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Table of Content - Volume 19 Issue 3 - September 2021


 

Study of efficacy of ultrasonography guided erector spinae plane block for abdominothoracic surgeries

 

Amol B Sasane1, Rahul D Kore2*, Pushpa I Agrawal3

 

1Senior Resident, 2Associate Professor, 3Professor and HOD, Department of Anaesthesiology, Dr. V M Government Medical College and SCSMSR, Solapur, Maharashtra, INDIA.

Email: Rahuldkorefb@yahoo.com

 

Abstract     Background: Erector spinae block (ESPB) provides analgesia by targeting the dorsal and ventral rami of the spinal nerves, performed in the lumbar region for postoperative analgesia of abdomino-thoracic surgeries. This study was aimed to assess the efficacy of Erector spinae block (ESPB) on postoperative analgesia in patients undergoing abdominothoracic surgeries under general anesthesia. Material and Methods: Present study was prospective, randomized, comparative study, conducted in patients with 18-70 years age, ASA grade- I/II, posted for abdominothoracic surgeries, Mallampatti scores - I and II, consented for participation. 120 patients were randomly assigned into two groups of 60 each, to either Erector spine block group (Group 1) or conventional pain killers (Group 2). Results: General characteristics such as age, height, weight, BMI were comparable in both groups and difference was not statistically significant. The postoperative systolic blood pressure, diastolic blood pressure, heart rate and Mean post-operative VAS score difference was statistically significant, from 30 minutes post-operative to 480 mins (8 hours). Group 1 have significantly less amount opioid requirement as none of the patients required inj tramadol more than 100 mg and only 5 (8.33%) cases required 100 mg whereas in the Group 2 73.33% required inj tramadol more than 100 mg and 8.55% required 175 mg. Group 1 have significantly long period of opioid free time as during first 2 hours none of the patients required inj tramadol whereas in the Group 2 83.33% required inj tramadol in the first 2 hours. Conclusion: In our study we concluded that the analgesic efficacy of Ultrasound guided Erector spinae block is an effective procedure over systemic analgesics and provide better patient satisfaction and compliance

Keywords: Erector spinae block.

 

INTRODUCTION

Erector spinae block (ESPB) provides analgesia by targeting the dorsal and ventral rami of the spinal nerves, performed in the lumbar region for postoperative analgesia of abdomino-thoracic surgeries.1 Adequate postoperative analgesia is essential to prevent complications such as systemic hypertension, myocardial ischemia or infarction, cardiac arrhythmias, respiratory compromise, pneumonia, postoperative ileus and delayed wound healing.2 Moreover, the severity of acute pain may lead on to distressing postsurgical chronic pain.3 Erector spinae block (ESPB) gained wide attention as it is a faster procedure that carries a lower risk of hypotension, can be used in patients with coagulopathy, is easy to perform, and requires less training.1 Erector spinae block performed at low thoracic levels was recently shown to provide satisfactory analgesia for gynecologic and abdominal surgery in case reports and series describing lower segment cesarean section, ventral hernia repair, and abdominoplasty.4 This study was aimed to assess the efficacy of Erector spinae block (ESPB) on postoperative analgesia in patients undergoing abdominothoracic surgeries under general anesthesia.

              

MATERIAL AND METHODS

Present study was prospective, randomized, comparative study, conducted in Department of Anaesthesiology, Dr. V M Government. Medical College, Solapur, India. Study duration was of 2 years (Dec 2018 to Oct 2020). The study was conducted after obtaining Ethics committee approval.

Inclusion criteria: Age - 18-70 years, ASA grade- I/II, posted for abdominothoracic surgeries, Mallampatti scores - I and II, consented for participation

Exclusion criteria: BMI >35 kg/m. Skin infection at the puncture site, Patients posted for emergency surgery, Patients with difficult airway, Severe coagulopathy, Chronic hepatic or renal failure, Preoperative opioid or non-steroidal anti-inflammatory drugs for chronic pain treatment.

Patients who satisfied the inclusion criteria were explained about the nature of the study and the anesthetic procedure and written informed consent was taken. The patients were familiarized with 10 cm visual analogue scale (VAS) for pain during preanesthetic visit.

