ADDITION OF PANCURONIUM AND NITROGLYCERIN TO LIDOCAINE FOR INTRAVENOUS REGIONAL ANESTHESIA IN UPPER EXTREMITY SURGERY: BLOCK CHARACTERISTICS AND POSTOPERATIVE ANALGESIA

Document Type : Original Article

Authors

Anesthesia and Intensive Care Department, Faculty of Medicine, Al-Azhar University, Cairo, Egypt

Abstract

Background: Intravenous regional anesthesia (IVRA) provides reliable and rapid analgesia with good muscle relaxation of the extremity distal to the tourniquet, but tourniquet pain and absence of post-operative analgesia are major drawbacks. Nitroglycerine and muscle relaxants are known to potentiate peripheral nerve blocks. Objective: Comparing nitroglycerine and pancuronium as adjuvants to IVRA with respect, block characteristics, and post- operative analgesia. Patient and Methods: This study was carried out in Al- Azhar University Hospitals for 6 months ( from 1/4/2016 to 1/10/2016 ) on 60 patients of both sexes aged 20-50 years, and belonging to ASA I & II  undergoing forearm and hand surgeries. Patients were randomely divided into three equal groups ( 20 patients at each group ) . Group I received 40 cc of 3 mg/kg of lidocaine diluted in normal saline (0.9 % NaCl), Group II recieved 40 cc of 1.5 mg/kg of lidocaine diluted in normal saline (0.9% NaCl) with 200 µg nitroglycerine, and Group III received 40 cc of 1.5 mg/kg of lidocaine diluted in normal saline (0.9 % NaCl with 200 µg nitroglycerin and 0.5 mg pancuronium. Results: Group I has the slowest sensory and motor onset time, but the shortest sensory and motor recovery time. There was no significant difference between Group II and III as regarding sensory onset and recovery times, but Group III  has shoter motor onset time and more prolonged motor recovery  time  than Group II. As regard postoperative analgesic requirements, Group II and III needed less analgesic doses than Group I, but there was no significant difference between Group II and III. Conclusion: Addition of 0.5 mg  pancuronium and 200 µg nitroglycerin as adjuvant to lidocaine for intravenous regional anesthesia reduced the dose of lidocaine used for IVRA, shortened the sensory and motor block onset times, prolonged the sensory and motor block recovery times, and reduced the postoperative analgesic requirement and improved the quality of intravenous regional anesthesia with no side effects.

Keywords


ADDITION OF PANCURONIUM AND NITROGLYCERIN TO LIDOCAINE FOR INTRAVENOUS REGIONAL ANESTHESIA IN UPPER EXTREMITY SURGERY: BLOCK CHARACTERISTICS AND POSTOPERATIVE ANALGESIA

 

By

 

Mostafa M. Mahdy, Abdulla M. Ahmed, Mostafa M. Sabra

and Ahmed S. Hamada

                                                                                                              

Anesthesia and Intensive Care Department, Faculty of Medicine,

Al-Azhar University, Cairo, Egypt

 

ABSTRACT

Background: Intravenous regional anesthesia (IVRA) provides reliable and rapid analgesia with good muscle relaxation of the extremity distal to the tourniquet, but tourniquet pain and absence of post-operative analgesia are major drawbacks. Nitroglycerine and muscle relaxants are known to potentiate peripheral nerve blocks. Objective: Comparing nitroglycerine and pancuronium as adjuvants to IVRA with respect, block characteristics, and post- operative analgesia. Patient and Methods: This study was carried out in Al- Azhar University Hospitals for 6 months ( from 1/4/2016 to 1/10/2016 ) on 60 patients of both sexes aged 20-50 years, and belonging to ASA I & II  undergoing forearm and hand surgeries. Patients were randomely divided into three equal groups ( 20 patients at each group ) . Group I received 40 cc of 3 mg/kg of lidocaine diluted in normal saline (0.9 % NaCl), Group II recieved 40 cc of 1.5 mg/kg of lidocaine diluted in normal saline (0.9% NaCl) with 200 µg nitroglycerine, and Group III received 40 cc of 1.5 mg/kg of lidocaine diluted in normal saline (0.9 % NaCl with 200 µg nitroglycerin and 0.5 mg pancuronium. Results: Group I has the slowest sensory and motor onset time, but the shortest sensory and motor recovery time. There was no significant difference between Group II and III as regarding sensory onset and recovery times, but Group III  has shoter motor onset time and more prolonged motor recovery  time  than Group II. As regard postoperative analgesic requirements, Group II and III needed less analgesic doses than Group I, but there was no significant difference between Group II and III. Conclusion: Addition of 0.5 mg  pancuronium and 200 µg nitroglycerin as adjuvant to lidocaine for intravenous regional anesthesia reduced the dose of lidocaine used for IVRA, shortened the sensory and motor block onset times, prolonged the sensory and motor block recovery times, and reduced the postoperative analgesic requirement and improved the quality of intravenous regional anesthesia with no side effects.

