Celiac plexus block: an anatomical study and simulation using computed tomography (2024)

  • Journal List
  • Radiol Bras
  • v.47(5); Sep-Oct 2014
  • PMC4341398

As a library, NLM provides access to scientific literature. Inclusion in an NLM database does not imply endorsem*nt of, or agreement with, the contents by NLM or the National Institutes of Health.
Learn more: PMC Disclaimer | PMC Copyright Notice

Celiac plexus block: an anatomical study and simulation using computedtomography (1)

HomeAboutSubmitSearchContactCBRRadiologia BrasileiraCBR

Radiol Bras. 2014 Sep-Oct; 47(5): 283–287.

PMCID: PMC4341398

PMID: 25741102

Language: English | Portuguese

Gabriela Augusta Mateus Pereira,1 Paulo Tadeu Campos Lopes,2 Ana Maria Pujol Vieira dos Santos,2 Adriane Pozzobon,3 Rodrigo Dias Duarte,4 Alexandre da Silveira Cima,5 and Ângela Massignan5

Author information Article notes Copyright and License information PMC Disclaimer

Abstract

Objective

To analyze anatomical variations associated with celiac plexus complex by means ofcomputed tomography simulation, assessing the risk for organ injury as thetranscrural technique is utilized.

Materials and Methods

One hundred eight transaxial computed tomography images of abdomen were analyzed.The aortic-vertebral, celiac trunk (CeT)-vertebral, CeT-aortic andceliac-aortic-vertebral topographical relationships were recorded. Two needleinsertion pathways were drawn on each of the images, at right and left, 9 cm and4.5 cm away from the midline. Transfixed vital organs and gender-relatedassociations were recorded.

Results

Aortic-vertebral - 45.37% at left and 54.62% in the middle; CeT-vertebral - T12,36.11%; T12-L1, 32.4%; L1, 27.77%; T11-T12, 2.77%; CeT-aortic - 53.7% at left and46.3% in the middle; celiac-aortic-vertebral - L-l, 22.22%; M-m, 23.15%; L-m,31.48%; M-l, 23.15%. Neither correspondence on the right side nor significantgender-related associations were observed.

Conclusion

Considering the wide range of abdominal anatomical variations and thecharacteristics of needle insertion pathways, celiac plexus block should not bestandardized. Imaging should be performed prior to the procedure in order toreduce the risks for injuries or for negative outcomes to patients. Gender-relatedanatomical variations involved in celiac plexus block should be more deeplyinvestigated, since few studies have addressed the subject.

Keywords: Celiac plexus block, Transcrural pathway, Computed tomography, Anatomy

Abstract

Objetivo

Analisar variações anatômicas relacionadas ao bloqueio do plexo celíaco por meioda simulação por tomografia computadorizada e avaliar a possibilidade detransfixação de órgãos pelo método transcrural.

Materiais e Métodos

Cento e oito imagens de tomografias computadorizadas transaxiais abdominais foramanalisadas. As relações aorto-vertebral, tronco celíaco (TCe)-vertebral,TCe-aórtica e celíaco-aorto-vertebral foram registradas. Em cada imagem foramdispostas duas trajetórias de agulhas, a 9 cm e a 4,5 cm à esquerda e à direita dalinha média. Os órgãos vitais transfixados e associações relacionadas ao gêneroforam registrados.

Resultados

Aorto-vertebral - 45,37% esquerda e 54,62% central; TCe-vertebral - T12, 36,11%;T12-L1, 32,4%; L1, 27,77%; T11-T12, 2,77%; TCe-aórtica - 53,7% esquerda e 46,3%central; celíaco-aorto-vertebral - L-l, 22,22%; M-m, 23,15%; L-m, 31,48%; M-l,23,15%. Em nenhum dos critérios analisados houve correspondência no lado direito enem associação significativa entre os gêneros.

Conclusão

O bloqueio do plexo celíaco não deve ser padronizado, em razão das amplasvariações anatômicas abdominais e das características próprias de cada acesso,sendo necessário o registro de imagem prévio ao procedimento para cada paciente,visando diminuir riscos de lesão. Registros sobre a variação anatômica quanto aogênero, relacionados ao bloqueio do plexo celíaco, devem ser aprofundados.

