Skip to main content
PMC home page
BMC Anesthesiology logoLink to BMC Anesthesiology
. 2017 Jan 17;17:8. doi: 10.1186/s12871-017-0300-z

Intrathecal magnesium sulfate does not reduce the ED50 of intrathecal hyperbaric bupivacaine for cesarean delivery in healthy parturients: a prospective, double blinded, randomized dose-response trial using the sequential allocation method

Fei Xiao 1,2, Wenping Xu 2, Ying Feng 1, Feng Fu 1, Xiaomin Zhang 2, Yinfa Zhang 2, Lizhong Wang 2, Xinzhong Chen 1,✉
PMCID: PMC5240204  PMID: 28095795

Abstract

Background

Addition of intrathecal magnesium sulfate to local anesthetics has been reported to potentiate spinal anesthesia and prolong analgesia in parturients. The current study was to determine whether intrathecal magnesium sulfate would reduce the dose of hyperbaric bupivacaine in spinal anesthesia with bupivacaine and sufentanil for cesarean delivery.

Methods

Sixty healthy parturients undergoing scheduled cesarean delivery were randomly assigned to receive spinal anesthesia with 0.5% hyperbaric bupivacaine and 5 μg sufentanil with either 0.9% sodium chloride (Control group) or 50% magnesium sulfate (50 mg) (Magnesium group). Effective anesthesia was defined as a bilateral T5 sensory block level achieved within 10 min of intrathecal drug administration and no additional epidural anesthetic was required during surgery. Characteristic of spinal anesthesia and the incidence of side effects were observed. The ED50 for both groups was calculated using the Dixon and Massey formula.

Results

There was no significant difference in the ED50 of bupivacaine between the Magnesium group and the Control group (4.9 mg vs 4.7 mg) (P = 0.53). The duration of spinal anesthesia (183 min vs 148 min, P < 0.001) was longer, the consumption of fentanyl during the first 24 h postoperatively (343 μg vs 550 μg, P < 0.001) was lower in the Magnesium group than that in the Control group.

Conclusions

Intrathecal magnesium sulfate (50 mg) did not reduce the dose requirement of intrathecal bupivacaine, but can extend the duration of spinal anesthesia with no obvious additional side effects.

Trial registration

This study was registered with Chinese Clinical Trial Registry (ChiCTR) on 15 Jul. 2014 and was given a trial ID number ChiCTR-TRC-14004954.

Keywords: Anesthesia, Spinal, Magnesium sulfate, Cesarean delivery

Background

Spinal anesthesia is the most widely used technique for cesarean delivery mainly due to its rapid onset and reliable effect [1, 2]. The main limitations of spinal anesthesia are the relatively short duration of anesthesia and analgesia, and high incidence of hypotension. To minimize these limitations, intrathecal adjuncts such as opioids, clonidine, neostigmine and epinephrine have been reportedly used for prolonging analgesia and reducing the dose of intrathecal local anesthetic, and subsequently reducing the incidence of spinal anesthesia-induced hypotension [3–5]. However, intrathecal opioids such as fentanyl and sufentanil, which are commonly used as adjuncts to intrathecal local anesthetic, are associated with a number of undesirable side-effects, including delayed respiratory depression, urinary retention, and pruritus [6–8]. In addition, other adjuncts, such as clonidine, neostigmine and epinephrine, also exhibit adverse effects such as sedation and so on [9, 10].

Magnesium ion is a natural calcium antagonist, which is critical to numerous physiological activities. Animal studies showed that intrathecal magnesium could produce an analgesic effect and enhance opioid’s antinociceptive activity, presumably due to magnesium’s possible block of the N-methyl-D-aspartate (NMDA) receptor and regulate calcium influx into cells in the central nervous system [11, 12]. Several recent studies [13, 14] investigated the utility of magnesium as an adjunct to intrathecal local anesthetics for both obstetrical and nonobstetrical surgery, aiming to overcome the limitations of spinal anesthesia, which main findings are that the addition of magnesium sulfate to intrathecal local anesthetics with or without opioids could prolong the duration of analgesia, reduce postoperative analgesic requirements, and improve perioperative shivering without significant side effects. No previous studies have assessed whether the addition of intrathecal magnesium sulfate can reduce the dose of intrathecal local anesthetic required for spinal anesthesia for cesarean delivery. We therefore designed the present prospective, randomized, double blinded study to investigate the hypothesis that intrathecal magnesium sulfate (MgSO4) 50 mg would decrease the median effective dose (ED50, which means the dose that would be necessary to provide effective anesthesia for 50% of the patients treated) of intrathecal hyperbaric bupivacaine in spinal bupivacaine-sufentanil anesthesia for cesarean delivery using an up-down sequential allocation method.

Methods

Design

We conducted a prospective, double-blinded, up-down sequential allocation study to determine the ED50 of intrathecal hyperbaric bupivacaine combined with or without MgSO4, in spinal bupivacaine-sufentanil anesthesia for cesarean delivery in healthy parturients.