Keywords: Lidocaine, nitroglycerine, pancuronium, intravenous regional anesthesia.

 

 

INTRODUCTION

    Intravenous regional anesthesia (IVRA) or Bier’s block is an ideal technique for outpatient undergoing extremity surgery lasting less than one hour. (Sardesai et al., 2015) It is easy to be administered, lower cost compared with general anesthesia, no need for deep sedation and can be used for emergency operations for patients with full stomach. IVRA shortens hospital length of stay when compared with general anesthesia (Celik et al., 2016).

    IVRA has also disadvantages such as tourniquet pain, insufficient postoperative analgesia, poor muscle relaxation, local anesthesia toxicity (Honarmand et al., 2015).

    Lidocaine is amino amide local anaesthetic. The main action of lidocaine is via sodium channel inactivation. Also it inactivate potassium, calcium channels and it has the ability to block NMDA receptors. (Van der Wal et al., 2015) Because of safety and effectiveness, it has become the most common local anesthesia to be used. It has intermediate duration of action  and  its cardiotoxicity is one ninth bupivacaine. (Maruthingal et al., 2015) The ideal solution for IVRA should have rapid onset to reduce the dose of LA, prolong post deflation analgesia, and decrease tourniquet pain. (Batra et al., 2008) To achieve this, other drugs including narcotics, non-steroidal anti-inflammatory drugs (NSAIDs), clonidine, nitroglycerin (TNG), dexmedetomidine,  magnesium, and neostigmine were used in combination with lidocaine in different studies (Abbasivash et al., 2009).

    Nitroglycerin has been used as an adjuvant with many anesthetic drugs to induce fast effect in controlling acute and chronic pains. (Hassani et al., 2015) It was proved that nitroglycerine (TNG), nitric oxide generator, helps in distribution of local anesthetic agents to neuron trunks by vasodilatation and  also it has been demonstrated that, when nitroglycerine is used with other drugs, analgesic effect is increased (Cakmak et al., 2014).

    Various neuromuscular blocking agents have been used with IVRA to improve the operating conditions and reduce the local anesthetic dose and possible systemic toxicity. Administration of neuromuscular blocking drugs including pancuronium (0.5 mg) with local anesthetics in upper limb IVRA improves surgical conditions in Adults and no reported complications from using adjuvant neuromuscular blocking drugs in IVRA (Dominic and Barry , 2007) .

    The present work aimed to compare nitroglycerine and pancuronium as adjuvant to IVRA.

PATIENTS AND METHODS

    The study was designed as a prospec-tive, double-blinded clinical trial. This study was carried out in Al-Azhar University Hospitals for 6 months (from 1/4/2016 to 1/10/2016) on 60 patients of both sexes aged 20 -50 years belonging to ASA I & II undergoing forearm and hand surgeries. After obtaining approval from ethical committee, a written consents were obtained from the patients after they were informed about the procedure.

     Exclusion criteria included patient refusal, liver disease,  Reynauld’s disease, sickle cell disease, crush injuries and hand infection. The 60 Patients were be randomely divided into three equal groups (computer generated with sealed envelope technique ) : Group I recieved 40 cc of 3mg/kg of lidocaine diluted in normal saline (0.9 % NaCl), Group II recieved 40 cc of 1.5mg/kg of lidocaine diluted in normal saline (0.9% NaCl) with 200 µg Nitroglycerine, and Group III recieved 40 cc of 1.5mg/kg of lidocaine diluted in normal saline (0.9 % NaCl) with 200 µg Nitroglycerin and 0.5 mg pancuronium.