120 patients were randomly assigned into two groups of 60 each. Randomization done by alternating patients to either Erector spine block group (Group 1) or conventional pain killers (Group 2)

Group 1: - Postoperative ultrasound guided erector spine block with 0.25 % bupivacaine 20 cc.

Group 2: - Postoperative No Block given, Conventional drug-based pain management

In the operating room, all basic monitors were connected to the patient (ECG, SPO2, EtCO2, non-invasive BP). Baseline vitals were recorded. Postoperative as per randomization, anaesthesia was given accordingly.

Primary Outcome was Post-operative visual analogue scale pain score and Post-operative hemodynamic characteristics. Secondary Outcome was Post-operative opioid requirement.

Descriptive statistics was done for all data and suitable statistical tests of comparison were done. Continuous variables were analysed with the T test and categorical variables were analysed with the Chi-Square Test and Fisher Exact Test. Statistical significance was taken as P < 0.05. The data was analysed using SPSS version 26 software and Microsoft Excel 2010

 

RESULTS

General characteristics such as age, height, weight, BMI were comparable in both groups and difference was not statistically significant.

 

Table 1: General characteristics of study population

Characteristics

Group 1

Group 2

P value

Mean age (years)

37.05 ± 15

43.25 ± 14.21

>0.05

Mean Height (cm)

162.33 ± 4.78

163.06 ± 3.79

>0.05

Mean weight (kgs)

61.41 ± 9.25

63.00 ± 8.61

>0.05

Mean BMI (kg/m2)

23.36 ± 3.77

23.72 ± 3.34

>0.05

The postoperative systolic blood pressure ranged from 126 to 172 mm of Hg the Group 2 have higher mean systolic blood pressure than the Group 1, the effect on systolic blood pressure is considered to be statistically significant since p < 0.05, from 30 minutes post-operative to 480 mins (8 hours)


 

Table 2: Systolic Blood Pressure distribution

Post-Operative time

(in minutes)

Group 1

Group 2

Mean

Std. Deviation

Mean

Std. Deviation

0 mins

128.9167

2.21162

129

2.16286

30 mins

128.9333

2.05737

136.2

6.93749

60 mins

137.8167

6.46632

151.4333

8.20163

120 mins

141.2833

5.43713

156.9167

6.14318

180 mins

147.35

6.11424

162.4167

6.81049

240 mins

150.4833

4.11896

165.9

4.96325

300 mins

143.9167

6.27422

160.1

6.91032

360 mins

139.3667

4.6903

156.5833

5.46264

420 mins

128.8833

1.92302

141.8333

4.34592

480 mins

128.7667

2.01155

133.7667

4.58578

540 mins

128.95

1.96085

129.2333

2.06969

720 mins

128.6

1.98469

128.8167

2.0126

The postoperative diastolic blood pressure ranged from 82 to 114 mm of Hg the Group 2 have higher mean diastolic blood pressure than the Group 1, the effect on diastolic blood pressure is considered to be not statistically significant since p > 0.05. from 30 minutes post-operative to 480 mins (8 hours).

 

 

Table 3: Diastolic Blood Pressure distribution in study population

Post-Operative time

(in minutes)

Group 1

Group 2

Mean

Std. Deviation

Mean

Std. Deviation

0 mins

85.65

2.41342

86.05

2.15048

30 mins

85.0833

2.27955

90.1833

4.88683

60 mins

91.35

4.64621

100.05

5.38493

120 mins

92.7667

3.72971

102.5833

4.66248

180 mins

96.7167

4.19884

106.25

4.55708

240 mins

98.6333

3.83546

109.0833

3.8939

300 mins

95.0167

3.82007

104.4167

4.98911

360 mins

91.8833

3.79157

102.3833

4.15011

420 mins

85.55

2.30272

93.4667

3.60539

480 mins

85.4

2.35206

88.8167

2.9943

540 mins

85.1333

2.1821

85.4333

2.37477

720 mins

85.5833

2.38137

85.6667

2.25243

The postoperative heart rate ranged from 61 to 94 per minute, the Group 2 have higher mean heart rate than the Group 1, the effect on heart rate is considered to be not statistically significant since p > 0.05, from 30 minutes post-operative to 480 mins (8 hours)

 

Table 4: Heart rate distribution in study population

Group Statistics

Post Operative time (in minutes)