Subjects and setting

Sixty healthy (ASA PS I, II) parturients at term pregnancy, undergoing elective cesarean section, were enrolled in the current study, which was conducted from July 2014 to August 2014. Subjects were enrolled after our hospital’s (Women’s Hospital, School of Medicine, Zhejiang University) ethical review board approval (No: 20140069. Approval date: 2014 Jul 15) and written informed consent have been obtained. Exclusion criteria were patients with obesity (body mass index (BMI) > 35 kg/m2), gestational age < 37 weeks, active labor, early labor, ruptured membranes, history of previous cesarean deliveries, diabetes or gestational diabetes, hypertension or pre-eclampsia, intrauterine growth restriction, placenta previa, significant coexisting maternal disease, any contraindication to spinal or epidural anesthesia such as local infection or bleeding disorders. This study was registered in a Chinese Clinical Trial Registry (ChiCTR) (registration number is ChiCTR-TRC-14004954).

Study protocol

Patients were randomized into one of two groups, Control group (n = 30) and Magnesium group (n = 30), based on a computer-generated random number list (Microsoft, Excel) which was kept in sealed opaque envelopes before the start of the study (prepared by FX).

No premedication was administered. On arrival in operating theatre, all patients were preloaded with 10 mL · kg−1 of 37 °C Lactate Ringer’s solution at the speed of 10 ml · kg−1 · h−1 with an 18-G intravenous cannula through an arm vein before anesthesia. Standard monitoring including non-invasive blood pressure (NIBP), heart rate (HR), oxygen saturation (SpO2) and electrocardiogram (ECG) were applied and recorded.

Combined spinal-epidural (CSE) technique (using the needle-through-needle technique) was performed in the left lateral position for all the patients studied. In brief, epidural puncture was performed with an 18-G Tuohy needle at the estimated L2-3 interspace and the method of loss-of-resistance-to-air technique (the air volume is not more than 2 ml) was used to identify the epidural space. A 27-G spinal needle with pencil tip was then passed via the Tuohy needle to enter the subarachnoid space. One of two pre-mixed study solutions was injected at a rate of 0.25 mL · S−1through the spinal needle. After the injection, the spinal needle was removed and an epidural catheter was then inserted 3-4 cm into the epidural space. No drugs were injected via the epidural catheter. The patient was then turned to supine with a 15-degree tilt to the left side.

The mixed solutions for spinal anesthesia were prepared before anesthesia by an anesthesia assistant (XZ), who did not participate in the subsequent patient assessment, and administered by a second attending anesthesiologist (FX and WX) who remained blinded to the mixed solution contents. The mixed solution for patients in Control group was: 0.5% bupivacaine + sufentanil 5 μg +0.5 mL 10% dextrose, diluted with 0.9% sodium chloride to a total volume of 3 mL. The mixed solution for patients in Magnesium group was: 0.5% bupivacaine + sufentanil 5 μg + 0.5 ml 10% dextrose + 0.1 ml 50% preservative-free magnesium sulfate (50 mg) (WuXi Pharmaceutical Company, China; Production batch: 1307201.) diluted with 0.9% sodium chloride to a total volume of 3 ml. An insulin syringe (1 ml) was used to measure volumes less than 1 ml.

The dose of intrathecal bupivacaine administered to patients varied according to the up-and-down allocation method [15]. In each group, for the first patient, the dose of intrathecal bupivacaine was 8 mg. For the next patient, the dose of intrathecal bupivacine was determined by the response (effective or ineffective) of the previous patient to the mixed intrathecal solution for spinal anesthesia in the same group. If the response of the previous patient was effective, the dose of intrathecal bupivacaine for the next patient was decreased by 1 mg in that group. Conversely, if the response of the patient was ineffective, the dose of intrathecal bupivacaine for the next patient was increased by 1 mg in that group. Effective anesthesia was defined as a bilateral T5 or above sensory block level achieved within 10 min of intrathecal drug administration and no additional epidural anesthetic was required for intraoperative pain. Ineffective anesthesia was defined as a bilateral T5 sensory block level was not achieved within 10 min of intrathecal drug administration, or an additional epidural anesthetic was needed to deal with intraoperative pain (VAS ≥ 3) despite a T5 sensory level being obtained. Additional epidural anesthetic was 5 ml of 2% lidocaine, repeated every 10 min if necessary.

Measurements

Automatic measurements of non-invasive arterial pressure (NIBP) and heart rate (HR) were recorded from the beginning of spinal anesthesia at 2-min intervals for 10 min, and then at 5-min intervals until the end of the surgery. An average of three consecutive measurements at the time when patient arrived in operating theatre with a supine position was defined as basal NIBP and basal HR. Hypotension was defined as a systolic arterial pressure below 90 mmHg, or a decrease of more than 20% of basal systolic blood pressure. Hypotension was treated with a boluse of 40 μg intravenous phenylephrine, repeatedly if needed. Bradycardia, defined as heart rate less than 55 beats per min, was treated with 0.5 mg of atropine intravenously.