     Close monitoring of the patient should be done. A 22 Gauge intravenous cannula was inserted in the dorsum of operative hand (as distal as possible) for injection of the study drugs, another 20 Gauge intravenous cannula was inserted in the controlateral hand for crystalloid infusion. A double pneumatic tourniquet was placed on the upper arm on operative side and then it was exanguated by 2 min. elevation and wrapping with an Esmarch bandage. The proximal tourniquet was then inflated to 100 mmHg above the systolic blood pressure or to a minimum of 250 mmHg, then selected local anesthetic solution was injected. After adequate block, distal tourniquet was inflated and the proximal tourniquet was deflated.

    Sensory block was assessed every 1 min. by ice cube, while motor block by modified Bromage scale. Sensory and motor block recovery times were  assessed. Postoperative pain evaluation using NRS was assessed every 1 hr or need for analgesics. If NRS > 3, patient received 10 mg/kg of paracetamol by IV infusion as a first dose . After 60 minutes, if he still in pain and NRS was >3, the patient received a second dose of 5 mg/kg. Patient's and surgeon's satisfaction score were recorded. Any local or systemic complications were recorded.

Statistical analysis: Data were analyzed using IBM SPSS software package  version  20.0 (Aujla et al., 2009 and Elmetwaly et al., 2010) . Comparison between groups regarding categorical variables was tested using Chi-square test. When more than 20% of the cells have expected count less than 5, correction for chi-square was conducted using Fisher’s Exact test or Monte Carlo correction. The distributions of   quantitative   variables   were   tested   for   normality    using Kolmogorov-Smirnov test, Shapiro-Wilk test and D'Agstino test. For normally distributed data, comparison between more than two population were analyzed F-test (ANOVA) to be used and Post Hoc test (Tukey). For abnormally distributed data, Kruskal Wallis test was used to compare between different groups  and  pair  wise  comparison  was  assessed  using  Mann-Whitney  test. p value > 0.05 was considered significant .

RESULTS

● There was no statistically significant difference between the three groups as regards age, weight, sex, ASA physical status, duration of surgery and percentage of types of surgeries (Table 1).

 

Table (1): Demographic data in the studied groups.

Groups

Parameters

Group I (n=20)

Group II (n=20)

Group III (n=20)

Test of sig.

P value

Age (ys)

Range

19-49

19-49

19-49

F = 0.359

0.700

Mean ±SD

29.80 ±8.62

29.65 ±9.20

27.70 ±8.39

 

Sex

Male

No.

15

16

15

 

χ2 = 0.275

 

1.000

%

75

80

75

Female

No.

5

4

5

%

25

20

25

Weight (kg)

Range

60 -95

65- 98

69 -95

F = 0.547

0.581

Mean ±SD

78.10 ±9.95

79.35 ±8.35

81.0 ±7.95

 

ASA

I

No.

18

18

18

 

χ2 = 0.223

 

1.000

%

90

90

90

II

No.

2

2

2

%

10

10

10

Duration of surgery (min)

Range

30 -55

38- 57

34 -55

F = 0.613

0.545

Mean ±SD

45.25 ±7.08

46.50 ±5.57

44.40 ±5.31

c2: Chi square test Sig. bet. groups was done using Chi square test or Fisher Exact

F, p: F and p values for ANOVA test, Sig. bet. grps was done using Post Hoc Test (LSD)

 

 

 

● There was a statistically significant decrease in sensory block onset time of Gr II (3.65 ± 0.99 min.) and Gr III (4.0 ± 0.97 min.) compared with Gr  I (6.3 ± 1.53 min.), but there was no significant difference between Gr II and Gr III (Table 2).


 

Table (2): Comparison between the three studied groups according to sensory block onset times.  

Groups

 

Sensory Block onset

Times (min )

Sensory Block Onset Times (min.)

 

Group I

 

Group II

 

Group III

Min.(min)

4.0

2.0

2.0

Max.(min)

9.0

6.0

6.0

Mean

6.30

3.65

4.0

±SD.

1.53

0.99

0.97

Median

6.0

4.0

4.0

F

29.259*

P

<0.001*

p1

<0.001*

p2

<0.001*

p3

0.356

F, P: F and P values for ANOVA test, Sig. bet. grps was done using Post Hoc Test (LSD).

p1: p value for comparing between Group I and Group II.

p2: p value for comparing between Group I and Group III.

p3: p value for comparing between Group II and Group III.

