
A1  - Chen, Qiao Yi
A1  - Dang, Jingxia
SP  - ePub
EP  - ePub
VL  - ePub
IS  - ePub
N2  - BACKGROUND AND OBJECTIVE: The early clinical features of nitrous oxide (N(2) O)-induced neuropathy were mimicking that of Guillain-Barré Syndrome (GBS). We aimed to explore clinical and laboratory characteristics of N(2) O-induced neuropathy in comparison with GBS. <br><br>METHODS: We retrospectively reviewed data of 15 patients with N(2) O-induced neuropathy and compared them with 15 GBS patients. <br><br>RESULTS: The age of the N(2) O-induced neuropathy group was significantly younger than that in the GBS group (22 ± 5 vs 45 ± 17). Paresthesia was more common in N(2) O-induced neuropathy group (100% vs 53.3%). The proportion of distal upper limbs weakness was lower than that in GBS group (20.0% vs 93.3%). There was no significant difference in distal weakness of the lower limbs (100% vs 80.0%). The incidence of motor conduction block and compound muscle action potential amplitude reduction in upper limbs was lower than that in GBS group (6.7% vs 60.0%; 26.7% vs 80.0%). The sensory nerve action potential amplitude drop in the lower limbs was more severe than that in GBS group (53.3% vs 0). The increase of Mean corpuscular volume (MCV) was more pronounced compared to GBS group (96.97 ± 6.00 vs 88.55 ± 5.41). High homocysteine levels were more common in N(2) O-related group [29.80(11.60, 70.50) vs 14.35(9.22, 19.30)]. <br><br>CONCLUSION: Typical clinical features of the acute N(2) O neuropathy appears to be a myeloneuropathy, affecting the lower limbs more than the upper limbs, mixed axonal-demyelinating electrophysiological performance, higher homocysteine level and larger MCV and common posterior spinal cord involvement in cervical segment. This article is protected by copyright. All rights reserved.<p />  <p>Language: en</p>
LA  - en
SN  - 1085-9489
UR  - http://dx.doi.org/10.1111/jns.12503
ID  - ref1
ER  -