Sensory level was assessed bilaterally along the mid clavicular line using a 17-G needle (patient was asked to report pain sensation, if the block was not even bilaterally, the lower side was chosen). The onset time of sensory block was defined as the time between intrathecal injection and a T10 sensory block level being achieved. The duration of sensory block was defined as the time between the onset time of sensory block and the recovery of sensory level of T10. Motor block in the lower limbs was graded by a Bromage Score [16] (0 = able to lift extended leg; 1 = able to flex knee but not lift extended leg; 2 = able to move foot only; and 3 = unable to move foot). The onset time of motor block was defined as the time between intrathecal injection and a Bromage Score of 1 being reached. The duration of motor block was defined as the period between the time of motor block onset and a Bromage Score of 0. The duration of spinal anesthesia [17] was defined as the period from spinal injection to the first requirement of bolus of fentanyl 10 μg postoperatively with patient-controlled analgesia (PCA) pump, which was set with a bolus of 10 μg fentanyl and 10 min of locking time and without a background dose. And patient did not received any other analgesics after surgery Both the sensory and motor block characteristics were noted every 1 min for the first 10 min after spinal anesthesia, followed thereafter by 10-min intervals until the end of the surgery and then by 30-min intervals after surgery before the patient full recovery.

Subjective pain was assessed with a visual analogue scale (VAS) ranged from 0 to 10 (0 = no pain, 10 = maximum undersirable pain) at the following timepoints: skin incision, fetal delivery, peritoneal closure, skin closure, and 1, 4, 8, 12, 24 h postoperatively. At the end of the surgery, patients were asked to grade the level of satisfaction during surgery (1 = excellent; 2 = good; 3 = bad).

Side effects and complications of spinal anesthesia including pruritus, shivering, severe sedation, nausea and vomiting, post dural puncture headache (PDPH) and respiratory depression (defined as breath rate < 12 bpm or SpO2 < 90%) during surgery and the first 24 h postoperatively were also recorded by a fixed anesthesia assistant. Sedation was ranked as none = awake and alert, mild = awake but drowsy, moderate = asleep but arousable, severe = not arousable. Any symptoms and signs of neurological deficit were also recorded. Umbilical arterial blood was drawn for blood gas analysis immediately after delivery. The neonatal Apgar score was assessed at 1 min and 5 min after delivery by a pediatrician who was not involved in this study.

Statistical analysis

The Dixon and Massey formula [15, 18] was applied to calculate the ED50 for both groups. Sample size estimation was calculated using the G*Power software. The primary outcome of the present study which is ED50 of intrathecal bupivacaine for cesarean delivery. An estimated ‘average’ SD of difference of the ED50 of intrathecal bupivacaine between groups is 0.5 mg, and power was given at 0.95 to detect a difference of 1.6 SD (0.8 mg) at P < 0.05. A minimum of 12 subjects was then necessary in each of the two groups. Because the Dixon and Massey technique requires the sample size to be approximately twice this number (as the estimations of ED50, SE and confidence interval (CI) 95% are based on the number and distribution of the lesser occurring outcome, which will be approximately 50% of the observations), therefore, 30 subjects were enrolled finally in each of the two groups, allowing for possible drop-outs and a potential deviation of the initial dose from the center of the effective dose distribution.

Demographic data were collected and are presented as count or mean ± SD as appropriate. Nominal data were analyzed using the Chi-square test, normally distributed continuous data were analyzed using Student’s t test and non-normallly distributed continuous data (such as epidural supplementations which were presented as median) were analyzed using non-parametric Wilcoxon rank sum test. Normal distribution was determined using the Kolmogorov–Smirnov test. Duration of spinal anesthesia was also analyzed using Kaplan-Meier survival analysis. Statistical analysis was performed with Graphpad Prism 5 (Version 5.01). Statistical significance was defined as P < 0.05 (two-sided).

Results

The CONSORT diagram of the present study is showed in Fig. 1. A total of 66 patients were assessed for eligibility, among them 60 patients were enrolled and randomly assigned into the Control group (n = 30) or the Magnesium group (n = 30). All 60 patients finished the study and were included into the final analysis.

Fig. 1.

Fig. 1

Open in a new tab

CONSORT diagram

There were no significant differences in the demographic and obstetric characteristics between the Control group and the Magnesium group (Table 1).

Table 1.