*: Statistically significant at p ≤ 0.05.

 

● There was a statistically significant differences in motor block onset time between the three groups. The shortest time was in Gr III (7.80 ± 1.36 min.) followed by Gr II (10.65 ± 2.01 min.), while the longest time was  Gr I (13.35 ± 1.04 min. - Table 3).


Table (3): Comparison between the three studied groups according to motor block onset times.

Groups

Motor Block Onset

Times (min.)

Motor Block Onset Times (min.)

Group I

Group II

Group III

Min.(min)

12.0

7.0

5.0

Max.(min)

15.0

14.0

10.0

Mean

13.35

10.65

7.80

±SD.

1.04

2.01

1.36

F

66.371*

P

<0.001*

p1

<0.001*

p2

<0.001*

p3

<0.001*

F, P: F and P values for ANOVA test, Sig. bet. grps was done using Post Hoc Test (LSD).

p1: p value for comparing between Group I and Group II.

p2: p value for comparing between Group I and Group III.

p3: p value for comparing between Group II and Group III.

*: Statistically significant at p ≤ 0.05

 

 

● There was a statistically significant increase in motor block intensity i.e. lesser Modified Bromage Scale in Gr II (1.85 ± 0.37 min.) and Gr III ( 2.0 ± 0.0 min.) compared with Gr I (1.50 ± 0.51 min.), but there was no significant difference between Gr II and Gr III (Table 4).


 

Table (4): Intensity of motor block according to Modified Bromage Scale in studied groups.

Groups

Modified Bromage Scale

Modified Bromage Scale

Group I

Group II

Group III

Min.

1.0

1.0

2.0

Max.

2.0

2.0

2.0

Mean

1.50

1.85

2.0

±SD.

0.51

0.37

0.0

Median

1.50

2.0

2.0

KWc2

15.257*

P

<0.001*

p1

0.020*

p2

<0.001*

p3

0.075

KWc2: Chi square for Kruskal Wallis test Sig. bet. grps was done using Mann Whitney test

p1: p value for comparing between Group I and Group II.

p2: p value for comparing between Group I and Group III.

p3: p value for comparing between Group II and Group III.

*: Statistically significant at p ≤ 0.05

 

● There was a statistically significant increase in sensory block recovery time of Gr II (10.45 ± 1.85 min.) and III (11.0 ± 1.89 min.) compared  with Gr I (6.85 ± 1.46 min.) but there was no significant difference between Gr II and Gr III (p3  0.323 - Table 5 ).


 

Table (5): Comparison between the three studied groups according to sensory block recovery times

Groups

Sensory

Block Recovery Times (min.)

Sensory Block Recovery Times (min.)

 

Group I

 

Group II

 

Group III

Min.(min)

5.0

4.0

8.0

Max.(min)

9.0

12.0

15.0

Mean

6.85

10.45

11.0

±SD.

1.46

1.85

1.89

F

33.384*

P

<0.001*

p1

<0.001*

p2

<0.001*

p3

0.323

F, P: F and P values for ANOVA test, Sig. bet. grps was done using Post Hoc Test (LSD).

p1: p value for comparing between Group I and Group II.

p2: p value for comparing between Group I and Group III.

p3: p value for comparing between Group II and Group III.

*: Statistically significant at p ≤ 0.05

 

 

● There was a statistically significant difference between the three groups in motor block recovery time. The longest recovery time was in Gr III  (21.65 ± 2.03 min.) followed by Gr II (13.30 ± 1.81 min.), while the shortest was in Gr I (11.60 ± 1.73 min. - Table 6).


 

Table (6): Comparison between the three studied groups according to motor block recovery times

Groups

Motor

Block Recovery Times (min.)

Motor Block Recovery Times (min.)

 

Group I

 

Group II

 

Group III

Min.(min)

9.0

10.0

18.0

Max.(min)

14.0

16.0

25.0

Mean

11.60

13.30

21.65

±SD.