GROUP

N

Mean pulse rate (per minute)

Std. Deviation

Std. Error Mean

0 mins

Group 1

60

65.0833

2.50621

0.32355

Group 2

60

65.0333

2.62302

0.33863

30 mins

Group 1

60

65.5667

2.36763

0.30566

Group 2

60

69.6333

4.83268

0.6239

60 mins

Group 1

60

70.0167

4.61938

0.59636

Group 2

60

79.1

5.51024

0.71137

120 mins

Group 1

60

72.4167

3.79693

0.49018

Group 2

60

81.9667

4.86414

0.62796

180 mins

Group 1

60

75.9

4.19321

0.54134

Group 2

60

86.2667

4.98087

0.64303

240 mins

Group 1

60

78.3

3.98003

0.51382

Group 2

60

88.4333

4.24011

0.5474

300 mins

Group 1

60

74.45

4.09392

0.52852

Group 2

60

84.5333

5.01681

0.64767

360 mins

Group 1

60

71.7

3.85016

0.49705

Group 2

60

82.2167

4.39218

0.56703

420 mins

Group 1

60

64.8833

2.41529

0.31181

Group 2

60

73.1

3.443

0.44449

480 mins

Group 1

60

64.7333

2.60291

0.33603

Group 2

60

67.8

3.73168

0.48176

540 mins

Group 1

60

64.9333

2.29123

0.2958

Group 2

60

64.45

2.72107

0.35129

720 mins

Group 1

60

64.85

2.68596

0.34676

Group 2

60

65.0667

2.52356

0.32579

Mean post-operative VAS score at 0 mins, 30mins 1,2,3,4,5,6,7,8 9 and 12 hrs. (Group 1 vs Group 2s) was considered to be statistically significant since p < 0.05

 

Table 5: VAS Score distribution in study population

Post-Operative time

Group 1

Group 2

Mean

Std. Deviation

Mean

Std. Deviation

0 mins

0

0

0.8333

0.37582

30 mins

0.45

0.50169

1.9667

0.80183

60 mins

2.1333

0.76947

3.75

0.98506

120 mins

2.5

0.62436

4.4333

0.76727

180 mins

3.2833

0.71525

5.1667

0.80605

240 mins

3.6833

0.53652

5.65

0.57711

300 mins

2.8167

0.70089

4.8667

0.85304

360 mins

2.35

0.54695

4.4333

0.67313

420 mins

0.65

0.48099

2.5833

0.49717

480 mins

0

0

1.5833

0.49717

540 mins

0

0

0.7667

0.42652

720 mins

0

0

0.1167

0.32373

Group 1 have significantly less amount opioid requirement as none of the patients required in j tramadol more than 100 mg and only 5 (8.33%) cases required 100 mg whereas in the Group 2 73.33% required in j tramadol more than 100 mg and 8.55% required 175 mg. the mean dose of opioid in group 1 is 63.3333 ± 16.25190 mg whereas in Group 2 127.0833 ± 25.33323mg. By conventional criteria the association between the treatment groups, first dose of Injection Tramadol is considered to be statistically significant since p < 0.05.

 

Table 6: Use of Injection Tramadol

Injection Tramadol (mg)

Group 1 (n=60)

%

Group 2 (n=60)

%

50

33

55.00%

1

1.67%

75

22

36.67%

1

1.67%

100

5

8.33%

14

23.33%

125

0

0.00%

25

41.67%

150

0

0.00%

14

23.33%

175

0

0.00%

5

8.33%

Mean dose of tramadol (mg)

63.33 ± 16.25

 

127.08 ± 25.33

 

Group 1 have significantly long period of opioid free time as during first 2 hours none of the patients required inj tramadol whereas in the Group 2 83.33% required inj tramadol in the first 2 hours. the mean time of first dose of opioid in Group 1 is 4.0500 ± 1.12634 hours whereas in Group 2 1.6167 ± 0.80447 hours. By conventional criteria the association between the treatment groups, first dose of Injection Tramadol is considered to be statistically significant since p < 0.05.

 

Table 7: First dose of Injection Tramadol

First Injection Tramadol (hours)

Group 1

(n=60)

%

Group 2s

(n=60)

%

1-2

0

0.00%

50

83.33%

3-4

43

71.67%

10

16.67%

5-6

17

28.33%

0

0.00%

time of 1st dose of Inj Tramadol (hrs.)