Patient’s demographic, obstetric and surgical data

Magnesium group
(n = 30)		 Control group
(n = 30)		 P-value*
Age (y) 25 ± 3 26 ± 3 0.41
Height (cm) 162 ± 3 162 ± 3 0.42
Weight (kg) 72 ± 4 72 ± 4 0.84
Gestational age (week) 39 ± 1 39 ± 1 0.60
Duration of surgery (min) 45 ± 7 47 ± 7 0.41
Open in a new tab

Data are presented as mean ± SD. *Student t test

The ED50 of intrathecal hyperbaric bupivacaine for cesarean delivery, determined using Dixon and Massay up-down sequential method [19, 20], was 4.7 mg (95% CI, 4.4–5.0 mg) in the Control group, and 4.9 mg (95% CI, 4.6–5.2 mg) in the Magnesium group. There was no significant difference in the ED50 of bupivacaine between the Magnesium group and the Control group (P = 0.53). The individual responses (effective or ineffective anesthesia) to the corresponding intrathecal hyperbaric bupivacaine dose are showed in Fig. 2. Thirteen patients in each group required additional epidural 2% lidocaine to complement intra-operative analgesia,and the mean total dose of additional epidural 2% lidocaine was similar in the two groups [5 ml (5–10 ml) vs. 5 ml (5–10 ml)].

Fig. 2.

Fig. 2

Open in a new tab

Individual response to intrathecal hyperbaric bupivacaine at corresponding dose. Unfilled square (□) represents an ineffective response to the corresponding dose of intrathecal bupivacaine for spinal anesthesia. Filled square (■) represents an effective response to the corresponding dose of intrathecal bupivacaine for spinal anesthesia. Solid line represents the ED50 (dashed lines represent the 95% confidence interval, CI) of intrathecal hyperbaric bupivacaine for caesarean delivery

Characteristics and efficacy of spinal anesthesia in patients with “effective anesthesia” are presented in Table 2. The onset and duration of sensory and motor blockade were longer in the Magnesium group than in the Control group (P < 0.001). Moreover, the duration of spinal anesthesia was also significantly longer in the Magnesium group than in the Control group (183 ± 11 min vs 148 ± 9 min, P < 0.001) (Fig.3). The consumption of fentanyl during the first 24 hours postoperatively were significantly less in the Magnesium group than in Control group (343 ± 42 μg vs 550 ± 49 μg, P < 0.001). The Magnesium group has higher rate of excellent satisfaction during intraoperative period than that in the Control group (94.1% vs 52.9%, P = 0.017).

Table 2.

Characteristics and efficacy of spinal anesthesia in patients with effective anesthesia

Magnesium group
(n = 17)		 Control group
(n = 17)		 P-value
Sensory block (to pinprick)
 Onset time to T10 (min) 4 ± 0 3 ± 0 <0.001*
 Duration (min) 140 ± 9 121 ± 9 <0.001*
Motor block
 Onset time (min) 4 ± 0 2 ± 0 <0.001*
 Duration (min) 148 ± 12 125 ± 10 <0.001*
Duration of anesthesia (min) 183 ± 11 148 ± 9 <0.001*
Consumption of fentanyl (μg) 343 ± 42 550 ± 49 <0.001*
Patient Satisfaction
 Excellent [number (%)] 16 (94.1) 9 (52.9) 0.017#
 Good [number (%)] 1 (5.9) 8 (47.1) 0.017#
Open in a new tab

Data are presented as mean ± SD or number (%). *Student t test, #Chi-square test

Fig. 3.

Fig. 3

Open in a new tab

Duration of spinal anesthesia. Cumulative percentages of patient remaining no pain after spinal injection in patients with “effective anesthesia” in the Magnesium group (solid line, red area) and in the Control group (dotted line, blue area), obtained using the Kaplan–Meier survival analysis. Log-rank differences between the two groups were significant (P < 0.001)

The incidence of side effects of spinal anesthesia, such as hypotension, nausea and vomiting, shivering, pruritus, post dural puncture headache (PDPH), severe sedation and respiratory depression during perioperative period, were similar between groups (Table 3). Neonatal Apgar score at 5 min after delivery and umbilical arterial pH immediately after delivery were also comparable between groups (Table 3). No neurological deficit was observed in any patient in both groups during the first postoperative week.

Table 3.

Side effects of anesthesia and neonatal Apgar score and umbilical arterial pH

Magnesium group
(n = 30)		 Control group
(n = 30)		 P -Value
Hypotension 6(20.0) 8(26.7) 0.76#
Nausea and vomiting 12(40.0) 9(30.0) 0.59#
Shivering 5 (16.7) 6 (20.0) 1.00#
Pruritus 8(26.7) 7(23.3) 1.00#
PDPH 0 (0%) 1 (3.3) 1.00#
Severe sedation 0 0
Respiratory depression 0 0
Apgar score 10.0 ± 0.0 10.0 ± 0.0 1.00*
Umbilical artery pH 7.37 ± 0.04 7.38 ± 0.06 0.22*
Open in a new tab

Data are presented as number (percent) or mean ± SD. PPDH = post dural puncture headache. *Student t test, #Chi-square test

Discussion

We demonstrated that intrathecal magnesium sulfate (50 mg) did not reduce the median effective dose (ED50) of intrathecal bupivacaine, for cesarean delivery under spinal anesthesia with bupivacaine coadministered with 5 μg sufentanil in healthy parturients.