INTRODUCTION

Celiac plexus block (CPB) is prescribed in cases of upper abdomen cancer, chronicpancreatitis, metastases, painful retroperitoneal tumors and chronic abdominal pain inpatients who do not respond to treatment regimens based on high-dose narcoticanalgesia(1-3). Since the beginning of the 20th century, the CPBtechnique has been adapted, giving rise to a variety of techniques that differ mainly inthe type of access, the instruments used, sedation, neurolytic solutions, imagingguidance and timing in the course of the disease. The variations and combinations oftechniques stand as a means to increase the chances of success in the procedure as wellas to reduce the occurrence of complications and morbidity(4-8).

The celiac plexus (CP) is deeply located in the retroperitoneum, overlying theanterolateral surface of the aorta, at the level of the celiac trunk (CeT), comprising adense network of ganglia that varies considerably in size, number andpositioning(6-13). It originates from sympathetic fibers of splanchnicnerves, extending from T5 to T12, and containing preganglionic splanchnic afferentfibers, preganglionic parasympathetic fibers and postganglionic sympathetic fibers. TheCP is found in the epigastrium, posteriorly to the stomach and the pancreas, andanteriorly to the diaphragmatic pillars, where it surrounds the CeT, the superiormesenteric arteries and the aorta. The visceral pain transmitted by the CP is related tothe pancreas, diaphragm, stomach, liver, spleen, small bowel, transverse colon,suprarenal glands, kidneys, abdominal aorta and mesenterium(7,13,14).

The retrocrural, transcrural, transaortic and anterior approaches are the most commonlyutilized in CPB, differing from each other in needle directioning, insertion angulationand pathway, as well as in patient positioning, among other factors that involve risksand benefits peculiar to each technique. In CPB, the imaging guidance utilized tovisualize the correct insertion of the needle and to confirm contrast medium spread ismost commonly done with either computed tomography (CT), ultrasonography orfluoroscopy(6-8,12,15-18). The decisionon which individual technique to adopt should be based on the available facilities,clinical expertise, the patients' physical condition, and on the diseaseseverity(18).

CPB may pose risks to the patient, depending on the technique employed and on abdominalanatomical variations(19). Althoughcomplications have been recorded in less than 2% of patients submitted to CPB,diaphragmatic irritation, orthostatic hypotension, pneumothorax, pericarditis,intervertebral disc injury, retroperitoneal abscess, transient diarrhea, arterydissection, pleuritis and neurologic damage have been reported(8,17). In spite of that, reports in the literature confirm thesignificant benefits to the quality of life of patients who undergo thisprocedure(4,17,18,20,21).

The variation in CPB techniques adopted since 1919(3) and the scarcity of studies reporting problems after thisprocedure such as organ transfixion and neurologic injury, or even discussing theanatomical variations of structures involved in CPB unveil the need for furtherinformation regarding this relevant analgesic resource.

The present study was aimed at analyzing the anatomical variations of structuresinvolved in CPB and implementing one of the techniques described in the literature bymeans of simulations utilizing CT. Axial CT sections of the abdomen of adult patientswere analyzed to assess one of the main risks involved in this procedure, i.e., injuryto organs or structures caused by the needle insertion towards the CP region.

MATERIALS AND METHODS

Transaxial contrast-enhanced abdominal CT images (one-centimeter-thick slices) of 108adult patients (72 women and 36 men), recovered from the Siemens Syngo®system were analyzed. The CPB simulation was based on an adapted version of thetranscrural method(22).

For each patient, an axial section at the level of the CeT was utilized to assess theaorta in the craniocaudal direction, from the diaphragm aortic hiatus to the firstanterior branch of the abdominal aorta. The celiac trunk was identified according to thefollowing criteria: 1) the first anterior branch of the abdominal aorta; 2) divided intoleft gastric artery, common hepatic artery, and splenic artery; 3) different from thesuperior mesenteric artery.

The location of the aorta was determined in relation to the vertebral body at the levelof the CeT emergence, and defined as follows: anterior to the left third (l); anteriorto the middle third (m); and anterior to the right third ® of the vertebral body.

