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MBBS, MD (Pathology),
Sanjay Gandhi institute of trauma and orthopedics,
Bengaluru.
On Aug 2018




Dr. Mamta Gupta,
"It gives me great pleasure to be associated with JCDR, since last 2-3 years. Since then I have authored, co-authored and reviewed about 25 articles in JCDR. I thank JCDR for giving me an opportunity to improve my own skills as an author and a reviewer.
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Dr. Mamta Gupta
Consultant
(Ex HOD Obs &Gynae, Hindu Rao Hospital and associated NDMC Medical College, Delhi)
Aug 2018




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Thanking you
With sincere regards
Dr. Rajendra Kumar Ghritlaharey, M.S., M. Ch., FAIS
Associate Professor,
Department of Paediatric Surgery, Gandhi Medical College & Associated
Kamla Nehru & Hamidia Hospitals Bhopal, Madhya Pradesh 462 001 (India)
E-mail: drrajendrak1@rediffmail.com
On May 11,2011




Dr. Shankar P.R.

"On looking back through my Gmail archives after being requested by the journal to write a short editorial about my experiences of publishing with the Journal of Clinical and Diagnostic Research (JCDR), I came across an e-mail from Dr. Hemant Jain, Editor, in March 2007, which introduced the new electronic journal. The main features of the journal which were outlined in the e-mail were extensive author support, cash rewards, the peer review process, and other salient features of the journal.
Over a span of over four years, we (I and my colleagues) have published around 25 articles in the journal. In this editorial, I plan to briefly discuss my experiences of publishing with JCDR and the strengths of the journal and to finally address the areas for improvement.
My experiences of publishing with JCDR: Overall, my experiences of publishing withJCDR have been positive. The best point about the journal is that it responds to queries from the author. This may seem to be simple and not too much to ask for, but unfortunately, many journals in the subcontinent and from many developing countries do not respond or they respond with a long delay to the queries from the authors 1. The reasons could be many, including lack of optimal secretarial and other support. Another problem with many journals is the slowness of the review process. Editorial processing and peer review can take anywhere between a year to two years with some journals. Also, some journals do not keep the contributors informed about the progress of the review process. Due to the long review process, the articles can lose their relevance and topicality. A major benefit with JCDR is the timeliness and promptness of its response. In Dr Jain's e-mail which was sent to me in 2007, before the introduction of the Pre-publishing system, he had stated that he had received my submission and that he would get back to me within seven days and he did!
Most of the manuscripts are published within 3 to 4 months of their submission if they are found to be suitable after the review process. JCDR is published bimonthly and the accepted articles were usually published in the next issue. Recently, due to the increased volume of the submissions, the review process has become slower and it ?? Section can take from 4 to 6 months for the articles to be reviewed. The journal has an extensive author support system and it has recently introduced a paid expedited review process. The journal also mentions the average time for processing the manuscript under different submission systems - regular submission and expedited review.
Strengths of the journal: The journal has an online first facility in which the accepted manuscripts may be published on the website before being included in a regular issue of the journal. This cuts down the time between their acceptance and the publication. The journal is indexed in many databases, though not in PubMed. The editorial board should now take steps to index the journal in PubMed. The journal has a system of notifying readers through e-mail when a new issue is released. Also, the articles are available in both the HTML and the PDF formats. I especially like the new and colorful page format of the journal. Also, the access statistics of the articles are available. The prepublication and the manuscript tracking system are also helpful for the authors.
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Overall, the publishing process with JCDR has been smooth, quick and relatively hassle free and I can recommend other authors to consider the journal as an outlet for their work."



Dr. P. Ravi Shankar
KIST Medical College, P.O. Box 14142, Kathmandu, Nepal.
E-mail: ravi.dr.shankar@gmail.com
On April 2011
Anuradha

Dear team JCDR, I would like to thank you for the very professional and polite service provided by everyone at JCDR. While i have been in the field of writing and editing for sometime, this has been my first attempt in publishing a scientific paper.Thank you for hand-holding me through the process.