1.73

1.81

2.03

F

166.980*

P

<0.001*

p1

0.005*

p2

<0.001*

p3

<0.001*

F, p: F and p values for ANOVA test, Sig. bet. grps was done using Post Hoc Test (LSD).

p1: p value for comparing between Group I and Group II.

p2: p value for comparing between Group I and Group III.

p3: p value for comparing between Group II and Group III.

*: Statistically significant at p ≤ 0.05

 

● There was a significant increase of NRS for postoperative pain at 1 hr and 2 hour in Gp I than Gr II or Gr III, and increase of NRS for postoperative pain after 3 hours in Gr II and Gr III, no significant difference between study groups after 4 hours (Table 7).


 

Table (7): Changes in postoperative NRS in studied groups.

Groups

 

Postoperative NRS

Postoperative NRS

1 hr

2 hrs

3 hrs

4 hrs

Group I

 

 

 

 

Min.

1.0

2.0

1.0

1.0

Max.

4.0

4.0

3.0

4.0

Mean

2.80

3.10

2.10

2.15

±SD.

1.06

1.02

0.45

0.67

Median

3.0

4.0

2.0

2.0

Group II

 

 

 

 

Min.

0.0

1.0

1.0

0.0

Max.

2.0

3.0

4.0

4.0

Mean

1.30

1.90

3.10

2.55

±SD.

0.80

0.45

1.07

1.47

Median

1.50

2.0

4.0

2.0

Group III

 

 

 

 

Min.

0.0

2.0

0.0

0.0

Max.

2.0

3.0

4.0

4.0

Mean

1.0

2.10

3.20

2.65

±SD.

0.92

0.31

1.20

1.27

Median

1.0

2.0

4.0

2.0

KWc2

23.533*

20.131*

14.681*

1.833

P

<0.001*

<0.001*

0.001*

0.400

p1

<0.001*

<0.001*

0.002*

0.369

p2

<0.001*

0.001*

<0.001*

0.139

p3

0.296

0.107

0.682

0.840

KWc2: Chi square for Kruskal Wallis test Sig. bet. grps was done using Mann Whitney test.

p1: p value for comparing between Group I and Group II.

p2: p value for comparing between Group I and Group III.

p3: p value for comparing between Group II and Group III.

*: Statistically significant at p ≤ 0.05

 

 

● There was a significant decrease of postoperative analgesic requirements in Gr II (10.50 ± 1.54 mg/kg) and Gr III (10.75 ± 1.83 mg/kg) compared with Gr I (13.25 ± 2.45 mg/kg) but there was no significant difference between Gr II and Gr III (p3 0.691 - Table 8).

 

 

 

 

Table (8):  Comparison between the three studied groups according to P.O analgesic requirements (paracetamol iv infusion 10-15 mg/kg).

Groups

 

 

Paracetamol IV infusion

(mg/kg)

P.O Analgesic Requirements paracetamol (mg/kg)

 

Group I

 

Group II

 

Group III

Min.(mg/kg)

10.0

10.0

10.0

Max.(mg/kg)

15.0

15.0

15.0

Mean

13.25

10.50

10.75

±SD.

2.45

1.54

1.83

F

11.848*

P

<0.001*

p1

<0.001*

p2

<0.001*

p3

0.691

F, p: F and p values for ANOVA test, Sig. bet. grps was done using Post Hoc Test (LSD).

p1: p value for comparing between Group I and Group II.

p2: p value for comparing between Group I and Group III.

p3: p value for comparing between Group II and Group III.

*: Statistically significant at p ≤ 0.05

 



DISCUSSION

    Intravenous regional anesthesia (IVRA) is a technically simple, reliable and cost-effective method of regional anesthesia for short operative procedures of  the extremities (Sethi and Wason, 2010). IVRA is a suitable technique for short elective surgical procedures performed on the distal arm , but it can also be used in the case of an emergency procedures (Ali et al., 2016). Disadvantages of this block include tourniquet pain , poor muscle relaxation, short duration of block and absence of post-operative analgesia (Esha et al., 2016).

    The ideal IVRA solution should have the following features: rapid onset, reduced dose of LA, reduced tourniquet pain, and prolonged post deflation analgesia (Nasr and Waly, 2011). Different additives such as opioids, non- steroidal anti-inflammatory drugs (NSAIDs), dexmedetomidine, and muscle relaxants have been combined with LAs to improve block quality, prolong post- operative analgesia and decrease tourniquet pain (Sethi and Wason, 2010). Intravenous regional anesthesia acts by diffusion of local anesthetic into the small veins surrounding the nerves, leading to a centrifugal conduction block in the nerves involved (Eapen et al., 2015).