4.05 ± 1.13

 

1.62 ± .80

 

 


DISCUSSION

Ultrasound guided erector spinae (ESP) block is a regional anesthesia technique, recently described by Forero et al.,1 for use in thoracic neuropathic pain. ESP block is reported to lead to analgesic effect on somatic and visceral pain by effecting the ventral rami and rami communicants that include sympathetic nerve fibers, as LA spreads through the paravertebral space.1,4 When performed bilaterally it has been reported to be as effective as thoracic epidural analgesia.4 In present study, mean age in case group was 37.05 ± 15.00 years, in control group the mean age was 43.25 ± 14.22 years, similar findings were seen by Peker et al.,5 in his study the case and control group have age 48 ±15.91 and 48.44 ± 14.32 respectively , Krishna et al.,6 found the case and control group have age 48.321±1.7 and 49.62 ± 1.51 years respectively and Aksu et al.,7 found the case and control group have age 49.26±14.18 and 47.26±13.461 years respectively, Systolic Blood Pressure distribution in study population ranged from 126 to 172 mm of Hg the control group have higher mean systolic blood pressure than the cases group,. Ciftci et al.,8 reported similar results. Effect on systolic blood pressure was considered to be statistically significant from 30 minutes post-operative to 480 mins (8 hours) similar findings were also seen by S. Tulgar et al.,9 Aksu et al.,7 and Krishna et al.,6 Postoperative diastolic blood pressure ranged from 82 to 114 mm of Hg the control group have higher mean diastolic blood pressure than the cases group, Elyazed et al.,10 and Krishna et al.,7 reported similar results. Effect on diastolic blood pressure is considered to be not statistically significant. from 30 minutes post-operative to 480 mins (8 hours) like S. Tulgar et al.,9 Aksu et al.,7 and Elyazed et al.,10 also reported similar results. Post operative heart rate ranged from 61 to 94 per minute, the control group have higher mean heart rate than the cases group, the effect on heart rate was considered to be statistically significant from 30 minutes post-operative to 480 mins (8 hours) similar findings were also seen by S. Tulgar et al.,9 Aksu et al.,7 and Krishna et al.,6 For VAS Score the post-operative analgesia was considered to be better in study group and difference was statistically significant, similar reports are given by almost all the studies like S. Tulgar et al.,9 Aksu et al.,6, Elyazed et al.,10 and Krishna et al.,6 Total dose of Inj Tramadol given to the patients post op, cases group have significantly less amount opioid requirement as none of the patients required inj tramadol more than 100 mg and only 5 (8.33%) cases required 100 mg whereas in the control group 73.33% required inj tramadol more than 100 mg and 8.55% required 175 mg. Similar findings are reported by Aksu et al.,7 Elyazed et al.,10 Krishna et al.,6 and Altiparmak et al.,11 Total dose of Injection Tramadol was more in control group as compared to cases and difference was statistically significant, similar findings are shown with systemic pain killers by Koo et al.,12 Singh et al.,13 and a systemic review of RCT conducted by Mostafa et al.,14 In distribution of time of 1st dose of Inj Tramadol, cases group have significantly long period of opioid free time as during first 2 hours none of the patients required inj tramadol whereas in the control group 83.33% required inj tramadol in the first 2 hours, similar findings were reported by Aksu et al.,7 Elyazed et al.,10 Krishna et al.,6 and Altiparmak et al.,11 First dose of Injection Tramadol was earlier required in control group as compared to cases and difference was statistically significant, similar findings are reported by Koo et al.,12 Singh et al.,13 Aksu et al.,7 and Elyazed et al.,10Erector spinae block (ESPB) provides extensive, potent unilateral analgesia, is performed by local anesthetic injection in the plane between the erector spinae muscle and the Transverse process. The local anesthetic diffuses into the paravertebral space through spaces between adjacent vertebrae and blocks both the dorsal and ventral branches of the thoracic spinal nerves.3,4In our study, the analgesic efficacy of Ultrasound guided Erector spinae block in patients undergoing abdominothoracic surgeries is highly improved than with systemic analgesics.