Dr. Anuradha
E-mail: anuradha2nittur@gmail.com
On Jan 2020

Important Notice

Original article / research
Year : 2023 | Month : August | Volume : 17 | Issue : 8 | Page : UC01 - UC04 Full Version

Ultrasound-guided versus Conventional Caudal Blocks in Children: A Randomised Clinical Study


Published: August 1, 2023 | DOI: https://doi.org/10.7860/JCDR/2023/60772.18262
Mythreyi Muthukrishnan, Nischala Dixit, Karthik Jain, Anjali TM Ollapally

1. Senior Resident, Department of Anaesthesiology, St. John’s Medical College, Bengaluru, Karnataka, India. 2. Professor, Department of Anaesthesiology, St. John’s Medical College, Bengaluru, Karnataka, India. 3. Associate Professor, Department of Anaesthesiology, St. John’s Medical College, Bengaluru, Karnataka, India. 4. Assistant Professor, Department of Anaesthesiology, St. John’s Medical College, Bengaluru, Karnataka, India.

Correspondence Address :
Dr. Anjali TM Ollapally,
Assistant Professor, Department of Anaesthesiology, St. John’s Medical College, Bengaluru-560034, Karnataka, India.
E-mail: dr.anjaliollapally@gmail.com

Abstract

Introduction: Caudal epidural block is a popular regional anaesthetic technique in children undergoing infraumbilical surgeries. Conventionally, a landmark-guided method is used to perform caudal epidural blocks. Although widely practiced, this method is associated with procedural difficulties such as multiple attempts, decreased success rates at the first puncture, as well as higher rates of complications including dural puncture, rectal injury, and intraosseous/intravenous (i.v.)/subcutaneous injections. In order to overcome the shortcomings of the conventional technique, various other methods have been described in clinical practice, including imaging-assisted techniques with fluoroscopy and Ultrasound (US).

Aim: To compare the overall block success rates between the conventional and US-guided methods of caudal blocks in children.

Materials and Methods: The present randomised clinical study was conducted in the Department of Anaesthesiology, St. John’s Medical College, Bengaluru, Karnataka, India, from November 2019 to September 2021. Sixty-four children, aged 1-8 years, belonging to the American Society of Anaesthesiologists (ASA) physical status grade I and II, and undergoing elective inguinal hernial surgery were included in the study. After induction of general anaesthesia, the children were administered caudal blocks based on the assigned groups: group A (conventional)- patients were given 0.5 mL/kg of 0.25% bupivacaine after the needle entered the sacral canal, and group B (USG)- patients were given 0.5 mL/kg of 0.25% bupivacaine immediately after the needle was visualised piercing the sacrococcygeal ligament in the longitudinal view. The parameters studied were overall block success rates, block performance times, and the number of attempts taken. Descriptive statistics were reported using mean±Standard Deviation (SD) for continuous variables and number or percentage for categorical variables. Independent t-test and Mann-Whitney U test were used for normally distributed and non-normally distributed variables, respectively. Chi-square test was used to analyse differences between categorical variables.

Results: A total of 64 children of both genders, aged 1-8 years, belonging to ASA physical status I and II, were included in the study. Overall block success rates were comparable between the two groups, with 28 (87.5%) in group A and 30 (93.8%) in group B. The mean block performance time was longer in group B (2.781±1.2439 minutes) compared to group A (1.578±0.5835 minutes) (p-value <0.001). The number of attempts was lower in group B, with 100% success in the first attempt, as opposed to 68.8% in group A (p-value <0.05).

Conclusion: Ultrasound-guided caudal block does not improve overall block success rates or block performance time, but it does improve success rates at the first attempt and thereby reduces the number of attempts.

Keywords

Attempts, Bupivacaine, Block performance, Inguinal hernia

Caudal epidural block is a regional anaesthetic modality that can be used to provide analgesia and anaesthesia in both adults and children. The technique has found widespread use in the pediatric population for intraoperative and postoperative pain relief in surgeries performed below the level of the umbilicus. Affecting the dermatomes T10 to S5, it is a useful adjunct and alternative to systemic methods of analgesia. Originally discovered by French physicians Fernand Cathelin and Jean-Anthanase Sicard and was introduced into practice prior to lumbar epidural block (1). Initially, it lacked popularity due to significant variations in the anatomy of the sacrococcygeal region, which were further exaggerated in the paediatric age group, especially infants and young children.