    Nitroglycerine helps in distribution of local anesthetic agents to neuron trunks by vasodilatation (Biricik et al., 2014). NTG exerts its analgesic effect as it is metabolized to nitric oxide (NO) in the cell. NO causes an increase in the intracellular concentration of cyclic guanosine monophosphate, which produces pain modulation in the central and peripheral nervous systems. NO generators also induce anti-inflammatory and analgesic effect (Asadi and Mehri, 2013).

    Various neuromuscular blocking agents have been used with IVRA to improve the operating conditions and reduce the local anesthetic dose and possible systemic toxicity. Administration of neuromuscular blocking drugs including pancuronium (0.5 mg) with local anesthetics in upper limb IVRA improves surgical conditions in Adults and no reported complications  from using adjuvant neuromuscular blocking drugs in IVRA (Aujla et al., 2009). Addition of muscle relaxants to lidocaine for IVRA has shown to shorten the motor block onset time, prolong the motor block recovery time and improve the muscle relaxation and operative conditions (Esmaoglu et al., 2006). Muscle relaxants act at the level of the muscle spindle and reduce the central input from these structures resulting in loss of muscle tone and spasm (Aujla et al., 2009).

    The aim of the present study is to reduce the dose of lidocaine to decrease toxicity potentials and to improve postoperative analgesia by the use of pancuronium and nitroglycerin with lidocaine for intravenous regional  anesthesia for upper extremity surgery.

    As regard onset time of sensory block, there was significant decrease in sensory block onset time in Gr II (3.65 ± 0.99) and Gr III (4.0 ± 0.97) when compared with Gr I (6.30 ± 1.53). Also, the present study revealed that sensory block recovery time was significantly prolonged in Gr II (10.45 ± 1.85) and Gr III (11.0 ± 1.89) when compared with Gr I (6.85 ± 1.46).

    Asadi and Mehri (2013) studied the addition of 200 μg nitroglycerin to lidocaine for IVRA in patients scheduled for hand and forearm surgery and they found that sensory block onset time was shorter in nitroglycerin group when compared to lidocaine group.

    Moreover, Abbasivash et al. (2009) studied Forty-six patients scheduled   for closed reduction of forearm fractures. The study group received 200 μg NTG mixed with 0.5% lidocaine. They found that adding nitroglycerin to lidocaine in IVRA leads to shorter sensory block onset time. The recovery time of sensory block was prolonged.

    Also, Sen et al.(2006), Asadi and Mehri (2013) and Cakmak et al. (2014) studied the effect of adding 200 μg nitoglycerin to 3 mg/kg lidocaine for IVRA on patients undergoing hand surgery in two groups and they found that the addition of nitroglycerin to lidocaine in IVRA shortened the onset time of sensory block with prolonged sensory block recovery time.

    In addition, Elmetwaly et al. (2010) studied the analgesic effect of 200 μg nitroglycerin when added to 3 mg/kg 0.5% lidocaine (maximum 200 mg) for IVRA on patients scheduled for elective forearm and hand surgery and agreed the present study results by reporting shorter sensory block onset time and delay in sensory block recovery time after tourniquet release in the nitroglycerin  group.

    Sen et al. (2006), Elmetwaly et al. (2010), Asadi and Mehri (2013) and Cakmak et al. (2014) studied the effect of adding 200 μg nitoglycerin to 0.5% lidocaine for IVRA on patients undergoing hand surgery and they found shortened the onset time of motor block with prolonged recovery time which  was in agreement with the present study.

    Moreover, Abbasivash et al. (2009) found that adding 200 μg nitroglycerin to 0.5% lidocaine in IVRA leads to shorter motor block onset time. The  recovery time of motor block was prolonged which was in agreement with the present study results.

    In the present study we used 1.5 mg/kg lidocaine and it gave the same results of all previous studies which used 3 mg/kg lidocaine, the present study show that the use of nitroglycerine shortens the sensory and motor block onset times and delays the sensory and motor block recovery times.