Several previous studies [13, 19, 21, 22] reported that the duration of spinal anesthesia was significantly prolonged by intrathecal magnesium sulfate, which is consistent with the findings in the present study. The present study also showed that adding magnesium sulfate intrathecally could significantly prolong the duration of spinal anesthesia with bupivacaine and sufentanil (184 min vs 148 min, P < 0.001). Evidence is conflicting regarding the usage of intrathecal magnesium sulfate in obstetric patients for prolonging the duration of spinal anesthesia [13, 17, 22, 23], the study designs with or without opioids may contribute to this discrepancy. This synergistic effect has been already demonstrated in a rat model by Kroin and colleagues [12] who found that the addition of intrathecal magnesium increased the peak effect and area under the analgesic curve of intrathecal morphine. The potentiation of opioid antinociception by magnesium sulfate may last in the postoperative period, explaining the decrease in consumption of postoperative fentanyl found in the present study.

NMDA-receptor antagonists can diminish the activation of C-fibers which leads to neuronal excitation, prevent central sensitization elicited by peripheral nociceptive stimulation [20, 24]. Magnesium sulfate, a noncompetitive NMDA-receptor antagonist, has both independent and synergistic analgesic properties. Kroin et al. demonstrated in an animal study that intrathecal magnesium sulfate potentiated the antinociceptive effect of morphine to noxious thermal and mechanical stimulation at an incisional pain site at the level of the spinal cord in a dose-dependent fashion [12]. Mercieri et al. found that systemic magnesium sulfate infusion (i.e. intravenous route), even with large doses, did not increase cerebrospinal fluid (CSF) magnesium concentrations, suggesting magnesium sulfate exhibits insufficient blood-brain barrier penetration [25, 26]. Hence, intrathecal route would be better for magnesium sulfate administration to potentiate spinal anesthesia than systemic route by which effective CSF concentrations of magnesium required large doses that may result in severe side effects.

Because intrathecal magnesium alone has been showed to produce sensory and motor block, [27, 28] it might be expected that magnesium potentiates the spinal block via a synergistic interaction between NMDA antagonists and local anesthetics, resulting in a reduction in the dose of local anesthetics required for achieving effective spinal anesthesia for certain surgical procedures. Unexpectedly, the present study demonstrated that the ED50 of intrathecal bupivacaine for cesarean delivery in the Magnesium group was not reduced when compared with the Control group, suggesting that intrathecal 50 mg magnesium sulfate exhibits little or no effect on efficacy of spinal anesthesia with local anesthetics for cesarean delivery. In contrast to the lack of effect of magnesium on the median effective dose of intrathecal bupivacaine in the current study, previous studies suggested that intrathecal fentanyl or sufentanil significantly reduce the dose (ED50 or ED95) of spinal local anesthetics for cesarean delivery [3, 29, 30]. The possible underlying mechanism is that magnesium may be removed from extracellular fluid more rapidly than opioids, or that it may be specific to the NMDA receptor channel and therefore has no influence on the channels the local anesthetics act and opioid receptor sites [14, 17]. Moreover, intrathecal magnesium sulfate exerts its spinal action in a localized manner, [17] whereas, fentanyl or sufentanil bind strongly to opioid receptors in the dorsal horn of spinal cord, and may also exert a supraspinal action by intrathecal cephalad spread, [31] hence both fentanyl and sufentanil exhibit a significant synergistic effect on local anesthetics. In addition, the dosage of intrathecal magnesium sulfate should be taken into account. The dose of magnesium sulfate of 50 mg we choose in the current study was based on majority of the studies [13, 14, 17, 32] on clinical investigation of intrathecal magnesium sulfate for cesarean delivery publically published so far. However, whether higher dose of intrathecal magnesium sulfate could reduce the dose (ED50 or ED95) of intrathecal local anesthetics for cesarean delivery remains unknown. Hence, it is warrant to conduct further studies on optimal dose of magnesium sulfate for cesarean delivery.

The onset of sensory and motor blockade in the Magnesium group in the present study were found to be significantly delayed when compared with the Control group, which was in agreement with the findings of previous studies [13, 21]. The clinical significance of this delay is questionable because the delayed time was only about 1 min for both sensory and motor blockade onset in the present study. It is difficult to explain this phenomenon on mechanism of magnesium action upon central nervous system. The effect of adding magnesium sulfate on the pH and baricity of the spinal solution might be considered as a possibility for this delay [22, 33]. Pascual-Ramirez suggested that the onset delay when magnesium was added could also indicate there is a modulation of the neuronal electrical conduction blockade [34].

Concerns about the safety of intrathecal administration of magnesium sulfate have been being considered. Preclinical studies showed the impact of intrathecal magnesium sulfate on neurological structure and functions appears inconsistent among species [33]. In rats, intrathecal magnesium sulfate resulted in transient motor and sensory block with no obvious adverse clinical and histological consequences. In canines, intrathecal magnesium sulfate of 45–60 mg produced no neurological deficit and histopathological change in spinal cord [35]. In clinical studies, intrathecal magnesium sulfate 50 mg was found to be safe and effective, [13, 14, 17, 21, 22] which are similar to the findings of the present study, in which we also did not find any obvious symptoms and signs of dysfunction in nervous system, reinforcing the safety of maternal intrathecal magnesium. However, safety of intrathecal magnesium sulfate would be argued because our study is a small study and no specific assessments to assess safety were done. Hence, the safety of intrathecal magnesium sulfate with larger sample size and specific assessment variables, or with large dose should be carefully evaluated in both animals and humans, especially in pregnant populations.