The site of CeT emergence was determined in relation to the vertebral column. As theaxial CT sections were analyzed in the craniocaudal direction, the CeT origin wasidentified taking the aorta as a reference, at the level of either a vertebral body oran intervertebral space, and recorded as follows: at left (L); at the middle (M); atright ® of the aortic wall. The celiac-aortic-vertebral topographic relationship wasanalyzed and divided into the groups L-l, M-m, L-m or M-l, L-r and R-l.

Lines representing the needles pathway were drawn on the axial image where the CeTorigin was identified. From the midline defined as the vertebral spinous process, twolines were drawn on each side of the vertebral body. The original image was rotated 180°so as to simulate the prone position of a patient during the virtual procedure. Thefirst line (L9) was drawn starting 9 cm away from the midline on the skin surface,tangentially to the vertebral body and crossing the diaphragmatic pillars. The secondline was drawn accordingly, though 4.5 cm away from the midline (L4.5). The vital organstransfixed by L9 and L4.5 as well as the correlation between patients' gender and theanalyzed criteria were recorded.

Descriptive statistics were utilized in the data analysis and the data are expressed asmeans ± standard deviation. The CeT emergence sites and their topographic relationshipsare presented as percent values. The exact Fisher test was used to analyze theassociation between patients' gender, CeT emergence site and topographic relationships.The software Bioestat 5.00® was utilized in the statistical analysis,considering 0.05 as significance level (p ≤ 0.05).

RESULTS

In the present study, CT images of 108 individuals, 72 women and 36 men, were analyzed.Most patients presented normal CT findings. In the cases where alterations weredetected, the following conditions were most commonly diagnosed: renal cyst (12.03%,n = 13); renal lithiasis (8.33%, n = 9); hepaticcyst (5.55%%, n = 6); liver metastasis (4.6%, n = 5);colon diverticula (3.7%, n = 4); hepatic nodules (2.77%,n = 3); and retroperitoneal lymph node enlargement (2.77%,n = 3). Renal carcinoma and hepatocellular carcinoma were alsodiagnosed.

As regards CeT emergence site in relation to the vertebra, in 36.11% of the cases itemerged at the level of T12; in 32.4%, between T12 and L1; in 27.77%, at the level ofL1; and only in 2.77%, between T11 and T12.

The results regarding celiac-aortic-vertebral topographic relationship showedcorrespondence at the left aortic wall (L-l) in 22.22% of cases, at the middle (M-m) in23.15%, at the left-middle (L-m) in 31.48%, and central-left (M-l) in 23.15% of cases.No correspondence at the right side of the aortic wall was observed.

The percentages of organs transfixed by lines L9 and L4.5 are demonstrated on Table 1. Table2 shows the results regarding organ transfixion by L9 and L4.5 describing aneedle's pathway observed in the present study and in the study developed by Yang etal.(22). Images of sometransfixed organs are shown on Figure 1.

Table 1

Occurrence of organs and structures transfixion by needle insertion lines L9 andL4.5.

L9L4.5
Organs and structuresRight sideLeft sideRight sideLeft side
Liver12.03%8.33%
Kidneys19.44%23.15%0.92%0.92%
Spleen4.62%0.92%
Aorta68.51%97.22%2.7%78.7%
Inferior vena cava25%0.92%
Portal vein0.92%
Lungs67.59%51.85%54.62%44.44%
Tumor mass1.85%1.85%0.92%

Open in a separate window

L9, line 9 cm; L4.5, line 4.5 cm.

Table 2

Organs transfixion by the two needle insertion pathways, L9 and L4.5, observed inthe present study and in the study developed by Yang et al.(22).

OrganPresent studyYanget al.(22)
L9L4.5L9L4.5
Right sideLeft sideRight sideLeft sideRight sideLeft sideRight sideLeft side
Kidneys19.44%23.15%0.92%0.92%58%64%4%4%
Aorta68.51%97.22%2.7%78.7%68%90%10%84%
Inferior vena cava25%0.92%4%6%48%
Lungs67.59%51.85%54.62%44.5%
Liver12.03%8.33%24%4%

Open in a separate window

L9, line 9 cm; L4.5, line 4.5 cm.