    Regarding pancuronium, Flamer and Peng (2011) evaluated thirty one studies with data collected on 1523 subjects and use of muscle relaxants (pancuronium, atracurium, mivacurium and cisatracu-rium) that revealed that the use of muscle relaxants as adjuvant in IVRA enhances motor block and shortens its onset time with delay of its recovery time. In addition to making the surgery easier, addition of muscle relaxant as an adjuvant in IVRA reduces the dose of LA to a nontoxic range.

    Aujla et al. (2009) evaluated the effect of lignocaine alone versus mixture of lignocaine, pancuronium for intravenous regional anesthesia on 100 patients divided into two equal groups of 50 each scheduled for elective upper limb surgery, they revealed that the addition of muscle relaxant (0.5 mg  pancuronium) to IVRA anesthetic solution improved the muscle relaxation and operative conditions.

    The present study show that the use of pancuronium shortens the motor block onset times and delays motor block recovery time and it gave the same effect of all previous studies although we use 1.5 mg/kg of lidocaine.

    Sen et al. (2006) and Honarmand et al. (2011) studied the effects of adding 200 μg nitoglycerin to 3 mg/kg lidocaine 0.5 % for IVRA and they found that postoperative analgesic requirements were significantly smaller in NTG groups (P < 0.0001).

    In addition, Abbasivash et al. (2009) , Elmetwaly et al. (2010) and Cakmak et al. (2014) studied the effects of adding 200 μg nitroglycerin to 3 mg/kg lidocaine 0.5 % for IVRA on patients undergoing hand surgery and they found that postoperative analgesic requirement was lower for the first 4 hours in the nitroglycerine group. There was significant difference in paracetamol requirement between the groups L (lidocaine) and LL-N (lidocaine and nitroglycerine): P = 0.001.

    In the present study, postoperative analgesic requirement (paracetamol iv infusion) showed a significant decrease in Gr II (10. 50 ± 1.54) and Gr III (10.75 ± 1.83) compared with Gr I (13.25 ± 2.45).

    In the present study, neither patients' satisfaction about the operation nor surgeons' opinion of the operative conditions showed significant difference between the three groups.

    No adverse effects or complications were reported in this study. No evidence of central nervous system or cardiac complications were seen after local anesthetic administration, before and during surgery and after release of  the tourniquet. This could be due to, the small dose of lidocaine (1.5 mg/kg), pancuro-nium (0.5 mg) and nitroglycerin (200 μg/kg), deflation of tourniquet 60 minutes after inflation and by the cyclic deflation technique.

    Abbasivash et al. (2009) found that there were no side effects from using lidocaine 0.5% with 200 μg nitroglycerin for IVRA.

CONCLUSIONS

    Addition of pancuronium and nitroglycerin improve the quality of intravenous regional anesthesia with no side effects, shortens the sensory and motor block onset times, prolongs the sensory and motor block recovery times, and reduce the postoperative analgesic requirement with satisfaction for patient and surgeon.

REFERENCES

1. Abbasivash R, Hassani E, Aghdashi MM and Shirvani M. (2009): The effect of nitroglycerin as an adjuvant to lidocaine in intravenous regional anesthesia. Middle East J Anesthesiol., 20(2):265-269.

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 إستخدام البانکیوریوم والنیتروجلیسرین مع اللیدوکیین فى التخدیر الموضعی الوریدی عند البالغین الخاضعین لجراحات الطرف العلوی للجسم

 

مصطفى محمد مهدى  _عبد الله محمد احمد _ مصطفى محمد صبره _ احمد سعد حمادة

 

قسم التخدیر و العنایة المرکزة - کلیة الطب - جامعة الأزهر

 

خلفیة البحث: التخدیر الناحی الوریدی تقنیة بسیطة و فعالة من حیث التکلفة و الذى یستخدم لإجراء العملیات القصیرة فی الأطراف. و هناک بعض القیود المرتبطة بالتخدیر الناحی الوریدی و التی تشمل سمّیة المخدر الموضعی، و تأخر العمل، و سوء استرخاء العضلات، و آلام العاصبة، و محدودیة التسکین للألم  بعد العملیة الجراحیة . و کی یکون محلول التخدیر الناحی الوریدی مثالیا، فیجب أن یشمل الممیزات الآتیة: سرعة التخدیر, وأقل کمیة ممکنة من المخدر الموضعی, وأقل ألم للعاصبة وطول مدة تسکین الألم بعد العملیة الجراحیة. و قد إستخدمت الإضافات المختلفة مع المخدر الموضعی لتحسین جودة التخدیر، والحد من آلام العاصبة، وإطالة مدة تسکین الألم بعد تفریغ العاصبة من الهواء کالمخدرات،والعقاقیر غیر الستیرویدیة المضادة للالتهاب، ومرخیات العضلات، والنیوستیجمین.