 

CONCLUSION

In our study we concluded that the analgesic efficacy of Ultrasound guided Erector spinae block is an effective procedure over systemic analgesics and provide better patient satisfaction and compliance

 

REFERENCES

  1. Forero M, Adhikary SD, Lopez H, Tsui C, Chin KJ. The Erector Spinae Plane Block: A Novel Analgesic Technique in Thoracic Neuropathic Pain. Reg Anesth Pain Med 2016;41:621-7.
  2. Liu SS, Wu CL. Effect of postoperative analgesia on major postoperative complications: a systematic update of the evidence. Anesth Analg 2007;104:689-702.
  3. Sundararaman LV, Edwards RR, Ross EL, Jamison RN. Integration of Mobile Health Technology in the Treatment of Chronic Pain: A Critical Review. Reg Anesth Pain Med 2017;42:488-98.
  4. Chin K, Adhikary S, Sarwani N, Forero M. The analgesic efficacy of pre‐operative bilateral erector spinae plane (ESP) blocks in patients having ventral hernia repair. Anaesthesia 2017;72:452-60.
  5. Peker K, Akcaboy ZN, Aydin G, et al. The Effect of Erector Spinae Plane Block on Laparoscopic Cholecystectomy Anesthesia: Analysis of Opioid Consumption, Sevoflurane Consumption, and Cost. J Laparoendosc Adv Surg Tech A 2020;30:725-9.
  6. Krishna SN, Chauhan S, Bhoi D, et al. Bilateral Erector Spinae Plane Block for Acute Post-Surgical Pain in Adult Cardiac Surgical Patients: A Randomized Controlled Trial. J Cardiothorac Vasc Anesth 2019;33:368-75.
  7. Aksu C, Kuş A, Yörükoğlu HU, Tor Kılıç C, Gürkan YJJ. Erektor Spina Plan Bloğunun Laparoskopik Kolesistektomi Sonrası Postoperatif Ağrı Üzerine Etkisi: Randomize Kontrollü Çalışma. JARSS 2019, 27:9-14.
  8. Ciftci B, Ekinci M, Celik EC, Tukac IC, Bayrak Y, Atalay YO. Efficacy of an Ultrasound-Guided Erector Spinae Plane Block for Postoperative Analgesia Management After Video-Assisted Thoracic Surgery: A Prospective Randomized Study. J Cardiothorac Vasc Anesth 2020;34:444-9.
  9. Tulgar S, Kapakli MS, Senturk O, Selvi O, Serifsoy TE, Ozer Z. Evaluation of ultrasound-guided erector spinae plane block for postoperative analgesia in laparoscopic cholecystectomy: A prospective, randomized, controlled clinical trial. J Clin Anesth 2018;49:101-6.
  10. Abu Elyazed MM, Mostafa SF, Abdelghany MS, Eid GM. Ultrasound-Guided Erector Spinae Plane Block in Patients Undergoing Open Epigastric Hernia Repair: A Prospective Randomized Controlled Study. Anesth Analg 2019;129:235-40.
  11. Altıparmak B, Toker MK, Uysal AI, Kuşçu Y, Demirbilek SG Ultrasound-guided erector spinae plane block versus oblique subcostal transversus abdominis plane block for postoperative analgesia of adult patients undergoing laparoscopic cholecystectomy: randomized, controlled trial. Journal of clinical anesthesia 2019;57:31-6.
  12. Koo CH, Hwang JY, Shin HJ, Ryu JH. The Effects of Erector Spinae Plane Block in Terms of Postoperative Analgesia in Patients Undergoing Laparoscopic Cholecystectomy: A Meta-Analysis of Randomized Controlled Trials. J Clin Med 2020;9:2928.
  13. Singh S, Kumar G, Akhileshwar. Ultrasound-guided erector spinae plane block for postoperative analgesia in modified radical mastectomy: A randomised control study. Indian J Anaesth 2019;63:200-4.
  14. Mostafa SF, Abdelghany MS, Abdelraheem TM, Abu Elyazed MM. Ultrasound-guided erector spinae plane block for postoperative analgesia in pediatric patients undergoing splenectomy: A prospective randomized controlled trial. Paediatr Anaesth 2019;29:1201-7.
























 








 




 








 

 









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