The anatomical landmarks important in this mode of regional anaesthesia include the Posterior Superior Iliac Spines (PSIS), sacral cornua, and sacral hiatus. The sacral vertebrae, while fusing to form the sacrum, retain discrete anterior and posterior intervertebral foramina. The laminae of S4 and S5 do not fuse, resulting in the sacral hiatus, which can be palpated as a groove above the coccyx along the midline. The sacral cornua, PSIS, and sacral hiatus form an equilateral triangle, which is the main landmark for performing and administering the caudal block. Both the PSIS and sacral cornua can be used as guides to identify the hiatus, through which the caudal block is performed using various techniques.

Conventionally, a landmark guided method is used to perform caudal epidural blocks. The above mentioned anatomical structures are utilised to locate the sacral hiatus, through which a needle is inserted to pierce the sacrococcygeal ligament and inject local anaesthetic drugs (2). Although widely practiced, this method is associated with procedural difficulties such as multiple attempts, decreased success rates at the first puncture, and higher rates of complications such as dural puncture, rectal injury, and intraosseous/IV/subcutaneous injections (3). To overcome the shortcomings of the conventional technique, various other methods have been described in clinical practice. These include imaging-assisted techniques with fluoroscopy and Ultrasound (US) (4). US-guided caudal epidural blocks offer advantages as they improve visualisation of the sacrococcygeal ligament and sacral hiatus, allowing for visualisation of the drug spread during injection. This ultimately improves success rates, success rates at the first attempt, reduces the number of attempts, and decreases associated complications (5).

The present study aims to understand the difficulties encountered during the performance of conventional and US-guided caudal blocks and compare the advantages and disadvantages of the two methods, with the goal of introducing more effective techniques for routine clinical practice. Traditionally, conventional caudal blocks have a success rate of 75%, and the use of US is expected to increase this rate.

The aim of the present study was to compare landmark-guided versus US-guided caudal blocks, with the primary outcome being overall success rates and the secondary outcomes being block performance times, success rates at the first puncture, and the number of attempts.

Material and Methods

This randomised clinical study was conducted in the Department of Anaesthesiology at St. John’s Medical College Hospital in Bengaluru, India, from November 2019 to September 2021. The study received approval from the Institutional Ethics Committee (IEC Study Ref no: 292/2019) and was registered with the ISRCTN registry (https://doi.org/10.1186/ISRCTN10599628).

Sample size calculation: The sample size was determined based on a study by Karaca O et al., in 2019 (3). To detect a minimum difference of 24% between the two groups, with 80% power and a significance level of 5%, a total of 64 patients (32 in each group) were required. The sample size was calculated using nMaster 2.0 software.

Inclusion criteria: The study included patients aged 1-8 years, without any contraindications for caudal block, scheduled for elective inguinal hernia surgeries, and classified as ASA physical status I or II. Written informed consent was obtained from the guardians.

Exclusion criteria: Patients who refused to give consent, had infections at the injection site, had coagulation abnormalities, or had known hypersensitivity to the drugs used were excluded from the study.

Study Procedure

The children were kept Nil Per Os (NPO) prior to surgery in accordance with standard guidelines. They received intravenous fluids at maintenance rates (based on the Holliday Segar formula) during the NPO period. The operation theatres were prepared with checked anaesthesia workstations and ASA-recommended monitors. Measures were taken to maintain normothermia. Depending on the presence/absence of intravenous access, the child either received premedicated with 7 mcg/kg glycopyrrolate intravenously with/without 0.03 mg/kg midazolam intravenously and 0.15 mg/kg ondansetron intravenously, or intravenous access was established under inhalational sevoflurane. General Anaesthesia (GA) was induced using inhalational or intravenous sevoflurane, intravenous fentanyl 2-3 mcg/kg, and intravenous propofol 1-2 mg/kg. Under adequate depth of anaesthesia, an appropriate-sized Laryngeal Mask Airway (LMA) was inserted, and the child was maintained on isoflurane with spontaneous or assisted ventilation and intravenous Ringer’s lactate as fluid support.

The child was then positioned in the lateral position, and caudal block was performed under strict aseptic precautions using either the conventional landmark-guided method or the Ultrasound-Guided (USG) method. The block was performed by a trained anaesthesiologist with at least five years of practical experience. Due to the nature of the study design, blinding was not possible. The children were assigned to the following two groups using the envelope method (Table/Fig 1):

Group A: Caudal block performed using the conventional method guided by anatomical landmarks. The Posterior Superior Iliac Spines (PSIS) and sacral cornua were palpated to locate the sacral hiatus using the equilateral triangle method. A 22G needle was inserted at an angle of 60-80 degrees until the sacrococcygeal ligament was punctured (resulting in a popping sensation). The angle was then reduced to 20-30 degrees, and the needle was advanced by 2-3 mm. Negative aspiration of Cerebrospinal Fluid (CSF) or blood was confirmed, and 0.5 mL/kg of 0.25% bupivacaine was injected (6).