الهدف من البحث: مقارنة وقت بدء ووقت إنتهاء التخدیر، و مقدار الألم ، و المسکنات بعد الجراحة عند إضافة النیتروجلیسرین أو عقار البانکرونیم بالورید  إلى عقار اللیدوکایین فی التخدیر الناحی الوریدی لجراحة الطرف العلوی.

المرضى و طرق البحث:هذا البحث تم تنفیذه فى مستشفیات جامعة الأزهر لمدة 6 أشهر فى الفترة من
 1-4-2016 حتى 1-10-2016  على 60 مریض من عمر 20 حتى 50 سنة من الجنسیین خضعوا لعملیات إختیاریة فی الید أو الساعد ، و ذلک بعد الحصول على موافقة  لجنة الجودة وأخلاقیات البحث العلمی و موافقة خطیة من المرضى .

          وقد تم تقسیم المرضى إلى ثلاث مجموعات عشوائیة (بنظام الأظرف المغلقة)  متساویة العدد:

● المجموعة الأولى : تم إستخدام ٤٠سم ٣من اللیدوکایین بجرعة 3 مجم⁄ کجم ( المخفف فی محلول ملحی طبیعی) لإعطاء التخدیر الناحی الوریدی .

● المجموعة الثانیة : تم إستخدام ٤٠سم ٣من اللیدوکایین بجرعة 1,5 مجم⁄کجم مضافا إلیه 200 میکروجرام نیتروجلیسرین لإعطاء التخدیر الناحی الوریدی .

● المجموعة الثالثة : تم إستخدام  ٤٠سم ٣من اللیدوکایین بجرعة 1,5 مجم⁄کجم مضافا إلیه 0,5 مجم بانکرونیم و 200 میکروجرام نیتروجلیسرین لإعطاء التخدیر الناحی الوریدی .

          وقد شملت هذه الدراسة تقییموقت بدء وإنتهاء التخدیر الحسی و الحرکی , و جرعة المسکنات  بعد العملیة الجراحیة , و مدى إرتیاح المریض و الجراح للعملیة الجراحیة والأعراض الجانبیة أو المضاعفات أثناء أو بعد العملیة الجراحیة.

النتائج: کان وقت بدء التخدیرالحسی والحرکی فی مجموعة اللیدوکاییین بطیئا ، ووقت نهایتهما سریعا, بالإضافة إلى إستهلاک کمیة أکبر من المسکنات بعد العملیة الجراحیة. أما فى مجموعة النیتروجلیسرین ، فقدبدأ التخدیر الحسی فی وقت أقصر ، و إنتهى فی وقت أطول , مع إستهلاک وقت أطول لبدء التخدیر الحرکی و زواله فی وقت قصیر, بالإضافة إلى إستهلاک کمیة قلیلة من المسکنات وعدد أقل من المرضى الذین إشتکوا من الألم  بعد العملیة الجراحیة. أما المجموعة الأخیرة و هی مجموعة البانکرونیم و النیتروجلیسرین  فقد کانت مثل مجموعة النیتروجلیسرین , و باستثناء التخدیر الحرکی فقد کان وقت البدایة أسرع و الزوال فی مدة أطول ، و لم تحدث أی مضاعفات فی أی مجموعة مما سبق.

الاستنتاج : إضافة البانکرونیم والنیتروجلیسرین إلى اللیدوکایین فی التخدیر الناحی الوریدی قلل
الجرعة المطلوبة من اللیدوکایین للتخدیر، وقصر مدة بدء التخدیر الحسی والحرکی، وجعل
نھایتھما فی مدة أطول، وأقل شکوى من الألم و أقل إحتیاجاً للمسکنات بعد العملیة الجراحیة، وأفضل جودة للتخدیر دون حدوث أى مضاعفات للمرضى .