Open in a separate window

Figure 1

A: Needle insertion pathway 9.0 cm to the right of the midline,indicating transfixion of lungs. B: Needle insertion pathway 4.5 cmto the right and to the left of midline, indicating transfixion of lungs.

No significant correlation was observed between genders and celiac-vertebral,aortic-vertebral, celiac-aortic and celiac-aortic-vertebral topographicrelationships.

DISCUSSION

Scarce information is found in the literature on the radiographic anatomy of structuresinvolved in CPB. The anatomical variations in the CeT and adjacent structures in theabdomen, which play an essential role in the guidance of the needle during blockprocedures have not been duly investigated(5,22).

As regards the celiac-aortic-vertebral topographic relationship, Yang et al. havereported twice as many cases as compared with the present study, particularly for theL-l group(22). The present results donot reveal any correlation on the right side, which is corroborated by the low frequencyreported in the mentioned study (0.5% for both L-r and R-l).

The data of the present study regarding the site of CeT emergence from the aorta aresimilar to those reported by Yang et al.(22). On the other hand, as regards celiac-vertebral topographicrelationship, Yang et al. have observed CeT emergence site between T11-and T12 in 6.5%of cases, as compared with only 2.77% observed in the present study.

Data about gender-related associations reported by Puelma et al.(23) demonstrate correlation with T12 in 50%of male and in 52,9% of the female patients, and with L1 in 50% and 47.1%respectively.

A significant difference in the aortic-vertebral topographic relationship was observedas the data from de present study are compared with those reported by Yang etal.(22), who reported 70%anterior to the left third, 29% anterior to the middle third, and 1% anterior to theright third of the vertebral body.

The risk for organ injury by needles in CPB according to two lines drawn from themidline was analyzed. In the present study, the right and left lungs were transfixed bythe needle pathways corresponding to both lines (Figure1), while the results reported by Yang et al.(22) did not reveal any possibility of pneumothorax.Additionally, results regarding injury to kidneys, inferior vena cava, aorta and liverwere also very different from those reported by the mentioned study (Table 2). Such differences observed between the twostudies clearly reveal the key role played by anatomical variations in CPB.

Kidney transfixion is most likely to occur as the needles are inserted < 7.5 cm awayfrom the midline and as they run laterally to the vertebral body(6). Injury to the pancreas, stomach andliver as well as pneumothorax are rarely reported in the literature(5,7,17,24,25). Injury to kidneys andlungs, for example, has never exceeded 0.8%(24). The imaging guidance with CT may minimize the occurrence ofsuch complications(6).

In an effort to simulate new needle pathways to the CP to avoid organs injury, 7.5% ofthe 400 simulations on images were excluded from the study because of the occurrence oforgan transfixion(26). The same studyreported difference in the distance between the site where needles were inserted and themidline (IP-ML) in men and women; larger distances were observed in men. Significantdifferences were also observed between the right side (7.04 cm) and the left side (3.58cm) for this criterion. A distance of about 7.5 cm was suggested for both sides, thoughit might vary between 4 cm and 10 cm(27).

The IP-ML distance in male patients with pancreatitis was larger (7.47 cm on the rightside and 3.78 on the left side), as compared with female patients with the samecondition (6.64 cm on the right and 3.25 cm on the left side)(22,26). In thepresent study, the diseases detected on images did not have any influence on anatomicalaspects and therefore no change was required in the needle pathway up to the CP.

In the literature approaching CPB, there are scarce data about abdominal anatomicalvariations in men and women, which has been reported in a study developed by McCartneyet al.(5). In the present study, nocorrelation was observed between gender and CeT-vertebral, aortic-vertebral, CeT-aorticand celiac-aortic-vertebral topographic relationships. Similarly, data previouslypublished on the CeT-vertebral topographic relationship were not significant(23).

There is controversy about the most appropriate imaging method for guidance inCPB(3,5,6,18). In another study, Yang et al. recommend the use ofpreprocedural CT images and fluoroscopy during the procedure(28). Other authors understand that CT-guidance is moreappropriate both previously and during the procedure, considering that risks areconsiderably reduced with the use of this method(7,8,17,25,29,30).