Group B: Caudal block performed using USG. The sacral hiatus was identified in the transverse view at the level of the sacral cornua using a linear probe of a Sonosite portable US machine (Fujifilm, United States of America). The typical appearance of the sacral cornua, sacral body, sacrococcygeal ligament, and sacral hiatus (resembling frog eyes) was noted. After negative aspiration of blood or CSF, 0.5 mL/kg of 0.25% bupivacaine was injected, and the spread of the drug was visualised [7,8].

Surgery commenced 15 minutes after the caudal block was performed, and vital signs were monitored and recorded every five minutes. Baseline Heart Rate (HR), Respiratory Rate (RR), and Motor Movement (MM) were noted at 0 minutes, 5 minutes after induction, 10 minutes after block performance, 25 minutes after surgical incision, and 60 minutes postoperatively for all cases. The primary outcome assessed was the success rate of the block, and the secondary outcomes were block performance times and the number of attempts. A successful block was defined as the absence of significant motor movement at the time of surgical incision or a significant increase in HR/RR. The block performance time was calculated as the duration from the identification of structures to the completion of the local anaesthetic injection. In the case of an unsuccessful block, analgesia was supplemented with intravenous fentanyl and/or intravenous/per rectum paracetamol. After completion of surgery, the Laryngeal Mask Airways (LMA) were removed, and the child was monitored in the Post-Anaesthesia Care Unit (PACU).

Statistical Analysis

Statistical analysis was performed using the Statistical Package for the Social Sciences (SPSS) software. Descriptive statistics were reported, including mean±SD for continuous variables and number/percentage for categorical variables. An independent t-test was used to compare continuous variables, such as block performance time and age, if the variable was normally distributed. If the variable was not normally distributed, the Mann-Whitney U test was used. The Chi-square test was used to test differences between categorical variables, such as sex and number of attempts. A p-value <0.05 was considered statistically significant, indicating a probability that the result is true.

Results

In both groups A and B, the majority of children belonged to the 5-10 kg weight range. There were no observable differences between the two groups in terms of the ages, weights, ASA grades, and genders of the children (Table/Fig 2). The overall block performance rates were comparable and statistically insignificant between the two groups (Table/Fig 3).

There was a statistically significant difference in block performance times (mean) between the two groups, with the USG group having a higher time (Table/Fig 4). The overall block performance rates were comparable between the two groups, but there was a statistically significant difference in terms of the number of attempts and block performance times (Table/Fig 4). There was no statistical significance between the two groups in terms of Heart Rate (HR) and Respiratory Rate (RR) across all time points (Table/Fig 5),(Table/Fig 6).

Discussion

As early as the 1980s, Veyckemans F et al., observed that it was more challenging to locate anatomical landmarks in very small children, especially those weighing less than 10 kg (9). Three decades later, Abukawa Y et al., and Kim YH et al., independently found that the conventional equi-angular triangle method for locating the sacral hiatus was unreliable in younger children, and the use of imaging methods like ultrasound improved identification (8),(10). Liu JZ et al., further added that the use of ultrasound and direct visualisation of the sacral canal improved success rates and block performance times (11). Chen CP et al., determined that the identification of the sacral hiatus by ultrasound was as good as the gold standard fluoroscopy (12). Therefore, ultrasound-guided caudal blocks were chosen to be studied against conventional caudal blocks in this study population.

Park JH et al., studied and confirmed that an angle of 20 degrees for needle insertion in ultrasound-guided blocks was optimal, while Doo AR et al., stated that there was a statistically significant advantage in terms of block success rate if the drug was injected immediately after piercing the sacrococcygeal ligament in the ultrasound-guided group (13),(14). As a result, a sequential combination of these two techniques was chosen to perform caudal blocks in the ultrasound-guided group, resulting in good overall block success rates, better success rates at the first attempt, and a decreased number of total attempts.