Conclusions

In conclusion, in patients undergoing cesarean delivery with spinal anesthesia, the addition of intrathecal magnesium sulfate (50 mg) to spinal hyperbaric bupivacaine combined with sufentanil did not reduce the ED50 of intrathecal bupivacaine as determined with an up-down sequential method, but prolonged the duration of spinal anesthesia, reduced the consumption of post-operative fentanyl, delayed the onset of both sensory and motor blockade of spinal anesthesia. No obvious additional side effects were found.

Acknowledgements

The authors would thank all staffs in the department of anesthesia and operating room of Jiaxing Maternity and Child Care Hospital for their help in this study. The authors would also thank Cynthia A Wong, Department of Anesthesiology, Northwestern University, USA, for reviewing this manuscript before submitting to this journal for publication.

Fundings

This study was supported by the fund from National Natural Science Foundation of China (NSFC, No 81271237 and No 81471126) and the fund from Science Technology Department of Zhejiang Province (No 2014C33171) and the fund from Jiaxing Science and Technology Bureau in Zhejiang Province, China (No. 2016BY28031). The fundings played mainly role in the design of the study and data collection and analysis in the present study.

Availability of data and material

All data generated or analyzed during this study were included in this published article.

Authors’ contributions

FX helped in designing and conducting the study, collecting the data and writing the manuscript. WX helped in designing and conducting the study. YF helped in designing the study and analyzing the data. FF helped in analyzing the data. XZ helped in conducting the study and collecting the data. YZ helped in conducting the study and collecting the data. LW helped in designing the study. XC helped in designing the study, analyzing the data and writing the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

This study was approved by the ethical review board of Women’s Hospital, School of Medicine, Zhejiang University (No: 20140069. Approval date: 2014 Jul 23) and written informed consents have been obtained from all patients.

Abbreviations

BMI

Body mass index

ECG

Electrocardiograph

ED50

Median effective dose

HR

Heart rate

MgSO4

Magnesium sulfate

NIBP

Non-invasive blood pressure

NMDA

N-methyl-D-aspartate

PCA

Patient-controlled analgesia

PDPH

Post dural puncture headache

SpO2

Pulse oxygen saturation

VAS

Visual analogue scale

Contributor Information

Fei Xiao, Email: 1036230359@qq.com.

Wenping Xu, Email: 119165599@qq.com.

Ying Feng, Email: fengyingfly@tom.com.

Feng Fu, Email: fufeng@zju.edu.cn.

Xiaomin Zhang, Email: 95463941@qq.com.

Yinfa Zhang, Email: zhangyinfajx@163.com.

Lizhong Wang, Email: jxlzw@sina.com.

Xinzhong Chen, Email: chenxinz@zju.edu.cn.