CONCLUSION

CPB should not be standardized, considering the wide range of gender-related abdominalanatomical variations, laterality and pathologies, as well as the characteristics ofneedle insertion pathways. Imaging should be performed prior to the procedure in orderto reduce the risks for injuries or for negative outcomes to patients.

Gender-related anatomical variations of structures involved in celiac plexus blockshould be more deeply investigated, since few studies have addressed the subject.

The present study may contribute for the knowledge on the anatomy of abdominal arteriesrequired in other invasive surgical, diagnostic or therapeutic procedures.

Footnotes

*Study developed at Universidade Luterana do Brasil (Ulbra), Canoas, RS, Brazil.

Pereira GAM, Lopes PTC, Santos AMPV, Pozzobon A, Duarte RD, Cima AS, Massignan A.Celiac plexus block: an anatomical study and simulation using computed tomography.Radiol Bras. 2014 Set/Out;47(5):283–287.

REFERENCES

1. Gorbitz C, Leavens ME. Alcohol block of the celiac plexus for control of upper abdominal paincaused by cancer and pancreatitis. Technical note. J Neurosurg. 1971;34:575–579. [PubMed] [Google Scholar]

2. Singler RC. An improved technique for alcohol neurolysis of the celiacplexus. Anesthesiology. 1982;56:137–141. [PubMed] [Google Scholar]

3. Fugère F, Lewis G. Coeliac plexus block for chronic pain syndromes. Can J Anaesth. 1993;40:954–963. [PubMed] [Google Scholar]

4. Hastings RH, McKay WR. Treatment of benign chronic abdominal pain with neurolytic celiacplexus block. Anesthesiology. 1991;75:156–158. [PubMed] [Google Scholar]

5. McCartney CJL, Chambers WA. Coeliac plexus block. Curr Anaesth Crit Care. 1998;9:318–324. [Google Scholar]

6. Mercadante S, Nicosia F. Celiac plexus block: a reappraisal. Reg Anesth Pain Med. 1998;23:37–48. [PubMed] [Google Scholar]

7. Titton RL, Lucey BC, Gervais DA, et al. Celiac plexus block: a palliative tool underused byradiologists. AJR Am J Roentgenol. 2002;179:633–636. [PubMed] [Google Scholar]

8. Wang PJ, Shang MY, Qian Z, et al. CT-guided percutaneous neurolytic celiac plexus blocktechnique. Abdom Imaging. 2006;31:710–718. [PubMed] [Google Scholar]

9. Ward EM, Rorie DK, Nauss LA, et al. The celiac ganglia in man: normal anatomic variations . Anesth Analg. 1979;58:461–465. [PubMed] [Google Scholar]

10. Paz Z, Rosen A. The human celiac ganglion and its splanchnic nerves. Acta Anat (Basel) 1989;136:129–133. [PubMed] [Google Scholar]

11. Weber JG, Brown DL, Stephens DH, et al. Celiac plexus block. Retrocrural computed tomographic anatomy inpatients with and without pancreatic cancer. Reg Anesth. 1996;21:407–413. [PubMed] [Google Scholar]

12. Rathmell JP, Gallant JM, Brown DL. Computed tomography and the anatomy of celiac plexusblock. Reg Anesth Pain Med. 2000;25:411–416. [PubMed] [Google Scholar]

13. Loukas M, Klaassen Z, Merbs W, et al. A review of the thoracic splanchnic nerves and celiacganglia. Clin Anat. 2010;23:512–522. [PubMed] [Google Scholar]

14. Erdine S. Celiac ganglion block. Agri. 2005;17:14–22. [PubMed] [Google Scholar]

15. Boas RA. Sympathetic blocks in clinical practice. Int Anesthesiol Clin. 1978;16:149–182. [PubMed] [Google Scholar]

16. Montero Matamala A, Vidal Lopez F, Aguilar Sanchez JL, et al. Percutaneous anterior approach to the celiac plexus usingultrasound. Br J Anaesth. 1989;62:637–640. [PubMed] [Google Scholar]