The primary objective of this study was to compare the overall block success rates between the conventional and ultrasound-guided methods of caudal blocks. Although the ultrasound-guided group had a higher success rate of 93.8% compared to the conventional group’s 87.5%, the difference between the two groups was not statistically significant. Similar results were found in studies conducted by Karaca O et al., (96.2% vs 94.7%) and AhiskaliogluA et al., (97% vs 93%) (3),(15). Wang LZ et al., also noted comparable success rates between both groups, with slightly higher rates in the conventional group (95.7% vs 92.8%) (16).

The secondary objectives of the present study were to compare block performance times and the number of attempts, thereby noting the success rates at the first attempt. There was a statistically significant difference in mean block performance times between the two groups, with the conventional method being quicker. This finding is consistent with the study by Kollipara N et al., who also observed longer block performance times in the ultrasound-guided group (17). However, Karaca O et al., and Ahiskalioglu A et al., reported comparable times between the two groups (3),(15). On the contrary, Wang LZ et al., demonstrated quicker times in the ultrasound-guided group (16). The discrepancies in findings could be attributed to operator factors, such as unfamiliarity with using ultrasound and the learning curve. Additionally, the definition of block performance times varied among the studies, which could also contribute to the differences in outcomes.

Regarding the number of attempts and success rates at the first attempt, the authors noted a statistically significant difference between the two groups. All blocks in the ultrasound-guided group were successfully performed at the first attempt, resulting in a 100% success rate. In contrast, in the conventional group, only 68.8% of the blocks were successful on the first attempt. Similar advantages of ultrasound use were reported by Karaca O et al., (90.2% vs 66.2%), Wang LZ et al., (92.8% vs 60%), Ahiskalioglu A et al., (80% vs 63%), and Kollipara N et al., (90.6% vs 64.2%) (3),(15),(16),(17). Similar to these studies, the outcomes in the present study were not affected by the demographic profiles of the study population.

Conventional caudal blocks are associated with the risk of complications such as intraosseous injection, subcutaneous bulging, dural puncture, intravascular injection and systemic toxicity, subdural block, and rectal penetration. Wang LZ et al., reported a reduction in the number of bloody taps in the ultrasound-guided group compared to the conventional group (5.7% vs 18.6%). Subcutaneous bulging was observed in 6 patients in the conventional group and none in the ultrasound-guided group (16). Ahiskalioglu A et al., also reported similar rates of complications (15). Karaca O et al., noted 14 bloody taps, 10 subcutaneous bulges, and 32 intraosseous injections in their conventional group, but none in their ultrasound-guided group (3). In the present study, no complications were noted in the ultrasound-guided group due to the direct visualisation of the needle and sacral dilatation (18),(19).

Limitation(s)

The use of ultrasound was operator-dependent, and although an anaesthesiologist with five years of practical experience performed the block, there was still a learning curve involved in using ultrasound. Blinding was not possible in this study. The rates of direct needle visualisation and sacral canal dilatation were not noted and compared between the two views (transverse and longitudinal).

Conclusion

Upon analysing the results of this study, it was concluded that the use of ultrasound does not increase the overall success rates of caudal epidural blocks. However, Ultrasound-Guided (USG) blocks significantly decrease the number of attempts taken to perform the block, thereby increasing the success rate at the first attempt. Although an increase in block performance time was noted when using ultrasound, this could be attributed to unfamiliarity with using the apparatus and discrepancies in the definition of block performance time. Ultrasound also has the added advantage of decreasing the risk of complications.

Acknowledgement

To the Department of Radiology, we extend our gratitude for their assistance and training in ultrasound-guided caudal space identification prior to the start of the study.

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DOI and Others

DOI: 10.7860/JCDR/2023/60772.18262

Date of Submission: Oct 13, 2022
Date of Peer Review: Dec 26, 2022
Date of Acceptance: May 02, 2023
Date of Publishing: Aug 01, 2023

AUTHOR DECLARATION:
• Financial or Other Competing Interests: None
• Was Ethics Committee Approval obtained for this study? Yes
• Was informed consent obtained from the subjects involved in the study? Yes
• For any images presented appropriate consent has been obtained from the subjects. NA

PLAGIARISM CHECKING METHODS:
• Plagiarism X-checker: Oct 14, 2022
• Manual Googling: Mar 15, 2023
• iThenticate Software: Apr 18, 2023 (7%)

ETYMOLOGY: Author Origin

EMENDATIONS: 9

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