References

  • 1.Gizzo S, Noventa M, Fagherazzi S, Lamparelli L, Ancona E, et al. Update on best available options in obstetrics anaesthesia: perinatal outcomes, side effects and maternal satisfaction. Fifteen years systematic literature review. Arch Gynecol Obstet. 2014;290:21–34. doi: 10.1007/s00404-014-3454-7. [DOI] [PubMed] [Google Scholar]
  • 2.Palanisamy A. What’s new in Obstetric Anesthesia? The 2013 Gerard W. Ostheimer lecture. Anesth Analg. 2014;118:360–6. doi: 10.1213/ANE.0000000000000101. [DOI] [PubMed] [Google Scholar]
  • 3.Chen X, Qian X, Fu F, Lu H, Bein B. Intrathecal sufentanil decreases the median effective dose (ED50) of intrathecal hyperbaric ropivacaine for caesarean delivery. Acta Anaesthesiol Scand. 2010;54:284–90. doi: 10.1111/j.1399-6576.2009.02051.x. [DOI] [PubMed] [Google Scholar]
  • 4.Krukowski JA, Hood DD, Eisenach JC, Mallak KA, Parker RL. Intrathecal neostigmine for post-cesarean section analgesia: dose response. Anesth Analg. 1997;84:1269–75. doi: 10.1213/00000539-199706000-00018. [DOI] [PubMed] [Google Scholar]
  • 5.Farzi F, Mirmansouri A, Forghanparast K, Heydarzadeh A, Abdollahzadeh M, et al. Addition of intrathecal fentanyl or meperidine to lidocaine and epinephrine for spinal anesthesia in elective cesarean delivery. Anesthesiology and pain medicine. 2014;4 doi: 10.5812/aapm.14081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Brockway MS, Noble DW, Sharwood-Smith GH, McClure JH. Profound respiratory depression after extradural fentanyl. Br J Anaesth. 1990;64:243–5. doi: 10.1093/bja/64.2.243. [DOI] [PubMed] [Google Scholar]
  • 7.Campora E, Merlini L, Pace M, Bruzzone M, Luzzani M, et al. The incidence of narcotic-induced emesis. J Pain Symptom Manage. 1991;6:428–30. doi: 10.1016/0885-3924(91)90041-2. [DOI] [PubMed] [Google Scholar]
  • 8.Chilvers CR, Vaghadia H, Mitchell GW, Merrick PM. Small-dose hypobaric lidocaine-fentanyl spinal anesthesia for short duration outpatient laparoscopy. II. Optimal fentanyl dose. Anesth Analg. 1997;84:65–70. doi: 10.1213/00000539-199701000-00012. [DOI] [PubMed] [Google Scholar]
  • 9.Missant C, Teunkens A, Vandermeersch E, Van de Velde M. Intrathecal clonidine prolongs labour analgesia but worsens fetal outcome: a pilot study. Can J Anaesth. 2004;51:696–701. doi: 10.1007/BF03018428. [DOI] [PubMed] [Google Scholar]
  • 10.Gurbet A, Turker G, Kose DO, Uckunkaya N. Intrathecal epinephrine in combined spinal-epidural analgesia for labor: dose-response relationship for epinephrine added to a local anesthetic-opioid combination. Int J Obstet Anesth. 2005;14:121–5. doi: 10.1016/j.ijoa.2004.12.002. [DOI] [PubMed] [Google Scholar]
  • 11.Xiao WH, Bennett GJ. Magnesium suppresses neuropathic pain responses in rats via a spinal site of action. Brain Res. 1994;666:168–72. doi: 10.1016/0006-8993(94)90768-4. [DOI] [PubMed] [Google Scholar]
  • 12.Kroin JS, McCarthy RJ, Von Roenn N, Schwab B, Tuman KJ, et al. Magnesium sulfate potentiates morphine antinociception at the spinal level. Anesth Analg. 2000;90:913–7. doi: 10.1213/00000539-200004000-00025. [DOI] [PubMed] [Google Scholar]
  • 13.Malleeswaran S, Panda N, Mathew P, Bagga R. A randomised study of magnesium sulphate as an adjuvant to intrathecal bupivacaine in patients with mild preeclampsia undergoing caesarean section. Int J Obstet Anesth. 2010;19:161–6. doi: 10.1016/j.ijoa.2009.08.007. [DOI] [PubMed] [Google Scholar]
  • 14.Morrison AP, Hunter JM, Halpern SH, Banerjee A. Effect of intrathecal magnesium in the presence or absence of local anaesthetic with and without lipophilic opioids: a systematic review and meta-analysis. Br J Anaesth. 2013;110:702–12. doi: 10.1093/bja/aet064. [DOI] [PubMed] [Google Scholar]
  • 15.Dixon WJ. Staircase bioassay: the up-and-down method. Neurosci Biobehav Rev. 1991;15:47–50. doi: 10.1016/S0149-7634(05)80090-9. [DOI] [PubMed] [Google Scholar]
  • 16.Bromage PR. A comparison of the hydrochloride and carbon dioxide salts of lidocaine and prilocaine in epidural analgesia. Acta Anaesthesiol Scand Suppl. 1965;16:55–69. doi: 10.1111/j.1399-6576.1965.tb00523.x. [DOI] [PubMed] [Google Scholar]
  • 17.Unlugenc H, Ozalevli M, Gunduz M, Gunasti S, Urunsak IF, et al. Comparison of intrathecal magnesium, fentanyl, or placebo combined with bupivacaine 0.5% for parturients undergoing elective cesarean delivery. Acta Anaesthesiol Scand. 2009;53:346–53. doi: 10.1111/j.1399-6576.2008.01864.x. [DOI] [PubMed] [Google Scholar]
  • 18.Dixon WJ, Massey FJ. Introduction to statistical analysis. New York: McGraw-Hill; 1983. p. 11. [Google Scholar]
