2022
DOI: 10.2147/lra.s372903
|View full text |Cite
|
Sign up to set email alerts
|

Comparison Between Ultrasound-guided Caudal Analgesia versus Peripheral Nerve Blocks for Lower Limb Surgeries in Pediatrics: A Randomized Controlled Prospective Study

Abstract: Background and Aim: Ultrasound (US) guided regional analgesia is a safe and effective method in providing perioperative analgesia in pediatrics with a high success rate rapid onset and fewer side effects. The aim of this study was to compare the efficacy of US-guided caudal block versus US-guided peripheral nerve blocks (femoral and sciatic nerve blocks) in providing perioperative analgesia in pediatrics undergoing unilateral lower limb surgery. Methods: Children aged 1-12 years scheduled for unilateral lower … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
0
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 21 publications
(18 reference statements)
0
0
0
Order By: Relevance
“…The primary outcome of this study was the time to the first postoperative analgesia requirement. The sample size was calculated by PASS 15 program, based on the results of a study by Mahrous et al (15) in which the duration to the first postoperative opioid demand was significantly shorter in the caudal group compared to PNB group, with mean and standard deviation (SD) of 9.6 ± 2.9 vs. 15.1 ± 3.5; considering a 20% dropout rate, the calculated sample size of 15 patients per each study group achieved 97% power to reject the null hypothesis of equal means when the difference between population means is µ1-µ2 = 9.6-15.1 = -5.5, with SD of 2.9 for 1st group and 3.5 for the 2nd group and a significance level of 0.05, utilizing the 2-samples unequal variance z-test.…”
Section: Sample Sizementioning
confidence: 99%
“…The primary outcome of this study was the time to the first postoperative analgesia requirement. The sample size was calculated by PASS 15 program, based on the results of a study by Mahrous et al (15) in which the duration to the first postoperative opioid demand was significantly shorter in the caudal group compared to PNB group, with mean and standard deviation (SD) of 9.6 ± 2.9 vs. 15.1 ± 3.5; considering a 20% dropout rate, the calculated sample size of 15 patients per each study group achieved 97% power to reject the null hypothesis of equal means when the difference between population means is µ1-µ2 = 9.6-15.1 = -5.5, with SD of 2.9 for 1st group and 3.5 for the 2nd group and a significance level of 0.05, utilizing the 2-samples unequal variance z-test.…”
Section: Sample Sizementioning
confidence: 99%