17. Eisenberg E, Car DB, Chalmers TC. Neurolytic celiac plexus block for treatment of cancer pain: ameta-analysis. Anesth Analg. 1995;80:290–295. [PubMed] [Google Scholar]

18. Kambadakone A, Thabet A, Gervais DA, et al. CT-guided celiac plexus neurolysis: a review of anatomy, indications,technique, and tips for successful treatment. Radiographics. 2011;31:1599–1621. [PubMed] [Google Scholar]

19. Haaga JR, Kori SH, Eastwood DW, et al. Improved technique for CT-guided celiac ganglia block. AJR Am J Roentgenol. 1984;142:1201–1204. [PubMed] [Google Scholar]

20. Wong GY, Schroeder DR, Carns PE, et al. Effect of neurolytic celiac plexus block on pain relief, quality oflife, and survival in patients with unresectable pancreatic cancer: a randomizedcontrolled trial. JAMA. 2004;291:1092–1099. [PubMed] [Google Scholar]

21. Erdek MA, Halpert DE, González Fernández M, et al. Assessment of celiac plexus block and neurolysis outcomes andtechnique in the management of refractory visceral cancer pain. Pain Med. 2010;11:92–100. [PubMed] [Google Scholar]

22. Yang IY, Oraee S, Viejo C, et al. Computed tomography celiac trunk topography relating to celiac plexusblock. Reg Anesth Pain Med. 2011;36:21–25. [PubMed] [Google Scholar]

23. Puelma F, Olave E. Relaciones del origen del tronco celiaco, arteriasmesentéricas y renales con la columna vertebral en individuoschilenos. Int J Morphol. 2010;28:1227–1234. [Google Scholar]

24. Davis DD. Incidence of major complications of neurolytic coeliac plexusblock. J R Soc Med. 1993;86:264–266. [PMC free article] [PubMed] [Google Scholar]

25. Hol PK, Kvarstein G, Viken O, et al. MRI-guided celiac plexus block. J Magn Reson Imaging. 2000;12:562–564. [PubMed] [Google Scholar]

26. Yang IY, Oraee S, Viejo C, et al. Transcrural celiac plexus block simulates on 200 computed tomographyimages. Br J Anaesth. 2011;107:972–977. [PubMed] [Google Scholar]

27. Moore DC, Bush WH, Burnett LL. Celiac plexus block: a roentgenographic, anatomic study of techniqueand spread of solution in patients and corpses. Anesth Analg. 1981;60:369–379. [PubMed] [Google Scholar]

28. Yang IY, Oraee S. A modified approach to transcrural celiac plexus block. Reg Anesth Pain Med. 2005;30:303–307. [PubMed] [Google Scholar]

29. Gress F, Schmitt C, Sherman S, et al. A prospective randomized comparison of endoscopic ultrasound- andcomputed tomographyguided celiac plexus block for managing chronic pancreatitispain. Am J Gastroenterol. 1999;94:900–905. [PubMed] [Google Scholar]

30. Sekhadia M, Chekka K. Standarts of care for celiac plexus neurolysis: radiologic guidanceand fellowship training. J Support Oncol. 2009;7:89–90. [PubMed] [Google Scholar]

Articles from Radiologia Brasileira are provided here courtesy of Colegio Brasileiro De Radiologia

Celiac plexus block: an anatomical study and simulation using computed
tomography (2024)
Top Articles
Latest Posts
Article information

Author: Nicola Considine CPA

Last Updated:

Views: 5999

Rating: 4.9 / 5 (49 voted)

Reviews: 80% of readers found this page helpful

Author information

Name: Nicola Considine CPA

Birthday: 1993-02-26

Address: 3809 Clinton Inlet, East Aleisha, UT 46318-2392

Phone: +2681424145499

Job: Government Technician

Hobby: Calligraphy, Lego building, Worldbuilding, Shooting, Bird watching, Shopping, Cooking

Introduction: My name is Nicola Considine CPA, I am a determined, witty, powerful, brainy, open, smiling, proud person who loves writing and wants to share my knowledge and understanding with you.