  • 19.Kathuria B, Luthra N, Gupta A, Grewal A, Sood D. Comparative efficacy of two different dosages of intrathecal magnesium sulphate supplementation in subarachnoid block. Journal of Clinical and Diagnostic Research: JCDR. 2014;8:GC01–5. doi: 10.7860/JCDR/2014/8295.4510. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Pelissier T, Infante C, Constandil L, Espinosa J, Lapeyra CD, et al. Antinociceptive effect and interaction of uncompetitive and competitive NMDA receptor antagonists upon capsaicin and paw pressure testing in normal and monoarthritic rats. Pain. 2008;134:113–27. doi: 10.1016/j.pain.2007.04.011. [DOI] [PubMed] [Google Scholar]
  • 21.Ozalevli M, Cetin TO, Unlugenc H, Guler T, Isik G. The effect of adding intrathecal magnesium sulphate to bupivacaine-fentanyl spinal anaesthesia. Acta Anaesthesiol Scand. 2005;49:1514–9. doi: 10.1111/j.1399-6576.2005.00793.x. [DOI] [PubMed] [Google Scholar]
  • 22.Buvanendran A, McCarthy RJ, Kroin JS, Leong W, Perry P, et al. Intrathecal magnesium prolongs fentanyl analgesia: a prospective, randomized, controlled trial. Anesth Analg. 2002;95:661–6. doi: 10.1097/00000539-200209000-00031. [DOI] [PubMed] [Google Scholar]
  • 23.Shoeibi G, Sadegi M, Girozian A, Tabassomi F. The additional effect of magnesium sulfate to lidocaine in spinal anesthesia for cesarean section. Int J Pharmacol. 2007;3:425–7. doi: 10.3923/ijp.2007.425.427. [DOI] [Google Scholar]
  • 24.Urch CE, Rahman W, Dickenson AH. Electrophysiological studies on the role of the NMDA receptor in nociception in the developing rat spinal cord. Brain Res Dev Brain Res. 2001;126:81–9. doi: 10.1016/S0165-3806(00)00141-3. [DOI] [PubMed] [Google Scholar]
  • 25.Sullivan JT, Higgins N, Toledo P, Scavone BM, McCarthy RJ, et al. The effect of intravenous magnesium therapy on the duration of intrathecal fentanyl labor analgesia. Int J Obstet Anesth. 2012;21:212–6. doi: 10.1016/j.ijoa.2012.01.006. [DOI] [PubMed] [Google Scholar]
  • 26.Mercieri M, De Blasi RA, Palmisani S, Forte S, Cardelli P, et al. Changes in cerebrospinal fluid magnesium levels in patients undergoing spinal anaesthesia for hip arthroplasty: does intravenous infusion of magnesium sulphate make any difference? A prospective, randomized, controlled study. Br J Anaesth. 2012;109:208–15. doi: 10.1093/bja/aes146. [DOI] [PubMed] [Google Scholar]
  • 27.Bahar M, Chanimov M, Grinspun E, Koifman I, Cohen ML. Spinal anaesthesia induced by intrathecal magnesium sulphate. Anaesthesia. 1996;51:627–33. doi: 10.1111/j.1365-2044.1996.tb07843.x. [DOI] [PubMed] [Google Scholar]
  • 28.Najafi A, Akbari H, Khajavi MR, Etezadi F. Inadvertent intrathecal injection of large dose magnesium sulfate. Saudi journal of anaesthesia. 2013;7:464–6. doi: 10.4103/1658-354X.121049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Bouvet L, Da-Col X, Chassard D, Dalery F, Ruynat L, et al. ED(5)(0) and ED(9)(5) of intrathecal levobupivacaine with opioids for Caesarean delivery. Br J Anaesth. 2011;106:215–20. doi: 10.1093/bja/aeq296. [DOI] [PubMed] [Google Scholar]
  • 30.Qian XW, Chen XZ, Li DB. Low-dose ropivacaine-sufentanil spinal anaesthesia for caesarean delivery: a randomised trial. Int J Obstet Anesth. 2008;17:309–14. doi: 10.1016/j.ijoa.2008.01.018. [DOI] [PubMed] [Google Scholar]
  • 31.Choi DH, Ahn HJ, Kim MH. Bupivacaine-sparing effect of fentanyl in spinal anesthesia for cesarean delivery. Reg Anesth Pain Med. 2000;25:240–5. doi: 10.1097/00115550-200011000-00007. [DOI] [PubMed] [Google Scholar]
  • 32.Yousef AA, Amr YM. The effect of adding magnesium sulphate to epidural bupivacaine and fentanyl in elective caesarean section using combined spinal-epidural anaesthesia: a prospective double blind randomised study. Int J Obstet Anesth. 2010;19:401–4. doi: 10.1016/j.ijoa.2010.07.019. [DOI] [PubMed] [Google Scholar]
  • 33.Albrecht E, Kirkham KR, Liu SS, Brull R. The analgesic efficacy and safety of neuraxial magnesium sulphate: a quantitative review. Anaesthesia. 2013;68:190–202. doi: 10.1111/j.1365-2044.2012.07337.x. [DOI] [PubMed] [Google Scholar]
  • 34.Pascual-Ramirez J, Gil-Trujillo S, Alcantarilla C. Intrathecal magnesium as analgesic adjuvant for spinal anesthesia: a meta-analysis of randomized trials. Minerva Anestesiol. 2013;79:667–78. [PubMed] [Google Scholar]
  • 35.Simpson JI, Eide TR, Schiff GA, Clagnaz JF, Hossain I, et al. Intrathecal magnesium sulfate protects the spinal cord from ischemic injury during thoracic aortic cross-clamping. Anesthesiology. 1994;81:1493–9. doi: 10.1097/00000542-199412000-00025. [DOI] [PubMed] [Google Scholar]

Articles from BMC Anesthesiology are provided here courtesy of BMC

RESOURCES