Cover image of the article: The Effect of Needle Type, Duration of Surgery and Position of the Patient on the Risk of Transient Neurologic Symptoms

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The Effect of Needle Type, Duration of Surgery and Position of the Patient on the Risk of Transient Neurologic Symptoms

Authors

Farhad EtezadiFarhad Etezadi ORCID1, Kourosh Karimi Yarandi2, Aylar AhangaryAylar Ahangary ORCID1, Hajar ShokriHajar Shokri ORCID1, Farsad ImaniFarsad Imani ORCID1, Saeid Safari3, Mohammad Reza KhajaviMohammad Reza Khajavi ORCID1,*
1Department of Anesthesiology, Sina Hospital, Tehran University of Medical Sciences, khajavim@tums.ac.ir, Iran
2Department of Neurosurgery, Tehran University of Medical Sciences, Iran
3Department of Anesthesiology, Rasoul Akram Medical Center, Iran University of Medical Sciences (IUMS), Iran
*Corresponding Author: Department of Anesthesiology, Sina Hospital, Hassan Abad Sq.,Tehran University of Medical Sciences, khajavim@tums.ac.ir, Iran. Tel: +98-9123837096. Fax: +98-2166509059. Email: khajavim@tums.ac.ir

Anesthesiology and Pain Medicine:Vol. 2, issue 4; 154-8
Published online:Mar 26, 2013
Article type:Research Article
Received:Jun 22, 2012
Accepted:Oct 09, 2012
How to Cite:Etezadi F, Karimi Yarandi K, Ahangary A, Shokri H, Imani F, et al. The Effect of Needle Type, Duration of Surgery and Position of the Patient on the Risk of Transient Neurologic Symptoms. Anesth Pain Med. 2013;2(4):. doi: https://doi.org/10.5812/aapm.6916

Abstract

Background:

The incidence of transient neurologic symptoms (TNS) after spinal anesthesia with lidocaine is reported as high as 40%.

Objectives:

This prospective clinical trial was designed to determine the incidence of TNS in patients who underwent spinal anesthesia with two different needles, in two different surgical positions.

Patients and Methods:

The present randomized clinical trial was conducted on 250 patients (ASA I-II), who were candidates for surgery in supine or lithotomy positions. According to the needle type (Sprotte or Quincke) and local anesthetics (lidocaine and bupivacaine) all patients were randomly divided into four groups. After performing spinal anesthesia in sitting position, the position was changed into supine or lithotomy, according to surgical procedure. The patients were observed for complications of spinal anesthesia during the first five post-operative days. The primary end-point for this trial was to recognize the incidence of TNS among the four groups. Our secondary objective was to evaluate the effect of patient\'s position, needle type, and duration of surgery on the development of TNS following spinal anesthesia.

Results:

TNS was most commonly observed when lidocaine was used as anesthetic drug (P = 0.003). The impact of needle type, was not significant (P = 0.7). According to multivariate analysis, the duration of surgery was significantly lower in cases suffering from TNS (P = 0.04). Also, the risk of TNS increased following surgeries performed in lithotomy position (P = 0.00).

Conclusions:

According to the results of this clinical study, spinal anesthesia with lidocaine, and the lithotomy position in surgery increased the risk of TNS.

Highlights

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© 2013, Author(s). The Author(s) retain copyright in the Article. Upon acceptance, the Author(s) grant Brieflands the non-exclusive right of first publication and a worldwide, perpetual, royalty-free, non-exclusive license to copyedit, format, publish, reproduce, distribute, display, preserve, archive, index, promote, and make the Version of Record available in all formats and media. Brieflands and the relevant journal will be identified as the original publisher of the Version of Record. The Article will be published under the [Creative Commons Attribution 4.0 International License (CC BY 4.0)](https://creativecommons.org/licenses/by/4.0/). The Author(s) may immediately deposit and share the Version of Record in any repository or platform. No separate permission or fee is required for uses permitted under CC BY 4.0. CCC may provide optional customized reprint services.

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